Sarcoscypha dudleyi
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Sarcoscypha dudleyi, commonly known as the crimson cup or the scarlet cup, is a species of fungus in the Sarcoscyphaceae family of the Pezizales order. In addition to its main distribution in the central to eastern United States, the fungus has also been recorded once in Bulgaria. It has been frequently confused with Sarcoscypha coccinea, but can be distinguished from this and other related species in Sarcoscypha by differences in microscopic characteristics, such as the presence and number of oil droplets in the spores. The species Molliardiomyces dudleyi is an imperfect form of the fungus that lacks a sexually reproductive stage in its life cycle.
Taxonomy and phylogeny
The species was first collected by the botanist William Russell Dudley in October 1888, in Tompkins County, New York.[2] American mycologist Charles Horton Peck, who described it in the 1894 Annual Report of the New York State Botanist, named it Peziza Dudleyi after its discoverer. Peck noted a physical resemblance to P. aurantia (now known as Aleuria aurantia) and P. inaequalis, and said that it could be distinguished from those species by its yellow hymenium and larger spores.[3] Several mycologists have considered the species to be synonymous with S. coccinea.[4][5][6] However, as was later pointed out by Harrington (1990), "the importance of fresh material for species diagnosis, especially for noting ascospore guttulation, cannot be overstated. Although I had examined material (dried herbarium specimens) from western North America I was not prepared to recognize that group as a species distinct from the two, large eastern North American species until I saw fresh (living) material."[2] As is the case with many fungi, microscopic differences between similar species can only be accurately determined by examining fresh material. Harrington analyzed herbarium specimens and fresh material of North American specimens of "S. coccinea", and found that both S. dudleyi and S. austriaca were commonly misidentified. These results echoed a similar 1984 analysis of European specimens, performed by Hans-Otto Baral.[7]
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| Phylogeny and relationships of S. dudleyi and related species based on ITS sequences and morphological characteristics.[8] |
The phylogenetic relationships in the genus Sarcoscypha were analyzed by Francis Harrington in the late 1990s.[8][9] The cladistic analysis combined comparison of sequences from the internal transcribed spacer in the non-functional RNA with fifteen traditional morphological characters, such as spore features, fruit body shape, and degree of hair curliness. Based on this analysis, S. dudleyi is part of a clade of evolutionarily related taxa that includes the species S. occidentalis, S. emarginata, S. hosoyae, S. korfiana and S. mesocyatha.[8] All of these species contain large oil droplets in their spores, in contrast to the other major clade of Sarcoscypha (containing the type species S. coccinea), characterized by having smaller, more numerous droplets.[9]
Sarcoscypha dudleyi is commonly known as the "crimson cup" or the "scarlet cup",[10] although it shares this latter name with S. coccinea.[11]
Description
The fruit body is 2–6 cm (0.8–2.4 in) broad and shallowly to deeply cup-shaped. The exterior surface of the fruit body is covered with whitish, matted "hairs", while the interior fertile surface of the cup (the hymenium) is scarlet- to orange-red. The edge of the cup (or margin) is curved inwards in young fruit bodies. The stem, if present at all, is short.[10]
The asci are 400–500 by 12–14 µm, cylindrical, and operculate. The ascospores are elliptical to cylindrical with rounded ends, uniseriate, hyaline, and measure 26–40 by 10–12 µm. They contain two large oil drops at either end; the oil drops are useful taxonomic characters that may be used to help distinguish S. dudleyi from some other Sarcoscypha species. The spores are covered with a sheath of mucilage, which typically causes the eight spores of the ascus to be ejected together.[2] The paraphyses (sterile filamentous hyphal end cells in the hymenium) are slender, slightly enlarged above, and contain numerous red granules.[10] The granules contain carotenoid pigments such as plectaniaxanthine or beta carotene, and give the fruit body its color.[12]
Anamorph form
Anamorphic or imperfect fungi are those that seem to lack a sexual stage in their life cycle, and typically reproduce by the process of mitosis in structures called conidia. In some cases, the sexual stage—or teleomorph stage—is later identified, and a teleomorph-anamorph relationship is established between the species. The International Code of Botanical Nomenclature permits the recognition of two (or more) names for one and the same organisms, one based on the teleomorph, the other(s) restricted to the anamorph. The anamorphic state of S. coccinea is Molliardiomyces dudleyi.[2]
Habitat and distribution
Sarcoscypha dudleyi is a saprobic species,[13] and derives nutrients by breaking down the complex insoluble polysaccharides found in woody material, such as cellulose and lignin. Fruit bodies are found growing singly or in very small groups, and are attached to buried or partially buried sticks in forests. Basswood has been noted to be a preferred wood type for the species. Fruit bodies typically appear during early spring, but may occasionally also in late fall.[10] Although the distribution appears to be largely restricted to the eastern United States,[10] it was once reported in Bulgaria in 1994, representing the first European collection.[14]
References
- ↑ "Sarcoscypha dudleyi (Peck) Baral". Index Fungorum. CAB International. Retrieved 2010-08-25.
