Key to North American Collybioid Mushrooms
|1.||Stem with a long, root-like projection that extends into the substrate; mature cap usually at least 4 cm across.|
|1.||Stem without a root-like projection; cap variously sized.|
|2.||Growing in eastern North America or in the Rocky Mountains.|
|2.||Growing west of the Rocky Mountains.|
|3.||Cap becoming wrinkled over the center; gills remaining white in age (though one species develops rusty gill edges); spores 10 µ long or longer.|
|3.||Cap smooth; gills becoming flushed pinkish with age; spores 5.5-7 µ long.|
|4.||Stem brown, darkening with age; root-like projection fairly short; young cap convex; odor aromatic; under various conifers.|
|5.||Mushroom growing from decayed remains of other mushrooms, and/or arising from a small knot of tissue (a sclerotium); cap small (under 3 cm across), white to grayish or brownish.|
|5.||Mushroom growing from soil, forest litter, wood (sticks, logs, stumps, woodchips), or in grass; cap varying.|
|7.||Mushroom growing in grass.|
|7.||Mushroom growing from wood, woodchips, soil, cones, nut shells, leaf litter, or conifer duff.|
|8.||Cap pink to pinkish brown, 1-3 cm across; stem pink, with white fuzz; spores inamyloid; pileipellis a cutis.|
|8.||Cap and stem not pink; other features varying.|
|9.||Gills distant; cap bell-shaped, becoming flat with a central bump; spores smooth and inamyloid.|
|9.||Gills close or crowded; cap soon planoconvex or flat; spores ornamented and amyloid.|
|10.||Mushroom growing from fallen cones or nut shells.|
|10.||Mushroom growing from wood, woodchips, soil, leaf litter, or conifer duff.|
|11.||Growing from shells of hickory, walnut, and other hardwoods; cap bright yellow, fading to nearly whitish; hymenial cystidia fusiform.|
|11.||Growing from cones; cap whitish to brown; cystidia when present, varying.|
|12.||Growing from cones of magnolia trees.|
|12.||Growing from cones of other trees.|
|13.||Spores tiny (under 5 µ long) and amyloid; pileipellis a cutis; on cones of various conifers across North America.|
|13.||Spores often longer than 5 µ, inamyloid; pileipellis hymeniform; substrate and distribution varying.|
|14.||On cones of spruces in western North America.|
|14.||On cones of pines or Douglas-fir; distribution varying.|
|15.||On cones of Douglas-fir in western North America (or very rarely on western pines); hymenial cystidia with large apical masses that rupture and leave "colarettes"; cap often becoming slightly pinkish.|
|15.||On cones of eastern North American pines, western pines or Douglas-fir; cystidia without large apical masses or colarettes; cap usually not pinkish.|
|16.||Cap medium-sized to large (4-20 cm across when mature), grayish brown to brown or nearly black, radially streaked; stem pure white; stem 1-2 cm thick, base often (but not always) attached to white rhizomorphs; spores inamyloid, ellipsoid.|
|16.||Not completely as above.|
|17.||Cap dry, brownish orange to orangish brown; stem densely but finely fuzzy; growing from and near hardwood debris in late spring and early summer, eastern North America; spores amyloid and smooth.|
|17.||Not completely as above.|
|18.||Cap and stem conspicuously hairy; cap small (usually under 3.5 cm across), whitish to brown; growing from wood (sticks, logs, stumps).|
|18.||Cap and stem not both conspicuously hairy (though cap may be silky, or stem may conspicuously hairy in combination with a bald cap); cap size and color varying; substrate varying.|
|19.||On wood of conifers.|
|19.||On wood of hardwoods.|
|20.||Found on the West Coast; cap convex to planoconvex, whitish to buff or tawny, with a darker center.|
|20.||Found in northern North America; cap usually with a sharp central bump, brown to rusty brown.|
|21.||Mature cap 1-3.5 cm across, not becoming radially grooved (although hairs may aggregate into radial patterns); KOH red to black on cap surface.|
