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2,315 results for “Comparative analysis”
THE LINGUACULTURAL CONCEPT OF DOUBT: A COMPARATIVE ANALYSIS OF ENGLISH AND UZBEK LANGUAGES
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COMPARATIVE ANALYSIS OF THE CONCEPT "LOVE" IN THE PHRASEOLOGY OF ENGLISH AND UZBEKI LANGUAGES
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Comparative genomic analysis of the mutant Rhodotorula mucilaginosa JH-R23 provides insight into the high-yield carotenoid mechanism
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COMPARATIVE ANALYSIS OF INTONATION OF STATEMENTS IN ENGLISH AND UZBEK
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COMPARATIVE ANALYSIS OF SURGICAL TERMS IN UZBEK AND ENGLISH LANGUAGE
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Fig. 4 in Corosolic acid content and SSR markers in Lagerstroemia speciosa (L.) Pers.: A comparative analysis among populations across the Southern Western Ghats of India
Fig. 4. HPTLC profile of (a) MeOH extract of L. speciosa (LS1197) of population 7 (b) CRA standard.
Fig. 1 in Corosolic acid content and SSR markers in Lagerstroemia speciosa (L.) Pers.: A comparative analysis among populations across the Southern Western Ghats of India
Fig. 1. Chemical structure of corosolic acid (CRA).
COMPARATIVE ANALYSIS OF SEMANTIC MEANING OF RESPECT TERMS
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Comparative analysis of Dipodomys species indicates that kangaroo rat hindlimb anatomy is adapted for rapid evasive leaping
<p><span>Body size is a key factor that influences antipredator behavior. For animals that rely on jumping to escape from predators, there is a theoretical trade-off between jump distance and acceleration as body size changes at both the inter- and intraspecific levels. Assuming geometric similarity, acceleration will decrease with increasing body size due to a smaller increase in muscle cross-sectional area than body mass. Smaller animals will likely have a similar jump distance as larger animals due to their shorter limbs and faster accelerations. Therefore, in order to maintain acceleration in a jump across different body sizes, hind limbs must be disproportionately bigger for larger animals. We explored this prediction using four species of kangaroo rats (<i>Dipodomys </i>spp.), a genus of bipedal rodent with similar morphology across a range of body sizes (40–150 g). Kangaroo rat jump performance was measured by simulating snake strikes to free-ranging individuals. Additionally, morphological measurements of hind limb muscles and segment lengths were obtained from thawed frozen specimens. Overall, jump acceleration was constant across body sizes and jump distance increased with increasing size. Additionally, kangaroo rat hind limb muscle mass and cross-sectional area scaled with positive allometry. Ankle extensor tendon cross-sectional area also scaled with positive allometry. Hind limb segment length scaled isometrically, with the exception of the metatarsals, which scaled with negative allometry. Overall, these findings support the hypothesis that kangaroo rat hind limbs are built to maintain jump acceleration rather than jump distance. Selective pressure from single-strike predators, such as snakes and owls, likely drives this relationship.</span></p>
Supplementary material 1 from: Sun C-H, Huang Q, Zeng X-S, Li S, Zhang X-L, Zhang Y-N, Liao J, Lu C-H, Han B-P, Zhang Q (2022) Comparative analysis of the mitogenomes of two Corydoras (Siluriformes, Loricarioidei) with nine known Corydoras, and a phylogenetic analysis of Loricarioidei. ZooKeys 1083: 89-107. https://doi.org/10.3897/zookeys.1083.76887
COI sequences of Corydoras aeneus and C. paleatus Tables S1–S4, Figs S1–S4
Figure 2 from: Sun C-H, Huang Q, Zeng X-S, Li S, Zhang X-L, Zhang Y-N, Liao J, Lu C-H, Han B-P, Zhang Q (2022) Comparative analysis of the mitogenomes of two Corydoras (Siluriformes, Loricarioidei) with nine known Corydoras, and a phylogenetic analysis of Loricarioidei. ZooKeys 1083: 89-107. https://doi.org/10.3897/zookeys.1083.76887
Figure 2 K2P genetic distance a nucleotide diversity b Ka/Ks ratio c analyses of protein-coding genes among the eleven Corydoras mitogenomes.
Figure 3 from: Sun C-H, Huang Q, Zeng X-S, Li S, Zhang X-L, Zhang Y-N, Liao J, Lu C-H, Han B-P, Zhang Q (2022) Comparative analysis of the mitogenomes of two Corydoras (Siluriformes, Loricarioidei) with nine known Corydoras, and a phylogenetic analysis of Loricarioidei. ZooKeys 1083: 89-107. https://doi.org/10.3897/zookeys.1083.76887
Figure 3 Phylogenetic trees of 44 Siluriformes species using concatenated nucleotide sequences of 13 protein-coding genes and two rRNAs using the maximum likelihood method. Numbers in the ML tree represent SH-aLRT support/ultrafast bootstrap support values.
