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FIG. 7 in Anatomy, affinities, and evolutionary implications of new silicified stems of Sphenophyllum Brongniart, 1828 from the early Carboniferous (Mississippian) of France and Germany
FIG. 7. — Reconstruction of MN911 at the level of branching based on a series of transverse sections. Because only the base of the leaves is well known, their tips are represented in dashed lines. Sections 1-6 correspond to polished surfaces MN911-B1i, MN911-B1s, MN911-B2i, MN911-B2s, MN911-B3i, and MN911- B3s; sections 7 and 8 correspond to slides MN911-A1 and MN911-A2. Artwork by Bernard Terreaux.
FIG. 2 in Anatomy, affinities, and evolutionary implications of new silicified stems of Sphenophyllum Brongniart, 1828 from the early Carboniferous (Mississippian) of France and Germany
FIG. 2. — General aspect of the specimens in transverse section at the same scale. The primary xylem is in dark grey, the secondary xylem – when present – is in black. A, MN201(slide MN201-E2); B, same specimen as A at a level of branching (slide MN201-F1); C, largest axis resulting from the branching of MN911 with two leaf bases (slide MN911-A1); D, same axis as in C at another level with one leaf base and the production of two traces from one arm of the stele (slide MN911-A2); E, smallest axis resulting from the branching of MN911 (slide MN911-A2); F, MN864 showing secondary xylem all around the stele (slide MN864-C1); G, KLC3 showing a small amount of secondary xylem (slide KLC3-C); H, KLC4 showing a small amount of secondary xylem like KLC3 but a much smaller cortex (slide KLC4-B2). Scale bar: 2 mm.
FIG. 1 in Anatomy, affinities, and evolutionary implications of new silicified stems of Sphenophyllum Brongniart, 1828 from the early Carboniferous (Mississippian) of France and Germany
FIG. 1. — Maps showing the location of the localities in Southern France (A) and Thuringia, Germany (B). Detailed maps modified from Galtier et al. 1988 and Meyer-Berthaud & Rowe 1997.
Fig. 7 in Reproduction of two loricariid species in a confined river and implications for environmental impacts of dams
Fig. 7. Monthly changes in mean (± SE) gonadosomatic index (GSI; dots represent individual values) of Hemiancistrus fuliginosus (a. females; c. males) and Hypostomus isbrueckeri (b. females; d. males). Results of the Kruskal-Wallis tests: Hem. fuliginosus females, H = 47.5, df = 7, p <0.001; males, H = 6.9, df = 7, p <0.44; Hyp. isbrueckeri females, H = 14.4, df = 7, p <0.045, males H = 20.4, df = 7, p <0.005.
FIGURE 4 in Bite marks attributable to Tyrannosaurus rex: preliminary description and implications
FIGURE 4. Edmontosaurus proximal pedal phalanx (UCMP 140601) bearing tyrannosaur-like "puncture and pull" bite mark furrows. The specimen bears five such bite marks (three are visible). The furrows are deeper proximally suggesting the element was somewhat articulated at the time of feeding. Scale = 2.5 cm.
FIGURE 1 in Bite marks attributable to Tyrannosaurus rex: preliminary description and implications
FIGURE 1. Photographs of Tyrannosaurus rex bite marks on an adult Triceratops pelvis (MOR 799). Anterolateral view of the ventral surface of the sacrum and left ilium of the specimen. Arrows point to some of the more prominent tooth marks (over 58 definitive tooth marks are present on the pelvis). Furrows from "puncture and pull" biting and deep localized punctures are visible. Brackets encompass a region where the theropod(s) removed approximately one sixth of the anterior ilium via repetitive peripheral biting. Scale = 25 cm.
Reproduction package for the paper "The effects of surface fossil magnetic fields on massive star evolution - II. Implementation of magnetic braking in MESA and implications for the evolution of surface rotation in OB stars "
<p>This is a reproduction package for the paper "The effects of surface fossil magnetic fields on massive star evolution - II. Implementation of magnetic braking in MESA and implications for the evolution of surface rotation in OB stars" by Keszthelyi et al. (2020), https://doi.org/10.1093/mnras/staa237</p>
Fig. 1 in Is the Egyptian fruit-bat Rousettus aegyptiacus a pest in Israel? An analysis of the bat's diet and implications for its conservation
Fig. 1. Monthly mean number of droppings (with standard error bars) of Rousettus aegyptiacus in Nachash and Rakefet caves during 1994 and 1995. Samples collected from three 1 m2 sheets during 48 h each month.
