Recent Migration Events Research Articles

Discovery of a Nearctic vicariant bumblebee (Hymenoptera: Apidae) in Eurasia uncovers secondary trans-Beringian exchanges of insect faunas

Repeated emergence and disappearance of the Bering Land Bridge during the Quaternary triggered multiple faunal exchanges between northeast Asia and North America. Older (Early to Middle Pleistocene) dispersal events through the bridge followed by its submergence often lead to the vicariant origin of sister species, whose allopatric ranges are currently separated by the Bering Strait. Among bumblebees, examples of these pairs include Bombus balteatus Dahlbom 1832 – B. kirbiellus Curtis 1835, B. pyrrhopygus Friese 1902 – B. polaris Curtis 1835, and B. hyperboreus Schönherr 1809 – B. natvigi Richards 1931. However, integrative taxonomic analyses of new bumblebee samples from hard-to-reach areas of the Chukotka Peninsula (Russian Far East) reveal that the Nearctic B. kirbiellus is present at the north-eastern margin of Asia and that its Asian specimens share the COI haplotype with populations from Alaska. Although B. kirbiellus originated as a Nearctic relative of B. balteatus and was thought to be an endemic to North America, there was a Late Pleistocene (or more recent) expansion of this species from Alaska to Chukotka. Our findings indicate the possibility of secondary expansion of vicariant species through the Beringia during the Last Glacial Maximum or via a more recent migration event across the Bering Strait.

Inference of local invasion pathways in two invasive crayfish species displaying contrasting genetic patterns

Abstract The efficient management of invasive alien species (IAS) requires the identification of their introduction pathways. Genetic assessments have proven useful to inform invasion pathways at large (national to worldwide) scales, but studies at local scales are still rare, despite their importance for guiding management. In this study, genetic analyses were used to identify local invasion pathways of two invasive crayfish species (the spiny‐cheek crayfish Faxonius limosus and the red swamp crayfish Procambarus clarkii) in a dense network of artificial lakes. We first characterized the spatial patterns of genetic variability, effective population sizes (Ne) and among‐lakes recent migration events for each species using neutral microsatellite markers. We then identified the environmental factors affecting genetic variability and inferred the potential local invasion pathways. Results revealed different patterns of genetic variability between the two species: F. limosus displayed very low levels of genetic diversity, Ne and spatial structuring compared to P. clarkii, which displayed high genetic diversity, Ne and spatial genetic structuring. We also demonstrated context‐dependent effects of different environmental factors (fishery management, spatial distribution and lake size) on genetic variability indices. We did not identify local invasion pathways for F. limosus due to limited genetic variability, likely caused by a strong founder effect and potential parthenogenetic reproduction. Contrastingly, multiple invasion pathways (release, contaminant, unaided/corridor spread and stowaway) were identified for P. clarkii. Synthesis and applications. Although limited in some particular cases (e.g. for species having experienced strong shaping events and/or displaying asexual reproductive modes), neutral genetic variation assessments can provide important insights for inferring local invasion pathways in complex landscapes for invasive alien species displaying short generation times and complex invasion histories.

Geographical separation and ethnic origin influence the human gut microbial composition: a meta-analysis from a Malaysian perspective.

Ethnicity is consistently reported as a strong determinant of human gut microbiota. However, the bulk of these studies are from Western countries, where microbiota variations are mainly driven by relatively recent migration events. Malaysia is a multicultural society, but differences in gut microbiota persist across ethnicities. We hypothesized that migrant ethnic groups continue to share fundamental gut traits with the population in the country of origin due to shared cultural practices despite subsequent geographical separation. To test this hypothesis, the 16S rRNA gene amplicons from 16 studies comprising three major ethnic groups in Malaysia were analysed, covering 636 Chinese, 248 Indian and 123 Malay individuals from four countries (China, India, Indonesia and Malaysia). A confounder-adjusted permutational multivariate analysis of variance (PERMANOVA) detected a significant association between ethnicity and the gut microbiota (PERMANOVA R 2=0.005, pseudo-F=2.643, P=0.001). A sparse partial least squares – discriminant analysis model trained using the gut microbiota of individuals from China, India and Indonesia (representation of Chinese, Indian and Malay ethnic group, respectively) showed a better-than-random performance in classifying Malaysian of Chinese descent, although the performance for Indian and Malay were modest (true prediction rate, Chinese=0.60, Indian=0.49, Malay=0.44). Separately, differential abundance analysis singled out Ligilactobacillus as being elevated in Indians. We postulate that despite the strong influence of geographical factors on the gut microbiota, cultural similarity due to a shared ethnic origin drives the presence of a shared gut microbiota composition. The interplay of these factors will likely depend on the circumstances of particular groups of migrants.

