Home About us Contact | |||
Local Population Size (local + population_size)
Selected AbstractsTHE EVOLUTION OF DISPERSAL IN A LEVINS' TYPE METAPOPULATION MODELEVOLUTION, Issue 10 2007Vincent A.A. Jansen We study the evolution of the dispersal rate in a metapopulation model with extinction and colonization dynamics, akin to the model as originally described by Levins. To do so we extend the metapopulation model with a description of the within patch dynamics. By means of a separation of time scales we analytically derive a fitness expression from first principles for this model. The fitness function can be written as an inclusive fitness equation (Hamilton's rule). By recasting this equation in a form that emphasizes the effects of competition we show the effect of the local competition and the local population size on the evolution of dispersal. We find that the evolution of dispersal cannot be easily interpreted in terms of avoidance of kin competition, but rather that increased dispersal reduces the competitive ability. Our model also yields a testable prediction in term of relatedness and life-history parameters. [source] Habitat selection as a source of inter-specific differences in recruitment of two diadromous fish speciesFRESHWATER BIOLOGY, Issue 11 2008ROBIN HALE Summary 1For aquatic species with highly dispersive offspring, the addition of new individuals into an area (recruitment) is a key process in determining local population size so understanding the causes of recruitment variability is critical. While three general causative mechanisms have been identified (the supply of individuals, habitat selection and mortality), we have a limited understanding of how variation in each is generated, and the consequences this may have for the spatial and temporal distribution of recruits. 2We examined whether active habitat selection during settlement could be the cause of variability in populations of two diadromous fish species using a field survey and laboratory-based choice experiments. If larval behaviour is important, we predicted there would be inter-specific differences in abundance between sites during the survey, and that larvae would prefer water collected from sites with higher conspecific abundances during the experiments. 3During the field survey, significant differences were detected between two rivers (the Cumberland and Grey), with one species (Galaxias maculatus) found in higher abundances at one site (the Cumberland River) while comparable numbers of a closely related species (Galaxias brevipinnis) were caught at both sites. Laboratory choice experiments were conducted to determine whether larval preferences during settlement could be the cause of these differences. G. maculatus larvae showed a preference for freshwater over saltwater, indicating that the fish may be responding to reduced salinities around river mouths during settlement. The results of a second experiment were consistent with the notion that larval preferences could be the mechanism driving differences in the populations of the two rivers, with G. maculatus preferring water collected from the Cumberland River while G. brevipinnis did not prefer water from either river. 4These results demonstrate that active habitat selection may be important in establishing spatial patterns of larvae at settlement, and that multiple cues are likely to be involved. This study also demonstrates that the behaviours exhibited by individuals can strongly influence the structure and dynamics of populations of aquatic species with complex life cycles. [source] Impacts of sudden winter habitat loss on the body condition and survival of redshank Tringa totanusJOURNAL OF APPLIED ECOLOGY, Issue 3 2006NIALL H. K. BURTON Summary 1Recent theoretical modelling has provided important insights into how habitat loss may affect local populations through impacts on individual fitness (survival, body condition, fecundity). Despite this, attempts to provide empirical evidence of such impacts on displaced individuals have been limited. Using a before-after-control-impact (BACI) approach, we report how a sudden loss of wintering habitat impacted on the body condition and survival of redshank Tringa totanus. 2The intertidal mudflats of Cardiff Bay, UK, were inundated with freshwater in November 1999 following impoundment by a barrage, resulting in the displacement of c. 300 redshank to adjacent habitat on the Severn Estuary. Movements and the survival of these birds were monitored through observations of colour-marked individuals. Comparative survival rates were calculated for marked populations at the main recipient site, Rhymney, and a control site. 3Displaced redshank had difficulty maintaining their mass in the first winter post-barrage closure: adults previously only recorded at Cardiff Bay were significantly lighter than those previously recorded at Rhymney. 4Survival rates of displaced redshank also declined. The estimated annual survival of adult Cardiff Bay redshank fell from 0·846 in the 2 years pre-barrage closure to 0·778 in the 3 following years because of a significant decline in winter survival (P = 0·0006). In comparison, there was no significant change in the survival of adult Rhymney redshank, and adult survival at the control site was actually greater post-barrage closure than beforehand. The lack of decline in these rates and the similarity between those of Cardiff Bay adults pre-barrage closure and Rhymney adults indicate that the increase in winter mortality of Cardiff Bay birds resulted from their displacement. 5Synthesis and applications. This study provides the first conclusive empirical evidence that habitat loss can impact individual fitness in a bird population. Adult redshank displaced from Cardiff Bay experienced poor body condition and a 44% increase in mortality rate. Without an increase in the recruitment of first-winter birds, such a change is likely to reduce substantially local population size. The results reported here should help to inform governments, planners and non-governmental organizations (NGOs) seeking to understand how developments might impact on animal populations. [source] Modelling species diversity through species level hierarchical modellingJOURNAL OF THE ROYAL STATISTICAL SOCIETY: SERIES C (APPLIED STATISTICS), Issue 1 2005Alan E. Gelfand Summary., Understanding spatial patterns of species diversity and the distributions of individ-ual species is a consuming problem in biogeography and conservation. The Cape floristic region of South Africa is a global hot spot of diversity and endemism, and the Protea atlas project, with about 60 000 site records across the region, provides an extraordinarily rich data set to model patterns of biodiversity. Model development is focused spatially at the scale of 1, grid cells (about 37 000 cells total for the region). We report on results for 23 species of a flowering plant family known as Proteaceae (of about 330 in the Cape floristic region) for a defined subregion. Using a Bayesian framework, we developed a two-stage, spatially explicit, hierarchical logistic regression. Stage 1 models the potential probability of presence or absence for each species at each