CBD



CBDDistr.GENERALCBD/COP/14/INF/810 November 2018ENGLISH ONLYCONFERENCE OF THE PARTIES TO THE CONVENTION ON BIOLOGICAL DIVERSITYFourteenth meetingSharm El-Sheikh, Egypt, 17-29 November 2018Item 23 of the provisional agenda*Review of pollinators and pollination relevant to the conservation and sustainable use of biodiversity in all ecosystems, beyond their role in agriculture and food productionI.IntroductionThe present report is presented in response to decision XIII/15, paragraph 11, in which the Conference of the Parties to the Convention on Biological Diversity requested the Executive Secretary, subject to the availability of resources, in partnership with relevant organizations and indigenous peoples and local communities, to compile and summarize information on pollinators and pollination relevant to the conservation and sustainable use of biodiversity in all ecosystems, beyond their role in agriculture and food production for consideration by the Subsidiary Body on Scientific, Technical and Technological Advice (SBSTTA) at a meeting held prior to the fourteenth meeting of the Conference of the Parties. The Assessment on Pollinators, Pollination and Food Production of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services (IPBES), used literature available until July 2015. Since that point in time, a considerable amount of new literature has been made available. A workshop convened from 27?to 29 November 2017, in collaboration with IPBES, the University of Reading, and the Convention on Biological Diversity, brought together regional experts on pollinators to discuss and assess the role of pollinators and pollination services in supporting ecosystems beyond agricultural systems and in supporting ecosystem services beyond food production.A draft report was subsequently prepared, drawing on the contributions of researchers and partners around the world, and was made available to the Subsidiary Body on Scientific, Technical and Technological Advice at its twenty-second meeting (see CBD/SBSTTA/22/INF/21); the report’s main authors are listed in the annex below.In its recommendation 22/9, the Subsidiary Body took note of the draft full report on the relevance of pollinators and pollination to the conservation and sustainable use of biodiversity in all ecosystems beyond their role in agriculture and food production, and requested the Executive Secretary, subject to the availability of resources, to finalize the report, taking into account peer review comments, and make it available for the fourteenth meeting of the Conference of the Parties. A summary of the draft full report is provided as annex II to the draft decision on conservation and sustainable use of pollinators presented under item 23 in the compilation of draft decisions (CBD/COP/14/2).Pursuant to this request, the Executive Secretary issued notification 2018-068, requesting comments on the draft full report. Submissions in response to this notification were received from Argentina, Canada, the European Union, India, Japan, Mexico, New Zealand, the United Kingdom of Great Britain and Northern Ireland; other Governments; and the Food and Agriculture Organization of the United Nations. The revised report, taking into account peer-review comments, is provided in the present document. Section II of the document describes the roles and values of pollinators and pollinator-dependent plants beyond agriculture. Section III reports on the trends and status of pollinators and pollinator-dependent plants in all ecosystems. Section IV provides the status of the main drivers of shifts in pollinators, pollination and pollinator-dependent wild plants in all ecosystems. Finally, section V presents some response options for conservation and management of pollinators, their habitats and their food and water resources in all ecosystems. II. Roles and values of pollinators and pollinator-dependent plants beyond agriculture There is a wide diversity of values linked to pollinators and pollination beyond agriculture and food production. Pollinators and their habitats provide ecological, cultural, economic, health, human, and social values. Globally, nearly 90% of wild flowering plant species depend, at least in part, on the transfer of pollen by animals (IPBES 2016a). Pollinators also enhance the reproduction and genetic diversity of plants. More than half of plant species are self-incompatible or dioecious and completely dependent on biotic pollination. Pollinator-dependent plants are critical for the continued functioning of ecosystems as they provide food, form habitats and provide other resources for a wide range of species. Examples include mangroves, with many obligate outbreeder plants, which provide important services such as preventing coastal erosion, supporting fisheries, protecting from flood and salt intrusion, providing wood fuel and timber, as well as providing habitat and food for bees and many other species (e.g. birds, mudskippers) among others (Mukherjee et al. 2014). Another example is tropical forests, which contain a high number of dioecious species contributing to climate regulation, wild meat, malaria and other diseases regulation, fruits and seeds that support many other species in the forest, among other services. Furthermore, products from stingless bees, such as honey, wax, cerume (a mix of wax and propolis), propolis, pollen and the bees themselves are used by many indigenous people for different purposes, including nourishment, traditional medicine, activities related to their spiritual and contemplative life, and hand-crafting (Rodrigues 2006). Stingless bees are very diverse in the tropics and subtropics of the world, consisting of nearly 600 species (Meléndez Ramirez et al. 2018).2.1 Ecological and intrinsic valuesMost of the estimated 350,000 angiosperm species, as well as many gymnosperm species, depend on animal pollinators for production of seeds and the maintenance of their populations. Animal-mediated pollination usually leads to some degree of outcrossing and thus promotes and maintains genetic variation in populations, which in turn allows species to adapt to new and changing environments. For these two reasons - ensuring a supply of seed propagules and promoting genetic variation - pollinators are considered to be of fundamental importance for the maintenance of plant diversity and ecosystem functioning (Wilcock and Neiland 2002). However, plant species vary enormously in their degree of dependence on pollinators for seed production, and also in their degree of dependence on seeds for maintenance of populations (Bond 1994).Pollinators and other flower visitors utilize flowers for food in the form of nectar and pollen, and, in some cases, oils and resins, as well as for shelter and mating rendezvous sites (Simpson and Neff 1983). Some pollinators also use flowers as brood sites (Sakai 2002; Hembry and Althoff 2016). Thus, mutualisms between plants and their floral visitors sustain not only plant diversity, but also the diversity of an estimated 350,000 described animal pollinator species, mainly various insects, birds and mammals (Ollerton 2017) and many more awaiting scientific discovery. The degree of ecological dependence of these animals on the flowers ranges from completely obligate, as in species that use particular flowers as brood sites or sources of food, to facultative, as in species that have generalist diets that include some food from flowers. Generalized pollinator species are usually network keystone species because they interact with many plant species and thus play an important role in maintaining the whole network (Gonzalez et al. 2010).Plant dependence on animal pollinators for seed productionThe great majority (c. 87.5%) of flowering plants are adapted for pollination by animals (Ollerton et al. 2011), with the remainder of species being either wind-pollinated (Linder 1998; Friedman and Barrett 2009) or completely reliant on autonomous seed production. The degree of ecological dependence of plants on pollen-vectors for seed production depends on their breeding systems. Plants that are dioecious (including some gymnosperms such as cycads) or that are genetically self-incompatible are wholly dependent on cross-pollination for seed production (Richards 1997). It has been estimated that about 50% of angiosperms fall into this category of obligate dependence on pollen vectors (Fryxell 1957; de Nettancourt 1997). The remaining plant species are genetically self-compatible, but these often have an obligate dependence on pollen vectors for seed production on account of spatial or temporal separation of their reproductive parts (Richards 1997). Self-compatible plants that are capable of autonomous self-fertilization often undergo some outcrossing due to pollinator visits. Data from molecular markers show that most self-compatible plants experience mixed-mating and fall along a continuum from selfing to outcrossing (Schemske and Lande 1985; Vogler and Kalisz 2001). Only a very small proportion of plant species produce seeds entirely through autonomous self-fertilization or through non-sexual processes such as apomixis (Moldenke 1979). Cross-pollination is not only essential for seed production for around half of all plant species, but also results in higher seed production and performance of progeny in many self-compatible species (Aizen and Harder 2007). This is because cross-fertilization reduces the likelihood of inbreeding depression which is commonly observed in the self-fertilized progeny of plants (Darwin 1895; Husband and Schemske 1996; Keller and Waller 2002). Cross-fertilization also promotes the build-up of genetic variation and thus the ability of plant species to adapt to new and changing environments (Jump and Penuelas 2005; Morran et al. 2009). Studies involving supplemental hand-pollination of flowers have shown that seed production of plants is often limited by the quantity and quality of pollen received naturally (Knight et al. 2005). This phenomenon of pollen limitation of fecundity occurs naturally in relatively undisturbed ecosystems, but is often exacerbated when plant populations become small and fragmented (?gren 1996; Wilcock and Neiland 2002). It can arise because pollinators are rare or because plants have too few mating partners and pollinators carry inadequate amounts or quality of pollen. Because self-incompatible plants cannot use their own pollen to produce seeds, they are more likely to experience pollen-limitation than self-compatible plants (Larson and Barrett 2000). The availability of effective pollinators in plant communities is an obvious requirement for successful seed production in most plant species. It is often shown experimentally that selective exclusion of a single group of effective pollinators to which plants are adapted can result in failure of plants to produce fruits or seeds. Pollinator diversity has been linked to seed production in plant species with generalist pollination systems (Albrecht et al. 2012); while a global meta-analysis showed an average of 63% loss of fruit or seed production when vertebrate pollinators were excluded from the flowering plants they visited (Ratto et al. 2018).Demographic dependence of plants on seeds Plants vary in their dependence on seeds for demographic viability of their populations. Many plants are obligate reseeders and replace their populations entirely from seeds. Such plants include annuals and plants in fire-prone habitats that are killed by fire. Pollen limitation of seed production in small populations of the annual plant species Clarkia concinna (Onagraceae) was associated with reduced population persistence, suggesting links between pollination, seed population and demographic viability in this species (Groom 1998). However, even plants that are not short-lived or killed by fire usually depend on seeds for establishing new populations and for demographic replacement due to age-dependent mortality of adults. The effects of pollination failure on the demographics of long-lived woody species may not be obvious for decades, even though the demographic consequences may be just as serious in the long term (Janzen 1974). While it is obvious that a complete cessation of seed production would have a negative impact on most plant populations, it is also important to ask whether quantitative variation in seed production due to differing levels of pollination service will affect plant demography (Groom 1998; Lundgren et al. 2016). An older view was that plant recruitment was limited by microsites or by self-thinning processes, such as that variation in propagule supply would have little effect on plant recruitment (Harper 1977). However, recent meta-analyses suggest that the maintenance and establishment of plant populations is often limited by the supply of propagules (Clark et al. 2007). Experimental augmentation of the number of seeds at sites or introduction of seeds into sites where populations are absent have clearly shown that seed supply is important for plant demography (Turnbull et al. 2000; Clark et al. 2007). Seed limitation of plant demography is most evident for plants in disturbed habitats, for those with large seeds, and for those with short-lived seed banks (Turnbull et al. 2000; Clark et al. 2007). Variation in seed supply is less demographically important where there is a high background density of seedlings or adults, as is often the case for woody species with self-thinning among saplings (Turnbull et al. 2000). For example, seed predation which reduces the supply of seeds in a manner similar to lack of pollination has been shown to have limited demographic consequences in some shrubs that occur in dense populations with self-thinning of seedlings (Hoffmann and Moran 1991). Scaling the ecological importance of pollination to the landscape levelIf pollinators are ecologically important for plant demography at local scales, we can predict that plant distribution should correlate with the availability of pollinators and that plants that do not depend on pollinators should be better colonizers.Indirect evidence for the ecological importance of pollinators comes from evidence that pollinator availability can restrain the geographical distribution of plant species. In one study, niche models that include availability of key pollinator mutualists do a better job of explaining actual plant distributions than do niche models that include only abiotic factors (Duffy and Johnson 2017). This suggests that pollinators are part of the fundamental ecological niche of certain plant species. This is also supported by translocation studies which show that pollination success of some plants with specialized pollination systems drops close to zero when plants are moved beyond the range of their pollinator species (Waterman et al. 2011). A corollary of this finding is that the geographical ranges of plants which are capable of facultative self-fertilization should not be constrained by pollinator distributions. Indeed, the success of self-fertilizing species as weeds and as colonizers of islands is testimony to the strong role of pollinators as an ecological filter of the distribution of plant species that lack the capacity for uniparental reproduction, including autonomous self-fertilization (Rambuda and Johnson 2004; Van Kleunen et al. 2008; Pannell et al. 2015; Grossenbacher et al. 2017). Breakdown in mutualisms and extinction Failure of pollination mutualisms can be defined as a catastrophic decrease in the frequency of interactions between plants and pollinators, which has the potential to result in extinctions of one or more partners in the mutualism. This may arise when there are too few plants to support the energetic or brood site requirements of key pollinator species or when plants produce too few seeds for demographic replacement on account of a paucity of pollinators (Kearns et al. 1998; Neuschulz et al. 2016).Failure of mutualisms leading to lower seed production and sometimes also extirpation of plant populations have been recorded in several studies (Groom 1998; Wilcock and Neiland 2002). Bond (1994) argued that the overall risk of extinction through mutualism failure could be predicted by the probability of mutualism failure (such as the level of specialization), reproductive dependence on the mutualism (such as the breeding system) and the degree of dependence on seeds (for example, whether a species is an obligate reseeder). Few studies have examined all of these factors together and the failure of mutualisms has generally been assessed in terms of the deleterious effects of habitat fragmentation on plant fecundity. Mutualism failure does not seem more likely overall to occur in plants with specialized pollination systems than in those with generalized pollination systems (Ashworth et al. 2004). It has been suggested that this is due to the asymmetry of pollination systems whereby plants with specialized pollination systems often rely on generalist animals (Ashworth et al. 2004). Another possible explanation is that plants with specialized pollination systems often have compensatory mechanisms that assure seed production, such as facultative self-fertilization (Bond 1994; Fenster and Marten-Rodriguez 2007). Indeed, genetic self-incompatibility has emerged as a predictor of the magnitude of mutualism failure as measured by declines in fecundity (Aguilar et al. 2006; Merrett et al. 2007). Changes in plant community composition arising from mutualism failure have been documented in a guild of orchids specialized for pollination by an oil-collecting bee in South Africa (Pauw and Bond 2011). Plant species richness in the guild decreases with declining pollination success and the species that persist when pollination fails completely are all clonal, suggesting that non-clonal species are most prone to local extinction through failure of the pollination system (Pauw and Bond 2011). Ecological reliance of pollinators on plant food resourcesA very large number of insect and vertebrate species depend on flowers as a source of food (Ollerton 2017). Their dependence on food from flowers varies from obligate, as applies to almost all bees, hawkmoths, long-proboscid flies, and specialist avian nectarivores such as hummingbirds and sunbirds, to facultative, as applies to many short-tongued flies, beetles, and opportunistic avian nectarivores. Among the animals that have an obligate dependence on flowers for food, only some depend on a specific plant taxon for food. Estimates of the percentage of bees in various communities that are oligolectic (i.e. depend on a particular plant taxon, usually a genus, for food) range from 15%?to 60% (Minckley and Roulston 2006). This form of specialization usually involves collection of pollen and univoltine reproduction that is synchronized with flowering of the host plants (Minckley and Roulston 2006). The flowers utilized by oligolectic bees are often morphologically unspecialized and abundant (and are often also used and pollinated by many polylectic bees). This may reflect that specialization by bees on rare and ephemeral plant species is unlikely to persist through evolutionary time. A landscape devoid of a diversity of flowers, such as a monoculture of cereal crops, will lose many of the animal species that visit flowers for food. A positive relationship between floral abundance and diversity of flower-visiting animals at the habitat scale is now very well established (Potts et al. 2003; Hines and Hendrix 2005; Scheper et al. 2015). However, such relations may in some cases reflect local aggregation of animals and not necessarily a change in population sizes (Roulston and Goodell 2011). Declines of bee species at the countrywide scale have been shown to be correlated with declines in specific host plants (Biesmeijer et al. 2006; Scheper et al. 2014), but it is not easy to establish causality in such large-scale correlative studies. In Europe, specialist long-tongued bumblebees have narrower host plant ranges than generalist short-tongued bumblebees and have also declined more rapidly, suggesting that lack of floral resources, particularly of pollen-rich legumes, has been a causal factor in their decline (Goulson and Darvill 2004; Goulson et al. 2005). The most convincing evidence for an effect of floral resources on pollinator populations comes from demographic studies which show that colony growth and reproduction in bees can reflect the availability of floral resources (Crone and Williams 2016; Spiesman et al. 2017). There is some evidence that oligolectic bees are more vulnerable to habitat fragmentation and changes in particular floral resources than are polylectic bees. Detailed demographic studies have shown that population persistence of oligolectic bees can be strongly correlated with availability of particular floral host plants, implying that survival and reproduction of the bees is pollen-limited (Williams and Kremen 2007; Franzen and Nilsson 2010; Palladini and Maron 2014) (Figure 1). Figure 1. The relationship between local extinctions and the size of local female beeNote: A. hattorfiana populations the year before the extinction events occurred, and the local pollen plant population size (number of K. arvensis stalks), over 3 consecutive years ((a) 2003–2004, (b) 2004–2005 and (c) 2005–2006). Extinct local bee populations are denoted by an open dot and local bee population present both years are denoted by a filled dot. Logistic regression 2003–2004, all variables included in the model: patch area: B = ?0.24, p = 0.82; bee population size: B = ?2.99, p?=?0.035, plant population size: B = ?4.58, p = 0.003; bees in surrounding 3 km2 in 2003: B = ?0.009, p = 0.24. Logistic regression 2005–2006, all variables included in the model: patch area: B = ?2.87, p = 0.15; bee population size: B =??5.39, p = 0.009; plant population size: B = ?5.83, p = 0.044; bees in surrounding 3?km2 in 2005: B?=??0.06, p = 0.34. Extinctions in 2005 were not analysed statistically owing to few observations. From Franzen and Nilsson 2010. (A. = Andrena, K. = Krautia)In his discussion of the putative relationship between a Malagasy orchid and giant hawkmoth, Darwin (1862) originally proposed the idea that the extinction of a particular plant species could lead to extinction of a pollinator species that depended on food from its flowers. While there is strong evidence for local extirpation of pollinator populations due to a lack of floral resources (Franzen and Nilsson 2010) and several examples of country-wide extinctions of flower-visiting insect species (cf. Ollerton et al. 2014), we are not yet aware of any cases where an animal species has become globally extinct because of a lack of floral resources. However, given the extent of habitat fragmentation, the large number of plant species that have become extinct or nearly so in the past 100 years and the paucity of our knowledge about host plant usage by flower-visiting animals, the possibility that this is occurring without being documented is very real. Data on population changes in wild flower-visiting animals are notoriously hard to obtain and the causes of these changes even harder to establish.2.2 Economic and non-economic valuesAs has been shown, pollinators provide a full range of benefits, including cultural (e.g. identity), financial (e.g., honey sales), health (e.g. pharmaceutical properties of bee products), human (e.g., employments in beekeeping), and social (e.g., beekeepers associations) dimensions (Potts et al. 2016). Some examples of the vast contribution of pollinators to different dimensions of human wellbeing, including economic and non-economic values, will be presented below. CulturalPollinators, pollinator habitats, and pollinator products are sources of inspiration for art, education, literature, music, religion, traditions, and technology. Honey-hunting and beekeeping practices based on indigenous and local knowledge have been documented in more than 50 countries (Crane 1999; Gupta et al. 2014). Bees have inspired imagery and texts in religions all over the world; these have including the three-bee motif of Pope Urban VIII, the Surat An-Na?l in the Qur’an, and sacred passages within Buddhism, Hinduism, and Chinese traditions such as the Chuang Tzu (Potts et al. 2016). Many of the fruits, berries, and other non-cultivated plants that we enjoy in gardens, parks, and semi-natural habitats depend on wild pollinators for their propagation. Indeed, home gardens provide a large set of ecosystem services, cultural services being the category most valued, including aesthetic information, recreation and tourism, inspiration for culture, art and design, and spiritual experience (Calvet-Mir, Gómez-Baggethun and Reyes-García 2012). Pollinators are among the national symbols of some countries (e.g., such as hummingbirds in Jamaica and sunbirds in Singapore) and contribute directly to cultural identity (IPBES 2016a) and also indirectly, for example by supporting aesthetically important flowers in landscapes (Junge et al. 2015). Furthermore, many sites listed under the Convention Concerning the Protection of the World Cultural and Natural Heritage depend on pollination to maintain their values, while the Convention for the Safeguarding of the Intangible Cultural Heritage recognizes several practices that rely on pollinator-dependent plants as globally important (IPBES 2016; Potts et al. 2016).Pollinators play an important role in the life of indigenous peoples and in their environment, underpinning spiritual beliefs and practices. Such relationships can be deeply important and complex but are rarely described in detail. Box 1 provides an example of the interwoven relationships between Māori people, pollinators and the products that result from the pollination process. It also highlights a more recent focus on the inclusion of Māori values and knowledge in assisting the safeguarding of this relationship.FinancialBee products, such as honey, propolis and beeswax contribute to increased income for beekeepers around the globe. Beekeeping is critical for local development as it typically requires minimal investment, generates diverse products, can occur without land ownership or rent, and provides flexibility in timing and locations of activities (Hilmi et al. 2011). Pollinators and pollinator-dependent plants also support technological and knowledge advances through inspiration and application of their biology to human innovations such as visually guided robot flight (IPBES 2016a).Native bees have an innate ability to buzz pollinate crops with poricidal anthers like tomato, capsicum and brinjal (Nunes-Silva et al. 2013). The estimated cost of pollination using electric vibrators by the labourers in tomato under greenhouses was $82.25/year/0.25 acre (Hanna 2004). This labour-dependent activity of sonicating the anthers could be managed by domestication of some native bee species.Moreover, pollinator-dependent plants contribute to several material and non-material services with important financial value such as ornamentals, medicines, biofuels, fibres, construction materials, musical instruments, arts, crafts, and recreation activities (Potts et al. 2016). For example, in the Nilgiri Biosphere Reserve in India, it was found that 40% of plants that provide non-timber forest products, including construction materials and medicine, benefit to some extent from biotic pollination (Rehel et al. 2009).HealthMany medicinal plant species depend on pollinators for their reproduction. In addition, pollinator-dependent plants recycle carbon dioxide, regulate climate, and improve air and water quality. Furthermore, several micronutrients, including vitamins A and C, calcium, fluoride and folic acid, are obtained primarily from pollinator-dependent plants (Smith et al. 2015). Also, pollinator products (e.g. honey, propolis, bee sting) are employed for improving health, such as anti-bacterial, anti-fungal, and anti-diabetic agents derived from honey (Jull et al. 2015). Pollinator insects, including the larvae of bees, beetles, moths, and palm weevils, constitute an important proportion of the approximately 2,000 insect species consumed globally, being high in protein, vitamins and minerals (IPBES 2016a).Other human/ socialBeekeeping provides jobs for hundreds of thousands of families all over the world (Hilmi et al. 2011; Gupta et al. 2014; Johannsmeier 2001). Beekeeping can also form the basis for gaining and transmitting knowledge about ecological processes (IPBES 2016a). Furthermore, understanding of flowers and pollinators is part of the knowledge base for indigenous people and local communities, for example, in some regions flowering phenology provides indications for decisions regarding weather predictions. Beekeeping associations can enhance social bonds among beekeepers that facilitate cooperative actions and social connections, having potential to increase or exchange knowledge, improve livelihoods, and long-term resilience (Garibaldi et al. 2016). Furthermore, beekeeping can be a potentially effective intervention tool for reducing relapses in youth criminal behaviour, and for empowering youth to link biodiversity, culture and society and take action on issues of environmental impacts on pollinators and pollination (IPBES 2016a). Pollinators are also critical for the subsistence of many home gardens, which contribute to the creation and maintenance of social relations (Calvet-Mir et al. 2012). Box 1. New Zealand – Māori pollination values, impacts and policyBird pollinators and the plants they pollinate are extremely important to the Māori. Native birds are well recognized both by Māori and other researchers as key pollinators of many native plant species (Doherty and Tumarae-Teka 2015). These included the kōparapara (bellbird, Anthornis melanura), tūī (Prosthemadera novaezelandiae), kererū (Hemiphaga novaeseelandiae), hihi (stitchbird, Notiomystis cincta), kākā (Nestor meridionalis) and tieke (saddleback, Philestrunus carunculatus) (Craig et al. 1981; Clout and Hay 1989). Bird pollinated plants include kōwhai (Sophora spp.) and rātā (Metrosideros spp.), which was used by Māori to treat skin diseases and wounds, while the pūriri (Vitex lucens) was used for ulcers and was sometimes boiled and used to remedy backache (Brooker et al. 1987). Harakeke (Phormium tenax) was an important source of muka (fibre) to make cloth and rope (Carr et al. 2005). Wild-growing and cultivated flax grown in a pā harakeke (a site for the planting of selected varieties of harakeke based on their muka or raranga (weaving/plaiting qualities) had a number of uses, including for clothing, cordage, fishing nets, bird snares and baskets (Murray 1836; Best 1942; McAllum 2005). Beyond the value that bird-pollination brought to the forest plants many of the bird pollinators were hunted by Māori for food and feathers (Best 1942; Lyver et al. 2008) and were fundamental to cultural identity and heritage values expressed through language, knowledge systems, and customary management regimes (Timoti et al. 2017). The skin and feathers of bird pollinators were often used for making garments such as korowai (traditional cloaks; Harwood 2011). Feathers from the kererū, kākā, and kākāriki (parakeet, Cyanoramphus spp.) frequently adorned korowai in the early nineteenth century (as listed by Harwood 2011). The biological and cultural impacts of bird declines have impacted Māori. Since European settlement in New Zealand, predation by introduced mammalian predators such as rats (e.g. ship rat, Rattus rattus), feral cats (Felis catus), and mustelids (e.g. stoats, Mustela erminea) and habitat degradation have significantly reduced the populations of native bird species, such as the kōkō (traditional name for tūī) and kererū (Kelly et al. 2010; García et al. 2014). Biocultural indicators such as flock size and harvest tallies of kōkō and kererū in Te Urewera have been used by Tuawhenua over the last century to monitor the declines of these two species (Lyver et al. 2017). The large-scale declines of cultural (and ecological) keystone native birds around New Zealand have had a significant impact on the cultural identity and heritage of many Māori tribes. The losses affect cultural diversity as much as the biological diversity of New Zealand.The role of Māori values and mātauranga (indigenous knowledge) in the management and conservation of native ecosystems has become increasingly recognized over the past three decades in New Zealand (Taiepa et al. 1997; Awatere and Harmsworth 2014) and governmental agencies are increasingly mandating for its inclusion in decision-making (Ministry for the Environment & Statistics New Zealand 2015). For example, the Te Kawa o Te Urewera and Whirinaki Te Pua-a-Tāne Conservation Management Plans incorporate the principles of kaitiakitanga (customary guardianship regimes), whanaungatanga (interrelationships where all things live and interact as whanau (family)), tuakana–teina (positive and supportive relationships), he tangata (people as an essential part of the ecosystem) and mauri reflecting the life essence of ecosystems and tribes (Te Uru Taumatua 2017; Ngati Whare and Department of Conservation 2017). The arrangement gives effect to the treaty of Waitangi (ensuring consultation with iwi regarding management including access to sites and resources, establishing protocols for tree removal and pest control, regeneration, collection and propagation of seeds and seedlings, concessions to use cultural information and for identification of business opportunities that are consistent with natural, historical and cultural heritage values (Ngati Whare and Department of Conservation 2017)).III. Trends and status of pollinators and pollinator-dependent plants in all ecosystemsGlobal trends and status of pollinators, their habitats and biomes A lack of global Red List assessments specifically for insect pollinators and, in most parts of the world, the lack of long-term population data or benchmark data with which to compare the present status of wild pollinator populations makes it difficult to discern any temporal trend. Evidence of changes in species richness or abundance along a habitat degradation gradient can be used as a proxy for temporal changes if the more pristine areas in the gradient today are seen as what the degraded areas used to be in the past. In a global meta-analysis, Aguilar et al. 2006 found that local declines in pollinator abundance and diversity were linked to decreasing trends in wild plant pollination and seed production in habitat fragments. Morales and Traveset (2009) evaluated data from 40 global studies on the effects of invasive plant species on pollinator visitation and reproduction of native co-flowering species; an overall significantly negative effect of invasive species on visitation and reproduction of native plants was detected. Montero-Casta?o and Vila (2012), using 143 studies, showed that habitat alteration and invasions affected pollinators by decreasing visitation rates. Visitation rates by vertebrates in altered landscapes and by insects (excluding bees) in invaded areas were the most affected.While it has not yet been possible to carry out a comprehensive global monitoring of pollinator or pollination trends, two global databases lend themselves to visualizing some key global patterns. The first such visualization is a map depicting the IUCN Red List status of vertebrate pollinators globally (Figure?2). Population numbers of vertebrate pollinators are easier to track than invertebrates, and thus their status does not represent pollinators in general, but they nonetheless provide indicators of regions where some pollinator groups and their floral resources are under different levels of risk.The second is a world map showing the annual growth rate in the number of honeybee hives for countries reporting those data to the Food and Agriculture Organization of the United Nations (FAO) between 1961 and 2012 (Figure 3). However, there have been regional changes in the numbers of colonies since 2012 which are not captured here; for instance, the number of colonies in the United States of America has risen over the last decade. Managed bee colonies can pollinate both crop plants and wild plants, and thus their trends are relevant for this report, although causes in each case are complex. Figure 2. The International Union for Conservation of Nature (IUCN) Red List status of vertebrate pollinators (including mammals and birds) across IUCN regions. IUCN relative risk categories: EW = Extinct in the wild; CR?=?Critically Endangered; EN = Endangered; VU = Vulnerable; NT = Near Threatened; LC = Least Concern; DD?=?Data Deficient; NE = Not Evaluated. Adapted from IUCN 2016b. Disclaimer: The designations employed and the presentation of material on this map do not imply the expression of any opinion whatsoever on the part of the Secretariat of the Convention on Biological Diversity concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Figure 3. World map showing the annual growth rate (% change per year) in the number of honeybee hives for countries reporting those data to FAO between 1961 and 2012 (IPBES 2016b).Regional trends and status of pollinators, their habitats and biomes Current knowledge on trends and status of pollinators in different regions and their respective biomes is detailed below. Each subsection features what is known of both wild pollinators and managed pollinators, recognizing that managed pollinators also have important roles beyond agriculture, foraging in natural and semi-natural habitats. Information on declines of pollinators is available for agrosystems, but such information is scarce for wild plants. 3.2.1 African regionHabitats and biomes vulnerable to pollinator declines Tropical forest: Pollination dependence is poorly documented in African tropical forests. High vulnerability might be expected, however, given that for lowland forests globally, over?98% of flowering species are animal pollinated, with effective visitors limited to one or two classes of visitor, usually from the same order ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "author" : [ { "dropping-particle" : "", "family" : "Bawa", "given" : "K. S.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Annual Review of Ecology and Systematics", "id" : "ITEM-1", "issue" : "1990", "issued" : { "date-parts" : [ [ "1990" ] ] }, "page" : "399-422", "title" : "Plant-pollinator interactions in tropical rain forests", "type" : "article-journal", "volume" : "21" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Bawa 1990)", "plainTextFormattedCitation" : "(Bawa 1990)", "previouslyFormattedCitation" : "(Bawa 1990)" }, "properties" : { }, "schema" : "" }(Bawa 1990).Dry deciduous forest: A number of Madagascan forest species are pollinated by lemurs ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "author" : [ { "dropping-particle" : "", "family" : "Sussman", "given" : "Robert W", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Raven", "given" : "Peter H", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Science", "id" : "ITEM-1", "issue" : "4343", "issued" : { "date-parts" : [ [ "1978" ] ] }, "page" : "731-736", "title" : "Pollination by lemurs and marsupials: an archaic coevolutionary system", "type" : "article-journal", "volume" : "200" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Sussman and Raven 1978)", "plainTextFormattedCitation" : "(Sussman and Raven 1978)", "previouslyFormattedCitation" : "(Sussman and Raven 1978)" }, "properties" : { }, "schema" : "" }(Sussman and Raven 1978), many of which are threatened, suggesting vulnerability of the system.Subtropical forest: Most trees are insect pollinated ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "author" : [ { "dropping-particle" : "", "family" : "Griffiths", "given" : "Megan E", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Lawes", "given" : "Michael J", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Griffiths", "given" : "Megan E", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Lawes", "given" : "Michael J", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "id" : "ITEM-1", "issue" : "4", "issued" : { "date-parts" : [ [ "2006" ] ] }, "page" : "614-622", "title" : "Biogeographic, environmental , and phylogenetic influences on reproductive traits in subtropical forest trees , South Africa", "type" : "article-journal", "volume" : "29" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Griffiths et al. 2006)", "plainTextFormattedCitation" : "(Griffiths et al. 2006)", "previouslyFormattedCitation" : "(Griffiths et al. 2006)" }, "properties" : { }, "schema" : "" }(Griffiths et al. 2006), so declines in insects would be detrimental.Mediterranean: Cape Floristic Region, South Africa: High vulnerability – many asymmetrical interactions – i.e. many specialized species reliant on a single species or functional group of pollinator ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1098/rstb.2009.0243", "ISBN" : "0962-8436", "ISSN" : "0962-8436", "PMID" : "20047876", "abstract" : "The flora of southern Africa has exceptional species richness and endemism, making it an ideal system for studying the patterns and processes of evolutionary diversification. Using a wealth of recent case studies, I examine the evidence for pollinator-driven diversification in this flora. Pollination systems, which represent available niches for ecological diversification, are characterized in southern Africa by a high level of ecological and evolutionary specialization on the part of plants, and, in some cases, by pollinators as well. These systems are asymmetric, with entire plant guilds commonly specialized for a particular pollinator species or functional type, resulting in obvious convergent floral evolution among guild members. Identified modes of plant lineage diversification involving adaptation to pollinators in these guilds include (i) shifts between pollination systems, (ii) divergent use of the same pollinator, (iii) coevolution, (iv) trait tracking, and (v) floral mimicry of different model species. Microevolutionary studies confirm that pollinator shifts can be precipitated when a plant species encounters a novel pollinator fauna on its range margin, and macroevolutionary studies confirm frequent pollinator shifts associated with lineage diversification. As Darwin first noted, evolutionary specialization for particular pollinators, when resulting in ecological dependency, may increase the risk of plant extinction. I thus also consider the evidence that disturbance provokes pollination failure in some southern African plants with specialized pollination systems.", "author" : [ { "dropping-particle" : "", "family" : "Johnson", "given" : "S. D.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Philosophical Transactions of the Royal Society B: Biological Sciences", "id" : "ITEM-1", "issue" : "1539", "issued" : { "date-parts" : [ [ "2010" ] ] }, "page" : "499-516", "title" : "The pollination niche and its role in the diversification and maintenance of the southern African flora", "type" : "article-journal", "volume" : "365" }, "uris" : [ "" ] }, { "id" : "ITEM-2", "itemData" : { "DOI" : "10.1111/jbi.12453", "ISBN" : "1365-2699", "ISSN" : "13652699", "PMID" : "22752187", "abstract" : "We aimed to produce the first complete pollination network for Africa to test (1) whether South African plants are unusually specialized in their interactions with pollinators, and (2) whether the South African data conform with global patterns of specialization.\\n\\n\\nLocation\\n\\nCederberg, Cape Floristic Region, South Africa (32\u00b004\u203231.52\u2033 S, 19\u00b004\u2032 48.42\u2033 E; elevation 320 m).\\n\\n\\nMethods\\n\\nWe sampled all plant\u2013pollinator interactions within a 1-ha plot to assemble a network of 62 plant species linked to 217 pollinators species by 10,314 visits. We calculated the standardized Kullback\u2013Leibler distance (d\u2032) as an estimate of plant and animal specialization, and standardized two-dimensional Shannon entropy (\u0394H2\u2032) as an estimate of network-wide specialization. We compared these metrics with those calculated for 58 other networks from across the world.\\n\\n\\nResults\\n\\nIn a global context, the South African plant species had an unusually high number of interaction partners (mean = 6.32) while the animal species had unusually few (mean = 1.81). Animal diversity was high relative to plant diversity (network asymmetry = 0.56). Nevertheless, the South African plants, pollinators and network overall were more specialized than any previously studied community (weighted mean d\u2032 plants = 0.824 and animals = 0.807, community \u0394H2\u2032 = 0.834), suggesting functional specialization. Overall, specialization was found to increase sharply with latitude in the Southern Hemisphere, whereas no relationship was found in the Northern Hemisphere.\\n\\n\\nMain conclusions\\n\\nThe findings that South African plants have a high diversity of pollinators and that specialization of pollination networks increases with latitude in the Southern Hemisphere only are in contradiction to expectations derived from earlier literature. Long-term climatic stability in the Southern Hemisphere might have allowed phenotypic and functional specialization to manifest and persist.