Conservation biology of parasites explained
A large proportion of living species on Earth live a parasitic way of life.[1] Parasites have traditionally been seen as targets of eradication efforts, and they have often been overlooked in conservation efforts. In the case of parasites living in the wild – and thus harmless to humans and domesticated animals – this view is changing. The conservation biology of parasites is an emerging and interdisciplinary field that recognizes the integral role parasites play in ecosystems. Parasites are intricately woven into the fabric of ecological communities, with diverse species occupying a range of ecological niches and displaying complex relationships with their hosts.
The rationale for parasite conservation extends beyond their intrinsic value and ecological roles. Parasites offer potential benefits to human health and well-being. Many parasites produce bioactive compounds with pharmaceutical properties, which can be utilized in drug discovery and development. Understanding and conserving parasite biodiversity not only contributes to the preservation of ecosystems but also holds promise for medical advancements and novel therapeutic interventions.
Parasite role in ecosystems
Ranging from microscopic pathogens to larger organisms such as worms and arthropods, parasites exhibit remarkable diversity in their life cycles, transmission strategies, and host relationships. They can be found in virtually every ecosystem on Earth, including terrestrial, freshwater, and marine environments. Parasites often rely on one or multiple host species to complete their life cycle, and their presence can have profound effects on host populations, communities, and even entire ecosystems.[2] [3] One of the fundamental aspects of parasite ecology is their role as a trophic level within the food web.[4] Parasites can occupy various positions within the trophic hierarchy, acting as predators, consumers, or even decomposers.[5] They regulate host populations by influencing host behavior, growth, and reproduction. Furthermore, parasites can indirectly shape community dynamics by mediating interactions between host species and influencing the distribution and abundance of other organisms within the ecosystem.
Despite their ecological significance, parasites have historically received less attention in conservation efforts compared to other groups of organisms. However, in recent years, there has been a growing recognition of the importance of parasite conservation. Ecologists and conservation biologists have emphasized the need for research to understand the ecological roles of parasites, as well as the threats they face and the potential consequences of their decline or extinction. Integrating parasite conservation into broader conservation frameworks is crucial for maintaining the integrity and functionality of ecosystems.
Conservation approaches
Conservation approaches for animal parasites encompass a range of strategies tailored to their unique characteristics and conservation requirements. Assessing the conservation status of parasites poses challenges, as traditional criteria such as those developed by the IUCN may not adequately capture the specific threats and vulnerabilities of these organisms. Efforts often focus on conserving host species, recognizing that protecting the host also benefits associated parasites. This includes habitat conservation, management of host populations, and minimizing anthropogenic impacts.
Nuances arise in parasite conservation when considering translocating species or implementing captive breeding programs. It is essential to consider the potential effects on parasite populations and ensure that appropriate measures are in place to safeguard their survival. In situ conservation, which involves the preservation and management of parasites within their natural habitats, is a key approach. Additionally, ex situ conservation methods, such as maintaining parasite populations in controlled environments, can serve as a safety net for critically endangered species.
Endangered parasite species
A note published in 1990 pointed out that the captive breeding and reintroduction program to save the black-footed ferret would cause the loss of its specific parasites and demanded "equal rights for parasites".[6] A paper in 1992 warned that not only the loss of certain host species from the wild, but host population bottlenecks or the fragmentation of host populations would predictably lead to the extinction of host-specific parasites.[7] The paper also noted that parasites exert selective pressures upon their host populations that increase host genetic diversity. At first, this view met with open scepticism.[8] However, it became clear that the co-extinction of hosts and their specific parasites is likely to increase the current estimates of extinction rates significantly.[9] A decade later, a study focusing on highly host-specific groups such as fig wasps, parasites, butterflies, and myrmecophil butterflies estimated the number of parasites put at risk by the endangered status of the host at about 6300.[10] Other authors argued that host-specific parasite faunae have an unexpected advantage for conservation scientists. Their genealogies and population genetic patterns may help to illuminate their hosts' evolutionary and demographic history.[11] Recently, scientists suggested that rich parasite faunae are inevitably needed for healthy ecosystem functioning[12] and also that parasites and mutualists are the most endangered species on Earth.[13] Even vets have started to argue about the conservational values of parasite species.[14]
A recent study on parasites of coral reef fish suggested that extinction of a coral reef fish species would eventually result in the coextinction of at least ten species of parasites. Although this number might seem high, the study included only large parasites such as parasitic worms and crustaceans, but not microparasites such as Myxosporea and Microsporidia.[15]
Examples of parasite conservation
The list below follows that of Mey (2005)[16]
- Acutifrons caracarensis, parasite of the extinct Guadalupe caracara (Caracara lutosa), Guadalupe Island, Mexico.
