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Metapopulation
Terms modified by Metapopulation Selected AbstractsCOALESCENCE IN A METAPOPULATION WITH RECURRENT LOCAL EXTINCTION AND RECOLONIZATIONEVOLUTION, Issue 5 2003John R. Pannell Abstract Many species exist as metapopulations in balance between local population extinction and recolonization. The effect of these processes on average population differentiation, within-deme diversity, and specieswide diversity has been considered previously. In this paper, coalescent simulations of Slatkin's propagule-pool and migrant-pool models are used to characterize the distribution of neutral genetic diversity within demes (,s), diversity in the metapopulation a whole (TTT), the ratio FST= (,t,,S)/,T, Tajima's D statistic, and several ratios of gene-tree branch lengths. Using these distributions, power to detect differences in key metapopulation parameter values is determined under contrasting sampling regimes. The results indicate that it will be difficult to use sequence data from a single locus to detect a history of extinctions and recolonizations in a metapopulation because of high genealogical variance, the loss of diversity due to reductions in effective population size, and the fact that a genealogy of lineages from different demes under Slatkin's model differs from a neutral coalescent only in its time scale. Genetic indices of gene-tree shape that capture the effects of extinction/recolonization on both external branches and the length of the genealogy as a whole will provide the best indication of metapopulation dynamics if several lineages are sampled from several different demes. [source] Is the matrix a sea?ECOLOGICAL ENTOMOLOGY, Issue 1 2005Habitat specificity in a naturally fragmented landscape Abstract., 1. Metapopulation and island biogeography theory assume that landscapes consist of habitat patches set in a matrix of non-habitat. If only a small proportion of species conform to the patch,matrix assumptions then metapopulation theory may only describe special cases rather than being of more general ecological importance. 2. As an initial step towards understanding the prevalence of metapopulation dynamics in a naturally fragmented landscape, the distribution of beetle species in three replicates of three habitat types was examined, including rainforest and eucalypt forest (the habitat patches), and buttongrass sedgeland (the matrix), in south-west Tasmania, Australia. 3. Ordination methods indicated that the buttongrass fauna was extremely divergent from the fauna of forested habitats. Permutation tests showed that the abundance of 13 of 17 commonly captured species varied significantly among habitats, with eight species confined to eucalypts or rainforest, and three species found only in buttongrass. Approximately 60% of species were confined to forested habitat implying that metapopulation theory has the potential to be very important in the forest,buttongrass landscape. 4. Although floristically the rainforest and eucalypts were extremely distinct, the beetle faunas from eucalypts and rainforests overlapped substantially. Therefore rainforest patches connected by eucalypt forest represent continuous habitat for most species. 5. Other studies report a wide range of values for the proportion of patch-specific species in fragmented landscapes. Understanding the environmental or historical conditions under which a high proportion of species become patch specialists would help to identify where spatial dynamic theory may be especially applicable, and where habitat loss and fragmentation poses the greatest threat to biodiversity. [source] The Cost Efficiency of Wild Dog Conservation in South AfricaCONSERVATION BIOLOGY, Issue 4 2005P. A. LINDSEY crianza de especies cinegéticas; financiamiento de donantes; Lycaon pictus; metapoblación; reintroducción Abstract:,Aside from Kruger National Park, no other suitable reserves of sufficient size exist in South Africa that will hold a viable population of wild dogs (Lycaon pictus). Consequently, conservation efforts have been focused on creating a metapopulation through a series of wild dog reintroductions into isolated fenced reserves. Additional potential exists for conserving wild dogs on private ranch land. Establishing the metapopulation was an expensive process, accounting for approximately 75% of the US$380,000 spent on wild dog conservation in South Africa during 1997-2001. The principal goal of the metapopulation project was to reduce the risk of catastrophic population decline. Now that this has been achieved, we developed a uniform cost-efficiency index to estimate the cost efficiency of current and potential future conservation strategies in South Africa. Conserving wild dogs in large protected areas was predicted to be the most cost-efficient conservation strategy (449 packs/$100,000 expenditure). Establishing the metapopulation has been less cost efficient (23 packs/$100,000), and expansion of the metapopulation was predicted to be even less cost efficient if predation by wild dogs results in additional costs, as is to be expected if private reserves are used for reintroductions (3-13 packs/$100,000). Because of low logistical costs, conserving wild dogs in situ on private ranch land was potentially more cost efficient than reintroducing wild dogs (14-27 packs/$100,000). We recommend that donor funding be used to reintroduce wild dogs into transfrontier parks, when they are established, to maintain the existing metapopulation and to establish conservation programs involving wild dogs on private ranch land. Investing in the expansion of the metapopulation should be limited to state-owned nature reserves willing to carry predation costs without compensation. Resumen:,Además del Parque Nacional Kruger, en África del Sur no existen otras reservas de suficiente tamaño como para mantener una población viable de perros salvajes (Lycaon pictus). En consecuencia, los esfuerzos de conservación se han enfocado en la creación de una metapoblación por medio de una serie de reintroducciones en pequeñas reservas cercadas. Hay un potencial adicional para la conservación de perros salvajes en terrenos privados. El establecimiento de la metapoblación fue un proceso costoso, ,75% de US $380,000 que fueron gastados en la conservación de perros salvajes entre 1997 y 2001 en África del Sur. La meta principal del proyecto de metapoblación fue la reducción del riesgo de una declinación catastrófica de la población. Ya que esto se ha logrado, desarrollamos un índice de rentabilidad uniforme para estimar la rentabilidad de las actuales y potenciales estrategias de conservación en África del Sur. Se predijo que la estrategia de conservación de más rentable (449manadas/$100,000 de gasto) era la conservación de perros salvajes en áreas protegidas grandes. El establecimiento de la metapoblación ha sido menos rentable (23 manadas/$100,000), y se predijo que la expansión de la metapoblación sería aun menos rentable si la depredación por perros salvajes resulta