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159 results for “genetic heterogeneity”

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zenodo28/100

Figure 7 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)

Figure 7. Eucyclops taiwanensis sp. n., female, ZIN RN 55090 (holotype): (A) P1; (B) P2; (C) P3; (D) P4; caudal side; Scale bar: 100 μm.

opencc-by-4.0Jun 2015View details →
zenodo28/100

Figure 6 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)

Figure 6. Eucyclops taiwanensis sp. n., female, ZIN RN 55090 (holotype): (A) antenna; (B) mandible; (C) maxillula; (D) maxilla; (E) maxilliped. Scale bar: A = 67 μm, B–E = 50 μm.

opencc-by-4.0Jun 2015View details →
zenodo28/100

Figure 5 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)

Figure 5. Eucyclops taiwanensis sp. n., female, ZIN RN 55090 (holotype): (A) habitus, dorsal; (B) urosome with P5, ventral side; (C) antennule with aesthetascs indicated by arrows; (D) hyaline membrane on segments 10–12 of antennule. Scale bar: A = 150 μm; B = 100 μm, C = 75 μm; D =37 μm.

opencc-by-4.0Jun 2015View details →
zenodo28/100

Figure 4 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)

Figure 4. Distribution of Eucyclops serrulatus (Fischer) females from different localities on the base of caudal rami index INseta/OUTseta, and P4 exo Lseg/Sp1 (see Table 4 and text). Populations from Dniester Liman; Zakarpattia region; and from the type locality in Orlov Pond, Saint Petersburg: individuals from Orlov Pond resembling the Zakarpattia population ▲; individuals from Orlov Pond resembling Dniester Liman ♦ and individuals from Orlov Pond ○ looking like hybrids between the two Ukrainian populations.

opencc-by-4.0Jun 2015View details →
zenodo28/100

Figure 1 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)

Figure 1. The localities of the Eucyclops serrulatus (Fischer) and Eucyclops taiwanensis sp. n., populations studied. Locality names are listed in Table 1.

opencc-by-4.0Jun 2015View details →
zenodo28/100

Figure 2 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)

Figure 2. Phylogenetic tree constructed based on data from mitochondrial cytochrome c oxidase subunit I (CO1) region (651 bp) by the Bayesian method using the TPM1uf +G model. Numbers beside nodes indicate Bayesian posterior probabilities (BPP) and bootstrap values. Clade 1 includes sequences of Eucyclops serrulatus (Fischer) from the Zakarpattia region of Ukraine, Orlov Pond and Tavricheskii Pond in Saint Petersburg, Creteil Lake in Paris and the pond in Oslo; Clade 2: Eucyclops serrulatus sequences from the Dniester Liman in Ukraine, Orlov Pond in Saint Petersburg and Central Russia (Udmurtia). Clade 3: Eucyclops taiwanensis sp. n. sequences from ponds in Taiwan. Clade 4: Eucyclops cf. serrulatus sequences from the Xucar River in Spain.

opencc-by-4.0Jun 2015View details →
dryad28/100

Evolutionary stability, landscape heterogeneity, and human land-usage shape population genetic connectivity in the Cape Floristic Region biodiversity hotspot

<p>As human-induced change eliminates natural habitats, it impacts genetic diversity and population connectivity for local biodiversity. The South African Cape Floristic Region (CFR) is the most diverse extratropical area for plant biodiversity, and much of its habitat is protected as a UNESCO World Heritage site. There has long been great interest in explaining the underlying factors driving this unique diversity, especially as much of the CFR is endangered by urbanization and other anthropogenic activity. Here, we use a population and landscape genetic analysis of SNP data from the CFR endemic plant <i>Leucadendron salignum</i> or "common sunshine conebush" as a model to address the evolutionary and environmental factors shaping the vast CFR diversity. We found that high population structure, along with relatively deeper and older genealogies, are characteristic of the southwestern CFR, whereas, low population structure and more recent lineage coalescence depicts the eastern CFR. Population network analyses show genetic connectivity is facilitated in areas of lower elevation and higher seasonal precipitation. These population genetic signatures corroborate CFR species-level patterns consistent with high Pleistocene biome stability and landscape heterogeneity in the southwest, but with coincident instability in the east. Finally, we also find evidence of human land-usage as a significant gene flow barrier, especially in severely-threatened lowlands where genetic connectivity has been historically the highest. These results help identify areas where conservation plans can prioritize protecting high genetic diversity threatened by contemporary human activities within this unique cultural UNESCO site.</p>

opencc-zeroDec 2020View details →
dryad28/100

Data from: Quantitative genetic variance in experimental fly populations evolving with or without environmental heterogeneity

