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1,061 results for “115”
Figure 1 from: Fujimoto S, Jimi N (2020) A new marine tardigrade genus and species (Arthrotardigrada, Styraconyxidae) with unique pockets on the legs. Zoosystematics and Evolution 96(1): 115-122. https://doi.org/10.3897/zse.96.49676
Figure 1 Drawings of Cyaegharctus kitamurai gen. et sp. nov., holotype KUZ Z2624. A. Habitus (ventral view). B. Leg IV pocket organ. an anus, bt buccal tube, ca cavity, cE cirrus E, db dense body, ec external cirrus, go female gonopore (detail not available), ic internal cirrus, lc lateral cirrus, mc median cirrus, pc primary clava, pl placoid, op opening, sc secondary clava, soI, IV legs I and IV sensory organs, sr seminal receptacles, ss stylet support, st stylet.
Figure 2 from: Fujimoto S, Jimi N (2020) A new marine tardigrade genus and species (Arthrotardigrada, Styraconyxidae) with unique pockets on the legs. Zoosystematics and Evolution 96(1): 115-122. https://doi.org/10.3897/zse.96.49676
Figure 2 DIC and PhC micrographs of Cyaegharctus kitamurai gen. et sp. nov., adult female. A. Habitus (dorsal view). B. cephalic region (ventral view). C. Lateral cirrus. D. Buccal apparatus. E. Caudal region (ventral view) (epicuticle pillars visible). F. Leg I sensory organ and pocket organ. G. Leg II pocket organ (arrowhead indicates protruding portion). H. Leg II digits and claws. I. Leg III pocket organ. J. Leg IV pocket organ. K. female gonopore. L. Legs I–III sensory organs. M. Leg III digits and claws. A–J. holotype KUZ Z2624, K. paratype KUZ Z2625, L, M. paratype KUZ Z2626. an anus, bt buccal tube, ca cavity, cE cirrus E, db dense body, ec external cirrus, go gonopore, ic internal cirrus, lc lateral cirrus, mc median cirrus, pc primary clava, pei,e peduncles of internal and external digits, pl placoid, poI–IV legs I–IV pocket organs, pp proximal pad, sc secondary clava, soI–IV legs I–IV sensory organs, sr seminal receptacles, ss stylet support, st stylet.
Figure 3 from: Fujimoto S, Jimi N (2020) A new marine tardigrade genus and species (Arthrotardigrada, Styraconyxidae) with unique pockets on the legs. Zoosystematics and Evolution 96(1): 115-122. https://doi.org/10.3897/zse.96.49676
Figure 3 SEM micrographs of Cyaegharctus kitamurai gen. et sp. nov., four-claw juvenile paratype KUZ Z2627. A. Habitus (lateral view). B. Cephalic region (frontal view). C. Cephalic region (ventral view). D. Anus. E. Leg I sensory organ. F. Leg II sensory organ. G. Leg III sensory organ. H. Leg IV sensory organ. I. Leg IV pocket organ. J. Leg III digits and claws. ah accessory hook, an anus, cE cirrus E, ec external cirrus, fe femur, ic internal cirrus, lc lateral cirrus, mc median cirrus, pc primary clava, ph primary hook, poIII, IV legs III and IV pocket organs, pp proximal pad, sc secondary clava, sh secondary hook, soI–IV legs I–IV sensory organs, ti tibia.
Figure 4 from: Luo T, Xiao N, Gao K, Zhou J (2020) A new species of Leptobrachella (Anura, Megophryidae) from Guizhou Province, China. ZooKeys 923: 115-140. https://doi.org/10.3897/zookeys.923.47172
Figure 4 Holotype of Leptobrachella suiyangensis sp. nov. (GZNU20180606007) in preservative. A Dorsal view B Ventral views C Lateral views.
Figure 3 from: Luo T, Xiao N, Gao K, Zhou J (2020) A new species of Leptobrachella (Anura, Megophryidae) from Guizhou Province, China. ZooKeys 923: 115-140. https://doi.org/10.3897/zookeys.923.47172
Figure 3 Holotype of Leptobrachella suiyangensis sp. nov. (GZNU20180606007) in life. A Dorsal view B Dorsolateral view C Ventral view D Right eye shown iris coloration E Volar view of the left hand F Plantar view of the left foot.
