identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
669D9355CC795394BBFC366804C49C57.text	669D9355CC795394BBFC366804C49C57.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Blastobotrys sasensis M. Kolarik & R. Vadkertiova 2026	<div><p>Blastobotrys sasensis M. Kolařík &amp; R. Vadkertiová sp. nov.</p><p>Fig. 8</p><p>Etymology.</p><p>The epithet sasensis is derived from the acronym SAS (Slovak Academy of Sciences) combined with the Latin suffix - ensis (i. e., originating from). The name honours the institution’s role in advancing scientific research in Slovakia.</p><p>Diagnosis.</p><p>Blastobotrys sasensis differs from the closely related species B. muscicola by its ability to utilise d-xylose, erythritol, sorbose, glucitol, and ribitol. Another related species, B. robertii, differs by its ability to assimilate glycerol (Suppl. material 13: table SS 1). It also differs from both closely related species in its origin. B. muscicola was isolated from a moss growing on a fallen log in USA (Kurtzman 2007) and B. robertii was isolated from rotten pine wood ( Pinus sylvestris) in the Netherlands (Middelhoven and Kurtzman 2007).</p><p>Type.</p><p>SLOVAKIA • Zvolen region, <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=19.029675&amp;materialsCitation.latitude=48.627396" title="Search Plazi for locations around (long 19.029675/lat 48.627396)">Tŕnie</a>, 48.627397°N, 19.029675°E; alt. 665 m.; from thorax of Treptoplatypus oxyurus feeding in the base (40 cm diam) of a decaying Abies alba; 10. June 2024; leg. M. Knížek, J. Vakula, M. Zúbrik, isol. M. Kolařík Tox- 13 (holotype CCY 100-1-1, culture preserved in a metabolically inactive state in the Culture Collection of Yeasts, Bratislava, Slovakia, ex-type culture CCF 6841). Sequence Accessions: ITS – PX 523827, LSU - PX 591253, WGS - ERZ 28669457 .</p><p>Description.</p><p>On YMA, after 7 days of incubation at 28 ° C, the culture is slightly beige, dry and wrinkled. On MEA under the same incubation conditions, the culture is white, dry and powdery. On YMA, after 21 days of cultivation, the colony is raised, crateriform, cerebriform, with an undulate margin and a cream-coloured centre. On MEA, after 21 days of cultivation, the colony is raised, filamentous, and fluffy, with an undulate margin and a cream-coloured centre (Fig. 8 E, F). In both ME medium and YM, after 7 days of incubation at 28 ° C, the cells are oval to elongate, often spindle-shaped, 1.5–3 × 2.5–17 µm (Fig. 8 A, B). A sediment and a thick pellicle are formed in both media after 7 days of incubation at 28 ° C. Conidiophores with primary and secondary conidia are formed on MEA after 7 days, abundant hyphae are present. Multiple budding of mother cells occurs (Fig. 8 C, D). No sexual reproduction is observed.</p><p>Physiological and biochemical characteristics. Fermentation of glucose and d-xylose is absent. The following carbon compounds are assimilated: glucose, fructose, mannose, galactose, maltose, saccharose, lactose, raffinose, d-xylose, cellobiose, trehalose, soluble starch, melibiose, l-sorbose, salicin, ribitol, d-mannitol, d-glucitol, erythritol, glycerol, n-acetyl-d-glucosamine (w), succinic acid, and citrate. The other compounds- melezitose, l-arabinose, inulin, l-rhamnose, d-arabinose, d-ribose, xylitol, myo - inositol, ethanol, methanol, glycerol and dl-lactate - are not assimilated. The nitrogen compounds - ethylamine, l-lysine, cadaverine and n-acetyl-d-glucosamine are assimilated, whereas nitrate, nitrite, and creatinine are not assimilated. The urease reaction is negative. Starch-like polysaccharides are not produced. Growth in a vitamin-free medium (w), 10 % NaCl + 5 % glucose and 50 % glucose is positive. Growth at a temperature range from 5 ° C to 30 ° C is positive, growth at 35 ° C is negative.</p><p>Distribution.</p><p>The species is currently known only from a culture at the type locality in Slovakia. The NCBI GenBank contains the LSU sequence KF 617761, which has a 99.4 % identity and may represent our species. It is a sequence of an uncultured fungus obtained from Picea mariana forest soil in Alaska by Taylor et al. (2014). Based on the GlobalFungi exact hit, it was found in 54 samples, all originating from deadwood of Picea abies (53 samples) or an undetermined tree (one sample) collected in Finland (53 samples) by Ovaskainen (2010) and Korhonen (2022) and in the Asian part of Russia (Mikryukov et al. 2021). This suggests that it is associated with conifers in temperate and boreal Eurasia, not necessarily with T. oxyurus, which is specific to Abies alba .