Mesopredator release hypothesis

Raccoons (Procyon lotor) and skunks (Mephitis mephitis) are mesopredators. Here they share cat food in a suburban backyard.

The mesopredator release hypothesis is an ecological theory used to describe the interrelated population dynamics between apex predators and mesopredators within an ecosystem, such that a collapsing population of the former results in dramatically increased populations of the latter. This hypothesis describes the phenomenon of trophic cascade in specific terrestrial communities.

A mesopredator is a medium-sized, middle trophic level predator, which both preys and is preyed upon. Examples are raccoons, skunks,[1] snakes, cownose rays, and small sharks.

The hypothesis

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The term "mesopredator release" was first used by Soulé and colleagues in 1988 to describe a process whereby mid-sized carnivorous mammals became far more abundant after being "released" from the control of a larger carnivore.[2] This, in turn, resulted in decreased populations of still smaller prey species, such as birds.[3][4][5] This may lead to dramatic prey population decline, or even extinction, especially on islands. This process arises when mammalian top predators are considered to be the most influential factor on trophic structure and biodiversity in terrestrial ecosystems.[6] Top predators may feed on herbivores and kill predators in lower trophic levels as well.[7] Thus, reduction in the abundance of top predators may cause the medium-sized predator population to increase, therefore having a negative effect on the underlying prey community.[8] The mesopredator release hypothesis offers an explanation for the abnormally high numbers of mesopredators and the decline in prey abundance and diversity.[9] The hypothesis supports the argument for conservation of top predators because they protect smaller prey species that are in danger of extinction.[4] This argument has been a subject of interest within conservation biology for years, but few studies have adequately documented the phenomenon.[10]

Criticism

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One of the main criticisms of the mesopredator release hypothesis is that it argues in favor of the top-down control concept and excludes the possible impacts that bottom-up control could have on higher trophic levels.[10] This means that it supports the argument that top predators control the structure and population dynamics of an ecosystem, but it does not take into account that prey species and primary producers also have an effect on the ecosystem's structure. Furthermore, populations of smaller predators do not always increase after the removal of top predators; in fact, they sometimes decline sharply.[3] Another problem is that the hypothesis is offered as an explanation after large predators have already become rare or extinct in an ecosystem. Consequently, there is no data on the past ecosystem structure and the hypothesis cannot be tested.[11] As a result, information on the past conditions has been inferred from studies of the present conditions. However, contemporary examples of mesopredator release exist, such as the culling of cats on Macquarie Island.[12]

The hypothesis is sometimes also applied to humans as apex predators that produce top-down effects on lower trophic levels. However, it fails to recognize bottom-up effects that anthropogenic land transformations can have on landscapes on which primary producers, prey species, and mesopredators dwell.[13][14] Possible bottom-up effects on an ecosystem can be from bioclimatic impacts on ecosystem productivity and from anthropogenic habitat alterations.[10] Examples of anthropogenic habitat change include agriculture, grazing land, and urbanization. More importantly, the hypothesis does not take into account that higher trophic levels are affected by primary productivity. It also does not mention that trophic interactions operate at different strengths according to the ecosystem.[15][16] Therefore, the roles of predation and food/nutrient processes in influencing ecosystem structures remain open to controversy and further testing.[17]

Other release hypotheses

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The mesopredator release hypothesis has also inspired other "release hypotheses". For example, the "mesoscavenger release hypothesis", which proposes that when large, efficient, scavenger populations decline (such as vultures), small, less efficient, mesoscavenger populations increase (such as rats).[18] However, this type of release is different. In the mesoscavenger release hypothesis, mesoscavengers are being released from competition for food, whereas, in the mesopredator release hypothesis, mesopredators are being released from direct predation from the apex predators.

