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2,445 results for “Genetics: population”
Fig. 1 in Genetic And Morphological Variability Of Small Vendace (Coregonus Albula (Linnaeus, 1758)) Population In Three Latvian Lakes
Fig. 1. The location of sampling sites. - Lake Sventes, Lake Nirzas and Lake Rāznas.
Fig. 6. RAPD band patterns and mean heterozygosity across S in MORPHOLOGICALAND GENETIC DIFFERENTIATION OF SAXIFRAGA HIRCULUS L. (SAXIFRAGACEAE) POPULATIONS IN LITHUANIA Edita Meškauskaitė, Donatas Naugžemys, Donatas Žvingila, Jonas Remigijus
Fig. 6. RAPD band patterns and mean heterozygosity across S. hirculus populations in Lithuania
Fig. 2 in MORPHOLOGICALAND GENETIC DIFFERENTIATION OF SAXIFRAGA HIRCULUS L. (SAXIFRAGACEAE) POPULATIONS IN LITHUANIA Edita Meškauskaitė, Donatas Naugžemys, Donatas Žvingila, Jonas Remigijus
Fig. 2. Variation in morphologic features of S. hirculus generative individuals in Lithuania
Fig. 1 in MORPHOLOGICALAND GENETIC DIFFERENTIATION OF SAXIFRAGA HIRCULUS L. (SAXIFRAGACEAE) POPULATIONS IN LITHUANIA Edita Meškauskaitė, Donatas Naugžemys, Donatas Žvingila, Jonas Remigijus
Fig. 1. The location of S. hirculus research sites in Lithuan
Fig. 3 in MORPHOLOGICALAND GENETIC DIFFERENTIATION OF SAXIFRAGA HIRCULUS L. (SAXIFRAGACEAE) POPULATIONS IN LITHUANIA Edita Meškauskaitė, Donatas Naugžemys, Donatas Žvingila, Jonas Remigijus
Fig. 3. Frequency distribution of runners per S. hirculus floral shoot in the studied populations
Figure 1 in Unveiling the genetic diversity of bicolored-spined porcupines (Rodentia: Erethizontidae): a novel karyotype, population structuring, and evolutionary insights
Figure 1. Map of part of South America with collecting localities of C. bicolor specimens with sequences on the GenBank (Black circles), generated in the present study (triangle), others register of occurrences (white circles), and type locality (star). Gray area represents the Amazon Biome. ARG = Argentina, BOL = Bolivia, BRA = Brazil, PER = Peru.
Figure 4 in Unveiling the genetic diversity of bicolored-spined porcupines (Rodentia: Erethizontidae): a novel karyotype, population structuring, and evolutionary insights
Figure 4. Topology of median joining on top of the map showing the current separation of C. bicolor populations by the rivers Ucayali and Beni/Madre de Dios. Circles are haplotypes and its dimension are proportional to the number of shared sequences. Numbers in the segments connecting the circles are nucleotide substitutions and black circle is the median vector. For haplotypes localities see figure 2. BOL = Bolivia, BRA = Brazil, PER = Peru.
Figure 3 in Unveiling the genetic diversity of bicolored-spined porcupines (Rodentia: Erethizontidae): a novel karyotype, population structuring, and evolutionary insights
Figure 3. Maximum likelihood phylogenetic tree. Symbols near nodes represent Bootstrap values: black circles (90-100%), white circles (80-89%), white squares (70-79%), black square (66%). BOL = Bolivia, BRA = Brazil, COL = Colombia, ECU = Ecuador, GUF = French Guiana, MEX = Mexico, PAR = Paraguay, PER = Peru.
Figure 2 in Unveiling the genetic diversity of bicolored-spined porcupines (Rodentia: Erethizontidae): a novel karyotype, population structuring, and evolutionary insights
Figure 2. Conventional stained karyotypes of Coendou (Sphiggurus) bicolor male LBCE21287 (above) and female LBCE21289 (below) from Brazilian Acre state with 2n = 52 and FN = 82. The X and Y are sexual chromosomes.