- 1 2 3 4 Harrington FA. (1990). "Sarcoscypha in North America (Pezizales, Sarcoscyphaceae)". Mycotaxon 38: 417–58. Retrieved 2010-04-04.
- ↑ Peck CH. (1894). "Report of the Botanist (1893)". Annual Report on the New York State Museum of Natural History 47: 23. Retrieved 2010-08-25.
- ↑ Seaver FJ. (1928). The North American Cup-Fungi (Operculates). New York: Self published. pp. 191–92.
- ↑ Kanouse BC. (1948). "The genus Plectania and its segregates in North America". Mycologia 40 (4): 482–97. doi:10.2307/3755155. JSTOR 3755155.
- ↑ Pfister DH. (1979). "Type studies in the genus Peziza. VI. Species described by C. H. Peck". Mycotaxon 8: 333–38. Retrieved 2010-08-25.
- ↑ Baral HO. (1984). "Taxonomische und ökologische Studien über Sarcoscypha coccinea agg., Zinnoberrote Kelchbecherlinge". Zeitschrift für Mykologie (in German) 50: 117–45.
- 1 2 3 Harrington FA. (1998). "Relationships among Sarcoscypha species: evidence from molecular and morphological characters". Mycologia 90 (2): 235–43. doi:10.2307/3761299. JSTOR 3761299.
- 1 2 Harrington FA, Potter D. (1997). "Phylogenetic relationships within Sarcoscypha based upon nucleotide sequences of the internal transcribed spacer of nuclear ribosomal DNA". Mycologia 89 (2): 258–67. doi:10.2307/3761080. JSTOR 3761080.
- 1 2 3 4 5 Healy RA, Huffman DR, Tiffany LH, Knaphaus G. (2008). Mushrooms and Other Fungi of the Midcontinental United States (Bur Oak Guide). Iowa City: University of Iowa Press. p. 291. ISBN 1-58729-627-6. Retrieved 2010-08-25.
- ↑ Arora, David (1986). Mushrooms Demystified: a Comprehensive Guide to the Fleshy Fungi. Berkeley, California: Ten Speed Press. p. 836. ISBN 0-89815-169-4. Retrieved 2010-09-01.
- ↑ Arpin N. (1968). "Les caroténoïdes des Discomycètes: essai chimiotaxinomique" [Carotenoids of the Discomycetes: chemotaxonomic analysis]. Bulletin Mensuel de la Société Linnéenne de Lyon (in French) 28 (suppl): 1–169.
- ↑ Kuo M. (2002). "Sarcoscypha dudleyi & Sarcoscypha austriaca". MushroomExpert.Com. Retrieved 2010-08-25.
- ↑ Dimitrova EG. (1994). "A contribution to the study of the Discomycetes fungi in Bulgaria. II". Fitologija 47: 74–77. ISSN 0324-0975.
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