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Figure 1 in The second Mecistocephalus centipede without a spiculum: Mecistocephalus aspiculus sp. n. from south China (Chilopoda: Geophilomorpha: Mecistocephalidae)
Figure 1. Mecistocephalus aspiculus sp. n. (CMMI-20201217113): a, forcipular segment and anterior leg-bearing segments, dorsal; b, median part of body, dorsal; c, posterior part of body, dorsal. Scale bar: 1 mm.
Database of upper ocean mixing enhanced by tropical cyclones in the northern South China Sea in 2023
<p>Data reported in the manuscript "Identification and quantification of upper ocean mixing enhanced by tropical cyclones in the northern South China Sea" can be downloaded here.</p> <p>Matlab (versions later than 9.12.0.1884302 (R2022a)) is necessary to run the postprocessing codes.</p>
Table 1. Main differential characters between M in The second Mecistocephalus centipede without a spiculum: Mecistocephalus aspiculus sp. n. from south China (Chilopoda: Geophilomorpha: Mecistocephalidae)
<p><b>Table 1.</b> Main differential characters between <i>M. aspiculus</i> Jiang and You, <b>sp. n.</b> and <i>M. yanagiharai</i> Takakuwa, 1936. Character states of <i>M. yanagiharai</i> are based on the description and reference pictures published by Uliana <i>et al.</i> (2007) and Takakuwa (1936a).</p><table><tbody><tr><th></th><th><i>Mecistocephalus yanagiharai</i></th><th><i>Mecistocephalus aspiculus</i></th></tr></tbody><tbody><tr><th>Species</th><td>Takakuwa, 1936</td><td>Jiang and You, <b>sp. n.</b></td></tr><tr><th>Clypeus: width/length</th><td>1.2</td><td>1.6</td></tr><tr><th>Clypeus: areolate part length/non-</th><td>1.45</td><td>0.45</td></tr><tr><th>areolate (plagulae) part length</th><td></td><td></td></tr><tr><th>Sensilla of clypeal plagulae</th><td>Absent</td><td>Present</td></tr><tr><th>Labral mid-piece: shape of posterior</th><td>Sub-fusiform</td><td>Inverted triangular</td></tr><tr><th>margin</th><td></td><td></td></tr><tr><th>Labral side-piece: shape of anterior</th><td>Almost straight, with external margins</td><td>Sinuous, with external margins</td></tr><tr><th>margin</th><td>slightly convergent backwards</td><td>evidently convergent forwards</td></tr><tr><th>Labral side-piece: shape of posterior</th><td>Straight</td><td>Convex close to the internal and</td></tr><tr><th>margin</th><td></td><td>external ends</td></tr><tr><th>Additional sclerite on the external of</th><td>Absent</td><td>Present (comma-shaped)</td></tr><tr><th>side-piece</th><td></td><td></td></tr><tr><th>First maxillary coxal projection: shape</th><td>Clavate, sub-triangular</td><td>Sub-trapezoid</td></tr><tr><th>of distal lobe</th><td></td><td></td></tr><tr><th>Article I of second maxillary</th><td>4.5</td><td>4</td></tr><tr><th>telopodite: length/width</th><td></td><td></td></tr></tbody></table>
Paleomagnetic Constraints on the Timing of Alteration Associated with the Emplacement of the Leqingla Pb-Zn Deposit, South Tibet, China
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FIGURE 4. The paratypes SYS a009350 in A new species of the genus Boulenophrys from South China (Anura, Megophryidae)
FIGURE 4. The paratypes SYS a009350 (A–D) and GEP a209 (E–F) of Boulenophrys pepe sp. nov. in life: A. dorsal view; B. dorsolateral view; C. ventral view; D. lateral view of head, with an arrow showing swollen lips and protrude jaws; E. dorsolateral view; F. ventral view.
FIGURE 3 in A new species of the genus Boulenophrys from South China (Anura, Megophryidae)
FIGURE 3. The holotype (GEP a207) of Boulenophrys pepe sp. nov. in life: A. dorsal view; B. dorsolateral view; C. ventral view; D. ventral view of head, arrows showing swollen lips and protrude jaws; E. ventral view of hand; F. ventral view of foot.
FIGURE 2 in A new species of the genus Boulenophrys from South China (Anura, Megophryidae)
FIGURE 2. ML tree based on the partial DNA sequences of the mitochondrial 16S and COI genes, with Bootstrap Support (BS) and Posterior Probabilities (BPP) at nodes.