Whole-Genome Sequencing of a 900-Year-Old Human Skeleton Supports Two Past Migration Events from the Russian Far East to Northern Japan.

Recent studies on paleogenomics have reported some Paleolithic and Neolithic genomes that have provided new insights into the human population history in East and Northeast Asia. However, there remain some cases where more recent migration events need to be examined to elucidate the detailed formation process of local populations. Although the area around northern Japan is one of the regions archaeologically suggested to have been affected by migration waves after the Neolithic period, the genetic source of these migrations are still unclear. Thus, genomic data from such past migrant populations would be highly informative to clarify the detailed formation process of local populations in this region. Here, we report the genome sequence of a 900-year-old adult female (NAT002) belonging to the prehistoric Okhotsk people, who have been considered to be the past migrants to northern Japan after the Neolithic period. We found a close relationship between NAT002 and modern Lower Amur populations and past admixture events between the Amur, Jomon, and Kamchatka ancestries. The admixture dating suggested migration of Amur-related ancestry at approximately 1,600 BP, which is compatible with the archaeological evidence regarding the settlement of the Okhotsk people. Our results also imply migration of Kamchatka-related ancestry at approximately 2,000 BP. In addition, human leukocyte antigen (HLA) typing detected the HLA-B*40 allele, which is reported to increase the risk of arthritis, suggesting the genetic vulnerability of NAT002 to hyperostosis, which was observed around her chest clavicle.

Morphological and molecular evidence of population divergence in a widespread shorebird across its southern mainland Australian distribution

We characterize geographical variation in the genetics, ecology, morphology and plumage of the Hooded Plover Charadrius cucullatus, a threatened shorebird widespread on coasts (south-east) and saltlakes (south-west) across the southern mainland of Australia. We confirm the distinctness of populations on either side of the Nullabor Plain/Great Australian Bight indicating that this apparent biogeographic barrier to terrestrial flora and fauna also influenced the phylogeographic pattern of a resident shorebird which is dependent on access to saline/hypersaline water. Western birds are genetically distinct, larger and have darker plumage than those in the east. Distinct ecological differences also exist, with eastern birds being resident, usually occurring on ocean beaches, with generalised diets and seasonal, solitary breeding. Western birds are nomadic, breeding when suitable conditions prevail, and exhibit more specialized diets, and may at times breed semi-colonially. Within the extensive eastern population, genetic analyses revealed an isolation by distance pattern, as well as genetic evidence of a long distance dispersal event. South Australian birds are distinct from Victorian birds, but cluster closely with Victorian birds in all genetic analyses. The western population features little genetic structuring, consistent with nomadism and congregatory behavior associated with drought/flood events. The distinctness of western populations found using multiple lines of evidence and the lack of evidence for any recent migration events across the Nullabor Plain, suggests that previously described subspecies warrant reinstatement, and that these evolutionary units require conservation assessment, as has been recognized by national conservation authorities. Conservation management of the eastern population should occur across its distribution, taking care to capture the genetic variability which is evident within this population. Further exploration of genetic variation between Eastern states is suggested.

You Will Never Walk Alone: Codispersal of JC Polyomavirus with Human Populations.

