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.
1,287
datasets available to search
ShareScore release 0.7.1
Dataset results
1,287 results for “species identity”
FIGURES 1–6 in The identity of Equatobursa, with proposal of new genus and species level synonymies (Hemiptera: Heteroptera: Heterogastridae)
FIGURES 1–6. Types of Equatobursa nigra Zou, 1985, and their labels. Fig. 1, holotype, dorsal view; Fig. 2, same, ventral view; Fig. 3, same, labels; Fig. 4, allotype, dorsal view; Fig. 5, same, ventral view; Fig. 6, same, labels. Scales in mm. © NKUM.
FIGURES 7–12 in The identity of Equatobursa, with proposal of new genus and species level synonymies (Hemiptera: Heteroptera: Heterogastridae)
FIGURES 7–12. Genitalia of Equatobursa nigra Zou, 1985, male allotype (Figs. 7–11) and a non-type female (Fig. 12). Fig. 7, genital capsule, lateral view; Fig. 8, same, posterior view, left paramere removed; Fig. 9–11, left paramere, three different aspects; Fig. 12, apical portion of spermatheca. Lettering: ar = apical receptacle of spermatheca; cs = cuplike sclerite; ip = intermediate part of spermatheca; rp = right paramere; sd = spermathecal duct. Scales in mm.
FIGURE 7. A–C in Typhlocarcinus kerala, a new species of rhizopine crab from southwestern India, and the identity of T. craterifer Rathbun, 1914 (Crustacea: Brachyura: Pilumnidae)
FIGURE 7. A–C, Typhlocarcinus craterifer Rathbun, 1914, holotype female (13.4 × 9.5 mm) (USNM 46397), Philippines; D– I, Typhlocarcinus kerala sp. nov., paratype male (18.3 × 13.0 mm) (DABFUK), Kerala, India. A, right side of carapace (denuded); B, frontal margin (denuded); C, left third maxilliped (denuded); D, right third maxilliped (denuded); E, ventral view of left G1; F, dorsal view of left G1; G, ventral view of distal part of left G1; H, dorsal view of distal part of left G1; I, left G2. Scales: A = 1.0 mm; B–I = 0.5 mm.
FIGURE 6 in Typhlocarcinus kerala, a new species of rhizopine crab from southwestern India, and the identity of T. craterifer Rathbun, 1914 (Crustacea: Brachyura: Pilumnidae)
FIGURE 6. Typhlocarcinus kerala sp. nov. A–C, paratype male (18.3 × 13.0 mm) (DABFUK), Kerala, India; D–G, paratype female (19.6 ×13.0 mm) (DABFUK), Kerala, India; G, H, holotype male (17.0 ×11.4 mm) (ZSI/WGRC/IR-INV 8237), Kerala, India. A, anterior thoracic sternum, telson, and pleonal somites 5 and 6; B, E, thoracic sternum and pleonal somites 1–6; C, posterior thoracic sternum and pleonal somites 1–5; F, thoracic sternum and vulvae; G, lateral side of carapace showing granules; H, posterior thoracic sternites and sternopleonal cavity showing G1, G2 and pleonal locking tubercle on sternite 5.
FIGURE 4 in Typhlocarcinus kerala, a new species of rhizopine crab from southwestern India, and the identity of T. craterifer Rathbun, 1914 (Crustacea: Brachyura: Pilumnidae)
FIGURE 4. Typhlocarcinus kerala sp. nov. A, E, paratype male (18.3 × 13.0 mm) (DABFUK), Kerala, India; B–D, F, paratype female (19.6 ×13.0 mm) (DABFUK), Kerala, India. A, C, D, frontal view of cephalothorax; B, right dorsal surface of carapace (denuded); E, F, outer view of chelae.
FIGURE 2. Typhlocarcinus craterifer Rathbun, 1914 in Typhlocarcinus kerala, a new species of rhizopine crab from southwestern India, and the identity of T. craterifer Rathbun, 1914 (Crustacea: Brachyura: Pilumnidae)
FIGURE 2. Typhlocarcinus craterifer Rathbun, 1914, holotype female (13.4 × 9.5 mm) (USNM 46397), Philippines. A, posterior view of thoracic sternum and pleonal somites 1–4; thoracic sternum and pleonal somites 1–6; C, thoracic sternum and vulvae; D, dorsal view of right cheliped; E, outer view of right chela; F, outer view of left chela; G, right last ambulatory leg; H, right second or third ambulatory leg.
