scholarly journals Pollinator enhancement in agriculture: comparing sown flower strips, hedges and sown hedge herb layers in apple orchards

Author(s):  
Vivien von Königslöw ◽  
Felix Fornoff ◽  
Alexandra-Maria Klein

AbstractIn intensive agricultural landscapes semi-natural habitats for pollinators are often limited, although willingness to establish pollinator habitat is increasing among farmers. A common pollinator enhancement measure is to provide flower strips, but existent or improved hedgerows might be more effective. In this study, we compare the effectiveness of three pollinator enhancement measures at edges of conventional apple orchards: (i) perennial flower strips, (ii) existent hedgerows, and (iii) existent hedgerows complemented with a sown herb layer. We used orchard edges without any enhancement as control. The study took place over three consecutive years in Southern Germany. Wild bee abundance and species richness were highest in flower strips followed by improved hedges. Hoverflies were also most abundant in flower strips, but not more species rich than at control sites. Wild bee but not hoverfly community composition differed between control and enhancement sites. The overall pollinator community included only few threatened or specialized species. Flower abundance was the main driver for wild bee diversity, whereas hoverflies were largely unaffected by floral resources. Pollinator enhancement had neither an effect on the abundance or species richness within the orchards nor on apple flower visitation. Perennial flower strips seem most effective to enhance wild bees in intensive agricultural landscapes. Additionally, flower-rich hedgerows should be promoted to complement flower strips by extending the flowering period and to increase connectivity of pollinator habitat in agricultural landscapes.

2021 ◽  
Author(s):  
Nicole Beyer ◽  
Felix Kirsch ◽  
Doreen Gabriel ◽  
Catrin Westphal

Abstract Context Pollinator declines and functional homogenization of farmland insect communities have been reported. Mass-flowering crops (MFC) can support pollinators by providing floral resources. Knowledge about how MFC with dissimilar flower morphology affect functional groups and functional trait compositions of wild bee communities is scarce. Objective We investigated how two morphologically different MFC, land cover and local flower cover of semi-natural habitats (SNH) and landscape diversity affect wild bees and their functional traits (body size, tongue length, sociality, foraging preferences). Methods We conducted landscape-level wild bee surveys in SNH of 30 paired study landscapes covering an oilseed rape (OSR) (Brassica napus L.) gradient. In 15 study landscapes faba beans (Vicia faba L.) were grown, paired with respective control landscapes without grain legumes. Results Faba bean cultivation promoted bumblebees (Bombus spp. Latreille), whereas non-Bombus densities were only driven by the local flower cover of SNH. High landscape diversity enhanced wild bee species richness. Faba bean cultivation enhanced the proportions of social wild bees, bees foraging on Fabaceae and slightly of long-tongued bumblebees. Solitary bee proportions increased with high covers of OSR. High local SNH flower covers mitigated changes of mean bee sizes caused by faba bean cultivation. Conclusions Our results show that MFC support specific functional bee groups adapted to their flower morphology and can alter pollinators` functional trait composition. We conclude that management practices need to target the cultivation of functionally diverse crops, combined with high local flower covers of diverse SNH to create heterogeneous landscapes, which sustain diverse pollinator communities.


2021 ◽  
Vol 9 ◽  
Author(s):  
Panlong Wu ◽  
Piaopiao Dai ◽  
Meina Wang ◽  
Sijie Feng ◽  
Aruhan Olhnuud ◽  
...  