Heterogeneous environments are typically expected to maintain more genetic variation in fitness within populations than homogeneous environments. However, the accuracy of this claim depends on the form of heterogeneity as well as the genetic basis of fitness traits and how similar the assay environment is to the environment of past selection. Here we measure quantitative genetic variance for three traits important for fitness using replicated experimental populations of Drosophila melanogaster evolving under four selective regimes: constant salt-enriched medium (Salt), constant cadmium-enriched medium (Cad), and two heterogeneous regimes that vary either temporally (Temp) or spatially (Spatial). As theory predicts, we found that Spatial populations tend to harbor more genetic variation than Temp populations or those maintained in a constant environment that is the same as the assay environment. Contrary to expectation, Salt populations tend to have more genetic variation than Cad populations in both assay environments. We discuss the patterns for quantitative genetic (QG) variances across regimes in relation to previously reported data on genome-wide sequence diversity. For some traits, the QG patterns are similar to the diversity patterns of ecological selected SNPs whereas the QG patterns for some other traits resembled that of neutral SNPs.

opencc-zeroDec 2014View details →
dryad28/100

Data from: Detecting spatial genetic signatures of local adaptation in heterogeneous landscapes

The spatial structure of the environment (e.g., the configuration of habitat patches) may play an important role in determining the strength of local adaptation. However, previous studies of habitat heterogeneity and local adaptation have largely been limited to simple landscapes, which poorly represent the multi-scale habitat structure common in nature. Here, we use simulations to pursue two goals: (1) we explore how landscape heterogeneity, dispersal ability, and selection affect the strength of local adaptation, and (2) we evaluate the performance of several genotype-environment association (GEA) methods for detecting loci involved in local adaptation. We found that the strength of local adaptation increased in spatially aggregated selection regimes, but remained strong in patchy landscapes when selection was moderate to strong. Weak selection resulted in weak local adaptation that was relatively unaffected by landscape heterogeneity. In general, the power of detection methods closely reflected levels of local adaptation. False positive rates (FPRs), however, showed distinct differences across GEA methods based on levels of population structure. The univariate GEA approach had high FPRs (up to 55%) under limited dispersal scenarios, due to strong isolation by distance. By contrast, multivariate, ordination-based methods had uniformly low FPRs (0-2%), suggesting these approaches can effectively control for population structure. Specifically, constrained ordinations had the best balance of high detection and low FPRs, and will be a useful addition to the GEA toolkit. Our results provide both theoretical and practical insights into the conditions that shape local adaptation and how these conditions impact our ability to detect selection.

opencc-zeroDec 2014View details →
dryad28/100

Data from: Genome-wide association analysis for blood lipid traits measured in three pig populations revealed a substantial level of genetic heterogeneity

Serum lipids are associated with myocardial infarction and cardiovascular disease in humans. Here we dissected the genetic architecture of blood lipid traits by applying genome-wide association studies (GWAS) in 1,256 pigs from Laiwu, Erhualian and Duroc × (Landrace × Yorkshire) populations, and a meta-analysis of GWAS in more than 2,400 pigs from five diverse populations. A total of 22 genomic loci surpassing the suggestive significance level were detected on 11 pig chromosomes (SSC) for six blood lipid traits. Meta-analysis of GWAS identified 5 novel loci associated with blood lipid traits. Comparison of GWAS loci across the tested populations revealed a substantial level of genetic heterogeneity for porcine blood lipid levels. We further evaluated the causality of nine polymorphisms nearby or within the APOB gene on SSC3 for serum LDL-C and TC levels. Of the 9 polymorphisms, an indel showed the most significant association with LDL-C and TC in Laiwu pigs. But the significant association was not identified in the White Duroc × Erhualian F2 resource population, in which the QTL for LDL-C and TC was also detected on SSC3. This indicates that population-specific signals may exist for the SSC3 QTL. Further investigations are warranted to validate this assumption.

