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Figure 3 in The anatomy, phylogenetic relationships, and stratigraphic position of the Tithonian-Berriasian Spanish sauropod dinosaur Aragosaurus ischiaticus
Figure 3. The 'Fault in the Zabacheras area' – Mesozoic syn-rift faults affecting the Villar del Arzobispo Formation ('Unit 2' and 'Unit 3') fossilized by the Castellar Formation ('Unit 4'). Abbreviations: U2, Villar del Arzobispo Formation dominantly carbonate facies; U3, Villar del Arzobispo Formation dominantly siliciclastic facies; U4, El Castellar Formation; U5, Camarillas Formation; ZH, Las Zabacheras site; black lines crossing U2 and U3, Mesozoic syn-rift faults; black lines perpendicular to the latter only in U2, Cenozoic faults; contact between U2 and U3, sedimentary contact; contact between units U3 and U4, unconformable contact; contact between units U4 and U5, sedimentary contact.
Figure 7 in The anatomy, phylogenetic relationships, and stratigraphic position of the Tithonian-Berriasian Spanish sauropod dinosaur Aragosaurus ischiaticus
Figure 7. Pectoral girdle elements of Aragosaurus ischiaticus: A–D, left coracoid (IG 482) in lateral (A), ventral (B), medial (C), and anterior (D) views; E, right scapula (ZH-1) in medial view and partial left coracoid in lateral view; F, anatomical articulation between the coracoid and scapula in lateral view.
Figure 2 in The anatomy, phylogenetic relationships, and stratigraphic position of the Tithonian-Berriasian Spanish sauropod dinosaur Aragosaurus ischiaticus
Figure 2. General stratigraphic section indicating the stratigraphic settings for localities in the Villar del Arzobispo Formation from Galve and the section of the Las Zabacheras site. Modified from Díaz-Molina & Yebenes (1987).
Figure 5 in The anatomy, phylogenetic relationships, and stratigraphic position of the Tithonian-Berriasian Spanish sauropod dinosaur Aragosaurus ischiaticus
Figure 5. Dorsal ribs of Aragosaurus ischiaticus: A–D, anterior dorsal distal rib (IG 492 Uls) in lateral (A), posterior (B), medial (C), and distal (D) views; E–H, posterior dorsal distal rib (IG 481) in medial (E), posterior (F), lateral (G), and distal (H) views.
Figure 1 in The anatomy, phylogenetic relationships, and stratigraphic position of the Tithonian-Berriasian Spanish sauropod dinosaur Aragosaurus ischiaticus
Figure 1. Geological map showing the locality where Aragosaurus was found in Spain. Modified from Díaz-Molina & Yebenes (1987), Soria de Miguel (1997), and with data from Peropadre, Meléndez & Liesa (2012): 1, Upper Triassic (Keuper facies); 2, Cortes de Tajuña, Cuevas Labradas and Barahona formations; 3, Turmiel Formation; 4, Chelva Formation; 5, Loriguilla Formation; 6, Higueruelas Formation; 7, Villar del Arzobispo Formation; 8, El Castellar Formation; 9, Camarillas Formation; 10, Artoles Formation; 11, Morella Formation; 12, Areniscas de las Parras de Martín Formation; 13, Utrillas Formation; 14, Upper Cretaceous; 15, Cenozoic; 16, Quaternary.