Bees provide key pollination services for a wide range of crops. Accumulating evidence shows the effect of semi-natural habitats at the landscape level and local management practices on bee diversity in fields. However, most of the evidence is derived from studies in North America and Europe. Whether this paradigm is applicable in China, which is characterized by smallholder-dominated agricultural landscapes, has rarely been studied. In this study, we aimed to investigate how bee diversity affected apple production, and how landscape and local variables affected bee diversity and species composition on the Northern China Plain. The results showed that bees significantly increased apple fruit set compared to bagged controls. Wild bee diversity was positively related to apple seed numbers. Higher seed numbers reduced the proportion of deformed apples and thus increased fruit quality. Wild bee abundance was positively correlated with flowering ground cover, and both the abundance and species richness of wild bees were positively affected by the percentage of semi-natural habitats. We conclude that apple quality can benefit from ecological intensification comprising the augmentation of wild bees by semi-natural habitats and flowering ground cover. Future pollination management should therefore reduce the intensification level of management at both the local and landscape scales.


Insects ◽  
2020 ◽  
Vol 11 (11) ◽  
pp. 812
Author(s):  
Justine Rivers-Moore ◽  
Emilie Andrieu ◽  
Aude Vialatte ◽  
Annie Ouin

Loss of semi-natural habitats (SNH) in agricultural landscapes affects wild bees, often negatively. However, how bee communities respond varies and is still unclear. To date, few studies have used precise descriptors to understand these effects. Our aim was to understand the respective and complementary influences of different wooded and herbaceous habitats on wild bee communities. We selected thirty 500-m radius landscapes on a gradient of a percentage of wooded SNH in south-western France. At each landscape, we sampled wild bees in spring 2016 and plants in spring 2015 and 2016 at the forest edge, in a hedgerow, and in a permanent grassland. Pollen carried by the most abundant bee species was collected and identified. Using beta diversity indices, we showed that wild bee community composition differs between the three SNH types, and especially between herbaceous and wooded SNH. Based on Jacobs’ selection index, we showed that pollen of some plant species recorded in wooded SNH are preferentially selected by wild bees. Studying the impact of the loss of each SNH type on the global bee-pollen interaction network, we found that wooded SNH contributed to its resilience, enabling specific plant–bee interactions. Overall, our results underline the non-negligible contribution of wooded SNH to the diversity of wild bees in agricultural landscapes, and thus the importance of maintaining different types of SNH.


2013 ◽  
Vol 2013 ◽  
pp. 1-38 ◽  
Author(s):  
M. B. Théodore Munyuli

This study was conducted in 2006 in central Uganda to provide baseline data on relationships between bee community variables and local, climatic, landscape and regional drivers affecting bee community abundance and diversity in agricultural landscapes. Bee abundance and species richness increased significantly () with increase in percent cover of semi-natural habitats and the abundance of wild and cultivated floral resources in the landscape. There were strong linear declines () in bee species richness and abundance with cultivation intensity. Bee species richness declined very steeply with forest distance. Bee species richness and abundance were negatively affected by land-use intensity (). Bee species richness and abundance were strongly negatively correlated () with increase in mean annual temperatures in the previous years than in current years indicating potential vulnerability of local bee species to future climate changes. The percent cover of semi-natural habitats and natural in the farmland predicted best the occurrence and distribution in central Uganda. It is therefore recommended to policy-makers and to farmers to invest in the protection of forest fragments (and related semi-natural habitats) acting as buffer in the mitigation of negative effects of climate change on bee biodiversity and pollination services delivery.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Cheng Gong ◽  
Liangtao Li ◽  
Jan C. Axmarcher ◽  
Zhenrong Yu ◽  
Yunhui Liu

AbstractIn the intensively farmed, homogenous agricultural landscape of the North China Plain, family graveyards form distinct cultural landscape features. In addition to their cultural value, these graveyards represent semi-natural habitat islands whose potential roles in biodiversity conservation and ecological functioning has remained poorly understood. In this study, we investigated plant species richness on 199 family graveyards of different ages and sizes. In accordance with biogeography theory, both overall and insect-pollinated plant species richness increased with area and age of graveyards. Even small graveyards show a strong potential for conserving local plant richness, and a mosaic of both large and small family graveyards could play an important role in the conservation of farmland biodiversity and related ecosystem functions. The launch of agri-environmental measures that conserve and create semi-natural habitats, in turn benefitting agricultural biodiversity and ecological functioning, has proven difficult in China due to the shortage of dispensable arable land. Given the great value of family graveyards as semi-natural habitats reflected in our study, we propose to focus preliminary efforts on conserving these landscape features as existing, widespread and culturally important semi-natural habitat islands. This would represent an effective, complementary policy to a subsequent re-establishment of other semi-natural habitats for the conservation of biodiversity and ecological functioning in agricultural landscapes.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Károly Lajos ◽  
Ferenc Samu ◽  
Áron Domonkos Bihaly ◽  
Dávid Fülöp ◽  
Miklós Sárospataki

