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zenodo40/100

FIG. 6 in Modern taxonomic approaches to identifying diatrypaceous fungi from marine habitats, with a novel genus Halocryptovalsa Dayarathne & K.D.Hyde, gen. nov.

FIG. 6. — Asexual morph of Cryptosphaeria avicenniae Devadatha & V.V.Sarma, sp. nov. (AMH-9952 – holotype): A, conidiomata on host (Avicennia marina); B, C, horizontal section through conidioma; D, peridium; E, F, conidiophores and conidiogenous cells; G-L, conidia. Scale bars: B-C, 100 μm; D, 50 μm; E-L, 10 μm.

opencc-zeroMar 2020View details →
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FIG. 6. — Russula nigrocarpa S.Y.Zhou, Y.Song & L.H in Three novel species of Russula Pers. subg. Compactae (Fr.) Bon from Dinghushan Biosphere Reserve in southern China

FIG. 6. — Russula nigrocarpa S.Y.Zhou, Y.Song & L.H.Qiu, sp. nov. (GDGM 79720, holotype): A, basidia; B, cheilocystidia; C, pleurocystidia; D, terminal elements of pileipellis; E, pileocystidia. Scale bars: A-E, 10 μm.

opencc-zeroNov 2020View details →
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FIG. 1 in Three novel species of Russula Pers. subg. Compactae (Fr.) Bon from Dinghushan Biosphere Reserve in southern China

FIG. 1. — Maximum Likelihood tree of Russula Pers. subg. Archaeae Buyck & V.Hofst. and Compactae (Fr.) Bon based on ITS sequences, bootstrap values higher than 70% were displayed around nodes. Scale bar: 0.03 substitutions.

opencc-zeroNov 2020View details →
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FIG. 5. — Russula nigrocarpa S.Y.Zhou, Y.Song & L.H in Three novel species of Russula Pers. subg. Compactae (Fr.) Bon from Dinghushan Biosphere Reserve in southern China

FIG. 5. — Russula nigrocarpa S.Y.Zhou, Y.Song & L.H.Qiu, sp. nov. (GDGM 79720, holotype): A, B, fruiting bodies; C-E, pleurocystidia; F-H, pileocystidia; I, J, scanning electronic micrographs of basidiospores. Scale bars: A, B, 1 cm; C-H, 10 μm; I, J, 1 μm.

opencc-zeroNov 2020View details →
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FIG. 8. — Russula ochrobrunnea S.Y.Zhou, Y.Song & L.H in Three novel species of Russula Pers. subg. Compactae (Fr.) Bon from Dinghushan Biosphere Reserve in southern China

FIG. 8. — Russula ochrobrunnea S.Y.Zhou, Y.Song & L.H.Qiu, sp. nov. (GDGM 79718, holotype): A, basidia; B, pleurocystidia; C, cheilocystidia; D, caulocystidia; E, terminal elements of pileipellis. Scale bars: A-D, 10 μm.

opencc-zeroNov 2020View details →
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FIG. 2 in Three novel species of Russula Pers. subg. Compactae (Fr.) Bon from Dinghushan Biosphere Reserve in southern China

FIG. 2. — Maximum Likelihood tree of Russula Pers. subg. Archaeae Buyck & V.Hofst. and Compactae (Fr.) Bon based on LSU-mtSSU-tef1-rpb2-rpb1 combined sequences, bootstrap values higher than 70% were displayed around nodes. Scale bar: 0.02 substitutions.

opencc-zeroNov 2020View details →
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FIG. 4. — Russula latolamellata Y.Song & L.H in Three novel species of Russula Pers. subg. Compactae (Fr.) Bon from Dinghushan Biosphere Reserve in southern China

FIG. 4. — Russula latolamellata Y.Song & L.H.Qiu, sp. nov. (GDGM 79561, holotype): A, basidia; B, cheilocystidia; C, terminal elements of pileipellis; D, pleurocystidia. Scale bars: A-D, 10 μm.

opencc-zeroNov 2020View details →
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FIG. 7. — Russula ochrobrunnea S.Y.Zhou, Y.Song & L.H in Three novel species of Russula Pers. subg. Compactae (Fr.) Bon from Dinghushan Biosphere Reserve in southern China

FIG. 7. — Russula ochrobrunnea S.Y.Zhou, Y.Song & L.H.Qiu, sp. nov. (GDGM 79718, holotype): A-D, fruiting bodies; E, F, scanning electronic micrographs of basidiospores. Scale bars: A-D, 1 cm; E, F, 1 μm.

opencc-zeroNov 2020View details →
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FIG. 3. — Russula latolamellata Y.Song & L.H in Three novel species of Russula Pers. subg. Compactae (Fr.) Bon from Dinghushan Biosphere Reserve in southern China

FIG. 3. — Russula latolamellata Y.Song & L.H.Qiu, sp. nov. (GDGM 79561, holotype): A-D, fruiting bodies; E, F, scanning electronic micrographs of basidiospores. Scale bars: A-D, 1 cm; E, F, 1 μm.

opencc-zeroNov 2020View details →
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FIG. 15. — B, C, F, H, I, K, M-P, R, S in Modern taxonomic approaches to identifying diatrypaceous fungi from marine habitats, with a novel genus Halocryptovalsa Dayarathne & K.D.Hyde, gen. nov.