</p><p>Notes.</p><p>Based on the phylogenomic and ITS- LSU rDNA analyses, it forms a lineage sister to B. muscicola and B. robertii (Figs 4, 5).</p></div>	https://treatment.plazi.org/id/669D9355CC795394BBFC366804C49C57	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Kolařík, Miroslav;Vadkertiová, Renata;Knížek, Miloš;Sklenář, František;Vakula, Jozef;Zúbrik, Milan;Kolář, Michal;Hulcr, Jiří	Kolařík, Miroslav, Vadkertiová, Renata, Knížek, Miloš, Sklenář, František, Vakula, Jozef, Zúbrik, Milan, Kolář, Michal, Hulcr, Jiří (2026): The ambrosial mycobiota of Treptoplatypus oxyurus (Coleoptera, Platypodidae): a unique island of fungal diversity revealing Wilhelmdebeerea oxyuri gen. et sp. nov. (Ophiostomatales), and two new yeast species Blastobotrys sasensis sp. nov., and Sugiyamaella casensis sp. nov. (Dipodascales). IMA Fungus 17: e 177075, DOI: 10.3897/imafungus.17.177075
7C291BBFAB6A5C34B3212612CB9A89BE.text	7C291BBFAB6A5C34B3212612CB9A89BE.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Sugiyamaella casensis M. Kolarik & R. Vadkertiova 2026	<div><p>Sugiyamaella casensis M. Kolařík &amp; R. Vadkertiová sp. nov.</p><p>Fig. 8</p><p>Etymology.</p><p>The epithet casensis is derived from the acronym CAS (Czech Academy of Sciences) combined with the Latin suffix - ensis (i. e., originating from). The name honours the institution’s role in advancing scientific research in the Czech Republic.</p><p>Diagnosis.</p><p>Sugiyamaella casensis differs from the closely related species Sugiyamaella mastotermitis in its inability to ferment saccharides and to grow at 40 ° C. Moreover, unlike S. mastotermitis, it assimilates d-ribose, ribitol and glycerol (Suppl. material 13). The strain of S. mastotermitis was isolated from the gut contents of the termite Mastotermes darwiniensis (laboratory culture) in Germany (Handel et al. 2016), whereas S. casensis was isolated from the larvae of Treptoplatypus oxyurus in Slovakia.</p><p>Type.</p><p>SLOVAKIA • Zvolen region, <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=19.029675&amp;materialsCitation.latitude=48.627396" title="Search Plazi for locations around (long 19.029675/lat 48.627396)">Tŕnie</a>, 48.627397°N, 19.029675°E; alt. 665 m.; from thorax of Treptoplatypus oxyurus feeding in the base (40 cm diam) of a decaying Abies alba; 10. June 2024; leg. M. Knížek, J. Vakula, M. Zúbrik, isol. M. Kolařík Tox- 17 (holotype CCY 101-1-1, culture preserved in a metabolically inactive state in the Culture Collection of Yeasts, Bratislava, Slovakia, ex-type culture CCF 6842). Sequence accessions: ITS – PX 523828, LSU - PX 591254, WGS - ERZ 28669458 .</p><p>Description.</p><p>On YMA, after 7 days of incubation at 28 ° C, the culture is white, soft and slightly wrinkled. On MEA, under the same incubation conditions, the culture is white, dry and powdery. On YMA, after 21 days of cultivation, the colony is soft, with a flat undulate margin and a raised, rugose centre, cream in colour. On MEA, after 21 days of cultivation, the colony is cream-coloured, raised, with a flat, undulate margin and an elevated centre, slightly wrinkled, with a filamentous growth in the upper layer (Fig. 8 K). In both ME and YM media, after 7 days of incubation at 28 ° C, the cells are globose, oval to ovoidal (1.1–4.2 × 2.7–12 µm), some of them with a blunt end, and occur singly or in pairs. Short hyphae with blastoconidia occur (Figs 8 G, 8 H). Sediment and slight cloudiness are formed in both media. True hyphae with blastoconidia, arising from denticles, are formed on MEA after 7 days at 28 ° C (Fig. 6 I). Lipid particles of various shapes and sizes are formed after 21 days at 25 ° C (Fig. 6 J). No sexual reproduction is observed.