Sánchez-Bayo, F. & Wyckhuys, K. A. Worldwide decline of the entomofauna: A review of its drivers. Biol. Conserv. 232, 8–27. https://doi.org/10.1016/j.biocon.2019.01.020 (2019).
Google Scholar
van Klink, R. et al. Meta-analysis reveals declines in terrestrial but increases in freshwater insect abundances. Science 368, 417–420. https://doi.org/10.1126/science.aax9931 (2020).
Google Scholar
Wagner, D. L. Insect declines in the anthropocene. Annu. Rev. Entomol. 65, 457–480. https://doi.org/10.1146/annurev-ento-011019-025151 (2020).
Google Scholar
Goulson, D. The insect apocalypse, and why it matters. Curr. Biol. 29, R967–R971. https://doi.org/10.1016/j.cub.2019.06.069 (2019).
Google Scholar
Cardoso, P. et al. Scientists’ warning to humanity on insect extinctions. Biol. Conserv. 242, 108426. https://doi.org/10.1016/j.biocon.2020.108426 (2020).
Google Scholar
Potts, S. G. et al. Global pollinator declines: Trends, impacts and drivers. Trends Ecol. Evol. 25, 345–353. https://doi.org/10.1016/j.tree.2010.01.007 (2010).
Google Scholar
Goulson, D., Nicholls, E., Botías, C. & Rotheray, E. L. Bee declines driven by combined stress from parasites, pesticides, and lack of flowers. Science 347, 1255957. https://doi.org/10.1126/science.1255957 (2015).
Google Scholar
Ollerton, J. Pollinator diversity: Distribution, ecological function, and conservation. Annu. Rev. Ecol. Evol. Syst. 48, 353–376. https://doi.org/10.1146/annurev-ecolsys-110316-022919 (2017).
Google Scholar
Klein, A.-M. et al. Importance of pollinators in changing landscapes for world crops. Proc. Biol. Sci. 274, 303–313. https://doi.org/10.1098/rspb.2006.3721 (2007).
Google Scholar
Ollerton, J., Winfree, R. & Tarrant, S. How many flowering plants are pollinated by animals?. Oikos 120, 321–326. https://doi.org/10.1111/j.1600-0706.2010.18644.x (2011).
Google Scholar
Ollerton, J., Erenler, H., Edwards, M. & Crockett, R. Pollinator declines. Extinctions of aculeate pollinators in Britain and the role of large-scale agricultural changes. Science 346, 1360–1362. https://doi.org/10.1126/science.1257259 (2014).
Google Scholar
Wenzel, A., Grass, I., Belavadi, V. V. & Tscharntke, T. How urbanization is driving pollinator diversity and pollination—A systematic review. Biol. Conserv. 241, 108321. https://doi.org/10.1016/j.biocon.2019.108321 (2020).
Google Scholar
Senapathi, D., Goddard, M. A., Kunin, W. E. & Baldock, K. C. R. Landscape impacts on pollinator communities in temperate systems: Evidence and knowledge gaps. Funct. Ecol. 31, 26–37. https://doi.org/10.1111/1365-2435.12809 (2017).
Google Scholar
Fenoglio, M. S., Rossetti, M. R. & Videla, M. Negative effects of urbanization on terrestrial arthropod communities: A meta-analysis. Glob. Ecol. Biogeogr. 29, 1412–1429. https://doi.org/10.1111/geb.13107 (2020).
Google Scholar
Ives, C. D. et al. Cities are hotspots for threatened species. Glob. Ecol. Biogeogr. 25, 117–126. https://doi.org/10.1111/geb.12404 (2016).
Google Scholar
Soanes, K. & Lentini, P. E. When cities are the last chance for saving species. Front. Ecol. Evol. 17, 225–231. https://doi.org/10.1002/fee.2032 (2019).
Google Scholar
Lynch, L. et al. Changes in land use and land cover along an urban-rural gradient influence floral resource availability. Curr. Landsc. Ecol. Rep. 6, 46–70. https://doi.org/10.1007/s40823-021-00064-1 (2021).
Google Scholar
Hall, D. M. et al. The city as a refuge for insect pollinators. Conserv. Biol. 31, 24–29. https://doi.org/10.1111/cobi.12840 (2017).
Google Scholar
Buchholz, S. & Egerer, M. H. Functional ecology of wild bees in cities: Towards a better understanding of trait-urbanization relationships. Biodivers. Conserv. 29, 2779–2801. https://doi.org/10.1007/s10531-020-02003-8 (2020).
