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Figure 5 in Ionic homeostasis, biochemical components and yield of Italian zucchini under nitrogen forms and salt stress
Figure 5. Italian zucchini plants fertilized with different forms of nitrogen and irrigated with saline waters.
Figure 2 in Ionic homeostasis, biochemical components and yield of Italian zucchini under nitrogen forms and salt stress
Figure 2. Accumulation of nitrogen (N) (A), phosphorus (P) (B), potassium (K) (C), calcium (Ca) (D) and magnesium (Mg) (E) in Italian zucchini plants irrigated with saline waters. * - Significant at 0.05 probability level (p<0.05).
Figure 4. Chlorophyll b in Ionic homeostasis, biochemical components and yield of Italian zucchini under nitrogen forms and salt stress
Figure 4. Chlorophyll b content (A) and electrolyte leakage (B) in Italian zucchini plants nourished with different forms of nitrogen and irrigated with saline waters. Means followed by different letters indicate significant difference by Tukey test at 0.05 probability level.
Figure 3 in Ionic homeostasis, biochemical components and yield of Italian zucchini under nitrogen forms and salt stress
Figure 3. Accumulation of sodium (Na+) (A), sodium/potassium ratio (Na+/K+) (B), sodium/calcium ratio (Na+/Ca++) (C and D) and sodium/ magnesium ratio (Na+/Mg++) (E and F) in Italian zucchini plants nourished with different forms of nitrogen and irrigated with saline waters. Means followed by different letters indicate significant difference by Tukey test at 0.05 probability level. * and ns - Significant at 0.05 probability level (p<0.05) and not significant (p>0.05), respectively.
Figure 4 in Comparative anatomical studies on the cranial nerves of the fully formed embryos of the Nile tilapia Oreochromis niloticus (Ostiechthyes-Cichlidae). I. Nervus glossopharyngeus
Figure 4. Photomicrograph of part of a transverse section of Oreochromis niloticus through the postotic region showing the position of the glossopharyngeal nerve extracranially. X60. AU.C. Auditory capsule.EXO. Exooccipital bone.F.GP. Glossopharyngeal foramen. IJV.internal jugular vein.G.EB.X 1 The epibranchial ganglion of the 1st branchial vagal trunk.G.EB.X The epibranchial ganglion 2 of the 2nd branchial vagal trunk. MO. Medulla Oblongata. N.CSY. Cranial sympathetic nerve. N.IX Nervus glossopharyngeus RO.IX Glossopharyngeal root.
Figure 1 in Ionic homeostasis, biochemical components and yield of Italian zucchini under nitrogen forms and salt stress
Figure 1. Accumulation of nitrogen - N (A), phosphorus - P (B), potassium - K (C), calcium - Ca (D) and magnesium - Mg (E) in Italian zucchini plants fertilized with different forms of nitrogen and irrigated with saline water. Means followed by different letters indicate significant difference by Tukey test at 0.05 probability level.
Programming codes for obtaining components by means of Single Point Incremental Forming using a Kuka Robot
<p>Programming codes for obtaining components by means of Single Point Incremental Forming using a Kuka Robot, adopting different strategies</p>
Data used in "The Backscatter Gating method for time, energy, and position resolution characterization of long form factor organic scintillators" by Hunter N. Ratliff et al.
<p>This repository contains the raw experimental and PHITS-simulated data used in the JINST article “The Backscatter Gating method for time, energy, and position resolution characterization of long form factor organic scintillators” by Hunter N. Ratliff et al., available at <a href="https://doi.org/10.1088/1748-0221/19/07/P07002">https://doi.org/10.1088/1748-0221/19/07/P07002</a> (the accepted manuscript can also be found at <a href="https://hdl.handle.net/11250/3145287">https://hdl.handle.net/11250/3145287</a> and <a href="https://hratliff.com/publications/">https://hratliff.com/publications/</a>).</p> <p> </p> <p>The data consists of three top-level directories, each with various subdirectories. Within the “PHITS-simulated-data” directory are the PHITS simulations (including input and output files) used in producing Figures 4 and 5 in the manuscript, showing energy spectra in the bar for BSG events from a Cs-137 emission for placement of the source on the bar and on the BSG detector and with spacings between the bar and BSG detector of 20, 80, and 150 mm, along with the energy-dependent spatial distribution of these recoil electrons in the bar.</p> <p> </p> <p>The other two top-level directories contain raw data produced by the CAEN CoMPASS software when acquiring data experimentally. In the analysis for each measurement, the contents of the “RAW” folders were used. The “Energy-calibrations-of-CeBr3” directory contains the energy spectra of the CeBr3 detector (used as the BSG detector) when exposed to a variety of radioactive sources, used together to energy-calibrate the CeBr3 detector. The “Backscatter-gating-measurements” directory contains all of the list-mode data acquired with CoMPASS used for all of the other experimental measurements presented in the manuscript. It contains subdirectories for varied sources, source positions along the bar, distances between the bar and BSG detector, measurements with the source affixed to the BSG detector instead, and a few miscellaneous measurements. The “images” directories within each measurement’s directory (at the same level as the “RAW” folders) contain images produced by the analysis script written for this work used for diagnostics and presenting analyzed data.</p> <p> </p>
Fig. 2 in The local forms of Zootecus (Gastropoda: Pulmonata: Subulinidae) of Pakistan: an archaeomalacological case study
Fig. 2 - WP 199, N 25 44. 760 E 66 37.190 with Zootecus shells emerging from sediments (photo by P. Biagi, R. Nisbet, A. Girod).