FIG. 15. — B, C, F, H, I, K, M-P, R, S, Halodiatrype salinicola Dayarathne & K.D.Hyde (MFLU 15-0179 – holotype); A, D, E, G, J, L, O, P, T, U, Halodiatrype avicenniae Dayarathne & K.D.Hyde (MFLU 16-1185 – holotype and MFLU – 16-1197):A, B, horizontal section of ascoma (MFLU 16-1185,MFLU 15-0179);C, D, vertical section through ascoma (MFLU 15-0179, MFLU 16-1185); E, F, peridium (MFLU 16-1185, MFLU 15-0179); G, H, section through neck (MFLU 16-1185, MFLU 15-0179); I, J, asci (MFLU 15-0179 (in Congo red), MFLU 16-1185); K, L, paraphyses (MFLU 15-0179, MFLU 16-1185); M-P, ascospores (MFLU 15-0179, MFLU 16-1185); Q, conidia from culture on PDA (MFLU 18-0150); R-U, culture on PDA (MFLU 15-0179, MFLU 16-1185) Scale bars: A, 1000 µm; B, 500 µm; C, D, I-L, 100 μm; E, F, Q, 20 μm; G-H, 50 μm; M-P, 10 μm

opencc-zeroMar 2020View details →
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Swiss German Novel Collection (ELTeC-gsw)

<pre># ELTeC-CH This is the Swiss novel collection for the ELTeC, the European Literary Text Collection, produced by the COST Action &quot;Distant Reading for European Literary History&quot; (CA16204, https://distant-reading.net). ## Release notes General information about ELTeC releases is available at https://github.com/COST-ELTeC/ELTeC. The ELTeC-gsw collection will contain 100 novels encoded at level 1. The corpus composition criteria are fulfilled. ## Contributors * Collection editor(s): Giulia Grisot, Berenike Herrmann * Sources: Textgrid Repository, Deutsches Textarchiv, KOLIMO, Project-gutenberg.de, e-rara.ch ## Licence All texts included in this collection are in the public domain. The textual markup is provided with a Creative Commons Attribution International 4.0 licence (CC 0, https://creativecommons.org/publicdomain/zero/1.0/).</pre>

opencc-by-4.0Apr 2021View details →
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Novel metagenome assembled genomes (MAGs) that best represent novel species level taxa within the phylum Chloroflexota

<p>1280 Chloroflexita MAGs from the study &quot;Taxonomic re-classification and expansion of the phylum Chloroflexota based on over 5000 genomes and metagenome-assembled genomes&quot;. Only MAGs that improved the representation of a species-level genome cluster within the phylum <em>Chloroflexota</em> were included in this deposition.</p> <p>Most of these MAGs were assembled from publicly availabe metagenome sequence data obtained from the NCBI sra database.</p> <p>An overview of the here deposited MAGs can be found in <a href="https://zenodo.org/api/files/2a6a7fa1-489c-426d-8e05-ada23038dfdf/Zenodo_deposited_MAGS_overview.xlsx?versionId=9cde1488-8388-4fdb-a45e-2d48dc066f9a"> Zenodo_deposited_MAGS_overview.xlsx</a>, for more details please refer to the abive mentioned publication.</p> <p>MAG assemblies are deposited as gzip compressed tar.archive. Three tar.gz archives have been deposited, containing the same MAG assemblies but sorted by different criteria:</p> <ol> <li>All MAGs sorted by category of the source environment</li> <li>All MAGs sorted by class designation</li> <li>All MAGs sorted by MIMAG quality (high or moderate)</li> </ol>

opencc-by-4.0Dec 2022View details →
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Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta

<p>(i) PCR-sequencing: Chromatograms were generated by PCR-sequencing of a region within exon 4 of MBTPS2 using DNA extracted from a healthy control and the proband&#39;s fibroblasts</p> <p>(ii) Gene expression was quantified by qRT-PCR using RNA extracted from fibroblasts. Transcript levels of each gene of interest was&nbsp;calculated using the 2^-deltaCt method with normalization to the average Ct values of endogenous control genes GAPDH, IPO8 and TBP.</p> <p>(iii) Cellular fatty acid content was quantified by GC-MS/MS. Each table represents one technical replicate. Absolute values of each fatty acid are listed in the tables; relative ratios of various fatty acids are calculated at the bottom of each table.&nbsp;</p> <p>(iv) Immunocytochemistry images of ECM proteins (COL1 = collagen type I; COL4 = collagen type IV; COL5 = collagen type V; a2b1 = integrin a2b1)&nbsp;and binding of collagen-hybridising peptide (R-CHP).</p>

opencc-by-4.0May 2023View details →
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Data from: A novel strategy based on Zn(II) porphyrins and silver nanoparticles to photoinactivate Candida albicans

<p>Data supporting&nbsp;the figures presented in the research article &quot;A novel strategy based on Zn(II) porphyrins and silver nanoparticles to photoinactivate <em>Candida albicans&quot;</em></p> <p><strong>Background:</strong> Photodynamic inactivation (PDI) has been an attractive alternative to treat <em>Candida albicans</em> infections, especially considering the spread of resistant strains. The combination of the photophysical advantages of Zn(II) porphyrins (ZnPs) and the plasmonic effect of silver nanoparticles (AgNPs) has the potential to further improve PDI. In this context, this study aimed to evaluate PDI action in <em>C. albicans</em> using ZnTnHex-2-PyP<sup>4+</sup> or ZnTE-2-PyP<sup>4+</sup> associated with AgNPs. <strong>Methods:</strong> AgNPs stabilized with polyvinylpyrrolidone (PVP) were chosen to allow for (i) overlap between NP extinction and ZnP absorption spectra and (ii) favor AgNPs-ZnPs contact; prerequisites for exploring the plasmonic effect. Optical and zeta potential (&zeta;) characterizations were performed, and ROS generation was also evaluated. Yeasts were incubated with ZnPs alone or in combination with AgNPs (AgNPs-ZnPs systems), at various concentrations of ZnPs and two proportions of AgNPs, then irradiated with a blue LED. Interactions between yeasts and the systems (ZnP alone or AgNPs-ZnPs) were evaluated by fluorescence microscopy. <strong>Results:</strong> Subtle spectroscopic changes were observed for ZnPs after association with AgNPs, and the &zeta; analyses confirmed AgNPs-ZnPs interaction. PDI using ZnP-hexyl (0.8 &micro;M) and ZnP-ethyl (5.0 &micro;M) promoted a 3 and 2 log<sub>10</sub> reduction of yeasts, respectively. On the other hand, AgNPs-ZnP-hexyl (0.2 &micro;M) and AgNPs-ZnP-ethyl (0.6 &micro;M) systems led to complete fungal eradication under the same parameters and lower porphyrin concentrations. An increase in the ROS level was observed when ZnPs were associated with AgNPs. Enhanced interaction of yeasts with AgNPs-ZnPs was observed, when compared with ZnPs alone. <strong>Conclusion:</strong> We hypothesize that the plasmonic effect combined with the greater interactions between cells and AgNPs-ZnPs systems resulted in an efficient and improved <em>C. albicans</em> yeast PDI, encouraging further developments toward inactivation of resistant <em>Candida</em> spp.</p> <p>&nbsp;</p>

opencc-by-4.0Jan 2023View details →
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Biometeorological Dataset for 'Novel algorithms for high resolution prediction of canopy evapotranspiration in grapevine'

<p>A&nbsp;head trained <strong><em>Vitis vinifera</em></strong> L. cv. Zinfandel vine was grafted on St. George rootstock (<em>V. rupestris</em>) then planted in a 1.1 m<sup>3</sup> plastic container&nbsp;filled with Yolo County, CA sourced sandy loam.<br> <br> To estimate evapotranspiration, we measured the wind speed, air temperature and relative humidity in vine canopies by mounting each vine with a suite of research grade sensors. We measured wind speed (units m ᐧ s<sup>-1</sup>) inside the vine canopy using a single needle anemometer (<em>East 30 Sensors</em>; Pullman, WA) that took instantaneous wind speed measurements every 10 seconds and recorded the average of the previous 12 instantaneous measurements for every 2-minute interval.</p> <p>We measured temperature (units <sup>o</sup>C) and relative humidity (units %) using HMP60L sensors (Campbell Scientific; Logan, UT) mounted both inside and outside of each vine canopy and recorded instantaneous measurements at each 2-minute interval. We filtered all biometeorological data using a 3-hour moving average to remove noise without causing any significant over or under-approximation of daily maxima and minima.</p> <p>We automated all data collection using two CR1000 data loggers (<em>Campbell Scientific</em>; Logan, UT), with 1 or 2 vines and associated sensors per logger, using custom CR1 programs. &nbsp;A single 30W solar cell and 12V lead acid battery powered the entire vine-sensor system.</p> <p>This dataset represents all sensor data from a single vine, as measured in August 2020. Columns are named accordingly and include&nbsp;units.</p> <p><strong>Please Note</strong>: The column named &#39;load_cell_kg&#39; is not named accurately. The values given are in units of millivolts, and need&nbsp;to be translated from&nbsp;millivolts to kilograms. The 2020 calibration coefficient is&nbsp;0.00330693663 millivolts per kilogram.</p>

