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Fig. 4 in Infestation and seasonal fluctuation of chigger mites on the Southeast Asian house rat (Rattus brunneusculus) in southern Yunnan Province, China
Fig. 4. Seasonal fluctuation of infestations of the Southeast Asian house rat (R. brunneusculus) with Leptotrombidium (L.) deliense at Jingha, southern Yunnan of China (April 2016–March 2017).
Fig. 6 in Infestation and seasonal fluctuation of chigger mites on the Southeast Asian house rat (Rattus brunneusculus) in southern Yunnan Province, China
Fig. 6. Seasonal fluctuation of infestations of the Southeast Asian house rat (R. brunneusculus) with Leptotrombidium (L.) scutellare at Jingha, southern Yunnan of China (April 2016–March 2017).
Fig. 3 in Infestation and seasonal fluctuation of chigger mites on the Southeast Asian house rat (Rattus brunneusculus) in southern Yunnan Province, China
Fig. 3. Seasonal fluctuation of infestations of the Southeast Asian house rat (R. brunneusculus) with Ascoschoengastia indica at Jingha, southern Yunnan of China (April 2016–March 2017).
Fig. 2 in Temporal variations of larval digenean assemblages parasitizing Heleobia parchappii (Mollusca: Cochliopidae) in two shallow lakes from the Buenos Aires province, Argentina
Fig. 2. Seasonal variation in the Overall prevalence (mean ± S.D) of larval digeneans parasitizing Heleobia parchappii (D'Orbigny, 1835) in Los Padres and La Brava lakes, Buenos Aires province, Argentina.
Fig. 3 in Temporal variations of larval digenean assemblages parasitizing Heleobia parchappii (Mollusca: Cochliopidae) in two shallow lakes from the Buenos Aires province, Argentina
Fig. 3. Seasonal variation in Species richness (mean ± S.D) of larval digeneans parasitizing Heleobia parchappii (D'Orbigny, 1835) in Los Padres and La Brava lakes, Buenos Aires province, Argentina.
Fig. 2 in New dinosaur egg material from Yunxian, Hubei Province, China resolves the classification of dendroolithid eggs
Fig. 2. Clutches of dendroolithid eggs of Placoolithus tumiaolingensis (Zhou, Ren, Xu, and Guan, 1998) comb. nov. from the Upper Cretaceous of the Tumiaoling outcrop, Yunxian, Hubei Province, China. A. TML 4; A1, general view; A2, the lower eggs; A3, higher egg and egg impressions. B. TML 7. C. TML 9. D. TML 10. E. TML 14; E1, general view; E2, egg groups. Scale bars 20 cm.
Fig. 1. A, B in New dinosaur egg material from Yunxian, Hubei Province, China resolves the classification of dendroolithid eggs
Fig. 1. A, B. Map of the location of dendroolithid eggs (asterisk) in Yunxian, Hubei Province, China.
Fig. 4 in New dinosaur egg material from Yunxian, Hubei Province, China resolves the classification of dendroolithid eggs
Fig. 4. Radial thin sections showing variety of dendroolithid eggshell microstructure of Placoolithus tumiaolingensis (Zhou, Ren, Xu, and Guan, 1998) comb. nov. from the Upper Cretaceous of the Tumiaoling outcrop, Yunxian, Hubei Province, China. A. TML 9, few branches. B. TML 10, fasciculate branches. C. TML 4, thinner eggshell. D. Eggshell from TML 4 with the Dendroolithus tumiaolingensis (Zhou, Ren, Xu, and Guan, 1998) microstructure from the Upper Cretaceous of the Tumiaoling outcrop, Yunxian, Hubei Province, China. E. Eggshell from TML 4 with Dendroolithus hongzhaiziensis (Zhou, Ren, Xu, and Guan, 1998) microstructure from the Upper Cretaceous of the Tumiaoling outcrop, Yunxian, Hubei Province, China. F. Eggshell from TML 8 with Paradendroolithus qinglongshanensis (Zhou, Ren, Xu, and Guan, 1998) microstructure from the Upper Cretaceous of the Tumiaoling outcrop, Yunxian, Hubei Province, China. Scale bars 400 μm.
Fig. 5 in A new capybara from the late Miocene of San Juan Province, Argentina, and its phylogenetic implications
Fig. 5. Schematic occlusal view of upper teeth of Cardiatherium (A–C) and Phugatherium (D–E). A. Cardiatherium calingastaense sp. nov. (late Miocene, Puchuzum, San Juan Province, Argentina), INGEO-PV 87, right P4–M3. B. Cardiatherium patagonicum (late Miocene, Estancia Rincón Chico, Chubut Province, Argentina), MPEF-PV 740/22, reversed left P4; MPEF-PV 740/23, reversed left M1 or M2; MPEF-PV 740/18, right M3. C. Cardiatherium paranense (late Miocene, Ituzaingó Formation, Entre Ríos Province, Argentina), MLP 87-XI-1-27, right P4–M3. D. Phugatherium novum (middle Pliocene, Chapadamalal Formation, Buenos Aires Province, Argentina), MMP 492-S, right P4–M1. E. Phugatherium cataclisticum late Miocene–Early Pliocene, Monte Hermoso Formation, Buenos Aires Province, Argentina), MLP 15-231a, right M1.
