Next Article in Journal
Cave Communities: From the Surface Border to the Deep Darkness
Next Article in Special Issue
Landscape-Level Effects of Forest on Pollinators and Fruit Set of Guava (Psidium guajava L.) in Orchards across Southern Thailand
Previous Article in Journal
Attraction and Avoidance between Predators and Prey at Wildlife Crossings on Roads
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Editorial

Land-Use and Climate Impacts on Plant–Pollinator Interactions and Pollination Services

Center for Macroecology, Evolution and Climate, GLOBE Institute, University of Copenhagen, 2100 Copenhagen Ø, Denmark
Diversity 2020, 12(5), 168; https://doi.org/10.3390/d12050168
Submission received: 21 April 2020 / Accepted: 23 April 2020 / Published: 25 April 2020
(This article belongs to the Special Issue Land-Use and Climate Impacts on Plant-Pollinator Interactions)

Abstract

:
Most flowering plants rely on animals for pollination and most animal pollinators rely on flowering plants for food resources. However, there is an ongoing concern that anthropogenic-induced global change threatens the mutualistic association between plants and pollinators. Two of the most important factors of global change are land-use and climate change. Land-use and climate change may affect species distributions and species phenologies, leading to spatial and temporal mismatches between mutualistic partners. Land-use and climate change may also influence species abundances, nesting habitats, floral resources and the behaviors of pollinators. Thus, mutualistic plant–pollinator interactions should be more susceptible to global change than simple measures of biodiversity, such as species richness and species composition. The potential negative impacts of land-use and climate change on plant–pollinator interactions may have large consequences for the conservation of threatened plants and pollinators and economically by diminishing crop productivity. Here I highlight ‘fruitful avenues’ for research into better understanding the influence of land-use and climate change on plant–pollinator interactions.

The majority of the world’s angiosperms rely on animals for pollination and likewise most pollinators rely on flowering plants for food resources [1,2]. Thus, plant–pollinator interactions are crucial for plants, pollinators, and the functioning of terrestrial ecosystems [3]. Pollination is also essential for the productivity of many of our crops [4,5], with an estimated annual economic value of 235–577 billion US dollars [6]. Plant–pollinator interactions are therefore important for both humans and nature.
However, plant–pollinator interactions are altered by anthropogenic-induced global change, notably land-use and climate change [4,5,6,7,8,9]. Land-use and climate change impact species distributions and species phenologies, which may lead to spatial and temporal mismatches between mutualistic partners. Land-use and climate change may also influence species abundances, nesting habitats, floral resources and behaviors of pollinators, with unknown effects on plant–pollinator interactions [8,9,10,11]. Thus, mutualistic plant–pollinator interactions should be more susceptible to global change and give an “early warning” signal before simple measures of biodiversity, such as species richness and species composition [9]. Despite recent advances, we are still far from understanding how land-use and climate change influence plant–pollinator interactions.
Here I present some ‘fruitful avenues’ for better understanding the influence of land-use and climate change on plant–pollinator interactions. To identify the exact mechanisms in which land-use and climate change impact plant–pollinator interactions, one may take an experimental approach [9], manipulating the land-use and/or climate to detect the mechanisms causing an impact on plant–pollinator interactions. Alternatively to an experimental approach, studies may take either a temporal or a spatial approach. By using a temporal approach, one is able to examine how historical changes in land-use and climate have influenced a given plant–pollinator system. For instance, it is possible to examine changes in species phenology and temporal plant–pollinator co-occurrence patterns in relation to changes in climate [12] and/or in relation to land-use effects on spatial co-occurrence patterns of plants and pollinators, and thus plant–pollinator interactions [13]. Temporal studies are thus useful to link historical changes in land-use and climate to changes in plant–pollinator interactions [13]. Temporal studies should preferably be conducted over long time periods and be repeated across a variety of localities; however, such data rarely exist. An alternative ‘fruitful avenue’ is to take a spatial approach to understand land-use and climate change impacts on plant–pollinator interactions. When taking a spatial approach, it is important to sample throughout wide gradients of land-use and climate conditions. Land-use impacts can be examined in several ways. Notably, one may focus on the linear distance to a given habitat type or, alternatively, one can examine the proportion of a specific habitat type within a buffer surrounding each study site [4,5,14]. If taking the approach of estimating the linear distance to a patch of a given habitat type, one has to define the minimum patch size required to sustain pollinators and pollination services or, better, use several threshold values for the minimum patch size [4]. When taking the buffer approach, you can likewise use several diameters within which you estimate landscape level measures of each habitat type [14]. In both cases, it is important to pick spatial distances that make sense for the biological organism in question. When using a spatial approach to examine the impact of climate, one can use either large continental-scale gradients or smaller scale gradients [10,15]. Continental-scale gradients have the advantage that it is possible to examine the potential impact of historical changes in climate [10], whereas smaller spatial-scale gradients focus on contemporary variation in climate [15]. Mountains may be particularly useful laboratories to understand climate-driven changes to plant–pollinator interactions [15,16], as climate changes along elevation gradients and mountains encompass large variations in climatic conditions [17]. No matter whether taking an experimental, temporal, or spatial approach to understand land-use and climate change impacts on plant–pollinator interactions, it is important to have a standardized sampling protocol or take sampling efforts into account when comparing across space or time [18]. Finally, land-use and climate change may interact and jointly shape plant–pollinator interactions—more so than each driver alone [16]. Thus, it is important to focus on either a land-use or a climate gradient, keeping the other driver constant, or to have a setup that makes it possible to examine the interaction effects of land-use and climate change on plant–pollinator interactions.
Identifying the impacts of land-use and climate change on plant–pollinator interactions can have practical applications, such as for the conservation of endangered plants. Plants that are highly dependent on pollinators and have a specialized association with their pollinators are particularly at risk of suffering of lack of reproduction if their pollinators change in their temporal appearance, change their feeding behavior, become less abundant, or fully disappear from the localities of the plant [12,15]. Many crops around the world are also dependent on pollinators, and thus it is important to understand the effects of land-use and climate change on crop production and its economic value [4,5]. There may well be a trade-off between ensuring sufficient pollination of crops and saving endangered pollinators and plants. From a farming perspective, abundant common pollinators may sufficiently pollinate at least some crops, while land-use and climate change threatens endangered pollinators and plants in the surrounding landscape. This possible trade-off between farming and nature conservation is another fruitful avenue to understand to maximize the benefit for both humans and nature.