\\n", "author" : [ { "dropping-particle" : "", "family" : "Pauw", "given" : "Anton", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Stanway", "given" : "Rosanne", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Journal of Biogeography", "id" : "ITEM-2", "issue" : "4", "issued" : { "date-parts" : [ [ "2015" ] ] }, "page" : "652-661", "title" : "Unrivalled specialization in a pollination network from South Africa reveals that specialization increases with latitude only in the Southern Hemisphere", "type" : "article-journal", "volume" : "42" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Johnson 2010; Pauw and Stanway 2015)", "plainTextFormattedCitation" : "(Johnson 2010; Pauw and Stanway 2015)", "previouslyFormattedCitation" : "(Johnson 2010; Pauw and Stanway 2015)" }, "properties" : { }, "schema" : "" }(Johnson 2010; Pauw and Stanway 2015).Mountain grasslands: Pollination systems in mountain (C4) grasslands are quite highly specialized (Johnson et al. 2009). Tropical and subtropical savannas and grasslands: Some groups have quite marked reliance on one or a couple of species. For example, Convolvulus hawkmoth, Agrius convolvuli is the most important pollinator of African plants with very long-tubed (>8 cm long) flowers. More than 70 grassland and savanna plant species in Africa belong to the Agrius pollination guild (Johnson and Raguso 2016).Drylands and deserts:In the semi-arid areas of South Africa (Namaqualand), bees are prone to reproductive failure during drought (Mayer and Kuhlmann 2004). Many of the dominant daisies that appear to be generalists actually require specialist pollinators (Bombyllid flies) (Ellis and Johnson 2009; De Jager and Ellis 2014). Monkey beetles (Scarabaeidae: Hopliini) carry high pollen loads, so are likely important pollinators in some systems, e.g. Succulent Karoo, monkey beetle community composition has been found to change in response to heavy grazing (Mayer et al. 2006).Wetlands and dambos: These are often habitats for orchids with specialized pollinators (Burgoyne et al. 2000; Johnson 2006) and breeding sites for some important pollinators (this is a knowledge gap). Urban and peri-urban: Vulnerable – decline in rare butterflies associated with urbanization in South Africa (Mecenero et al. 2015), decline in visitation to bird-pollinated Erica perspicua near roads (Geerts and Pauw 2011). There is a loss of bird pollinator functional diversity along a gradient of increasing urbanization (Pauw and Louw 2012).Coastal areas:Many mangrove species are bird or insect pollinated (Noske 1993; Okoth 2010).tatus of pollinators and pollinationWild pollinators: A lack of data on spatial and temporal changes in wild pollinators in Africa, combined with poorly known taxonomy, hampers assessment of the trends and status of Africa’s pollinators, although some ongoing initiatives may help address this issue. Certain trends can be predicted from studies that substitute space for time, however. Bees (Apidae): Data sets on the trends and status of bees on the continent are not yet available. Some work has been conducted on how bees might be affected by climate change: in a region with high bee endemism in South Africa, range contractions are expected for half of the 12 species considered ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1111/j.1472-4642.2011.00877.x", "ISBN" : "1366-9516", "ISSN" : "13669516", "PMID" : "23610622", "abstract" : "Aim Bees are the most important pollinators of flowering plants and essential ecological keystone species contributing to the integrity of most terrestrial ecosystems. Here, we examine the potential impact of climate change on bees geographic range in a global biodiversity hotspot. Location South Africa with a focus on the Cape Floristic Region (CFR) diversity hotspot. Methods similar to Geographic ranges of 12 South African bee species representing dominant distribution types were studied, and the climate change impacts upon bees were examined with A2 and B2 climate scenarios of HadCM3 model, using MaxEnt for species distribution modelling. Results The predicted levels of climate change-induced impacts on species ranges varied from little shifts and range expansion of 550% for two species to substantial range contractions between 32% and 99% in another six species. Four species show considerable range shifts. Bees of the winter rainfall area in the west of South Africa generally have smaller range sizes than in the summer rainfall area and generally show eastward range contractions toward the dry interior. Bee species prevalent in summer rainfall regions show a tendency for a south-easterly shift in geographic range. Main conclusions The bee fauna of the CFR is identified as the most vulnerable to climate change due to the high level of endemism, the small range sizes and the island-like isolation of the Mediterranean-type climate region at the SW tip of Africa. For monitoring climate change impact on bees, we suggest to establish observatories in the coastal plains of the west coast that are predicted to be worst affected and areas where persistence of populations is most likely. Likely impacts of climate change on life history traits of bees (phenology, sociality, bee-host plant synchronization) are discussed but require further investigation", "author" : [ { "dropping-particle" : "", "family" : "Kuhlmann", "given" : "Michael", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Guo", "given" : "Danni", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Veldtman", "given" : "Ruan", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Donaldson", "given" : "John", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Diversity and Distributions", "id" : "ITEM-1", "issue" : "9", "issued" : { "date-parts" : [ [ "2012" ] ] }, "page" : "885-897", "title" : "Consequences of warming up a hotspot: Species range shifts within a centre of bee diversity", "type" : "article-journal", "volume" : "18" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Kuhlmann et al. 2012)", "plainTextFormattedCitation" : "(Kuhlmann et al. 2012)", "previouslyFormattedCitation" : "(Kuhlmann et al. 2012)" }, "properties" : { }, "schema" : "" }(Kuhlmann et al. 2012). Butterflies and moths (Lepidoptera): Since the late 1980s, South Africa has produced three red data assessments of the approximately 800 species of butterfly found in the country. A comparison of the two most recent assessments found an increase in severity of threat status of Lepidoptera. In the 2009 assessment, 60 (7.5%) of the total 801 species were considered threatened (i.e., vulnerable, endangered or critically endangered), and in the 2013 assessment ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "ISBN" : "9780620553575", "author" : [ { "dropping-particle" : "", "family" : "Mecenero", "given" : "S.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Ball", "given" : "J.B.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Edge", "given" : "David A", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Hamer", "given" : "Michelle", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Henning", "given" : "G.A.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Kruger", "given" : "M.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Pringle", "given" : "E.L.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Terblanche", "given" : "R.F.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Williams", "given" : "M.C.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "id" : "ITEM-1", "issue" : "May 2016", "issued" : { "date-parts" : [ [ "2013" ] ] }, "title" : "Conservation assessment of butterflies of South Africa, Lesotho and Swaziland: Red List and Atlas", "type" : "book" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Mecenero et al. 2013)", "plainTextFormattedCitation" : "(Mecenero et al. 2013)", "previouslyFormattedCitation" : "(Mecenero et al. 2013)" }, "properties" : { }, "schema" : "" }(Mecenero et al. 2013), although this number was unchanged ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1007/s10841-015-9758-5", "ISSN" : "15729753", "author" : [ { "dropping-particle" : "", "family" : "Edge", "given" : "David A.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Mecenero", "given" : "Silvia", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Journal of Insect Conservation", "id" : "ITEM-1", "issue" : "2", "issued" : { "date-parts" : [ [ "2015" ] ] }, "page" : "325-339", "title" : "Butterfly conservation in Southern Africa", "type" : "article-journal", "volume" : "19" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Edge and Mecenero 2015)", "plainTextFormattedCitation" : "(Edge and Mecenero 2015)", "previouslyFormattedCitation" : "(Edge and Mecenero 2015)" }, "properties" : { }, "schema" : "" }(Edge and Mecenero 2015), the severity of threat had increased. Six species new to science were considered to be under immediate threat from ongoing habitat destruction, suggesting that species may go extinct before being described ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "ISBN" : "9781919976518", "author" : [ { "dropping-particle" : "", "family" : "Henning", "given" : "G A", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Terblanche", "given" : "R F", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Ball", "given" : "J B", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "SANBI Biodiversity Series", "id" : "ITEM-1", "issue" : "13", "issued" : { "date-parts" : [ [ "2009" ] ] }, "title" : "South African Red Data Book : Butterflies", "type" : "book", "volume" : "3" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Henning et al. 2009)", "plainTextFormattedCitation" : "(Henning et al. 2009)", "previouslyFormattedCitation" : "(Henning et al. 2009)" }, "properties" : { }, "schema" : "" }(Henning et al. 2009). Furthermore, the 2013 assessment considered three species to be extinct ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "ISBN" : "9780620553575", "author" : [ { "dropping-particle" : "", "family" : "Mecenero", "given" : "S.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Ball", "given" : "J.B.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Edge", "given" : "David A", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Hamer", "given" : "Michelle", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Henning", "given" : "G.A.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Kruger", "given" : "M.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Pringle", "given" : "E.L.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Terblanche", "given" : "R.F.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Williams", "given" : "M.C.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "id" : "ITEM-1", "issue" : "May 2016", "issued" : { "date-parts" : [ [ "2013" ] ] }, "title" : "Conservation assessment of butterflies of South Africa, Lesotho and Swaziland: Red List and Atlas", "type" : "book" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Mecenero et al. 2013)", "plainTextFormattedCitation" : "(Mecenero et al. 2013)", "previouslyFormattedCitation" : "(Mecenero et al. 2013)" }, "properties" : { }, "schema" : "" }(Mecenero et al. 2013). When rare or very rare species are also considered, 151 species (18.8% - one in every six Lepidoptera) are of high conservation concern in the region ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1007/s10841-015-9758-5", "ISSN" : "15729753", "author" : [ { "dropping-particle" : "", "family" : "Edge", "given" : "David A.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Mecenero", "given" : "Silvia", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Journal of Insect Conservation", "id" : "ITEM-1", "issue" : "2", "issued" : { "date-parts" : [ [ "2015" ] ] }, "page" : "325-339", "title" : "Butterfly conservation in Southern Africa", "type" : "article-journal", "volume" : "19" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Edge and Mecenero 2015)", "plainTextFormattedCitation" : "(Edge and Mecenero 2015)", "previouslyFormattedCitation" : "(Edge and Mecenero 2015)" }, "properties" : { }, "schema" : "" }(Edge and Mecenero 2015). The IUCN red list for Lepidoptera for the whole of Africa includes red list assessments for only 355 species. Many of the species listed in the IUCN red list are also included in the South African assessment, including two of the three species listed as extinct for Africa. The third species listed as extinct for Africa is the nymphalid Libythea cinyras, which was endemic to Mauritius. Excluding the extinct species, 96?species (27.3%) are threatened or near threatened, and almost 12% (42 species) are data deficient. Some of the data are also dated: one quarter of the species assessed in the IUCN redlist were last assessed over two decades ago; the remainder were assessed during or after 2011. Population trends for the African Lepidoptera indicated that 10% were stable, 9% were decreasing, and trends for the remaining 81% were unknown. Pollinating birds: A number of bird families in Africa may be instrumental in pollination, including Zosteropidae and Icteridae, but their effectiveness in this role may be fairly minor. Therefore, we consider here the sunbirds (Nectariniidae) and sugarbirds (Promeropidae). The IUCN lists 11 (12%) of the 93 sunbird species included in their database as threatened or near-threatened; there are only two species of sugarbird, and one of these (Promerops gurneyi) is considered near threatened. For sunbirds, 22% are considered to be decreasing and the remainder are considered stable; none are increasing. Of the sugarbirds, one species is decreasing, the other is stable. The two Southern African Bird Atlas Projects (SABAP1, 1987-1991; and SABAP2, 2007-2017) allow comparison of reporting rates over the two different time periods. This comparison shows that 15 out of the 23 species (i.e., 65%), show declines over time, while the remainder showed increases. As with many other species, habitat transformation is largely responsible for these losses. Pteropodid bats: The role of bats in pollination in Africa is poorly studied. The IUCN red list provides assessments for 42 species of the Pteropodidae in Africa, the bats most likely to be pollinators. Thirty of these are found on the mainland and 12 on islands. The threat status of the island species is more severe than that of the continental species: 11 of the 12 island species are threatened compared to 3 of the 30 mainland species, although 5 of the mainland species are considered data deficient. Almost half (45%) of island species and 27% of mainland species are declining, but we lack data for 40% of the continental species, so the proportion of species in decline could be much greater. None of the mainland species seem to be increasing, although two (18%) island species appear to be increasing.Managed pollinators - honeybees (Apis mellifera): In a study assessing managed honeybee colonies in South Africa, losses were almost 30% in 2009-2010 and 46.2% in 2010-2011 ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.3896/IBRA.1.53.1.03", "ISBN" : "20786913", "ISSN" : "0021-8839", "abstract" : "This study reports honey bee, Ap i s m e lf l i e ra L., colony losses that occurred in South Africa over two consecutive years. The total losses were 29.6% (95% CI: 22.8-37.5) in 2009-2010 and 46.2% (95% CI: 37.3-55.0) in 2010-2011. Furthermore, the study shows that the cape n si s worker social parasite, a problem unique to southern Africa, is the main perceived cause, and could explain the significant differences in the number of losses between beekeepers using the subspecies A. m . sc u t e l l at a and those using the subspecies A. m . cape n si s . In contrast to previous studies in North America and Europe, we find a significant negative effect of migratory beekeeping practices on the extent of colony losses. Migratory beekeepers lost on average more colonies (35.5% (95% CI 29.7-47.2)) than did stationary beekeepers (17.2% (95% CI 11.2-22.3)). This was especially pronounced when the beekeepers were migrating for the pollination of apples/cherries, eucalyptus, onions and/or sunflowers. The major beekeeper-perceived causes of mortality were small hive beetles, varroa mites, absconding (non-reproductive swarming), and chalkbrood disease. Those listing chalkbrood disease lost significantly fewer colonies than those who did not list chalkbrood. 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None of the beekeepers surveyed indicated that these losses were threatening their livelihoods ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.3896/IBRA.1.53.1.03", "ISBN" : "20786913", "ISSN" : "0021-8839", "abstract" : "This study reports honey bee, Ap i s m e lf l i e ra L., colony losses that occurred in South Africa over two consecutive years. The total losses were 29.6% (95% CI: 22.8-37.5) in 2009-2010 and 46.2% (95% CI: 37.3-55.0) in 2010-2011. Furthermore, the study shows that the cape n si s worker social parasite, a problem unique to southern Africa, is the main perceived cause, and could explain the significant differences in the number of losses between beekeepers using the subspecies A. m . sc u t e l l at a and those using the subspecies A. m . cape n si s . In contrast to previous studies in North America and Europe, we find a significant negative effect of migratory beekeeping practices on the extent of colony losses. Migratory beekeepers lost on average more colonies (35.5% (95% CI 29.7-47.2)) than did stationary beekeepers (17.2% (95% CI 11.2-22.3)). This was especially pronounced when the beekeepers were migrating for the pollination of apples/cherries, eucalyptus, onions and/or sunflowers. The major beekeeper-perceived causes of mortality were small hive beetles, varroa mites, absconding (non-reproductive swarming), and chalkbrood disease. Those listing chalkbrood disease lost significantly fewer colonies than those who did not list chalkbrood. 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Honeybees are native to Africa; their health and ability to reproduce in swarms is key to both their survival and their use in beekeeping and pollination. A survey of the health of Africa’s pollinators, carried out in 2016, suggested that aside from an outbreak of American foul?brood in the Western Cape, South Africa, largescale colony losses had not been observed on the continent ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1007/s13592-015-0406-6", "ISBN" : "0044-8435 1297-9678", "ISSN" : "12979678", "abstract" : "Honeybee (Apis mellifera L.) pathogens and parasites and the negative effects thereof on honeybee populations remain an issue of public concern and the subject of active research. Africa with its high genetic diversity of honeybee sub-species and largewild population is also exposed to various factors responsible for colony losses in other parts of the world.Apart fromthe currentAmerican foulbrood epidemic in theWestern Cape of South Africa, no large-scale colony losses have been reported elsewhere on the continent. We discuss the presence of pathogens, parasites, pests and predators of African honeybees as well as the threats they face in relation to habitat changes arising from the impact of increased human populations. 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A recent study suggests that although deformed wing virus has a long evolutionary history with A. mellifera, the parasitic mite, Varroa destructor, spread by human transport of colonies from Europe and North America to other regions, makes the disease far more virulent ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1126/science.aac9976", "ISBN" : "1498224114983", "ISSN" : "1095-9203", "PMID" : "26912700", "abstract" : "Deformed wing virus (DWV) and its vector, the mite Varroa destructor, are a major threat to the world's honeybees. Although the impact of Varroa on colony-level DWV epidemiology is evident, we have little understanding of wider DWV epidemiology and the role that Varroa has played in its global spread. A phylogeographic analysis shows that DWV is globally distributed in honeybees, having recently spread from a common source, the European honeybee Apis mellifera. 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Their contribution to floral biodiversity and conservation, by virtue of their pollination of indigenous flowering plants is unknown, but certain to be considerable. Economically, honeybees are critical for the pollination of a host of commercial crop plants as well as being the source of energy and livelihood for many thousands of mostly small-scale beekeepers. In the past, honeybee pests and problems have been of limited importance in Africa. More recently, however, an increasing number of exotic diseases and pests as well as home-grown problems threaten honeybees, beekeeping and honeybee-pollination in Africa. Two problems in South Africa, the capensis problem and varroa mites, have severely curtailed beekeeping in that country and may well have impact on bees and beekeeping throughout the continent. R\u00e9sum\u00e9. Pour des raisons \u00e9cologiques et \u00e9conomiques, les abeilles rev\u00eatent une tr\u00e8s grande importance en Afrique. Ecologiquement, leur contribution r\u00e9elle au maintien de la biodiversit\u00e9 florale par l'activit\u00e9 de pollinisation n'est pas r\u00e9ellement connue, mais elle est assur\u00e9ment consid\u00e9rable. Economiquement, les abeilles jouent un r\u00f4 le cl\u00e9 dans la pollinisation des plantes cultiv\u00e9es et repr\u00e9sentent une source d'\u00e9nergic et un appoint de revenus \u00e0 des millers d'apiculteurs modestes. Dans le pass\u00e9, l'impact des maladies et des pestes apicoles n'ont pas pos\u00e9 de s\u00e9rieux probl\u00e8mes en Afrique. En revanche, l'\u00e9mergence r\u00e9cente de maladies et de parasites exotiques, associ\u00e9e aux probl\u00e8mes qui se sont d\u00e9velopp\u00e9s sur place, menance s\u00e9rieusement aussi bien les abeilles que l'apiculture et la pollinisation. Deux dangers, plus sp\u00e9cifiquement sud-africains, respectivement le Probl\u00e8me Capensis et la varroase, qui ont consid\u00e9rablement affaibli l'apiculture dans ce pays, pourraient m\u00eame s'\u00e9tendre \u00e0 l'ensemble du continent.", "author" : [ { "dropping-particle" : "", "family" : "Allsopp", "given" : "Mike", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "International Journal of Tropical Insect Science", "id" : "ITEM-2", "issue" : "1", "issued" : { "date-parts" : [ [ "2004" ] ] }, "page" : "87\u201394", "title" : "Cape honeybee (<i>Apis mellifera capensis</i> Eshscholtz) and varroa mite (<i>Varroa destructor</i> Anderson & Trueman) threats to honeybees and beekeeping in Africa", "type" : "article-journal", "volume" : "24" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Allsopp 2004; Wilfert et al. 2016)", "plainTextFormattedCitation" : "(Allsopp 2004; Wilfert et al. 2016)", "previouslyFormattedCitation" : "(Allsopp 2004; Wilfert et al. 2016)" }, "properties" : { }, "schema" : "" }(Allsopp 2004; Wilfert et al. 2016), so its full effect on disease virulence may not yet be fully manifest, making it a future concern for Africa, and necessitating close monitoring. In Kenya, where only remote apiaries were free of Varroa destructor, remote colonies were also free of deformed wing virus (DWV), acute bee paralysis virus (ABPV) and black queen cell virus (BQCV) ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1371/journal.pone.0094459", "ISBN" : "10.1371/journal.pone.0094459", "ISSN" : "19326203", "PMID" : "24740399", "abstract" : "In East Africa, honey bees (Apis mellifera) provide critical pollination services and income for small-holder farmers and rural families. While honey bee populations in North America and Europe are in decline, little is known about the status of honey bee populations in Africa. We initiated a nationwide survey encompassing 24 locations across Kenya in 2010 to evaluate the numbers and sizes of honey bee colonies, assess the presence of parasites (Varroa mites and Nosema microsporidia) and viruses, identify and quantify pesticide contaminants in hives, and assay for levels of hygienic behavior. Varroa mites were present throughout Kenya, except in the remote north. Levels of Varroa were positively correlated with elevation, suggesting that environmental factors may play a role in honey bee host-parasite interactions. Levels of Varroa were negatively correlated with levels of hygienic behavior: however, while Varroa infestation dramatically reduces honey bee colony survival in the US and Europe, in Kenya Varroa presence alone does not appear to impact colony size. Nosema apis was found at three sites along the coast and one interior site. Only a small number of pesticides at low concentrations were found. Of the seven common US/European honey bee viruses, only three were identified but, like Varroa, were absent from northern Kenya. The number of viruses present was positively correlated with Varroa levels, but was not correlated with colony size or hygienic behavior. Our results suggest that Varroa, the three viruses, and Nosema have been relatively recently introduced into Kenya, but these factors do not yet appear to be impacting Kenyan bee populations. Thus chemical control for Varroa and Nosema are not necessary for Kenyan bees at this time. 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There was also a significant correlation between viral diversity and Varroa loads ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1371/journal.pone.0094459", "ISBN" : "10.1371/journal.pone.0094459", "ISSN" : "19326203", "PMID" : "24740399", "abstract" : "In East Africa, honey bees (Apis mellifera) provide critical pollination services and income for small-holder farmers and rural families. While honey bee populations in North America and Europe are in decline, little is known about the status of honey bee populations in Africa. We initiated a nationwide survey encompassing 24 locations across Kenya in 2010 to evaluate the numbers and sizes of honey bee colonies, assess the presence of parasites (Varroa mites and Nosema microsporidia) and viruses, identify and quantify pesticide contaminants in hives, and assay for levels of hygienic behavior. Varroa mites were present throughout Kenya, except in the remote north. 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Apart from the relatively recent introduction of Varroa to Africa, part of the African honeybees’ resistance to disease may lie in their large wild populations ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1051/apido/2009013", "ISSN" : "0044-8435", "abstract" : "\u2013 Honeybees are native to Africa and Europe but have been spread worldwide as the basis for an apicultural industry. To date, large and diverse wild populations only remain in Africa. On this continent the beekeeping industry is relatively undeveloped and relies on trapping swarms from wild populations to constitute the managed stocks. Bee breeding is seldom practiced. The situation is therefore different from that of Europe or North America where wild or feral honeybees have almost disappeared and this distinction is important when assessing the conservation status of African honeybees. While African honeybees appear to be more resistant to major diseases, the history of honeybee populations worldwide suggests that their conservation is a necessity. 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Of these, the para-sitic mite, Varroa destructor Anderson and Truman (Acari:Varroidae), is considered by many as the most devastating. We found this mite in honeybee colonies throughout Kenya and in Tanzania for the first time in early 2009. Beekeepers surveyed were neither aware of the mite's presence nor had they observed any negative impact on the survival and/or productivity of their bees. In March of 2009, we sampled 38 honeybee colonies (likely A. m. scutellata, and possibly A. m. scutellata hybrids) in seven locations in Central and Eastern Kenya. We employed a common sam-pling technique to determine mite presence/absence that utilizes powdered sugar to dislodge mites from adult bees (Macedo et al., 2002). An average of 717 \u00b1 43 bees per colony were sampled and Var-roa mites were found in all 38 colonies examined with numbers ranging from 3\u2013108 per sample and averaging 26.3 \u00b1 25.9 per colony. In a further sim-ilar survey (April\u2013May, 2009) of 125 additional colonies located in the eastern, western and coastal regions of Kenya (69 colonies in 18 locations), coastal Tanzania (18 colonies in 4 locations) includ-ing Ugunja and Pemba Islands, collectively referred to as Zanzibar (likely A.m. litorea), and Western Uganda (14 colonies in 4 locations), 87% of the", "author" : [ { "dropping-particle" : "", "family" : "Frazier", "given" : "Maryann", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Muli", "given" : "Eliud", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Conklin", "given" : "Tracy", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Schmehl", "given" : "Daniel", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Torto", "given" : "Baldwyn", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Frazier", "given" : "James", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Tumlinson", "given" : "James", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Evans", "given" : "Jay D", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Raina", "given" : "Suresh", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Apidologie", "id" : "ITEM-1", "issued" : { "date-parts" : [ [ "2009" ] ] }, "page" : "463-465", "title" : "A scientific note on Varroa destructor found in East Africa; threat or opportunity?", "type" : "article-journal", "volume" : "41" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Frazier et al. 2009)", "manualFormatting" : "( i.e., finding and removing parasites from hives; Frazier et al. 2009)", "plainTextFormattedCitation" : "(Frazier et al. 2009)", "previouslyFormattedCitation" : "(Frazier et al. 2009)" }, "properties" : { }, "schema" : "" }(i.e., finding and removing parasites from hives; Frazier et al. 2009) may give them some immunity to diseases. Figure 4 depicts the current status of documentation of the presence of the three main pathogen groups (bacteria, fungi and viruses) associated with honeybees, as reported by national governments in Africa.Figure 4. Distribution of pathogen groups (bacteria, fungi and viruses) associated with honeybees (from Pirk et al. 2016). White = none or no data; pink = one of these pathogen groups present; red = two of these pathogen groups present; maroon = all three of these pathogen groups present. Managed pollinators - stingless bees: A survey of stingless bee species in Tanzania found them to be present in relatively low densities, attributed to threats from fire, honey hunting and logging activities ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "author" : [ { "dropping-particle" : "", "family" : "Hamisi", "given" : "Issa", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "id" : "ITEM-1", "issued" : { "date-parts" : [ [ "2016" ] ] }, "number-of-pages" : "69", "publisher" : "Sokoine University of Agriculture, Morogoro, Tanzania", "title" : "Diversity, status and threats to stingless bees (Apidae: Meliponini) of Ipembampazi Forest Reserve, Tabora - Tanzania", "type" : "thesis" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Hamisi 2016)", "plainTextFormattedCitation" : "(Hamisi 2016)", "previouslyFormattedCitation" : "(Hamisi 2016)" }, "properties" : { }, "schema" : "" }(Hamisi 2016). Managed pollinators - bumblebees (Bombus spp.): As yet, bumblebees have not been introduced to Africa and it is advisable to avoid such introductions, as they can introduce diseases and have been associated with declines of native Bombus species in South America ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1111/1365-2656.12185", "ISBN" : "0021-8790", "ISSN" : "13652656", "PMID" : "24256429", "abstract" : "The Palaearctic Bombus ruderatus (in 1982/1983) and Bombus terrestris (1998) have both been introduced into South America (Chile) for pollination purposes. We here report on the results of sampling campaigns in 2004, and 2010-2012 showing that both species have established and massively expanded their range. Bombus terrestris, in particular, has spread by some 200\u00a0km\u00a0year(-1) and had reached the Atlantic coast in Argentina by the end of 2011. Both species, and especially B.\u00a0terrestris, are infected by protozoan parasites that seem to spread along with the imported hosts and spillover to native species. Genetic analyses by polymorphic microsatellite loci suggest that the host population of B.\u00a0terrestris is genetically diverse, as expected from a large invading founder population, and structured through isolation by distance. Genetically, the populations of the trypanosomatid parasite, Crithidia bombi, sampled in 2004 are less diverse, and distinct from the ones sampled later. Current C.\u00a0bombi populations are highly heterozygous and also structured through isolation by distance correlating with the genetic distances of B.\u00a0terrestris, suggesting the latter's expansion to be a main structuring factor for the parasite. Remarkably, wherever B.\u00a0terrestris spreads, the native Bombus dahlbomii disappears although the reasons remain unclear. Our ecological and genetic data suggest a major invasion event that is currently unfolding in southern South America with disastrous consequences for the native bumblebee species.", "author" : [ { "dropping-particle" : "", "family" : "Schmid-Hempel", "given" : "Regula", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Eckhardt", "given" : "Michael", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Goulson", "given" : "David", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Heinzmann", "given" : "Daniel", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Lange", "given" : "Carlos", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Plischuk", "given" : "Santiago", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Escudero", "given" : "Luisa R.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Salath\u00e9", "given" : "Rahel", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Scriven", "given" : "Jessica J.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Schmid-Hempel", "given" : "Paul", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Journal of Animal Ecology", "id" : "ITEM-1", "issue" : "4", "issued" : { "date-parts" : [ [ "2014" ] ] }, "page" : "823-837", "title" : "The invasion of southern South America by imported bumblebees and associated parasites", "type" : "article-journal", "volume" : "83" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Schmid-Hempel et al. 2014)", "plainTextFormattedCitation" : "(Schmid-Hempel et al. 2014)", "previouslyFormattedCitation" : "(Schmid-Hempel et al. 2014)" }, "properties" : { }, "schema" : "" }(Schmid-Hempel et al. 2014) as well as reduced native plant seed and fruit set ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1016/j.biocon.2006.07.023", "author" : [ { "dropping-particle" : "", "family" : "Kenta", "given" : "Tanaka", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Inari", "given" : "Naoki", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Nagamitsu", "given" : "Teruyoshi", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Goka", "given" : "Koichi", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Hiura", "given" : "Tsutom", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Forestry", "id" : "ITEM-1", "issued" : { "date-parts" : [ [ "2007" ] ] }, "page" : "298-309", "title" : "Commercialized European bumblebee can cause pollination disturbance : An experiment on seven native plant species in Japan", "type" : "article-journal", "volume" : "134" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Kenta et al. 2007)", "plainTextFormattedCitation" : "(Kenta et al. 2007)", "previouslyFormattedCitation" : "(Kenta et al. 2007)" }, "properties" : { }, "schema" : "" }(Kenta et al. 2007). Wild plants dependent on pollinators in Africa: In many African ecosystems, there is a high degree of pollinator-plant specialization, particularly in the global biodiversity hotspots. For example, the majority of species in the Orchidaceae and Iridaceae of southern Africa are pollinated by a single species, and plants adapted to pollination by oil-collecting bees, long-proboscid flies and the Aeropetes butterfly are usually pollinated by a single species ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "ISSN" : "00382353", "abstract" : "Data assembled from recent publications on plant\u2013pollinator systems in southern African plants reveal a pattern of remarkable specialization by the plants. Analysis of plant species in two large families \u2014 the Orchidaceae and Iridaceae \u2014 showed that most have been found to be pollinated by a single animal species. Similar levels of specialization are evident in southern African plants pollinated by oil-collecting bees, long-proboscid flies, butterflies and hopliine beetles. By contrast, analysis of published data for the Orchidaceae and Polemoniaceae in the northern hemisphere showed that most species have relatively generalized pollination systems (median number of pollinator species=3.5 and 5, respec- tively). Claims made in the literature that generalization is the rule rather than the exception in plant pollination systems have been based solely on studies in cool temperate ecosystems in the northern hemisphere and may be premature if there are strong regional differences in the degree of specialization in plants. This highlights theneedformorestudies of pollination systems across a range of ecosystemsandgeographical regions in order to obtain an accurate global view of the diversity of plant pollination systems.", "author" : [ { "dropping-particle" : "", "family" : "Johnson", "given" : "Steven D.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Steiner", "given" : "Kim E.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "South African Journal of Science", "id" : "ITEM-1", "issue" : "7-8", "issued" : { "date-parts" : [ [ "2003" ] ] }, "page" : "345-348", "title" : "Specialized pollination systems in southern Africa", "type" : "article-journal", "volume" : "99" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Johnson and Steiner 2003)", "plainTextFormattedCitation" : "(Johnson and Steiner 2003)", "previouslyFormattedCitation" : "(Johnson and Steiner 2003)" }, "properties" : { }, "schema" : "" }(Johnson and Steiner 2003), or some plants are pollinated by a small group of species ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "ISSN" : "00382353", "abstract" : "Data assembled from recent publications on plant\u2013pollinator systems in southern African plants reveal a pattern of remarkable specialization by the plants. Analysis of plant species in two large families \u2014 the Orchidaceae and Iridaceae \u2014 showed that most have been found to be pollinated by a single animal species. Similar levels of specialization are evident in southern African plants pollinated by oil-collecting bees, long-proboscid flies, butterflies and hopliine beetles. By contrast, analysis of published data for the Orchidaceae and Polemoniaceae in the northern hemisphere showed that most species have relatively generalized pollination systems (median number of pollinator species=3.5 and 5, respec- tively). Claims made in the literature that generalization is the rule rather than the exception in plant pollination systems have been based solely on studies in cool temperate ecosystems in the northern hemisphere and may be premature if there are strong regional differences in the degree of specialization in plants. This highlights theneedformorestudies of pollination systems across a range of ecosystemsandgeographical regions in order to obtain an accurate global view of the diversity of plant pollination systems.", "author" : [ { "dropping-particle" : "", "family" : "Johnson", "given" : "Steven D.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Steiner", "given" : "Kim E.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "South African Journal of Science", "id" : "ITEM-1", "issue" : "7-8", "issued" : { "date-parts" : [ [ "2003" ] ] }, "page" : "345-348", "title" : "Specialized pollination systems in southern Africa", "type" : "article-journal", "volume" : "99" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Johnson and Steiner 2003)", "plainTextFormattedCitation" : "(Johnson and Steiner 2003)", "previouslyFormattedCitation" : "(Johnson and Steiner 2003)" }, "properties" : { }, "schema" : "" }(Johnson and Steiner 2003). In the semi-arid Succulent Karoo, even daisies, which phenotypically may appear very generalized, often have specialist pollinators ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.3732/ajb.0800222", "ISBN" : "0002-9122", "ISSN" : "00029122", "PMID" : "21628234", "abstract" : "One of the most widely accepted explanations for floral diversification in angiosperms is the pollinator-shift model developed by Verne Grant and Ledyard Stebbins. According to this model, the most profound changes in floral traits (such as morphology, color, patterning and scent) occur when plants undergo adaptive shifts between pollinator classes. We tested this model through investigations of geographical variation in floral form and pollinator assemblages in the South African annual daisy Gorteria diffusa. This species has elaborate insect-like ornaments on the capitulum, which attract bee flies belonging to the genus Megapalpus. We found unprecedented levels of geographically structured intraspecific variation and identified 14 discrete forms that vary in the morphology and ornamentation of the capitulum. This variation is not due to phenotypic plasticity because differences among forms were maintained in plants grown from seed in a common garden experiment. Contrary to predictions from the pollinator-shift model, all populations, regardless of floral phenotype, were pollinated primarily by a single species of Megapalpus bee fly. Much of the extensive variation in floral form in G. diffusa therefore appears to have arisen without evolutionary shifts between pollinator types.", "author" : [ { "dropping-particle" : "", "family" : "Ellis", "given" : "Allan G.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Johnson", "given" : "Steven D.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "American Journal of Botany", "id" : "ITEM-1", "issue" : "4", "issued" : { "date-parts" : [ [ "2009" ] ] }, "page" : "793-801", "title" : "The evolution of floral variation without pollinator shifts in <i>Gorteria diffusa</i> (Asteraceae)", "type" : "article-journal", "volume" : "96" }, "uris" : [ "" ] }, { "id" : "ITEM-2", "itemData" : { "DOI" : "10.1093/aob/mct189", "ISBN" : "0305-7364", "ISSN" : "03057364", "PMID" : "24052554", "abstract" : "Floral polymorphism is frequently attributed to pollinator-mediated selection. Multiple studies, however, have revealed the importance of non-pollinating visitors in floral evolution. Using the polymorphic annual daisy Ursinia calenduliflora, this study investigated the importance of different insect visitors, and their effects on fitness, in the maintenance of floral polymorphism. The spatial structure of a discrete floral polymorphism was characterized based on the presence/absence of anthocyanin floret spots in U. calenduliflora. A 3-year observational study was then conducted in polymorphic populations to investigate differences in visitation rates of dominant visitors to floral morphs. Experiments were performed to explore the floral preference of male and female Megapalpus capensis (the dominant insect visitor) and their effectiveness as pollinators. Next, floral damage by antagonistic florivores and the reproductive success of the two floral morphs were surveyed in multiple populations and years. Floral polymorphism in U. calenduliflora was structured spatially, as were insect visitation patterns. Megapalpus capensis males were the dominant visitors and exhibited strong preference for the spotted morph in natural and experimental observations. While this may indicate potential fitness benefits for the spotted morph, female fitness did not differ between floral morphs. However, as M. capensis males are very efficient at exporting U. calenduliflora pollen, their preference may likely increase the reproductive fitness of the spotted morph through male fitness components. The spotted morph, however, also suffered significantly greater costs due to ovule predation by florivores than the spotless morph. The results suggest that pollinators and florivores may potentially exert antagonistic selection that could contribute to the maintenance of floral polymorphism across the range of U. calenduliflora. The relative strength of selection imposed by each agent is potentially determined by insect community composition and abundance at each site, highlighting the importance of community context in the evolution of floral phenotypes.", "author" : [ { "dropping-particle" : "", "family" : "Jager", "given" : "Marinus L.", "non-dropping-particle" : "De", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Ellis", "given" : "Allan G.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Annals of Botany", "id" : "ITEM-2", "issue" : "2", "issued" : { "date-parts" : [ [ "2014" ] ] }, "page" : "213-222", "title" : "Floral polymorphism and the fitness implications of attracting pollinating and florivorous insects", "type" : "article-journal", "volume" : "113" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Ellis and Johnson 2009; De Jager and Ellis 2014)", "manualFormatting" : "(e.g., Ellis and Johnson 2009; De Jager and Ellis 2014)", "plainTextFormattedCitation" : "(Ellis and Johnson 2009; De Jager and Ellis 2014)", "previouslyFormattedCitation" : "(Ellis and Johnson 2009; De Jager and Ellis 2014)" }, "properties" : { }, "schema" : "" }(e.g., Ellis and Johnson 2009; De Jager and Ellis 2014). Such specialization suggests a marked susceptibility to pollinator loss ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1007/BF00989056", "ISBN" : "0378-2697", "ISSN" : "0378-2697", "abstract" : "Ixianthes retzioides is a rare South African shrub with large yellow oil-secret- ing flowers. Populations studied previously revealed low levels of reproductive success and the absence of a specialized oil-collecting pollinator. We report the discovery of a population in which the predicted specialist pollinator, Rediviva gigas, is present. The presence of this oil-collecting bee resulted in a mean fruit set per plant of 97.2 + 8.3% (N = 9) and a mean seed set of 331.6 + 162.6 (N = 52). This represents a 7.4-fold increase in fruit set and a 7.8-fold increase in seed set over a previously studied population lacking the specialist pollinator. The contrast between populations with and without the specialist pollinator dramatically illustrates the potential benefits and costs of specialization for pol- lination, respectively.", "author" : [ { "dropping-particle" : "", "family" : "Steiner", "given" : "Kim E.