|21.||Mature cap 0.5-1 cm across, becoming radially grooved; KOH negative on cap surface.|
|22.||Odor and taste not reminiscent of garlic or onions.|
|23.||Growing in woodchips in eastern North America; mature cap 1-5 cm across, becoming conspicuously lined/pleated.|
|23.||Not growing in woodchips; distribution varying; cap variously sized, not becoming conspicuously lined (but perhaps developing faint lines along the margin).|
|24.||Mature cap 3-7 cm across; gills crowded; growing on leaf litter of hardwoods east of the Rocky Mountains; pileipellis a cutis.|
|24.||Mature cap usually under 3 cm across; gills close, nearly distant, or distant; substrate and distribution varying; pileipellis varying.|
|25.||Stem finely hairy to finely velvety, at least near the base; distribution varying.|
|26.||Substrate varying; pileipellis hymeniform.|
|27.||Growing east of the Rocky Mountains.|
|28.||Fresh cap purple to lavender.|
|28.||Fresh cap not purple to lavender.|
|29.||Growing on the ground.|
|30.||Gills crowded and lavender, with edges colored like the faces; fresh cap lavender.|
|31.||Under conifers in western North America; gills yellowish; KOH negative on cap surface.|
|31.||Under hardwoods or conifers in southeastern North America (north to Massachusetts and Missouri); gills purplish; KOH green to blue on cap surface.|
|32.||Under conifers across North America; cap whitish, 4-12 cm; gills crowded; cap, gills, and stem developing reddish spots with age; spores nearly round, dextrinoid (at least a few).|
|32.||Not completely as above.|
|33.||Growing from wood (sticks, logs, stumps, woodchips, etc.).|
|33.||Growing from soil, leaf litter, or conifer duff.|
|34.||Flesh yellow or yellowish.|
|34.||Flesh white, whitish, brownish, or grayish.|
|35.||Cap reddish to purplish red.|
|35.||Cap yellow, yellowish, olive, or yellowish brown.|
|36.||On wood of conifers; cap covered with reddish to purplish red scruffies over a yellow base color.|
|37.||Cap bald or nearly so--or if tiny scales are present, scales yellowish to olive.|
|38.||Cap clear to bright yellow.|
|39.||Found only in the Pacific Northwest; cap margin sometimes fringed; spores 7-9 µ long.|
|39.||Found in the Pacific Northwest and in eastern North America; cap margin not fringed; spores 5.5-6.5 µ long.|
|40.||Fresh cap sticky; mature stem becoming brown and velvety to finely velvety, from the base upwards.|
|40.||Fresh cap not normally sticky; mature stem bald to hairy or scaly, but not velvety and brown.|
|41.||Cap more highly colored; variously distributed.|
|42.||Growing at high altitude in Mexico, from buried wood of Senecio cineraroides, a woody plant.|
|42.||Growing elsewhere; substrate not as above.|
|43.||Growing on the wood of various hardwoods; widely distributed in North America; spores 7-9 µ long.|
|44.||Cap and stem covered with dark brick red scales; cap 5-8 cm across; odor and taste strong and unpleasant.|
|44.||Not completely as above.|
|45.||Fresh cap whitish to buff, pale tan, or pale grayish brown.|
|45.||Fresh cap more highly colored.|
|46.||Usually growing in dense clusters of many mushrooms; caps pale grayish brown, streaked-looking, often with a tiny central depression; spores amyloid.|
|46.||Growing gregariously or in loose clusters of a few mushrooms; caps white to pale tan, not streaked, convex to planoconvex; spores inamyloid.|
|47.||Found in western North America on wood of conifers (often near melting snowbanks); cap whitish; mature stem length about equal to cap width.|
|47.||Found in eastern North America on wood of hardwoods; cap buff to pale tan; mature stem long in proportion to cap.|
|48.||Growing in dense clusters of many mushrooms on the wood of conifers; caps convex, reddish brown, soon fading to pinkish buff and then contrasting starkly with the bald, reddish stems; spores inamyloid.|
