Skip to main content
Powered by ShareScore

Find research datasets worth reusing

Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.

23

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

23 results for “Hymenoscyphus”

Learn how ShareScore rates datasets ↗
zenodo40/100

Fig. 7 Hymenoscyphus imberbis. a Habitus. b in Emendations to tissue typology in discomycetes

Fig. 7 Hymenoscyphus imberbis. a Habitus. b Textura intricata typica in medullary excipulum. Photographs by L.C.A.F. Rommelaars (coll. L.C.A.F. Rommelaars s.n.; 2013; Netherlands, Tilburg, "Kaaistoep"; on dead deciduous wood; herb. Rommelaars)

opencc-by-4.0May 2020View details →
zenodo40/100

Fig. 9 Hymenoscyphus epiphyllus var. acarius. a Habitus. b in Emendations to tissue typology in discomycetes

Fig. 9 Hymenoscyphus epiphyllus var. acarius. a Habitus. b Textura globulosa typica in ectal excipulum. Photographs by L.C.A.F. Rommelaars (coll. L.C.A.F. Rommelaars s.n.; 2012; Netherlands, Tilburg, "Kaaistoep"; on mixture of Pinus sylvestris needles and deciduous leaves; herb. Rommelaars)

opencc-by-4.0May 2020View details →
zenodo40/100

Fig. 5 Hymenoscyphus fructigenus var. carpini. a Habitus. b in Emendations to tissue typology in discomycetes

Fig. 5 Hymenoscyphus fructigenus var. carpini. a Habitus. b Textura porrecta typica in the medullary excipulum. c Textura prismatica typica in the ectal excipulum. Drawing and photographs by the author (coll. J. Hengstmengel no. 443; 28.9.1979; Netherlands, Leiden, Botanical garden; on fallen fruits of Carpinus betulus; herb. L 977.215–219

opencc-by-4.0May 2020View details →
zenodo36/100

Comparative analyses of the Hymenoscyphus fraxineus and Hymenoscyphus albidus genomes reveals potentially adaptive differences in secondary metabolite and transposable element repertoires

<p><strong>Background&nbsp;</strong>The dieback epidemic decimating common ash (<em>Fraxinus excelsior</em>) in Europe is caused by the invasive fungus&nbsp;<em>Hymenoscyphus fraxineus</em>. In this study we analyzed the genomes of&nbsp;<em>H. fraxineus</em>&nbsp;and&nbsp;<em>H. albidus</em>, its native but, now essentially displaced, non-pathogenic sister species, and compared them with several other members of&nbsp;<em>Helotiales</em>. The focus of the analyses was to identify signals in the genome that may explain the rapid establishment of&nbsp;<em>H. fraxineus</em>&nbsp;and displacement of&nbsp;<em>H. albidus</em>.</p> <p><strong>Results</strong>&nbsp;The genomes of&nbsp;<em>H. fraxineus</em>&nbsp;and&nbsp;<em>H. albidus&nbsp;</em>showed a high level of synteny and identity. The assembly of&nbsp;<em>H. fraxineus&nbsp;</em>is 13 Mb&nbsp;longer than that of&nbsp;<em>H. albidus&rsquo;,&nbsp;</em>most of this&nbsp;difference can be attributed to higher dispersed repeat content ((i.e transposable elements&nbsp;[TEs]) in&nbsp;<em>H. fraxineus</em>. In general, TE families in&nbsp;<em>H. fraxineus</em>showed more signals of repeat-induced point mutations (RIP) than in&nbsp;<em>H. albidus</em>, especially in Long-terminal repeat (LTR)/Copia and LTR/Gypsy elements.&nbsp;Comparing gene family expansions and 1:1 orthologs, relatively few genes show signs of positive selection between species. However, several of those that did appeared to be associated with secondary metabolite genes families, including&nbsp;gene families&nbsp;containing two of the genes in the&nbsp;<em>H. fraxineus-</em>specific,&nbsp;<em>hymenosetin&nbsp;</em>biosynthetic gene cluster (BGC).</p> <p><strong>C</strong><strong>onclusion&nbsp;</strong>The genomes of&nbsp;<em>H. fraxineus</em>&nbsp;and&nbsp;<em>H. albidus</em>&nbsp;show a high degree of synteny, and are rich in both TEs and BGCs, but&nbsp;the genomic signatures also indicated that&nbsp;<em>H. albidus</em>&nbsp;may be less well equipped to adapt&nbsp;and maintain its ecological niche in a rapidly changing environment.&nbsp;</p> <p><strong>Data included</strong></p> <p>This post contains the alternate structural and functional annotations of the genomes of Helotealean fungi&nbsp;used in the study.</p>

opencc-by-4.0Dec 2020View details →
zenodo32/100

Supplementary material 1 from: Pourmoghaddam MJ, Lambert C, Surup F, Khodaparast SA, Krisai-Greilhuber I, Voglmayr H, Stadler M (2020) Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon spp. against the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture. MycoKeys 66: 105-133. https://doi.org/10.3897/mycokeys.66.50946

Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon species towards the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture

opencc-zeroMay 2020View details →
zenodo32/100

Datasets for "Meteorological factors associated with the timing and abundance of Hymenoscyphus fraxineus spore release" by Burns, Timmermann and Yearsley.

<p>======++++++++++++++++++++++++++++++==============<br> <br> # Data Files:<br> <br> File: burns_etal_preprocessed_data.Rdata<br> <br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; This file contains the pre-processed spore count data and the cleaned meteorological data<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; The file contains:<br> <br> stations&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; The longitude and latitude of the two weather stations used for the metro data<br> varStr_mean&nbsp;&nbsp;&nbsp; Names of the meteorological variables<br> windowStr&nbsp; &nbsp; &nbsp; &nbsp; Names of the three time windows<br> <br> emission&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; The main data frame containing the spore and meteorological data<br> &nbsp;&nbsp;&nbsp;&nbsp; date&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Date of a spore count recording. (POSIXlt)<br> &nbsp;&nbsp;&nbsp;&nbsp; year&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Year of spore count recording<br> &nbsp;&nbsp;&nbsp;&nbsp; month&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Month of spore count recording&nbsp;<br> &nbsp;&nbsp;&nbsp;&nbsp; day&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Day of year of spore count recording<br> &nbsp;&nbsp;&nbsp;&nbsp; total&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; The total daily spore count<br> &nbsp;&nbsp;&nbsp;&nbsp; peak&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;The maximum spore count each day&nbsp;&nbsp;&nbsp;&nbsp;<br> &nbsp;&nbsp;&nbsp;&nbsp; peak_time&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; The time (hours after midnight) of the maximum spore count each day<br> &nbsp;&nbsp;&nbsp;&nbsp; peak_time_raw&nbsp;&nbsp;&nbsp; Raw value for time of maximum spore count each day<br> &nbsp;&nbsp;&nbsp;&nbsp; peak_time_date&nbsp;&nbsp; Date and time (POSIXct) for maximum spore count each day<br> ===================================================<br> <br> File: results_burns_etal_daily_emission_analysis_2010_2011_prop0.8.Rdata<br> <br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; This file gives the results for the total daily emission of spores<br> <br> File: results_burns_etal_daily_peaktime_analysis_2010_2011_prop0.8.Rdata<br> <br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; This file gives the results for the time of the daily per in spore counts<br> <br> ================<br> Both files have the same variables, which are listed below.<br> <br> # Setup parameters<br> use.prop&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; Proportion of the data to use for fitting model<br> colinear_threshold&nbsp; The correlation threshold to identify collinear covariates<br> frost_var&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;The name of the variable to use as a frost covariate (three possible windows)<br> k.use&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; The dimension of the basis for the smoothing thin-plate splines in the GAM<br> nIter&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; Number of Monte-Carlo random subsamples of the data<br> seed&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;The random number seed at the start of the analysis<br> years&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; The years of data to use for fitting the GAM models.<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Leaving a year out allows it to be used as independent validation data<br> <br> # Outputs from the analysis<br> var.use&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; The names of covariate used in the final analysis after removing collinear covariates<br> models&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;A list (of length nIter) giving all the fitted models<br> d&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; A data frame with a summary of the nIter model results.<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; There are nIter rows. Each row summarises the results from one GAM<br> &nbsp;&nbsp;&nbsp; The data frame contains:<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; r2&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; r-squared between the model and the validation data.<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Validation data are the (1-use.prop) proportion not used for fitting<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; r2_fitted.&nbsp; &nbsp; &nbsp;r-squared for the data used to fit the model<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; dev.exp.&nbsp; &nbsp; &nbsp; The explained deviance from the fitted GAM<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; nTerm.&nbsp; &nbsp; &nbsp; &nbsp; The number of smooth terms in the fitted GAM<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; term1&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; The smooth term with the smallest p-value (number is an index for var.use)<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; term2&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; The smooth term with the second smallest p-value (number is an index for var.use)<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; term3&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; The smooth term with the third smallest p-value (number is an index for var.use)<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; termF&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; The smooth term with the largest F-value (number is an index for var.use)<br> pValues&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;p values for each of the smooth terms (columns) for each of the nIter models (rows)<br> FValues&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;F values for each of the smooth terms (columns) for each of the nIter models (rows)<br> edf&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Estimated degrees of freedom for each of the smooth terms (columns) for each of the nIter models (rows)<br> pValue_param&nbsp;&nbsp;&nbsp;p values for each of the parametric terms (columns) in each of nIter models (rows)<br> tVal_param.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;t statistics for each of the parametric terms (columns) in each of nIter models (rows)<br> &nbsp;</p>