Fig. 5 in The local forms of Zootecus (Gastropoda: Pulmonata: Subulinidae) of Pakistan: an archaeomalacological case study
Fig. 5 - Rohri Hills, site 59. Section through the deposits: a) Zootecus sp. shells (modified from Biagi & Pessina. 1994).
Fig. 1 in The local forms of Zootecus (Gastropoda: Pulmonata: Subulinidae) of Pakistan: an archaeomalacological case study
Fig. 1 - Left: map of Pakistan with the areas of the studied sites. A) Balochistan, sites WP16, WP 31, Uthal. B) Upper Sindh, Rohri Hills, site 59, site 480. Right: satellite view of the area of Balochistan, South of Uthal with location of the Lake Siranda and the lagoon of Miani Hor.
Fig. 11 in The local forms of Zootecus (Gastropoda: Pulmonata: Subulinidae) of Pakistan: an archaeomalacological case study
Fig. 11 - Comparison between the linear regression of the five samples and the shapes described in the past literature. 1) Z. pullus. 2) Z. chion gracilor minor. 3) Z. insularis chion. 4) Z. polygyratus. 5) Z. chion. 6) Z. chion from Hyderabad. 7) Z. agrensis. 8) Z. estellus. 9) Z. pertica.
Fig. 4 in The local forms of Zootecus (Gastropoda: Pulmonata: Subulinidae) of Pakistan: an archaeomalacological case study
Fig. 4 - Left: view of shell heaps. WP 16, Zootecus sp. with fresh-water malacofauna. Right: WP 31, shells of Zootecus sp. only (photo by A. Girod).
Fig. 9 in The local forms of Zootecus (Gastropoda: Pulmonata: Subulinidae) of Pakistan: an archaeomalacological case study
Fig. 9 - Linear regression analyses of the height - diameter relationships in the samples; x-axis = diameter in mm; y-axis = height in mm.
Fig. 3 in The local forms of Zootecus (Gastropoda: Pulmonata: Subulinidae) of Pakistan: an archaeomalacological case study
Fig. 3 - Hills around the River Windar and some living specimens of Zootecus cfr. insularis (photo by A. Girod).
Sulfaguanidine Solid-State forms: An Experimental and Computational Study
<p><span>Computational data:</span></p> <ul> <li><span>Crystal structure prediction anhydrates</span></li> <li><span>Crystal structure prediction monohydrates</span></li> </ul> <p><span>Experimental data:</span></p> <ul> <li><span>IR spectra (dat files)</span></li> <li><span>Moisture sorption/desorption data</span></li> <li><span>C16 Solubility data</span></li> </ul> <p> </p> <p> </p>
◂Fig.15 Scanning electron micrographs (SEM) showing transverse rows of dentition on Dinaride Zospeum and Iberozospeum radulae; (a) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia, transverse rows of teeth on long, slender basal plates (bp), rachidian (r) and lateral teeth (l), arrows indicate medial grooves on mesocones of individual teeth; (b) Z. isselianum, NMBE 553389, Turjeva jama, Slovenia, ibid.; (c) Iberozospeum sp. (RMNH.MOL.234,116), Cueva a Sul, straight transverse rows of small, seemingly bi-cuspid lateral teeth (l) with reduced mesocones on compact basal plates; (d) ibid., close up view of rachidian teeth (r), lateral fang-like teeth (l) and transitional teeth (t); (e) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili, rachidian teeth (r) flanked by 4-cuspid lateral teeth (l), C. ibazoricum-like in form; (f) Iberozospeum sp. (RMNH. MOL.234108), Cueva la Torcona, lateral teeth showing reduced mesocones (me) flanked by long, fang-like endo- and ectocones (e), rachidian tooth (r) (flipped over in upper righthand corner of image); (g) I. zaldivarae (AJC 1876a), Cueva de Las Paúles, transverse rows of teeth showing varying cusp lengths; (h) ibid., close up view (left to right) of marginal (m) and transitional teeth (t) on short, compact basal plates (bp). — Magnification varies for each perspective, see scale bars; all Figs taken by M. Ruppel, (ret.) Goethe University Frankfurt am Main in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig.15 Scanning electron micrographs (SEM) showing transverse rows of dentition on Dinaride Zospeum and Iberozospeum radulae; (a) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia, transverse rows of teeth on long, slender basal plates (bp), rachidian (r) and lateral teeth (l), arrows indicate medial grooves on mesocones of individual teeth; (b) Z. isselianum, NMBE 553389, Turjeva jama, Slovenia, ibid.; (c) Iberozospeum sp. (RMNH.MOL.234,116), Cueva a Sul, straight transverse rows of small, seemingly bi-cuspid