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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).
Fig. 2 in Genetic variability in four samples of Neoplecostomus yapo (Teleostei: Loricariidae) from the rio Paranapanema basin, Brazil
Fig. 2. Lateral view of four specimens of Neoplecostomus yapo from the following localities: A, ribeirão Atlântico, 85.9 mm SL; B) ribeirão Uraí, 93.3 mm SL; C) rio Verde, 96.0 mm SL; and D) rio Fortaleza, 97.4 mm SL (type locality of N. yapo).
Fig. 1 in Genetic variability in four samples of Neoplecostomus yapo (Teleostei: Loricariidae) from the rio Paranapanema basin, Brazil
Fig. 1. Partial map of South America showing the collecting sites of Neoplecostomus yapo. Circle = ribeirão Atlântico, município de Mandaguaçu; triangle = ribeirão Uraí, mun. Londrina; lozenge = rio Fortaleza, mun. Tibagi; and star = rio Verde, mun. Ponta Grossa, Paraná State.
Fig. 3 in A multi-approach analysis of the genetic diversity in populations of Astyanax aff. bimaculatus Linnaeus, 1758 (Teleostei: Characidae) from Northeastern Brazil
Fig. 3. Giemsa-stained karyotypes of Astyanax aff. bimaculatus (2n = 50, FN = 96) from sites A (a), B (b) and C (c). In (d), a somatic metaphase after silver nitrate staining in a specimen from Contas River, showing four positive signals (arrows). The bar equals 5µm.
Fig. 2 in A multi-approach analysis of the genetic diversity in populations of Astyanax aff. bimaculatus Linnaeus, 1758 (Teleostei: Characidae) from Northeastern Brazil
Fig. 2. Partial view of collection sites of Astyanax aff. bimaculatus in the State of Bahia, Brazil: (a) Contas River, upstream Pedra Dam, Porto Alegre County – site A, (b) Contas River, downstream Pedra Dam, city of Jequié – site B, and (c) Mineiro stream, Recôncavo Sul Basin, city of Itamari – site C. In (d), view of Pedra Dam reservoir in Middle Contas River, city of Jequié.
Fig. 1 in A multi-approach analysis of the genetic diversity in populations of Astyanax aff. bimaculatus Linnaeus, 1758 (Teleostei: Characidae) from Northeastern Brazil
Fig. 1. Map of the studied area in the State of Bahia, Brazil, showing the hydrographic system and collection sites of Astyanax aff. bimaculatus: (a) site A - Contas River, upstream of Pedra Dam, Porto Alegre County (b) site B - Contas River, downstream of Pedra Dam, city of Jequié (Contas River Basin), (c) site C - Mineiro stream, city of Itamari (Recôncavo Sul Basin) and (*) location of Pedra Dam in Contas River. A specimen of Astyanax aff. bimaculatus is illustrated in detail (total length = 6.65 cm).
Fig. 1 in Fish passage ladders from Canoas Complex - Paranapanema River: evaluation of genetic structure maintenance of Salminus brasiliensis (Teleostei: Characiformes)
Fig. 1. Partial view of the Paranapanema River and its principal affluents (Tibagi and Cinzas Rivers). Featured are the two collection sites: HEP Canoas I and HEP Canoas II.
Figure 10 in Species diversity and endemism in the Daphnia of Argentina: a genetic investigation
Figure 10. UPGMA tree based on allozyme variation at seven loci in Daphnia spinulata populations from Argentina and D. exilis populations from North America. Data for most of the D. exilis populations are from Hebert & Finston (1993), but trimmed to the same seven loci surveyed in the Argentine populations. Codes for their populations are in capital letters and indicate the state where each was collected. Codes in small letters represent new D. exilis data and are found in Appendix 2, while the D. spinulata codes are in Appendix 1. The scale bar represents Nei's genetic distance.
Figure 6 in Species diversity and endemism in the Daphnia of Argentina: a genetic investigation
Figure 6. Collection sites for Argentine populations belonging to the subgenus Ctenodaphnia. Photographs are included for a single individual of each species. Species assignments are based on genetic analyses (see text and subsequent figures). Animals are not shown to scale, and not all sites are shown (see Appendix 1 for the complete collection list).
Figure 7 in Species diversity and endemism in the Daphnia of Argentina: a genetic investigation
Figure 7. NJ tree based on COI sequence variation among all unique haplotypes of Argentine populations belonging to the subgenus Ctenodaphnia. Two members of the subgenus Daphnia (D. obtusa and D. pulex) were included to root the tree. Bootstrap values are presented for major clusters, and K2P distances are indicated by the scale bar. The collection site of each individual is indicated by its population code (see Appendix 1). Individuals morphologically identified as D. notacantha are indicated by an asterisk. This tree is not intended to represent a phylogenetic hypothesis for the subgenus.
Figure 9 in Species diversity and endemism in the Daphnia of Argentina: a genetic investigation
Figure 9. NJ tree based on COI sequence variation among a sample of Daphnia spinulata populations from Argentina and D. exilis populations from North America. The scale bar represents K2P distance. The codes for Argentine populations are provided in Appendix 1, while D. exilis codes are found in Appendix 2.