en costos adicionales, como se esperaría si se utilizan reservas privadas para las reintroducciones (3-13 manadas/$100,000). Debido a los bajos costos de logística, la conservación de perros salvajes in situ en terrenos privados fue potencialmente más rentable que reintroducir a los perros salvajes (14-27 manadas/$100,000). Recomendamos que el financiamiento de donantes sea utilizado para reintroducir perros salvajes en parque transfronterizos, cuando sean establecidos, para mantener a la metapoblación existente y para establecer programas de conservación que involucren a perros salvajes en terrenos privados. La inversión en la expansión de la metapoblación deberá limitarse a reservas naturales propiedad del estado que estén dispuestas a absorber los costos de la depredación sin ser compensadas. [source] Patch Occupancy and Potential Metapopulation Dynamics of Three Forest Mammals in Fragmented Afromontane Forest in South AfricaCONSERVATION BIOLOGY, Issue 4 2000Michael J. Lawes We recorded patch occupancy of blue duiker ( Philantomba monticola), tree hyrax ( Dendrohyrax arboreus), and samango monkey (Cercopithecus mitis labiatus) in 199 forest patches. Their rarity is ascribed to the fragmentation and destruction of their forest habitat. Incidence functions, derived from presence and absence data, were formulated as generalized linear models, and environmental effects were included in the fitted logistic models. The small and mostly solitary hyrax and duiker persisted in smaller patches than the large and social monkey. Although this result follows expectations based on relative home-range sizes of each species, the incidence probability of the samango monkey was invariant with increasing isolation, whereas a gradual decrease with increasing isolation was observed for the hyrax and duiker. Group dynamics may inhibit dispersal and increase the isolation effect in social species such as samango monkeys. A mainland-island metapopulation model adequately describes patterns of patch occupancy by the hyrax and duiker, but the monkeys' poor dispersal ability and obvious area-dependent extirpation suggest that they exist in transient, nonequilibrium (declining) metapopulations. Through identification of large forest patches for careful protection and management, the survival of all three species,especially the monkey,could be prolonged. Because no functional metapopulation may exist for the monkey, however, this is an emergency measure. For the duiker and hyrax, larger patches should form part of a network of smaller and closer patches in a natural matrix. Resumen: Investigamos la persistencia de tres mamíferos forestales raros de tamaño mediano (2,9 kg) en los bosques fragmentados de cinturón de niebla Podocarpus en la región central de la provincia KwaZulu-Natal, Sudáfrica. Registramos la ocupación del duiker azul ( Philantomba monticola), el hyrax arborícola ( Dendrohyrax arboreus) y el mono samango (Cercopithecus mitis labiatus) en 199 parches forestales. Su rareza se atribuye a la fragmentación y destrucción de su hábitat forestal. Las funciones de incidencia, derivadas de datos de presencia y ausencia, fueron formuladas como modelos lineales generalizados, y los efectos ambientales fueron incluidos en los modelos logísticos ajustados. Los pequeños y mayormente solitarios hyrax y duiker persistieron en parches más pequeños que los monos, que son más grandes y más sociables. A pesar de que este resultado obedece a expectativas basadas en tamaños de rango de hogar relativos de cada especie, la probabilidad de incidencia del mono samango no cambió con un incremento en el aislamiento, mientras que una disminución gradual al crecer el aislamiento se observó en hyrax y duiker. Las dinámicas de grupos podrían inhibir la dispersión e incrementar el efecto de aislamiento en especies sociables como lo es el mono samango. Un modelo de metapoblación continente-isla describe adecuadamente los patrones de la ocupación de parches por hyrax y duiker; sin embargo, la pobre capacidad de dispersión de los monos y la obvia extirpación área-dependente sugiere que estos existen en metapoblaciones transitorias, desequilibradas (en disminución). Mediante la identificación de parches forestales grandes para la protección y manejo cuidadosos, la supervivencia de las tres especies ( pero especialmente la de los monos) podría ser prolongada. Sin embargo, debido a que no existen metapoblaciones funcionales de monos, esta es una medida de emergencia. Para el duiker y el hyrax, los parches grandes deberán formar parte de una red de parches más pequeños y más cercanos en una matriz natural. [source] Long-distance dispersal of seeds in the fire-tolerant shrub Banksia attenuataECOGRAPHY, Issue 4 2009Tianhua He Long-distance dispersal (LDD) of seeds enables alleles, individuals and species of plants to (re)colonize suitable but remote habitats. Banksia attenuata is a long-lived resprouting shrub restricted to dune crests in fire-prone sclerophyll shrublands of the Eneabba sandplain, southwestern Australia. Highly polymorphic microsatellite DNA genetic markers and population assignment tests were employed to identify LDD immigrants among 788 individuals from 27 stands of B. attenuata comprising a metapopulation. Of the 487 (61.8% of the total) individuals unambiguously assigned to a unique source population, 27 (5.5%) were identified as immigrants by assignment to a known population other than that from which they were sampled, while the remaining 460 were assigned to the population from which they were sampled. The distance between source and sink populations for these immigrants ranged from 0.2 to 2.6,km, averaging 1.4,km, and broadly trending in the direction of seasonal winds. These results suggest that B. attenuata has similar long-distance seed dispersal properties as its co-occurring shorter-lived and fire-sensitive congener, B. hookeriana, despite fewer, larger and less mobile seeds. The frequency and distance of LDD for seeds observed in both species (5.5,6.8%) helps explain the persistence of populations on these geographically isolated dunes, where they are subject to local extinction from recurrent fire and severe summer drought, and will remain important under predicted climate change conditions. Analysis also revealed that species richness of the functional group to which B. attenuata belongs was positively correlated with the number of immigrants identified per dune, and such correlation was likely driven by environmental properties of the dunes, particularly water availability. [source] Local host ant specificity of Phengaris (Maculinea) teleius butterfly, an obligatory social parasite of Myrmica antsECOLOGICAL ENTOMOLOGY, Issue 5 2010MAGDALENA WITEK 1. Phengaris butterflies are obligatory social parasites of Myrmica ants. Early research suggested that there is a different Myrmica host species for each of the five European Phengaris social parasites, but more recent studies have shown that this was an oversimplification. 