1. A. submaculata - Bryer Tract, Abington, PA M. R. Goldman
2. A. submaculata - near Glasboro, NJ RET
3. A. submaculata - Jamesburg Park, NJ RET
After more than 30 years of collecting in the eastern United States, RET has found only one entity
that could correspond to Peck's description of A. submaculata. Nevertheless,
because of the limited description of the present species (provided below), the
identification has not been formally published. The candidate has simply
been called "Amanita sp. 18" (Tulloss et al., 1995)
among other temporary designations.
The cap is 48 - 192 mm wide, grayish-brown to dark brown over the center, grayish brown to brownish or umbrinous gray to
umbrinous elsewhere, sometimes pallid at the margin, with appearance of having
brown or gray-brown innate fibrils, often with depigmented small spots
or short radial lines (hence Peck's epithet), at first often irregularly
rounded conic to irregularly convex to plano-convex to plane, with a
broad umbo, subshiny to shiny when dry, tacky to waxy when moist, with a
nonappendiculate and nonstriate margin (slightly striate, to 15% of the
radius with age), incurved at first, then down curved, finally straight.. The volva is absent
or present as irregular warts of varying size or filamentous thin
squamules, white or off-white or pallid becoming grayish or grayish
brown or brown, often over the center only, pulverulent, friable and
detersile.. The flesh is white, grayish at the center, 4 - 5 mm thick, thinning evenly to the margin,
and then membranous to the margin.
The gills are free to very narrowly adnate, subcrowded to crowded,
off-white to white to pale cream to cream, staining red brick, rounded
on the outer end, 4 - 8.5 mm broad, with or without a decurrent line on
the stipe apex.. The short gills are truncate to subtruncate to rounded truncate to
subattenuate to attenuate in steps, rather narrow, of diverse lengths,
some free from both the stem and margin.
The stem is (38-) 105 - 198 × (5.5-) 11.5 - 26 mm, slightly narrowing upward, flaring at the top, satiny white to
whitish to pale ground to blackish to brownish, pale orange-brown with
handling, sometimes with vertical red-brown dashes of staining on lower
stipe and upper bulb, sometimes sinuous, sparsely pulverulent above the
ring, satiny or fibrillose (sometimes coarsely squamulose) below partial
veil, with fibrils white or pallid in the topmost quarter of stem, brown
to gray brown below, with some fibrils becoming darker from handling,
with faintly longitudinally striations at maturity.. The bulb is (13-) 36 - 45 × (13-) 24 - 44 mm,
irregularly ovoid to fusiform to napiform to subnapiform, sometimes very small and
slender, staining brick red in old insect damage or staining with
red-brown marks.. The stem flesh is whitish to pale grayish cream, staining as in
other tissues, and solid.. The ring is white, sometimes brownish with age or staining brick red,
subapical to apical, superior, membranous, skirt-like (often suggesting
a broad, mid-19th Cent. ball gown), copious, striate
above, eventually collapsing on stipe, and tearing.. The volva is absent
or present as one or two thin whitish to gray rings around the top of the stipe's bulb
or as a loose limb against stipe or as loose patches easily overlooked
in the substrate, more membranous and more likely to be collected attached
to the specimen than in the case (for example) of Amanita
flavoconia G. F. Atk.
The species has a distinctive range of odors varying from fruit-like to anise-like, sometimes with both
elements present, sometimes with a chlorine-like addition.
The spores measure (6.3-) 7.0 - 9.8 (-13.3) × (4.5-) 4.9 - 6.6 (-8.4) µm and are broadly ellipsoid to
ellipsoid to elongate (rarely cylindric) and amyloid. Basidia lack clamps.
Originally collected in North Carolina where it was reported to occur scattered or clustered in "thin woods" and
"open places." In New Jersey it is often collected in Pine-Oak (Pinus-Quercus) barrens on sandy soil of the Atlantic Coastal Plain.
This species is often misidentified in North America. RET has been told that A. excelsa (Fr. : Fr.) Bertillon in Dechambre
has a fruity odor in North America, which is not true so far as we know. This error
is probably due to the confusion of A. submaculata, A.
morrisii Peck, and other often fruity-smelling taxa from the Americas, with the European species.
The information below is derived from the original description (Peck, 1900)
supplemented by the description of the type by Jenkins (1978).
The cap of Amanita submaculata is 70 - 90 mm wide, convex or somewhat bell-shaped, dark brown, more or less marked by whitish stripes or spots, and shiny when dry. The volval remnants are present as a single, floccose patch.
The gills are free, subdistant, white, and thin.
The stem is approximately 70 - 90 × 6 - 12mm, cylindric, white, and solid. The ring is large, white, flaring, very thin, persistent, and membranous. An ovoid bulb is present at the stem base without volval remnants.