Figure 4 in The anatomy, phylogenetic relationships, and stratigraphic position of the Tithonian-Berriasian Spanish sauropod dinosaur Aragosaurus ischiaticus
Figure 4. Caudal vertebrae of Aragosaurus ischiaticus: A, the series of caudals in their relative positions from Cd1 to Cd14 in lateral view; B, C fragment (IG 453, Cd1) of anterior caudal vertebral centrum in anterior (B) and posterior (C) views; D, E, fragment (IG 474, Cd2) of anterior caudal vertebral centrum in lateral (D) and posterior (E) views; F, anterior caudal vertebral centrum (IG 473, Cd3) in anterior view from Lapparent (1960); G–I, anterior caudal vertebra (ZH- 18, Cd4) in left lateral (G), right lateral (H), and anterior (I) views; J–L, anterior caudal neural spine (IG 493, Cd1) in posterior (J), anterior (K), and lateral (L) views; LL, M, middle caudal vertebra (ZH-17, Cd 6) in left lateral (LL) and anterior (M) views; N, anterior caudal neural spine (IG 493, Cd1) in dorsal view; O, P, posterior caudal vertebra (ZH-15, Cd 10) in left lateral (O) and posterior (P) views; Q, distal caudal vertebrae (ZH-12 and 16, Cd 13 and 14) in left lateral view. Arrow 1: a bulge on the lateroventral surface below the caudal rib. Arrow 2: anterior caudal vertebrae possess neural spine summits with shallow, dorsolaterally facing concavities on either side of the midline. Arrow 3: small epipophysislike protuberances on the dorsal surfaces of middle caudal vertebral postzygapophyses.
FIGURE 1 in Osteology, natural history notes, and phylogenetic relationships of the poorly known Caribbean frog Leptodactylus nesiotus (Anura, Leptodactylidae)
FIGURE 1. Graphical representation of skull showing the dimensions measured. (A) dorsal, (B) ventral and (C) lateral views.
FIGURE 2 in Osteology, natural history notes, and phylogenetic relationships of the poorly known Caribbean frog Leptodactylus nesiotus (Anura, Leptodactylidae)
FIGURE 2. Skull of Leptodactylus nesiotus, dorsal view of the male specimen. c: cartilage; p: process; r: ramus.
FIGURE 10 in Osteology, natural history notes, and phylogenetic relationships of the poorly known Caribbean frog Leptodactylus nesiotus (Anura, Leptodactylidae)
FIGURE 10. Topology of most parsimonious trees and bootstrap/GC/bremer support relative values under concavities K = 3. Question marks in GC values represent negatives values, which are an artifact of the method, assigned to weakly supported nodes.
FIGURE 11 in Osteology, natural history notes, and phylogenetic relationships of the poorly known Caribbean frog Leptodactylus nesiotus (Anura, Leptodactylidae)
FIGURE 11. "latrans-melanonotus" clade with the synapomorphies for each node. Numbers above nodes are character numbers. Numbers below nodes are character states. Empty and filled hashmarks indicate homoplastic and nonhomoplastic characters, respectively.
FIGURE 2. A in Species boundaries in the Rana arfaki group (Anura: Ranidae) and phylogenetic relationships to other New Guinean Rana
FIGURE 2. A) An UPGMA phenogram produced from a matrix of the percentage of loci showing fixed allelic differences between OTUs. Scale bar represents 10% fixed allelic differences. Numbers at the beginning of each terminal label refer to locations in Fig. 1. B) A NJ tree of evolutionary relationships among New Guinean ranid frogs based on CSE genetic distances. Numbers at nodes are bootstrap proportions from 100 pseudoreplicates found with a heuristic search under the maximum parsimony criterion of optimality. Scale bar represents a CSE distance of 0.1.
FIGURE 3 in Species boundaries in the Rana arfaki group (Anura: Ranidae) and phylogenetic relationships to other New Guinean Rana
FIGURE 3. Lateral view of head of preserved specimens A) R. arfaki ABTC 44639 and B) R. jimiensis AMS R105974, illustrating the difference in relative size and degree of wartiness of the tympanum.