Fig. 2 in Molecular phylogeny of Blaberidae (Dictyoptera, Blattodea), with implications for taxonomy and evolutionary scenarios
Fig. 2. Conflicting results among different molecular markers. The phylogenetic relationships of four species are detailed for separate and combined analyses performed in Maximum Likelihood (ML) and Bayesian Inference (BI). Boxes colored as 'Untested or unresolved' refer to missing data and multifurcation, respectively.
Fig. 1 in Molecular phylogeny of Blaberidae (Dictyoptera, Blattodea), with implications for taxonomy and evolutionary scenarios
Fig. 1. [part 2 on next page] Optimal phylogenetic tree reconstructed in Maximum Likelihood with the combined dataset. Bootstrap values and posterior probabilities are reported for each node (bootstrap values below 25% are not displayed). The color of internal branches is proportional to bootstrap values. Geographic origin of the specimens sequenced is provided in brackets after the species names. In purple, monophyletic group congruent with morphological hypotheses; in blue, monophyletic group with geographic consistency at the continental level; in brown, incertae sedis species; in green, four species with conflicting and supported positions (Thanatophyllum akinetum Grandcolas, 1991 and Phoetalia pallida (Brunner von Wattenwyl, 1865) or congruent, but weakly supported positions (Laxta sp. and Pronauphoeta cf. viridula (Palisot de Beauvois, 1805)). The four latter species are discussed in the text (see also Fig. 2). The subfamilies indicated on the right of the tree are derived from traditional morphology-based classifications. Units for the branch length scale at the bottom right: number of expected substitutions per site.
Raw data for: Sex and Power: Sexual dimorphism in trait variability and its eco-evolutionary and statistical implications
<p>This is a dataset obtained from the EBI in August 2018. The full code, analyses and processed data that are associated with the paper that is based on this large dataset can be found here: <a href="https://github.com/itchyshin/mice_sex_diff">https://github.com/itchyshin/mice_sex_diff</a></p> <p> </p>
Tectono-stratigraphic and thermal evolution of the western Betic flysch: implications for the geodynamics of South Iberian margin and Alboran Domain
<p>Table and Figure from article "<strong>Tectono-stratigraphic and thermal evolution of the western Betic flysch: implications for the geodynamics of South Iberian margin and Alboran Domain" accepted to AGU, Tectonics</strong></p>
Fig. 7 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 7 (opposite page). Kalloconus canariensis sp. nov. A–B. Holotype (dorsal and ventral views), 89.0 mm (MNCN 15.05/200091H). C. Paratype 1, 85.3 mm (MNCN 15.05/200091P). D. Paratype 5, 76.3 mm (MNCN 15.05/200092). E. Paratype 3, 92.1 mm (MNCN 15.05/200093). F. Paratype 2, 132.0 mm (MNCN 15.05/200094). G. Paratype 4, 93.9 mm (MNCN 15.05/200092). H. Paratype 6, 47.4 mm (MNCN 5.05.200091P). I. Paratype 7, 43.3 mm (MNCN 15.05/200095). J–K. Radular tooth. K. K. canariensis sp. nov., paratype 1. K. K. pulcher ([Lightfoot], 1786), Joal Fadiouth, Senegal (MJT), SL = 96.7 mm. Scale bars = 10 mm unless otherwise indicated
Fig. 8 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 8. Plot of maximum diameter (MD, mm) versus shell length (SL, mm) for K. canariensis sp. nov. (Ɨ) and K. pulcher ([Lightfoot], 1786) (-). The lectotype of K. siamensis (Hwass in Bruguiére, 1792) (A) is also shown.
