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FIGURE 6 in The intriguing shapes of the ammonoid whorl
FIGURE 6. Boxplots for the first three principal components for the subtaxa used in this work. A) Subtaxa against PC1. B) Subtaxa against PC2. C) Subtaxa against PC3.
FIGURE 6. DMNH 2013-07-1942 in A revision of "Trinitichelys" maini (Testudinata: Baenidae) and additional material of its new genus from the Lewisville Formation (Woodbine Group, Cenomanian), Texas, USA
FIGURE 6. DMNH 2013-07-1942, Gehennachelys maini comb. nov. shoulder girdle and forelimb bones. Partial left scapula of DMNH 2013-07-1942 in A, posteromedial, and B, anterolateral views. Partial right scapula of DMNH 2013- 07-1942 in C, posteromedial, and D, anterolateral views. Partial right scapula of DMNH 2013-07-0601 in E, posteromedial, and F, anterolateral views. Right coracoid of DMNH 2013-07-1942 in G, dorsal, and H, ventral views. Partial left coracoid of DMNH 2013-07-1942 in I, dorsal, and J, ventral views. Right humerus in K, posterior, L, dorsal, M, proximal, N, distal, O, ventral, and P, posterior views. M and N are oriented with B.
FIGURE 6 in A Pliocene goodeid fish of the Paleolake Amajac, Sanctórum, Hidalgo, Mexico
FIGURE 6. μCT imagens of IGM 13127, paratype of Paleocharacodon guzmanae gen. and sp. nov., from the lacustrine sediments of the Paleolake Amajac, in Sanctórum, Atotonilco El Grande Municipality, Hidalgo, central Mexico. A) Left side of the head and anterior part of the trunk. B) Quadrate and bones of both jaws exposed on the right side. C) Close-up of bones involved in the articulation quadrate-lower jaw showing the bilobed head of the quadrate and the articular facet of the anguloarticular in which there is a central participation of the retroarticular (here disarticulate and displaced from its normal position) and two enveloping projections of the anguloarticular. D) Right view of the hyoid arch. The scale only applies to A, B and D. Abbreviations: 1, 2a, 2b, 3, pores of the supraorbital sensory canal; aa, anguloarticular; bh, basihyal; br, brachiostegal ray; bst, bicuspid sharp tooth; cha, ceratohyal anterior; chp, ceratohyal posterior; cl, cleitrum; co, coronomeckelian; id; cor, coracoid; d, dentary; dsp, dermosphenotic; entp, entopterygoid; epi, epioccipital; fr, frontal; hy, hyomandibula; ih, interhyal; iop, infraopercle; let, lateral ethmoid; mx, maxilla; na, nasal; op, opercle; pa, parietal; pcli, postcleitrum inferior; pmx, premaxilla; pop, preopercle; psp, parasphenoid; ptt, posttemporal; q, quadrate; r, rib; rar, retroarticular; scl, supracleitrum; soc, supraoccipital; sp, sphenotic; sop, subopercle; sy, symplectic; uh, urohyal; ust, unicuspid sharp tooth; utt, unicuspid truncated tooth; vhh, ventral hypohyal; dubious elements; within parenthesis: i, internal view (if it is not indicated, the structures show the right view); l, left; r, right; va, ventroanterior view; vp, ventroposterior view.
FIGURE 6 in Middle Eocene cartilaginous fishes (Vertebrata: Chondrichthyes) of the Dnieper-Donets Basin, northern Ukraine
FIGURE 6. Lamniform shark teeth from the middle Eocene deposits of Vyshhorod: A-H – Macrorhizodus praecursor (Leriche, 1905), anterior teeth NMNHU-G 391/101 (A-B), anterolateral teeth NMNHU-G 391/103 (C-D), 391/69 (E-F), anterior tooth NMNHU-G 391/68 (G-H); I-P – Otodus (Carcharocles) sp., upper lateral tooth NMNHU-G 391/32 (I-J), lower anterolateral teeth, NMNHU-G 391/35 (K-M), lower anterolateral tooth NMNHU-G 391/26 (N-P). Labial view in A, C, E, G, I, K, and N, lingual view in B, D, F, H, J, M, and O, mesial view in L and P.
