Hackl, Jürgen

6 files · 132 MB · parquet, tiffdeclared

EuroFlood is an open, cloud-native index over the JRC/Copernicus CEMS-EFAS Satellite-Derived Flood Depth Maps for Europe (Betterle & Salamon, 2025; CC-BY-4.0) - ~3,280 satellite-derived observed flood-depth maps across Europe, 2015-2024. The bundle is a sparse Cloud-Optimized GeoTIFF encoding, per pixel, the set of flood events that inundated it, plus a combo_id -sorted GeoParquet dictionary and a small events table. Query by region and time via HTTP range reads (GDAL /vsicurl + DuckDB) to retrieve matching events, then fetch only the source depth rasters needed. Built with the open-source EuroFlood Python package ( pip install euroflood ).

COSTEA, MARIA

1 files · 81 KB · jpegdeclared

COSTEA, Maria (2003, article), "Momente de convergență în relațiile româno-bulgare," Anuarul Arhivelor Mureșene , nr. 2, 2003, p. 258-263, ISSN 1583-1337 .

Geisler, Jan · Rakhimberdiev, Eldar · Boom, Michiel P. · et al.

29 files · 124 MB · csv, shapefiledeclared

1. Many migratory birds now reach their Arctic breeding grounds earlier in order to keep pace with advancing springs and shifting nutrient peaks, either by departing earlier from non-breeding grounds or by travelling faster. For dark-bellied brent geese, there is limited potential to travel faster, as their migration to the Siberian breeding grounds is already among the fastest of Arctic geese and swans. Earlier departure would require reaching departure body mass earlier, either through a faster accumulation of energy stores during spring staging or via adjustments earlier in the annual cycle. 2. We examined long-term shifts in spring staging phenology and changes in winter and spring body mass trajectories of brent geese at the population level, with particular emphasis on the effects of winter temperature on body mass and spring body mass on departure timing. 3. We used more than five decades of body mass measurements from individuals caught in the United Kingdom and France, and in the Dutch Wadden Sea to reconstruct changes in spring and winter mass trajectories, respectively. These data were combined with over five decades of migration counts in the Netherlands and more than two decades of counts in Denmark to quantify changes in spring staging phenology. 4. We found that brent geese have not shifted their spring arrival in the Wadden Sea but have advanced departure timing. Furthermore, brent geese were heavier during and after milder winters, and have changed mass trajectories over recent decades. They no longer lose mass during winter and the second spring staging phase, and fuelling rates in the first spring staging phase have declined. Annual variation in body mass was not related to annual departure timing. 5. These results suggest that milder winters have relaxed energetic constraints and improved body condition in brent geese throughout the non-breeding season. Our findings highlight the importance of considering the full annual cycle when assessing how animals with limited capacity to adjust migration timing or speed respond to global change.

Pairon, Marie · Dufrêne, Marc

1 files · 1.7 MB · jpegdeclared

Land-use and land-cover (LULC) changes following artificialisation between 2007 and 2018

Agudelo-Restrepo, Manuela · Dibouloul, Patrick · Harms, Karen · et al.

1 files · 143 KB · jpegdeclared

Figure 4 Key NOESY (a) and HMBC (b) correlations in 1a.

Agudelo-Restrepo, Manuela · Dibouloul, Patrick · Harms, Karen · et al.

1 files · 142 KB · jpegdeclared

Figure 3 Structures of compounds 1–7.

Agudelo-Restrepo, Manuela · Dibouloul, Patrick · Harms, Karen · et al.

1 files · 706 KB · jpegdeclared

Figure 2 Schizothecium keniense (ex-type strain CCF 6931). A. Ascoma; B. Groups of agglutinated hairs in the upper part of the ascoma; C. Ascomatal wall of textura angularis to globulosa; D, E. Ascospores; F. Ascospore with upper and lower cell (arrow indicates germ pore of the upper cell); G. Ascospore with mucilaginous appendage in the upper cell. Scale bars: 100 µm (A); 50 µm (B); 10 µm (C–G).

Agudelo-Restrepo, Manuela · Dibouloul, Patrick · Harms, Karen · et al.

1 files · 512 KB · jpegdeclared

Figure 1 Randomized accelerated maximum likelihood (RAxML) phylogram obtained from the combined sequences of the internal transcribed spacer region (ITS), the nuclear rDNA large subunit (LSU), and fragments of ribosomal polymerase II subunit 2 (rpb2) and β-tubulin (tub2) genes of type and reference strains belonging to the Schizotheciaceae. Bootstrap support values ≥ 70 / Bayesian posterior probability scores ≥ 0.95 are indicated along branches. Branch lengths are proportional to distance. New species proposed in the present study is indicated in bold. T indicates ex-type strains.

Xiong, YinRu · Manawasinghe, Ishara S. · Zhang, MiaoMiao · et al.

1 files · 869 KB · jpegdeclared

Figure 4 Lentimurispora arundinis (holotype, HKAS 155057). a, b. Appearance of sporodochia on host substrate. c–f. Conidiogenous cells and developing conidia. g–l. Conidiogenous cells and developing conidia. m. Germinated conidium. n. Culture on PDA from above and reverse. Scale bars: 50 μm (c); 20 μm (d, e); 10 μm (f–m).

Xiong, YinRu · Manawasinghe, Ishara S. · Zhang, MiaoMiao · et al.