FIGURE 1 in A new species of the genus Boulenophrys from South China (Anura, Megophryidae)
FIGURE 1. Map showing the distribution sites of Boulenophrys pepe sp. nov. and its phylogenetic close species, B. obesa and B. ombrophila.
TABLE 1 in A new species of the genus Boulenophrys from South China (Anura, Megophryidae)
<p><b>TABLE 1.</b> Literature for morphological characters of 67 recognized species of <i>Boulenophrys</i>.</p><table><tbody><tr><th><b>ID</b></th><th><i>Boulenophrys species</i></th><th><b>References</b></th></tr></tbody><tbody><tr><th>1</th><td><i>B. acuta</i> (Wang, Li and Jin, 2014)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>2</th><td><i>B. angka</i> (Wu, Suwannapoom, Poyarkov, Pawangkhanant, Xu, Jin, Murphy and Che, 2019)</td><td>Wu <i>et al</i>. 2019</td></tr><tr><th>3</th><td><i>B. anlongensis</i> (Li, Lu, Liu and Wang, 2020)</td><td>Li <i>et al</i>. 2020; Lyu <i>et al.</i> 2023</td></tr><tr><th>4</th><td><i>B. baishanzuensis</i> (Wu, Li, Liu, Wang and Wu, 2020)</td><td>Wu <i>et al</i>. 2020</td></tr><tr><th>5</th><td><i>B. baolongensis</i> (Ye, Fei and Xie, 2007)</td><td>Ye <i>et al</i>. 2007; Fei and Ye 2016</td></tr><tr><th>6</th><td><i>B. binchuanensis</i> (Ye and Fei, 1995)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>7</th><td><i>B. binlingensis</i> (Jiang, Fei and Ye, 2009)</td><td>Fei <i>et al.</i> 2009; Lyu <i>et al.</i> 2023</td></tr><tr><th>8</th><td><i>B. boettgeri</i> (Boulenger, 1899)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>9</th><td><i>B. brachykolos</i> (Inger and Romer, 1961)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>10</th><td><i>B. caobangensis</i> (Nguyen, Pham, Nguyen, Luong and Ziegler, 2020)</td><td>Nguyen <i>et al</i>. 2020</td></tr><tr><th>11</th><td><i>B. caudoprocta</i> (Shen, 1994)</td><td>Shen 1994; Lyu <i>et al.</i> 2023</td></tr><tr><th>12</th><td><i>B. congjiangensis</i> (Luo, Wang, Wang, Lu, Wang, Deng and Zhou, 2021)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>13</th><td><i>B. cheni</i> (Wang and Liu, 2014)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>14</th><td><i>B. chishuiensis</i> (Xu, Li, Liu, Wei and Wang, 2020)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>15</th><td><i>B. daiyunensis</i> (Lyu, Wang and Wang, 2021)</td><td>Lyu <i>et al</i>. 2023</td></tr><tr><th>16</th><td><i>B. daoji</i> (Lyu, Zeng, Wang and Wang, 2021)</td><td>Lyu <i>et al</i>. 2023</td></tr><tr><th>17</th><td><i>B. daweimontis</i> (Rao and Yang, 1997)</td><td>Rao and Yang 1997</td></tr><tr><th>18</th><td><i>B. dongguanensis</i> (Wang and Wang, 2019)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>19</th><td><i>B. elongata</i> Zeng, Wang, Chen, Xiao, Zhan, Li and Lin, 2024</td><td>Zeng <i>et al.</i> 2024</td></tr><tr><th>20</th><td><i>B. fengshunensis</i> Wang, Zeng, Lyu and Wang, 2022</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>21</th><td><i>B. fanjingmontis</i> (Zhang, Liang, Ran and Shen, 2012)</td><td>Lyu <i>et al</i>. 2023</td></tr><tr><th>22</th><td><i>B. fansipanensis</i> (Tapley, Cutajar, Mahony, Nguyen, Dau, Luong, Le, Nguyen, Nguyen, Portway, Luong and Rowley, 2018)</td><td>Tapley <i>et al</i>. 2018a</td></tr><tr><th>23</th><td><i>B. frigida</i> (Tapley, Cutaja, Nguyen, Portway, Mahony, Nguyen, Harding, Luong and Rowley, 2021)</td><td>Tapley <i>et al</i>. 2021</td></tr><tr><th>24</th><td><i>B. hoanglienensis</i> (Tapley, Cutajar, Mahony, Nguyen, Dau, Luong, Le, Nguyen, Nguyen, Portway, Luong and Rowley, 2018)</td><td>Tapley <i>et al</i>. 2018a</td></tr><tr><th>25</th><td><i>B. hungtai</i> Wang, Zeng, Lyu, Xiao and Wang, 2022</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>26</th><td><i>B. hengshanensis</i> Qian, Hu, Mo, Gao, Zhang and Yang, 2023</td><td>Qian <i>et al.</i> 2023</td></tr><tr><th>27</th><td><i>B. insularis</i> (Wang, Liu, Lyu, Zeng and Wang, 2017)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>28</th><td><i>B. jiangi</i> (Liu, Li, Wei, Xu, Cheng, Wang and Wu, 2020)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>29</th><td><i>B. jingdongensis</i> (Fei and Ye, 1983)</td><td>Lyu <i>et al</i>. 