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FIGURE 2 in A revised dichotomous key to the snakes of Italy (Reptilia, Squamata, Serpentes), according to recent systematic updates: SUPPLEMENTARY FILE
FIGURE 2. Nomenclature of belly and tail scales in Eryx jaculus (A) and Vipera berus (B). Photo credits: Di Nicola M. R.
Fig. 5 in Ancient divergence and recent population expansion in a leaf frog endemic to the southern Brazilian Atlantic forest
Fig. 5 Model checking in ABC analyses of Phyllomedusa distincta. Ordination plots show summary statistics vectors of simulated (gray circles) and observed (black triangles) data after the rejection step. We conducted the rejection step per locus and for all loci jointly (see text for details)
Fig. 4 in Ancient divergence and recent population expansion in a leaf frog endemic to the southern Brazilian Atlantic forest
Fig. 4 Extended Bayesian Skyline plots of Phyllomedusa distincta groups: a Northern group and b Southern group. Dashed line represents the median population size (multiply by thousand and by generation time of 1 year) and the lightly shaded gray the 95 % HPD. The accumulation of green lines represents the full posterior distribution. The y-axis is in logarithmic scale
Fig. 3 Neochromadora aff. poecilosoma, a in Nematode succession at deep-sea hydrothermal vents after a recent volcanic eruption with the description of two dominant species
Fig. 3 Neochromadora aff. poecilosoma, a female, specimen no.7, reproductive system; b female, no. 7 total view; c male, no. 1, cuticle on the level of the pharynx; d male, no. 1, cuticle on the level of the midbody; e male, no.1, cuticle on the level of the tail. Scale in μm
Fig. 2 Neochromadora aff. poecilosoma, a in Nematode succession at deep-sea hydrothermal vents after a recent volcanic eruption with the description of two dominant species
Fig. 2 Neochromadora aff. poecilosoma, a male, specimen no.1, head region; b male, specimen no. 2; c male, no.1, anterior end; d female, specimen no. 6; e male, no. 1, posterior end; f male, no.1, spicule. Scale in μm
Fig. 1 in Nematode succession at deep-sea hydrothermal vents after a recent volcanic eruption with the description of two dominant species
Fig. 1 Examples of habitat types analyzed in this study. a Newly established active vent site colonized by the tubeworm foundation species Tevnia jerichonana and a few large Riftia pachyptila tubeworms at P-Vent in 2007. b Old inactive vent at the site East Wall showing empty tubeworm tubes and mussel shells in 2007. c Newly bare basalt adjacent to the vent site Tica in 2007. In each habitat artificial settlement devices (referred to as "sponge;" see Fig. 1c) were deployed
FIG. 3 in Phylogeny of African Long-Fingered Frogs (Arthroleptidae: Cardioglossa) Reveals Recent Allopatric Divergences in Coloration
FIG. 3. Chronogram displaying divergence times within Cardioglossa and the Arthroleptidae based on the concatenated dataset. Bars at nodes represent 95% highest posterior density estimates and asterisk (*) denotes the nodes anchored with a secondary calibration. All nodes have support values.0.95 unless otherwise noted. In addition, Bayesian species delimitation probabilities are depicted in the box at each node within Cardioglossa under three different combinations of priors: left, large population sizes (Ne; H ¼ 3, 0.02) with deep divergences (s ¼ 3, 0.3); center, small Ne (H ¼ 3, 0.0002) with shallow divergences (s ¼ 3, 0.003); right, large Ne (H ¼ 3, 0.02) with shallow divergences (s ¼ 3, 0.003). Support values below 0.95 are colored red. See Data Accessibility for tree file.
FIG. 1 in Phylogeny of African Long-Fingered Frogs (Arthroleptidae: Cardioglossa) Reveals Recent Allopatric Divergences in Coloration
FIG. 1. Map showing the currently recognized distributions (range polygons based on IUCN, 2020) of the 18 species of Cardioglossa in this study showing the locations of our samples. For details on sampling, see Supplemental Table 1 (see Data Accessibility).
FIG. 2 in Phylogeny of African Long-Fingered Frogs (Arthroleptidae: Cardioglossa) Reveals Recent Allopatric Divergences in Coloration
FIG. 2. Maximum likelihood phylogeny of Cardioglossa based on the multilocus concatenated, partitioned dataset of mitochondrial and nuclear data. A black dot at each node indicates high support (e.g., Bayesian posterior probability.0.95, maximum likelihood bootstrap.70). Tip labels of individuals used for divergence time analysis are indicated in boldface. Photographs are not scaled to size. (Photo credits: D.C.B.: C. melanogaster, C. oreas manengouba, C. pulchra, C. schioetzi; M.B.: C. annulata, C. escalerae, C. leucomystaX 1; Brian Freiermuth: C. leucomystaX 2, C. oreas oreas; E.G.: C. congolia, C. cyaneospila; V.G.: C. alsco; M.H.: C. nigromaculata, C. Venusta; Greg Jongsma: C. gracilis; P.J.M.: C. nigromaculata 'Bioko'; Dan Portik: C. elegans, C. occidentalis; M.-O.R.: C. gratiosa, C. trifasciata; images available via https://doi.org/10.7479/3yje-r341). See Data Accessibility for tree file.
