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Figure 1 in Fregetta lineata (Peale, 1848) is a valid extant species endemic to New Caledonia
Figure 1. Map showing all locations mentioned in the text, including the breeding location of New Zealand Storm Petrel F. maoriana; and the locations where specimens of New Caledonian Storm Petrel F. lineata were collected, at-sea sightings made, and the fledgling found. There has been discussion about the origin of the specimen NHMUK 1895.2.11.1 (Galbreath 2018).
Figure 6 in Fregetta lineata (Peale, 1848) is a valid extant species endemic to New Caledonia
Figure 6. Comparative measurements of New Caledonian Storm Petrel Fregetta lineata (black), White-bellied Storm Petrel F. grallaria (red) and Black-bellied Storm Petrel F. tropica (green). Data are presented as a correlation matrix for each pair of morphometric variables, with the diagonal in the matrix showing the distribution of each variable per taxon. Colour chart as in Fig. 4F.
Figure 4 in Fregetta lineata (Peale, 1848) is a valid extant species endemic to New Caledonia
Figure 4. Top row: results of Principal Component Analyses performed on six biometrics (bill width, bill depth at gonys, and culmen, wing, tail and tarsus lengths) taken from specimens of Black-bellied Storm Petrel Fregetta tropica (11 populations), small White-bellied Storm Petrels F. grallaria (six populations), the large Titan Storm Petrel F. [g.] titan (Rapa Island) and F. maoriana (New Zealand). The two Brisbane specimens and the specimens ('lineata') from Samoa and ('guttata') from Ua Pou were treated individually. (A) All taxa, plus the four museum specimens. (B) Same analysis performed on individual skins showing distinct taxa and breeding localities. (C) Same analysis for only the five recognised taxa. Bottom row: results of Discriminant Analyses performed on individual specimens from New Caledonian Storm Petrel 'Fregetta lineata' (a regrouping of 'lineata, guttata and QM 14391'), small White-bellied Storm Petrels F. grallaria, Black-bellied Storm Petrel F. tropica (including QM 31216), New Zealand Storm Petrel F. maoriana, and the large Titan Storm Petrel F. [g.] titan. (D) Grouped by nine breeding localities. (E) Same analysis performed on the five taxa as a priori groups. (F) Same analysis performed on a reduced set of taxa (lineata, grallaria and tropica). In all plots, each point represents a specimen, except in 4A.
Figure 10 in Fregetta lineata (Peale, 1848) is a valid extant species endemic to New Caledonia
Figure 10. New Caledonian Storm Petrel Fregetta lineata, Port Bouraké, New Caledonia, 26 September 2014; the first documented fledgling; note traces of down on head, stripes on belly diagnostic of F. lineata, narrow white fringes on dorsal feathers and upperwing (the latter most typical of F. grallaria) (photographer unknown, images supplied by L. Renaudet)
Figure 11 in Fregetta lineata (Peale, 1848) is a valid extant species endemic to New Caledonia
Figure 11. New Caledonian Storm Petrel Fregetta lineata held at the American Museum of Natural History, New York (AMNH 194110); the annotations demonstrate that the middle toe and claw measure 32 mm, and the published measurement of 22 mm is incorrect (Hadoram Shirihai)
Fig. 7. Acetes spiniger Hansen, 1919 in Taxonomic Assessment of Acetes indicus H. Milne Edwards, 1830 (Crustacea, Decapoda, Sergestoidea) as Revealed from Molecular and Morphological Analyses: Re-validation of A. spiniger Hansen, 1919 and Designation of a New Species
Fig. 7. Acetes spiniger Hansen, 1919. (a–e) male (cl 4.3 mm) and (f–i) female (cl. 5.8 mm) from off Kuala Selangor, Malaysia (NSMT-Cr 31637): a, anterior part of cephalothorax, lateral; b, posterior part of abdomen, lateral; c, right left lower antennular flagellum; d, basal segments of third pereopod and genital coxa, ventral; e, capitulum of right petasma; f, anterior part of cephalothorax, lateral; g, basal segments of third pereopod and third and fourth thoracic sternites, ventral; h, lateral profile showing channels and sternites between third and fourth thoracic somites, i, posterior part of telson, dorsal. Abbreviations: gc, genital coxa; iiist, ivst, third and fourth thoracic sternites, respectively.
