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Fig. 3. Tommotiid Camenella reticulosa Conway Morris, 1990 in The tommotiid Camenella reticulosa from the early Cambrian of South Australia: Morphology, scleritome reconstruction, and phylogeny
Fig. 3. Tommotiid Camenella reticulosa Conway Morris, 1990 from lower Cambrian Hawker Group, Flinders Ranges, Arrowie Basin, South Australia, mitral sclerites. A. SAMP 43164 (sinistral), Wilkawillina S; oblicate/accrescent view of sclerite showing wide radial ribs. B. SAMP 43165 (sinistral), MMF 0.0; obplicate/accrescent view of specimen with deep radial folds. C. SAMP 43166 (sinistral), Wilkawillina Q; C1, obplicate/ accrescent view of specimen with pointed apex; C2, decrescent view showing strong curvature of the aperture; C3, detail of shell ornament on accrescent side showing co−marginal ribs capped by nodes and a superimposed reticulation; C4, detail of smoothly rounded apex showing a circular depression. D. SAMP 43167 (sinistral), MMF 0.0; D1, oblique obplicate/accrescent view of small specimen; D2, apical view showing the almost equal development of radial ribs on plicate (lowermost in picture) and obplicate sides. E. SAMP 43168 (sinistral), MMF 0.0; oblique obplicate/accrescent view of specimen with minimal helical twist. F. SAMP 43169 (dextral), Bunyeroo 4b; F1, oblique apical/obplicate/decrescent view of abraded specimen with strong helical twist; F2, oblique apical/plicate/decrescent view showing angular deflection of strongly developed radial ribs on plicate side.
Fig. 1 in The tommotiid Camenella reticulosa from the early Cambrian of South Australia: Morphology, scleritome reconstruction, and phylogeny
Fig. 1. Simplified locality map showing sample localities within the Wilkawillina Limestone that yielded Camenella at Bunyeroo Gorge, Wilkawillina Gorge and the MMF section in the central Flinders Ranges (A). The regional context of all localities within South Australia is also depicted (B, C).
Fig. 3 in Taxonomy, phylogeny, and functional morphology of the foraminiferal genus Involutina
Fig. 3. Structural model of Involutina (in axial section). The presence of a semitube, as defined by Piller (1978), is only barely discernible in few of our specimens.
Fig. 1. A in Taxonomy, phylogeny, and functional morphology of the foraminiferal genus Involutina
Fig. 1. A. Map of Europe locating Austria (dark gray). B. Map showing the location of the Northern Calcareous Alps in the territories of Austria and Germany (grey). C. Enlargement of the area of Salzburg showing the Adnet locality. D. Location of the sampled quarry (Quarry XXXI). The quarry numbering follows that of Kieslinger (1964). E. Lithologic section of the quarry XXXI and samples location within the "marmorea-crust" (arrow).
Fig. 2 in A new Eliomys from the Late Miocene of Spain and its implications for the phylogeny of the genus
Fig. 2. The glirid mammals Eliomys yevesi sp. nov. (A–L) and Eliomys intermedius Friant, 1953 (M–U) from Spain, Villatoya-Venta del Moro Formation, Miocene (see Table 1 for locality name abbreviations). A. VVmA-42 (MGUV-27256), right p4. B. VVmA-1 (MGUV-27215), right m1, m2. C. VVmA- 6 (MGUV-27220), right m1, m2. D. VVmBC-5 (MGUV-27490), right m3. E. VVmA-40 (MGUV-27254), left P4. F. VVmA-16 (MGUV-27230), right M1, M2. G. VVmA-25 (MGUV-27239), right M1, M2. H. VVmA-13 (MGUV-27227), left M3. I. VVmA-14 (MGUV-27228), left M3. J. ABS3A-38 (MGUV-23529), right m1, m2. K. AF1'06-190 (MGUV-28334), right m1, m2. L. AF1'07-36 (MGUV-28427), left M1, M2. M. AC0-88 (MGUV-28551), right m3. N. LB2B-176 (MGUV-28727), right m1, m2. O. LB2B-241 (MGUV-28727), left M1, M2. P. LB2B-177 (MGUV-28728), left M3. Q. LB2B- 178 (MGUV-28729), left P4. R. AL2D-290 (MGUV-28063), left m1, m2. S. AL2D-356 (MGUV-28129), left m3. T. AL2D-291 (MGUV-28064), right M1, M2. U. AL2D-293 (MGUV-28066), left M1, M2.
Fig. 1 in A new Eliomys from the Late Miocene of Spain and its implications for the phylogeny of the genus
Fig. 1. Location of the Venta del Moro, Alcoy, Purcal, and Calicasas sites (stars) that have yielded specimens of Eliomys yevesi sp. nov. The dormouse symbol indicates the location of Venta del Moro, the type locality of E. yevesi. Abbreviations: ABS-3A, Alcoi Barranc Sud 3A; AF-1, Alcoi Forn 1; CLC-3B, Calicasas 3B; PUR-4, Purcal 4; VVm, Venta del Moro.