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Whitehead", "given" : "V. B.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Plant Systematics and Evolution", "id" : "ITEM-1", "issue" : "1", "issued" : { "date-parts" : [ [ "1996" ] ] }, "page" : "131-138", "title" : "The consequences of specialization for pollination in a rare South African shrub, <i> Ixianthes retzioides </i> (Scrophulariaceae)", "type" : "article-journal", "volume" : "2" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Steiner and Whitehead 1996)", "manualFormatting" : "(e.g., Steiner and Whitehead 1996)", "plainTextFormattedCitation" : "(Steiner and Whitehead 1996)", "previouslyFormattedCitation" : "(Steiner and Whitehead 1996)" }, "properties" : { }, "schema" : "" }(e.g., Steiner and Whitehead 1996). This susceptibility has been demonstrated in studies where habitat fragmentation adversely impacts pollinator species, and has a striking effect on plant seed set, particularly those species dependent on particular pollinator species ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "author" : [ { "dropping-particle" : "", "family" : "Donaldson", "given" : "John", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "N\u00e4nni", "given" : "Ingrid", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Zachariades", "given" : "Costas", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Kemper", "given" : "Jessica", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Conservation Biology", "id" : "ITEM-1", "issue" : "5", "issued" : { "date-parts" : [ [ "2002" ] ] }, "page" : "1267-1276", "title" : "Effects of habitat fragmentation on pollinator diversity and plant reproductive success in Renosterveld shrublands of South Africa", "type" : "article-journal", "volume" : "16" }, "uris" : [ "" ] }, { "id" : "ITEM-2", "itemData" : { "DOI" : "10.1890/06-1383.1", "ISBN" : "0012-9658", "ISSN" : "00129658", "PMID" : "17645022", "abstract" : "A suspected global decline in pollinators has heightened interest in their ecological significance. In a worst-case scenario, the decline of generalist pollinators is predicted to trigger cascades of linked declines among the multiple specialist plant species to which they are linked, but this has not been documented. I studied a portion of a pollination web involving a generalist pollinator, the oil-collecting bee Rediviva peringueyi, and a community of oil-secreting plants. Across 27 established conservation areas located in the Cape Floral Region, I found substantial variation in the bees' occurrence in relation to soil type and the successional stage of the vegetation. Anthropogenic declines were detectable against this background of naturally occurring variation: R. peringueyi was absent from small conservation areas (<385 ha) in an urban matrix. In the absence of the bee, seed set failed in six specialist plant species that are pollinated only by R. peringueyi but remained high in a pollination generalist, which had replacement pollinators. The findings are consistent with theoretical predictions of the importance of generalist pollinators in maintaining the structure of pollination webs. [PUBLICATION ABSTRACT];A suspected global decline in pollinators has heightened interest in their ecological significance. In a worst-case scenario, the decline of generalist pollinators is predicted to trigger cascades of linked declines among the multiple specialist plant species to which they are linked, but this has not been documented. I studied a portion of a pollination web involving a generalist pollinator, the oil-collecting bee Rediviva peringueyi, and a community of oil-secreting plants. Across 27 established conservation areas located in the Cape Floral Region, I found substantial variation in the bees' occurrence in relation to soil type and the successional stage of the vegetation. Anthropogenic declines were detectable against this background of naturally occurring variation: R. peringueyi was absent from small conservation areas (<385 ha) in an urban matrix. In the absence of the bee, seed set failed in six specialist plant species that are pollinated only by R. peringueyi but remained high in a pollination generalist, which had replacement pollinators. The findings are consistent with theoretical predictions of the importance of generalist pollinators in maintaining the structure of pollination webs.;A suspected global decline in pollinators has \u2026", "author" : [ { "dropping-particle" : "", "family" : "Pauw", "given" : "Anton", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Ecology", "id" : "ITEM-2", "issue" : "7", "issued" : { "date-parts" : [ [ "2007" ] ] }, "page" : "1759-1769", "title" : "Collapse of a pollination web in small conservation areas", "type" : "article-journal", "volume" : "88" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Donaldson et al. 2002; Pauw 2007)", "plainTextFormattedCitation" : "(Donaldson et al. 2002; Pauw 2007)", "previouslyFormattedCitation" : "(Donaldson et al. 2002; Pauw 2007)" }, "properties" : { }, "schema" : "" }(Donaldson et al. 2002; Pauw 2007). Very few data sets exist to enable comparison of current with historical pollination rates. An elegant study comparing century-old herbarium specimens with more current specimens in highly fragmented habitat in an urban matrix found the rate of flower visitation to the orchid Pterygodium catholicum had declined significantly post 1950 and was associated with a decline in abundance of this and other non-clonal species ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1111/j.1600-0706.2010.19039.x", "ISBN" : "0030-1299", "ISSN" : "00301299", "abstract" : "Widespread reports of low pollination rates suggest a recent anthropogenic decline in pollination that could threaten natural and agricultural ecosystems. Nevertheless, unequivocal evidence for a decline in pollination over time has remained elusive because it was not possible to determine historical pollination rates. Here we demonstrate a widely applicable method for reconstructing historical pollination rates, thus allowing comparison with contemporary rates from the same sites. We focused on the relationship between the oil-collecting bee Rediviva peringueyi (Melittidae) and the guild of oil-secreting orchid species (Coryciinae) that depends on it for pollination. The guild is distributed across the highly transformed and fragmented lowlands of the Cape Region of South Africa. We show that rehydrated herbarium specimens of Pterygodium catholicum, the most abundant member of the guild, contain a record of past pollinator activity in the form of pollinarium removal rates. Analysis of a pollination time series showed a recent decline in pollination on Signal Hill, a small urban conservation area. The same herbaria contain historical species occurrence data. We analyzed this data and found that there has been a contemporaneous shift in orchid guild composition in urban areas due to the local extirpation of the non-clonal species, consistent with their greater dependence on seeds and pollination for population persistence.", "author" : [ { "dropping-particle" : "", "family" : "Pauw", "given" : "Anton", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Hawkins", "given" : "Julie A.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Oikos", "id" : "ITEM-1", "issue" : "3", "issued" : { "date-parts" : [ [ "2011" ] ] }, "page" : "344-349", "title" : "Reconstruction of historical pollination rates reveals linked declines of pollinators and plants", "type" : "article-journal", "volume" : "120" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Pauw and Hawkins 2011)", "plainTextFormattedCitation" : "(Pauw and Hawkins 2011)", "previouslyFormattedCitation" : "(Pauw and Hawkins 2011)" }, "properties" : { }, "schema" : "" }(Pauw and Hawkins 2011). Plant-pollinator networks: Plant-pollinator networks confirm high specialization in some systems, e.g., the Cape Floristic Region ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1111/jbi.12453", "ISBN" : "1365-2699", "ISSN" : "13652699", "PMID" : "22752187", "abstract" : "We aimed to produce the first complete pollination network for Africa to test (1) whether South African plants are unusually specialized in their interactions with pollinators, and (2) whether the South African data conform with global patterns of specialization.\\n\\n\\nLocation\\n\\nCederberg, Cape Floristic Region, South Africa (32\u00b004\u203231.52\u2033 S, 19\u00b004\u2032 48.42\u2033 E; elevation 320 m).\\n\\n\\nMethods\\n\\nWe sampled all plant\u2013pollinator interactions within a 1-ha plot to assemble a network of 62 plant species linked to 217 pollinators species by 10,314 visits. We calculated the standardized Kullback\u2013Leibler distance (d\u2032) as an estimate of plant and animal specialization, and standardized two-dimensional Shannon entropy (\u0394H2\u2032) as an estimate of network-wide specialization. We compared these metrics with those calculated for 58 other networks from across the world.\\n\\n\\nResults\\n\\nIn a global context, the South African plant species had an unusually high number of interaction partners (mean = 6.32) while the animal species had unusually few (mean = 1.81). Animal diversity was high relative to plant diversity (network asymmetry = 0.56). Nevertheless, the South African plants, pollinators and network overall were more specialized than any previously studied community (weighted mean d\u2032 plants = 0.824 and animals = 0.807, community \u0394H2\u2032 = 0.834), suggesting functional specialization. Overall, specialization was found to increase sharply with latitude in the Southern Hemisphere, whereas no relationship was found in the Northern Hemisphere.\\n\\n\\nMain conclusions\\n\\nThe findings that South African plants have a high diversity of pollinators and that specialization of pollination networks increases with latitude in the Southern Hemisphere only are in contradiction to expectations derived from earlier literature. Long-term climatic stability in the Southern Hemisphere might have allowed phenotypic and functional specialization to manifest and persist.\\n", "author" : [ { "dropping-particle" : "", "family" : "Pauw", "given" : "Anton", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Stanway", "given" : "Rosanne", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Journal of Biogeography", "id" : "ITEM-1", "issue" : "4", "issued" : { "date-parts" : [ [ "2015" ] ] }, "page" : "652-661", "title" : "Unrivalled specialization in a pollination network from South Africa reveals that specialization increases with latitude only in the Southern Hemisphere", "type" : "article-journal", "volume" : "42" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Pauw and Stanway 2015)", "plainTextFormattedCitation" : "(Pauw and Stanway 2015)", "previouslyFormattedCitation" : "(Pauw and Stanway 2015)" }, "properties" : { }, "schema" : "" }(Pauw and Stanway 2015). At various sites in Africa, flower visitor network studies have confirmed the value of natural vegetation to agriculture in supporting agricultural pollinators ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1016/j.biocon.2010.03.036", "ISSN" : "00063207", "author" : [ { "dropping-particle" : "", "family" : "Hagen", "given" : "Melanie", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Kraemer", "given" : "Manfred", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Biological Conservation", "id" : "ITEM-1", "issue" : "7", "issued" : { "date-parts" : [ [ "2010", "7" ] ] }, "page" : "1654-1663", "publisher" : "Elsevier Ltd", "title" : "Agricultural surroundings support flower\u2013visitor networks in an Afrotropical rain forest", "type" : "article-journal", "volume" : "143" }, "uris" : [ "" ] }, { "id" : "ITEM-2", "itemData" : { "DOI" : "10.1016/j.agee.2017.11.002", "ISSN" : "01678809", "abstract" : "As the Anthropocene advances, understanding the complex web of interactions between species has become a central theme in the maintenance of biodiversity, ecosystem functions, and agricultural systems. Plant-flower visitor networks yield insights into how natural vegetation supports crop pollination. Although crops themselves also support pollinators, the importance of spillover of flower-visiting pollinators from natural vegetation into croplands is increasingly appreciated. Natural vegetation not only provides forage and nesting sites, but can also support crop flower visitors when the crop is not flowering. We evaluated indirect effects between mango (the dominant tropical fruit crop globally) and wild plant species in neighbouring vegetation, and the factors determining these indirect effects, by constructing flower visitor networks. We constructed these networks for transects that included mango fields and neighbouring natural vegetation in north-eastern South Africa. Surveys were conducted before, during and after mango flowering, to allow evaluation of the importance of pollinator support when the crop was not in flower. Network analysis showed that potential indirect effects of other plant species on mango increased with flower abundance of those species, although this increase was less marked for species growing in natural vegetation. The cumulative (total, i.e. indirect effects summed) effect of natural vegetation on mango flower visitation was greater both during mango flowering and when it was not flowering. This is likely because of the greater plant diversity in natural systems, and because the combination of these species provided flowers over a protracted period. These positive indirect effects among plants flowering over extended periods of time have to date rarely been considered in crop pollination studies. Given the rapid expansion of high-intensity, high-yield monoculture plantings, such effects warrant further investigation.", "author" : [ { "dropping-particle" : "", "family" : "Simba", "given" : "Lavhelesani D.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Foord", "given" : "Stefan H.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Th\u00e9bault", "given" : "Elisa", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Veen", "given" : "F.J.Frank", "non-dropping-particle" : "van", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Joseph", "given" : "Grant S.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Seymour", "given" : "Colleen L.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Agriculture, Ecosystems & Environment", "id" : "ITEM-2", "issue" : "October 2017", "issued" : { "date-parts" : [ [ "2018" ] ] }, "page" : "148-156", "publisher" : "Elsevier", "title" : "Indirect interactions between crops and natural vegetation through flower visitors: the importance of temporal as well as spatial spillover", "type" : "article-journal", "volume" : "253" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Hagen and Kraemer 2010; Simba et al. 2018)", "plainTextFormattedCitation" : "(Hagen and Kraemer 2010; Simba et al. 2018)", "previouslyFormattedCitation" : "(Hagen and Kraemer 2010; Simba et al. 2018)" }, "properties" : { }, "schema" : "" }(Hagen and Kraemer 2010; Simba et al. 2018) and that alien invasion in grassland fragments can reduce modularity of networks (Hansen et al. 2018). Within grasslands and savannas in Kenya and South Africa, hundreds of long-tubed flowered species have become adapted for pollination by a single abundant species, the convolvulus hawkmoth, Agrius convolvuli ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1111/1365-2435.12753", "ISSN" : "13652435", "abstract" : "1.Proboscis length has been proposed as a key dimension of plant pollination niches, but this niche space has not previously been explored at regional and global scales for any pollination system. Hawkmoths are ideal organisms for exploring pollinator niches as they are important pollinators in most of the biodiverse regions of the earth and vary greatly in proboscis length, with some species having the longest proboscides of all insects. 2.Using datasets for nine biogeographical regions spanning the Old and New World, we ask whether it is possible to identify distinct hawkmoth pollination niches based on the frequency distribution of proboscis length, and whether these niches are reflected in the depths of flowers that are pollinated by hawkmoths. We also investigate the levels of specialization in hawkmoth pollination systems at the regional and community level using data from interaction network studies. 3.We found that most regional hawkmoth assemblages have bimodal or multimodal distributions of proboscis length, and that these are matched by similar distributions of floral tube lengths. Hawkmoths, particularly those with longer proboscides, are polyphagous and at the network level show foraging specialization equivalent to or less than that of bees and hummingbirds. In the case of plants, shorter-tubed flowers are usually visited by numerous hawkmoth species, while those that are longer-tubed tend to exclude shorter-proboscid hawkmoths and thus become ecologically specialized on longer-proboscid hawkmoth species. Longer-tubed flowers tend to have greater nectar rewards and this promotes short-term constancy by long-proboscid hawkmoths. 4.Our results show that pollinator proboscis length is a key niche axis for plants and can account for patterns of evolution in functional traits such as floral tube length and nectar volume. We also highlight a paradoxical trend for nectar resource niche breadth to increase according to proboscis length of pollinators, while pollinator niche breadth decreases according to the tube length of flowers. This article is protected by copyright. All rights reserved.", "author" : [ { "dropping-particle" : "", "family" : "Johnson", "given" : "Steven D.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Mor\u00e9", "given" : "Marcela", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Amorim", "given" : "Felipe W.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Haber", "given" : "William A.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Frankie", "given" : "Gordon W.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Stanley", "given" : "Dara A.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Cocucci", "given" : "Andrea A.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Raguso", "given" : "Robert A.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Functional Ecology", "id" : "ITEM-1", "issue" : "1", "issued" : { "date-parts" : [ [ "2017" ] ] }, "page" : "101-115", "title" : "The long and the short of it: a global analysis of hawkmoth pollination niches and interaction networks", "type" : "article-journal", "volume" : "31" }, "uris" : [ "" ] }, { "id" : "ITEM-2", "itemData" : { "DOI" : "10.1093/aob/mcv137", "author" : [ { "dropping-particle" : "", "family" : "Johnson", "given" : "Steven D", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Raguso", "given" : "Robert A", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Annals of Botany", "id" : "ITEM-2", "issue" : "January", "issued" : { "date-parts" : [ [ "2016" ] ] }, "page" : "25-36", "title" : "The long-tongued hawkmoth pollinator niche for native and invasive plants in Africa", "type" : "article-journal", "volume" : "117" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Johnson and Raguso 2016; Johnson et al. 2017)", "plainTextFormattedCitation" : "(Johnson and Raguso 2016; Johnson et al. 2017)", "previouslyFormattedCitation" : "(Johnson and Raguso 2016; Johnson et al. 2017)" }, "properties" : { }, "schema" : "" }(Johnson and Raguso 2016; Johnson et al. 2017). Reliance on a single species of pollinator is potentially risky in the face of global change. Around the globe, anthropogenic disturbance has been found to simplify pollination networks, and Africa is no exception. Pollination networks for heathland habitats in Madagascar in which hand-weeding of invasive species had helped restore native flora over 20 years had almost twice as many flowers as were found at an unrestored site, and a plant-pollinator web with a visitation rate by flower visitors about 1.8?times that of the unrestored site, suggesting far greater network complexity at the restored site ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1016/j.ppees.2009.04.001", "ISBN" : "1433-8319", "ISSN" : "14338319", "abstract" : "Pollination webs have recently deepened our understanding of complex ecosystem functions and the susceptibility of biotic networks to anthropogenic disturbances. Extensive mutualistic networks from tropical species-rich communities, however, are extremely scarce. We present fully quantitative pollination webs of two plant-pollinator communities of natural heathland sites, one of which was in the process of being restored, on the oceanic island of Mauritius. The web interaction data cover a full flowering season from September 2003 to March 2004 and include all flowering plant and their pollinator species. Pollination webs at both sites were dominated by a few super-abundant, disproportionately well-connected species, and many rare and specialised species. The webs differed greatly in size, reflecting higher plant and pollinator species richness and abundance at the restored site. About one fifth of plant species at the smaller community received <3 visits. The main pollinators were insects from diverse taxonomic groups, while the few vertebrate pollinator species were abundant and highly linked. The difference in plant community composition between sites appeared to strongly affect the associated pollinator community and interactions with native plant species. Low visitation rate to introduced plant species suggested little indirect competition for pollinators with native plant species. Overall, our results indicated that the community structure was highly complex in comparison to temperate heathland communities. We discuss the observed differences in plant linkage and pollinator diversity and abundance between the sites with respect to habitat restoration management and its influence on pollination web structure and complexity. For habitat restoration to be successful in the long term, practitioners should aim to maintain structural diversity to support a species-rich and abundant pollinator assemblage which ensures native plant reproduction. \u00a9 2009 R\u00fcbel Foundation, ETH Z\u00fcrich.", "author" : [ { "dropping-particle" : "", "family" : "Kaiser-Bunbury", "given" : "Christopher N.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Memmott", "given" : "Jane", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "M\u00fcller", "given" : "Christine B.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Perspectives in Plant Ecology, Evolution and Systematics", "id" : "ITEM-1", "issue" : "4", "issued" : { "date-parts" : [ [ "2009" ] ] }, "page" : "241-254", "title" : "Community structure of pollination webs of Mauritian heathland habitats", "type" : "article-journal", "volume" : "11" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Kaiser-Bunbury et al. 2009)", "plainTextFormattedCitation" : "(Kaiser-Bunbury et al. 2009)", "previouslyFormattedCitation" : "(Kaiser-Bunbury et al. 2009)" }, "properties" : { }, "schema" : "" }(Kaiser-Bunbury et al. 2009). Environmentally friendly agricultural practices have been found to reduce or even circumvent network homogenization ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1007/s10841-014-9659-z", "ISSN" : "1366638X", "abstract" : "Plant and animal communities, as well as their interaction networks in agricultural landscapes, face threats of biotic homogenization due mostly to intensive man- agement and cropland expansion. It is unclear whether agri-environmental schemes that promote environmentally friendly farming approaches can reduce the effects of these threats which cause reduction in regional (beta) diversity. Here, we examined biotic homogenization of insect\u2013flower interactions in vineyards managed under agri-environ- mental schemes in the Cape Floristic Region (CFR). The interaction networks studied are of significant conservation value in the fragmented CFR agricultural landscape. Assessment was done using permutational distance-based test for homogeneity of multivariate dispersion to deter- mine whether vineyards contributed to loss of diversity across the landscape through homogenization of their insect\u2013flower interaction networks and flower visitor community. Vineyards did not show significant homoge- nization of interaction networks and flower-visitor com- munity when compared to natural sites. Organic viticulture, integrated vineyard management and on-going protection of natural vegetation close to vineyards, as practiced in the CFR, are possibly contributing to the reduction in biotic homogenization observed here. Further vineyard expansion must however be prevented to avoid future biotic losses. These measures should be supported by all stakeholders in the conservation sector to achieve wine production while at the same time conserving the natural complement of biodiversity.", "author" : [ { "dropping-particle" : "", "family" : "Kehinde", "given" : "Temitope", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Samways", "given" : "Michael J.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Journal of Insect Conservation", "id" : "ITEM-1", "issue" : "3", "issued" : { "date-parts" : [ [ "2014" ] ] }, "page" : "469-477", "title" : "Effects of vineyard management on biotic homogenization of insect-flower interaction networks in the Cape Floristic Region biodiversity hotspot", "type" : "article-journal", "volume" : "18" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Kehinde and Samways 2014)", "plainTextFormattedCitation" : "(Kehinde and Samways 2014)", "previouslyFormattedCitation" : "(Kehinde and Samways 2014)" }, "properties" : { }, "schema" : "" }(Kehinde and Samways 2014). 3.2.2 Asian and Pacific regionHabitats and biomes vulnerable to pollinator declines Tropical dry evergreen forests (TDEF) are a unique forest type found along the east coast of India. They mostly occur as small isolated fragments of varying sizes (0.5 to ≈10 ha) and are considered as endangered forests types in peninsular India. Nayak and Davidar (2010) studied the reproductive biology of the woody species of this forest. Of the 14 woody species found in these forests, four species were self-incompatible and six species were self-compatible. The majority of plants species (85%) had a generalized pollination system, receiving visits from diverse insects, such as social bees, solitary bees, wasps, moths, and ?ies, of which Apis cerana, Apis dorsata, Braunsapis picitarius and Trigona sp. seemed to be the important pollinators. Two plant species, namely Capparis brevispina and C. zeylanica, had butter?ies and birds, respectively, as their main pollinators. Selwyn and Parthasarathy (2006) reported bees to be the most important pollinators in this type of forest.In a long-term study spanning 10 years Devy and Davidar (2003) recorded the pollination systems of 86 tree species (80% of all the arborescent trees) in a mid-elevation wet evergreen forest in the Indian Western Ghats, a region rich in endemic flora and a biodiversity hotspot. Approximately 75% of these species were specialized to a single pollinator group such as bee, beetle, or moth, revealing the vulnerability of the reproductive system.Trends and status of pollinators and pollinationPresent status and temporal changes in pollinators: Only one species of leafcutter (Megachilid) bees from the entire Asia-Pacific region (Megachile pluto) from Indonesia has a mention in the IUCN Red data list (marked as vulnerable). In comparison, butterflies of this region are relatively better assessed by IUCN. Of 270 species of butterflies that have been reported in IUCN Red Data list, 3?species have been reported to be Critically Endangered, 21 species to be Endangered, 30 species to be Near Threatened and 42 species to be vulnerable. However, nothing is known about the status of thousands of other butterfly species that are reported from the region.As part of an attempt to identify populations trends among pollinating insects, Smith et al. (2017) reported a decline of a number of wild pollinators in Eastern India based on farmers’ perception. Partap and Verma (2000) observed declines of native populations of A. cerana in the Himalayan region of Nepal. Crane (1992) reported the onset of local extinctions of A. cerana in the hilly areas of Bhutan, Afghanistan, Bangladesh, China, Myanmar, Pakistan and to some extent in India. A study in Japan reported disappearance of endemic small bees from an archipelago due to introduced lizard predation (Abe 2006). In another study, Xiong et al. (2013) reported pollinator scarcity to be the reason for delayed selfing of Himalayan mayapple (Podophyllum hexandrum) in China. But apart from these few studies no other assessment reporting any temporal change in wild pollinator species populations is available from this region, save some general observations regarding threats to the bee fauna (Krishnan et al. 2012; Teichroew et al. 2016). The sole available study on the trend of genetic diversity change of a single species is by Nagamitsu et al. (2016) that show low genetic diversity of the Japanese subspecies of A.?cerana, A.?cerana japonica. South-west Pacific islands have been reported to have a depauperate bee fauna and an even smaller endemic bee fauna (Groom et al. 2015). However, a recent study by da Silva et al. (2016) reported current status of Braunsapis puangensis, an introduced species in Papua New Guinea, and found the species to be effectively contributing to the existing plant species in the island and therefore seeming to have a positive impact. Lee et al. (2016) reported on the diversity of the stingless bees (Meliponinae) for the first time from Cambodia and Laos. Wild invertebrate pollinators: Basu et al. (2016) found areas with more natural vegetation or forested areas to have greater bee diversity in a region adjacent to the Eastern Himalayan biodiversity hotspot. In another study, Thomas et al. (2009) reported wet forests of the Western Ghats to have a greater diversity of social bees than relatively degraded and drier forest sites. Bee abundance, particularly among Apidae, was greater in large primary forests than in degraded forests in Malaysia and Singapore (Liow et al. 2001). In a changing tropical landscape in southern Yunnan, south-western China, wild bee diversity was reported to be significantly greater in primary forests (Meng et al. 2012), although the same study reported hoverfly diversity to be higher in early successional forests than in the primary forests. Plantations with greater tree diversity have been reported to host higher nest densities of honeybees in Sumatra (Salmah et al. 2014). Agricultural areas close to forested areas have been found to be more species diverse for bees (Krishnan et al. 2012; Klein et al. 2006; Klein et al. 2009) and wasps (Klein et al. 2006). On the other hand, the opposite trend has also been observed, where opening up of landscapes from forested areas to open land or agroforestry in Sulawesi, Indonesia, increased the diversity of bees due to greater availability of bee-associated herbs in open areas (Hoehn et al. 2010). Managed bees - Apis mellifera: the European honeybee and A. cerana are the two major managed bees in the Asia-Pacific region, apart from Trigona spp. that are managed for honey production in some parts of the region. Aizen et al. (2009a) reported an overall rise in the global stock of managed honeybees, but apart from China, which followed the trend, there was no specific mention of other countries in the Asia-Pacific region in the report. Kohsaka et al. (2017) reports declines in honey production by managed bees in Japan and the Republic of Korea, although the same study reports a gradual increase in numbers of beekeepers and bee colonies in Japan in recent years. According to the same study, managed colonies of A. cerana have declined significantly both in the Republic of Korea and Japan. Xie (2011) reported a nearly 3-fold increase in managed honey colonies and honey production in China during the past 50 years. However, Chen et al. (2017) reported A. cerana colony losses in China. Similar colony losses were also reported from Japan for A. mellifera (Gutierrez 2009; Taniguchi 2012). An overall increase in beekeeping has been reported in Malaysia (Ismail 2016) and the practice of beekeeping with stingless bees (Trigona itama and T. thoracica) has also been reported to be on the rise (Ismail 2016). Melipone bee culture has also been reported to be on the rise in Thailand (Chuttong et al. 2015). Vertebrate pollinators: Pteropus hypomelanus, a nectarivorous bat known as a pollinator of durian (Durio zibethinus) in Malaysia has been reported to be locally endangered (Aziz et al. 2017). Among other reports apart from population trends include specific associations of bat pollinators with Parkia spp. in Thailand (Bumrungsri et al. 2009) and Mucuna sp. in China (Kobayashi et al. 2016). Kobayashi et al. (2016) also reported Mucuna pollination by squirrels in Taiwan. Japanese macaque (Macaca fuscata) and Japanese marten (Martes melampus) have been reported to be the effective pollinators of Mucuna macrocarpa found in Japan (Kobayashi et al. 2015). As reported in Devy and Davidar (2003) birds seemed to play an important role in pollinating the epiphytic plants belonging to Loranthaceae and many ground herbs in mid elevation wet evergreen forests in the Indian Western Ghats. A fruit bat, Eonycteris spelaea, has been identified as the legitimate pollinator of a late-successional tree, Oroxylum indicum (Bignoniaceae), in Thailand (Srithongchuay et al. 2008). Yoshikawa and Isagi (2014) reported recording 24 terrestrial bird species, including three exotic bird species, as acting as pollinators in Japan. The same study reported 4 flower feeding bird species. Liu et al. (2002) reported long-tongued fruit bats (Macroglossus sobrinus) and sunbirds (Arachnothera longirostris) to be the major pollinators of Musa itinerans (Musaceae), a pioneer species in tropical rain forests of Yunnan, China.Wild plants: A rich body of information exists on pollination biology of specific wild plants from across the Asia-Pacific region. A number of studies have highlighted the pollination biology of plants of conservation concerns that attract remarkably high diversity of pollinators. A number of species of beetles and bees – Trigona sp. in particular – were reported to be potential pollinators of eight species of Amorphophalus found in the Northern Western Ghats that are endemic to this region (Punekar and Kumaran 2010). Murali (1993) reported several species of carpenter bees to be the pollinators of Casia fistula, a common understory tree found across India. Pittosporum dasycaulon, a self-incompatible rare medicinal plant found in the Indian Western Ghats, is pollinated chiefly by Apis cerana and Apis dorsata (Gopalakrishnan and Thomas 2014). Myristica dactyloides is a vulnerable swamp species found in the Western Ghats and has been reported to be pollinated by a range of insects: thysanopterans (thrips), coleopterans (beetles), halictid bees, and dipterans (syrphid and phorid flies) (Sharma and Shivanna 2011). Terminalia pallida Brandis (Combretaceae), an endemic and medicinal tree species of India is pollinated by A. dorsata and wasps (Raju et al. 2012). A recent review (Ollerton et al. 2017) has listed various Dipteran species that are responsible for pollination of Cercopagia spp. found across various countries of the Asia-Pacific region. A. dorsata and Nomia spp. seem to be the effective pollinators of Decaspermum parviflorum (Lam.) A.?J.?Scott (Myrtaceae), a cryptically dioecious plant reported from Sulawesi, Indonesia (Kevan and Lack 1985). Eomecon chionantha Hance (Papaveraceae), an endemic species in China, has been reported to be most effectively pollinated by A. cerana, Bombus atripes and Episyrphus sp. (Syrphidae: Diptera) (Xiao et al. 2016). Trillium tschonoskii Maxim. (Trilliaceae), a wideranging plant species reported from Japan to the Korean archipelago and Taiwan, reportedly has a diverse set of pollinating insects including Scatophagiae (Diptera), Oedemera lucidicollis (Coleoptera) and Andrena species (Hymenoptera). Gastrodia elata, a mycoheterotrophic Japanese orchid has been reported to be pollinated by a number of insects, including 20 species belonging to Dermaptera, Thysanoptera, Diptera and Lepidoptera and 10 species of bees (Sugiura et al. 2017). Sugiura (2012) reported a number of insect taxa, including 9 species of bees, 3 species of Diptera, and 1 species each of Lepidoptera and Coleoptera, to be the potential pollinators of 2 species of understory Rhododendron in secondary forests in central Japan. Reports on pollination of ecologically important plants include Raju and Rao (2016), who described Pavetta tomentosa, a keystone shrub species found in the southern Eastern Ghats forests to be pollinated most effectively by Papillinoid and Pierid butterflies and the Sphingid moths. Fiala et al. (2011) studied the pollination systems of pioneer species of Macaranga in Malaysian rain forests, and found thrips and heteropterans to be the most effective pollinators. Schima superba Gardn. et Champ. is a perennial evergreen tree valued for its eco-protection and commercial values in China. Apis cerana and two species of beetles (Protaetia brevitarsis Lewis, and Popillia mutans Newman) have been identified as the most effective pollinators of this tree (Yang et al. 2017).Pollination biology of some economically important plants outside of crops has been reported. Callistemon citrinus, an ornamental Australian plant with high nectar content, was reported to be visited by a wide array of animals, including insects, birds and squirrels. While Apis dorsata was found to be the dominant potential pollinator, sunbirds, parrots, oriental white-eye sparrow and squirrels were reported to be occasional pollinators (Chauhan et al. 2017). Deka et al. (2011) reported bumblebee (Bombus haemorrhoidalis Smith) to be the only effective pollinator of large cardamom (Amomum subulatum Roxb.) in the Western Ghats, India. Rao and Raju (2002) reported A. dorsata to be the only effective pollinator of red sanders (Pterocarpus santalinus), an endangered tree species endemic to Indian Eastern Ghats. Aquilaria spp. (Thymelaeaceae), important commercial trees in Indonesia and the principal source of gaharu, a valuable resin, were reported to be essentially dependent upon cross-pollination and were visited by 20 different insect species (Soehartono and Newton 2001). Ghazoul and McLeash (2001) reported Trigona spp. to be the sole effective pollinator of self-incompatible Shorea siamensis, an important commercial timber species found in Thailand.A number of studies also report noteworthy pollination syndromes or systems. Ruchisansakun et al. (2017) described a new and endangered species in Myanmar, Impatiens tanintharyiensis (Balsaminaceae), to have a bee pollination syndrome. Koshy et al. (2001) report bee visits in bamboo flowers in the Western Ghats in India and infer possible bee pollination. Pedicularis chamissonis, a nectarless plant from Japan, has been reported to be self-incompatible and is pollinated effectively by buzz pollinating Bombus hypocrita sapporoensis (Kawai and Kudo 2009). Plants of the genus Mucuna (Fabaceae) are vine plants that are distributed primarily in tropical and subtropical regions. Mucuna macrocarpa found in the northern limit of its distribution, in the Japanese archipelago, has been reported to be pollinated by the Japanese macaque (Macaca fuscata) and the Japanese marten (Martes melampus), which force open the flowers (Kobayashi et al. 2015). Kawai and Kudo (2009) report buzz pollination by bumblebees of the Japanese plant Pedicularis chamissonis. Plant-pollinator network: A few studies are available from this region that report plant-pollinator interaction networks. In a study conducted in a biodiverse meadow in south-western China, Fang and Huang (2016) looked at temporal network stability and found the network to be stable across years. In another study Zhang and He (2017) documented the plant-pollinator network of a subtropical forest in China. In this network, comprising 84 pollinator species and 28 plant species (9 dioecious and 19 monomorphic), plant reproductive systems seemed to influence the network structure, in that dioecious plants were reported to have more generalized pollinators. Chakraborty et al. (2016) investigated a nocturnal pollen transport network focused on hawkmoths and found the hawkmoths to predominantly associate with non-crop plants in the agrarian landscape. Yoshikawa and Isagi (2014) is the only available study reporting bird pollinator–plant network in Japan. Abe (2006) reported that domination and expansion of introduced honeybees have the potential for disruption of the native pollination network in the two main islands, and several satellite islands, of the Ogasawara Islands in Japan.3.2.3 Latin American regionHabitats and biomes vulnerable to pollinator declines Pollinator-dependent floras prevail across ecoregions in Latin America (Ollerton 2011). Intensive agriculture has been identified as the most important cause of local bee decline in this region (de Palma 2016), probably followed by invasive bees (Aizen et al. 2018). Therefore, the biomes likely to be experiencing the highest rates of disruptions of plant-pollinator interactions are those undergoing the highest destruction rates, for instance due to soybean expansion (e.g. see Altieri and Pengue 2006). These include the subtropical Chaco forest, the Cerrado savannah, the Pantanal wetland, and the Amazonian forest (e.g. Fearnside 2001; Grau et al. 2005; Pacheco 2006). Increasing soybean cultivation has also impacted long-time highly modified biomes like the Pampas grasslands, where much agricultural diversity has been lost due to the increasing dominance of this crop (Aizen et al. 2009b). Another highly menaced biome rich in plant-pollinator mutualisms is the Atlantic forest (Ribeiro et al. 2009) of which only 29% of its original forest cover remains. The extreme fragmentation of this biome has implied a differential loss of plant species with relatively specialized pollination and sexual systems that only survive in the interior of large remnants (Lopes et al. 2009). Impacts of extensive deforestation of cloud forests along the Andes and the Mesoamerican mountains (e.g. Dirzo and Garcia 1992) as well as destruction and degradation of high-altitude Paramo vegetation (e.g. Podwojewski et al. 2002) on plant-pollinator interactions can be predicted but require further investigation. Finally, bumblebee invasion has been seen to disrupt plant-pollinator interactions in the temperate forests of South America (Aizen et al. 2008), increasing flower damage and causing the decline of the giant Patagonian bumblebee Bombus dahlbomii (reviewed in Aizen et al. 2018; see Box 2). Bee surveys have been conducted in Brazil since the end of the 1960s and these observations became a standardized methodology to perform bee surveys and allowing comparisons between the different localities and biomes (Sagakami et al. 1967). In Brazil, Africanized honeybees (Apis mellifera scutellata) are present and well adapted to urban areas, forests borders and open vegetation. A recent study (Brown et al. 2016) compared the presence of Africanized honeybee within and outside forests across Rondonia state in Brazil, recording 187 areas inside and outside forest fragments. Their presence was significantly higher outside forest cover. These findings agree with previous studies documenting the spread of Africanized honeybees in the Amazon in their preference for deforested areas. Native bees have resisted competition with Africanized honeybees, but there are still concerns about the installation and management of Apis colonies in natural areas and reserves. On the one hand, the introduction of Africanized honeybees helped to increase the honey production in Brazil from 5,000 tons/year to 40,000 tons/year (Morais 2012). On the other hand, the impacts of competition between Africanized honeybees and native bees, their relations with plants in natural environments and impacts on the reproduction of native plants are still unclear (Silveira et al. 2002). Trends and status of pollinators and pollinationWild insect pollinators: Most of the area of the Neotropics occurs within the boundaries of Latin America. This biogeographical region hosts one of the highest species diversity worldwide, including plant and insect pollinator diversity, due to its extensive tropical biomes, abrupt climatic gradients, high landscape heterogeneity, and complex geological history (Morrone 2006; Kreft and Jetz 2007; Freitas et al. 2009). For instance, a study from just one site in Colombia reports close to 300 different bee species (Smith-Pardo and Gonzalez 2007), a figure that has not yet been surpassed by any other study on any other continent (de Palma et al. 2016). At a more continental scale, some typical boreal bee groups like the bumblebees (Bombus) are poorly represented in Latin America (Williams 1998). However, the region is extremely species-rich in highly diversified groups of tropical bees like the stingless bees (Meliponini) (Rasmussen and Cameron 2009) and the exclusively Neotropical and charismatic orchid bees (Euglossini) (Cameron 2004). Although long-term studies are needed to establish some clear trends, this biodiversity, and that of plants and pollinators in particular, is threatened by a combination of large-scale drivers, including land clearing and conversion to cattle pasture and extensive monocultures, pesticide and herbicide use, climate change, and invasive bees (Bradshaw 2009; IPBES 2016a). Regarding invasive bees, two major bee invasions have been recorded in this region. In the 1950s, the African honeybee, Apis mellifera scutellata, was introduced into Brazil to produce colonies more resistant to tropical conditions through hybridization with European subspecies. However, the Africanized honeybee rapidly escaped confinement and in less than 50 years invaded most of tropical and subtropical America, from central Argentina to the southern United States (Moritz et al. 2005). Nowadays the Africanized honeybee dominates most flower insect-visiting assemblages in a wide variety of biomes (reviewed in Morales et al. 2017). Recorded in more detail is the invasion of southern South America by two European bumblebees, a long-tongued species, Bombus ruderatus, and a short-tongued species, B. terrestris, introduced into Chile for crop pollination in 1982 and 1997, respectively, and the related decline of the giant Patagonian bumblebee B. dahlbomii (see Box 2). The distribution of B. terrestris now extends from Tierra del Fuego to northern Chile and probably southern Peru (reviewed in Aizen et al. 2018). Box 2. Policy coordination needed on introduced bumblebee species in South AmericaChile has allowed continuous importation of introduced bumblebees to pollinate agricultural crops. Since 1997, this policy has authorized the importation of more than a million colonies of Bombus terrestris from Europe. In?2015 alone, more than 200,000 colonies and queens were imported. Unfortunately, bumblebees are mobile and do not respect international boundaries, even those established along major geographic barriers. As a consequence, this introduced species has spread widely in Chile and Argentina, and it is now on the verge of entering Bolivia and Peru. The invasion of Argentina across the Andes, and its unintended consequences, has occurred despite Argentina having banned importation of non-native bumblebees (Aizen et al. 2018). The most serious biological impact of this invasion is the decline of Bombus dahlbomii, the only native bumblebee in southern South America and one of the world’s largest bumblebees (Figure 5). The alien invaders, Bombus ruderatus, another European bumblebee that was brought from New Zealand to Chile in 1982 and 1983, and especially Bombus terrestris, are potent competitors and carry foreign bee diseases (Arbetman et al. 2013; Schmid-Hempel et al. 2014). As they spread, Bombus dahlbomii disappeared from much of Chile and Argentina (Morales et al. 2013; Aizen et al. 2018). The demise of Bombus dahlbomii is so severe that it is now recognized in Chile and internationally as an endangered species (; Morales et al. 2016). The invasion of Bombus terrestris has also caused detrimental effects on native and crop plants. To access nectar this bee damages flowers of many plant species (nectar robbing), reducing nectar for other flower visitors but often not pollinating flowers effectively (Combs 2011). Nectar robbing and other flower damage caused by Bombus terrestris in commercial raspberry fields reduces fruit quality and might compromise honey production by honeybees (Sáez et al. 2014, 2017). Invasion by Bombus terrestris also promotes the spread of alien plants, which compete with native species (Morales et al. 2014). For example, in Argentina pollination by Bombus?terrestris increases seed production and establishment of scotch broom, a pernicious plant invader. The environmental costs of this invasion should alert governments about the consequences of importing bumblebees or any other pollinator. Despite these costs, Chile still allows unabated importation of this introduced bumblebee. A retrospective lesson of the Bombus terrestris case is that coordinated risk assessment and cautious implementation are essential components of regional and global policy development to avoid transnational species invasions. In particular, policies concerning the importation of potentially invasive species must be established regionally among neighbouring countries with suitable habitat. Unilateral investments and efforts will be futile if the countries involved adopt conflicting policies. The South American example also points to the need for stricter international regulations of the bumblebee trade, regulations that should involve not only the importing but also the exporting countries.54038534290Native bumblebee B. dahlbomiiFlowers of Alstroemeria aureaNative bumblebee B. dahlbomiiFlowers of Alstroemeria aureaFigure 5. Visitation to flowers of Alstroemeria aurea changes over time amongst one native bumblebee (B.?dahlbomii) and two introduced bumblebees (B. ruderatus and B. terrestis). Source: The graphic is reproduced from Morales et al. (2013).Vertebrate pollinators: The most diversified and emblematic group of vertebrate pollinators in Latin America are the hummingbirds (family Trochilidae), which include about 240 species of relatively specialized pollinators (Bleiweiss 1998), followed by the New World glossophagine bats (family Phyllostomidae), which include close to 40 nectarivorous species (Fleming 2009). Although a comprehensive database to evaluate invertebrate pollinator decline is still missing for almost all Latin America, it is estimated that 12 and 8% of the vertebrate pollinator fauna for South America and Mesoamerica, respectively, are threatened with extinction (Aslan et al. 2013). This list includes several species of hummingbirds, whose decline could cause the demographic collapse of many plant species that coevolved with them (Martin-González et al. 2015). A list of vertebrate pollinators in Brazil was published by Buzato et al. (2012), who registered 338 species of effective pollinators, distributed in 25?families and 135 genera. Among them were 84 species of hummingbirds, 48 species of bats (Phyllostomidae), 54 species of non-flying mammals, 111 species of passeriform birds, and 39 species of non-passeriform birds. Most of them (65%) were in forests. There were also 2 reptile species that were pollinators. The Atlantic rainforest presented a higher number of plant-vertebrate pollinator interactions.Managed pollinators: Despite the introduction of bee species, there has been a recent trend in Latin America to rear native bee species for commercial purposes. This is case for several species of stingless bees for honey production and/or pollination services in Brazil, Paraguay, Bolivia, Peru, Venezuela, Costa Rica, and Mexico (Cortopassi-Laurino et al. 2006). Also, several species of large bees have started to be reared to provide pollination services for specific crops. This includes Bombus epiphiatus in Mexico (Vergara and Fonseca-Buendía 2012) and Bombus atratus in Argentina and Colombia mostly for greenhouse crops (Velozo 2013; Cruz et al. 2017), and solitary bees of the genera Xylocopa and Centris for pollination of passion fruit and acerola in Brazil (Freitas and Oliveira Filho 2003; Oliveira and Schlindwein 2009; Junqueira et al. 2013).Managed pollinators: the introduction of Apis species in mangrovesThe introduction of Apis species in mangroves to produce honey and bee bread has been explored in many countries such as India, the United States, China, and Cuba (Pi?eiro 1989; Krishnamurthy 1990; Yao et al. 2006; Singh and Kar 2011). Although mangrove vegetation is present in a considerable area of Brazil, covering 13,000 km2 of the Brazilian coast from North to South (Spalding et al. 2010), mangrove apicultural activities have not been significantly explored yet. Assessing the potential contribution of the mangrove vegetation to apiculture as well as the impacts on the ecosystems is fundamental as apiculture in forests has the potential to be developed as a conservationist activity with many associated benefits (Luz and Barth 2012). Managed pollinators: MeliponicultureThe main social pollinators of tropical areas are the stingless bees, the Meliponini. They live in tropical and subtropical areas of the world. In Latin America, the Catalogue of Bees in the Neotropical Region (Moure et al. 2007) mentions 417 species in the Neotropics, with many others yet to be described; more than 500 species have been described worldwide (Michener 2013). They have perennial colonies and are generalists for food collection (Kleinert et al. 2013). They do not have functional stings, but can defend themselves using resin and biting, and some species produce caustic substances that burn enemies. They generally have large distribution areas and common traits that allow local management, despite their diversity in size, behaviour and preferences for resources utilization. Beekeeping with stingless bees is called meliponiculture (Nogueira-Neto 1953, 1997; Cortopassi-Laurino et al. 2006; Jaffé et al. 2016; Vit et al. 2013; Heard 2016). Meliponiculture presents a global opportunity for tropical countries, and for smallholder farmers. Stingless bees are useful pollinators for crops and also for wild fruits (Heard 1999; Slaa et al. 2006; Nunes-Silva et al. 2013; Giannini et al. 2015; Venturieri et al. 2013; Freitas et al. 2017; Campbell et al. 2018). Most of them produce a tasteful honey that is more liquid than that of honeybees. It was the first honey known and used by traditional populations in the Americas; it is used much more as medicine than as a sweetener (Cortopassi-Laurino et al. 2006).Beekeeping with stingless bees was originally seen as an indigenous activity and curiosity for many people. Mayan Indians and others in Central America have been known for keeping Melipona beecheii in natural trunks. The beekeeping of Scaptotrigona over history has also been part of the traditions coming from ancestors of indigenous communities. Practices involving stingless bees practices have been extensively documented, for instance in the Lévi-Strauss anthropological studies on Brazilian indigenous peoples and in work on the Kayapó people in the Amazon (Posey and Camargo 1985; Camargo and Posey 1990), the Guarani (Rodrigues 2006), the Enawene-Nawe (dos Santos and Antonini 2008) and the Pankararé (Costa Neto 1998; Costa Neto 1999; Castro et al. 2017). For those peoples, their holistic view considers bees as part of the ecosystem and there are no forests without bees or vice versa.?These studies showed the diverse and rich knowledge that different indigenous peoples have about bees and wasps, with more than 25 ethnospecies divided into these two groups of insects. Their traditional knowledge go beyond the taxonomic system: they consider a range of aspects which include morphologic, ethological, ecological and social characteristics (description, distribution, nest building, seasonality, dispersion, practical aspects of handling and manipulation for the extraction of products, preservation and semi-domestication of species, and the use of their products) (Rodrigues 2006; Quezada-?uan et al. 2018). Such indigenous knowledge has supported science to clarify the biology of some species, and some species of stingless bees have their popular and scientific names based on indigenous origins. For instance, Melipona mandacaia?(manda = guard, sai = pretty) describes a behaviour found in that species, which always has a guard at the hive entrance (Nogueira-Neto 1997).Another example is the observations of the Enawenê-Nawê people in the western region of Brazil. They recognize 48 species of stingless bees. They suggest a mutualism between the stingless bees (Scaptotrigona species) and the harpy eagle (Harpia harpyja). This bee is attracted to excrement and preys that remain on this bird and the bees visit its beak, nostrils and cloaca to nourish themselves (dos Santos and Antonini 2008). These observations go along with a passage in a publication of Claude Lévi-Strauss which includes the observation made by the naturalist Henry Bates suggesting that stingless bees from the Amazon obtain less of their nutrition from flowers and more of it from tree sap and from bird excrement. Meliponiculture is generally undertaken by indigenous and local communities, and particularities can be observed according to regional and traditional knowledge. For instance, when the Kayapós open natural nests to collect food, some brood, pollen and honey is left for the spirit “Bepkororoti”, and this allows recovery of the colony. The Kayapós use smoke for managing aggressive bees, such as Oxytrigona, and also use a common toxic liana (Tanaecium nocturnum, Bignoniaceae) to manage the bees, which causes bees to sleep after 1 or 2 minutes. All knowledge on bees is passed orally from generation to generation. Large-scale rearing of stingless bees is a current challenge as it must be aligned with sustainable development.Modern meliponiculture in Brazil began with Nogueira-Neto (1953, 1970, 1997), and has now spread to all continents (Vit et al. 2013). A very modern and technically developed meliponiculture has arisen recently (Menezes et al. 2013; Venturieri et al. 2013). Nests are obtained with trap nests instead of by cutting down trees (Oliveira et al. 2013), and colonies are multiplied with established beekeeping practices. Techniques to allow laboratory in vitro queen production are available (Menezes et al. 2013). Research on meliponiculture has included many experiments concerning pesticides effects on bees such as that of Rosa et al. 2016, and has supported programmes of large scale production of local bees. New developments in landscape genomics are showing how important is to recognize the diverse populations adapted to different environmental conditions (as shown in studies with Melipona subnitida in Brazil, in review).Stingless bees are very diverse in size and habits, which allows them to pollinate a large diversity of plant species. Very small bees as Plebeia minima and Aparatrigona, for instance, pollinate cupua?u (Theobroma grandiflorum), a fruit from the Amazon forest that is of great local importance (Venturieri 1997). A range of insect species visit and pollinate a?aí palm (Euterpe oleracea), currently one of the most important fruits in the Amazon (Campbell et al. 2018), with a growing commercial importance. Large bees from the Melipona genus “buzz” pollinate (a specialized form of pollination for certain crops) and are as effective as Bombus in the pollination of eggplants (Nunes-Silva et al. 2013). Their habitat tends to be forested land, and they are generalists, with roles in pollination both within and beyond agriculture. A big gap remains, however, in southern hemisphere knowledge on the breeding of these bees and their ecological importance, although their honey is appreciated and has high value in Latin America countries (Vit et al. 2013).Wild plant pollination: Pollinator dependence is high in most floras of this region, including not only floras from tropical biomes (Ollerton et al. 2011), but also floras from higher latitudes (Aizen and Ezcurra 1998) and altitudes (Arroyo et al. 1983). Characteristic of many floras of the region is the relatively high proportion of hummingbird-pollinated plant species (Stiles 1978; del Coro Arizmendi and Ornelas 1990; Aizen and Ezcurra 1998; Buzato et al. 2000). Bat-pollination can be also relatively common in some neotropical floras, encompassing species in about 160 genera across the Neotropics, twice as many genera as in the Paleotropics (Fleming et al. 2009). Even a case of rodent pollination has been documented in the Andes (Cocucci and Sersic 1998). Some relatively common plant-pollinator interactions in the Neotropics involve fragance-seeking bees, such as those existing between many orchids and male euglossine bees (Ramírez et al. 2011), and oil collecting-bees, including species in the genera Centris and Chalepogenus and plants in the genus Calceolaria and family Malpighiaceae (Ramussen and Olesen 2000). Differential loss of plant species with relatively specialized pollination and sexual systems has been documented in highly fragmented biomes like the Atlantic forest (Lopes et al. 2009) and it has been suggested that an increase in selfing could be associated with the invasion of Africanized bees (Aizen and Feinsinger 1994a,?b).Wild relatives of crops: Latin America hosts the wild germplasm of many food crops that directly or indirectly depend on pollinators for high yield (Klein et al. 2007). These crops include pumpkins, squash, potato, tomato, pepper, cacao, strawberry, quinoa, amaranth, avocado, sweet potato, a?aí, palmito, Brazil nut, guarana, passion fruit, and yuca, among others. Germplasm of these, and perhaps of hundreds of wild species with agricultural potential, persists in remnants of natural and seminatural habitats (Smith et al. 1992), and is managed by local indigenous communities in this region (e.g. Zimmerer 1991). Therefore, diverse pollinator assemblages are important to ensure not only the reproduction of wild plants in general, but also the persistence of this germplasm. Yet, perhaps with a few exceptions, the occurrence and diversity of this germplasm and its current conservation status are unknown.Plant-pollinator networks: A diversity of studies looking at changes in the structure and dynamics of plant-pollinator networks along different environmental gradients have been conducted in Latin America. Relevant findings include a loss of network connectivity along an elevation gradient in the Andes of central Chile (Ramos-Jiliberto et al. 2010) and with decreasing habitat size in a system of isolated hills in the Argentine Pampas (Sabatino et al. 2010). In this latter system, plant-pollinator interactions are non-randomly lost, the most vulnerable being those interactions characterized as specialized and rare (Aizen et al. 2012). A similar result was recently reported in a long-term study of a plant-pollinator network from the Monte desert (Chacoff et al. 2018). At larger geographical scales, higher biotic specialization with decreasing latitude has been reported in plant-hummingbird pollination webs (Dalsgaard et al. 2011), a trend that replicates a global pattern in plant-pollinator interactions (Olesen and Jordano 2002). Relatively specialized neotropical mutualisms, like those existing between Malpighiaceae flowers and their oil-collecting bees, might be highly persistent due to exhibition of more cohesive, and presumably resilient, webs than the whole plant-pollinator network in which these subwebs are immersed (Bezerra et al. 2009). A network approach has also been followed to infer patterns of coevolution between orchids and orchid bees (Euglossini) across the Neotropics, finding that orchid diversification has apparently tracked the diversification of orchid bees leading to asymmetric specialization (Rámirez et al. 2011). Analysis of the structure of plant-pollinator network from the temperate forests of the southern Andes showed that mutualism disruption can be associated with the introduction of ungulates (Vázquez and Simberloff 2003) and invasive plants and bees (Aizen et al. 2008).3.2.4 Europe, Canada, the United States, Australia and New ZealandHabitats and biomes vulnerable to pollinator declinesThe European Red List of Habitats (Janssen et al. 2016) reports the highest percentage of threatened types (categories Critically Endangered, Endangered, Vulnerable) in the European Union (EU28) was found among mires and bogs (85%), followed by grasslands (53%), heathland (29%), and scrub (14%), all of which are considered important habitats for pollinators and contain flowering plants dependent upon biotic pollination. Vogiatzakis et al. (2014) used an expert elucidation process to assign quality scores to European Corine land-use classes for wild bees; the habitats with the highest ranked quality were mixed forest, sclerophylous vegetation, natural grassland, moors and heathland. Senapathi et al. (2015) analysed land cover changes in 14 sites across in England over more than 80 years, and found significant effects on richness and composition of bee and wasp species, with changes in edge habitats between major land classes also having a key influence. Sites surrounded primarily by arable expansion showed a greater decline in species richness than sites that did not, and sites surrounded by landscapes with urban expansion lost proportionally fewer species.Koh et al. (2016) estimated the shifts in the relative abundance of wild bees between 2008 and 2013 across the United States using a spatial habitat model, national land-cover data, and expert knowledge. High likelihoods of declines were associated with areas where corn and grain cropland mostly replaced grasslands and pasture; high likelihoods of increases were associated with areas where grasslands, pastures, and corn/soy fields were converted to higher-quality habitat, such as shrublands or fallow crop fields.Data for New Zealand and Australia are largely limited to studies assessing impacts of pollinator decline on the fitness of specific plant species (e.g. reduced pollination rates as mentioned earlier) or risks to pollinators and associated habitats due to environmental change (e.g. land clearance or climate change). In Australia, ongoing land clearance across multiple habitat types threatens a wide range of animal species (Reside et al. 2017). The resulting habitat fragmentation also impacts the pollination of plants depending on the size and shape of fragments (Cunningham 2000) while pollinator abundance and distribution can also be impacted (Eby 2016). Trends and status of pollinators and pollinationWild invertebrate pollinators: Wild invertebrate pollinators in the Western European and Others Group (WEOG) region include bees, butterflies, moths, wasps, beetles and other insects. Bees are considered the most important wild pollinators through much of WEOG, with an estimated 1,965 species in Europe, 3,622 in North America (United States and Canada), and 1,687 in Australia and New Zealand (Nieto et al. 2014; Discover Life’s bee species guide and world checklist). Regional and national assessments indicate high levels of threat for some bees and butterflies. In Europe, 9% of bee species (Nieto et al. 2014) and 9% of butterfly species (van Swaay et al. 2010) are threatened and populations are declining for 37% of bees and 31% of butterflies (excluding data deficient species, which includes 57% of bees). Numbers of threatened species tend to be much higher at national levels than at regional levels, e.g., more than 50% for bees in some European countries.Many wild bees and butterflies have been declining in abundance, occurrence and diversity at local and regional scales in north-western Europe (Biesmeijer et al. 2006; Carvalheiro et al. 2013; Ollerton et al. 2014) and in North America (Cameron et al. 2011; Bartomeus et al. 2013; Burkle et al. 2013); data for New Zealand and Australia are currently insufficient to draw general conclusions.Bees (Apidae): Kerr et al. (2015) analysed long-term shifts in bumblebee species ranges in Europe and North America and found consistent trends regarding bumblebees failing to track warming through time at their northern range limits, range losses from southern range limits, and shifts to higher elevations among southern species. Some species have declined severely, such as Franklin’s bumblebee (Bombus franklini) in the western United States (Thorp 2005) and the great yellow bumblebee (Bombus distinguendus) in Europe (Bommarco et al. 2012). Butterflies and moths (Lepidoptera): The diversity and abundance of Lepidoptera species have declined in the United Kingdom (Fox 2013; Thomas et al. 2004). In North America, almost 60 species are Red Listed by the Xerces Society as Vulnerable, Imperiled or Critically Imperiled, and there is particular concern about the iconic monarch butterfly.Other invertebrates: Trends for other wild pollinator species are variable (e.g. European hoverflies, Keil et al. 2011), unknown or are only known for a small part of the species’ distribution. Managed pollinators: The main managed pollinators in Europe, North America and Australia and New Zealand are western honeybees (Apis mellifera) and bumblebees (Bombus terrestris in Europe and New Zealand, and B. impatiens in North America), although other bee species are or have been managed such as the world’s most intensively managed solitary bee Megachilerotundata used for commercial alfalfa production in USA (Pitts-Singer and Cane 2011), and Megachile, Osmia, Nomia and stingless bees (Australia only), but to a much lesser extent.FAO data show that the number of managed western honeybee hives has been increasing at the global scale over the last 50 years (IPBES 2016b); however, contrasting trends (increases, decreases, no change) are found among countries within Europe, North America and Australia/New Zealand (Figure 3). Between 2005 and 2015 there have been severe declines in some European countries (Potts et al. 2010) and seasonal colony loss is high in some European countries and in North America (Neumann and Carreck 2010).Information on current numbers of other managed pollinators traded annually is problematic because such information is often withheld by rearing companies and there is no obligation to report commercially sensitive information. However, an estimated two million Bombus colonies were traded annually across the world for pollination in 2006 (Velthuis and van Doorn 2006) and an estimated 800?million alfalfa leafcutter bees are traded commercially per year in North America (Reisen et al. 2009). While trends in western honeybees are captured in national statistics, trends at the subnational level, and for other managed pollinators, are poorly understood.Vertebrate pollinators: There are also vertebrate pollinators in North America (e.g. hummingbirds), Australia (e.g. some birds, marsupial, rodents and bats) and New Zealand (birds, one bat). There are no vertebrate pollinators reported in Europe. An IUCN Red List assessment shows that 16.5% of vertebrate pollinators are threatened with global extinction (Figure 2), with similar proportions documented for North America and Europe but higher proportions for Oceania (Aslan et al. 2013).Wild plants and plant-pollinator networks: Biesmeijer et al. (2006) found a decline since 1980 of outcrossing plant species that rely on pollinators, when compared to self-compatible or wind-pollinated plants, in Britain and the Netherlands. This decline was strongly correlated with (but not necessarily caused by) loss of bee diversity. Burkle et al. (2013) analysed changes in plant-pollinator interactions over 120 years in Illinois, USA, and found only 50% of the bee species originally recorded in the late 1800s by Charles Robertson remained; although novel interactions had arisen, the total number of interactions in the remaining network was only half that of the original. In addition, the overall network structure had become less nested, indicating that pollination is more vulnerable to future perturbations. In New Zealand, decline in local pollinator numbers has been associated with decreased cross-pollination in a number of plant species, including Dactylanthus taylorii (Cummings et al. 2014) and Sophora microphylla (Etten et al. 2015). Local extinction of bird pollinators reduced pollination, seed production, and plant density in the shrub Rhabdothamnus solandri (Gesneriaceae) on the North Island of New Zealand, but not on three nearby island bird sanctuaries where birds remain abundant (Anderson et al. 2011).A number of global meta-analyses as cited in section 3.1 above (based on considerable data from the WEOG region) indicate linkages between local declines in pollinator abundance and diversity, and decreasing wild plant pollination and seed production (Aguilar et al. 2006), noted effects of invasive plant species on visitation and reproduction of native plants (Morales and Traveset 2009), and showed the impacts on visitation rates of pollinators from habitat alteration and invasions (Montero-Casta?o and Vila 2012). In most cases, however, historical baseline data are lacking and researchers have used space-for-time substitution. Detecting historical trends in plant reproduction is difficult given the paucity of long-term studies, and many gaps remain in our understanding.IV.Status of the main drivers of shifts in pollinators, pollination and pollinator-dependent wild plants in all ecosystemsThe IPBES assessment (IPBES 2016a) highlighted some direct and indirect drivers of change that are affecting the abundance, diversity and health of pollinators. As a consequence, the negative impact on the provision of pollination services generates risks to societies and ecosystems. Indirect drivers of change include institutions and governance systems, and direct drivers includes land-use change, intensive agricultural management and pesticide use, environmental pollution, invasive alien species, pathogens, and climate change. As the IPBES assessment concluded, explicitly linking pollinator declines to individual or combinations of direct drivers is limited by data availability or complexity, yet case studies worldwide suggests that these direct drivers often affect pollinators negatively.This report considers the following drivers: Land-use change: habitat destruction, fragmentation and degradation, pollution, along with conventional intensive land management and agricultural practices.Managed pollinators, invasive alien species, pests and diseases: Impacts on native pollinators and pollination may result from alien flowering plants, introduced alien pollinators and alien predators. Wild pollinators and their pollination services might be impacted by managed pollinators in different ways, mainly through competition and spillover of diseases. Commercial management, mass breeding, transport and trade in pollinators outside their original ranges have resulted in new invasions, transmission of pathogens and parasites, and regional extinctions of native pollinator species.Pesticides: the risk to pollinators from pesticides arises through a combination of toxicity (compounds vary in toxicity to different pollinator species) and the level of exposure.Climate change: Some pollinator species have moved their ranges, altered their abundance and shifted their seasonal activities in response to observed climate change over recent decades, with impacts on their populations and overall distribution.Other drivers of disturbance: Include fire and grazing, and genetically modified organisms (GMOs).4.1 Land-use changePollinator richness generally declined with decreasing landscape heterogeneity (Andersson et al. 2013), and habitat destruction and fragmentation are likely to negatively affect pollinators ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1079/IJT20049", "ISBN" : "1742-7584", "ISSN" : "1742-7584", "abstract" : "There is now considerable evidence for disruption of plant-pollinator mutualisms in fragmented landscapes. The causes can be myriad, and vary from lack of nesting sites for key insect pollinators, to a decline in pollinator visits when plant population sizes are reduced by fragmentation. One important and well-documented consequence of disruption in pollination systems is reduced seed production in plant populations in fragments as a result of pollen-limitation. When reduced seed production, in turn, has a negative effect on seedling recruitment, populations may enter a spiral towards extinction. Some pollination systems, on the other hand, are surprisingly resilient to anthropogenic changes, and pollen flow between trees in fragments separated by several kilometres has been reported recently. Understanding how reproductive attributes of plants, such as breeding systems and specificity of pollination systems, affect the outcome of habitat fragmentation remains a key challenge.", "author" : [ { "dropping-particle" : "", "family" : "Harris", "given" : "L. Fabienne", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Johnson", "given" : "Steven D.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "International Journal of Tropical Insect Science", "id" : "ITEM-1", "issue" : "01", "issued" : { "date-parts" : [ [ "2004" ] ] }, "page" : "29-43", "title" : "The consequences of habitat fragmentation for plant\u2013pollinator mutualisms", "type" : "article-journal", "volume" : "24" }, "uris" : [ "" ] }, { "id" : "ITEM-2", "itemData" : { "author" : [ { "dropping-particle" : "", "family" : "Donaldson", "given" : "John", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "N\u00e4nni", "given" : "Ingrid", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Zachariades", "given" : "Costas", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Kemper", "given" : "Jessica", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Conservation Biology", "id" : "ITEM-2", "issue" : "5", "issued" : { "date-parts" : [ [ "2002" ] ] }, "page" : "1267-1276", "title" : "Effects of habitat fragmentation on pollinator diversity and plant reproductive success in Renosterveld shrublands of South Africa", "type" : "article-journal", "volume" : "16" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Donaldson et al. 2002; Harris and Johnson 2004)", "plainTextFormattedCitation" : "(Donaldson et al. 2002; Harris and Johnson 2004)", "previouslyFormattedCitation" : "(Donaldson et al. 2002; Harris and Johnson 2004)" }, "properties" : { }, "schema" : "" }(Donaldson et al. 2002; Harris and Johnson 2004). Areas where habitats are not completely transformed, such as with heavy livestock grazing, can also negatively impact pollinators ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1079/IJT20047", "ISSN" : "1742-7584", "abstract" : "A study was conducted to investigate whether a lack of pollinators, pollination and therefore, a shortage of fruit set of perennial plants is more likely to occur in overgrazed land than farmland without grazing pressure, as this could have considerable effects on the reproduction of certain plant species. The study was conducted at two adjacent BIOTA biodiversity observatories (<url>biota-</url>) in Namaqualand, South Africa. Individuals of certain plant species of the family of Aizoaceae were measured and flower and fruit production recorded. Malaise traps and transect walks were used to document insect diversity. Preliminary results indicate that not all plant species show reduced flower production but that fruit set is indeed compromised on overgrazed land. Insect diversity and abundance is partially reduced under heavy grazing pressure, especially in locations where the vegetation cover is low and dominated by unpalatable plant species.", "author" : [ { "dropping-particle" : "", "family" : "Mayer", "given" : "Carolin", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "International Journal of Tropical Insect Science", "id" : "ITEM-1", "issue" : "1", "issued" : { "date-parts" : [ [ "2004" ] ] }, "page" : "95-103", "title" : "Pollination services under different grazing intensities", "type" : "article-journal", "volume" : "24" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Mayer 2004)", "plainTextFormattedCitation" : "(Mayer 2004)", "previouslyFormattedCitation" : "(Mayer 2004)" }, "properties" : { }, "schema" : "" }(Mayer 2004), changing the dominant guilds ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1023/A:1014520226989", "ISBN" : "0960-3115", "ISSN" : "09603115", "PMID" : "188", "abstract" : "Species turnover of monkey beetle (Scarabaeidae: Hopliini) assemblages along disturbance and environmental gradients was examined at three sites within the arid, winter rainfall Namaqualand region of the succulent Karoo, South Africa. At each site two study plots with comparable vegetation and soils but contrasting management (grazing) histories were chosen, the disturbed sites having fewer perennial shrubs and generally more annuals and bare ground. Beetles collected using coloured pan-traps showed a consistently higher abundance in disturbed sites. Lepithrix, Denticnema and Heterochelus had higher numbers in disturbed plots, while Peritrichia numbers were lower in disturbed areas. Measures of species richness and diversity were consistently higher in the undisturbed sites. Distinctive assemblages of monkey beetles and plants occurred at each site. A high compositional turnover ($\u03b2$ diversity) was recorded for both monkey beetles and plants along a rainfall gradient; between-site $\u03b2$ diversity values ranged from 0.7 to 0.8 (out of a maximum of 1.0). Species turnover of beetles was higher between the disturbed sites along the environmental gradient than the corresponding undisturbed sites. The high monkey beetle species turnover is probably linked to the high plant species turnover, a distinctive feature of succulent Karoo landscapes. Monkey beetles are useful indicators of overgrazing disturbance in Namaqualand, as their pollinator guilds are apparently disrupted by overgrazing. A shift away from perennial and bulb pollinator guilds towards those favouring weedy annuals was observed in disturbed areas. The consequences to ecosystem processes due to the effects of disturbance on monkey beetle communities and the role of monkey beetles as indicators of disturbance is discussed, as well as the implications of disturbance on monkey beetle pollination guilds.", "author" : [ { "dropping-particle" : "", "family" : "Colville", "given" : "J.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Picker", "given" : "M. 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Although livestock grazing is not often seen as a driver of fragmentation, grazing can reduce flower availability of palatable plants, leading to changes in seed set and demography ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "DOI" : "10.1007/BF00045574", "ISBN" : "0042-3106", "ISSN" : "00423106", "PMID" : "549", "abstract" : "A three-year study involving 1300 marked shrubs of three species differing in palatability to sheep provided evidence that changes in the demographic structure of shrub populations in arid rangelands are a function of seed availability. Sheep reduced canopy size and flowering of their preferred forage species but had no effect on survivorship of seedlings or established plants during the study. Although annual turnover in all populations was low (< 6 %), abundant recent recruitment of non-forage species was observed on degraded rangeland. Natality of all three species was positively correlated with flower abundance. Mortality was correlated with natality because seedlings had a low probability of surviving their first year. Recruitment of both forage and non-forage species, appeared to be inhibited by competition and seedlings seldom survived near adult plants of the same growth form.", "author" : [ { "dropping-particle" : "", "family" : "Milton", "given" : "S. J.", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Vegetatio", "id" : "ITEM-1", "issue" : "1", "issued" : { "date-parts" : [ [ "1994" ] ] }, "page" : "17-27", "title" : "Growth, flowering and recruitment of shrubs in grazed and in protected rangeland in the arid Karoo, South Africa", "type" : "article-journal", "volume" : "111" }, "uris" : [ "" ] }, { "id" : "ITEM-2", "itemData" : { "DOI" : "10.1079/IJT20047", "ISSN" : "1742-7584", "abstract" : "A study was conducted to investigate whether a lack of pollinators, pollination and therefore, a shortage of fruit set of perennial plants is more likely to occur in overgrazed land than farmland without grazing pressure, as this could have considerable effects on the reproduction of certain plant species. The study was conducted at two adjacent BIOTA biodiversity observatories (<url>biota-</url>) in Namaqualand, South Africa. Individuals of certain plant species of the family of Aizoaceae were measured and flower and fruit production recorded. Malaise traps and transect walks were used to document insect diversity. Preliminary results indicate that not all plant species show reduced flower production but that fruit set is indeed compromised on overgrazed land. Insect diversity and abundance is partially reduced under heavy grazing pressure, especially in locations where the vegetation cover is low and dominated by unpalatable plant species.", "author" : [ { "dropping-particle" : "", "family" : "Mayer", "given" : "Carolin", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "International Journal of Tropical Insect Science", "id" : "ITEM-2", "issue" : "1", "issued" : { "date-parts" : [ [ "2004" ] ] }, "page" : "95-103", "title" : "Pollination services under different grazing intensities", "type" : "article-journal", "volume" : "24" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Milton 1994; Mayer 2004)", "plainTextFormattedCitation" : "(Milton 1994; Mayer 2004)", "previouslyFormattedCitation" : "(Milton 1994; Mayer 2004)" }, "properties" : { }, "schema" : "" }(Milton 1994; Mayer 2004).However, fallow farmland can provide resources for pollinators and be associated with greater bee diversity ADDIN CSL_CITATION { "citationItems" : [ { "id" : "ITEM-1", "itemData" : { "ISBN" : "19207603", "ISSN" : "1920-7603", "PMID" : "123197374", "abstract" : "\u2014Bees provide important pollination services that maintain native plant populations and ecosystem resilience, which is critical to the conservation of the rich and endemic biodiversity of Kaya forests along the Kenyan Coast. This study examined bee composition and floral resources from the forest core to the surrounding farmlands around Kaya Muhaka forest. In total, 755 individual bees, representing 41 species from three families were recorded: Apidae, Halictidae and Megachilidae. Overall, Apidae were the most abundant with a proportion of 76% of the total bee individuals, Halictidae at 14% and Megachilidae at 10%. Bee composition was similar between forest edge and crop fields as compared to forest core and fallow farmlands. We found a significant decrease in bee diversity with increasing distance from the forest to the surrounding farming area. A high abundance of bees was recorded in fallow farmland, which could be explained by the high abundance of floral resources in the habitat. We found floral resources richness to significantly affect bee species richness. These findings are important for understanding the effects of land use change on insect pollinators and their degree of resilience in disturbed habitats.", "author" : [ { "dropping-particle" : "", "family" : "Chiawo", "given" : "David O", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Ogol", "given" : "Callistus K P O", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Kioko", "given" : "Esther N", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Otiende", "given" : "Verrah A", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" }, { "dropping-particle" : "", "family" : "Gikungu", "given" : "Mary W", "non-dropping-particle" : "", "parse-names" : false, "suffix" : "" } ], "container-title" : "Journal of Pollination Ecology", "id" : "ITEM-1", "issue" : "6", "issued" : { "date-parts" : [ [ "2017" ] ] }, "page" : "51-59", "title" : "Bee diversity and floral resources along a disturbance gradient in Kaya Muhaka Forest and surrounding farmlands of coastal Kenya", "type" : "article-journal", "volume" : "20" }, "uris" : [ "" ] } ], "mendeley" : { "formattedCitation" : "(Chiawo et al. 2017)", "plainTextFormattedCitation" : "(Chiawo et al. 2017)", "previouslyFormattedCitation" : "(Chiawo et al. 2017)" }, "properties" : { }, "schema" : "" }(Chiawo et al. 2017) and bee species richness in wildflower strips on arable land is likely to increase with the amount of semi-natural habitats (Scheper et al. ADDIN EN.CITE <EndNote><Cite ExcludeAuth="1"><Author>Scheper</Author><Year>2015</Year><RecNum>2149</RecNum><DisplayText>(2015)</DisplayText><record><rec-number>2149</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1446148717">2149</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Scheper, Jeroen</author><author>Bommarco, Riccardo</author><author>Holzschuh, Andrea</author><author>Potts, Simon G.</author><author>Riedinger, Verena</author><author>Roberts, Stuart P. M.</author><author>Rundlof, Maj</author><author>Smith, Henrik G.</author><author>Steffan-Dewenter, Ingolf</author><author>Wickens, Jennifer B.</author><author>Wickens, Victoria J.</author><author>Kleijn, David</author></authors></contributors><titles><title>Local and landscape-level floral resources explain effects of wildflower strips on wild bees across four European countries</title><secondary-title>Journal of Applied Ecology</secondary-title></titles><periodical><full-title>Journal of Applied Ecology</full-title><abbr-1>J. Appl. Ecol.</abbr-1><abbr-2>J Appl Ecol</abbr-2></periodical><pages>1165-1175</pages><volume>52</volume><number>5</number><dates><year>2015</year><pub-dates><date>Oct</date></pub-dates></dates><isbn>0021-8901</isbn><accession-num>WOS:000361186500007</accession-num><urls><related-urls><url>&lt;Go to ISI&gt;://WOS:000361186500007</url></related-urls></urls><electronic-resource-num>10.1111/1365-2664.12479</electronic-resource-num></record></Cite></EndNote>2015). Global meta-analyses have shown how proximity to natural habitat can be important for wild pollinators, with pollinator species richness, visitation, and overall stabilization of pollination services found to decrease with isolation from natural areas PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5SaWNrZXR0czwvQXV0aG9yPjxZZWFyPjIwMDg8L1llYXI+

