name | Amanita subfrostiana |
name status | nomen acceptum |
author | Zhu L. Yang |
english name | "False Frost's Amanita" |
images | |
cap |
The cap of A. subfrostiana is 40 - 70 mm wide, convex to applanate, red over disc, and becoming pale orange towards the margin. The volval remnants on pileus are floccouse to felty, yellow to yellowish or orange; the margin has long striations. |
gills |
The lamellae are white to cream-colored, and the short lamelullae are usually truncate. |
stem |
The stem is 60 - 100 × 10 - 15 mm, subcylindric or tapering upwards. The basal bulb is subglobose to ovoid, 10 - 30 mm wide; its upper part is covered with yellowish floccose volval remnants often forming a short limb. The ring is membranous, its upper surface is whitish and its lower surface is yellowish. |
odor/taste | double click in markup mode to edit. |
spores |
The spores of A. subfrostiana are (8.0-) 8.5 - 10.5 (-12.0) x (7.0-) 8.0 - 10.0 (-10.5) µm, globose to subglobose, inamyloid, colorless, hyaline, thin-walled, smooth. There are clamps at bases of basidia. |
discussion |
Amanita subfrostiana grows in coniferous or mixed forests. To date it has been found only in southwestern China. Amanita frostiana (Peck) Sacc. is similar to the present species. However, A. frostiana, originally described from North America, usually has a less saturated, yellow-orange to orange-yellow cap, shorter striations along the cap margin, and paler-colored volval remnants on the cap.—Zhu L. Yang |
brief editors | RET |
name | Amanita subfrostiana | ||||||||||||||||
author | Zhu L. Yang. 1997. Biblioth. Mycol. 170: 12, figs. 1-4. | ||||||||||||||||
name status | nomen acceptum | ||||||||||||||||
english name | "False Frost's Amanita" | ||||||||||||||||
MycoBank nos. | 444653 | ||||||||||||||||
GenBank nos. |
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holotypes | HKAS 32513 | ||||||||||||||||
intro |
The following text may make multiple use of each data field. The field may contain magenta text presenting data from a type study and/or revision of other original material cited in the protolog of the present taxon. Macroscopic descriptions in magenta are a combination of data from the protolog and additional observations made on the exiccata during revision of the cited original material. The same field may also contain black text, which is data from a revision of the present taxon (including non-type material and/or material not cited in the protolog). Paragraphs of black text will be labeled if further subdivision of this text is appropriate. Olive text indicates a specimen that has not been thoroughly examined (for example, for microscopic details) and marks other places in the text where data is missing or uncertain. NOTE: Spore data from papers by Z. L. Yang are presented following his use of the "Times New Roman" face for "Q" and "Q'"—respectively, " | ||||||||||||||||
basidiospores |
From protolog: [240/8/5] (8.0-) 8.5 - 10.5 (-12.0) × (7.0-) 8.0 - 10.0 (-10.5) μm, ( | ||||||||||||||||
ecology | Solitary or in small groups. At 2360± m elev. In conifer forest or in mixed forest. | ||||||||||||||||
material examined |
from protolog: CHINA: XIZANG AUTONOMOUS REGION (TIBET)—Unkn. Prefecture. - Unkn. Co., unkn. loc., 20.viii.1983 Y. G. Su (paratype, HKAS 16416).
YUNNAN—Dali Bai Autonomous Prefecture - Binchuan Co., Jizushan, 2.viii.1985 G. P. Xiao 89 (paratype, HKAS 15431), 9.viii.1985 G. P. Xiao 470 (paratype, HKAS 17038), 1.ix.1992 Y. Xiang 4 (holotype, HKAS 32513); Binchuan Co., Jizushan, 2360 m elev., 4.viii.1985 G. P. Xiao 296 (paratype, HKAS, 17266). Zhang et al. (2004) voucher for sequencing: CHINA: YUNNAN—Unkn. loc., s.d. unkn. coll. s.n. (HKAS 34551). | ||||||||||||||||
citations | —Zhu L. Yang | ||||||||||||||||
editors | RET | ||||||||||||||||
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name | Amanita subfrostiana |
bottom links | [ Keys & Checklists ] |
name | Amanita subfrostiana |
bottom links | [ Keys & Checklists ] |
Each spore data set is intended to comprise a set of measurements from a single specimen made by a single observer; and explanations prepared for this site talk about specimen-observer pairs associated with each data set. Combining more data into a single data set is non-optimal because it obscures observer differences (which may be valuable for instructional purposes, for example) and may obscure instances in which a single collection inadvertently contains a mixture of taxa.