taxonID	type	format	identifier	references	title	description	created	creator	contributor	publisher	audience	source	license	rightsHolder	datasetID
0396E61D4D36FFD5FF10F91D2A1FFAF5.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/17987460/files/figure.png	https://doi.org/10.5281/zenodo.17987460	FIG. 1. — Map of France with stars pointing to locations where the strains of the present study originated from.	FIG. 1. — Map of France with stars pointing to locations where the strains of the present study originated from.	2025-12-16	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana		Zenodo	biologists	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana			
0396E61D4D36FFD5FF10F91D2A1FFAF5.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/17987464/files/figure.png	https://doi.org/10.5281/zenodo.17987464	FIG. 2. — FungANI analyses of the Podospora Rabenh. strains PSN1303, PSN1705, PSN1871 and PSN1899. The Average Nucleotide Identities (ANIs) are at the top, and at the bottom are given the ANIs obtained when comparing the genomes in the two directions (reference and tested genome IDs are given below the graphic), as well as the percentages of zero hits, the estimated size of the region specific for each genome and the numbers of BLAST made during the analysis. The graphic represents the number of BLAST detecting sequences with the color-coded percentages and in the boxes are the actual number of BLAST with such hit percentages.In all cases, ANIs were higher than 99.5% and the strains had less than 1.5% of specific sequences.These were scattered all over the genomes. For more information see (Lalanne & Silar 2025).	FIG. 2. — FungANI analyses of the Podospora Rabenh. strains PSN1303, PSN1705, PSN1871 and PSN1899. The Average Nucleotide Identities (ANIs) are at the top, and at the bottom are given the ANIs obtained when comparing the genomes in the two directions (reference and tested genome IDs are given below the graphic), as well as the percentages of zero hits, the estimated size of the region specific for each genome and the numbers of BLAST made during the analysis. The graphic represents the number of BLAST detecting sequences with the color-coded percentages and in the boxes are the actual number of BLAST with such hit percentages.In all cases, ANIs were higher than 99.5% and the strains had less than 1.5% of specific sequences.These were scattered all over the genomes. For more information see (Lalanne & Silar 2025).	2025-12-16	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana		Zenodo	biologists	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana			
0396E61D4D36FFD5FF10F91D2A1FFAF5.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/17987470/files/figure.png	https://doi.org/10.5281/zenodo.17987470	FIG. 3. — Main morphological features of PSN1303, PSN1705, PSN1871 and PSN1899. Scale bars: Perithecia on M0 + miscanthus, rosettes of asci, 250 µm; ascus, ascospores, 50 µm.	FIG. 3. — Main morphological features of PSN1303, PSN1705, PSN1871 and PSN1899. Scale bars: Perithecia on M0 + miscanthus, rosettes of asci, 250 µm; ascus, ascospores, 50 µm.	2025-12-16	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana		Zenodo	biologists	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana			
0396E61D4D36FFD5FF10F91D2A1FFAF5.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/17987474/files/figure.png	https://doi.org/10.5281/zenodo.17987474	FIG. 4. — FungANI analysis of the genome of Podospora reunionensis Silar, sp. nov. strain PSN1158 with those of all type strains of the P. anserina (Rabenh.) Niessl species complex. The layouts are the same as on Figure 2.	FIG. 4. — FungANI analysis of the genome of Podospora reunionensis Silar, sp. nov. strain PSN1158 with those of all type strains of the P. anserina (Rabenh.) Niessl species complex. The layouts are the same as on Figure 2.	2025-12-16	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana		Zenodo	biologists	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana			