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ADDIN EN.CITE.DATA (Ricketts et al. 2008; Garibaldi et al. 2011; Kennedy et al. 2013). Landscape configuration can play an important role in the maintenance of diverse pollinator communities. Decreased patch size, loss of habitat area and reduced connectivity have all been identified as important drivers of species richness declines ADDIN EN.CITE <EndNote><Cite><Author>Marini</Author><Year>2014</Year><RecNum>2333</RecNum><DisplayText>(Marini<style face="italic"> et al.</style> 2014)</DisplayText><record><rec-number>2333</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1448127534">2333</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Marini, Lorenzo</author><author>Ockinger, Erik</author><author>Bergman, Karl-Olof</author><author>Jauker, Birgit</author><author>Krauss, Jochen</author><author>Kuussaari, Mikko</author><author>Poyry, Juha</author><author>Smith, Henrik G.</author><author>Steffan-Dewenter, Ingolf</author><author>Bommarco, Riccardo</author></authors></contributors><titles><title>Contrasting effects of habitat area and connectivity on evenness of pollinator communities</title><secondary-title>Ecography</secondary-title></titles><periodical><full-title>Ecography</full-title><abbr-1>Ecography</abbr-1><abbr-2>Ecography</abbr-2></periodical><pages>544-551</pages><volume>37</volume><number>6</number><dates><year>2014</year><pub-dates><date>Jun</date></pub-dates></dates><isbn>0906-7590</isbn><accession-num>WOS:000337694100004</accession-num><urls><related-urls><url>&lt;Go to ISI&gt;://WOS:000337694100004</url></related-urls></urls><electronic-resource-num>10.1111/j.1600-0587.2013.00369.x</electronic-resource-num></record></Cite></EndNote>(Marini et al. 2014). Furthermore, they negatively affect the ecological network link richness, leading to network contraction ADDIN EN.CITE <EndNote><Cite><Author>IPBES</Author><Year>2016</Year><RecNum>3119</RecNum><DisplayText>(IPBES 2016a)</DisplayText><record><rec-number>3119</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518442386">3119</key></foreign-keys><ref-type name="Report">27</ref-type><contributors><authors><author>IPBES</author></authors><secondary-authors><author>S.G. Potts</author><author>V. L. Imperatriz-Fonseca</author><author>H. T. Ngo</author></secondary-authors><tertiary-authors><author>Secretariat of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services</author></tertiary-authors></contributors><titles><title>The assessment report of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services on pollinators, pollination and food production.</title></titles><dates><year>2016</year></dates><pub-location>Bonn, Germany</pub-location><urls></urls></record></Cite></EndNote>(IPBES 2016a).While existing linear landscape elements in intensively used farmland (such as in Flanders, Belgium) may act as functional biological corridors facilitating pollen dispersal through pollinator movements ADDIN EN.CITE <EndNote><Cite><Author>Van Geert</Author><Year>2010</Year><RecNum>2337</RecNum><DisplayText>(Van Geert<style face="italic"> et al.</style> 2010)</DisplayText><record><rec-number>2337</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1448127534">2337</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Van Geert, Anja</author><author>Van Rossum, Fabienne</author><author>Triest, Ludwig</author></authors></contributors><titles><title>Do linear landscape elements in farmland act as biological corridors for pollen dispersal?</title><secondary-title>Journal of Ecology</secondary-title></titles><periodical><full-title>Journal of Ecology</full-title><abbr-1>J. Ecol.</abbr-1><abbr-2>J Ecol</abbr-2></periodical><pages>178-187</pages><volume>98</volume><number>1</number><dates><year>2010</year><pub-dates><date>Jan</date></pub-dates></dates><isbn>0022-0477</isbn><accession-num>WOS:000272657400019</accession-num><urls><related-urls><url>&lt;Go to ISI&gt;://WOS:000272657400019</url></related-urls></urls><electronic-resource-num>10.1111/j.1365-2745.2009.01600.x</electronic-resource-num></record></Cite></EndNote>(Van Geert et al. 2010), increasing wildflower patch size can lead to increases in wild bee density and result in greater seed set in wild flowers within agricultural landscapes, as found in Michigan, USA ADDIN EN.CITE <EndNote><Cite><Author>Bennett</Author><Year>2014</Year><RecNum>2332</RecNum><DisplayText>(Bennett &amp; Isaacs 2014)</DisplayText><record><rec-number>2332</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1448127534">2332</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Bennett, Ashley B.</author><author>Isaacs, Rufus</author></authors></contributors><titles><title>Landscape composition influences pollinators and pollination services in perennial biofuel plantings</title><secondary-title>Agriculture Ecosystems &amp; Environment</secondary-title></titles><periodical><full-title>Agriculture Ecosystems &amp; Environment</full-title><abbr-1>Agric. Ecosyst. Environ.</abbr-1><abbr-2>Agri. Ecosys. Env.</abbr-2></periodical><pages>1-8</pages><volume>193</volume><dates><year>2014</year><pub-dates><date>Aug 1</date></pub-dates></dates><isbn>0167-8809</isbn><accession-num>WOS:000338618400001</accession-num><urls><related-urls><url>&lt;Go to ISI&gt;://WOS:000338618400001</url></related-urls></urls><electronic-resource-num>10.1016/j.agee.2014.04.016</electronic-resource-num></record></Cite></EndNote>(Bennett and Isaacs 2014). There is also evidence from Great Britain that long-term declines in richness at local site levels may be buffered by the heterogeneity of the surrounding habitat ADDIN EN.CITE <EndNote><Cite><Author>Senapathi</Author><Year>2015</Year><RecNum>1835</RecNum><DisplayText>(Senapathi<style face="italic"> et al.</style> 2015)</DisplayText><record><rec-number>1835</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1427881949">1835</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Senapathi, Deepa</author><author>Carvalheiro, Luísa G.</author><author>Biesmeijer, Jacobus C.</author><author>Dodson, Cassie-Ann</author><author>Evans, Rebecca L.</author><author>McKerchar, Megan</author><author>Morton, R. Daniel</author><author>Moss, Ellen D.</author><author>Roberts, Stuart P. M.</author><author>Kunin, William E.</author><author>Potts, Simon G.</author></authors></contributors><titles><title>The impact of over 80 years of land cover changes on bee and wasp pollinator communities in England</title></titles><pages>20150294</pages><volume>282</volume><number>1806</number><dates><year>2015</year><pub-dates><date>2015-05-07 00:00:00</date></pub-dates></dates><work-type>Journal Article</work-type><urls><related-urls><url>;(Senapathi et al. 2015). Thus a combination of large high-quality patches and heterogeneous landscapes may help to maintain high bee species richness and communities with diverse trait composition, which might stabilize pollination services provided to both crops and wild plants on local and landscape scales ADDIN EN.CITE <EndNote><Cite><Author>Senapathi</Author><Year>2017</Year><RecNum>3189</RecNum><DisplayText>(Senapathi<style face="italic"> et al.</style> 2017)</DisplayText><record><rec-number>3189</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1519679303">3189</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Senapathi, Deepa</author><author>Goddard, Mark A.</author><author>Kunin, William E.</author><author>Baldock, Katherine C. R.</author></authors></contributors><titles><title>Landscape impacts on pollinator communities in temperate systems: evidence and knowledge gaps</title><secondary-title>Functional Ecology</secondary-title></titles><periodical><full-title>Functional Ecology</full-title><abbr-1>Funct. Ecol.</abbr-1><abbr-2>Funct Ecol</abbr-2></periodical><pages>26-37</pages><volume>31</volume><number>1</number><keywords><keyword>agri-environment</keyword><keyword>habitat characteristics</keyword><keyword>policy</keyword><keyword>pollinator conservation</keyword><keyword>spatial scales</keyword><keyword>species abundance</keyword><keyword>species richness</keyword></keywords><dates><year>2017</year></dates><isbn>1365-2435</isbn><urls><related-urls><url>;(Senapathi et al. 2017).The data on pollinator decline in Africa are scarce and only a few studies reporting on declines at a local scale are available (Pauw and Hawkins 2011). In Africa, many species of pollinators in subSaharan Africa are found in forest habitats. Deforestation continues to occur on the continent (Keenan et al. 2015). Reasons for deforestation are conversion of land for agriculture (Haines-Young 2009), and use of timber for construction and fuel (IEA 2016). Regions with less forest cover also show patterns of significant land-use change. In South Africa, grassland is often converted to commercial plantations, resulting in a loss of foraging habitat leading to pollen limitation for plant species ultimately affecting the demographic structure of plant species as shown for Brunsvigia radulosa (Ward and Johnson 2005). In Durban, South Africa, the tree Oxyanthus pyriformis?subsp.?pyriformis is pollinated exclusively by a hawkmoth. The tree occurs in a few suburban habitat fragments but is rarely visited by the hawkmoths and it shows almost complete absence of seed and fruit set, with more than a thousand-fold increase by means of hand-pollination (Johnson et al. 2004). In Asia, significant changes in landscape structure are created by oil palm plantations that cause large natural areas to be deforested. One policy response to such concerns is the pressure being applied to the buyers of these products to modify their practices to attain a sustainability certification (Carlson et al. 2018).In Latin America, deforestation is a major driver in this respect. Three of the major biomes from South America have suffered intense deforestation mainly for conventional agriculture: the Amazonia biome (with a loss of more than 20% of its forests over the past 30 years); the Cerrado biome (nearly half of the biome has been converted to pasture or cropland and only approximately 8% is formally protected by parks or indigenous reserves); and the Chaco biome (its deforestation rates are among the highest in the world, extending to an estimated 8 million ha deforested from 2000 to 2012). The Atlantic forest is recognized for its high degree of species richness and rates of endemism, but only 29% of its original forest cover remains. Moreove, the Atlantic forest biome is highly fragmented, with more than 80% of the forest patches less than 50 ha in size, revealing a serious situation. Nature reserves protect only 9% of the remaining forest and 1% of the original forest. Some specific locations of Amazonia, the Atlantic forest and the Chaco have exhibited a slow recovery over the last 10 years, as secondary forests become established (Teixeira et al. 2009; Yanai et al. 2017; Khanna et al. 2017; Noojipady et al. 2017; Fehlenbert et al. 2017). Habitat loss and reduction of connectivity for pollinators in Brazil, Argentina and Costa Rica has had documented negative effects on pollinators (e.g., Aguilar et al. 2006; Gon?alves et al. 2014; Ferreira et al. 2015; Nemésio et al. 2016; Boscolo et al. 2017; Rocha et al. 2017; Hadley et al. 2018). Social bees from the Atlantic forest of the north-east region of Brazil showed negative effects of changes in forest cover at a local scale depending on regional forest cover (<35%; Ferreira et al. 2015). In addition, the reduction of habitat quality and landscape heterogeneity can cause species loss and can reduce robustness and resilience of plant-pollinator networks (data from Brazil and Argentina; Moreira et al. 2017). Hummingbirds have also declined ca. 40-50% across the deforestation gradient in Costa Rica (Hadley et al. 2018). In Amazonia, it was shown that smaller fragments had fewer species of bats and higher levels of dominance than continuous forest, and also a well conserved vegetation structure is a good predictor of bat abundance regardless of landscape configuration (Rocha et al. 2017). Management strategies and conservation practices must integrate proper actions that consider both local and regional scales. For existing fragmented landscapes, it is important to increase forest availability at the regional scale, while also maintaining high environmental heterogeneity at the local scale (Yanai et al. 2017; Khanna et al. 2017; Noojipady et al. 2017; Fehlenberget al. 2017).Stingless bee nests in nature are in danger of depletion due to logging practices. In Malaysia (Eltz et al. 2003) and in the Brazilian Amazon (Venturieri, unpubl. data) it has been shown that logging reduces stingless bee nests and, as a consequence, native pollinators, which has implications for forest recovery or restoration. Villanueva-Gutiérrez et al. (2005) remarked that logging also reduces forest habitat that contains suitable, unoccupied nesting sites. Eltz et al. (2003) considered that the loss of pollinators occurs even if the rules for certified wood management are taken into account. Attention to the need for general pollinator conservation among the rules for forest management needs to be established.4.2 Managed pollinators, invasive alien species, pests and diseases Impacts of introduced and managed pollinatorsIn Latin America, one example is the two species of bumblebees (Bombus ruderatus and Bombus terrestris) that were introduced into continental Chile and later arrived into Argentina and also crossed to Navarino Island in southern Chile with disastrous consequences for the native bumblebee Bombus dahlbomii. Bombus terrestris has spread by some 200 km/year from Chile and had reached the Atlantic coast in Argentina in a short period of around 15 years (Torretta et al. 2006; Morales et al. 2013; Schmid-Hempel et al. 2014; Morales et al. 2017; Mallinger et al. 2017; Rendoll-Carcamo et al. 2017). These invasive species are infected by protozoan parasites that seem to spread along with the imported hosts and spread to native species (Schmid-Hempel et al. 2014). A large-scale investigation in Patagonia showed that after only 5 years post-arrival, B. terrestris had increased its populations with concurrent geographic retraction of the native B. dahlbomii (Morales et al. 2013, 2017).For some plant species (e.g. Alstroemeria aurea) invasive bumblebees have replaced B.?dahlbomii, which was the most abundant pollinator of this endemic herb few years ago (Morales et al. 2013). Stakeholders should consider the continuous evaluation of adequate densities of managed colonies for different regions, the relative resource availability for pollinators (i.e. native species and flowering crops), the health status of the managed bee colonies monitoring for pathogens and parasites, and performing baselines to evaluate declines in wild bee species.Management of stingless bees in Africa is still in its infancy (Cortopassi-Laurino et al. 2006). Management of colonies, including artificial reproduction and queen rearing, needs to be advanced in order to use natural resources in a sustainable way. A mismanagement error helped to spread the Cape honeybee, A. mellifera capensis, from its native range around the Western Cape region into the region of the adjacent subspecies A. mellifera scutellata (Greeff 1997). When moved into the range of A. mellifera scutellata, the Cape honeybee workers invade colonies, kill the resident queen and establish themselves as egg-laying workers producing female offspring (Neumann and Moritz 2002). As these bees are all essentially reproductives, there is little or no foraging in these colonies, and they soon run out of nectar and pollen reserves. These colonies then dwindle in size to only a few hundred bees, which then either die out or invade other scutellata colonies, thus repeating the cycle (Allsopp 2004). The spread of the Cape honeybee workers has been facilitated by keeping colonies at high densities, thus enhancing parasite transmission, and by frequent transportation, enhancing long-distance petition between managed bees, mainly the honeybee, and wild pollinators has been documented in several contexts. In Kenya, it has been observed that honeybees outcompete wild bees specialized on a few plant species during seasons with scarce floral resources (Martins 2004). In South Africa it has been shown that honeybees start foraging early, diminishing the pool of pollen available for dispersal by bird pollinators that start foraging at later time points (Hargreaves et al. 2010). In Mauritius honeybees compete with endemic nectarivorous birds, the grey white-eye,?Zosterops borbonicus mauritianus?Gmelin, and the olive white-eye,?Z. chloronothos?Viellot, for nectar on two endemic trees (Hansen et al. 2002).Another invasive alien species is the dwarf honeybee Apis florea, introduced via air transport from Pakistan into Khartoum, Sudan, in 1985 (Lord and Nagi 1987). Since then, this bee has spread along the river Nile and the Ethiopian highlands up to Djibouti in 2014 (Steiner 2017). A second introduction occurred in 2017 in Egypt (Shebl 2017). In its current distribution range, it is coexisting with A. mellifera and no threats have been observed. The honeybee A. mellifera does not appear to be competing over resources with the dwarf honeybee (El Shafie et al. 2002) and pathogen spillover has not been reported. Impact on the wild bee fauna of the invaded areas has not yet been documented.In Asia, the erosion of traditional knowledge systems (management of local bees, including honeybees and stingless bees), particularly in tropical countries, may contribute to local declines. The management and keeping of the Asian hive bee, Apis cerana has revolved around a number of traditional practices, such as the use of wall hives. These practices are now less and less common in the region.Impact of other invasive alien species, pests and diseases on pollinators With respect to the impacts of invasive alien species on pollinators, recent research on a global level has documented that these are spread as a consequence of the global growth in economic wealth, trade, commerce, and transport efficiency (Mack et al. 2000; Hulme 2009; Dawson et al. 2017). Invasive alien species create risks and opportunities for pollinator nutrition, reorganize species interactions to affect native pollination and community stability, and spread and select for virulent diseases (Vanbergen et al. 2018). For example, invasive alien species possessing generalized ecological traits or that are evolutionarily close to natives are readily incorporated into species networks and ecosystems. When attaining great abundance, they substantially modify structure and function of pollination systems, often negatively for native species (Vanbergen et al. 2018). Invasive alien species thus tend to represent a significant biological risk to pollinators and pollination, but effects are complex and contingent on the abundance of the invader and the ecological function and evolutionary history of both the invader and the recipient ecosystem.Abundant invasive alien plant species can provide a substantial food resource that dominates pollinator diet (Figure 6) (Praz et al. 2008; Bartomeus et al. 2010; Pysek et al. 2011; Chrobock et al. 2013; Masters and Emery 2015; Russo et al. 2016; Montero-Casta?o and Vilà 2017; Stiers and Triest 2017). This may produce risks for pollinator health such as by altering the nutritional quality of the landscape. Pollinators require a specific balance of essential nutrients (Sedivy et al. 2011; Stabler et al. 2015; Vaudo et al. 2016) and if a plant invasion reduces the availability or diversity of particular nutrients provided by diverse floral resources, then nutritional deficits for pollinators might arise (Vanbergen et al. 2018). Other potential risks to pollinators from alien plants are from novel plant chemicals in alien pollen and nectar that can be toxic to native pollinator species (Praz et al. 2008; Arnold et al. 2014; Tiedeken et al. 2016); or alteration of flowering phenology at the community level, affecting availability of floral resources to foraging insects (Vanbergen et al. 2018). Figure 6. Invasive alien plant impact on pollinator visitation and network structure. An example of an alien plant species (a)?Himalayan balsam, Impatiens glandulifera, native to Asia and invasive in Europe. This plant attains high densities, produces copious nectar and pollen and possesses a large, enduring floral display, all of which enables it to readily penetrate and dominate plant-pollinator networks by co-opting pollinators, such as (b)?the honeybee and (c)?syrphid hoverflies. In turn, alien plant invasions can alter the composition and structure of native plant-pollinator networks from (d) to?(e). This raises the risk of (e)?pollinator nutritional deficits due to reductions in availability of essential nutrients from diverse floral resources, poorly matched mutualisms and impaired native plant pollination. Source of images: Dan Chapman and Claire Carvell. Adapted from Vanbergen et al. 2018.However, there are comparatively few recorded examples of alien plant invasions, consistently lowering overall pollinator diversity or abundance (Lopezaraiza-Mikel et al. 2007; Moron et al. 2009; Nienhuis et al. 2009). This suggests that either pollinators can compensate for IAS-associated changes in floral quality or availability (Harmon-Threatt and Kremen 2015) or effects are subtle, chronic (possibly undetected), or only adversely affect pollinators in combination with other stressors (Schweiger et al. 2010; Vanbergen and Insect Pollinators Initiative 2013).While direct links between invasive alien plants and pollinator decline are unproven, there is much evidence that invasive alien plant species are incorporated readily into, and often assume a key role in, native community networks (Bartomeus et al. 2008; Ramos-Jiliberto et al. 2012; Albrecht et al. 2014; CaraDonna et al. 2017; Goodell and Parker 2017; Kaiser-Bunbury et al. 2017). Once the invasive alien is established and abundant in the network, then it may affect pollination of coflowering native plants generally by outcompeting them for pollination services (Brown et al. 2002; Morales and Traveset 2009; Dietzsch et al. 2011; Thijs et al. 2012), although there are situations where they facilitate native pollination (McKinney and Goodell 2011; Masters and Emery 2015; Albrecht et al. 2016; Russo et al. 2016) Whether facilitation or local competition predominates depends on the relative abundance and distribution of the alien plant and the species composition of the recipient ecosystem or habitat (Montero-Castano and Vila 2012; Carvalheiro et al. 2014; Albrecht et al. 2016; Russo et al. 2016).Invasive alien plants can disrupt native pollination by improper native pollen transfer or reproductive interference (stigma clogging or chemical inhibition of pollen germination) ultimately reducing native plant reproduction (Chittka and Schurkens 2001; Brown et al. 2002; Morales and Traveset 2008; Thijs et al. 2012; Bruckman and Campbell 2016b). Yet this may be mitigated by plant compensatory mechanisms, e.g. self-reproduction, that can assure reproduction (Morales and Traveset 2009; Dietzsch et al. 2011; Emer et al. 2015). Overall, pollinator sharing and impacts on native plant pollination and reproduction tend to be greater where, relative to the native flora, the alien plant produces higher densities of flowers, where they are related, or where they have similar flower phenology or morphology (Pysek et al. 2011; Thijs et al. 2012; Carvalheiro et al. 2014; Bruckman and Campbell 2016a; Herron-Sweet et al. 2016). Humans have globally translocated many different bee species for apiculture and crop pollination services, mostly from the European region (IPBES 2016a), and in some cases (e.g. Apis mellifera) these species are considered naturalized in other WEOG regions (North America, Australasia). The principal managed pollinators (the western honeybee Apis mellifera and the bumblebee Bombus terrestris) possess traits (sociality, generalist diet and nesting flexibility) that coupled with recurrent introduction of managed colonies and frequent establishment of feral populations risk impacts on native pollinators and pollination. Compared to the situation in other world regions, there is less evidence that translocation and establishment of European bees across much of WEOG has competitively excluded native pollinators or disrupted native pollination (Thomson 2004; Kenis et al. 2009; IPBES 2016a). One explanation might be that any impacts occurred long ago (e.g. about 200?years ago in North America) and so went unrecorded. The introduction exotic bees into Australia and New Zealand occurred in the nineteenth century (Doull 1973; Donovan 2007), but evidence of their impact on native flora and their pollinators is also limited (Howlett and Donovan 2010). In Australia, reduced seed set in the endemic shrub?Melastoma affine?was associated with high abundances of Apis mellifera, which in turn disturbed the foraging activity of native bees (Gross 1998).In the WEOG region, the greatest risk to native pollinators from alien pollinators probably comes from transcontinental movement of pollinating bees leading to pathogen and parasite spillover into native pollinators, with potential implications for community epidemiology (IPBES 2016a; Vanbergen et al. 2018). Sustained movement by humans of managed honeybee (A. mellifera) colonies into Asia led to the host shift of the parasitic Varroa mite from Asian honeybee (A. cerana) populations and its subsequent worldwide spread, as part of trade in managed A. mellifera, along with a complex of viral pathogens it transmits among bee hosts (Martin et al. 2012; IPBES 2016a; Wilfert et al. 2016). This Varroa host shift appears to have allowed eco-evolutionary changes that increased virulence of strains of deformed wing virus (DWV) infecting honeybees, which contribute to colony losses (Martin et al. 2012; Ryabov et al. 2014; McMahon et al. 2016; Wilfert et al. 2016; Brosi et al. 2017). This sort of process may lead to future risks for native pollinators where bees (managed or feral) are introduced because there are indications of pathogen sharing among a broad spectrum of flower-visiting insect hosts (Singh et al. 2010; Furst et al. 2014; McMahon et al. 2015; Wilfert et al. 2016). Where predators of pollinators are introduced beyond their native range they typically exert strong top-down pressure on plant pollination and fitness by consumption of pollinators (IPBES 2016a). In the WEOG region, the accidental introduction (2004) into Europe from Asia and subsequent spread of the predatory yellow-legged hornet (Vespa velutina) represents a new threat to already stressed European honeybee populations (Monceau et al. 2014; Keeling et al. 2017b). In California, invasive ant species that are more aggressive or competitive than native ants deter pollinators and seed dispersers thereby reducing plant fitness (Hanna et al. 2015). Effects of invasive alien predators on the web of interspecific interactions affecting native pollination can be highly complex and is well illustrated by the case of the invasive predatory wasp (Vespula pensylvanica) in Hawaii (Hanna et al. 2013, 2014). This wasp is a generalist predator of arthropods, but also behaves as a nectar thief to compete with native Hylaeus bees and the intriduced honeybee A. mellifera. This predator thereby lowers pollination and fruit production of native tree Metrosideros polymorpha (Hanna et al. 2013, 2014). Experimental removal of the wasp revealed that the alien A. mellifera was the most effective pollinator in this system, in all likelihood fulfilling the niche of extinct or declining bird pollinators, themselves reduced by introduced vertebrate predators (Hanna et al. 2013). In a similar case, predatory alien wasps from Europe in New Zealand beech forests outcompeted native bird pollinators and the introduced honeybees (A. mellifera) for energy-rich honeydew secretions produced by native scale insects and thus threatened the native bird pollinators (Moller et al. 1991; Markwell et al. 1993). Several invasive alien species have been recognized in Africa, although the impacts on pollinators have been found for a few species only. As invasive plant species are often capable of selfing, interactions with pollinators are not expected and hence direct effects might be negligible. The prime examples of invasive plant species are Parthenium hysterophorus and plants of the genus Prosopis, also known as Mesquite. The latter one was introduced as beneficial plant to provide fodder, fuel and shade in arid regions. Especially in water scarce areas Prosopis turned into an undesirable invasive alien weed due to its huge water usage and occurrence in dense stands (Le Maitre et al. 2000). P. hysterophorus has a high potential to disrupt natural ecosystems resulting in grassland and woodlands dominated by P.?hysterophorus reducing the number of indigenous plants. The genus Prosopis is highy attractive to pollinators, providing both a concentrated nectar and abundant pollen. However, direct effects on pollinators have not been described. In contrast, the invasive Rubus cuneifolius in South Africa puts remnant grassland patches under threat. R. cuneifolius reduces the ecological complexity of remnant grassland patches, which otherwise are valuable contributors to regional biodiversity by promoting intact flower visitor networks (Hansen et al. 2018).Sunbirds in Namaqualand have adapted to the invasive tree tobacco Nicotiana glauca by pollinating through hovering, as do New World hummingbirds; sunbirds usually pollinate by perching. N.?glauca flowers pollinated by hovering sunbirds show higher seed set (Geerts and Pauw 2009).Invasive alien animal species acting as competitors or predators could set pollinators at risk, but so far there are only very few invasive alien insect species being reported in Africa. The invasive paper wasp Polistes dominula, introduced in 2008 to South Africa (Eardley et al. 2009), hunts bee species, but major impacts on native wild pollinators have not been reported, especially as several parasitoids of native species also use P. dominula as their host (Benadé et al. 2014). 4.3 PesticidesThe risk to pollinators from pesticides occurs through a combination of toxicity and level of exposure. This risk varies according to the species’ biology (for example, ability to metabolize toxins, foraging ecology), between chemical compounds, with the type and scale of land management, interactions with other stressors, and with landscape ecological infrastructure. Herbicides used to control weeds pose an indirect risk because they reduce the abundance and diversity of flowering plants providing pollen and nectar to pollinators (IPBES 2016; Potts et al. 2016). Under controlled experimental conditions, pesticides, particularly insecticides like neonicotinoids, have a broad range of lethal and sublethal (for example, behavioural and physiological) effects on pollinators (IPBES 2016; Potts et al. 2016). Below we highlight studies published since the IPBES assessment.Recent laboratory studies on the impact of neonicotinoids (e.g. thiamethoxam, clothianidin) on bumblebee species and the honeybee (Apis mellifera) increasingly employ doses (~1.5-5 ppb) in experimental treatments that accurately simulate field-realistic exposure levels. Such experiments have revealed sublethal reductions in feeding rate, lifespan, and reproductive capacity (i.e. ovary development, sperm viability, egg production) of queen and male (drone) bees (Baron et al. 2017a,?b; Straub et al. 2016). Semi-field experiments (where insects are subject to a treatment and then allowed to forage freely) continue to reveal complex, subtle effects of neonicotinoids on bumblebee foraging behaviour (e.g. floral choice, foraging duration, pollen collection rates), although the level and directions of effects often varies among studies (Stanley and Raine 2016; Stanley et al. 2016; Arce et al. 2017). A controlled landscape experiment implemented across three countries (Hungary, Germany, and the United Kingdom) that employed oilseed rape (canola) treated with neonicotinoids (clothianidin or thiamethoxam) showed that wild bee reproduction (B. terrestris and Osmia bicornis) was negatively related with neonicotinoid residues in the bee nests (Woodcock et al. 2017), broadly in agreement with Rundlof et al. (2015). Honeybee colony performance varied geographically, with negative (Hungary and United Kingdom) or positive (Germany) responses recorded. Only in Hungary did this translate into reduced colony viability (24% decline in workers in the following spring) (Woodcock et al. 2017). This complexity in honeybee responses follows overall equivocal results from earlier honeybee field experiments in Sweden and North America (Rundlof et al. 2015; IPBES 2016a). Recent distribution modelling integrating long-term citizen science records of wild bee species occurrence across the British landscape revealed that while the bee species benefit from the pollen and nectar provided by the oilseed rape crop, they were on average three times more negatively affected by exposure to neonicotinoids than species that did not forage on the treated crop, leading to increased population extinction rates (Woodcock et al. 2016). Similarly, analysis of long-term butterfly population data from northern California revealed a negative association between butterfly populations and increasing neonicotinoid application, even after controlling for land use and other factors (Forister et al. 2016).Fungicides, in combination with other agrichemicals (e.g. insecticides), have impacts on bee health, for an example by impeding resistance to disease (IPBES 2016a). Recent studies have produced further correlative evidence of the role of fungicides in range contractions of North American bumblebee species, potentially due to interactions with pathogens (Nosema bombi) and/or climate (McArt et al. 2017b). The risk to honeybees from fungicide exposure extends beyond the cropped area (McArt et al. 2017a). Gene function and cellular metabolism of honeybees experimentally exposed to diets containing triazole fungicides is disrupted, with implications for the bee’s capacity to extract sufficient energy from and detoxify secondary plant compounds in food (Mao et al. 2017). Pervasive neonicotinoid and fungicide contamination of floral resources and honey stores mean it is likely that there is a risk to wild pollinators from chronic exposure to sublethal doses of multiple pesticides (David et al. 2016; Hladik et al. 2016; Mogren and Lundgren 2016; Colwell et al. 2017; McArt et al. 2017a; Mitchell et al. 2017). Experiments show a risk of synergy between chemical and other stressors (nutritional state, pathogen presence) that could have implications for pollinator health and survival, for instance via reduced immunocompetence (Brandt et al. 2016; IPBES 2016; Brandt et al. 2017; Tosi et al. 2017).There is experimental evidence linking pesticides with negative effects on pollinators in Brazil and Argentina. For example, Apis mellifera is used as the test species in environmental risk assessments, and it is generally considered to be extremely sensitive to pesticides. A recent meta-analysis showed that when compared to honeybees, stingless bees (M. scutellaris,?N. perilampoides,?S. postica,?T. iridipennis,?T. nigra?and?T. spinipes) are more sensitive to different pesticides than other bee species (e.g., bumblebees, etc.) (Arena and Sgolastra 2014). Nevertheless, evidence is based mainly on dose–response toxicity bioassays, with scant information on field sublethal effects of pesticides (del Sarto et al. 2014; Balbuena et al. 2015; Barbosa et al. 2015). An experimental study performed in Brazil, using the technique of vitro-reared queens in a neotropical social bee species (Plebeia droryana) also showed high larval mortality after exposure to an organophosphate pesticide (chlorpyrifos) via larval food, and workers were produced instead of queens (dos Santos et al. 2016).Experimental studies performed with the great fruiteating bat (Artibeus lituratus) from Brazil indicate that the chronic exposure of fruit bats to environmentally relevant concentrations of endosulfan can lead to significant bioaccumulation, which may affect the health of this important seed disperser in neotropical forests (Brinati et al. 2016). 4.4 Climate changeWith respect to global patterns in relation to climate change, regional studies show variation in species responses. A global study by Urban ADDIN EN.CITE <EndNote><Cite ExcludeAuth="1"><Author>Urban</Author><Year>2015</Year><RecNum>3144</RecNum><DisplayText>(2015)</DisplayText><record><rec-number>3144</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518449199">3144</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Urban, M.C. </author></authors></contributors><titles><title>Accelerating extinction risk from climate change.</title><secondary-title>Science</secondary-title></titles><periodical><full-title>Science</full-title></periodical><pages>571-573</pages><volume>348</volume><dates><year>2015</year></dates><urls></urls></record></Cite></EndNote>(2015) suggests that extinction risks will accelerate with future global temperatures, threatening up to one in six species under current policies with extinction risks highest in South America, Australia, and New Zealand.Climate change has been documented as impacting various taxa at multiple levels, including causing range shifts in species and populations across the globe including Europe and North America PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5LZXJyPC9BdXRob3I+PFllYXI+MjAxNTwvWWVhcj48UmVj