Google Scholar
Theodorou, P. et al. Urban areas as hotspots for bees and pollination but not a panacea for all insects. Nat. Commun. 11, 576. https://doi.org/10.1038/s41467-020-14496-6 (2020).
Google Scholar
Khalifa, S. A. M. et al. Overview of bee pollination and its economic value for crop production. Insects https://doi.org/10.3390/insects12080688 (2021).
Google Scholar
Doyle, T. et al. Pollination by hoverflies in the Anthropocene. Proc. Biol. Sci. 287, 20200508. https://doi.org/10.1098/rspb.2020.0508 (2020).
Google Scholar
Rader, R. et al. Non-bee insects are important contributors to global crop pollination. Proc. Natl. Acad. Sci. USA. 113, 146–151. https://doi.org/10.1073/pnas.1517092112 (2016).
Google Scholar
Persson, A. S., Ekroos, J., Olsson, P. & Smith, H. G. Wild bees and hoverflies respond differently to urbanisation, human population density and urban form. Landsc. Urban Plan. 204, 103901. https://doi.org/10.1016/j.landurbplan.2020.103901 (2020).
Google Scholar
Gathof, A. K., Grossmann, A. J., Herrmann, J. & Buchholz, S. Who can pass the urban filter? A multi-taxon approach to disentangle pollinator trait-environmental relationships. Oecologia 199, 165–179. https://doi.org/10.1007/s00442-022-05174-z (2022).
Google Scholar
Baldock, K. C. R. et al. Where is the UK’s pollinator biodiversity? The importance of urban areas for flower-visiting insects. Proc. Biol. Sci. 282, 20142849. https://doi.org/10.1098/rspb.2014.2849 (2015).
Google Scholar
Ramírez-Restrepo, L. & MacGregor-Fors, I. Butterflies in the city: A review of urban diurnal Lepidoptera. Urban Ecosyst. 20, 171–182. https://doi.org/10.1007/s11252-016-0579-4 (2017).
Google Scholar
Kuussaari, M. et al. Butterfly species’ responses to urbanization: Differing effects of human population density and built-up area. Urban Ecosyst. 24, 515–527. https://doi.org/10.1007/s11252-020-01055-6 (2020).
Google Scholar
Theodorou, P. The effects of urbanisation on ecological interactions. Curr. Opin. Insect. Sci. 52, 100922. https://doi.org/10.1016/j.cois.2022.100922 (2022).
Google Scholar
Martins, K. T., Gonzalez, A. & Lechowicz, M. J. Patterns of pollinator turnover and increasing diversity associated with urban habitats. Urban Ecosyst. 20, 1359–1371. https://doi.org/10.1007/s11252-017-0688-8 (2017).
Google Scholar
Theodorou, P. et al. The structure of flower visitor networks in relation to pollination across an agricultural to urban gradient. Funct. Ecol. 31, 838–847. https://doi.org/10.1111/1365-2435.12803 (2017).
Google Scholar
Geslin, B., Gauzens, B., Thébault, E. & Dajoz, I. Plant pollinator networks along a gradient of urbanisation. PLoS ONE 8, e63421. https://doi.org/10.1371/journal.pone.0063421 (2013).
Google Scholar
Udy, K. L., Reininghaus, H., Scherber, C. & Tscharntke, T. Plant–pollinator interactions along an urbanization gradient from cities and villages to farmland landscapes. Ecosphere https://doi.org/10.1002/ecs2.3020 (2020).
Google Scholar
Jędrzejewska-Szmek, K. & Zych, M. Flower-visitor and pollen transport networks in a large city: Structure and properties. Arthropod. Plant Interact. 7, 503–516. https://doi.org/10.1007/s11829-013-9274-z (2013).
Google Scholar
von der Lippe, M., Buchholz, S., Hiller, A., Seitz, B. & Kowarik, I. CityScapeLab Berlin: A research platform for untangling urbanization effects on biodiversity. Sustainability 12, 2565. https://doi.org/10.3390/su12062565 (2020).
Google Scholar
Dylewski, Ł, Maćkowiak, Ł & Banaszak-Cibicka, W. Are all urban green spaces a favourable habitat for pollinator communities? Bees, butterflies and hoverflies in different urban green areas. Ecol. Entomol. 44, 678–689. https://doi.org/10.1111/een.12744 (2019).
Google Scholar
Grossmann, A. J., Herrmann, J., Buchholz, S. & Gathof, A. K. Dry grassland within the urban matrix acts as favourable habitat for different pollinators including endangered species. Insect Conserv. Divers. https://doi.org/10.1111/icad.12607 (2022).