See also

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References

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  1. ^ Helgen, K.; Reid, F. (2016). "Mephitis mephitis". IUCN Red List of Threatened Species. 2016: e.T41635A45211301. doi:10.2305/IUCN.UK.2016-1.RLTS.T41635A45211301.en. Retrieved 12 November 2021.
  2. ^ Soulé, Michael E.; Bolger, Douglas T.; Alberts, Allison C.; Wright, John; Sorice, Marina; Hill, Scott (March 1988). "Reconstructed Dynamics of Rapid Extinctions of Chaparral-Requiring Birds in Urban Habitat Islands" (PDF). Conservation Biology. 2 (1): 75–92. Bibcode:1988ConBi...2...75S. doi:10.1111/j.1523-1739.1988.tb00337.x. hdl:2027.42/74761.
  3. ^ a b Prugh, L.R.; Stoner, C.J.; Epps, C.W.; Bean, W.T.; Ripple, W.J.; LaLiberte, A.S.; Brashares, J.S. (October 2009). "The Rise of the Mesopredator" (PDF). BioScience. 59 (9): 779–791. doi:10.1525/bio.2009.59.9.9. ISSN 0006-3568. S2CID 40484905. Retrieved 22 September 2015.
  4. ^ a b Sanicola, S. (2007). "Mesopredator Release". Retrieved 23 May 2007.
  5. ^ Courchamp, F.; Langlais, M.; Sugihara, G. (1999). "Cats protecting birds: modelling the mesopredator release effect". Journal of Animal Ecology. 68 (2): 282–292. Bibcode:1999JAnEc..68..282C. doi:10.1046/j.1365-2656.1999.00285.x.
  6. ^ Hebblewhite, M; White, CA; Nietvelt, CG; McKenzie, JA; Hurd, TE; Fryxell, JM (2005). "Human activity mediates a trophic cascade caused by wolves" (PDF). Ecology. 86 (8): 2135–2144. Bibcode:2005Ecol...86.2135H. doi:10.1890/04-1269. S2CID 11581675. Retrieved 22 September 2015.
  7. ^ Palomares, E.; Caro, T.M. (1999). "Interspecific killing among mammalian carnivores" (PDF). Am. Nat. 153 (5): 492–508. doi:10.1086/303189. hdl:10261/51387. PMID 29578790. S2CID 4343007.
  8. ^ Crooks, K.R.; Soulé, M.E. (1999). "Mesopredator release and avifaunal extinctions in a fragmented system". Nature. 400 (6744): 563–566. Bibcode:1999Natur.400..563C. doi:10.1038/23028. S2CID 4417607.
  9. ^ Terborgh, J., Estes, J.A., Paquet, P., Ralls, K., Boyd-Heger, D., Miller, B.J. 1999. The role of top carnivores in regulating terrestrial ecosystems. In: Continental conservation: design and management principles for long-term, regional conservation networks. (eds Soulé, M. & Terborgh, J.). Island Press, Covelo, CA; Washington DC. pp. 39–64
  10. ^ a b c Elmhagen, B.; Rushton, S. (2007). "Trophic control of mesopredators in terrestrial ecosystems: top-down or bottom-up?". Ecology Letters. 10 (3): 197–206. doi:10.1111/j.1461-0248.2006.01010.x. PMID 17305803.
  11. ^ Sæther, B.E. (1999). "Top dogs maintain diversity". Nature. 400 (6744): 510–511. Bibcode:1999Natur.400..510S. doi:10.1038/22889. S2CID 5125870.
  12. ^ Bergstrom, D.M.; Lucieer, A.; Kiefer, K.; Wasely, J.; Belbin, L.; Pedersen, T.K.; Chown, S.L. (2009). "Indirect effects of invasive species removal devastate world heritage island" (PDF). Journal of Applied Ecology. 46 (1): 73–81. Bibcode:2009JApEc..46...73B. doi:10.1111/j.1365-2664.2008.01601.x.
  13. ^ Larivière, S (2004). "Range expansion of raccoons in the Canadian prairies: review of hypotheses". Wildl. Soc. Bull. 32 (3): 955–963. doi:10.2193/0091-7648(2004)032[0955:reorit]2.0.co;2. S2CID 86325289.
  14. ^ COVE, MICHAEL V.; JONES, BRANDON M.; BOSSERT, AARON J.; CLEVER, DONALD R.; DUNWOODY, RYAN K.; WHITE, BRYAN C.; JACKSON, VICTORIA L. (2012). "Use of Camera Traps to Examine the Mesopredator Release Hypothesis in a Fragmented Midwestern Landscape". The American Midland Naturalist. 168 (2): 456–465. doi:10.1674/0003-0031-168.2.456. ISSN 0003-0031. JSTOR 23269832. S2CID 84331827.
  15. ^ Oksanen, L.; Oksanen, T. (2000). "The logic and realism of the hypothesis of exploitation ecosystems". Am. Nat. 155 (6): 703–723. doi:10.1086/303354. PMID 10805639. S2CID 4440865.
  16. ^ Pardo Vargas, Lain E.; Cove, Michael V.; Spinola, R. Manuel; de la Cruz, Juan Camilo; Saenz, Joel C. (2016-04-01). "Assessing species traits and landscape relationships of the mammalian carnivore community in a neotropical biological corridor". Biodiversity and Conservation. 25 (4): 739–752. Bibcode:2016BiCon..25..739P. doi:10.1007/s10531-016-1089-7. hdl:11056/17406. ISSN 1572-9710. S2CID 16607291.
  17. ^ Pace, M.L.; Cole, J.J.; Carpenter, S.R.; Kitchell, J.F. (1999). "Trophic cascades revealed in diverse ecosystems". Trends Ecol. Evol. 14 (12): 483–488. doi:10.1016/s0169-5347(99)01723-1. PMID 10542455.
  18. ^ O'Bryan, Christopher J.; Holden, Matthew H.; Watson, James E. M. (2019). "The mesoscavenger release hypothesis and implications for ecosystem and human well-being". Ecology Letters. 22 (9): 1340–1348. Bibcode:2019EcolL..22.1340O. doi:10.1111/ele.13288. ISSN 1461-0248. PMID 31131976. S2CID 167209009.
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