Figure 2 from: Luo T, Xiao N, Gao K, Zhou J (2020) A new species of Leptobrachella (Anura, Megophryidae) from Guizhou Province, China. ZooKeys 923: 115-140. https://doi.org/10.3897/zookeys.923.47172
Figure 2 Bayesian inference tree derived from partial DNA sequences of the mitochondrial 16S r RNA gene. Numbers before slashes indicate Bayesian posterior probabilities (displayed >0.60 values), and numbers after slashes are ultrafast bootstrap support for maximum likelihood (2000 replicates) analyses (>60 retained). The symbol "–" represents value below 0.60/60. The scale bar represents 0.05 nucleotide substitutions per site.
Figure 5 from: Luo T, Xiao N, Gao K, Zhou J (2020) A new species of Leptobrachella (Anura, Megophryidae) from Guizhou Province, China. ZooKeys 923: 115-140. https://doi.org/10.3897/zookeys.923.47172
Figure 5 Paratypes of Leptobrachella suiyangensis sp. nov. in life. A GZNU20180606005, adult male (A), (B) GZNU20180606002, adult male C GZNU20180606003, adult female.
Figure 1 from: Luo T, Xiao N, Gao K, Zhou J (2020) A new species of Leptobrachella (Anura, Megophryidae) from Guizhou Province, China. ZooKeys 923: 115-140. https://doi.org/10.3897/zookeys.923.47172
Figure 1 Collection locality (red circle) of Leptobrachella suiyangensis sp. nov. from Suiyang County, Guizhou province, China used in this study.
Figures 115-126 from: Zhang R-N, van Achterberg C, Tian X-X, Tan J-L (2020) Review of the Bobekia-group (Braconidae, Alysiinae, Alysiini), with description of a new genus and a new subgenus. ZooKeys 926: 25-51. https://doi.org/10.3897/zookeys.926.47270
Figures 115-126 Separatatus carinatus Chen & Wu, ♀, holotype 115 wings 116 mesosoma, dorsal aspect 117 mandible, full view of first tooth 118 head, dorsal aspect 119 hind leg 120 mandible, full view of third tooth (fourth tooth arrowed) 121 head, anterior aspect 122 first–third metasomal tergites, dorsal aspect 123 basal antennal segments 124 antenna 125 habitus, lateral aspect 126 outer hind claw, lateral aspect.
Supplementary material 1 from: Fiorillo BF, Silva BR, Menezes FA, Marques OAV, Martins M (2020) Composition and Natural History of Snakes from Etá Farm region, Sete Barras, south-eastern Brazil. ZooKeys 931: 115-153. https://doi.org/10.3897/zookeys.931.46882
Specimen identifications
Figure 5 from: Fiorillo BF, Silva BR, Menezes FA, Marques OAV, Martins M (2020) Composition and Natural History of Snakes from Etá Farm region, Sete Barras, south-eastern Brazil. ZooKeys 931: 115-153. https://doi.org/10.3897/zookeys.931.46882
Figure 5 AEchinanthera undulataBErythrolapmprus aesculapiiCE. miliarisDHelicops carinicaudusEImantodes cenchoa (photo: Ricardo J. Sawaya) FOxyrhopus clathratusGSiphlophis pulcherHSordellina punctata.
Figure 6 from: Fiorillo BF, Silva BR, Menezes FA, Marques OAV, Martins M (2020) Composition and Natural History of Snakes from Etá Farm region, Sete Barras, south-eastern Brazil. ZooKeys 931: 115-153. https://doi.org/10.3897/zookeys.931.46882
Figure 6 ATaeniophallus bilineatusBT. persimilisCThamnodynastes nattereriDTomodon dorsatusETropidodryas serraFXenodon neuwiediiGMicrurus corallinusHTropidophis paucisquamis.
Figure 4 from: Fiorillo BF, Silva BR, Menezes FA, Marques OAV, Martins M (2020) Composition and Natural History of Snakes from Etá Farm region, Sete Barras, south-eastern Brazil. ZooKeys 931: 115-153. https://doi.org/10.3897/zookeys.931.46882
Figure 4 AClelia plumbeaBDipsas albifronsCD. alternans (photo: Arthur Abegg) DD. indica petersiED. neuwiediFD. variegataGEchinanthera cephalostriataHE. cyanopleura (photograph Marcos Di-Bernardo).
Figure 2 from: Fiorillo BF, Silva BR, Menezes FA, Marques OAV, Martins M (2020) Composition and Natural History of Snakes from Etá Farm region, Sete Barras, south-eastern Brazil. ZooKeys 931: 115-153. https://doi.org/10.3897/zookeys.931.46882
Figure 2 Satellite images (source: Google Earth) A the region where the study area (light orange rectangle) is located in the southern São Paulo State and the group of continuous protected areas (in light green) that encompasses most of the primary forests of this region (AR = Parque Estadual Turístico do Alto Ribeira; CB = Parque Estadual Carlos Botelho; IV = Parque Estadual Intervales; XI = Estação Ecológica de Xituê) as well as the location of the Etá Farm region (rectangle) B the region of the Etá Farm, Sete Barras Municipality where 1 indicates the Etá Farm administrative buildings, 2–4 indicate areas of forest, 5 and 6 indicate peach palm plantations; 7 indicates abandoned banana plantation, and 8 indicates an agricultural settlement.