JC polyomavirus (JCPyV) is one of the most prevalent human viruses. Findings based on the geographic distribution of viral subtypes suggested that JCPyV codiverged with human populations. This view was however challenged by data reporting a much more recent origin and expansion of JCPyV. We collected information on ∼1,100 worldwide strains and we show that their geographic distribution roughly corresponds to major human migratory routes. Bayesian phylogeographic analysis inferred a Subsaharan origin for JCPyV, although with low posterior probability. High confidence inference at internal nodes provided strong support for a long-standing association between the virus and human populations. In line with these data, pairwise FST values for JCPyV and human mtDNA sampled from the same areas showed a positive and significant correlation. Likewise, very strong relationships were found when node ages in the JCPyV phylogeny were correlated with human population genetic distances (nuclear-marker based FST). Reconciliation analysis detected a significant cophylogenetic signal for the human population and JCPyV trees. Notably, JCPyV also traced some relatively recent migration events such as the expansion of people from the Philippines/Taiwan area into Remote Oceania, the gene flow between North-Eastern Siberian and Ainus, and the Koryak contribution to Circum-Arctic Americans. Finally, different molecular dating approaches dated the origin of JCPyV in a time frame that precedes human out-of-Africa migration. Thus, JCPyV infected early human populations and accompanied our species during worldwide dispersal. JCPyV typing can provide reliable geographic information and the virus most likely adapted to the genetic background of human populations.

The largest fish in the world's biggest river: Genetic connectivity and conservation of Arapaima gigas in the Amazon and Araguaia-Tocantins drainages.

Arapaima, pirarucu or paiche (Arapaima gigas) is one of the largest freshwater fish in the world, and has a long history of commercial exploitation in the Amazon region. To estimate levels of genetic variability and historical and recent connectivity in Arapaima, we examined variation in eleven microsatellite DNA markers in individuals from 22 localities in Brazil, Colombia, and Peru. The results of analysis of molecular variance, Bayesian clustering and discriminant analysis of principal components showed that Arapaima in our samples represents two major populations, one in the Amazonas and one in the Araguaia-Tocantins River basins. The Amazonas population is further structured by isolation-by-distance with the hydrologically largely unconnected Amapá locality representing the eastern-most extreme of this continuum; gene flow predominates at distances of less than 1500 km with localities separated by over 2000 km dominated by genetic drift and effectively forming different populations. We saw no evidence of multiple species of Arapaima in the Amazonas basin, and analysis of pairwise genetic divergence (FST) with Mantel tests and correlograms indicated that this largest population exhibits a large-scale pattern of isolation-by-distance, with which results from MIGRATE-N agreed. The degree and significance of genetic divergence indicates that most sampled localities represent demographically independent sub-populations, although we did identify several recent migration events between both proximal and more distant localities. The levels of genetic diversity were heterogeneous across sites, including low genetic diversity, effective population sizes, and evidence of genetic bottlenecks in several places. On average the levels of gene diversity and rarefied allelic richness were higher for localities along the Amazonas mainstem than in the tributaries, despite these being the areas of highest fishing pressure, while the lowest values were found in tributary headwaters, where landscape modification is a significant threat. We recommend that managers consider the regional and local threats to these populations and tailor strategies accordingly, strategies which should ensure the ability of young A. gigas to disperse through floodplain corridors to maintain genetic diversity among otherwise sedentary adult sub-populations.

Multilocus Genotypes of the Wheat Leaf Rust Fungus Puccinia triticina in Worldwide Regions Indicate Past and Current Long-Distance Migration.