Fig. 4 in A new capybara from the late Miocene of San Juan Province, Argentina, and its phylogenetic implications
Fig. 4. Occlusal dental details of the holotype (INGEO-PV 87) of the hydrochoerine rodent Cardiatherium calingastaense sp. nov., late Miocene, Puchuzum, San Juan Province, Argentina. Right P4–M3 (A1), left P4–M1 (A2), left M1–M2 (A3), posterior part of right M3 (A4), left p4–m3 (A5), right m1 (A6), left m3 (A7), left p4 (A8), right p4 (A9).
Fig. 3 in A new capybara from the late Miocene of San Juan Province, Argentina, and its phylogenetic implications
Fig. 3. Holotype (INGEO-PV 87) of the hydrochoerine rodent Cardiatherium calingastaense sp. nov., late Miocene, Puchuzum, San Juan Province, Argentina. A. Skull in dorsal (A1) and ventral (A2) views, and detail of the scars for masseter medialis muscle (A3); correspondence indicated by lines. B. Mandible in occlusal (B1) and left lateral (B2) views.
Fig. 2 in A new capybara from the late Miocene of San Juan Province, Argentina, and its phylogenetic implications
Fig. 2. Dental nomenclature (occlusal view). A–C, E. Cardiatherium calingastaense sp. nov. A. Right p4. B. Right m1. C. Right m3. E. Right M1. D. Cardiatherium patagonicum, right p4. Abbreviations: c, column; he, external fissure (or flexid); HFI, fundamental internal fissure (hypoflexus); hfe, fundamental external fissure; hi, internal fissure; HPE, primary external fissure; hpi, primary internal fissure; HSE/hse, secondary external fissure; hsi, secondary internal fissure; hsni, internal supernumerary fissure; hti, tertiary internal fissure; pr, prism; prIIa/b, anterior and posterior lobes of pr II; prsa, anterior secondary prism.
Fig. 6 in A new capybara from the late Miocene of San Juan Province, Argentina, and its phylogenetic implications
Fig. 6. Schematic occlusal view of lower teeth of Cardiatherium. A. Cardiatherium calingastaense sp. nov. (late Miocene, Puchuzum, San Juan Province, Argentina), holotype, INGEO-PV 87, right p4–m2 and reversed left m3. B. Cardiatherium patagonicum (late Miocene, Estancia Rincón Chico, Chubut Province, Argentina), MPEF-PV 740/9, reversed left p4; MPEF-PV 740/24, right m1–m2; MPEF-PV 740/7, reversed left m3. C. Cardiatherium paranense (late Miocene, Ituzaingó Formation, Entre Ríos Province, Argentina), MLP 40-XI-15-1, right p4–m3. D. Cardiatherium orientalis (late Miocene, Camacho Formation, San Gregorio, Uruguay), SPV-FHC-27-XI-64-20, right p4–m3. E. Cardiatherium chasicoense (late Miocene, Arroyo Chasicó, Buenos Aires Province, Argentina), MMP 300-M, right p4–m2; MMH-CH 88-6-71, reversed left m3.
Fig. 7 in A new capybara from the late Miocene of San Juan Province, Argentina, and its phylogenetic implications
Fig. 7. Stratigraphic adjustment of the strict consensus tree for the phylogenetic analysis of Hydrochoerinae (333 MPTs of 3364 steps). Upper case letters indicate the nodes within Hydrochoerinae, as described in the main text. Silhouettes reflect external aspect and relative size of representatives of the main clades within Hydrochoerinae.
Fig. 3 in Burgess Shale-type microfossils from the middle Cambrian Kaili Formation, Guizhou Province, China
Fig. 3. Sclerites of the problematic lophotrochozoan Wiwaxia (NIGP 153962–153977) from the middle Cambrian Kaili Formation, Guizhou, China. A. KAIL−05−01−N28. B. KAIL−GTBM−9−2−a−M38. C. KAIL−05−01−S43. D. KAIL−GTBM−9−35M−02−F25. E. KAIL−05−01−T15. F. KAIL−A−01−R33. G. KAIL−05−03−L36. H. KAIL−GTBM−9−2−b−D40. I. KAIL−GTBM−9−2−d−P33. J. KAIL−GTBM−9−2−d−N34. K. KAIL−GTBM−9−35M−02−J34. L. KAIL− GTBM−9−37M−01−S46 (image reversed). M. KAIL−07−01−L24. N. KAIL−A−01−P37. O. KAIL−05−05−T6. P. KAIL−GTBM−9−37M−01−M22. Scale bars: A 200 µm, B–P 100 µm.
