name | Amanita sturgeonii | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
author | Tulloss, Q. Cai & Kudzma nom. prov. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
name status | nomen provisorum | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
english name | "Sturgeon's Destroying Angel" | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
etymology | Honoring the first and primary collector, Walter Sturgeon. He insisted this was a new species until molecular studies proved him right. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
GenBank nos. |
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intro |
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. The following is based on original research by the authors of this tab. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
pileus | 50 - 100 mm wide, white, with pale yellow to pale yellowish tan to tan to sordid tan to olivaceous?? areas developing particularly over disc; broadly rounded-conic or campanulate (often with vertical sides) at first, then convex to plano-convex to planar, viscid when moist, matte when dry; context white, 4.5 - 7 mm thick above stipe, unchanging when cut or bruised, frim, dense, thinning slowly toward margin, still 1± mm thick within 4 mm of margin; margin nonstriate, nonappendiculate, incurved at first; universal veil absent. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
lamellae | free to narrowly adnate with very faint decurrent lines near stipe apex (requiring 10× lens), crowded, white to off-white in mass, white to off-white to pale cream in side view, unchanging when cut or bruised, rounded at pileus margin, acute at stipe, 4.5 - 8.5 mm broad, broadest at 75% of pileus radius from stipe, with edges white and fimbriate and becoming tan when bruised; lamellulae truncate to rounded truncate (shortest) or attenuate (longest), plentiful, of diverse lengths, unevenly distributed. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
stipe | 43 - 100 × 10 - 15 mm (length includes bulb), white, unchanging when cut or bruised, cylindric, furfuraceous near apex, fibrillose or minutely fibrillose below partial veil; bulb 12 - 29 × 15 - 23 mm, napiform, marginate, firmer than in (e.g.) A. bisporigera; context solid, white, unchanging when cut or bruised, concolorous in insect tunnels; partial veil subapical to apical, skirt-like, white, thin, fragile, often tearing during development of basidiome, often deciduous, striate above, smooth below; universal veil irregularly limbate, white or whitish, membranous, enclosing stipe bulb, 20 - 30 mm from stipe base to uppermost point on limb, with 8± mm of limb free, with upper portion of limbs very thin, with limb base having triangular cross-section up to 2 mm thick at base, with only very narrow sinus separating limb from stipe base. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
odor/taste |
Odor Faintly of old potates or pungent unpleasant and meat-like. Taste not recorded. POISONOUS. A death following an intoxication with the symptomology of amanitin poisoning has been reliably attributed to ingestion of this species. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
macrochemical tests |
5% and 10% KOH soln. - quickly strong yellow on pileus. Test vouchers: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
lamella trama | bilateral, divergent; ?? | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
subhymenium | pseudoparenchymatous (cellular), with abrupt interface to subhymenial tree. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
basidia | 38± × 9.0 - 11.5 μm, 4-sterigmate, with sterigmata up to ?? × ?? μm, arising from ??; clamps not observed. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
universal veil | On pileus: absent. On stipe base, exterior layer of limb: dominated by gelatinized interwoven filamentous hyphae. On stipe base, interior of limb: filamentous undifferentiated hyphae 3.1 - 17.3 μm wide, dominant, commonly branching, single or in fascicles of up to at least 7 hyphae, with walls dominantly thin (occasionally up to 0.5 μm thick) and sometimes yellowish and refractive; inflated cells locally common, broadly clavate to narrowly clavate to nearly cylindric, up to 224 × 80 μm, with walls usually thin (occasionally up to 0.7 μm thick); vascular hyphae not observed; clamps not observed. On stipe base, inner surface layer of limb: thin, similar to interior, but gelatinized. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
lamella edge tissue | sterile; ?? | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
basidiospores | [53/1/1] (6.8-) 7.5 - 9.5 (-10.2) × (6.2-) 7.0 - 9.0 (-9.2) μm, (L = 8.5 μm; W = 7.9 μm; Q = 1.0 - 1.14 (-1.20); Q =1.07), hyaline, colorless, smooth, thin-walled, weakly amyloid to amyloid, globose to subglobose or (occasionally) broadly ellipsoid, usually at least somewhat adaxially flattened; apiculus sublateral, trucate conic to cylindric; contents granular to mono- to multiguttulate; color in deposit not recorded. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ecology | Gregarious to scattered. Ohio: With Quercus (often Q. rubra) in somewhat open areas such as cemeteries and parks. New Jersey: In lawn between single Quercus and single 40-year-old Pinus, ca. 5 m distant from each other. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
material examined |
U.S.A.: NEW JERSEY—Hunterdon
Co. - Sergeantsville, Reading Rd., 28.ix.2014 poisoning
victim's family s.n. [Tulloss 9-29-14-A] (RET 648-2,
nrITS seq'd.), 1.x.2014 R. E. Tulloss [10-1-14-A] (RET
648-3, nrITS seq'd.). Monmouth Co., Hazlet, 07.ix.2021 poisoning victims s.n. [RET 931-6, nrLSU seq’d.). Morris Co. - ca. Morristown,
24.x.2015 poisoning victim s.n. (RET 725-1, specimens
labeled A-D). Somerset Co. - Franklin Twp.,
28.viii.2008 Dr. Anthony Nici s.n.
