Figures
Abstract
The Andes of South America hosts perhaps the highest amphibian species diversity in the world, and a sizable component of that diversity is comprised of direct-developing frogs of the genus Pristimantis (Anura: Craugastoridae). In order to better understand the initial stages of species formation in these frogs, this study quantified local-scale spatial genetic structuring in three species of Pristimantis. DNA sequences of two mitochondrial gene fragments (16S and COI) were obtained from P. brevifrons, P. palmeri and P. jubatus at different locations in the Cordillera Occidental. We found high levels of genetic diversity in the three species, with highly structured populations (as measured by FST) in P. brevifrons and P. palmeri while P. jubatus showed panmixia. Large effective population sizes, inferred from the high levels of genetic diversity, were found in the three species and two highly divergent lineages were detected within P. jubatus and P. palmeri. Estimated divergence times among populations within P. brevifrons and P. palmeri coincide with the Pleistocene, perhaps due to similar responses to climatic cycling or recent geological history. Such insights have important implications for linking alpha and beta diversity, suggesting regional scale patterns may be associated with local scale processes in promoting differentiation among populations in the Andes.
Citation: García-R JC, Crawford AJ, Mendoza ÁM, Ospina O, Cardenas H, Castro F (2012) Comparative Phylogeography of Direct-Developing Frogs (Anura: Craugastoridae: Pristimantis) in the Southern Andes of Colombia. PLoS ONE 7(9): e46077. https://doi.org/10.1371/journal.pone.0046077
Editor: Norman Johnson, University of Massachusetts, United States of America
Received: March 18, 2012; Accepted: August 28, 2012; Published: September 25, 2012
Copyright: © García-R et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This research was supported by Universidad del Valle (Convocatoria Interna CI-746). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
The Andes of South America contain the highest levels of total species richness in the world [1], [2]. The high biodiversity of tropical montane regions may be due to their old age [3], higher rates of adaptive divergence across elevation gradients [4], [5], greater opportunities for vicariant speciation [6], [7], [8] or a mixture of factors [9], [10]. Montane diversity is often spatially partitioned, i.e., beta diversity (species composition between sites) is quite high compared to the lowlands, while alpha diversity (species within a community) is relatively low [11]. The observation that sister species, at least in vertebrates, tend to be in similar habitats [8] suggests that simple vicariance models [12] could potentially account for much montane diversity compared with models invoking ecological gradients [5]. Indeed, mountain ridges and valleys have long been considered as agents of allopatric speciation by acting as effective barriers to dispersal [13].
A given geographic barrier may not have the same effect on all species, however. Organismal biology and natural history interact with landscape features to determine to what extent a potential barrier will affect dispersal [6], [14]. Over evolutionary time the context-specific dispersal capacity of an organism will determine spatial genetic patterns [15], [16]. Even congeneric species may have contrasting ecological requirements that result in distinct phylogeographic histories [17].
Using molecular data it is possible to quantify the magnitude of genetic variation within populations and patterns of gene flow among conspecific populations. Moreover, if shared past events led to the formation of current genetic patterns, then comparing phylogeographic patterns of sympatric species may enhance our understanding of the relative roles performed by the forces of climatic, geological and ecological conditions in structuring within-species genetic variation [18], [19], [20]. Molecular studies of different amphibians in the montane Neotropics have revealed high levels of genetic diversity across small geographic areas [21], [22], [23]. However, in South America and especially in Colombia, there are only a few molecular studies on genetic diversity of widely distributed montane amphibian taxa endemic to particular regions [9]. The mountains of southwestern Colombia are considered hotspots of diversity for their unique assemblages of anurans and other taxa [24]. The number of species of anurans in the Cordillera Occidental of Colombia is steadily increasing [24], with over 150 species currently found at elevations above 1,000 meters [25].
The genus Pristimantis (Anura: Terrarana: Craugastoridae) is the dominant component of the total amphibian fauna of Colombia, with 200 species, i.e., 27% of the country’s 750 species [26]. Nevertheless, little is known about their ecology, phylogenetic relationships [27], population genetic structure, or levels of genetic polymorphism. This study focused on three species of Pristimantis with distributions in the Cordillera Occidental of Colombia. Pristimantis jubatus [28] is found at 2,450–2,750 meters above sea level (masl) in Munchique National Park, with a total range less than 5,000 km2 in the department of Cauca. This species is considered to be locally abundant, inhabits forests with high (>90%) average humidity and dense vegetation cover (>80%) and appears to be intolerant of habitat modifications [28], [29]. In contrast, Pristimantis palmeri [30] and P. brevifrons [31] are sympatric in the Cordillera Occidental, ranging from the departments of Cauca to Risaralda, with elevational ranges of 900 to 2,400 masl and 1,140–3,200 masl, respectively. They are common species with apparently stable populations, most frequently found in disturbed situations, and are considered as generalist species and easily adaptable to modified landscapes.
