Browse Subject Areas

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Pattern of genetic differentiation of an incipient speciation process: The case of the high Andean killifish Orestias

  • Claudia Jimena Guerrero-Jiménez ,

    Affiliations Departamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de Chile, Ñuñoa, Santiago, Región Metropolitana, Chile, Escuela de Medicina Veterinaria, Facultad de Recursos Naturales y Medicina Veterinaria, Universidad Santo Tomás, Talca, Región del Maule Chile, Escuela de Medicina Veterinaria, Facultad de Recursos Naturales y Ciencias Silvoagropecuarias, Universidad Iberoamericana de Ciencias y Tecnología, Santiago, Santiago, Región Metropolitana, Chile

  • Fabiola Peña,

    Affiliation Faculty of Life Science, Utrecht University, Utrecht, Netherlands

  • Pamela Morales,

    Affiliation Departamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de Chile, Ñuñoa, Santiago, Región Metropolitana, Chile

  • Marco Méndez,

    Affiliation Departamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de Chile, Ñuñoa, Santiago, Región Metropolitana, Chile

  • Michel Sallaberry,

    Affiliation Departamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de Chile, Ñuñoa, Santiago, Región Metropolitana, Chile

  • Irma Vila,

    Affiliation Departamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de Chile, Ñuñoa, Santiago, Región Metropolitana, Chile

  • Elie Poulin

    Affiliations Departamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de Chile, Ñuñoa, Santiago, Región Metropolitana, Chile, Instituto de Ecología y Biodiversidad de Chile, Universidad de Chile, Ñuñoa, Santiago, Región Metropolitana, Chile

Pattern of genetic differentiation of an incipient speciation process: The case of the high Andean killifish Orestias

  • Claudia Jimena Guerrero-Jiménez, 
  • Fabiola Peña, 
  • Pamela Morales, 
  • Marco Méndez, 
  • Michel Sallaberry, 
  • Irma Vila, 
  • Elie Poulin


8 May 2017: Guerrero-Jiménez CJ, Peña F, Morales P, Méndez MA, Sallaberry M, et al. (2017) Correction: Pattern of genetic differentiation of an incipient speciation process: The case of the high Andean killifish Orestias. PLOS ONE 12(5): e0177498. View correction


During the Pleistocene and Holocene, the southwest Andean Altiplano (17°-22°S) was affected by repeated fluctuations in water levels, high volcanic activity and major tectonic movements. In the early Holocene the humid Tauca phase shifted to the arid conditions that have lasted until the present, producing endorheic rivers, lakes, lagoons and wetlands. The endemic fish Orestias (Cyprinodontidae) represents a good model to observe the genetic differentiation that characterizes an incipient speciation process in allopatry since the morphospecies described inhabit a restricted geographic area, with present habitat fragmentation. The genetic diversity and population structure of four endemic morphospecies of Orestias (Cyprinodontidae) found in the Lauca National Park (LNP) analyzed with mitochondrial markers (Control Region) and eight microsatellites, revealed the existence of genetic groups that matches the fragmentation of these systems. High values of genetic and phylogeographic differentiation indices were observed between Chungará Lake and Piacota lagoon. The group composed of the Lauca River, Copapujo and Chuviri wetlands sampling sites showed a clear signal of expansion, with a star-like haplotype network. Levels of genetic differentiation were lower than in Chungará and Piacota, suggesting that these localities would have differentiated after the bottlenecks linked to the collapse of Parinacota volcano. The Parinacota sample showed a population signal that differed from the other localities revealing greater genetic diversity and a disperse network, presenting haplotypes shared with other LNP localities. A mixing pattern of the different genetic groups was evident using the microsatellite markers. The chronology of the vicariance events in LNP may indicate that the partition process of the Orestias populations was gradual. Considering this, and in view of the genetic results, we may conclude that the morphospecies from LNP are populations in ongoing differentiation process.


Speciation is a continuous process during which differentiation and reproductive isolation are established [1]. In allopatry, geographic isolation impedes gene flow between local populations, while microevolutionary processes such as local adaptation and genetic drift proceed [2,3,4]. These processes enhance morphological variations [5,6], high genetic structuring of populations [7,8,9] and differences in karyotypes as a consequence of the new chromosome rearrangements that may cause reproductive incompatibility, [10,11], among others [12,13].

Fishes exhibit great morphological and ecological diversity, inhabiting very diverse aquatic habitats. These characteristics have made them a speciose and diversified group. They are used for the study of processes implicit in the generation of species [14,15,16,17,18,19]. Some fish show unusually high speciation rates and have received special attention. The family Cichlidae is the classical model to study an adaptive radiation and diversification in lake systems [20,21]. One example of this group is haplochromine cichlids from the Lake Victoria region in Africa, where there are species with low genetic differentiation but with different morphological characteristics. It is postulated that the diversification would be related to the variation in the water level of the large lakes produced 18000–15000 YBP (years before present); cichlids that had been isolated in small nearby lakes and creeks would then have colonized the large lakes [20, 22, 23]. Barluenga & Meyer [7] studied the speciation processes of the Midas cichlid in the lakes of Nicaragua; they found that the large lakes had genetically more ancestral populations, while species ensembles that inhabit crater lakes were younger and had less genetic variation. In spite of their recent origin (<25000 YBP), the isolation of the populations that inhabit crater lakes combined with the selective pressures to which they are exposed (physicochemical conditions of the water, size and depth) suggest a speciation process in these lakes.

Similar to the cichlids in Africa and Central America, Orestias is a speciose group of biogeographic interest due to its endemism and adaptation to the aquatic systems of the Altiplano [24,25,26]. This extensive flatland between 9° S and 22° S at more than 3000 m elevation has diverse aquatic systems formed since the Quaternary [27,28,29,30]. The current distribution of Orestias extends from Lago Lascha (9°S) in the center of Perú to the Salar de Ascotán in northern Chile (22°S) [26]. Of the 44 species described, 23 inhabit Titicaca lake (Bolivia-Peru), while the other 21 species inhabit rivers, lagoons, lakes, wetlands and salt pans of the Altiplano.

The long-term climate variations in this region, which have included alternation of wet and dry periods, generated a succession of paleolakes that covered extensive areas and included several vast salt flats and localized and fragmented watersheds [31]. Simultaneously, intense volcanic activity and strong tectonic movements formed large closed watersheds in the eastern Altiplano (currently Titicaca lake, Desaguadero river and the Uyuni and Coipasa salt pans), and in the western part, watersheds with small, isolated lakes, wetlands, salt pans and rivers [32, 33]. These geological and climatic changes, along with changes in the size of lakes, determined the current distribution of Orestias [26]; in this scenario the populations of fish that inhabit the lakes were divided into multiple isolated populations, producing different degrees of divergence and finally different species [34].