opencc-by-4.0Jan 2021View details →
dryad32/100

Data from: A versatile method for assessing pathogenicity of Hymenoscyphus fraxineus to ash foliage

We describe a method for inoculating rachises of Fraxinus excelsior (European or common ash) with Hymenoscyphus fraxineus, which is faster than previous methods and allows associated foliar symptoms to be assessed on replicate leaves. A total of ten ash seedlings were inoculated with five isolates of H. fraxineus and lesion development assessed over four weeks. A five‐point disease progress scale of symptom development was developed from no lesion (0), lesion on rachis (1), "pre‐top dead," with curling of distal leaflets and bending of the rachis (2), top dead, with wilting and death of distal leaflets (3) to leaf abscission (4). The method revealed variation in aggressiveness of H. fraxinus isolates and may be suitable for assessing the resistance of F. excelsior and other Fraxinus species to dieback. The in vitro growth rate of H. fraxineus isolates was highly correlated with both disease progress and the length of rachis lesions on susceptible plants, indicating that it can be used as a preliminary step in selecting isolates with high aggressiveness for use in resistance screening.

opencc-zeroDec 2017View details →
dryad32/100

Data from: Adaptive potential of ash (Fraxinus excelsior) populations against the novel emerging pathogen Hymenoscyphus pseudoalbidus

An emerging infectious pathogen Hymenoscyphus pseudoalbidus has spread across much of Europe within recent years causing devastating damage on European common ash trees (Fraxinus excelsior) and associated plant communities. The present study demonstrates the presence of additive genetic variation in susceptibility of natural F. excelsior populations to the new invasive disease. We observe high levels of additive variation in the degree of susceptibility with relatively low influence of environmental factors (narrow sense heritability = 0.37-0.52). Most native trees are found highly susceptible, and we estimate that only around 1% has the potential of producing offspring with expected crown damage of less than 10% under the present disease pressure. The results suggest that the presence of additive genetic diversity in natural F. excelsior populations can confer the species with important ability to recover, but that low resistance within natural European populations is to be expected due to a low frequency of the hypo-sensitive trees. Large effective population sizes will be required to avoid genetic bottlenecks. The role of artificial selection and breeding for protection of the species is discussed based on the findings.

opencc-zeroDec 2010View details →
dryad32/100

Data from: Population structure of the invasive forest pathogen Hymenoscyphus pseudoalbidus

Understanding the genetic diversity and structure of invasive pathogens in source and introduced areas is crucial to reveal hidden biological aspects of an organism, to reconstruct the course of invasions and to establish effective control measures. Hymenoscyphus pseudoalbidus (anamorph: Chalara fraxinea) is an invasive and highly destructive fungal pathogen on common ash Fraxinus excelsior in Europe and occurs natively in east Asia. To get insights into the dispersal mechanism and the history of invasion, we used microsatellite markers and characterized the genetic structure and diversity of H. pseudoalbidus populations at three spatial levels: (i) in Europe; (ii) at the epidemic front and (iii) between Europe and Japan. The 1208 European strains form one large population as no evident structure was detected using Bayesian and multivariate clustering analysis. Only the distribution of genetic diversity in space, pairwise population differentiation (GST) and the spatial analysis of principal components revealed a faint geographic pattern around Europe. A significant allele deficiency in most European populations pointed to a recent genetic bottleneck whereas no pattern of isolation by distance was found. Populations from Japan harbored a higher genetic diversity and were genetically differentiated from European ones. Nevertheless, phylogenetic and network analysis clearly demonstrated that individuals from both regions are conspecific. Our data suggest that H. pseudoalbidus was introduced only once by a minimum of two individuals. The potential source region of H. pseudoalbidus is huge and further investigations are required for a more accurate localization of the source population.