Fig. 6 in Taxonomic Assessment of Acetes indicus H. Milne Edwards, 1830 (Crustacea, Decapoda, Sergestoidea) as Revealed from Molecular and Morphological Analyses: Re-validation of A. spiniger Hansen, 1919 and Designation of a New Species
Fig. 6. Acetes omorii Hanamura, Imai & Hardianto sp. nov. (a) holotype male (cl 5.3 mm) (NSMT-Cr 31621), and (b–d) paratype female (cl 6.0 mm) (NSMT-Cr 31622) from Matang Mangrove, Malaysia: a, b, right lower antennular flagellum of male and female, respectively; c, basal segments of third pereopod and third and fourth abdominal sternites, ventral; d, lateral profile showing channels and sternites between third and fourth thoracic somites. Abbreviations: iiist, ivst, third and fourth thoracic sternites, respectively.
Fig. 3 in Taxonomic Assessment of Acetes indicus H. Milne Edwards, 1830 (Crustacea, Decapoda, Sergestoidea) as Revealed from Molecular and Morphological Analyses: Re-validation of A. spiniger Hansen, 1919 and Designation of a New Species
Fig. 3. Map showing sampling localities and distribution ranges of Acetes indicus, A. omorii sp. nov. and A. spiniger recognised in this study with certainty: blue solid circles (nos. 1–2) for A. indicus, green solid squares and open square (museum vouchered specimens) for A. spiniger, and red solid triangles for A. omorii sp. nov. Numerals indicating sampling locations: 1, Chiringa; 2, Kumira-Sandwip Ship Ghat; 3, Merbok Mangrove; 4; Matang Mangrove, 5; Kuala Selangor; 6, Malacca; 7, Samut Prakan; 8, Setarap Estuary, South Kalimantan; and 9, Goa.
Fig. 2 in Taxonomic Assessment of Acetes indicus H. Milne Edwards, 1830 (Crustacea, Decapoda, Sergestoidea) as Revealed from Molecular and Morphological Analyses: Re-validation of A. spiniger Hansen, 1919 and Designation of a New Species
Fig. 2. Haplotype network (implemented in PopART) of the Acetes indicus, A. omorii sp. nov., and A. spiniger based on the mitochondrial 16S (a) and mitochondrial COI (b) markers using minimum spanning network (MSN) analysis with outgroups of congeneric species. Circles with different colours represent different species.
Fig. 1 in Taxonomic Assessment of Acetes indicus H. Milne Edwards, 1830 (Crustacea, Decapoda, Sergestoidea) as Revealed from Molecular and Morphological Analyses: Re-validation of A. spiniger Hansen, 1919 and Designation of a New Species
Fig. 1. Bayesian inference trees of Acetes indicus, A. omorii sp. nov., and A. spiniger with the outgroups of other congeneric species based on the mitochondrial 16S (a) and mitochondrial COI (b) markers. Values at the nodes are Bayesian posterior probabilities/Maximum Likelihood/Neighbor Joining support values. For the haplotype abbreviations, see Table 1.
Fig. 5 in Taxonomic Assessment of Acetes indicus H. Milne Edwards, 1830 (Crustacea, Decapoda, Sergestoidea) as Revealed from Molecular and Morphological Analyses: Re-validation of A. spiniger Hansen, 1919 and Designation of a New Species
Fig. 5. Acetes omorii Hanamura, Imai and Hardianto sp. nov. (a–g) holotype male (cl 5.3 mm) (NSMT-Cr 31621), and (b–d) paratype female (cl 6.0 mm) from Matang Mangrove, Malaysia (NSMT-Cr 31622): a, cephalothorax, lateral; b, same, anterior part enlarged; c, right posterior part of abdomen, lateral; d, posterior part of telson, dorsal; e, basal segments of third pereopod and genital coxa; f, capitulum of petasma, posterior; g, right endopod of second pleopod, mesial; h, anterior part of body.