Many plant pathogenic fungi have a global distribution across diverse ecological zones and agricultural production systems. Puccinia triticina, the wheat leaf rust fungus, is a major pathogen in many wheat production areas of the world. The objective of this research was to determine the genetic relatedness of P. triticina in different worldwide regions. A total of 831 single-uredinial isolates collected from 11 regions were characterized for multilocus genotype at 23 simple sequence repeat loci and for virulence to 20 lines of wheat with single genes for leaf rust resistance. A total of 424 multilocus genotypes and 497 virulence phenotypes were found. All populations had high heterozygosity and significant correlation between virulence and molecular variation, which indicated clonal reproduction. The populations from North America and South America, Central Asia and Russia, and the Middle East and Europe were closely related for multilocus genotypes and many individual isolates from other continental regions were closely related. Twenty-seven multilocus genotypes were found in more than one continental region, and 13 of these had isolates with identical virulence phenotypes. The wide geographic distribution of identical and highly related multilocus genotypes of P. triticina indicated past and more recent migration events facilitated by the spread of clonally produced urediniospores.

The divergence history of European blue mussel species reconstructed from Approximate Bayesian Computation: the effects of sequencing techniques and sampling strategies.

Genome-scale diversity data are increasingly available in a variety of biological systems, and can be used to reconstruct the past evolutionary history of species divergence. However, extracting the full demographic information from these data is not trivial, and requires inferential methods that account for the diversity of coalescent histories throughout the genome. Here, we evaluate the potential and limitations of one such approach. We reexamine a well-known system of mussel sister species, using the joint site frequency spectrum (jSFS) of synonymous mutations computed either from exome capture or RNA-seq, in an Approximate Bayesian Computation (ABC) framework. We first assess the best sampling strategy (number of: individuals, loci, and bins in the jSFS), and show that model selection is robust to variation in the number of individuals and loci. In contrast, different binning choices when summarizing the jSFS, strongly affect the results: including classes of low and high frequency shared polymorphisms can more effectively reveal recent migration events. We then take advantage of the flexibility of ABC to compare more realistic models of speciation, including variation in migration rates through time (i.e., periodic connectivity) and across genes (i.e., genome-wide heterogeneity in migration rates). We show that these models were consistently selected as the most probable, suggesting that mussels have experienced a complex history of gene flow during divergence and that the species boundary is semi-permeable. Our work provides a comprehensive evaluation of ABC demographic inference in mussels based on the coding jSFS, and supplies guidelines for employing different sequencing techniques and sampling strategies. We emphasize, perhaps surprisingly, that inferences are less limited by the volume of data, than by the way in which they are analyzed.

Porcine Y-chromosome variation is consistent with the occurrence of paternal gene flow from non-Asian to Asian populations.

Pigs (Sus scrofa) originated in Southeast Asia and expanded to Europe and North Africa approximately 1 MYA. Analyses of porcine Y-chromosome variation have shown the existence of two main haplogroups that are highly divergent, a result that is consistent with previous mitochondrial and autosomal data showing that the Asian and non-Asian pig populations remained geographically isolated until recently. Paradoxically, one of these Y-chromosome haplogroups is extensively shared by pigs and wild boars from Asia and Europe, an observation that is difficult to reconcile with a scenario of prolonged geographic isolation. To shed light on this issue, we genotyped 33 Y-linked SNPs and one indel in a worldwide sample of pigs and wild boars and sequenced a total of 9903 nucleotide sites from seven loci distributed along the Y-chromosome. Notably, the nucleotide diversity per site at the Y-linked loci (0.0015 in Asian pigs) displayed the same order of magnitude as that described for autosomal loci (~0.0023), a finding compatible with a process of sustained and intense isolation. We performed an approximate Bayesian computation analysis focused on the paternal diversity of wild boars and local pig breeds in which we compared three demographic models: two isolation models (I models) differing in the time of isolation and a model of isolation with recent unidirectional migration (IM model). Our results suggest that the most likely explanation for the extensive sharing of one Y-chromosome haplogroup between non-Asian and Asian populations is a recent and unidirectional (non-Asian > Asian) paternal migration event.

Population genetic structure of Helicobacter pylori strains from Portuguese-speaking countries.

