Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
1,040
datasets available to search
ShareScore release 0.9.0
Dataset results
1,040 results for “belonging”
Figure 6 in The family Aeolidiidae Gray, 1827 (Gastropoda Opisthobranchia) from Brazil, with a description of a new species belonging to the genus Berghia Trinchese, 1877
Figure 6. Berghia marcusi sp. nov. A, dorsal view of the external morphology; scale bar = 5 mm. B, lateral view of a specimen, showing the arrangement of the cerata; scale bar = 1 mm. C, D, radular teeth (Praia dos Ossos, 5-mm-long specimen); scale bars = 10 Mm. E, detail of a tooth with piled up denticles (16.5-mm-long specimen, from Praia de Aramaçao). F, detail of a tooth with denticles ending in either two or more tips (16.5-mm long specimen, from Praia de Aramaçao).
Figure 5. Berghia creutzbergi. A in The family Aeolidiidae Gray, 1827 (Gastropoda Opisthobranchia) from Brazil, with a description of a new species belonging to the genus Berghia Trinchese, 1877
Figure 5. Berghia creutzbergi. A, lateral view of a specimen, showing the arrangement of the cerata; scale bar = 1 mm. B, radular tooth (13-mm-long specimen, from Praia de Armação); scale bar = 100 Mm.
Figure 4. Berghia benteva. A in The family Aeolidiidae Gray, 1827 (Gastropoda Opisthobranchia) from Brazil, with a description of a new species belonging to the genus Berghia Trinchese, 1877
Figure 4. Berghia benteva. A, dorsal view of the external morphology; scale bar = 5 mm. B, lateral view of a specimen, showing the arrangement of the cerata; scale bar = 5 mm. C, D, radular teeth (10-mm-long specimen, from Praia de Armação); scale bars = 100 Mm.
Figure 2 in The family Aeolidiidae Gray, 1827 (Gastropoda Opisthobranchia) from Brazil, with a description of a new species belonging to the genus Berghia Trinchese, 1877
Figure 2. Anteaeolidiella indica from Praia dos Ossos (10-mm-long specimen). A, the largest radular tooth. B, one median tooth. C, the smallest tooth. Scale bars = 10 Mm.
Figure 3 in The family Aeolidiidae Gray, 1827 (Gastropoda Opisthobranchia) from Brazil, with a description of a new species belonging to the genus Berghia Trinchese, 1877
Figure 3. SEM images of radulae and jaws. A, radula of Anteaeolidiella indica from Praia dos Ossos; scale bar = 10 Mm. B, jaw of A. indica; scale bar = 100 Mm. C, radula of Berghia benteva from Praia dos Ossos (18-mm-long specimen); scale bar = 50 Mm. D, central part of the tooth of B. benteva; scale bar = 10 Mm. E, detail of the tooth of Berghia creutzbergi from Praia de Armação (13-mm-long specimen); scale bar = 10 Mm. F, jaw of B. creutzbergi (13-mm-long specimen); scale bar = 200 Mm.
Figure 1. Living animals. A, Anteaeolidiella indica from Praia dos Ossos. B in The family Aeolidiidae Gray, 1827 (Gastropoda Opisthobranchia) from Brazil, with a description of a new species belonging to the genus Berghia Trinchese, 1877
Figure 1. Living animals. A, Anteaeolidiella indica from Praia dos Ossos. B, Berghia benteva from Praia de Armação (10-mm-long specimen). C, D, Berghia benteva from Praia dos Ossos (18- and 19-mm-long specimens). E, Berghia creutzbergi from Praia de Armação (13-mm-long specimen). F, Berghia marcusi sp. nov., from Praia de Armação (dorsal view, 12-mm-long specimen). G, Berghia marcusi sp. nov. (ventral view of the same specimen). H–J, Spurilla neapolitana from Praia de Armação. K, Spurilla neapolitana from Praia dos Ossos.
Fig. 3 in Report of a Feather Mite Species (Acariformes: Astigmata) from the Oriental White Stork, Ciconia boyciana (Ciconiiformes: Ciconiidae), Belonging to the Japanese Native Population
Fig. 3. Pelargolichus orientalis, male (A) and female (B). A, right setae se and si on prodorsal shield, dorsal view; B, posterior part of hysterosoma, dorsal view. Scale bars: 10 µm.