The highest region of the southwest Altiplano is found in the Lauca National Park, Chile (LNP), which is mostly above 4000 m elevation; the paleolakes did not cover this region. However, advances and retreats of glaciers and volcanic events produced changes in the landscape and fragmentation of the watersheds [35,36,37,38]. During the Holocene, about 12500 YBP, the collapse of the cone of the Parinacota volcano modified the watershed of the Lauca River, in different aquatic systems such as lakes, lagoons and wetlands [35,38]. Paleoclimate records indicate an increase in volcanic activity from 7800 to 1000 YBP, along with the establishment of a dry period that maintained the watersheds of Lauca and Chungará isolated until now [36,38]. This fragmentation would have produced the isolation of various populations, allowing differentiation. The four morphospecies described reflect this process: O. chungarensis Vila & Pinto 1986 in Chungará lake, O. piacotensis Vila 2006 in the Piacota lagoon, O. parinacotensis Arratia 1982 in the Parinacota wetland and O. laucaensis Arratia 1982 in the Lauca River and the Cotacotani Lagoon (Fig 1).

Studies of the species of Orestias have been mainly focused on morphological analysis in the context of traditional systematics, initially associated with taxonomic descriptions [39, 40, 41]. More recently, Vila et al 2010 [26] compared the morphology of Orestias that inhabit the Chilean Altiplano using linear and meristic (rays in fin, number of vertebrae) measurements; their results showed that some nominal species in the LNP were differentiated morphologically, (O. laucaensis and O. chungarensis), although meristic data showed high overlap between nominal species and could not distinguish them. Recent trophic studies of Orestias in the LNP watersheds showed low prey richness and dietary range, which was related to the reduced size and shallow depth of these systems, with mostly microinvertebrates inhabiting the macrophyte belt. Thus, the local populations of Orestias showed similar dietary habits associated with prey availability [42, 43].

From a phylogenetic point of view, a previous study suggested that diversification of Orestias in the southern Altiplano may be linked to historical vicariant events and contemporary variation in water level [34]. In this study the four morphospecies of the LNP formed a monophyletic group with good statistical support, however, they do not form monophyletic clades within this lineage, challenging the validity of these taxa under a phylogenic species concept [34]. A preliminary review of the number and morphology of chromosomes and the distribution of constitutive heterochromatin in the karyotypes of the morphospecies of the LNP compared to the other Chilean species showed that these four taxa form a distinct chromosome lineage, characterized by abundant constitutive heterochromatin in chromosome pair one. However, in contrast with the phylogenetic evidence, the four LNP morphospecies exhibited karyotype differences in the number of telocentric and subtelocentric chromosomes and microchromosomes [26]. In spite of the karyotype differences found, studies have not been performed to test the existence of reproductive barriers among these taxa.

In summary, the different analyses of the nominal species of the LNP have shown contrasting results in terms of their differentiation. Morphometric measurements and karyotypes have allowed distinguishing them as separate entities, while meristic measurements and molecular phylogeny have indicated that these nominal species do not constitute distinguishable groups. This discrepancy between different morphological and genetic approximations has been interpreted to be the result of incomplete sorting [34, 44], that is not enough time has elapsed for allopatric genetic differentiation to be translated into reciprocal monophyly between these taxa. In this context, our study adds more samples and uses more variable markers (Dloop, microsatellites against Cyt b, ND2 in the previous study) to further investigate the genetic relationship among LNP morphospecies.

In the present study, we hypothesize that all four morphospecies would have been formerly part of a unique Lauca River basin population that was fragmented in different bodies of water due to an intense volcanic activity during Holocene time. The presence of four Orestias morphospecies described in a restricted geographic area, each one occupying a different body of water, would therefore reflect an incipient allopatric speciation process. Under this hypothesis, we would expect to find genetic differentiation between the different bodies of water, at least for the most isolated ones, and an incomplete lineage sorting due to the short time elapsed since the fragmentation process.

Materials and method

Sampling sites and DNA isolation

The samples (n = 270) were collected in eight localities of the Lauca National Park (LNP) including the sites where the four morphospecies of Orestias were described. These locations represent the diverse aquatic systems shaped by the fragmentation of the Lauca River (Fig 1, Table 1, S1 File). Chungará Lake and Piacota lagoon represent the most isolated sites while do not connect with any other body of water. In contrast, the aquatic systems such as the wetlands of Parinacota, Chuviri, Copapujo as well as Cotacotani lagoon may be temporarily connected with Lauca River [45]. All specimens were euthanized using 100 mg/L tricaine methanosulfonate and fixed in 95% ethanol. DNA was extracted using the saline method [46]. For this study, samples were collected under permit from the Subsecretaria de Pesca, Chile, Resolución Exenta # 2231, 19 August 2011, and approved by the Bioethical Committee at the Universidad de Chile.

Table 1. Sampling localities at Lauca National Park.

N: sample size. Habitats: Type of aquatic systems.

Mitochondrial DNA (D-loop)

The control region of mitochondrial DNA (D-loop) was amplified by PCR using specific primers for the genus: (Forward 5’ ACC CCT AAC TCC CAA AGC T 3’) (Reverse 5’ TGA TAG TAA AGT CAG GAC CAA 3’) [47]. The PCR reaction was standardized in a total volume of 25 μl 10 X PCR buffer (50mM KCl, 10mM Tris-HCl, pH 8.0), MgCl2 50 mM, each primer 10 pm/μl, dNTP 2.5 mM, 0.5 μl Taq (Invitrogen), 9 μl ultrapure water, 1 μl DMSO and 10 ng/μl DNA.

The PCR cycle consisted of an initial denaturation for 5 min at 94°C, followed by 38 cycles of 45 sec at 94°C, 90 sec at 66°C and 90 sec at 72°C, with a final extension of 10 min at 72°C. PCR products were visualized in 2% agarose gel stained with ethidium bromide. Amplification products were sent for sequencing to Macrogen Inc. (South Korea). D-loop sequences were aligned, edited and assembled using the Proseq v.2.9.1 program [48]. Using the D-loop sequences we estimated diversity indices for each locality, including number of haplotypes (K), number of polymorphic sites (S), haplotype diversity (H), mean number of differences between pairs of sequences (Π) and nucleotide diversity (π) in the DnaSP v.5 program [49]. Coalescent analysis was be based on single locus, the genealogical relations among haplotypes were graphed by constructing an haplotype network using the median-joining algorithm implemented in the Network version 4.501 software [50].

