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2,268 results for “myanmar”
Fig. 7 in Primitive New Ants in Cretaceous Amber from Myanmar, New Jersey, and Canada (Hymenoptera: Formicidae)
Fig. 7. Facial view of holotype worker of †Haidomyrmex cerberus Dlussky (NHML In.20182).
Fig. 2 in An Unusual, Primitive Piesmatidae (Insecta: Heteroptera) in Cretaceous Amber from Myanmar (Burma)
Fig. 2. Dorsal habitus of holotype of Cretopiesma suukyiae, new genus and species.
Figs. 5–6 in Early Cretaceous Snakefly Larvae in Amber from Lebanon, Myanmar, and France (Raphidioptera)
Figs. 5–6. Photomicrographs of larval snakeflies in Burmese amber. 5. Head capsule of AMNH Bu-507
Fig. 4 in Early Cretaceous Snakefly Larvae in Amber from Lebanon, Myanmar, and France (Raphidioptera)
Fig. 4. Line illustration of specimen MNHN- ARC-328.4 in French amber. Scale bar 5 0.25 mm.
Sri Ksetra, Bago, Myanmar. Map of Sri Ksetra, phase 2.
<p>Sri Ksetra, Bago, Myanmar. Map of Sri Ksetra, phase 2.</p>
Sri Ksetra, Bago, Myanmar. Map of Sri Ksetra, phase 1.
<p>Sri Ksetra, Bago, Myanmar. Map of Sri Ksetra, phase 1.</p>
Agroforestry-based community forestry as a large-scale strategy to reforest agricultural encroachment areas in Myanmar: ambition vs. local reality
<p>Abstract: <br> Context: <br> The high rate of deforestation in Myanmar is mainly due to agricultural expansion. One task of the Forest Department is to increase tree cover in the encroaching farmland by establishing large-scale agroforestry-based community forests (ACFs).<br> Aim: <br> The objectives of this study were to analyze the adoption and performance of the ACFs in the agricultural encroachment areas in the Bago-Yoma region, Myanmar; and to provide recommendations to enhance the adoption of ACFs by farmers.<br> Methods: <br> We inventoried 42 sample plots and surveyed 291 farmers. Survey responses were analyzed by binary logistic regression, one-way ANOVA, and non-parametric correlation tests to evaluate factors influencing the adoption of ACFs. Stand characteristics were calculated from the inventory data to evaluate the performance of ACFs.<br> Results: <br> Our results show that farmer participation in ACFs was lower than stated in the registry of the Forest Department. Farmers practiced four different agroforestry designs in ACFs with different outcomes. The Forest Department strongly determined tree species and planting designs, farmers’ perception and participation in ACFs. Farmland size, unclear and insufficient information on ACFs, and a negative perception of raising trees in crop fields were the major factors limiting the adoption rates of ACFs. <br> Conclusion: <br> We recommend capacity building for farmers and Forest Department staff and raising awareness about the benefits of planting designs and trees on farmland. A stronger consideration of farmers’ preferences for design and species selection could increase their motivation to adopt ACFs and improve the long-term sustainability of ACFs.</p> <p> </p>
FIGURE 7 in Multigene phylogeny reveals the ribbed shell morphotypes in the land snail genus Sarika (Eupulmonata: Ariophantidae), with description of two new species from Thailand and Myanmar
FIGURE 7 Shell and body variation in Sarika siamensis.
Fig. 6 in Middle Eocene ungulate mammals from Myanmar: A review with description of new specimens
Fig. 6. Cenogram of the Pondaung fauna.
Data from: Middle Permian fusulines from the Thitsipin Formation of Shan State, Myanmar and their palaeobiogeographical and palaeogeographical implications
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Data from: Gastrodia putaoensis sp. nov. (Orchidaceae, Epidendroideae) from North Myanmar
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Nothapodytes burmanica (Icacinaceae), a new species from Kachin State, Myanmar
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Fig. 7 in New remarkable hell ants (Formicidae: Haidomyrmecinae stat. nov.) from mid-Cretaceous amber of northern Myanmar
Fig. 7. Overview and details of females of Linguamyrmex brevicornis gen. et sp. nov. Gyne specimen LA01 (AeB), worker specimen RM4 (C), worker holotype NIGP172001 (D). Habitus (A, C), head and mesosoma in dorsal view (B), head in ventrolateral view (D). Scale bars: 0.5 mm.
Fig. 1 in New remarkable hell ants (Formicidae: Haidomyrmecinae stat. nov.) from mid-Cretaceous amber of northern Myanmar
Fig. 1. Measurements of cranial structures shown on 3D models. A, head of Dhagnathos gen. nov. in full facial view. B, head of Dhagnathos gen. nov. in lateral view. C, head of Aquilomyrmex gen. nov. in dorsal view. D, head of Aquilomyrmex gen. nov. in lateral view. Scale bars: 1 mm.