cell, given species attributes, grid cell (site level) environmental data with species level coefficients, and a spatial random effect. The second level of the hierarchy models the probability of observing each species in each cell given that it is present. Because the atlas data are not evenly distributed across the landscape, grid cells contain variable numbers of sampling localities. Thus this model takes the sampling intensity at each site into account by assuming that the total number of times that a particular species was observed within a site follows a binomial distribution. After assigning prior distributions to all quantities in the model, samples from the posterior distribution were obtained via Markov chain Monte Carlo methods. Results are mapped as the model-estimated probability of presence for each species across the domain. This provides an alternative to customary empirical ,range-of-occupancy' displays. Summing yields the predicted richness of species over the region. Summaries of the posterior for each environmental coefficient show which variables are most important in explaining the presence of species. Our initial results describe biogeographical patterns over the modelled region remarkably well. In particular, species local population size and mode of dispersal contribute significantly to predicting patterns, along with annual precipitation, the coefficient of variation in rainfall and elevation. [source] Local forest environment largely affects below-ground growth, clonal diversity and fine-scale spatial genetic structure in the temperate deciduous forest herb Paris quadrifoliaMOLECULAR ECOLOGY, Issue 14 2005HANS JACQUEMYN Abstract Paris quadrifolia (herb Paris) is a long-lived, clonal woodland herb that shows strong differences in local population size and shoot density along an environmental gradient of soil and light conditions. This environmentally based structuring may be mediated by differences in clonal growth and seedling recruitment through sexual reproduction. To study the interrelationship between environmental conditions and spatial patterns of clonal growth, the spatial genetic structure of four P. quadrifolia populations growing in strongly contrasting sites was determined. In the first place, plant excavations were performed in order to (i) determine differences in below-ground growth of genets, (ii) investigate connectedness of ramets and (iii) determine total genet size. Although no differences in internode length were found among sites, clones in moist sites were much smaller (genets usually consisted of 1,3 interconnected shoots, most of them flowering) than genets in dry sites, which consisted of up to 15 interconnected shoots, the majority of which were vegetative. Further, amplified fragment length polymorphism (AFLP) markers were used. Clonal diversity was higher in populations located in moist and productive ash,poplar forests compared to those found in drier and less productive mixed forest sites (G/N: 0.27 and 0.14 and Simpson's D: 0.84 and 0.75, respectively). Patterns of spatial population genetic structure under dry conditions revealed several large clones dominating the entire population, whereas in moist sites many small genets were observed. Nevertheless, strong spatial genetic structure of the genet population was observed. Our results clearly demonstrate that patterns of clonal diversity and growth form of P. quadrifolia differ among environments. Limited seedling recruitment and large clone sizes due to higher connectedness of ramets explain the low clonal diversity in dry sites. In moist sites, higher levels of clonal diversity and small clone sizes indicate repeated seedling recruitment, whereas strong spatial genetic structure suggests limited seed dispersal within populations. [source] Spatial population structure in a patchily distributed beetleMOLECULAR ECOLOGY, Issue 4 2001Tomas Roslin Abstract The dynamics and evolution of populations will critically depend on their spatial structure. Hence, a recent emphasis on one particular type of structure , the metapopulation concept of Levins , can only be justified by empirical assessment of spatial population structures in a wide range of organisms. This paper focuses on Aphodius fossor, a dung beetle specialized on cattle pastures. An agricultural database was used to locate nearly 50 000 local populations of A. fossor in Finland. Several independent methods were then used to quantify key processes in this vast population system. Allozyme markers and mitochondrial DNA (mtDNA) sequences were applied to examine genetic differentiation of local populations and to derive indirect estimates of gene flow. These estimates were compared to values expected on the basis of direct observations of dispersing individuals and assessments of local effective population size. Molecular markers revealed striking genetic homogeneity in A. fossor. Differentiation was only evident in mtDNA haplotype frequencies between the isolated Åland islands and the Finnish mainland. Thus, indirect estimates of gene flow agreed with direct observations that local effective population size in A. fossor is large (hundreds of individuals), and that in each generation, a substantial fraction (approximately one-fifth) of the individuals move between populations. Large local population size, extreme haplotype diversity and a high regional incidence of A. fossor all testify against recurrent population turnover. Taken together, these results provide strong evidence that the whole mainland population of A. fossor is better described as one large ,patchy population', with substantial movement between relatively persistent local populations, than as a classical metapopulation. [source] DIFFERENTIATION AMONG POPULATIONS WITH MIGRATION, MUTATION, AND DRIFT: IMPLICATIONS FOR GENETIC INFERENCEEVOLUTION, Issue 1 2006Seongho Song Abstract Populations may become differentiated from one another as a result of genetic drift. The amounts and patterns of differentiation at neutral loci are determined by local population sizes, migration rates among populations, and mutation rates. We provide exact analytical expressions for the mean, variance, and covariance of a stochastic model for hierarchically structured populations subject to migration, mutation, and drift. In addition to the expected correlation in allele frequencies among populations in the same geographic region, we demonstrate that there is a substantial correlation in allele frequencies among regions at the top level of the hierarchy. We propose a hierarchical Bayesian model for inference of Wright's F -statistics in a two-level hierarchy in which we estimate the among-region correlation in allele frequencies by substituting replication across loci for replication across time. We illustrate the approach through an analysis of human microsatellite data, and we show that approaches ignoring the among-region correlation in allele frequencies underestimate the amount of genetic differentiation among major geographic population groups by approximately 30%. Finally, we discuss the implications of these results for the use and interpretation of F -statistics in evolutionary studies. [source] |