In the original description, Peck says the specimen he was sent "yielded no spores." According to Jenkins' type study, the spores measure 7.0 - 8.6 × 4.7 - 6.4 µm and are broadly ellipsoid to ellipsoid to elongate and amyloid. Clamps are absent at bases of basidia.
Miss M. L. Wilson, Peck's North Carolina correspondent, included a rough watercolor of the material which is preserved at the
New York State Museum (Albany).—R. E. Tulloss and L. Possiel
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 material not directly from the protolog of the present taxon and not cited as the work of another researcher is based on original research by R. E. Tulloss.
48 - 192 mm wide, grayish brown to dark brown (e.g., 5F7-8) over disc, grayish-brown to brownish or umbrinous gray to umbrinous elsewhere (e.g., 5C-D5)), pallid at margin, staining reddish-brown in streaks and in older insect bites or staining brick red and becoming dark red-brown with time, virgate (with brown or gray-brown, apparently innate, radial fibrils), at first often irregularly rounded conic, then irregularly convex to plano-convex to plane, with broad umbo, sometimes slightly undulate, sometimes splitting at margin, subshiny to shiny when dry, tacky to waxy when moist; context mostly white, often with grayish area in disc, staining pale rust to brick red to ochraceous in larva tunnels, 4 - 15 mm thick, thinning evenly to within 4 - 5 mm of margin, then membranous to margin; margin nonstriate becoming striate in age (0.15R), incurved at first, then downcurved to straight, nonappendiculate; universal veil absent or as irregular warts of varying sizes or filamentous thin squamules, white or off-white or pallid becoming grayish or brown or brownish gray, often over disc only, minutely verrucose (10× lens), pulverulent, friable, detersile.
free to very narrowly adnate, some with decurrent tooth at stipe apex, with or without decurrent line on stipe, subcrowded to crowded, rounded on outer end, with even width for most of length, off-white to white to pale cream to cream in mass and in side view, staining brick red, 4 - 8.5 mm broad, sometimes forking near margin; lamellulae truncate to subtruncate to rounded truncate to subattenuate to attenuate in steps, rather narrow,
common, of diverse length, some free from both stipe and margin.
(38-) 105 - 198 × (5.5-) 11.5 - 26 mm, satiny white to whitish to pale ground to blackish to brownish, pale orange-brown with handling, sometimes with vertical red-brown dashes of staining on lower stipe and upper bulb, slightly narrowing upward, flaring at apex, sometimes sinuous, sparsely pulverulent above partial veil, satiny or fibrillose (sometimes coarsely squamulose) below partial veil, with fibrils white or pallid in the topmost 1/4 of stipe, brown to gray brown below, with some fibrils becoming darker from handling, becoming faintly longitudinally striatulate at maturity; bulb (13-) 36 - 45 × (13-) 24 - 44 mm, irregularly ovoid to fusiform to napiform to subnapiform, sometimes very small and slender, staining brick red in old insect damage or taking on superficial red-brown marks; context whitish to pale grayish cream, staining as in other tissues, solid, with larva tunnels concolorous to watery brown to brick red or ochraceous; partial veil white, browning with age or staining brick red, subapical to apical, superior, membranous, skirt-like, copious, striate above, with outer half becoming free first and creating fold around the ring at about mid-radius and (consequently) resembling a great mid-19th Cent. ball gown when full free, eventually collapsing on stipe, often tearing; universal veil absent or as one or two thin whitish to gray rings around top of bulb or as loose limb against stipe or loose patches easily overlooked in substrate, more membranous and more likely to be collected attached to specimen than in the volva of (e.g.) A. flavoconia.
Odor Pleasant, fruity or flowery or strongly anise-like, rarely with an additional chlorine-like odor or like an automobile tire.
L-tyrosine (aqueous sat. sol.) - positive on stipe surface and stipe context (spot testing only). Voucher collections: Tulloss 7-21-85-F, 8-1-86-F, and 8-16-85-E.
bilateral, divergent, with shallow angle of divergence, with subhymenial base comprised of narrow elements (clavate to subcylindric to narrowly subfusiform, up to 64 × 26 µm) often in chain of two between central stratum and subhymenium; wcs =
??; filamentous, undifferentiated hyphae
?? µm wide,
??, occasionally with yellowish subrefractive walls; terminal, inflated cells,
??; vascular hyphae
?? µm wide,
?? µm; wst-far =
?? µm; pseudoparenchymatous, 3 to 4 cells deep, with smallest cells nearest basidia, with largest cells (globose to clavate) up to 28 × 15.5 µm, with basidia arising from
from type study of Jenkins (1978a): [-/-/1]
7.0 - 8.6 × 4.7 - 6.4 μm, (Q = 1.22 - 1.83; Q' = 1.59),
hyaline, thin-walled, amyloid, broadly ellipsoid to elongate, often adaxially flattened; apiculus sublateral, cylindric; contents guttulate;
color in deposit not recorded.