opencc-zeroDec 2014View details →
dryad28/100

Genetic homogeneity in the face of morphological heterogeneity in the harbor porpoise from the Black Sea and adjacent waters (Phocoena phocoena relicta)

<p>Absence of genetic differentiation is usually taken as an evidence of panmixia, but can also reflect other situations including even nearly complete demographic independence among large-sized populations. Deciphering which situation applies has major practical implications (e.g., in conservation biology). The endangered harbor porpoises in the Black Sea illustrates well this point. While morphological heterogeneity suggested that population differentiation may exist between individuals from the Black and Azov seas, no genetic study provided conclusive evidence or covered the entire subspecies range. Here, we assessed the genetic structure at ten microsatellite loci and a 3,904 base-pairs mitochondrial fragment in 144 porpoises across the subspecies range (i.e., Aegean, Marmara, Black, and Azov seas). Analyses of the genetic structure including <i>F<sub>ST</sub></i>, Bayesian clustering, and multivariate analyses revealed a nearly complete genetic homogeneity. Power analyses rejected the possibility of underpowered analyses (power to detect <i>F<sub>ST</sub></i>≥0.008 at microsatellite loci). Simulations under various demographic models, evaluating the evolution of <i>F<sub>ST</sub></i>, showed that a time-lag effect between demographic and genetic subdivision is also unlikely. With a realistic effective population size of 1000 individuals, the expected "<i>grey zone"</i> would be at most 20 generations under moderate levels of gene flow (≤10 migrants per generation). After excluding alternative hypotheses, panmixia remains the most likely hypothesis explaining the genetic homogeneity in the Black Sea porpoises. Morphological heterogeneity may thus reflect other processes than population subdivision (e.g., plasticity, selection). This study illustrates how combining empirical and theoretical approaches can contribute to understanding patterns of weak population structure in highly mobile marine species.</p>

opencc-zeroNov 2019View details →
dryad28/100

Data from: Do genetic structure and landscape heterogeneity impact color morph frequency in a polymorphic salamander?

Landscape heterogeneity plays an important role in population structure and divergence, particularly for species with limited vagility. Here, we used a landscape genetic approach to identify how landscape and environmental variables affect genetic structure and color morph frequency in a polymorphic salamander. The Eastern Red-backed Salamander, Plethodon cinereus, is widely distributed in northeastern North America and contains two common color morphs, striped and unstriped, that are divergent in ecology, behavior, and physiology. To quantify population structure, rates of gene flow, and genetic drift, we amplified 10 microsatellite loci from 648 individuals across 28 sampling localities. This study was conducted in northern Ohio, where populations of P. cinereus exhibit an unusually wide range of morph frequency variation. To test whether genetic distance was more correlated with morph frequency, elevation, canopy cover, waterways, ecological niche, or geographic distance, we used resistance distance and least cost path analyses. We then examined whether landscape and environmental variables, genetic distance, or geographic distance were correlated with variation in morph frequency. Tests for population structure revealed three genetic clusters across our sampling range, with one cluster monomorphic for the striped morph. Rates of gene flow and genetic drift were low to moderate across sites. Genetic distance was most correlated with ecological niche, elevation, and a combination of landscape and environmental variables. In contrast, morph frequency variation was correlated with waterways and geographic distance. Thus, our results suggest that selection is also an important evolutionary force across our sites, and a balance between gene flow, genetic drift, and selection interact to maintain the two color morphs.

opencc-zeroDec 2018View details →
dryad28/100

Data from: Bayesian inference of selection in a heterogeneous environment from genetic time-series data

