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1 better management and utilization of bees as pollinators.
2 crops have focused on reducing the need for pollinators.
3 n restores pollination accuracy and fit with pollinators.
4 major group of wild and commercially-reared pollinators.
5 ductive services provided by animals such as pollinators.
6 oadening the drivers of floral traits beyond pollinators.
7 in mediating interactions between plants and pollinators.
8 icide flupyradifurone than other managed bee pollinators.
9 ce of floral morphology in relation to their pollinators.
10 g concern over current and future impacts on pollinators.
11 d in areas with high abundance of vertebrate pollinators.
12 creased specificity between plants and their pollinators.
13 adaptation to selection imposed by distinct pollinators.
14 with pollinator dependence in the absence of pollinators.
15 n co-evolutionary process between plants and pollinators.
16 fee-suitable areas will also be suitable for pollinators.
17 species-specific mutualism system with wasp pollinators.
18 defenses to limit pollen loss to generalist pollinators.
19 produced by nectaries to attract and reward pollinators.
20 and to declines in the abundance of dipteran pollinators.
21 d among populations, compared to less mobile pollinators.
22 al resources to produce nectar that attracts pollinators [3], but toxins in this reward could disrupt
23 ly term "migrant hoverflies." Adults are key pollinators [7-10] and larvae are significant biocontrol
24 sehold income was positively associated with pollinator abundance in gardens, highlighting the influe
25 plant-pollinator interactions by decreasing pollinator abundance with implications for pollination a
26 Management practices increasing not just pollinator abundance, but also functional divergence, co
28 short growing seasons, low temperatures, low pollinator activity or unstable weather may hamper sexua
29 iation, and one intuitive hypothesis is that pollinators affect rates of plant diversification throug
30 in landscapes with high edge density, 70% of pollinator and 44% of natural enemy species reached high
33 y bees are agriculturally important, both as pollinators and by providing products such as honey.
35 of size matching among Asteraceae and their pollinators and its relationship with foraging efficienc
38 ortant negative side effects, especially for pollinators and other beneficial insects feeding on nect
39 ow naturally occurring extreme events impact pollinators and pollination has not yet been synthesized
40 the potential impacts of natural hazards on pollinators and pollination in natural and cultivated sy
41 ersity and species richness of phytophagous, pollinators and predators arthropods, as well as the per
42 rsification exerted the strongest effects on pollinators and predators, suggesting these management s
43 plexity impacts interactions between plants, pollinators, and co-flowering competitors is unknown.
47 on of self-pollination, attraction of animal pollinators, and the effective use of wind pollination.
49 behaviour of the introduced super-generalist pollinator are implicated as key in determining the role
54 functional redundancy and complementarity of pollinator assemblages and, therefore, might alter the p
57 ecosystem function and the global decline in pollinators attenuates the resistance of natural areas a
62 en predators and prey and between plants and pollinators, but studies have rarely demonstrated signif
63 gate visitors of plants, like bees and other pollinators, but these impacts can be difficult to inter
65 These results demonstrate that competing pollinators can take advantage of alarm signal informati
68 at sexually dimorphic traits would evolve if pollinators changed behavior depending on the traits of
70 in sensory drive probably play out in plant-pollinator communication, the theory has not been formal
72 tensive designed greenspaces, the support of pollinator communities hinges significantly on floral re
78 d the effects of mass flowering apple on the pollinator community and yield of co-blooming strawberry
79 asynchronous range shifts in an alpine plant-pollinator community by transplanting replicated alpine
80 om bark beetle outbreaks may drive shifts in pollinator community composition through cascading effec
83 These studies suggest that highly mobile pollinators conduct greater gene flow within and among p
85 in urban planning recommendations to enhance pollinator conservation, using increasing city-scale com
87 whether wildflower gardens, while benefiting pollinators, could also hasten the extinction of native
88 volved interactions between plants and their pollinators, could be causing plant reproduction to be l
96 ecause infectious diseases are implicated in pollinator declines worldwide, a better understanding of
101 e populations with generalist pollination or pollinator dependence were less pollen limited than nati
104 and availability, breeding programs for many pollinator-dependent crops have focused on reducing the
105 nd that the positive effects emerge only for pollinator-dependent crops, while pollinator-independent
106 favouring early reproductive effort, to less pollinator-dependent plants favouring a prolonged phenol
107 ong trait trade-offs, which ranged from more pollinator-dependent plants favouring early reproductive
108 stic insights into how phytochemicals affect pollinator diseases and (2) the restriction to few, comm
109 eveloped Bayesian network models integrating pollinator dispersal and resource switching to estimate
110 nsive area, and allotments due to their high pollinator diversity and leverage on city-scale plant-po
112 edictions, we surveyed visitation frequency, pollinator effectiveness (pollen deposition ability) and
113 mpact of plant removal on flower visitation, pollinator effectiveness and insect foraging in several
116 trade often involves movement of many insect pollinators, especially bees, beyond their natural range
121 variation in the prevalence of mutualism and pollinators feeding upon resources in addition to reward
122 e results demonstrate that alkaloids enhance pollinator flower constancy, opening new perspectives in
123 ired for plant defense as well as to attract pollinators for the successful reproduction of plumeria.