</p><p>Physiological and biochemical characteristics. Fermentation of glucose and d-xylose is absent. The following carbon compounds are assimilated: glucose, fructose, mannose, galactose, maltose, saccharose, raffinose, melezitose, d - xylose, l - arabinose, cellobiose, trehalose, soluble starch, melibiose, l-rhamnose, d - sorbose, d - ribose, salicin, xylitol, ribitol, d - mannitol, d - glucitol, erythritol, myo - inositol, ethanol, glycerol, n-acetyl- d - glucosamine, succinic acid, and citrate. The other carbon compounds - lactose, inulin, d - arabinose, methanol and dl-lactate- are not assimilated. The nitrogen compounds: ethylamine and n-acetyl- d - glucosamine are assimilated, whereas nitrate, nitrite, l-lysine, cadaverine, and creatinine are not assimilated. The urease reaction is negative. Starch-like polysaccharides are not produced. Growth in a vitamin-free medium, 10 % NaCl + 5 % glucose (w) and 50 % glucose is positive. Growth at 5 and 10 ° C is weak. Growth at a range from 20 ° C to 30 ° C is positive. Growth at 35 ° C is negative.</p><p>Distribution.</p><p>It is currently documented solely from the type locality in Slovakia. Further investigations are required to determine whether its distribution corresponds to the range of its insect vector, T. oxyurus . No identical or similar (≥ 90 %) sequences were found in the GlobalFungi database.</p><p>Notes.</p><p>Based on the phylogenomic and ITS- LSU rDNA analyses, it forms a lineage sister to S. mastotermitis (Fig. 4, 6).</p></div>	https://treatment.plazi.org/id/7C291BBFAB6A5C34B3212612CB9A89BE	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Kolařík, Miroslav;Vadkertiová, Renata;Knížek, Miloš;Sklenář, František;Vakula, Jozef;Zúbrik, Milan;Kolář, Michal;Hulcr, Jiří	Kolařík, Miroslav, Vadkertiová, Renata, Knížek, Miloš, Sklenář, František, Vakula, Jozef, Zúbrik, Milan, Kolář, Michal, Hulcr, Jiří (2026): The ambrosial mycobiota of Treptoplatypus oxyurus (Coleoptera, Platypodidae): a unique island of fungal diversity revealing Wilhelmdebeerea oxyuri gen. et sp. nov. (Ophiostomatales), and two new yeast species Blastobotrys sasensis sp. nov., and Sugiyamaella casensis sp. nov. (Dipodascales). IMA Fungus 17: e 177075, DOI: 10.3897/imafungus.17.177075
64628AFC8FA15D7EA44C68C81570884D.text	64628AFC8FA15D7EA44C68C81570884D.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Wilhelmdebeerea M. Kolarik 2026	<div><p>Wilhelmdebeerea M. Kolařík gen. nov.</p><p>Etymology.</p><p>In honour of Wilhelm de Beer, for his contributions to mycology.</p><p>Type species.</p><p>Wilhelmdebeerea oxyuri M. Kolařík .</p><p>Diagnosis.</p><p>Known from the asexual state only. It produces both hyalorhinocladiella-like and leptographium-like asexual states. Such a combination of characteristics is rare in Ophiostomatales and is known only in several phylogenetically unrelated species.</p></div>	https://treatment.plazi.org/id/64628AFC8FA15D7EA44C68C81570884D	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Kolařík, Miroslav;Vadkertiová, Renata;Knížek, Miloš;Sklenář, František;Vakula, Jozef;Zúbrik, Milan;Kolář, Michal;Hulcr, Jiří	Kolařík, Miroslav, Vadkertiová, Renata, Knížek, Miloš, Sklenář, František, Vakula, Jozef, Zúbrik, Milan, Kolář, Michal, Hulcr, Jiří (2026): The ambrosial mycobiota of Treptoplatypus oxyurus (Coleoptera, Platypodidae): a unique island of fungal diversity revealing Wilhelmdebeerea oxyuri gen. et sp. nov. (Ophiostomatales), and two new yeast species Blastobotrys sasensis sp. nov., and Sugiyamaella casensis sp. nov. (Dipodascales). IMA Fungus 17: e 177075, DOI: 10.3897/imafungus.17.177075
B85B9A0AAACF51B68AC807748CED13D0.text	B85B9A0AAACF51B68AC807748CED13D0.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Wilhelmdebeerea oxyuri M. Kolarik 2026	<div><p>Wilhelmdebeerea oxyuri M. Kolařík sp. nov.</p><p>Fig. 7</p><p>Etymology.</p><p>The epithet oxyuri refers to the specific beetle associated with this fungus.</p><p>Diagnosis.</p><p>Wilhelmdebeerea is a monotypic genus and the species and genus diagnoses are identical until additional species are found.</p><p>Type.