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Figure 12 in Two species representing a rare genus Sinaxonopsis (Acari, Hydrachnidiae, Aturidae) from China, with discussion of some taxonomic features
Figure 12 Sinaxonopsis unicucrus Yi & Jin, 2012, ♀ (HN-AT-202106110512), SEM photographs: A –Outer side of III-Leg-1–6; B – Inner side of III-Leg-1–6; C – Outer side of IV-Leg-1–6; D – Inner side of IV-Leg-1–6.
Cross section shape: circular elliptical unknown Siphuncle position: central marginal unknown Fig. 4 Morphometrics of orthoconic cephalopods from the Besano Formation. Measurements are compared with discrete characters of the shell. Orange circles represent definite and orange crosses likely orthoceratoids, while blue triangles represent definite and blue crosses likely coleoids. Black crosses are indeterminable. A Apical angle, calculated from length and diameters of the specimens. B Maximum diameter in Orthoceratoid and coleoid cephalopods from the Middle Triassic of Switzerland with an updated taxonomic framework for Triassic Orthoceratoidea
Cross section shape: circular elliptical unknown Siphuncle position: central marginal unknown Fig. 4 Morphometrics of orthoconic cephalopods from the Besano Formation. Measurements are compared with discrete characters of the shell. Orange circles represent definite and orange crosses likely orthoceratoids, while blue triangles represent definite and blue crosses likely coleoids. Black crosses are indeterminable. A Apical angle, calculated from length and diameters of the specimens. B Maximum diameter
Figure 2 in Rhyscotus subrisus Li & Jiang, sp. nov., representing a new record family Rhyscotidae from China (Isopoda: Oniscidea)
Figure 2. Appendages of Rhyscotus subrisus Li & Jiang, sp. nov., holotype. A. Antenna. B. Pereopod 1. C. Pereopod 7. D. Pleopod 1. E. Pleopod 2. F. Pleopod 3 exopodite. G. Pleopod 4 exopodite. H. Pleopod 5 exopodite. Scale bars = 0.1 mm.
Figure 1 in Rhyscotus subrisus Li & Jiang, sp. nov., representing a new record family Rhyscotidae from China (Isopoda: Oniscidea)
Figure 1. Habitus of Rhyscotus subrisus Li & Jiang, sp. nov., holotype. A. Dorsal view. B. Lateral view. C. Head in frontal view. D. Pleon in dorsal view. E. Pleon in ventral view. Scale bars: A–B = 1.0 mm; C–E = 0.5 mm.
Fig. 7 in An early Eocene pan-gekkotan from France could represent an extra squamate group that survived the K/Pg extinction
Fig. 7. SEM images of the jaw symphyseal region and details of tooth crowns in two extant gekkotans, Gonatodes albogularis (Duméril and Bibron, 1836) A) and Sphaerodactylus klauberi Grant, 1923 (B), showing a similar sulcus on the crown as present in Bauersaurus gen. nov.
Fig. 4 in An early Eocene pan-gekkotan from France could represent an extra squamate group that survived the K/Pg extinction
Fig. 4. Pan-gekkotan squamate Bauersaurus cosensis gen. et sp. nov. from Cos, France, early Eocene (MP 10–11). Tooth details of the holotype (UM- COS-1012) maxilla (A) and UM-COS-1013 dentary (B) in ventromedial (A1), ventral (A2), anteromedial (A3), dorsal (B1), anterior (B2) views (all micro-CT visualizations).
Fig. 6 in An early Eocene pan-gekkotan from France could represent an extra squamate group that survived the K/Pg extinction
Fig. 6. Maxillae of several gekkotans compared with Bauersaurus gen. nov. in lateral (left column) and medial (right column) views; 3D models of gekkotans were mirrored. Top to bottom, Sphaerodactylus grandisquamis spanius Stejneger, 1904, RT 14708 (Sphaerodactylidae), Holodactylus africanus Boettger, 1893, CAS 198932 (Eublepharidae), Paradelma orientalis (Günther, 1876) CAS 77652 (Pygopodide), Underwoodisaurus milii Bory de Saint-Vincent, 1823, CAS 74744 (Carphodactylidae), Pseudothecadactylus australis (Günther, 1877) MCZ Herp R- 35162 (Diplodactylide), Bauersaurus cosensis the holotype UM-COS-1012 (Pan-Gekkota). Bauersaurus cosensis is inferred as sister to Gekkota.