composite data from all material revised by RET: [406/19/16] (6.3-) 7.0 - 9.8 (-13.3) × (4.5-) 4.9 - 6.6 (-8.4) µm, (L = (7.2-) 7.8 - 8.8 (-8.9) µm; L’ = 8.4 µm; W = (5.2-) 5.5 - 6.2 µm; W’ = 5.7 µm; Q = (1.18-) 1.25 - 1.67 (-2.02); Q = (1.32-) 1.36 - 1.56 (-1.64); Q’ = 1.47), hyaline, colorless, thin-walled, smooth, amyloid, broadly ellipsoid to ellipsoid to elongate, rarely cylindric, often adaxially flattened, infrequently adaxially indented, infrequently expanded at one end; apiculus sublateral, cylindric; contents monoguttulate; white in deposit.
Connecticut: In sandy loam. Kentucky: In dry loam of lawn/ with Quercus alba L., Q. stellata Wangenh., and other Quercus spp. and Tsuga canadensis (L.) Carr. New Jersey: In dark loam of Quercus-Fagus-Carya forest or dark sand (having significant organic matter) in mixed forest or in sand of Pinus-Quercus barrens. New York: In loamy clay. South Carolina: In dark moist loam with Quercus muehlenbergii Engelm. and Pinus.
from type study of Jenkins (1978a):
U. S. A.: NORTH CAROLINA—Unkn. Co. - unkn. loc.,
1899 Miss M. L. Wilson s.n. (holotype, NYS).
CONNECTICUT—Middlesex Co. - East Haddam, Devil’s Hopyard St. Pk. [41°28'32" N/ 72°20'25" W, 72 m], 31.viii.1997 David Rose s.n. [Tulloss 8-31-97-L] (RET 269-9); Ivoryton 22.ix.1987 S. S. Ristich s.n. [Tulloss 9-27-87-SSR2] (RET 021-6); Middleton Twp., 25.vii.1992 Faith Hurd s.n. [Tulloss 7-25-92-M] (RET 067-8), 25.vii.1992 NEMF participant s.n. [Tulloss 7-25-92-G] (RET 064-8). New London Co. - Mystic, Pequot Woods, ca. Mystic Seaport, 2.viii.2008 Janet Blanchard s.n. [Tulloss 8-2-08-B] (RET 446-3).
GEORGIA—Forsyth Co. - unkn. loc., 7.v.2011 Timothy Kewin s.n. [mushroomobserver #94176] (RET 509-3).
INDIANA—Monroe Co. - Bloomington, Griffey Lk. , 9.ix.2012 Stephen Russell s.n. [mushroomobserver #110440] (RET 531-7, nrITS & nrLSU seq'd.). Owen Co. - Spencer, McCormick’s Creek St. Pk. [39.2982° N/ 86.7217° W, 218 m], 5.ix.2012 S. Russell s.n. [mushroomobserver #109802] (RET 531-6, nrITS & nrLSU seq'd.).
KENTUCKY—Laurel Co. - Levi Jackson Wilderness Trail St. Pk., 20.vii.1987 D. C. & R. E. Tulloss 7-20-87-B (RET 149-9).
MAINE—Cumberland Co. - Falmouth, 10.vii.1984 S. S. Ristich s.n. [RET 7-10-84-SSR] (RET ??);
N. Yarmouth, Nanovic Woods, 9.vii.1997 S. S. Ristich s.n. (RET 262-9).
Stratford Co. - Sanford, 22.vii.1988 S. S. Ristich s.n. [Tulloss 7-22-88-SSR] (RET 119-8).
MASSACHUSETTS—Berkshire Co. - Adams, 15.viii.1986 NEMF1986 participant s.n. [Tulloss 8-15-86-H] (RET 466-5); Hopkins Memorial Forest, 16.viii.1986 participant NEMF1986 s.n. [Tulloss 8-16-86-D] (RET 668-5). Middlesex Co. - Granton Conservation Area, 19.viii.1989 Peter Kukle s.n. [Tulloss 8-19-89-C] (RET 245-2).
Burlington Co. - Wharton St. For., Batsto Village, 12.vii.1985 D. C. & R. E. Tulloss 7-12-85-F (RET 202-8). Hunterdon Co. - Lebanon, Oakmoss Mycological Preserve [40°38'50.07" N/ 74°47'50.92" W], 25.vii.2007 Richard Balsley s.n. (in herb. Balsley; RET 409-7); Tewksbury Twp., 26.vii.1984 M. Hacker s.n. [Tulloss 7-26-84-S] (RET 243-8).
