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FIGURE 6 in Were terror birds the apex continental predators of Antarctica? New findings in the early Eocene of Seymour Island
FIGURE 6. Biplot of the Principal Component Analyses (PCA). A, Analysis without normalization of data; B, Analysis with variables converted into indexes. Abbreviations: BH, basal height; HAF, maximum height of the articular facet; ICA, inner curvature angle; LFT, flexor tubercle length; OCA, outer curvature angle; TL, total length; and WAF, maximum width of articular facet.
FIGURE 6. The handle form 1. A in The challenge of hard-to-reach spaces in mechanical fossil preparation: Development of the Wada air scribe, a novel short-bodied air scribe with an adjustable handle
FIGURE 6. The handle form 1. A, production process. The component numbers correspond to those in Figure 2; B, the handle in right lateral view; C, the handle in top view; D, the handle with the socket head screw (M4) in bottom view; E, the handle in left lateral view.
FIGURE 6. 3D in A reappraisal of the cranial and mandibular osteology of the spinosaurid Irritator challengeri (Dinosauria: Theropoda)
FIGURE 6. 3D renderings of the right maxilla of Irritator challengeri (SMNS 58022). A, lateral view; B, lateral view with maxillary bone rendered transparent; C, medial view; D, medial view with maxillary bone rendered transparent; E, ventral view of tooth row fragment; F, ventral view with maxillary bone rendered transparent. Note different scale for E–F. Also note that tooth positions are numerically labelled but refer to preserved tooth position from anterior to posterior, not to anatomical tooth positions, which are unknown. Replacement teeth are highlighted with dashed lines in D, and different generations are indicated with prime (') or double prime (''). Arrows in A and C indicate approximate original position of tooth-bearing fragment. Abbreviations: acp, ascending process; jr, jugal ramus; lac, lacrimal contact; mw-prmr, medial wall of promaxillary recess; palgr, palatine groove; pdl, paradental lamina; prmr, promaxillary recess; rt, replacement tooth.
FIGURE 6 in Pleistocene record of mammals and pollen from Mexico (Las Tazas, Valsequillo, Puebla) and their paleoenvironmental interpretation
FIGURE 6. Pollen diagram of the locality Las Tazas, Valsequillo, Puebla, Mexico. Showing on the right in dark green the arboreal elements vs in light green the herbaceous elements. Area delimited by grey lines indicates the layers with the presence of vertebrate remains (bone silhouette). Diagram was made in Tilia 3.0.1.
FIGURE 6 in An early Cambrian pelago-benthic acorn worm and the origin of the hemichordate larva
FIGURE 6. Inferred phylogenetic relationships: Phylogenetic position of Cambrobranchus pelagobenthos and other Cambrian ambulacrarians using majority-rules Bayesian analysis of 113 characters and 27 taxa. Numbers at nodes represent posterior probabilities. Pie charts indicate the results of an ancestral state reconstruction.
Figure 6 in Herbicide response and germination behavior of two goosegrass (Eleusine indica) populations in the Australian environment
Figure 6. Effect of burial depth on the seedling emergence of the two Australian populations (Gatton and Ingham) of Eleusine indica. The lines represent a gaussian model fit to the emergence data obtained at different seed burial depths.
Figure 3. – Average STRUCTURE results aggregated using CLUMPAK for populations 2–6 and 9. K in Landscape biogeography and population structuring of a facultatively amphidromous galaxiid fish, Galaxias brevipinnis
Figure 3. – Average STRUCTURE results aggregated using CLUMPAK for populations 2–6 and 9. K = 6 was selected as the most likely population estimate using Evanno's method. STRUCTURE initially separated the lakes draining to the east coast (L. Wānaka and L. Wakatipu) from all other sites at K = 2. The West Coast lakes were split away next (K = 3), with L. Moeraki and L. Paringa splitting at K = 4 and L. Cristabel at K = 5. East coast L. Wānaka and L. Wakatipu were split at K = 6. L. Paringa and L. Moeraki are split form each other at K = 9.
Figure 6 in Historical review of the computerization of the MNHN Fish Collection and its collaboration with FishBase
Figure 6. – Number of identifications by year in the MNHN Fish Collection, and percentage of total identifications by the top ten taxonomists' names.
Figure 6 in A simple framework for the exploration of functional biodiversity
Figure 6. – Boxplot of trophic levels by productivity group, for 31,148 species of fishes, with indication of median trophic level and number of species (n).
Figure 6 in Reproductive biology of Elops lacerta (Elopiformes: Elopidae) in the Gulf of Guinea, Côte d'Ivoire, West Africa
Figure 6. – Size at first sexual maturity (FL50) of males and females Elops lacerta caught from January 2019 to December 2020.
Figure 6 in Using deep-learning for automatic identification of images of marine benthic macro-invertebrate bycatch: a proof of concept
Figure 6. – Example of detection and classification obtained with an image including an Ophiuroid, a piece of coral and a sea star with network 2; red squares and annotations have been provided by the computer with no human action.