FIGURE 6 in Approaching the Khersonian Crisis: Fish otoliths from the upper Bessarabian (middle Sarmatian s.l.; Late Miocene) of Jurkine (Kerch Peninsula, Crimea)
FIGURE 6. Idealized block diagram depicting Bessarabian environmental settings and distribution of otolith-based taxa of the Gobiidae in the various environments of the middle Sarmatian s.l. (Bessarabian) (after Bratishko et al., 2017; Bratishko et al., 2023; and this study). Not to scale.
FIGURE 6 in Bioerosion traces on the Campanian turtle remains: New data from the lagoonal deposits of the Quseir Formation, Kharga Oasis, Egypt
FIGURE 6. Palaeoecology and post-mortem stages of the three turtle-bearing horizons in the Qarn Ganah area, Kharga Oasis, Egypt. (A) A sketch showing the proposed life of side-necked turtle (Bothremydidae) living in small isolated ponds during the Campanian time. (B‒D) A proposed model for the formation of the three horizons of turtle concentrations.
FIGURE 6. Caddisfly larva morphotype 3 in Unique fossils of caddisfly larvae from Baltic amber and in situ amber formation in aquatic ecosystems
FIGURE 6. Caddisfly larva morphotype 3, Leptoceridae, PED 1635, volume renders of µCT-scans. A, Lateral view. B, Lateral view, other side. C, Fronto-lateral view, case partially removed. D, Frontal view. E, Colour-marked version of D. F, labeled head. Abbreviations: at = antenna; md = possible mandibles.
FIGURE 6 in On the "screamer-like" birds from the British London Clay: An archaic anseriform-galliform mosaic and a non-galloanserine "barb-necked" species of Perplexicervix
FIGURE 6. Danielsavis nazensis Houde et al., 2023, comparison of tibiotarsus, tarsometatarsus, pedal phalanges with other galloanserine birds. A, D. nazensis (holotype, NMS.Z.2021.40.1), distal end of right tibiotarsus; the arrow denotes an enlarged detail of the bone. B, distal end of right tibiotarsus of the anseriform Saintandrea chenoides from the late Oligocene of France (holotype, NMB Mar. 874e). C, mirrored distal end of left tibiotarsus of an unnamed galliform from the early Eocene of Egem in Belgium (IRSNB Av 168); coated with ammonium chloride. D‒G, D. nazensis (holotype, NMS.Z.2021.40.1), right tarsometatarsus in distal (D), proximal (E), dorsal (F), and plantar (G) view; the arrow denotes an enlarged detail of the proximal end of the bone. H, I, D. nazensis (NMS.Z.2021.40.3), proximal end of right tarsometatarsus in proximal (H) and plantar (I) view. J, D. nazensis (NMS.Z.2021.40.3), distal end of right tarsometatarsus in plantar view; the arrow denotes an enlarged detail of the bone. K, D. nazensis (holotype, NMS.Z.2021.40.1), non-ungual pedal phalanges; the asterisk indicates a mirrored phalanx. L, mirrored left foot of Chauna torquata (Anhimidae, Anseriformes; SMF 19920). M, right foot of Pavo cristatus (Phasianidae, Galliformes; SMF 20342). N, mirrored distal end of left tarsometatarsus of Anachronornis anhimops (holotype, coated with ammonium chloride; from Houde et al., 2023: figure 2, published under a CC BY 4.0 license) in plantar view. The dotted lines in A‒C indicate the midline of the distal tibiotarsus. The arrows in K‒M denote the length of the third phalanx of the fourth toe. Abbreviations: cdl, condylus lateralis; cdm, condylus medialis; cmh, crista medialis hypotarsi; ext, sulcus extensorius; fdl, sulcus for musculus flexor digitorum longus; fhl, sulcus for musculus flexor hallucis longus; ltr, lateral rim of plantar articular surface of trochlea metatarsi III; mdr, medial rim of plantar articular surface of trochlea metatarsi III; pst, pons supratendineus. The scale bars equal 10 mm.
FIGURE 6. Fossil larva BUB 4436, specimen 3. A. Overview dorsal side. B in An overview of crawling water beetle larvae and a first possible record from 100-million-years-old Myanmar amber
FIGURE 6. Fossil larva BUB 4436, specimen 3. A. Overview dorsal side. B. Colour-marked version of B. C. Ventral side. D. Close-up on anterior region in ventral view. E. Close-up on head. F. Close-up on very terminal end. Abbreviations: ad = abdomen; at = antenna; hc = head capsule; ms = mesothorax; mt = metathorax; pt = prothorax; te = trunk end.
