bee abundance
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2022 ◽  
Author(s):  
Vera Wilder Pfeiffer ◽  
David W. Crowder ◽  
Janet Silbernagel

Abstract Wild bee communities persist in cities despite major disruption of nesting and food resources by urban development. Bee diversity and abundance is key for urban agriculture and maintenance of plant diversity, and assessing what aspects of cities enhance bee populations will promote our capacity to retain and provision bee habitat. Here, we assessed how variation in land cover and neighborhood development history affected bee communities in the midwestern US urban landscape of Madison, Wisconsin. We sampled bee communities across 38 sites with relatively high (> 55%) or low (< 30%) levels of impervious surface, and assessed effects of land use and neighborhood development history on bee abundance and species richness. We show abundance and richness of bees was lower in recently developed neighborhoods, with particularly strong negative effects on soil nesting bees. Soil nesting bees and bee community richness decreased as cover of impervious surface increased, but above ground nesting bees were minimally impacted. Bee community similarity varied spatially and based on dissimilar local land cover, only for soil nesting bees, and the overall bee community. Impervious surface limited bee abundance and diversity, but new neighborhoods were associated with greater negative effects. We suggest that enhancing the structural diversity of new neighborhoods in urban ecosystems may imitate the structural benefits of older neighborhoods for bee populations.


2021 ◽  
Author(s):  
Vera W Pfeiffer ◽  
David W Crowder ◽  
Janet Silbernagel

Wild bee communities persist in cities despite major disruption of nesting and food resources by urban development. Bee diversity and abundance is key for urban agriculture and maintenance of plant diversity, and assessing what aspects of cities enhance bee populations will promote our capacity to retain and provision bee habitat. Here, we assessed how variation in land cover and neighborhood development history affected bee communities in the midwestern US urban landscape of Madison, Wisconsin. We sampled bee communities across 38 sites with relatively high (> 55%) or low (< 30%) levels of impervious surface, and assessed effects of land use and neighborhood development history on bee abundance and species richness. We show abundance and richness of bees was lower in recently developed neighborhoods, with particularly strong negative effects on soil nesting bees. Soil nesting bees and bee community richness decreased as cover of impervious surface increased, but above ground nesting bees were minimally impacted. Bee community similarity varied spatially and based on dissimilar local land cover, only for soil nesting bees, and the overall bee community. Impervious surface limited bee abundance and diversity, but new neighborhoods were associated with greater negative effects. We suggest that enhancing the structural diversity of new neighborhoods in urban ecosystems may imitate the structural benefits of older neighborhoods for bee populations.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Szymon Smoliński ◽  
Aleksandra Langowska ◽  
Adam Glazaczow

AbstractVarroa destructor is the main pest of the honey bee Apis mellifera, causing colony losses. We investigated the effect of temperature on the autumn abundance of V. destructor in bee colonies over 1991–2020 in Central Europe. We tested the hypothesis that temperature can affect autumn mite populations with different time-lags modulating the bee abundance and brood availability. We showed that raised spring (March–May) and autumn (October) temperatures reinforce autumn V. destructor infestation in the bee colonies. The critical temperature signals embrace periods of bee activity, i.e., just after the first cleansing flights and just before the last observed bee flights, but no direct effects of phenological changes on V. destructor abundance were found. These effects were potentially associated with increased bee reproduction in the specific periods of the year and not with the extended period of activity or accelerated spring onset. We found significant effects of autumn bee abundance, autumn capped brood abundance, and the number of colonies merged on autumn mite infestation. We also observed differences in V. destructor abundance between bees derived from different subspecies. We indicated that climatic effects, through influence on the bee abundance and brood availability, are one of the main drivers regulating V. destructor abundance.


2021 ◽  
Vol 288 (1960) ◽  
Author(s):  
Hamutahl Cohen ◽  
Gordon P. Smith ◽  
Hillary Sardiñas ◽  
Jocelyn F. Zorn ◽  
Quinn S. McFrederick ◽  
...  

As the global agricultural footprint expands, it is increasingly important to address the link between the resource pulses characteristic of monoculture farming and wildlife epidemiology. To understand how mass-flowering crops impact host communities and subsequently amplify or dilute parasitism, we surveyed wild and managed bees in a monoculture landscape with varying degrees of floral diversification. We screened 1509 bees from 16 genera in sunflower fields and in non-crop flowering habitat across 200 km 2 of the California Central Valley. We found that mass-flowering crops increase bee abundance. Wild bee abundance was subsequently associated with higher parasite presence, but only in sites with a low abundance of non-crop flowers. Bee traits related to higher dispersal ability (body size) and diet breadth (pollen lecty) were also positively related to parasite presence. Our results highlight the importance of non-crop flowering habitat for supporting bee communities. We suggest monoculture alone cannot support healthy bees.