The genetic structure as a function of the geographic component was analyzed using SAMOVA (Spatial Analysis of Molecular VAriance), which identifies the groups of genetically homogeneous and geographically close localities that maximize the variance of genetic diversity among these groups [51]. To estimate the level of genetic differentiation between the different groups identified by SAMOVA, we used two indices: FST, based on the differences in haplotype frequencies and ΦST, based on the number of differences between pairs of sequences, with the Arlequin v. program [52]. The statistical significance of FST and ΦST was based on 10000 permutations; we used the false discovery rate [53] correction for multiple tests. We used the PERMUT program [54] to calculate the estimators of population differentiation GST and NST among groups. NST takes into account the genetic distance between haplotypes, while GST only considers the difference in frequency. NST significantly greater than GST suggests phylogeographic structure. We performed 1000 permutations to determine its significance; if more than 5% of the permuted values of NST are greater than GST the null hypothesis GST = NST is rejected.

We performed the Tajima [55] and Fu [56] tests in each genetic group defined by SAMOVA, to detect deviations from the mutation-drift equilibrium expected with the Wright-Fisher model that could indicate population expansions or bottlenecks under the assumption that the sequence variants are selectively neutral.

We used three different models to evaluate past demographic changes. First, we constructed the mismatch distribution for each group, and when pertinent we estimated the demographic parameters of the expansion using the Sudden demographic expansion model of Schneider & Excoffier [57] with the Arlequin v.3.5 program. In the cases where this match did occur, we estimated the parameter of demographic expansion Tau: τ = 2, which is the time when growth began measured in mutational time. t is the time in generations and μ is the mutation rate per sequence per generation. The initial value of Theta is given by θ0 = 2Niμ where Ne0 is the initial effective population size estimated before population growth, while the final value is assumed to be infinite, θ1 = ∞, according with the Sudden demographic expansion model of Schneider & Excoffier [57].

Second, we reconstructed the demographic history of each genetic group using the LAMARC 2.1.5 program [58]. This program constructs coalescence trees using maximum likelihood; from these trees several population parameters are estimated. The growth rate g and the value of θ are estimated with the assumption of exponential growth, following θt = θ0egt, where θt is the value of θ at time t and θ0 is the current value of θ. Using these parameter s we estimated the time since the beginning of demographic expansion in units of mutational time. The time of the initiation of expansion was estimated as the moment when θt was 1% of θ0, as recommended by the author of the program [58].

Third, the demographic history of the groups was inferred using a Bayesian Skyline Plot (BSP) analysis with the BEAST program version 1.7.1 [59], which assume a demographic model just not one of constant size. The assumption used to generate coalescence trees was a relaxed molecular clock; trees were generated with the exponential distribution. These analyses were performed with MCMC chains of 300 million iterations; parameters and trees were sampled every 1000 generations, discarding the first 100 million generations as burn-in. The results were graphed with the Tracer program version 1.7 [60].

The only study for the estimation of freshwater fish mutations rates including time dependency in molecular rates was introduced by Ho (2005). He dates changes in river drainages and isolation of fish populations to document rates of mitochondrial DNA change over a range of temporal scales. He utilizes precise spatio-temporal disruptions of linear freshwater systems and hence avoids many of the limitations associated with typical DNA calibration methods involving fossil data.

We used a mutation rate of 6% per million years proposed by Burridge et al. [61]; their study were based on a robust calibration system applied to closely related taxa in the Galaxidae.


We amplified eight microsatellite loci, originally optimized in O. agassii of Bolivia by Esquer-Garrigos et al. [62], for each of the localities (Table A in S2 File). PCR reactions were standardized in a 10 μl volume that contained: 5X PCR buffer (50mM KCl, 10mM Tris-HCl, pH 8.0), MgCl2 25 mM, BSA 0,1mg/μl, primers 50 pm/μl, dNTP 2.5 mM, 0.1 μl Taq (Promega Inc.) and 50 ng/μl DNA. The PCR conditions were: initial denaturation for 5 min at 94°C, followed by 35 cycles of 30 sec at 92°C, 30 sec at the locus-specific aligning temperature (T° a) (Table A in S2 File) and extension at 72°C for 60 sec, with a final extension of 20 min at 72°C. PCR products were visualized in 3% agarose gels stained with ethidium bromide to verify positive amplification. Amplification products were sent for genotyping to Macrogen Inc. (South Korea). The analysis of fragments was performed in the software GENEMAPPER 3.0 (Applied Biosystems). For each locus we calculated allele frequencies, observed (Ho) and expected (He) heterozygosity with the Genetix v. 4.05 software [63]. The values of FIS were calculated in Genetix; we performed an exact test in Genepop 4.2 to determine possible deviations from Hardy-Weinberg equilibrium for each locus and locality [63, 64].

The degree of genetic structure between localities was analyzed by calculating FST [65] between pairs of localities with 10000 permutations in Genetix, using the false discovery rate for multiple tests. Localities that didn't show any signal of genetic difference (Fst: NS) were assigned to a same population. To determine if the genotyped individuals correspond to the population groups defined in the structure analysis, we performed an assignment test with the Geneclass 2.0 program [66], using the frequency method described by Paetkau et al. [67].

We then performed a Bayesian analysis to infer the number of genetic populations (K) with individual genotype data using the software STRUCTURE V.2.0 [68]. The program was run 10 times, discarding the first 10000 iterations as burn-in, followed by 500,000 MCMC iterations; these parameters were calculated for each value of K under the admixture model and correlated allele frequencies between populations. The value of α, the degree of mixture between the K populations, was evaluated for each population separately. We analyzed K values from 1 to 8 population based on LnP (D), the logarithm of the likelihood of the observed data as a function of K. We also calculated ΔK based on the rate of the change of log likelihood between successive values of K, to identify the number of genetic cluster in the data set [69].


Mitochondrial control region

We obtained a total of 270 samples in the eight sampling sites representing 890 nucleotide positions (GenBank Accesion Numbers BankIt1931003:KX498091-KX498358). The descriptive indices of genetic diversity showed 42 polymorphic sites (S); the number of haplotypes was K = 51; the haplotype diversity was Hd = 0.747 and the mean number of differences between pairs of sequences was Π = 1.593 (Table 2). The sample of Piacota lagoon had the smallest number of haplotypes (K = 4 with N = 46), the lowest haplotype diversity (Hd = 0.128) and the least number of differences between pairs of sequences (Π = 0.174). By contrast, the sample of the Parinacota wetland showed a high number of haplotypes (K = 11 with N = 29), the greatest haplotype diversity (Hd = 0.79) and the largest number of differences between pairs of sequences (Π = 2.192) (Table 2). The haplotype network revealed a small but clear differentiation between Piacota and Chungará (4 substitutions); both sites had a central haplotype with short branches. By contrast, Parinacota showed haplotypes much more dispersed in the network (Fig 2).

