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Figure 1 from: Wang WY, Yamada A, Yamane S (2020) Maritime trap-jaw ants (Hymenoptera, Formicidae, Ponerinae) of the Indo-Australian region – redescription of Odontomachus malignus Smith and description of a related new species from Singapore, including first descriptions of males. ZooKeys 915: 137-174. https://doi.org/10.3897/zookeys.915.38968
Figure 1 Cluster dendrogram of COI (313 bp) barcodes of Odontomachus litoralis and O. malignus from (near) sympatric populations in Singapore, specimens collected from Borneo (KU146009.1), Palau (KU146082.1), and the Philippines (KU504894.1), and additional reference barcodes of O. rixosus, O. pararixosus, and O. simillimus. Nodes are annotated with numbers indicating percentage (%) uncorrected p-distance thresholds at which sequences diverge.
Figure 10 from: Wang WY, Yamada A, Yamane S (2020) Maritime trap-jaw ants (Hymenoptera, Formicidae, Ponerinae) of the Indo-Australian region – redescription of Odontomachus malignus Smith and description of a related new species from Singapore, including first descriptions of males. ZooKeys 915: 137-174. https://doi.org/10.3897/zookeys.915.38968
Figure 10 A Distribution of Odontomachus malignus and O. litoralis in Singapore B map of intertidal and terrestrial habitat types in Pulau Semakau (by Feng Yikang, for RMBR [Raffles Museum of Biodiversity Research]) and locations where O. malignus males were collected (indicated by red-filled circles).
Figure 137 from: Wood JR.I, Muñoz-Rodríguez P, Williams BR.M, Scotland RW (2020) A foundation monograph of Ipomoea (Convolvulaceae) in the New World. PhytoKeys 143: 1-823. https://doi.org/10.3897/phytokeys.143.32821
Figure 137 Ipomoea chenopodiifolia subsp. chenopodiifoliaA habit showing corolla shape and exsertion of stamens and style. Subsp. signataB habit showing corolla shape and exsertion of stamens and style. Subsp. bellatorC habit showing included stamens and style D outer sepal E inner sepal. Drawn by Rosemary Wise A from Olazo 1132; B from from Martínez & García 22197; C from Nuñez 11826; D, E from de Avila 143.
Figure 2 from: Likhitrakarn N, Golovatch SI, Thach P, Chhuoy S, Ngor PB, Srisonchai R, Sutcharit C, Panha S (2020) Two new species of the millipede genus Plusioglyphiulus Silvestri, 1923 from Cambodia (Diplopoda, Spirostreptida). ZooKeys 938: 137-151. https://doi.org/10.3897/zookeys.938.51234
Figure 2 Plusioglyphiulus biserratus sp. nov., ♂ paratype A–C anterior part of body, lateral, dorsal and ventral views, respectively D, E midbody segments, dorsal and lateral views, respectively F cross-section of a midbody segment G–I posterior part of body, lateral, dorsal and ventral views, respectively.
Figure 5 from: Likhitrakarn N, Golovatch SI, Thach P, Chhuoy S, Ngor PB, Srisonchai R, Sutcharit C, Panha S (2020) Two new species of the millipede genus Plusioglyphiulus Silvestri, 1923 from Cambodia (Diplopoda, Spirostreptida). ZooKeys 938: 137-151. https://doi.org/10.3897/zookeys.938.51234
Figure 5 Plusioglyphiulus khmer sp. nov. A, B ♂ paratype C–L ♂ holotype A gnathochilarium, ventral view B collum, dorsal view C antenna, lateral view D, E ♂ legs 1, anterior and posterior views, respectively F ♂ legs 2, posterior view G ♂ legs 3, posterior view H, I anterior gonopods, anterior and posterior views, respectively J, K posterior gonopods, posterior and anterior views, respectively L midbody leg, anterior view. Abbreviations: cxp1 1st coxosternal process cxp2 2nd coxosternal process te telopodites d terminal medial spike k a small bifid process. Scale bars: 0.1 mm.
Figure 1 from: Likhitrakarn N, Golovatch SI, Thach P, Chhuoy S, Ngor PB, Srisonchai R, Sutcharit C, Panha S (2020) Two new species of the millipede genus Plusioglyphiulus Silvestri, 1923 from Cambodia (Diplopoda, Spirostreptida). ZooKeys 938: 137-151. https://doi.org/10.3897/zookeys.938.51234
Figure 1 Habitus, live coloration APlusioglyphiulus boutini Mauriès, 1970, ♂ from Prasat Phnom Totong Temple BPlusioglyphiulus biserratus sp. nov., ♀ paratype CPlusioglyphiulus khmer sp. nov., ♂ paratype. All pictures by R. Srisonchai, not taken to scale.