2023</td></tr><tr><th>30</th><td><i>B. jinggangensis</i> (Wang, 2012)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>31</th><td><i>B. jiulianensis</i> (Wang, Zeng, Lyu and Wang, 2019)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>32</th><td><i>B. kuatunensis</i> (Pope, 1929)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>33</th><td><i>B. leishanensis</i> (Li, Xu, Liu, Jiang, Wei and Wang, 2018)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>34</th><td><i>B. lushuiensis</i> (Shi, Li, Zhu, Jiang, Jiang and Wang, 2021)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>35</th><td><i>B. liboensis</i> (Zhang, Li, Xiao, Li, Pan, Wang, Zhang and Zhou, 2017)</td><td>Zhang <i>et al</i>. 2017</td></tr><tr><th>36</th><td><i>B. lini</i> (Wang and Yang, 2014)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>37</th><td><i>B. lishuiensis</i> (Wang, Liu and Jiang, 2017)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>38</th><td><i>B. minor</i> (Stejneger, 1926)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>39</th><td><i>B. mirabilis</i> (Lyu, Wang and Zhao, 2020)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>40</th><td><i>B. mufumontana</i> (Wang, Lyu and Wang, 2019)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>41</th><td><i>B. nankunensis</i> (Wang, Zeng and Wang, 2019)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>42</th><td><i>B. nanlingensis</i> (Lyu, Wang, Liu and Wang, 2019)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>43</th><td><i>B. obesa</i> (Wang, Li and Zhao, 2014)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>44</th><td><i>B. ombrophila</i> (Messenger and Dahn, 2019)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>45</th><td><i>B. omeimontis</i> (Liu, 1950)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>46</th><td><i>B. palpebralespinosa</i> (Bourret, 1937)</td><td>Fei <i>et al.</i> 2009; Lyu <i>et al.</i> 2023</td></tr><tr><th>47</th><td><i>B. puningensis</i> Wang, Zeng, Lyu, Xiao and Wang, 2022</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>48</th><td><i>B. qianbeinsis</i> (Su, Shi, Wu, Li, Yao, Wang and Li, 2020)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>49</th><td><i>B. rubrimera</i> (Tapley, Cutajar, Mahony, Chung, Dau, Nguyen, Luong and Rowley, 2017)</td><td>Tapley <i>et al</i>. 2017, 2018b</td></tr><tr><th>50</th><td><i>B. sangzhiensis</i> (Jiang, Ye and Fei, 2008)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>51</th><td><i>B. sanmingensis</i> (Lyu and Wang, 2021)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>52</th><td><i>B. shimentaina</i> (Lyu, Liu and Wang, 2020)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>53</th><td><i>B. shuichengensis</i> (Tian and Sun, 1995)</td><td>Tian and Sun 1995; Tian <i>et al</i>. 2000; Fei and Ye 2016</td></tr><tr><th>54</th><td><i>B. shunhuangensis</i> (Wang, Deng, Liu, Wu and Liu, 2019)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>55</th><td><i>B. spinata</i> (Liu and Hu, 1973)</td><td>Hu <i>et al.</i> 1973; Lyu <i>et al.</i> 2023</td></tr><tr><th>56</th><td><i>B. tongboensis</i> (Wang and Lyu, 2021)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>57</th><td><i>B. tuberogranulatus</i> (Shen, Mo and Li, 2010)</td><td>Mo <i>et al</i>. 2010; Fei and Ye 2016; Lyu <i>et al.</i> 2023</td></tr><tr><th>58</th><td><i>B. wugongensis</i> (Wang, Lyu and Wang, 2019)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>59</th><td><i>B. wuliangshanensis</i> (Ye and Fei, 1995)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>60</th><td><i>B. wushanensis</i> (Ye and Fei, 1995)</td><td>Ye and Fei 1995; Fei and Ye 2016; Lyu <i>et al.