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Figure 1 in Helminth fauna of the invasive American red-eared slider Trachemys scripta in eastern Spain: potential implications for the conservation of native terrapins
Figure 1. Sampling localities of the American red-eared slider, Trachemys scripta in eastern Spain. (A) Protected wetland 'Marjal de Peñíscola'; (B) 'Cabanes-Torreblanca' Natural Park; (C) Protected Landscape 'Desembocadura del Mijares'; (D) Protected wetland 'Marjal de Gandía'; (E) Site of Community Importance 'Marjal de La Safor'.
Figure 4 in Phylogeography of the Eurasian red squirrel (Sciurus vulgaris orientis) on the boreal island of Hokkaido, Japan
Figure 4. Network of the 29 cytochrome b gene haplotypes of Sciurus vulgaris orientis in Hokkaido Island, Japan, using statistical parsimony. Haplotype names correspond to Appendix 1. Missing haplotypes are indicated by open circles. Lines connecting haplotypes indicate the relationship. Numbers in parentheses indicate the number of individuals. Haplotypes without parentheses are from just one individual.
Figure 5 in Phylogeography of the Eurasian red squirrel (Sciurus vulgaris orientis) on the boreal island of Hokkaido, Japan
Figure 5. Observed (solid lines with solid diamonds) and expected (dotted lines with open squares) mismatch distributions of Sciurus vulgaris orientis haplotypes: A) northern population; B) southern population; C) over all of Hokkaido population.
Figure 3 in Phylogeography of the Eurasian red squirrel (Sciurus vulgaris orientis) on the boreal island of Hokkaido, Japan
Figure 3. Phylogeny of Sciurus vulgaris constructed with the Bayesian inference (BI) under a HKY + G model for the cytochrome b sequences. Numbers above branches represent posterior probability supports in Bayesian analysis followed by bootstrap values from 300 replicates of ML analysis. Hyphens mean no data because clades were absent. Symbols indicate phylogroups, and correspond to those in Figure 2.
Data from: Dynamics of diet-egg transfer of fatty acids in the teleost fish, red drum (Sciaenops ocellatus)
<p>Eggs of marine organisms are increasingly being recognized as important components of marine food webs. The degree to which egg fatty acid profiles reflect maternal diet fatty acid profiles, and therefore the value of fatty acids in eggs as trophic biomarkers, depends on the species' reproductive strategy and the extent of modification of ingested fatty acids. We measured the dynamics of transfer of recently ingested fatty acids to spawned eggs in a batch-spawning teleost, red drum (<em>Sciaenops ocellatus</em>). Results of 21 dietshift experiments, from which the fatty acid profiles of the diets and eggs were compared, showed that 15 of 27 fatty acids measured (one saturated, two monounsaturated and 12 polyunsaturated fatty acids) in eggs were correlated with their levels in the recent diet, and the rate of incorporation into eggs was proportional to the magnitude of the diet shift. Large shifts in diet might occur naturally during spawningmigrations or when prey communities vary over time. Results of this study indicate that fatty acids in red drum eggs can be useful for studying adult diet and exploring trophic linkages in marine systems.</p> <p>This article is part of the theme issue 'The next horizons for lipids as 'trophic biomarkers': evidence and significance of consumer modification of dietary fatty acids'.</p>
Figure 1 in Coccidian parasites of red squirrels (Sciurus vulgaris) and grey squirrels (Sciurus carolinensis) in England
Figure 1. Outline map of England indicating collection sites. 1. Isle of Wight; 2. Fursey Island; 3. Epping Forest; 4. Thetford Chase; 5. Formby; 6. Cumbria.
Reflectance and emission spectra of Earth-like planets orbiting red giant stars
<p>Spectra of red giant stellar hosts and reflectance/emission planetary spectra as described in Kozakis & Kaltenegger (2020). File names and content are explained in 0readme.txt. Please email theakozakis@gmail.com with any questions.</p> <p> </p>
Data for investigation of Ugandan red colobus monkey response to Hepatocystis parasites
<p>Supplemental data for analysis of gene expression response of Ugandan red colobus monkeys (<em>Piliocolobus tephrosceles</em>) to <em>Hepatocystis</em>, a malaria-like parasite.</p>
Fig. 112. T2. A in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 112. T2. A. Lasioglossum (D.) petrellum (Cockerell, 1903), ♂, with weaker microsculpture and distinct punctures throughout. B. L. (D.) droegei Gibbs, 2009, ♂, with strong microsculpture and obscure punctures towards apical rim. Scale bars: 0.5 mm.
