name | Amanita sororcula |
name status | nomen acceptum |
author | Tulloss, Ovrebo & Halling |
english name | "Little Sister Ringless Amanita" |
images | |
cap |
The cap of Amanita sororcula is 35 - 60 mm wide, bell-shaped at first, eventually nearly flat, sometimes with an umbo, with margin striate (25 - 35% of the radius). The cap ranges from gray to grayish brown and is paler toward the margin. The flesh is white, but black under the cap skin. The cap is 4 - 5 mm thick. The volva is present in scattered patches that are white to tannish gray. |
gills |
The gills are free, ranging from white to gray or dark brownish gray with age, and 6 - 7.5 mm broad. |
stem |
The stem is 70 - 150 × 7 - 10 mm, white, sometimes gray toward base, exannulate, and decorated with fine, appressed gray to brownish gray fibrils. The flesh is white and hollow. The volva may be sac-like, membranous to submembranous, white to gray, extending up to 30 mm from the bottom of the stem, or it may be in scattered gray patches or bands on the lower stem; in the latter cases, there may also be a white cup surrounding the stem base. |
spores |
The spores measure (7.8-) 9.5 - 14.0 (-17.0) × (7.2-) 8.8 - 12.8 (- 15.5) µm and are globose to subglobose (occasionally broadly ellipsoid) and inamyloid. Clamps are not present or rare at bases of basidia. |
discussion |
Amanita sororcula is known from Costa Rica to Andean Colombia and occurs in this region in cloud forests with oak (Quercus). Prior to description of A. sororcula, collections of this species were commonly assigned to A. ceciliae (Berk. & Broome) Bas, which also has a weakly structured volva and graying gills, but, among other differences, the latter has a strong yellow tint in the pileus when young. As far as is known, A. ceciliae is restricted to Europe and neighboring regions of Asia. Several Western Hemisphere species with a weakly structured volva and graying lamellae remain to be formally described.—R. E. Tulloss |
brief editors | RET |
name | Amanita sororcula | ||||||||
author | Tulloss, Ovrebo & Halling. 1992. Mem. New York Bot. Gard. 66: 17, figs. 11-12. | ||||||||
name status | nomen acceptum | ||||||||
english name | "Little Sister Ringless Amanita" | ||||||||
synonyms |
The editors of this site owe a great debt to Dr. Cornelis Bas whose famous cigar box files of Amanita nomenclatural information gathered over three or more decades were made available to RET for computerization and make up the lion's share of the nomenclatural information presented on this site. | ||||||||
etymology | sororcula "little sister" Metaphorically intended to be the "little sister" of Amanita ceciliae, which was named for a daughter of Berkeley. Motivated by past confusion of this species and similar species from the Americas with A. ceciliae. | ||||||||
MycoBank nos. | 359390 | ||||||||
GenBank nos. |
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holotypes | HUA | ||||||||
revisions | Tulloss, here. | ||||||||
selected illustrations | Tulloss. 2000a. Boll. Gruppo Micol. G. Bresadola 43(2): 15, fig. 4. | ||||||||
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 material is based upon original research by R. E. Tulloss. | ||||||||
pileus | PILEUS: 35 - 85 mm wide, gray to smoky gray (61 g Br.) to brownish gray (7E3) to grayish brown (6D-F4) or to "soapstone" (MP) to dark brown (6F8 or 7F5) to chocolate to fuscous to deep fuscous to dark grayish brown (7F3); usually darkest over disc (e.g., 6F4 to 8F3), sometimes uniformly pigmented, at first rounded subconic to convex, then broadly convex to campanulate, subumbonate to umbonate, dry, subpolished to shiny; context white, but blackish under pileipellis, unchanging when cut, 4 - 5 mm thick; margin sulcate or pectinate (0.25R - 0.5R), sometimes decurved, flaring upward at maturity, nonappendiculate; universal veil as scattered appressed patches or truncate conic or conic warts, white or whitish at first, becoming orangish gray to brownish gray (6B-C2) to grayish to tannish gray (5C3) to dark grayish brown (6F4), sometimes paler on sides than on upper surface, sometimesly nearly black in exsiccata. | ||||||||
lamellae | LAMELLAE: free, close to crowded, white to whitish buff, becoming gray from margin inward, with white to grayish to dark gray to brownish gray (6C2) to dark brownish gray (7E3) to dark grayish brown (8F3) to "soapstone" (MP) fimbriate edges, drying 4A3 or slightly grayer than 4A4 to 5B4 or dark gray to yellowish gray (5Y 7/4) and always retaining brownish edge, rather thin to rather thick, 3 - 8 mm broad; lamellulae truncate to subtruncate, of diverse lengths, unevenly distributed. | ||||||||