Figure 3 from: Fiorillo BF, Silva BR, Menezes FA, Marques OAV, Martins M (2020) Composition and Natural History of Snakes from Etá Farm region, Sete Barras, south-eastern Brazil. ZooKeys 931: 115-153. https://doi.org/10.3897/zookeys.931.46882
Figure 3 ACorallus cropaniiBC. hortulanusCChironius bicarinatus (photo: Arthur Abegg) DC. exoletusEC. foveatusFC. fuscusGC. laevicollisHSpilotes pullatus.
Fig. 115 in Illustrated identification guide to the Nordic aphids feeding on Conifers (Pinophyta) (Insecta, Hemiptera, Sternorhyncha, Aphidomorpha)
Fig. 115. Cinara (Cupressobium) juniperi (De Geer, 1773). Colonies on current and previous year's twigs of Juniperus communis, in F attended by Myrmica rubra (Linnaeus, 1758).
Figures 115-119 from: Astafurova YuV, Proshchalykin MYu, Schwarz M (2020) New and little-known species of the genus Sphecodes Latreille (Hymenoptera, Halictidae) from Southeast Asia. ZooKeys 937: 31-88. https://doi.org/10.3897/zookeys.937.51708
Figures 115-119 Sphecodes sauteri Meyer, female 115 head, frontal view 116, 118 mesosoma, dorsal view (116), lateral view (118) 117 metasoma, dorsal view 119 propodeum, dorsal view. Scale bars: 1.0 mm.
Figure 4 from: Zhang X, Liang X, Chen X, Wang X (2020) Three new species of the genus Chilocorellus Miyatake (Coleoptera, Coccinellidae, Sticholotidini) from the Philippines. ZooKeys 937: 115-127. https://doi.org/10.3897/zookeys.937.50139
Figure 4 Distribution map. C. luzonicus Miyatake, 1994 (♦); C. quadrimaculatus Wang & Ren, 2010 (); C. protuberans Wang & Ren, 2010 (●); C. tenuous Wang & Ren, 2010 (■); C. seleuyensis Wang & Ren, 2011 (▲); C. uncinacanthus Zhang et Wang, sp. nov. (▲); C. denspinulifer Zhang et Wang, sp. nov. (●); C. fistulachaetodontus Zhang et Wang, sp. nov. (■).
Figure 3 from: Zhang X, Liang X, Chen X, Wang X (2020) Three new species of the genus Chilocorellus Miyatake (Coleoptera, Coccinellidae, Sticholotidini) from the Philippines. ZooKeys 937: 115-127. https://doi.org/10.3897/zookeys.937.50139
Figure 3 Chilocorellus fistulachaetodontus sp. nov. a dorsal habitus b lateral habitus c frontal habitus d head, ventral e head, ventral f antenna g labrum h left mandible i right mandible j maxilla k labium l prothorax, ventral m mesoventrite and metaventrite n metendosternite o front leg p mid leg q hind leg r male abdomen s female abdomen t tegmen, ventral view u tegmen, lateral view v penis, lateral w apex of penis x female genitalia (ovipositor). Scale bars: 0.5 mm (a–c, m, r–s); 0.2 mm (d–e, l, n–q, t–v); 0.1 mm (f, j–k, x); 0.05 mm (g, h–i, w).
Figure 2 from: Zhang X, Liang X, Chen X, Wang X (2020) Three new species of the genus Chilocorellus Miyatake (Coleoptera, Coccinellidae, Sticholotidini) from the Philippines. ZooKeys 937: 115-127. https://doi.org/10.3897/zookeys.937.50139
Figure 2 Chilocorellus denspinulifer sp. nov. a dorsal habitus b lateral habitus c frontal habitus d head, ventral f antenna g labrum h left mandible i right mandible j maxilla k labium l prothorax, ventral m mesoventrite and metaventrite n metendosternite o front leg p mid leg q hind leg r male abdomen s female abdomen t tegmen, ventral view u tegmen, lateral view v penis, lateral w apex of penis x female genitalia (ovipositor). Scale bars: 0.5 mm (a–c, m, r–s, v); 0.2 mm (d, l, n–q, t–u; f), 0.1 mm (h–k, x); 0.05 mm (g, w).
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