Fig. 1 in Report of a Feather Mite Species (Acariformes: Astigmata) from the Oriental White Stork, Ciconia boyciana (Ciconiiformes: Ciconiidae), Belonging to the Japanese Native Population
Fig. 1. The taxidermy specimen of the Oriental White Stork Ciconia boyciana sampled in Toyooka City, Hyogo Prefecture, Japan.
Fig. 1 in Lectotypification of taxa belonging to the "Festuca circummediterranea" group
Fig. 1. – Lectotypus of Festuca ovina subsp. laevis Hack. [Todaro s.n., W] [© Naturhistorisches Museum Wien. Reproduced with permission]
Fig. 2 in Lectotypification of taxa belonging to the "Festuca circummediterranea" group
Fig. 2. – Lectotypus of Festuca duriuscula var. campana N. Terracc. [Terracciano s.n., W] [© Naturhistorisches Museum Wien. Reproduced with permission]
Source data belonged to "Geometric flow control in lateral flow assays: Macroscopic single-phase modeling"
<p>This record contains all the necessary data to obtain the results of the study "Geometric flow control in lateral flow assays: Macroscopic single-phase modeling" (<a href="https://doi.org/10.1063/5.0093316">https://doi.org/10.1063/5.0093316</a>).</p>
Data belonging to the article: Estimating pre-harvest density, adult sex ratio and fecundity of white-tailed deer using wildlife cameras
<p>Adult sex ratio and fecundity (juveniles per female) are key population parameters in sustainable wildlife management, but inferring these requires abundance estimates of at least three age/sex classes of the population (male and female adults and juveniles). Prior to harvest, we used an array of 36 wildlife camera traps during 2 and 3 weeks in the early autumn of 2016 and 2017 respectively. We recorded white-tailed deer adult males, adult females and fawns from the pictures. Simultaneously, we collected fecal DNA (fDNA) from 92 20mx20m plots placed in 23 clusters of four plots between the camera traps. We identified individuals from fDNA samples with microsatellite markers and estimated the total sex ratio and population density using Spatial Capture Recapture (SCR). The fDNA-SCR analysis concluded equal sex ratio in the first year and female bias in the second year, and no difference in space use between sexes (fawns and adults combined). Camera information was analyzed in a Spatial Capture (SC) framework assuming an informative prior for animals' space use, either (1) as estimated by fDNA-SCR (same for all age/sex classes), (2) as assumed from the literature (space use of adult males larger than adult females and fawns), (3) by inferring adult male space use from individually-identified males from the camera pictures. These various SC approaches produced plausible inferences on fecundity, but also inferred total density to be lower than the estimate provided by fDNA-SCR in one of the study years. SC approaches where adult male and female were allowed to differ in their space use suggested the population had a female-biased adult sex ratio. In conclusion, SC approaches allowed estimating the pre-harvest population parameters of interest and provided conservative density estimates.</p>
Text-fig. 4. a: Conglomeratic to massive sandstone facies 1, facies A are composed of Andesit (AF), Clay (CF) and Sandstone (SF) fragments lain on medium-sandstone. b: Conglomeratic to massive sandstone facies, outcropping of massive sandstone facies comprises of fine to medium grain size of grey to yellowish sandstone. c: Heterolithic sandstone-mudstone facies, intercalation of fine sand with silt and shale as type form of heterolithic sandstone mudstone as indicated by a high sand/shale ratio. d: Example outcrops of heterolithic sandstone-mudstone 2 indicated by low sand/shale ratio. e: Heterolithic fine sand and mudstone and mudstone facies, intercalation of thin sandstone and shale. f: Representative of slump deposits outcrops belong to conglomeratic to massive sandstone facies, which is indicated by the intercalation of sandstone and shale and some disturbed beds or layers as seen in slump deposits. The facies type is normally deposited within the basin floor, channel margin or as a product of the overbank deposits. In this figure the slump deposit is shown as internal bedding, some occurred on the bedding-plane. Trend slope measurement of the fold-axis revealed values N 135°E and N 108°E. in Lithofacies And Ichnofacies Of Turbidite Deposits, West Java, Indonesia
Text-fig. 4. a: Conglomeratic to massive sandstone facies 1, facies A are composed of Andesit (AF), Clay (CF) and Sandstone (SF) fragments lain on medium-sandstone. b: Conglomeratic to massive sandstone facies, outcropping of massive sandstone facies comprises of fine to medium grain size of grey to yellowish sandstone. c: Heterolithic sandstone-mudstone facies, intercalation of fine sand with silt and shale as type form of heterolithic sandstone mudstone as indicated by a high sand/shale ratio. d: Example outcrops of heterolithic sandstone-mudstone 2 indicated by low sand/shale ratio. e: Heterolithic fine sand and mudstone and mudstone facies, intercalation of thin sandstone and shale. f: Representative of slump deposits outcrops belong to conglomeratic to massive sandstone facies, which is indicated by the intercalation of sandstone and shale and some disturbed beds or layers as seen in slump deposits. The facies type is normally deposited within the basin floor, channel margin or as a product of the overbank deposits. In this figure the slump deposit is shown as internal bedding, some occurred on the bedding-plane. Trend slope measurement of the fold-axis revealed values N 135°E and N 108°E.