Evolutionary geneticists have sought to characterize the causes and molecular targets of selection in natural populations for many years. Although this research program has been somewhat successful, most statistical methods employed were designed to detect consistent, weak to moderate selection. In contrast, phenotypic studies in nature show that selection varies in time and that individual bouts of selection can be strong. Measurements of the genomic consequences of such fluctuating selection could help test and refine hypotheses concerning the causes of ecological specialization and the maintenance of genetic variation in populations. Herein, I proposed a Bayesian non-homogenous hidden Markov model to estimate effective population sizes and quantify variable selection in heterogeneous environments from genetic time-series data. The model is described and then evaluated using a series of simulated data, including cases where selection occurs on a trait with a simple or polygenic molecular basis. The proposed method accurately distinguished neutral loci from non-neutral loci under strong selection, but not from those under weak selection. Selection coefficients were accurately estimated when selection was constant or when the fitness values of genotypes varied linearly with the environment, but these estimates were less accurate when fitness was polygenic or the relationship between the environment and the fitness of genotypes was non-linear. Past studies of temporal evolutionary dynamics in lab populations have been remarkably successful. The proposed method makes similar analyses of genetic time-series data from natural populations more feasible, and thereby could help answer fun damental questions about the causes and consequences of evolution in the wild.

opencc-zeroDec 2014View details →
dryad28/100

Data from: Cis- and trans-acting genetic factors contribute to heterogeneity in the rate of crossing over between the Drosophila simulans clade species

In the genus Drosophila, variation in recombination rates has been found within and between species. Genetic variation for both cis- and trans-acting factors has been shown to affect recombination rates within species, but little is known about the genetic factors that affect differences between species. Here we estimate rates of crossing over for seven segments that tile across the euchromatic length of the X chromosome in the genetic backgrounds of three closely related Drosophila species. We first generated a set of Drosophila mauritiana lines each having two semi-dominant visible markers on the X chromosome and then introgressed these doubly marked segments into the genetic backgrounds of its sibling species, D. simulans and D. sechellia. Using these 21 lines (7 segments, 3 genetic backgrounds) we tested whether recombination rates within the doubly marked intervals differed depending on genetic background. We find significant heterogeneity among intervals and among species backgrounds. Our results suggest that a combination of both cis- and trans-acting factors have evolved among the three D. simulans clade species and interact to affect recombination rate.

opencc-zeroDec 2011View details →
dryad28/100

Data from: The genetics of adaptation to discrete heterogeneous environments: frequent mutation or large-effect alleles can allow range expansion

Range expansions are complex evolutionary and ecological processes. From an evolutionary standpoint, a populations' adaptive capacity can determine the success or failure of expansion. Using individual-based simulations, we model range expansion over a two-dimensional, approximately continuous landscape. We investigate the ability of populations to adapt across patchy environmental gradients and examine how the effect sizes of mutations influence the ability to adapt to novel environments during range expansion. We find that genetic architecture and landscape patchiness both have the ability to change the outcome of adaptation and expansion over the landscape. Adaptation to new environments succeeds via many mutations of small effect or few of large effect, but not via the intermediate between these cases. Higher genetic variance contributes to increased ability to adapt, but an alternative route of successful adaptation can proceed from low genetic variance scenarios with alleles of sufficiently large effect. Steeper environmental gradients can prevent adaptation and range expansion on both linear and patchy landscapes. When the landscape is partitioned into local patches with sharp changes in phenotypic optimum, the local magnitude of change between subsequent patches in the environment determines the success of adaptation to new patches during expansion.

opencc-zeroDec 2015View details →
dryad28/100

Data from: Bayesian inference of selection in a heterogeneous environment from genetic time-series data

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publicJul 2015View details →
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Data from: No effect of environmental heterogeneity on the maintenance of genetic variation in wing shape in Drosophila melanogaster

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publicJul 2010View details →
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Data from: Phylogeography and paleodistribution models of a widespread birch (Betula platyphylla Suk.) across East Asia: multiple refugia, multidirectional expansion, and heterogeneous genetic pattern

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publicJun 2019View details →
dryad28/100

Data from: Genome-wide association analysis for blood lipid traits measured in three pig populations revealed a substantial level of genetic heterogeneity

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publicJun 2016View details →
dryad28/100

Evolutionary stability, landscape heterogeneity, and human land-usage shape population genetic connectivity in the Cape Floristic Region biodiversity hotspot

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publicDec 2020View details →

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dandi-nwb
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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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Last verified 2026-04-29Open record