Fig. 1 in An early Eocene pan-gekkotan from France could represent an extra squamate group that survived the K/Pg extinction
Fig. 1. Pan-gekkotan squamate Bauersaurus cosensis gen. et sp. nov. from Cos, France, early Eocene (MP 10–11). Holotype (UM-COS-1012), right maxilla, in lateral (A1), medial (A2), dorsal (A3), ventral (A4), anteromedial (A5), and dorsomedioposterior (A6) views (all micro-CT visualizations).
Fig. 3 in An early Eocene pan-gekkotan from France could represent an extra squamate group that survived the K/Pg extinction
Fig. 3. Pan-gekkotan squamate Bauersaurus cosensis gen. et sp. nov. from Cos, France, early Eocene (MP 10–11). Photographs of the holotype (UM- COS-1012) maxilla (A) and UM-COS-1013 dentary (B) in lateral (A1, B1) and medial (A2, B2) views.
Fig. 5. A in An early Eocene pan-gekkotan from France could represent an extra squamate group that survived the K/Pg extinction
Fig. 5. A. Reconstruction of the complete skull of an early Eocene pan-gekkotan squamate Bauersaurus cosensis gen. et sp. nov. from Cos, France, using a D model of a living gekkotan with similar morphology and proportions of bones, Pseudothecadactylus australis (MCZ Herp R- 35162), grey silhouette; Bauersaurus, micro-CT visualizations of jaws in lateral view. B–F. Comparison of the overall shape of the facial process with other gekkotans, i.e. the Late Jurassic Eichstaettisaurus schroederi (the holotype BSPG 1937 I; modified from Simões et al. 2017), (B) the early Eocene (MP 10) Laonogekko lefevrei (the holotype MNHN PMT 5; modified from Augé 2005) (C), the middle Eocene (MP 12 and MP 13) Geiseleptes delfinoi (the holotype GMH Ce IV-4057-1933; modified from Villa et al. (2022) (D), the middle–late Eocene (MP 16–19) Cadurcogekko piveteaui (the right maxilla MNHN QU 17734; modified from Augé 2005) (E), and Cadurcogekko cf. piveteaui (mirror inverted left maxilla NHMW 2019/0052/0001 originally described by Georgalis et al. 2021) (F).
Fig. 2 in An early Eocene pan-gekkotan from France could represent an extra squamate group that survived the K/Pg extinction
Fig. 2. Pan-gekkotan squamate Bauersaurus cosensis gen. et sp. nov. from Cos, France, early Eocene (MP 10–11). UM-COS-1013, right dentary, in lateral (A1), medial (A2), dorsal (A3) views (all micro-CT visualizations).
Fig. 8. Representative mammalian teeth from the J&M in New Late Cretaceous microvertebrate assemblage from the Campanian-Maastrichtian Williams Fork Formation, northwestern Colorado, USA, and its paleoenvironmental implications
Fig. 8. Representative mammalian teeth from the J&M site, Colorado, USA, Williams Fork Formation, Campanian–Maastrichtian, Upper Cretaceous. A. Meniscoessus sp., MWC 8848, incisor crown in labial (A1) and lingual (A1) views. B. Multituberculata indet., MWC 8863, tooth crown in occlusal (B1), lingual (B2), and distal (B3) views. C. cf. Cimolodon nitidus Marsh, 1889, MWC 8860, left p4 tooth crown in occlusal (C1), labial (C2), and lingual (C3) views. D.?Leptalestes cooki (Clemens, 1966), MWC 8859, tooth crown in occlusal (D1), labial (D2), and lingual (D3) views.
Fig. 3. Representative non-batoid chondrichthyans from the J&M in New Late Cretaceous microvertebrate assemblage from the Campanian-Maastrichtian Williams Fork Formation, northwestern Colorado, USA, and its paleoenvironmental implications
Fig. 3. Representative non-batoid chondrichthyans from the J&M site, Colorado, USA, Williams Fork Formation, Campanian–Maastrichtian, Upper Cretaceous. A–D. Lonchidion griffisi Case, 1987. A. MWC 8851, tooth crown in labial (A1) and occlusal (A2) views. B. MWC 9580, fragmentary tooth crown in labial (B1) and occlusal (B2) views. C. MWC 9581, fragmentary tooth crown in lingual (C1), labial (C2), and occlusal (C3) views. D. MWC 9582, fragmentary tooth crown in labial (D1) and occlusal (D2) views. E, F. Cantioscyllium markaguntensis Kirkland, Eaton, and Brinkman, 2013. E. MWC 8866, tooth crown in labial (E1) and occlusal (E2) views. F. MWC 9586, tooth crown in labial (F1) and lingual (F2) views. G, H. cf. Chilloscyllium sp. G. MWC 8850, morph 1 tooth crown in mesial (G1) and labial (G2) views. H. MWC 9576, morph 2 tooth crown in mesial (H1) and labial (H2) views. I . Hybodontoidea gen. et sp. indet., MWC 9800, dorsal fin spine in lateral view.