Mercer Co. - Hopewell Twp., 3.vii.1991 R. E. Tulloss 7-3-91-B (RET 112-2); Hopewell Twp., off Carter Road, woods behind AT&T/Lucent research labs [40°21’39” N/ 74°43’29” W, 63 m], 1.viii.1985 R. E. Tulloss 8-1-85-F (RET 223-1). Middlesex Co. - Jamesburg Twp., Jamesburg Twp. Pk., ca. Helmetta [40°23’07” N/ 74°25’48” W],
21.viii.1983 M. A. King & R. E. Tulloss 8-21-83-E (RET 469-6), 29.vii.1984 R. E. Tulloss 7-29-84-F (RET 011-7), -J (RET 242-7), -K (RET 243-6), 16.viii.1984 R. E. Tulloss 8-16-84-E (RET 232-5), 14.vii.1996 B. 24.vii.1996 Britt Carlson & R. E. Tulloss [Tulloss] 7-24-96-H (RET 200-3).
Monmouth Co. - Upper Freehold Twp., Assunpink Wildlife Mgmt. Area [40°12’36” N/ 74°28’42” W], 10.viii.1986 M. A. King & R. E. Tulloss 8-10-86-C (RET 222-10); Shark River Co. Pk. [40°12’18” N/ 74°05’44” W, 16 m], 17.vii.1988 Robert Hosh s.n. [Tulloss 7-17-88-B] (RET 124-3). Morris Co. - Hackettstown Reservoir, 26.vii.1984 G. Kibby, R. Peabody, J. Richards, & R. E. Tulloss [Tulloss] 7-26-84-O (RET 242-6); Mendham, Meadowood Twp. Pk. [40°47'31" N/ 74°38'43" W, 214 m], 22.vii.1984 NJMA foray participant s.n. [Tulloss 7-22-84-G] (RET 243-4),
19.vii.1992 Hanna Tschekenow s.n. [Tulloss 7-19-92-C] (RET 063-3).
Cayuga Co. - Fair Haven St. Pk., 4.viii.1995 NEMF participant s.n. [Tulloss 8-4-95-C] (RET 154-7). Dutchess Co. - Pine Plains, Thompson Pond Preserve [41°57’52” N/ 73°40’57” W, ca. 140-410 m elev.], 6.vii.2011 Wm. Bakaitis s.n. (RET 480-10). Otsego Co. - Gilbert Lake St. Pk., 16.viii.1985 E. Cherniack [Tulloss 8-16-85-E] (RET ??). Tompkins Co. - Ithaca, 27.viii.1981 S. S. Ristich s.n. [Tulloss 8-27-81-RB] (RET 166-8).
NORTH CAROLINA—McDowell Co. - Little Switzerland, ca. Wildacres Retreat, Armstrong Crk. [35º48’41.69” N/ 82º04’24.22” W], 26.ix.2009 NAMA foray participant s.n. [Justice NC-AM-21] (RET 452-9).
PENNSYLVANIA—Union Co. - R. B. Winter St. Pk., 13.viii.1984 D. C., M. H., & R. E. Tulloss 8-13-84-E (RET 242-10).
SOUTH CAROLINA—Greenville Co. - Roper Mtn. Pk., 23.viii.1991 Emily & Erin Luetkemeier & R. E. Tulloss 8-23-91-B (RET 032-2).
TEXAS—Newton Co. - Bleakwood, Co. Rd. 3062, Lewis prop. [30°42.509’ N/ 93°49.630’ W], 9.viii.2009 David P. Lewis 9172 (RET 461-2), 26.ix.2009 David P. Lewis 9277 (RET 462-1). Tyler Co. - Big Thicket Nat. Preserve, Beech Creek Unit, 25.x.1986 Jay Justice s.n. [Tulloss 10-25-86-G] (RET 467-3).
WEST VIRGINIA—Greenbrier Co. - Monongahela Nat. For., Lake Sherwood Recreation Area [38°00'24" N/ 80°06'40" W, 825 m], 2.ix.1982 M. H. & R. E. Tulloss 9-2-82-A (RET 214-6). Tucker Co. - Fernow Exp. For., 4.ix.1992 S. L. Stephenson, R. P. Bhatt & A. Kumar WS13-110 (FWVA).
—R. E. Tulloss
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"Ball Gown Amanita"
1. A. submaculata - Bryer Tract, Abington, PA M. R. Goldman
2. A. submaculata - near Glasboro, NJ RET
3. A. submaculata - Jamesburg Park, NJ RET
Dr. Mitchell R. Goldman - (1) Pennsylvania, U.S.A.
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.