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.
9,029
datasets available to search
ShareScore release 0.9.0
Dataset results
9,029 results for “Asia”
FIGURE 43. A–K in New taxa and records of Gryllacrididae (Orthoptera, Stenopelmatoidea) from South East Asia and New Guinea with a key to the genera
FIGURE 43. A–K, Asarcogryllacris (Pseudasarca) arborea sp. nov.: Habitus dorsal view male (A) and female (G), do. lateral view female (H), face (B), male abdominal apex in apical (C–D), oblique lateral (E) and ventral view (F), female seventh abdominal sternite, subgenital plate and base of ovipositor (I–J), stridulatory pegs on second and third abdominal tergites (front is left, K).—(B–C holotype, others paratypes).—L, Asarcogryllacris (A.) macilenta macilenta (Pictet & Saussure, 1891): Habitus dorsal view (lectotype). Abbreviations: 9th ninth abdominal tergite, ce cercus, e epiproct, pa paraproct, ph phallus, pr process of ninth tergite, sg subgenital plate, sp spermatophore (specimen from alcohol).
FIGURE 4 in New taxa and records of Gryllacrididae (Orthoptera, Stenopelmatoidea) from South East Asia and New Guinea with a key to the genera
FIGURE 4. Genus Eugryllacris: Habitus dorsal view: A–B, E. trabicauda sp. nov. female holotype (A) and male paratype (B); C–D, E. vermicauda sp. nov. female holotype (C) male paratype (D); E, E. serricauda sp. nov. male holotype; F, E. guomashan sp. nov. female holotype; G, E. crassicauda sp. nov. female paratype; H, E. crassicauda cambodiana ssp. nov. female holotype; I, E. malaccensis (Griffini, 1908) male; J, E. serricauda sp. nov. female paratype. Scales 10 mm.
FIGURE 3 in New taxa and records of Gryllacrididae (Orthoptera, Stenopelmatoidea) from South East Asia and New Guinea with a key to the genera
FIGURE 3. Genus Caustogryllacris: A–E, C. p. podocausta (Haan, 1842) male (A–C) and female (D–E); F–J, C. p. pallidior (Pictet & Saussure, 1891) male.—Habitus dorsal view (A, F), face (B, G), male abdominal apex with ninth tergite and subgenital plate in apico-ventral (C, H) and ventral view (I), stridulatory pegs on second and third abdominal tergites (front is right, J), female subgenital plate (D), ovipositor (E).
FIGURE 2. A in New taxa and records of Gryllacrididae (Orthoptera, Stenopelmatoidea) from South East Asia and New Guinea with a key to the genera
FIGURE 2. A, Melaneremus sikkimensis sp. nov. male holotype; B, Papuogryllacris ligata bundi ssp. nov. male holotype; C, Gryllacris signifera signifera (Stoll, 1813); D, Papuogryllacris leeuweni (Karny, 1930) male; E, Eugryllacris serricauda sp. nov. female; F, Capnogryllacris (C.) e. erythrocephala Gorochov, 2003; G, Asarcogryllacris (A.) parapat sp. nov. female holotype; H, Asarcogryllacris (A.) macilenta macilenta (Pictet & Sauss., 1891) female lectotype; I, Zalarnaca (Zalarnaca) maninjau sp. nov. male holotype.—A–B, body and legs ventral view showing the ventral tibial spines (arrows); C–D, habitus lateral view with the ventral tibial spines (black arrow) and the presence (C, also F) or absence (D) of ventral pre-apical spines on hind tibia (blue arrow); E–F, abdominal apex with ovipositor in lateral view, red arrows mark the widened (E) or simple (F) ovipositor apical area, the green arrow marks the lateral furrow of the ovipositor with widened apical area; G, venation of left tegmen; H, venation of right tegmen; I, apical area of right hind tibia and tarsus. Abbreviations of veins as in Fig. 1.
FIG. 13 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 13. PCA of nine external and cranial characters of R. affinis specimens from southern Malay Peninsula (green shaded Zone A in Fig. 1) (black squares) and northern Malay Peninsula (orange shaded Zone B in Fig. 1) (grey circles)
FIG. 11 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 11. Maximum likelihood tree based on COI. Scores on the branches refer to bootstrap support values (1,000 iterations) derived from maximum likelihood (1st score) and Bayesian posterior probabilities (2nd score); -- = no support value. Specimens are labeled by specimen codes (IS, HM, HZM and MZB) and collecting localities. The symbols of clades correspond to the genetic distribution map, Fig. 12
FIG. 10 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 10. Distribution of Cytb clades of R. affinis within the Sundaic subregion. The shape of the symbols corresponds to clades defined in Fig. 9. Black symbols are sequences from the current study whereas grey symbols are sequences from GenBank. Localities of sequences not listed in the methods and materials of the current study are listed for the first time as following, BA = Jambusan Cave, Bau, Sarawak; GB = Gunung Berumput, Sarawak; GG = Gunung Gading NP, Sarawak; KM = Kabumen, Central Java and PC = Prachuap Kiri Khan. unK = unknown specific locality from Borneo (sequences from GenBank). Dashed arrows indicate the type localities of subspecies. Black solid arrows indicate the transition zones of biota in the peninsula
FIG. 7 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 7. Ventral view of R. affinis skulls from Borneo (A — TK168483, ♀), Sumatra (B — MZB35882, ♀), Java (C — MZB34475, ♀), Malay Peninsula (D — IS110823.10, ♂; E — IS120122.1, ♂) and India (F — HZM4.28148). Scale = 5 mm
FIG. 4 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 4. Noseleaf variation of R. affinis in the Sundaic subregion (specimen from northern India included for comparison). Kabumen, Central Java (A — MZB34475, ♀); Musoorie, northern India (B — HZM.4.28148, ♂); Sarawak, northwest Borneo (C — TK152216, ♀); Lampung, southwestern Sumatra (D — MZB34965, ♀); Narathiwat, southern Malay Peninsula (E — IS120122.1, ♂); Songkhla, southern Malay Peninsula (F — IS110823.10, ♂). Scale = 5 mm
