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Fig. 3 in Close relationship of Plasmodium sequences detected from South American pampas deer (Ozotoceros bezoarticus) to Plasmodium spp. in North American white-tailed deer
Fig. 3. Phylogenetic relationship of Plasmodium sequences from Brazilian pampas deer within ungulate Plasmodium spp. The tree was constructed using concatenated partial nucleotide sequences of cytb and cox1 by maximum likelihood (ML) method based on the GTR + I + G model. Bootstrap values (BV) for ML with 1000 replicates of ultrafast bootstrap analysis and Bayesian posterior probability (BPP) are indicated for each internal branch. The compositions of collapsed clades are described in Fig. 2 legend. The length for the substitutions/site (0.07) is indicated.
Fig. 2 in Close relationship of Plasmodium sequences detected from South American pampas deer (Ozotoceros bezoarticus) to Plasmodium spp. in North American white-tailed deer
Fig. 2. Phylogenetic relationships of Plasmodium sequences from Brazilian pampas deer within Haemosporidia. The tree was constructed using ∼3.4 kb of partial mitochondrial nucleotide sequences by the maximum likelihood (ML) method based on the GTR + I + G model. Bootstrap values (BV) for ML with 1000 replicates of ultrafast bootstrap analysis and Bayesian posterior probability (BPP) are indicated for each internal branch. The compositions of collapsed clades are Leucocytozoon (L. fringillinarium, L. majoris, and L. sabrasezi); Haemoproteus and Parahaemoproteus (Haemoproteus sp. jb1.JA27, Haemoproteus sp. jb2.SEW5141, and Parahaemoproteus vireonis); and bird, lizard and non-ungulate mammalian Plasmodium (P. gallinaceum, P. relictum, P. juxtinucleare, P. lutzi, P. floridense, P. mexicanum, P. falciparum, P. vivax, P. malariae, P. ovale, P. coatneyi, P. cynomolgi, P. fieldi, P. gonderi, P. inui, P. knowlesi, P. fragile, P. simiovale, P. simium, P. hylobati, P. reichenowi, P. billicollinsi, P. billbrayi, P. berghei, P. chabaudi, P. vinckei, and P. yoelii). Mitochondrial DNA sequences (including cytb and cox1) used in this study were listed in the Supplementary Table S1 of Templeton et al. (2016a). Nucleotide sequences of Plasmodium sp. in the North American white-tailed deer was based on Table S4 of Martinsen et al. (2016). Nucleotide positions containing indels or undetermined nucleotides, or those where the alignment was not clearly made were excluded. Nucleotide positions corresponding to the P. falciparum mtDNA (NC_002375.1) 974–1502, 1509–1576, 1578–1628, 1637–1678, 1698–1760, 1762–1769, 1774–1800, 1806–1831, 1834–1867, 1870–1909, 1914–2031, 2050–3474, and 3486–4444 were used. The length for the substitutions/site (0.04) is indicated.
Figs 13-18 in A revision of Trisunius III. Three new species from North India and Nepal, and additional records (Coleoptera: Staphylinidae: Paederinae)
Figs 13-18: Trisunius tenuincisus nov.sp.: (13) habitus; (14) forebody; (15) male sternite VII; (16) male sternite VIII; (17-18) aedeagus in lateral and in ventral view. Scale bars: 13: 1.0 mm; 14: 0.5 mm; 15-16: 0.2 mm; 17-18: 0.1 mm.
Map 1 in A revision of Trisunius III. Three new species from North India and Nepal, and additional records (Coleoptera: Staphylinidae: Paederinae)
Map 1: Distribution of the genus Trisunius in the Himalaya and in North India. Trisunius monticola (filled and open triangles); T. volans (open triangle); T. manasluensis and T. opaciceps (filled circle); T. perpusillus (open diamond); T. alesi (star); T. tenuincisus (open circle); T. borailicus (filled diamond).