2. The pattern of host ant specificity within a Phengaris teleius metapopulation from southern Poland is reported. A combination of studying the frequency distribution of Phengaris occurrence and morphometrics on adult butterflies were used to test whether use of different host species is reflected in larval development. 3. Phengaris teleius larvae were found to survive in colonies of four Myrmica species: M. scabrinodis, M. rubra, M. ruginodis, and M. rugulosa. Myrmica scabrinodis was the most abundant species under the host plant but the percentage of infested nests was similar to other host ant species at two sites and lower in comparison to nests of M. rubra and M. ruginodis at the other two sites. Morphometric measurements of adult butterflies reared by wild colonies of M. scabrinodis and M. ruginodis showed that wing size and number of wing spots were slightly greater for adults eclosing from nests of M. ruginodis. 4. Our results suggest that P. teleius in the populations studied is less specialised than previously suggested. The results are consistent with the hypothesis that P. teleius is expected to be the least specific of the European Phengaris species, as it has the largest and best defended fourth-instar caterpillars and, as a predatory species, it spends less time in the central larval chambers of the host colonies. The fact that individuals reared by M. ruginodis had wider hind wings may suggest that P. teleius had better access to resources in M. ruginodis than in M. scabrinodis colonies. [source] Dispersal and egg shortfall in Monarch butterflies: what happens when the matrix is cleaned up?ECOLOGICAL ENTOMOLOGY, Issue 1 2010MYRON P. ZALUCKI 1. We use an individual-based model describing the life of a monarch butterfly, which utilises milkweeds both aggregated in patches and scattered across the wider landscape as a substrate for laying eggs. The model simplifies the metapopulation of milkweed habitat patches by representing them as a proportion of the overall landscape, with the rest of the landscape considered matrix, which may contain some low density of milkweed plants. 2. The model simulates the number of eggs laid daily by a butterfly as it searches for hosts. The likelihood of finding hosts is related to the density of plants and the search ability of the butterfly. For an empty matrix, remaining in a habitat patch results in more eggs laid. However individuals that are good searchers have almost equivalent success without remaining in a habitat patch. These individuals are most affected by the presence of hosts in the matrix. 3. Given realistic values of habitat patch availability, our model shows that the presence of plants at a low density in the matrix has a substantial impact on the number of eggs laid; removing these plants can reduce lifetime potential fecundity by ca. 20%. These results have implications for monarch butterflies inhabiting agricultural landscapes, in which genetically modified soybean that is resistant to herbicides has resulted in the decimation of milkweeds over large areas. [source] Dynamics in a butterfly,plant,ant system: influence of habitat characteristics on turnover rates of the endangered lycaenid Maculinea alconECOLOGICAL ENTOMOLOGY, Issue 5 2007JAN CHRISTIAN HABEL Abstract 1.,Maculinea alcon, a myrmecophilic, stenotopic lycaenid butterfly is restricted to wet heathlands, bogs, and nutrient-poor hay meadows. Due to intensification of agriculture and decrease of extensively grazed meadows, many suitable habitats have disappeared and the remaining ones are highly fragmented and deteriorated. 2.,Historical distribution data and a comparison with the present occupation of patches show the decline of this critically endangered butterfly in north-west Germany. Most of the populations in north-west Germany are small and often geographically isolated. 3.,In summer 2002, two-thirds of 77 investigated potential patches were unoccupied as a result of unsuitable habitat structure and habitat fragmentation. 4.,Several habitat parameters were highly significantly correlated with the presence of M. alcon, in particular the distribution pattern of the host plant Gentiana pneumonanthe. Furthermore, butterflies were absent from many patches with an incidence probability below 50% with respect to patch size and isolation. 5.,In the nature reserve Lüneburger Heide, part of the study area, M. alcon populations have been observed since 1995. Typical turnover of local populations could be detected during these years. Extinctions and re-colonisations have stabilised the presence of this species in a metapopulation in this nature reserve. 6.,These data show the importance of different factors on different spatial levels influencing the presence of this endangered butterfly. [source] Dispersal ability and host-plant characteristics influence spatial population structure of monophagous beetlesECOLOGICAL ENTOMOLOGY, Issue 1 2005Matthew J. St Pierre Abstract., 1. Dispersal plays an integral role in determining spatial population structure and, consequently, the long-term survival of many species. Theoretical studies indicate that dispersal increases with population density and decreasing habitat stability. In the case of monophagous insect herbivores, the stability of host-plant populations may influence their spatial population structure. 2. The tallgrass prairie in Iowa, U.S.A. is highly fragmented and most prairie insects face a landscape with fewer habitat patches and smaller host-plant populations than 150 years ago, potentially making dispersal between patches difficult. Some herbivores, however, use native plant species with weedy characteristics that have increased in abundance because of disturbances. 3. Mark,recapture data and presence,absence surveys were used to examine dispersal and spatial population structure of two monophagous beetles with host plants that exhibit different population stability and have responded differently to fragmentation of tallgrass prairie. 4. Chrysochus auratus Fabricius exhibits a patchy population structure and has relatively large dispersal distances and frequencies. Its host plant is variable locally in time and space, but is more abundant than 150 years ago. The other species, Anomoea laticlavia Forster, exhibits a metapopulation or non-equilibrium population structure and has relatively small dispersal distances and frequencies. Its host-plant populations are stable in time and space. 