These species were chosen because the accessibility of the area, availability of samples, their co-distribution in the Cordillera Occidental, and their contrasting ecological requirements. Thus, they should provide a useful opportunity to investigate the local historical demographic processes behind the larger scale biogeographic patterns in an ecoregion with a dynamic geologic history [32]. Information on intraspecific genetic variation is also important to inform conservation plans at the level of communities and biogeographic subregions [33], because data on population sizes and migration rates may be useful for predicting the effects of disease, climate change and isolation by habitat fragmentation on amphibian populations [34], [35], [36].
Determining the processes promoting diversification and the geographic and temporal scales at which they operate is key to understanding how this group of direct-developing frogs has attained such remarkable levels of beta diversity across the Andes mountains [27]. This study investigates the population histories on different spatial scales of three species of Pristimantis and focuses on the following questions: 1. Is genetic diversity randomly distributed in each species with respect to geography? 2. Do species with broad versus narrow distributions show similar patterns in the distribution of genetic variation? 3. Do sympatric species have common phylogeographic patterns because they share similar environmental histories, or do species with contrasting life histories show distinct phylogeographic patterns?
Results
MtDNA Diversity
The 16S alignment contained 536 base pairs (bp) for P. brevifrons (N = 19 individuals), and 537 bp for P. palmeri (N = 32) and P. jubatus (N = 30). This locus showed the number of segregating sites, S = 18 for P. brevifrons, S = 12 for P. palmeri, and S = 26 for P. jubatus. The COI alignment contained 658 bp for P. brevifrons (N = 16), and 618 bp for P. palmeri (N = 35) and P. jubatus (N = 31). Pristimantis brevifrons showed S = 30 polymorphic sites, while P. palmeri and P. jubatus contained S = 110 and S = 50 sites, respectively. The translation of amino acids using the genetic code for vertebrates showed that COI variants were synonymous (silent).
Haplotype relationships were illustrated in a median-joining network (Fig. 1). The two sampling localities for P. brevifrons (Los Paraguas and Peñas Blancas), located 151.8 km apart and about at roughly same altitude, did not share haplotypes (each locality contained unique haplotypes) either in 16S or COI, which is consistent with a long period of isolation. As expected from the geography (Fig. 2), for P. palmeri the Serranía de Los Paraguas had the greatest differentiation as compared to the other two more proximal localities (Peñas Blancas and Chicoral) (Fig. 1). Chicoral and Peñas Blancas sites are separated by 18 km, while the northern population of Los Paraguas is more than 134 km apart from those sites.
Branches represent inferred mutational steps, where more than three mutations are denoted by the number of substitutions. The size of the circle is proportional to the number of individuals found for each haplotype. The two highly divergent specimens from Peñas Blancas in P. palmeri and one from Munchique National Park in P. jubatus were included in the networks.
There was a highly divergent COI haplotype found in two specimens (UVC15845 and UVC15857) within Peñas Blancas population of P. palmeri that were 17% (p-distance) diverged from what were presumably conspecific samples found at the same site. We were unable to amplify 16S from these same two specimens, unfortunately. Furthermore, there was one haplotype from the Chicoral population closely related to samples found at Peñas Blancas, indicating recent gene flow between these populations (Fig. 1). Pristimantis jubatus showed relatively low mtDNA divergences among sampling sites, with a total of four haplotypes for both genes. One individual of P. jubatus (UVC15842) from the site Observatorio was highly diverged (4% and 8%, p-distances for 16S and COI, respectively) from its conspecifics, with 22 nucleotide differences at 16S and 46 differences at COI from others at the same locality (Fig. 1). These divergence haplotypes within P. palmeri and P. jubatus may be migrants from an unsampled locality or cryptic species considering the intra-specific threshold values of divergence proposed by Vences et al. [37] and Fouquet et al. [38] of 3–5% at 16S and 10% at COI.
