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Fig. 16 Scolopocryptops sukuyan n in An unknown segment number in centipedes: a new species of Scolopocryptops (Chilopoda: Scolopendromorpha) from Trinidad with 25 leg-bearing segments
Fig. 16 Scolopocryptops sukuyan n. sp., paratype, AMNH IZ 00357039, Trinidad. Segment 25 showing the coxopleuron, lateral view. Scale bar 1 mm
Fig. 12 Scolopocryptops sukuyan n in An unknown segment number in centipedes: a new species of Scolopocryptops (Chilopoda: Scolopendromorpha) from Trinidad with 25 leg-bearing segments
Fig. 12 Scolopocryptops sukuyan n. sp., paratype, AMNH IZ 00357039, Trinidad. Tergites 7 to 9, dorsal view. Scale bar 1 mm
Fig. 14 Scolopocryptops sukuyan n in An unknown segment number in centipedes: a new species of Scolopocryptops (Chilopoda: Scolopendromorpha) from Trinidad with 25 leg-bearing segments
Fig. 14 Scolopocryptops sukuyan n. sp., paratype, AMNH IZ 00357039, Trinidad. Tergite 25, dorsal view. Scale bar 1 mm
Fig. 6 Scolopocryptops sukuyan n in An unknown segment number in centipedes: a new species of Scolopocryptops (Chilopoda: Scolopendromorpha) from Trinidad with 25 leg-bearing segments
Fig. 6 Scolopocryptops sukuyan n. sp., holotype, AMNH IZ 00357038, Trinidad. Tergite 25, dorsal view. Scale bar 1 mm
Fig. 3 Scolopocryptops sukuyan n in An unknown segment number in centipedes: a new species of Scolopocryptops (Chilopoda: Scolopendromorpha) from Trinidad with 25 leg-bearing segments
Fig. 3 Scolopocryptops sukuyan n. sp., holotype, AMNH IZ 00357038, Trinidad. Cephalic plate, dorsal view. Scale bar 1 mm
Fig. 7 Scolopocryptops sukuyan n in An unknown segment number in centipedes: a new species of Scolopocryptops (Chilopoda: Scolopendromorpha) from Trinidad with 25 leg-bearing segments
Fig. 7 Scolopocryptops sukuyan n. sp., holotype, AMNH IZ 00357038, Trinidad. Sternite 25, ventral view. Scale bar 1 mm
Fig. 4 Scolopocryptops sukuyan n in An unknown segment number in centipedes: a new species of Scolopocryptops (Chilopoda: Scolopendromorpha) from Trinidad with 25 leg-bearing segments
Fig. 4 Scolopocryptops sukuyan n. sp., holotype, AMNH IZ 00357038, Trinidad. Forcipular coxosternum, ventral view. Scale bar 1 mm
Fig. 1 in An unknown segment number in centipedes: a new species of Scolopocryptops (Chilopoda: Scolopendromorpha) from Trinidad with 25 leg-bearing segments
Fig. 1 Phylogeny of Scolopendromorpha based on Bayesian and maximum likelihood analyses of transcriptomic data (Benavides et al., 2021), with Scolopocryptops sukuyan n. sp. placed on the tree based on previous morphological cladistic analysis of Scolopocryptops (Chagas-Jr., 2008)
Fig. 2 Scolopocryptops sukuyan n in An unknown segment number in centipedes: a new species of Scolopocryptops (Chilopoda: Scolopendromorpha) from Trinidad with 25 leg-bearing segments
Fig. 2 Scolopocryptops sukuyan n. sp., paratype, AMNH IZ 00357039, Trinidad. a Habitus dorsal. b Habitus ventral. Scale bar 5 mm
FIGURE 4. A–J in A new species of Paspalum, Notata group (Poaceae, Paspaleae), from the Cerrado biome, Brazil: description, chromosome number, and leaf blade anatomy
FIGURE 4. A–J. Transverse sections of the leaf blades of Paspalum species. A–C. P. cerradoense R.C. Oliveira & Valls, Oliveira et al. 2693 (holotype). D–F. P. cromyorhizon Trin. ex Döll, Valls et al. 9668. G–J. P. ionanthum Chase, Valls et al. 14288. A, D, G. Parenchyma in the midrib adaxial region (m) present (A) or absent (D, G) in the midvein region. B, E, I. Colorless cells (cc) under bulliform cells (bc) present (B) or absent (E, I). C, F, J. Fiber fascicle (ff) fills the leaf margin (C) or not (F, I). H. Adaxial leaf side, showing a stoma (arrow). Scales: A. 200 μm; D, G. 100 μm; B–C, E–F, H–J. 50 μm.
FIGURE 3 in A new species of Paspalum, Notata group (Poaceae, Paspaleae), from the Cerrado biome, Brazil: description, chromosome number, and leaf blade anatomy
FIGURE 3. Chromosomes of Paspalum cerradoense R.C. Oliveira & Valls, Oliveira & Fagg 2787 (paratype). Scale: 10 μm.
FIGURE 1. Paspalum cerradoense R.C. Oliveira & Valls. A. Habit. B. Inflorescence.A. Habit. B. Inflorescence. C in A new species of Paspalum, Notata group (Poaceae, Paspaleae), from the Cerrado biome, Brazil: description, chromosome number, and leaf blade anatomy
FIGURE 1. Paspalum cerradoense R.C. Oliveira & Valls. A. Habit. B. Inflorescence.A. Habit. B. Inflorescence. C. Segment of rachis with pedicels. D. Ligule region. E. Upper glume, detail of the subapical teeth in dorsal view. F. Upper glume, ventral view. G. Spikelet, dorsal view, showing upper glume. H. Spikelet, ventral view, showing lower lemma. I. Upper anthecium, ventral view. J. Upper anthecium, dorsal view.