124 st contributions by natural habitats of wild pollinators - forests - to plot-level crop revenue, wher
126 etween practitioners' bumblebee-friendly and pollinator-friendly lists: r = 0.75), appropriateness an
129 ween BeeWatch records and the practitioners' pollinator-friendly plant list (465 plants from 9 differ
131 as led to numerous recommendations of which "pollinator-friendly" plants to grow and help turn urban
132 y and population-level impacts to plants and pollinators from seven hazard types, including climatolo
135 pis mellifera, is the most important managed pollinator globally and has recently experienced unsusta
136 nown pollination syndrome(s) with functional pollinator group(s) that are attracted to blue flowers,
138 ong plant species, the redistribution of the pollinator guild affected mostly the other plants with h
140 and national initiatives aimed at restoring pollinator habitats and populations have been developed.
141 this change in the natural habitats of wild pollinators has reduced crop revenue possibly by as much
144 re, field observations show that bee and fly pollinators have opposite colour preferences; this resul
145 despread reports of declining populations of pollinators have raised concerns that plant populations
147 cological stressors are drivers of declining pollinator health and responsible for observed populatio
148 lights the potential of CRP lands to improve pollinator health and the utility of colony-level molecu
152 e-induced chemical defenses and signaling on pollinators (herbivore-induced pollinator limitation).
153 rdens and allotments (community gardens) are pollinator 'hotspots': gardens due to their extensive ar
154 The attractiveness of ornamental plants to pollinators, however, cannot be presumed, and some studi
155 our study supports the pooling of different pollinators (hummingbirds, bats, rodents and flowerpierc
157 ies, reproduction appears to be dependent on pollinator identity such that reduced reproduction may b
159 ffectiveness (pollen deposition ability) and pollinator importance (the product of visitation frequen
161 ell-replicated study of floral resources and pollinators in 360 sites incorporating all major land us
163 represent a new floral cue that could assist pollinators in the recognition and learning of rewarding
165 ransmission involving economically important pollinators, including honey bees (Apis mellifera), has
166 ompanied by a reduction in traits attracting pollinators, including reduced emission of floral scent.
169 contrasting between pollinator-dependent and pollinator-independent crops, we find that the positive
171 ow available in the market with the label of pollinator-independent, the real dependence of these var
173 ; abundance and species richness of Diptera, pollinator insects, spiders, and predators (predator ins
176 t the loss of generalist plants alters plant-pollinator interactions by decreasing pollinator abundan
177 for restoration to re-establish native plant-pollinator interactions critical for production of outcr
178 hypothesis that impacts of climate on plant-pollinator interactions operate through changes in water
179 ent plant traits, such as light driven plant-pollinator interactions or light emitting plant-based se
180 hanges in water availability to impact plant-pollinator interactions through pollinator responses to
181 velop a framework of sensory drive for plant-pollinator interactions, identifying similarities and di
187 mptions about the cognitive abilities of bat pollinators, invoke Weber's law inappropriately, and can
188 al and physiological coadaptation with their pollinators involving terpenoid- and benzenoid-derived c
190 pecific pollen (HP) transfer by their shared pollinators is common and has consequences for plant rep
197 flow across the landscape, distinct types of pollinators may cause different opportunities for allopa
198 plants exhibited species-specific direct and pollinator-mediated indirect responses to frost, thus su
202 that the induction of sequential behavior in pollinators might be crucial to the evolution of sexual
203 onsumer-resource mechanisms underlying plant-pollinator mutualisms can increase persistence, producti
204 ts of forest conservation, as this preserves pollinators' natural habitats, and by extension its inha
207 ns, we constructed 16 hybrid herbivore-plant-pollinator networks along an agricultural intensificatio
208 delling and data from eleven bipartite plant-pollinator networks observed along a landscape simplific
211 ify key traits associated with the different pollinators of 19 Merianieae species and estimated the p
213 etting was more effective at capturing known pollinators of alfalfa, especially those belonging to th
215 toes, including Aedes aegypti, are effective pollinators of the Platanthera obtusata orchid, and demo
217 ions when the goal of a study is to identify pollinators or link pollinator decline to food productio
220 and services by decreasing the overlap among pollinators' phenologies within European assemblages, ex
221 Despite evidence that climate warming shifts pollinator phenology, a general assessment of these shif
222 ets to examine relationships among land use, pollinator phylogenetic structure, and crop production.