Figure 4 from: Likhitrakarn N, Golovatch SI, Thach P, Chhuoy S, Ngor PB, Srisonchai R, Sutcharit C, Panha S (2020) Two new species of the millipede genus Plusioglyphiulus Silvestri, 1923 from Cambodia (Diplopoda, Spirostreptida). ZooKeys 938: 137-151. https://doi.org/10.3897/zookeys.938.51234
Figure 4 Plusioglyphiulus khmer sp. nov., ♂ paratype A–C anterior part of body, lateral, dorsal and ventral views, respectively D, E midbody segments, dorsal and lateral views, respectively F cross-section of a midbody segment G–I posterior part of body, lateral, dorsal and ventral views, respectively.
Figure 3 from: Likhitrakarn N, Golovatch SI, Thach P, Chhuoy S, Ngor PB, Srisonchai R, Sutcharit C, Panha S (2020) Two new species of the millipede genus Plusioglyphiulus Silvestri, 1923 from Cambodia (Diplopoda, Spirostreptida). ZooKeys 938: 137-151. https://doi.org/10.3897/zookeys.938.51234
Figure 3 Plusioglyphiulus biserratus sp. nov., ♂ holotype A gnathochilarium, ventral view B collum, dorsal view C antenna, lateral view D, E ♂ legs 1, anterior and posterior views, respectively F ♂ legs 2, posterior view G ♂ legs 3, posterior view H, I anterior gonopods, posterior and anterior views, respectively J, K posterior gonopods, posterior and anterior views, respectively L midbody leg, anterior view. Abbreviations: cxp2 coxosternal process te telopodites ap anterior coxal processes pp paramedian coxal processes. Scale bar: 0.1 mm.
Figure 8 from: Lemos-Espinal JA, Smith GR (2020) A conservation checklist of the amphibians and reptiles of the State of Mexico, Mexico with comparisons with adjoining states. ZooKeys 953: 137-159. https://doi.org/10.3897/zookeys.953.50881
Figure 8 Proportion of A) amphibians and B) reptiles listed in protected categories on the IUCN Red List, SEMARNAT, and high EVS for the State of Mexico. Green is proportion in Data Deficient and Least Concern (IUCN); Not Listed and Subject to Special Protection (we regarded the category of Subject to Special Protection in SEMARNAT equivalent to Least Concern in IUCN) (SEMARNAT); or low or medium EVS. Red is percentage in protected categories or high EVS. N is the number of species assessed.
Figure 7 from: Lemos-Espinal JA, Smith GR (2020) A conservation checklist of the amphibians and reptiles of the State of Mexico, Mexico with comparisons with adjoining states. ZooKeys 953: 137-159. https://doi.org/10.3897/zookeys.953.50881
Figure 7 Species accumulation curves for total herpetofauna, amphibians, and reptiles of the State of Mexico, Mexico.
Figure 6 from: Lemos-Espinal JA, Smith GR (2020) A conservation checklist of the amphibians and reptiles of the State of Mexico, Mexico with comparisons with adjoining states. ZooKeys 953: 137-159. https://doi.org/10.3897/zookeys.953.50881
Figure 6 AAmbystoma lermaenseBChiropterotriton orculusCAbronia deppiiD juvenile Sceloporus sugillatusECrotalus transversus. Photos by Eric Centenero-Alcalá
Figure 5 from: Lemos-Espinal JA, Smith GR (2020) A conservation checklist of the amphibians and reptiles of the State of Mexico, Mexico with comparisons with adjoining states. ZooKeys 953: 137-159. https://doi.org/10.3897/zookeys.953.50881
Figure 5 Climate map of the State of Mexico, Mexico (modified from García – Comisión Nacional para el Conocimiento y Uso de la Biodiversidad 1998).
Figure 4 from: Lemos-Espinal JA, Smith GR (2020) A conservation checklist of the amphibians and reptiles of the State of Mexico, Mexico with comparisons with adjoining states. ZooKeys 953: 137-159. https://doi.org/10.3897/zookeys.953.50881
Figure 4 Vegetation map of the State of Mexico, Mexico (modified from Dirección General de Geografía – INEGI 2016).
Figure 3 from: Lemos-Espinal JA, Smith GR (2020) A conservation checklist of the amphibians and reptiles of the State of Mexico, Mexico with comparisons with adjoining states. ZooKeys 953: 137-159. https://doi.org/10.3897/zookeys.953.50881
Figure 3 Physiographic provinces of the State of Mexico, Mexico (modified from Cervantes-Zamora et al. 1990).
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
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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.