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5,145 results for “CO₂”
Multiple climatic factors co-regulate the accumulation and geospatial distribution of bufogenins in Bufo bufo gargarizans Cantor poison glands
<p>The eight main climatic factors included TEM_Avg, TEM_Max, TEM_Min, RHU_Avg, PRE_Time, PRE_Max, GST_Max and GST_Min. Data of related climatic factors were obtained from China Meteorological Administration.</p>
FIGURE 5. Drapetis males. Left mid femur, SEM images showing modified cuticle. A. D in Co-existing species of Drapetis Meigen in Skåne (S Sweden) with description of a new species and a key to males of NW European species (Diptera: Hybotidae)
FIGURE 5. Drapetis males. Left mid femur, SEM images showing modified cuticle. A. D. completa Kovalev; B. D. exilis Meigen; C. D. infitialis Collin; D. D. exilis, detail of anterior cuticle; E. D. infitialis, detail of anterior cuticle. Scales: A = 1 μm, C = 10 μm.
FIGURE 6. Drapetis males. Left mid femur, SEM images showing modified cuticle. A. D in Co-existing species of Drapetis Meigen in Skåne (S Sweden) with description of a new species and a key to males of NW European species (Diptera: Hybotidae)
FIGURE 6. Drapetis males. Left mid femur, SEM images showing modified cuticle. A. D. parilis Collin; B. D. pusilla Loew; C. D. parilis, detail of anterior cuticle; D. D. pusilla, detail of antero-dorsal cuticle. Scales: C, D = 10 μm.
FIGURE 4 in Co-existing species of Drapetis Meigen in Skåne (S Sweden) with description of a new species and a key to males of NW European species (Diptera: Hybotidae)
FIGURE 4. Drapetis abrollensis sp. nov. Right midleg, SEM images showing modified cuticle. A. Femur and tibia; B. Subapical cuticle of femur; C. Ventral edge of tibia; D. Detail of C showing accumulations of brochosomes. Scales: A = 0.1 mm; C = 1 μm.
FIGURE 3. Drapetis males. Legs. A. D in Co-existing species of Drapetis Meigen in Skåne (S Sweden) with description of a new species and a key to males of NW European species (Diptera: Hybotidae)
FIGURE 3. Drapetis males. Legs. A. D. assimilis (Fallén), right hind femur; B. D. pusilla Loew, left fore femur; C. D. abrollensis sp. nov., right mid femur and tibia. Scale = 0.1 mm.
FIGURE 2. Drapetis males. Right wing. A. D in Co-existing species of Drapetis Meigen in Skåne (S Sweden) with description of a new species and a key to males of NW European species (Diptera: Hybotidae)
FIGURE 2. Drapetis males. Right wing. A. D. assimilis (Fallén); B. D. abrollensis sp. nov.; C. D. incompleta Collin. Scale = 0.1 mm.
FIGURE 1 in Co-existing species of Drapetis Meigen in Skåne (S Sweden) with description of a new species and a key to males of NW European species (Diptera: Hybotidae)
FIGURE 1. Drapetis abrollensis sp. nov. Male terminalia. A. Right epandrial lamella with projections on apical border, right lateral view; B. Epandrium with cerci, dorsal view; C. Left surstylus, left lateral view; D. Epandrium and hypandrium, ventral view. Abreviations: ej = ejaculatory apodeme; hy = hypandrium; lc = left cercus; lel = left epandrial lamellae; ls 1 = left surstylus 1; ls 2 = left surstylus 2; p1, p2 = projections of the right epandrial lamella; rc = right cercus; rel = right epandrial lamella. Scale = 0.1 mm.
FIGURE 4 in Biogeography and co-occurrence of 16 planktonic species of Keratella Bory de St. Vincent, 1822 (Rotifera, Ploima, Brachionidae) in lakes and reservoirs of the United States
FIGURE 4. Co-occurrence matrix for ten Keratella species. All other taxon pair combinations showed no significant negative or positive co-occurrence correlations. (Abbreviations: Amer = K. americana, Tect = K. tecta, Quad = K. quadrata, Taur = K. taurocephala, Trop = K. tropica, Cras = K. crassa, Disp = K. quadrata dispersa, Earl = K. earlinae, Test = K. testudo, Coch = K. cochlearis)
FIGURE 2 in Biogeography and co-occurrence of 16 planktonic species of Keratella Bory de St. Vincent, 1822 (Rotifera, Ploima, Brachionidae) in lakes and reservoirs of the United States
FIGURE 2. Distributions of 15 species of Keratella within nine agglomerated ecoregions of the continental U.S. Each circle represents one sample; circle size represents total biomass (µg dry weight L-1) for that species in a sample. Biomass values for each species are set to individual scales.
