Fomitopsis cajanderi

A look at the upper surface of the sessile polypore Fomitopsis cajanderi (P. Karst) Kotl. & Pouzar., commonly known as the "rosy conk".
Photo credit: Darvin Deshazer
Source: Mushroom Observer (CC-by-nc-sa-2.5)
Classification
Kingdom Fungi
Phylum Basidiomycota
Class Basidiomycetes
Order Polyporales
Family Fomitopsidaceae
Genus Fomitopsis
Fomes cajanderi P. Karst.
Finl. Basidsvamp. 46(11): 8 (1904) [1903-1904]
Fomes subroseus (Weir) Overh.
Bulletin of the Penn. State College 316: 11 (1935)
Fomitopsis roseozonata (Lloyd) S. Ito
Mycol. Fl. Japan 2(4): 309 (1955)
Fomitopsis subrosea (Weir) Bondartsev & Singer
Annls mycol. 39(1): 55 (1941)
Polystictus mimicus (P. Karst.) Sacc. & Trotter
Syll. fung. (Abellini) 21: 322 (1912)
Pycnoporus mimicus P. Karst.
Trudy Troitsk. Otd. imp. russk. geogr. obsc. 8: 62 (1906)
Trametes roseozonata Lloyd
Mycol. Writ. 7: 1144 (1922)
Trametes subrosea Weir
Rhodora 25: 217 (1923)
Ungulina subrosea (Weir) Murashk.
Trudy omsk. sel'sk Chozj. Kirova 17: 86 (1939)
Rosy conk
This fungus is the causative agent of a tree disease called "brown top rot". As early as 1926, Zeller identified this fungus as the organism largely responsible for large economic losses resulting from damage to peach and prune trees in orchards from central California to British Columbia (Zeller, 1926). In the early stages of decay, the wood develops a faint brownish or yellow-brown stain, while more advanced stages of decay appear as soft, irregular, yellowish or reddish-brown cubes. Thin, white or faintly rose-colored mycelial felts may develop in the cracks between the cubes. In both the natural environment and in culture the vegetative mycelium of F. cajanderi forms a primordial mat, a basidiocarp primordium and a sporulating basidiocarp. The fundamental structural unit is the same in both laboratory culture and in nature: the clamped, generative hypha functions initially in nutrient absorption, then produces unbranched or branched skeletal cells and basidia, and later develops irregularly thickened walls and swollen clamp connections (Kennedy and Wong, 1978).
Fruiting bodies: 2-10 cm in diameter, perennial, woody, and bracket or hoof-shaped, typically glabrous; often found in overlapping clusters, upper surface typically rough and brown or black in color, often zonate; the sterile border is rounded and blunt.
Pore surface: rose-colored, sometimes with greenish-brown zone lines, pores are thick-walled and shallow, 3-5 pores/mm; flesh concolorous with pore surface.

The thick, pink pores of the rosy conk.
Photo credit and source: as above. Original image
Spores: smooth, allantoid, 5.5-7.0 x 1.5-2.0 µm.
Spore print: off-white.
Habitat: found on conifer wood (or "broad-leaved trees" in China, see He et al., 2003; 2006)
Distribution: widespread.
Odor and taste: not distinguishable.
Edibility: inedible.
A study of secondary metabolites from F. cajanderi led to the isolation of three novel acetal lactones named fomlactones A, B, and C from the neutral ether extracts (He et al., 2003).

Structure of ketal lactone triterpenes from F. cajanderi. Fomlactone A (R=OAc), fomlactone B (R=OH), fomlactone C (R= ═O).
Later work by the same research group (He et al., 2006) revealed additional compounds including:
- ergosterol
- ergosterol peroxide
- ergosta-4,6,8 (14),22-tetraen-3-one
- 16-acetoxy-24-methylene- 3-oxolanosta-8-en-21-oic acid (R= ═O)
- the novel lanostane-type triterpenoid 24-methyl- lanost-8,24-dien- 23S,26-lactone
- methyl 24-methylene-3-oxolanost-8-en-26-oic ester
- 3β-acetoxy-24-methylene- 8-en-26-oic ester
- methyl 3α-acetoxy-24-methylene 23-oxylanost-8-en-26-oic ester
Links
References
He J, Feng XZ, Lu Y, Zhao B.
Fomlactones A-C, novel triterpene sactones from Fomes cajanderi.
J Nat Prod. 2003 66(9):1249-51.
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He J, Feng XZ, Ji TF, Lu Y, Zhao B.
Secondary metabolites from fungus Fomes cajanderi.
Nat Prod Res. 2006 20(6):598-605.
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Hogberg N, Hermansson JO.
Fomitopsis cajanderi in Europe - Evidence from mating experiments.
Mycotaxon. 1999 70:69-71.
Kennedy LL, Wong WM.
Fomitopsis cajanderi - development in nature and in culture.
Can J Bot. 1978 56(19):2319-27.
Madhosin C.
A serological comparison of isolates of Fomes roseus and Fomes subroseus.
Can J Bot. 1964 42(12):1677&.
Tsuneda I, Kennedy LL.
Basidiospore germination and substrate preference in Fomes fomentarius and Fomitopsis cajanderi.
Mycologia 1980. 72(1):204-8.
Zeller SM.
The brown-pocket heart rot of stone-fruit trees caused by Trametes subrosea Weir.
J Agric Res. 1926 33:687-93.
Last modified: 23-Nov-2008

November 17th, 2009 at 9:25 pm
Fomitopsis Pinicola is also a powerful one in this family. The mission/content of your site is fantastic, and you seem to missing a few of the major ones that I've been working with- maitake, cordyceps, chaga, reishi, lion's mane, and Turkey Tail, to name a few. Please add these to your list if you can find time to research them. I'd love to use your site as a reference for ALL my favorite mushrooms. Regardless, GREAT work. Fantastic resource.
December 12th, 2009 at 9:20 am
Yeah, my list is over 800 species long! The ones you've listed I'm working on, but as you might imagine, the body of research and published literature on each is so immense that it will take some time to synthesize it and figure out how to present it. Thanks for the comments!