Fig. 5 in A new Eliomys from the Late Miocene of Spain and its implications for the phylogeny of the genus
Fig. 5. Early Vallesian (early Tortonian) to early Villanyan (Piacenzian) stratigraphic distribution and proposed phylogenetic relationships of the genus Eliomys (modified from García-Alix et al. 2008a). Abbreviations: ABS, Alcoi Barranc Sud; AC, Alcoy Cristian; AF, Alcoi Forn; AL, Alcoy; ALJ, Aljezar; ARQ, Arquillo; BLS, Barranco de Blas; CA/MN, Calatayud-Montalbán Basin; CB/AL, Cabriel and Alcoy Basins; CLC, Calicasas; DHS, Dehesa; ELMA, European Land Mammal Age; FOU, Lo Fournas; FRA, France; GER, Germany; GR/GU, Granada and Guadix Basins; HAU, Hautimagne; Ham, Hammerschmiede; LB, La Bullana; LC, Lomas de Casares; LG, La Gloria; LM, Los Mansuelos; MN, Mammal Neogene Units; ORR, Orrios; OTU, Otura; PE-2A, Pedregueras 2A; PUR, Purcal; SAR, Sarrión; SET, Sète; SOL, Solera; TCH, Tollo de Chiclana; TER, Teruel Basin; VAL, Villaba Alta; VVm, Venta del Moro; VP, Viveros de Pino. The double-headed arrow indicates the range of uncertainty.
Fig. 4. 50 in A new Eliomys from the Late Miocene of Spain and its implications for the phylogeny of the genus
Fig. 4. 50% majority rule consensus of the seven most parsimonious trees (L = 21, retention index = 0.619, consistency index = 0.619) resulting from the phylogenetic analysis. Numbers next to clades indicate the percentage of most parsimonious trees in which the clade was recovered. The extant glirid Dryomys nitedula, a form closely related to Eliomys, was chosen as outgroup.
Fig. 3 in A new Eliomys from the Late Miocene of Spain and its implications for the phylogeny of the genus
Fig. 3. Comparison of length and width measurements (in mm) of p4 (A), P4 (B), m1, m2 (C), M1, M2 (D), m3 (E), and M3 (F) of Eliomys truci from Aljezar B, Hautimagne, Los Mansuetos, Orrios, Sarrión, Sete, Villalba Alta (Adrover 1986), Concud 2 and 3, Concud Barranco de los Calaveros, Los Mansuetos, Masada del Valle 2, 5 and 7, Tortojada A and C (Weerd 1976), DHS-1 and 16, PUR-23, 24, and 25A, OTU-1, TCH-1B and 13 (García-Alix et al. 2008a), Negratín-1 (Minwer-Barakat et al. 2009); Moreda 1A, 1B, Rambla Seca 1 (Castillo 1990) and Puente Minero (Alcalá et al. 1991); Eliomys yevesi sp. nov. from VVm-A, B, BC, C, and D, ABS-3A, AF-1'06, AF-1'07, CLC-3B, and PUR-4; Eliomys intermedius from Arquillo 3, Sete, Orrios 3, Villalba Alta (Adrover 1986), Escorihuela, Orrios (Weerd 1976), PUR-13, TCH-1 and 1B, TCH3, TCH-13 (García-Alix et al. 2008), Moreda 1A, 1B, Bélmez 1 and Rambla Seca A1 and A2 (Castillo 1990) and Alozaina (Aguilar et al. 1993); Eliomys quercinus from Vallparadís and Cal Guardiola (Minwer-Barakat et al. 2011, Baños de Mula (Agustí et al. 1990), Peña de Estebanvela (Sesé 2006b), Valdocarros (Sesé et al. 2011), Sima de los Huesos (Cuenca-Bescós et al. 1997), Bois Roche (Sesé and Villa 2008), Santenay (Chaline 1972); and Eliomys aff. quercinus from Huétor Tájar 1 and 8.
Fig. 6. Two contrasting pterosaur phylogenies. A in The extent of the pterosaur flight membrane
Fig. 6. Two contrasting pterosaur phylogenies. A. Phylogeny from Lü et al. (2009). B. A simplified version of that presented by Wang et al. (2005). Thick black lines indicate species or groups of taxa for which the fossil evidence supports an ankle attachment of the wing.
Fig. 1 in Size does not matter: molecular phylogeny reveals one of the largest trematodes from vertebrates, the enigmatic Ithyoclinostomum dimorphum, as a species of Clinostomum (Trematoda: Clinostomidae)
Fig. 1. Metacercariae of Clinostomum dimorphum found in the erythrinid fish, Hoplias intermedius from Brazil: (A) Whole view of a paragenophore specimen. B) Detail of reproductive structures of a hologenophore specimen.