FIGURE 6 in Wear-dependent molar morphology in hypsodont rodents: The case of the spalacine Pliospalax
FIGURE 6. Three-dimensional model visualizing the sequence of the wear stages (6.1-6.12) for the m1 of Pliospalax tourkobouniensis (TB1-901), from the locality of Tourkobounia-1 in Greece (De Bruijn and Van der Meulen, 1975). Labial and occlusal view. The scale bars apply to all panels of the figure.
FIGURE 6 in Report from the 8th Symposium on Fossil Decapod Crustaceans, Zaragoza (Spain), June 2022
FIGURE 6 (left). Brachyuran Distefania incerta (Bell, 1863) from the Koskobilo quarry (Navarra). FIGURE 7 (right). Javier Luque (University of Cambridge) showing two specimens of Joer- anina gaspari Van Bakel et al., 2012 from the lower upper Albian of Egiarreta outcrop preserved in concretions (Navarra).
FIGURE 4. Fossil larvae BUB 4436, specimens 1 and 6. A–D. Specimen 1. A in An overview of crawling water beetle larvae and a first possible record from 100-million-years-old Myanmar amber
FIGURE 4. Fossil larvae BUB 4436, specimens 1 and 6. A–D. Specimen 1. A. View on one side. B. Colour-marked version of A. C. View on other side. D. Very terminal end, with different contrasting to highlight the setae. E–G. Specimen 6. E. Overview. F. Colour-marked version of E. G. Close-up on very terminal end. Abbreviations: ad = abdomen; at = antenna; hc = head capsule; ms = mesothorax; mt = metathorax; pt = prothorax; te = trunk end.
FIGURE 6 in Dental ecomorphology and macroevolutionary patterns of North American Late Cretaceous metatherians
FIGURE 6. Patterns of taxonomic diversity and dietary diversity of NALK metatherians. Top: Known taxonomic diversity (gray squares and line) of NALK metatherians and the metatherian diversity sampled in this study (black circles and line). Middle: Dietary diversity of NALK metatherians through time (out of six dietary categories). Judithian diversity count is based on our DFA classification of Iugomortiferum thoringtoni as a carnivore. Bottom: Hypothesized phylogenetic relationships of NALK metatherians sampled in this study (the deltatheriid Atokatheridium boreni was removed). The phylogeny is modified from Williamson et al. (2014), Wilson et al. (2016), and Cohen et al. (2020). Thick horizontal bars represent the known temporal range of each species. Bar colors represent the dietary categories assigned to each taxon in this study. For cases in which specimens of the same species were classified differently, we include both classifications in this figure, with the exception of Iugomortiferum thoringtoni and Didelphodon vorax. Our DFA classification for Iugomortiferum thoringtoni (carn) contradicts additional lines of evidence that suggests it is a plant-dominated omnivore (see Discussion), and thus we classify it here as 'carn/pdo.' Our DFA classifies the two Didelphodon vorax specimens as an animal-dominated omnivore and an invertivore, but additional lines of evidence suggest that it is an animal-dominated omnivore (see Discussion). Abbreviations for diet categories: ado = animaldominated omnivore; carn = carnivore; frug = frugivore; inv = invertivore; pdo = plant-dominated omnivore; sis = softinvertebrate specialist. Abbreviations for NALMAs: Aquil = Aquilan; La = Lancian.
FIGURE 6 in Morphospace dynamics and intraspecies variety of Sorex araneus and S. tundrensis according to recent and fossil data
FIGURE 6. Hemimandible shape transformation along of PC1 (morphospace see on Figure 5B). A1, Shape transformation toward of the negative end of PC1 (corresponding to S. tundrensis). A2, Hemimandible of S. tundrensis (ZIN 107833/1149, PtU) in medial view, with an impose mandibular ramus contour of S. araneus (B2). B1, Shape transformation toward of the positive end of PC1 (corresponding to S. araneus). B2, Hemimandible of S. araneus (ZIN 96960; Ser'ga Riv., Mid. Ural). C, Inset from Figure 5B: result of PCA. Key: a, shape change in the posterior shift of the whole cheek-teeth row, with shortening the 'angle' between the m3 posterior alveolus and the mandibular ramus base; b, shape change in the anterior overall inclination of the mandibular ramus; c, shape change in the anterior shift of the condylar process.
FIGURE 6 in First report of rodents from the Miocene Siwalik locality of Dunera, Pathankot District, Punjab, India
FIGURE 6. Scatterplot of molar size (sq. root of width*length) vs. shape (max. width/length) in Siwalik murid specimens. A) M1; B) M2; C) m1; D) m2; E) m3. See Appendix for data used in the plots.