The human gastric colonizer Helicobacter pylori is useful to track human migrations given the agreement between the bacterium phylogeographic distribution and human migrations. As Portugal was an African and Brazilian colonizer for over 400years, we hypothesized that Portuguese isolates were likely genetically closer with those from countries colonized by Portuguese in the past. We aimed to characterize the population structure of several Portuguese-speaking countries, including Portugal, Brazil, Angola, and Cape Verde. We included strains isolated in Portugal from Portuguese and from former Portuguese colonies. These strains were typed by multilocus sequence typing (MLST) for seven housekeeping genes. We also retrieved from Multi Locus Sequence Typing Web site additional housekeeping gene sequences, namely from Angola and Brazil. We provided evidence that strains from Portuguese belong to hpEurope and that the introgression of hpEurope in non-European countries that speak Portuguese is low, except for Brazil and Cape Verde, where hpEurope accounted for one quarter and one half of the population, respectively. We found genetic similarity for all strains from Portuguese-speaking countries that belong to hpEurope population. Moreover, these strains showed a predominance of ancestral Europe 2 (AE2) over ancestral Europe 1 (AE1), followed by ancestral Africa 1. H. pylori is a useful marker even for relative recent human migration events and may become rapidly differentiated from founder populations. H. pylori from Portuguese-speaking countries assigned to hpEurope appears to be a hybrid population resulting from the admixture of AE1, AE2 and ancestral hpAfrica1.

Population structure and coalescence in pedigrees: Comparisons to the structured coalescent and a framework for inference

Contrary to what is often assumed in population genetics, independently segregating loci do not have completely independent ancestries, since all loci are inherited through a single, shared population pedigree. Previous work has shown that the non-independence between gene genealogies of independently segregating loci created by the population pedigree is weak in panmictic populations, and predictions made from standard coalescent theory are accurate for populations that are at least moderately sized. Here, we investigate patterns of coalescence in pedigrees of structured populations. We find that the pedigree creates deviations away from the predictions of the structured coalescent that persist on a longer timescale than in the case of panmictic populations. Nevertheless, we find that the structured coalescent provides a reasonable approximation for the coalescent process in structured population pedigrees so long as migration events are moderately frequent and there are no migration events in the recent pedigree of the sample. When there are migration events in the recent sample pedigree, we find that distributions of coalescence in the sample can be modeled as a mixture of distributions from different initial sample configurations. We use this observation to motivate a maximum-likelihood approach for inferring migration rates and mutation rates jointly with features of the pedigree such as recent migrant ancestry and recent relatedness. Using simulation, we show that our inference framework accurately recovers long-term migration rates in the presence of recent migration events in the sample pedigree.

Genetic diversity and structure of remnant Magnolia stellata populations affected by anthropogenic pressures and a conservation strategy for maintaining their current genetic diversity

Understanding the factors shaping rare species’ current genetic diversity and structure, particularly the impact of recent anthropogenic pressures, is important in order to develop appropriate conservation strategies based on robust predictions. Thus, we have genotyped all 585 surviving individuals of Magnolia stellata from six remnant populations and seven isolated tree sites in northern Mie Prefecture, Japan, using nuclear and chloroplast microsatellites. Three genetic clusters were detected by STRUCTURE analysis, with an oldest divergence time between pairs within 25 generations according to coalescent analysis. We attribute this recent divergence to recent anthropogenic environmental changes. Evidence of only one significant recent migration event between pairs of the six populations was detected, indicating that most of the remnant populations are isolated now. Their future genetic status was predicted using Monte Carlo simulations, under four scenarios. It declined more than twice as rapidly in a scenario assuming variations in fecundity among both female and male parents than in a scenario assuming no fecundity variations, but strongly improved in a scenario including promotion of migrations between adjacent pairs of populations. These predictions indicate that sexual reproduction of the species should be promoted by providing more suitable habitats and migration between populations should be enhanced by restoring remnant isolated tree sites and extinct populations. In addition, all the remnant populations should be conserved because they host current genetic variation that may be important for coping with future climate change, and they could provide important stepping-stones for gene flow.

