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4,619 results for “identical”
FIGURE 2 in The identity of Chelodina oblonga Gray 1841 (Testudines: Chelidae) reassessed
FIGURE 2. Illustration of Chelodina oblonga by Gray (1841), based on BMNH 1947.3.5.89. Compare with photographs of the same specimen in Figure 1.
FIGURE 1 in The identity of Chelodina oblonga Gray 1841 (Testudines: Chelidae) reassessed
FIGURE 1. Ventral, left lateral and dorsal views of the lectotype of Chelodina oblonga Gray (BMNH 1947.3.5.89). The lateral image is slightly dorsally angled, affecting the profile of the carapace. (Image courtesy of P. Campbell, BMNH).
FIG. 2. — Ophiorrhiza medogensis H.Li in Taxonomic studies on Indian Ophiorrhiza L. (Rubiaceae): with a new variety, new distributional record of O. medogensis H.Li for India and the identity of O. recurvipetala Bhuyan, Baruah & Mehmud
FIG. 2. — Ophiorrhiza medogensis H.Li: A, a twig with inflorescence (inset: part of inflorescence enlarged); B, inflorescence (long-styled); C, inflorescence (shortstyled); D, E, floral parts of long-styled flower: D, corolla showing stamens; E, calyx with style, stigma and bracts; F, G, floral parts of short-styled flower: F, splitopened corolla showing stamens; G, calyx with style and stigma. Scale bars: 5 mm. Photos by V.S. Hareesh.
FIG. 1. — Ophiorrhiza medogensis H.Li var. shiyomiense Hareesh & M in Taxonomic studies on Indian Ophiorrhiza L. (Rubiaceae): with a new variety, new distributional record of O. medogensis H.Li for India and the identity of O. recurvipetala Bhuyan, Baruah & Mehmud
FIG. 1. — Ophiorrhiza medogensis H.Li var. shiyomiense Hareesh & M.Sabu, var. nov.: A, habit; B, a twig with inflorescence; C, inflorescence side view; D, inflorescence (short-styled); E, inflorescence (long-styled); F, G, floral parts of short-styled flower: F, split-opened corolla showing stamens; G, calyx with style and stigma; H, I, floral parts of long-styled flower: H, corolla showing stamens; I, calyx with style and stigma; J, infructescence. Scale bars: 5 mm. Photos by V.S. Hareesh.
Fig. 7. – Palisota cristalensis E in Novitates Gabonenses 90: Palisota (Commelinaceae) revisited: description of eight new species from Central Africa and notes on the identity of P. satabiei and P. bogneri
Fig. 7. – Palisota cristalensis E. Bidault & Burg (A– D) and P. fadenii Burg & E. Bidault (E–F). A. Living plant in habitat; B. Inflorescence showing closed flowers; C. Detail of an open flower; D. Detail of pubescence on the upper side of the lamina; E. Detail of an open bisexual flower showing the reflexed lower stamen still in place, and the two upper stamens removed; F. Detail of an open bisexual flower from the outside, showing the reflexed lower stamen still in place, one of the upper stamens, and the calyx with one larger sepal. [A, C: Bidault et al. 3379; B, D: Bidault et al. 3309; E–F: Sita 535] [Photos: A–E:E. Bidault; F: W.J. van der Burg]
Exceptional variation in the appearance of Common Murre eggs reveals their potential as identity signals
<p>We studied the ground colors and maculations of 161 Common Murre (Uria aalge) eggs laid by 43 females in 3 small breeding groups on the cliffs of Skomer Island, Wales, in 2016–2018. Both the colors and maculations varied much more among than within females, providing quantitative evidence for the egg traits that might facilitate the parents' ability to identify their own eggs on the crowded breeding ledges where the density is typically ~20 eggs m–2. Ground colors had a trimodal distribution of hue values (whitish to pale brown, pale blue, or vivid blue-green) and maculations ranged from none to complex squiggles and blotches. The eggs laid by each female in different years were similar to one another, and replacement eggs laid by females within years were also more similar to their first egg than to other eggs in the same breeding group. Egg appearance did not differ among the 3 breeding groups that we studied. Our findings thus support anecdotal observations that, within and between years, female Common Murres lay eggs that have similar ground colors and maculations. We do not, however, find evidence that there is much difference among the eggs laid in different parts of a colony.</p>
Raw data: quantum interference of identical photons from remote GaAs quantum dots
<p>This is the raw data supporting the findings in the letter titled "<em>Quantum Interference of Identical Photons from Remote GaAs Quantum Dots</em>" that is published in <em>Nature Nanotechnology.</em></p>
Supplementary data for Plutniak, S. 2022. "What makes the identity of a scientific method? A history of the 'Structural and analytical typology' in the growth of evolutionary and digital archaeology in southwestern Europe (1950s–2000s)", Journal of Paleolithic Archaeology, vol. 5, 10.
<p>Supplementary data for Plutniak, S. 2022. “What makes the Identity of a Scientific Method? A History of the ‘Structural and analytical typology’ in the Growth of Evolutionary and Digital Archaeology in Southwestern Europe (1950s–2000s)”, <em>Journal of Paleolithic Archaeology</em>. vol 5, 10. DOI: <a href="https://doi.org/10.1007/s41982-022-00119-7">10.1007/s41982-022-00119-7</a>.</p> <p> </p> <p> </p> <p> </p>
Fig. 9 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 9. Lebertia (Pilolebertia) gibbosa Lundblad, 1926, holotype, ♂ (NHRS). A. Venter. B. Palp. C. I-L. D. II-L. E. III-L. F. IV-L. Scale bars = 100 µm.
