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FIGURE 2 in Comparative analysis of the diet composition and its relation to morphological characteristics in Achirus mazatlanus and Syacium ovale (Pleuronectiformes: Osteichthyes) from a Mexican Pacific coastal lagoon
FIGURE 2 | A. Dendrogram showing the result of numerical classification of stomach contents. B. Principal coordinate analysis plot. Vector overlay shows food categories with Spearman's correlation values of 0.5 or higher with ordination axes. Data pooled by species (Am: Achirus mazatlanus; So: Syacium ovale) and size classes (1 for LT <10 cm; 2 for LT ≥ 10 cm and LT ≤ 15 cm; 3 for LT> 15 cm).
Fig. 6 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 6. Four examples of the tissue expression profiling of unknown distinct unigenes (>500 bp) expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis. Relative expression levels were determined as described in Fig. 5.
Fig. 4 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 4. Kyoto encyclopedia of gene and genomes (KEGG) analysis of unigenes expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis. Each category contains more than 1 unigene sequences.
Fig. 2 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 2. Clusters of orthologous groups (COG) functional classification of unigenes expressed highly and specifically in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis.
Fig. 1 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 1. Statistics of sequences expressed specifically in each analyzed tissue of Bactrocera dorsalis.
Fig. 5 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 5. Six examples of the tissue expression profiling of predicted distinct unigenes (>500 bp) expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis. Relative expression levels were determined by qRT-PCR in head (HE), thorax (TH), abdomen (AB), midgut (MG), fat body (FB), Malpighian tubules (MT), testes (TE), and male accessory glands and ejaculatory duct (MAG) samples from B. dorsalis males. Relative expression levels were calculated based on the value in head, which was ascribed an arbitrary value of 1. Different letters above the bars indicate significant differences based on Tukey's test (P ≤ 0.05).
Fig. 3 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 3. Gene ontology (GO) classification of unigenes expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis.
Fig. 1 in A comparative analysis of resistance testing methods in Aedes albopictus (Diptera: Culicidae) from St. Johns County, Florida
Fig. 1. Collection site locations in St. Johns County, Florida, for the 3 Aedes albopictus field strains tested for resistance in this study. RAYS is 14.7 km from ELKTON. RAYS is 6.6 km from BEACH. ELKTON and BEACH are 18.0 km apart. ELKTON and RAYS were the F1 and F2 sites in Marcombe et al. (2014).
Fig. 6 in Comparative Analysis of Complete Mitogenomes of Two Gobies and Their Phylogenetic Implication.
Fig. 6. Termination-associated sequences (TAS), conserved sequence blocks (CSB-1, CSB-2, and CSB-3) and central conserved sequences (CSB-D) and GTGGG box in control region of two Oxyurichthys species mitogenomes.
Fig. 8 in Comparative Analysis of Complete Mitogenomes of Two Gobies and Their Phylogenetic Implication.
Fig. 8. Phylogenetic trees of goby derived from Maximum Likelihood (ML) method based on 13 PCGs + 2 rRNAs. The numbers at nodes are ultrafast bootstrap values. GenBank accession numbers are placed in front of species names.
Fig. 7 in Comparative Analysis of Complete Mitogenomes of Two Gobies and Their Phylogenetic Implication.
Fig. 7. Phylogenetic trees of goby derived from Bayesian Inference (BI) method based on 13 PCGs + 2 rRNAs. The numbers at nodes are posterior probability values. GenBank accession numbers are placed in front of species names.
Fig. 5 in Comparative Analysis of Complete Mitogenomes of Two Gobies and Their Phylogenetic Implication.
Fig. 5. The putative origin of L-strand replication (OL) of Oxyurichthys ophthalmonema (a) and Oxyurichthys microlepis (b).
A Meta-Analysis on the Reliability of Comparative Judgement Data
<p>This is the data and R analysis script with the article "A Meta-Analysis on the Reliability of Comparative Judgement"</p>
Supplementary information for D4.6 CEMCAP comparative techno-economic analysis of CO2 capture in cement plants
<p>Supplementary information for D4.6 CEMCAP comparative techno-economic analysis of CO2 capture in cement plants</p>
Fig. 2 in Comparative analysis of the diet of Arctocephalus gazella (Pinnipedia), at two localities of the South Shetland Islands, with emphasis on the fish component
Fig. 2. Estimated standard length frequency distribution of Gymnoscopelus nicholsi (Gilbert, 1911), preyed on by Antarctic fur seals Arctocephalus gazella (Peters, 1875), at Stranger Point and Duthoit Point, South Shetland Islands, in February 2012.
Fig. 1 in Comparative analysis of the diet of Arctocephalus gazella (Pinnipedia), at two localities of the South Shetland Islands, with emphasis on the fish component
Fig. 1. The study area at South Shetland Islands: Stranger Point, King George Island/Isla 25 de Mayo and Duthoit Point, Nelson Island (modified from MALVÉ et al., 2014 and BRAUN et al., 2017).
Fig. 4 in Comparative analysis of the diet of Arctocephalus gazella (Pinnipedia), at two localities of the South Shetland Islands, with emphasis on the fish component
Fig. 4. Estimated standard length frequency distribution of Electrona antarctica (Gunther, 1878) preyed on by Arctocephalus gazella (Peters, 1875), at both sampling sites, Stranger Point and Duthoit Point, South Shetland Islands, in February 2012.
Fig. 3 in Comparative analysis of the diet of Arctocephalus gazella (Pinnipedia), at two localities of the South Shetland Islands, with emphasis on the fish component
Fig. 3. Estimated standard length frequency distribution of Pleuragramma antarctica (Boulenger, 1902) preyed on by Arctocephalus gazella (Peters, 1875), at both sampling sites, Stranger Point and Duthoit Point, South Shetland Islands, in February 2012.
Fig. 25 in Faunal dynamics across the Silurian-Devonian positive isotope excursions (δ C, δ O) in Podolia, Ukraine: Comparative analysis of the Ireviken and Klonk events
Fig. 25. Scheme of main environmental changes and faunal responses across the Klonk Event and the S–D transition carbon isotope excursion (SIDECIE) in the Dnistrove succession. Sea−level pattern after Walliser (1996: fig. 1; see other sea−level curves in Haq and Schutter 2008: fig. 2; Brett et al. 2009: fig. 20; Johnson 2010: fig. 1; Munnecke et al. 2010: fig. 2); for discussion of differently recorded eustasy, as well as climatic setting see Buggisch and Joachimski (2006) and Małkowski and Racki (2009). Shades of gray denote two slices of the SIDECIE.
Fig. 24 in Faunal dynamics across the Silurian-Devonian positive isotope excursions (δ C, δ O) in Podolia, Ukraine: Comparative analysis of the Ireviken and Klonk events
Fig. 24. Scheme of main environmental changes and faunal responses across the Ireviken Event and early Sheinwoodian carbon isotope excursion (ESCIE) in the Kytayhorod succession. Overall eustatic pattern and climatic events compiled from Johnson (2010: fig. 2; see other sea−level curves in Lüning et al. 2000: fig. 9; Cramer and Saltzman 2007: fig. 5; Brett et al. 2009: fig. 20; Ray and Butcher 2010: fig. 1) and Lehnert et al. (2010: figs. 1–3), respectively. Regional bathymetric curve modified from Koren et al. (1989: fig. 1). Note a distinctive discrepancy of the both sea−level patterns in some intervals, probably mostly controlled by regional epeirogenic activity in the Podolian shelf domain. Shades of gray denote three slices of the ESCIE.
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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.