History of settlement of villages from Central Tunisia by studying families sharing a common founder Glycogenosis type III mutation

Glycogen storage disease type III (GSD III; Cori disease; Forbes disease) is an autosomal recessive inherited metabolic disorder resulting from deficient glycogen debrancher enzyme activity in liver and muscle. In this study, we focused on a single AGL gene mutation p.W1327X in 16 Tunisian patients from rural area surrounding the region of Mahdia in Central Tunisia. This constitutes the largest pool of patients with this mutation ever described. This study was performed to trace the history of the patients’ ancestries in a single region. After extraction of genomic DNA, exon 31 of AGL gene was sequenced. The patients were investigated for the hypervariable segment 1 of mitochondrial DNA and 17 Y-STR markers. We found that the p.W1327X mutation was a founder mutation in Tunisia Analysis of maternal lineages shows an admixture of autochthonous North African, sub-Saharan and a predominance of Eurasian haplogroups. Heterogeneity of maternal haplogroups indicates an ancient settlement. However, paternal gene flow was highly homogeneous and originates from the Near East. We hypothesize that the p.W1327X mutation was introduced into the Tunisian population probably by a recent migration event; then the mutation was fixed in a small region due to the high rate of consanguineous marriages and genetic drift. The screening for this mutation should be performed in priority for GSD III molecular diagnosis, for patients from the region of Mahdia and those from regions sharing the same settlement history.

Complete Mitochondrial Genomes of New Zealand's First Dogs.

Dogs accompanied people in their migrations across the Pacific Ocean and ultimately reached New Zealand, which is the southern-most point of their oceanic distribution, around the beginning of the fourteenth century AD. Previous ancient DNA analyses of mitochondrial control region sequences indicated the New Zealand dog population included two lineages. We sequenced complete mitochondrial genomes of fourteen dogs from the colonisation era archaeological site of Wairau Bar and found five closely-related haplotypes. The limited number of mitochondrial lineages present at Wairau Bar suggests that the founding population may have comprised only a few dogs; or that the arriving dogs were closely related. For populations such as that at Wairau Bar, which stemmed from relatively recent migration events, control region sequences have insufficient power to address questions about population structure and founding events. Sequencing mitogenomes provided the opportunity to observe sufficient diversity to discriminate between individuals that would otherwise be assigned the same haplotype and to clarify their relationships with each other. Our results also support the proposition that at least one dispersal of dogs into the Pacific was via a south-western route through Indonesia.

Sample Planning Optimization Tool for conservation and population Genetics (SPOTG): a software for choosing the appropriate number of markers and samples

Summary Genetic data are frequently used to make inferences about evolutionary and ecological processes, but the choice of the number of genetic markers and samples for such studies is usually ad hoc. Unfortunately, suboptimal sampling routinely leads to ambiguous results. spotg is a user-friendly software for optimizing sampling strategy for five common genetic study topics: hybridization, temporal sampling, bottlenecks, connectivity and assignment. spotg facilitates formal evaluation of the expected statistical power of proposed sampling strategies before project implementation, by using stochastic genetic simulations of realistic population scenarios and various sampling schemes. We demonstrate use of the tool with two example species (lynx and bison) in which demographic history differs; the appropriate sampling strategy for detecting a genetic bottleneck differs dramatically between the two cases, with important implications for sample planning. spotg has an interactive graphical tool for exploring results, and extensive documentation, tips and tutorials to enable use by conservation managers, ecologists beginning to use genetics and students.

Genetic structure of house mouse (Mus musculusLinnaeus 1758) populations in the Atlantic archipelago of the Azores: colonization and dispersal

We analyzed the genetic structure and relationships of house mouse (Mus musculus) populations in the remote Atlantic archipelago of the Azores using nuclear sequences and microsatellites. We typed Btk and Zfy2 to confirm that the subspecies Mus musculus domesticus was the predominant genome in the archipelago. Nineteen microsatellite loci (one per autosome) were typed in a total of 380 individuals from all nine Azorean islands, the neighbouring Madeiran archipelago (Madeira and Porto Santo islands), and mainland Portugal. Levels of heterozygosity were high on the islands, arguing against population bottlenecking. The Azorean house mouse populations were differentiated from the Portuguese and Madeiran populations and no evidence of recent migration between the three was obtained. Within the Azores, the Eastern, Western, and Central island groups tended to act as separate genetic units for house mice, with some exceptions. In particular, there was evidence of recent migration events among islands of the Central island group, whose populations were relatively undifferentiated. Santa Maria had genetically distinctive mice, which may relate to its colonization history. © 2013 The Linnean Society of London