</i> 2023</td></tr><tr><th>61</th><td><i>B. xiangnanensis</i> (Lyu, Zeng and Wang, 2020)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>62</th><td><i>B. xianjuensis</i> (Wang, Wu, Peng, Shi, Lu and Wu, 2020)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>63</th><td><i>B. xuefengmontis</i> Lyu and Wang, 2023</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>64</th><td><i>B. yangmingensis</i> (Lyu, Zeng and Wang, 2020)</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>65</th><td><i>B. yaoshanensis</i> Qi, Mo, Lyu, Wang and Wang, 2021</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>66</th><td><i>B. yingdeensis</i> Qi, Lyu, Wang and Wang, 2021</td><td>Lyu <i>et al.</i> 2023</td></tr><tr><th>67</th><td><i>B. yunkaiensis</i> Qi, Wang, Lyu and Wang, 2021</td><td>Lyu <i>et al.</i> 2023</td></tr></tbody></table><p>......continued on the next page</p><p>......continued on the next page</p>
Long-term Changes in Salinity in the South China Sea due to Anthropogenic Forcing
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The history of the El Niño‒Southern Oscillation and sea surface salinity during 1376‒1500 CE reconstructed by Porites coral δ18O from Huangyan Island, South China Sea
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The origin of late Cenozoic magmatism in the South China Sea and Southeast Asia
<p>Table S1 Chemical and isotopic compositions for South China Sea seamount lava and standard sample</p> <p>Table S2 Major and trace element contents and He isotope compositions for South China Sea seamount glass</p> <p>Table S3 Major element compositions of melt inclusion in olivine from South China Sea seamount lavas</p> <p>Table S4 Major and trace element compositions of olivines analyzed by EPMA (wt. %) and LA-ICP-MS (ppm)</p> <p>Table S5 Chemical compositions of spinel inclusions and their host olivines analyzed and calculated Al-in-ol-sp temperatures and log(fO2) FMQ.</p> <p>Table S6 U-Th-Pb isotopic ratios and ages of zircons</p> <p>Table S7 Compositions of International standards</p>
Data for: "Possible link between decadal variability in precipitation in the South China Sea and the North Atlantic Oscillation during the 20th century: A perspective from coral geochemical records"
<p>This dataset includes all the data for the paper "Possible link between decadal variability in precipitation in the South China Sea and the North Atlantic Oscillation during the 20th century: A perspective from coral geochemical records" by Cui et al.</p>
Bulk and amino acid nitrogen specific isotope data from particulate organic matter and mesozooplankton (1000-2000 µm) from the Mekong River plume and southern South China Sea
<p><strong><span><span>The mean trophic position (TP) of mesozooplankton largely determines how much mass and energy is available for higher trophic levels like fish. Unfortunately, the ratio of herbivores to carnivores in mesozooplankton is difficult to identify in field samples. Here we investigated changes in the mean TP of mesozooplankton in a highly dynamic environment encompassing four distinct habitats in </span></span></strong>the southern South China Sea:<strong> </strong><span>the </span>Mekong River plume, coastal upwelling region, shelf waters, and offshore oceanic waters<strong><span>. </span></strong><span>We used a set of parameters derived from bulk and amino acid nitrogen stable isotopes from particulate organic matter (POM) and four mesozooplankton size fractions to identify changes in the nitrogen source and structure of the planktonic food web across these habitats.</span> We found clear indications of a shift in N sources for biological production from nitrate in near-coastal waters towards an increase in diazotroph-N inputs in oceanic waters where diazotrophs shaped the phytoplankton community. The shift in N source was accompanied by a lengthening of the food chain (increase in the TP), which may provide further support for the connection between diazotrophy and the indirect routing of N through the marine food web. Our combined bulk and amino acid δ<sup>15</sup>N approach also allowed us to estimate the trophic enrichment (TE) of mesozooplankton across the entire regional ecosystem. When put in the context of literature values, our high TE of 5.1‰ suggested a link between ecosystem heterogeneity and the less efficient transfer of mass and energy across trophic levels.</p>