Table 2. Genetic diversity indices for the D-loop in different samples of Orestias.

N: sample size; S: Polymorphic sites; K: Number of haplotypes; []: Rarefaction of the number of haplotypes; Hd: Haplotype diversity; π: Nucleotide diversity; Π: Mean number of differences between pairs of sequences.

Fig 2. Median joining network of mitochondrial control region haplotypes including 270 mtDNA d-loop control region sequences in the 8 sampling sites.

Each haplotype is represented by a colored circle indicating the main site where it was collected; the size of the circle is proportional to its frequency in the whole sampling effort.

The SAMOVA showed that the variation between groups was maximized with four groups (59.92%); the corresponding variance between sample within groups was low (2.14%) but significant. The four genetic groups in the LNP were: Group 1: Chungará; Group 2: Parinacota; Group 3: Piacota and Group 4: Lauca, Misituni, Cotacotani, Copapujo and Chuviri (Table B in S2 File). The values of ΦST and FST among groups were low but significant for the majority of the comparisons (Table 3a and 3b).

Table 3. Genetic differentiation among groups defined by SAMOVA based on (a) differences of haplotype frequencies FST and (b) number of differences among sequencesΦST.

Group1: Chungará; Group 2: Parinacota; Group 3: Piacota; Group 4: Lauca, Misituni, Cotacotani, Chuviri and Copapujo. Corrected significance is shown above the diagonal *** P<0.0001.

The structure index Nst (0.576) based on the number of differences between pairs of sequences was significantly greater than Gst (0.462) calculated from the haplotype frequencies (p = 0.0034), indicating the existence of a phylogeographic structure among the groups of the LNP.

Tajima’s D index was negative but not significant for Parinacota. In concordance, the mismatch distribution for the Parinacota group was multimodal (Fig 3) and didn’t show any evidence of demographic expansion, i.e, no deviation to mutation-drift equilibrium. Demographic inference analyses were performed only on groups which showed negative and significant value of Tajima’s D index as well as unimodal mismatch distribution: Chungará, Piacota and the Lauca groups. The parameters estimated for Chungará under the Sudden demographic expansion model (τ = 1.67[0–2.24]) indicate that the expansion would have occurred 12000 YBP, with values of Νe0 = 0 that indicate the reduced initial effective population size in the locality (Table 4). The parameters of the model for Piacota and the Lauca group showed that expansion beginning 3200 YBP for the Lauca group and 1600 YBP for Piacota (Table 4, Fig 3).

Table 4. Estimation of effective population sizes and expansion times under instantaneous, sudden demographic expansion and exponential growth models of the different genetic groups with unimodal distribution of Orestias in the Lauca National Park.

Nei: Initial effective population size; Nef: Final effective population size.[]: confidence intervals.

Fig 3. Median joining haplotype networks and the distribution of pairwise differences between haplotypes (mismatch distribution) analyses for each group obtained by SAMOVA.

a) Chungará b) Lauca Group c) Piacota d) Parinacota.

Assuming exponential growth, the rates of growth G and population sizes obtained using the maximum likelihood analysis (LAMARC 2.1.5 program) indicated that the growth of the populations of Chungará (Nei = 30000; Nef = 370000), the Lauca group (Nei = 24000; Nef = 220000) began from 8000–4300 YBP with effective sizes of one or two orders of magnitude lower in Piacota (Nei = 700; Nef = 60000) (Table 4).

The Bayesian skyline plots for the genetic groups also showed patterns of population growth and differences in expansion times. The expansion began approximately 5000 YBP in Parinacota, with an increase of population size of 40000 and a mean of 100000 individuals (Fig 4d); the expansion in Chungará began 17000 YBP and the Lauca group 8000 YBP, with an increase in effective population size from 100000 to 1 million individuals respectively (Fig 4a and 4b). In Piacota the increase in mean population size was much less than in the other localities (from 5000 to 100000 individuals), with that expansion beginning 2500 YBP (Fig 4c). The mean time to the most recent common ancestor (TMRCA) of the groups is shown in Table C in S2 File.

Fig 4. Historical demographic trends of the effective population size (Ne) constructed using a Bayesian skyline plot approach based on control region haplotypes of groups of Orestias (a. Chungará, b. Lauca, c. Piacota, d. Parinacota).

The y-axis is the product of effective population size (Ne) and generation length in a log scale (Population size (Net)) while the x-axis is the time before present (years). The median estimate (black solid line) and 95% highest probability density (HPD) limits are shown (in purple). The color lines represent the time of the most recent ancestor (TRCMA) in the Orestias population. The thin dashed line represents time for the expansion in the species.


We obtained multilocus genotypes in 261 of 270 samples of Orestias the samples for 8 loci (Table E in S2 File). Loci A116, D110 and A106 had the largest numbers (14 to 15) of alleles. Locus C102 had the smallest number (2 or 3) of alleles in all localities. Global evaluation of the microsatellite data set using Micro-checker indicated no evidence of non-amplified (null) alleles. Further tests for errors in the data showed no evidence of stuttering or large allele dropout. No significant deviations from Hardy—Weinberg equilibrium across populations were detected. No linkage disequilibrium was found between loci per population after Bonferroni correction.

All FST between pairs of samples were significant with and without the FDR correction, except for Lauca/Misituni and Cotacotani/Chuviri/Copapujo (Table 5). The sampling site that did not have significant differences was grouped in the Lauca (Lauca-Misituni) and the CCC (Cotacotani-Chuviri-Copapujo) populations.

Table 5. Measures of genetic differentiation (FST) between pairs of Orestias populations based on information of 8 microsatellite loci.

Above diagonal; Bonferroni-corrected degrees of significance. *** = P<0.0001. NS = Not significant.

The descriptive indices of genetic diversity of the 8 microsatellite loci are shown in Table 6. The mean number of alleles per locus was similar in all populations; the largest number was in the CCC population with 9.3 alleles and the smallest number was in Piacota with 5 alleles. Parinacota had the highest allelic richness (6.6) and Piacota the smallest richness (4.1). FIS values were not significantly different from zero (p values > 0.05) for any locus in any population (Table D in S2 File). Pairwise comparisons among loci did not show any linkage disequilibrium for population-specific analyses (p values > 0.05). Intermediate values of heterozygosity (0.47–0.60) were found for all populations; Chungará had the greatest mean heterozygosity (0.60) and Piacota had the lowest (0.47).

Table 6. Genetic diversity measures for 8 microsatellite loci for genetic populations of Orestias of the LNP.

N = Number of individuals analyzed per locus; A: Mean number of alleles per locus; Hobs: Observed heterozygosity; Hexp: Expected heterozygosity; FIS: Endogamy index; NeC: Contemporary effective population size; AR: Allelic richness. Chung: Chungará; CCC: Chuviri.-Copapujo- Cotacotani; Lau: Lauca group; Pari: Parinacota; Pia: Piacota. Braquets []: Standard deviation. NS = not significant.