Population Genetic Structure
For two of the three species, mtDNA variation showed patterns of population subdivision. Population genetic structure was high among localities for the widespread, generalist species P. palmeri and P. brevifrons (Table 1). For P. palmeri the minimum estimated pairwise FST among populations was found between Chicoral and Peñas Blancas (FST = 0.682, probability of the null hypothesis of panmixa, p<0.01), which are geographically closer. The greatest population structuring was observed between Paraguas and Peñas Blancas (the two most distant sampling sites) in both P. brevifrons (FST = 0.98, p<0.01) and P. palmeri (FST = 0.95, p<0.01). However, substantial polymorphism within populations resulted in low but significant proportions of the total variation partitioned among localities in the AMOVA (29.9%, p<0.01 and 21.6%, p<0.01, for P. brevifrons and P. palmeri, respectively). In the more range-restricted and habitat-specialized species P. jubatus, in contrast, we observed low mtDNA sequences divergence among all three localities (FST = 0.0076–0.2749) and a low percentage of the total variation partitioned among localities (1.34%, p>0.05). These results suggest that the three sampling localities 3 km apart, Observatorio, Santa Ana and Charguayaco (Table 2) within the Munchique National Park (Fig. 2) form a single genetic population.
Tajima’s D statistic for P. jubatus for the combined Observatorio-Santa Ana-Charguayaco data (treated as one population, based on the above results), showed a significantly site-frequency skew for the mitochondrial dataset (DT ≤ - 2.5 for both genes, Table 3). These values were due to the sample UVC15842 (found in Observatorio, see above), which increased the number of singleton sites and caused a rejection of the standard neutral model. If this sample was excluded, neutrality was not rejected (Table 3). Summary statistics of genetic polymorphisms for all populations of the three species of Pristimantis are provided in Table 3.
Estimation of Historical Demographic Parameters
Gene flow (Nm) since initial divergence was very low between the two sampling localities of P. brevifrons, and within P. palmeri between the northerly Los Paraguas and the two southern sites. In contrast, significant and asymmetric gene flow was detected between the two adjacent populations of P. palmeri, with migration from Chicoral into Peñas Blancas being lower than in the reverse direction (Table 4, Fig. S1).
Based on estimates of θ for the combined mitochondrial gene sequences and using an inheritance scalar of 0.25 and a mutation rate estimated from closely related frogs (see Methods), we calculated an effective population size (Ne) for P. brevifrons of 38,000 (90% HPD 6,000–150,000) and 68,000 (90% HPD 21,000–181,000) reproductive individuals in Paraguas and Peñas Blancas, respectively. For P. palmeri we estimated Ne at 10,000 (90% HPD 500–73,000) individuals in Paraguas, 50,000 (90% HPD 12,000–145,000) for Peñas Blancas and 100,000 (90% HPD 40,000–280,000) at Chicoral (Table 4, Fig. S2). To be more conservative in our estimates of Ne we removed the unusually divergent specimens of P. palmeri (UVC15857 and UVC15845) from Peñas Blancas. Including these samples would inflate the number of segregating sites and bias estimates of Ne upwards. Because the three collecting localities for P. jubatus apparently represented a single genetic population, their effective population size was obtained using MIGRATE [39]. As the specimen UVC15842 of P. jubatus caused significant departures from standard neutral expectations (see above), we removed this sample prior to calculating Ne, yielding a more conservative estimated effective population size for this species of 94,000 (95% C.I. 15,600–470,000) individuals.
The upper tail of the posterior distribution for divergence times did not reach zero probability so we were unable to estimate a strict 90% HPD value for this parameter for any species. The partial posterior distributions, however, suggested the following tentative approximations of divergence times. The mode of the posterior distribution of divergence time among P. palmeri populations was about 0.58 million years ago (Mya) (90% HPD roughly 0.40–1.8 Mya) between Paraguas and Peñas Blancas, and divergence time between adjacent populations Chicoral and Peñas Blancas was 0.14 Mya (0.06–0.90 Mya) (Table 4, Fig. S3). Divergence times across the same terrain (Paraguas to Peñas Blancas) were slightly older in P. brevifrons (0.80 Mya; 90% HPD 0.56–1.4 Mya) than in P. palmeri (0.58).