Google Scholar
Settele, J., Steiner, R., Feldmann, R. & Hermann, G. Schmetterlinge. Die Tagfalter Deutschlands: 720 Farbfotos. 3rd ed. (2015).
Amiet, F. Hymenoptera Apidae, 1. Teil. Allgemeiner Teil, Gattungsschlüssel – Die Gattungen Apis, Bombus und Psithyrus (Centre Suisse de Cartographie de la Faune, 1996).
Amiet, F., Müller, A. & Neumeyer, R. Apidae 2. Colletes, Dufourea, Hylaeus, Nomia, Nomioides, Rhophitoides, Rophites, Sphecodes, Systropha (Fauna Helvetica, 1999).
Amiet, F., Herrmann, M., Müller, A. & Neumeyer, R. Apidae 3. Halictus, Lasioglossum (Centre Suisse de Cartographie de la Faune, 2001).
Amiet, F., Herrmann, M., Müller, A. & Neumeyer, R. Apidae 4. Anthidium, Chelostoma, Coelioxys, Dioxys, Heriades, Lithurgus, Megachile, Osmia, Stelis (Centre Suisse de Cartographie de la Faune, 2004).
Amiet, F., Herrmann, M., Müller, A. & Neumeyer, R. Apidae 5. Ammobates, Ammobatoides, Anthophora, Biastes, Ceratina, Dasypoda, Epeoloides, Epeolus, Eucera, Macropis, Melecta, Melitta, Nomada, Pasites, Tetralonia, Thyreus, Xylocopa (Centre Suisse de Cartographie de la Faune, 2007).
Amiet, F., Herrmann, M., Müller, A. & Neumeyer, R. Apidae 6. Andrena, Melliturga, Panurginus, Panurgus (Centre Suisse de Cartographie de la Faune, 2010).
Gokcezade, J. F., Gereben-Krenn, B.-A., Neumayer, J. & Krenn, H. W. Feldbestimmungsschlüssel für die Hummeln Österreichs, Deutschlands und der Schweiz (Hymenoptera, Apidae). Linzer biologische Beiträge 47, 5–42 (2015).
Bartsch, H. Tvåvingar: Blomflugor. Diptera: Syrphidae: Syrphinae: denna volym omfattar samtliga nordiska arter (ArtDatabanken Sveriges lantbruksuniversitet, 2009).
Bartsch, H. Tvåvingar: Blomflugor. Diptera: Syrphidae: Eristalinae & Microdontinae: denna volym omfattar samtliga nordiska arter (ArtDatabanken Sveriges lantbruksuniversitet, 2009).
Bot, S. & van de Meutter, F. Veldgids zweefvliegen (KNNV Uitgeverij, 2019).
Jäger, E. J. Rothmaler-Exkursionsflora von Deutschland. Gefäßpflanzen: Grundband 20th edn. (Springer Spektrum, 2011).
Senate Department for Urban Development and Housing. Berlin Environmental Atlas. 06.01 Actual Use of Built-up Areas/06.02 Inventory of Green and Open Spaces 2010 (2011).
Holland, J. D., Bert, D. G. & Fahrig, L. Determining the spatial scale of species’ response to habitat. Bioscience 54, 227. https://doi.org/10.1641/0006-3568(2004)054[0227:DTSSOS]2.0.CO;2 (2004).
Google Scholar
Senate Department for Urban Development and Housing. Berlin Environmental Atlas. 05.08 Biotope Types (2014).
Hanski, I. A practical model of metapopulation dynamics. J. Anim. Ecol. 63, 151. https://doi.org/10.2307/5591 (1994).
Google Scholar
Hanski, I. Habitat connectivity, habitat continuity, and metapopulations in dynamic landscapes. Oikos 87, 209. https://doi.org/10.2307/3546736 (1999).
Google Scholar
Senate Department for Urban Development and Housing. Berlin Environmental Atlas. 06.10 Building and Vegetation Heights (2014).
Saura, S. & Torné, J. Conefor Sensinode 2.2: A software package for quantifying the importance of habitat patches for landscape connectivity. Environ. Model. Softw. 24, 135–139. https://doi.org/10.1016/j.envsoft.2008.05.005 (2009).
Google Scholar
Saure, C. Rote Liste und Gesamtartenliste der Bienen und Wespen (Hymenoptera part.) von Berlin mit Angaben zu den Ameisen. In Rote Listen der gefährdeten Pflanzen und Tiere von Berlin.