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ADDIN EN.CITE.DATA (Fitter and Fitter 2002; Parmesan and Yohe 2003; Both and te Marvelde 2007), causing mismatches in phenological events PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5WaXNzZXI8L0F1dGhvcj48WWVhcj4yMDEyPC9ZZWFyPjxS

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RW5kTm90ZT4A

ADDIN EN.CITE.DATA (Visser et al. 2012; Chevillot et al. 2017) and increasing extinction risks PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5SYXNtb250PC9BdXRob3I+PFllYXI+MjAxMjwvWWVhcj48

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ADDIN EN.CITE.DATA (Thomas et al. 2004; Butchart et al. 2010; Rasmont and Iserbyt 2012). Alterations in physiology and phenology can desynchronize ecological interactions and thereby threaten ecosystem function PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5UaGFja2VyYXk8L0F1dGhvcj48WWVhcj4yMDE2PC9ZZWFy

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dGU+

ADDIN EN.CITE.DATA (Thackeray et al. 2016). These changes may also affect pollinators via changes in their spatial distribution, physiology and/or seasonal phenology through spatial and temporal mismatches between plants and their pollinators PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5IZWdsYW5kPC9BdXRob3I+PFllYXI+MjAwOTwvWWVhcj48

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ADDIN EN.CITE.DATA (Hegland et al. 2009; Kerr et al. 2015).Increasing temperatures may either increase or decrease synchrony between species, depending on their respective starting positions ADDIN EN.CITE <EndNote><Cite><Author>Singer</Author><Year>2010</Year><RecNum>3147</RecNum><DisplayText>(Singer &amp; Parmesan. 2010)</DisplayText><record><rec-number>3147</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518451345">3147</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Singer, M.C.</author><author>C. Parmesan.</author></authors></contributors><titles><title>Phenological asynchrony between herbivorous insects and their hosts: signal of climate change or pre-existing adaptive strategy? &#xD;</title><secondary-title>Philosophical Transactions of the Royal Society B-Biological Sciences</secondary-title></titles><periodical><full-title>Philosophical Transactions of the Royal Society B-Biological Sciences</full-title></periodical><pages>3161-3176</pages><volume>365</volume><number>1555 </number><dates><year>2010</year></dates><urls></urls></record></Cite></EndNote>(Singer and Parmesan. 2010). Bartomeus et al. ADDIN EN.CITE <EndNote><Cite ExcludeAuth="1"><Author>Bartomeus</Author><Year>2011</Year><RecNum>1537</RecNum><DisplayText>(2011)</DisplayText><record><rec-number>1537</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1357569056">1537</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Bartomeus, Ignasi</author><author>Ascher, John S.</author><author>Wagner, David</author><author>Danforth, Bryan N.</author><author>Colla, Sheila</author><author>Kornbluth, Sarah</author><author>Winfree, Rachael</author></authors></contributors><titles><title>Climate-associated phenological advances in bee pollinators and bee-pollinated plants</title><secondary-title>Proceedings of the National Academy of Sciences of the United States of America</secondary-title></titles><periodical><full-title>Proceedings of the National Academy of Sciences of the United States of America</full-title><abbr-1>Proc. Natl. Acad. Sci. U. S. A.</abbr-1><abbr-2>Proc Natl Acad Sci U S A</abbr-2></periodical><pages>20645-20649</pages><volume>108</volume><number>51</number><dates><year>2011</year><pub-dates><date>Dec 20</date></pub-dates></dates><isbn>0027-8424</isbn><accession-num>WOS:000298289400077</accession-num><urls><related-urls><url>;(2011) reported that the phenology of 10 bee species from north-eastern North America has advanced by about 10 days over about 130 years, with most of this advance occurring since 1970. Parmesan (2007) found that butterflies showed spring advancement three times stronger than that for herbs and grasses. Because most butterflies use herbs and grasses as host plants, this suggests an increasing asynchrony between these two interacting groups. Observations that show the phenological decoupling of plants and their pollinators are also presented by Gordo and Sanz ADDIN EN.CITE <EndNote><Cite ExcludeAuth="1"><Author>Gordo</Author><Year>2006</Year><RecNum>1568</RecNum><DisplayText>(2006)</DisplayText><record><rec-number>1568</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1357569056">1568</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Oscar Gordo</author><author>Juan Jose Sanz</author></authors></contributors><titles><title>Temporal trends in phenology of the honey bee Apis mellifera (L.) and the small white Pieris rapae (L.) in the Iberian Peninsula (1952-2004)</title><secondary-title>Ecological Entomology</secondary-title></titles><periodical><full-title>Ecological Entomology</full-title><abbr-1>Ecol. Entomol.</abbr-1><abbr-2>Ecol Entomol</abbr-2></periodical><pages>261-268</pages><volume>31</volume><keywords><keyword>Appearance date</keyword><keyword>climate change</keyword><keyword>long-term study</keyword><keyword>Mediterranean region</keyword><keyword>temperature response</keyword></keywords><dates><year>2006</year></dates><urls><related-urls><url>;(2006) and McKinney et al. ADDIN EN.CITE <EndNote><Cite ExcludeAuth="1"><Author>McKinney</Author><Year>2012</Year><RecNum>3148</RecNum><DisplayText>(2012)</DisplayText><record><rec-number>3148</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518451429">3148</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>McKinney, A. M.</author><author>P. J. CaraDonna</author><author>D. W. Inouye</author><author>B. Barr</author><author>D. Bertelson</author><author>N. M. Waser</author></authors></contributors><titles><title>Asynchronous</title></titles><dates><year>2012</year></dates><urls></urls></record></Cite></EndNote>(2012). While such long-term studies may be rare due to lack of historic data, experimental studies such as the one by Shenk et al. (2018), on Osmia bicornis show that even short temporal mismatches can cause clear fitness losses in solitary bees. Moreover, evidence suggests that climate constitutes a significant driver of plant-pollinator interactions, even within relatively narrow latitudinal gradients ADDIN EN.CITE <EndNote><Cite><Author>Petanidou</Author><Year>2018</Year><RecNum>3120</RecNum><DisplayText>(Petanidou<style face="italic"> et al.</style> 2018)</DisplayText><record><rec-number>3120</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518446233">3120</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Petanidou, T.</author><author>Kallimanis, A. S.</author><author>Lazarina, M.</author><author>Tscheulin, T.</author><author>Devalez, J.</author><author>Stefanaki, A.</author><author>Hanlidou, E.</author><author>Vujic, A.</author><author>Kaloveloni, A.</author><author>Sgardelis, S. P.</author></authors></contributors><titles><title>Climate drives plant-pollinator interactions even along small-scale climate gradients: the case of the Aegean</title><secondary-title>Plant Biology</secondary-title></titles><periodical><full-title>Plant Biology</full-title></periodical><pages>176-183</pages><volume>20</volume><dates><year>2018</year><pub-dates><date>Jan</date></pub-dates></dates><isbn>1435-8603</isbn><accession-num>WOS:000419106200017</accession-num><urls><related-urls><url>&lt;Go to ISI&gt;://WOS:000419106200017</url></related-urls></urls><electronic-resource-num>10.1111/plb.12593</electronic-resource-num></record></Cite></EndNote>(Petanidou et al. 2018).At ecosystem level, historical phenology data generate conflicting results, with some studies predicting plant-pollinator interactions will be vulnerable to future climate changes ADDIN EN.CITE <EndNote><Cite><Author>Burkle</Author><Year>2013</Year><RecNum>1857</RecNum><DisplayText>(Burkle<style face="italic"> et al.</style> 2013)</DisplayText><record><rec-number>1857</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1433761206">1857</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Burkle, Laura A.</author><author>Marlin, John C.</author><author>Knight, Tiffany M.</author></authors></contributors><titles><title>Plant-Pollinator Interactions over 120 Years: Loss of Species, Co-Occurrence, and Function</title><secondary-title>Science</secondary-title></titles><periodical><full-title>Science</full-title></periodical><pages>1611-1615</pages><volume>339</volume><number>6127</number><dates><year>2013</year><pub-dates><date>Mar 29</date></pub-dates></dates><isbn>0036-8075</isbn><accession-num>WOS:000316731600050</accession-num><urls><related-urls><url>&lt;Go to ISI&gt;://WOS:000316731600050</url></related-urls></urls><electronic-resource-num>10.1126/science.1232728</electronic-resource-num></record></Cite></EndNote>(Burkle et al. 2013), while others argue that these interactions will remain robust ADDIN EN.CITE <EndNote><Cite><Author>Hegland</Author><Year>2009</Year><RecNum>1572</RecNum><DisplayText>(Hegland<style face="italic"> et al.</style> 2009)</DisplayText><record><rec-number>1572</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1357569056">1572</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Stein Joar Hegland</author><author>Anders Nielsen</author><author>Amparo Lázaro</author><author>Anne-Line Bjerknes</author><author>?rjan Totland</author></authors></contributors><titles><title>How does climate warming affect plant-pollinator interactions?</title><secondary-title>Ecology Letters</secondary-title></titles><periodical><full-title>Ecology Letters</full-title><abbr-1>Ecol. Lett.</abbr-1><abbr-2>Ecol Lett</abbr-2></periodical><pages>184-195</pages><volume>12</volume><number>2</number><keywords><keyword>Abundance</keyword><keyword>climate warming</keyword><keyword>distribution</keyword><keyword>global change</keyword><keyword>interaction</keyword><keyword>mismatch</keyword><keyword>mutualism</keyword><keyword>network</keyword><keyword>phenology</keyword><keyword>pollination</keyword></keywords><dates><year>2009</year></dates><urls><related-urls><url>;(Hegland et al. 2009). A modelling study (Memmott et al. ADDIN EN.CITE <EndNote><Cite ExcludeAuth="1"><Author>Memmott</Author><Year>2007</Year><RecNum>1375</RecNum><DisplayText>(2007)</DisplayText><record><rec-number>1375</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1344509526">1375</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Memmott, Jane</author><author>Craze, Paul G.</author><author>Waser, Nickolas M.</author><author>Price, Mary V.</author></authors></contributors><titles><title>Global warming and the disruption of plant-pollinator interactions</title><secondary-title>Ecology Letters</secondary-title></titles><periodical><full-title>Ecology Letters</full-title><abbr-1>Ecol. Lett.</abbr-1><abbr-2>Ecol Lett</abbr-2></periodical><pages>710-717</pages><volume>10</volume><number>8</number><dates><year>2007</year><pub-dates><date>Aug</date></pub-dates></dates><isbn>1461-023X</isbn><accession-num>WOS:000247561100009</accession-num><urls><related-urls><url>;(2007) using a highly resolved empirical network of interactions in England found that diet breadth (i.e., number of plant species visited) of the pollinators might decrease due to the reduced phenological overlap between plants and pollinators and that extinctions of plant, pollinators and their crucial interactions could be expected as consequences of these disruptions. An increasing number of observational and experimental studies across many organisms provides strong evidence that climate change has contributed to the overall spring advancement observed especially in the northern hemisphere ADDIN EN.CITE <EndNote><Cite><Author>Settele</Author><Year>2014</Year><RecNum>3143</RecNum><DisplayText>(Settele<style face="italic"> et al.</style> 2014)</DisplayText><record><rec-number>3143</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518449039">3143</key></foreign-keys><ref-type name="Report">27</ref-type><contributors><authors><author>Settele, J.</author><author>R. Scholes </author><author>R. Betts</author><author>S. Bunn</author><author>P. Leadley</author><author>D. Nepstad</author><author>J.T. Overpeck</author><author>M.A. Taboada</author></authors><secondary-authors><author>Field, C. B. </author><author>Barros, V. R.</author><author>Dokken, D. J. </author><author>Mach, K. J.</author><author>Mastrandrea, M. D. </author><author>Bilir, T. E.</author><author>Chatterjee, M.</author><author>Ebi, K. L.</author><author>Estrada, Y. O.</author><author>Genova, R. C. </author><author>Girma, B. </author><author>Kissel, E. S. </author><author>Levy, A. N.</author><author>MacCracken, S. </author><author>Mastrandrea, P. R.</author><author>White, L. L.</author></secondary-authors><tertiary-authors><author>Cambridge University Press</author></tertiary-authors></contributors><titles><title>Terrestrial and Inland Water Systems.</title><secondary-title>Climate Change 2014: Impacts, Adaptation, and Vulnerability. Part A: Global and Sectoral Aspects. Contribution of Working Group II to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change </secondary-title></titles><dates><year>2014</year></dates><pub-location>Cambridge, United Kingdom and New York, NY, USA</pub-location><urls></urls></record></Cite></EndNote>(Settele et al. 2014). Additionally, there is some evidence that daily activity patterns may change with climate change in the United States ADDIN EN.CITE <EndNote><Cite><Author>Rader</Author><Year>2013</Year><RecNum>1982</RecNum><Prefix>e.g. </Prefix><DisplayText>(e.g. Rader<style face="italic"> et al.</style> 2013)</DisplayText><record><rec-number>1982</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1433765657">1982</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Rader, R.</author><author>Reilly, J.</author><author>Bartomeus, I.</author><author>Winfree, R. </author></authors></contributors><titles><title>Native bees buffer the negative impact of climate warming on watermelon crop pollination by honey bees</title><secondary-title>Global Change Biology</secondary-title></titles><periodical><full-title>Global Change Biology</full-title><abbr-1>Glob. Change Biol.</abbr-1><abbr-2>Glob Change Biol</abbr-2></periodical><pages>3103-3110</pages><volume>19</volume><dates><year>2013</year></dates><urls></urls></record></Cite></EndNote>(e.g. Rader et al. 2013). However, the effects of these shifts in terms of interacting species are still not well understood and require further investigation PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5CdXJrbGU8L0F1dGhvcj48WWVhcj4yMDExPC9ZZWFyPjxS

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ADDIN EN.CITE.DATA (Bartomeus et al. 2011; Burkle and Alarcón 2011).Although research on other insects clearly shows that autumn/winter temperature shifts can drastically alter the diapause or overwintering behaviour or prevent emergence ADDIN EN.CITE <EndNote><Cite><Author>Coleman</Author><Year>2014</Year><RecNum>1755</RecNum><DisplayText>(Coleman<style face="italic"> et al.</style> 2014)</DisplayText><record><rec-number>1755</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1417794702">1755</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Coleman, P. C.</author><author>Bale, J. S. </author><author>Hayward, S. A. L.</author></authors></contributors><titles><title>Cross generation plasticity in cold hardiness is associated with diapause, but not the non-diapause developmental pathway, in the blow fly, Calliphora vicina.</title><secondary-title>Journal of Experimental Biology </secondary-title></titles><periodical><full-title>Journal of Experimental Biology</full-title><abbr-1>J. Exp. Biol.</abbr-1><abbr-2>J Exp Biol</abbr-2></periodical><pages>1454-1461</pages><volume>217</volume><dates><year>2014</year></dates><urls></urls></record></Cite></EndNote>(Coleman et al. 2014; ADDIN EN.CITE <EndNote><Cite><Author>Bale</Author><Year>2010</Year><RecNum>1535</RecNum><DisplayText>(Bale &amp; Hayward 2010)</DisplayText><record><rec-number>1535</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1357569056">1535</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>J. S. Bale</author><author>S. A. L. Hayward</author></authors></contributors><titles><title>Insect overwintering in a changing climate</title><secondary-title>Journal of Experimental Biology</secondary-title></titles><periodical><full-title>Journal of Experimental Biology</full-title><abbr-1>J. Exp. Biol.</abbr-1><abbr-2>J Exp Biol</abbr-2></periodical><pages>980-994</pages><volume>213</volume><keywords><keyword>insect</keyword><keyword>cold hardiness</keyword><keyword>diapause</keyword><keyword>climate change</keyword><keyword>distributions</keyword><keyword>invasive species</keyword></keywords><dates><year>2010</year></dates><urls><related-urls><url> and Hayward 2010), quantitative data on key pollinators is severely lacking. However, experimental studies on Bombus terrestris show that diapause is already being disrupted, with queens attempting to establish winter colonies ADDIN EN.CITE <EndNote><Cite><Author>Stelzer</Author><Year>2010</Year><RecNum>1752</RecNum><DisplayText>(Stelzer<style face="italic"> et al.</style> 2010)</DisplayText><record><rec-number>1752</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1415894136">1752</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Ralph J. Stelzer</author><author>Lars Chittka</author><author>Marc Carlton</author><author>Thomas C. Ings </author></authors></contributors><titles><title>Winter Active Bumblebees (Bombus terrestris) Achieve High Foraging Rates in Urban Britain</title><secondary-title>Plos One</secondary-title></titles><periodical><full-title>Plos One</full-title></periodical><pages>e9559</pages><volume>5</volume><number>3</number><dates><year>2010</year></dates><urls><related-urls><url>;(Stelzer et al. 2010) and weight loss, survival, and emergence times being impacted in the mason bee Osmia cornuta ADDIN EN.CITE <EndNote><Cite><Author>Bosch</Author><Year>2004</Year><RecNum>3136</RecNum><DisplayText>(Bosch &amp; Kemp 2004)</DisplayText><record><rec-number>3136</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518447674">3136</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Bosch, J.</author><author>Kemp, W. P.</author></authors></contributors><titles><title>Effect of pre-wintering and wintering temperature regimes on weight loss, survival, and emergence time in the mason bee Osmia cornuta (Hymenoptera: Megachilidae)</title><secondary-title>Apidologie</secondary-title></titles><periodical><full-title>Apidologie</full-title><abbr-1>Apidologie</abbr-1><abbr-2>Apidologie</abbr-2></periodical><pages>469-479</pages><volume>35</volume><number>5</number><dates><year>2004</year></dates><urls></urls><electronic-resource-num>10.1051/apido:2004035</electronic-resource-num></record></Cite></EndNote>(Bosch and Kemp 2004).Some of the clearest examples of climate-related changes in species populations come from high-latitude ecosystems where non-climate drivers are of lesser importance PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5TZXR0ZWxlPC9BdXRob3I+PFllYXI+MjAxNDwvWWVhcj48

