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639 results for “eastern China”
FIGURES 15–17 in Four new species of Oedalea (Diptera, Empidoidea, Hybotidae, Oedaleinae) from China with a key to south eastern Asian species
FIGURES 15–17. Oedalea wulingshana sp. nov. (male). 15. Adult habitus, lateral view; 16. Head, lateral view; 17. Wing.
FIGURES 11–14 in Four new species of Oedalea (Diptera, Empidoidea, Hybotidae, Oedaleinae) from China with a key to south eastern Asian species
FIGURES 11–14. Oedalea wenliangi sp. nov. (male). 11. Genitalia, dorsal view; 12. Left epandrial lamella, lateral view; 13. Right epandrial lamella, lateral view; 14. Hypandrium and phallus, ventral view. Abbreviations: see Material and methods.
FIGURES 1–3 in Four new species of Oedalea (Diptera, Empidoidea, Hybotidae, Oedaleinae) from China with a key to south eastern Asian species
FIGURES 1–3. Oedalea linzhiensis sp. nov. (male). 1. Adult habitus, lateral view; 2. Head, lateral view; 3. Wing.
FIGURES 8–10 in Four new species of Oedalea (Diptera, Empidoidea, Hybotidae, Oedaleinae) from China with a key to south eastern Asian species
FIGURES 8–10. Oedalea wenliangi sp. nov. (male). 8. Adult habitus, lateral view; 9. Head, lateral view; 10. Wing.
FIGURES 22–24 in Four new species of Oedalea (Diptera, Empidoidea, Hybotidae, Oedaleinae) from China with a key to south eastern Asian species
FIGURES 22–24. Oedalea yangi sp. nov. (male). 22. Adult habitus, lateral view; 23. Head, lateral view; 24. Wing.
Original data of diatom communities in two alpine lakes of eastern China
<p>This study explored ecological responses of Erye and Sanye lakes to climate change and atmospheric deposition based on multi-proxy sedimentary records in the Taibai Mountain (eastern China). Diatom communities of the two study lakes shifted from large-sized benthic taxa to small fragilariod species after the mid-20th century, synchronous with an increase in diatom production and a decrease in mean length of diatom valves. Changes in diatom communities were significantly correlated with nitrogen deposition in both lakes and climate warming in the upstream lake. </p>
On following pages: 507. Cansdale's Swamp Rat (Malacomys cansdalel); 508. Edwards's Swamp Rat (Malacomys edwards); 509. Alpine Field Mouse (Apodemus alpicola), 510. Long-tailed Field Mouse (Apodemus sylvaticus); 511. Striped Field Mouse (Apodemus agrarius); 512. Western Broad-toothed Field Mouse (Apodemus epimelas); 513. Hyrcanian Field Mouse (Apodemus hyrcanicus); 514. Caucasus Field Mouse (Apodemus ponticus); 515. Herb Field Mouse (Apodemus uralensis); 516. Yellow-necked Field Mouse (Apodemus flavicollis); 517. Eastern Broad-toothed Field Mouse (Apodemus mystacinus), 518. Steppe Field Mouse (Apodemus witherbyi); 519. Nepalese Field Mouse (Apodemus gurkha); 520. Himalayan Field Mouse (Apodemus pallipes); 521. Kashmir Field Mouse (Apodemus rusiges); 522. Chevrier's Field Mouse (Apodemus chevrieri); 523. South China Field Mouse (Apodemus draco); 524. Large-eared Field Mouse (Apodemus latronum); 525. Taiwan Field Mouse (Apodemus semotus); 526. Korean Field Mouse (Apodemus peninsulae); 527. Small Japanese Field Mouse (Apodemus argenteus); 528. Large Japanese Field Mouse (Apodemus speciosus); 529. Okinawa Island Spiny Rat (Tokudaia muenninki); 530. Amami Spiny Rat (Tokudaiaosimensis); 531. Tokunoshima Spiny Rat (Tokudaia tokunoshimensis). in Muridae
On following pages: 507. Cansdale's Swamp Rat (Malacomys cansdalel); 508. Edwards's Swamp Rat (Malacomys edwards); 509. Alpine Field Mouse (Apodemus alpicola), 510. Long-tailed Field Mouse (Apodemus sylvaticus); 511. Striped Field Mouse (Apodemus agrarius); 512. Western Broad-toothed Field Mouse (Apodemus epimelas); 513. Hyrcanian Field Mouse (Apodemus hyrcanicus); 514. Caucasus Field Mouse (Apodemus ponticus); 515. Herb Field Mouse (Apodemus uralensis); 516. Yellow-necked Field Mouse (Apodemus flavicollis); 517. Eastern Broad-toothed Field Mouse (Apodemus mystacinus), 518. Steppe Field Mouse (Apodemus witherbyi); 519. Nepalese Field Mouse (Apodemus gurkha); 520. Himalayan Field Mouse (Apodemus pallipes); 521. Kashmir Field Mouse (Apodemus rusiges); 522. Chevrier's Field Mouse (Apodemus chevrieri); 523. South China Field Mouse (Apodemus draco); 524. Large-eared Field Mouse (Apodemus latronum); 525. Taiwan Field Mouse (Apodemus semotus); 526. Korean Field Mouse (Apodemus peninsulae); 527. Small Japanese Field Mouse (Apodemus argenteus); 528. Large Japanese Field Mouse (Apodemus speciosus); 529. Okinawa Island Spiny Rat (Tokudaia muenninki); 530. Amami Spiny Rat (Tokudaiaosimensis); 531. Tokunoshima Spiny Rat (Tokudaia tokunoshimensis).