Speight, M. C. D. Species Accounts of European Syrphidae (Diptera) (Syrph the Net Publications, 2014).
Middleton-Welling, J. et al. A new comprehensive trait database of European and Maghreb butterflies, Papilionoidea. Sci. Data 7, 351. https://doi.org/10.1038/s41597-020-00697-7 (2020).
Google Scholar
Dormann, C. F., Fründ, J., Blüthgen, N. & Gruber, B. Indices, graphs and null models: Analyzing bipartite ecological networks. Open Ecol. J. 2, 7–24. https://doi.org/10.2174/1874213000902010007 (2009).
Google Scholar
Kaiser-Bunbury, C. N. & Blüthgen, N. Integrating network ecology with applied conservation: A synthesis and guide to implementation. AoB Plants https://doi.org/10.1093/aobpla/plv076 (2015).
Google Scholar
Almeida-Neto, M., Guimarães, P., Guimarães, P. R., Loyola, R. D. & Ulrich, W. A consistent metric for nestedness analysis in ecological systems: Reconciling concept and measurement. Oikos 117, 1227–1239. https://doi.org/10.1111/J.0030-1299.2008.16644.X (2008).
Google Scholar
Dormann, C. F. & Strauss, R. A method for detecting modules in quantitative bipartite networks. Methods Ecol. Evol. 5, 90–98. https://doi.org/10.1111/2041-210X.12139 (2014).
Google Scholar
Blüthgen, N., Menzel, F. & Blüthgen, N. Measuring specialization in species interaction networks. BMC Ecol. 6, 9. https://doi.org/10.1186/1472-6785-6-9 (2006).
Google Scholar
Patefield, W. M. Algorithm AS 159: An efficient method of generating random R × C tables with given row and column totals. J. Appl. Stat. 30, 91. https://doi.org/10.2307/2346669 (1981).
Google Scholar
Stein, K. et al. Plant–pollinator networks in Savannas of Burkina Faso, West Africa. Diversity 13, 1. https://doi.org/10.3390/d13010001 (2021).
Google Scholar
Escobedo-Kenefic, N. et al. Disentangling the effects of local resources, landscape heterogeneity and climatic seasonality on bee diversity and plant–pollinator networks in tropical highlands. Oecologia 194, 333–344. https://doi.org/10.1007/s00442-020-04715-8 (2020).
Google Scholar
Renaud, E., Baudry, E. & Bessa-Gomes, C. Influence of taxonomic resolution on mutualistic network properties. Ecol. Evol. 10, 3248–3259. https://doi.org/10.1002/ece3.6060 (2020).
Google Scholar
Ropars, L., Dajoz, I., Fontaine, C., Muratet, A. & Geslin, B. Wild pollinator activity negatively related to honey bee colony densities in urban context. PLoS ONE 14, e0222316. https://doi.org/10.1371/journal.pone.0222316 (2019).
Google Scholar
Egerer, M. & Kowarik, I. Confronting the modern gordian knot of urban beekeeping. Trends Ecol. Evol. 35, 956–959. https://doi.org/10.1016/j.tree.2020.07.012 (2020).
Google Scholar
Zuur, A. F., Ieono, E. N., Walker, N., Saveliev, A. A. & Smith, G. M. Mixed Effects Models and Extensions in Ecology with R (Springer, 2009).
Google Scholar
Bartón, K. MuMIn. multi-model inference, R package version 1.42.1 (2018).
Paradis, E., Claude, J. & Strimmer, K. APE: Analyses of phylogenetics and evolution in R language. Bioinformatics 20, 289–290. https://doi.org/10.1093/bioinformatics/btg412 (2004).
Google Scholar
Wood, T. J., Kaplan, I. & Szendrei, Z. Wild bee pollen diets reveal patterns of seasonal foraging resources for honey bees. Front. Ecol. Evol. https://doi.org/10.3389/fevo.2018.00210 (2018).
Google Scholar
Proske, A., Lokatis, S. & Rolff, J. Impact of mowing frequency on arthropod abundance and diversity in urban habitats: A meta-analysis. Urban For Urban Green 76, 127714. https://doi.org/10.1016/j.ufug.2022.127714 (2022).
Google Scholar
Bates, A. J. et al. Changing bee and hoverfly pollinator assemblages along an urban-rural gradient. PLoS ONE 6, e23459. https://doi.org/10.1371/journal.pone.0023459 (2011).
