Most marine organisms disperse via ocean currents as larvae, so it is often assumed that larval-stage duration is the primary determinant of geographic range size. However, empirical tests of this relationship have yielded mixed results, and alternative hypotheses have rarely been considered. Here we assess the relative influence of adult and larval-traits on geographic range size using a global dataset encompassing 590 species of tropical reef fishes in 47 families, the largest compilation of such data to date for any marine group. We analyze this database using linear mixed-effect models to control for phylogeny and geographical limits on range size. Our analysis indicates that three adult traits likely to affect the capacity of new colonizers to survive and establish reproductive populations (body size, schooling behavior, and nocturnal activity) are equal or better predictors of geographic range size than pelagic larval duration. We conclude that adult life-history traits that affect the postdispersal persistence of new populations are primary determinants of successful range extension and, consequently, of geographic range size among tropical reef fishes.eographic range size is a fundamental biogeographic variable that, among other effects (1, 2), strongly influences a species susceptibility to extinction (3, 4). Because most marine organisms disperse as larval propagules transported by ocean currents, it is often assumed that the duration of the larval stage is the fundamental determinant of their dispersal ability, and hence their range size (5, 6). Tropical reef fishes have geographic ranges that vary greatly in size, from a few square kilometers around tiny isolated islands to entire ocean basins (7-9). Given that pelagic larval duration (PLD) also varies greatly among such fishes, from only a few days to many months, the effects of PLD on dispersal potential became an early focus of investigation on general determinants of range size among those fishes and other near-shore marine species (10-12). However, although it has become evident that PLD is unlikely to be a primary determinant of geographic range size (13-16), alternative hypotheses have only recently begun to be considered (9).To expand its geographic range, a species must successfully colonize new areas following the dispersal of its propagules (17). Consequently, attributes other than pelagic dispersal capacity may largely determine how widely reef fishes are distributed geographically (9). Here we assess the relative importance of seven adult and larval traits in influencing geographic range sizes of tropical reef fishes at the global scale. We do so using data from 590 species of tropical reef fishes in 47 families, the largest compilation of such data currently available for any marine group (Dataset S1). Traits directly linked to larval dispersal potential include PLD and spawning mode. Adult traits include maximum body size, schooling behavior, nocturnal activity, use of multiple habitat types, and adult depth range. The adultbiology tra...
Seagrasses structure some of the world's key coastal ecosystems presently in decline due to human activities and global change. The ability to cope with environmental changes and the possibilities for shifts in distribution range depend largely on their evolvability and dispersal potential. As large-scale data usually show strong genetic structure for seagrasses, finer-grained work is needed to understand the local processes of dispersal, recruitment and colonization that could explain the apparent lack of exchange across large distances. We aimed to assess the fine-grained genetic structure of one of the most important and widely distributed seagrasses, Zostera marina, from seven meadows in Brittany, France. Both classic population genetics and network analysis confirmed a pattern of spatial segregation of polymorphism at both regional and local scales. One location exhibiting exclusively the variety 'angustifolia' did not appear more differentiated than the others, but instead showed a central position in the network analysis, confirming the status of this variety as an ecotype. This phenotypic diversity and the high allelic richness at nine microsatellites (2.33-9.67 alleles/locus) compared to levels previously reported across the distribution range, points to Brittany as a centre of diversity for Z. marina at both genetic and phenotypic levels. Despite dispersal potential of several 100 m, a significant pattern of genetic differentiation, even at fine-grained scale, revealed 'genetic patchiness'. Meadows seem to be composed of a mosaic of clones with distinct origins in space and time, a result that calls into question the accuracy of the concept of populations for such partially clonal species.
Theoretically, the dynamics of clonal and genetic diversities of clonal plant populations are strongly influenced by the competition among clones and rate of seedling recruitment, but little empirical assessment has been made of such dynamics through temporal genetic surveys. We aimed to quantify 3 years of evolution in the clonal and genetic composition of Zostera marina meadows, comparing parameters describing clonal architecture and genetic diversity at nine microsatellite markers. Variations in clonal structure revealed a decrease in the evenness of ramet distribution among genets. This illustrates the increasing dominance of some clonal lineages (multilocus lineages, MLLs) in populations. Despite the persistence of these MLLs over time, genetic differentiation was much stronger in time than in space, at the local scale. Contrastingly with the short-term evolution of clonal architecture, the patterns of genetic structure and genetic diversity sensu stricto (that is, heterozygosity and allelic richness) were stable in time. These results suggest the coexistence of (i) a fine grained (at the scale of a 20 Â 30 m quadrat) stable core of persistent genets originating from an initial seedling recruitment and developing spatial dominance through clonal elongation; and (ii) a local (at the scale of the meadow) pool of transient genets subjected to annual turnover. This simultaneous occurrence of initial and repeated recruitment strategies highlights the different spatial scales at which distinct evolutionary drivers and mating systems (clonal competition, clonal growth, propagule dispersal and so on) operate to shape the dynamics of populations and the evolution of polymorphism in space and time. Keywords: clonality; seagrass; spatio-temporal genetic structure; Zostera marina INTRODUCTION Clonality is a life history trait widely distributed among taxa and habitats, particularly in photosynthetic organisms. Partially clonal organisms are characterized by a mixed system allowing the combination of two reproductive strategies: the production of new genetically identical modules through vegetative growth or fragmentation and the production of new genetic individuals through sexual recombination. As a consequence, their population dynamics and evolutionary trajectories are profoundly affected by their rate and mode of clonal reproduction. Populations of clonal plants are composed of genetic individuals, or genets occupying space and dispersing locally through the production of modular shoots, or ramets (Harper, 1977). As genets are able to persist through time and space, the composition and evolution of populations of clonal plants is largely affected by the level of intraspecific competition (Eriksson, 1989(Eriksson, , 1993Pan and Price, 2001;Travis and Hester, 2005).Depending on the turnover of genets and intensity of inter-genet competition for space, two extreme recruitment strategies have been defined (Eriksson, 1993): (i) the 'Initial Seedling Recruitment' (ISR) strategy, characterizing populations originating fro...
Partial clonality is commonly used in eukaryotes and has large consequences for their evolution and ecology. Assessing accurately the relative importance of clonal vs. sexual reproduction matters for studying and managing such species. Here, we proposed a Bayesian approach, ClonEstiMate, to infer rates of clonality c from populations sampled twice over a short time interval, ideally one generation time. The method relies on the likelihood of the transitions between genotype frequencies of ancestral and descendent populations, using an extended Wright-Fisher model explicitly integrating reproductive modes. Our model provides posterior probability distribution of inferred c, given the assumed rates of mutation, as well as inbreeding and selfing when occurring. Tested under various conditions, this model provided accurate inferences of c, especially when the amount of information was modest, that is low sample sizes, few loci, low polymorphism and strong linkage disequilibrium. Inferences remained robust when mutation models and rates were misinformed. However, the method was sensitive to moderate frequencies of null alleles and when the time interval between required samplings exceeding two generations. Misinformed rates on mating modes (inbreeding and selfing) also resulted in biased inferences. Our method was tested on eleven data sets covering five partially clonal species, for which the extent of clonality was formerly deciphered. It delivered highly consistent results with previous information on the biology of those species. ClonEstiMate represents a powerful tool for detecting and inferring clonality in finite populations, genotyped with SNPs or microsatellites. It is freely available at https://www6.rennes.inra.fr/igepp_eng/Productions/Software.
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