stipe | STIPE: 70 - 150 × 7 - 15+ mm, subcylindric or tapering upwards, with ground color white (at least above) to sometimes grayish toward base, with surface decorated with fine appressed grayish to brownish gray to grayish brown (6-7E3) fibrils often in belts; context white, unchanging when cut or bruised, stuffed, becoming hollow; exannulate; universal veil as complete or incomplete short limb of membranous to submembranous tissue about 20 - 30 mm from stipe base [white to whitish to orangish white (6A2) at first, becoming pale ashgray to gray to brownish gray (8E2)] or in scattered grayish patches or dark gray-brown (nearly black in exsiccata) bands low on stipe, with color change occurring from uppermost portion downward, sometimes with whitish rather small cupulate portion enclosing base of stipe. | ||||||||
odor/taste | Odor mild or lacking or fungoid or slightly disagreeable (not strong). Taste mild. | ||||||||
macrochemical tests |
MACROCHEMICAL TESTS: Ammonia soln. - negative on lamellae. KOH soln. - negative on pileipellis and on lamellae. Spot test for laccase (syringaldazine) - negative throughout basidiome. Spot test for tyrosinase (paracresol) - throughout basidiome. Phenol (also tyrosinase indicator) - negative on pileipellis [obscured because of pileus color?], turning flesh directly chocolate. Test vouchers: Franco-M. 534, 905, 906; Gómez & Alfaro 24759; Mueller 4642. | ||||||||
pileipellis | 80 - 160 µm thick overall (145 - 235 µm in material in which sporulation just beginning when dried); suprapellis 5 - 35 µm thick (20 - 60 µm in material in which sporulation just beginning when dried), colorless, with hyphae gelatinized or partially gelatinized; subpellis 75 - 125 µm thick (120 -175 µm in material in which sporulation just beginning when dried), with hyphae partially gelatinized or ungelatinized yellow-brown to orange-brown, with pigment sometimes extending short distance into pileus context; filamentous, undifferentiated hyphae 1.8 - 7.5 µm wide, branching, interwoven, subradially arranged in part, with intracellular pigment sometimes becoming guttulate in 2% KOH; vascular hyphae 1.0 - 11.5 µm wide, locally tangled loosely, common to plentiful, rarely branching, sinuous. | ||||||||
pileus context | filamentous, undifferentitated hyphae 1.8 - 10.0 µm wide, branching, plentiful, dominating in tissue nearest pileipellis and nearest lamellae, with walls thin to slightly thickened, often in fascicles, interwoven in moderately open lattice; acrophysalides plentiful, dominating in region away from pileipellis and lamellae, clavate to pyriform to subovoid to ovoid to ellipsoid to elongate (subfusiform or narrowly subfusiform), to 136 × 49 µm (mostly under 100 µm long), with walls thin or slightly thickened, sometimes with penultimate hyphal segment partially inflated, sometimes in chains of two; vascular hyphae 1.0 - 15.5 µm wide, branching, infrequent to locally common to locally plentiful, locally in coils and knots. | ||||||||
lamella trama | obscurely bilateral; wcs = (30-) 55 - 95 (-105) µm; subhymenial base poorly or not differentiated from subhymenium; central stratum containing plentiful intercalary inflated cells [clavate to ellipsoid to subfusiform, up to 80 × 34 µm (mostly under 65 × 25 µm), sometimes with wall slightly thickened at least in apical region]; filamentous, undifferentiated hyphae 1.5 - 10.0 µm wide, branching; diverging, terminal inflated cells not observed; vascular hyphae 2.2 - 15.0 µm wide, sinuous, scarce to locally common. | ||||||||
subhymenium | wst-near = (5-) 15 - 45 (-50) µm; wst-far = (25-) 35 - 70 µm; pseudoparenchymatous, occasionally locally showing some branching of chains of cells or slightly inflated hyphal segments, with inflated cells (to 35 × 26 µm) in one to three (below bases of longest basidia/-oles) to four or five (below bases of shortest basidia/-oles) layers with larger cells nearest central stratum, with basidia arising from inflated cells or slightly inflated short hyphal segments or occasionally directly from a hypha of the central stratum. | ||||||||
basidia | 45 - 82 × 9.5 - 20 µm thin-walled, but rather commonly with wall up to 0.8 µm thick in apical region, 4- or occasionally 3- or 2-sterigmate, with sterigmata up to 17.5 × 7.5 µm (largest by far in matural in which sporulation just beginning); clamps rare to locally common, somewhat difficult to detect because of thin wall. | ||||||||
