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1,040 results for “belonging”
Fig. S3 in High Genetic Diversity of Amoebae Belonging to the Genus Mayorella (Amoebozoa, Discosea, Dermamoebida) in Natural Habitats
Fig. S3
Fig. S1 in High Genetic Diversity of Amoebae Belonging to the Genus Mayorella (Amoebozoa, Discosea, Dermamoebida) in Natural Habitats
Fig. S1
Breaking Barriers: Investigating the Sense of Belonging Among Women and Non-Binary Students in Software Engineering
<p>This is a package published with the paper "Breaking Barriers: Investigating the Sense of Belonging Among Women and Non-Binary Students in Software Engineering" at the Software Engineering Education and Training track of the 2024 International Conference on Software Engineering (<a href="https://conf.researchr.org/track/icse-2024/icse-2024-software-engineering-education-and-training-track">ICSE-SEET 2024</a>).</p> <p>The data includes the data used in a study about Sense of Belonging among women and non-binary students in software engineering Education.</p>
FIGURE 5 in A new species of planthopper belonging to the genus Oecleus Stål, 1862 (Hemiptera Fulgoroidea: Cixiidae) from coconut palm (Cocos nucifera L) in Jamaica
FIGURE 5. Male terminalia of Oecleus mackaspringi sp. n.; A. lateral view, B. ventral view, and C. dorsal view.
FIGURE 3 in A new species of planthopper belonging to the genus Oecleus Stål, 1862 (Hemiptera Fulgoroidea: Cixiidae) from coconut palm (Cocos nucifera L) in Jamaica
FIGURE 3. Adult male Oecleus mackaspringi sp. n.; A. head frontal view, B. head, pronotum, and mesonotum lateral view, C. head, pronotum, and mesonotum dorsal view, scale=1mm.
FIGURE 9 in A new species of planthopper belonging to the genus Oecleus Stål, 1862 (Hemiptera Fulgoroidea: Cixiidae) from coconut palm (Cocos nucifera L) in Jamaica
FIGURE 9. Maximum Likelihood phylogenetic tree based on 18S sequence data. Branch support was assessed using 1,000 bootstrap replicates with Haplaxius, Myndus, and Nymphomyndus representing outgroups within the Oecleini.
Figure 6 in Revision of freshwater shrimps belonging to Caridina weberi complex (Crustacea: Decapoda: Atyidae) from Polynesia with discussion on their biogeography
Figure 6. Caridina rapaensis. (MNHN-IU-2016-11771; DNA: CA2115), (a). first pereiopod; (b). first pereiopod, detail of the fingertips; (c). second pereiopod; (d). third pereiopod; e. fifth pereiopod; f. dactylus of fifth pereiopod; (g). dactylus of third pereiopod; (h). cephalothorax; (i). preanal carina; (k). uropodal diaeresis; (l). telson. (MNHN-IU-2015-1921: ♀ ovig, 4.0 mm), (j). eggs. (MNHN-IU-2015- 1921: ♂, cl 2.9 mm), m. first pleopod; n. second pleopod.
Figure 4. Caridina marquesensis n in Revision of freshwater shrimps belonging to Caridina weberi complex (Crustacea: Decapoda: Atyidae) from Polynesia with discussion on their biogeography
Figure 4. Caridina marquesensis n. sp. Paratype (MNHN-IU-2017–71; DNA: CA2071), (a). first pereiopod; (b). first pereiopod detail of the fingertips; (c). second pereiopod; (d). third pereiopod; (c). fifth pereiopod; (f). dactylus of fifth pereiopod; (g). dactylus of third pereiopod; h. cephalothorax; (i). preanal carina; (k). uropodal diaeresis; (l). telson. Paratype (MNHN-IU-2017-69; DNA: CA2075), j. eggs. Holotype (MNHN-IU-2017-66), m. first pleopod; n. second pleopod.
Figure 8 in Revision of freshwater shrimps belonging to Caridina weberi complex (Crustacea: Decapoda: Atyidae) from Polynesia with discussion on their biogeography
Figure 8. Distribution map of the four species studied with oceanic currents of Southern Polynesia (from Martinez et al. 2009) represented: SEC. South Equatorial Current. SECC. South Equatorial Countercurrent. MCC. Marquesas Countercurrent. STCC. South Tropical Countercurrent. GYRE. South Pacific Gyre.