opencc-zeroDec 2013View details →
dryad32/100

Data from: A versatile method for assessing pathogenicity of Hymenoscyphus fraxineus to ash foliage

Open the record for dataset details and reuse information.

publicDec 2018View details →
dryad32/100

Data from: Adaptive potential of ash (Fraxinus excelsior) populations against the novel emerging pathogen Hymenoscyphus pseudoalbidus

Open the record for dataset details and reuse information.

publicNov 2011View details →
dryad32/100

Data from: Population structure of the invasive forest pathogen Hymenoscyphus pseudoalbidus

Open the record for dataset details and reuse information.

publicJun 2014View details →
zenodo28/100

Figure 7 from: Pourmoghaddam MJ, Lambert C, Surup F, Khodaparast SA, Krisai-Greilhuber I, Voglmayr H, Stadler M (2020) Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon spp. against the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture. MycoKeys 66: 105-133. https://doi.org/10.3897/mycokeys.66.50946

Figure 7 Illustration of antagonist test by dual culture technique of Hypoxlon spp. and Hymenoscyphus fraxineus on barley-malt agar in 9-cm diam. plates A dual culture of H. rubiginosum (MUCL 47152) against Hym. fraxineus (STMA 18166) after 1 wk of incubation B dual culture of H. rubiginosum (MUCL 47152) against Hym. fraxineus (STMA 18166) after 2 wk of incubation C dual culture of H. rubiginosum (MUCL 47152) against Hym. fraxineus (STMA 18166) after 3 wk of incubation D dual culture of H. rubiginosum (MUCL 47152) against Hym. fraxineus (STMA 18166) after 4 wk of incubation E–H (Hypoxylon aff. rubiginosumMUCL 57724) against Hym. fraxineus after 1, 2, 3, 4 wk I–LH. texense (DSM 107933) against Hym. fraxineus after 1, 2, 3, 4 wk M–PH. guilanense (MUCL 57726) against Hym. fraxineus after 1, 2, 3, 4 wk.

opencc-by-4.0May 2020View details →
zenodo28/100

Figure 4 from: Pourmoghaddam MJ, Lambert C, Surup F, Khodaparast SA, Krisai-Greilhuber I, Voglmayr H, Stadler M (2020) Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon spp. against the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture. MycoKeys 66: 105-133. https://doi.org/10.3897/mycokeys.66.50946

Figure 4 Hypoxylon aff. rubiginosum (GUM 1587) A, B stromatal habit C close-up view of stromatal surface, with stromatal pigments in 10% KOHD stroma in section showing perithecia and ostioles E mature and immature asci in water F ascus in water G ascus in Melzer's reagent H ascus tip in Melzer's reagent I ascospores in 10% KOH with dehiscent perispore J ascospore in water, with germ-slit K ascospore under SEM. Scale bars: 5 mm (A, B); 1 mm (C); 0.5 mm (D); 20 µm (E–G); 10 µm (H–J); 2 µm (K).

opencc-by-4.0May 2020View details →
zenodo28/100

Figure 11 from: Pourmoghaddam MJ, Lambert C, Surup F, Khodaparast SA, Krisai-Greilhuber I, Voglmayr H, Stadler M (2020) Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon spp. against the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture. MycoKeys 66: 105-133. https://doi.org/10.3897/mycokeys.66.50946

Figure 11 HPLC-UV chromatograms at 210 nm from mono cultural barley-malt agar extracts of MUCL 47152 (H. rubiginosum), STMA 18166 (Hym. fraxineus), STMA 13090 (H. fuscum) and one dual culture experiment thereof. UV/Vis spectra are shown for phomopsidin (5), 10-hydroxyphomopsidin (6), orthosporin (9), daldinone B (10), 1,8-dimethoxynaphthalene (11), daldinin F (12), 5–methylmellein (13), viridiol (14) and an unidentifiable compound (UC 6) after comparison of data with internal databases. The UV signal of UC 6 was enhanced in the dual culture extract.

opencc-by-4.0May 2020View details →
zenodo28/100

Figure 6 from: Pourmoghaddam MJ, Lambert C, Surup F, Khodaparast SA, Krisai-Greilhuber I, Voglmayr H, Stadler M (2020) Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon spp. against the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture. MycoKeys 66: 105-133. https://doi.org/10.3897/mycokeys.66.50946