Figure 4 from: Sun C-H, Huang Q, Zeng X-S, Li S, Zhang X-L, Zhang Y-N, Liao J, Lu C-H, Han B-P, Zhang Q (2022) Comparative analysis of the mitogenomes of two Corydoras (Siluriformes, Loricarioidei) with nine known Corydoras, and a phylogenetic analysis of Loricarioidei. ZooKeys 1083: 89-107. https://doi.org/10.3897/zookeys.1083.76887
Figure 4 Phylogenetic tree of 44 Siluriformes species using concatenated nucleotide sequences of 13 protein-coding genes and two rRNAs via the Bayesian interference method. Applicable posterior probability values are shown.
Comparative analysis of passerine feather traits: data and script
<p></p> <p class="Normln1"><span>Tropical bird species are characterised by a comparatively slow pace of life, being predictably different from their temperate zone counterparts in their investments in growth, survival and reproduction. In birds, <span>the development of functional plumage is often considered energetically demanding investment, with consequences on individual fitness and survival. However, </span>current knowledge of interspecific variation in feather growth patterns is mostly based on species of the northern temperate zone. We<span> evaluated patterns in tail feather growth rates (FGR) and feather quality (</span>stress-induced <span>fault bar occurrence; FBO), </span>using<span> </span>1518 individuals of 167 species and 39 passerine families inhabiting Afrotropical and northern temperate zones. We <span>detected</span> a clear difference in feather traits between species breeding in the temperate and tropical zones, with the latter having significantly slower FGR and three times higher FBO. Moreover, trans-Saharan latitudinal migrants resembled temperate zone residents in that they exhibited a comparatively fast FGR and low FBO, despite sharing moulting environments with tropical species. Our results reveal convergent latitudinal shifts in feather growth investments (latitudinal syndrome) across unrelated passerine families and underscore the importance of breeding latitude in determining cross-species variation in key avian life-history traits.</span></p>
Figure 9 from: Chen Z-T (2022) Comparative mitogenomic analysis of two earwigs (Insecta, Dermaptera) and the preliminary phylogenetic implications. ZooKeys 1087: 105-122. https://doi.org/10.3897/zookeys.1087.78998
Figure 9 Predicted structural elements in the control regions of Challia fletcheri, Euborellia arcanum, Eudohrnia metallica, and Paratimomenus flavocapitatus.
Figure 4 from: Chen Z-T (2022) Comparative mitogenomic analysis of two earwigs (Insecta, Dermaptera) and the preliminary phylogenetic implications. ZooKeys 1087: 105-122. https://doi.org/10.3897/zookeys.1087.78998
Figure 4 Evolutionary rates of PCGs in six species of earwigs. The bar indicates each gene's Ka/Ks value.
Figure 5 from: Chen Z-T (2022) Comparative mitogenomic analysis of two earwigs (Insecta, Dermaptera) and the preliminary phylogenetic implications. ZooKeys 1087: 105-122. https://doi.org/10.3897/zookeys.1087.78998
Figure 5 Secondary structures of tRNA genes in the mitogenome of Apachyus feae. Mismatched base pairs are indicated by red circles; reduced arms are indicated by red arrowheads.
Figure 6 from: Chen Z-T (2022) Comparative mitogenomic analysis of two earwigs (Insecta, Dermaptera) and the preliminary phylogenetic implications. ZooKeys 1087: 105-122. https://doi.org/10.3897/zookeys.1087.78998
Figure 6 Secondary structures of tRNA genes in the mitogenome of Diplatys flavicollis. Mismatched base pairs are indicated by red circles; reduced arms are indicated by red arrowheads.
Figure 1 from: Chen Z-T (2022) Comparative mitogenomic analysis of two earwigs (Insecta, Dermaptera) and the preliminary phylogenetic implications. ZooKeys 1087: 105-122. https://doi.org/10.3897/zookeys.1087.78998
Figure 1 Mitochondrial maps of Apachyus feae and Diplatys flavicollis. Genes outside the map are transcribed clockwise, whereas those inside the map are transcribed counterclockwise. Names and other details of the genes are listed in Tables 2 and 3. The inside circles show the GC content and the GC skew. GC content and GC skew are plotted as the deviation from the average value of the entire sequence.
Figure 10 from: Chen Z-T (2022) Comparative mitogenomic analysis of two earwigs (Insecta, Dermaptera) and the preliminary phylogenetic implications. ZooKeys 1087: 105-122. https://doi.org/10.3897/zookeys.1087.78998
Figure 10 Phylogenetic relationships within Dermaptera inferred by Bayesian inference and maximum likelihood analysis. Numbers at the nodes are posterior probabilities (left) and bootstrap values (right). The family names are listed after the species. Infraorders and parvorders are indicated below each family name.
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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.