Fig. 6 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 6 (opposite page). A. Conus navarroi navarroi Rolán, 1986, holotype, 16 mm (MNCN 15.05/1008). B. Africonus angeluquei Tenorio, Abalde & Zardoya, 2018 (= perrineae Cossignani & Fiadeiro, 2018), holotype, 30.0 mm (MNCN 15.05/78710). C. Conus raulsilvai Rolán, Monteiro & Fernandes, 1998, holotype, 19.7 mm (MNCN 15.05/27230). D. Conus regonae Rolán & Trovão, 1990, holotype, 32.7 mm (MNCN 15.05/1092). E. Conus roeckeli Rolán, 1980, holotype, 13.2 mm (MNCN 15.05/1049). F. Africonus salletae Cossignani, 2014, holotype, 15.5 mm (MMM). G. Africonus santaluziensis Cossignani & Fiadeiro, 2015, paratype, 28.1 mm (Paul Kersten coll.). H. Africonus santanaensis Afonso & Tenorio, 2014, holotype, 17.1 mm (MNCN 15.05/60118). I. Conus saragasae Rolán, 1986, holotype, 21.8 mm (MNCN 15.05/1009). J. Africonus verdensis (Trovão, 1979), 22.5 mm (MNCN 15.05/78864). K. Conus vulcanus Tenorio & Afonso, 2004, holotype, 25.2 mm (MNCN 15.05/46652). L. Chelyconus ermineus (Born, 1778), 54.3 mm (MNCN 15.05/80014). M. Genuanoconus genuanus (Linnaeus, 1758), 50.2 mm (MNCN 15.05/78547). N. Kalloconus ateralbus (Kiener, 1850), 40.1 mm (MNCN 15.05/79649). O. Kalloconus byssinus (Röding, 1798), 56.4 mm (MNCN 15.05/90429). Scale bars = 10 mm.
Fig. 2 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 2. Phylogenetic relationships of West African cones and species delimitation. A time tree (relaxed molecular clock) was reconstructed following methods and calibrations in Abalde et al. (2017a). Dates are in million years. Bold names indicate new mitogenomes. A red line indicates the threshold (uncorrected p distance of 0.2%, based on the divergences between Africonus verdensis (Trovão, 1979) and its sister group and Varioconus guanche (Lauer, 1993) and its sister group) for species delimitation.
Fig. 10 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 10 (opposite page). A. Conus ambiguus Reeve, 1844, neotype, 39.3 mm (NBC). B. Conus bellocqae van Rossum, 1996, paratype, 60 mm (F. Gubbioli coll., Marbella, Spain). C. Monteiroconus tabidus (Reeve, 1844), 33.6 mm (MNCN 15.05/78864). D. Conus belairensis Pin & Leung Tack in Pin, 1989, holotype, 36.7 mm (MNHN IM-2000-32668). E. Varioconus bruguieresi (Kiener, 1846) comb. nov., 32.1 mm (MNCN 15.05/78497). F. Varioconus cloveri (Walls, 1978) comb. nov., 23.2 mm (MNCN 15.05/78457). G. Varioconus echinophilus (Petuch, 1975b) comb. nov., 22.0. mm (MNCN 15.05/90430). H. Conus franciscanus Hwass in Bruguière, 1792, lectotype, 56.6 mm (MHNG-MOLL-52625). I. Varioconus franciscanus (Hwass in Bruguière, 1792) comb. nov., 53.6 mm (MNCN 15.05/78491). J. Varioconus franciscanus f. hybridus (Kiener, 1847), 40.0 mm (MNCN 15.05/78427). K. Conus guanche Lauer, 1993, holotype, 34.0 mm (MNHN IM-2000-2553). L. Conus guinaicus Hwass in Bruguière, 1792, lectotype, 43.0 mm (MHNG-MOLL-52638). M. Varioconus guinaicus (Hwass in Bruguière, 1792) comb. nov., 50.2 mm (MNCN 15.05/78443). N. Lautoconus wolof Petuch & Berschauer, 2018, holotype, 21.1 mm (MNHN IM-2000-34015). O. Conus pineaui Pin & Leung Tack in Pin, 1989, holotype, 28.7 mm (MNHN IM-2000-2528). P. Conus dorotheae Monnier & Limpalaër, 2010, holotype, 26.8 mm (MNHN IM-2009-8702). Scale bars = 10 mm.