5. The results indicate that dispersal ability of monophagous beetles reflects the life-history dynamics of their host plants, but the spatial population structure exhibited today is strongly influenced by how the host plants have responded to the fragmentation process over both time and space. [source] Meta-ecosystems: a theoretical framework for a spatial ecosystem ecologyECOLOGY LETTERS, Issue 8 2003Michel Loreau Abstract This contribution proposes the meta-ecosystem concept as a natural extension of the metapopulation and metacommunity concepts. A meta-ecosystem is defined as a set of ecosystems connected by spatial flows of energy, materials and organisms across ecosystem boundaries. This concept provides a powerful theoretical tool to understand the emergent properties that arise from spatial coupling of local ecosystems, such as global source,sink constraints, diversity,productivity patterns, stabilization of ecosystem processes and indirect interactions at landscape or regional scales. The meta-ecosystem perspective thereby has the potential to integrate the perspectives of community and landscape ecology, to provide novel fundamental insights into the dynamics and functioning of ecosystems from local to global scales, and to increase our ability to predict the consequences of land-use changes on biodiversity and the provision of ecosystem services to human societies. [source] FEMALE SOLDIER BEETLES DISPLAY A FLEXIBLE PREFERENCE FOR SELECTIVELY FAVORED MALE PHENOTYPESEVOLUTION, Issue 5 2005Denson Kelly Mclain Abstract In Georgia (USA) the soldier beetle, Chauliognathus pennsylvanicus (Coleoptera; Cantharidae), exhibits clinal variation in the length of the spot on its elytron. This suggests that the viability of phenotypes varies by habitat. Evidence of viability selection comes from within-site changes in the spot length distribution across a breeding season. When males with spots of intermediate length became less frequent, they became disproportionately less likely to mate, consistent with either a loss of vigor among remaining males or female rejection of disfavored phenotypes. Persistent, daily courtship by males provides females with the opportunity to track changes in male phenotype frequency and to exercise choice for phenotypes favored under natural selection. A laboratory experiment in which the frequency of one spot morph (long) or the other (short) was increased from 25% to 75% over a period of 30 days revealed that females possess a flexible preference that leads them to prefer whichever spot type has become more common over time. A haploid genetic model demonstrates that a flexible female preference for the locally favored male phenotype can be selected for when different viability alleles, genetically correlated with the male trait, are favored in different habitats that are linked by gene flow. Thus, migration between different kinds of habitat patches of a metapopulation could maintain the variation in male quality. This variation favors female choice for any trait that is directly or indirectly favored by natural selection. Such choice imparts positive frequency-dependent selection that could rapidly fix traits pleiotropically linked to viability. Rapid fixation would cause differentiation between populations of colonizing species as females exercise choice for mates favored under new ecological conditions. [source] THE EVOLUTION OF ENVIRONMENTAL AND GENETIC SEX DETERMINATION IN FLUCTUATING ENVIRONMENTSEVOLUTION, Issue 12 2003Tom J. M. Van Dooren Abstract Twenty years ago, Bulmer and Bull suggested that disruptive selection, produced by environmental fluctuations, can result in an evolutionary transition from environmental sex determination (ESD) to genetic sex determination (GSD). We investigated the feasibility of such a process, using mutation-limited adaptive dynamics and individual-based computer simulations. Our model describes the evolution of a reaction norm for sex determination in a metapopulation setting with partial migration and variation in an environmental variable both within and between local patches. The reaction norm represents the probability of becoming a female as a function of environmental state and was modeled as a sigmoid function with two parameters, one giving the location (i.e., the value of the environmental variable for which an individual has equal chance of becoming either sex) and the other giving the slope of the reaction norm for that environment. The slope can be interpreted as being set by the level of developmental noise in morph determination, with less noise giving a steeper slope and a more switchlike reaction norm. We found convergence stable reaction norms with intermediate to large amounts of developmental noise for conditions characterized by low migration rates, small differential competitive advantages between the sexes over environments, and little variation between individual environments within patches compared to variation between patches. We also considered reaction norms with the slope parameter constrained to a high value, corresponding to little developmental noise. For these we found evolutionary branching in the location parameter and a transition from ESD toward GSD, analogous to the original analysis by Bulmer and Bull. Further evolutionary change, including dominance evolution, produced a polymorphism acting as a GSD system with heterogamety. Our results point to the role of developmental noise in the evolution of sex determination. [source] COALESCENCE IN A METAPOPULATION WITH RECURRENT LOCAL EXTINCTION AND RECOLONIZATIONEVOLUTION, Issue 5 2003John R. Pannell Abstract Many species exist as metapopulations in balance between local population extinction and recolonization. The effect of these processes on average population differentiation, within-deme diversity, and specieswide diversity has been considered previously. In this paper, coalescent simulations of Slatkin's propagule-pool and migrant-pool models are used to characterize the distribution of neutral genetic diversity within demes (,s), diversity in the metapopulation a whole (TTT), the ratio FST= (,t,,S)/,T, Tajima's D statistic, and several ratios of gene-tree branch lengths. Using these distributions, power to detect differences in key metapopulation parameter values is determined under contrasting sampling regimes. The results indicate that it will be difficult to use sequence data from a single locus to detect a history of extinctions and recolonizations in a metapopulation because of high genealogical variance, the loss of diversity due to reductions in effective population size, and the fact that a genealogy of lineages from different demes under Slatkin's model differs from a neutral coalescent only in its time scale. Genetic indices of gene-tree shape that capture the effects of extinction/recolonization on both external branches and the length of the genealogy as a whole will provide the best indication of metapopulation dynamics if several lineages are sampled from several different demes. [source] A metapopulation model for the introgression from genetically modified plants into their wild relativesEVOLUTIONARY APPLICATIONS (ELECTRONIC), Issue 2 2009Patrick G. Meirmans Abstract Most models on introgression from genetically modified (GM) plants have focused on small spatial scales, modelling gene flow from a field containing GM plants into a single adjacent population of a wild relative. Here, we present a model to study the effect of introgression from multiple plantations into the whole metapopulation of the wild relative. The most important result of the model is that even very low levels of introgression and