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2,402 results for “East Asia”
FIGURES 76–79 in Nepticulidae (Lepidoptera) of East Asia (1). Re-examination of the male genitalia of types deposited at the Russian Academy of Sciences
FIGURES 76–79. Male genitalia of Stigmella ussurica Puplesis (a junior syn. of Stigmella tranocrossa Kempermen & Wilkinson), paratype, slide no. AG 410 (ZIN). 76, general view; 77, other view with inner lobe of valva; 78, view with vinculum and uncus exposed; 79, aedeagus. Scale bar 100 µm.
FIGURE 1 in Species of the genus Eurydema (Hemiptera: Heteroptera: Pentatomidae) in Far East Asia: An integrated approach using morphological, molecular, and data crossing analyses for taxonomy
FIGURE 1. Eurydema species in Far East Asia distinguished by the traditional key (see introduction). A, E. pulchra (exocorium with a black spot, red coloration); B, E. dominulus (exocorium entirely pale); C, E. gebleri (legs partly pale; pronotum with 6 dark spots); D, E. rugosa (legs entirely black; pronotum with 2 dark spots). E, E. pulchra (exocorium with a black spot, yellow coloration); F, E. dominulus or E. pulchra (exocorium with a small dark spot); G, E. gebleri or E. rugosa (legs partly pale; pronotum with 2 dark spots); H, E. gebleri or E. rugosa (legs partly pale; pronotum with fused dark spots). A–E, Eurydema species possibly identified by the traditional key to species (see introduction); F–H, examples of color variation in each species leading to misidentification or the lack of identification, scale: 1mm.
FIGURE 4 in Species of the genus Eurydema (Hemiptera: Heteroptera: Pentatomidae) in Far East Asia: An integrated approach using morphological, molecular, and data crossing analyses for taxonomy
FIGURE 4. Interspecific copulation and life cycle of the gebleri–group. A, copulating scene (the upper species is E. gebleri (female) and the lower one is E. rugosa (male) as determined by the traditional key); B, 1st instars and eggs; C, 2nd instars; D, 3rd and 4th instars; E, final instars; F, mixed stage nymphs and adult.
FIGURES 33–38. Stenoloba spp., male genitalia. 33. S in Fourteen new species of the genus Stenoloba Staudinger, 1892 from South East Asia (Lepidoptera: Noctuidae, Bryophilinae)
FIGURES 33–38. Stenoloba spp., male genitalia. 33. S. pendleburyi, genit. slide GB5645, Indonesia, Sumatra; 34. S. ansari, holotype, genit. slide 3-150510, Indonesia, Java; 35. S. wolfgangi, holotype, genitalia slide 7212GB, Indonesia, Sumatra; 36. S. albibasis, holotype, genit. slide 5320GB, Indonesia, Sumatra; 37. S. elegans (after Holloway 2009), Malaysia, Borneo; 38. S. futii, genit. prep. 5321 DB, Indonesia, Sumatra.
FIGURES 25–32. Stenoloba spp., adults. 25. S in Fourteen new species of the genus Stenoloba Staudinger, 1892 from South East Asia (Lepidoptera: Noctuidae, Bryophilinae)
FIGURES 25–32. Stenoloba spp., adults. 25. S. siamensis, female, holotype, Thailand; 26. S. mossy, female, holotype, Vietnam; 27. S. ronkayi, male, holotype, Vietnam; 28. S. matovi, male, holotype, Vietnam 29, 30. S. sacculata (29 = male, holotype, 30 = female, paratype), Vietnam; 31, 32. S. pinratanai (31 = male, holotype, 32 = female, paratype), Thailand.
FIGURES 1–8. Stenoloba spp., adults. 1, 2. S in Fourteen new species of the genus Stenoloba Staudinger, 1892 from South East Asia (Lepidoptera: Noctuidae, Bryophilinae)
FIGURES 1–8. Stenoloba spp., adults. 1, 2. S. pendleburyi, male, Indonesia, Sumatra; 3. S. ansari, male, holotype, Indonesia, Java; 4. S. ansari, male, Indonesia, Sulawesi; 5, 6. S. wolfgangi (5 = male, holotype, 6 = female, paratype), Indonesia, Sumatra; 7, 8. S. albibasis (7 = male, holotype, 8 = female, paratype), Indonesia, Sumatra.