FIG. 3 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 3. Lateral view of R. affinis skulls from Borneo (A — TK168483, ♀), Sumatra (B — MZB35882, ♀), Central Java (C — MZB34475, ♀), Malay Peninsula (D — IS110823.10, ♂; E — IS120122.1, ♂) and India (F — HZM4.28148, ♂). Scale = 5 mm
FIG. 12 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 12. Distribution of COI clades of R. affinis in the Sundaic subregion. The shape of the symbols corresponds to clades defined in Fig. 11. Black symbols are sequences from the current study and Ith et al. (in review) whereas grey symbols are sequences from GenBank. Localities of the sequences not listed in the methods and materials of the current study are listed for the first time as following, ER = Endau Rompin National Park, Peninsular Malaysia; KL = Kuala Lompat, Pahang; NS = Negeri-Sembilan; TT = Thaninthary Div, Myanmar. Dashed arrows indicate the type localities of subspecies. Black solid arrows indicate the transition zones of biota in the peninsula
FIG. 9 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 9. Baysian phylogenetic tree based on Cytb gene. Scores on the branches refer to bootstrap support values (1,000 iterations) derived from maximum likelihood (1st score) and Bayesian posterior probabilities (2nd score); -- = no support value. The horizontal bars on the tree branches represent the 95% highest posterior density intervals for the divergence estimates. Specimens are labeled by specimen codes (CHGTK, EF, EU, JN, IS, MZB, PS and TK) and collecting localities. The symbols of clades correspond to the genetic distribution map, Fig. 10
FIG. 2 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 2. PCA of 12 external and cranial characters for R. affinis specimens from Borneo (black squares), Sumatra (black diamonds), southern Malay Peninsula (black circles) and northern Malay Peninsula (open circles)
FIG. 6 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 6. Dorsal view of R. affinis skulls from Borneo (A — TK168483, ♀), Sumatra (B — MZB35882, ♀), Java (C — MZB34475, ♀), Malay Peninsula (D — IS110823.10, ♂; E — IS120122.1, ♂) and India (F — HZM4.28148, ♂). Scale = 5 mm
FIG. 1 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 1. Sample localities and echolocation frequencies of R. affinis in the Sundaic subregion. M = Peninsular Malaysia, Sa = Sarawak, S = Sumatra, and T = Thailand. Abbreviations for localities are given in the methods and materials. The grey shading indicates the Sundaic biogeographic subregion following Woodruff (2010), green (zone A) and orange (B) shadings are the echolocation zones recognized in the Malay Peninsula. Dashed arrows indicate type localities and subspecies names, solid arrows indicate the transition zone of biota within the Malay Peninsula, dashed lines indicate the echolocation frequencies (min–max), and the two-headed arrows indicate the echolocation frequencies (min–max) as a whole from each echolocation zone. Note: the northern boundary of the Sundaic subregion is sometimes placed at the Isthmus of Kra (e.g., Lekagul and McNeely, 1988 and Corbet and Hill, 1992)
FIG. 5 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 5. Sella variation of R. affinis in the Sundaic Subregion (specimen from northern India included for comparison). Kabumen, Central Java (A — MZB34475, ♀); Musoorie, northern India (B — HZM.4.28148, ♂); Sarawak, northwest Borneo (C — TK152216, ♀); Lampung, southwestern Sumatra (D — MZB34965, ♀); Narathiwat, southern Malay Peninsula (E — IS120122.1, ♂); Songkhla, southern Malay Peninsula (F — IS110823.10, ♂). Scale = 5 mm
FIG. 8 in Geographical variation of Rhinolophus affinis (Chiroptera: Rhinolophidae) in the Sundaic subregion of Southeast Asia, including the Malay Peninsula, Borneo and Sumatra
FIG. 8. Bacula of R. affinis from the Sundaic Subregion in lateral view (l), ventral view (v) and dorsal view (d); Sarawak, northwestern Borneo (A — TK152217); Lampung, southwestern Sumatra (B — MZB31501); Narathiwat, southern Malay Peninsula (C — IS120124.1). Scale = 1 mm
Mobile Connectivity Index Europe Asia
<p>The file combines data from various sources that provide insight into indicators that can be used to characterize broadband connectivity in Montenegro, Malaysia, and Thailand. Indicators for changes in the number and annual growth of the rural population, indicators showing Internet penetration and use of social networks, number of fixed broadband subscriptions, number of secured Internet servers, and number of fixed and mobile phone subscribers are covered. In addition, some other data that can be used to characterize the DESI index in the broader context of digitization (for example, infrastructure, affordability, 2G-5G coverage, Internet connection speeds, etc.) are given.</p>
FIGURE 41 in Contribution to the knowledge of the Ichneumoninae (Hymenoptera, Ichneumonidae) from Maritime Southeast Asia
FIGURE 41. Virgichneumon stegemanni (Heinrich, 1934) ♂. A face, frontal view, B propodeum, frontal view, C basal tergites, frontal view.
FIGURE 36. Setanta albimaculata n in Contribution to the knowledge of the Ichneumoninae (Hymenoptera, Ichneumonidae) from Maritime Southeast Asia
FIGURE 36. Setanta albimaculata n. sp. HT ♀. A face, frontal view, B metasomal apex, lateral view, C propodeum, dorsal view, D basal tergites, dorsal view.
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.