selection can lead to a high probability that the transgene goes to fixation in the metapopulation. Furthermore, the overall frequency of the transgene in the metapopulation, after a certain number of generations of introgression, depends on the population dynamics. If there is a high rate of migration or a high rate of population turnover, the overall transgene frequency is much higher than with lower rates. However, under an island model of population structure, this increased frequency has only a very small effect on the probability of fixation of the transgene. Considering these results, studies on the potential ecological risks of introgression from GM plants should look not only at the rate of introgression and selection acting on the transgene, but also at the metapopulation dynamics of the wild relative. [source] Metapopulation ecology in the sea: from Levins' model to marine ecology and fisheries scienceFISH AND FISHERIES, Issue 2 2004Jacob P Kritzer Abstract Marine and fisheries scientists are increasingly using metapopulation concepts to better understand and model their focal systems. Consequently, they are considering what defines a metapopulation. One perspective on this question emphasizes the importance of extinction probability in local populations. This view probably stems from the focus on extinction in Levins' original metapopulation model, but places unnecessary emphasis on extinction,recolonization dynamics. Metapopulation models with more complex structure than Levins' patch-occupancy model and its variants allow a broader range of population phenomena to be examined, such as changes in population size, age structure and genetic structure. Analyses along these lines are critical in fisheries science, where presence,absence resolution is far too coarse to understand stock dynamics in a meaningful way. These more detailed investigations can, but need not, aim to assess extinction risk or deal with extinction-prone local populations. Therefore, we emphasize the coupling of spatial scales as the defining feature of metapopulations. It is the degree of demographic connectivity that characterizes metapopulations, with the dynamics of local populations strongly dependent upon local demographic processes, but also influenced by a nontrivial element of external replenishment. Therefore, estimating rates of interpopulation exchange must be a research priority. We contrast metapopulations with other spatially structured populations that differ in the degree of local closure of their component populations. We conclude with consideration of the implications of metapopulation structure for spatially explicit management, particularly the design of marine protected area networks. [source] Myths and moderation in marine ,metapopulations'?FISH AND FISHERIES, Issue 1 2002R Kent Smedbol Abstract The metapopulation concept is appearing with increasing frequency in the marine population dynamics and genetics literature, though its applicability to marine systems remains an open question. Moreover, in recent years, the meaning of the term ,metapopulation' has become blurred, concomitant with its increasing use. In this paper, we summarize the concept of metapopulation dynamics and the associated theoretical assumptions. We call for a stricter definition and use of the term ,metapopulation', critically evaluate the applicability of metapopulation theory to marine population dynamics and its use in the related literature, and consider two published case-studies that investigate metapopulation structuring in specific marine populations. Finally, we urge scientists to carefully articulate what is meant by the term ,metapopulation' and to use appropriate citations in the primary literature to circumvent the potential for nebulous (and possibly damaging) conclusions in the future. [source] Spatial population structure of a specialist leaf-mining mothJOURNAL OF ANIMAL ECOLOGY, Issue 4 2008Sofia Gripenberg Summary 1The spatial structure of natural populations may profoundly influence their dynamics. Depending on the frequency of movements among local populations and the consequent balance between local and regional population processes, earlier work has attempted to classify metapopulations into clear-cut categories, ranging from patchy populations to sets of remnant populations. In an alternative, dichotomous scheme, local populations have been classified as self-sustaining populations generating a surplus of individuals (sources) and those depending on immigration for persistence (sinks). 2In this paper, we describe the spatial population structure of the leaf-mining moth Tischeria ekebladella, a specialist herbivore of the pedunculate oak Quercus robur. We relate moth dispersal to the distribution of oaks on Wattkast, a small island (5 km2) off the south-western coast of Finland. 3We build a spatially realistic metapopulation model derived from assumptions concerning the behaviour of individual moths, and show that the model is able to explain part of the variation in observed patterns of occurrence and colonization. 4While the species was always present on large trees, a considerable proportion of the local populations associated with small oaks showed extinction,recolonization dynamics. The vast majority of moth individuals occur on large trees. 5According to model predictions, the dominance of local vs. regional processes in tree-specific moth dynamics varies drastically across the landscape. Most local populations may be defined broadly as ,sinks', as model simulations suggest that in the absence of immigration, only the largest oaks will sustain viable moth populations. Large trees in areas of high oak density will contribute most to the overall persistence of the metapopulation by acting as sources of moths colonizing other trees. 6No single ,metapopulation type' will suffice to describe the oak,moth system. Instead, our study supports the notion that real populations are often a mix of earlier identified categories. The level to which local populations may persist after landscape modification will vary across the landscape, and sweeping classifications of metapopulations into single categories will contribute little to understanding how individual local populations contribute to the overall persistence of the system. [source] Lifetime reproductive success in relation to morphology in the house sparrow Passer domesticusJOURNAL OF ANIMAL ECOLOGY, Issue 4 2004Henrik Jensen Summary 1In this study we relate variation in lifetime reproductive success (LRS) of male and female house sparrows Passer domesticus to morphological characteristics. 2Our analyses demonstrated no sex-specific difference in the distribution of LRS. The variance in LRS was influenced mainly by variation in individual annual reproductive success, and to a lesser extent by variation in individual lifespan. 3Phenotypic traits explained a significant proportion of the variation in LRS in males, but not in females. The effect of male morphology on LRS operated mainly through an effect on the number of recruiting daughters. 