AbstractMass-flowering crop monocultures, like sunflower, cannot harbour a permanent pollinator community. Their pollination is best secured if both managed honey bees and wild pollinators are present in the agricultural landscape. Semi-natural habitats are known to be the main foraging and nesting areas of wild pollinators, thus benefiting their populations, whereas crops flowering simultaneously may competitively dilute pollinator densities. In our study we asked how landscape structure affects major pollinator groups’ visiting frequency on 36 focal sunflower fields, hypothesising that herbaceous semi-natural (hSNH) and sunflower patches in the landscape neighbourhood will have a scale-dependent effect. We found that an increasing area and/or dispersion of hSNH areas enhanced the visitation of all pollinator groups. These positive effects were scale-dependent and corresponded well with the foraging ranges of the observed bee pollinators. In contrast, an increasing edge density of neighbouring sunflower fields resulted in considerably lower visiting frequencies of wild bees. Our results clearly indicate that the pollination of sunflower is dependent on the composition and configuration of the agricultural landscape. We conclude that an optimization of the pollination can be achieved if sufficient amount of hSNH areas with good dispersion are provided and mass flowering crops do not over-dominate the agricultural landscape.


2020 ◽  
Vol 49 (2) ◽  
pp. 502-515 ◽  
Author(s):  
Brianne Du Clos ◽  
Francis A Drummond ◽  
Cynthia S Loftin

Abstract Homogeneous, agriculturally intense landscapes have abundant records of pollinator community research, though similar studies in the forest-dominated, heterogeneous mixed-use landscape that dominates the northeastern United States are sparse. Trends of landscape effects on wild bees are consistent across homogeneous agricultural landscapes, whereas reported studies in the northeastern United States have not found this consistency. Additionally, the role of noncrop habitat in mixed-use landscapes is understudied. We assessed wild bee communities in the mixed-use lowbush blueberry (Vaccinium angustifolium Ait.) production landscape of Maine, United States at 56 sites in eight land cover types across two regional landscapes and analyzed effects of floral resources, landscape pattern, and spatial scale on bee abundance and species richness. Within survey sites, cover types with abundant floral resources, including lowbush blueberry fields and urban areas, promoted wild bee abundance and diversity. Cover types with few floral resources such as coniferous and deciduous/mixed forest reduced bee abundance and species richness. In the surrounding landscape, lowbush blueberry promoted bee abundance and diversity, while emergent wetland and forested land cover strongly decreased these measures. Our analysis of landscape configuration revealed that patch mixing can promote wild bee abundance and diversity; however, this was influenced by strong variation across our study landscape. More surveys at intra-regional scales may lead to better understanding of the influence of mixed-use landscapes on bee communities.


1987 ◽  
Vol 119 (7-8) ◽  
pp. 735-745 ◽  
Author(s):  
Cynthia D. Scott-Dupree ◽  
Mark L. Winston

AbstractWild bee pollinators were collected in tree-fruit orchards and uncultivated habitats in the Okanagan Valley. Higher abundance and diversity of wild bee pollinators were found at uncultivated sites than on tree-fruit crops. Wild bees were not abundant enough in orchard habitats to provide adequate tree-fruit pollination. Variable flower visitation patterns by polylectic bees in orchard and uncultivated habitats make it difficult to predict floral visitation patterns. Therefore, orchardists cannot rely on a substantial and predictable contribution to pollination of fruit crops by wild bee species. Research into the use of wild bees as managed pollinators for tree-fruit crops in the Okanagan Valley may have potential. Future studies should consider three wild bee species collected in Okanagan Valley orchards, Bombus terricola occidentalis Greene, Bombus bifarius nearcticus Handlirsch, and Osmia lignaria propinqua Cresson, for pollination management.


