Table 1.
List of Chrysosporium and related species examined.
| Strain1 | Species | Notes1,2 | Origin | GenBank No. |
|---|---|---|---|---|
| CBS 593.71 | Amauroascus aureus | Clade IV Neotype of Gymnoascus aureus |
Decayed wood, Cryptomeria japonica, Mt. Yudono, Japan | KC989708 |
| CBS 342.64 | Aphanoascus terreus | Clade II (no living ex-type culture available) | Lawn soil, India. Anamorph, C. indicum (H.S. Randhawa & R.S. Sandhu) Garg | KC989709 |
| CBS 272.66 | Arthroderma ciferrii (Isotype) | Clade VII | Soil, Arkansas, USA. Anamorph, C. georgiae (Varsavsky & Ajello) Oorschot | KC989711 |
| CBS 473.77 | Arthroderma tuberculatum (Type) | Clade VII | Feather of Turdus americanus, Urbana, IL, USA | KC989710 |
| FRR 4958 | C. botryoides (Type3) | = CBS 492.91 | Nest of Osmia cornifrons, Nagano region, Japan | KC989712 |
| CBS 643.79 | C. carmichaelii (Type) | Clade VI | Michigan, USA | KC989713 |
| CBS 688.71 | Bettsia alvei (Type) | Pollen in honeycomb, Zeeland, Denmark | KC989714 | |
| FRR 2000 | C. farinicola | = UAMH 4688 | Prunes, Young, NSW, Australia | KC989715 |
| CBS 298.95 | C. farinicola | Prune processing equipment, UK | KC989716 | |
| FRR 77 | C. fastidium (Type) | = IMI 126288, CBS 154.67, ATCC 18053, ATCC 36783, UAMH 2369 | Dried prunes, Leeton, NSW, Australia | KC989717 |
| FRR 376 | C. fastidium | Dried prunes, Australia | KC989718 | |
| FRR 81 | C. fastidium | Identified as C. fastidium, appearance and LSU sequence of C. farinicola (Table 3, Fig. 1) | Dried prunes, Australia | KC989725 |
| J211 | C. fastidium | Identified as C. fastidium, appearance and LSU sequence of C. farinicola (Table 3, Fig. 1) | Dried prunes, Australia | KC989734 |
| FRR 4953 | C. globiferum (Type) | = CBS 454.91 | Nest cells of Osmia cornifrons, Nagano region, Japan | KC989719 |
| FRR 4957 | C. globiferum var. articulatum (Type) | = CBS 493.91 | Nest cells of Osmia cornifrons, Nagano region, Japan | KC989720 |
| FRR 4956 | Chrysosporium globiferum var. niveum (Type) | = CBS 455.91 | Nest cells of Osmia cornifrons, Nagano region, Japan | KC989721 |
| FRR 4954 | C. hispanicum (Type) | = CBS 486.91 | Nest cells of Osmia cornuta, Valladolid, Spain | KC989722 |
| FRR 4955 | C. holmii (Type) | = CBS 487.91 | Nest cells of Osmia rufa, Glostrup, Denmark | KC989723 |
| FRR 2357 | C. inops | Chopped Chinese dates, Australia | KC989724 | |
| CBS 297.95 | C. inops | Chinese five spice powder, Sheffield, UK | JF922024 | |
| FRR 4952 | C. medium (Type) | = CBS 488.91 | Nest cells of Osmia rufa, Tåstrup, Denmark | KC989726 |
| FRR 4949 | C. medium var. spissescens (Type) | = CBS 489.91 | Nest cells of Osmia rufa, Tåstrup, Denmark | KC989727 |
| CBS 388.68 | C. merdarium (Type species) | Soil | KC989728 | |
| FRR 4950 | C. minus (Type) | = CBS 490.91 | Nest cells of Osmia rufa, Karlslunde, Denmark | KC989729 |
| FRR 4951 | C. pyriforme (Type) | = CBS 491.91 | Nest cells of Osmia rufa, Sweden | KC989730 |
| CBS 634.79 | C. sulfureum | Clade VI | Cheese rind, Switzerland | KC989731 |
| CBS 640.79 | C. synchronum (Type) | Clade VIII Sordariomycetes | Commercially grown Agaricus bisporus, Edmonton, Alberta, Canada | KC989732 |
| CBS 171.62 | C tropicum (Isotype) | Clade I | Woollen overcoat, Guadalcanal, Solomon Is. | KC989733 |
| CBS 153.67 | C. xerophilum | = ATCC 18052, IMI 126287, UAMH 2368 | Dried prunes, Sydney, NSW, Australia | JF922023 |
| CBS 437.88 | C. zonatum (Type) | Clade I | Horse dung, Kuwait | KC989735 |
| CBS 407.71 | Nannizziopsis vriesii | Clade IV Status: Isotype of Rollandina vriesii |
Ameiva (lizard) skin and lung, Netherlands | KC989736 |
| CBS 708.79 | Renispora flavissima | Clade IV | Soil in barn housing Myotis velifer, Kansas, USA | KC989737 |
| CBS 120.77 | Uncinocarpus reesii (Type) | Clade III | Feather, Australia | KC989738 |
1Culture collections of CBS (Centraalbureau voor Schimmelcultures, Utrecht, The Netherlands), FRR (CSIRO Animal, Food and Health Sciences, North Ryde, Australia); J (Dept of Microbiology, Swedish University of Agricultural Sciences, Uppsala, Sweden).
2Clade numbers refer to the groupings of Vidal et al. (2000).
3All types studies were ex-type cultures.