Conflicts of Interest

The author declares no conflict of interest.

References

  1. Ollerton, J.; Winfree, R.; Tarrant, S. How many flowering plants are pollinated by animals? Oikos 2011, 120, 321–326. [Google Scholar] [CrossRef]
  2. Rech, A.R.; Dalsgaard, B.; Sandel, S.; Sonne, J.; Svenning, J.-C.; Holmes, N.; Ollerton, J. The macroecology of animal versus wind pollination: Ecological factors are more important than historical climate stability. Plant Ecol. Divers. 2016, 9, 253–262. [Google Scholar] [CrossRef]
  3. Kearns, C.A.; Inouye, D.W.; Waser, N.M. Endangered mutualisms: The conservation of plant–pollinator interactions. Annu. Rev. Ecol. Evol. Syst. 1998, 29, 83–112. [Google Scholar] [CrossRef]
  4. Ricketts, T.H.; Daily, G.C.; Ehrlich, P.R.; Michener, C.D. Economic value of tropical forest to coffee production. Proc. Natl. Acad. Sci. USA 2004, 101, 12579–12582. [Google Scholar] [CrossRef] [Green Version]
  5. Klein, A.M.; Vaissière, B.E.; Cane, J.H.; Steffan-Dewenter, I.; Cunningham, S.A.; Kremen, C.; Tscharntke, T. Importance of pollinators in changing landscapes for world crops. Proc. Biol. Sci. B 2007, 274, 303–313. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Potts, S.G.; Imperatriz-Fonseca, V.L.; Ngo, H.T.; Biesmeijer, J.C.; Breeze, T.D.; Dicks, L.V.; Garibaldi, L.A.; Hill, R.; Settele, J.; Vanbergen, A.J.; et al. (Eds.) IPBES: Summary for Policymakers of the Assessment Report of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services on Pollinators, Pollination and Food Production; Secretariat of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services: Bonn, Germany, 2016; p. 36. [Google Scholar]
  7. Burkle, L.A.; Alarcón, R. The future of plant-pollinator diversity: Understanding interaction networks across time, space, and global change. Am. Bot. 2011, 98, 528–538. [Google Scholar] [CrossRef] [PubMed]
  8. Hegland, S.J.; Nielsen, A.; Làzaro, A.; Bjerknes, A.L.; Totland, Ø. How does climate warming affect plant-pollinator interactions? Ecol. Lett. 2009, 12, 184–195. [Google Scholar] [CrossRef]
  9. Tylianakis, J.M.; Didham, R.K.; Bascompte, J.; Wardle, D.A. Global change and species interactions in terrestrial ecosystems. Ecol. Lett. 2008, 11, 1351–1363. [Google Scholar] [CrossRef] [PubMed]
  10. Dalsgaard, B.; Trøjelsgaard, K.; Martín González, A.; Nogués-Bravo, D.; Ollerton, J.; Petanidou, I.; Sandel, B.; Schleuning, M.; Wang, Z.; Rahbek, C.; et al. Historical climate-change influences modularity and nestedness of pollination networks. Ecography 2013, 36, 1331–1340. [Google Scholar] [CrossRef] [Green Version]
  11. Sonne, J.; Martín González, A.M.; Maruyama, P.M.; Sandel, B.; Vizentin-Bugoni, J.; Schleuning, M.; Abrahamczyk, S.; Alarcón, R.; Araujo, C.C.; Araújo, F.P.; et al. High proportion of smaller ranged hummingbird species coincides with ecological specialization across the Americas. Proc. R. Soc. B 2016, 283, 20152512. [Google Scholar] [CrossRef] [PubMed]
