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Figs 137-140 in Classification, Natural History, and Evolution of the Subfamily Peloniinae O (Coleoptera: Cleroidea: Cleridae). Part IX. Taxonomic revision of the New World genus Muisca S
Figs 137-140: Habitus. (137) Muisca hexa. (138) M. maculosa. (139) M. anachyma. (140) M. mestolinea.
Figure 1 from: Qiu Z-J, Zhang J, Baskaran X-R, Hu J, Li Z-Y, Liu Z-Y (2020) Petrocosmea nanchuanensis (Gesneriaceae), a new species from Chongqing, China. 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: 137-144. https://doi.org/10.3897/phytokeys.157.33625
Figure 1 Drawing of Petrocosmea nanchuanensis Z.Y. Liu, Z.Y. Li & Z.J. Qiu, sp. nov. A habit B stamens C dissected corolla D calyx and pistil.
Figure 2 from: Qiu Z-J, Zhang J, Baskaran X-R, Hu J, Li Z-Y, Liu Z-Y (2020) Petrocosmea nanchuanensis (Gesneriaceae), a new species from Chongqing, China. 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: 137-144. https://doi.org/10.3897/phytokeys.157.33625
Figure 2 Petrocosmea nanchuanensis Z.Y. Liu, Z.Y. Li & Z.J. Qiu A habitat B flowering plants C flower, front view D flower, side view E flower, front view, showing pistil and anthers F hairs on abaxial leaves G stamens H hairs on the pistil.
Figure 3 from: Qiu Z-J, Zhang J, Baskaran X-R, Hu J, Li Z-Y, Liu Z-Y (2020) Petrocosmea nanchuanensis (Gesneriaceae), a new species from Chongqing, China. 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: 137-144. https://doi.org/10.3897/phytokeys.157.33625
Figure 3 Drawing of the most parsimonious tree generated from six cpDNA and two nrDNA regions (partial & unpublished). Bootstrap values are shown above branches and Bayesian posterior probabilities are indicated below branches.
Figure 1 from: Yao G, Song Z-Q, Xue B-E, Shi S, Li Y-L, Luo S-X (2020) Taxonomic revision of the genus Glochidion (Phyllanthaceae) in Taiwan, China. PhytoKeys 159: 137-159. https://doi.org/10.3897/phytokeys.159.54839
Figure 1 A holotype of Glochidion assamicum var. magnicapsulum Croiatz & Hara (A. Henry 117, A) B holotype of G. kusukusense Hayata (B. Hayata & S. Sasaki s.n., TI) C lectotype of G. lanceolatum Hayata (T. Makino s.n., TI) D holotype of G. chademenosocarpum Hayata (B. Hayata s.n., TI) E isotype of G. rubrum Blume (C.L. von Blume s.n., NY) F isolectotype of G. suishaense Hayata (B. Hayata s.n., TI).
Figure 4 from: Yao G, Song Z-Q, Xue B-E, Shi S, Li Y-L, Luo S-X (2020) Taxonomic revision of the genus Glochidion (Phyllanthaceae) in Taiwan, China. PhytoKeys 159: 137-159. https://doi.org/10.3897/phytokeys.159.54839
Figure 4 Glochidion lanyuense Gang Yao & S.X. Luo, sp. nov. (based on the holotype, drawn by Y.X. Liu) A habit B ovary and style C female flower D male flower.
Figure 3 from: Yao G, Song Z-Q, Xue B-E, Shi S, Li Y-L, Luo S-X (2020) Taxonomic revision of the genus Glochidion (Phyllanthaceae) in Taiwan, China. PhytoKeys 159: 137-159. https://doi.org/10.3897/phytokeys.159.54839
Figure 3 Holotype of Glochidion ovalifolium F.Y. Lu & Y.S. Hsu. (F.Y. Lu & Y.S. Hsu 242, NCAI!).
