TL;DR: Morphological and molecular data suggest that two distinct groups of gyrodactylids infect goodeids, one of which shares a common ancestor with gyrodACTylids parasitizing poeciliids, and the second most abundant parasite group infecting G. atripinnis.
Abstract: Goodeid topminnows are live-bearing fishes endemic to the Mexican Highlands (Mesa Central, MC). Unfortunately, in the MC, environmental degradation and introduced species have pushed several goodeid species to the brink of extinction. Invasive fishes can introduce exotic parasites, and the most abundant goodeid, blackfin goodea Goodea atripinnis Jordan, is parasitised by six exotic helminths. Poeciliids are widely dispersed invasive fishes, which exert negative ecological effects on goodeids. Poeciliids host several species of the monogenean genus Gyrodactylus von Nordmann, 1832, including pathogenic, invasive parasites. Here, we looked for evidence of Gyrodactylus species switching hosts from poeciliids to goodeids. Fish were collected in rivers draining the MC into both sides of the continental divide. Hosts were screened for gyrodactylid parasites in localities where G. atripinnis and poeciliids occurred sympatrically. Gyrodactylus specimens were characterised morphologically (attachment apparatus) and molecularly (internal transcribed spacer region, ITS). A Bayesian phylogenetic tree using ITS sequences established relationships between gyrodactylids collected from goodeid fishes and those from parasites infecting poeciliids. Gyrodactylids were collected from G. atripinnis in six localities on both sides of the watershed where exotic poeciliids occurred sympatrically. Morphological and molecular analyses indicated the presence of four undescribed species of Gyrodactylus infecting this goodeid host. Gyrodactylus tomahuac n. sp., the most abundant and geographically widespread species, is described here. The other three Gyrodactylus spp. are not described, but their ITS sequences are used as molecular data presented here, are the only available for gyrodactylids infecting goodeid fishes. Morphological and molecular data suggest that two distinct groups of gyrodactylids infect goodeids, one of which shares a common ancestor with gyrodactylids parasitizing poeciliids. No evidence was found of gyrodactylids switching hosts from invasive poeciliids to endemic goodeids, nor vice versa. Moreover, considering that G. atripinnis is known to host both Gyrodactylus lamothei Mendoza-Palmero, Sereno-Uribe & Salgado-Maldonado, 2009 and Gyrodactylus mexicanus Mendoza-Palmero, Sereno-Uribe & Salgado-Maldonado, 2009, with the addition of G. tomahuac n. sp. and the three undescribed Gyrodactylus spp. reported, at least six gyrodactylids may infect this host. This would make monogeneans the second most abundant parasite group infecting G. atripinnis, which to date is known to harbour 22 helminth species: nine digeneans, five nematodes, four cestodes, three monogeneans and one acanthocephalan.
Abstract: The development of viviparity in animals has produced in both maternal female and young many morphological and physiological adaptations, some simple antd some highly specialized. Teleosts are no exception to this generalization. The family Goodeidae (order Cyprinodontes), a family of viviparous freshwater fishes from Mexico, illustrates excellently many such adaptive changes exhibited by both mother and young during gestation. The reader is referred to the work of Meek ( '04) and Hubbs and Turner ( '39) f o r historical data concerning the family, to Hubbs and Turner ('39) for the most recent taxonomic revision of the family, to L41varez ( '50) for the most recent key of the Goodeidae and to numerous articles by Turner and Nendoza f o r structural, histological, physiological anld taxonomic aspects of reproduction in this family. The ovary in the females of this family acts as a comhination ovary-uterus since the eggs are discharged from the follicle into the ovarian cavity at the time of fertilization and the embryo develops there until birth. Furthermore, since the amount of yolk is very limited, the embryo must obtain its nutritive materials and oxygen from the ovarian fluid and release its excretory wastes into the ovarian lumen. To better effect this interchange of substances, the ovary has become highly vascular (Turner, '33, '47; Mendoza, '40, '%), it has increased its internal surface enormously by forming conipli-
TL;DR: This species has a wide distribution across the Pacific Slope of Mexico, including the Lerma-Grande de Santiago basin, Ameca River, Magdalena Lake and the Balsas and Armeria basins.
Abstract: A population of blackfin goodea Goodea atripinnis was encountered in the Metztitlan Canyon Biosphere Reserve (Panuco Basin, Hidalgo, Mexico). This species has a wide distribution across the Pacific Slope of Mexico, including the Lerma-Grande de Santiago basin, Ameca River, Magdalena Lake and the Balsas and Armeria basins. Biometric data were used for identification and comparison to those of other putative members of the genus. The taxonomic identification and systematic position of this species are discussed. Goodea luitpoldii and G. gracilis are confirmed as synonyms with G. atripinnis. Comments on conservation implications of this species and their Panuco Basin populations are given.
TL;DR: In this paper, the authors analyzed variation in the mitochondrial cytochrome b gene to evaluate the phylogeographic relationships, genetic structure, genetic diversity and demographic history of Goodea from across its distribution range.
Abstract: Central Mexico is characterized by a complex topography that is the result of historic and contemporary tectonic and climatic factors. These events have influenced the evolutionary history of numerous freshwater fishes in the region. Nonetheless, recent studies have shown that life-history traits and ecological characteristics of species may influence dispersal capabilities and the degree of genetic connectivity. Goodea (Cyprinodontiformes: Goodeidae) is one of the most widely distributed and environmentally tolerant genera of goodeids. In this study, the authors analysed variation in the mitochondrial cytochrome b gene to evaluate the phylogeographic relationships, genetic structure, genetic diversity and demographic history of Goodea from across its distribution range. They found low genetic differentiation and identified shared haplotypes among several regions. Geographic segregation was found in samples southwest and northeast of the Lower Lerma region, with some internal isolated groups showing phylogeographic differentiation and unique haplotypes. The AMOVA best explained genetic structure when grouped by haplogroups rather than when grouped by recognized biogeographic regions. Several regions showed null genetic diversity, raising the possibility of dispersal mediated by humans. Finally, Bayesian Skyline Plot analysis showed a population expansion for the Southwest haplogroup, except for the Armeria population and sub-group II of the Northeast haplogroup. All this suggests a recent colonization of Goodea atripinnis throughout some of the biogeographic regions currently inhabited by this species.