0396E61D4D36FFD5FF10F91D2A1FFAF5.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/17987478/files/figure.png	https://doi.org/10.5281/zenodo.17987478	FIG. 5. — Morphology of Podospora reunionensis Silar, sp. nov: A, mycelium morphology after eight days of incubation on M2; B, M0 + Guibourtia demeusii L. wood shavings;C, M0 + miscanthus;on the right are enlargements to see the presence/absence and positions of the perithecia;D, Perithecia on M0 + miscanthus; E, rosettes of asci; F, peridium showing a textura intricata; G, ascus; H, ascospores; I, cladorrhinum-like anamorph; J, spermatia. Scale bars: A-C, 1 cm; D, E, 250 µm; F-H, 50 µm; I, J, 10 µm.	FIG. 5. — Morphology of Podospora reunionensis Silar, sp. nov: A, mycelium morphology after eight days of incubation on M2; B, M0 + Guibourtia demeusii L. wood shavings;C, M0 + miscanthus;on the right are enlargements to see the presence/absence and positions of the perithecia;D, Perithecia on M0 + miscanthus; E, rosettes of asci; F, peridium showing a textura intricata; G, ascus; H, ascospores; I, cladorrhinum-like anamorph; J, spermatia. Scale bars: A-C, 1 cm; D, E, 250 µm; F-H, 50 µm; I, J, 10 µm.	2025-12-16	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana		Zenodo	biologists	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana			
0396E61D4D36FFD5FF10F91D2A1FFAF5.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/17987490/files/figure.png	https://doi.org/10.5281/zenodo.17987490	FIG. 6. — Comparison of Podospora reunionensis Silar, sp. nov. and Podospora comata Milovtz.: A, production of perithecia; B, production of ascospores (right: ejected on the lid) on M0 and Guibourtia demeusii L. wood shavings; A, arrows point to where PSN1158 differentiated perithecia that ejected ascospores on the lid (arrowheads). C, D, ascospores; C,The arrows point towards the conspicuous secondary appendages in PSN1158. These are also present in the P. comata Milovtz. strain T, but are shorter and rarer (i.e., they appear to be missing on most ascospores). Scale bars: 50 µm.	FIG. 6. — Comparison of Podospora reunionensis Silar, sp. nov. and Podospora comata Milovtz.: A, production of perithecia; B, production of ascospores (right: ejected on the lid) on M0 and Guibourtia demeusii L. wood shavings; A, arrows point to where PSN1158 differentiated perithecia that ejected ascospores on the lid (arrowheads). C, D, ascospores; C,The arrows point towards the conspicuous secondary appendages in PSN1158. These are also present in the P. comata Milovtz. strain T, but are shorter and rarer (i.e., they appear to be missing on most ascospores). Scale bars: 50 µm.	2025-12-16	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana		Zenodo	biologists	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana			
0396E61D4D3FFFD6FC36F9D72B4AFB49.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/17987478/files/figure.png	https://doi.org/10.5281/zenodo.17987478	FIG. 5. — Morphology of Podospora reunionensis Silar, sp. nov: A, mycelium morphology after eight days of incubation on M2; B, M0 + Guibourtia demeusii L. wood shavings;C, M0 + miscanthus;on the right are enlargements to see the presence/absence and positions of the perithecia;D, Perithecia on M0 + miscanthus; E, rosettes of asci; F, peridium showing a textura intricata; G, ascus; H, ascospores; I, cladorrhinum-like anamorph; J, spermatia. Scale bars: A-C, 1 cm; D, E, 250 µm; F-H, 50 µm; I, J, 10 µm.	FIG. 5. — Morphology of Podospora reunionensis Silar, sp. nov: A, mycelium morphology after eight days of incubation on M2; B, M0 + Guibourtia demeusii L. wood shavings;C, M0 + miscanthus;on the right are enlargements to see the presence/absence and positions of the perithecia;D, Perithecia on M0 + miscanthus; E, rosettes of asci; F, peridium showing a textura intricata; G, ascus; H, ascospores; I, cladorrhinum-like anamorph; J, spermatia. Scale bars: A-C, 1 cm; D, E, 250 µm; F-H, 50 µm; I, J, 10 µm.	2025-12-16	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana		Zenodo	biologists	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana			