Text-fig. 21. Femur head from White Patch Bone Site belonging to a large mammal approximately the size of a pygmy hippopotamus, probably an embrithopod. View of ligamentary fossa. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 21. Femur head from White Patch Bone Site belonging to a large mammal approximately the size of a pygmy hippopotamus, probably an embrithopod. View of ligamentary fossa.
Fig. 2 in The Strongylidae belonging to Strongylus genus in horses from southeastern Poland
Fig. 2 The buccal cavity of large strongyles from the genus Strongylus: S. vulgaris, S. edentatus, and S. equinus
Figs 100–108 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)
Figs 100–108. Epipharynx (100, 103, 106) and aedeagus (dorsal and lateral view) (101–102, 104–105, 107–108) of: 100–102 = Ammoecius mimus (PÉRINGUEY, 1901), 103–105 = A. lugubris BOHEMAN, 1857, 106–108 = A. terminatus HAROLD, 1869
Figs 96–99 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)
Figs 96–99. Habitus of: 96 = Ammoecius incultus (PETROVITZ, 1961) (male, length 3.0 mm, South Africa: S. W. Cape, Gansbaa 10 km NE), 97 = A. terminatus HAROLD, 1869 (male, length 3.5 mm, South Africa: S. W. Cape, Brackfontein farm), 98 = A. mimus (PÉRINGUEY, 1901) (male, length 4.5 mm, South Africa: Cape, Karroo, Olifantsulei farm), 99 = A. lugubris BOHEMAN, 1857 (male, length
Figs 69–80 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)
Figs 69–80. Epipharynx (69, 73, 77), apex of corypha (lateral view) (70, 74, 78) and aedeagus (dorsal and lateral view) (71–72, 75–76, 79–80) of: 69–72 = Ammoecius amplicollis (PEYERIMHOFF, 1939),
Figs 81–84 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)
Figs 81–84. Habitus of: 81 = Ammoecius brevis ERICHSON, 1848 (male, length 4.0 mm, Italy: Piedmont, Ghislarengo), 82 = A. frigidus BRISOUT, 1866 (male, length 5.0 mm, Portugal: Castelo Branco, Covilhã, Beida Baixa), 83 = A. lusitanicus ERICHSON, 1848 (male, length 5.0 mm, Spain: Cadiz, Sierra de Aljibe), 84 = A. rugifrons AUBÉ, 1850 (male, length 4.5 mm, Algeria: Mechroha)
Figs 65–68 in Systematic Redefinition Of Taxa Belonging To The Genera Ahermodontus Báguena, 1930 And Ammoecius Mulsant, 1842, With Description Of The New Genus Vladimirellus (Coleoptera: Aphodiidae)
Figs 65–68. Habitus of: 65 = Ammoecius numidicus MULSANT, 1851 (male, length 4.5 mm, Algeria: Mahouna), 66 = A. franzi (PETROVITZ, 1964) (male, length 5.5 mm, Morocco: Oukaïmeden), 67 = A. amplicollis (PEYERIMHOFF, 1939) (male, length 5.0 mm, Morocco: Oukaïmeden), 68 = A. meur-
ScienceDex guides
Understand access before you commit
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.