FIGURE 1 in Biogeography and co-occurrence of 16 planktonic species of Keratella Bory de St. Vincent, 1822 (Rotifera, Ploima, Brachionidae) in lakes and reservoirs of the United States
FIGURE 1. Dorsal views of the loricas of 15 species of Keratella. a) Keratella americana, b) Keratella cochlearis, c) Keratella crassa, d) Keratella earlinae, e) Keratella mixta, f) Keratella testudo, g) Keratella hiemalis, h) Keratella quadrata, i) Keratella quadrata dispersa, j) Keratella serrulata, k) Keratella taurocephala, l) Keratella tecta, m) Keratella ticinensis, n) Keratella tropica, o) Keratella valga. Scale bar represents 50 µm.
text-fig. 32. Furculae of theropod dinosaurs. A, Allosaurus fragilis; UMNH VP 7408; anterior view. B, Segisaurus halli; UCMP V 338; pectoral girdle as preserved in lateral view. Abbreviations: co, coracoid; fu, furcula; sc, scapula. Scale bars represent 10 mm. in The interrelationships and evolution of basal theropod dinosaurs
text-fig. 32. Furculae of theropod dinosaurs. A, Allosaurus fragilis; UMNH VP 7408; anterior view. B, Segisaurus halli; UCMP V 338; pectoral girdle as preserved in lateral view. Abbreviations: co, coracoid; fu, furcula; sc, scapula. Scale bars represent 10 mm.
Supplementary Videos S1-S2 3D co-culture spheroid formation containing A498-ST cells
<p><strong>Supplementary Videos S1-S2</strong></p> <p><strong>3D co-culture spheroid formation containing A498-ST cells </strong></p> <p>Representative movies (<strong>S1</strong>, bright field and <strong>S2,</strong> fluorescence stained) recorded for 24 hours of an A498-ST 3D co-culture capturing the kinetic formation of a 3D spheroid. 3D co-cultures harbor 70% tumor cells (A498-ST, green), 20% fibroblasts (NHDFα, blue) and 10% endothelial cells (ECRF24, red). Scalebar represents 1000 µm. </p>
Datasets for "Constraints on the geometry and frictional properties of the Main Himalayan Thrust using co-, post- and interseismic deformation in Nepal" "
<p>This contains GNSS and InSAR data used in the publication "Constraints on the geometry and frictional properties of the Main Himalayan Thrust using co-, post- and interseismic deformation in Nepal". GNSS data come as separate text files for east and north displacements and errors. Each text file consists of a number of columns. Each file has 40 columns, where the first column is time in decimal years after the Gorkha earthquake and the following columns correspond to each GNSS station. The time series are those obtained after the removal of "non-postseismic" deformation such as linear and sinusoidal terms</p> <p>The InSAR data are in the form of GMT GRD files at 200m resolution. Data are from Sentinel-1a track 19 and are a derived work of Copernicus data, subject to the ESA use and distribution conditions. The name of each GRD file is as follows: t19_{date1}_{date2}_hgt_ramp_200m.grd. Date 1 and date 2 are the dates of the two images used to make each interferogram.</p>
Fig. 2 in Absence of co-phylogeny indicates repeated diatom capture in dinophytes hosting a tertiary endosymbiont
Fig. 2 Polyphyletic endosymbionts of Durinskia, Galeidinium and Kryptoperidinium with closest relatives among free-ranging diatoms. Maximum likelihood (ML) tree (−ln = 14,945) of all 77 Bacillariaceae operational taxonomic units available, derived from the comparison of concatenated rRNA and plastid sequences. Highlighted endosymbiont taxa were scattered along up to ten only distantly related lineages over the Bacillariaceae phylogeny. Note that accessions of neither Durinskia nor Kryptoperidinium constituted monophyletic groups. Within such lineages, endosymbionts were usually closer related to free-ranging diatoms than to other endosymbionts (though statistical support was not always high). Some endosymbionts were phylogenetically isolated from free-living diatoms exhibiting long branches (e.g. D. kwazulunatalensis N.Yamada, Sym & T.Horig., D. oculata and G. rugatum Tam. & T.Horig.). Branch lengths are drawn to scale, with the scale bar indicating the number of nt substitutions per site. The numbers on the branches are statistical support values (ML bootstrap values, values <50 are not shown, posterior probabilities below branches, values <90 are not shown; asterisks indicate maximal support)