4The size of the patch of black feathers on the chest of males (badge size) and male bill length were both positively associated with LRS. Lifespan and bill length were positively related and reproductive success increased with badge size. In females, number of recruiting daughters was positively related to bill length, body mass and body condition index due to the positive effect of these traits on annual production of daughters. 5These results indicate that identifying factors causing the large individual variation in LRS, which is likely to be closely related to fitness, will be important to understand microevolutionary processes in this metapopulation, and hence their demographic feedbacks. [source] Dynamics of regional coexistence for more or less equal competitorsJOURNAL OF ANIMAL ECOLOGY, Issue 1 2003C. Patrick Doncaster Summary 1Competition between two species in a metapopulation involves each inhibiting the other's ability firstly to colonize an already occupied area and then to persist in it. Models for regional competition of this kind have 3-D dynamics, from which it has proved difficult to extract useful predictions except for special conditions. We introduce a 2-D general model for species that are equally vigorous at inhibiting the ability of others to remain in an occupied patch as to arrive there. The model covers the full spectrum of competitive interactions, from weak to strong and symmetrical to asymmetrical. Its Lotka,Volterra dynamics extend the general theory of competitive coexistence by generating clear predictions for community structure, amenable to cross-system comparisons and experimental manipulations. 2Previous 2-D models of interactions between dominant and fugitive species are special cases of the 2-D general model. Moderately asymmetrical competition has two outcomes distinctly different from dominant,fugitive interactions, at both the scale of metapopulation and population: (i) slow growing and weak competitors coexist with faster growing superior competitors, albeit at reduced densities; and (b) habitat removal always yields relative gains in abundance for species with higher growth capacity, but the gains are absolute only for species subjected to competitive impacts that exceed within-species impacts. Extinctions of slow growing and weak competitors provide the most sensitive indication of habitat degradation, and their losses also have the least effect on community structure. 3The 2-D general model further predicts that highly productive communities will tolerate differences between species in their capacity for population growth, whereas less productive communities will tolerate stronger competitive interactions between species. This prediction applies equally to a population of resource consumers as to a metapopulation of colonists. The model explicitly links local and regional population dynamics to r,K selection in community structure by predicting a prevalence of growth-orientated species in resource-poor habitats and competition-orientated species in resource-rich habitats. [source] The equilibrium assumption in estimating the parameters of metapopulation modelsJOURNAL OF ANIMAL ECOLOGY, Issue 1 2000Atte Moilanen 1.,The construction of a predictive metapopulation model includes three steps: the choice of factors affecting metapopulation dynamics, the choice of model structure, and finally parameter estimation and model testing. 2.,Unless the assumption is made that the metapopulation is at stochastic quasi-equilibrium and unless the method of parameter estimation of model parameters uses that assumption, estimates from a limited amount of data will usually predict a trend in metapopulation size. 3.,This implicit estimation of a trend occurs because extinction-colonization stochasticity, possibly amplified by regional stochasticity, leads to unequal numbers of observed extinction and colonization events during a short study period. 4.,Metapopulation models, such as those based on the logistic regression model, that rely on observed population turnover events in parameter estimation are sensitive to the implicit estimation of a trend. 5.,A new parameter estimation method, based on Monte Carlo inference for statistically implicit models, allows an explicit decision about whether metapopulation quasi-stability is assumed or not. 6.,Our confidence in metapopulation model parameter estimates that have been produced from only a few years of data is decreased by the need to know before parameter estimation whether the metapopulation is in quasi-stable state or not. 7.,The choice of whether metapopulation stability is assumed or not in parameter estimation should be done consciously. Typical data sets cover only a few years and rarely allow a statistical test of a possible trend. While making the decision about stability one should consider any information about the landscape history and species and metapopulation characteristics. [source] Temporal and spatial genetic variation in a metapopulation of the annual Erysimum cheiranthoides on stony river banksJOURNAL OF ECOLOGY, Issue 1 2009Olivier Honnay Summary 1Metapopulation dynamics , the recurrent extinction and colonization in spatially discrete habitats , is expected to strongly affect within and between population genetic diversity. So far, however, accounts of true plant metapopulations are extremely scarce. 2We monitored the colonization and extinction dynamics of an assemblage of populations of the annual Erysimum cheiranthoides on stony river banks during three consecutive years. Each year, winter flooding drives some populations to extinction, while vacant banks may become colonized. We describe the dynamics of these ephemeral populations using amplified fragment length polymorphism (AFLP) markers to quantify changes in the metapopulation genetic structure over time, and assessing the direction and relative amount of migration and colonization events. 3Average extinction and colonization rates were high (0.39 and 0.34, respectively). While population genetic differentiation (FST) tripled from 0.06 in 2005 to 0.17 in 2007, total metapopulation genetic diversity remained fairly constant through the years. Genetic assignment analyses allowed assigning more than 50% of the genotyped individuals to populations extant the year before. Colonizing individuals originated from different source populations (, << 1) and there was considerable evidence of upstream seed dispersal. 4The degree and pattern of spatial genetic structure varied between years and was related to variation in the flooding intensity of the Meuse River through the years. Possibly, activation of the soil seed bank also played a role in structuring the genetic make-up of the populations. 5Because migration and colonization events were qualitatively equal, and colonizing individuals originated from different sources, the increase in FST was in agreement with previous theoretical work. Very high migration and colonization rates, and the short monitoring period, may explain why there was no loss of genetic diversity from the metapopulation through recurrent extinction and colonization events. 