Figure 5 from: Yao G, Song Z-Q, Xue B-E, Shi S, Li Y-L, Luo S-X (2020) Taxonomic revision of the genus Glochidion (Phyllanthaceae) in Taiwan, China. PhytoKeys 159: 137-159. https://doi.org/10.3897/phytokeys.159.54839
Figure 5 Morphological comparison between Glochidion lanyuense Gang Yao & S.X. Luo and G. lanceolatum Hayata A, C, E, G, I, LG. lanyuenseB, D, F, H, J, K, MG. lanceolatumA, B female flower C, D ovary and style E, F pedicle of female flower G, H general view of style I–K female flowers (shown by arrowheads) L, M fruit. Scar bars: 1 mm (A–H); 3 mm (I–K); 5 mm (L).
Figure 2 from: Yao G, Song Z-Q, Xue B-E, Shi S, Li Y-L, Luo S-X (2020) Taxonomic revision of the genus Glochidion (Phyllanthaceae) in Taiwan, China. PhytoKeys 159: 137-159. https://doi.org/10.3897/phytokeys.159.54839
Figure 2 General morphology of GlochidionA–CG. acuminatum var. acuminatum Müll. Arg D, E, HG. ellipticum Wight F, GG. lanceolatum Hayata I–KG. philippicum (Cav.) C.B. Rob L, PG. puberum (L.) Hutch M–OG. rubrum Blume Q–SG. zeylanicum var. zeylanicum (Gaertn.) A. Juss T–VG. zeylanicum var. tomentosum Trimen A, D, F, I, M, R, T female flowers B, E, J, S, U male flowers C, G, H, K, N–Q, V fruits L female flowers and male flowers N male flowers and fruits. Photographs: A–C, F, G, I–K, M–O, Q–U by A. Kawakita (Kyoto University, Japan) D–E, H, L, P by G. Yao V Z.Q. Song.
Figure 7 from: Li Y, Liu C, Lin L, Li Y, Xiao J, Loh K-H (2020) Pleistocene isolation caused by sea-level fluctuations shaped genetic characterization of Pampus minor over a large-scale geographical distribution. ZooKeys 969: 137-154. https://doi.org/10.3897/zookeys.969.52069
Figure 7 BSPs showing NefT (Nef = effective population size; T = generation time) changes over time for P. minor based on Cytb sequences. The upper and lower limits of the blue line represent the 95% confidence intervals of highest posterior densities (HPD) analysis. The solid black line represents median estimates of NefT.
Figure 5 from: Li Y, Liu C, Lin L, Li Y, Xiao J, Loh K-H (2020) Pleistocene isolation caused by sea-level fluctuations shaped genetic characterization of Pampus minor over a large-scale geographical distribution. ZooKeys 969: 137-154. https://doi.org/10.3897/zookeys.969.52069
Figure 5 Matrix of pairwise FST values between 11 P. minor populations based on Cytb sequences. * significant at p < 0.05 by the permutation test, ** extremely significant at p < 0.01 by the permutation test.
Figure 6 from: Li Y, Liu C, Lin L, Li Y, Xiao J, Loh K-H (2020) Pleistocene isolation caused by sea-level fluctuations shaped genetic characterization of Pampus minor over a large-scale geographical distribution. ZooKeys 969: 137-154. https://doi.org/10.3897/zookeys.969.52069
Figure 6 The expected mismatch distributions under a sudden expansion model (solid gray line) and the observed pairwise difference (black bars) of Cytb haplotypes of P. minor.
Figure 4 from: Li Y, Liu C, Lin L, Li Y, Xiao J, Loh K-H (2020) Pleistocene isolation caused by sea-level fluctuations shaped genetic characterization of Pampus minor over a large-scale geographical distribution. ZooKeys 969: 137-154. https://doi.org/10.3897/zookeys.969.52069
Figure 4 Unrooted minimum spanning tree showing the genetic relationships among the Cytb haplotypes of P. minor. Circle sizes are proportional to haplotype frequency. Perpendicular tick marks on the lines joining the haplotypes represent the number of nucleotide substitutions.
