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1,337 results for “genetic variations”
Fig. 5. Misgolas maxhicksi n in Trapdoor Spiders of the Genus Misgolas (Mygalomorphae: Idiopidae) from Eastern New South Wales, With Notes on Genetic Variation
Fig. 5. Misgolas maxhicksi n.sp. A–G?, holotype AM KS38635: (A), right palp retrolateral. (B,C), right bulb: B, dorsal; C, prolateral. (D,E), right tarsus/metatarsus joint I: D, prolateral; E, retrolateral. (F,G), right tarsus/metatarsus joint II: F, prolateral; G, retrolateral. (H)?, paratype AM KS48650, venter.
Fig. 4. Misgolas dougweiri n in Trapdoor Spiders of the Genus Misgolas (Mygalomorphae: Idiopidae) from Eastern New South Wales, With Notes on Genetic Variation
Fig. 4. Misgolas dougweiri n.sp. A–H?, holotype AM KS50006: (A), right palp retrolateral. (B,C), right bulb: B, dorsal; C, prolateral. (D,E), right tarsus/metatarsus joint I: D, prolateral; E, retrolateral. (F,G), right tarsus/metatarsus joint II: F, prolateral; G, retrolateral. (H), venter.
Fig. 3. Misgolas tarnawskiae n in Trapdoor Spiders of the Genus Misgolas (Mygalomorphae: Idiopidae) from Eastern New South Wales, With Notes on Genetic Variation
Fig. 3. Misgolas tarnawskiae n.sp. A–H?, holotype AM KS92879: (A), right palp retrolateral. (B,C), right bulb: B, dorsal; C, prolateral. (D,E), right leg I: D, prolateral; E, retrolateral. (F,G), right leg II: F, prolateral; G, retrolateral. (H), venter.
Fig. 2. Misgolas thompsonae n in Trapdoor Spiders of the Genus Misgolas (Mygalomorphae: Idiopidae) from Eastern New South Wales, With Notes on Genetic Variation
Fig. 2. Misgolas thompsonae n.sp. A–H?, holotype AM KS36705: (A), right palp retrolateral. (B,C), right bulb: B, dorsal; C, prolateral. (D), venter. (E,F), right leg I: E, prolateral; F, retrolateral. (G,H), right leg II: G, prolateral; H, retrolateral.
Fig. 15. Misgolas raveni n in Trapdoor Spiders of the Genus Misgolas (Mygalomorphae: Idiopidae) from Eastern New South Wales, With Notes on Genetic Variation
Fig. 15. Misgolas raveni n.sp. A–G?, holotype AM KS50007: (A), right palp retrolateral. (B,C), right bulb: B, dorsal; C, prolateral. (D), right leg I prolateral. (E), right bifid apophysis prolateral. (F), right leg IV retrolateral. (G), venter.
Fig. 1. Misgolas mudfordae n in Trapdoor Spiders of the Genus Misgolas (Mygalomorphae: Idiopidae) from Eastern New South Wales, With Notes on Genetic Variation
Fig. 1. Misgolas mudfordae n.sp. A–J?, holotype AM KS50037: (A), right palp retrolateral. (B,C), right bulb: B, dorsal; C, prolateral. (D), venter. (E,F), right leg I: E, prolateral; F, retrolateral. (G,H), right leg II: G, prolateral; H, retrolateral. (I), right leg IV retrolateral. (J), carapace.
Fig. 23. Misgolas milledgei n in Trapdoor Spiders of the Genus Misgolas (Mygalomorphae: Idiopidae) from Eastern New South Wales, With Notes on Genetic Variation
Fig. 23. Misgolas milledgei n.sp. A–H?, holotype AM KS21570: (A), right palp retrolateral. (B,C), right bulb: B, dorsal; C, prolateral. (D), body dorsum. (E), venter. (F,G), right leg IV: F, prolateral; G, retrolateral. (H), right cymbium dorsal.
Fig. 10. Misgolas taiti n in Trapdoor Spiders of the Genus Misgolas (Mygalomorphae: Idiopidae) from Eastern New South Wales, With Notes on Genetic Variation
Fig. 10. Misgolas taiti n.sp. A–F?, holotype AM KS5209: (A) right palp retrolateral. (B,C), right bulb: B, dorsal; C, prolateral. (D), right leg IV retrolateral. (E), right tarsus I ventral. (F), venter.
Fig. 19. Misgolas macei n in Trapdoor Spiders of the Genus Misgolas (Mygalomorphae: Idiopidae) from Eastern New South Wales, With Notes on Genetic Variation
Fig. 19. Misgolas macei n.sp. A–F?, holotype AM KS38643: (A), right palp retrolateral. (B,C), right bulb: B, dorsal; C, prolateral. (D), right cymbium dorsal. (E), right tarsus/metatarsus IV retrolateral. (F), venter.
Fig. 4 in Patterns Of Genetic Variation In The Little Spiderhunter (Arachnothera Longirostra) In Southeast Asia
Fig. 4. Frequency distribution of pairwise sequence differences among little spiderhunter individuals from the Malay Peninsula and Borneo populations.