Study on the mating systems of wild rice Oryza rufipogon and O. nivara and their effects on population genetic variation
<p>As the wild ancestors of Asian cultivated rice,<em> Oryza rufipogon</em> Griff. and <em>O. nivara</em> Sharma et Shastry serve as valuable germplasms for rice breeding. Mating systems are important in shaping the level and pattern of population genetic variation, and are crucial for germplasm conservation. We genotyped 12 simple sequence repeats (SSR) markers for a large number of maternal plants and seeds collected from <em>O</em>.<em> rufipogon</em> and <em>O. nivara</em> populations distributed in Southeast Aisa and South China. Based on the 12 SSR markers, we estimated the outcrossing rates and other parameters of the mixed-mating model for the two wild rice species. We also assessed the level of genetic diversity and population structure for parental populations of <em>O</em>.<em> rufipogon</em> and <em>O. nivara</em>. Our study could facilitate <em>in situ</em> and <em>ex situ</em> conservation, and the utilization of these valuable germplasm resources.</p>
Figure 6 in Infraspecific genetic variation and population structure of Salvia nemorosa L. (Lamiaceae) in Iran
Figure 6. UPGMA tree of the studied populations based on Nei's genetic distance.
Figure 5 in Infraspecific genetic variation and population structure of Salvia nemorosa L. (Lamiaceae) in Iran
Figure 5. STRUCTURE plot of the studied populations of S. nemorosa based on k = 7 of ISSR results.
Fig. 1 in Worldwide sampling reveals low genetic variability in populations of the freshwater ciliate Paramecium biaurelia (P. aurelia species complex, Ciliophora, Protozoa)
Fig. 1 Th_ origin (N = 92) of Paramecium biaurelia strains us_d in pr_s_nt studi_s
Genotyping measures and population genetic indices for assesing reproductive modes of polyploid Ludwigia grandiflora subsp. hexapetala in western Europe
<p>Raw data used to assess reproductive modes in 53 sampled populations in western Europe (France and northern Spain).</p> <p><em>Ludwigia grandiflora </em>subsp.<em> hexapetala</em> (<em>Lgh</em>) is a hermaphrodite, polyploid, partially clonal and heteromorphic plant that recently colonized multiple countries worldwide. Individuals in this species are either self-incompatible caused by a late-acting self-incompatible (LSI) system developing long-styled flowers, or self-compatible (SC) developing short-styled flowers. We used a SNP approach allowing confident allele dosage to genotype 53 LSI and SC populations of <em>Lgh</em> in France and northern Spain. We measured their genetic diversity and assessed their reproductive modes using methods adapted to autopolyploid species. </p>
Figure 3 in Genetic variability and population structure of some Iranian Salvia limbata C. A. Mey. populations
Figure 3. Results of AMOVA analysis among and within the studied populations.
Fig. 1 in Soluble proteins in Messor structor (Latreille, 1798) (Hymenoptera: Formicidae) populations from Bulgaria - genetic variability and possible usage as population-genetic markers
Fig. 1. Sampling locations.
Fig. 1 in Trypanosomes genetic diversity, polyparasitism and the population decline of the critically endangered Australian marsupial, the brush tailed bettong or woylie (Bettongia penicillata)
Fig. 1. Geographical origin of the different species of marsupials trapped in this study.
Anthropogenic pressures drive population genetic structuring across a Critically Endangered lemur species range
<p>Includes initial input landscape surfaces (.acs) and final resistance surfaces (.out) generated during the current study.</p>
Figure 4 in Determination of genetic variations between Apodemus mystacinus populations distributed in Turkey inferred from mtDNA PCR-RFLP
Figure 4. UPGMA dendrogram of the composite data by combining cytb and D-loop regions.
Figure 1 in Microsatellite based genetic diversity of Mediterranean fruit fly (Ceratitis capitata, Diptera: Tephritidae) populations from Southwest Turkey
Figure 1. Map of Turkey with sampling sites.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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