Figure 1 from: Li Y, Liu C, Lin L, Li Y, Xiao J, Loh K-H (2020) Pleistocene isolation caused by sea-level fluctuations shaped genetic characterization of Pampus minor over a large-scale geographical distribution. ZooKeys 969: 137-154. https://doi.org/10.3897/zookeys.969.52069
Figure 1 Sampling locations of P. minor. Populations are marked by abbreviations that correspond to Table 1.
Figure 2 from: Li Y, Liu C, Lin L, Li Y, Xiao J, Loh K-H (2020) Pleistocene isolation caused by sea-level fluctuations shaped genetic characterization of Pampus minor over a large-scale geographical distribution. ZooKeys 969: 137-154. https://doi.org/10.3897/zookeys.969.52069
Figure 2 Composition and distribution of 22 Cytb haplotypes in the Chinese and Malaysian populations.
Figure 3 from: Li Y, Liu C, Lin L, Li Y, Xiao J, Loh K-H (2020) Pleistocene isolation caused by sea-level fluctuations shaped genetic characterization of Pampus minor over a large-scale geographical distribution. ZooKeys 969: 137-154. https://doi.org/10.3897/zookeys.969.52069
Figure 3 NJ tree and distribution of Cytb haplotypes among populations for P. minor. Bootstrap supports of > 50 in 1000 replicates are shown.
Figures 137-144 from: Wood TJ, Michez D, Cejas D, Lhomme P, Rasmont P (2020) An update and revision of the Andrena fauna of Morocco (Hymenoptera, Apoidea, Andrenidae) with the description of eleven new North African species. ZooKeys 974: 31-92. https://doi.org/10.3897/zookeys.974.54794
Figures 137-144 Andrena (Margandrena) menahemella Scheuchl & Pisanty, 2016 (Israel) 137 female profile 138 female face 139 female dorsum 140 female tergites (Morocco) 141 female profile 142 female face 143 female dorsum 144 female tergites.
Figure 4 from: Qi S, Wang J, Grismer LL, Chen H-H, Lyu Z-T, Wang Y-Y (2020) The Stoor Hobbit of Guangdong: Goniurosaurus gollum sp. nov., a cave-dwelling Leopard Gecko (Squamata, Eublepharidae) from South China. ZooKeys 991: 137-153. https://doi.org/10.3897/zookeys.991.54935
Figure 4 Comparisons of iris color with three closely related congeners AGoniurosaurus gollum sp. nov. (holotype, SYS r002420) BGoniurosaurus varius (holotype, SYS r002333) CGoniurosaurus yingdeensis (holotype SYSr000504) DGoniurosaurus zhelongi (holotype, SYS r000770). Photographs by Shuo Qi and Ying-Yong Wang.
Figure 3 from: Qi S, Wang J, Grismer LL, Chen H-H, Lyu Z-T, Wang Y-Y (2020) The Stoor Hobbit of Guangdong: Goniurosaurus gollum sp. nov., a cave-dwelling Leopard Gecko (Squamata, Eublepharidae) from South China. ZooKeys 991: 137-153. https://doi.org/10.3897/zookeys.991.54935
Figure 3 Type series of Goniurosaurus gollum sp. nov. A holotype, male, SYS r002420 B paratype, male, SYS r002421 C paratype, female, SYS r002421; (1) dorsal view; (2) dorsal view of head; (3) ventral view of head; (4) close-up of the precloacal region, the Arabic number refer to the number of precloacal pores. Photographs by Shuo Qi.
Figure 2 from: Qi S, Wang J, Grismer LL, Chen H-H, Lyu Z-T, Wang Y-Y (2020) The Stoor Hobbit of Guangdong: Goniurosaurus gollum sp. nov., a cave-dwelling Leopard Gecko (Squamata, Eublepharidae) from South China. ZooKeys 991: 137-153. https://doi.org/10.3897/zookeys.991.54935
Figure 2 A The general aspect of the adult male holotype of Goniurosaurus gollum sp. nov. (SYS r002420) in life B scalation and coloration characters of the head of the holotype. Photographs by Shuo Qi.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.