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Figure 4 from: Likhitrakarn N, Golovatch SI, Jeratthitikul E, Srisonchai R, Sutcharit C, Panha S (2020) A remarkable new species of the millipede genus Trachyjulus Peters, 1864 (Diplopoda, Spirostreptida, Cambalopsidae) from Thailand, based both on morphological and molecular evidence. ZooKeys 925: 55-72. https://doi.org/10.3897/zookeys.925.49953
Figure 4 Trachyjulus magnus sp. nov., ♂ holotype. A Antenna, lateral view B gnathochilarium, ventral view C, D legs 1, caudal and frontal view, respectively E, F legs 2, caudal and frontal view, respectively G midbody leg, frontal view H legs 3, frontal view I, J anterior gonopods, frontal and caudal views, respectively K, L posterior gonopods, frontal and caudal views, respectively. Scale bars: 0.2 mm.
Figure 3 from: Likhitrakarn N, Golovatch SI, Jeratthitikul E, Srisonchai R, Sutcharit C, Panha S (2020) A remarkable new species of the millipede genus Trachyjulus Peters, 1864 (Diplopoda, Spirostreptida, Cambalopsidae) from Thailand, based both on morphological and molecular evidence. ZooKeys 925: 55-72. https://doi.org/10.3897/zookeys.925.49953
Figure 3 Trachyjulus magnus sp. nov., ♂ paratype. A, B Legs 1, frontal and caudal views, respectively C legs 2, caudal view D penes, caudal view E legs 3, frontal view F, G anterior gonopods, caudal and frontal views, respectively H telopodite tips of anterior gonopods I, J posterior gonopods, caudal and frontal views, respectively K, L telopodite tips of anterior gonopods, caudal and frontal views, respectively.
Figure 1 from: Likhitrakarn N, Golovatch SI, Jeratthitikul E, Srisonchai R, Sutcharit C, Panha S (2020) A remarkable new species of the millipede genus Trachyjulus Peters, 1864 (Diplopoda, Spirostreptida, Cambalopsidae) from Thailand, based both on morphological and molecular evidence. ZooKeys 925: 55-72. https://doi.org/10.3897/zookeys.925.49953
Figure 1 Trachyjulus magnus sp. nov., habitus, live coloration. A ♂ holotype B paratypes. Scale bars: 1 cm.
Figure 2 from: Likhitrakarn N, Golovatch SI, Jeratthitikul E, Srisonchai R, Sutcharit C, Panha S (2020) A remarkable new species of the millipede genus Trachyjulus Peters, 1864 (Diplopoda, Spirostreptida, Cambalopsidae) from Thailand, based both on morphological and molecular evidence. ZooKeys 925: 55-72. https://doi.org/10.3897/zookeys.925.49953
Figure 2 Trachyjulus magnus sp. nov., A–C, I–P ♀ paratype, D–H ♂ paratype. A, B anterior part of body, lateral and dorsal views, respectively C collum, dorsal view D cephalic capsule, dorsal view E gnathochilarium, ventral view F antenna, lateral view G tip of antenna H bacilliform sensilla on antennomere 5, lateral view I cross-section of midbody ring J midbody rings, ventral view K claw of midbody leg L enlarged ozopore region, lateral view M midbody prozona, dorsal view N–P posterior part of body, lateral, dorsal and ventral views, respectively.
Supplementary material 2 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426
Figure S1–S7, Tables S2–S6. Partial morphological and molecular results
Figure 6 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426
Figure 6 Principal component analysis of dorsal view (a), ventral view (b), lateral view (c) of skull, and lateral view of the mandible (d) of the three clades.
Figure 1 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426
Figure 1 Distribution of phylogenetic clades of N. confucianus species complex obtained from Cytb. The numbers correspond to the locality code in Suppl. material 1, Table S1.
Figure 7 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426
Figure 7 Thin plate splines of dorsal view (a), ventral view (b), lateral view (c) of skull, and lateral view of the mandible (d) of N. sacer, N. confucianus, and N. lotipes.