Fig. 4 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 4 (opposite page). A. Conus felitae Rolán, 1990, holotype, 12.7 mm (MNCN 15.05/1099). B. Africonus fernandesi (Tenorio, Afonso & Rolán, 2008), 14.5 mm (MNCN 15.05/78598). C. Africonus freitasi Tenorio, Afonso, Rolán, Pires, Vasconcelos, Abalde & Zardoya, 2018, holotype, 13.7 mm (MNCN 15.05/200008) D. Conus verdensis furnae Rolán, 1990, holotype, 21.1 mm (MNCN 15.05/1097). E. Africonus fuscoflavus (Röckel, Rolán & Monteiro, 1980), 22.3 mm (MNCN 15.05/80407). F. Conus damottai galeao Rolán, 1990, holotype, 21.3 mm (MNCN 15.05/1093). G. Africonus gonsaloi Afonso & Tenorio, 2014, holotype, 19.3 mm (MNCN 15.05/60119). H. Africonus grahami (Röckel, Cosel & Burnay, 1980), 24.0 mm (MNCN 15.05/78549). I. Conus infinitus Rolán, 1990, holotype, 20.8 mm (MNCN, 15.05/1095). J. Conus isabelarum Tenorio & Afonso, 2004, holotype, 22.8 mm (MNCN 15.05/46654). K. Conus josephinae Rolán, 1980, holotype, 25.8 mm (MNCN 15.05/1050). L. Africonus kersteni (Tenorio, Afonso & Rolán, 2008), holotype, 20.8 mm (MNCN 15.05/47051). M. Africonus longilineus (Röckel, Rolán & Monteiro, 1980), 21.7 mm (MNCN 15.05/79738). N. Africonus lugubris (Reeve, 1849), 14.5 mm (MNCN 15.05/90431). O. Africonus maioensis (Trovão, Rolán & Félix-Alves, 1990), 29.5 mm (MNCN 15.05/78689). P. Africonus miruchae (Röckel, Rolán & Monteiro, 1980), 12.9 mm (MNCN 15.05/79789). Scale bars = 10 mm.
Fig. 3 in New acoustic and molecular data shed light on the poorly known Amazonian frog Adenomera simonstuarti (Leptodactylidae): implications for distribution and conservation
Fig. 3. Preserved male of nominal Adenomera simonstuarti (Angulo & Icochea, 2010) (= genetic lineage 3): call voucher INPA-H 40967 (SVL = 23.4 mm) from the upper Juruá River, in Tarauacá, Brazilian state of Acre. This specimen corresponds to a call voucher (see Fig. 5). A−B. Body in dorsal and ventral views, not to scale. C−D. Detail of the ventral surface of right foot and hand, respectively. Note the nearly solid, dark-colored stripe along the underside of the forearm. Photographs by J. Magnusson. Scale bar = 5 mm.
FIG. 2 in On the morphology of the astragalus and calcaneus of the amphicyonids (Carnivora, Mammalia) from the Paleogene of Europe: implications for the ecology of the European bear-dogs
FIG. 2. — Tarsal bones of Cynodictis lacustris from Aubrelong (France; Rupelian, MP21): A-E, MNHN.F.Au994, left astragalus (reversed views); A, dorsal view; B, ventral view; C, lateral view; D, distal view; E, proximal view; F-J, MNHN.F.Au2044, right calcaneus; F, dorsal view; G, lateral view; H, medial view; I, distal view; J, proximal view. Abbreviations: cf, cuboid facet; ef, ectal facet; f, foramen; ff, fibular facet; h, head; ll, lateral lip; lp, lateral process; lpt, lateral process of tuber; ml, medial lip; mpt, medial process of tuber; n, neck; ppt, proximal plantar tuberosity; plt, plantar tubercle; pp, peroneal process; ptg, plantar tendon groove; sf, sustentacular facet; sg, sagittal groove; sit, sinus of the tarsus; st, sustentaculum tali; tc, tuber calcanei; tr, trochlea. Scale bar: 1 cm.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.