Figs 7-12 in A revision of Trisunius III. Three new species from North India and Nepal, and additional records (Coleoptera: Staphylinidae: Paederinae)
Figs 7-12: Trisunius borailicus nov.sp.: (7) habitus; (8) forebody; (9) male sternite VII; (10) male sternite VIII; (11-12) aedeagus in lateral and in ventral view. Scale bars: 7: 1.0 mm; 8: 0.5 mm; 9- 10: 0.2 mm; 11-12: 0.1 mm.
FIGURE 2 in Additional Notes on North American Acanthaceae: Biogeography, Distributions, Taxonomy, Lectotypifications, and Catalog of Species
FIGURE 2. Justicia spp. (A, B) and Pseuderanthemum variabile (C, D). A. Flower of J. americana (Daniel & Lott 10530) showing limb of corolla with lateral lobes of lower lip widely spreading from lower-central lobe. B. Flower of J. lanceolata (Daniel 11762) showing limb of corolla with lateral lobes of lower lip barely spreading from lower-central lobe. There is variation in color of the corolla in both species of Justicia. C. Spontaneous plant of P. variabile at San Francisco Conservatory of Flowers (Daniel s.n.). D. Front view of limb of corolla.
Figures 22–23 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figures 22–23. Lateral habitus of Dieunomia heteropoda (Say). 22. Female. 23. Male. Images courtesy of Laurence Packer.
Figures 10–15 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figures 10–15. Males of Dufourea novaeangliae (Robertson) (10–12) and D. monardae (Viereck) (13–15). 10, 13. Propodea. 11, 14. Metatrochanters. 12, 15. Metasomal sterna six. Modified from Dumesh & Sheffield (2012).
Figures 6–9 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figures 6–9. Females of Dufourea novaeangliae (Robertson) (6, 7) and D. monardae (Viereck) (8, 9). 6, 8. Head and mouthparts in lateral view. 7, 9. Mesobasitarsi. Modified from Dumesh & Sheffield (2012).
Figures 4–5 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figures 4–5. Faces of female Dufourea Lepeletier de Saint Fargeau. 4. Dufourea novaeangliae (Robertson). 5. D. harveyi (Cockerell). Modified from Dumesh & Sheffield (2012).
Figures 2–3 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figures 2–3. Lateral habitus of male Dufourea Lepeletier de Saint Fargeau. 2. Dufourea maura (Cresson). 3. D. harveyi (Cockerell). Modified from Dumesh & Sheffield (2012).
Figure 1 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figure 1. Face of female Dufourea maura (Cresson). Modified from Dumesh & Sheffield (2012). Scale bar = 1 mm.
FIGURE 14. A-G in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia
FIGURE 14. A-G. Amamriabatis heni nov gen. nov. sp. A. anterior tooth KEB 1-218, A1. Occlusal view, A2. Basal view, A3. Lingual view, B. antero-lateral tooth KEB 1-219 (Holotype), B1. Occlusal view, B2. Lingual view, B3. Basal view, C. juvenile tooth KEB 1-220, occlusal view, D. antero-lateral tooth KEB 1-221, D1. Occlusal view, D2. Basal view, D3. Labial view, E. lateral tooth KEB 1-222, E1. Occlusal view, E2. Lingual view, E3. Basal view, F. antero-lateral tooth KEB 1-223, F1. Occlusal view, F2. Basal view, F3. Labial view, G. lateral tooth KEB 1-224, G1. Occlusal view, G2. Basal view, G3. Lingual view; H. Archaeomanta sp. KEB 1-225, H1. Lateral view, H2. Labial view.