|48.||Not completely as above.|
|49.||Spores amyloid; cap often streaked-looking; most species (but not all) growing in dense clusters of many mushrooms.|
|49.||Spores inamyloid or dextrinoid; cap not normally streaked; growing alone, scattered, gregariously, or in loose clusters.|
|50.||Mature cap usually over 5 cm across, dark brown, vase-shaped; gills whitish to very pale gray, running down the stem; stem 6-12 cm tall; found in the Pacific Northwest.|
|50.||Mature cap smaller and paler than above, not vase-shaped; gills varying; stem much shorter than above; variously distributed.|
|51.||Mature cap 2-6 cm across, gray to gray-brown; gills distant; growing in loose clusters of a few mushrooms; spores 6-8 µ long.|
|51.||Mature cap smaller and paler than above; gills close; usually growing in dense clusters of many mushrooms; spores 3.5-6.5 µ long.|
|52.||Spores globose, 3.5-4.5 (-5) µ long; cap not usually developing a pronounced central depression (a "belly button"); found east of the Rocky Mountains on the wood of conifers.|
|52.||Spores broadly ellipsoid to subglobose, 4.5-6.5 µ long; cap usually developing a pronounced central depression; ecology and distribution varying.|
|53.||Found only on the wood of hardwoods, east of the Rocky Mountains; stem finely scaly to finely hairy overall; spores 5-6.5 µ long.|
|53.||Found on the wood of hardwoods or conifers; widely distributed in North America; stem bald or finely silky near the apex; spores 4.5-6 µ long.|
|54.||Growing from woodchips in introduced settings, usually in clusters; mature cap 4-12 cm across, dark reddish brown fading to tan; stem 0.5-1 cm thick.|
|54.||Growing from sticks, logs, or stumps in woodland settings; cap and stem varying.|
|55.||Cap pale (pale brown to cinnamon buff) when fresh; gills nearly distant; stem about twice as long as the cap is wide, usually grooved and finely velvety; spores narrow (5.5-8 x 2-3 µ) and inamyloid.|
|55.||Fresh cap usually darker than above; gills, stem, and spores varying.|
|56.||Gills usually very crowded; stem bald and pliant; cap moist to greasy when fresh; stem base attached to rhizomorphs; spores inamyloid.|
|56.||Not completely as above.|
|57.||Spores round or nearly so; spores (at least a few) dextrinoid.|
|57.||Spores not round; spores dextrinoid or inamyloid.|
|58.||Found in eastern North America; gills faintly pinkish with iron salts after 10 minutes.|
|59.||Fresh cap purple-brown; spores (at least a few) dextrinoid; spores 5.5-7 x 3-4.5 µ.|
|59.||Cap usually not purple-brown; spores inamyloid; spore dimensions varying.|
|60.||Found in western North America.|
|60.||Found in eastern North America.|
|61.||Young gills whitish; cap becoming lined nearly to the center, medium brown when young; stem inconspicuously fuzzy; cheilocystidia to about 80 µ long, often chained, apices usually lacking knoblike projections.|
|61.||Young gills brownish; cap becoming radially wrinkled or somewhat lined about halfway to the center, dark brown when young; stem conspicuously fuzzy when fresh; cheilocystidia up to about 40 µ long, with short, knoblike projections.|
|62.||Stem tough and finely to densely fuzzy; flesh tough; gills with age becoming pinkish and/or developing reddish spots; pileipellis a cutis.|
|62.||Stem pliant and bald; flesh insubstantial; gills remaining whitish to creamy throughout development; pileipellis a hymeniform layer of broom cells.|
|63.||Fresh cap yellow, orangish yellow, or yellowish (but not yellowish brown).|
|63.||Fresh cap not yellow or yellowish.|
|64.||Appearing in spring or early summer in eastern North America under hardwoods; gills crowded and yellow; stem base attached to pinkish rhizomorphs.|
