Laccaria laccata var. proxima

 

History of name:
Laccaria laccata var. proxima

Clitocybe proxima Boudier, Bull. Soc. Bot. France 28: 91. 1881. Laccaria proxima (Boudier) Patouillard, Hymeno. Eur.: 97. 1887. Laccaria laccata var. proxima (Boudier) Maire, Bull. Soc. Mycol. France 24: 16. 1908. Clitocybe laccata var. proxima (Boudier) Bresadola. 1927. Icon. Mycologia.: 43. 1927.

Type: Plate II, fig. 2 in Boudier, Bull. Soc. Bot France 28. 1881 (lectotype, fide Mueller, 1991a). Epitype: FRANCE: Montemorency, November l9O4, Boudier s.n. (as C. proxima) (PC! "neotype" fide Mueller, 1987).

Species Synopsis:



Pileus mostly 15-70 mm diam, not striate, reddish brown to orange brown. Lamellae pinkish flesh color. Stipe mostly 24-72 X 3-10 mm, often finely longitudinal-striate, concolorous with pileus; basal mycelium white. Basidia 4 sterigmate. Cheilocystidia 19-66.5 X 2.5-8.5 µm, undifferentiated to subclavate, often abundant. Basidiospores 8-11 X 7-9 µm (excluding ornamentation), mostly broadly ellipsoid to ellipsoid, echinulate; spines mostly 0.5-1 µm long. Found throughout North America.

Habitat and Distribution:



Scattered to gregarious; terrestrial, associated most commonly with Pinaceae, occasionally among mosses including Sphagnum; disturbed areas, early succession forests or under young planted pines in reforested areas. Cosmopolitan; common. Found throughout North America. See Specimens Examined for a list of the specimens studied.

Observations:


Laccaria proxima can be distinguished from L. laccata by its more robust, more strongly colored basidiomata, non-striate and slightly scaly to scaly pilei, and more elongate, finely echinulate basidiospores. Laccaria proxima is separated from L. montana in having smaller, more finely echinulate basidiospores and the more robust habit of its basidiomata. Collections of L. proxima can be differentiated from those of L. oblongospora by having less elongate, larger basidiospores, white basal mycelium, and culture mats that are white on MMN, PDA and N6:5 media. A discussion of various interpretations of the name L. proxima is presented in the section on type specimens.
Mueller (1982, 1984, 1985) reported that cultures of some L. proxima were violet to purple on PDA and MMN media. Upon further analysis of the collections from which these violet culture mats were derived, it was determined that these specimens were L. bicolor and not L. proxima. The basidiospores observed from these collections were much smaller and had longer echinulae than those from other collections referable to L. proxima. The basidiospore dimensions and cultural characteristics fit my circumscription of L. bicolor.
Intra- and interspecific pairing studies have supported treatment of L. proxima as a discrete species. No isolate of L. proxima has been found to mate with any other putative taxa and no intraspecific intersterility groups have been detected (Fries & Mueller, 1984; Mueller, unpublished data). Further support for recognizing L. proxima as an autonomous species was obtained during analyses of mtDNA and rDNA RFLPs of select species of Laccaria (Gardes et al., 1990, 1991a). A low level of intraspecific heterogenity in mtDNA and rDNA RFLPs was detected among the three isolates of L. proxima used in these analyses while their RFLPs were distinct from the other tested taxa.
Laccaria proxima has been reported from throughout North America. It has also commonly been collected in Europe (Clémençon, 1984; Contu, 1986; Mueller, 1991a). Watling (1987) reported that L. proximella Singer is the alpine equivalent of L. proxima. As discussed previously (Mueller, 1991a), I cannot support this contention based on the large number of collections referable to L. proxima that I have examined from alpine and boreal habitats in Europe and North America. My interpretation of L. proximella is that it differs from L. proxima by having violet stains (or mycelium?) at the stipe base and grows in very poor, rocky soil. I have collected material referable to L. proximella in southern Argentina and Chile.