Google Scholar
Geslin, B. et al. The proportion of impervious surfaces at the landscape scale structures wild bee assemblages in a densely populated region. Ecol. Evol. 6, 6599–6615. https://doi.org/10.1002/ece3.2374 (2016).
Google Scholar
Birdshire, K. R., Carper, A. L. & Briles, C. E. Bee community response to local and landscape factors along an urban-rural gradient. Urban Ecosyst. 23, 689–702. https://doi.org/10.1007/s11252-020-00956-w (2020).
Google Scholar
Goddard, M. A., Benton, T. G. & Dougill, A. J. Beyond the garden fence: Landscape ecology of cities. Trends Ecol. Evol. 25, 202–203. https://doi.org/10.1016/j.tree.2009.12.007 (2010).
Google Scholar
Theodorou, P. et al. Bumble bee colony health and performance vary widely across the urban ecosystem. J. Anim. Ecol. 91, 2135–2148. https://doi.org/10.1111/1365-2656.13797 (2022).
Google Scholar
Potts, S. G., Vulliamy, B., Dafni, A., Ne’eman, G. & Willmer, P. Linking bees and flowers: How do floral communities structure pollinator communities?. Ecology 84, 2628–2642. https://doi.org/10.1890/02-0136 (2003).
Google Scholar
Ebeling, A., Klein, A.-M., Schumacher, J., Weisser, W. W. & Tscharntke, T. How does plant richness affect pollinator richness and temporal stability of flower visits?. Oikos 117, 1808–1815. https://doi.org/10.1111/j.1600-0706.2008.16819.x (2008).
Google Scholar
Theodorou, P. et al. Urban fragmentation leads to lower floral diversity, with knock-on impacts on bee biodiversity. Sci. Rep. 10, 21756. https://doi.org/10.1038/s41598-020-78736-x (2020).
Google Scholar
Potts, S. G. et al. Role of nesting resources in organising diverse bee communities in a Mediterranean landscape. Ecol. Entomol. 30, 78–85. https://doi.org/10.1111/j.0307-6946.2005.00662.x (2005).
Google Scholar
Fründ, J., Linsenmair, K. E. & Blüthgen, N. Pollinator diversity and specialization in relation to flower diversity. Oikos 119, 1581–1590. https://doi.org/10.1111/j.1600-0706.2010.18450.x (2010).
Google Scholar
Fornoff, F. et al. Functional flower traits and their diversity drive pollinator visitation. Oikos 126, 1020–1030. https://doi.org/10.1111/oik.03869 (2017).
Google Scholar
Hofmann, M. M. & Renner, S. S. One-year-old flower strips already support a quarter of a city’s bee species. J. Hymenopt. Res. 75, 87–95. https://doi.org/10.3897/jhr.75.47507 (2020).
Google Scholar
Verboven, H. A., Uyttenbroeck, R., Brys, R. & Hermy, M. Different responses of bees and hoverflies to land use in an urban–rural gradient show the importance of the nature of the rural land use. Landsc. Urban Plan. 126, 31–41. https://doi.org/10.1016/j.landurbplan.2014.02.017 (2014).
Google Scholar
Luder, K., Knop, E. & Menz, M. H. M. Contrasting responses in community structure and phenology of migratory and non-migratory pollinators to urbanization. Divers. Distrib. 24, 919–927. https://doi.org/10.1111/ddi.12735 (2018).
Google Scholar
Merckx, T. & van Dyck, H. Urbanization-driven homogenization is more pronounced and happens at wider spatial scales in nocturnal and mobile flying insects. Glob. Ecol. Biogeogr. 28, 1440–1455. https://doi.org/10.1111/geb.12969 (2019).
Google Scholar
Tzortzakaki, O., Kati, V., Panitsa, M., Tzanatos, E. & Giokas, S. Butterfly diversity along the urbanization gradient in a densely-built Mediterranean city: Land cover is more decisive than resources in structuring communities. Landsc. Urban Plan. 183, 79–87. https://doi.org/10.1016/j.landurbplan.2018.11.007 (2019).
Google Scholar
Krauss, J., Steffan-Dewenter, I. & Tscharntke, T. How does landscape context contribute to effects of habitat fragmentation on diversity and population density of butterflies?. J. Biogeogr. 30, 889–900. https://doi.org/10.1046/j.1365-2699.2003.00878.x (2003).