FIGURE 3 in New country records for three species of frog from Myanmar including two genera (Nasutixalus and Oreolalax)
FIGURE 3. Bayesian matrilineal genealogy of Nasutixalus (A) resulting from DNA sequences of a 16S rRNA gene fragment and external features of Nasutixalus jerdonii in life from Myanmar (B). "*" denotes Bayesian posterior probabilities (BPP) ≥0.95; "#" denotes nodes with 90
Subspecies and Distribution. H. a. ater Templeton, 1848 - India and Sri Lanka. H. a. amboinensis Peters, 1871 — Ambon I, Moluccas. H. a. antricola Peters, 1861 — Philippines. H. a. aruensisj. E. Gray, 1858 — New Guinea, Bismarck Archipelago, Woodlark I, and E Australia (Queensland). H. a. gilberti D. H. Johnson, 1959 - Western Australia and Northern Territory, Australia. H. a. naUamalaensis. Srinivasulu & B. Srinivasulu, 2006 - Eastern Ghats, Andhra Pradesh, India. H. a. saevus K. Andersen, 1918 - Myanmar S to Peninsular Malaysia, Sumatra, N Borneo, Java, Lesser Sunda Is (Bali and Lombok), Sulawesi, Moluccas, and Kai Is. Range of this subspecies is tentative and needs revision. in Family Hipposideridae (Old World Leaf-nosed Bats)
Subspecies and Distribution. H. a. ater Templeton, 1848 - India and Sri Lanka. H. a. amboinensis Peters, 1871 — Ambon I, Moluccas. H. a. antricola Peters, 1861 — Philippines. H. a. aruensisj. E. Gray, 1858 — New Guinea, Bismarck Archipelago, Woodlark I, and E Australia (Queensland). H. a. gilberti D. H. Johnson, 1959 - Western Australia and Northern Territory, Australia. H. a. naUamalaensis. Srinivasulu & B. Srinivasulu, 2006 - Eastern Ghats, Andhra Pradesh, India. H. a. saevus K. Andersen, 1918 - Myanmar S to Peninsular Malaysia, Sumatra, N Borneo, Java, Lesser Sunda Is (Bali and Lombok), Sulawesi, Moluccas, and Kai Is. Range of this subspecies is tentative and needs revision.
Subspecies and Distribution. R. p. perniger Hodgson, 1843 - N, C & SW India (Uttarakhand, Sikkim, West Bengal, Assam, Meghalaya, Nagaland, Madhya Pradesh, Karnataka, and Kerala), C & E Nepal, Bhutan, Bangladesh, Myanmar, S China (Yunnan), N Thailand, Laos, Vietnam, and Cambodia. . p. lanosus K. Andersen, 1905 — C & SE China (Sichuan, Guizhou, Guangxi, Anhui Zhejiang,Jiangxi, Fujian, and Guangdong). R.p. spurcus G. M. Allen, 1928 - Hainan I, China. Possibly also peninsular Thailand, according to recorded calls. in Rhinolophidae
Subspecies and Distribution. R. p. perniger Hodgson, 1843 - N, C & SW India (Uttarakhand, Sikkim, West Bengal, Assam, Meghalaya, Nagaland, Madhya Pradesh, Karnataka, and Kerala), C & E Nepal, Bhutan, Bangladesh, Myanmar, S China (Yunnan), N Thailand, Laos, Vietnam, and Cambodia. . p. lanosus K. Andersen, 1905 — C & SE China (Sichuan, Guizhou, Guangxi, Anhui Zhejiang,Jiangxi, Fujian, and Guangdong). R.p. spurcus G. M. Allen, 1928 - Hainan I, China. Possibly also peninsular Thailand, according to recorded calls.
Subspecies and Distribution. R. t. trifoliatus Temminck, 1834 —Sumatra, Belitung I, Borneo, WJava, and Banta I. R. t. edax K. Andersen, 1918 - NE India (two records in West Bengal and Assam), S China (one record in Guizhou), S Myanmar, C & S Thailand, Peninsular Malaysia, and Singapore. R. t. niasensis K. Andersen, 1906 — Nias I. R. t. solitarius K Andersen, 1905 - Bangka I. in Rhinolophidae
Subspecies and Distribution. R. t. trifoliatus Temminck, 1834 —Sumatra, Belitung I, Borneo, WJava, and Banta I. R. t. edax K. Andersen, 1918 - NE India (two records in West Bengal and Assam), S China (one record in Guizhou), S Myanmar, C & S Thailand, Peninsular Malaysia, and Singapore. R. t. niasensis K. Andersen, 1906 — Nias I. R. t. solitarius K Andersen, 1905 - Bangka I.
Subspecies and Distribution. R. p. pearsonii Horsfield, 1851 - N India (Uttarakhand, Sikkim, West Bengal, Assam, Meghalaya, and Mizoram), Nepal, Bhutan, Bangladesh,, S & SE China (Xizang, Sichuan, Yunnan, Shaanxi, Guizhou, Guangxi, Hubei, Hunan, and Guangdong), Myanmar, Thailand, Laos, Vietnam, and Cambodia. R.p. chinensisK. Andersen, 1905 - SE China (Anhui, Zhejiang, Jiangxi, and Fujian). in Rhinolophidae
Subspecies and Distribution. R. p. pearsonii Horsfield, 1851 - N India (Uttarakhand, Sikkim, West Bengal, Assam, Meghalaya, and Mizoram), Nepal, Bhutan, Bangladesh,, S & SE China (Xizang, Sichuan, Yunnan, Shaanxi, Guizhou, Guangxi, Hubei, Hunan, and Guangdong), Myanmar, Thailand, Laos, Vietnam, and Cambodia. R.p. chinensisK. Andersen, 1905 - SE China (Anhui, Zhejiang, Jiangxi, and Fujian).
Distribution. NC, C & SE Myanmar, Thailand (including Tarutao I), C Laos, and NW Peninsular Malaysia (including Langkawi I). in Rhinolophidae
Distribution. NC, C & SE Myanmar, Thailand (including Tarutao I), C Laos, and NW Peninsular Malaysia (including Langkawi I).
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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.