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398 results for “Malay”
Fig. 7 in Two new species of Barbodes from the Malay Peninsula and comments on 'cryptic species' in the B. binotatus group (Teleostei: Cyprinidae)
Fig. 7. Distribution of Barbodes sellifer, new species (green marks) and B. zakariaismaili, new species (orange marks) on Malay Peninsula and Sumatra, based on examined material. Stars are type localities. Each mark may consist of more than one locality. (K. K. P. Lim).
Fig. 8 in Two new species of Barbodes from the Malay Peninsula and comments on 'cryptic species' in the B. binotatus group (Teleostei: Cyprinidae)
Fig. 8. The forest stream (a) inhabited by Barbodes sellifer, new species, in the type locality, Nee Soon swamp-forest in Singapore; and a view from the surface (b) showing a congregation of many individuals of B. sellifer (with the distinct black subdorsal blotch) with a few Rasbora elegans (with the two black spots on the side). (Photographs by K. K. P. Lim, March 2005).
Fig. 5. a in Two new species of Barbodes from the Malay Peninsula and comments on 'cryptic species' in the B. binotatus group (Teleostei: Cyprinidae)
Fig. 5. a, Barbodes sellifer, new species, CMK 6027, paratype, 59.5 mm SL; b, B. zakariaismaili, new species, ZRC 52347, holotype, 66.3 mm SL. Note differences in snout shape, and in size and position of eye. (Photographs by M. Kottelat).
Fig. 4 in Two new species of Barbodes from the Malay Peninsula and comments on 'cryptic species' in the B. binotatus group (Teleostei: Cyprinidae)
Fig. 4. Barbodes sellifer, new species, about 60 mm SL; Singapore: Nee Soon swamp forest (type locality). Live specimen, in situ, January 2005, not preserved. (Photograph by Nick Baker).
Fig. 1 in Two new species of Barbodes from the Malay Peninsula and comments on 'cryptic species' in the B. binotatus group (Teleostei: Cyprinidae)
Fig. 1. Barbodes sellifer, new species, Singapore; a, ZRC 12354, holotype, 97.8 mm SL; b, ZRC 54462, paratype, 47.9 mm SL. (Photographs by M. Kottelat).
Fig. 14 in Two new species of Barbodes from the Malay Peninsula and comments on 'cryptic species' in the B. binotatus group (Teleostei: Cyprinidae)
Fig. 14. Barbodes zakariaismaili, new species, Malaysia: Pahang: Cameron Highlands; a, b, CMK 27384, paratypes: 27.8 mm SL (a) and 33.7 mm SL (b); c, d, ZRC 62315, paratypes: 30.1 mm SL (c) and 35.5 mm SL (d). (Photographs by M. Kottelat).
Fig. 2 in Two new species of Barbodes from the Malay Peninsula and comments on 'cryptic species' in the B. binotatus group (Teleostei: Cyprinidae)
Fig. 2. Barbodes sellifer, new species, ZRC 1242, paratypes, Singapore; a, 13.3 mm SL; b, 21.1 mm SL; c, 30.8 mm SL; d, 33.6 mm SL; e, 42.7 mm SL. (Photographs by M. Kottelat).
Fig. 3 in Two new species of Barbodes from the Malay Peninsula and comments on 'cryptic species' in the B. binotatus group (Teleostei: Cyprinidae)
Fig. 3. Barbodes sellifer, new species, ZRC 21699, 42.4 mm SL; Malaysia: Terengganu: Sekayu. (Photograph by M. Kottelat).
Fig. 6 in Two new species of Barbodes from the Malay Peninsula and comments on 'cryptic species' in the B. binotatus group (Teleostei: Cyprinidae)
Fig. 6. Scales at caudal-fin base in: a, Barbodes sellifer, new species, ZRC 12355, 69.2 mm SL; and b, B. zakariaismaili, new species, ZRC 62315, 67.4 mm SL. Edge of posteriormost scales enhanced. (Photographs by M. Kottelat).
Fig. 6 in ThegenusKanigara Distant(Heteroptera:Lygaeoidea: Rhyparochromidae) from Malay Peninsula and Thailand, with description of a new species
Fig. 6. Distribution of Kanigara nebulosa, new species, Kanigara oculata Scudder, 1969, and Kanigara punctata Scudder, 1969.
Fig. 2 in ThegenusKanigara Distant(Heteroptera:Lygaeoidea: Rhyparochromidae) from Malay Peninsula and Thailand, with description of a new species
Fig. 2. Male and female genitalia of Kanigara nebulosa, new species. A, pygophore, dorsal view; B–E, right paramere, four different aspects; F, G, phallus (F, dorsal view; G, lateral view); H, sperm reservoir; I, spermatheca. Scale bars = 0.1 mm.
Fig. 5 in ThegenusKanigara Distant(Heteroptera:Lygaeoidea: Rhyparochromidae) from Malay Peninsula and Thailand, with description of a new species
Fig. 5. Male and female genitalia of Kanigara punctata Scudder, 1969. A, pygophore, dorsal view; B–E, right paramere, four different aspects; F, G, phallus (F, dorsal view; G, lateral view); H, sperm reservoir; I, spermatheca. Scale bars = 0.1 mm.