Genetic structure of an endangered endemic fish (Gobiocypris rarus) in the upper Yangtze River

The goal of this study was to examine the genetic diversity and structure of wild populations of rare minnow (Gobiocypris rams) in the upper Yangtze River. Individuals from nine locations were sampled and genotyped at eight microsatellite markers. Populations differed from each other on allelic frequency, although there were no significant differences on other genetic diversity indices. Our results further suggested low to moderate levels of population differentiation (F-ST: 0.0130-0.1537). Specifically, two distinct genetic clusters (C1 and C2) were found, which may be highly correlated with the evolution of water systems. In addition, a weak but significant isolation-by-distance pattern was best explained by riparian distance through man-made channels. It suggested that fish might use man-made channels for gene flow in history, although no significant recent migration event was found. Therefore, this study highlights the need to consider the genetic specificities of G. rams for sustaining long-term survival of this species. (C) 2012 Elsevier Ltd. All rights reserved.

Local contamination in relation to population genetic diversity and resilience of an arctic marine amphipod

The objective of this study was to investigate whether populations inhabiting a contaminated environment are affected in terms of decreased genetic diversity due to selection of tolerant genotypes and if such effect carries a cost. Marine arctic amphipod populations (Orchomenella pinguis) were collected from sites within a contaminated fjord, as well as from sites outside the fjord on the west-coast of Greenland over three years (2006–2008). Impacts on genetic diversity, effects on resilience such as development of tolerance and cost were determined. AFLP-analysis was used to explore within and between population genetic diversity, and exposure studies were performed where the populations were subjected to known and unknown stressors to assess resilience. Populations collected at three contaminated sites all had reduced genetic diversity in 2007 compared to populations outside the fjord. This pattern was different in 2008 as all contaminated site populations increased in diversity, whereas a decrease in diversity occurred at the outer sites. However, tolerance, but even more so, cost, was related to contamination exposure in 2008, in spite of the shift in genetic diversity. We suggest that contamination rapidly induces effects that can be captured as tolerance and associated cost, whereas effects on genetic diversity can be difficult to separate from recent migration events that dilute eventual decreases in diversity due to contamination pressure. As long as impacted populations can be influenced by migration events that increase the genetic diversity and add health to an affected population, populations in contaminated areas may have enhanced probability of survival.

Mitochondrial DNA analysis of an immigrant basque population: Loss of diversity due to founder effects

The Basques have a well-documented history of migration and settlement in the Americas, and they often retain cultural identity across generations. Numerous genetic studies have been carried out on European Basques; thus, immigrant Basques are an ideal population for investigating the genetic consequences of a recent human migration event. We have sampled 53 unrelated individuals with Basque ancestry in Boise, Idaho and determined the mitochondrial DNA (mtDNA) sequence variation of the first and second hypervariable regions. Thirty-six mtDNA haplotypes were detected in our sample. We found evidence of genetic changes consistent with founder effects, which is compatible with the known history of migration. Compared with the European Basque population, the immigrant Basques are significantly different in terms of haplogroup frequency distribution and diversity. They have a lower measure of weighted intralineage mean pairwise diversity (WIMP) and greater genetic distance from other European populations. These data indicate that this immigrant Basque population has experienced a reduction in genetic diversity compared with the putative source population. However, this loss of diversity is not detectable using indices of demographic history such as Tajima's D and Fu's F. This study represents the first description of mtDNA diversity in an immigrant Basque population, and our findings indicate that founder effects accompanying this relatively recent migration event have shaped the genetic diversity of this population.