Individual assignment (GeneClass) to the populations delimited by pairwise Fst analysis showed that the greatest percentage of correct assignments was found in the Chungará and Piacota populations, with 100% and 96%, respectively. In the CCC and Lauca populations the correct assignments were 75% and 76%, respectively; the incorrectly assigned individuals of these two populations were assigned to the other population. Parinacota had the lowest percentage of correct assignments (68%); individuals incorrectly assigned were mainly assigned to CCC (12%) and Lauca group (12%).

The STRUCTURE analysis found the lowest value of LnP for K = 4 (Fig 5b), thus indicating four genetic clusters. The first group was composed mostly of individuals from Lago Chungará; the second group with individuals from the Cotacotani lagoons and the wetlands of Chuviri and Copapujo; the third group with individuals from the two river sites (Lauca and Misituni) and the fourth of individuals from the Piacota lagoon (Fig 5a). Although each locality had a predominance of only one genetic group (especially Chungará and Piacota), the individuals collected in the Parinacota wetland belonged indiscriminately to the different groups and showed high levels of admixture (Fig 5a).

Fig 5.

a. Results of the admixture analysis of Orestias for K = 4. Each individual is represented by a thin vertical line, which is partitioned into K colored segments that represent the individual’s estimated membership probabilities in K clusters. Black lines separate individuals of different populations. Populations are labeled below the plot. b. ΔK (1) and (2) ln (P) analysis.


Our results showed the existence of various genetic groups in the localities of the LNP that coincide with the fragmentation of the aquatic systems due to the volcanic and climate events that originated closed systems such as Lago Chungará and the Piacota lagoon [37, 38]. Genetic analyses performed with mtDNA and microsatellites coincided in separating clearly Chungará and Piacota, which are the most disconnected systems in the study area (Fig 1). This pattern is supported by the high values of genetic and phylogeographic differentiation between these two systems and with the rest of the localities (Tables 2, 3 and 6). These two localities harbor different morphospecies, O. chungarensis in Lake Chungará and O. piacotensis in Piacota lagoon.

The populations of these two localities show signs of growth after 12000 YBP, which may be related to the main volcanic events that occurred in the Pleistocene-Holocene boundary, which originated these lentic systems. The formation of the Chungará subwatershed (12000 YBP) as a product of the collapse of the Parinacota volcano isolated Lago Chungará from the Lauca watershed, which has probably lasted until the present. The low genetic variation of Chungará population, in particular the low number of differences between haplotypes, may indicate a founder effect during the separation and later appearance of new haplotypes during population growth in this large lake. The closed system of the Piacota lagoon has been disconnected from the Parinacota wetland during the arid period of the mid-Holocene (8000–4000 YBP). The small size of the lagoon would have limited the population size of Orestias (S3 Table), thus genetic drift may have acted more strongly, retaining a smaller number of new haplotypes. This difference in diversity between lakes of different sizes has also been documented in cichlids in the region of Lake Victoria in Africa [19, 23] and in the lakes of Nicaragua [7]. In these cases, the genetic diversity be associated with the size and depth of the lakes; populations in larger, older lakes have greater diversity than smaller, more recently formed lakes [7, 19].

The analysis of mitochondrial sequences identified a third group including the two sites of the Lauca river with those of Cotacotani lagoon and the wetlands of Copapujo and Chuviri. In the same way as the previous groups, this group shows a clear sign of expansion illustrated by a star-like haplotype network. During the volcanic processes (12000–4000 YBP) the Lauca river was probably affected by landslides from the collapse of the volcano dome, the pyroclastic rain, lahars and inundations, which may have generated population bottlenecks as has been reported for recent eruptions in other parts of Chile [70]. The analyses of genetic differentiation and assignment with microsatellite markers separated this group into two, one corresponding to the sites from the Lauca river and the other to the wetland of Copapujo and Chuviri and Cotacotani lagoons. However, the levels of genetic differentiation of the later two groups (Lauca River and CCC) appear to be lower than those estimated for the populations of Chungará and Piacota, suggesting that these localities would have differentiated after the bottlenecks linked to the collapse of Parinacota volcano.

The population of Parinacota showed a different population signal than the rest of the localities. Based on mitochondrial sequences showed greater genetic diversity and a disperse network with the presence of low-frequency haplotypes (Fig 3), several of them were shared with other localities of the LNP (Fig 2). The star-like haplotypes observed in the other localities may thus reflect founder effects associated with bottlenecks or recolonization events from the Parinacota population (Fig 3). In this scenario, the Parinacota site, that was an integral part of the Lauca paleoriver, would have been less affected by the volcanic events associated with the collapse of the Parinacota volcano and the population of Orestias have remained in situ in the wetlands that were separated from the river [37], safeguarding its genetic diversity. Based on our results, the Parinacota locality may thus be considered as a refuge of the population of the Lauca paleoriver when the catastrophic events affected the LNP zone at the beginning of the Holocene. Although the theory of refuges has been developed mainly in relation to the glacial cycles of the Quaternary [71], the Parinacota population fulfills the characteristics described in this model, such as the detection of greater diversity and the presence of haplotypes shared with peripheral populations that show an expansion signal.

The results based on the microsatellite markers identified Parinacota as a singular population in terms of its genetic diversity. However, in contrast to the mtDNA information that identified Parinacota as a source population for the historical colonization of the other sites, microsatellites markers indicated that Parinacota would correspond currently to a point of admixture of the different genetic groups of the LNP (Fig 5a). In the STRUCTURE analysis, Parinacota population that did not form part of a genetic cluster, instead almost all individuals sampled showed an admixture of the different groups identified (Fig 5a). As the lowest point in the system, the Parinacota wetlands may receive migrants from the other localities in years with inundations, allowing asymmetrical gene flow from the other aquatic systems to the wetlands. This particular connectivity pattern among the different environments suggests that the Parinacota locality is a sink population, receiving the current genetic diversity of the other populations.

The chronology of the vicariance events in the LNP determined that the separation of the populations of Orestias was stepwise. First, the volcanic collapse of Parinacota (12500 YBP) [3538] would have initiated the separation of the populations of the watershed of the Lauca paleoriver in Chungará, Cotacotani and Lauca. Later, at the end of the Pleistocene, the wet episodes would have facilitated the arrival of individuals to the Chungará subwatershed, which is when the separation of O. laucaensis (Lauca) and O. chungarensis (Chungará) apparently occurred. Volcanic eruptions processes in the Holocene (8000–4000 YBP) maintained the populations separated, facilitating genetic differentiation between them. During this time there was also a drastic climate change with the arid episode (7000–6000 YBP), in which the connections between the rivers, wetlands and lagoons would have been affected. This is the case of the Piacota lagoon, which was probably separated from the Parinacota wetland by the decrease in water between them and also the eruption of the Ajata volcano, leaving the Piacota lagoon with an isolated population described as O. piacotensis. Finally, the return of wet periods after 4000 YBP allowed the re-connection of the Cotacotani lagoons with the Lauca river, which is shown by the presence of O. laucaensis in the different systems as one genetic group.