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ADDIN EN.CITE.DATA (see Hegland et al. 2009; Settele et al. 2014). However, research on neotropical orchid bee species revealed changes in effective population size in response to climate change since the last glacial maximum, highlighting the potential vulnerability and plasticity of pollinator population responses to future climate change ADDIN EN.CITE <EndNote><Cite><Author>López-Uribe</Author><Year>2014</Year><RecNum>3149</RecNum><DisplayText>(López-Uribe<style face="italic"> et al.</style> 2014)</DisplayText><record><rec-number>3149</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518451561">3149</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>López-Uribe, M.M.</author><author>K.R. Zamudio</author><author>C.F. Cardoso </author><author>B.N. Danforth</author></authors></contributors><titles><title>Climate, physiological tolerance, and sexbiased dispersal shape genetic structure of Neotropical orchid bees.</title><secondary-title>Molecular Ecology</secondary-title></titles><periodical><full-title>Molecular Ecology</full-title><abbr-1>Mol. Ecol.</abbr-1><abbr-2>Mol Ecol</abbr-2></periodical><pages>1874-1890</pages><volume>23</volume><number>7</number><dates><year>2014</year></dates><urls></urls></record></Cite></EndNote>(López-Uribe et al. 2014). There is substantial evidence that terrestrial plant and animal species’ ranges have moved in response to warming over the last several decades and this movement will accelerate over the coming decades ADDIN EN.CITE <EndNote><Cite><Author>Settele</Author><Year>2014</Year><RecNum>3143</RecNum><DisplayText>(Settele<style face="italic"> et al.</style> 2014)</DisplayText><record><rec-number>3143</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518449039">3143</key></foreign-keys><ref-type name="Report">27</ref-type><contributors><authors><author>Settele, J.</author><author>R. Scholes </author><author>R. Betts</author><author>S. Bunn</author><author>P. Leadley</author><author>D. Nepstad</author><author>J.T. Overpeck</author><author>M.A. Taboada</author></authors><secondary-authors><author>Field, C. B. </author><author>Barros, V. R.</author><author>Dokken, D. J. </author><author>Mach, K. J.</author><author>Mastrandrea, M. D. </author><author>Bilir, T. E.</author><author>Chatterjee, M.</author><author>Ebi, K. L.</author><author>Estrada, Y. O.</author><author>Genova, R. C. </author><author>Girma, B. </author><author>Kissel, E. S. </author><author>Levy, A. N.</author><author>MacCracken, S. </author><author>Mastrandrea, P. R.</author><author>White, L. L.</author></secondary-authors><tertiary-authors><author>Cambridge University Press</author></tertiary-authors></contributors><titles><title>Terrestrial and Inland Water Systems.</title><secondary-title>Climate Change 2014: Impacts, Adaptation, and Vulnerability. Part A: Global and Sectoral Aspects. Contribution of Working Group II to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change </secondary-title></titles><dates><year>2014</year></dates><pub-location>Cambridge, United Kingdom and New York, NY, USA</pub-location><urls></urls></record></Cite></EndNote>(Settele et al. 2014). A synthesis of range shifts ADDIN EN.CITE <EndNote><Cite><Author>Chen</Author><Year>2011</Year><RecNum>3137</RecNum><DisplayText>(Chen<style face="italic"> et al.</style> 2011b)</DisplayText><record><rec-number>3137</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518447674">3137</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Chen, I. C.</author><author>Hill, J. K.</author><author>Ohlemüller, R.</author><author>Roy, D. B.</author><author>Thomas, C. D.</author></authors></contributors><titles><title>Rapid range shifts of species associated with high levels of climate warming</title><secondary-title>Science</secondary-title></titles><periodical><full-title>Science</full-title></periodical><pages>1024-1026</pages><volume>333</volume><number>6045</number><dates><year>2011</year></dates><urls></urls><electronic-resource-num>10.1126/science.1206432</electronic-resource-num></record></Cite></EndNote>(Chen et al. 2011b) indicates that terrestrial species (e.g. butterflies) have moved poleward about 11 to 17 km per decade across various sites including Europe and North America. Kerr et al.’s ADDIN EN.CITE <EndNote><Cite ExcludeAuth="1"><Author>Kerr</Author><Year>2015</Year><RecNum>2374</RecNum><DisplayText>(2015)</DisplayText><record><rec-number>2374</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1448748984">2374</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Kerr, Jeremy T.</author><author>Pindar, Alana</author><author>Galpern, Paul</author><author>Packer, Laurence</author><author>Potts, Simon G.</author><author>Roberts, Stuart M.</author><author>Rasmont, Pierre</author><author>Schweiger, Oliver</author><author>Colla, Sheila R.</author><author>Richardson, Leif L.</author><author>Wagner, David L.</author><author>Gall, Lawrence F.</author><author>Sikes, Derek S.</author><author>Pantoja, Alberto</author></authors></contributors><titles><title>Climate change impacts on bumblebees converge across continents</title><secondary-title>Science</secondary-title></titles><periodical><full-title>Science</full-title></periodical><pages>177-180</pages><volume>349</volume><number>6244</number><dates><year>2015</year><pub-dates><date>July 10, 2015</date></pub-dates></dates><urls><related-urls><url>;(2015) study on bumblebees across Europe and North America (using over 110 years of observed data) found cross-continentally consistent trends in failures to track warming through time at species’ northern range limits, range losses from southern range limits, and shifts to higher elevations among southern species. These effects were found to be independent of changing land uses or pesticide applications and underscore the need to test for climate impacts at both leading and trailing latitudinal and thermal limits for species.There is tremendous variation in range shifts among species and species groups. Much of this variation can be explained by large differences in regional patterns of temperature trends over the last several decades ADDIN EN.CITE <EndNote><Cite><Author>Burrows</Author><Year>2011</Year><RecNum>3150</RecNum><DisplayText>(Burrows<style face="italic"> et al.</style> 2011)</DisplayText><record><rec-number>3150</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518451790">3150</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Burrows, M.T.</author><author>D.S. Schoeman</author><author>L.B. Buckley</author><author>P. Moore</author><author>E.S. Poloczanska</author><author>K.M. Brander</author><author>C. Brown</author><author>J.F. Bruno</author><author>C.M. Duarte</author><author>B.S. Halpern</author><author>J. Holding</author><author>C.V. Kappel</author><author>W. Kiessling</author><author>M.I. O’Connor</author><author>J.M. Pandolfi</author><author>C.?Parmesan</author><author>F.B. Schwing, </author><author>Sydeman, W. J. </author><author>A.J. Richardson.</author></authors></contributors><titles><title>The pace of shifting climate in marine and terrestrial ecosystems.</title><secondary-title>Science</secondary-title></titles><periodical><full-title>Science</full-title></periodical><pages>652-655</pages><volume>334</volume><number>6056</number><dates><year>2011</year></dates><urls></urls></record></Cite></EndNote>(Burrows et al. 2011) and by differences in species dispersal capacity, life history and behaviour ADDIN EN.CITE <EndNote><Cite><Author>Devictor</Author><Year>2012</Year><RecNum>3151</RecNum><DisplayText>(Devictor<style face="italic"> et al.</style> 2012)</DisplayText><record><rec-number>3151</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518451940">3151</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Devictor, V.</author><author>C. van Swaay</author><author>T. Brereton</author><author>L. Brotons</author><author>D. Chamberlain </author><author>J. Heliola</author><author>S. Herrando</author><author>R. Julliard</author><author>M. Kuussaari</author><author>A. Lindstrom</author><author>J. Reif</author><author>D.B. Roy</author><author>O. Schweiger</author><author>J. Settele</author><author>C. Stefanescu</author><author>A. Van Strien</author><author>C. Van Turnhout</author><author>Z. Vermouzek</author><author>M. Wallis DeVries</author><author>I. Wynhoff </author><author>F. Jiguet.</author></authors></contributors><titles><title>Differences in the climatic debts of birds and butterflies at a continental scale.</title><secondary-title>Nature Climate Change, 2, 121-124.</secondary-title></titles><periodical><full-title>Nature Climate Change, 2, 121-124.</full-title></periodical><pages>121-124</pages><volume>2</volume><dates><year>2012</year></dates><urls></urls></record></Cite></EndNote>(Devictor et al. 2012). While the rate of climate change in Europe was equal to a shift of 249?km northward between 1990 and 2008 ADDIN EN.CITE <EndNote><Cite><Author>IPBES</Author><Year>2016</Year><RecNum>3119</RecNum><DisplayText>(IPBES 2016a)</DisplayText><record><rec-number>3119</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518442386">3119</key></foreign-keys><ref-type name="Report">27</ref-type><contributors><authors><author>IPBES</author></authors><secondary-authors><author>S.G. Potts</author><author>V. L. Imperatriz-Fonseca</author><author>H. T. Ngo</author></secondary-authors><tertiary-authors><author>Secretariat of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services</author></tertiary-authors></contributors><titles><title>The assessment report of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services on pollinators, pollination and food production.</title></titles><dates><year>2016</year></dates><pub-location>Bonn, Germany</pub-location><urls></urls></record></Cite></EndNote>(IPBES 2016a), butterfly and bird community composition only made average shifts of 114 km and 37 km northward, respectively, thus leading to an accumulated climatic debt of 212 km for birds and 135 km for butterflies ADDIN EN.CITE <EndNote><Cite><Author>Devictor</Author><Year>2012</Year><RecNum>3151</RecNum><DisplayText>(Devictor<style face="italic"> et al.</style> 2012)</DisplayText><record><rec-number>3151</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518451940">3151</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Devictor, V.</author><author>C. van Swaay</author><author>T. Brereton</author><author>L. Brotons</author><author>D. Chamberlain </author><author>J. Heliola</author><author>S. Herrando</author><author>R. Julliard</author><author>M. Kuussaari</author><author>A. Lindstrom</author><author>J. Reif</author><author>D.B. Roy</author><author>O. Schweiger</author><author>J. Settele</author><author>C. Stefanescu</author><author>A. Van Strien</author><author>C. Van Turnhout</author><author>Z. Vermouzek</author><author>M. Wallis DeVries</author><author>I. Wynhoff </author><author>F. Jiguet.</author></authors></contributors><titles><title>Differences in the climatic debts of birds and butterflies at a continental scale.</title><secondary-title>Nature Climate Change, 2, 121-124.</secondary-title></titles><periodical><full-title>Nature Climate Change, 2, 121-124.</full-title></periodical><pages>121-124</pages><volume>2</volume><dates><year>2012</year></dates><urls></urls></record></Cite></EndNote>(Devictor et al. 2012).Over longer periods, habitat types or biomes may shift their distributions due to climate change or may disappear entirely ADDIN EN.CITE <EndNote><Cite><Author>Settele</Author><Year>2014</Year><RecNum>3143</RecNum><DisplayText>(Settele<style face="italic"> et al.</style> 2014)</DisplayText><record><rec-number>3143</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518449039">3143</key></foreign-keys><ref-type name="Report">27</ref-type><contributors><authors><author>Settele, J.</author><author>R. Scholes </author><author>R. Betts</author><author>S. Bunn</author><author>P. Leadley</author><author>D. Nepstad</author><author>J.T. Overpeck</author><author>M.A. Taboada</author></authors><secondary-authors><author>Field, C. B. </author><author>Barros, V. R.</author><author>Dokken, D. J. </author><author>Mach, K. J.</author><author>Mastrandrea, M. D. </author><author>Bilir, T. E.</author><author>Chatterjee, M.</author><author>Ebi, K. L.</author><author>Estrada, Y. O.</author><author>Genova, R. C. </author><author>Girma, B. </author><author>Kissel, E. S. </author><author>Levy, A. N.</author><author>MacCracken, S. </author><author>Mastrandrea, P. R.</author><author>White, L. L.</author></secondary-authors><tertiary-authors><author>Cambridge University Press</author></tertiary-authors></contributors><titles><title>Terrestrial and Inland Water Systems.</title><secondary-title>Climate Change 2014: Impacts, Adaptation, and Vulnerability. Part A: Global and Sectoral Aspects. Contribution of Working Group II to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change </secondary-title></titles><dates><year>2014</year></dates><pub-location>Cambridge, United Kingdom and New York, NY, USA</pub-location><urls></urls></record></Cite></EndNote>(Settele et al. 2014), and climates with no analog in the past can be expected to occur in the future ADDIN EN.CITE <EndNote><Cite><Author>Wiens</Author><Year>2011</Year><RecNum>3154</RecNum><DisplayText>(Wiens<style face="italic"> et al.</style> 2011)</DisplayText><record><rec-number>3154</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518452362">3154</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Wiens, J.A.</author><author>N.E. Seavy</author><author>D. Jongsomjit</author></authors></contributors><titles><title>Protected areas in climate space: what will the future bring?</title><secondary-title>Biological Conservation</secondary-title></titles><periodical><full-title>Biological Conservation</full-title><abbr-1>Biol. Conserv.</abbr-1><abbr-2>Biol Conserv</abbr-2></periodical><pages>2119-2125</pages><volume>144</volume><number>8</number><dates><year>2011</year></dates><urls></urls></record></Cite></EndNote>(Wiens et al. 2011). However, because species can show substantial capacity to adapt to novel habitats, the consequences of this non-analogy on species abundance and extinction risk are difficult to quantify ADDIN EN.CITE <EndNote><Cite><Author>Willis</Author><Year>2009</Year><RecNum>3155</RecNum><DisplayText>(Oliver<style face="italic"> et al.</style> 2009; Willis &amp; Bhagwat 2009)</DisplayText><record><rec-number>3155</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518452456">3155</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Willis, K.J.</author><author>S.A. Bhagwat</author></authors></contributors><titles><title>Biodiversity and climate change.</title><secondary-title>Science</secondary-title></titles><periodical><full-title>Science</full-title></periodical><pages>806-807</pages><volume>326</volume><number>5954</number><dates><year>2009</year></dates><urls></urls></record></Cite><Cite><Author>Oliver</Author><Year>2009</Year><RecNum>3156</RecNum><record><rec-number>3156</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518452551">3156</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Oliver, T.</author><author>J.K. Hill</author><author>C.D. Thomas</author><author>T. Brereton</author><author>D.B. Roy</author></authors></contributors><titles><title>Changes in habitat specificity of species at their climatic range boundaries. </title><secondary-title>Ecology Letters</secondary-title></titles><periodical><full-title>Ecology Letters</full-title><abbr-1>Ecol. Lett.</abbr-1><abbr-2>Ecol Lett</abbr-2></periodical><pages>1091-1102</pages><volume>12</volume><number>10</number><dates><year>2009</year></dates><urls></urls></record></Cite></EndNote>(Oliver et al. 2009; Willis and Bhagwat 2009).The attribution of extinctions to climate change is much more difficult, but there is a growing consensus that it is the interaction of other global change pressures with climate change that poses the greatest threat to species PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Hb256YWxlei1WYXJvPC9BdXRob3I+PFllYXI+MjAxMzwv

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ADDIN EN.CITE.DATA (Gonzalez-Varo et al. 2013a; Vanbergen et al. 2013). While there is no scientific consensus concerning the magnitude of direct impact of climate change on extinction risk, there is broad agreement that climate change will contribute to and result in shifts in species abundances and ranges. In the context of other global change pressures this will contribute substantially to increased extinction risks over the coming century ADDIN EN.CITE <EndNote><Cite><Author>Settele</Author><Year>2014</Year><RecNum>3143</RecNum><DisplayText>(Settele<style face="italic"> et al.</style> 2014)</DisplayText><record><rec-number>3143</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518449039">3143</key></foreign-keys><ref-type name="Report">27</ref-type><contributors><authors><author>Settele, J.</author><author>R. Scholes </author><author>R. Betts</author><author>S. Bunn</author><author>P. Leadley</author><author>D. Nepstad</author><author>J.T. Overpeck</author><author>M.A. Taboada</author></authors><secondary-authors><author>Field, C. B. </author><author>Barros, V. R.</author><author>Dokken, D. J. </author><author>Mach, K. J.</author><author>Mastrandrea, M. D. </author><author>Bilir, T. E.</author><author>Chatterjee, M.</author><author>Ebi, K. L.</author><author>Estrada, Y. O.</author><author>Genova, R. C. </author><author>Girma, B. </author><author>Kissel, E. S. </author><author>Levy, A. N.</author><author>MacCracken, S. </author><author>Mastrandrea, P. R.</author><author>White, L. L.</author></secondary-authors><tertiary-authors><author>Cambridge University Press</author></tertiary-authors></contributors><titles><title>Terrestrial and Inland Water Systems.</title><secondary-title>Climate Change 2014: Impacts, Adaptation, and Vulnerability. Part A: Global and Sectoral Aspects. Contribution of Working Group II to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change </secondary-title></titles><dates><year>2014</year></dates><pub-location>Cambridge, United Kingdom and New York, NY, USA</pub-location><urls></urls></record></Cite></EndNote>(Settele et al. 2014). A recent modelling study on hoverfly species in Europe has shown how species adapted to high mountains are projected to almost vanish from the Balkans, and only regions of the Alps would remain suitable for them ADDIN EN.CITE <EndNote><Cite><Author>Radenkovic</Author><Year>2017</Year><RecNum>3126</RecNum><DisplayText>(Radenkovic<style face="italic"> et al.</style> 2017)</DisplayText><record><rec-number>3126</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518446233">3126</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Radenkovic, S.</author><author>Schweiger, O.</author><author>Milic, D.</author><author>Harpke, A.</author><author>Vujic, A.</author></authors></contributors><titles><title>Living on the edge: Forecasting the trends in abundance and distribution of the largest hoverfly genus (Diptera: Syrphidae) on the Balkan Peninsula under future climate change</title><secondary-title>Biological Conservation</secondary-title></titles><periodical><full-title>Biological Conservation</full-title><abbr-1>Biol. Conserv.</abbr-1><abbr-2>Biol Conserv</abbr-2></periodical><pages>216-229</pages><volume>212</volume><dates><year>2017</year><pub-dates><date>Aug</date></pub-dates></dates><isbn>0006-3207</isbn><accession-num>WOS:000407186000024</accession-num><urls><related-urls><url>&lt;Go to ISI&gt;://WOS:000407186000024</url></related-urls></urls><electronic-resource-num>10.1016/j.biocon.2017.06.026</electronic-resource-num></record></Cite></EndNote>(Radenkovic et al. 2017). Another modelling study on butterflies in Britain has showed that while widespread drought-sensitive butterfly population extinctions could occur as early as 2050, measures to manage landscapes for pollinators and in particular to reduce habitat fragmentation could significantly improve the probability of persistence ADDIN EN.CITE <EndNote><Cite><Author>Oliver</Author><Year>2015</Year><RecNum>2832</RecNum><DisplayText>(Oliver<style face="italic"> et al.</style> 2015)</DisplayText><record><rec-number>2832</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1510691262">2832</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Oliver, Tom H.</author><author>Marshall, Harry H.</author><author>Morecroft, Mike D.</author><author>Brereton, Tom</author><author>Prudhomme, Christel</author><author>Huntingford, Chris</author></authors></contributors><titles><title>Interacting effects of climate change and habitat fragmentation on drought-sensitive butterflies</title><secondary-title>Nature Climate Change</secondary-title></titles><periodical><full-title>Nature Climate Change</full-title></periodical><pages>941</pages><volume>5</volume><dates><year>2015</year></dates><publisher>Nature Publishing Group</publisher><urls><related-urls><url><style face="underline" font="default" size="100%"> face="normal" font="default" size="100%">10.1038/nclimate2746&#xD;</style><style face="underline" font="default" size="100%">;(Oliver et al. 2015). While regional studies show variation in species responses, a global study by Urban ADDIN EN.CITE <EndNote><Cite ExcludeAuth="1"><Author>Urban</Author><Year>2015</Year><RecNum>3144</RecNum><DisplayText>(2015)</DisplayText><record><rec-number>3144</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1518449199">3144</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Urban, M.C. </author></authors></contributors><titles><title>Accelerating extinction risk from climate change.</title><secondary-title>Science</secondary-title></titles><periodical><full-title>Science</full-title></periodical><pages>571-573</pages><volume>348</volume><dates><year>2015</year></dates><urls></urls></record></Cite></EndNote>(2015) suggests that extinction risks will accelerate with future global temperatures, threatening up to one in six species under current policies, with extinction risks highest in South America, Australia, and New Zealand.The African continent is strongly exposed to the effects of climate change, especially through unpredictability and disrupted equilibria. For bees in the Cape Floristic Region diversity hotspot in South Africa it has been shown, applying modelling approaches, that most bees will show range shifts and/or range contractions under realistic models for increasing temperatures, while only a minority of species might show range expansions (Kuhlmann et al. 2012). Tropical insects might be affected more strongly by even a small increase in temperature than are insects at higher latitudes; tropical insects are often already living at the higher ranges of optimal temperatures. In contrast, species in higher latitudes have broader temperature tolerance and live in cooler climates well within broader physiological optima (Deutsch et al. 2008).In all ecosystems, however, frequencies of fires affect the ability for some plant species to mature and produce flowers (pyrophytes) (Jackson et al. 1999; Cavender-Bares et al. 2004), indirectly affecting pollinators that might specialize on such species. In regions where pollinators are scarce, plants competing heavily for pollinators resulting in specialized relationships between plant and pollinator species, making them more vulnerable to environmental disturbances as fires. Despite the importance of the frequency of fires, the spatial scale of the fire is equally important. Over the past two decades, the area burnt per year has slightly decreased in northern-hemisphere Africa, while it has increased in southern-hemisphere Africa (Giglio et al. 2013). Climate change models suggest that fires might increase in frequency, as the length of the fire weather season will increase (Jolly et al. 2015). The recruiting and re-establishment of plant and pollinator populations is easier after small-scale than after large-scale fires, which will take longer time to be reinvaded by pollinator species (Brown et al. 2017).In Latin America, models show that climate change will impact native stingless bees (e.g. Melipona subnitida, Melipona bicolor and Melipona scutellaris, which are locally important pollinator of wild and crop plants in north-east Brazil and are also exploited for honey production by regional beekeepers), disconnecting suitable habitats in the future which can threaten species dispersal and gene flow (Giannini et al. 2012, 2017). Bombus bellicosus is a South American species whose populations have disappeared from their northern distribution. Changes in land uses and climate are stressors believed to cause species declines. Climate change models have shown that suitable climatic conditions for B. bellicosus will cause their populations to retreat southwards (Martins et al. 2015). Bees’ habitats also will be at risk with climate change (Giannini et al. 2013).4.5 Other drivers of disturbanceFire and grazingUnexpected disturbances of natural habitats might affect pollinators directly or indirectly via direct effects on their foraging plants or nesting habitats. In particular Mediterranean-type environments (which occur in different regions on the continent, in both southern and northern Africa) are sensitive to the frequency of fires (LeHouerou 1974), which in turn affect the reseeding and resprouting of plants. The replenishment of the vegetation depends on the juvenile periods of certain plants and might be restored after ten years in Mediterreanean-type ecosystems (Burrows et al. 2008). By contrast, grassland savannahs might be less vulnerable (Staver et al. 2011), as there might be plants adapted to rapid resprouting (Higgins et al. 2000). Grazing in grasslands might represent another kind of disturbance, which can affect pollinator species (Mayer 2005) and pollination services (Mayer 2004). Grasslands are generally adapted to grazing. Grazing might affect the availability of high-value nutritious flowering plants as forage resources for pollinators. However, grazing might contribute to removal of vegetation cover, which might create nesting habitats for ground-nesting pollinator species. Positive as well as negative effects might occur as a resonse to grazing depending on the pollinator species’ biology resulting in shifts in community structure of invertebrates (Seymour and Dean 1999) and specifically pollinator insects (Mayer et al. 2006).Genetically modified organisms (GMOs)Genetically modified (GM) crops have allowed increased yields and, to some extent, have reduced pesticide usage. However, since 1996, when glyphosate-tolerant crops were introduced, 32?glyphosate-resistant weed species have been identified worldwide (Heap 2016), contributing to the considerable increase of herbicide usage (Mortensen et al. 2012). Therefore, GM crops remain an important topic due to the actual and perceived environmental, ecological and health risks linked to their use (e.g. Tsatsakis et al. 2017). The increase in the number and types of traits being engineered into crops, as well as the effect of stacked traits, indicates a need for assessments that account for different types of potential environmental effects beyond those associated with herbicide tolerance (HT) and insect resistance (IR) (Woodbury 2017). Established but incomplete studies have shown that cultivation of GM crops could affect pollinators and pollination services through unintended impacts on ecosystem health and biodiversity. The potential adverse effects posed by GM crops directly or indirectly impacting pollinators and pollination in ecosystems beyond agricultural systems and the consequences remain a concern. Indirect impacts of GMOs on pollinators and pollination services beyond agricultureThe IPBES assessment (IPBES 2016a) reported many clear indirect threats to pollinators and pollination. Land-use change for GM crop cultivation (e.g. deforestation; shift to monoculture) is a major indirect threat that destroys or degrades pre-existing pollinator populations, communities and the pollination functions they deliver in the landscape (IPBES 2016a). HT crops are associated with high herbicide use that eliminates many agricultural weeds that provide food for pollinators, resulting in a reduction in available floral resources in the landscape (IPBES 2016a). The cessation of insecticide use with adoption of IR crops may have benefited some pollinator species by reducing risks from pesticide exposure. However, the emergence of pest resistance or outbreaks of secondary pests often leads to resumption of insecticide use and return of attendant risks to pollinators (IPBES 2106a).Direct impacts of GMOs on pollinators and pollination services beyond agricultureScientific evidence of a direct hazard to and impacts on pollinators from contact with GM crops is conflicting and/or inconclusive (Malone and Burgess 2009; Woodbury et al. 2017) or does not currently address potential sublethal effects (IPBES 2016a). Toxicity to pollinatorsThe western honeybee (Apis mellifera) is the most studied domesticated pollinator and has been a standard organism for laboratory toxicity tests and assessing the impacts of chemical pesticides for agriculture. Recent studies showed no clear negative effects of Cry Bt?toxins (used in IR crops) or HT proteins on honeybees (Lima et al. 2011; Ricroch et al. 2017). Apart from honeybees, only a few other bee species, wild but sometimes also managed, such as bumblebees (e.g. Bombus terrestris) and solitary bees (e.g. Osmia spp.), have been studied; other managed or wild pollinator species have been less considered. One example is the monarch butterfly (Danaus plexippus), a non-target insect pollinator affected by the consumption of pollen of Bt?corn (Losey et al. 1999; Hansen Jesse and Obrycki 2000). Research on non-target effects of transgenic crop plants has focused primarily on bitrophic, tritrophic and indirect effects of entomotoxins from Bacillus thuringiensis (Bt), but little work has considered intergenerational transfer of Cry proteins. Paula et al. (2014) reported that Bt?toxin was transferred by a butterfly (Chlosyne lacinia) to its eggs and this had effects on its offspring, with impacts on mortality and development time.In additional to the direct contact with GMO plants, pollen substitutes are also an object of study. Bee feed supplements are currently widely used in apiculture to supplement natural forage. A recent experimental study showed that a supplementary diet with GMO corn (transgenic AG8088YG) negatively impacted bee health (Nicodemo et al. 2018).?In order to assess toxicity effect on pollinators caused by GMO crops, it is important to take into account not only all development stages of insect pollinators like honeybees (egg-larvae-pupa-adult) but also other wild or managed pollinator species. Biological characteristics of different species or developmental stages can respond differently to toxicity tests; for example, the response to novel proteins in pollen diets can differ between honeybee larvae and larvae of bumblebees and solitary bees due to the fact that the laststage honeybee larvae consume mainly secretions from nurse honeybees instead of pollen (Malone and Burgess 2009). Gene flow and pollination servicesPollinator species can collect and transport pollen between GM and non-GM plants, and mediate the transfer of transgenes (Malone and Burgess 2009); thus, pollinators represent important potential vectors for the transfer of genes from GM crops to related native plants in other ecosystems beyond agriculture. This may promote contamination of non-GM seeds and wild relatives, as well as contamination of honey products with GM ingredients.Pollen-mediated gene flow has been reported at various levels in most GM crops (Ford et al. 2006; Han et al. 2015; Yan et al. 2015). Honeybees and bumblebees are very important vectors of oilseed rape pollen, even though substantial wind-pollination occurs too. The relationships between the four major commercialized GM crops (maize, soybeans, cotton, oilseed rape) and pollen dispersal by insects have been reported in different studies. With many crop species, most cross-pollination occurs within a few meters of the source plant (Ramsay et al. 2003; Funk et al. 2006). However, for oilseed rape some longer-range field studies have recorded cross-pollination events 5 to 26 km from source at two Scottish sites (Ramsay et al. 2003) and events at up to 3 km at three different Australian sites (Rieger et al. 2002). In Kenya, carpenter bees (Xylocopa spp.) fly distances of at least 7 km and are capable of carrying GMO pollen from cultivated to wild cowpea flowers (Pasquet et al. 2008). Soybean is autogamous, but studies shown that about 5% of plants have been cross-pollinated (McGregor 1976). Recent studies in Brazil have shown that insect pollination is beneficial for soybean (Chiari et al. 2005; Milfont et al. 2013). Thus, the possibility of bee-mediated cross-pollination between GM and non-GM soybean exists and warrants further investigation (Malone and Burgess 2009).The persistence of transgenes in nature has been documented in central Argentina, implying that gene flow and introgression between feral populations of GM Brassica napus and wild B. rapa can occurr (Pandolfo et al. 2017). A study in China with eastern honeybees (Apis cerana cerana?Fabricius) and a herbicide-resistant GM strain of Brassica napus (Z7B10) examined the effects of honeybee short-range foraging on oilseed rape gene flow and honey composition (Liu et al. 2017). Results showed variable frequencies of gene flow between GM and non-GM oilseed rape cultivars, suggesting the important role of honeybees in gene flow of GMOs; GM pollen grains were found in honey collected from honeybees foraging on both GM and non-GM oilseed rape cultivars (Lui et al. 2017). Evidence from Mexico demonstrates that honeybees visit the flowers of soybean and that pollen of GMO soybean flowers is present in honey harvested by beekeepers (Borrell and Vandame 2012; Gálvez 2013; Villanueva-Gutiérrez et al. 2014; Gálvez 2016). Beside bees, Richards et al. (2005) found that nectar-feeding moths could travel hundreds of kilometres and it was concluded that this posed a potential risk for movement of Bt?cotton transgenes to non-GM cotton plants. Taken together, these studies demonstrate the importance of a good understanding of crop pollination biology for making robust assessments of transgene flow risk from GM plants.Other potential impacts of GMOs on pollinators and pollination services beyond agricultureRisk assessments of GMOs need to address the wider environmental and sociopolitical dimensions of risk taking into account a wide range of actors (Binimelis and Wickson 2018). The potential socioeconomic impacts go beyond agricultural sectors, since the expansion of GM genes to the environment can also cause potential adverse effects on indigenous peoples and their cultural ways of living and traditional practices (Bellevue 2017), which includes a reliance on natural pest control and seed integrity for their basic food resources. Additionally, beekeeper livelihoods can be impacted by the risk of GM ingredients contaminating their honey products which could exclude them from certain markets due to residue regulations. Beehive products have been considered as good indicators for monitoring environmental contamination (Bargańska et al. 2016; Conti and Botre 2001; Porrini et al. 2003; Ruiz et al. 2013) and the risks of contamination is creating a displacement of beekeepers and a restriction of the spaces in which they can operate (Binimelis and Wickson 2018).V.Response options to conserve and manage pollinators, their habitats and their food and water resources in all ecosystemsThe main gap for underdeveloped countries on shaping landscape management policies to benefit pollinators is the lack of knowledge on local pollinators and on their contributions to improving biodiversity and agricultural yields. Additionaly, the role of wild insects and other wild animals as pollinators, which have great importance for the maintenance of biodiversity (e.g. birds, bats and other small mammals, moths, butterflies, flies and beetles), should also be better recognized as providers of this important ecosystem service. For most of these countries, the management of native bees and appropriate beekeeping practices should have more attention. The lack of knowledge and the lack of monitoring contribute to the informal commercialization and introduction of pollinators that could become invasive species. In Latin America, data on pollinators are partially available. It is possible to identify areas that have not been thoroughly sampled, and also areas under threat of deforestation. An example of deforestation on a large scale is the Amazon region in the last 50 years. Figure 7 shows the deforestation in this region from 1978 to 2015. Studies report that tropical deforestation has impacted bee communities and their foraging characteristics (Campbell et al. 2018; Lichtenberg et al. 2017; Hipólito et al. 2018), but measures to mitigate these impacts are hampered by insufficient taxonomic knowledge and research in those regions where pressures are the greatest. Figure 7. Map of current status of deforestation in the Amazon Basin, provided courtesy of Dr. Luiz Gylvan Meira, Instituto Tecnológico Vale - Desenvolvimento Sustentável.Landscape approaches to pollinator conservation and climate changeClimate and land-use change are among the most important processes driving biodiversity loss, especially in the tropics (Gutierrez et al. 2017). Although the potential impacts of each threat have been widely studied in isolation, few studies have assessed the impacts of climate and land cover change in combination. Giannini et al. proposed a methodological framework, which integrates species distribution forecasts and graph theory to identify key conservation areas, to help design novel conservational and agricultural practices that can be crucial to conserve pollination services by buffering the joint effect of habitat configuration and climate change (Giannini et al. 2015b). Approaches to promote conservation of pollinators and their habitats can be integrated into land-use planning (Pufal et al. 2017; Potts et al. 2016). As most natural areas are under pressure due to anthropogenic uses, the ranges for pollinators’ activities are changing. Modelling is a very important tool for restoration and also to predict impacts of global change, which can support the development of protection policies for pollinators in future (Giannini et al. 2013a; Giannini et al. 2015b; Giannini et al. 2017; Costa et al. 2018).Recent studies considering landscape structure show how pollinator communities are linked to the health of ecosystems (e.g. Campbell et al. 2018, a study with a?aí palm in the Amazon; Hipólito et al. 2018, for coffee crops under forest). The maintainance of natural vegetation and corridors between crop fields, together with more diversified production systems, could help to conserve pollinators and to sustain pollination services. Where extensive natural area is lacking, small stands of traditional diversified farming systems already present in different regions of Latin America serve as an alternative to support native pollinators (Garibaldi et al. 2014; Garibaldi et al. 2016). In drylands, such as the semiarid region of north-eastern Brazil, populations of native bees can be jeopardized by climate change. Models show a possible shift in pollinators’ poplulations to areas more climatically suitable for them, with consequences for species dispersal and gene flow. One strategy could be the reconnection of the remaining suitable areas through conservation and restoration programmes based on the distribution of the plant species that are used by pollinators as sources of pollen and nectar (Giannini et al. 2017).Landscape genetics is a useful tool to support landscape management. Landscape genetics can determine population characteristics of pollinators, as well as genetic consequences of bee management in large areas, inside or outside their distribution areas (Jaffé et al. 2016 a,?b; Brito et al. 2010; Byatt et al. 2015; Quezada-?uan et al. 2012). On the east coast of Australia, a study showed the impact of anthropogenic displacement of colonies on the genetic structure of a stingless bee (Tetragonula carbonaria) (Chapman et al. 2017). There are some mitigation opportunities for pollinators (Settele et al. 2016; Scheffers et al. 2016); for example, assisted displacement of managed colonies of social pollinators and solitary pollinators taking into account the genetic composition of local populations, avoiding disturbances to their natural genetic patrimony (Toledo et al. 2017). This issue needs attention, and methods should be developed to evaluate the adaption of pollinators to new environments. Another point of concern regarding significant changes in landscape is related to crops such as oil palm that causes a large natural area to be deforested. One policy response to such concerns could be the incorporation of pollinator-friendly practices into existing certification schemes.Land or habitat restoration with pollinator considerationsCommunity and indigenous conserved areas – Options for pollinator conservationNatural or semi-natural habitats managed by local communities, particularly indigenous communities by means of customary laws/rules are important conservation hotspots (ICCA 2012). These areas are often outside state-regulated conservation protected area networks and are important biodiversity refuges providing valuable ecosystem services including pollination (Bhagwat 2009; Blicharska et al. 2013). Bodin et al. (2006) report that community-managed forests in Madagascar improved crop pollination in adjacent farming landscapes. Sacred groves are excellent examples of such community-protected forests and previously existed in Asia, Africa, Europe and Americas but their present occurrence is mostly restricted to Africa and Asia (Chandran et al. 1998). Sacred groves have been extensively documented in Nigeria (Onyekwelu and Olusola 2014) and in India (Malhotra et al. 2007), Thailand (Wangpakkapattanawong et al. 2010), the Philippines (Rebancos and Buot 2007) and several other south and south-east Asian countries (Ramakrishnan et al. 2012 in Parotta and Trosper 2012). Habitat enhancement might be necessary for improving conditions for pollinators, such as by introducing artificial nests (“bee hotels”). Several reports indicate open forests to harbor larger numbers of pollinator populations compared to closed-canopy forests (Taki et al. 2013; Wratten et al. 2012; Winfree et al. 2007). Areas where shifting cultivation practices exist often host a series of forests in different successional stages; their pollinator fauna should to be studied so that suitable management strategies for better pollinator fauna can be informed by such studies. Financial schemes and insurance programmes may be conceived that would further incentivize management of such forests by the local communities.Provision of indirect and direct economic incentivesIncentives for supporting biodiversity in farmlands have been proactively used in the United Kingdom (Dicks et al. 2015) and other European Union countries through agri-environment schemes. These schemes have so far been the best known examples of protecting biodiversity through providing incentives (Batary et al. 2015). A number of studies have linked increased pollinator abundance and/or diversity to such schemes. The US Farm Bill (2008) made specific economic provisions for pollinator conservation when it was further ratified in the 2014 Farm Bill. These models show the potential of conserving non-cropped land in agricultural landscapes that can go a long way in conserving pollinators (Morandin and Winston 2006). While such schemes are generally non-existent in the developing world, economic incentive models for forest protection have emerged from India. Joint Forest Management (JFM), a participatory forest management programme, was launched in the early 1990s in West Bengal, an eastern Indian state that involved local communities in forest protection. The Forest Department extended revenue shares to the forest protection committees constituted by the villagers. This model later spread across other Indian states and has since been adopted in other developing countries too for protection or afforestation (Klooster and Masera 2000; Pagdee et al. 2006; Ellis and Bolland 2008; Porter-Bolland et al. 2012).Although such programmes have not explicitly included pollinator conservation as a focal theme, the incentivized community-protected forests outside the protected area network do contribute significantly to pollinator conservation as well. Similar models can and should be developed with a more clearly stated objective of conserving pollinators. Maderson and Wynne-Jones 2016 make a point about harnessing beekeepers’ knowledge and involving them in participatory bee conservation programme. Direct or indirect provisioning of incentives can be a mechanism through which this can work. Village-level Biodiversity Management Committees (BMC) are an integral part of India’s regulation of biodiversity. These BMCs are the custodians of biodiversity knowledge at the local community level. These bodies can be vehicles for incentivizing the conservation of pollinators and/or their habitats. Similar bodies exist in other developing countries as well. Disaster risk management and climate changePollinator conservation can be synonymous with habitat conservation and restoration or regeneration of natural habitats. Habitats in floodplain regions face recurrent floods, and the frequency of floods is increasing in the climate change scenario (Arnell and Gosling 2016). Tree planting is often identified as an important activity in climate change adaptation programmes (Pramova, et al. 2012) and pollinator-friendly shrubs or trees can be selected in such tree-planting programmes. Managed pollinatorsOften, managed pollinators are transported over long distances for the purpose of pollination (Cavigli et al. 2016). They are even transported outside of their natural distribution range (e.g. African honeybees into Brazil, and European bumblebees into Australia, Asia and South America) (Moritz et al. 2005). Trade and transportation of managed pollinatorsTrade and transport of managed pollinators, whether local, regional or global, appears to be uncoordinated and unregulated. There is an urgent need to set up and harmonize regulations for the trade in managed pollinators, which in turn affects the transportation of pollinators and should aim at preventing the relocation of species or their genetic material from their native range into non-native habitats, where species might compete with and spill over diseases to native and endemic pollinators, setting them and their pollination services at risk. In order to prevent catastrophic introductions into non-native ranges, some countries have set up national regulations; for instance, South Africa has restricted imports of non-native species and requires a preliminary environmental impact assessment (NEMBA 2004). Placement of managed pollinators in or close to protected areas should be better understood and carefully planned to protect wild pollinators from competition (Campbell and Motton 1985; Goulson 2003; Lopezaraiza-Mikel et al. 2007), avoid the spread of diseases (Fürst et al. 2014) and hence prevent negative impacts on wild plant pollination.Regulation of international trade in pollinatorsWhen regulating the international trade with species, colonies and queens (noting that trade with queens is quite common in the honeybee industry) it has been recommended to first promote and support the use of native/local alternatives for pollination purposes (Jaffé et al. 2015), before the need for trade is accepted. Regulations, policies and best management practices on pollinator movement need to consider the economic value of the pollinator movement, which might represent a trade-off, recognizing that movement of pollinators might be required for pollination purposes in agricultural production, e.g. pollination of almonds, apples and melons (Kremen 2005). If, however, quarantine requirements to prevent spillover and transmittal of bee pests and disease are instituted for importing or exporting pollinators, this might also create incentives to support local wild pollinators. In addition to any regulation, there is a need to elaborate a set of best management practices (BMP) for the transportation of bees, which must be based on an assessment of the appropriate use of different transportation structures (roadways, railways, as air cargo, etc.).Best practices in pollinator managementAside from large-scale transportation of managed pollinators, management within the apiaries of managed bees may play a role in the transmission and spread of diseases between colonies (Brosi et al. 2017). For this purpose, best management practices (BMP), similar to the Good Agricultural Practices (GAP) promoted by FAO, need to be developed that respect local differences in beekeeping and hive management. BMPs have been developed at a country level, e.g. in Australia (Somerville 2007), the United States (for crop pollination in California) (Heintz et al. 2011), and some other voluntary recommendations have been put forward (Ritter 2013), but overall international harmonization is lacking. Establishment of BMPs should be based on rigorous education of beekeepers and farmers on interactions between managed and wild pollinators and the requirements of wild pollinator communities and wild plant pollination. Risk managementPreventive measures put in place should be accompanied by a set of effective responses to current and emerging risks, such as diseases and invasive alien species. Introductions of non-native species can happen accidentally, but the spread of an invasive species or pathogen might be suppressed by early measures and activities, like the establishment of quarantine areas etc. There are a few regions in the world (parts of Australia, Seychelles) that are not affected by the ectoparasitic mite Varroa destructor (Locke 2016), the most detrimental honeybee pest. This mite also acts as vector for a number of bee viruses, which might spill over to wild bee species (McMahon et al. 2015). Effective countermeasures need to be put in place to prevent the invasion of these areas by the mite, if it is ever introduced. Australia has set up an information platform that aims at disseminating information relevant to all relevant stakeholders.Biosecurity incursions that affect a plant’s ability to produce flowering bodies for pollinators can significantly alter plant species composition (Pegg et al. 2017). This could then further affect the abundance and complexity of pollinator assemblages. In Australia, Austropuccinia psidii (myrtle rust) is an introduced fungal pathogen that inhibits the development of new shoots, leaves, flowering and fruiting bodies and seed (Pegg et al. 2014). The pathogen affects plant species in the family Myrtaceae, including paperbarks (Melaleuca spp.), tea-trees (Leptospermum spp.), eucalypts (Eucalyptus spp.), and lillipillies (Syzigium spp.), that are among the most dominant species found across many Australian ecosystems (Pegg et al. 2014). As the prevalence of the disease increases, declines are being observed across entire populations of individual plant species (Carnegie et al. 2016; Pegg et al. 2017). Declining plant diversity within ecosystems has been linked with declining insect diversity (herbivores and predators) (Knops et al. 1999). Therefore, a reduction in flowering caused by increased Austropuccinia?psidii infection rates may not only reduce plant diversity within ecosystems but also reduce nectar and pollen resources which many pollinating species may rely on. A subsequent reduction in pollinator abundance and diversity may further reduce pollination of other native plant species that exist within the same ecological communities but are not themselves directly susceptible to myrtle rust.MonitoringThe spread of pests and pathogens among managed pollinators and the spillover to wild pollinators, and its prevention and management, requires continuous monitoring of both managed pollinators and wild pollinators. The state institutions that are in charge of the monitoring need to be reinforced and maintained. In additional, a harmonized reporting procedure, data management strategy, and data storage including accessibility needs to be established, so that current and emerging risks and threats can be detected almost in real time and across borders, so that respective countermeasures can be activated. Over the last several years, the COLOSS network, whose activities depend on voluntary engagement of stakeholders, has set up surveillance networks and task force teams to enforce and standardize research, build capacity, create awareness for sustainable bee management, and inform policymakers.Knowledge managementThere are three key areas where knowledge and data management are crucial to supporting the role of pollinators in conservation and sustainable use of biodiversity in all ecosystems: (a)?knowledge about the status of pollinators; (b)?knowledge about the risks to human well-being generated by pollinator decline; and (c)?knowledge about what the best responses are, and where and when they should be implemented.Knowledge about the status of pollinatorsAs described in section III above, there is a severe lack of long-term data on the status of wild pollinator populations and communities in much of the world, especially for invertebrate pollinators. For example, in the European Red List of bees, 57% of the European bee species were classed as “data deficient”, with not enough information to assign a threatened status ADDIN EN.CITE <EndNote><Cite><Author>Nieto</Author><Year>2014</Year><RecNum>699</RecNum><DisplayText>(Nieto et al. 2014)</DisplayText><record><rec-number>699</rec-number><foreign-keys><key app="EN" db-id="e2s5p0e5ix0v9iefzw6ves2md20d90dz2we9" timestamp="1442742478">699</key></foreign-keys><ref-type name="Report">27</ref-type><contributors><authors><author>A. Nieto</author><author>Stuart P.M. Roberts,</author><author>James Kemp,</author><author>Pierre Rasmont,</author><author>Michael Kuhlmann,</author><author>Mariana García Criado,</author><author>Jacobus C. Biesmeijer,</author><author>Petr Bogusch, </author><author>Holger H. Dathe,</author><author>Pilar De la Rúa,</author><author>Thibaut De Meulemeester,</author><author>Manuel Dehon,</author><author>Alexandre Dewulf,</author><author>Francisco Javier Ortiz-Sánchez,</author><author>Patrick Lhomme,</author><author>Alain Pauly,</author><author>Simon G. Potts,</author><author>Christophe Praz,</author><author>Marino Quaranta,</author><author>Vladimir G. Radchenko,</author><author>Erwin Scheuchl,</author><author>Jan Smit,</author><author>Jakub Straka,</author><author>Michael Terzo,</author><author>Bogdan Tomozii,</author><author>Jemma Window,</author><author>Denis Michez</author></authors></contributors><titles><title>European Red List of Bees</title></titles><dates><year>2014</year></dates><pub-location>Luxembourg: Publication Office of the European Union</pub-location><urls><related-urls><url>;(Nieto et al. 2014). Addressing this data shortfall requires a combination of taxonomic training and capacity-building, standardized long-term monitoring at national scales and accessible, well-curated databases.An exemplary response has been demonstrated by the JRS Biodiversity Foundation pollinators programme. This funds projects in African countries. It aims to increase the accessibility and quality of pollinator biodiversity data, through long-term investment in collecting baseline data, developing technologies and methods to do so, and creating data-sharing platforms relevant at regional and local levels. The programme has already funded projects to develop long-term monitoring and accessible databases.Many initiatives, like the IABIN Thematic Pollinators Network, the BIOTA Program, the Global Biodiversity Information Facility (GBIF) and Species 2000, have been supporting the digitalization of pollinator-related biodiversity collections, offering possibilities to open access for biodiversity data. Most tropical biodiversity is poorly known, and an effort to use new tools to access information on pollinators has assisted in this.Notable tools and efforts include DNA barcoding; biodiversity informatics tools; geographical referencing for the museum specimens; and a focus on small collections. As yet, however, open access to data from most regional collections is not completely available to the general public, making it difficult to map the occurrences of better studied groups and to provide evidence on areas not sampled until now.TaxonomyThe support of basic scientific projects to increase the taxonomic knowledge of pollinators may be important for pollinator conservation; however, taxonomy is only a priority for invertebrate pollinators. In comparison, vertebrate pollinators, which include birds, mammals and reptiles ADDIN EN.CITE <EndNote><Cite><Author>Ratto</Author><Year>2018</Year><RecNum>1525</RecNum><DisplayText>(Ratto et al. 2018)</DisplayText><record><rec-number>1525</rec-number><foreign-keys><key app="EN" db-id="e2s5p0e5ix0v9iefzw6ves2md20d90dz2we9" timestamp="1513617636">1525</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Ratto, F.,</author><author>Simmons, B.I.,</author><author>Spake, R.,</author><author>Zamora-Gutierrez, V.,</author><author>MacDonald, M.A.,</author><author>Merriman, J.C.,</author><author>Tremlett, C.J.,</author><author>Poppy, G.M.,</author><author>Peh, Kelvin S. H.</author><author>Dicks, L.V.</author></authors></contributors><titles><title>Global importance of vertebrate pollinators for plant reproductive success: a meta-analysis</title><secondary-title>Frontiers in Ecology and the Environment</secondary-title></titles><periodical><full-title>Frontiers in Ecology and the Environment</full-title></periodical><dates><year>2018</year></dates><urls></urls></record></Cite></EndNote>(Ratto et al. 2018), are extremely well known taxonomically.Reviews of regional conservation needs for native bees have identified a shortage of taxonomic expertise as a constraint to effective conservation action. Many regions have many species not yet described and a shortage of experts to identify species, even when descriptions exist PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5CYXRsZXk8L0F1dGhvcj48WWVhcj4yMDA5PC9ZZWFyPjxS