Discussion
Studies on the intraspecific genetic differentiation and population structure of anurans in montane regions are sorely needed, considering that work in montane areas lags behind work done in low elevation environments of the Neotropics (e.g. Central America and Amazonia) [40], [41], [42]. We argue here that much interspecific diversity was likely derived from within-species diversity through vicariance processes, and these processes in term were actively promoted by millions of years of remarkable geological dynamism of the Andean Cordillera [21], [40]. Thus, an understanding of interspecific diversity patterns is informed by the study of within-species historical demographic processes [40], [43].
This study characterizes the genetic diversity, population structure and phylogeography of P. brevifrons, P. palmeri and P. jubatus using the mitochondrial markers COI and 16S. Estimates of gene flow, population sizes, and divergence time revealed important aspects of the historical demography of these three Neotropical montane species. Our data highlighted the undifferentiated structure of P. jubatus at a local geographical scale as well as the similar phylogeographic structure in P. brevifrons and P. palmeri, two species with similar life histories.
Comparative Phylogeographic of Pristimantis Frogs
For P. brevifrons and P. palmeri analyses of the two mitochondrial loci revealed high genetic differentiation in space cross the same geographic scale landscape (approx. 150 km.) and a similar inferred age of population differentiation in both species (around 0.80 Mya) (Fig. 1, Table 4). This implies that the two widespread species responded similarly to shared environmental processes producing similar population histories at the same spatial scale. Because these species are similar in terms of their ecological requirements, their parallel phylogeographic patterns suggest an eco-geological explanation of the geographical pattern during the Pleistocene [18], [19], [44].
The northern population of Los Paraguas showed low migration rates with the two southern sites, and a corresponding high pairwise population differentiation. This population appears to have split from the other locations during the Mid-Pleistocene (0.58–0.80 Mya), i.e., following the last episode of uplift of the northern portion of the Andes in the Pliocene (5.0–2.0 Mya) [45], [46]. The Serranía de Los Paraguas is a mountain formation that follows the western flank of the Cordillera Occidental, diverging from the main mountain range. This geological separation may be the cause of the restricted gene flow with the southern localities, thereby promoting the divergence of the Los Paraguas population. In the Cordillera Oriental of Colombia a similar pattern of isolation by ridges is found in unrelated frog species [9], [47].
Despite the dearth of ecological data for species of Pristimantis, these frogs are thought to have small home ranges along with low vagility [29], [48], which is supported by genetic data in a few species [40], [42]. At a smaller spatial scale (∼3 km), our analysis for the narrowly distributed P. jubatus, showed no significant spatial differentiation. We expected that the habitat specialist P. jubatus would show high structure but we likely need more geographically extensive sampling. On the other hand, we might have expected direct-developing frogs to show minimal population structuring as these amphibians do not require a water source for ovipositing or mating, so they may breed anywhere within a continuous forest of high relative humidity [40]. Pristimantis palmeri perhaps fits this prediction an intermediate spatial scale, i.e., the 18 km between Chicoral and Peñas Blancas. We estimated the asymmetric migration rates at 1.2 (90% HPD 0.003–13.9) and 0.004 (0.001–10.0), thus we could not reject the hypothesis of substantial levels of gene flow at this distance.
To date, there is a limited yet growing number of studies on genetic structure at local or regional scales in Neotropical frogs e.g., [40], [42], [49]. In other studies of terraranid frogs, Elmer et al. [42] found genetic structure at 4 km but Crawford [40] found no mitochondrial or nuclear differentiation between populations separated by 10 km. Also, Guarnizo et al. [9] found identical DNA sequences in localities as far away as 26 km in the high-elevation Andean hylid frog, Dendropsophus labialis. These results indicate that Andean frogs may disperse long distances at least in some cases or in some geographic context [27] and their range limits may be perhaps closely associated to altitude due to thermal limitations [50], [51], that may increase opportunities for speciation and high beta diversity in the Andes [52].
