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11 results for “meta-populations”

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zenodo40/100

figure 1 in Spatial genetic structure in the Eurasian otter (Lutra lutra) meta-population from its core range in Italy

figure 1 The area surveyed for collection of otter samples (40° 40' N, 39° 37' N). Red spots indicate the location of the collected samples. The blue lines highlight the main rivers (order 1) and their tributaries (order 2, 3 and 4 according to waterway hierarchy). The continuous red lines represent regional boundaries. In the inset, the current otter distribution (inferred from Balestrieri et al., 2016, modified) is reported in orange and the study area is defined by the black bold square.

opencc-by-4.0Aug 2020View details →
zenodo40/100

figure 4 in Spatial genetic structure in the Eurasian otter (Lutra lutra) meta-population from its core range in Italy

figure 4 Principal Component Analysis (pca) performed on microsatellite genotypes (dots). Circles show the well-defined spatial groups. A) pca according to the belonging of genotypes to the six river basins: the Cilento basin (green dots); the Agri basin (pink dots); the Sinni basin (blue dots); the Lao basin (red dots); the Basento basin (orange dots); the Abatemarco basin (violet dots); black dots indicate the samples outside of the main river basins. Dashed line indicates geographically contiguous but genetically different genotypes. B) pca according to clusters inferred by STRUCTURE: genotypes assigned unambiguously to K2 (green dots), to K3 (yellow dots), to K5 (violet dots). Grey dots represent samples with mixed genotypes assignable to K1 and K4.

opencc-by-4.0Aug 2020View details →
zenodo40/100

figure 3 in Spatial genetic structure in the Eurasian otter (Lutra lutra) meta-population from its core range in Italy

figure 3 Genetic structure and distribution of the Italian otter genotypes in the study area. A) Estimated population structure based on the analysis of 11 microsatellite loci according to STRUCTURE (K = 5). Each bar represents a sample analysed. B) Geographic visualisation of genotypes in the study area performed using QGIS 3.4.1 software with base layers acquired from http://www.pnc.miniambiente. it/. Each circle represents a sample analysed. The colours indicate the percentage of assignment of an individual to each cluster: in blue, K1; in green, K2; in orange, K3; in red, K4; in violet, K5. The bold blue lines highlight the main rivers, while the tiny blue lines show all other waterways.

opencc-by-4.0Aug 2020View details →
zenodo40/100

figure 6 Mantel test for A in Spatial genetic structure in the Eurasian otter (Lutra lutra) meta-population from its core range in Italy

figure 6 Mantel test for A) the correlation between geographic distance (GGDsq) and genetic distance (LinGD) (Rxy = 0.264, P = 0.0001) and for B) the correlation between resistance distance (a measure of ecological distance) (ECO500) and LinGD (Rxy = 0.217, P = 0.0001).

opencc-by-4.0Aug 2020View details →
dryad36/100

Data from: Multi-generation genetic contributions of immigrants reveal cryptic elevated and sex-biased effective gene flow within a natural meta-population

<p>Impacts of immigration on micro-evolution and population dynamics fundamentally depend on net rates and forms of resulting gene flow into recipient populations. Yet, the degrees to which observed rates and sex ratios of physical immigration translate into multi-generational genetic legacies have not been explicitly quantified in natural meta-populations, precluding inference on how movements translate into effective gene flow and eco-evolutionary outcomes. Our analyses of three decades of complete song sparrow (<em>Melospiza melodia</em>) pedigree data show that multi-generational genetic contributions from regular natural immigrants substantially exceeded those from contemporary natives, consistent with heterosis-enhanced introgression. Further, while contributions from female immigrants exceeded those from female natives by up to three-fold, male immigrants' lineages typically went locally extinct soon after arriving. Both the overall magnitude, and the degree of female bias, of effective gene flow therefore greatly exceeded those which would be inferred from observed physical arrivals, reshaping the eco-evolutionary implications of immigration.</p>

opencc-zeroDec 2023View details →
dryad36/100

Data from: Multi-generation genetic contributions of immigrants reveal cryptic elevated and sex-biased effective gene flow within a natural meta-population

Open the record for dataset details and reuse information.

publicJan 2024View details →
dryad36/100

Local sub-population dynamics of a Central European Grey Partridge meta-population support a large-scale conservation approach to halt its ongoing decline

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publicSep 2024View details →
dryad32/100

Data from: Tigers in the Terai: strong evidence for meta-population dynamics contributing to tiger recovery and conservation in the Terai Arc Landscape

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publicMar 2018View details →
zenodo28/100

figure 5 in Spatial genetic structure in the Eurasian otter (Lutra lutra) meta-population from its core range in Italy

figure 5 Cumulative current map, based on all possible pairs of sampling locations, representing the amount of current flowing through each pixel. Higher current flow represents higher connectivity, and vice versa.

opencc-by-4.0Aug 2020View details →
zenodo28/100

figure 2 in Spatial genetic structure in the Eurasian otter (Lutra lutra) meta-population from its core range in Italy

figure 2 Definition of the six main river basins by drawing a buffer area of 1 km around all waterways connected to the main rivers: in green, the Cilento basin; in pink, the Agri basin; in blue, the Sinni basin; in red, the Lao basin; in orange, the Basento basin; in violet, the Abatemarco basin. Red spots indicate the location of the collected samples. The bold blue lines highlight the main rivers, while the tiny blue lines show all other waterways.

opencc-by-4.0Aug 2020View details →
zenodo24/100

Meta-population structure and the evolutionary transition to multicellularity

<p>The evolutionary transition to multicellularity has occurred on numerous occasions, but transitions to complex life forms are rare. While the reasons are unclear, relevant factors include the intensity of within- versus between-group selection that are likely to shape the course of life cycle evolution. A highly structured environment eliminates the possibility of mixing between evolving lineages, thus ensuring strong competition between groups. Less structure intensifies competition within groups, decreasing opportunity for group-level evolution. Here, using populations of the bacterium <em>Pseudomonas fluorescens</em>, we report the results of experiments that explore the effect of lineage mixing on the evolution of nascent multicellular groups. Groups were propagated under regimes requiring reproduction via a life cycle replete with developmental and dispersal (propagule) phases, but in one treatment lineages never mixed, whereas in a second treatment, cells from different lineages experienced intense competition during the dispersal phase. The latter treatment favoured traits promoting cell growth at the expense of traits underlying group fitness, a finding that is supported by results from a mathematical model. Together our results show that the transition to multicellularity benefits from ecological conditions that maintain discreteness not just of the group (soma) phase, but also of the dispersal (germline) phase.</p>

opencc-by-4.0Oct 2018View details →

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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OpenNeuro

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