FIGURE 1. Typhlocarcinus craterifer Rathbun, 1914 in Typhlocarcinus kerala, a new species of rhizopine crab from southwestern India, and the identity of T. craterifer Rathbun, 1914 (Crustacea: Brachyura: Pilumnidae)
FIGURE 1. Typhlocarcinus craterifer Rathbun, 1914, holotype female (13.4 × 9.5 mm) (USNM 46397), Philippines. A, overall view; B, dorsal view of carapace (right side denuded); C, frontal view of cephalothorax (partially denuded); D, ventral view of cephalothorax showing buccal cavity and pleon.
FIGURE 5 in Typhlocarcinus kerala, a new species of rhizopine crab from southwestern India, and the identity of T. craterifer Rathbun, 1914 (Crustacea: Brachyura: Pilumnidae)
FIGURE 5. Typhlocarcinus kerala sp. nov., paratype male (18.3 × 13.0 mm) (DABFUK), Kerala, India. A, right last ambulatory leg; B, right second or third ambulatory leg; C, ventro-mesial view of second and fourth ambulatory dactyli and propodi; D, dorsal view of right cheliped; E, outer view of merus and carpus of right cheliped.
FIGURE 3 in Typhlocarcinus kerala, a new species of rhizopine crab from southwestern India, and the identity of T. craterifer Rathbun, 1914 (Crustacea: Brachyura: Pilumnidae)
FIGURE 3. Typhlocarcinus kerala sp. nov. A, holotype male (17.0 × 11.4 mm) (ZSI/WGRC/IR-INV 8237); Kerala, India; B, D, paratype male (18.3 × 13.0 mm) (ZSI), Kerala, India; C, paratype female (19.6 × 13.0 mm) (DABFUK), Kerala, India. A–C, overall dorsal view; D, dorsal view of carapace right side (denuded).
FIGURES 4–18 in Identity of the oribatid mite Oribata curva and transfer to Trichogalumna (Acari, Oribatida, Galumnidae), with discussion of nomenclatural and biogeographical issues in the ' curva ' species-group
FIGURES 4–18. Trichogalumna curva (Ewing, 1907). Permanently slide-mounted historical adult specimens (see text). Photomicrographs (except 4) with transmitted, differential interference contrast illumination: 4—cotype slide of Oribata curva Ewing, 1907; 5—dorsal habitus of cotype, with egg on right side; 6—distal part of right bothridial seta of cotype; 7—distal part of left bothridial seta of cotype; 8—left notogastral seta p3 of cotype; 9—left porose area Aa of cotype at surface focus, with insert below at deep focus; 10—right porose area A1 of cotype (surface focus); 11—right porose area A2 of cotype (surface focus); 12—left porose area Aa of Ewing specimen from Missouri at surface (top, with base of seta lm) and deep (bottom insert) focus; 13—porose area A1 (surface focus) of Ewing specimen from Arcola, Illinois, showing absence of slits; 14— porose area A1 of Ewing specimen from Missouri at surface focus (and lyrifissure im), with insert at deep focus; 15—right porose area Aa of Jacot specimen from North Carolina at surface (top) and deep (bottom insert) focus; 16—same, but different specimen from North Carolina, showing absence of slits; 17—partial right pteromorph of Jacot specimen from North Carolina (anterior to top); pteromorph of Ewing specimen from Urbana, Illinois (deteriorated glycerin medium, anterior to right), showing accentuated striae. Scale bars: 100 µm (5), 10 µm (6–18); 6–16 to same scale.
FIGURES 1–3 in Identity of the oribatid mite Oribata curva and transfer to Trichogalumna (Acari, Oribatida, Galumnidae), with discussion of nomenclatural and biogeographical issues in the ' curva ' species-group
FIGURES 1–3. Trichogalumna curva (Ewing, 1907) adult (specimen from Columbia, Missouri): 1—dorsal view (legs omitted); 2—ventral view (legs omitted, gnathosoma represented only by slightly raised subcapitular mentum); 3—lateral view (gnathosoma and legs omitted). Scale bar: 100 µm.