Figure 6 in The fisheries of the sea around Saint-Pierre and Miquelon: from cod to sea cucumber
Figure 6. – Contrasting the growth of Atlantic cod (Gadus morhua) with that of orange-footed sea cucumber (Cucumaria frondosa) as representative of two, radically different fisheries in St Pierre and Miquelon. The growth parameters of G. morhua (L∞ = 98 cm total length, K = 0.15 year–1 and t = –0.5 year) are from May et al. 0 (1966), with W = 0.0075·L3 (g; cm) from Mello and Rose (2005) used for the conversion to growth in weight. Those for C. frondosa (L = 20 cm mouth-to-vent, K = 0.18 year–1 and t = –0.7 year) ∞ 0 were computed by the authors based on data in figure 7 of Hamel and Mercier (1996), with W = 16·L1.34 (g; cm, caliper length) from Harper et al. (2020) used for growth in weight.
Figure 6. – The R in French research on fisheries in the Northwest Atlantic, from its origins to the present
Figure 6. – The R/V Président Théodore Tissier of the Office Scien-Scien- tifique et Technique des Pêches Maritimes carried out surveys in the North West Atlantic mainly during the 1950s (source: www.lepetit-manchot.fr).
Figure 6 in The lungs of extinct and extant coelacanths: a morphological and histological review
Figure 6. – †Axelrodichthys araripensis from the Cretaceous of Brazil ("Josa collection"; specimen deposited at the MNHN, Paris). Sections of bony plates of the lung. A: Section of a bony plate showing the central artefactual fracture (black arrowheads), as on Latimeria plates (see Fig. 4A). B: Detail of a section of a bony plate showing the artefactual fracture (black arrowheads) and the Liesegang lines (black arrows) indi- cating a spheritic mineralization process. C: Section of a bony plate showing the histological organization with regu- lar collagenous layers and osteocytes with canalicles crossing the extracellular matrix. D: Horizontal ground section of a bony plate showing numerous star-shape osteocytes with cytoplasmic processes. Inset: detail of an osteocyte with its ramified canalicles. E: Ground section showing some large vascular cavities (white asterisks). F: Cross- ground section of a bony plate showing Liesegang lines (black arrowheads) and some mineralized spherules (black arrows). G: Horizontal ground section of a bony plate showing an osteocyte with its cytoplasmic processes (on the left, black arrow) and some mineralized spherules (on the right). Scale bars: A = 100 μm; B, C = 25 μm; D, F = 20 μm; inset D, E, G = 10 μm. Deposited at the Laboratoire de Paléontologie, MNHN, Paris.
Figure 6. – A in Review of Giuris (Teleostei: Eleotridae) from Indo-Pacific islands, with description of three new species
Figure 6. – A: Giuris laglaizei, male; in MNHN 2019-0211, Lake Taal, Philippines (Photo M. Gaulke). B: G. laglaizei, male; in MNHN 2019-0211, Lake Taal, Philippines; LS 140 mm (Photo M. Gaulke). C: G. laglaizei, male; in MNHN 2020-0147, Lake Mainit, Philippines; LS 106 mm (Photo M. Gaulke). D: G. laglaizei, female; in MNHN 2020-0147, Lake Mainit, Philippines; LS 96 mm (Photo M. Gaulke). E: G. agilis, drawing from Herre (1927).
Figure 6. – Significant French ichthyological records for 2018 in French ichthyological records for 2018
Figure 6. – Significant French ichthyological records for 2018 (continued). A: Parablennius pilicornis, ~8 cm TL, 6 May 2018 (reversed photograph); B: Parablennius pilicornis, ~10 cm TL, 7 Jun. 2018; C: Parablennius ruber, ~12 cm TL, 5 Aug. 2018; D: Parablennius ruber, ~8-9 cm TL, 4 Sep. 2018; E: Parablennius ruber, ~9-10 cm TL, 4 Oct. 2018.
Figure 6 in Effects of dams on demographic structures of amphidromous fish and crustacean species in Caribbean rivers
Figure 6. – Individual number histograms of each species broken down by size classes (mm) for the three stations (top chart) and porosity chart of the Pérou River water intake (bottom chart). Bottom chart: arrow indicates the optimal size at crossing; dotted black line indicates 50% crossing; dotted grey lines indicate the mean crossing rate for these size classes. The size of the downstream and upstream population of Macrobrachium faustinum is too small and fragmented to be presented.
Figure 6 in Life history traits and exploitation of Hampala barb (Hampala macrolepidota - Cyprinidae) in a subtropical reservoir (Lao PDR)
Figure 6. – Percentage of mature Hampala macrolepidota females in 20 mm standard length intervals from the Nam Theun 2 Reservoir in Lao PDR in 2016 fitted to a logistic function.
Figure 6 in A third European species of grayling (Actinopterygii, Salmonidae), endemic to the Loire River basin (France), Thymallus ligericus n. sp.
Figure 6. – Dorsal fin on a live paratype of Thymallus ligericus n. sp. MNHN 2018-0726, 290 mm SL ♀, Lignon River at Boën-surLignon, 29 May 2015, Persat, Juglaret and Buttazzoni coll.
FIGURE 6 in Palaeoecology and sea level changes: Decline of mammal species richness during late Quaternary island formation in the Montebello Islands, north-western Australia
FIGURE 6. Species accumulation curve for Morgan's Cave, showing increasing species with increased sampling effort (cumulative NISP). Further sampling effort could have yielded more species.
ScienceDex guides
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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.