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Figure 3 in A new species of Cletocamptus (Copepoda: Harpacticoida) from Chile and some notes on Cletocamptus axi Mielke, 2000
Figure 3. Cletocamptus cecsurirensis sp. nov. Female. (A) Antennule; (B) urosome, ventral (P5-bearing somite omitted); (C) P6; (D) left caudal ramus, ventral. Scale bar: 46 Mm (A); 107 Mm (B); 32 Mm (C); 64 Mm (D).
Figure 5 in A new species of Cletocamptus (Copepoda: Harpacticoida) from Chile and some notes on Cletocamptus axi Mielke, 2000
Figure 5. Cletocamptus cecsurirensis sp. nov. Female. (A) Maxilliped; (B) P5. Scale bar: 60 Mm (A); 100 Mm (B).
Figure 2 in A new species of Cletocamptus (Copepoda: Harpacticoida) from Chile and some notes on Cletocamptus axi Mielke, 2000
Figure 2. Cletocamptus cecsurirensis sp. nov. Female. (A–H) Spinular ornamentation along posterior margin of P2– P5-bearing somites (A–D), genital double-somite (E, F), and fourth and fifth urosomites (G, H); (I) anal somite and right caudal ramus, lateral; (J) anal somite and caudal rami, dorsal. Scale bar: 100 Mm.
Visual Tracking of Entire Bumblebee Colonies Using Novel Pipeline Finds No Evidence of Gut-Brain Axis (Replicates 1, 2)
<p>This archive contains raw data processed from video files taken of bumblebee colonies during replicates 1 and 2 of a study on the effect of the gut microbiome on social behaviour. Files ending with "_raw.csv" contain data on read tags, while ones ending with "_noID.csv" contain data on potential tags. Files are named as follows: R[replicate number][Baseline/Data][Day]R[recording session][HiveID][VideoID]</p>
MPIData: Easy Axis Orientation Estimation
<p>This data repository contains magnetic particle imaging data. The files are stored in the <a href="https://arxiv.org/pdf/1602.06072.pdf">MDF file format</a> and the folder structure is organized as an <a href="https://github.com/MagneticParticleImaging/MPIFiles.jl">MDF store</a>. The data is used in <a href="https://github.com/IBIResearch/EasyAxisOrientationEstimation">this</a> code example.</p>
Text-fig. 4. Ratio diagrams of total length of p3–m3. Parasorex depereti from BRS 25 (data from Fanfani 1999), Parasorex depereti (data from Crochet 1986), Parasorex ibericus, type locality Otura-1, Spain (Mein and Martín-Suárez 1993), Parasorex pristinus (Ziegler 2003), Apulogalerix pusillus, Gargano (fissure filling F32), Italy (Masini and Fanfani 2013). On the horizontal axis are reported the element of the series, in ordinates the ratio of the average lengths on the standard Parasorex socialis from La Grive, France (data from Masini and Fanfani 2013). in New Light On Parasorex Depereti (Erinaceomorpha: Erinaceidae: Galericini) From The Late Messinian (Mn 13) Of The Monticino Quarry (Brisighella, Faenza, Italy)
Text-fig. 4. Ratio diagrams of total length of p3–m3. Parasorex depereti from BRS 25 (data from Fanfani 1999), Parasorex depereti (data from Crochet 1986), Parasorex ibericus, type locality Otura-1, Spain (Mein and Martín-Suárez 1993), Parasorex pristinus (Ziegler 2003), Apulogalerix pusillus, Gargano (fissure filling F32), Italy (Masini and Fanfani 2013). On the horizontal axis are reported the element of the series, in ordinates the ratio of the average lengths on the standard Parasorex socialis from La Grive, France (data from Masini and Fanfani 2013).
Fig. 5. Correlation between PCA axis 1 in Fish assemblages of tropical floodplain lagoons: exploring the role of connectivity in a dry year
Fig. 5. Correlation between PCA axis 1 and species richness (a), density (b), and biomass (c) in connected [February (), May (), November ()] and disconnected lagoons, May (), August (), November ()]. Arrows indicate the direction of the limnological variables influence.
Figure 5. Head capsule EES plots. A, axis 2 in Termite soldier defence strategies: a reassessment of Prestwich's classification and an examination of the evolution of defence morphology using extended eigenshape analyses of head morphology
Figure 5. Head capsule EES plots. A, axis 2 vs. axis 1. B, axis 2 vs. axis 3. C, modelled mode of dorsal head capsule shape change along axes 1, 2 and 3.