FIGURE 12. A-C in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia
FIGURE 12. A-C. Mecotrygon asperodentulus nov. gen nov. sp. A. anterior tooth KEB 1-188, A1. occlusal view, A2. Profile, A3. Basal view; B. lateral tooth KEB 1-189, B1. occlusal view, B2. labial view, B3. Profile; C. lateral tooth KEB 1-190, HOLOTYPE, C1. Occlusal view, C2. Lingual view, C3. Basal view, C4. Profile; D-M. Himantura souarfortuna nov. sp. D.?posterior tooth KEB 1-191, D1. Occlusal view, D2. Profile, D3. Basal view; E. antero-lateral tooth KEB 1- 192, occlusal view; F. anterior tooth KEB 1-193, F1. Occlusal view, F2. Labial view; G. antero-lateral tooth KEB 1-194, G1. Occlusal view, G2. Profile; H. anterior tooth KEB 1-195, occlusal view; I. lateral tooth KEB 1-196, occlusal view; J. A. anterior tooth KEB 1-197, occlusal view; K. lateral tooth KEB 1-198, K1. Occlusal view, K2. Basal view; L. A. anterior tooth KEB 1-199, occlusal view; M. lateral tooth KEB 1-200, occlusal view. N-O. Dasyatoid indet. N. antero-lateral tooth KEB 1-201, N1. Occlusal view, N2. Basal view; O. A. antero-lateral tooth KEB 1-202, occlusal view; P-Q. Arechia sp. P. lateral tooth KEB 1-203, occlusal view; Q. A. anterior tooth KEB 1-204, Q1. Occlusal view, Q2. Lingual view.
FIGURE 10. A-D in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia
FIGURE 10. A-D: Propristis cf. schweinfurti. A. Rostral denticle KEB 1-172, A1. Profile, A2. dorsal view; B. Rostral denticle KEB 1-173, Profile; C. Rostral denticle KEB 1-174, C1. Profile, C2. Dorsal view, C3. basal view; D. Rostral denticle KEB 1-175, D1. profile. D2. dorsal view; E: Pristis sp. Rostral denticle, KEB 1-165, dorsal view; F-G. Rhynchobatus cf. vincenti. F. anterior tooth KEB 1-176, F1. Occlusal view, F2. Basal view; G. anterior tooth KEB 1-177, occlusal view; H-I.?Torpedo sp. H. lateral tooth KEB 1-178, occlusal view, I. lateral tooth KEB 1-179, occlusal view.
FIGURE 9. A-F in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia
FIGURE 9. A-F: Propristis cf. schweinfurti, A. Anterior oral tooth KEB 1-166, A1. Lingual view, A2. Occlusal view, A3. profile; B. Antero-lateral oral tooth KEB 1-167, B1. Occlusal view, B2. Lingual view, B3. Labial view; C. Anterior oral tooth KEB 1-168, C1. Lingual view, C2. Basal view, C3. Profile; D. lateral tooth KEB 1-169, D1. Lingual view, D2. Occlusal view, D3. Basal view, D4. Magnificence of crown-root boundary of D3; E.?male lateral tooth KEB 1-170, E1. Occlusal tooth, E2. Basal view; F.?male anterior tooth KEB 1-171, F1. Lingual view, F2. Occlusal view; G-L: Pristis sp. G. porterior tooth KEB 1-158, G1. Occlusal view, G2. Basal view; H. anterior tooth KEB 1-159, occlusal view; I. lateral tooth KEB 1-160, I1 occlusal view, I2., lingual view. J lateral tooth KEB 1-161, occlusal view; K. anterior tooth KEB 1-162, occlusal view; L. lateral tooth of?juvenile KEB 1-163, L1. Occlusal view, L2. Basal view; M. lateral tooth of juvenile KEB 1-164, M1. Occlusal view, M2. Profile.
FIGURE 1 in Diversity and renewal of tropical elasmobranchs around the Middle Eocene Climatic Optimum (MECO) in North Africa: New data from the lagoonal deposits of Djebel el Kébar, Central Tunisia
FIGURE 1. Paleotemperatures (ice-free deep-ocean T°/ tropical sea surface T°) and Thermic events during the "doubthouse" conditions of Eocene period (from Cramwinckel et al., 2018 modified with events dating from Hollis et al., 2019). Stratigraphically and geographical locations of the main deposits with Elasmobranch associations along the southwestern Tethys. Abbreviations: DAK: Dakhla (Adnet et al., 2010), GEN: Genam (Zouhri et al., 2017, in press); AZ: Aznag (Tabuce et al., 2005) PM: Phosphate ores (see Noubhani and Cappetta, 1997), Morocco; GAF: Gafsa basin (see Arambourg, 1952); KEBAR: Kébar (this work and Adnet et al., 2019); MBK: Mabrouk (see Sweydan et al., 2019), Tunisia; EG: ElGedida (see Strougo et al., 2007); KM: KM11 (see Adnet et al., 2011) MT: Minqar Tabaghbagh (see Zalmout et al., 2012); BQ: Birquet Qarun QS: Quar et Sa; GE: Genahamm Fm.; MI: Midawara FM. from Wadi al Hitan, see Underwood et al., 2011), Egypt; QD: Qa Faydat al Dahikya, Jordania, see Mustafat and Zalmout, 2002).