2021 ◽  
Vol 2 ◽  
Author(s):  
Ola Olsson ◽  
Mark V. Brady ◽  
Martin Stjernman ◽  
Henrik G. Smith

Most landscapes are comprised of multiple habitat types differing in the biodiversity they contain. This is certainly true for human modified landscapes, which are often a mix of habitats managed with different intensity, semi-natural habitats and even pristine habitats. To understand fundamental questions of how the composition of such landscapes affects biodiversity conservation, and to evaluate biodiversity consequences of policies that affect the composition of landscapes, there is a need for models able to translate information on biodiversity from individual habitats to landscape-wide predictions. However, this is complicated by species richness not being additive. We constructed a model to help analyze and solve this problem based on two simple assumptions. Firstly, that a habitat can be characterized by the biological community inhabiting it; i.e., which species occur and at what densities. Secondly, that the probability of a species occurring in a particular unit of land is dictated by its average density in the associated habitats, its spatial aggregation, and the size of the land unit. This model leads to a multidimensional species-area relation (one dimension per habitat). If the goal is to maximize species diversity at the landscape scale (γ-diversity), within a fixed area or under a limited budget, the model can be used to find the optimal allocation of the different habitats. In general, the optimal solution depends on the total size of the species pool of the different habitats, but also their similarity (β-diversity). If habitats are complementary (high β), a mix is usually preferred, even if one habitat is poorer (lower α diversity in one habitat). The model lends itself to economic analyses of biodiversity problems, without the need to monetarize biodiversity value, i.e., cost-effectiveness analysis. Land prices and management costs will affect the solution, such that the model can be used to estimate the number of species gained in relation to expenditure on each habitat. We illustrate the utility of the model by applying it to agricultural landscapes in southern Sweden and demonstrate how empirical monitoring data can be used to find the best habitat allocation for biodiversity conservation within and between landscapes.


2020 ◽  
Vol 57 (5) ◽  
pp. 1468-1479 ◽  
Author(s):  
Matias I Dufek ◽  
Dario D Larrea ◽  
Miryam P Damborsky ◽  
Pablo R Mulieri

Abstract Sarcophagidae (Diptera) are of great interest from a veterinary, medical, and forensic viewpoint, and are potential bioindicators for environmental impact assessments. In this study, we evaluated changes in abundance, species richness, and diversity of flesh flies in different habitat types in the Humid Chaco ecoregion of South America: 1) anthropized habitats: urban, cattle farm, and alfalfa crop, and 2) natural habitats: savanna and forest. We hypothesized that sarcophagid fly community parameters are affected by the anthropization and that spatial turnover will contribute more to the overall beta diversity than nestedness between habitats. In each habitat, samplings were conducted monthly from March 2015 to February 2016 in 25 sites, 5 per habitat, totaling 300 independent samples at the end of the study. We collected 5,790 Sarcophagidae (55 species). Community parameters of Sarcophagidae were evaluated and compared. The ecological effects of anthropization and habitat type were observed in the present study. As expected, our results showed the highest abundance, species richness, and diversity in the savanna and forest habitats (natural), whereas the lowest values were registered in the urban and alfalfa crop habitats, supporting the hypotheses of anthropization as the main driver of diversity loss. In addition, sarcophagid assemblages differed between all habitats and the overall dissimilarity was structured by spatial turnover. The main conclusion of this research is that flesh fly community structure is greatly affected by anthropization and habitat type, and this would be related to canopy cover and microclimate conditions of each environment.


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