|64.||Appearing in summer and fall; distribution and ecology varying; gills close, whitish to yellowish or yellow; stem base not attached to rhizomorphs.|
|65.||Cap 0.5-3 cm across, yellow to orangish yellow or bright brownish yellow; appearing under conifers in the Rocky Mountains and under alder or conifers in northern North America; spores tiny (3-4 µ long).|
|65.||Cap larger than above--or, if under 3 cm across when mature, yellowish brown; ecology and range varying; spores longer than 4 µ.|
|66.||Under hardwoods in eastern North America; spores ellipsoid to subfusiform, inamyloid; pileipellis varying.|
|67.||Cap 3-7 cm across, yellow when fresh; widely distributed and common under various hardwoods east of the Rocky Mountains; pileipellis hymeniform.|
|67.||Cap 0.5-2.5 cm across, yellowish brown; found under birch in northeastern North America; rare; pileipellis a cutis.|
|68.||Mature stem usually at least twice as long as the width of the cap, covered with fine whitish fuzz; cap soon fading to pale tan or buff; gills crowded; often growing in loose clusters of a few mushrooms.|
|68.||Not completely as above.|
|69.||Mature stem typically 5 mm wide or wider.|
|69.||Mature stem typically under 5 mm wide.|
|70.||Cap pale brown to whitish, with a brown center, 3-11 cm; gills close or nearly distant; growing in eastern North America; pileipellis hymeniform.|
|70.||Not completely as above.|
|71.||Spores (or at least a few of them) dextrinoid.|
|72.||Gills conspicuously serrated in all stages of development (reminiscent of gills in Lentinellus); growing under spruce in eastern North America; stem more or less equal (not swollen toward the base).|
|72.||Not completely as above.|
|73.||Odor heavy and sweet, like almonds or benzadehyde; cap at first dark purplish brown; gills staining reddish with age; stem often rooting somewhat; found on the West Coast.|
|73.||Not completely as above.|
|74.||Spores round or nearly so, 3.5-5 µ; found in the Pacific Northwest and northern California.|
|75.||Cap pale (pale brown to cinnamon buff) when fresh; gills nearly distant; stem about twice as long as the cap is wide, usually grooved and finely velvety; spores narrow (5.5-8 x 2-3 µ) and inamyloid.|
|75.||Fresh cap usually darker than above; gills, stem, and spores varying.|
|76.||Gills usually very crowded; stem bald and pliant; mature cap up to 7.5 cm across; stem base attached to rhizomorphs; widely distributed in North America; spores 5-6.5 x 2.5-3.5 µ.|
|76.||Gills close or nearly distant; stem whitish-fuzzy to velvety near the base; mature cap to 3.5 cm across; rhizomorphs lacking; known from Connecticut and Massachusetts; spores 8.5-10 x 3.5-4.5 µ.|
|77.||Young gills pale to dark brown.|
|77.||Young gills not brown.|
|78.||Cap turning green with ammonia or KOH; stem brown, bald except for a fuzzy base; spores 5-8 x 2.5-4 µ.|
|78.||Cap not turning green with ammonia or KOH; stem brown or whitish, finely to densely fuzzy; spores varying.|
|79.||Spores 6-8.5 x 3.5-4 µ; cheilocystidia cylindric to clavate, with short knoblike projections; stem brownish overall; known from California.|
|79.||Spores 9-10 x 3.5-4 µ; cheilocystidia absent; stem whitish overall; known from the Pacific Northwest and Michigan.|
|80.||Gills conspicuously serrated in all stages of development (reminiscent of gills in Lentinellus); growing under spruce in eastern North America; spores (at least a few of them) dextrinoid.|
|80.||Not completely as above.|
|81.||Cap pale (pale brown to cinnamon buff) when fresh; gills nearly distant; stem about twice as long as the cap is wide, usually grooved and finely velvety; spores narrow (5.5-8 x 2-3 µ) and inamyloid.|
|81.||Not completely as above.|
|82.||Stem fuzzy or minutely hairy over the lower third or more.|
|82.||Stem bald, or with only a fuzzy base and/or minute pubescence near the apex.|