- Archaeocroton sphenodoni, parasite of the tuatara (Sphenodon punctatus), New Zealand.
- Coloceras hemiphagae, parasite of the extinct Norfolk Island pigeon (Hemiphaga novaeseelandiae spadicea), Norfolk Island, New Zealand.
- Coloceras restinctus, parasite of the extinct Norfolk Island pigeon (Hemiphaga novaeseelandiae spadicea), Norfolk Island, New Zealand.
- Colpocephalum californici, parasite of the California condor (Gymnogyps californianus), western North America. The host was saved by a captive breeding and repatriation program, but the parasite was driven to extinction, deliberately killed whenever it was found during the program to ensure condor survival.
- Columbicola extinctus, parasite of the extinct passenger pigeon (Ectopistes migratorius), eastern North America. However, recent taxonomic studies show that it is conspecific with the lice living on band-tailed pigeon (Patagioenas fasciata), thus it is not extinct.[17]
- Felicola isidoroi, parasite of the endangered Iberian lynx. Similarly to C. californici, it is thought extinct after conservation efforts deloused captive lynxes.
- Longimenopon dominicanum, parasite of the extinct Guadalupe storm petrel (Oceanodroma macrodactyla), Guadelupe Island, Mexico.
- Philopteroides xenicus, parasite of the extinct bushwren (Xenicus longipes), New Zealand.
- Psittacobrosus bechsteini, parasite of the extinct Cuban red macaw (Ara tricolor), Cuba.
- Rallicola piageti, parasite of the possibly extinct New Caledonian rail (Cabalus lafresnayanus), New Caledonia.
- Rallicola extinctus, parasite of the extinct huia (Heteralocha acutirostris), New Zealand.[18]
See also
Notes and References
- 10.1016/S0020-7519(98)00153-2 . Windsor DA. 1998. Most of the species on Earth are parasites. International Journal for Parasitology . 28 . 12 . 1939–1941 . 9925276.
- Carlson . Colin J. . Hopkins . Skylar . Bell . Kayce C. . Doña . Jorge . Godfrey . Stephanie S. . Kwak . Mackenzie L. . Lafferty . Kevin D. . Moir . Melinda L. . Speer . Kelly A. . Strona . Giovanni . Torchin . Mark . Wood . Chelsea L. . 2020-10-01 . A global parasite conservation plan . Biological Conservation . en . 250 . 108596 . 10.1016/j.biocon.2020.108596 . 225345547 . 0006-3207. 10919/102428 . free .
- Dougherty . Eric R. . Carlson . Colin J. . Bueno . Veronica M. . Burgio . Kevin R. . Cizauskas . Carrie A. . Clements . Christopher F. . Seidel . Dana P. . Harris . Nyeema C. . August 2016 . Paradigms for parasite conservation: Parasite Conservation . Conservation Biology . en . 30 . 4 . 724–733 . 10.1111/cobi.12634. 26400623 . 2027.42/133571 . 4853514 . free .
- Web site: Everything in Moderation: Principles of Parasite Control for Wildlife Conservation . 2023-07-12 . BioScience . 2014 . 10.1093/biosci/biu135 . Stringer . Andrew Paul . Linklater . Wayne . 64 . 10 . 932–937 .
- Kwak . Mackenzie L. . Heath . Allen C. G. . Cardoso . Pedro . 2020-08-01 . Methods for the assessment and conservation of threatened animal parasites . Biological Conservation . en . 248 . 108696 . 10.1016/j.biocon.2020.108696 . 225517357 . 0006-3207.
- 10.1038/348104c0 . Windsor DA. 1990. Heavenly hosts. Nature . 348 . 6297 . 104 . . free .