universal veil | On pileus, exterior surface: often strongly gelatinized or eroded away. On pileus, interior: filamentous, undifferentiated hyphae 1.5 - 11.5 µm wide, frequently branching, loosely interwoven, often in fascicles, plentiful, partially gelatinized, more common near pileipellis; inflated cells subglobose to ellipsoid to ovoid to clavate to broadly fusiform to narrowly subfusiform, up to 72 × 55 µm, terminal dominating, pale gray to gray to grayish brown to brown to brownish gray, collapsing, with walls thin or up to 0.8 µm thick; vascular hyphae 1.8 - 11.0 µm wide, scattered, slightly more common than on stipe base. On pileus, adjacent to pileipellis: filamentous, undifferentiated hyphae as in interior, gelatinized; inflated cells smaller than in interior, gelatinized. On stipe base, exterior surface: somewhat to extensively gelatinized, sometimes eroded away, with inflated cells collapsing, with orange-brown or brown intracellular pigment in some hyphal segments and some inflated cells, dominated (at least locally) by filamentous, undifferentiated hyphae. On stipe base, interior: similar to interior of pileal warts, but with hyphae somewhat more plentiful; filamentous, undifferentiated hyphae 1.5 - 9.5 µm wide, branching, hyaline, colorless, loosely interwoven, sometimes in fascicles, with walls thin or slightly thickened (0.5± µm, in those of larger diameter); inflated cells with walls thin or up to 0.5 µm thick, sometimes colorless, otherwised colored as on pileus, subglobose to subovoid to ovoid to ellipsoid to subclavate to elongate, terminal or in short chains, to 70 × 52 (-62) µm, dominant away from inner surface; vascular hyphae 1.0 - 6.0 µm wide, not common; clamps absent or infrequent. On stipe base, inner surface: filamentous, undifferentiated hyphae dominating. | ||||||||
stipe context | longitudinally acrophysalidic; filamentous, undifferentiated hyphae 1.5 - 11.2 µm wide, branching, plentiful, with walls thin or up to 0.8 µm thick; acrophysalides to 375 × 50 µm, but most less than half that length, of nearly cylindric, dominating, with walls thin to 1.2 µm thick, sometimes subtended by partially inflated hyphal segment; vascular hyphae 2.5 - 14.5 µm wide, infrequent or so plentiful as to partially obscure other structures at times, locally in coils and knots branching, with those of largest diameter having slightly thickened walls. | ||||||||
basidiospores | composite of all material revised by RET: [420/18/14] (7.8-) 9.5 - 14.0 (-17.0) × (7.2-) 8.8 - 12.8 (-15.5) µm, (L = (10.2-) 10.3 - 12.1 (-13.0) µm; L' = 11.2 µm; W = (9.5-) 9.6 - 11.5 (-12.2) µm; W' = 10.5 µm; Q = (1.0-) 1.02 - 1.16 (-1.33); Q = 1.05 - 1.11 (-1.15); Q' = 1.07), hyaline, colorless, thin-walled, smooth, inamyloid, globose to subglobose, occasionally broadly ellipsoid, rarely ellipsoid, slightly to distinctly adaxially flattened, sometimes somewhat irregularly shaped; apiculus sublateral, truncate conic to cylindric, to 3.5 µm broad at the base, sometimes appearing splintered; contents monoguttulate; white with or without yellowish cast in deposit. | ||||||||
ecology | Colombia: Solitary to subgregarious, 2500± - 3000 m elev. In Q. humboldtii forest (Overbo 2426 & 2507; Franco-M. 534, 905, & 906) or under Q. colombiana Cuatrec. and Q. humboldtii (Singer B 3596). Costa Rica: Solitary, 1800 - 2880 m. In Quercus forest (Gómez 24759, Singer B 12397) or in Quercus dominated forest (Franco-M. 1104 & 1157; Mueller 4642) or with Q. copeyensis (Franco-M. 1158) or with Q. copeyensis and Q. seemannii (Franco-M. 1153) or with Q. seemannii (Franco-M. 1161) or "in magnolietum" (Gómez 18449). Honduras: Subgregarious, at 1800 m elev. Under Quercus (Mueller 4127). | ||||||||
material examined |
COLOMBIA:
ANTIOQUIA—Mpio. Santa Rosa de Osos - vereda "El Chaquiro," Finca "La Española," prop. Arcángel Perez, 1.vi.1992 A. E. Franco-M. 905 (COL; NY; RET 086-1), 906 (COL; NY), 908 (COL; NY); vereda "El Chaquiro," road from Santa Rosa de Osos to Aragon, near Llanos de Cuivá, 5.xi.1986 Ovrebo 2426 (paratype, HUA), 14.xi.1986 Ovrebo 2507 (holotype, HUA; isotype, RET 042-6), 22.vi.1990, Franco-M. 534 (paratypes, HUA & NY).
BOYACÁ—Mpio. Arcabuco - 26.iv.1992 A. E. Franco-M. 781 (COL; NY), 781A (COL; NY); Tunja, 29.vii.1960 Singer B 3596 (paratype, BAFC 31.974).
COSTA RICA:
ALAJUELA—Ctn. Unkn. - Palmira,
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discussion |
Amanita inaurata f. americana sensu Singer and possible synonymy are mentioned in Garrido
and Bresinsky (1985). The synonymy proposed was with A.
gemmata sensu Guzmán & Varela which is clearly not a
member of section Vaginatae. RET concurs with Tulloss et
al. (1992) that the latter taxon can be identified as A. xylinivolva Tulloss et al.. There were no mature basidia on the basidiomes of Gómez 18449; however, the anatomy of these specimens matches well with that of the present species. | ||||||||
citations | —R. E. Tulloss | ||||||||
editors | RET | ||||||||
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name | Amanita sororcula |
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name | Amanita sororcula |
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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.