|83.||Known from California; cap 1.5-4 cm, lined nearly to the center; cheilocystidia to about 80 µ long, often chained, apices usually lacking projections; spores 8-10 x 4-5 µ`;.|
|83.||Growing in eastern North America; cap, cheilocystidia, and spores varying.|
|84.||Cap at first brown to reddish brown or orangish brown, but soon fading to pale tan or buff, contrasting with the darker, reddish brown stem; KOH on cap and stem surfaces strongly olive to green or black.|
|84.||Cap brown to reddish brown or orangish brown, fading (if at all) to cinnamon or tan; KOH negative to dull olive on cap and stem surfaces.|
|85.||Appearing in spring and early summer; stem fuzzy only over roughly the lower 1/3; gills nearly distant; hyphae of the stem encrusted with dark brown material in a water mount.|
|85.||Appearing in late summer and fall; stem fuzzy nearly to the apex; gills close; hyphae of the stem not encrusted with dark brown material in a water mount.|
|86.||Usually growing directly from soil; spores under 9 µ long; cheilocystidia present.|
|86.||Usually growing from hardwood leaf litter; spores 8.5-11 µ long; cheilocystidia present or absent.|
|87.||Known from Connecticut and Massachusetts; cheilocystidia absent; pileipellis elements mostly smooth, or inconspicuously encrusted.|
|87.||Widely distributed and common east of the Great Plains; cheilocystidia present; pileipellis elements frequently encrusted with conspicuous brown pigment.|
|88.||Known from California; cap brown, becoming lined and upturned, often darker in the center and lighter at the margin; odor foul, like rotting cabbage; lower stem dark brown to black; cheilocystidia absent; pileipellis a cutis with brown-encrusted elements.|
|88.||Not completely as above.|
|89.||Spores round or nearly so; spores (at least a few) dextrinoid.|
|89.||Spores not round; spores dextrinoid or inamyloid.|
|90.||Found in eastern North America; gills faintly pinkish with iron salts after 10 minutes.|
|91.||Appearing in spring and early summer in eastern North America (and reported, perhaps erroneously, from California); gills and stem pale yellow; cap very dark brown becoming reddish brown; stem attached to orangish to reddish brown rhizomorphs; pileipellis a cutis.|
|91.||Not completely as above.|
|92.||Pileipellis a cutis or layer of tangled branching hyphae.|
|93.||Found on leaf litter of birch in the northeastern United States; gills close or nearly distant; cap and stem yellowish brown; stem base without rhizomorphs; spores 9.5-11 µ long.|
|93.||Widely distributed and common across North America; found in diverse ecosystems; gills usually very crowded; cap and stem various shades of brown; stem base attached to whitish rhizomorphs; spores 5-6.5 µ long.|
Antonín, V., R. E. Halling & M. E. Noordeloos (1997). Generic concepts within the groups of Marasmius and Collybia sensu lato. Mycotaxon 63: 359-368.
Antonín, V. & J. Herink (1999). Notes on the variability of Gymnopus luxurians (Tricholomataceae). Czech Mycology 52: 41-49.
Arnolds, E. (2006). A confusing duo: Calocybe cerina and Callistosporium pinicola (Agaricales). Acta Mycologica 41: 29-40.
Bandala, V. M., R. Ryoo, L. Montoya & K. Kang-Hyeon (2012). New species and new records of Crinipellis from tropical and subtropical forests of the east coast of Mexico. Mycologia 104: 733-745.
Barrasa, J. M, F. Esteve-Raventos & R. M. Dahncke (2006). Clitocybula canariensis (Tricholomataceae), a new brown-rot fungus from the Canary Islands (Spain). Fungal Diversity 22: 1-11.
Bigelow, H. E. (1973). The genus Clitocybula. Mycologia 65: 1101-1116.
Brunner, I. L. & O. K. Miller, Jr. (1988). Calocybe fallax: Its ecology and cultural behavior. Mycotaxon 33: 41-50.
Coker, W. C. & H. C. Beardslee (1921). The collybias of North Carolina. Journal of the Elisha Mitchell Scientific Society 37: 83-107.