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ADDIN EN.CITE.DATA (Batley and Hogendoorn 2009; Eardley et al. 2009a; Freitas et al. 2009). There are excellent examples of training courses in bee taxonomy. The American Museum of Natural History has conducted a training course annually since 1999, training over 250 people. The European COST (Cooperation in Science and Technology) Action Super-B has funded three annual European bee taxonomy courses, in 2016, 2017 and 2018, targeted towards European early career researchers. The funding for these courses ends in 2018.Provision of such courses in developing countries is limited by the availability of funding. Taxonomy training is perhaps best delivered by National Museums with entomology collections. Financial support for these institutions in data-poor regions (Africa, Latin America and Asia-Pacific) could be used to support taxonomy capacity-building.Standardized long-term monitoringMuch of our current understanding of declines in pollinator species comes from analysis of temporal trends in distributional data gleaned from ad hoc records of species presence collected by amateur naturalists PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5CYXJ0b21ldXM8L0F1dGhvcj48WWVhcj4yMDEzPC9ZZWFy

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ADDIN EN.CITE.DATA (Nieto et al. 2014; Regan et al. 2015). Standardized long-term monitoring of pollinators and pollination services is urgently needed to provide good quality information about patterns of decline and to target interventions ADDIN EN.CITE <EndNote><Cite><Author>IPBES</Author><Year>2016</Year><RecNum>1514</RecNum><DisplayText>(IPBES 2016a)</DisplayText><record><rec-number>1514</rec-number><foreign-keys><key app="EN" db-id="e2s5p0e5ix0v9iefzw6ves2md20d90dz2we9" timestamp="1513617634">1514</key></foreign-keys><ref-type name="Report">27</ref-type><contributors><authors><author>IPBES,</author></authors></contributors><titles><title>The assessment report of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services on pollinators, pollination and food production</title></titles><dates><year>2016</year></dates><pub-location>Bonn, Germany</pub-location><urls></urls></record></Cite></EndNote>(IPBES 2016a). The Government of the United Kingdom has funded the development of a Pollinator Monitoring and Research Partnership (PMRP), which aims to combine improved analyses of long-term records with new systematic survey activity to establish how insect pollinator populations are changing across Great Britain. This is funded initially for two years (2017 and 2018) as part of the National Pollinator Strategies for Scotland, England and Wales.The UK’s Pollinator Monitoring Research Advisory Group (PMRAG) recently conducted a stocktaking of pollinator monitoring programmes around the world, which identified 73 monitoring programmes. The vast majority (47) were in Europe, with only 2 in Africa and 1 in Asia. For example, in 2017 JRS Biodiversity Foundation funded the College of African Wildlife Management (CAWM) in Mweka, Tanzania, to develop and implement a monitoring programme for Tanzanian bee species. The most frequently included taxa across all these monitoring programmes were bumblebees (Bombus spp.) and butterflies. The majority of the initiatives (51/73) depend on data collected by volunteers, or “citizen scientists”. A number of these used standardized monitoring methods such as transect walks or pan traps. This indicates the feasibility of such monitoring programmes, but a dearth of activity in the data-poor areas of the world.The majority of existing literature focuses on specific hymenopteran groups, but there is a lack of information on the impact of landscape changes on non-bee taxa ADDIN EN.CITE <EndNote><Cite><Author>Senapathi</Author><Year>2017</Year><RecNum>3189</RecNum><DisplayText>(Senapathi<style face="italic"> et al.</style> 2017)</DisplayText><record><rec-number>3189</rec-number><foreign-keys><key app="EN" db-id="tw2des2aczdzaoeff22xe9arrp9se250eap5" timestamp="1519679303">3189</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Senapathi, Deepa</author><author>Goddard, Mark A.</author><author>Kunin, William E.</author><author>Baldock, Katherine C. R.</author></authors></contributors><titles><title>Landscape impacts on pollinator communities in temperate systems: evidence and knowledge gaps</title><secondary-title>Functional Ecology</secondary-title></titles><periodical><full-title>Functional Ecology</full-title><abbr-1>Funct. Ecol.</abbr-1><abbr-2>Funct Ecol</abbr-2></periodical><pages>26-37</pages><volume>31</volume><number>1</number><keywords><keyword>agri-environment</keyword><keyword>habitat characteristics</keyword><keyword>policy</keyword><keyword>pollinator conservation</keyword><keyword>spatial scales</keyword><keyword>species abundance</keyword><keyword>species richness</keyword></keywords><dates><year>2017</year></dates><isbn>1365-2435</isbn><urls><related-urls><url>;(Senapathi et al. 2017). Most studies have taken a “spatial” approach (as evidenced above) while very few studies have assessed changes over time by resampling sites across multiple habitat and land cover types and comparing findings to historical data sets PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5CdXJrbGU8L0F1dGhvcj48WWVhcj4yMDEzPC9ZZWFyPjxS

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ADDIN EN.CITE.DATA (see Carvalheiro et al. 2013) but are required to obtain a comprehensive understanding of land-use changes on pollinator communities.Accessible databasesGood taxonomy, volunteer recording and long-term monitoring of pollinator populations are only useful to policy in the long term if the data they generate are stored and curated in accessible databases.Several international biodiversity information centres carry information on pollinators, although their remit is far broader. For example, the International Union for Conservation of Nature (IUCN) holds a number of conservation databases, including the Red List of threatened species, which has assessed the threat status of all European bee species ADDIN EN.CITE <EndNote><Cite><Author>Nieto</Author><Year>2014</Year><RecNum>699</RecNum><DisplayText>(Nieto et al. 2014)</DisplayText><record><rec-number>699</rec-number><foreign-keys><key app="EN" db-id="e2s5p0e5ix0v9iefzw6ves2md20d90dz2we9" timestamp="1442742478">699</key></foreign-keys><ref-type name="Report">27</ref-type><contributors><authors><author>A. Nieto</author><author>Stuart P.M. Roberts,</author><author>James Kemp,</author><author>Pierre Rasmont,</author><author>Michael Kuhlmann,</author><author>Mariana García Criado,</author><author>Jacobus C. Biesmeijer,</author><author>Petr Bogusch, </author><author>Holger H. Dathe,</author><author>Pilar De la Rúa,</author><author>Thibaut De Meulemeester,</author><author>Manuel Dehon,</author><author>Alexandre Dewulf,</author><author>Francisco Javier Ortiz-Sánchez,</author><author>Patrick Lhomme,</author><author>Alain Pauly,</author><author>Simon G. Potts,</author><author>Christophe Praz,</author><author>Marino Quaranta,</author><author>Vladimir G. Radchenko,</author><author>Erwin Scheuchl,</author><author>Jan Smit,</author><author>Jakub Straka,</author><author>Michael Terzo,</author><author>Bogdan Tomozii,</author><author>Jemma Window,</author><author>Denis Michez</author></authors></contributors><titles><title>European Red List of Bees</title></titles><dates><year>2014</year></dates><pub-location>Luxembourg: Publication Office of the European Union</pub-location><urls><related-urls><url>;(Nieto et al. 2014). The Global Biodiversity Information Facility collates global biodiversity data for over 1.5 million species and has been used to investigate spatial patterns in plant-pollinator interactions, such as between oil-collecting bees in the genus Centris and flowers that produce oil PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5HaWFubmluaTwvQXV0aG9yPjxZZWFyPjIwMTM8L1llYXI+

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ADDIN EN.CITE.DATA (Giannini et al. 2013b). The Integrated Taxonomic Information System (ITIS) has a checklist of the world’s bee species, providing details of all synonyms and subspecies.Three projects funded by the JRS Biodiversity Foundation provide Africa-focused examples. The National Museums of Kenya were funded to collect and disseminate data on Lepidoptera in critical habitats in East Africa. This includes digitizing records of species occurrence held by partner institutions across the region and publishing those data to make them available for use by managers and conservationists. A second project, led by the Royal Museum for Central Africa, is funded to assemble, enhance, and mobilize data on the diversity and distribution of Diptera. Figure 8. Drivers of pollinator decline (central boxes) relate to the key risks associated with pollinator decline (right boxes), and how these drivers are addressed by three important sets of responses (left boxes) that ultimately reduce the risks. Arrows are thick if there is clear evidence that at least one of the responses can reduce the impact of the driver on pollinators, or clear evidence that the driver generates the impact underlying the risk, at least in some circumstances. Arrows are thin if the link between response and driver, or driver and risk, is suspected or inferred by current evidence, but direct empirical evidence of it taking place is either sparse or lacking. Source: ADDIN EN.CITE <EndNote><Cite><Author>Potts</Author><Year>2016</Year><RecNum>1523</RecNum><DisplayText>(Potts et al. 2016)</DisplayText><record><rec-number>1523</rec-number><foreign-keys><key app="EN" db-id="e2s5p0e5ix0v9iefzw6ves2md20d90dz2we9" timestamp="1513617636">1523</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Potts, Simon G.</author><author>Imperatriz-Fonseca, Vera</author><author>Ngo, Hien T.</author><author>Aizen, Marcelo A.</author><author>Biesmeijer, Jacobus C.</author><author>Breeze, Thomas D.</author><author>Dicks, Lynn V.</author><author>Garibaldi, Lucas A.</author><author>Hill, Rosemary</author><author>Settele, Josef</author><author>Vanbergen, Adam J.</author></authors></contributors><titles><title>Safeguarding pollinators and their values to human well-being</title><secondary-title>Nature</secondary-title></titles><periodical><full-title>Nature</full-title><abbr-1>Nature</abbr-1></periodical><pages>220-229</pages><volume>540</volume><number>7632</number><dates><year>2016</year><pub-dates><date>12/08/print</date></pub-dates></dates><publisher>Macmillan Publishers Limited, part of Springer Nature. All rights reserved.</publisher><isbn>0028-0836</isbn><work-type>Review</work-type><urls><related-urls><url> et al. 2016.Knowledge of risks to human well-beingWhen it comes to knowledge of links between pollinator decline and human well-being, the main challenges for knowledge management are complexity and lack of relevant knowledge in many areas (Figure 8 above illustrates both).In the case of invasive species and pesticides, risk assessment and tiered approaches to mitigate the risks are well established policy processes PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5LZWVsaW5nPC9BdXRob3I+PFllYXI+MjAxNzwvWWVhcj48

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ADDIN EN.CITE.DATA (Keeling et al. 2017; Keeling et al. 2017a; IPBES 2016a,?b), developed in response to complexity and large uncertainties.Horizon scanning garners knowledge from across society as broadly as possible to identify emerging risks that can feed into risk assessment processes PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Ccm93bjwvQXV0aG9yPjxZZWFyPjIwMTY8L1llYXI+PFJl

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ADDIN EN.CITE.DATA (Brown et al. 2016b; Roy et al. 2014; Sutherland et al. 2017). This process has identified specific pollinator-related risks, such as the potential for Bombus terrestris to invade in southern Africa and Australia ADDIN EN.CITE <EndNote><Cite><Author>Sutherland</Author><Year>2017</Year><RecNum>1535</RecNum><DisplayText>(Sutherland, Barnard, et al. 2017)</DisplayText><record><rec-number>1535</rec-number><foreign-keys><key app="EN" db-id="e2s5p0e5ix0v9iefzw6ves2md20d90dz2we9" timestamp="1513617638">1535</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Sutherland, William J.</author><author>Barnard, Phoebe</author><author>Broad, Steven</author><author>Clout, Mick</author><author>Connor, Ben</author><author>C?té, Isabelle M.</author><author>Dicks, Lynn V.</author><author>Doran, Helen</author><author>Entwistle, Abigail C.</author><author>Fleishman, Erica</author><author>Fox, Marie</author><author>Gaston, Kevin J.</author><author>Gibbons, David W.</author><author>Jiang, Zhigang</author><author>Keim, Brandon</author><author>Lickorish, Fiona A.</author><author>Markillie, Paul</author><author>Monk, Kathryn A.</author><author>Pearce-Higgins, James W.</author><author>Peck, Lloyd S.</author><author>Pretty, Jules</author><author>Spalding, Mark D.</author><author>Tonneijck, Femke H.</author><author>Wintle, Bonnie C.</author><author>Ockendon, Nancy</author></authors></contributors><titles><title>A 2017 Horizon Scan of Emerging Issues for Global Conservation and Biological Diversity</title><secondary-title>Trends in Ecology &amp; Evolution</secondary-title></titles><periodical><full-title>Trends in Ecology &amp; Evolution</full-title><abbr-1>Trends Ecol Evol</abbr-1></periodical><pages>31-40</pages><volume>32</volume><dates><year>2017</year></dates><publisher>Elsevier</publisher><isbn>0169-5347</isbn><urls><related-urls><url>;(Sutherland et al. 2017).Knowledge about appropriate responsesKnowledge about appropriate responses to mitigate or reverse pollinator decline, or to reduce its impacts on biodiversity and ecosystems, comprises knowledge about (a) what responses are available and (b)?how effective those responses are at delivering their specific objectives. Information about available responses can be generated by sharing best practice guidelines, or case studies, among international networks. Many examples of sharing best practices for pollinator conservation beyond food production are provided by the existing national pollinator strategies. For example, the National Pollinators Strategy for England has defined and widely shared “Five simple actions for pollinators”, and an accompanying set of case studies. Further action to catalyse an international network that collates best practice guidelines and case studies to support wild pollinators would be valuable in this context.Strictly, best practices should be identified by benchmarking, based on outcome metrics that compare practices carried out in a similar context, to find out which perform best. This is where the second area of knowledge about appropriate responses is important. Knowledge about the relative effectiveness of responses at delivering their objectives must be rigorously synthesized and shared as widely as possible.Systematic review, synthesis and summarizing of evidence relating to environmental management is rapidly developing PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5EaWNrczwvQXV0aG9yPjxZZWFyPjIwMTQ8L1llYXI+PFJl

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ADDIN EN.CITE.DATA (Scheper et al. 2013; Dicks et al. 2010; Humbert et al. 2012; James et al. 2016; Villemey et al. 2018; Blowers et al. 2017) have already been published online and are fully open access. For example, Villemey et al. ADDIN EN.CITE <EndNote><Cite><Author>Villemey</Author><Year>2018</Year><RecNum>1828</RecNum><DisplayText>(Villemey et al. 2018)</DisplayText><record><rec-number>1828</rec-number><foreign-keys><key app="EN" db-id="e2s5p0e5ix0v9iefzw6ves2md20d90dz2we9" timestamp="1519309343">1828</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Villemey, Anne</author><author>Jeusset, Arzhva?l</author><author>Vargac, Marianne</author><author>Bertheau, Yves</author><author>Coulon, Aurélie</author><author>Touroult, Julien</author><author>Vanpeene, Sylvie</author><author>Castagneyrol, Bastien</author><author>Jactel, Hervé</author><author>Witte, Isabelle</author><author>Deniaud, Nadine</author><author>Flamerie De Lachapelle, Frédérique</author><author>Jaslier, Emmanuel</author><author>Roy, Véronique</author><author>Guinard, Eric</author><author>Le Mitouard, Eric</author><author>Rauel, Vanessa</author><author>Sordello, Romain</author></authors></contributors><titles><title>Can linear transportation infrastructure verges constitute a habitat and/or a corridor for insects in temperate landscapes? A systematic review</title><secondary-title>Environmental Evidence</secondary-title></titles><periodical><full-title>Environmental Evidence</full-title></periodical><pages>5</pages><volume>7</volume><number>1</number><dates><year>2018</year><pub-dates><date>2018/02/05</date></pub-dates></dates><isbn>2047-2382</isbn><urls><related-urls><url>;(2018) found that globally, terrestrial verges along linear transport infrastructure (road, rail, pipelines and powerlines) host similar or richer pollinator communities than habitats away from linear transport features. These resources, and the rigorous knowledge synthesis methods that underlie them, represent a gold standard for management of scientific knowledge. They are not necessarily appropriate for synthesizing other forms of knowledge, such as indigenous and local knowledge or tacit, experiential knowledge held by practitioners such as land managers and conservationists.In addition to information about effectiveness of practices at supporting pollinators, relative impacts of pollinator-friendly versus unfriendly practices (or landscapes) on the full range of benefits provided by pollinators should be evaluated. These benefits include cultural (e.g. identity), financial (e.g. honey sales), health (e.g. pharmaceutical properties of bee products), human (e.g. employments in beekeeping), and social (e.g. beekeepers associations) dimensions. The sum and balance of these benefits are the foundation for future development and sustainable rural livelihoods. Therefore, evaluating how the full range of benefits change would be a robust approach to valuing pollinator changes in both monetary and non-monetary terms PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5HYXJpYmFsZGk8L0F1dGhvcj48WWVhcj4yMDE3PC9ZZWFy

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GaribaldiUniversidad Nacional de Río Negro, ArgentinaBarbara Gemmill-HerrenWorld Agroforestry Center, KenyaBrad G. HowlettThe New Zealand Institute for Plant & Food Research Limited, New ZealandSteven JohnsonSchool of Life Sciences, University of KwaZulu-Natal, South AfricaMonica KobayashiSecretariat of the Convention on Biological Diversity, CanadaMichael LattorffInternational Centre of Insect Physiology and Ecology, KenyaPhilip O’B. LyverLandcare Research, New ZealandHien NgoIntergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services (IPBES), GermanySimon G. PottsReading University, United KingdomDeepa SenapathiReading University, United KingdomColleen SeymourSouth African National Biodiversity Institute, South Africa?Adam VanbergenAgroecologie, AgroSup Dijon, INRA, Univ. Bourgogne Franche-Comte, F-21000 Dijon, France & NERC Centre for Ecology & Hydrology, United Kingdom__________ ................
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