Fig. 2 in A report of 22 unrecorded bacterial species in Korea, isolated from the North Han River basin in 2017
Fig. 2. Transmission electron micrographs of cells of the strains isolated in the study. Strains: 1, IMCC34522 (0.5 μm); 2, IMCC34590 (0.2 μm); 3, IMCC34630 (0.2 μm); 4, IMCC34661 (0.2 μm); 5, IMCC34666 (0.5 μm); 6, IMCC34578 (0.5 μm); 7, IMCC34610 (0.5 μm); 8, IMCC34605 (1.0 μm); 9, IMCC34726 (0.2 μm); 10, IMCC34658 (0.5 μm); 11, IMCC34655 (0.5 μm); 12, IMCC34711 (0.2 μm); 13, IMCC34728 (0.5 μm); 14, IMCC34689 (0.2 μm); 15, IMCC34713 (0.2 μm); 16, IMCC34644 (0.2 μm); 17, IMCC34656 (0.2 μm); 18, IMCC34688 (0.5 μm); 19, IMCC34510 (0.5 μm); 20, IMCC34659 (0.5 μm); 21, IMCC34607 (0.2 μm); 22, IMCC34525 (0.5 μm). Scale bars are indicated in parenthesis after strain ID.
Figs. 1-6 in Rediscovery of Zubovskya morii (Bey-Bienko, 1931) (Orthoptera: Acrididae), the nearly forgotten endemic grasshopper in North Korea with revised checklist from its type locality, Mount Baekdusan
Figs. 1-6. Habitus of Zubovskya morii (Bey-Bienko, 1931). 1. Male, dorsal view; 2. Male, ventral view; 3. Female, dorsal view; 4. Female, ventral view; 5. Male, lateral view; 6. Female, lateral view.
Telescopus finkeldeyi Haacke, 2013 DAMARA TIGER SNAKE Telescopus finkeldeyi Haacke 2013:281. Holotype: TM 53542 (collector J.A. van Rooyen). Type locality: "Rössing Uranium mine area, Swako- mund [sic] district (2214Db) Namibia." Global conservation status (IUCN): Not Evaluated. Global distribution: The species is known from Angola and Namibia. Ocurrences in Angola (Map 364): The species occurs in southwestern Angola. Namibe: "5 km north Namibé" [-15.20000, 12.15000] (Haacke 2013:285). Taxonomic and distributional notes: Some earlier records of T. semiannulatus polystictus in Namibia actually refer to this recently described species. MAP 364. Distribution of Telescopus finkeldeyi in Angola. in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)
Telescopus finkeldeyi Haacke, 2013 DAMARA TIGER SNAKE Telescopus finkeldeyi Haacke 2013:281. Holotype: TM 53542 (collector J.A. van Rooyen). Type locality: "Rössing Uranium mine area, Swako- mund [sic] district (2214Db) Namibia." Global conservation status (IUCN): Not Evaluated. Global distribution: The species is known from Angola and Namibia. Ocurrences in Angola (Map 364): The species occurs in southwestern Angola. Namibe: "5 km north Namibé" [-15.20000, 12.15000] (Haacke 2013:285). Taxonomic and distributional notes: Some earlier records of T. semiannulatus polystictus in Namibia actually refer to this recently described species. MAP 364. Distribution of Telescopus finkeldeyi in Angola.
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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.