Fig. 1 in Absence of co-phylogeny indicates repeated diatom capture in dinophytes hosting a tertiary endosymbiont
Fig. 1 Polyphyletic endosymbionts of freshwater Unruhdinium with closest relatives among free-ranging diatoms. Maximum likelihood (ML) tree (−ln = 21,700) of all 37 Stephanodiscaceae operational taxonomic units available, derived from the comparison of concatenated rRNA and plastid sequences. Endosymbiont taxa are highlighted. Note that we did not observe any contradictory tree topologies between separated analyses of nuclear and plastid loci (not shown). Endosymbionts of Unruhdinium segregated into two distinct lineages. Four identical sequences of different U. penardii (Lemmerm.) Gottschling strains clustered together (94LBS, .98BPP) and built a well-supported (99LBS, 1.00BPP) sister group relationship with free-living Discostella nipponica (Skvortzov) A.Tuji & D.M.Williams (strain TNS:AL-5776). A second lineage (100LBS, 1.00BPP) did not include endosymbiont sequences of U. cf. kevei (G.X.Liu & Z.Y.Hu) Gottschling and U. jiulongense (H. Gu) Gottschling only, but also those of the free-living strains L435 and LO4-2. All sequences of this lineage were nearly identical. Branch lengths are drawn to scale, with the scale bar indicating the number of nt substitutions per site. The numbers on the branches are statistical support values (ML bootstrap values, values <50 are not shown, posterior probabilities below branches, values <90 are not shown; asterisks indicate maximal support)
Fig. 2 in Flowering phenology of co-occurring Asteraceae: a matter of climate, ecological interactions, plant attributes or of evolutionary relationships among species?
Fig. 2 Number of Asteraceae species growing in Chaco Serrano forests of La Serranita-Los Aromos that bear flowers during each month of the year; for calculation, see text in Material and methods Section
Fig. 1 in Flowering phenology of co-occurring Asteraceae: a matter of climate, ecological interactions, plant attributes or of evolutionary relationships among species?
Fig. 1 Diagram of phylogenetic relationships between Asteraceae taxa studied in this work (adapted from Panero and Crozier 2008; Panero and Funk 2008)
Fig. 4 in Flowering phenology of co-occurring Asteraceae: a matter of climate, ecological interactions, plant attributes or of evolutionary relationships among species?
Fig. 4 Plot of PCA scores for 43 co-occurring Asteraceae species in Chaco Serrano forests of La Serranita-Los Aromos, showing first two principal component axes from analysis of flowering phenology considering plant traits and taxonomic membership. Vectors corre-
Fig. 2 in Molecular footprint of parasite co-introduction with Nile tilapia in the Congo Basin
Fig. 2 Median-joining haplotype networks constructed using COI sequences (314 bp) for a Cichlidogyrus sclerosus, b Cichlidogyrus thurstonae and c Cichlidogyrus tilapiae collected in DRC, Madagascar and Burundi
Fig. 1 in Molecular footprint of parasite co-introduction with Nile tilapia in the Congo Basin
Fig. 1 Map of sampling localities with the native range of Nile tilapia in pink (Teugels & Thys van den Audenaerde, 2003; Trewavas & Teugels, 1991). Localities 1–4 are in Lower Congo (1, Tondé; 2, Monzi; 3, Ndimba Leta; 4, Pond near Kila Kindinga), 5 in Middle Congo (Djugu-Djugu ponds), 6–12 in Upper Congo (6, Futuka Farm; 7, Lake Kipopo; 8, Zoo Lubumbashi; 9, Bumaki Farm; 10, Kiswishi River off Futuka Farm; 11, Luapula River off Kashiobwe; 12, Lake Tshangalele); 13 Pond adjacent to Lake Tanganyika, Burundi; 14-16 are in Madagascar (14, Lake Andranotapahina; 15, Ankafarantsika National Park, Lake Ravelobe; 16 Anjingo River near Antsohihy) and 17 is in Lake Kariba, Zimbabwe. Pool Malebo and Boyoma Falls (black bar) divide the Congo Basin in the above-mentioned sections. More info about the sampling localities in Addendum 1
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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.