Figure 5 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426
Figure 5 Principal component analysis and discriminant analysis of external and skull morphological indices. Principal component plots of external and skull indices are shown in a and b. Discriminant function plots of external and skull indices are shown in c and d, respectively.
Supplementary material 1 from: Li Y, Li Y, Li H, Wang J, Rong X, Li Y (2020) Niviventer confucianus sacer (Rodentia, Muridae) is a distinct species based on molecular, karyotyping, and morphological evidence. ZooKeys 959: 137-159. https://doi.org/10.3897/zookeys.959.53426
Tables S1. Sampling and Genbank sequences information
Figure 1 from: Chen W-H, Wen F, Ren M-X, Yang L, Hong X, Qiu Z-J, Shui Y-M (2020) Gesneriaceae in China and Vietnam: Perfection of taxonomy based on comprehensive morphological and molecular evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 1-5. https://doi.org/10.3897/phytokeys.157.56842
Figure 1 Flowers of some species of Gesneriaceae in China and Vietnam ABournea sinensis Oliv. (photographed by Yu-Min Shui) BOreocharis guileana (B.L. Burtt) Li H. Yang & F. Wen, comb. nov. (by Li-Hua Yang) COreocharis baolianis (Q.W. Lin) Li H. Yang & M. Kang, comb. nov. (by Li-Hua Yang) DOreocharis jasminina S.J.Ling, F.Wen & M.X. Ren, sp. nov. (by Shao-Jun Ling) EOreocharis flavovirens Xin Hong (by Xin Hong) FOreocharis wumengensis Lei Cai & Z.L.Dao, sp. nov. (by Lei Cai) GOreocharis fulva W.H.Chen & Y.M.Shui, sp. nov. (by Yu-Min Shui) HAllocheilos rubroglandulosus W.H. Chen & Y.M. Shui, sp. nov. (by Yu-Min Shui) IPetrocodon rubiginosus Y.G.Wei & R.L.Zhang, sp. nov. (by Fang Wen) JPetrocodon luteoflorus Lei Cai & F. Wen, sp. nov. (by Fang Wen) KDeinostigma fasciculatum W.H.Chen & Y.M.Shui, sp. nov. (by Yu-Min Shui) LPrimulina xuansonensis W.H.Chen & Y.M.Shui, sp. nov. (by Yu-Min Shui) MDidymocarpus lobulatus F. Wen, Xin Hong &W.Y. Xie, sp. nov. (by Jia-Jun Zhou) NParaboea myriantha Y.M. Shui & W.H. Chen, sp. nov. (by Yu-Min Shui) OParaboea sinensis var. glabrissima W.H.Chen & Y.M.Shui, var. nov. (by Yu-Min Shui) PPetrocosmea nanchuanensis Z.Y. Liu, Z.Y. Li & Z.J. Qiu, sp. nov. (by Zhi-Jing Qiu).
Supplementary material 4 from: Chen W-H, Zhang Y-M, Guo S-W, Zhang Z-R, Chen L, Shui Y-M (2020) Reassessment of Bournea Oliver (Gesneriaceae) based on molecular and palynological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 27-41. https://doi.org/10.3897/phytokeys.157.55254
Supporting materials
Supplementary material 2 from: Chen W-H, Zhang Y-M, Guo S-W, Zhang Z-R, Chen L, Shui Y-M (2020) Reassessment of Bournea Oliver (Gesneriaceae) based on molecular and palynological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 27-41. https://doi.org/10.3897/phytokeys.157.55254
Figure S1
Figure 4 from: Chen W-H, Zhang Y-M, Guo S-W, Zhang Z-R, Chen L, Shui Y-M (2020) Reassessment of Bournea Oliver (Gesneriaceae) based on molecular and palynological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 27-41. https://doi.org/10.3897/phytokeys.157.55254
Figure 4 The morphology of pollen grains of Bournea sinensis Oliv. (A–D) and B. leiophylla (W. T. Wang) W. T. Wang (E–H) by SEM. A polar view showing pollen grain with three equatorial, colporus apertures B equatorial view showing single free, prolate pollen grain C equatorial view show apertures and granular aperture membrane D detail showing verrucate tectum with granular E polar view showing pollen grain with three equatorial, colporus apertures F equatorial view showing single free, oblate pollen grain G equatorial view show apertures and granular aperture membrane H detail showing verrucate tectum with granular.
