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398 results for “Malay”
Fig. 6 in Brevibora Cheeya, A New Species Of Cyprinid Fish From Malay Peninsula And Sumatra
Fig. 6: Type locality of Brevibora cheeya at Rantau Abang, Terengganu, Malaysia (February 2009).
Annotated Dataset for Bilingual Code-Mixed English-Malay Sentiment Analysis and Sarcasm Detection in Public Security Domain
<p>Tweets from X, and post with comment from TikTok was acquired <span>from 11 September until 21 September 2022</span>. Data from both platforms was merged and selected. Three annotators manually labelling the selected data for sentiment and sarcasm. Sentiment labels are ‘positive’, ‘negative’, and ‘neutral’. Sarcasm label is ‘sarcastic’ and ‘not sarcastic’. Majority voting is considered for each label. Language identification label produced for each data. </p>
Fig. 6 in A New Species Of Rana (Amphibia: Anura: Ranidae) From The Highlands Of The Malay Peninsula, With Diagnostic Larval Descriptions
Fig. 6. Lateral (a) and dorsal (b) aspects of advanced (Stage 43) larval Rana banjarana.
Fig. 5 in A New Species Of Rana (Amphibia: Anura: Ranidae) From The Highlands Of The Malay Peninsula, With Diagnostic Larval Descriptions
Fig. 5. Lateral (a) and dorsal (b) aspects of early (Stage 27) larval Rana banjarana.
Fig. 1 in The habitat preference of dung beetle species associated with elephant dung of the Malay Peninsula
Fig. 1. Map of all the localities where dung beetle sampling was carried out.
Fig. 7. Baruna Jaya VIII, 2015 in History of collection and discovery of polychaetes (Annelida), including a bibliography, from the Indo-Malay-Philippines Archipelago and surrounding seas
Fig. 7. Baruna Jaya VIII, 2015. Photo: LIPI, Jakarta.
Fig. 5 in History of collection and discovery of polychaetes (Annelida), including a bibliography, from the Indo-Malay-Philippines Archipelago and surrounding seas
Fig. 5. Syllis ramosa, original illustration of McIntosh (1885, pl. 31).
Fig. 3 in History of collection and discovery of polychaetes (Annelida), including a bibliography, from the Indo-Malay-Philippines Archipelago and surrounding seas
Fig. 3. Amphinome rostrata, original illustrations from Pallas (1766), pl. 8, figs. 14–18.
Fig. 4 in History of collection and discovery of polychaetes (Annelida), including a bibliography, from the Indo-Malay-Philippines Archipelago and surrounding seas
Fig. 4. Sternapis spinosa, original illustrations from Sluiter (1882: pl. 1).
Fig. 2 in History of collection and discovery of polychaetes (Annelida), including a bibliography, from the Indo-Malay-Philippines Archipelago and surrounding seas
Fig. 2. Georg Eberhand Rumphius, engraved portrait as reproduced in Rumphius (1705).
Conservation prioritisation through genomic reconstruction of demographic histories applied to two endangered suids in the Malay Archipelago
<p><strong>Aim</strong>: The biodiversity of the Malay Archipelago is the product of the region's rich biogeographical history with periods of island connectivity and isolation during the Pleistocene glacial cycles. Here, the case of two endemic suid species, the Javan (<em>Sus verrucosus</em>) and Bawean (<em>S. blouchi</em>) warty pigs, was used to illustrate how biogeographic processes and recent anthropogenic pressures can shape demographic histories with significant implications for species conservation.</p> <p><strong>Location</strong>: Malay Archipelago, with focus on Bawean and Java.</p> <p><strong>Methods</strong>: We employed genome-wide single nucleotide polymorphisms from the Porcine SNP60 v2 BeadChip to assess interspecific genetic differentiation, to estimate divergence times, and to perform demographic model selection.</p> <p><strong>Results</strong>: In contrast to the hypothesis of recent divergence during the last glacial maximum, <em>S. blouchi</em> was found to have diverged from <em>S. verrucosus</em> at least 166k years ago following a founder event. The contemporary <em>S. blouchi</em> population was characterised by a recent bottleneck that reduced the effective population size to less than 20. The genomic assessment supports the single species status of <em>S. blouchi</em>, as was previously proposed based on morphometrics. The demographic history of <em>S. verrucosus</em> showed evidence of secondary contact with the sympatric banded pig (<em>S. scrofa vittatus</em>) that colonised Java 70k years ago.</p> <p><strong>Main</strong> <strong>conclusions</strong>: While the Javan and Bawean warty pigs have persisted throughout the Pleistocene climatic oscillations, contemporary pressures from human activities threaten their survival and immediate action should be taken to grant legal protection to both <em>S. verrucosus</em> and <em>S. blouchi</em>. This study highlighted the use of demographic history modelling using genomic data to identify evolutionary significant units and inform conservation.</p>
Malaysian Malay E-line data
<p>Data on Photogrammetric and Cephalometric Analyses of Ricketts' Esthetic Line in Malaysian Malay Adults: A Cross-sectional Study</p>
Conservation prioritisation through genomic reconstruction of demographic histories applied to two endangered suids in the Malay Archipelago
Open the record for dataset details and reuse information.