The combination of the chronology of the vicariance processes in the LNP and the genetic analyses allows us to conclude that although the localities of the LNP analyzed are not evolutionarily separated units, they are groups in the process of differentiation. The short time since the events that originated this process has not allowed a complete lineage sorting among these populations in spite of the morphological differences that have been described and that motivated the description of different nominal species. In spite of the genetic and phylogeographic differentiation detected in this study, up to now there is no evidence of reproductive isolation among the groups and they do not appear to have developed ecological specialization, at least not at the trophic level [43]. There are also indications that individuals of these groups could maintain contact in the Parinacota wetland by sporadic migrations. It is probable that the different populations of Orestias in the LNP are illustrating an uncertain phase of speciation in which sudden changes in the environmental conditions, in this case mainly hydrographic, could reinforce or revert this speciation process, indicating the reticulate nature of evolution [72]. In this context, despite the differences reported in karyotypes in a previous study (Vila et al. 2011), our results support the hypothesis that the morphospecies described in LNP may just correspond to genetically differentiated populations of a same species, together with the overlap of meristic, lack of monophyly and similar dietary habits. Finally, Orestias from the LNP appear as an ideal model to exemplify the processes of genetic, morphological, ecological differentiation that accompany an incipient geographic isolation, and thus understand incipient steps of the allopatric speciation process.

Supporting information

S1 File. Google Earth Placemark.

Google Earth Placemark file that contains latitudinal and longitudinal coordinates of our sampling sites.


S2 File. Characterístics of the microsatellite loci used for Orestias of the Parque Nacional Lauca.

Modified from Esquer et al. 2011. T°a: annealing temperature (°C) (Table A). SAMOVA analysis Spatial molecular analysis of variance (SAMOVA) of D-loop sequences in different geographic groups (Table B). TMRCA. Time to most recent common ancestor using Bayesian skyline analysis for the three genetic groups with expansion signal (Table C). FIS-values for eight microsatellite loci in populations of Orestias of the Lauca National Park (Table D). Genotypes of each sample in each localities of LNP (Table E).



We thank Dr. Sergio Scott, MSc Juan Pablo Oyanedel, MSc Christian Araya and Dr. Gonzalo Collado for his support in field trips and collection of individuals and Lafayette Eaton for the English correction. This research is part of a Ph.D. thesis. This study is part of the objectives of the projects FONDECYT Project 1110243 and 1140543. The samples of this study, were collected under permit from the Subsecretaria de Pesca RES 2231 on 19 August 2011, and approved by the Bioethical Committee at the Universidad de Chile. Fondecyt Project 1110243. Support was provided by Fondecyt Projects 1110243,1140543, 1080390 and 1110188 . the Instituto de Ecología y Biodiversidad de Chile IEB, ICM-P05-002 and PFB 023.

Author Contributions

  1. Conceptualization: CJGJ EP IV.
  2. Data curation: CJGJ FP PM EP IV.
  3. Formal analysis: CJGJ EP IV MM MS FP.
  4. Funding acquisition: EP IV.
  5. Investigation: CJGJ FP EP IV.
  6. Methodology: CJGJ EP.
  7. Project administration: CJGJ EP IV.
  8. Resources: CJGJ EP MM IV.
  9. Software: CJGJ EP IV.
  10. Supervision: CJGJ EP IV.
  11. Validation: CJGJ.
  12. Visualization: CJGJ EP IV.
  13. Writing – original draft: CJGJ EP IV.
  14. Writing – review & editing: CJGJ PM FP EP MM IV MS.