FIGURE 6 in Trilobite moulting behaviour variability had little association with body proportions
FIGURE 6. Scatterplots of the total dataset, for each metric morphometry variable. Data is grouped by mode of moulting (see legend). Linear regression lines represent the MANCOVA analysis models (see text).
FIGURE 6. A in An intriguing new species of dabbling duck (Aves: Anseriformes) from the middle Miocene of Austria
FIGURE 6. A, skull and pelvis of Lavanttalornis hassleri gen. et sp. nov., holotype, specimen LMK-Pal 7453c from Lavanttal, Austria, middle Miocene (preserved on slab C); B, pelvis of Anas platyrhynchos (Anatinae: Anatini); C, pelvis of Aythya fuligula (Anatinae: Aythyni). Abbreviations: ant, antitrochanter; fin, foramina intertransversaria; isc, ala ischii; nos, nostril; poi, ala postacetabularis ilii; pri, ala preacetabularis ilii; ram, ramus mandibulae (inside surface of right branch). Scale bars equal 10 mm.
FIGURE 6 in Ethological interpretation of making the pellet designs by the bubbler crab Dotilla on the modern intertidal beaches: A study from the Bay of Bengal coast, Eastern India
FIGURE 6. Other pellet structures produced by the crab Dotilla on the upper intertidal flat of the Bakkhali beach, Bay of Bengal coast of Eastern India. (A) Petaloid pellet design produced by petal shaped radial rows of pellets and conjugate petals formed around burrow opening. (B) The line tracing corresponding to A shows SI value 100% as the burrow mouth is closed. (C) Leaf-shaped pellet design and (D) its corresponding line tracing shows very poor SI value (13.89%). (E) Asteroid pellet design contains several radiating runways that are well enclosed within the pellet spread areas and (F) its corresponding line tracing shows 100% SI value. (G, J and K) Different stages of formation of pellet mat design in pellet – microzone 1 wherein entire surface is covered by dense population of pellets leaving no space for the predators to sneak into burrow opening (SI = 100%). Note high population density and small size of the pellet designs. (H) Mossy pellet design formed by the crab community. Several burrow openings and corresponding runways are partially to fully covered by pellet spread zones. (I) Line tracing shows variable SI values of the individual structures (marked here by red, yellow and green circles having SI values <70%, 70% - 90% and> 90% respectively) averaged at 85% for the community structure. Arrows indicate possible entry routes of predators into the burrows. (L and M) Concentric radial and concentric pellet structures formed on rippled surface. (N) At times, pellets are formed selectively along the ripple troughs. (O) Beach profile showing extends of lower, middle and upper intertidal flats, besides mudground, supratidal flat and coastal dunes. Note smaller size of the structures (G, H, J, K) due to increased population density and predation pressure.
FIGURE 6 in The earliest fossil evidence of spiny feather (pinnate-leaved) palms from the K-Pg of Gondwana
FIGURE 6. Spines on the rachises of different species of modern pinnate palms. (A) Astrocaryum sciophilum (Miq.) Pulle, 1916; (B) Plectocomia dransfieldiana Madulid, 1981; (C) Aiphanes horrida (Jacq.) Burret, 1932; (D) Acrocomia totai Martius, 1944; (E) Astrocaryum murumuru Martius, 1824; (F) Bactris gasipaes Kunth, 1816; (G) Desmoncus chinantlensis Liebm. ex Martius, 1853; (H) Aiphanes verrucosa Borchsenius and Balslev, 1990; (I) Astrocaryum mexicanum Liebm. ex Martius, 1853 (scale bars = 1 cm, source: The Herbarium Catalogue, Royal Botanic Garden, Kew, published on the internet http://www.kew.org/herbcat).
FIGURE 6 in A feeding organ the basihyal and thyrohyal tells which size of prey do true baleen whales (Cetacea, Chaeomysticeti) eat
FIGURE 6. Morphological traits of the basihyal and thyrohyal among the Chaeomysticeti separated by prey types. Boxes gray in colour are extinct baleen whales, which ID number 4, 8, 11, 33, 40, 53, 61, 70 in Table 2 are used here. Piscobalaena nana shows two different types of phylogenetic hypotheses (see in cladogram section).
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Allen Brain Atlas
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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.
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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.
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