Figure 6 Hypoxylon aff. rubiginosum (GUM 1588) A stromatal habit B close-up view of stromatal surface, with stromatal pigments in 10% KOHC section of stroma showing perithecia and ostioles D ascus in Melzer's reagent E ascospores in 10% KOH with dehiscent perispore. Scale bars: 2.5 mm (A); 0.5 mm (B, C); 20 µm (D); 10 µm (E).

opencc-by-4.0May 2020View details →
zenodo28/100

Figure 5 from: Pourmoghaddam MJ, Lambert C, Surup F, Khodaparast SA, Krisai-Greilhuber I, Voglmayr H, Stadler M (2020) Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon spp. against the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture. MycoKeys 66: 105-133. https://doi.org/10.3897/mycokeys.66.50946

Figure 5 Culture and anamorphic structures of Hypoxylon aff. rubiginosum (GUM 1587) on OAA, B surface of colony after 1 and 8 wk of incubation (respectively, left to right) C–G general view of anamorph structure with virgariella-like branching patterns H, I conidiogenous cells and immature conidia J mature conidia. Scale bars: 20 µm (C–G); 10 µm (H–J).

opencc-by-4.0May 2020View details →
zenodo28/100

Figure 3 from: Pourmoghaddam MJ, Lambert C, Surup F, Khodaparast SA, Krisai-Greilhuber I, Voglmayr H, Stadler M (2020) Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon spp. against the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture. MycoKeys 66: 105-133. https://doi.org/10.3897/mycokeys.66.50946

Figure 3 Hypoxylon rubiginosum (GUM 1586) A, B stromatal habit C close-up view of stromatal surface D close-up view of stromatal surface, with stromatal pigments in 10% KOHE ascospores in 10% KOH with dehiscent perispore F mature and immature asci in water G immature ascus in water H mature ascus in water I ascus in Melzer's reagent J ascospores in water K ascus tip in Melzer's reagent. Scale bars: 2 cm (A); 1 cm (B); 4 mm (C); 2 mm (D); 10 µm (E); 20 µm (F–I), 10 µm (J, K).

opencc-by-4.0May 2020View details →
zenodo28/100

Figure 10 from: Pourmoghaddam MJ, Lambert C, Surup F, Khodaparast SA, Krisai-Greilhuber I, Voglmayr H, Stadler M (2020) Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon spp. against the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture. MycoKeys 66: 105-133. https://doi.org/10.3897/mycokeys.66.50946

Figure 10 HPLC-UV profiles at 210 nm derived from barley-malt agar (A–C, E) and stromal (E) extracts and compound standard (F). UV/Vis spectra are shown for identified compounds in mono- and dual culture (C) experiments of STMA 18166 (Hym. fraxineus, A) and DSM 107933 (H. texense, B; UC 2, 4 – unknown compounds); stromal metabolites (4 – mitorubrinol; URg – unknown rubiginosin A derivative; 3 – rubiginosin A; 2 – mitorubrinol acetate; 7 – mitorubrin; UC2 – Unknown compound 2 of GLM-F116101 (H. texense, D), and ... ESI mass spectra of 8 in positive and negative modes... of 8 8 (rickiol A, F) identified in the mono culture extract of MUCL 54624 (H. rubiginosum, E).

opencc-by-4.0May 2020View details →
zenodo28/100

Figure 2 from: Pourmoghaddam MJ, Lambert C, Surup F, Khodaparast SA, Krisai-Greilhuber I, Voglmayr H, Stadler M (2020) Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon spp. against the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture. MycoKeys 66: 105-133. https://doi.org/10.3897/mycokeys.66.50946

Figure 2 Hypoxylon guilanense (Holotype GUM 989) A stromatal habit B close-up view of stromatal surface, with stromatal pigments in 10% KOHC, H, I ascospores in water, with germ-slits D, E ascospores in 10% KOH with dehiscent perispore F, G ascospore under SEMJ, K culture on 9 cm OA plates after 1 and 3 wk of incubation (left to right). Scale bars: 2.5 mm (A), 1 mm (B); 10 µm (C–E); 2 µm (F, G); 10 µm (H, I).

opencc-by-4.0May 2020View details →

ScienceDex guides

Understand access before you commit

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

Compare curated datasets

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