  1. 1. Nossil P, Feder JL. Genomic divergence during speciation: causes and consequences. Philosophical Transactions of the Royal Society of London B: Biological Sciences. 2012;367: 332–42. pmid:22201163
  2. 2. Coyne JA, Orr HA. Speciation. Sunderland, MA: Sinauer Associates; 2004. 545 p.
  3. 3. Bolnick DI, Fitzpatrick BM. Sympatric Speciation: Models and Empirical Evidence. Annual Review of Ecology, Evolution, and Systematics. 2007;38: 459–87.
  4. 4. Nossil P. Speciation with gene flow could be common. Mol Ecol. 2008;17: 2103–6. pmid:18410295
  5. 5. Beltman JB, Haccou P, Cate C. Learning and colonization of new niches: a first step toward speciation. Evolution. 2004;58: 35–46. pmid:15058717
  6. 6. Burbrink FT, Pyron RA. How does ecological opportunity influence rates of speciation, extinction, and morphological diversification in New World ratsnakes (tribe Lampropeltini)? Evolution. 2010;64: 934–43. pmid:19895554
  7. 7. Barluenga M, Meyer A. Phylogeography colonization and population history of the Midas cichlid species complex (Amphilophus spp.) in the Nicaraguan crater lakes. BMC Evol Biol. 2010;10: 326. pmid:20977752
  8. 8. Marko PB, Hart MW. The complex analytical landscape of gene flow inference. Trends in Ecology and Evolution. 2011;26(448–456).
  9. 9. April J, Hanner RH, Dion-Côté A-M, Bernatchez L. Glacial cycles as an allopatric speciation pump in north-eastern American freshwater fishes. Mol Ecol. 2012;22(2): 409–22. pmid:23206322
  10. 10. Moyle LC, Muir CD, Han MV, Hahn MW. The contribution of gene movement to the "two rules of speciation". Evolution. 2010;64: 1541–57. pmid:20298429
  11. 11. Butlin R, Debelle A, Kerth C, Snook RR, Beukeboom LW, Castillo Cajas RF, et al. What do we need to know about speciation? Trends Ecol Evol. 2012;27: 27–39. pmid:21978464
  12. 12. Dhuyvetter H, Hendrickx F, Gaublomme E, Desender K. Differentiation between two salt marsh beetle ecotypes: Evidence for ongoing speciation. Evolution. 2007;61: 184–93. pmid:17300437
  13. 13. Fitzpatrick BM, Fordyce JA, Gavrilets S. Pattern, process and geographic modes of speciation. J Evol Biol. 2009;22: 2342–7. pmid:19732257
  14. 14. Herdegen M, Alexander HJ, Babik W, Mavárez J, Breden F, Radwan J. Population structure of guppies in north-eastern Venezuela, the area of putative incipient speciation. BMC Evol Biol. 2014;14: 28. pmid:24533965
  15. 15. Ribbink AJ. Is the Species Flock Concept Tenable? In: Echelle AA, Kornfield I, editors. Evolution of Fish Species Flocks. Orono: University of Maine; 1984. p. 21–5.
  16. 16. Kornfield I, Smith PF. African Cichlid Fishes: Model Systems for Evolutionary Biology. Annu Rev Ecol Syst. 2000;31: 163–96.
  17. 17. Hudson AG, Vonlanthen P, Müller R, Seehausen O. Review: The geography of speciation and adaptive radiation in coregonines. Adv Limnol. 2005;60: 111–46.
  18. 18. Mehner T, Pohlmann K, Elkin C, Monaghan MT, Nitz B, Freyhof J. Genetic population structure of sympatric and allopatric populations of Baltic ciscoes (Coregonus albula complex, Teleostei, Coregonidae). BMC Evol Biol. 2010;10: 85. pmid:20350300
  19. 19. Bezault E, Mwaiko S, Seehausen O. Population genomic tests of models of adaptive radiation in Lake Victoria region cichlid fish. Evolution. 2011;65: 3381–7. pmid:22133213
  20. 20. Kocher TD. Adaptive evolution and explosive speciation: the cichlid fish model. Nature Reviews Genetics. 2004;5: 288–98. pmid:15131652
  21. 21. Seehausen O. African cichlid fish: a model system in adaptive radiation research. Proceedings of the Royal Society B: Biological Sciences. 2006;273: 1987–98. pmid:16846905
  22. 22. Danley PD, Kocher TD. Speciation in rapidly diverging systems: lessons from Lake Malawi. Mol Ecol. 2001;10: 1075–86. pmid:11380867
  23. 23. Elmer KR, Reggioa C, Wirtha T, Verheyenb E, Salzburgera W, Meyera A. Pleistocene desiccation in East Africa bottlenecked but did not extirpate the adaptive radiation of Lake Victoria haplochromine cichlid fishes. PNAS. 2009;106: 13404–9. pmid:19651614
  24. 24. Parker A, Kornfield I. Molecular Perspective on Evolution and Zoogeography of Cyprinodontid Killifishes (Teleostei; Atherinomorpha). Copeia. 1995;1995: 8–21.
  25. 25. Dejoux C, Iltis A. El lago Titicaca: Síntesis del conocimiento limnológico actual. La Paz, Bolivia: Orstom/Hisbol; 1991. 584 p.
  26. 26. Vila I, Scott S, Iturra P, Lam N, Mendez M. Karyological and morphological analysis of divergence among species of the killifish genus Orestias (Teleostei: Cyprinodontidae) from the Southern Altiplano. In: Nelson JS, Schultze HP, Wilson MVH, editors. Origin and Phylogenetic Interrelationships of Teleosts. Munich, Verlag. 2010. p. 471–80.
  27. 27. Lavenu A, Fornari M, Sebrier M. Existence de deux nouveaux épisodes lacustres quaternaires dans l'Altiplano péruvo-bolivien. Cahiers ORSTOM, Série Géologie. 1984;14: 103–14.
  28. 28. Fornari M, Risacherb F, Férauda G. Dating of paleolakes in the central Altiplano of Bolivia. Palaeogeogr, Palaeoclimatol, Palaeoecol. 2001;172: 269–82.
  29. 29. Fritz SC, Baker PA, Lowenstein TK, Seltzer GO, Rigsby CA, Dwyer GS, et al. Hydrologic variation during the last 170,000 years in the southern hemisphere tropics of South America. Quatern Res. 2004;61: 95–104.
  30. 30. Rigsby CA, Bradbury JP, Baker PA, Rollins SM, Warren MR. Late Quaternary palaeolakes, rivers, and wetlands on the Bolivian Altiplano and their palaeoclimatic implications. Journal of Quaternary Science. 2005;20: 671–91.
  31. 31. Placzek C, Quade J, Patchett PJ. Geochronology and stratigraphy of late Pleistocene lake cycles on the southern Bolivian Altiplano: Implications for causes of tropical climate change. Geological Society of America Bulletin. 2006;118: 515–32.
  32. 32. Chong G. The Cenozoic saline deposits of the Chilean Andes between 18°00' and 27°00' south latitude. In: Bahlburg H, Breitkreuz C, Geise P, editors. The Southern Andes Lecture Notes in Earth Sciences. Berlin: Springer Verlag; 1988. p. 137–51.
  33. 33. Núñez L, Grosjean M, Cartajena I. Human occupations and climate change in the Puna de Atacama, Chile. Science. 2002;298: 821–4. pmid:12399589
  34. 34. Vila I, Morales P, Scott S, Poulin E, Véliz D, Harrod C, et al. Phylogenetic and phylogeographic analysis of the genus Orestias (Teleostei: Cyprinodontidae) in the southern Chilean Altiplano: the relevance of ancient and recent divergence processes in speciation. J Fish Biol. 2013;82: 927–43. pmid:23464552
  35. 35. Clavero JE, Sparks RSJ, Huppert HE, Dade WB. Geological constraints on the emplacement mechanism of the Parinacota debris avalanche, northern Chile. Bulletin of Volcanology. 2002;64: 40–54.
  36. 36. Clavero JE, Sparks SJ, Polanco E, Pringle MS. Evolution of Parinacota volcano, Central Andes, Northern Chile. Revista Geológica de Chile. 2004;31: 317–47.
