Biology:Poeciliidae
| Poeciliidae | |
|---|---|
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| Green swordtail, Xiphophorus hellerii | |
Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Actinopterygii |
| Order: | Cyprinodontiformes |
| Superfamily: | Poecilioidea |
| Family: | Poeciliidae Bonaparte, 1831[1] |
| Subfamilies & Genera | |
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See text | |
The Poeciliidae are a family of freshwater fishes of the order Cyprinodontiformes, the tooth-carps, and include well-known live-bearing aquarium fish, such as the guppy, molly, platy, and swordtail. The original distribution of the family was the Southeastern United States to north of Río de la Plata, Argentina , and Africa, including Madagascar . Due to release of aquarium specimens and the widespread use of species of the genera Poecilia and Gambusia for mosquito control, though, poeciliids can today be found in all tropical and subtropical areas of the world. In addition, Poecilia and Gambusia specimens have been identified in hot springs pools as far north as Banff, Alberta.[2]
Live-bearing
Although the whole family Poeciliidae is known as "live bearers" (viviparous), some species are egg-scattering with external fertilization. All African species are egg-layers, and (with the exception of the members of the genus Tomeurus), all American species are live-bearers. Among the three subfamilies, the Aplocheilichthyinae are restricted to Africa, the Poeciliinae are primarily from the Americas (the only exception is the African Rhexipanchax), and the Procatopodinae are mainly from Africa (the South American Fluviphylax and Pseudopoecilia are the only exceptions). This distribution suggests that the Poeciliidae antedate the split between Africa and South America 100 million years ago, and that live-bearing subsequently evolved in South America. Poeciliids colonized North America through the Antilles, while they were connected 44 million years ago. Poeciliids then moved to Central America by the Aves land bridge on the Caribbean Plate. When South America connected to Central America three million years ago, some further dispersal southward occurred, but South American species did not move into Central America.[3]
Among the live-bearing species, differences are seen in the mode and degree of support the female gives the developing larvae. Many members of the family Poeciliidae are considered to be lecithotrophic (the mother provisions the oocyte with all the resources it needs prior to fertilization, so the egg is independent of the mother), but others are matrotrophic (literally "mother feeding": the mother provides the majority of resources to the developing offspring after fertilization). Lecithotrophy and matrotrophy are not discrete traits. Most scientific studies quantify matrotrophy using a matrotrophy index (MI), which is the dry mass of fully developed offspring divided by the dry mass of a fertilized egg.[4]
Members of the genus Poeciliopsis, for example, show variable reproductive life history adaptations. Poeciliopsis monacha, P. lucida, and P. prolifica form part of the same clade within that genus. However, their modes of maternal provisioning vary greatly. P. monacha can be considered to be lecithotrophic because it does not really provide any resources for its offspring after fertilization - the pregnant female is basically a swimming egg sac. P. lucida shows an intermediate level of matrotrophy, meaning that to a certain extent the offspring's metabolism can actually affect the mother's metabolism, allowing for increased nutrient exchange. P. prolifica is considered to be highly matrotrophic, and almost all of the nutrients and materials needed for fetal development are supplied to the oocyte after it has been fertilized. This level of matrotrophy allows Poeciliopsis to carry several broods at different stages of development, a phenomenon known as superfetation. Because the space for developing embryos is limited, viviparity reduces brood size. Superfetation can compensate for this loss by keeping embryos at various stages and sizes during development.[5]
P. elongata, P. turneri, and P. presidionis form another clade that could be considered an outgroup to the P. monacha, P.lucida, and P. prolifica clade. These three species are very highly matrotrophic - so much so that in 1947, C. L. Turner described the follicular cells of P. turneri as "pseudo-placenta, pseudo-chorion, and pseudo-allantois".[citation needed] The greater degree of matrotrophy in a species is linked with a higher degree of placentation, including "a thicker maternal follicle, higher degree of vascularization, and greater number of villi in the placenta".[4]
The reason for placental evolution in Poeciliids is controversial, and involves two major groups of hypotheses, adaptive and conflict hypotheses.[6] Adaptive hypotheses, including the locomotor hypothesis,[7] Trexler-DeAngelis Model[8] (reproductive allotment), and life-history facilitation,[9][6] broadly suggest that the placenta evolved to facilitate the evolution of another advantageous trait in the fish's environment. The conflict hypothesis suggests the placenta is a nonadaptive byproduct of genetic "tug-o-war" between the mother and the offspring for resources.[10]