6Synthesis. This study gives one of the first accounts of the dynamics of a true plant metapopulation. Temporal monitoring of genetic variation gave evidence of extensive and bidirectional seed dispersal, highly variable and increasing genetic differentiation, and rather constant within population genetic diversity. An important suggestion from this research is to include a dormant seed stage in further theoretical work on (meta) population genetics. [source] Spatially heterogeneous stochasticity and the adaptive diversification of dormancyJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 10 2009E. Rajon Abstract Diversified bet-hedging, a strategy that leads several individuals with the same genotype to express distinct phenotypes in a given generation, is now well established as a common evolutionary response to environmental stochasticity. Life-history traits defined as diversified bet-hedging (e.g. germination or diapause strategies) display marked differences between populations in spatial proximity. In order to find out whether such differences can be explained by local adaptations to spatially heterogeneous environmental stochasticity, we explored the evolution of bet-hedging dormancy strategies in a metapopulation using a two-patch model with patch differences in stochastic juvenile survival. We found that spatial differences in the level of environmental stochasticity, restricted dispersal, increased fragmentation and intermediate survival during dormancy all favour the adaptive diversification of bet-hedging dormancy strategies. Density dependency also plays a major role in the diversification of dormancy strategies because: (i) it may interact locally with environmental stochasticity and amplify its effects; however, (ii) it can also generate chaotic population dynamics that may impede diversification. Our work proposes new hypotheses to explain the spatial patterns of bet-hedging strategies that we hope will encourage new empirical studies of this topic. [source] Detecting local adaptation in a natural plant,pathogen metapopulation: a laboratory vs. field transplant approachJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 5 2007ANNA-LIISA LAINE Abstract Antagonistic coevolution between hosts and parasites in spatially structured populations can result in local adaptation of parasites. Traditionally parasite local adaptation has been investigated in field transplant experiments or in the laboratory under a constant environment. Despite the conceptual importance of local adaptation in studies of (co)evolution, to date no study has provided a comparative analysis of these two methods. Here, using information on pathogen population dynamics, I tested local adaptation of the specialist phytopathogen, Podosphaera plantaginis, to its host, Plantago lanceolata at three different spatial scales: sympatric host population, sympatric host metapopulation and allopatric host metapopulations. The experiment was carried out as a field transplant experiment with greenhouse-reared host plants from these three different origins introduced into four pathogen populations. In contrast to results of an earlier study performed with these same host and parasite populations under laboratory conditions, I did not find any evidence for parasite local adaptation. For interactions governed by strain-specific resistance, field studies may not be sensitive enough to detect mean parasite population virulence. Given that parasite transmission potential may be mediated by the abiotic environment and genotype-by-environment interactions, I suggest that relevant environmental variation should be incorporated into laboratory studies of parasite local adaptation. [source] Spatial scale of local adaptation in a plant-pathogen metapopulationJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 4 2005A.-L. LAINE Abstract The rate and scale of gene flow can strongly affect patterns of local adaptation in host,parasite interactions. I used data on regional pathogen occurrence to infer the scale of pathogen dispersal and to identify pathogen metapopulations in the interaction between Plantago lanceolata and its specialist phytopathogen, Podosphaera plantaginis. Frequent extinctions and colonizations were recorded in the metapopulations, suggesting substantial gene flow at this spatial scale. The level of pathogen local adaptation was assessed in a laboratory inoculation experiment at three different scales: in sympatric host populations, in sympatric host metapopulations and in allopatric host metapopulations. I found evidence for adaptation to sympatric host populations, as well as evidence indicating that local adaptation may extend to the scale of the sympatric host metapopulation. There was also variation among the metapopulations in the degree of pathogen local adaptation. This may be explained by regional differences in the rate of migration. [source] Spatio-temporal variation in the strength and mode of selection acting on major histocompatibility complex diversity in water vole (Arvicola terrestris) metapopulationsMOLECULAR ECOLOGY, Issue 1 2009MATTHEW K. OLIVER Abstract Patterns of spatio-temporal genetic variation at a class II major histocompatibility complex (MHC) locus and multiple microsatellite loci were analysed within and between three water vole metapopulations in Scotland, UK. Comparisons of MHC and microsatellite spatial genetic differentiation, based on standardised tests between two demographically asynchronous zones within a metapopulation, suggested that spatial MHC variation was affected by balancing selection, directional selection and random genetic drift, but that the relative effects of these microevolutionary forces vary temporally. At the metapopulation level, between-year differentiation for MHC loci was significantly correlated with that of microsatellites, signifying that neutral factors such as migration and drift were primarily responsible for overall temporal genetic change at the metapopulation scale. Between metapopulations, patterns of genetic differentiation implied that, at large spatial scales, MHC variation was primarily affected by directional selection and drift. Levels of MHC heterozygosity in excess of Hardy,Weinberg expectations were consistent with overdominant balancing selection operating on MHC variation within metapopulations. However, this effect was not constant among all samples, indicating temporal variation in the strength of selection relative to other factors. The results highlight the benefit of contrasting variation at MHC with neutral markers to separate the effects of stochastic and deterministic microevolutionary forces, and add to a growing body of evidence showing that the mode and relative strength of selection acting on MHC diversity varies both spatially and temporally. [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] Maintenance of genetic variation