  37. 37. Sáez A, Valero-Garcés BL, Moreno A, Bao R, Pueyo JJ, González-Sampériz P, et al. Lacustrine sedimentation in active volcanic settings: the Late Quaternary depositional evolution of Lake Chungará (northern Chile). Sedimentology. 2007;54: 1191–222.
  38. 38. Giralt S, Moreno A, Bao R, Sáez A, Prego R, Valero-Garcés BL, et al. A statistical approach to disentangle environmental forcings in a lacustrine record: the Lago Chungará case (Chilean Altiplano). J Paleolimnol. 2008;40: 195–215.
  39. 39. Vila I. A New Species of Killifish in the Genus Orestias (Teleostei: Cyprinodontidae) from the Southern High Andes, Chile. Copeia. 2006;2006: 471–7.
  40. 40. Arratia G. Peces del Altiplano de Chile. In: Veloso A, Bustos E, editors. El Hombre y los Ecosistemas de Montaña. Montevideo, Uruguay: Oficina Regional de Ciencia y Tecnología de la UNESCO para América Latina y el Caribe; 1982. p. 93–133.
  41. 41. Parenti L. Biogeography of the Andean killifish genus Orestias with comments on the species flock concept. In: Echelle AA, Kornfield I, editors. Evolution of Fish Species Flocks. Orono, Maine: University of Maine 1984. p. 85–92.
  42. 42. Dorador C, Pardo R, Vila I. Variaciones temporales de parámetros físicos, químicos y biológicos de un lago de altura: el caso del lago Chungará. Rev Chil Hist Nat. 2003;76: 15–22.
  43. 43. Guerrero CJ, Poulin E, Méndez MA, Vila I. Caracterización trófica de Orestias (Teleostei: Cyprinodontidae) en el Parque Nacional Lauca. Gayana. 2015;79: 18–25.
  44. 44. Esquer-Garrigos Y, Hugueny B, Koerner K, Ibañez C, Bonillo C, Pruvost P, et al. Non-invasive ancient DNA protocol for fluid-preserved specimens and phylogenetic systematics of the genus Orestias (Teleostei: Cyprinodontidae). Zootaxa. 2013;3640: 373–94. pmid:26000423
  45. 45. Marquez M, Vila I, Hinojosa F, Méndez M, Carvajal J, Sabando C. Distribution and seasonal fluctuations in the aquatic biodiversity of th southern Altiplano. Limnologica.2009; 39: 314–318.
  46. 46. Aljanabi SM, Martinez I. Universal and rapid salt-extraction of high quality genomic DNA for PCR-based techniques. Nucleic Acids Res. 1997;25: 4692–3. pmid:9358185
  47. 47. Morales P, Vila I, Poulin E. Genetic structure in remnant populations of an endangered cyprinodontid fish, Orestias ascotanensis, endemic to the Ascotán salt pan of the Altiplano. Conserv Genet. 2011;12: 1639–43.
  48. 48. Filatov DA. PROSEQ: A software for preparation and evolutionary analysis of DNA sequence data sets. Mol Ecol Notes. 2002;2: 621–4.
  49. 49. Librado P, Rozas J. DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics. 2009;25: 1451–2. pmid:19346325
  50. 50. Bandelt HJ, Forster P, Röhl A. Median-joining networks for inferring intraspecific phylogenies. Mol Biol Evol. 1999;16: 37–48. pmid:10331250
  51. 51. Dupanloup I, Schneider S, Excoffier L. A simulated annealing approach to define the genetic structure of populations. Mol Ecol. 2002;11: 2571–81. pmid:12453240
  52. 52. Excoffier L, Lischer HEL. Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Molecular Ecology Resources. 2010;10: 564–7. pmid:21565059
  53. 53. Pike N. Using false discovery rates for multiple comparisons in ecology and evolution. Methods in Ecology and Evolution. 2011;2: 278–82.
  54. 54. Pons O, Petit R. Measuring and testing genetic differentiation with ordered Versus unordered alleles. Genetics. 1996;144: 1237–45. pmid:8913764
  55. 55. Tajima F. Statistical methods to test for nucleotide mutation hypothesis by DNA polymorphism. Genetics. 1989;123: 85–595.
  56. 56. Fu Y. Statistical Tests of Neutrality of Mutations Against Population Growth, Hitchhiking and Background Selection. Genetics Society of America. 1997;147: 915–25.
  57. 57. Schneider S, Excoffier L. Estimation of past demographic parameters from the distribution of pairwise differences when the mutation rates vary among Sites: application to human mitochondrial DNA. Genetics. 1999. 152: 1079–1089. pmid:10388826
  58. 58. Kuhner MK. LAMARC 2.0: maximum likelihood and Bayesian estimation of population parameters. Bioinformatics. 2006;22: 768–70. pmid:16410317
  59. 59. Drummond AJ, Rambaut A. BEAST: Bayesian evolutionary analysis by sampling trees. BMC Evol Biol. 2007;7: 214. pmid:17996036
  60. 60. Rambaut A, Drummond A. Tracer v1.5. 2009.
  61. 61. Burridge CP, Craw D, Fletcher D, Waters JM. Geological dates and molecular rates: fish DNA sheds light on time dependency. Mol Biol Evol. 2008;25: 624–33. pmid:18281273
  62. 62. Esquer-Garrigos Y, Lambourdière J, Ibañez C, Gaubert P. Characterization of ten polymorphic microsatellite loci in the Andean pupfish Orestias agassizii, with cross-amplification in the sympatric O. luteus. Conservation Genetics Resources. 2011;3: 17–9.
  63. 63. Belkhir K, Borsa P, Chikhi L, Raufaste N, Bonhomme F. GENETIX 4.05, logiciel sous Windows TM pour la génétique des populations. 1996–2004 Laboratoire Génome, Populations, Interactions, CNRS UMR 5171, Université de Montpellier II, Montpellier (France).
  64. 64. Rousset F. GWNWPOP’007: a complete re-implementation of the genepop software for Windows and Linux. Molecular Ecology Resources. 2008;8: 103–6. pmid:21585727
  65. 65. Weir BS, Cockerham CC. Estimating F-statistics forthe analysis of population structure. Evolution. 1984;38: 1358–70.
  66. 66. Piry S, Alapetite A, Cornuet J M, Paetkau D, Baudouin L, Estoup A. GeneClass2: A Software for Genetic Assignment and First-Generation Migrant Detection. Journal of Heredity. 2004 95:536–539. pmid:15475402
  67. 67. Paetkau D, Calvert W, Stirling I, Strobeck C. Microsatellite analysis of population structure in Canadian polar bears. Mol Ecol. 1995;4: 347–54. pmid:7663752
  68. 68. Pritchard JK, Stephens M, Donnelly P. Inference of Population Structure Using Multilocus Genotype Data. Genetics. 2000;155: 945–59. pmid:10835412
  69. 69. Evanno G, Regnaut S, Goudet J. Detecting the number of clusters of individuals using the software STRUCTURE: a simulation study. Mol Ecol. 2005;14: 2611–20. pmid:15969739
  70. 70. De la Barrera F, Reyes-Paecke S, Meza L. Análisis del paisaje para la evaluación ecológica rápida de alternativas de relocalización de una ciudad devastada. Rev Chil Hist Nat. 2011;84: 181–94
  71. 71. Maggs CA, Castilho R, Foltz D, Henzler C, Jolly MT, Kelly J, et al. Evaluating signature of glacial refugia for north atlantic benthic marine taxa. Ecoloy. 2009;89(11 Suplement): S108–S22.
  72. 72. Turgeon J, Bernatchez L. Reticulate evolution and phenotypic diversity in North American ciscoes, Coregonus ssp. (Teleostei: Salmonidae): implications for the conservation of an evolutionary legacy. Conserv Genet. 2003;4: 67–81.