Fig. 4. Acetes indicus H. Milne Edwards, 1830 in Taxonomic Assessment of Acetes indicus H. Milne Edwards, 1830 (Crustacea, Decapoda, Sergestoidea) as Revealed from Molecular and Morphological Analyses: Re-validation of A. spiniger Hansen, 1919 and Designation of a New Species
Fig. 4. Acetes indicus H. Milne Edwards, 1830. (a–g) male (cl 5.6 mm) from Kumia-Sandwip Ship Ghat Bangladesh, and (h–j) female (cl 7.3 mm) from same locality (NSMT-Cr 31616): a, anterior part of cephalothorax, lateral; b, posterior part of abdomen, lateral; c, posterior part of telson, dorsal; d, left lower antennular flagellum; e, basal segments of third pereopod and genital coxa, ventral; f, right petasma, posterior; g, same, capitulum; h, anterior part of cephalothorax, lateral; i, basal segments of third pereopod and third and fourth abdominal sternites, ventral; j, lateral profile showing channels and sternites between third and fourth thoracic somites. Abbreviations: gc, genital coxa; iiist and ivst, third and fourth thoracic sternites, respectively.
Figure 4 in A discussion on the validity of the genus Abalakeus (Acari: Erythraeidae) with a redescription of A. gonabadensis
Figure 4 Abalakeus gonabadensis (larva). A – Scutum circular with striations and cheliceral bases with punctations and faint striations; B – Semi-rectangular scutum; C – Scutum and cheliceral bases with striations; D – Dorsal idiosomal setae.
Figure 1 in A discussion on the validity of the genus Abalakeus (Acari: Erythraeidae) with a redescription of A. gonabadensis
Figure 1 Abalakeus gonabadensis(larva). A – Dorsal view of idiosoma; B – Ventral view of idiosoma; C – Gnathosoma.
Figure 2 in A discussion on the validity of the genus Abalakeus (Acari: Erythraeidae) with a redescription of A. gonabadensis
Figure 2 Abalakeus gonabadensis(larva). A – BFe-Ge I; B – Ti and Ta I; C – BFe-Ge II; D – Ti and Ta II.
Figs 7a–f in Taxonomic Assessment of Three North American Trichodinids by Reevaluating the Taxon Validity of Trichodina heterodentata Duncan, 1977 (Peritrichia)
Figs 7a–f. Comparisons of denticles redrawn from micrographs taken of a – Trichodina heterodentata Duncan, 1977, Population A, b – T. heterodentata Duncan, 1977, Population B, c – T. heterodentata Duncan, 1977, Population C, d – T. hypsilepis Wellborn, 1967, e – T. salmincola Wellborn, 1967 and f – T. vallata Wellborn, 1967 paratypes housed at the Smithsonian Museum, USA.
The state-of-the-art machine learning model for Plasma Protein Binding Prediction: computational modeling with OCHEM and experimental validation
<p><span>Institute of Materia Medica, Chinese Academy of Medical Sciences purchased 10,000 ChemDiv databases.</span></p>
Data from: Geomorphological signatures of known hurricanes and validation of theoretical emplacement formulations: coastal boulder deposits on Cuban low-lying marine terraces
<p>Here we show the models made from SfM photogrammetry for 5 boulders found on the Cuban island emplaced by three hurricanes on the low marine terrace. To generate a 3D-scaled SfM point cloud of each studied boulder, we adapted an easy SfM workflow using Agisoft Metashape software (version 1.7.2). We surveyed each CBD obtaining pictures between 0.5 m - 3 m distance from the boulder and also climbing on the boulder to maximise the diversity of picture angles. The survey was carried over a time lapse of ~30 minutes and under cloudy conditions to avoid shadows created by direct sunlight. For scaling SfM results and assessing the quality of measurements, we used six wooden balls as photogrammetric targets. The diameter of the balls is 30 ± 0.2 x 10-3 m, as verified by repeated caliper measurements. We complemented these targets with two 70 x 10 cm wooden scales. All these targets were used as reference scale bars to correct the spherical distortion inherent to the camera optics and perform an auto-calibration. We further used these targets to check possible distortion after post processing and the generation of the resulting 3D model. In order to create a point cloud and a solid volume, we followed the software workflow: we first aligned the images to identify tiepoints, which were then used in bundle adjustment to compute the 3D dense clouds in a second step.</p>
FIGURE 2 in Late Pleistocene and Holocene pikas (Mammalia, Lagomorpha) from Europe and the validity of Ochotona spelaea: New insights based on mtDNA analysis
FIGURE 2. Haplotype network of species of the genus Ochotona based on the analysis of cytochrome b mtDNA sequences.
FIGURE 1 in Late Pleistocene and Holocene pikas (Mammalia, Lagomorpha) from Europe and the validity of Ochotona spelaea: New insights based on mtDNA analysis
FIGURE 1. Phylogenetic tree of the genus Ochotona based on the analysis of cytochrome b mtDNA sequences.
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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.