Fig. 1. Kanigara nebulosa, new species. A, B in ThegenusKanigara Distant(Heteroptera:Lygaeoidea: Rhyparochromidae) from Malay Peninsula and Thailand, with description of a new species
Fig. 1. Kanigara nebulosa, new species. A, B, holotype, male (A, dorsal view; B, ventral view); C, D, paratype, female (C, dorsal view; D, ventral view). Scale bars = 1.0 mm.
Fig. 3. Kanigara oculata Scudder, 1969. A, B in ThegenusKanigara Distant(Heteroptera:Lygaeoidea: Rhyparochromidae) from Malay Peninsula and Thailand, with description of a new species
Fig. 3. Kanigara oculata Scudder, 1969. A, B, female (A, dorsal view; B, ventral view); C, spermatheca. Scale bars: A, B = 1.0 mm; C = 0.1 mm.
Fig. 4. Kanigara punctata Scudder, 1969. A, B in ThegenusKanigara Distant(Heteroptera:Lygaeoidea: Rhyparochromidae) from Malay Peninsula and Thailand, with description of a new species
Fig. 4. Kanigara punctata Scudder, 1969. A, B, male (A, dorsal view; B, ventral view); C, D, female (C, dorsal view; D, ventral view). Scale bars = 1.0 mm.
Fig. 3 in Phylogeography of Long-spined Sea Urchin Across the Indo-Malay Archipelago.
Fig. 3. Diadema setosum. Minimum-spanning network of COI gene haplotypes. Area of circle proportional to haplotype frequency in total sample; length of branch proportional to number of mutations (scale bar: one mutational step) except alternative links between haplotypes, where number of mutational steps is represented by a series of perpendicular dashes. A few such links between distant haplotypes were omitted for better readability. White: haplotype sampled from Group-1 D. setosum; hachured white: Group-2; black: Sub-group-3a; grey: Sub-group-3b.
Fig. 2 in Phylogeography of Long-spined Sea Urchin Across the Indo-Malay Archipelago.
Fig. 2. Phylogeographic structure of Diadema setosum in the Indo-Malay archipelago. A: Multidimensional scaling plot based on the matrix of pairwise ФST (T92+G model; Arlequin). Ellipses delineate groups of samples designated by hierarchical clustering. Abbreviations for samples as in table 1. B: Pairwise estimates of genetic differentiation plotted against the logarithm of geographic distance [ln(gD), gD in km]. Black circles (●) intra-group comparisons; open circles (○) (resp. triangles): inter-group comparisons involving Group 1 (resp. Group 2).
Fig. 1 in Phylogeography of Long-spined Sea Urchin Across the Indo-Malay Archipelago.
Fig. 1. Diadema setosum sampling locations. Colours refer to the results of MDS analysis (see RESULTS). Bold dotted lines indicate inferred geographic barriers. SoM Strait of Malacca; Mak. Str. Makassar Strait; other abbreviations as in table 1. Table 1. Diadema setosum sampling details and GenBank accession numbers by sample. N sample size
Audio file of Malay diphthong (dataset)
<p>This dataset provides the spoken audio for the diphthong /au/, /ai/, /oi/ and /ui/ from district regions of Selangor (standard), Perlis, Kedah, and Pulau Pinang located in Malaysia. The overall recording of the audio spontaneous speech is approximately 4 hours. A total of 193 diphthongs were extracted from the spoken words and the file was grouped into district and diphthong as shown below. This is the clean and processed data with clear pronunciation of the diphthongs. The dataset have been used to analyze the pronunciation of the diphthong between the districts regions in Malaysia and can be used further for camparing between other languages.</p> <p> </p> <p>DiphData.zip contains all of these file:</p> <p> </p> <p>Selangor’s diphthong file</p> <p>S(au).file</p> <p>S(ai).file</p> <p>S(oi).file</p> <p> </p> <p>Perlis’s diphthong file</p> <p>P(au).file</p> <p>P(ai). file</p> <p>P(oi).file</p> <p>P(ui).file</p> <p> </p> <p>Kedah’s diphthong file</p> <p>K(au).file</p> <p>K(ai).file</p> <p>K(oi).file</p> <p>K(ui).file</p> <p> </p> <p>Pulau Pinang’s diphthong file</p> <p>PP(au).file</p> <p>PP(ai).file</p> <p>PP(oi).file</p> <p>PP(ui).file</p> <p> </p>
Fig. 4 in A New Species Of Rana (Amphibia: Anura: Ranidae) From The Highlands Of The Malay Peninsula, With Diagnostic Larval Descriptions
Fig. 4. Ventral aspects of left forelimb (a) and left hindlimb (b) of adult male Rana banjarana (illustrated from holotype: ZRC.1.8325). Note nuptial pad (unpigmented, non-constricted) on inner face of first finger. Scale bar = 5mm.
ScienceDex guides
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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.