lateral teeth (l) with reduced mesocones on compact basal plates; (d) ibid., close up view of rachidian teeth (r), lateral fang-like teeth (l) and transitional teeth (t); (e) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili, rachidian teeth (r) flanked by 4-cuspid lateral teeth (l), C. ibazoricum-like in form; (f) Iberozospeum sp. (RMNH. MOL.234108), Cueva la Torcona, lateral teeth showing reduced mesocones (me) flanked by long, fang-like endo- and ectocones (e), rachidian tooth (r) (flipped over in upper righthand corner of image); (g) I. zaldivarae (AJC 1876a), Cueva de Las Paúles, transverse rows of teeth showing varying cusp lengths; (h) ibid., close up view (left to right) of marginal (m) and transitional teeth (t) on short, compact basal plates (bp). — Magnification varies for each perspective, see scale bars; all Figs taken by M. Ruppel, (ret.) Goethe University Frankfurt am Main
◂Fig. 14 Scanning electron micrographs (SEM) showing radular ribbon form, middle adhesive zone (az) and rows of dentition (rd) of Dinaride and Iberian individuals (notation denotes aspects on one Dinaride Zospeum and one Iberozospeum ribbon); (a) Z. exiguum (NMBE 553384), Križna jama, Slovenia (45.7452, 14.4673), long and narrow, tapered anterior end (tae), short adhesive zone (az), bottom furled with narrow obtuse or straight base (nosb); (b) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia (44.2701, 15.8855), ibid., with straight base; (c) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili (42.9994, -2.4381), moderately long and broad, tapered anterior end (tae), prominent adhesive zone (az), straight base (sb); (d) I. zaldivarae, (AJC 1876), Cueva de Las Paúles (43.1282, -2.7362), ibid.; (e) Iberozospeum sp. (RMNH.MOL. 234,109), Cueva de la Foz, long and broad, ibid; (f) Iberozospeum sp., (RMNH.MOL. 234,144), Cueva de Rales, very long and broad, ibid; (g) Iberozospeum sp., (RMNH.MOL. 234,116), Cueva a Sul, long and broad, ibid; (h) Iberozospeum sp., (RMNH.MOL. 234,108), Cueva de Torcona, very long and broad, ibid. — Magnification varies for each perspective, see scale bars; all Figs imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig. 14 Scanning electron micrographs (SEM) showing radular ribbon form, middle adhesive zone (az) and rows of dentition (rd) of Dinaride and Iberian individuals (notation denotes aspects on one Dinaride Zospeum and one Iberozospeum ribbon); (a) Z. exiguum (NMBE 553384), Križna jama, Slovenia (45.7452, 14.4673), long and narrow, tapered anterior end (tae), short adhesive zone (az), bottom furled with narrow obtuse or straight base (nosb); (b) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia (44.2701, 15.8855), ibid., with straight base; (c) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili (42.9994, -2.4381), moderately long and broad, tapered anterior end (tae), prominent adhesive zone (az), straight base (sb); (d) I. zaldivarae, (AJC 1876), Cueva de Las Paúles (43.1282, -2.7362), ibid.; (e) Iberozospeum sp. (RMNH.MOL. 234,109), Cueva de la Foz, long and broad, ibid; (f) Iberozospeum sp., (RMNH.MOL. 234,144), Cueva de Rales, very long and broad, ibid; (g) Iberozospeum sp., (RMNH.MOL. 234,116), Cueva a Sul, long and broad, ibid; (h) Iberozospeum sp., (RMNH.MOL. 234,108), Cueva de Torcona, very long and broad, ibid. — Magnification varies for each perspective, see scale bars; all Figs imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main
Fig. 4 in Ground beetles (Coleoptera: Carabidae) from the region of Cape Emine (Central Bulgarian Black sea coast). Part I. Taxonomic and zoogeographic structure, life forms, habitat and humidity preferences
Fig. 4. Proportions of the subclasses of life forms in the carabid complex (I – class Zoophaga, II – class Mixophytophaga).
Fig. 17 in Revision of (Coutière, 1897) and Allied Forms (Decapoda: Caridea: Alpheidae).
Fig. 17. Salmoneus alius sp. nov., holotype, non-ovigerous specimen (cl 2.7 mm) from New Caledonia (MNHN-IU-2019-3495): A, third maxilliped, lateral view; B, same, ultimate article, mesial view; C, second pereiopod, lateral view; D, third pereiopod, lateral view; E, fourth pereiopod, lateral view; F, fifth pereiopod, lateral view.
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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.