Fig. 3 A in Recent progress in reconstructing lophotrochozoan (spiralian) phylogeny
Fig. 3 A hypothesis of lophotrochozoan phylogeny as discussed in this review. This topology shows a summary of different phylogenomic studies (Weigert et al. 2014; Wey-Fabrizius et al. 2014; Schiffer et al. 2018; Marlétaz et al. 2019). *Please note that several taxa formerly regarded to be placed outside Annelida (Echiura, Myzostomida, Orthonectida, Pogonophora, Sipuncula and Vestimentifera) are now firmly placed as annelid ingroups. Annelida relationships are (mostly) well resolved, see discussion in the text and Struck (2019) for review
Fig. 2 in Recent progress in reconstructing lophotrochozoan (spiralian) phylogeny
Fig. 2 Hypotheses of lophotrochozoan relationships. a State-of-the-art review from Telford et al. (2015) summarizing the knowledge at that point. b Phylogenomic analysis of Lophotrochozoa based on 638 orthologs by Kocot et al. (2017). c Phylogenomic analysis of Lophotrochozoa based on 1/6 of 638 orthologs selected to mini- mize the patristic distance across taxa by Kocot et al. (2017). d Phylogenomic analysis of 267 orthologs with amino acids recoded according 6 Dayhoff groups to reduce saturation by Marlétaz et al. (2019)
FIGURE 1 in Counting counts: revised estimates of numbers of accepted species of flowering plants, seed plants, vascular plants and land plants with a review of other recent estimates
FIGURE 1. Accepted names at species rank as a function of all published species names for selected seed plant families (all published in WCSP).
FIGURE 4 in The hybrid origin of Phai Liang, a bamboo of recent introduction into horticulture in Southeast Asia, and a new nothogenus, ×Thyrsocalamus (Bambuseae: Bambusinae)
FIGURE 4. Characteristics in the type collection (K.M. Wong & D. Ohrnberger WKM 3555) of × Thyrsocalamus liang from the Mae Hia Bamboo Collection, Royal Project Foundation, Chiang Mai, Thailand. A. Culm internode with scattered white hairs at the uppermost part; B. Culm leaves with erect blades, leafy branches, and branches with inflorescences at the peak of anthesis. Photographs by K.M. Wong.
FIGURE 1 in The hybrid origin of Phai Liang, a bamboo of recent introduction into horticulture in Southeast Asia, and a new nothogenus, ×Thyrsocalamus (Bambuseae: Bambusinae)
FIGURE 1. Schematic diagram showing the position of haplotype-specific primers and their site numbers in the partial GBSSI gene. Arrows indicate the directions of primers.
FIGURE 3 in The hybrid origin of Phai Liang, a bamboo of recent introduction into horticulture in Southeast Asia, and a new nothogenus, ×Thyrsocalamus (Bambuseae: Bambusinae)
FIGURE 3. Phai Liang cultivated in the Rimba Ilmu Botanic Garden of the University of Malaya (A–C) and Penang Botanical Garden (D–H). A. Clump habit; B. Internodes and elliptic branch buds; C. Culm sheaths with pale brown hairs; D. Clump habit; E. Subrotundovate primary branch bud at a culm node; F. Spreading culm-sheath blades on a shoot; G. Foliage leaves; H. Pseudospikelets with purpleblue to maroon anthers extruded from florets. Photographs by K.M. Wong.
FIGURE 2 in The hybrid origin of Phai Liang, a bamboo of recent introduction into horticulture in Southeast Asia, and a new nothogenus, ×Thyrsocalamus (Bambuseae: Bambusinae)
FIGURE 2. Phylogenetic tree reconstructed based on partial nuclear GBSSI marker. Numbers above nodes are bootstrap values for maximum parsimony analysis; numbers below nodes are posterior probabilities for Bayesian inference.
FIGURE 5. Thyrsostachys siamensis. A in The hybrid origin of Phai Liang, a bamboo of recent introduction into horticulture in Southeast Asia, and a new nothogenus, ×Thyrsocalamus (Bambuseae: Bambusinae)
FIGURE 5. Thyrsostachys siamensis. A. Planted clump at Gurun, Kedah, Malaysia; B. Clump base showing persistent culm sheaths, planted clump (WKM 3511) along Holland Road, Singapore; C. Dense silvery white appressed hairs on culm sheaths of a shoot (WKM 3511); D. Subrotund-ovate primary branch bud (WKM 3511); E. Stiffly erect clump habit, Kuching, Malaysia. Photographs by K.M. Wong.
FIGURE 1. Chresta artemisiifolia. A. Habit with synflorescences. B in Chresta artemisiifolia (Vernonieae, Asteraceae), a new endangered species from a recently created protected area in the Brazilian Caatinga
FIGURE 1. Chresta artemisiifolia. A. Habit with synflorescences. B. Adaxial surface of leaf. C–D. Syncephalia. E. Floret with pappus. F–I. Phyllaries from most internal to most external. K–M: Pappus series, from most internal to most external. J. Cypsela.
FIGURE 3 in Chresta artemisiifolia (Vernonieae, Asteraceae), a new endangered species from a recently created protected area in the Brazilian Caatinga
FIGURE 3. Known distribution of Chresta artemisiifolia in relation to the proposed area of the mosaic of conservation units in Boqueirão da Onça. The detail on the bottom left represents the distribution of C. harleyi, C. hatschbachii, C. martii and C. subverticillata in relation to C. artemisiifolia.
FIGURE 2. Chresta artemisiifolia. A. Habit. B–C in Chresta artemisiifolia (Vernonieae, Asteraceae), a new endangered species from a recently created protected area in the Brazilian Caatinga
FIGURE 2. Chresta artemisiifolia. A. Habit. B–C. Details of branches showing the leaves with constricted blades. D. Comparison between leaves of C. martii (left) and C. artemisiifolia (right). E–F. Syncephalia with open florets. G. Microscopic section showing the cells of the carpopodium wall, the glands above the carpopodium and the twin-hairs. H. Microscopic section showing the tips of the petals, with short, simple trichomes and globular glandular trichomes. A.–H. by C.M. Siniscalchi.
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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.