FIGURE 4 in Jianghuaimon dabiense gen. nov. et sp. nov (Crustacea: Decapoda: Potamidae), a new genus and new species of freshwater crab from eastern-central China
FIGURE 4. Bayesian inference (BI) tree based on the 16SrDNA gene. Support values represented at nodes. Only values ≥ 60% and ≥ 50% are shown for BI and MP, respectively (- not supported).
FIGURE 5 in Jianghuaimon dabiense gen. nov. et sp. nov (Crustacea: Decapoda: Potamidae), a new genus and new species of freshwater crab from eastern-central China
FIGURE 5. Jianghuaimon dabienese gen. nov. et sp. nov. (A) general habitat; (B) on land under and among rocks (circled in red); (C) burrow in mountain seepage (circled in red); (D) color in life.
FIGURE 3 in Jianghuaimon dabiense gen. nov. et sp. nov (Crustacea: Decapoda: Potamidae), a new genus and new species of freshwater crab from eastern-central China
FIGURE 3. Jianghuaimon dabienese gen. nov. et sp. nov. (A–C, F–G, H–I) male holotype (20.4 × 15.7 mm), SYSBM002003; (D) male paratype (16.9 × 12.9 mm), NNU 20105JD1; (E) male paratype (17.5 × 13.2 mm), SYSBM002008; (A) right third maxilliped; (B) left G2, ventral view; (C–E) left G1s, ventral view; (F) major chela (right); (G) minor chela (left); (H) left G1 terminal segment, dorsal view; (I) left G1 terminal segment, ventral view. Scale bars: A–G = 2.0 mm; H–I = 1.0 mm.
FIGURE 2 in Jianghuaimon dabiense gen. nov. et sp. nov (Crustacea: Decapoda: Potamidae), a new genus and new species of freshwater crab from eastern-central China
FIGURE 2. Jianghuaimon dabiense gen. nov. et sp. nov. (A–D) male holotype (20.4 × 15.7 mm), SYSBM002003; (E–F) female paratype (16.4 × 13.0 mm), SYSBM002007; (A) Cephalothorax, anterior view; (B) anterior thoracic sternum; (C) anterior thoracic sternum and pleon, ventral view; (D) sterno-pleonal cavity with G1 in situ, ventral view. Female paratype (mm): (E) pleon, ventral view; (F) vulvae, ventral view.
FIGURE 1 in Jianghuaimon dabiense gen. nov. et sp. nov (Crustacea: Decapoda: Potamidae), a new genus and new species of freshwater crab from eastern-central China
FIGURE 1. Jianghuaimon dabiense gen. nov. et sp. nov., dorsal habitus. (A) male holotype SYSBM002003; (B) female paratype SYSBM002007.
Data from : Soil pH determines bacterial distribution and assembly processes in natural mountain forests of eastern China
<p><b>Aim: </b>There have been numerous studies of forest-soil microbial biogeography, but an integrated view of edaphic factors, plant, climatic factors, and geographic distance in determining the variation of bacterial community and assembly processes remains unclear at large spatial scales. Here, we analyzed the factors affecting the biogeographic pattern and assembly processes of soil bacterial communities under 58 tree species in five natural mountain forests.</p> <p><b>Location: </b>Eastern China.</p> <p><b>Major taxa studied: </b>Bacterial communities.</p> <p><b>Methods: </b>Hierarchical partitioning analysis and distance decay models were performed to evaluate the relative contributions of plant phylogeny, environmental, and spatial variables to the composition of bacterial communities. We applied the Nearest Taxon Index (NTI), β-Nearest Taxon Index (βNTI), and the modified Raup-Crick metric to reveal the mechanisms of bacterial assembly processes.</p> <p><b>Results: </b>We found that plant phylogeny accounted for a significant, but minor, fraction (0.7%) of the variation in composition of bacterial communities. In contrast, soil pH was the primary determinant of bacterial diversity and community composition, independently explaining 68.6% and 69.9% of the variation, respectively. Based on the NTI analysis, bacterial community assembly was more phylogenetically clustered with increasing soil pH. Variable selection was the predominant process explaining bacterial community assembly when differences in soil pH were ≥ 0.83, whereas homogenizing dispersal dominated when differences in soil pH were < 0.83. However, there was no significant relationship between plant phylogenetic distance and βNTI.</p> <p><b>Main conclusions: </b>Our findings provide strong evidence that soil pH predominantly determines bacterial distribution and mediates the relative impact of stochasticity and determinism in soil bacterial community assembly. This suggests that climate-change associated forest soil acidification could have a dramatic impact on soil bacterial diversity, composition, and function.</p>
FIGURE 16 in Diversity of cave-dwelling pseudoscorpions from eastern Yunnan in China, with the description of eleven new species of the genus Lagynochthonius (Pseudoscorpiones, Chthoniidae)
FIGURE 16. Lagynochthonius minimus sp. nov., A. Holotype male, habitus (dorsal view); B. Paratype female, habitus (dorsal view).