FIGURES 79–86. Stenoloba spp., distribution maps. 79. S in Fourteen new species of the genus Stenoloba Staudinger, 1892 from South East Asia (Lepidoptera: Noctuidae, Bryophilinae)
FIGURES 79–86. Stenoloba spp., distribution maps. 79. S. benjamini; 80. S. dentilinea; 81. S. siamensis; 82. S. mossy; 83. S. ronkayi; 84. S. matovi; 85. S. sacculata; 86. S. pinratanai.
FIGURES 49–54 in Fourteen new species of the genus Stenoloba Staudinger, 1892 from South East Asia (Lepidoptera: Noctuidae, Bryophilinae)
FIGURES 49–54. Stenoloba spp., tip of male abdomen. 49. S. ansari; 50. S. wolfgangi, Vietnam; 51. S. futii; 52. S. futioides; 53. S. benjamini; 54. S. javensis.
FIGURE 7 in Morphological and molecular identification of three new resupinate species of Hyphoderma (Hyphodermataceae, Agaricomycetes) from East Asia
FIGURE 7. Basidiomata of Hyphoderma yunnanense. Bars: A = 1 cm, B = 1 mm (Holotype: CLZhao 8845). Photo plate by: Zi-Yan Duan.
Figure 5 in Multilocus phylogeny and historical biogeography of the Crematogaster inflata-group (Hymenoptera: Formicidae) in South-East Asia
Figure 5. Evolution of antennal club (A), propodeal inflation (B), propodeal spines (C) and metapleural gland opening (D) in the Crematogaster inflata-group. Ancestral state reconstructions as estimated with corHMM under the ER model. Pie charts represent ancestral reconstructions of number of antennal club, inflation of propodeum, propodeal spines and metapleural gland opening.
Figure 2 in Multilocus phylogeny and historical biogeography of the Crematogaster inflata-group (Hymenoptera: Formicidae) in South-East Asia
Figure 2. Maximum likelihood (ML) phylogeny for 38 taxa using six nuclear (ArgK, CAD, EF1αF1, LWRh, Top1, Wg) and two mitochondrial (12S, COI) genes in an IQ-TREE analysis. Values at each node are bootstrap value of the IQ-TREE analysis and posterior probability of the MRBAYES analysis, respectively; '–' indicates that this node is not found in the MRBAYES topology. Data were partitioned by PARTITIONFINDER and analysed using a best fit model for each gene and codon position. Inset, Crematogaster inflata specimen in profile view.
Figure 3 in Multilocus phylogeny and historical biogeography of the Crematogaster inflata-group (Hymenoptera: Formicidae) in South-East Asia
Figure 3. Phylogenetic relationships and species groups within the Crematogaster inflata-group from maximum likelihood (ML) and Bayesian (BI) analyses. Bootstrap value and posterior probability are shown at each node.
FIGURE 2 in Integrative taxonomic revision of the genus Phaselia Guenée, [1858] (Geometridae: Ennominae) in the Middle East and Central Asia
FIGURE 2: Wing venation of male specimen of genus Phaselia (based on P. serrularia) with magnification of the costal part of the forewing (section A). Sc = subcostalis; R = radial veins; Rs = radial sector; M = medial veins; CuA = cubital veins; A = anal veins.
FIGURES 98–100 in Integrative taxonomic revision of the genus Phaselia Guenée, [1858] (Geometridae: Ennominae) in the Middle East and Central Asia
FIGURES 98–100: Variation of the male genitalia of Phaselia sihvoneni sp. nov. 98: Holotype, from: N Pakistan, N Karimabad (g. prep. 0153/2021 M. Werner); 99: Paratype, from: Tajikistan, Rushan, Shipad (g. prep. 0130/2021 M. Werner); 100: Paratype, from: N Pakistan, N Sost (g. prep. 0159/2021 M. Werner). a = genitalia capsule; b = aedeagus. Scalebar = 1 mm.
FIGURE 6 in Review of the genus Zelleria Stainton (Lepidoptera, Yponomeutidae, Yponomeutinae) in East Asia, with description of a new species
FIGURE 6. Wing venation of Zelleria, female, Gangwon Province, Korea (Paratype from INU).
Figs 802. Teutamus fertilis n in Forest Spiders of South East Asia With a revision of the sac and ground spiders (Araneae: Clubionidae, Corinnidae, Liocranidae, Gnaphosidae, Prodidomidae and Trochanteriidae).
Figs 802. Teutamus fertilis n. sp., male, habitus.