- Rózsa L. 1992. Endangered parasite species. International Journal for Parasitology . 22 . 3 . 265–266 . 1639560 . 10.1016/S0020-7519(05)80002-5.
- 10.1016/0020-7519(94)90199-6 . Bush AO, Kennedy CR . 1994. Host fragmentation and helminth parasites: Hedging your bets against extinction. International Journal for Parasitology . 24 . 8 . 1333–1343 . 7729985.
- 10.1038/366307a0 . Stork NE, Lyal CH . 1993. Extinction or 'co-extinction' rates?. Nature. 366 . 6453. 307–8 . . free.
- Koh LP, Dunn RR, Sodhi NS, Colwell RK, Proctor HC, Smith VS. 2004. Species Coextinctions and the Biodiversity Crisis. Science. 305. 5690. 1632–1634. 15361627. 10.1126/science.1101101. 30713492.
- Whiteman NK, Parker PG . 2005. Using parasites to infer host population history: a new rationale for parasite conservation. Animal Conservation . 8 . 175–181 . 10.1017/S1367943005001915 . 2. 43057262.
- Hudson PJ, Dobson AP, Lafferty KD . 2006. Is a healthy ecosystem one that is rich in parasites? . Trends in Ecology & Evolution. 21 . 381–385 . 10.1.1.79.9080 . 10.1016/j.tree.2006.04.007 . 16713014. 7.
- 10.1098/rspb.2009.0413 . Dunn RR, Harris NC, Colwell RK, Koh LP, Sodhi NS . 2009. The sixth mass coextinction: are most endangered species parasites and mutualists? . Proceedings of the Royal Society B . 276 . 1670. 3037–3045 . 19474041 . 2817118 .
- Pizzi R. 2009. Veterinarians and Taxonomic Chauvinism: The Dilemma of Parasite Conservation . Journal of Exotic Pet Medicine . 18. 279–282 . 10.1053/j.jepm.2009.09.005 . 4.
- Justine . J.-L. . Beveridge . I. . Boxshall . G. A. . Bray . R. A. . Miller . T. L. . Moravec . F. . Trilles . J.-P. . Whittington . I. D. . 2012 . An annotated list of fish parasites (Isopoda, Copepoda, Monogenea, Digenea, Cestoda, Nematoda) collected from Snappers and Bream (Lutjanidae, Nemipteridae, Caesionidae) in New Caledonia confirms high parasite biodiversity on coral reef fish . Aquatic Biosystems . 8 . 22 . 10.1186/2046-9063-8-22 . 22947621 . 3507714 . free .
- Mey. Eberhard. 2005. Psittacobrosus bechsteini: ein neuer ausgestorbener Federling (Insecta, Phthiraptera, Amblycera) vom Dreifarbenara Ara tricolor (Psittaciiformes), nebst einer annotierten Übersicht über fossile und rezent ausgestorbene Tierläuse. Psittacobrosus bechsteini: a new extinct chewing louse (Insecta, Phthiraptera, Amblycera) off the Cuban Macaw Ara tricolor (Psittaciiformes), with an annotated review of fossil and recently extinct animal lice. Anzeiger des Vereins Thüringer Ornithologen. 5. 201–217. 2017-10-31. https://web.archive.org/web/20131227095139/http://phthiraptera.info/Publications/46150.pdf. 2013-12-27. dead.
- Clayton . Dale H. . Roger D. Price . 1999 . Taxonomy of New World Columbicola (Phthiraptera: Philopteridae) from the Columbiformes (Aves), with Descriptions of Five New Species . dead . Annals of the Entomological Society of America . . 92 . 5 . 675–85 . 10.1093/aesa/92.5.675 . https://web.archive.org/web/20120425124314/http://darwin.biology.utah.edu/PubsHTML/PDF-Files/42.pdf . 2012-04-25 . 2011-12-03.
- Mey E. 1992. Eine neue ausgestorbene Vogel-Ischnozere von Neuseeland, Huiacola extinctus (Insecta, Phthiraptera). Zoologischer Anzeiger. 224. 49–73. dead. https://web.archive.org/web/20071012042110/http://www.phthiraptera.org/Publications/0472.pdf. 2007-10-12.