Macromorphology:



Pileus (7-)15-69(-83) mm broad, campanulate to convex, often becoming plane to uplifted, some depressed, not striate, occasionally translucent-striate when faded, finely fibrillose to fibrillose, some becoming fibrillose-scaly to scaly or squarrose in age, hygrophanous, reddish brown to orange brown ("Auburn," "Sanford's Brown," "Orange Rufous," "Hazel," "Cinnamon-Rufous"), fading lighter ("Apricot Buff"); margin incurved to decurved, sometimes becoming plane, entire to undulate, occasionally becoming eroded with age; context thin, tapering quickly to margin, pinkish flesh color ("Japan Rose" to "Shell Pink"). Lamellae sinuate to adnate, occasionally arcuate, subdistant to distant, up to 10 mm broad, pinkish flesh color ("Flesh Color," "Pale Salmon Color"). Stipe (12-)24-72(-155) x 3-11 mm, equal to subclavate, often slightly bulbous, dry, fibrillose, often longitudinally striate, striations moderate to pronounced, most of stipe concolorous with pileus; base occasionally darker ("Rood's Brown"), striations concolorous with pileus or darker red ("Hay's Russet," "Pecan Brown" or "Onion-skin Pink"). Basal mycelium white. Basidiospores white in mass.

Micromorphology:


Pileipellis of interwoven hyphae with scattered to numerous large fascicles of ± perpendicular hyphae; fascicles composed of 15-30 or more hyphae; terminal cells of fascicular hyphae 27.5-92 x 4.5-16(-30) µm, filamentous, subclavate, clavate, broadly clavate, capitate or ventricose-rostrate; walls up to 0.5 µm thick, light to moderate yellowish brown; contents hyaline to light yellowish brown. Pileus trama tightly interwoven, morphologically undifferentiated, hyaline, light yellowish brown toward pileipellis. Lamellar trama parallel; hyphae mostly 3-19 µm diam, thin-walled, hyaline to light yellowish brown; cells filamentous to barrel-shaped. Subhymenium morphologically undifferentiated. Basidia (23-)33-62 x 8-15 µm, clavate, hyaline; sterigmata 4, up to 7 µm long. Cheilocystidia 19-66.5(-92) x 2-8.5(-16.5) µm, filamentous to subclavate, occasionally subcapitate, often abundant, thin-walled, hyaline. Basidiospores (excluding ornamentation) [265/20] 8-11(-12.5) x (6.5-)7-8.7(-9.2) µm [ = (8.7-)9-11.5 x 6.7-8(-8.8) µm], Q = (1.07-)1.16-1.49(-1.58) [ = 1.24-1.34(-1.43)], broadly ellipsoid, ellipsoid or occasionally oblong, hyaline, echinulate; echinulae 0.5-1 µm long, occasionally with one or two long echinulae (up to 2 µm long) at apex, crowded; hilar appendix 1.3-2 µm long, prominent, truncate, plage present; contents occasionally uniguttulate. Basal mycelium hyphae mostly 2.5-17.5 µm diam, tightly interwoven, hyaline; cells filamentous to barrel-shaped.

Somatic Culture Mat Morphology
(n=4; Appendix B):



PDA: Radius at week 3 = 3-17 mm, week 6 = 25.6-43 mm; mat felty, thick, tightly interwoven, not translucent, most of uniform thickness or with slightly thicker area near plug, in one (GMM 1525) forming concentric thicker-thinner bands, white to light tan; margin 1-2 mm broad, abruptly thinner or not well differentiated, silky to subfelty, thin, uneven, white; plug white or becoming olive; hyphae morphologically undifferentiated. MMN: Radius at week 3 = (6.3-)16-32 mm, week 6 = (18-)43-64 mm, mat subfelty to felty, relatively thin to moderately thick, interwoven, translucent to not translucent, thicker near plug, uniform or thinner towards margin, white; margin abruptly thinner or not well differentiated, silky to subfelty, white; plug white; hyphae morphologically undifferentiated. MEA: Radius at week 3 = 11-26 mm, week 6 = 30-51 mm; mat subfelty to felty, thin to relatively thick, translucent, white; margin not well differentiated, somewhat thinner, white; plug white; hyphae morphologically undifferentiated, occasionally irregularly swollen.