Fig. 2 in Size does not matter: molecular phylogeny reveals one of the largest trematodes from vertebrates, the enigmatic Ithyoclinostomum dimorphum, as a species of Clinostomum (Trematoda: Clinostomidae)
Fig. 2. Maximum likelihood phylogram based on the concatenated ITS1-5.8S-ITS2 + 28S + cox1 datasets of Clinostomum dimorphum (in bold) and selected species of the family Clinostomidae. Clade formed by isolates of 'Ithyoclinostomum' yamagutii (incertae sedis) is highlighted in grey. Taxon names are followed by GenBank accession numbers of ITS, 28S, and cox1, respectively, and country of record. Branch length scale bar indicates number of substitutions per site. Abbreviations: HON, Honduras; ITA, Italy; KEN, Kenya; MEX, Mexico; THAI, Thailand; USA, United States of America.
Fig. 5 in Morphology, molecular characterization and phylogeny of Bolbosoma nipponicum Yamaguti, 1939 (Acanthocephala: Polymorphidae), a potential zoonotic parasite of human acanthocephaliasis
Fig. 5. Phylogenetic relationships of representatives of the family Polymorphidae using Bayesian inference based on the 18S + ITS +28S + cox1 sequence data. Centrorhynchus clitorideus (Polymorphida: Centrorhynchidae) was chosen as outgroup. Bayesian posterior probabilities values> 0.70 are shown in the phylogenetic tree.
Fig. 4 in Morphology, molecular characterization and phylogeny of Bolbosoma nipponicum Yamaguti, 1939 (Acanthocephala: Polymorphidae), a potential zoonotic parasite of human acanthocephaliasis
Fig. 4. Phylogenetic relationships of representatives of the family Polymorphidae using maximum likelihood method based on the 18S + ITS +28S + cox1 sequence data. Centrorhynchus clitorideus (Polymorphida: Centrorhynchidae) was chosen as outgroup. Bootstrap values> 50 are shown in the phylogenetic tree.
Fig. 3 in Morphology, molecular characterization and phylogeny of Bolbosoma nipponicum Yamaguti, 1939 (Acanthocephala: Polymorphidae), a potential zoonotic parasite of human acanthocephaliasis
Fig. 3. Scanning electron micrographs of Bolbosoma nipponicum collected from Callorhinus ursinus (Linnaeus) (Carnivora: Otariidae) in St. Paul Island, Alaska. A: anterior part of male; B: trunk spines; C: proboscis; D: hooks.
Fig. 2 in Morphology, molecular characterization and phylogeny of Bolbosoma nipponicum Yamaguti, 1939 (Acanthocephala: Polymorphidae), a potential zoonotic parasite of human acanthocephaliasis
Fig. 2. Photomicrographs of Bolbosoma nipponicum collected from Callorhinus ursinus (Linnaeus) (Carnivora: Otariidae) in St. Paul Island, Alaska. A: anterior part of male; B: proboscis; C: posterior part of male; D: posterior part of female.
Fig. 1 in Morphology, molecular characterization and phylogeny of Bolbosoma nipponicum Yamaguti, 1939 (Acanthocephala: Polymorphidae), a potential zoonotic parasite of human acanthocephaliasis
Fig. 1. Bolbosoma nipponicum collected from Callorhinus ursinus (Linnaeus) (Carnivora: Otariidae) in St. Paul Island, Alaska. A: female; B: hooks; C: proboscis; D: male; E: trunk spines; F: testes and cement-glands; G: poster part of female. Scale bars: A, D = 1000 μm; B = 100 μm; C = 200 μm; E = 50 μm; F, G = 500 μm.
Fig. 3 in Characterization of the mitochondrial genome of Tetrameres grusi and insights into the phylogeny of Spirurina
Fig. 3. Phylogenetic relationships of Tetrameres grusi with other 24 Spirurina species based on concatenated amino acid sequences of 12 PCGs analyzed by BI and ML using Bunostomum phlebotomum as outgroup. Posterior probability values are indicated.
Fig. 2 in Characterization of the mitochondrial genome of Tetrameres grusi and insights into the phylogeny of Spirurina
Fig. 2. Mitogenome arrangement in Tetrameres grusi compared with those in Spirurina nematodes. The circular mitogenomes were linearized at the 5′ end of cox1 gene for illustration purpose. Non-coding regions were not shown. Triangular markers of the same color represent the corresponding duplicated genes. The purple frames represent the duplicated gene fragments.
Fig. 1 in Characterization of the mitochondrial genome of Tetrameres grusi and insights into the phylogeny of Spirurina
Fig. 1. Gene map of the mitogenome of Tetrameres grusi. PCGs are colour-coded (cox: lavender; nad: yellow; atp: green; cyt: purple); rRNAs are in red; tRNAs are in dark blue. Abbreviations of PCGs are: atp6 for ATP synthase subunits 6, cox1–3 for cytochrome oxidase subunits 1–3, cytb for cytochrome b, nad1–6 and nad4L for NADH dehydrogenase subunits 1–6 and 4L, rrnL and rrnS for large and small rRNA subunits, 22 tRNAs are designated by the one-letter code for the corresponding amino acid, with numerals differentiating each of the two leucine and serine-specifying tRNAs (L1 and L2 for codon families CUN and UUR, respectively; S1 and S2 for codon families UCN and AGN, respectively), NCR refers to Noncoding region. All genes are transcribed in the clockwise direction.
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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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