FIGURES 19–31 in Identity of the oribatid mite Oribata curva and transfer to Trichogalumna (Acari, Oribatida, Galumnidae), with discussion of nomenclatural and biogeographical issues in the ' curva ' species-group
FIGURES 19–31. Trichogalumna curva (Ewing, 1907), dissected adult specimens. Photomicrographs with transmitted, differential interference contrast illumination: 19—left porose area A1 (surface focus) and surrounding region of specimen from Florida; 20—same specimen, but right A1; 21—left porose area A1 of second Florida specimen; 22—left area A1 of third Florida specimen; 23—right area Aa of same specimen; 24 left area A2 of same specimen; 25—North Carolina specimen, anterior view of rostrum showing M-shaped inner excavation and inner rostral tooth (irt) by transparency (damage includes vertical crack * and broken edge of thin rostral lobe); 26—same, but deeper focus to show rostrophragma (rp); 27—same, lateral view, showing deep inner excavation of rostral lobe into which tooth irt projects; 28—central region of notogaster, Florida specimen, showing transverse band of larger tubercles, with central region of longitudinal striae (arrow); 29—left genital region of New York specimen showing fine granules and minute striae (arrow) on epimeres 3 and 4, and long striae near genital plate; 30—same, but deep focus to show apodemes 3 and 4 (on either side of seta 3b) and streaks (arrows) on inner cuticular surface in striate region; 31—same specimen, showing transverse band of large tubercles between aggenital seta (ag) and anal plate. Scale bars: 10 µm (19–24 to same scale).
Effects of tree species identity on soil microbial communities in Juglans nigra and Quercus rubra plantations.
<p>Black walnut (<i>Juglans nigra </i>L.) forestry within the Central Hardwoods Region (CHR) has progressed primarily based on studies of trial and error among plantations. Although <i>J. nigra</i> wood has been used for everything from gunstocks in the Revolutionary War to the artfully crafted furniture of today, gaps exist in our knowledge base regarding the impact of this hardwood species on the soil. We aim to evaluate and analyze how <i>J. nigra</i> modified soil bacterial and fungal structure in conjunction with soil properties after 10 years of establishment. Additionally, we used another hardwood tree Northern red oak (<i>Quercus rubra </i>L.) for contrast. Our results showed soil microbial structure is influenced primarily by plant species; then by season, and lastly depth. The alpha-diversity index was increased in <i>J. nigra</i> compared to bulk soil values, whereas <i>Q. rubra</i> decreased the index. The most significant disparities in microbiomes were observed between plant species with <i>J. nigra</i> displaying greater enrichment in <i>Nitrospira</i>, <i>Geobacter</i>, <i>Steroidobacter</i>, <i>Bacillus</i>, and <i>Perlucidibaca</i> while<i> Q. rubra </i>more enriched in <i>Acidobacteria</i> (<i>GP1</i>, <i>GP2</i>, and <i>GP3</i>) and ectomycorrhizal fungi (<i>Tuber</i>, <i>Inocybe</i>, <i>Amanita</i>, and <i>Russula</i>). Finally, the co-occurrence networks showed that <i>J. nigra</i> increased node numbers while <i>Q. rubra</i> increased connection (edge) numbers. Additionally, the<i> Q. rubra </i>network displayed the highest mean degree, density, and clustering coefficient while <i>J. nigra</i> exhibited the highest modularity and average connectivity. In conclusion, our findings highlight the intricate interplay between CHR tree species and soil microbiota.</p>
FIGURE 4 in Male flowers reveal the true identity of a new species of Hechtia (Bromeliaceae) from the Mexican state of Jalisco
FIGURE 4. Illustration of Hechtia carrilloi. A. Branch with pistillate flowers. B. Female plant with inflorescence. C. Male plant with inflorescence. D. Branch with staminate flowers. D. Detail of staminate flowers. E. Branch with immature fruits. Illustration by Alberto Guerra.
FIGURE 1 in Male flowers reveal the true identity of a new species of Hechtia (Bromeliaceae) from the Mexican state of Jalisco
FIGURE 1. Geographical distribution of Hechtia carrilloi (black triangles), and H. santanae (white dots).
FIGURE 3. Hechtia carrilloi. A. Staminate inflorescence. B. Staminate flowers. C. Pistillate flowers. D in Male flowers reveal the true identity of a new species of Hechtia (Bromeliaceae) from the Mexican state of Jalisco
FIGURE 3. Hechtia carrilloi. A. Staminate inflorescence. B. Staminate flowers. C. Pistillate flowers. D. Line drawing of staminate (above) and pistillate (below) flowers. E. Fruits. F. Rosette showing a central infructescence with strict sympodial growth pattern. (Credits: A, B. Ivón Ramírez-Morillo. C. Juan Pablo Ortiz-Brunel. D. Alberto Guerra. E, F. Katya Romero-Soler).