225 rm the conservation benefit of hedgerows for pollinator populations and demonstrate the importance of
230 o explain mechanisms underlying variation in pollinator preferences across populations, and how envir
231 r cosmopolitan status to understand how wild pollinator preferences change across different continent
232 atching between floral nectar tube depth and pollinator proboscis length of interacting species, such
233 community subsets, such as known tree fruit pollinators, rare pollinator species, and bees collected
234 A fundamental question is how generalist pollinators recognize "flower objects" in vastly differe
236 increase confidence in existing measures of pollinator redundancy at the community level using visit
241 impact plant-pollinator interactions through pollinator responses to differences in floral attractant
242 nonpollinator agents can reinforce or oppose pollinator selection, and, therefore, affect floral trai
246 on average, the mean flight date of European pollinators shifted to be 6 d earlier over the last 60 y
250 urs are more chromatic where there are fewer pollinators, solar radiation is high, precipitation and
252 we quantify pollen dispersal for individual pollinator species across more than 690 ha of tropical f
253 l networks, we discovered that few plant and pollinator species acted as connectors or hubs, both wit
254 cies, provide food and nesting resources for pollinator species and other beneficial arthropods.
255 ience) data, with the possibility to specify pollinator species or group, to powerfully support trans
256 , such as known tree fruit pollinators, rare pollinator species, and bees collected during apple bloo
257 ttributable to decreased visitation from key pollinator species, such as bumble bees, at warmer sites
258 restoration resulted in a marked increase in pollinator species, visits to flowers and interaction di
262 on non-target organisms, including important pollinators such as the European honeybee Apis mellifera
267 Plants ecologically specialized on a single pollinator taxon were extremely pollen limited across la
268 Floral syndromes are complex adaptations to pollinators that include color, nectar, and shape variat
269 n for having elaborate arms races with their pollinators that result in intricate morphologies in bot
272 , we find the holistic dynamic of plants and pollinators to be remarkably coherent across years, allo
276 th overlaps substantially with that of other pollinators, to survey the utilization of ornamental pla
277 show substantial inter-specific variation in pollinator trends, based on occupancy models for 353 wil
278 to open-pollinated varieties, but, even so, pollinators typically enhance seed production of both ty
280 potential distributions of coffee and coffee pollinators under current and future climates in Latin A
281 flowers appear to manipulate the behavior of pollinators using sexually dimorphic traits in the dioec
282 r animal pollination, understanding how wild pollinators utilize resources across environments can en
283 in Aconitum spp. nectar affect rates of both pollinator visitation and robbery but may have co-evolve
286 ility, in this bumblebee-pollinated species, pollinator visitation peaked at intermediate water level
287 es appears to be primarily driven by overall pollinator visitation rate, regardless of pollinator ide
288 rather than specific plant species, promotes pollinator visitation, and that diverse landscapes promo
292 tomato, Solanum peruvianum, herbivory limits pollinator visits, which reduces individual plant fitnes
293 During apple bloom, the known tree fruit pollinators were more frequently captured in the orchard
294 flowers present a higher-quality reward for pollinators, whereas male flowers have a more conspicuou
295 eton to keep their structures on display for pollinators, which has important implications for both t
297 M. sexta Hence, the hawkmoth is an important pollinator while the M. sexta larvae are specialized her
299 ble bees are important and widespread insect pollinators who face many environmental challenges.
300 power of the western honey bee, a generalist pollinator whose diet breadth overlaps substantially wit