Subfamilies and tribes
The family is divided into subfamilies and tribes as follows:[1][11]
- Subfamily Aplocheilichythinae Myers, 1928 (Banded lampeyes)
- Genus Aplocheilichthys Bleeker, 1863
- Genus Hylopanchax Poll & J. G. Lambert,1958
- Subfamily Procatopodinae Fowler, 1916 (Lampeyes)
- Tribe Fluviphylacini Roberts, 1970
- Genus Fluviphylax Whitley, 1920
- Tribe Procatopodini Fowler, 1916
- Genus Laciris Huber, 1981
- Genus Micropanchax Myers, 1924
- Genus Lacustricola Myers, 1924
- Genus Poropanchax Clausen, 1967
- Genus Platypanchax Ahl, 1928
- Genus Lamprichthys Regan 1911
- Genus Pantanodon Myers, 1955
- Genus Hypsopanchax Myers, 1924
- Genus Procatopus Boulenger, 1904
- Genus Plataplochilus Ahl, 1928
- Genus Rhexipanchax Huber, 1999
- Tribe Fluviphylacini Roberts, 1970
- Subfamily Poeciliinae Bonaparte, 1831 (Livebearers)
- Tribe Alfarini Hubbs, 1924
- Genus Alfaro Meek, 1912
- Tribe Gambusini Gill, 1889
- Genus Belonesox Kner, 1860
- Genus Brachyrhaphis Regan, 1913
- Genus Gambusia Poey, 1854
- Genus Heterophallus Regan, 1914
- Tribe Heterandriini Hubbs, 1924
- Genus Heterandria Agassiz, 1853
- Genus Neoheterandria Henn 1916
- Genus Poeciliopsis Regan 1913
- Genus Priapichthys Regan 1913
- Genus Pseudopoecilia Regan 1913
- Genus Xenophallus Hubbs, 1924
- Tribe Poeciliini Bonaparte, 1831
- Genus Limia Poey, 1854
- Genus Micropoecilia Hubbs, 1926
- Genus Pamphorichthys Regan, 1913
- Genus Phallichthys Hubbs, 1924
- Genus Poecilia Bloch & Schneider, 1801
- Genus Xiphophorus Heckel, 1848
- Tribe Cnesterodontini Hubbs, 1924
- Genus Cnesterodon Garman, 1895
- Genus Phalloceros Eigenmann, 1907
- Genus Phalloptychus Eigenmann, 1907
- Genus Phallotorynus Henn, 1916
- Genus Tomeurus Eigenmann, 1909
- Tribe Scolichthyini Rosen, 1967
- Genus Scolichthys Rosen, 1967
- Tribe Xenodexini Hubbs, 1950
- Genus Xenodexia Hubbs, 1950
- Tribe Alfarini Hubbs, 1924
References
- "Poeciliidae". Integrated Taxonomic Information System. https://www.itis.gov/servlet/SingleRpt/SingleRpt?search_topic=TSN&search_value=165876.
- ↑ 1.0 1.1 Richard van der Laan; William N. Eschmeyer; Ronald Fricke (2014). "Family-group names of Recent fishes". Zootaxa 3882 (2): 001–230. doi:10.11646/zootaxa.3882.1.1. PMID 25543675. https://biotaxa.org/Zootaxa/article/view/zootaxa.3882.1.1/10480.
- ↑ "Archived copy". http://srd.alberta.ca/FishWildlife/FisheriesManagement/documents/CostsAndThreatsOfInvasiveSpeciesInAlberta-Mar-04.pdf.
- ↑ Hrbek, T., J. Seekinger, and A. Meyer. 2007. A phylogenetic and biogeographic perspective on the evolution of poeciliid fishes. Molecular Phylogenetics and Evolution 43:986-998.
- ↑ 4.0 4.1 Kwan, Lucia; Fris, Megan; Rodd, F. Helen; Rowe, Locke; Tuhela, Laura; Panhuis, Tami M. (2015-03-12). "An examination of the variation in maternal placentae across the genusPoeciliopsis(Poeciliidae)". Journal of Morphology 276 (6): 707–720. doi:10.1002/jmor.20381. ISSN 0362-2525. PMID 25765517. http://dx.doi.org/10.1002/jmor.20381.
- ↑ Thibault, R. E., and R. J. Schultz. 1978. Reproductive adaptations among viviparous fishes (Cyprinodontiformes Poeciliidae). Evolution 32:320-333.
- ↑ 6.0 6.1 Furness, Andrew I.; Avise, John C.; Pollux, Bart J.A.; Reynoso, Yuridia; Reznick, David N. (May 2021). "The evolution of the placenta in poeciliid fishes". Current Biology 31 (9): 2004–2011.e5. doi:10.1016/j.cub.2021.02.008. ISSN 0960-9822. PMID 33657405.
- ↑ Thibault, Roger E.; Schultz, R. Jack (June 1978). "Reproductive Adaptations Among Viviparous Fishes (Cyprinodontiformes: Poeciliidae)". Evolution 32 (2): 320–333. doi:10.2307/2407600. ISSN 0014-3820. PMID 28563744. http://dx.doi.org/10.2307/2407600.
- ↑ Trexler, Joel C.; DeAngelis, Donald L. (November 2003). "Resource Allocation in Offspring Provisioning: An Evaluation of the Conditions Favoring the Evolution of Matrotrophy". The American Naturalist 162 (5): 574–585. doi:10.1086/378822. ISSN 0003-0147. PMID 14618536. http://dx.doi.org/10.1086/378822.
- ↑ Pires, Marcelo N.; Bassar, Ronald D.; McBride, Kevin E.; Regus, John U.; Garland, Theodore; Reznick, David N. (2011-03-24). "Why do placentas evolve? An evaluation of the life-history facilitation hypothesis in the fish genus Poeciliopsis". Functional Ecology 25 (4): 757–768. doi:10.1111/j.1365-2435.2011.01842.x. ISSN 0269-8463. http://dx.doi.org/10.1111/j.1365-2435.2011.01842.x.
- ↑ Crespi, Bernard; Semeniuk, Christina (May 2004). "Parent‐Offspring Conflict in the Evolution of Vertebrate Reproductive Mode". The American Naturalist 163 (5): 635–653. doi:10.1086/382734. ISSN 0003-0147. PMID 15122484. http://dx.doi.org/10.1086/382734.
- ↑ J. S. Nelson; T. C. Grande; M. V. H. Wilson (2016). Fishes of the World (5th ed.). Wiley. pp. 371. ISBN 978-1-118-34233-6. https://sites.google.com/site/fotw5th/.
Wikidata ☰ Q463057 entry
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