Fig. 1 in Patterns Of Genetic Variation In The Little Spiderhunter (Arachnothera Longirostra) In Southeast Asia
Fig. 1. Map showing sampling sites. The sites are numbered as follows: 1=Thale Ban National Park, Thailand; 2=Taman Negara National Park, Malaysia; 3=Matang Wildlife Centre and Kubah National Park, Sarawak; 4=Poring Hot Springs, Sabah; 5=Tawau Hills Park, Sabah; 6=Palawan; 7=South Mindanao; and 8=East Mindanao.
Fig. 3 in Patterns Of Genetic Variation In The Little Spiderhunter (Arachnothera Longirostra) In Southeast Asia
Fig. 3. Minimum spanning network of 38 haplotypes found by sequencing the mtDNA control region of little spiderhunter. Each hatch on branches corresponds to one mutation. Numbers in circles represent haplotype numbers (Table 1). The area of the circles in the network reflects haplotype frequency, with the smallest circle equal to one and the largest equal to eight. Haplotypes are shaded to match respective populations on the map (Fig. 1). Haplotypes without intervening branches differ by gaps.
Fig. 14 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 14. Additive tree (phenogram), based on Mahalanobis D2 distances (table 13), depicting meristic resemblance among nine groups of Aspidoscelis tesselata. Distances (similarities) between groups are computed by adding lengths of nodes between groups of interest. Terminal nodes represent the nine groups, and internal nodes represent horizontal distances between clusters. As an interpretation example, the resemblance between Conchas 6CE and Conchas 1CE is 7.2 + 3.2 + 2.2 + 2.8 + 5.6 = 21.0, while the resemblance between Conchas 6CE and Macho EC is 7.2 + 1.0 + 1.9 + 3.1 = 13.2.
Fig. 3 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 3. Electrophoretic phenotypes of sACOH, a monomeric enzyme, from liver homogenates of nine specimens of A. tesselata of pattern class CE from Conchas Lake State Park, New Mexico. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Lanes for individual lizards are labeled beside their patterns on the gel. Anode is to the right.
Fig. 11 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 11. Pattern of multivariate morphological variation among Aspidoscelis tesselata of pattern classes C (N = 44), E (N = 32), and New Mexico D (N = 5) from the vicinity of Sumner Lake State Park, De Baca County, New Mexico. Canonical variate scores were derived from a canonical variate analysis using meristic characters identified in table 10.
Fig. 2 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 2. Electrophoretic phenotypes of GPI, a dimeric enzyme, from erythrocyte hemolysates of six specimens of Aspidoscelis. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Note the very slight difference in migration between the products of the ballele versus callele. Lanes for individual lizards are labeled beside their patterns on the gel as follows: TESC, A. tesselata of pattern class CE from Conchas Lake State Park, New Mexico; and TESE, A. tesselata of pattern class E from Sandoval County, New Mexico. Anode is to the right.
Fig. 1 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 1. Geographic relationships among four northern collecting localities of Aspidoscelis tesselata of color pattern classes C, New Mexico D, and E and convenience classes CE and EC. Color patterns found at the four sites are (1) Conchas Lake State Park: CE and New Mexico D; (2) Sumner Lake State Park: C, New Mexico D, and E; (3) Puerto de Luna: E; and (4) Arroyo del Macho: EC.
Fig. 7 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 7. Color pattern variation in Aspidoscelis tesselata of pattern class CE from the vicinity of Conchas Lake State Park, San Miguel County, New Mexico. Morphological subgroup 6CE: A (RU 0002, 93 mm SVL); B (RU 0029, 96 mm SVL); morphological subgroup 1CE: C (RU 0013, 95 mm SVL); D (RU 0030, 89 mm SVL); E (RU 0021, 95 mm SVL); morphological subgroup 8CE: F (RU 0027, 86 mm SVL).
Fig. 4 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 4. Electrophoretic phenotypes of MPI, a monomeric enzyme, from liver homogenates of 11 specimens of Aspidoscelis. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Lanes for individual lizards are labeled beside their patterns on the gel (with genotype) as follows: NEOTESA, B, and C, different pattern classes of the triploid A. neotesselata from Colorado; TESC and D, A. tesselata of pattern classes CE and D from Conchas Lake State Park, New Mexico; TESE, A. tesselata of pattern class EC from Arroyo del Macho, New Mexico; TESF, A. dixoni from New Mexico; TESF × PUN, triploid hybrid of A. dixoni × A. tigris punctilinealis from New Mexico; and TESG and H, A. dixoni of two pattern classes from Texas. Anode is to the right.
Fig. 2 in Microsatellite variation and population genetic structure of a neotropical endangered Bryconinae species Brycon insignis Steindachner, 1877: implications for its conservation and sustainable management
Fig. 2. UPGMA clustering of the Nei's genetic distance (1972) of the Brycon insignis sampling locations based on six microsatellite loci. Bootstrap values above 50% are shown above branches indicating percentage support in 5000 permutations. Power Company Hatchery (PCH), São João River (SJR), Paraíba do Sul River (PSR), Imbé River (IMR), Muriaé River (MUR) and Itabapoana River (ITR).
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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.