Figure 3 from: Chen W-H, Zhang Y-M, Guo S-W, Zhang Z-R, Chen L, Shui Y-M (2020) Reassessment of Bournea Oliver (Gesneriaceae) based on molecular and palynological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 27-41. https://doi.org/10.3897/phytokeys.157.55254
Figure 3 The Bayes inference (BI) and Maximum likelihood (ML) tree inferred from six cp DNA markers (atpB-rbcL, ndhH-rps15-ycf1, rpl132, trnC-trnD, trnL-F, trnT-trnL) and ITS of the expanded genus Oreocharis s.l. in Gesneriaceae. Note 1) the red clade indicates the position of Bournea in phylogenetic trees; 2) the number of the node respectively indicates posterior probability values in BI and bootstrap values in ML, ※ indicates < 50%.
Figure 1 from: Chen W-H, Zhang Y-M, Guo S-W, Zhang Z-R, Chen L, Shui Y-M (2020) Reassessment of Bournea Oliver (Gesneriaceae) based on molecular and palynological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 27-41. https://doi.org/10.3897/phytokeys.157.55254
Figure 1 The morphology of Bournea sinensis Oliv. (A–E) and B. leiophylla (W. T. Wang) W. T. Wang (F–J). A plant B inflorescence C calyx and disc D stigma E front view of corolla showing the anthers and the style and stamens F plant G inflorescence H pistil and disc I stigma J front view of corolla showing the anthers.
Supplementary material 3 from: Chen W-H, Zhang Y-M, Guo S-W, Zhang Z-R, Chen L, Shui Y-M (2020) Reassessment of Bournea Oliver (Gesneriaceae) based on molecular and palynological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 27-41. https://doi.org/10.3897/phytokeys.157.55254
Figure S2
Supplementary material 1 from: Chen W-H, Zhang Y-M, Guo S-W, Zhang Z-R, Chen L, Shui Y-M (2020) Reassessment of Bournea Oliver (Gesneriaceae) based on molecular and palynological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 27-41. https://doi.org/10.3897/phytokeys.157.55254
Tables S1, S2
Figure 2 from: Chen W-H, Zhang Y-M, Guo S-W, Zhang Z-R, Chen L, Shui Y-M (2020) Reassessment of Bournea Oliver (Gesneriaceae) based on molecular and palynological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 27-41. https://doi.org/10.3897/phytokeys.157.55254
Figure 2 The Bayes inference (BI) and Maximum likelihood (ML) tree inferred from six cp DNA markers (atpB-rbcL, ndhH-rps15-ycf1, rpl132, trnC-trnD, trnL-F, trnT-trnL) of the expanded genus Oreocharis s.l. in Gesneriaceae. Note 1) the red clade indicates the position of Bournea in phylogenetic trees; 2) the number of the node respectively indicates posterior probability values in BI and bootstrap values in ML, ※ indicates < 50%.
Figure 3 from: Tan K, Lu T, Ren M-X (2020) Gesneriaceae in China and Vietnam: Perfection of taxonomy based on comprehensive morphological and molecular evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 7-26. https://doi.org/10.3897/phytokeys.157.34032
Figure 3 Species distributions pattern of the Asian Gesneriaceae. Black circles indicate diversification centers with highest species richness and the red grids are the evolutionary hotspots (at least 25% species are neoendemics). The species distribution information is obtained from http://www.gbif.org. The map was drawn using DIVA-GIS7.5.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.