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464 results for “Population Genetic Diversity”
Figure 1 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Figure 1 Distribution map of Usnea subfloridana in Estonia (light grey squares) and study populations (black circles) on Hiiumaa island in the western region (W), in the south-eastern region (SE) and in the northern region of Estonia; the map of Scandinavia was taken from free map resource http://d-maps.com/carte.php?num_car=5977&lang=en.
Figure 6 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Figure 6 Alleles of Usnea subfloridana and explanatory variables mean annual air temperature ('Temp') and geographical longitude of populations ('Long') in the bi-plot of the redundancy analysis (RDA) of the first and second axes. Labels of alleles prefixed by '8' or '9' indicate that these alleles belong to loci Us08 or Us09, respectively; for example, 8201 means that allele 201 is from Us08
Figure 4 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Figure 4 Usnea subfloridana multilocus genotypes (Us02, Us03, Us04, Us05, Us06, Us08, Us09) and explanatory variables mean annual air temperature ('Temp') and the presence of thamnolic acid ('Tham') in a lichen sample in the bi-plot of the redundancy analysis (RDA) of the first and second axes.
Figure 5 from: Degtjarenko P, Jüriado I, Mandel T, Tõrra T, Saag A, Scheidegger C, Randlane T (2019) Microsatellite based genetic diversity of the widespread epiphytic lichen Usnea subfloridana (Parmeliaceae, Ascomycota) in Estonia: comparison of populations from the mainland and an island. MycoKeys 58: 27-45. https://doi.org/10.3897/mycokeys.58.36557
Figure 5 Sample populations of Usnea subfloridana and explanatory variables mean annual air temperature ('Temp') and geographical longitude of populations ('Long') in the bi-plot of the redundancy analysis (RDA) of the first and second axes. The shape of symbols indicates the geographical location of studied populations (square – south-eastern region of mainland, circle - western island and diamond – north-eastern region) and the size of symbols indicates the number of different alleles found in the studied populations.
Figure 2 in Genetic diversity of codling moth Cydia pomonella L. (Lepidoptera: Tortricidae) populations in Turkey
Figure 2. Maximum likelihood tree of the COI gene haplotypes of C. pomonella. Numbers above the branches indicate the bootstrap values (>50) for nodes (1000 replications).
Figure 3. K in Microsatellite based genetic diversity of Mediterranean fruit fly (Ceratitis capitata, Diptera: Tephritidae) populations from Southwest Turkey
Figure 3. K = 4 clustering assignment depending on the Bayesian method under an admixture model obtained by Structure software. Individuals are represented by a vertical line and each color indicates a different cluster. 1: Muğla; 2: Aydın; 3: Antalya; 4: İzmir; 5: Adana; 6: Yalova; 7: Mersin.
Genetic diversity of farmed and wild Rufiji tilapia (Oreochromis urolepis urolepis) populations
<p>Rufiji tilapia (<em>Oreochromis urolepis urolepis</em>) is an endemic cichlid in Tanzania. In addition to its importance for biodiversity conservation, Rufiji tilapia is also attractive for farming due to its high growth-rate, salinity tolerance, and the production of all-male hybrids when crossed with Nile tilapia (<em>Oreochromis niloticus</em>). The aim of the current study was to assess the genetic diversity and population structure of both wild and farmed Rufiji tilapia populations in order to inform conservation and aquaculture practices.</p>
Figure 2 from: Liu D, Lan F, Xie S, Diao Y, Zheng Y, Gong J (2021) Dynamic genetic diversity and population structure of Coreius guichenoti. ZooKeys 1055: 135-148. https://doi.org/10.3897/zookeys.1055.70117
Figure 2 Phylogenetic trees of the mtDNA control region haplotypes in C. guichenoti reconstructed with Bayesian inference. Numbers at nodes represent Bayesian posterior probabilities and neighbor-joining tree. At the right side of the figure, the numbers represent the total of individuals from different sampling locations in each haplotype.
Figure 3 from: Liu D, Lan F, Xie S, Diao Y, Zheng Y, Gong J (2021) Dynamic genetic diversity and population structure of Coreius guichenoti. ZooKeys 1055: 135-148. https://doi.org/10.3897/zookeys.1055.70117
Figure 3 Median-joining network of the mtDNA control region haplotypes of C. guichenoti. The size of each circle indicates the relative frequency of the corresponding haplotype in the whole data set.
Supplementary material 1 from: Liu D, Lan F, Xie S, Diao Y, Zheng Y, Gong J (2021) Dynamic genetic diversity and population structure of Coreius guichenoti. ZooKeys 1055: 135-148. https://doi.org/10.3897/zookeys.1055.70117
Tables S1, S2, Figures S1, S2
Figure 4 from: Liu D, Lan F, Xie S, Diao Y, Zheng Y, Gong J (2021) Dynamic genetic diversity and population structure of Coreius guichenoti. ZooKeys 1055: 135-148. https://doi.org/10.3897/zookeys.1055.70117
Figure 4 Isolation by distance (IBD) relationship among C. guichenoti wild populations in five populations collected in 2009 a and seven populations collected in 2019 b.
Figure 1 from: Liu D, Lan F, Xie S, Diao Y, Zheng Y, Gong J (2021) Dynamic genetic diversity and population structure of Coreius guichenoti. ZooKeys 1055: 135-148. https://doi.org/10.3897/zookeys.1055.70117
Figure 1 Sampling localities of China (solid triangles indicate sites in 2009; solid circle indicate sites in 2019) of C. guichenoti. For full names of populations, see Table 1.
Figure 2 in Genetic diversity of Atherina hepsetus (Osteichthyes: Atherinidae) populations as determined by RFLP analysis of three mtDNA regions
Figure 2. Neighbor-joining (Saitou and Nei 1987) cladogram, based on the net nucleotide divergence.
Figure 2 in Genetic diversity, population structure and demographic history of Dugesia japonica in Taihang Mountains
Figure 2. Mismatch distribution of Dugesia japonica from Taihang Mountains based on mitochondrial COI.
Genetic Counseling Service Delivery and Outcomes in Diverse and Underserved Populations
ClinicalTrials.gov study NCT06212310. IPD Sharing: NO. Countries: 1. Publications: 0.
Data from: Elevated genetic diversity of mitochondrial genes in asexual populations of bark lice ("Psocoptera": Echmepteryx hageni)
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Data from: A single migrant enhances the genetic diversity of an inbred puma population
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Data from: Genetic diversity does not explain variation in extra-pair paternity in multiple populations of a songbird
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Data from: Genetic diversity and population structure of wild sunflower (Helianthus annuus L.) in Argentina: reconstructing its invasion history
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Data from: The contrasting roles of host species diversity and parasite population genetic diversity in the infection dynamics of a keystone parasitic plant
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International Brain Laboratory public data
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