[www.mushroomobserver.org #10221]
(HKAS 77816, nrITS & nrLSU seq'd.; RET
422-8, nrITS-LSU seq'd.).
OHIO—Colombiana Co. - Colombiana, Colombiana
Cemetery, | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
discussion |
The first material of this species seen by RET was sent from Mahoning Co., Ohio by Walter Sturgeon in 1980. Sturgeon also has reported this species from Colombiana, Lake, and Licking Counties (Ohio) and from Letchworth State Park in New York. He reports the species is largely associated with Quercus rubra. The present species can be distinguished from A. bisporigera by the lack of two-spored basidia in A. sturgeonii and the latter's spores having narrower range of Q values. A sporograph comparison of the present species with A. bisporigera is provided below. Spore shape is also useful in segregating the present species from A. suballiacea, which has 4-spored basidia: In the following image the sporograph of the present species is compare with those of A. amerivirosa and A. sp-bisporigera05. These two species have very similar spores (from the limited data we have to date); and the spores of both are notably larger than those of A. sturgeonii. It should be noted that data is limited at present. The molecular work of Cai et al. (2014) determines the present species as the probable cause of death in a poisoning case reported from the former Princeton Medical Center (Princeton, New Jersey, U.S.A.). At the time, the poisoning was attributed to A. bisporigera by RET. Cai et al. (2014) called this species "Amanita sp. 5 Yang 2014." One of the specimens of Tulloss 10-1-14-A was distorted in a manner that I have seen once or twice before on white species of the Phalloideae in eastern North America: One side of the cap had split open and seemed to be covered with brownish black tar. This was not so far as I could tell a staining reaction of the basidiome tissues. Therefore, I propose to call it the "tar syndrome." The brown stain on the top of the cap in image 5 on the brief tab is an extension of the staining from the dark mass on the opposite side of the cap. This mass is shown in image 6 on the brief tab. Until DNA sequences proved otherwise, the Hunterdon County material was treated (briefly) on this site as Amanita sp-O01 and as a distinct ("A. debilivenenum"). | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
citations | —R. E. Tulloss and L. V. Kudzma | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
editors | RET | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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name | Amanita sturgeonii |
name status | nomen provisorum |
author | Tulloss, Q. Cai & Kudzma |
english name | "Sturgeon's Destroying Angel" |
images |
1. Amanita sp-O01, Colombiana Co., Ohio, U.S.A. 2. Amanita sp-O01, Colombiana Co., Ohio, U.S.A. 3. Amanita sp-O01, from poisoning case, Somerset Co., New Jersey, U.S.A. 4. Amanita sp-O01, 10% KOH on emergency room specimen, Sergeantsville, Hunterdon Co., New Jersey, U.S.A. (RET 648-2) 5. Amanita sp-O01, mature specimen without half affected by the 'tar syndrome,' Sergeantsville, Hunterdon Co., New Jersey, U.S.A. (RET 648-3) 6. Amanita sp-O01, mature specimen showing the 'tar syndrome,' Sergeantsville, Hunterdon Co., New Jersey, U.S.A. (RET 648-3) |
photo |
Walter Sturgeon - (1-2) Colombiana County, Ohio, U.S.A. [www.mushroomobserver.org #79375] Dr. Naci - (3) from poisoning case, Somerset County, New Jersey, U.S.A. [www.mushroomobserver.org #10221] RET - (4) Sergeantsville, Hunterdon County, New Jersey, U.S.A. (RET 648-2) (5-6) Sergeantsville, Hunterdon County, New Jersey, U.S.A. (RET 648-3) |
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.