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854 results for “Disparity”
Racial Disparities in Epigenetic Aging of the Right versus the Left Colon
GEO Series GSE151732. Homo sapiens. 256 samples. Type: Methylation profiling by genome tiling array.
DNA supercoiling differences in bacteria result from disparate DNA gyrase activation by polyamines
GEO Series GSE150757. Salmonella enterica subsp. enterica serovar Typhimurium str. 14028S. 4 samples. Type: Expression profiling by high throughput sequencing.
Skewing in Arabidopsis roots involves disparate environmental signaling pathways
GEO Series GSE83242. Arabidopsis thaliana. 18 samples. Type: Expression profiling by array.
FIGURE 2. a in Description of the larva of Leptagrion dispar Selys, 1876 (Odonata: Coenagrionidae) with notes on distribution and ecology of the specie
FIGURE 2. a—Collection area, EPA Lagoa Encantada in Ilhéus, Bahia: the area is formed by several bromeliad agglomerates of various ages in the soil; b—bromeliads in a mangrove area in Itacaré, Bahia; c—Exuvia on the bromeliad leaf; d—Collection of larvae in the bromeliads with one handmade collector that sucks the accumulated water in the plants; e—Adult individual, male perched on a bromeliad.
FIGURE 1 in Description of the larva of Leptagrion dispar Selys, 1876 (Odonata: Coenagrionidae) with notes on distribution and ecology of the specie
FIGURE 1. Map with the collection sites of Leptagrion dispar in Ilhéus, Uruçuca—Serra Grande, and Itacaré, Brazil.
Fig. 1 in Morphology-based phylogenetic analysis of South American Sericini chafers (Coleoptera, Scarabaeidae) contrasts patterns of morphological disparity and current classification
Fig. 1. Characters illustrated: Heads and mouthparts. A F) Heads, dorsal view; G I) Heads, lateral view; J) Head, ventral view; K L) Maxilla, ventral view; M O) Mentum, ventral view. A) Astaena aequatorialis; B) A. boliviensis; C) A. catharinensis; D) A. fuscipennis; E) A. pilosa; F) A. saylori; G) Miotemna singularis; H) A. santaecrucis; I) A. schneblei; J) A. tridentata; K, M) Sayloria bicoloripes; L, O) Parasymmela amazonica; N) Symmela instabilis. Scale bars: A-I) 1 mm; J) 0.5 mm; K–O) 0.2 mm.
Examining the influence of sociodemographics, residential segregation, and historical redlining on eBird and iNaturalist data disparities in three US cities
<p>Code and data for the manuscript "Examining the influence of sociodemographics, residential segregation, and historical redlining on eBird and iNaturalist data disparities in three US cities<strong></strong><strong>"</strong></p>
Fig. 2 in A geometric morphometric approach for disparity of the sulcus acusticus of sagitta in species of Gerreidae (Teleostei: Perciformes)
Fig. 2 Sets of landmarks (LMs, black dots filled) and semi-landmarks (SLMs, black dots empty) designed to capture the shape of the sulcus acusticus from the 18 Gerreidae species sampled. The illustration is a vector graphic of a Diapterus auratus specimen (Chollet-Villalpando et al. 2019)
Fig. 3 in A geometric morphometric approach for disparity of the sulcus acusticus of sagitta in species of Gerreidae (Teleostei: Perciformes)
Fig. 3 Visualization of the variation of the morphospace volume occupied by genera in the Gerreidae. a–f Scatter plots of scores from PC1 vs. PC2 that represent the morphospace occupied by a Deckertichthys, with one species; b Diapterus (three spp.); c Eucinostomus (eight spp.); d Eugerres (four spp.); e Gerres (two spp.); f the complete set of 18 species analyzed in a single morphospace. Species are labeled as follows: filled black squares, Deckertichthys aureolus (Dau); empty black circles, Diapterus auratus (Da); gray equis, D. brevirostris (Db); black stars, D. rhombeus (Drh); gray plus, Eucinostomus argenteus (Ear); filled gray diamonds, E. currani (Ec);
Fig. 12 in New fossil data and phylogenetic inferences shed light on the morphological disparity of Mesozoic Sinoalidae (Hemiptera, Cicadomorpha)
Fig. 12 Fifty percent majority-rule consensus tree of Sinoalidae inferred from Bayesian inference analysis based on 34 morphological characters, with representatives of fore- and hind wings illustrated. Numbers above the nodes indicate posterior probabilities. Numbers above branches
Fig. 11 in New fossil data and phylogenetic inferences shed light on the morphological disparity of Mesozoic Sinoalidae (Hemiptera, Cicadomorpha)