FIGURE 44 in Diversity of cave-dwelling pseudoscorpions from eastern Yunnan in China, with the description of eleven new species of the genus Lagynochthonius (Pseudoscorpiones, Chthoniidae)
FIGURE 44. Lagynochthonius yaowangguensis sp. nov., holotype male (A–D), paratype female (E): A. Left chela (lateral view); B. Carapace (dorsal view); C. Left chelicera (dorsal view); D. Male genital area (ventral view); E. Female genital area (ventral view).
FIGURE 46 in Diversity of cave-dwelling pseudoscorpions from eastern Yunnan in China, with the description of eleven new species of the genus Lagynochthonius (Pseudoscorpiones, Chthoniidae)
FIGURE 46. Comparison of the chela of some cave-dwelling species of Lagynochthonius and Tyrannochthonius from Yunnan (black dotted bordered rectangles refer to the narrowed chelal hands and the sclerotized apodeme of movable chelal fingers). A. Left chela of L. crassus sp. nov. (lateral view); B. Left chela of L. fengi sp. nov. (lateral view); C. Left chela of L. magnidentatus sp. nov. (lateral view); D. Left chela of L. minimus sp. nov. (lateral view); E. Left chela of L. retrorsus sp. nov. (lateral view); F. Left chela of L. serratus sp. nov. (lateral view); G. Left chela of L. spinulentus sp. nov. (lateral view); H. Left chela of L. xiaolinensis sp. nov. (lateral view); I. Left chela of L. xibaiensis sp. nov. (lateral view); J. Left chela of L. xinjiaoensis sp. nov. (lateral view); K. Left chela of L. yaowangguensis sp. nov. (lateral view); L. A modified accessory tooth (td) present on dorso-antiaxial face of fixed chelal finger of L. yaowangguensis sp. nov. (red arrow, dorsal view); M–N. Left chela of Tyrannochthonius sp. nov. (lateral view). Scale bars: 0.25 mm (A–C, E–K, M–N); 0.10 mm (D, L).
FIGURE 43 in Diversity of cave-dwelling pseudoscorpions from eastern Yunnan in China, with the description of eleven new species of the genus Lagynochthonius (Pseudoscorpiones, Chthoniidae)
FIGURE 43. Lagynochthonius yaowangguensis sp. nov., A. Holotype male, habitus (dorsal view); B. Paratype female, habitus (dorsal view).
FIGURE 45 in Diversity of cave-dwelling pseudoscorpions from eastern Yunnan in China, with the description of eleven new species of the genus Lagynochthonius (Pseudoscorpiones, Chthoniidae)
FIGURE 45. Lagynochthonius yaowangguensis sp. nov., holotype male: A. Carapace (dorsal view), with a detail of anterior margin; B. Left chelicera (dorsal view), with details of teeth; C. Coxal spines on coxae II (ventral view); D. Rallum; E. Left pedipalp (minus chela, dorsal view); F. Left chela (lateral view), with details of teeth and with trichobothrial pattern, finger tips and modified tooth (abbreviations explained in Materials and methods); G. Left chela (dorsal view), with details of chemosensory setae and modified tooth; H. Leg I (lateral view); I. Leg IV (lateral view). Scale bars: 0.25 mm (A–B, E–I); 0.10 mm (C–D).
FIGURE 42. Unnamed Cave 4 in Diversity of cave-dwelling pseudoscorpions from eastern Yunnan in China, with the description of eleven new species of the genus Lagynochthonius (Pseudoscorpiones, Chthoniidae)
FIGURE 42. Unnamed Cave 4, type locality of Lagynochthonius yaowangguensis sp. nov., A. Entrance; B. Inside the cave entrance; C–D. Peculiar landscapes inside the cave; E. Area where L. yaowangguensis sp. nov. specimens were collected; F–G. Live individuals of L. yaowangguensis sp. nov. (F: male, G: female) in their natural environment.
FIGURE 40 in Diversity of cave-dwelling pseudoscorpions from eastern Yunnan in China, with the description of eleven new species of the genus Lagynochthonius (Pseudoscorpiones, Chthoniidae)
FIGURE 40. Lagynochthonius xinjiaoensis sp. nov., holotype male (A–D): A. Left chela (lateral view); B. Carapace (dorsal view); C. Left chelicera (dorsal view); D. Male genital area (ventral view).
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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.