in plants and pathogens involves complex networks of gene-for-gene interactionsMOLECULAR PLANT PATHOLOGY, Issue 4 2009SHARON A. HALL SUMMARY The RPP13 [recognition of Hyaloperonospora arabidopsidis (previously known as Peronospora parasitica)] resistance (R) gene in Arabidopsis thaliana exhibits the highest reported level of sequence diversity among known R genes. Consistent with a co-evolutionary model, the matching effector protein ATR13 (A. thaliana -recognized) from H. arabidopsidis reveals extreme levels of allelic diversity. We isolated 23 new RPP13 sequences from a UK metapopulation, giving a total of 47 when combined with previous studies. We used these in functional studies of the A. thaliana accessions for their resistance response to 16 isolates of H. arabidopsidis. We characterized the molecular basis of recognition by the expression of the corresponding ATR13 genes from these 16 isolates in these host accessions. This allowed the determination of which alleles of RPP13 were responsible for pathogen recognition and whether recognition was dependent on the RPP13/ATR13 combination. Linking our functional studies with phylogenetic analysis, we determined that: (i) the recognition of ATR13 is mediated by alleles in just a single RPP13 clade; (ii) RPP13 alleles in other clades have evolved the ability to detect other pathogen ATR protein(s); and (iii) at least one gene, unlinked to RPP13 in A. thaliana, detects a different subgroup of ATR13 alleles. [source] Population genetic structure of Plasmopara viticola in the Western Cape Province of South AfricaMOLECULAR PLANT PATHOLOGY, Issue 6 2007TREVOR KOOPMAN SUMMARY Plasmopara viticola populations in South Africa were studied for two consecutive grape growing seasons, in an organically managed and a conventional fungicide-sprayed vineyard. Three to four samplings in each season were genotyped with four microsatellite markers (GOB, CES, ISA and BER). Population differentiation (Fst) between the conventional fungicide-sprayed vineyard and organically managed vineyard was low (0.004 and 0.016) in both growing seasons, suggesting one metapopulation. However, differences in the relative contribution of the predominant and new genotypes to epidemics in the two vineyards suggested that fungicide applications may have selected for reduced pathogen diversity. In both years and vineyards, sexual (oosporic) reproduction and/or migration occurred throughout the year and contributed between 12 and 74% to the epidemic. Hardy,Weinberg analyses suggest that South African P. viticola populations are randomly mating. Epidemics in both years and vineyards were dominated by one or two genotypes that each contributed between 14 and 67% to the epidemic through asexual reproduction. The remaining genotypes showed low levels of asexual reproduction, with most genotypes never being able to reproduce asexually. However, for some genotypes asexual reproduction was important, as it enabled survival of the genotypes from one season to the next. In total, ten genotypes were able to survive asexually or vegetatively from one season to the next. The populations were further characterized by the presence of a high frequency of isolates that most likely have elevated ploidy levels. [source] Metapopulation dynamics across gradients , the relation between colonization and extinction in shaping the range edgeOIKOS, Issue 10 2009Beáta Oborny We study the dynamics of a metapopulation in which the rates of colonization and/or extinction change along an environmental gradient. Spatially explicit simulations are applied to compare two cases: in parent-dependent colonization (PDC) the rate of colonization is limited by the production of new individuals; in offspring-dependent colonization (ODC) it is limited by the success of establishment of the offspring. Thus, PDC depends on the quality of the parent's site, while ODC is dependent on the offspring's site. We combine PDC and ODC in a spatially implicit model. We study the steady-state distribution of a metapopulation, and ask whether the local densities of occupied sites at each position x along the gradient could be predicted from the local rates of colonization c(x) and extinction e(x). This prediction is not trivial, since the sites are connected, enabling a flow of individuals from more favorable to less favorable sites. The results show that at ODC a single parameter, c(x)/e(x), is sufficient for the prediction. Therefore, different species and geographic regions can be directly compared by appropriate rescaling: choosing the local average lifetime of occupancy, 1/e(x), for a time unit at each point along the gradient. This permits generalizations about the shape of range edges, and can help to predict the position of the boundary of a species' distribution. At PDC, rescaling is not possible: the whole profile of c(x) and e(x) along the gradient has to be taken into consideration. Nevertheless, rescaling gives a good approximation when the parent-dependent component of colonization does not change abruptly across space. [source] Which traits promote persistence of feral GM crops?OIKOS, Issue 1 2005Part 2: implications of metapopulation structure Transgenes may spread from crops into the environment via the establishment of feral populations, often initiated by seed spill from transport lorries or farm machinery. Locally, such populations are often subject to large environmental variability and usually do not persist longer than a few years. Because secondary feral populations may arise from seed dispersal to adjacent sites, the dynamics of such populations should be studied in a metapopulation context. We study a structured metapopulation model with local dispersal, mimicking a string of roadside subpopulations of a feral crop. Population growth is assumed to be subject to local disturbances, introducing spatially random environmental stochasticity. Our aim is to understand the role of dispersal and environmental variability in the dynamics of such ephemeral populations. We determine the effect of dispersal on the extinction boundary and on the distribution of persistence times, and investigate the influence of spatially correlated disturbances as opposed to spatially random disturbances. We find that, given spatially random disturbances, dispersal slows down the decline of the metapopulation and results in the occurrence of long-lasting local populations which remain more or less static in space. We identify which life history traits, if changed by genetic modification, have the largest impact on the population growth rate and persistence times. For oilseed rape, these are seed bank survival and dormancy. Combining our findings with literature data on transgene-induced life history changes, we predict that persistence is promoted by transgenes for oil-modifications (high stearate or high laurate) and, possibly, for insect resistence (Bt). Transgenic tolerance to glufosinate herbicide is predicted to reduce persistence. 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