Desjardin, D. E. (1985). New marasmioid fungi from California. Mycologia 77: 894-902.
Desjardin, D. E. & R. E. Halling (1987). California Collybias. I. Collybia bakerensis: A common snowbank agaric. Mycotaxon 29: 321-327.
Desjardin, D. E. & R. H. Petersen (1989). Studies on Marasmius from eastern North America. II. New species. Mycotaxon 34: 71-92.
Desjardin, D. E. (1991). Studies on Marasmius from eastern North America. IV. Additions to Sect. Sicci. Mycologia 83: 30-39.
Desjardin, D. E., R. E. Halling & B. A. Perry (1997). Gymnopus villosipes--a common collybioid agaric from California. Mycotaxon 64: 141-147.
Desjardin, D. E., R. E. Halling & D. E. Hemmes (1999). Agaricales of the Hawaiian Islands. 5. The genera Rhodocollybia and Gymnopus. Mycologia 91: 166-176.
Desjardin, D. E. (2000). Strobilurus diminutivus: A new species from montane California, USA.. In: Associazione Micologica Bresadola, ed. Micologia 2000. Brescia, Italy: Grafica Sette, 137-142.
Fatto, R. M. & Bessette, A. E. (1996). A new species of Callistosporium. Mycotaxon 60: 125-128.
Gilliam, M. S. (1975). New North American species of Marasmius. Mycologia 67: 817-844.
Gilliam, M. S. (1976). The genus Marasmius in the northeastern United States and adjacent Canada. Mycotaxon 4: 1-144.
Gillman, L. S. & Miller, O. K. (1977). A study of the boreal, alpine, and arctic species of Melanoleuca. Mycologia 69: 927-951.
Halling, R. E. (1979). Notes on Collybia. I. Collybia alkalivirens. Mycotaxon 8: 453-458.
Halling, R. E. (1981). Notes on Collybia. II. Additional taxa that are green in alkaline solution. Mycologia 73: 634-642.
Halling, R. E. (1983). The genus Collybia (Agaricales) in the Northeastern United States and adjacent Canada. Germany: J. Cramer. 148 pp.
Halling, R. E. (1989). Notes on Collybia III. Three neotropical species of Subg. Rhodocollybia. Mycologia 81: 870-875.
Halling, R. E. (1996). Notes on Collybia V. Gymnopus section Levipedes in tropical South America, with comments on Collybia. Brittonia 48: 487-494.
Halling, R. E. (1997). A revision of Collyba s.l. in the Northeastern United States and adjacent Canada. http://www.nybg.org/bsci/res/col/colintro.html
Hughes, K. W., L. L. McGhee, A. S. Methven, J. E. Johnson & R.H. Petersen (1999). Patterns of geographic speciation in the genus Flammulina based on sequences of the ribosomal ITS1-5.8S-ITS2 area. Mycologia 91: 978-986.
Hughes, K. W., R. H. Petersen, J. E. Johnson, J.-M. Moncalvo, R. Vilgalys, S. A. Redhead, T. Thomas & L. L. McGhee (2001). Infrageneric phylogeny of Collybia s. str. based on sequences of ribosomal ITS and LSU regions. Mycological Research 105: 164-172.
Kauffman, C.H. (1918). The gilled mushrooms (Agaricaceae) of Michigan and the Great Lakes region, Volumes I and II. New York: Dover. 924 pp.
Kerekes, J. F. & D. E. Desjardin (2009). A monograph of the genera Crinipellis and Moniliophthora from Southeast Asia including a molecular phylogeny of the nrITS region. Fungal Diversity 37: 101-152.
Komorowska, H. (2000). A new diagnostic character for the genus Collybia (Agaricales). Mycotaxon 75: 343-346.
Lennox, J. W. (1979). Collybioid genera in the Pacific Northwest. Mycotaxon 9: 117-231.
Mata, J. L., R. E. Halling & R. E. Petersen (2004). New species and mating system reports in Gymnopus (Agaricales) from Costa Rica. Fungal Diversity 16: 113-129.