FIGURE 2. Hippeastrum euryphyllum. A–B in Hippeastrum euryphyllum (Amaryllidaceae), a microendemic species from northeastern Argentina: new combination, description, taxonomic identity and distribution
FIGURE 2. Hippeastrum euryphyllum. A–B. Habitat; C. Habit; D. Flower in frontal view; E. Flower in lateral view; F. Infructescence; G. Detail of dehiscent fruits and seed. Photos by W. Medina.
Subspecies and Distribution. P.c.capensisPallas,1766—SouthAfrica,includingLesothoandSwaziland. P.c.bamendaeBrauer,1913—CameroonandCentralAfricanRepublic. P.c.capillosaBrauer,1917—SEthiopia. P.c.erlanger:Neumann,1901—SSomalia. P.c.habessinicaHemprich&Ehrenberg,1832—Egypt,NSudan,Israel,SaudiArabia,andYemen. P.c.jacksoniThomas,1900—EKenya. P.c.jayakariThomas,1892—Oman. P.c.johnston:Thomas,1894—SWTanzania,Malawi,Mozambique,andZimbabwe. P.c.kerstingiMatschie,1899—TogoandBenin. P.c.mackinder:Thomas,1900—WKenya. P.c.matschietNeumann,1900—DRCongoandTanzania. P.c.pallidaThomas,1891—NSomalia. P.c.ruficepsHemprich&Ehrenberg,1832—NandWAfrica. P.c.scioanaGiglioli,1888—NEthiopia. P.c.sharicaThomas&Wroughton,1907—Chad. P.c.syriacaSchreber,1784—Syria,Lebanon,Jordan,andIsrael. P. c. welwitschii Gray, 1868 — SW Angola and Namibia. The distribution information for this species is still incomplete; the Rock Hyrax is also present in Eritrea, Niger, Nigeria, C & S Sudan, Uganda, Rwanda, Burundi, Zambia and E Botswana, but the subspecific identity of these populations still requires confirmation. in Procaviidae
Subspecies and Distribution. P.c.capensisPallas,1766—SouthAfrica,includingLesothoandSwaziland. P.c.bamendaeBrauer,1913—CameroonandCentralAfricanRepublic. P.c.capillosaBrauer,1917—SEthiopia. P.c.erlanger:Neumann,1901—SSomalia. P.c.habessinicaHemprich&Ehrenberg,1832—Egypt,NSudan,Israel,SaudiArabia,andYemen. P.c.jacksoniThomas,1900—EKenya. P.c.jayakariThomas,1892—Oman. P.c.johnston:Thomas,1894—SWTanzania,Malawi,Mozambique,andZimbabwe. P.c.kerstingiMatschie,1899—TogoandBenin. P.c.mackinder:Thomas,1900—WKenya. P.c.matschietNeumann,1900—DRCongoandTanzania. P.c.pallidaThomas,1891—NSomalia. P.c.ruficepsHemprich&Ehrenberg,1832—NandWAfrica. P.c.scioanaGiglioli,1888—NEthiopia. P.c.sharicaThomas&Wroughton,1907—Chad. P.c.syriacaSchreber,1784—Syria,Lebanon,Jordan,andIsrael. P. c. welwitschii Gray, 1868 — SW Angola and Namibia. The distribution information for this species is still incomplete; the Rock Hyrax is also present in Eritrea, Niger, Nigeria, C & S Sudan, Uganda, Rwanda, Burundi, Zambia and E Botswana, but the subspecific identity of these populations still requires confirmation.
FIGURE 2. A. Leaf abaxial B. Calyx with pistil C–D in Taxonomy of Ophiorrhiza pectinata: Indo-Lankan Species with Notes on Lectotypification and Identity of Ophiorrhiza falcata (RUBIACEAE)
FIGURE 2. A. Leaf abaxial B. Calyx with pistil C–D. Corolla splitting and close up villous at mouth E. Style F. Capsule.
FIGURE 11 in The taxonomic identity of the monocle bream Scolopsis vosmeri species complex (Perciformes: Nemipteridae), with comments on molecular phylogenetic relationships within the genus Scolopsis
FIGURE 11. Posterior margin of preopercle. A: Scolopsis vosmeri, NTM S.14230-001, 140 mm SL, Sandakan. Sabah, Malaysia; B: Scolopsis japonica, WAM P.31312-002, 127.7 mm SL, Bintan Island, Indonesia; C: Scolopsis curite, NTM S.13160-013, 132.2 mm SL, Chilaw, Sri Lanka; arrow showing more rugose margin of latter. Photos by B.C. Russell.
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.