Figure 8 in Species diversity and endemism in the Daphnia of Argentina: a genetic investigation
Figure 8. NJ tree based on COI sequences for two populations of North American and one population of South American Daphnia similis. Populations of Argentine D. spinulata and North American D. exilis are included for comparison. South American sequences are indicated in bold. The scale bar represents K2P distance.
Figure 5 in Species diversity and endemism in the Daphnia of Argentina: a genetic investigation
Figure 5. NJ tree based on COI sequence variation among Argentine populations identified as D. laevis and D. gessneri. The identifications, based on head morphology, are indicated in this tree, followed by the collection site numbers. Sequences from the North American members of the D. laevis complex (D. dubia, D. laevis, and D. magniceps) were included for comparison. D. mendotae, a Hyalodaphnia species belonging to a different species complex (Colbourne & Hebert, 1996), was used to root the tree. The scale bar represents K2P distance.
Figure 4 in Species diversity and endemism in the Daphnia of Argentina: a genetic investigation
Figure 4. Collection sites for Argentine populations belonging to the subgenus Hyalodaphnia. Photographs are included to demonstrate the several head morphologies encountered. The morphological, not genetic, forms encountered at each site are indicated on the map.
Figure 3 in Species diversity and endemism in the Daphnia of Argentina: a genetic investigation
Figure 3. UPGMA tree based on allozyme variation at seven loci in three species of the Daphnia obtusa complex from Argentina. The scale bar represents Nei's genetic distance.
Figure 2 in Species diversity and endemism in the Daphnia of Argentina: a genetic investigation
Figure 2. NJ tree based on COI sequence variation among all unique haplotypes found in Argentine populations of the subgenus Daphnia. D. mendotae, a North American species belonging to the subgenus Hyalodaphnia, was included to root the tree. Bootstrap values for major clusters and among clusters are presented. The scale bar indicates K2P distances. D. obtusa 1 haplotype A was found at sites 1, 13, 15, 16, 17, 18, 20, 22, 26, 27, 40, 42, 46, 48, 122, 243, 249, 250, and 256; haplotype B was found at sites 132b, 169, 172, 183, 193, 194, and 195. D. 'pulicaria' haplotype C was found at sites 135, 156, 171, 202, and 205. All site codes are listed in Appendix 1. The NJ algorithm is used here for the purpose of clustering only; this tree is not intended to represent a phylogenetic hypothesis for the species assemblage.
Figure 9 in Genets and 'genet-like' taxa (Carnivora, Viverrinae): phylogenetic analysis, systematics and biogeographic implications
Figure 9. Illustration of the phylogenetic relationships within the subfamily Viverrinae obtained here in; civet by courtesy of Delachaux & Niestlé (Dorst & Dandelot, 1976); Genetta johnstoni, Osbornictis, Poiana and Genetta spp. by courtesy of Academic Press (Kingdon, 1997)]
Figure 1 in Genets and 'genet-like' taxa (Carnivora, Viverrinae): phylogenetic analysis, systematics and biogeographic implications
Figure 1. Phylogenetic relationships of the extant carnivores according to Gregory & Hellman (1939; modified).
Figure 3 in Genets and 'genet-like' taxa (Carnivora, Viverrinae): phylogenetic analysis, systematics and biogeographic implications
Figure 3. Illustration of some ultrastructural hair characters (Ex indicates coding related to the intergeneric analysis; In indicates coding related to the intrageneric analysis). A: Cross-section of the GH1 spatula base of Genetta genetta (1) and Genetta abyssinica (2). B: GH1 medullar structure of Genetta genetta (1), Genetta johnstoni (2), Poiana richardsonii (3) and Viverricula indica (4). C: GH1 middle part of the spatula of Poiana richardsonii (1), Osbornictis piscivora (2), Nandinia binotata (3) and Genetta tigrina (4).
Figure 2 in Genets and 'genet-like' taxa (Carnivora, Viverrinae): phylogenetic analysis, systematics and biogeographic implications
Figure 2. Illustration of some cranial and plantar characters (Ex indicates coding related to the intergeneric analysis; In indicates coding related to the intrageneric analysis). A: Skull of Felis silvestris. B: Skull of Poiana richardsonii (Allen, 1924; by courtesy of the American Museum of Natural History). C: Skull of Genetta victoriae (Allen, 1924; by courtesy of the American Museum of Natural History). D: Skull of Osbornictis piscivora (Allen, 1924; by courtesy of the American Museum of Natural History). E: Skull of Genetta genetta (Rosevear, 1974; by courtesy of The Natural History Museum, London). F: Left hindfoot and forefoot of Genetta pardina (Allen, 1924; by courtesy of the American Museum of Natural History). G: Left hindfoot and forefoot of Civettictis civetta (Pocock, 1915; by courtesy of Cambridge University Press).
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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.