1 files · 330 KB · jpegdeclared

Figure 3 Phylogram generated from maximum likelihood analysis of selected Pleosporales based on the combined ITS, LSU, rpb2, and tef1-α sequence dataset, with one Neoroussoella taxon and one Pseudoroussoella taxon as the outgroup. Bootstrap support for maximum likelihood (ML) equal to or greater than 75% and Bayesian inference posterior probability (BIPP) equal to or greater than 0.90 are indicated above the branches as ML/BIPP. The scale bar indicates 0.04 nucleotide changes per site. Isolates from this study are marked in red, and ex-type strains are indicated in bold.

Xiong, YinRu · Manawasinghe, Ishara S. · Zhang, MiaoMiao · et al.

1 files · 892 KB · jpegdeclared

Figure 2 Stachylidium arundinis (holotype, HKAS 155056). a, b. Appearance of sporodochia on host substrate. c, d. Conidiophores and conidiogenous cells with conidia. e, f. Conidiogenous cells and developing conidia. g. Conidia. h. Culture on PDA from above and reverse. Scale bars: 50 μm (c); 20 μm (d); 10 μm (e–g).

Xiong, YinRu · Manawasinghe, Ishara S. · Zhang, MiaoMiao · et al.

1 files · 226 KB · jpegdeclared

Figure 1 Phylogram generated from maximum likelihood analysis of Trichosphaeriaceae based on the combined ITS, LSU, rpb2, and tef1-α sequence dataset, with two Brunneomyces taxa as the outgroup. Bootstrap support for maximum likelihood (ML) equal to or greater than 75% and Bayesian inference posterior probability (BIPP) equal to or greater than 0.90 are indicated above the branches as ML/BIPP. The scale bar indicates 0.04 nucleotide changes per site. Isolates from this study are marked in red, and ex-type strains are indicated in bold.

Nie, Yong · Huang, Bo

1 files · 161 KB · jpegdeclared

Figure 3 The developmental origin of primary conidiophores and the pattern of septation during primary conida formation between Basidiobolus meristosporus and Drechslerosporium cornellii.

Nie, Yong · Huang, Bo

1 files · 397 KB · jpegdeclared

Figure 2 Drechslerosporium cornellii ARSEF 7942. A, B. Mycelia and primary conidiophore with a propulsive distention at the tip; C, D, E, F. Conidia with an apical protrusion at the base; G, H, I, J. Secondary conidiophores bearing a single secondary conidium; K, L. Secondary conidiophores bearing a single capilliconidium; M, N. Elongated capilliconidia; O–R. A single conidiophore bearing a digitate terminal chlamydospore. Scale bars: 10 μm (A–R).

Nie, Yong · Huang, Bo

1 files · 526 KB · jpegdeclared

Figure 1 Phylogenetic tree of the family Basidiobolaceae based on 28S, ITS, and RPB2 loci. Olpidium brassicae (AFTOL-ID 633) and Powellomyces sp. (AFTOL-ID 32) were used as outgroups. Maximum likelihood bootstrap values (≥ 50%) / Bayesian posterior probabilities (≥ 0.80) are indicated along each branch. The scale bar at the bottom left indicates the number of substitutions per site. New species is indicated in bold and new genus is highlighted in red.

Vaughn, Morgan · Harper, Dekon · Reiter, Lexi · et al.

1 files · 450 KB · jpegdeclared

Figure 5 Distributions of Xylopia ochrantha, X. peruviana, and X. rubrolineata in South America. Green shading indicates forest cover as of January 2026. "World Countries" and "Environment Map" layers are shown.

Vaughn, Morgan · Harper, Dekon · Reiter, Lexi · et al.

1 files · 345 KB · jpegdeclared

Figure 4 Xylopia rubrolineata. A. Flower bud; B. Flower bud showing cauline attachment; C, D. Leaves; E. Seed, view of micropylar end; F. Seed, side view; G. Fruit; H. Outer petal, adaxial view; I. Inner petal, adaxial view; J. Stamen, abaxial view; K, L. Staminodes, abaxial view; M. Abscised stigma, side view; A, C. From Sperling et al. 5987 (NY); B, D. From Chatrou et al. 410 (OWU); E–G. From Silva & Souza 2334 (OWU); H, I. From Silva & Souza 2459 (OWU); J–M. From Sperling et al. 5987 (MO).

Vaughn, Morgan · Harper, Dekon · Reiter, Lexi · et al.

1 files · 753 KB · jpegdeclared

Figure 3 Xylopia rubrolineata (XY-peruviana clade). A. Cauliflory, Alta Floresta, Mato Grosso, Brazil, 12 October 2011, R. Hoyer; B. Flower at anthesis, apical view, Alta Floresta, Mato Grosso, Brazil, 12 October 2011, R. Hoyer; C. Fruit on trunk, Alta Floresta, Mato Grosso, Brazil, 19 August 2025, M. Z. Ferreira; D. Inflorescence on trunk, showing dehisced monocarp and seeds, and flower buds, Cristalino Lodge, Mato Grosso, Brazil, 12 August 2022, S. Freire. Photographs used under the terms of the Creative Commons license for iNaturalist.

Vaughn, Morgan · Harper, Dekon · Reiter, Lexi · et al.

1 files · 252 KB · jpegdeclared

Figure 2 Phylogenetic distribution of trunciflory in Xylopia sect. Xylopia. Species in which trunciflory has been documented are highlighted in blue. Phylogeny and dates are those determined by Nge et al. (2026): all branches are fully supported based on maximum likelihood (RAxML) and species-tree (ASTRAL) analyses unless otherwise indicated. Submaximal values are displayed as "bootstrap/local posterior probability;" an asterisk indicates full support for the undisplayed value; a hyphen indicates that the particular clade was not recovered in the ASTRAL analysis. Names in the right-hand column are clade names as used in Johnson et al. (2025) and Nge et al. (2026).