Fig. 11 Fifty percent majority-rule consensus tree of Sinoalidae inferred from maximum parsimony analysis based on 34 morphological characters. Numbers above the nodes indicate bootstrap support values. Numbers above branches indicate character numbers, and below branches indicate state changes. White circles indicate homoplasious
Fig. 6 in New fossil data and phylogenetic inferences shed light on the morphological disparity of Mesozoic Sinoalidae (Hemiptera, Cicadomorpha)
Fig. 6 Thorax of Mesodorus orientalis gen. et sp. nov.: a pronotum; b mesonotum; c left foreleg; d right middle leg (mirrored); e left hind leg (mirrored). Symbols: pro., pronotum; mes., mesonotum; ms., mesoscutal
Fig. 5 in New fossil data and phylogenetic inferences shed light on the morphological disparity of Mesozoic Sinoalidae (Hemiptera, Cicadomorpha)
Fig. 5 Head of Mesodorus orientalis gen. et sp. nov.: a dorsal view; b ventral view; c left antenna; d right antenna. Symbols: ant., antenna; cro., crown; ce., compound eye; oce., ocellus; pc., postclypeus; ac.,
Fig. 1 in New fossil data and phylogenetic inferences shed light on the morphological disparity of Mesozoic Sinoalidae (Hemiptera, Cicadomorpha)
Fig. 1 Palaeogeographic distribution of the Sinoalidae. Maps reconstructed for a the Middle Jurassic (164.5 Ma) and b Late Cretaceous (96.6 Ma) after Scotese 2014. 1, Middle-Upper Jurassic of northeastern China; 2, Lowermost Upper Cretaceous of Myanmar. Circles indicate the number of genera
Figure 1 in The evolution of Metriorhynchoidea (mesoeucrocodylia, thalattosuchia): an integrated approach using geometric morphometrics, analysis of disparity, and biomechanics
Figure 1. Two extinct marine crocodylians, and an ichthyosaur, showing the extensive morphological adaptations to a pelagic lifestyle in metriorhynchids: Platysuchus SMNS 9930 (A), a teleosaurid, displays the comparatively heavier body typical of semi-aquatic teleosaurids, goniopholidids, pholidosaurids and eusuchians; in contrast to the hydrodynamic metriorhynchids, such as Cricosaurus suevicus SMNS 9808 (B). The ichthyosaur Stenopterygius SMNS 81841 (C) has similar adaptations to metriorhynchids, i.e. hydrofoil-like forelimbs, hypocercal tail, and the reduction in limb girdle size. Scale bar = 50 mm.
Figure 11. A in The evolution of Metriorhynchoidea (mesoeucrocodylia, thalattosuchia): an integrated approach using geometric morphometrics, analysis of disparity, and biomechanics
Figure 11. A, relative warps cranial morphology morphospace, delimited by the first two axes. B, shape changes corresponding to the mean shape, and the extremes of both of the first two axes.
Figure 10 in The evolution of Metriorhynchoidea (mesoeucrocodylia, thalattosuchia): an integrated approach using geometric morphometrics, analysis of disparity, and biomechanics
Figure 10. Dorsal view of a generalized metriorhynchid skull, with the landmarks measured shown (see Table 4). Image redrawn from Frey et al. (2002).
Figure 12 in Morphological disparity in a hyperdiverse mammal clade: a new morphotype and tribe of Neotropical cricetids
Figure 12. Contrasting selected external features between two morphotypes evolved to face arboreal mode of life in sigmodontine rodents.
Figure 2 in Morphological disparity in a hyperdiverse mammal clade: a new morphotype and tribe of Neotropical cricetids
Figure 2. Selected features of the external morphology of Rhagomys: A, tail basally furred (f) of R. septentrionalis (MEPN 10898, holotype; dry skin in dorsal view); B, C, halluctal nails of R. rufescens (B; MZUFV-CM 3706) and R. septentrionalis (C; MECN 6172); D, frontal view of manal digit calluses of R. septentrionalis (MECN 6172); E, F, ventral view of right fore (E) and hind foot (F) of R. septentrionalis (MECN 6172). Abbreviations: dg, transverse digit grooves; h, hallux; p, pollex.
Figure 1 in Morphological disparity in a hyperdiverse mammal clade: a new morphotype and tribe of Neotropical cricetids
Figure 1. Phylogenetic trees obtained from maximum likelihood (ML) and Bayesian inference (BI) analyses of the combined mitochondrial cytochrome b locus and three nuclear loci for Sigmodontinae with emphasis on the position of Rhagomys. Numbers above each node indicate bootstrap and posterior probabilities support values obtained in the ML and BI analyses, respectively.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.