Fig. 5. Representative osteichthyan teeth from the J&M in New Late Cretaceous microvertebrate assemblage from the Campanian-Maastrichtian Williams Fork Formation, northwestern Colorado, USA, and its paleoenvironmental implications
Fig. 5. Representative osteichthyan teeth from the J&M site, Colorado, USA, Williams Fork Formation, Campanian–Maastrichtian, Upper Cretaceous. A, E. Paralbula casei Estes, 1969b. A. MWC 8855, tooth crown in occlusal (A1), basal (A2), and mesial (A3) views. E. MWC 8856, tooth crown in occlusal view. B. cf. Melvius sp., MWC 8867, tooth crown in labial view. C. Pycnodontiformes gen. et sp. indet., MWC 8873, tooth plate fragment in occlusal (C) view. D. Actinopterygii indet., MWC 8867, tooth crown in lateral (D) view. F. Dipnoi indet., MWC 8885, toothplate fragment in lateral view.
Fig. 7. Representative theropod dinosaur teeth from the J&M in New Late Cretaceous microvertebrate assemblage from the Campanian-Maastrichtian Williams Fork Formation, northwestern Colorado, USA, and its paleoenvironmental implications
Fig. 7. Representative theropod dinosaur teeth from the J&M site, Colorado, USA, Williams Fork Formation, Campanian–Maastrichtian, Upper Cretaceous. A. cf. Richardoestesia sp., MWC 8865, tooth crown in labial view (A1), mesial (A2) and distal (A3) serration detail views. B. Dromaeosauridae indet., MWC 8872, tooth crown fragment in lingual (B1), distal (B2) and mesial (B3) serration detail views. C. Hadrosauridae indet., MWC 8896, tooth crown in occlusal (C1) and lateral (C2) views.
Fig. 1 in The oldest representative of the bombyliid bee fly in the earliest Eocene French amber
Fig. 1. Bombyliid bee fly Eoconophorina delfineae gen. et sp. nov., holotype MNHN.F.A71306; earliest Eocene, Oise amber, France. Habitus above A 1), left wing (A 2), mid tibia (A 3, arrow indicates spur). Abbreviations: bm, basal medial cell; br, basal radial cell; cua, cubital cell; dm discal cell; dm-m discal-medial crossvein; m-m medial crossvein; r-m radial-median crossvein; M1, first branch of median vein; R2+3, second + third branch of radial vein; R4, fourth branch; R5, fifth branch.
Figures represent five groups respectively. In group, when the dispersal rate is equal to 1% values of the probability of disperser survival are 1, 0.9, 0.8, 0.7, 0.6, 0.5 respectively as in groups and in The Influence Of Dispersal On The Metapopulation Viability Of Giant Panda (Aliuropoda Melanoleuca) In The Minshan Mountains
Figures represent five groups respectively. In group, when the dispersal rate is equal to 1% values of the probability of disperser survival are 1, 0.9, 0.8, 0.7, 0.6, 0.5 respectively as in groups and
Figure 2. Representative trial format for showing side B in Avoidance of cold-, cool-, and warm-water fishes to Zequanox exposure
Figure 2. Representative trial format for showing side B (above centerline) treated first. Zequanox concentrations in mg/L as active ingredient (shaded area) for each side of the choice tank. One trial per species (n = 6) was sampled every 5 minutes during the control period and every 2 minutes thereafter. The control period was preceded by a 10-minute acclimation period.
Figure 1. a in Hirmoneura obscura (Wiedemann in Meigen, 1820) represents a family new to Albania
Figure 1. a. Black marking indicates the collecting locality of the Hirmoneura obscura (Wiedemann in Meigen, 1820) specimen. b. Habitus, dorsal view (scale bar = 10mm). c. Head, frontal view (scale bar = 1mm). d. Ovipositor, dorsal view (scale bar = 1mm).
FIGURE 1 in Representativity of the genus Asphondylia Loew, 1850 (Diptera, Cecidomyiidae) in Brazil
FIGURE 1: Distribution of the number of Asphondylia species (Diptera, Cecidomyiidae) per Brazilian biomes.
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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.