Fig. 7 in Burgess Shale-type microfossils from the middle Cambrian Kaili Formation, Guizhou Province, China
Fig. 7. Problematic metazoan microfossils (NIGP 153992–154010) from the middle Cambrian Kaili Formation, Guizhou, China. A–F. Ornamented spines cf. Rushtonites/Mongolitubulus. A. KAIL−04−05−M10. B. KAIL−GTBM−9−35M−02−G23. C. KAIL−BP−01−K41. D. KAIL−X−01−P42. E. KAIL−09−01−S31. F−J. Possible elements of a lophotrochozoan jaw apparatus. F. KAIL−05−01−U23. G. KAIL−04−2−T39 (G1); detail (G2). H. KAIL−GTBM−9−2−d−F6 (image reversed). I. KAIL−BP−01−N25 (image reversed). J. KAIL−GTBM−9−2−d−E9. K−O. Diverse spinose forms including possible elements of a radula−like apparatus (M, N). K. KAIL−04−07−Q33. L. KAIL−05−03−J25. M. KAIL−GTBM−9−35M−02−N41. N. KAIL−05−03−M17. O. KAIL−04−09−X27. P, Q. Possible arthropodan seta (P) and setal array (Q). P. KAIL−X−01−M28. Q. KAIL−GTBM−9−35M−01−W29. R, S. Complex forms of unknown affinity. R. KAIL− 05−03−U21. S. KAIL−05−01−F35. Scale bars: A–P, S 100 µm; Q, R 50 µm; G 2 40 µm.
Fig. 2 in Burgess Shale-type microfossils from the middle Cambrian Kaili Formation, Guizhou Province, China
Fig. 2. Biomineralizing taxa preserved as small carbonaceous fossils (NIGP 153954–153961) from the middle Cambrian Kaili Formation, Guizhou, China. A. Hyolithid helen (A1), with detail of rounded proximal end (A2), KAIL−BP−01−J38. B. Multi−rayed chancelloriid sclerite, KAIL−A−01−P39. C−E. Single−rayed or disarticulated chancelloriid sclerites. C. KAIL−GTBM− 9−2−b−E39. D. KAIL−05−05−O17 (image reversed). E. KAIL−09−01−U19. F–H. Brachiopod fragments (F1, G1, H1), with details of microstructure (F2, G2, G3, H2). F. KAIL−07−01−U38. G. KAIL−05−05−E17. H. KAIL−GTBM− 9−2−d−K41. Scale bars: A1, B–E 200 µm; A2 40 µm; F1 400 µm; F2 125 µm; G1 250 µm; G2 125 µm; G3 60 µm; H1 500 µm; H2 150 µm.
Fig. 4 in Burgess Shale-type microfossils from the middle Cambrian Kaili Formation, Guizhou Province, China
Fig. 4. Pterobranch periderm (NIGP 153978–153979) from the middle Cambrian Kaili Formation, Guizhou, China. A. KAIL−BP−01−N23. B. KAIL−A− 01−R36. A2 is a photographic detail of A1; A3 and B2 are camera lucida drawings highlighting the fusellar microstructure, including characteristic oblique sutures developed locally in a "zig−zag" arrangement. Scale bars: A1 200 µm; A2, A3 100 µm; B1, B2 400 µm.
Fig. 1 in Burgess Shale-type microfossils from the middle Cambrian Kaili Formation, Guizhou Province, China
Fig. 1. Filaments and acritarchs (NIGP 153940–153953) from the middle Cambrian Kaili Formation, Guizhou, China. A–G. Cyanobacterial filaments. A–C. Eomicrocoleus Horodyski and Donaldson, 1980/Siphonophycus Schopf, 1968 emended Knoll, Swett, and Mark, 1991 with multiple cellular trichomes enclosed within a common sheath (in C, a double sheath). D,E,G. Siphonophycus spp. exhibiting a variety of growth forms. F. Polytrichoides Hermann, 1974 emend. Knoll, Swett, and Mark, 1991. A. KAIL−04−03−L44. B. KAIL−05−02−V31. C. KAIL−05−05−D13. D. KAIL−GTBM−9−35M−01−T45. E. KAIL− GTBM−9−37M−01−J23. F. KAIL−A−01−K26. G. KAIL−GTBM−9−2−b−M37. H, I. Filaments of uncertain affinity. H. KAIL−GTBM−9−35M−01−E44. I. KAIL− 09−01−H12. J–N. Acritarchs, including forms with medial splitting (K, L) and possible vegetative colony growth (M). J. KAIL−A−01−O25. K. KAIL− 04−05−T17. L. KAIL−04−05−G17. M. KAIL−GTBM−2−9−c−D21. N. KAIL−GTBM−9−2−d−S14. Scale bars A–F, J–L 200 µm; G–I 400 µm; M, N 100 µm.
Fig. 2 in Late Ordovician trilobites from the Xiazhen Formation in Zhuzhai, Jiangxi Province, China
Fig. 2. Outcrop photographs of sampling localities. Hammer in C, E, and F is about 26 cm long. A. Mudstone outcrop at locality 2; water bottle in the elipse is about 20 cm high. B. Close−up view of mudstone at locality 2; pen is about 13.5 cm long. C. Mudstone outcrop at locality 1. D. Brachiopod lag deposit supposedly underlying mudstone at locality 1; camera lens cap is about 5 cm in diameter. E. Mudstone outcrop at locality 3; a trench was dug to collect specimens. F. Mudstone outcrop at locality 4.
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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.