Mata, J. L., R. E. Halling, K. W. Hughes & R. H. Petersen (2004). Rhodocollybia in neotropical montane forests. Mycological Progress 3: 337-351.
Mata, J. L., K. W. Hughes & R. H. Petersen (2006). An investigation of /omphalotaceae (Fungi: Euagarics) with emphasis on the genus Gymnopus. Sydowia 58: 191-289.
Methven, A. S., K. W. Hughes & R. H. Petersen (2000). Flammulina RFLP patterns identify species and show biogeographical patterns within species. Mycologia 92: 1064-1070.
Moser, M. (1983). Keys to Agarics and Boleti (Polyporales, Boletales, Agaricales, Russulales). Ed. Kibby, G. Transl. Plant, S. London: Roger Phillips. 535 pp.
Murphy, J. F. (1997). Intersterility groups in Collybia subnuda. Mycologia 89: 566-577.
Noordeloos, M. E. (1995). Genus Collybia. In: Bas, C., Th. W. Kuyper, M. E. Noordeloos & E. C. Vellinga (1995). Flora Agaricina Neerlandica. Volume 3. Rotterdam: A. A. Balkema. 106-123.
Redhead, S. A. & R. Singer (1978). On Calocybe names. Mycotaxon 6: 500-502.
Redhead, S. A. (1979). The genus Strobilurus (Agaricales) in Canada with notes on extralimital species. Canadian Journal of Botany 58: 68-83.
Redhead, S. A. (1982). The systematics of Callistosporium luteo-olivaceum. Sydowia, Ser. II 35: 223-235.
Redhead, S. A. (1987). The Xerulaceae (Basidiomycetes), a family with sarcodimitic tissues. Canadian Journal of Botany 65: 1551-1562.
Redhead, S. A., J. Ginns & R. A. Shoemaker (1987). The Xerula (Collybia, Oudesmansiella) radicata complex in Canada. Mycotaxon 30: 357-405.
Redhead, S. A. & R. H. Petersen (1999). New species, varieties and combinations in the genus Flammulina. Mycotaxon 71: 285-294.
Singer, R. (1942). A monographic study of the genera Crinipellis and Chaetocalathus. Lilloa 8: 441-533.
Smith, A. H. & M. B. Walters (1944). A new species of Crinipellis from Ohio. Mycologia 36: 276-278.
Smith, A. H. (1960). Tricholomopsis (Agaricales) in the Western Hemisphere. Brittonia 12: 41-70.
Vilgalys, R. & O. K. Miller, Jr. (1982). Observations on sexuality in Collybia butyracea using a simplified crossing technique. Mycotaxon 14: 305-308.
Vilgalys, R. & Miller, O. K. Jr. (1983). Biological species in the Collybia dryophila group in North America. Mycologia 75: 707-722.
Vilgalys, R. & O. K. Miller, Jr. (1987). Morphological studies on the Collybia dryophila group in Europe. Transactions of the British Mycological Society 88: 461-472.
Vilgalys, R. & O. K. Miller, Jr. (1987). Mating relationships within the Collybia dryophila group in Europe. Transactions of the British Mycological Society 89: 295-300.
Vilgalys, R. (1991). Speciation and species concepts in the Collybia dryophila complex. Mycologia 83: 758-773.
Villarruel-Ordaz, J. L. & J. Cifuentes (1998). Primer registro de Collybia cookei (Tricholomataceae, Agaricales) en Mexico. Revista Mexicana de Micologia 14: 61-63.
Wells, V. L. & Kempton, P. E. (1971). Studies on the fleshy fungi of Alaska. V. The genus Strobilurus with notes on extralimital species. Mycologia 63: 370-379.
Wilson, A. W. & D. E. Desjardin (2005). Phylogenetic relationships in the gymnopoid and marasmioid fungi (Basidiomycetes, euagarics clade). Mycologia 97: 667-679.
Cite this page as:
Kuo, M. (2013, February). Collybioid mushrooms. Retrieved from the MushroomExpert.Com Web site: http://www.mushroomexpert.com/collybioid.html