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).
APPENDIX III. Bayesian inference topology of COI gene with posterior probability values. Numbers at the nodes represent posterior probability support, other nodes with red circles has> 95%. Terminals with locality specification are species prior for understand the description of I. crassa sp. nov. (★). in A new species of Ischnocnema (Anura: Brachycephalidae) from the mountainous region of Atlantic Forest, southeastern Brazil, with a new phylogeny and diagnose for Ischnocnema parva series
APPENDIX III. Bayesian inference topology of COI gene with posterior probability values. Numbers at the nodes represent posterior probability support, other nodes with red circles has> 95%. Terminals with locality specification are species prior for understand the description of I. crassa sp. nov. (★).
FIG UR E 3 (a) Dated phylogeny of the genus Theodoxus constructed in BEAST based on COI, 16S and ATPα. Node labels denote divergence times in millions of years ago (Ma); node bars indicate the 95% credibility interval around these dates. Small squares at nodes indicate significant support of divergence events found with BEAST and other phylogenetic analyses (see Figures S2.1 and S2.2), as explained through the key. Where MOTUs (A–R) show conspecifics among a number of morphospecies, species names are given in order of their year of description. Morphospecies, incorporated from GenBank, where determination was potentially dubious are highlighted by an asterisk. Clades (C) and subclades (SC) are demarcated by dashed lines between MOTUs. (b) LTT plots indicating the build‐up of lineages in Theodoxus over geological time. Dashed lines surrounding the solid LTT lines indicate the 95% confidence intervals. Where intra‐ and interspecific diversity diverge, interspecific diversity is highlighted in blue and intraspecific diversity in red. Transitions in geological ages are highlighted by narrow grey lines, while the grey bar marks the period of pronounced glacial cycles (last 900 kyr) [Colour figure can be viewed at wileyonlinelibrary.com] in Contributions of biogeographical functions to species accumulation may change over time in refugial regions
FIG UR E 3 (a) Dated phylogeny of the genus Theodoxus constructed in BEAST based on COI, 16S and ATPα. Node labels denote divergence times in millions of years ago (Ma); node bars indicate the 95% credibility interval around these dates. Small squares at nodes indicate significant support of divergence events found with BEAST and other phylogenetic analyses (see Figures S2.1 and S2.2), as explained through the key. Where MOTUs (A–R) show conspecifics among a number of morphospecies, species names are given in order of their year of description. Morphospecies, incorporated from GenBank, where determination was potentially dubious are highlighted by an asterisk. Clades (C) and subclades (SC) are demarcated by dashed lines between MOTUs. (b) LTT plots indicating the build‐up of lineages in Theodoxus over geological time. Dashed lines surrounding the solid LTT lines indicate the 95% confidence intervals. Where intra‐ and interspecific diversity diverge, interspecific diversity is highlighted in blue and intraspecific diversity in red. Transitions in geological ages are highlighted by narrow grey lines, while the grey bar marks the period of pronounced glacial cycles (last 900 kyr) [Colour figure can be viewed at wileyonlinelibrary.com]
FIGURE 3. Theoretical diagrams showing a in Aspidistra paucitepala (Asparagaceae), a new species with occurrence of the lowest tepal number in flowers of Asparagales
FIGURE 3. Theoretical diagrams showing a fraction of variation of flower groundplan in Aspidistra in the framework of the pentacyclic interpretation. Outer whorl tepals and outer whorl stamens red, inner whorl tepals and inner whorl stamens blue. Gynoecium is a black circle (individual carpels not shown as gynoecium diversity requires further investigation). There are some examples of species (based on data from protologues, Liang & Tamura 2000, Tillich 2005) below diagrams. Note that no attempt was made to make species lists exhaustive; trimerous and tetramerous flowers are found in many species of the genus. An alternative interpretation implies that all flowers illustrated here possess a single whorl of tepals and a single whorl of stamens.
FIGURE 2 in Aspidistra paucitepala (Asparagaceae), a new species with occurrence of the lowest tepal number in flowers of Asparagales
FIGURE 2. Vegetative organs, pistil and fruits of A. paucitepala. a. fruiting plant; b. fruiting plant with vertical branched rhizome (young green leaves mark rhizome apices); c. rhizome with basal parts of petioles and a nearly mature fruit; d. pistil of anthetic flower with lobed stigma; e. vertical rhizome with flowers and fruits at different developmental stages.
FIGURE 1 in Aspidistra paucitepala (Asparagaceae), a new species with occurrence of the lowest tepal number in flowers of Asparagales
FIGURE 1. Flowers of A. paucitepala. a–c. longitudinal sections of flowers (a, c) and flower bud (b); d. flower with three tepals and supposedly three stamens (side view); e. flower with two tepals and two stamens (cross section at the level of anthers, above the stigma, scanning electron microscopy); f. flower with three tepals and three stamens (top view); g. flower with four tepals and four stamens (top view); h. flowers with four and three tepals occurring on the same individual plant.
FIGURES NJ27–NJ30. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ27, Scrobipalpa acuminatella; NJ28, Sophronia gelidella; NJ29, Anthophila fabriciana; NJ30, Phiaris bipunctana. in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES NJ27–NJ30. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ27, Scrobipalpa acuminatella; NJ28, Sophronia gelidella; NJ29, Anthophila fabriciana; NJ30, Phiaris bipunctana.
FIGURES NJ17–NJ19, NJ21. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ17, Agonopterix conterminella. NJ18, Depressaria depressana; NJ19, Coleophora atriplicis; NJ21, Coleophora granulatella. in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES NJ17–NJ19, NJ21. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ17, Agonopterix conterminella. NJ18, Depressaria depressana; NJ19, Coleophora atriplicis; NJ21, Coleophora granulatella.
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.