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637 results for “Population analysis”
Fig. 2 in Genetic diversity and population structure of endangered Neofinetia falcata (Orchidaceae) in South Korea based on microsatellite analysis
Fig. 2. Structure analyses for putative genetic clusters of N. falcata. A: Graphs of ΔK values to determine the ideal number of groups present in the accessions of N. falcata. B: Estimated genetic structure of the 3 populations of brinjal based on STRUCTURE analysis K = 2 and K = 3.
Fig. 5 in Population analysis of white grubs (Coleoptera: Melolonthidae) throughout the Brazilian Pampa biome
Fig. 5. Dendrogram representing results of a cluster analysis of Melolonthidae species showing Jaccard index among the 18 locations sampled throughout the Brazilian Pampa.
Fig. 3 in Population analysis of white grubs (Coleoptera: Melolonthidae) throughout the Brazilian Pampa biome
Fig. 3. Population density of white grubs pest and other species (mean ± SE) in cultivated areas of the Brazilian Pampa. Pairs of columns with the same letters do not differ significantly by bootstrap t-test (p ≤ 0.05).
Figures 5a–f in Trapping Records of Fruit Fly Pest Species (Diptera: Tephritidae) on Oahu (Hawaiian Islands): Analysis of Spatial Population Trends
Figures 5a–f. Mean (± S.E.) captures in different habitats for B. cucurbitae in cuelure and torula yeast (a, b), B. dorsalis in methyl eugenol and torula yeast (c, d) and C. capitata in trimedlure and torula yeast (e, f) traps. Units are flies per trap per day in male lure and per week in torula yeast traps.
Text-fig. 2. Taphonomic and pathological phenomena of bear bones from Middle Pleistocene deposits from Vykopaná chodba in Za Hájovnou Cave (Moravia, the Czech Republic). a – fragment of left mandibula with pathological condylar process; b – thoracic vertebra with pathological rib facet; c – Mc III dext. with exostoses; d – fragment of juvenile right ulna with bite marks; e – gnawed right tibia with bite marks on proximal part; f – gnawed left calcaneus with bite marks. in Basic Population And Taphonomic Analysis Of Bear Assemblages From Za Hájovnou Cave (Moravia, The Czech Republic): A Fossil Record From 1987-2007
Text-fig. 2. Taphonomic and pathological phenomena of bear bones from Middle Pleistocene deposits from Vykopaná chodba in Za Hájovnou Cave (Moravia, the Czech Republic). a – fragment of left mandibula with pathological condylar process; b – thoracic vertebra with pathological rib facet; c – Mc III dext. with exostoses; d – fragment of juvenile right ulna with bite marks; e – gnawed right tibia with bite marks on proximal part; f – gnawed left calcaneus with bite marks.
Text-fig. 5. Distribution of age classes of deningeri bears from Middle Pleistocene deposits from Za Hájovnou Cave (Moravia, the Czech Republic) based on wear stage of M2 dext. and m2 dext. (I–III: juveniles, IV–VII: prime adults, VIII–IX: senile adults; according to Stiner 1998). Juveniles distinctly outnumber adults. in Basic Population And Taphonomic Analysis Of Bear Assemblages From Za Hájovnou Cave (Moravia, The Czech Republic): A Fossil Record From 1987-2007
Text-fig. 5. Distribution of age classes of deningeri bears from Middle Pleistocene deposits from Za Hájovnou Cave (Moravia, the Czech Republic) based on wear stage of M2 dext. and m2 dext. (I–III: juveniles, IV–VII: prime adults, VIII–IX: senile adults; according to Stiner 1998). Juveniles distinctly outnumber adults.
Text-fig. 4. Taphonomic and pathological phenomena of bear bones from Middle Pleistocene deposits from Spojovací chodba – Narozeninová chodba in Za Hájovnou Cave (Moravia, the Czech Republic). a – Mc V sin. with a pathological phenomenon on the metapodial distal part (tuberosity/exostosis?); b – gnawed juvenile ulna; c – right tibia gnawed by a large rodent (porcupine?) with detail. in Basic Population And Taphonomic Analysis Of Bear Assemblages From Za Hájovnou Cave (Moravia, The Czech Republic): A Fossil Record From 1987-2007
Text-fig. 4. Taphonomic and pathological phenomena of bear bones from Middle Pleistocene deposits from Spojovací chodba – Narozeninová chodba in Za Hájovnou Cave (Moravia, the Czech Republic). a – Mc V sin. with a pathological phenomenon on the metapodial distal part (tuberosity/exostosis?); b – gnawed juvenile ulna; c – right tibia gnawed by a large rodent (porcupine?) with detail.
Text-fig. 3. Taphonomic and pathological phenomena of bear bones from Middle Pleistocene deposits from Chodba naděje in Za Hájovnou Cave (Moravia, the Czech Republic). a – gnawed lumbar vertebra with a bite mark on the body head; b – fragment of pelvis with a bite mark; c – femur head with a bite mark; d – Mc II dext. with a pathological phenomenon on the metapodial proximal part (tuberosity/exostosis?). in Basic Population And Taphonomic Analysis Of Bear Assemblages From Za Hájovnou Cave (Moravia, The Czech Republic): A Fossil Record From 1987-2007
Text-fig. 3. Taphonomic and pathological phenomena of bear bones from Middle Pleistocene deposits from Chodba naděje in Za Hájovnou Cave (Moravia, the Czech Republic). a – gnawed lumbar vertebra with a bite mark on the body head; b – fragment of pelvis with a bite mark; c – femur head with a bite mark; d – Mc II dext. with a pathological phenomenon on the metapodial proximal part (tuberosity/exostosis?).