Verifying OpenJDK's LinkedList using KeY: Additional artefacts belonging to master thesis
<p>The file testcases.tar.gz contains source code files w.r.t. 64 test cases carried out for this thesis. It also contains log files that contain output of these test cases. The latter are also contained in the file Appendix.pdf, which serves as an on-line appendix for the thesis. Other sources which are of importance for the thesis can be found in https://doi.org/10.5281/zenodo.3517081. Three proof files have been re-established for the purpose of describing these proofs in the thesis. Thus: they deviate from the ones that can be found in https://doi.org/10.5281/zenodo.3517081. These three can be found in the file "Three renewed proof files.zip". It concerns proof files for lastIndexOf(Object), linkFirst(Object), and addFirst(Object). https://doi.org/10.5281/zenodo.3517081 is a link that has been created to store artefacts w.r.t. a paper for the TACAS conference in April 2020 in Dublin, Ireland. The paper carries the same title as this thesis.</p>
FIGURES 33‒44 in Rhinusa Stephens: a taxonomic revision of the species belonging to the R. linariae R. herbarum, R. melas, and R. mauritii groups (Coleoptera Curculionidae)
FIGURES 33‒44. Spiculum ventrale of (33) Rhinusa linariae; (34) R. herbarum; (35) R. mateui; (36) R. melas; (37) R. korotyaevi; (38) R. mauritii. Spermatheca of (39) R. linariae; (40) R. herbarum; (41) R. mateui; (42) R. melas; (43) R. korotyaevi; (44) R. mauritii.
FIGURES 23‒32 in Rhinusa Stephens: a taxonomic revision of the species belonging to the R. linariae R. herbarum, R. melas, and R. mauritii groups (Coleoptera Curculionidae)
FIGURES 23‒32. Profemur and protibia of (23) Rhinusa bipustulata, male; (24) R. linariae, male; (25) R. tetra, male; (26) R. tetra, female. Penis in dorsal view of (27) R. linariae; (28) R. herbarum; (29) R. mateui; (30) R. melas; (31) R. korotyaevi; (32) R. mauritii.
Patent citation data for USPTO utility patents granted between 1976-2015 and for patents belonging to 30 technology domains
<p>These two data file contains information on patent citations for USPTO utility patents granted between 1976 and 2015 and for patents that have been classified in 30 specific technology domains.</p> <p>The file 'CITATION_INFO_no_neg_citlag.csv' is generated combining raw data <a href="https://www.patentsview.org/download/">freely dowloadable from patentsview.org</a> from which citations where the filing year of the citing patent is younger than the filing year of the cited one have been removed.</p> <p>The file 'CITATIONS_DOMAINS.csv' is a sample of the previous file that only includes citations made by patents belonging to one of 30 domains defined in the paper '<a href="https://www.sciencedirect.com/science/article/pii/S0040162520309264#ecom0001">Estimating technology performance improvement rates by mining patent data</a>' by Giorgio Triulzi, Jeff Alstott and Chris Magee.</p> <p>These two files complement another dataset <a href="http://dx.doi.org/10.17632/f4fj887y67.1">published on Mendeley Data</a>. The two datasets can be used, together with the code <a href="https://github.com/GiorgioTriulzi/TechnologyPerformanceImprovementEstimates">published on GitHub</a>, to replicate the main results from the paper.</p>
FIGURE 2. Marphysa baileybrockae n in Reinstatement of species belonging Marphysa sanguinea complex (Annelida Eunicidae) and description of new species from the mid-Pacific Ocean and the Adriatic Sea
FIGURE 2. Marphysa baileybrockae n. sp. A. Anterior end, dorsal view; B. Anterior end, ventral view; C. Anterior end, lateral view; D. Maxillary apparatus, dorsal view; E. Left MI-II-III-IV-V, lateral view; F. Mandible; G. Parapodium 3; H. Parapodium 8; I. Parapodium 16; J. Parapodium 250; K. Parapodium 308; L. Thin, isodont narrow, symmetric, with short and slender teeth, chaetiger 8; M. Thick, anodont wide, symmetric, with long and thick teeth, chaetiger 295; N. Thick, isodont wide, symmetric, with long and slender teeth, chaetiger 358; O. Compound spinigers, chaetiger 8; P. Subacicular hook unidentate, chaetiger 122; Q. Subacicular hook bidentate, chaetiger 152. A–O from holotype USNM 5444, P–Q from paratype AMNH 367. All chaetigers in anterior view; al-MIII: attachment lamella MIII; al-MIV: attachment lamella MIV. Scale bars: A–C, 2.9 mm; D–E, 1 mm; F, 0.8 mm; G–K, 0.1 mm; L–Q, 30 µm.
FIGURE 6 in Reinstatement of species belonging Marphysa sanguinea complex (Annelida Eunicidae) and description of new species from the mid-Pacific Ocean and the Adriatic Sea
FIGURE 6. Marphysa leidii de Quatrefages, 1866. Neotype USNM 71609. A. Anterior end, dorsal view; B. Anterior end, ventral view; C. Anterior end, lateral view; D. Maxillary apparatus, dorsal view; E. Left MI-II-III-IV-V, lateral view; F. Mandible; G. Parapodium 3; H. Parapodium 8; I. Parapodium 13; J. Parapodium 99; K. Parapodium 161; L. Thin, isodont narrow, symmetric, with long and slender teeth, chaetiger 8; M. Thick, isodont wide, symmetric, with short and slender teeth, chaetiger 37; N. Thick, pectinate chaetae, chaetiger 162; O. Thick, anodont wide, symmetric, with long and slender, chaetiger 134; P. Compound spinigers, chaetiger 8; Q. Subacicular hook, chaetiger 37. All chaetigers in anterior view; al-MIII: attachment lamella MIII; LMI-II: ligament between MI and MII; 1: Isodont wide with long and slender teeth; 2: Anodont wide with short and slender teeth; 3: Anodont wide with long and slender teeth. Scale bars: A–C, 1.6 mm; D, 0.7 mm; E, 0.4 mm; F, 1.3 mm; G–K, 0.2 mm; L–N, O, Q, 30 µm; P, 0.1 mm.