0396E61D4D3FFFD6FC36F9D72B4AFB49.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/17987490/files/figure.png	https://doi.org/10.5281/zenodo.17987490	FIG. 6. — Comparison of Podospora reunionensis Silar, sp. nov. and Podospora comata Milovtz.: A, production of perithecia; B, production of ascospores (right: ejected on the lid) on M0 and Guibourtia demeusii L. wood shavings; A, arrows point to where PSN1158 differentiated perithecia that ejected ascospores on the lid (arrowheads). C, D, ascospores; C,The arrows point towards the conspicuous secondary appendages in PSN1158. These are also present in the P. comata Milovtz. strain T, but are shorter and rarer (i.e., they appear to be missing on most ascospores). Scale bars: 50 µm.	FIG. 6. — Comparison of Podospora reunionensis Silar, sp. nov. and Podospora comata Milovtz.: A, production of perithecia; B, production of ascospores (right: ejected on the lid) on M0 and Guibourtia demeusii L. wood shavings; A, arrows point to where PSN1158 differentiated perithecia that ejected ascospores on the lid (arrowheads). C, D, ascospores; C,The arrows point towards the conspicuous secondary appendages in PSN1158. These are also present in the P. comata Milovtz. strain T, but are shorter and rarer (i.e., they appear to be missing on most ascospores). Scale bars: 50 µm.	2025-12-16	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana		Zenodo	biologists	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana			
0396E61D4D3FFFD6FC36F9D72B4AFB49.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/17987505/files/figure.png	https://doi.org/10.5281/zenodo.17987505	FIG. 7. — Additional features of the ex-type strain PSN1158 of Podospora reunionensis Silar, sp. nov: A, acellular microsclerotic-like structures differentiated on M0 + miscanthus; B, palm-like structures differentiated during appressorium-like-directed cellophane penetration; C, Per-gene synonymous divergence (dS) between the mat1-1 and mat1-2 homokaryotic genomes of the strain PSN1158 plotted against the location on P. anserina (Rabenh.) Niessl chromosome 1 carrying the mating-type locus, and the six other chromosomes; location of the mating-type locus is indicated with a green dotted vertical line and boundaries of the non-recombining region around the mating-type locus of the P. anserina strain S genome with red dotted vertical lines. High dS values indicate recombination suppression or outcrossing; D, hyphal interference visualized by accumulation of Evans Blue in dead cells (arrows) at the confrontation of Penicillium chrysogenum (Pc) and PSN1158 or P. comata Milovtz. strain T. Scale bars: A, B, 50 µm.	FIG. 7. — Additional features of the ex-type strain PSN1158 of Podospora reunionensis Silar, sp. nov: A, acellular microsclerotic-like structures differentiated on M0 + miscanthus; B, palm-like structures differentiated during appressorium-like-directed cellophane penetration; C, Per-gene synonymous divergence (dS) between the mat1-1 and mat1-2 homokaryotic genomes of the strain PSN1158 plotted against the location on P. anserina (Rabenh.) Niessl chromosome 1 carrying the mating-type locus, and the six other chromosomes; location of the mating-type locus is indicated with a green dotted vertical line and boundaries of the non-recombining region around the mating-type locus of the P. anserina strain S genome with red dotted vertical lines. High dS values indicate recombination suppression or outcrossing; D, hyphal interference visualized by accumulation of Evans Blue in dead cells (arrows) at the confrontation of Penicillium chrysogenum (Pc) and PSN1158 or P. comata Milovtz. strain T. Scale bars: A, B, 50 µm.	2025-12-16	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana		Zenodo	biologists	Valérie, Philippe Silar;Christophe, Valérie Gautier;Narumon, Christophe Lalanne;Marvyn, Narumon Tangthirasunun;Fanny, Marvyn Arthur;Hartmann, Fanny E.;Giraud, Tatiana			
