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Fig. 3 in The vascular plant diversity of Burkina Faso (West Africa) - a quantitative analysis and implications for conservation
Fig. 3. – Origin of introduced plant species in Burkina Faso. The majority of introduced species originates in the Americas.
Fig. 6 in The vascular plant diversity of Burkina Faso (West Africa) - a quantitative analysis and implications for conservation
Fig. 6. – Province species richness in relation to province characteristics. Species richness per province is shown dependent on 4 factors.
Fig. 1 in The vascular plant diversity of Burkina Faso (West Africa) - a quantitative analysis and implications for conservation
Fig. 1. – The provinces of Burkina Faso and their assignment to the phytogeographic zones used in this study. The classification of provinces to the PGZs is modified after WHITE (1983) and GUINKO (1984a). [1: Les Balé; 2: Bam; 3: Banwa; 4: Bazègua. 5: Bougouriba; 6: Boulgou; 7: Boulkiemdé; 8: Ganzourgou; 9: Gnagna; 10: Gourma; 11: Houet; 12: Ioba; 13: Kadiogo; 14: Kénédougou; 15: Comoé; 16: Komandjari; 17: Kompienga; 18: Kossi; 19: Koulpélogo; 20: Kouritenga; 21: Kourwéogo; 22: Léraba; 23: Loroum; 24: Mouhoun; 25: Nahouri; 26: Namentenga; 27: Nayala; 28: Oubritenga; 29: Oudalan; 30: Passoré; 31: Sanguié; 32: Sanmatenga; 33: Séno; 34: Sissili; 35: Soum; 36: Sourou; 37: Tapoa; 38: Tuy; 39: Yagha; 40: Yatenga; 41: Ziro; 42: Zondoma; 43: Zoundwéogo; 44: Poni; 45: Noumbiel]
FIG. 6. — Sindhochelys ragei n. gen., n in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications
FIG. 6. — Sindhochelys ragei n. gen., n. sp., holotype CPAG-RANKT-V-3, from the Paleocene of Ranikot, locality K18-12, Southern Pakistan: left anterior part of the shell in oblique posterolateral view showing the delimitation of marginals 2 and 3, and of plastral scutes by the indentation at the end of sulci border, and the ventral bulges of the scutes. Abbreviations: ax b, axillary buttress; 3d per, third peripheral. The arrows indicate ends of sulci at the border of the peripherals and anterior plastral lobe. Scale bar: 5 cm.
FIG. 9 in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications
FIG. 9. — Comparison of the decoration of Sindhochelys ragei n. gen., n. sp. from the Paleocene of Ranikot, locality K18-12, Southern Pakistan, and Taphrosphys sulcatus (Leidy, 1856) from the early Paleocene of New Jersey (United States): A-D, Sindhochelys ragei n. gen., n. sp., holotype CPAG-RANKT-V-3: A, nuchal part; B, left peripherals 2, dorsal face with smaller polygons than in other parts; C, suprapygal-pygal part, dorsal views; D, imprint of an isolated plate, ventral view; E-G, Taphrosphys sulcatus: E, AMNH 1470, "Barnsboro, N.J." (Cope collections), nuchal border of three plates, dorsal view; F, G, AMNH 2522, «Tinton Falls, N.J.», syntype: F, peripheral 6 (medial plate of three in Leidy (1856: pl. 19, fig.4), and in Gaffney et al. (2006: fig. 20), dorsal view; G, xiphiplastron, ventral view. Scale bars: A-C, E-G, 5 cm; D, 2 cm.
FIG. 10 in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications
FIG. 10. — Fragmentary part of a carapace of an undetermined Bothremydidae, from the Paleocene of Ranikot, locality K18-12, CPAG-RANKT-V4, Southern Pakistan: A, B, ventral and dorsal views; C, detail of the dorsal decoration. Abbreviations: cost3, costal 3; cost5, costal 5; pcs, suture of the peripheral border with the border of plastral processes; per 5-8, peripherals 5, 6, 7, 8; perf, pholad perforations. Scale bars: A, B, 4 cm; C, 1 cm.
FIG. 5. — Sindhochelys ragei n. gen., n in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications
FIG. 5. — Sindhochelys ragei n. gen., n. sp., holotype CPAG-RANKT-V-3, from the Paleocene of Ranikot, locality K18-12, Southern Pakistan: A, anterolateral part of the carapace after removal of a part of the costal 1 with part of the neural l and the costal 2, to show the imprints of the thoracic ribs 1 and 2, and axillary buttress, in dorsal view; B, same removed part in ventral view. Abbreviations: ax b, axillary buttress; cost 1, costal 1; n1, neural 1; nu, nuchal; per 2, peripheral 2; rib 1, rib 2, medial part of thoracic ribs 1 and 2. Scale bar: 4 cm.
FIG. 4. — Sindhochelys ragei n. gen., n in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications
FIG. 4. — Sindhochelys ragei n. gen., n. sp., holotype CPAG-RANKT-V-3, from the Paleocene of Ranikot, locality K18-12, Southern Pakistan: A, B, shell drawings, in dorsal (A) and ventral (B) views. Scale bars: 10 cm.
FIG. 1 in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications
FIG. 1. — Location and stratigraphic position of fossil material: A, location of the Laki Range in eastern Sindh Province, southern Pakistan, and simplified geological map of the Ranikot Fort area (adapted from Schelling 1999); B, stratigraphic position of the fossil assemblage within the Waddi Sawri section. Note that the base of this section is close to the base of the Khadro Formation; in this area the thickness of the Khadro Formation is c. 80 m, and the fossil locality K18-12 is in the lower Khadro Formation.
