Across the southern Andes on fin: glacial refugia, drainage reversals and a secondary contact zone revealed by the phylogeographical signal of Galaxias platei in Patagonia
Abstract:We employed DNA sequence variation at two mitochondrial (control region, COI) regions from 212 individuals of Galaxias platei (Pisces, Galaxiidae) collected throughout Patagonia (25 lakes/rivers) to examine how Andean orogeny and the climatic cycles throughout the Quaternary affected the genetic diversity and phylogeography of this species. Phylogenetic analyses revealed four deep genealogical lineages which likely represent the initial division of G. platei into eastern and western lineages by Andean uplift, … Show more
“…only present in one location) haplotype (H2), may be the result of past glaciation processes reported for this area. Genetic evidence of postglacial recolonization in this area has recently been documented in the kelps Durvilleae antarctica (Fraser et al 2010) and Macrocystis pyrifera (Macaya & Zuccarello 2010) and also in a variety of Patagonian freshwater taxa (Cussac et al 2004, Zemlak et al 2008). For A. monodon the observations of genetic isolation, absence of genetic diversity in the most southerly location, and the star-like haplotype network observed in Clade II (Fig.…”
“…only present in one location) haplotype (H2), may be the result of past glaciation processes reported for this area. Genetic evidence of postglacial recolonization in this area has recently been documented in the kelps Durvilleae antarctica (Fraser et al 2010) and Macrocystis pyrifera (Macaya & Zuccarello 2010) and also in a variety of Patagonian freshwater taxa (Cussac et al 2004, Zemlak et al 2008). For A. monodon the observations of genetic isolation, absence of genetic diversity in the most southerly location, and the star-like haplotype network observed in Clade II (Fig.…”
“…Several species in the wet tropics of NE Australia show multiple geographic clades with a range of genetic divergences going back into the Pliocene(Schneider et al 1998;Moritz et al 2009). Following pioneering phylogeographic work on some Amazonian small mammals(Patton and Da Silva 1998) there is now growing effort to understand the great diversity in Amazonia and elsewhere in South America and Mesoamerica (eg Quijada-Mascarenas et al 2007;Zemlak et al 2008;Daza et al 2009;. …”
The older history of hybrid zones is explored through consideration of recent advances in climatology, paleontology and phylogeography in the Late Cenozoic, particularly the Quaternary Period with its major climatic cycles. The fossil record shows that these ice ages and their nested millennial oscillations caused substantial changes in species distributions and with genetic evidence allows deduction of refugia and colonization routes in arctic, temperate, desert and tropical regions. The age of divergence between hybridizing lineages varies from the Late Pleistocene to the Late Miocene, implying much range change and varying selection on sister lineages. Hybridizing lineages in the Tropical and Temperate regions range in age from young to old, but those studied in the Arctic are no more than a few ice ages old and their refugial roots are not clear. Mid to low latitude regions often show parapatric patchworks of lineages and multiple refugia stable through many climatic oscillations. Particular hybrid zones may have formed more than once; while some expansions were not the same, producing reticulation and introgression in previous glacial cycles. Hybrid-zone roots are complex and deep, and considerations of their complexity can reveal evolutionary pathways of species. They are indeed windows on evolution.
“…In addition, 2 genetic clusters were inferred both for A. ingens and A. shackletoni that suggest long-term persistence and secondary contact after the 2 populations survived in different refugia, where the populations would have diverge d. It has been proposed that ice-free areas existed on the shelf in Prydz Bay during the LGM (Domack et al 1998, O'Brien et al 1999, and these could have provided habitat for benthic organisms. Refugial populations and post-recolonization secondary population admixture has been identified in the Ross Sea (East Antarctica) in Adèlie penguins (Ritchie et al 2004) and has been documented as a genetic legacy to glacial cycles in different species from both the Southern (Zemlak et al 2008) and Northern (Hewitt 2000) Hemispheres. Additionally, the low genetic diversity and low effective population size observed for the 3 species could be associated with a relatively recent recolonization of the area.…”
Patterns of fine-scale spatial population structure in Antarctic benthic species are poorly understood. There is a high proportion of brooding species in the Antarctic benthos, and a brooding life history strategy is expected to restrict their dispersal abilities and therefore foster population structure. Additionally, genetic structuring of populations can preserve signals of historic processes (such as Pleistocene glaciations) on species distributions and abundances. We developed a set of 7 microsatellite markers to examine population genetic variation and infer the demographic history of 3 sympatric Antarctic sea urchin species from the order Spatangoida (Abatus ingens, A. shackletoni and A. philippii), all with brooding life history strategies. Samples were collected at 5 sites separated by up to 5 km, in the near-shore area surrounding Davis Station in the Vestfold Hills area of the Australian Antarctic Territory. We found evidence of a long-term population decline in all 3 species, and the estimated timing of the decline precedes anthropogenic activities and is compatible with long-term climate variability. Two genetic clusters in A. ingens and A. shackletoni suggest secondary contact after population differentiation in glacial refugia. Life history is not a good predictor of fine-scale population structure in these species, with gene flow possible at distances of 5 km. Finally, no evidence was found for a potential impact of pollution from Davis Station on genetic variation. The reduced effective population size observed for these Antarctic benthic species highlights their fragility and the need for conservation concern.
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