Subspecies and Distribution. H. g. galeritus Cantor, 1846 -SE Thailand, S Laos, C & S Vietnam, Cambodia, Malay Peninsula (including Tarutao and Penang Is), Sumatra, and Bangka I. H. g. brachyotis Dobson, 1874 -India (Gujarat, Madhya Pradesh, Maharashtra, Karnataka, Bihar, Odisha, and Andhra Pradesh), Bangladesh, and Sri Lanka. H. g. insolens Lyon, 1911 — Borneo. H. g. longicauda Peters, 1861 -W & Java. Also present on Sanana I (Sula Is), but subspecies involved not known. in Hipposideridae
Subspecies and Distribution. H. g. galeritus Cantor, 1846 -SE Thailand, S Laos, C & S Vietnam, Cambodia, Malay Peninsula (including Tarutao and Penang Is), Sumatra, and Bangka I. H. g. brachyotis Dobson, 1874 -India (Gujarat, Madhya Pradesh, Maharashtra, Karnataka, Bihar, Odisha, and Andhra Pradesh), Bangladesh, and Sri Lanka. H. g. insolens Lyon, 1911 — Borneo. H. g. longicauda Peters, 1861 -W & Java. Also present on Sanana I (Sula Is), but subspecies involved not known.
Subspecies and Distribution. H. c. ceruinus Gould, 1854 -Sulawesi and adjacent Is, Talaud, Moluccas, Kai, and Aru Is, New Guinea (including Waigeo and Yapen Is), Admiralty Is (Manus), Bismarck and Louisiade archipelagos, NE Australia (Cape York Peninsula and Moa and Albany Is), Solomon Is, and Vanuatu. H. c. labuanensisTomes, 1859-Malay Peninsula, Sumatra (includingMentawai, Enggano, and Bangka Is), Borneo, Kangean Is, and Philippines (Palawan and Mindanao Is). in Hipposideridae
Subspecies and Distribution. H. c. ceruinus Gould, 1854 -Sulawesi and adjacent Is, Talaud, Moluccas, Kai, and Aru Is, New Guinea (including Waigeo and Yapen Is), Admiralty Is (Manus), Bismarck and Louisiade archipelagos, NE Australia (Cape York Peninsula and Moa and Albany Is), Solomon Is, and Vanuatu. H. c. labuanensisTomes, 1859-Malay Peninsula, Sumatra (includingMentawai, Enggano, and Bangka Is), Borneo, Kangean Is, and Philippines (Palawan and Mindanao Is).
Distribution. Malay Peninsula and N & SW Borneo (Sabah, Sarawak, and Brunei); probably also occurs in the rest of Borneo (Kalimantan), but this has not yet been confirmed. in Family Hipposideridae (Old World Leaf-nosed Bats)
Distribution. Malay Peninsula and N & SW Borneo (Sabah, Sarawak, and Brunei); probably also occurs in the rest of Borneo (Kalimantan), but this has not yet been confirmed.
Subspecies and Distribution. R. a. afinis Horsfield, 1823 - Malay Peninsula (including Langkawi and Tioman Is), Sumatra, North Pagai I in Mentawai Is, and Java. R. a. hainanusJ. A. Allen, 1906 - Hainan I, China. R. a. himalayanus K Andersen, 1905 — N India (Uttarakhand, Uttar Pradesh, Sikkim, West Bengal, Assam, Meghalaya, Arunachal Pradesh, and Nagaland), Nepal, Bhutan, NE Bangladesh, N Myanmar, and C & S China (Sichuan, Yunnan, Shaanxi, Hubei, Hunan, and Guizhou). R. a. macrurus K. Andersen, 1905 - SE China (Jiangsu, Anhui, Zhejiang, Jiangxi, Fujian, Guangdong, Hong Kong, and Guangxi), S Myanmar, Thailand, Laos, and Vietnam (including Dao Tra Ban and Phu Quoc Is); possibly also Cambodia. R. a. nesites K. Andersen, 1905 - Borneo (including Laut, Sebuku, and Laut Kecil Is) and Anamba and Natuna Is. R. a. princeps K. Andersen, 1905 — Kangean (Kangean and Sepanjang Is), Lombok, Sumbawa, Flores, and Sumba Is. A morphologically distinct subspecies (still unnamed) is known from E Myanmar and N Vietnam. in Rhinolophidae
Subspecies and Distribution. R. a. afinis Horsfield, 1823 - Malay Peninsula (including Langkawi and Tioman Is), Sumatra, North Pagai I in Mentawai Is, and Java. R. a. hainanusJ. A. Allen, 1906 - Hainan I, China. R. a. himalayanus K Andersen, 1905 — N India (Uttarakhand, Uttar Pradesh, Sikkim, West Bengal, Assam, Meghalaya, Arunachal Pradesh, and Nagaland), Nepal, Bhutan, NE Bangladesh, N Myanmar, and C & S China (Sichuan, Yunnan, Shaanxi, Hubei, Hunan, and Guizhou). R. a. macrurus K. Andersen, 1905 - SE China (Jiangsu, Anhui, Zhejiang, Jiangxi, Fujian, Guangdong, Hong Kong, and Guangxi), S Myanmar, Thailand, Laos, and Vietnam (including Dao Tra Ban and Phu Quoc Is); possibly also Cambodia. R. a. nesites K. Andersen, 1905 - Borneo (including Laut, Sebuku, and Laut Kecil Is) and Anamba and Natuna Is. R. a. princeps K. Andersen, 1905 — Kangean (Kangean and Sepanjang Is), Lombok, Sumbawa, Flores, and Sumba Is. A morphologically distinct subspecies (still unnamed) is known from E Myanmar and N Vietnam.
Subspecies and Distribution. A r. robinsoni K. Andersen, 1918 - Malay Peninsula. A r. klossi K. Andersen, 1918 - Tioman, Pemanggil, and Aur Is off SE Malay Peninsula in Rhinolophidae
Subspecies and Distribution. A r. robinsoni K. Andersen, 1918 - Malay Peninsula. A r. klossi K. Andersen, 1918 - Tioman, Pemanggil, and Aur Is off SE Malay Peninsula
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. 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
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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.