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Component Population (component + population)
Selected AbstractsMINIMAL SELFING, FEW CLONES, AND NO AMONG-HOST GENETIC STRUCTURE IN A HERMAPHRODITIC PARASITE WITH ASEXUAL LARVAL PROPAGATIONEVOLUTION, Issue 3 2006Charles D. Criscione Abstract Little is known about actual mating systems in natural populations of parasites or about what constitutes the limits of a parasite deme. These parameters are interesting because they affect levels of genetic diversity, opportunities for local adaptation, and other evolutionary processes. We expect that transmission dynamics and the distribution of parasites among hosts should have a large effect on mating systems and demic structure, but currently we have mostly speculation and very few data. For example, infrapopulations (all the parasites in a single host) should behave as demes if parasite offspring are transmitted as a clump from host to host over several generations. However, if offspring are well mixed, then the parasite component population (all the parasites among a host population) would function as the deme. Similarly, low mean intensities or a high proportion of worms in single infections should increase the selfing rate. For species having an asexual amplification stage, transmission between intermediate and definitive (final) hosts will control the variance in clonal reproductive success, which in turn could have a large influence on effective sizes and rates of inbreeding. We examined demic structure, selfing rates, and the variance in clonal reproductive success in natural populations of Plagioporus shawi, a hermaphroditic trematode that parasitizes salmon. Overall levels of genetic diversity were very high. An a posteriori inference of population structure overwhelmingly supports the component population as the deme, rather than individual infrapopulations. Only a single pair of 597 adult individuals was identified as clones. Thus, the variance in clonal reproductive success was almost zero. Despite being hermaphroditic, P. shawi appears to be almost entirely outcrossing. Genetic estimates of selfing (<5%) were in accordance with the proportion of parasites from single infections. Thus, it appears that individual flukes outcross whenever possible and only resort to selfing when alone. Finally, our data support the hypothesis that aquatic transmission and the use of several intermediate hosts promotes high genetic diversity and well-mixed infrapopulations. [source] Cover Picture: Fabrication of Multicomponent Microsystems by Directed Three-Dimensional Self-Assembly (Adv. Funct.ADVANCED FUNCTIONAL MATERIALS, Issue 5 2005Mater. Abstract Directed three-dimensional self-assembly to assemble and package integrated semiconductor devices is demonstrated by Jacobs and Zheng on p.,732. The self-assembly process uses geometrical shape recognition to identify different components and surface-tension between liquid solder and metal-coated areas to form mechanical and electrical connections. The components (top left) self-assemble in a turbulent flow (center) and form functional multi-component microsystems (bottom right) by sequentially adding parts to the assembly solution. The technique provides, for the first time, a route to enable the realization of three-dimensional heterogeneous microsystems that contain non-identical parts, and connecting them electrically. We have developed a directed self-assembly process for the fabrication of three-dimensional (3D) microsystems that contain non-identical parts and a statistical model that relates the process yield to the process parameters. The self-assembly process uses geometric-shape recognition to identify different components, and surface tension between liquid solder and metal-coated areas to form mechanical and electrical connections. The concept is used to realize self-packaging microsystems that contain non-identical subunits. To enable the realization of microsystems that contain more than two non-identical subunits, sequential self-assembly is introduced, a process that is similar to the formation of heterodimers, heterotrimers, and higher aggregates found in nature, chemistry, and chemical biology. The self-assembly of three-component assemblies is demonstrated by sequentially adding device segments to the assembly solution including two hundred micrometer-sized light-emitting diodes (LEDs) and complementary metal oxide semiconductor (CMOS) integrated circuits. Six hundred AlGaInP/GaAs LED segments self-assembled onto device carriers in two minutes, without defects, and encapsulation units self-assembled onto the LED-carrier assemblies to form a 3D circuit path to operate the final device. The self-assembly process is a well-defined statistical process. The process follows a first-order, non-linear differential equation. The presented model relates the progression of the self-assembly and yield with the process parameters,component population and capture probability,that are defined by the agitation and the component design. [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] The role of genotypic diversity in determining grassland community structure under constant environmental conditionsJOURNAL OF ECOLOGY, Issue 5 2007RAJ WHITLOCK Summary 1A recent experiment varied the genetic diversity of model grassland communities under standardized soil and management conditions and at constant initial species diversity. After 5 years' growth, genetically diverse communities retained more species diversity and became more similar in species composition than genetically impoverished communities. 2Here we present the results of further investigation within this experimental system. We proposed that two mechanisms , the first invoking genetically determined and constant differences in plant phenotypes and the second invoking genotype,environment interactions , could each underpin these results. This mechanistic framework was used as a tool to interpret our findings. 3We used inter-simple sequence repeat (ISSR) DNA markers to confirm which of the individuals of six study species initially included in the model communities were unique genotypes. We then used the molecular markers to assess the survival and abundance of each genotype at the end of the 5-year experimental period. 4The DNA marker data were used to create, for the first time, a genotype abundance hierarchy describing the structure of a community at the level of genotypes. This abundance hierarchy revealed wide variation in the abundance of genotypes within species, and large overlaps in the performance of the genotypes of different species. 5Each genotype achieved a consistent level of abundance within genetically diverse communities, which differed from that attained by other genotypes of the same species. The abundance hierarchy of genotypes within species also showed consistency across communities differing in their initial level of genetic diversity, such that species abundance in genetically impoverished communities could be predicted, in part, by genotypic identity. 6Three species (including two canopy-dominants) experienced shifts in their community-level genotype abundance hierarchies that were consistent with an increased influence of genotype,environment interactions in genetically impoverished communities. 7Our results indicate that under relatively constant environmental conditions the species abundance structure of plant communities can in part be predicted from the genotypic composition of their component populations. Genotype,environment interactions also appear to shape the structure of communities under such conditions, although further experiments are needed to clarify the magnitude and mechanism of these effects. [source] Phenotypic tradeoffs between egg number and egg size in three parasitic anisakid nematodesOIKOS, Issue 10 2007M. Victoria Herreras Phenotypic tradeoffs between number and size of eggs were tested in three component populations of three marine anisakid nematodes: Anisakis simplex, Pseudoterranova decipiens and Contracaecum osculatum. Body and uterine volumes (as proxies of female size), and egg number, mean egg volume and clutch volume (as descriptors of reproductive output) were measured in 50 females of each species. Evidence of a phenotypic tradeoff was detected only in A. simplex; the first time that has been found in a parasite population. Comparison of feasible values inferred from the van Noordwijk and de Jong's model and current data showed that interindividual variation in egg size was narrower than expected in the three populations. Structural constrictions in response to optimal allocation rules might account for this pattern. In P. decipiens and C. osculatum variation in egg size was the lowest and independent of female size, suggesting that the tradeoff is absent, rather than being present but masked by unaccounted variables. Spatial constrictions imposed by uterine size seemed to play an important role determining the emergence of the tradeoffs. So factors accounting for the tradeoff in A. simplex are probably constructional rather than physiological. Individual variability in investment in clutch volume was similar to previous studies but variation in allocation between number and size of eggs was much smaller than that reported previously. Perhaps differences in life-history strategies might explain this because the nematodes studied are either semelparous or short-lived iteroparus organisms whereas previous data derive from long-lived iteroparous ones. Despite the perception that parasites live in resource-rich habitats, the present study indicates that patterns relating number and size of eggs might not differ much from those observed in free-living populations and thus the same range of factors would operate in both types of organisms. [source] | ||||||||||