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37 results for “Genetic assignment”
FIG. 1 in How do young bats find suitable swarming and hibernation sites? Assessing the plausibility of the maternal guidance hypothesis using genetic maternity assignment for two European bat species
FIG. 1. Left — drawing of 'Brunnen Meyer'; right — photo of the western side of the 'Brunnen Meyer' well house with window where bats enter
FIG. 2 in How do young bats find suitable swarming and hibernation sites? Assessing the plausibility of the maternal guidance hypothesis using genetic maternity assignment for two European bat species
FIG. 2. Simulation (10,000 iterations) of how often mother-offspring pairs are expected to arrive on the same night by chance for M. daubentonii (top) and M. nattereri (bottom); the observed number of pairs arriving on the same night is denoted by the arrow
Data from: SNPs reveal a genetic cline across the northeast Atlantic and enable powerful population assignment in the European lobster
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Data from: Genetic assignment of large seizures of elephant ivory reveals Africa’s major poaching hotspots
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Data from: Genetic sex assignment in wild populations using GBS data: a statistical threshold approach
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Data from: Seeds in motion: genetic assignment and hydrodynamic models demonstrate concordant patterns of seagrass dispersal
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Data from: Applications of random forest feature selection for fine-scale genetic population assignment
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Data from: Bayesian clustering analyses for genetic assignment and study of hybridization in oaks: effects of asymmetric phylogenies and asymmetric sampling schemes
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Data from: Sequencing improves our ability to study threatened migratory species: genetic population assignment in California's Central Valley Chinook salmon
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Data from: Genetic and individual assignment of tetraploid green sturgeon with SNP assay data
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Data from: RAD genotyping reveals fine-scale genetic structuring and provides powerful population assignment in a widely distributed marine species, the American lobster (Homarus americanus).
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Data from: Genetic assignment with isotopes and habitat suitability (GAIAH), a migratory bird case study
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Data from: The twenty amino acids are identified by unique numbers assigned to the uracil, cytosine, adenine, and guanine found in the three base positions of the sixty-four messenger RNA genetic codons
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Data from: Using probability modelling and genetic parentage assignment to test the role of local mate availability in mating system variation.
The formal testing of mating system theories with empirical data is important for evaluating the relative importance of different processes in shaping mating systems in wild populations. Here we present a generally applicable probability modelling framework to test the role of local mate availability in determining a population's level of genetic monogamy. We provide a significance test for detecting departures in observed mating patterns from model expectations based on mate availability alone, allowing the presence and direction of behavioural effects to be inferred. The assessment of mate availability can be flexible and in this study it was based on population density, sex ratio and spatial arrangement. This approach provides a useful tool for (1) isolating the effect of mate availability in variable mating systems and (2) in combination with genetic parentage analyses, gaining insights into the nature of mating behaviours in elusive species. To illustrate this modelling approach, we have applied it to investigate the variable mating system of the mountain brushtail possum (Trichosurus cunninghami) and compared the model expectations with the outcomes of genetic parentage analysis over an 18 year study. The observed level of monogamy was higher than predicted under the model. Thus, behavioural traits, such as mate guarding or selective mate choice, may increase the population level of monogamy. We show that combining genetic parentage data with probability modelling can facilitate an improved understanding of the complex interactions between behavioural adaptations and demographic dynamics in driving mating system variation.
Data from: Using probability modelling and genetic parentage assignment to test the role of local mate availability in mating system variation.
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Subspecies and Distribution. R. c.c clivosus Cretzschmar, 1828 - SWJordan, W & C Saudi Arabia, Yemen, and SW Oman. R c. acrotis Heuglin, 1862 — Eritrea, Ethiopia, Djibouti, and N Somalia. R c. augur ÌL. Andersen, 1904 — N & C South Africa. R c. brachygnathus K. Andersen, 1905 - Israel, Egypt, and N Sudan. R c. geoffmyii A. Smith, 1829 — SW South Africa. R c. keniensis Hollister, 1916 - SE Sudan, South Sudan, Uganda, NE DR Congo, Rwanda, Burundi, Kenya, and N Tanzania; other records throughout C Africa need further investigation. R c. schwarzi Heim de Balsac, 1934 - SE Algeria and W Libya. 7t c., socotranus Benda, Reiter & Vallo, 2017 - Socotra I, Yemen. AE c. zambesiensis K. Andersen, 1904 - S Tanzania, Malawi, Zambia, and SE DR Congo S to NE South Africa. R c. zuluensis K. Andersen, 1904 - E & S South Africa, Swaziland, and Lesotho. There is also a record from W DR Congo with no subspecific affinity and populations from Namibia and SW Angola are not currently assigned to any subspecies but might be associated with subspecies augur or geoffroyii following further morphological and genetic tests. in Rhinolophidae
Subspecies and Distribution. R. c.c clivosus Cretzschmar, 1828 - SWJordan, W & C Saudi Arabia, Yemen, and SW Oman. R c. acrotis Heuglin, 1862 — Eritrea, Ethiopia, Djibouti, and N Somalia. R c. augur ÌL. Andersen, 1904 — N & C South Africa. R c. brachygnathus K. Andersen, 1905 - Israel, Egypt, and N Sudan. R c. geoffmyii A. Smith, 1829 — SW South Africa. R c. keniensis Hollister, 1916 - SE Sudan, South Sudan, Uganda, NE DR Congo, Rwanda, Burundi, Kenya, and N Tanzania; other records throughout C Africa need further investigation. R c. schwarzi Heim de Balsac, 1934 - SE Algeria and W Libya. 7t c., socotranus Benda, Reiter & Vallo, 2017 - Socotra I, Yemen. AE c. zambesiensis K. Andersen, 1904 - S Tanzania, Malawi, Zambia, and SE DR Congo S to NE South Africa. R c. zuluensis K. Andersen, 1904 - E & S South Africa, Swaziland, and Lesotho. There is also a record from W DR Congo with no subspecific affinity and populations from Namibia and SW Angola are not currently assigned to any subspecies but might be associated with subspecies augur or geoffroyii following further morphological and genetic tests.
Distribution. NW Madagascar, found discontinuously from N of the Betsiboka River to the Mahajamba River. This is a much-reduced distribution compared to older accounts, but previous range descriptions were based on the incorrect assignment of a museum specimen; this new assessment is supported by strong genetic evidence. Further study is needed north of Ankarafantsika National Park to determine the N extent of the range. in Lepilemuridae
Distribution. NW Madagascar, found discontinuously from N of the Betsiboka River to the Mahajamba River. This is a much-reduced distribution compared to older accounts, but previous range descriptions were based on the incorrect assignment of a museum specimen; this new assessment is supported by strong genetic evidence. Further study is needed north of Ankarafantsika National Park to determine the N extent of the range.
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OpenNeuro
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