Research Compendium for: "Quina technology from Southwest China indicates diverse late-Pleistocene human dynamics in East Asia"
<div> <div> <div> <div> <p>✉ Correspondence: Hao Li <a href="mailto:lihao@itpcas.ac.cn">lihao@itpcas.ac.cn</a></p> <p>✉ Correspondence: Peiyuan Xiao <a href="mailto:xiaopeiyuan@itpcas.ac.cn">xiaopeiyuan@itpcas.ac.cn</a></p> <p>✉ Correspondence: Bo Li <a href="mailto:bli@uow.edu.au">bli@uow.edu.au</a></p> <p>✉ Correspondence: Davide Delpiano <a href="mailto:dlpdvd@unife.it">dlpdvd@unife.it</a></p> </div> </div> </div> <h3>Online access:</h3> <p>Zenodo DOI: <a href="https://doi.org/10.5281/zenodo.13762081">https://doi.org/10.5281/zenodo.13762081</a></p> <p>The files at the URL above will generate the results as found in the publication. The files hosted at <a href="https://github.com/PeiyuanXiao/Lithic-data-Longtan-site">https://github.com/PeiyuanXiao/Lithic-data-Longtan-site</a> are the development versions and may have changed since the paper was published.</p> <h3>Maintainer of this repository:</h3> <p>Peiyuan Xiao <a href="mailto:xiaopeiyuan@itpcas.ac.cn">xiaopeiyuan@itpcas.ac.cn</a></p> <p>Ben Marwick <a href="mailto:bmarwick@uw.edu">bmarwick@uw.edu</a></p> </div> <h3>Abstract:</h3> <p>The Late Pleistocene of Eurasia is key for understanding interactions between early modern humans and different types of archaic human groups. During this period, lithic technology shows more diversity and complexity, likely indicating flexible adaptative strategies. However, cultural variability as expressed by technological types remains vague in large parts of eastern Eurasia, like in China. Here we report a complete Quina technological system identified from the study of the Longtan site in Southwest China. This site has been securely dated to ca. 60–50 thousand years ago (ka), with compelling evidence of core exploitation, production of large and thick flakes, shaping and maintenance of scrapers exhibiting the whole Quina concept, typical of contemporary European Middle Paleolithic technologies developed by Neanderthal groups adapted to climatic oscillations during Marine Isotope Stage (MIS) 4 and early MIS 3. The finding of a Quina lithic assemblage in China not only demonstrates the existence of a Middle Paleolithic technology in the region, but also shows large-scale analogies with Neanderthal behaviors in western Europe. Longtan substantially extends the geographic distribution of this technical behavior in East Asia. Although its origin remains unclear, implications for Pleistocene hominin dispersal and adaptation to diverse ecological settings are considered. The Longtan lithic evidence also provides perspectives for understanding the cultural evolutionary situation before the large-scale arrivals of early modern humans in East Asia predating ~45 ka.</p> <h3>Keywords:</h3> <p>Middle Paleolithic; fluvial terrace; early MIS 3; Late Pleistocene; hominins</p> <div> <div> <h3>R packages and their versions:</h3> <p>Data processing & analyzing: <code>readxl (>= 1.4.3)</code>,<code>tidyverse (>= 2.0.0)</code>,<code>forcats (>= 1.0.0)</code>,<code>dunn.test (>= 1.3.6)</code>, other statistical testing methods use the corresponding functions in the R base package</p> <p>Plots creating: <code>tidyverse (>= 2.0.0)</code>,<code>ggpmisc (>= 0.5.6)</code>,<code>ggdist (>= 3.3.2)</code>,<code>MetBrewer (>= 0.2.0)</code>,<code>ggbeeswarm (>= 0.7.2)</code>,<code>cowplot (>= 1.1.3)</code>,<code>patchwork (>= 1.2.0)</code>,<code>ggtext (>= 0.1.2)</code>,<code>scales (>= 1.3.0)</code></p> </div> </div>
F in Biogeographic analysis of the ant genus Gnamptogenys Roger in South-East Asia-Australasia (Hymenoptera: Formicidae: Ponerinae)
F. 3. Distribution of the Gnamptogenys coxalis species group.
FIGURE 6 in Two new species of Cunaxa (Acari, Prostigmata, Cunaxidae) from South-East Asia with a world key to the genus
FIGURE 6. Cunaxa smileyi sp. nov., female (holotype), ventral view of idiosoma.
Assessing Genetic Diversity of Asian Salamanders (Hynobiidae) lived in Far East Asia using Transcriptome data
GEO Series GSE137677. Hynobius leechii; Hynobius yangi; Hynobius quelpaertensis; Hynobius unisacculus. 23 samples. Type: Expression profiling by high throughput sequencing.
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