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Supplementary material 2 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Appendix S2
Supplementary material 1 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Appendix S1
Supplementary material 4 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 1
Figure 3 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 3 The comparisons of dorsal head (row 1) and median dorsal (row 2) between Pareas macularius and P. margaritophorus. AP. margaritophorusBP. macularius.
Figure 2 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 2 Bayesian inference(left) and Maximum Likelihood(right) trees of the Pareidae based on mtDNA dataset. Branch support measures are Bayesian posterior probabilities and ML bootstrap support respectively. Branch support indices are not given for most intrageneric nodes to preserve clarity.
Supplementary material 3 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Appendix S3
Figure 1 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 1 Bayesian inference tree of the Pareidae based on nDNA dataset. Branch support measures are Bayesian posterior probabilities/ML bootstrap support (only where >50%). Branch support indices are not given for most intrageneric nodes to preserve clarity.
Figure 4 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 4 Holotype of Pareas menglaensis sp. nov. (YBU 14124). General view(A); dorsal (B), ventral (C), lateral (D) and frontal (E) views of the head; dorsal (F) and ventral (G) views of the median body.
Figure 5 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 5 Holotype of Pareas mengziensis sp. nov. (YBU 14252). Dorsal (A) and ventral (B) of general views; dorsal (C), ventral (D), and lateral (E) views of the head.
Figure 2 in Molecular evidence on evolutionary switching from particle-feeding to sophisticated carnivory in the calanoid copepod family Heterorhabdidae: drastic and rapid changes in functions of homologues
Figure 2. Phylogenetic tree based on the 18S + 28S rRNA genes of heterorhabdids. The numbers on branches indicate bootstrap values (maximum likelihood, ML) and posterior probability (Bayesian inference, BI). Two metridinids (Metridia effusa and Pleuromamma abdominalis) were chosen as the outgroup taxa. The star (Node ★) indicates the innovation of a poison-injection system.
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.
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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.