FIGURE 4. Marphysa brevibranchiata Treadwell, 1921 n. status. A in Reinstatement of species belonging Marphysa sanguinea complex (Annelida Eunicidae) and description of new species from the mid-Pacific Ocean and the Adriatic Sea
FIGURE 4. Marphysa brevibranchiata Treadwell, 1921 n. status. A. Anterior end, dorsal view; B. Anterior end, ventral view; C. Posterior view, dorsal view; D. Maxillary apparatus, dorsal view; E. Left MI-II-III-IV-V, lateral view; F. Mandible; G. Parapodium 3; H. Parapodium 8; I. Parapodium 25; J. Parapodium 125; K. Parapodium 266; L. Thick, isodont wide, asymmetric, with short and slender teeth, chaetiger 258; M. Thick, anodont wide, symmetric, with long and slender teeth, chaetiger 266; N. Thin, isodont narrow, asymmetric, with long and slender teeth, chaetiger 15; O. Thick, anodont wide, symmetric, with short and thick teeth, chaetiger 266; P. Compound spinigers, chaetiger 8; Q. Subacicular hook, chaetiger 258. A–C, GA–C, G–Q from lectotype AMNH 1358, D–F from paralectotype AMNH_IZC 00361334. All chaetigers in anterior view; LMI-II: Ligament between MI and MII; LMII-III: Ligament between MII and MIII. Scale bars: A–B, 2.9 mm; C, 2.4 mm; D–E, 0.9 mm; F, 1.3 mm; G–K, 0.2 mm; L–N, O, Q, 30 µm; P, 0.1 mm.
FIGURE 9 in Reinstatement of species belonging Marphysa sanguinea complex (Annelida Eunicidae) and description of new species from the mid-Pacific Ocean and the Adriatic Sea
FIGURE 9. Distribution of branchial filaments throughout the body in A. Marphysa americana Monro, 1933 n. status.; B. Marphysa baileybrockae n. sp.; C. Marphysa birgeri n. sp.; D. Marphysa brevibranchiata Treadwell, 1921 n. status.; E. Marphysa californica (Moore, 1909); F. Marphysa leidii de Quatrefages, 1866; G. Marphysa parishii Baird, 1869; H. Marphysa sanguinea (Montagu, 1813).
Data belonging to: Lining the nest with more feathers increases offspring recruitment probability: Selection on an extended phenotype in the blue tit
<p>Birds, among various other taxa, construct nests. Nests form an extended phenotype of the individual building it. Nests are used to extend control over the conditions in which offspring develop, and are therefore commonly considered to be shaped by selection. Nevertheless, scarcely any scientific evidence exist that nest composition is under selection. Here, we demonstrate with data from over 400 blue tit (<i>Cyanistes caeruleus</i>) nests collected over eight years that a higher proportion of feathers in the nest lining is positively associated with the probability of offspring to recruit as a breeding adult later in life. Strikingly, the extended phenotype (nest) was associated stronger with recruitment probability than phenotypic traits that have typically been considered important in selection (laying date, and female size and condition). Our findings suggest that the choice of nest material could be a maternal behaviour with potential lifelong effects on her offspring.</p>
FIGURE 2 in Report of a new genus Mirigryllus belonging to tribe Modicogryllini, with a new species M. nigrus from Zhejiang, China (Orthoptera: Gryllidae: Gryllinae Modicogryllini)
FIGURE 2. Mirigryllus nigrus sp. nov. in living condition. A, hatchling; B, junior instar; C, D, penultimate instar; E, F, ultimate instar; G, male (macropterous); H, female (macropterous); I, male (brachypterous); J, female (brachypterous).
FIGURE 1 in Report of a new genus Mirigryllus belonging to tribe Modicogryllini, with a new species M. nigrus from Zhejiang, China (Orthoptera: Gryllidae: Gryllinae Modicogryllini)
FIGURE 1. Phylogenetic relationship of Mirigryllus nigrus sp. nov. and allied lineages based on tandemly linked 18S-COI sequence. The gene tree was constructed by Maximum likelihood (ML) with JC model and rooted by two Loxoblemmus species as the outgroup. Topology supports (bootstrap value> 50) are indicated above each branch in this order: the SH-aLRT value, the Bayesian posterior probability and the bootstrap value. Sverc. is the abbreviation of Svercacheta.
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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.