opencc-by-4.0May 2023View details →
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FIG. 3 in Anatomy and morphology of Phaeomegaceros fimbriatus (Gottsche) R.J.Duff, J.C.Villarreal, Cargill & Renzaglia (Anthocerotophyta), a novel record for North America

FIG. 3. — Spores of Phaeomegaceros fimbriatus (Gottsche) R.J.Duff, J.C.Villarreal, Cargill &amp; Renzaglia under scanning electron microscopy: A-B, distal face varia- tion of the spores: A, five depressions surrounding a central depression on distal face of spores; B, six depressions surrounding a central depression on distal face of spores; C, proximal face with button-like verrucae confined to the center of triangular areas; D, spore tetrads (tesp) and pseudoelaters (ps). Scale bars: 10 µm.

opencc-zeroOct 2020View details →
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FIG. 2 in Anatomy and morphology of Phaeomegaceros fimbriatus (Gottsche) R.J.Duff, J.C.Villarreal, Cargill & Renzaglia (Anthocerotophyta), a novel record for North America

FIG. 2. — Phaeomegaceros fimbriatus (Gottsche) R.J.Duff, J.C.Villarreal, Cargill &amp; Renzaglia: A, female plant; B, transverse section of gametophyte thallus with band-like thickenings (eng) in cell walls; C, transverse section of gametophyte thallus with ventral tuber (tv) surrounded by rhizoids (ri); D, dorsal surface of a male plant with an antheridium (an) in each antheridial chamber; E, transverse section of a male plant with numerous antheridial chambers (can) and an antheridium (an); F, close up on antheridium (an); G, transverse section of involucre (i) with numerous lamellae (l); H, longitudinal section of the sporophyte foot (e) with placenta (pl); I, longitudinal section of sporophyte capsule with assimilative tissue (ta), spores (es) and central columella (c); J, transverse section of sporophyte with epidermis (ep), assimilative tissue (ta) and central columella (c); K, close up of spores (es), pseudoelaters and central columella (c); L, spores (es) and pseudoelaters (ps). Scale bars: A, 5 mm; B, I, K, 50 µm; C, F, H, J, 100 µm; D, E, G, 200 µm L, 30 µm.

opencc-zeroOct 2020View details →
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Fig. 1 in Novel distribution records and molecular data for species of Macrogyrodactylus Malmberg, 1957 (Monogenea: Gyrodactylidae) from Clarias gariepinus (Burchell) (Siluriformes: Clariidae) in southern Africa

Fig. 1. Map illustrating the sampling localities of Clarias gariepinus (Burchell) during the present study. A – Zambia; B – South Africa.

opencc-by-4.0Dec 2021View details →
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Fig. 2 in Novel distribution records and molecular data for species of Macrogyrodactylus Malmberg, 1957 (Monogenea: Gyrodactylidae) from Clarias gariepinus (Burchell) (Siluriformes: Clariidae) in southern Africa

Fig. 2. Micrographs showing the morphological features of Macrogyrodactylus clarii Gussev, 1961 (A–C), M. congolensis (Prudhoe, 1957) (D–F), and M. karibae Douëllou et Chishawa, 1995 (G, H). A, D, G – hamuli complex; B, E, H – sickle of marginal hook; C, F, I – cirrus with spines.

opencc-by-4.0Dec 2021View details →
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FIG. 9 in Newly discovered fossils provide novel insights on the biology of the South American Miocene snake Colombophis Hoffstetter & Rage, 1977

FIG. 9. — Comparison of vertebrae ratios for Colombophis spp.: A, pr-po/h, vertebra length to high ratio; B, pr-po/pr-pr vertebra length to width ratio; C, cl/naw, centrum length to neural arch width ratio; D, pr-pr/h vertebra width to high ratio; E, zw/ctw, zygosphene width to cotyle width ratio; F, pr-po/naw, vertebrae length to neural arch width ratio.

opencc-zeroJul 2023View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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Your academic CV and NIH biosketch

Make your CV in your school's format and your NIH biosketch from it, then download both as Word files.