FIG. 3. — Sindhochelys ragei n. gen., n in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications
FIG. 3. — Sindhochelys ragei n. gen., n. sp., holotype CPAG-RANKT-V-3, from the Paleocene of Ranikot, locality K18-12, Southern Pakistan: A, B, shell photographs in dorsal (A) and ventral (B) views. Scale bar: 10 cm.
FIG. 2 in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications
FIG. 2. — Turtle shell, CPAG-RANKT-V-3, holotype of Sindhochelys ragei n. gen., n. sp., in situ, during and after excavation at the locality K18-12: A, carapace in posterior view; A1, close-up of a lateral border showing the presence of a venerid bivalve in life position inside the carapace; B, carapace in dorsal view after excavation and split into three blocks. Scale bar: 30 cm.
Genetic diversity of wild and cultivated Coffea canephora in northeastern DR Congo and the implications for conservation - Additional Data
<p>List of wild and cultivated <em>Coffea canephora </em>accessions from northeastern Democratic Republic of the Congo included in Vanden Abeele et al. 2021 - American Journal of Botany, and the corresponding alleles for each of the 18 microsatellite markers (0 indicates missing alleles).</p>
Supporting Data for Drift Phase Structure Implications for Radiation Belt Transport by T.P. O'Brien et al. submitted to J. Geophysical Res.
<p>Datasets used in Drift Phase Structure Implications for Radiation Belt Transport by T.P. O'Brien et al. submitted to J. Geophysical Res.</p>
The impacts of management interventions on the sociality of African lions (Panthera leo): implications for lion conservation
<ol> <li>African lion (<em>Panthera leo</em>) populations normally consist of several neighbouring prides and multiple adult males or groups of males that interact competitively. In large, open systems, cub defence from infanticidal males and territory defence drive group living in lions. However, in smaller (< 1,000 km<sup>2</sup>), fenced wildlife reserves, opportunities for natural immigration and emigration are limited which means that the evolutionary drivers of lion sociality may collapse.</li> <li>Here, we use lion behavioural data collected from 16 wildlife reserves across South Africa to test how management-induced ecological conditions alter lion social dynamics.</li> <li>The number of lionesses observed together was best predicted by pride size, prey biomass and biome. Lionesses were less likely to group together as pride size increased, but more likely to group together as prey biomass and habitat productivity increased. In addition, adult males were observed more frequently with prides that had young (< 12 months) cubs in reserves that had unfamiliar adult males present compared to reserves without any unfamiliar adult males.</li> </ol> <p>Our results demonstrate how intra-specific competition between lions drives their sociality, and this may break down in small, fenced wildlife reserves where lions are actively managed. Although small, fenced reserves in South Africa have made a significant contribution to increasing lion numbers on the continent, our work highlights several important ecological implications of active lion management. For wildlife managers, mimicking the outcomes of different levels of intra-specific competition is likely a critical management tool for the persistence of lions in small reserves.</p>
FIG. 4 in Genetic diversity of Malagasy baobabs: implications for conservation
FIG. 4. — Observed nucleotide diversity PI (π) for the six Adansonia L. species endemic to Madagascar. Northern and southern populations of A. za Baill. are combined here. When distinguishing between geographic populations of A. za, nucleotide diversity was the same as combined for southern populations (π = 0.0029), but less for northern populations (π = 0.0026).
FIG. 3 in Genetic diversity of Malagasy baobabs: implications for conservation
FIG. 3. — Principal components analysis (PCA) of Malagasy Adansonia L. colored by species. Panels represent different PCA axes from: A, 2089 SNPs for all Malagasy Adansonia for axis 1 vs axis 2; B, axis 3 vs axis 4; C, 1873 SNPs for Longitubae taxa only for axis 1 vs axis 2; and D), axis 3 vs axis 4. Northern and southern populations of A. za Baill. labeled.
FIG. 2 in Genetic diversity of Malagasy baobabs: implications for conservation
FIG. 2. — SNP-based tree from 2089 biallelic SNPs as inferred by IQ-TREE. Values on the branches represent bootstrap support for the primary clades: A, broad scale relationships with monophyletic taxa collapsed and number of samples per clade indicated in parentheses; B, detailed phylogeny for the core Longitubae clade (A. perrieri Capuron, A. madagascariensis Baill., and A. za Baill.), with individual accessions mapped to their respective geographic localities in Madagascar (B). Adansonia za (Aza) accessions are listed in red; A. madagascariensis (Ama), in blue; and A. perrieri (Ape) accessions in yellow.
FIG. 1 in Genetic diversity of Malagasy baobabs: implications for conservation
FIG. 1. — Flowers of the six species of baobabs endemic to Madagascar: A, Adansonia grandidieri Baill.; B, A. madagascariensis Baill.; C, A. perrieri Capuron; D, A. rubrostipa Jum. & H. Perrier; E, A. suarezensis H. Perrier; F, A. za Baill. Photographs by David A. Baum and Nisa Karimi.
Water-soluble iron in PM2.5 in winter over six Chinese megacities: distributions, sources, and environmental implications
<p>We collected winter PM2.5 samples simultaneously in six Chinese megacities for analyzing ws‐Fe contents and speciation.</p>
Fig. 14 in Late Devonian-early Carboniferous ostracods (Crustacea) from South China: taxonomy, diversity and implications
Fig. 14. Location of the different ostracod mega-assemblages along the platform (modified from Crasquin & Horne 2018; redrawn, with minor modifications, from Casier 2008).
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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.