Text-fig. 44. Scanning electron microscope (SEM, a, b) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c, d) images of "Hexacarpellate flower". a) Lateral view of flower showing epigynous organization with remains of tepals inserted at top of the hypanthium; b) Detail of apical part of flower showing laminar structures (arrows) that may be stamen bases, adhering to, or fused with, the tepals; c) Longitudinal section (orthoslice yz0540) of flower through the median plane showing the epigynous organization and central axis with ovules (arrows); d) Transverse section (orthoslice xy1250) through the ovary of the flower showing the hexagonal outline, the six locules and ovules (arrows) borne near the center of the gynoecium. Specimen, Catefica 153-S174313 (a–d). Scale bars = 300 Μm (a, c), 100 Μm (b, d). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 44. Scanning electron microscope (SEM, a, b) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c, d) images of "Hexacarpellate flower". a) Lateral view of flower showing epigynous organization with remains of tepals inserted at top of the hypanthium; b) Detail of apical part of flower showing laminar structures (arrows) that may be stamen bases, adhering to, or fused with, the tepals; c) Longitudinal section (orthoslice yz0540) of flower through the median plane showing the epigynous organization and central axis with ovules (arrows); d) Transverse section (orthoslice xy1250) through the ovary of the flower showing the hexagonal outline, the six locules and ovules (arrows) borne near the center of the gynoecium. Specimen, Catefica 153-S174313 (a–d). Scale bars = 300 Μm (a, c), 100 Μm (b, d).
Text-fig. 22. Scanning electron microscope (SEM, a–c) and synchrotron radiation X-ray tomographic microscopy (SRXTM, d) images of Ibericarpus cuneiformis gen. et sp. nov.; Catefica locality, Portugal. a) Fruiting axis bearing an elongated receptacle with numerous diamond-shaped scars from detached fruitlets; note the absence of scars from bracts, tepals or stamens at the transition to the fruitlet scars and the stalk (arrow); b) Group of ten fruitlets detached from fruiting axis in (a) showing apical stigmatic region and distinctive bulging isodiametric epidermal cells; c) Detached fruitlet showing apical stigmatic region; d) Volume rendering of three adhering fruits showing apical stigmatic region and distinctive bulging isodiametric epidermal cells. Specimens, Catefica MM75-P0477 (a, b), Catefica 49-S115852 (c), Catefica 50-S174907 (d). Scale bars = 300 Μm (a–d). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 22. Scanning electron microscope (SEM, a–c) and synchrotron radiation X-ray tomographic microscopy (SRXTM, d) images of Ibericarpus cuneiformis gen. et sp. nov.; Catefica locality, Portugal. a) Fruiting axis bearing an elongated receptacle with numerous diamond-shaped scars from detached fruitlets; note the absence of scars from bracts, tepals or stamens at the transition to the fruitlet scars and the stalk (arrow); b) Group of ten fruitlets detached from fruiting axis in (a) showing apical stigmatic region and distinctive bulging isodiametric epidermal cells; c) Detached fruitlet showing apical stigmatic region; d) Volume rendering of three adhering fruits showing apical stigmatic region and distinctive bulging isodiametric epidermal cells. Specimens, Catefica MM75-P0477 (a, b), Catefica 49-S115852 (c), Catefica 50-S174907 (d). Scale bars = 300 Μm (a–d).
Text-fig. 28. Scanning electron microscope (SEM) images of stamens and pollen of Endressistemon cateficensis gen. et sp. nov.; Catefica locality, Portugal. a, b) Staminal structure with two lateral stamens and one median structure seen in ventral and dorsal view (orientation unknown) showing that each stamen has a prominent apical extension and two pairs of pollen sacs separated by a narrow connective; both stamens are borne on a common base together with the median structure and their anthers are sessile on the common stalk; note the apical projection of the median structure (asterisk) between the two stamens and the ribs over probable vascular bundles that extend from the common base into the apical projections of both stamens and the median structure (arrows); c) Staminal structure showing two stamens with prominent apical projections and median axis-like structure between the two stamens (arrow); d) Staminal structure showing two stamens with prominent apical projections borne on a common base; e) Staminal structure in (a) and (b), from the same orientation as (b), showing the ribs over probable vascular bundles (yellow) that extend into the apical projections; f) Detail of staminal structure in (a) and (b) showing the fused or strongly adhering apical projections of the two lateral stamens and the median structure (asterisk); g) Monocolpate, reticulate pollen grains from the pollen sacs of stamen in (d). Specimens, Catefica 49-S107778 (holotype, a, b, e, f), Catefica 49-S107769 (c), Catefica 49-S107751 (d, g). Scale bars = 600 Μm (a–d), 300 Μm (e), 100 Μm (f), 6 Μm (g). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 28. Scanning electron microscope (SEM) images of stamens and pollen of Endressistemon cateficensis gen. et sp. nov.; Catefica locality, Portugal. a, b) Staminal structure with two lateral stamens and one median structure seen in ventral and dorsal view (orientation unknown) showing that each stamen has a prominent apical extension and two pairs of pollen sacs separated by a narrow connective; both stamens are borne on a common base together with the median structure and their anthers are sessile on the common stalk; note the apical projection of the median structure (asterisk) between the two stamens and the ribs over probable vascular bundles that extend from the common base into the apical projections of both stamens and the median structure (arrows); c) Staminal structure showing two stamens with prominent apical projections and median axis-like structure between the two stamens (arrow); d) Staminal structure showing two stamens with prominent apical projections borne on a common base; e) Staminal structure in (a) and (b), from the same orientation as (b), showing the ribs over probable vascular bundles (yellow) that extend into the apical projections; f) Detail of staminal structure in (a) and (b) showing the fused or strongly adhering apical projections of the two lateral stamens and the median structure (asterisk); g) Monocolpate, reticulate pollen grains from the pollen sacs of stamen in (d). Specimens, Catefica 49-S107778 (holotype, a, b, e, f), Catefica 49-S107769 (c), Catefica 49-S107751 (d, g). Scale bars = 600 Μm (a–d), 300 Μm (e), 100 Μm (f), 6 Μm (g).
Text-fig. 2. Taimyria triassica NAUGOLNYKH et MOGUTCHEVA gen. et sp. nov., a – holotype 4287/6. Lateral female cones marked by orange arrows; main axis bearing lateral cones marked "Ax". Scale bar 1 cm. in Taimyria Gen. Nov., A New Genus Of Evolutionary Advanced Gymnosperms From Triassic Of The Taimyr Peninsula, Siberia, Russia
Text-fig. 2. Taimyria triassica NAUGOLNYKH et MOGUTCHEVA gen. et sp. nov., a – holotype 4287/6. Lateral female cones marked by orange arrows; main axis bearing lateral cones marked "Ax". Scale bar 1 cm.
Figure data to "Continuous similarity transformation for critical phenomena: easy-axis antiferromagnetic XXZ model"
<p>This collection of data is complementary to the publication "Continuous similarity transformation for critical phenomena: easy-axis antiferromagnetic XXZ model", Matthias R. Walther, Dag-Björn Hering, Götz S. Uhrig, Kai P. Schmidt, arXiv:2211.05689 (https://arxiv.org/abs/2211.05689).</p> <p>It contains the data points calculated by the method of Continuous Similarity Transformation(CST) used in Figures 3,5,6,7 and 8 in the CSV-Format.</p> <p>For details on the CST, the used error estimates and physical quantities we refer the the publication.</p> <p>For details on the format we recommend the README.md file.</p>
O2-O2, SO2, BrO, and IO differential slant column densities (dSCDs) measured by the University of Colorado Multi-AXis Differential Optical Absorption Spectroscopy (CU MAX-DOAS) instrument at Maido Observatory during April 29, 2018 and May 4, 2018
<p>Description: O<sub>2</sub>-O<sub>2</sub>, SO<sub>2</sub>, BrO, and IO differential slant column densities (dSCDs) measured by the University of Colorado Multi-AXis Differential Optical Absorption Spectroscopy (CU MAX-DOAS) instrument at Maido Observatory during April 29, 2018 and May 4, 2018.</p> <p>Instrument: University of Colorado Multi-AXis Differential Optical Absorption Spectroscopy (CU MAX-DOAS)<br> Instrument reference: Coburn et al. (2011); doi:10.5194/amt-4-2421-2011<br> Instrument contact: Christopher F. Lee (christopher.f.lee@colorado.edu)<br> Instrument PI: Rainer Volkamer (rainer.volkamer@colorado.edu)<br> <br> Measurement site: Maido Observatory, Reunion Island<br> Longitude: 55.384 degrees East<br> Latitude: 21.080 degrees South<br> Altitude: 2160 meters above sea level<br> Azimuth angle: Approximately 100 degrees clockwise from north<br> <br> The detection limit is defined as (2*Measured RMS) / (Maximum differential absorption cross section), where RMS = root-mean-square noise of spectral signal not accounted for by DOAS fit parameters [optical density units]. The maximum differential absorption cross sections used are 7.0e-21 [cm<sup>2</sup>] for SO<sub>2</sub>, 2.6e-17 [cm<sup>2</sup>] for BrO, and 3.5e-17 [cm<sup>2</sup>] for IO. Detection limits for SO<sub>2</sub> dSCDs, BrO dSCDs, and IO dSCDs are only reported during periods of significant SO<sub>2</sub> detection. BrO to SO<sub>2</sub> ratios are only reported during periods when both BrO dSCDs and SO<sub>2</sub> dSCDs are above the detection limit.</p> <p>Local time (RET) is UTC+4.<br> <br> Column 1: UTC start datetime (yyyy-mm-dd HH:MM:SS)<br> Column 2: UTC center datetime (yyyy-mm-dd HH:MM:SS)<br> Column 3: UTC stop datetime (yyyy-mm-dd HH:MM:SS)<br> Column 4: Elevation angle above the horizon (degrees)<br> Column 5: O<sub>2</sub>-O<sub>2</sub> dSCD [molec<sup>2</sup> cm<sup>-5</sup>]<br> Column 6: Spectral fit error for O<sub>2</sub>-O<sub>2</sub> dSCD [molec<sup>-2</sup> cm<sup>-5</sup>]<br> Column 7: SO<sub>2</sub> dSCD [molec cm<sup>-2</sup>]<br> Column 8: Spectral fit error for SO<sub>2</sub> dSCD [molec cm<sup>-2</sup>]<br> Column 9: Detection limit for SO<sub>2</sub> dSCD [molec cm<sup>-2</sup>]<br> Column 10: BrO dSCD [molec cm<sup>-2</sup>]<br> Column 11: Spectral fit error for BrO dSCD [molec cm<sup>-2</sup>]<br> Column 12: Detection limit for BrO dSCD [molec cm<sup>-2</sup>]<br> Column 13: IO dSCD [molec cm<sup>-2</sup>]<br> Column 14: Spectral fit error for IO dSCD [molec cm<sup>-2</sup>]<br> Column 15: Detection limit for IO dSCD [molec cm<sup>-2</sup>]<br> Column 16: Ratio of BrO dSCDs to SO<sub>2</sub> dSCDs<br> Column 17: Error in ratio of BrO dSCDs to SO<sub>2</sub> dSCDs</p>
Figure S50 in Supplementary Materials for Precipitation is the main axis of tropical plant phylogenetic turnover across space and time
Figure S50. Optimisation of tropical and temperate niches across the Mimosoid phylogeny. Ancestral niches were estimated using a complete metachronogram for Caesalpinioideae, including non-Mimosoid Caesalpinioideae taxa, but only the Mimosoid clade is shown here.
Figure S48 in Supplementary Materials for Precipitation is the main axis of tropical plant phylogenetic turnover across space and time
Figure S48. Speciation rates estimated across the Caesalpinioideae metachronogram under eight scenarios with different fixed extinction rates. Extinction rates are shown above each subfigure, while speciation rates are indicated by branch colours.
Figure S49 in Supplementary Materials for Precipitation is the main axis of tropical plant phylogenetic turnover across space and time
Figure S49. Top: Speciation rates in the Mimosoid clade through time, estimated under different extinction rate scenarios using BAMM. Middle: Paleotemperature inferred from delta O18 measurements, using data from Zachos et al. (179). Bottom: Phenogram of mean annual precipitation in the Mimosoid clade through time. Coloured lines with dots show the median, wettest, and driest reconstructed rainfall niche of all nodes in the phylogeny per time bin of one million years.
Figure S47 in Supplementary Materials for Precipitation is the main axis of tropical plant phylogenetic turnover across space and time
Figure S47. Ancestral range estimation of Caesalpinioideae, performed using BioGeoBEARS with the best-fitting model (i.e., DEC+J). Trans-oceanic dispersal events in the Mimosoid clade, based on a model with seven regions, are indicated with numbered green circles.
Figure S46 in Supplementary Materials for Precipitation is the main axis of tropical plant phylogenetic turnover across space and time
Figure S46. Optimisation of dry season length across the Mimosoid phylogeny. Inset shows the fraction of dry season length niche shifs per speciation event through time. See caption Figure 1 for explanation.
Figure S45 in Supplementary Materials for Precipitation is the main axis of tropical plant phylogenetic turnover across space and time
Figure S45. Variation partitioning results obtained using the genus-level Mimosoid phylogeny (rather than the metachronogram). See caption Figure 2 for explanation.
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