Google Scholar
Cozzi, G., Müller, C. B. & Krauss, J. How do local habitat management and landscape structure at different spatial scales affect fritillary butterfly distribution on fragmented wetlands?. Landsc. Ecol. 23, 269–283. https://doi.org/10.1007/s10980-007-9178-3 (2008).
Google Scholar
He, M. et al. Effects of landscape and local factors on the diversity of flower-visitor groups under an urbanization gradient, a case study in Wuhan, China. Diversity 14, 208. https://doi.org/10.3390/d14030208 (2022).
Google Scholar
Buchholz, S., Gathof, A. K., Grossmann, A. J., Kowarik, I. & Fischer, L. K. Wild bees in urban grasslands: Urbanisation, functional diversity and species traits. Landsc. Urban Plan. 196, 103731. https://doi.org/10.1016/j.landurbplan.2019.103731 (2020).
Google Scholar
Chapman, R. E. & Bourke, A. F. G. The influence of sociality on the conservation biology of social insects. Ecol. Lett. 4, 650–662. https://doi.org/10.1046/j.1461-0248.2001.00253.x (2001).
Google Scholar
Gaertner, M. et al. Non-native species in urban environments: Patterns, processes, impacts and challenges. Biol. Invasions 19, 3461–3469. https://doi.org/10.1007/s10530-017-1598-7 (2017).
Google Scholar
Kowarik, I. On the role of alien species in urban flora and vegetation. In Urban Ecology. An International Perspective on the Interaction Between Humans and Nature (ed. Marzluff, J. M.) 321–338 (2008).
Lorenz, S. & Stark, K. Saving the honeybees in Berlin? A case study of the urban beekeeping boom. Environ. Sociol. 1, 116–126. https://doi.org/10.1080/23251042.2015.1008383 (2015).
Google Scholar
Olesen, J. M., Bascompte, J., Dupont, Y. L. & Jordano, P. The modularity of pollination networks. Proc. Natl. Acad. Sci. USA 104, 19891–19896. https://doi.org/10.1073/pnas.0706375104 (2007).
Google Scholar
Thébault, E. & Fontaine, C. Stability of ecological communities and the architecture of mutualistic and trophic networks. Science 329, 853–856. https://doi.org/10.1126/science.1188321 (2010).
Google Scholar
Dormann, C. F., Fründ, J. & Schaefer, H. M. Identifying causes of patterns in ecological networks: Opportunities and limitations. Annu. Rev. Ecol. Evol. Syst. 48, 559–584. https://doi.org/10.1146/annurev-ecolsys-110316-022928 (2017).
Google Scholar
Tylianakis, J. M., Laliberté, E., Nielsen, A. & Bascompte, J. Conservation of species interaction networks. Biol. Conserv. 143, 2270–2279. https://doi.org/10.1016/j.biocon.2009.12.004 (2010).
Google Scholar
Grilli, J., Rogers, T. & Allesina, S. Modularity and stability in ecological communities. Nat. Commun. 7, 12031. https://doi.org/10.1038/ncomms12031 (2016).
Google Scholar
Grass, I., Jauker, B., Steffan-Dewenter, I., Tscharntke, T. & Jauker, F. Past and potential future effects of habitat fragmentation on structure and stability of plant–pollinator and host-parasitoid networks. Nat. Ecol. Evol 2, 1408–1417. https://doi.org/10.1038/s41559-018-0631-2 (2018).
Google Scholar
Kaiser-Bunbury, C. N. et al. Ecosystem restoration strengthens pollination network resilience and function. Nature 542, 223–227. https://doi.org/10.1038/nature21071 (2017).
Google Scholar
Bommarco, R. et al. Dispersal capacity and diet breadth modify the response of wild bees to habitat loss. Proc. Biol. Sci. 277, 2075–2082. https://doi.org/10.1098/rspb.2009.2221 (2010).
Google Scholar
Alarcón, R., Waser, N. M. & Ollerton, J. Year-to-year variation in the topology of a plant–pollinator interaction network. Oikos 117, 1796–1807. https://doi.org/10.1111/j.0030-1299.2008.16987.x (2008).
Google Scholar
Dupont, Y. L., Padrón, B., Olesen, J. M. & Petanidou, T. Spatio-temporal variation in the structure of pollination networks. Oikos 118, 1261–1269. https://doi.org/10.1111/j.1600-0706.2009.17594.x (2009).
Google Scholar
Santamaría, S. et al. Landscape effects on pollination networks in Mediterranean gypsum islands. Plant Biol. 20(Suppl 1), 184–194. https://doi.org/10.1111/plb.12602 (2018).
Google Scholar
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