Fig. 3. GenusLebertia Neuman, 1888 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 3. GenusLebertia Neuman, 1888, positions and shorthand labelling for morphological measurements. A. Example of segment length and height measurements for legs and palps. B. Measurements across the coxal shield. C. The dimensions of the claw; the centre of curvature (c) was defined to be the point opposite of the smaller claw. D. Distances among the long setae on the third segment of the palp. Abbreviations: Ac = acetabula; Cx = Coxa; Gn = gnathosomal bay; L = length; mL = median length; W = height; II-L = second leg. Roman numerals refer to the order of legs starting anteriorly, Arabic numerals refer to segment number starting proximally, for Ac starting anteriorly.
Fig. 1 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 1. Lebertia (Pilolebertia) porosa Thor, 1900 s. lat. A. Dorsal view. B. Ventral view showing acetabula. Photo: Reinhard Gerecke.
Fig. 2 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 2. Neighbor Joining tree based on COI barcodes of Norwegian specimens in the Lebertia porosa aggr. using the Kimura 2-Parameter substitution model. Bootstrap support (1000 replicates) above 70% is shown on branches.
Fig. 6 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 6. Lebertia (Pilolebertia) spp. Examples of observed differences in setation. A–B. High number of setae on segment five of legs three and four (III-L-5, IV-L-5) present in Lebertia aggr. spp. B and D. C. Gap in swimming setae on the fifth segment of the second leg (II-L-5) in Lebertia aggr. spp. A and B, and L. obscura Thor, 1900. D. Segment three of palp (P-3) with a double proximal long seta sometimes present in Lebertia aggr. spp. D. E–F. Segment five of the second leg (II-L-5), close-up: comparison of swimming setae with and without the large gap respectively.
Fig. 8 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 8. Lebertia (Pilolebertia) obscura Thor, 1900, ♂ from the type locality. A. Coxal field. B. Palp. C. I-L. D. II-L. E. III-L. F. IV-L. Scale bars = 100 µm.
Fig. 7 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 7. Lebertia (Pilolebertia) porosa Thor, 1900, ♂ from the type locality. A. Venter. B. Palp. C. I-L. D. II-L. E. III-L. F. IV-L. Scale bars = 100 µm.
Fig. 5 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 5. Lebertia (Pilolebertia) spp. from Norway. TCS haplotype network of COI sequences constructed with PopART.
Fig. 4 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 4. Lebertia (Pilolebertia) spp. in Norway. Maximum Likelihood tree from analysis of the concatenated dataset (COI, 18S, 28S) in RAxML-NG. Bootstrap support (500 replicates) above 50% on branches.
Graphs of redirection: an examination of URIs in identity graphs
<p>This is the dataset for our paper</p> <p><strong>What does it mean when your URIs are redirected? Examining identity and redirection in the LOD cloud</strong></p> <p> </p> <p>Redirection of URIs is widely used in the LOD cloud, and is even part of the best practice guidelines as an approach to the ``curation problem'' on the semantic web (i.e. how to repair imperfections). When dereferencing, one URI is redirected to another URI. Such a redirection could be the result of an update of the namespace, a different encoding scheme, or some other reasons. In this paper, we study the semantics of redirection and examine if redirection indicates how entities in the LOD cloud evolve. More specifically, we focus on entities in the identity graphs: subgraphs in the semantic web restricted to identity links. The entities we study are from sameAs.cc, an identity graph extracted from a crawl of the semantic web in 2015. Our analytical results include an examination of edges and chains of redirection as well as a statistical analysis of the redirection behavior of sampled entities. Additionally, we present properties of the graphs formed by redirection relations. </p> <p> </p> <p>The dataset contains the redirect relations of four sets of sampled entities. These sampled files are:</p> <ul> <li>ite_uniform... the edges of redirection graph corresponding to uniform samplings</li> <li>cc_sample_2... the sampling regarding connected components of size 2, 3-10, 10+, respectively.</li> </ul> <p>The Python scripts are open source online at:</p> <p>https://github.com/shuaiwangvu/redirection</p> <p>The paper is attached. In case of any questions, please contact Shuai Wang at shuai.wang@vu.nl.</p>
FIGURE 6 in Integrative systematics unveils the controversial identity of Engraulidae fishing stocks in a Neotropical estuary, northeast Brazil
FIGURE 6 | Bayesian topology and species delimitation using Generalized Mixed Yule-coalescent (GMYC), Bayesian Poisson Tree Process (bPTP) and Automatic Barcode Gap Discovery (ABGD) discriminating species denominated pilombetas.
FIGURE 3 in Integrative systematics unveils the controversial identity of Engraulidae fishing stocks in a Neotropical estuary, northeast Brazil
FIGURE 3 | Fresh specimens of the species identified in the study area. A. Anchoviella brevirostris (75.5 mm SL), B. Anchoviella cayennensis (90.3 mm SL), C. Anchoviella lepidentostole (83.2 mm SL), D. Anchovia clupeoides (120 mm SL), E. Cetengraulis edentulus (104.4 mm SL), F. Lycengraulis grossidens (98.7 mm SL). Photographs were taken by the first author.
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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.