Our IMa analyses produced robust historical demographic parameter estimates, with the exception of divergences times. Features of the evolutionary history of our three study species revealed by coalescent analyses are particularly informative because few data on historical demography are currently available for tropical amphibians. Demographic estimates of population size are not available for P. brevifrons, P. palmeri or P. jubatus to corroborate the genetic-based estimates, however, the estimated population sizes for P. brevifrons, P. palmeri and P. jubatus are quite similar compared to those obtained by Crawford [40] for the terraranid species Craugastor bransfordii (3.1×105) and C. stejnegerianus (1.0×105). Thus, the effective population sizes are potentially very large in our three species of Pristimantis. Large population sizes could be positively correlated to higher speciation rates [53], yet a more parsimonious explanation may be that the beta diversity of Pristimantis in montane regions has been promoted by barriers, such as the Peñas Blancas ridge. Our results here inform these biogeographic models by confirming that even localized and isolated populations of these relatively small frogs may hold substantial amounts of genetic diversity, thus contributing to the maintenance of viable populations through subsequent vicariant events during montane diversification [23]. MtDNA lineages within Pristimantis frogs showed signs of demographic changes associated with recent Pleistocene and geological events. It will be interesting to examine similarly widespread species to evaluate the generality of these patterns and conduct more fine-scaled phylogeographical analyses to explore the possible mechanisms leading to speciation within this group of direct-developing frogs.
Materials and Methods
Ethics Statement
This study was carried out in strict accordance with the evaluations of environmental, social, and educational impacts established for research projects under Universidad del Valle Convocatoria Interna number CI-746. Permit for sampling of specimens was obtained from Ministerio de Medio Ambiente, Vivienda y Desarrollo Territorial de Colombia (Resolución 573 del 10 de abril/08). Euthanasia of frogs was performed with Chloretone, and all efforts were made to minimize suffering. Specimens were deposited at Herpetological Collection – Universidad del Valle (Voucher numbers: UVC15812– UVC15954) (Table S1) and DNA sequences data have been submitted to Genbank: accession numbers JN104663– JN104683; JN370956– JN371118.
Sampling
Sampling was carried out at four localities (Fig. 2): La Serranía de Los Paraguas, municipality El Cairo, on the border of the departments of Valle del Cauca and Chocó, 2,000–2,200 masl (4.7333°, −76.3°); Chicoral, municipality La Cumbre, department of Valle del Cauca, 1,800–1,900 masl (3.5833°, −76.6°); Peñas Blancas, in Farallones de Cali National Park, municipality Cali, department of Valle del Cauca, 1,900–2,200 masl (3.4333°, −76.6667°); and Munchique National Park, municipality El Tambo, department of Cauca, 2,400–2,800 masl (2.6667°, −76.9167°).
At each locality we established approximately straight-line transects across which samples were collected. Samples sizes ranged from 7–15 individuals per location (Table 2). Pristimantis jubatus was sampled at three different locations in the Munchique National Park (Observatorio, Santa Ana and Charguayaco), while widespread, generalist species P. brevifrons and P. palmeri were sampled at La Serranía de Los Paraguas and Peñas Blancas, and Serranía de Los Paraguas, Peñas Blancas and Chicoral, respectively. Tissues were collected in the field and kept in a solution of 1 M Tris HCl, 0.5 M EDTA, 5 M NaCl and SDS to 20%. Specimen identification was confirmed by Dr. John D. Lynch, Curator of Amphibians at the Instituto de Ciencias Naturales, Universidad Nacional de Colombia, Bogotá.
Laboratory Techniques
Total DNA was extracted from liver or thigh tissue using the Qiagen Tissue DNeasy kit (Qiagen) following the manufacturer’s instructions. Mitochondrial DNA (mtDNA) fragments were amplified using PCR primers 16 Sbr plus 16 Sar for the ARN region of the 16S ribosomal RNA gene [54] and LCO1490 plus HCO2198 for the 5′ half of the cytochrome oxidase subunit I (COI), also known as the Folmer fragment or Barcode of Life fragment for animals [55], [56]. The DNA amplification reactions contained 2.5 mM MgCl2, 0.3 mM dNTPs, 0.3 µM of each Primer, 0.625 U of Taq polymerase and 1–2 µl total DNA. PCR conditions followed Goebel et al. [57] and Vences et al. [58]. Negative controls were used to monitor potential contamination in PCR. Amplification products were purified with QIAquick PCR clean-up kit (Qiagen). Both H (heavy) and L (light) strands were sequenced using the chemical reaction Big-Dye Terminator v. 3.1 reagents in an automated DNA sequencer (ABI 3730XL, Applied Biosystems Inc.). The sequences were deposited in GenBank (Table S1).
Analyses
DNA sequence analysis.