</p><p>SLOVAKIA • Zvolen region, <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=19.029675&amp;materialsCitation.latitude=48.627396" title="Search Plazi for locations around (long 19.029675/lat 48.627396)">Tŕnie</a>, 48.627397°N, 19.029675°E; alt. 665 m.; from larva of Treptoplatypus oxyurus feeding in the base (40 cm diam) of a decaying Abies alba; 10. June 2024; leg. M. Knížek, J. Vakula, M. Zúbrik, isol. M. Kolařík Tox- 2 (holotype PRM 963297 dried culture CCF 6802 on MEA, isotypes PRM 963298, 963299, dried culture CCF 6802 on MEA with cycloheximide, culture ex type CCF 6802) . Another representative strain – CCF 6803, the same source as CCF 6802, but isolated from mycangia of a female adult . Sequence accessions: ITS - PX 523832, LSU - PV 061845,, rpb 2 - PV 067587, tef 1-α - PV 067588, tub 2 - PV 067589, WGS - ERZ 28561635.</p><p>Description.</p><p>The species description is based on the type strain. The strain CCF 6803 has the same morphology. Cultural characteristics after 14 d: Colonies with optimal growth at 25 ° C (33 mm, 14 d). Growth at 5 ° C 8.5 mm, no growth at 35 ° C. Colonies at 25 ° C are cream with light brown zones, and the margin is narrow. Hyphae are hyaline to olive brown in colour, smooth, submerged in the medium; aerial mycelium is sparse, cream coloured. The strain grows well (32 mm in 14 d) on MEA with 500 mg / L of cycloheximide. Sexual morph is not observed. Asexual morph on MEA is mononematous, of the hyalorhinocladiella-like and leptographium-like type. Hyalorhinocladiella - like conidiophores, arising directly from submerged or aerial mycelium, are smooth, hyaline, micronematous or semimicronematous, 5.0–45.0 × 1.0–3.0 µm; conidia are variable in shape, hyaline, cylindrical, allantoid to broadly ellipsoidal, or clavate (1.5 –) 2.7–3.9 ± 0.66 (– 4.8) × (0.8 –) 1.0–2.0 ± 0.30 (– 3.0) µm. Leptographium - like anamorph. Conidiophores are macronematous, light olivaceous or olivaceous, smooth, arising from substrate hyphae, solitary or loosely compacted, resembling cream sporodochia, (100 –) 120–230 (– 450) μm in length. Stipe erect, olivaceous, 3–5 septate, (60 –) 80.0–180.0 (– 280.0) μm long and (3.0 –) 4.8–5.2 (– 6.2) μm wide at the base; basal cell is often swollen with a foot-like cell. Conidiogenous apparatus is (50.0 –) 55.0–65.0 (– 200.0) μm long (excluding conidial mass), consisting of 3–5 (mostly 3) series of branches-type B (more than two branches) (Jacobs and Wingfield 2001). Primary branches are (14.0 –) 15.5 – + 18.5 (– 24.0) × (4.0 –) 4.4 (– 5.0) μm in size. Conidiogenous cells are hyaline, tapering from base to apex, (6.0 –) 9.0 (– 15.0) × (0.7 –) 1.2 (– 1.3) μm in size. Conidia are hyaline, clavate (2.6 –) 3.3–5.9 ± 0.68 (– 7.5) × (1.1 –) 1.5–2.3 ± 0.25 (– 2.9) μm in size, accumulating around the conidiogenous apparatus as a creamy mucilaginous mass. Chlamydospores are absent.</p><p>Distribution.</p><p>Wilhelmdebeerea oxyuri was cultured from a single locality in Slovakia. Further investigations are required to determine the strength of its association with T. oxyurus . Based on GlobalFungi data, the species has been detected in 45 deadwood substrate samples from boreal forest ecosystems in Finland and Russia (Mikryukov et al. 2021; Korhonen et al. 2022) (see Biogeography section, Suppl. material 12). The host records suggest that W. oxyuri may be common, but poorly sampled, in coniferous wood in boreal Eurasia, not only in Abies, the exclusive host of T. oxyurus . Its distribution overlaps with B. sasensis and C. schatavii .</p><p>Notes.</p><p>The genomic sequence of monosporic ex-type strains contains both MAT gene idiomorphs, and the species can be considered homothallic. In particular, it possesses the MAT 1-1 gene sequence, which has an 83 % identity, and the MAT 1-2 gene, which has an 84 % identity, to the reference sequences of Ophiostoma montium .</p></div>	https://treatment.plazi.org/id/B85B9A0AAACF51B68AC807748CED13D0	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Kolařík, Miroslav;Vadkertiová, Renata;Knížek, Miloš;Sklenář, František;Vakula, Jozef;Zúbrik, Milan;Kolář, Michal;Hulcr, Jiří	Kolařík, Miroslav, Vadkertiová, Renata, Knížek, Miloš, Sklenář, František, Vakula, Jozef, Zúbrik, Milan, Kolář, Michal, Hulcr, Jiří (2026): The ambrosial mycobiota of Treptoplatypus oxyurus (Coleoptera, Platypodidae): a unique island of fungal diversity revealing Wilhelmdebeerea oxyuri gen. et sp. nov. (Ophiostomatales), and two new yeast species Blastobotrys sasensis sp. nov., and Sugiyamaella casensis sp. nov. (Dipodascales). IMA Fungus 17: e 177075, DOI: 10.3897/imafungus.17.177075