PLoS ONE ◽  
2021 ◽  
Vol 16 (7) ◽  
pp. e0254072
Author(s):  
Sergio Osorio-Canadas ◽  
Noé Flores-Hernández ◽  
Tania Sánchez-Ortiz ◽  
Alfonso Valiente-Banuet

‘Mexical’ scrubland is a sclerophyllous evergreen Mediterranean-like vegetation occurring in the leeward slopes of the main Mexican mountain ranges, under tropical climate. This biome occupies an elevational range approximately from 1900 to 2600 meters above sea level, which frequently is the upper-most part of the mountains range. This puts it at risk of extinction in a scenario of global warming in which an upward retraction of this type of vegetation is expected. The Mexical remains one of the least studied ecosystems in Mexico. For instance, nothing is known about pollinator fauna of this vegetation. Our main objective is to make a first insight into the taxonomic identity of the bee fauna that inhabits this biome, and to study how it is distributed along the elevational gradient that it occupies. Our results highlight that elevation gradient negatively affects bee species richness and that this relationship is strongly mediated by temperature. Bee abundance had no significant pattern along elevational gradient, but shows a significant relationship with flower density. Interestingly, and contrary to previous works, we obtained a different pattern for bee richness and bee abundance. Bee community composition changed strongly along elevation gradient, mainly in relation to temperature and flower density. In a global warming scenario, as temperatures increases, species with cold preferences, occupying the highest part of the elevation gradient, are likely to suffer negative consequences (even extinction risk), if they are not flexible enough to adjust their physiology and/or some life-story traits to warmer conditions. Species occupying mid and lower elevations are likely to extend their range of elevational distribution towards higher ranges. This will foreseeably cause a new composition of species and a new scenario of interactions, the adjustment of which still leaves many unknowns to solve.


2021 ◽  
Vol 2 (2) ◽  
Author(s):  
Marirose P. Kuhlman ◽  
Skyler Burrows ◽  
Daniel L. Mummey ◽  
Philip W. Ramsey ◽  
Philip G. Hahn

PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e10732
Author(s):  
Cassandra Vogel ◽  
Timothy L. Chunga ◽  
Xiaoxuan Sun ◽  
Katja Poveda ◽  
Ingolf Steffan-Dewenter

Background Landscape composition is known to affect both beneficial insect and pest communities on crop fields. Landscape composition therefore can impact ecosystem (dis)services provided by insects to crops. Though landscape effects on ecosystem service providers have been studied in large-scale agriculture in temperate regions, there is a lack of representation of tropical smallholder agriculture within this field of study, especially in sub-Sahara Africa. Legume crops can provide important food security and soil improvement benefits to vulnerable agriculturalists. However, legumes are dependent on pollinating insects, particularly bees (Hymenoptera: Apiformes) for production and are vulnerable to pests. We selected 10 pigeon pea (Fabaceae: Cajunus cajan (L.)) fields in Malawi with varying proportions of semi-natural habitat and agricultural area within a 1 km radius to study: (1) how the proportion of semi-natural habitat and agricultural area affects the abundance and richness of bees and abundance of florivorous blister beetles (Coleoptera: Melloidae), (2) if the proportion of flowers damaged and fruit set difference between open and bagged flowers are correlated with the proportion of semi-natural habitat or agricultural area and (3) if pigeon pea fruit set difference between open and bagged flowers in these landscapes was constrained by pest damage or improved by bee visitation. Methods We performed three, ten-minute, 15 m, transects per field to assess blister beetle abundance and bee abundance and richness. Bees were captured and identified to (morpho)species. We assessed the proportion of flowers damaged by beetles during the flowering period. We performed a pollinator and pest exclusion experiment on 15 plants per field to assess whether fruit set was pollinator limited or constrained by pests. Results In our study, bee abundance was higher in areas with proportionally more agricultural area surrounding the fields. This effect was mostly driven by an increase in honeybees. Bee richness and beetle abundances were not affected by landscape characteristics, nor was flower damage or fruit set difference between bagged and open flowers. We did not observe a positive effect of bee density or richness, nor a negative effect of florivory, on fruit set difference. Discussion In our study area, pigeon pea flowers relatively late—well into the dry season. This could explain why we observe higher densities of bees in areas dominated by agriculture rather than in areas with more semi-natural habitat where resources for bees during this time of the year are scarce. Therefore, late flowering legumes may be an important food resource for bees during a period of scarcity in the seasonal tropics. The differences in patterns between our study and those conducted in temperate regions highlight the need for landscape-scale studies in areas outside the temperate region.


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