  12. Schmidt, N.M.; Mosbacher, J.B.; Nielsen, P.S.; Rasmussen, C.; Høye, T.T.; Roslin, T. An ecological function in crisis? The temporal overlap between plant flowering and pollinator function shrinks as the Arctic warms. Ecography 2016, 39, 1250–1252. [Google Scholar] [CrossRef] [Green Version]
  13. Burkle, L.A.; Marlin, J.C.; Knight, T.M. Plant-pollinator interactions over 120 years: Loss of species, co-occurrence and function. Science 2013, 339, 1611–1615. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Sritongchuay, T.; Hughes, A.C.; Memmott, J.; Bumrungsrib, S. Forest proximity and lowland mosaic increase robustness of tropical pollination networks in mixed fruit orchards. Landsc. Urban Plan. 2019, 192, 103646. [Google Scholar] [CrossRef]
  15. Dalsgaard, B.; Kennedy, J.D.; Simmons, B.I.; Baquero, A.C.; Martín González, A.M.; Timmermann, A.; Maruyama, P.K.; McGuire, J.A.; Ollerton, J.; Sutherland, W.J.; et al. Trait evolution, resource specialisation and vulnerability to plant extinctions among Antillean hummingbirds. Proc. R. Soc. B. 2018, 285, 20172754. [Google Scholar] [CrossRef] [PubMed]
  16. Peters, M.K.; Hemp, A.; Appelhans, T.; Becker, J.N.; Behler, C.; Classen, A.; Detsch, F.; Ensslin, A.; Ferger, S.W.; Frederiksen, S.B.; et al. Climate–land-use interactions shape tropical mountain biodiversity and ecosystem functions. Nature 2019, 568, 88–92. [Google Scholar] [CrossRef] [PubMed]
  17. Rahbek, C.; Borregaard, M.K.; Colwell, R.K.; Dalsgaard, B.; Holt, B.G.; Morueta-Holme, N.; Nogues-Bravo, D.; Whittaker, R.J.; Fjeldså, J. Humboldt’s enigma: What causes global patterns of mountain biodiversity? Science 2019, 365, 1108–1113. [Google Scholar] [CrossRef] [PubMed]
  18. Dalsgaard, B.; Schleuning, M.; Maruyama, P.K.; Dehling, D.M.; Sonne, J.; Vizentin-Bugoni, J.; Zanata, T.B.; Fjeldså, J.; Böhning-Gaese, K.; Rahbek, C. Opposed latitudinal patterns of network-derived and dietary specialization in avian plant-frugivore interaction systems. Ecography 2017, 40, 1395–1401. [Google Scholar] [CrossRef] [Green Version]

Share and Cite

MDPI and ACS Style

Dalsgaard, B. Land-Use and Climate Impacts on Plant–Pollinator Interactions and Pollination Services. Diversity 2020, 12, 168. https://doi.org/10.3390/d12050168

AMA Style

Dalsgaard B. Land-Use and Climate Impacts on Plant–Pollinator Interactions and Pollination Services. Diversity. 2020; 12(5):168. https://doi.org/10.3390/d12050168

Chicago/Turabian Style

Dalsgaard, Bo. 2020. "Land-Use and Climate Impacts on Plant–Pollinator Interactions and Pollination Services" Diversity 12, no. 5: 168. https://doi.org/10.3390/d12050168

APA Style

Dalsgaard, B. (2020). Land-Use and Climate Impacts on Plant–Pollinator Interactions and Pollination Services. Diversity, 12(5), 168. https://doi.org/10.3390/d12050168

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop