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Рис. 2. Chagressia antis sp. nov.: A, B — генитаΛии самца (общий виΑ и эΑеагус); C — стернит и тергит 8-го сегмента брюшка самца, пучки анΑрокониаΛьных чешуек и пΛастинчатые скΛериты; D, E — генитаΛии самки (общий виΑ и обΛасть остиума); a. sc — анΑрокониаΛьные чешуйки; l. scl — пΛастинчатый скΛерит Fig. 2. Chagressia antis sp. nov.: A, B — male genitalia (general view and aedeagus); C — sternite and tergite of the 8thabdominal segment of the male, bundles of androconial scales and lamellar sclerites; D, E — female genitalia (general view and ostium area); a. sc — androconial scales; l. scl — lamellar sclerites in Chagressia antis gen. n., sp. n. (Lepidoptera: Gelechiidae, Gelechiinae) from Panama
Рис. 2. Chagressia antis sp. nov.: A, B — генитаΛии самца (общий виΑ и эΑеагус); C — стернит и тергит 8-го сегмента брюшка самца, пучки анΑрокониаΛьных чешуек и пΛастинчатые скΛериты; D, E — генитаΛии самки (общий виΑ и обΛасть остиума); a. sc — анΑрокониаΛьные чешуйки; l. scl — пΛастинчатый скΛерит Fig. 2. Chagressia antis sp. nov.: A, B — male genitalia (general view and aedeagus); C — sternite and tergite of the 8thabdominal segment of the male, bundles of androconial scales and lamellar sclerites; D, E — female genitalia (general view and ostium area); a. sc — androconial scales; l. scl — lamellar sclerites
72 white matter bundles segmented by 7 different methods in one HCP subject
<p>This dataset contains segmentations of 72 white matter tracts from 7 different automatic segmentation methods for one subject (623844) from the Human Connectome Project (HCP) young adult dataset (https://www.humanconnectome.org/study/hcp-young-adult). Segmentations are given for the original HCP data ("HCP Quality") and for a downsampled version of the HCP data with reduced resolution (2.5mm isotrop) and less gradients (32x b=1000mm/s^2) ("Clinical Quality").</p> <p>The data is part of the following project: https://github.com/MIC-DKFZ/TractSeg/<br> If you use the data please cite the paper mentioned on the project page.</p> <p>Each file is 4D nifti image. The 4th dimension determines the bundle:</p> <p>1: AF_left (Arcuate fascicle)<br> 2: AF_right<br> 3: ATR_left (Anterior Thalamic Radiation)<br> 4: ATR_right<br> 5: CA (Commissure Anterior)<br> 6: CC_1 (Rostrum)<br> 7: CC_2 (Genu)<br> 8: CC_3 (Rostral body (Premotor))<br> 9: CC_4 (Anterior midbody (Primary Motor))<br> 10: CC_5 (Posterior midbody (Primary Somatosensory))<br> 11: CC_6 (Isthmus)<br> 12: CC_7 (Splenium)<br> 13: CG_left (Cingulum left)<br> 14: CG_right <br> 15: CST_left (Corticospinal tract<br> 16: CST_right <br> 17: MLF_left (Middle longitudinal fascicle)<br> 18: MLF_right<br> 19: FPT_left (Fronto-pontine tract)<br> 20: FPT_right <br> 21: FX_left (Fornix)<br> 22: FX_right<br> 23: ICP_left (Inferior cerebellar peduncle)<br> 24: ICP_right <br> 25: IFO_left (Inferior occipito-frontal fascicle) <br> 26: IFO_right<br> 27: ILF_left (Inferior longitudinal fascicle) <br> 28: ILF_right <br> 29: MCP (Middle cerebellar peduncle)<br> 30: OR_left (Optic radiation) <br> 31: OR_right<br> 32: POPT_left (Parieto‐occipital pontine)<br> 33: POPT_right <br> 34: SCP_left (Superior cerebellar peduncle)<br> 35: SCP_right <br> 36: SLF_I_left (Superior longitudinal fascicle I)<br> 37: SLF_I_right <br> 38: SLF_II_left (Superior longitudinal fascicle II)<br> 39: SLF_II_right<br> 40: SLF_III_left (Superior longitudinal fascicle III)<br> 41: SLF_III_right <br> 42: STR_left (Superior Thalamic Radiation)<br> 43: STR_right <br> 44: UF_left (Uncinate fascicle) <br> 45: UF_right <br> 46: CC (Corpus Callosum - all)<br> 47: T_PREF_left (Thalamo-prefrontal)<br> 48: T_PREF_right <br> 49: T_PREM_left (Thalamo-premotor)<br> 50: T_PREM_right <br> 51: T_PREC_left (Thalamo-precentral)<br> 52: T_PREC_right <br> 53: T_POSTC_left (Thalamo-postcentral)<br> 54: T_POSTC_right <br> 55: T_PAR_left (Thalamo-parietal)<br> 56: T_PAR_right <br> 57: T_OCC_left (Thalamo-occipital)<br> 58: T_OCC_right <br> 59: ST_FO_left (Striato-fronto-orbital)<br> 60: ST_FO_right <br> 61: ST_PREF_left (Striato-prefrontal)<br> 62: ST_PREF_right <br> 63: ST_PREM_left (Striato-premotor)<br> 64: ST_PREM_right <br> 65: ST_PREC_left (Striato-precentral)<br> 66: ST_PREC_right <br> 67: ST_POSTC_left (Striato-postcentral)<br> 68: ST_POSTC_right<br> 69: ST_PAR_left (Striato-parietal)<br> 70: ST_PAR_right <br> 71: ST_OCC_left (Striato-occipital)<br> 72: ST_OCC_right</p>
Histological validation of per-bundle water diffusion metrics within a region of fiber crossing following axonal degeneration
<p>Interactive plots showing the correlation between histological parameters of optic nerves and chiasm, and metrics derived from diffusion MRI in a rat model of unilateral retinal ischemia.</p> <p> </p> <p>There are two .html files, each containing an interactive figure, one for data pertaining to the optic nerve, the other for the chiasm. The left panel shows the correlation matrix. Click on any cell to see the corresponding scatter plot on the right panel. </p>
Database of available existing wire spaced rod bundle experiments
<p><span>This report provides a literature review with respect to thermal-hydraulic experiments on rod bundles with wire spacers, representative of fuel assemblies in liquid-metal cooled fast reactors.<span> </span>Both isothermal and heated tests are evaluated, for nominal and non-nominal geometries. </span></p> <p><span>General acceptance criteria are defined for incorporating experiments into this review. The most relevant one is the related to the geometry: only the classical case with one wire per pin is considered. Further additional acceptance criteria are defined for each scenario. All rejected cases are listed in the appendix.</span></p> <p><span>Only publicly available data are considered, with a cut-off date of December 31<sup>st</sup>,<sup> </sup>2023. Ongoing activities are also mentioned, mostly from European collaborative projects, since results are expected to be published soon. A discussion on the comparison with simulation results is presented.</span></p>
Atlas of false-positive bundles for RecobundlesX
<p>This data is made to be used with the <a href="https://zenodo.org/record/4630660">Atlas for RecobundlesX</a>.</p> <p>In the study performed by <em>MaierHein et al. (2017)</em> about the ISMRM 2015 Tractography Challenge, several bundles from the submitted tractograms were labeled as false positives because they were not in the ground-truth tractogram. Quality control was performed on these bundles to select those with the most anatomical implausible trajectory. From these bundles, 44 were selected and refined to obtain smooth bundle models.</p> <p>v2. Streamlines outliers that were not removed with an automatic pruning step were removed manually.</p> <p><em>Maier-Hein KH, Neher PF, Houde J-C, Côté M-A, Garyfallidis E, Zhong J, et al. 2017. The challenge of mapping the human connectome based on diffusion tractography. Nat Commun 8:1349.</em></p>
Text-fig. 47. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of "One-seeded fruit sp. 1"; Catefica locality, Portugal. a, b) Lateral view of fruits showing slightly sinuous ventral margin and the curved stalk; c, d) Longitudinal sections perpendicular to each other through the median part of fruit and its single seed (c, orthoslice yz0652, d, xz0739) showing the bitegmic seed closely adhering to the fruit wall (fw); the several cell layer thick outer integument (oi) and the membranous inner integument (ii); note the vascular bundle (vb) branching into a dorsal and lateral bundle near the base of the fruit; e) Transverse section (orthoslice xy0600) showing fruit wall (fw) and outer (oi) and inner (ii) integuments of the seed; f) Longitudinal section (orthoslice yz0871) through the micropylar region showing micropyle (mi) formed from membranous inner integument (ii). Specimens, Catefica 49-S174927 (a), Catefica 49-S174923 (b, f), Catefica 49-S174769 (c–e). Scale bars = 300 Μm (a–d), 100 Μm (e, f). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 47. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of "One-seeded fruit sp. 1"; Catefica locality, Portugal. a, b) Lateral view of fruits showing slightly sinuous ventral margin and the curved stalk; c, d) Longitudinal sections perpendicular to each other through the median part of fruit and its single seed (c, orthoslice yz0652, d, xz0739) showing the bitegmic seed closely adhering to the fruit wall (fw); the several cell layer thick outer integument (oi) and the membranous inner integument (ii); note the vascular bundle (vb) branching into a dorsal and lateral bundle near the base of the fruit; e) Transverse section (orthoslice xy0600) showing fruit wall (fw) and outer (oi) and inner (ii) integuments of the seed; f) Longitudinal section (orthoslice yz0871) through the micropylar region showing micropyle (mi) formed from membranous inner integument (ii). Specimens, Catefica 49-S174927 (a), Catefica 49-S174923 (b, f), Catefica 49-S174769 (c–e). Scale bars = 300 Μm (a–d), 100 Μm (e, f).
Text-fig. 3. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of fruits of Canrightia foveolata sp. nov.; Catefica locality, Portugal. a) Volume rendering of fruit showing prominent rim around the middle of the fruit with reduced tepals (arrowheads) and partly abraded fruit wall exposing the pitted endotesta surface of one of two seeds (arrow); note two of the vascular bundles (vb) extending from the base of the fruit to the tepals; b) Voltex of fruit showing prominent rim around the fruit (arrowhead) and dense precipitation of crystals in the endothelium cells of one of the two seeds in the fruit; c) Longitudinal section of fruit (orthoslice yz0520) showing the inferred hypanthium rim (arrow head) and two seeds, one with a dense precipitation of crystals; note the prominent endothelium cells (asterisks) of the inner integument and the well-developed fruit wall above the seeds; d) Transverse section through basal part of fruit and seeds close to the micropyle (orthoslice xy0312) showing partly abraded fruit wall with five vascular bundles (vb) and details of the seed coat with endotesta (oi-end) surrounding the tegmen consisting of an outer epidermis (ii-o), middle layer (ii-m) and a distinct inner epidermis (endothelium) consisting of radially elongated cells (asterisk); e) Transverse section (orthoslice xy1680) through apical part of the fruit close to chalaza showing the tips of two seeds; note the endotesta (oi-end) surrounded by thick-walled cells of the exotesta (oi-o); f) Transverse section (orthoslice xy1485) through fruit in the region of the hypanthium rim showing sections through the two seeds close to the chalazal region; note endotesta (oi-end) surrounded by larger cells of exotesta (oi-o) and fruit wall (fr). Specimen, Catefica 49-S174249 (holotype, a–f). Scale bars = 300 Μm (a–c, e, f), 100 Μm (d). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 3. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of fruits of Canrightia foveolata sp. nov.; Catefica locality, Portugal. a) Volume rendering of fruit showing prominent rim around the middle of the fruit with reduced tepals (arrowheads) and partly abraded fruit wall exposing the pitted endotesta surface of one of two seeds (arrow); note two of the vascular bundles (vb) extending from the base of the fruit to the tepals; b) Voltex of fruit showing prominent rim around the fruit (arrowhead) and dense precipitation of crystals in the endothelium cells of one of the two seeds in the fruit; c) Longitudinal section of fruit (orthoslice yz0520) showing the inferred hypanthium rim (arrow head) and two seeds, one with a dense precipitation of crystals; note the prominent endothelium cells (asterisks) of the inner integument and the well-developed fruit wall above the seeds; d) Transverse section through basal part of fruit and seeds close to the micropyle (orthoslice xy0312) showing partly abraded fruit wall with five vascular bundles (vb) and details of the seed coat with endotesta (oi-end) surrounding the tegmen consisting of an outer epidermis (ii-o), middle layer (ii-m) and a distinct inner epidermis (endothelium) consisting of radially elongated cells (asterisk); e) Transverse section (orthoslice xy1680) through apical part of the fruit close to chalaza showing the tips of two seeds; note the endotesta (oi-end) surrounded by thick-walled cells of the exotesta (oi-o); f) Transverse section (orthoslice xy1485) through fruit in the region of the hypanthium rim showing sections through the two seeds close to the chalazal region; note endotesta (oi-end) surrounded by larger cells of exotesta (oi-o) and fruit wall (fr). Specimen, Catefica 49-S174249 (holotype, a–f). Scale bars = 300 Μm (a–c, e, f), 100 Μm (d).
Text-fig. 2. Scanning electron microscope (SEM, a, c–f) and synchrotron radiation X-ray tomographic microscopy (SRXTM, b, g) images of the flower of Mugideiriflora portugallica (a, b) and fruits, seeds and pollen of Canrightia resinifera (c–g); Catefica locality, Portugal. a) Oblique, apical view of flower showing multiparted organization with numerous laminar tepals, stamens that are rhomboidal and flattened in transverse section and carpels that are borne on the short conical apex of the receptacle; b) Transverse section (orthoslice xy0800) through basal part of flower showing the elongate bases of the laminar tepals and the flattened rhomboidal bases of the stamens; c) Fruit in lateral view showing irregular surface resulting from the abundant resin bodies in the fruit and hypanthium wall, scars from stamens on the rim of the hypanthium (arrowheads) and the lobed apical stigmatic region (st); d) Broken fruit with one or two seeds missing but showing three pendant, orthotropous seeds with pointed micropylar regions (mi) and a finely pitted crystalliferous endotesta; note the remains of the apical vascular bundles (vb); e) Single seed isolated from a fruit showing two distinct bundles (vb) still attached apically to the chalazal region of the seed, the pointed micropyle (mi) and the finely pitted surface of the crystalliferous endotesta; f) Monocolpate pollen from stigmatic region of fruit showing the long colpus and coarse reticulum; g) Transverse section (orthoslice xy0705) through a fruit showing four seeds all with radially elongated endothelium cells formed from the inner epidermis of the tegmen (asterisks). Specimens, Catefica 150-S174254 (a, b), Catefica 49-S170377 (c), Catefica 49-S170372 (d), Catefica 50-S170401 (e), Catefica 50-S170404 (f), Catefica 50-S174906 (g). Scale bars = 300 Μm (a–e, g), 6 Μm (f). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 2. Scanning electron microscope (SEM, a, c–f) and synchrotron radiation X-ray tomographic microscopy (SRXTM, b, g) images of the flower of Mugideiriflora portugallica (a, b) and fruits, seeds and pollen of Canrightia resinifera (c–g); Catefica locality, Portugal. a) Oblique, apical view of flower showing multiparted organization with numerous laminar tepals, stamens that are rhomboidal and flattened in transverse section and carpels that are borne on the short conical apex of the receptacle; b) Transverse section (orthoslice xy0800) through basal part of flower showing the elongate bases of the laminar tepals and the flattened rhomboidal bases of the stamens; c) Fruit in lateral view showing irregular surface resulting from the abundant resin bodies in the fruit and hypanthium wall, scars from stamens on the rim of the hypanthium (arrowheads) and the lobed apical stigmatic region (st); d) Broken fruit with one or two seeds missing but showing three pendant, orthotropous seeds with pointed micropylar regions (mi) and a finely pitted crystalliferous endotesta; note the remains of the apical vascular bundles (vb); e) Single seed isolated from a fruit showing two distinct bundles (vb) still attached apically to the chalazal region of the seed, the pointed micropyle (mi) and the finely pitted surface of the crystalliferous endotesta; f) Monocolpate pollen from stigmatic region of fruit showing the long colpus and coarse reticulum; g) Transverse section (orthoslice xy0705) through a fruit showing four seeds all with radially elongated endothelium cells formed from the inner epidermis of the tegmen (asterisks). Specimens, Catefica 150-S174254 (a, b), Catefica 49-S170377 (c), Catefica 49-S170372 (d), Catefica 50-S170401 (e), Catefica 50-S170404 (f), Catefica 50-S174906 (g). Scale bars = 300 Μm (a–e, g), 6 Μm (f).
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).
FIGURE 5 in Bundles of Sperm: Structural Diversity in Scorpion Sperm Packages Illuminates Evolution of Insemination in an Ancient Lineage
FIGURE 5. Sperm packages of Urodacidae Pocock, 1893 (A, B), Diplocentridae Karsch, 1880 (C, D), Scorpionidae Latreille, 1802 (E, F), and Bothriuridae Simon, 1880 (G–L) imaged with scanning electron microscopy (A–C, G, J) or light microscopy (D–F, H, I, K, L). A, B. Urodacus planimanus Pocock, 1893: ellipsoidal/ spherical. C. Diplocentrus lindo Stockwell and Baldwin, 2001: spiral/spherical. D. Nebo hierichonticus (Simon, 1872): bent. E. Pandinus imperator (C.L. Koch, 1841): straight. F. Scorpio fuliginosus (Pallary, 1928): ellipsoidal. G. Brachistosternus ferrugineus (Thorell, 1876): canelike. H. Brachistosternus pentheri Mello-Leitão, 1931: canelike. I. Lisposoma josehermana Lamoral, 1979: straight. J. Orobothriurus tamarugal Ochoa et al., 2011: straight. K. Rumikiru lourencoi (Ojanguren Affilastro, 2003): straight. L. Thestylus aurantiurus Yamaguti and Pinto-daRocha, 2003: straight. Scale bars: 25 µm.
FIGURE 4 in Bundles of Sperm: Structural Diversity in Scorpion Sperm Packages Illuminates Evolution of Insemination in an Ancient Lineage
FIGURE 4. Sperm packages of Chactidae Pocock, 1893 (A, B), Vaejovidae Thorell, 1876 (C–F), Heteroscorpionidae Kraepelin, 1905 (G, H), Hemiscorpiidae Pocock, 1893 (I), and Hormuridae Laurie, 1896 (J–L) imaged with scanning electron microscopy (A–J) or light microscopy (K, L). A, B. Uroctonus mordax Thorell, 1876: bent. C, D. Paravaejovis spinigerus (Wood, 1863): bent. E. Graemeloweus glimmei (Hjelle, 1972): bent. F. Vejovoidus longiunguis (Williams, 1969): bent. G, H. Heteroscorpion goodmani Lourenco, 1996: bent/double bent. I. Hemiscorpius lepturus Peters, 1861: bent. J. Hadogenes troglodytes (Peters, 1861): annular. K, L. Hormurus sp., Queensland, Australia: annular, double bent. Scale bars: 25 µm.
FIGURE 9 in Bundles of Sperm: Structural Diversity in Scorpion Sperm Packages Illuminates Evolution of Insemination in an Ancient Lineage
FIGURE 9. Schematic illustration summarizing the major types, shapes, and folding of sperm packages in Scorpiones with hypothesized evolutionary transformation from absence (free sperm), e.g., Buthida Soleglad and Fet 2003: A. Straight: fusiform, e.g., Parabuthus granulatus (Ehrenberg, 1831) (Buthidae C.L. Koch, 1837); straight, e.g., Iuridae Thorell, 1876, and Superstitioniidae Stahnke, 1940; or canelike, e.g., Bothriuridae Simon, 1880. B. Single fold: bent in half, e.g., Vaejovidae Thorell, 1876, Timogenes and Vachonia Abalos, 1954 (Bothriuridae). C. Multiple folds: ellipsoidal: double parallel fold, e.g., Tetratrichobothrius flavicaudis (De Geer, 1778), Nullibrotheas allenii (Wood, 1863); spiral, e.g., Euscorpiops longimanus (Pocock, 1893); double bent open gatefold, e.g., Broteochactas Pocock, 1893; annular: twisted, e.g., Hormuridae Laurie, 1896; or ringlike, e.g., Bothriurus Peters, 1861, and Timogenes Simon, 1880 (Bothriuridae).
FIGURE 1 in Bundles of Sperm: Structural Diversity in Scorpion Sperm Packages Illuminates Evolution of Insemination in an Ancient Lineage
FIGURE 1. Sperm packages of Bothriuridae Simon, 1880 (A, D, E, F), Superstitioniidae Stahnke, 1940 (B), Euscorpiidae Pocock, 1893 (C), and Buthidae C.L. Koch, 1837 (G–L), imaged with light microscopy (A–F) or scanning electron microscopy (G–L). A, D, E. Timogenes elegans (Mello-Leitão, 1931): bent, annular, straight. B. Superstitionia donensis Stahnke, 1940: straight. C. Tetratrichobothrius flavicaudis (De Geer, 1778): double bent/ellipsoidal; numbers represent folding that causes differences in shape. F. Brachistosternus ferrugineus (Thorell, 1876): straight. G. Zabius fuscus (Thorell, 1876): absent. H. Buthus paris (C.L. Koch, 1839): absent. I. Teruelius ankarana (Lourenço and Goodman, 2003): absent. J. Hottentotta conspersus (Thorell, 1876): absent. K. Babycurus jacksoni (Pocock, 1890): absent. L. Lychas obsti Kraepelin, 1913: absent. Arrows indicate folding of sperm packages described in text, including variations in conspecifics. Scale bars: 25 µm.
FIGURE 8 in Bundles of Sperm: Structural Diversity in Scorpion Sperm Packages Illuminates Evolution of Insemination in an Ancient Lineage
FIGURE 8. Transmission electron micrographs of spermatozoa from sperm packages of the bothriurid, Bothriurus bonariensis (C.L. Koch, 1842), sectioned at different points along an axis (A–D), and of sperm packages of four species of Bothriuridae Simon, 1880 sectioned in the middle (E–H). A. Head, middle piece, and flagella of different sperm packages. B. Nuclei of heads from different spermatozoa. C. Middle piece of different spermatozoa with paired mitochondria. D. Flagella of different spermatozoa. E. Bothriurus bonariensis. F. Timogenes elegans (Mello-Leitão, 1931). G. Brachistosternus ferrugineus (Thorell, 1876). H, I. Urophonius brachycentrus (Thorell, 1876). Inset in E–H illustrates details of axoneme. Abbreviations: axo, axoneme; f, flagellum; h, head; mit, mitochondria; mp, middle piece; n, nucleus. Scale bars: 0.5 µm (A–D); 2.5 µm (E–H).
FIGURE 3 in Bundles of Sperm: Structural Diversity in Scorpion Sperm Packages Illuminates Evolution of Insemination in an Ancient Lineage
FIGURE 3. Sperm packages of Caraboctonidae Kraepelin, 1905 (A, B), Superstitioniidae Stahnke, 1940 (C), Chactidae Pocock, 1893 (D–K), and Troglotayosicidae Lourenco, 1998 (L) imaged with scanning electron microscopy (A–C, E–G, K) or light microscopy (D, H–J, L). A. Caraboctonus keyserlingi Pocock, 1893: straight. B. Hadruroides lunatus (L. Koch, 1867): straight. C. Superstitionia donensis Stahnke, 1940: straight. D, E. Nullibrotheas allenii (Wood, 1863): ellipsoidal, double bent. F, G. Brotheas sp., Bartica District, Guyana: ellipsoidal, double bent. H. Broteochactas nitidus Pocock, 1893: double bent. I. Chactopsoides anduzei (González-Sponga, 1982): double bent. J. Chactas aequinoctialis (Karsch, 1879): ellipsoidal, spherical. K. Teuthraustes sp., Aguay Province, Ecuador: ellipsoidal. L. Troglotayosicus humiculum Botero-Trujillo and Francke, 2009: bent. Scale bars: 25 µm.
An Anesthesia-Centered Bundle to Reduce Postoperative Pulmonary Complications: The PRIME-AIR Study
ClinicalTrials.gov study NCT04108130. IPD Sharing: YES. Countries: 1. Publications: 11.
Building an Optimal Hand Hygiene Bundle
ClinicalTrials.gov study NCT02223455. IPD Sharing: YES. Countries: 1. Publications: 1.
Data from: 3D morphology of an outer-hair-cell hair bundle increases its displacement and dynamic range
Open the record for dataset details and reuse information.
Three-helix bundle structures
<p>Relevant data in "Enumeration and comprehensive in-silico modeling of three-helix bundle structures composed of typical αα-hairpins" : https://doi.org/10.1186/s12859-021-04380-5</p> <p>This repository contains following materials. </p> <p>(0) Decoy used in TM-score calculation</p> <p>(1) Centroid models of three-helix bundle structures sampled in backbone building simulations</p> <p>(2) Full-atom models of best designs</p> <p>(3) Resfile and Rosetta xml to reproduce design</p> <p> </p>
Archival bundle of the data used for "Predictive Auto-scaling with OpenStack Monasca" (UCC 2021)
<p>This archive contains the data used for the paper</p> <p><strong>Predictive Auto-scaling with OpenStack Monasca</strong><br> <a href="mailto:giacomo.lanciano@sns.it">Giacomo Lanciano</a>*, Filippo Galli, Tommaso Cucinotta, Davide Bacciu, Andrea Passarella<br> 2021 IEEE/ACM 14th International Conference on Utility and Cloud Computing (UCC)<br> <a href="https://doi.org/10.1145/3468737.3494104">10.1145/3468737.3494104</a></p> <p>Follow the instructions provided in the <a href="https://github.com/giacomolanciano/UCC2021-predictive-auto-scaling-openstack">companion repo</a> to automatically download and decompress the archive. The following files are included:</p> <table> <tbody> <tr> <td><strong>File</strong></td> <td><strong>Description</strong></td> </tr> <tr> <td> <p>amphora-x64-haproxy.qcow2</p> </td> <td> <p>Image used to create Octavia amphorae</p> </td> </tr> <tr> <td> <p>distwalk-{lin,mlp,rnn,stc}-<INCREMENTAL-ID>.log</p> </td> <td> <p>distwalk run log</p> </td> </tr> <tr> <td> <p>distwalk-{lin,mlp,rnn,stc}-<INCREMENTAL-ID>-pred.json</p> </td> <td> <p>Predictive metric data exported from Monasca DB</p> </td> </tr> <tr> <td> <p>distwalk-{lin,mlp,rnn,stc}-<INCREMENTAL-ID>-real.json</p> </td> <td> <p>Actual metric data exported from Monasca DB</p> </td> </tr> <tr> <td> <p>distwalk-{lin,mlp,rnn,stc}-<INCREMENTAL-ID>-times.csv</p> </td> <td> <p>Client-side response time for each request sent during a run</p> </td> </tr> <tr> <td> <p>model_dumps/*</p> </td> <td> <p>Dumps of the models and data scalers used for the validation</p> </td> </tr> <tr> <td> <p>predictor.log</p> </td> <td> <p>monasca-predictor log</p> </td> </tr> <tr> <td> <p>predictor-times.log</p> </td> <td> <p>monasca-predictor` log (timing info only)</p> </td> </tr> <tr> <td> <p>predictor-times-{lin,mlp,rnn}.{csv,log}</p> </td> <td> <p>monasca-predictor log (timing info only, group by predictor)</p> </td> </tr> <tr> <td> <p>super_steep_behavior.csv</p> </td> <td> <p>Dataset used to train MLP and RNN models</p> </td> </tr> <tr> <td> <p>test_behavior_02_distwalk-6t_last100.dat</p> </td> <td> <p>distwalk load trace</p> </td> </tr> <tr> <td> <p>ubuntu-20.04-min-distwalk.img</p> </td> <td> <p>Image used to create Nova instances for the scaling group</p> </td> </tr> </tbody> </table> <p>* <em>contact author</em></p>
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