Sequences were edited, assembled and aligned using the program Sequencher 4.6 (Gene Codes Corporation) and verified by eye. COI sequences were translated into amino acids with the program DnaSP 5.0 [59] to confirm the absence of inferred nonsense mutations. We used DnaSP to calculate the following summary statistics for genetic variation within each population: haplotype diversity (Hd), nucleotide diversity per site (π ) [60], the number of segregating sites (S), Watterson’s estimator of the per-site population mutation rate () [61] and Tajima’s D statistic (DT). Sites with indels or missing data were eliminated in pairwise sequence comparisons. Coalescence simulations were run in DnaSP to test for significant departures from the expected value DT = 0 under the standard neutral model using 5,000 replicates conditional on sample size and S.
Analysis of population differentiation.
We used the programs Arlequin 3.1 [62] and DnaSP 5.0 to conduct an Analysis of Molecular Variance (AMOVA) and calculate Lynch & Crease’s pairwise FST [63] to test the null hypothesis of panmixia between pairs of populations [64] using 1000 permutations and significance level of 0.05. FST was chosen as the metric parameter of the genetic differentiation among populations because it provides a more effective summary of the effects of population structure [65]. To visualize the relationship between the genealogy of haplotypes and geography, haplotype networks were inferred using median joining as implemented in the program Network 4.5.1.0 [66].
Estimation historical demographic parameters.
We estimated the effective population sizes (Ne), asymmetric pairwise migration rates (Nm) and time since population divergence (t) with the programs IMa [67] and MIGRATE [39]. To convert parameter estimates of IMa into demographic units, an inheritance scalar of 0.25 and generation time of one year were assumed. To obtain Ne from θ ( = 4Neμ, under the standard neutral model) we assumed a mutation rate, μ, of 1.9×10−8 per site per year, based on estimated rates of silent site divergence in a genus of frogs closely related to Pristimantis [68]. While the COI gene typically has higher overall rates of substitution relative to the more conserved 16S gene [37], [69], [70], we assume that these two mitochondrial genes experience comparable rates of mutation [71] (as opposed to substitution rates). We used an infinite-site model of substitution [72] for both genes, 16S and COI. Several preliminary MCMC simulations with broad priors were performed to set appropriate bounds for each parameter (θ, m, t). We compared the convergence of the marginal distributions of each parameter among multiple runs and obtained the credibility intervals based on 90% highest posterior density (HPD).
Supporting Information
Figure S1.
Posterior probability distributions for gene flow from IMa analysis.
https://doi.org/10.1371/journal.pone.0046077.s001
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Figure S2.
Posterior probability distributions for effective population sizes from IMa analysis.
https://doi.org/10.1371/journal.pone.0046077.s002
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Figure S3.
Posterior probability distributions for divergence times from IMa analysis.
https://doi.org/10.1371/journal.pone.0046077.s003
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Table S1.
Sample information for taxa analyzed in this study.
https://doi.org/10.1371/journal.pone.0046077.s004
(DOC)
Acknowledgments
We thank the Ministerio de Medio Ambiente, Vivienda y Desarrollo Territorial de Colombia for research permission (Resolución 573 del 10 de abril/08) and the Universidad del Valle for funding (Convocatoria Interna CI-746). The Programa de Postgrado de Ciencias-Biología and the Grupo de Estudios Ecogenéticos y Biología Molecular of the Universidad del Valle provided training in molecular techniques, support and academic assistance. Thanks to Ranulfo González and Guillermo Barreto for their advice, Diana López for access to software and literature at the Instituto de Investigaciones Alexander von Humboldt, John D. Lynch from the Instituto de Ciencias Naturales-UNAL for access to specimens, Luz Piedad Aguirre and Juan Esteban Zuluaga from the Vicerrectoria de Investigaciones of the Universidad del Valle for support, and to the rangers and inhabitants of La Romelia -Munchique National Park-, Peñas Blancas, Pichindé, El Cairo, Chicoral, and Loma Alta. Our work in Los Paraguas was facilitated by Serraniaguas. Wilmar Bolivar, Nelsy Pinto, Fernanda Castillo and an anonymous reviewer for insightful and helpful comments on various versions of the manuscript. Isabel Castro, Kyle Morrison and Alexander Wilson helped in the translation of the manuscript. This work partially fulfilled the requirements for the Masters degree of JCG-R at the Universidad del Valle.
Author Contributions
Conceived and designed the experiments: JCG AJC HC FC. Performed the experiments: JCG OO AM. Analyzed the data: JCG OO AM. Wrote the paper: JCG AJC.
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