The origin of late Cenozoic magmatism in the South China Sea and Southeast Asia
<p><strong>Table S1. Chemical and isotopic compositions for lavas from the South China Sea seamounts</strong></p> <p><strong>Table S2. Major and trace element contents and He isotope compositions for South China Sea seamount glass</strong></p> <p><strong>Table S3 Major element compositions of melt inclusion in olivine from lavas in the South China Sea seamounts</strong></p> <p><strong>Table S4. Major and trace element compositions of olivines analyzed by EPMA (wt. %) and LA-ICP-MS (ppm)</strong></p> <p><strong>Table S5 Chemical compositions of spinel inclusions and their host olivines analyzed and calculated Al-in-ol-sp temperatures and log(fO2) FMQ</strong></p> <p><strong>Table S6: U-Th-Pb isotopic ratios and ages, Hf isotopes of zircons</strong></p> <p><strong>Table S7 Compositions of International standards</strong></p>
FIGURE 1. Ribosomal DNA ITS2 in Molecular confirmation of Anopheles (Anopheles) lesteri from the Republic of South Korea and its genetic identity with An. (Ano.) anthropophagus from China (Diptera: Culicidae)
FIGURE 1. Ribosomal DNA ITS2 sequence for potential malaria vectors belonging to Anopheles (Anopheles) Hyrcanus Group from Korea, China, Japan and the Philippines. See Table 2 and text for sequence summaries and discussion. The following GenBank accession numbers correspond to the label numbers at the 5' end of the sequence: 1) AY375464; 2) AY375465; 3) AJ004942; 4) AY375466; 5) AF384172, AJ004941 and AF543860; 6) AY375467; 7) AY187728; 8) AY375468; 9) AY375469; 10) AY375470; 11) AY375471. The number of individuals sequenced, of those presented here for the first time, appears in parentheses
FIGURES 15–22 in One new species of scorpion belonging to the genus Euscorpiops Vachon, 1980 from South China (Scorpiones: Euscorpiidae, Scorpiopinae)
FIGURES 15–22. Euscorpiops yangi sp. nov. 15–18. Male holotype, 19–22. Female paratype. Chela, 15 and 19. dorsoexternal aspect, 16 and 20. external aspect, 17 and 21. ventral aspect, 18 and 22. internal aspect. Scale = 1mm.
FIGURES 2–14 in One new species of scorpion belonging to the genus Euscorpiops Vachon, 1980 from South China (Scorpiones: Euscorpiidae, Scorpiopinae)
FIGURES 2–14. Euscorpiops yangi sp. nov. 2–8, 14. Male holotype, 9–13. Female paratype. 2. Femur, dorsal aspect. 3–5. Patella (3. external, 4. dorsal and 5. ventral aspect). 6. Genital operculum and pectines, ventral aspect. 7–8. chelicera (7. dorsal, 8. ventral aspect). 9. Femur, dorsal aspect. 10–12. Patella (10. external, 11. dorsal, 12. ventral aspect). 13. Genital operculum and pectines, ventral aspect. 14. Telson, lateral aspect. Scale = 1mm.
FIGURE 1 in The genus Xylaria (Xylariaceae) in the south of China-6. A new Xylaria species based on morphological and molecular characters
FIGURE 1. Xylaria fusispora (from holotype): a. Stromata; b. Stromatal surface; c. Ascospores; d. Asci; e. Ascospore bearing appendage; f. Germ slit; g. Ascus apical ring; h. Ascospore by scanning-electron microscopy; i. Colony on OA after 4 weeks of incubation. Scale bars: a = 5 mm, b = 0.5 mm, c,d = 20 µm, e,f = 5 µm, g,i = 15 µm.
FIGURE 2 in The genus Xylaria (Xylariaceae) in the south of China-6. A new Xylaria species based on morphological and molecular characters
FIGURE 2. Strict consensus tree illustrating the phylogeny of Xylaria fusispora and selected Xylaria species generated by maximumlikelihood, maximum-parsimony and neighbour-joining analyses based on ITS sequences. Hypoxylon fragiforme and Camillea obularia were used as outgroup taxa. Name in bold indicates the new species. The bootstrap values (>50%) of maximum-likelihood, maximum-parsimony and neighbor-joining analyses of 1000 resampled datasets are shown (ML/MP/NJ).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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OpenNeuro
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