Figure 4 in CHD genes: a reliable marker for bird populations and phylogenetic analysis? Case study of the superfamily Sylvioidea (Aves: Passeriformes)
Figure 4. Maximum clade credibility trees for three data sets obtained by BI analysis in BEAST v1.8.0. MCC genealogy based on a Yule speciation process, summarized from the output of a Markov chain Monte Carlo chain run for 10 million iterations and sampled every 1000 iterations.
Figure 3 in CHD genes: a reliable marker for bird populations and phylogenetic analysis? Case study of the superfamily Sylvioidea (Aves: Passeriformes)
Figure 3. The ML tree for myoglobin gene (in blue) and for CHD-Z gene (in red); both trees are scaled in substitutions and the length of each tree and different topologies indicate that both of them are improper for phylogeny using a single gene.
Figure 1. Sex distribution for A. arundinaceus, A in CHD genes: a reliable marker for bird populations and phylogenetic analysis? Case study of the superfamily Sylvioidea (Aves: Passeriformes)
Figure 1. Sex distribution for A. arundinaceus, A. scirpaceus, and A. schoenobaenus, shown by sampling date.
Figure 2 in High genetic distinctiveness of wild and farm fox (Vulpes vulpes L.) populations in Poland: evidence from mitochondrial DNA analysis
Figure 2. Neighbor-joining haplotype network based on frequencies showing relationships between concatenated MT-CO1 and MTATP6 sequences of fur farm and wild red foxes.
Figure 1 in High genetic distinctiveness of wild and farm fox (Vulpes vulpes L.) populations in Poland: evidence from mitochondrial DNA analysis
Figure 1. Distribution of sampling sites of wild and fur-farm red foxes in Poland: light gray areas represent the provinces from which samples of wild foxes were taken; the darker gray area indicated with a black circle shows the location of investigated fox farms; the numbers represent fox fur-farms in particular voivodeships.
Figure 3 in Application of multifactorial discriminant analysis in the morphostructural differentiation of wild and cultured populations of Vieja Azul (Andinoacara rivulatus)
Figure 3. Cluster from Mahalanobis distances for cultured and wild populations of both sexes. HP: Cultured females; HS: wild females; MP: cultures males; MS: wild males.
Figure 2 in Application of multifactorial discriminant analysis in the morphostructural differentiation of wild and cultured populations of Vieja Azul (Andinoacara rivulatus)
Figure 2. Plot of the individual observation discriminant scores obtained with the canonical discriminant function. HP: Cultured females; HS: wild females; MP: cultures males; MS: wild males.
Figure 1 in Application of multifactorial discriminant analysis in the morphostructural differentiation of wild and cultured populations of Vieja Azul (Andinoacara rivulatus)
Figure 1. (a) Location of 25 anatomic landmark points designed on the left-side view of Andinoacara rivulatus; (b) 32 truss characters making up a truss network. 1- Commissure of the mouth; 2- most cranial point of the upper premaxilla; 3- origin of pelvic fin; 4- origin of dorsal fin; 5- origin of anal fin; 6- most cranial point of the base of the tenth spine of the dorsal fin; 7- ending of anal fin; 8- ending of dorsal fin; 9- ventral origin of caudal fin; 10- dorsal origin of caudal fin; 11- most cranial point of caudal peduncle; 12- most caudal point of caudal peduncle; 13- ending of pectoral fin; 14- end of operculum; 15- cranial edge of the eye; 16- caudal edge of the eye; 17- preoccipital (most posterior aspect of neurocranium); 18- below operculum; 19- origin of pectoral fin; 20- lower end of the head; 21- anal opening; 22- most cranial point of the lower premaxilla; 23- ending of 1st dorsal fin ray; 24- ending of the last anal fin ray; 25- ending of the pelvic fin radius.
Figure. Phylogram showing phylogenetic relationships estimated using maximum likelihood analysis of 16S rRNA and COXI gene revealed the grouping of Orthochirus iranus, O. farzanpay, O. stockwelli, O. zagrosensis, O. innesi (JQ514244.1 Morocco), and O. bicolor (KT716038.1 India), with the outgroup species Androctonus crassicauda (FJ217732). in A study of genetic diversity among different population of Orthochirus sp. based on cytochrome C oxidase subunit I and 16srRNA sequencing
Figure. Phylogram showing phylogenetic relationships estimated using maximum likelihood analysis of 16S rRNA and COXI gene revealed the grouping of Orthochirus iranus, O. farzanpay, O. stockwelli, O. zagrosensis, O. innesi (JQ514244.1 Morocco), and O. bicolor (KT716038.1 India), with the outgroup species Androctonus crassicauda (FJ217732).
Fig. 5 in Fossil population structure and mortality analysis of the cave bears from Urşilor Cave, north-western Romania
Fig. 5. Greatest length vs. width for the lower (A, N = 74) and upper (B, N = 105) cave bear canines from Urşilor (~45–40 calendar kyrs BP).
Fig. 6 in Fossil population structure and mortality analysis of the cave bears from Urşilor Cave, north-western Romania
Fig. 6. Percentage of juveniles vs. females (A) and old individuals vs. males (B) of cave bears from Urşilor, (~45–40 calendar kyrs BP). Data derived from SOM: tables 3 and 4.
Fig. 3 in Fossil population structure and mortality analysis of the cave bears from Urşilor Cave, north-western Romania
Fig. 3. Tripolar graphs showing the distribution of the teeth and mandibles (A) of cave bears from Urşilor (~45–40 calendar kyrs BP) in the three main age categories (according to Stiner 1994); and distribution of age classes (B) from different cave bear sites in the three main age categories, as proposed by Stiner (1994): NNVA (Normal Non-Violent Assemblage), grey dashed polygon; LS (Living age Structure), black dashed polygon.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.