There is growing interest in quantifying genetic population structure across the geographical ranges of species to understand why species might exhibit stable range limits and to assess the conservation value of peripheral populations. However, many assertions regarding peripheral populations rest on the long-standing but poorly tested supposition that peripheral populations exhibit low genetic diversity and greater genetic differentiation as a consequence of smaller effective population size and greater geographical isolation relative to geographically central populations. We reviewed 134 studies representing 115 species that tested for declines in within-population genetic diversity and/or increases in amongpopulation differentiation towards range margins using nuclear molecular genetic markers. On average, 64.2% of studies detected the expected decline in diversity, 70.2% of those that tested for it showed increased differentiation and there was a positive association between these trends. In most cases, however, the difference in genetic diversity between central and peripheral population was not large. Although these results were consistent across plants and animals, strong taxonomic and biogeographical biases in the available studies call for a cautious generalization of these results. Despite the large number of studies testing these simple predictions, very few attempted to test possible mechanisms causing reduced peripheral diversity or increased differentiation. Almost no study incorporated a phylogeographical framework to evaluate historical influences on contemporary genetic patterns. Finally, there has been little effort to test whether these geographical trends in putatively neutral variation at marker loci are reflected by quantitative genetic trait variation, which is likely to influence the adaptive potential of populations across the geographical range.
Rivers have been suggested to have played an important role in shaping present-day patterns of ecological and genetic variation among Amazonian species and communities. Recent molecular studies have provided mixed support for the hypothesis that large lowland Amazonian rivers have functioned as significant impediments to gene flow among populations of neotropical species. To date, no study has systematically evaluated the impact that riverine barriers might have on structuring whole Amazonian communities. Our analyses of the phylogeography of frogs and small mammals indicate that a putative riverine barrier (the Juruá River) does not relate to present-day patterns of community similarity and species richness. Rather, our results imply a significant impact of the Andean orogenic axis and associated thrust-and-fold lowland dynamics in shaping patterns of biotic diversity along the Juruá . Combined results of this and other studies significantly weaken the postulated role of rivers as major drivers of Amazonian diversification.
Mitochondrial DNA cytochrome b sequence data from a dart-poison frog, Epipedobates femoralis, were used to test two hypotheses of Amazonian diversi¢cation: the riverine barrier and the ridge hypotheses. Samples were derived from sites located on both banks of the Rio Jurua¨and on both sides of the Iquitos Arch in western Amazonia. The phylogeographic structure was inconsistent with predictions of the riverine barrier hypothesis. Haplotypes from opposite river banks did not form monophyletic clades in any of our phylogenetic analyses, nor was the topology within major clades consistent with the riverine hypothesis. Further, the greatest di¡erentiation between paired sites on opposite banks was not at the river mouth where the strongest barrier to gene £ow was predicted to occur. The results instead were consistent with the hypothesis that ancient ridges (arches), no longer evident on the landscape, have shaped the phylogeographic relationships of Amazonian taxa. Two robustly supported clades map onto opposite sides of the Iquitos Arch. The mean haplotypic divergence between the two clades, in excess of 12%, suggests that this cladogenic event dates to between ¢ve and 15 million years ago. These estimates span a period of major orogenesis in western South America and presumably the formation of these ancient ridges.
Latitudinal variation in patterns of evolution has fascinated biologists for over a century, but our understanding of latitudinal differences in evolutionary processes-such as selection and drift-remains limited. Here, we test for, and find, accelerated evolution of color patterns in bird taxa that breed at higher latitudes compared with those breeding in the tropics, analyzing data from seven diverse avian families. Most important, we show that the extent of overlap of species' breeding ranges (degree of sympatry) explains the elevated rate of color pattern evolution at higher latitudes. We suggest that the dynamic shifts in breeding ranges that accompanied climatic changes during the last 3 million years (Milankovitch Oscillations) resulted in more rapid and more frequent secondary contact at high latitudes. We argue that sympatry among diverging clades causes greater divergence of color traits in birds at higher latitudes through sexual, social, or ecological character displacement that accelerate rates of evolution, and through the selective elimination of weakly differentiated lineages that hybridize and fuse in sympatry (differential fusion). K E Y W O R D S :Character displacement, color patterns, differential fusion, latitudinal gradients, rates of evolution, reinforcement, speciation, sympatry.
Competitive partitioning of ‘community’ signal space has long been suggested to underlie diversification of mating signals. Selection or competitive exclusion is expected to reduce overlap of signals, minimizing destructive interference or reducing mismating. We used null models backed by simulation of type I and II error rates to test for evidence of structuring within 11 frog advertisement call assemblages. Within three assemblages, we found significant over‐dispersion and regularity‐of‐spacing in dominant frequency and in pulse rate, consistent with a signal interference hypothesis and signal confusion hypothesis, respectively. Observed partitioning could represent signal evolution or could result from selection on assemblage composition. Most assemblages showed no acoustic partitioning possibly because: (i) partitioning is more readily apparent in female preference, calling times or sites, rather than call attributes; (ii) assemblages have not yet accommodated recently arrived species, or are compositionally unstable so that acoustic accommodation cannot occur; and (iii) evidence of partitioning is only likely where the acoustic space is densely packed.
Patterns and levels of allozyme variation among populations of Amazonian frogs were used to test the riverine barrier hypothesis of species differentiation. Two frog species were sampled from each of the two main forest habitats on both banks of the Juruá River in the southwestern Brazilian Amazon Basin at various points along its course to contrast different barrier strengths. Scarthyla ostinodactyla and Scinax rubra were sampled from flooded forest (varzea), and Physalaemus petersi and Epipedobates femoralis from non‐flooded forest (terra firme). All species showed high levels of within‐population genetic variation. Average Nei's (1978) and Rogers’ (1972) genetic distances between sampled sites for all species were high indicating substantial among‐population differentiation. The observation of low gene flow between sampled sites within species was further substantiated with Slatkin's (1993) M̂ analyses. Randomization tests suggested that there was some population structure at a few assayed polymorphic loci that was consistent with the riverine barrier hypothesis. However, it was apparent from the raw allozyme frequency data that these results were largely driven by substantial differentiation at one or a few collecting localities rather than by basin‐wide patterns of riverine differentiation. Phenograms using genetic distance matrices supported this interpretation. Patterns of geographic variation are probably more consistent with the idea of this region being a zone of secondary contact.
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