FIGURE 1 in Phylogenetic relationships among Unionicola (Acari: Unionicolidae) mussel-mites of North America based on mitochondrial cytochrome oxidase I sequences
FIGURE 1. Maximum-parsimony (MP; PAUP*4.0b10, Swofford 2002) tree showing phylogenetic relationships among subgenera of Unionicola spp. from North American that occur in association with freshwater mussels based on morphological and life history characters, excluding those related to sites of egg deposition. The analysis revealed 17 parsimony informative characters. Heuristic searches yielded 8 equally parsimonious trees with a length of 39 steps (CI=0.72). Bootstrap (100 pseudoreplicates) support values>50% from MP analysis are reported above the branches.
FIGURE 3 in Phylogenetic relationships among Unionicola (Acari: Unionicolidae) mussel-mites of North America based on mitochondrial cytochrome oxidase I sequences
FIGURE 3. Maximum-likelihood tree showing phylogenetic relationships among representative species of North American Unionicola from subgenera that occur in association with mussels based on partial sequence data of the cox1 gene. Bootstrap support values>50% from MP and ML analysis are reported above the branches. The outgroup species, Unionicola crassipes, is a sponge-associated mite.
FIGURE 2 in Phylogenetic relationships among Unionicola (Acari: Unionicolidae) mussel-mites of North America based on mitochondrial cytochrome oxidase I sequences
FIGURE 2. Maximum-parsimony tree showing phylogenetic relationships among representative species of North American Unionicola from subgenera that occur in association with mussels based on partial sequence data of the cox1 gene. Bootstrap support values>50% from MP and ML analysis are reported above the branches. The outgroup species, Unionicola crassipes, is a sponge-associated mite.
FIGURE 1 in Phylogenetic relationships in the genus Astropecten Gray (Paxillosida: Astropectinidae) on a global scale: molecular evidence for morphological convergence, species-complexes and possible cryptic speciation
FIGURE 1. Phylogeny of the genus Astropecten as suggested by Döderlein (1917) presenting the relationships of species and species groups relevant to this study.
FIGURE 3 in Molecular phylogenetic analysis of a known and a new hydrothermal vent octopod: their relationships with the genus Benthoctopus (Cephalopoda: Octopodidae)
FIGURE 3. Maximum likelihood tree depicting the phylogenetic relationship of 14 species (15 individuals) of Octopodidae. The analysis employed a portion of the mitochondrial gene, 12S rDNA. Bayesian posterior probability support values are indicated below the nodes and maximum likelihood bootstrap values with 50% support or greater are indicated above the nodes.
FIGURE 2 in Molecular phylogenetic analysis of a known and a new hydrothermal vent octopod: their relationships with the genus Benthoctopus (Cephalopoda: Octopodidae)
FIGURE 2. Maximum likelihood tree depicting the phylogenetic relationship of 13 species (14 individuals) of Octopodidae. The analysis employed a portion of four mitochondrial genes (12S rDNA, 16S rDNA, COIII, cyt b) and a portion of the nuclear gene rhodopsin. Bayesian posterior probability support values are indicated below the nodes and maximum likelihood bootstrap values with 50% support or greater are indicated above the nodes.
FIGURE 1 in Molecular phylogenetic analysis of a known and a new hydrothermal vent octopod: their relationships with the genus Benthoctopus (Cephalopoda: Octopodidae)
FIGURE 1. The Manus Vent octopus specimen (FMNH 310455) in situ near a hydrothermal vent in the Manus Basin off Papua New Guinea, 1500 m depth.
FIGURE 3. Phylogenetic relationships among combined cytochrome b and 16S in First record of Hylomyscus walterverheyeni (Rodentia: Muridae) on the north-western side of the Sanaga River (western Cameroon)
FIGURE 3. Phylogenetic relationships among combined cytochrome b and 16S gene sequences of Hylomyscus inferred from a Bayesian Markov-chain Monte Carlo analysis. Values above branches indicate bootstrap supports obtained from distance and parsimony methods (NJ, MP) and Bayesian posterior probabilities. Hylomyscus waterverheyeni specimens are preceded by the locality code used in Fig. 1. For undescribed taxa, we followed Nicolas et al. (2006).
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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)
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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.