Fig. 115. Flagellomeres. A in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 115. Flagellomeres. A. Lasioglossum (D.) festinum sp. nov., ♂, long. B. L. (D.) imbriumbrae sp. nov., ♂, short. Scale bars: 1 mm. Arrows indicate relative lengths of F1 and F2.
Fig. 116 in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 116. Metasomal sterna, ♂. A. Lasioglossum (D.) zephyrus (Smith, 1853), with hair concentrated in apicolateral areas of S3–5. B. Typical red-tailed Lasioglossum (Dialictus), with hair evenly distributed and S5 straight. C. L. (D.) hudsoniellum (Cockerell, 1919), with S5 concave.
Fig. 107 in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 107. Pronotal angle (arrow and outline). A. Lasioglossum (D.) hudsoniellum (Cockerell, 1919), ♀, nearly 90 degrees. B. L. (D.) minckleyi sp. nov., ♀, obtuse. Scale bars: 0.5 mm.
Fig. 109 in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 109. Pronotal ridge (arrow). A. Lasioglossum (D.) kunzei (Cockerell, 1898), ♀, sharply carinate along full height of pronotum. B. L. (D.) eophilus (Ellis, 1914), ♀, absent. Scale bar: 0.5 mm.
Fig. 106. Ocellocular area. A in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 106. Ocellocular area. A. Lasioglossum (D.) clavicorne sp. nov., ♀, sparsely and distinctly punctate. B. L. (D.) clematisellum (Cockerell, 1904), ♀, densely punctate with punctures somewhat obscured by microsculpture. Scale bar: 0.25 mm.
Fig. 108. Mesepisternum. A in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 108. Mesepisternum. A. Lasioglossum (D.) eophilus (Ellis, 1914), ♀, entirely rugose. B. L. (D.) mesillense (Cockerell, 1898), ♀, ruguloso-punctate in dorsal half, smooth and distinctly punctate in ventral half. C. L. (D.) imbriumbrae sp. nov., ♀, entirely smooth and distinctly punctate. Scale bars: 0.5 mm.
Fig. 113. Clypeus. A in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 113. Clypeus. A. Lasioglossum (D.) miltolepoides sp. nov., ♂, sparsely punctate and entirely metallic. B. L. (D.) arenisaltans sp. nov., ♂, with dense punctures and yellow-orange apical rim. Scale bars: 0.5 mm.
Fig. 110. Mesoscutum punctures. A in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 110. Mesoscutum punctures. A. Lasioglossum (D.) vierecki (Crawford, 1904), ♂, all interspaces less than 1 puncture diameter. B. L. (D.) arenisaltans sp. nov., ♂, numerous interspaces of 1 puncture diameter or more. Scale bars: 0.5 mm.
Fig. 114. T1–3. A in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 114. T1–3. A. Lasioglossum (D.) cactorum sp. nov., ♂, convex with rims strongly downcurved (arrows). B. L. (D.) clematisellum (Cockerell, 1904), ♂, flat. Scale bars: 1 mm.
Fig. 105 in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 105. Dark spiracular spots (arrows) on the metasoma. A. Lasioglossum (D.) pictum (Crawford, 1902), ♀, present on T2–4. B. L. (D.) meteorum sp. nov., ♀, present on T3–4 only. Scale bars: 1 mm.
Fig. 100. Forewings. A in The 'red-tailed' Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic
Fig. 100. Forewings. A. Lasioglossum (D.) pallidellum (Ellis, 1914), ♂, with white hair, pale veins, and hyaline membrane. B. L. (D.) decorum sp. nov., ♀, with dark hair, dark veins, and lightly infuscated membrane. Scale bars: 1 mm.
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.