Paraphaeosphaeria pilleata | |
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Species: | P. pilleata |
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Paraphaeosphaeria pilleata Kohlm., Volkm.-Kohlm. & O.E.Erikss. (1996) | |
Known only from the Atlantic Coast of North Carolina |
Paraphaeosphaeria pilleata is a species of fungus in the Lophiostomataceae family. The species fruits exclusively in the lower parts of the culms of the black needlerush ( Juncus roemerianus ). It is found on the Atlantic Coast of North Carolina.
The species was first described by mycologists Jan Kohlmeyer, Brigitte Volkmann-Kohlmeyer, and Ove Eriksson in a 1996 Mycological Research publication. The specific epithet is derived from Latin pilleatus ("capped"), and refers to the small cap on the top of the ascus. [1]
The roughly spherical to ellipsoidal leathery fruit bodies (ascomata) are 120–300 μm high by 150–350 μm wide, with a short neck, and an ostiole (opening). The neck is 15–50 μm high, 42–70 μm in diameter, cylindrical to conical, and dark brown. The ascomata are immersed in the hard cortex of the host plant, with bases embedded in the pith. The ascomata are light brown in color, but darker around the ostiole. They are arranged in groups. The ascomata lack paraphyses; the ostiolar canal is formed when pseudoparenchymatous cells in the center of the neck dissolve or tear apart. In mature ascomata, the tips of the pseudoparaphyses reach into the canal. The peridium is 8–16 μm thick, and made of 3–5 layers of brown, thin-walled cells with large lumina that eventually merge with hyaline (translucent) cells to form a textura angularis—a pseudoparenchyma of very densely packed cells that appear angular in cross section. The hamathecium (a term referring to all hyphae that develop between asci of the hymenium) comprises unbranched pseudoparaphyses. These cells are septate, with constrictions at the septa, and measure 1.5–3 μm in diameter. In immature ascomata they are attached both at the top and the bottom, and fill the entire centrum before asci have developed; they join at the top under the neck before the ostiolar canal is formed. [1]
The asci (spore-bearing cells) are eight-spored, club-shaped to cylindrical, and measure 60–80 by 10–12 μm. Spores are arranged in two parallel rows in the ascus. They are supported on a short stalk, thick-walled, and fissitunicate, meaning the inner wall pops completely out of the outer wall during dehiscence. In this process, a small flat cap retracts to form a roughly spherical or irregular, temporary structure at the tip of the ascus. The ascospores are 15.5–23.5 by 4.5–6 μm, cylindrical to elongated ellipsoidal, two- (rarely three-) septate, constricted at the septa. Olive-brown in color, they are surrounded by a uniform gelatinous sheath about 6 μm thick, and have an umbilicus (a single compact strand of fused hyphae) at the top. The primary septum is initially laid down in the lower third of the ascospore, and the larger, upper hemispores are subsequently divided by a transverse septum. The ascospores germinate readily from one or several cells. When grown in pure culture, the fungus forms conidiomata that make ellipsoidal, one-celled, brown conidia, measuring 4.5–7 by 2.5–3.5 μm. [1]
Paraphaeosphaeria michotii has a rather similar morphology to P. pilleata, but can be distinguished microscopically by the lack of both an umbilicus and an evanescent cap on the tips of the asci. Additionally, P. michotti has narrower ascomata (up to 250 μm wide), a thinner peridium (16 μm), and branched pseudoparaphyses. [1]
Paraphaeosphaeria pilleata grows on the dead or dying culms of the rush Juncus roemerianus . The fungus is considered halotolerant because it is usually found 19 and 133 cm (7.5 and 52.4 in) above the rhizome, and is thus regularly exposed to salt spray. It is found on the Atlantic Coast of the United States. [1]
An ascocarp, or ascoma, is the fruiting body (sporocarp) of an ascomycete phylum fungus. It consists of very tightly interwoven hyphae and millions of embedded asci, each of which typically contains four to eight ascospores. Ascocarps are most commonly bowl-shaped (apothecia) but may take on a spherical or flask-like form that has a pore opening to release spores (perithecia) or no opening (cleistothecia).
An ascus is the sexual spore-bearing cell produced in ascomycete fungi. Each ascus usually contains eight ascospores, produced by meiosis followed, in most species, by a mitotic cell division. However, asci in some genera or species can occur in numbers of one, two, four, or multiples of four. In a few cases, the ascospores can bud off conidia that may fill the asci with hundreds of conidia, or the ascospores may fragment, e.g. some Cordyceps, also filling the asci with smaller cells. Ascospores are nonmotile, usually single celled, but not infrequently may be coenocytic, and in some cases coenocytic in multiple planes. Mitotic divisions within the developing spores populate each resulting cell in septate ascospores with nuclei. The term ocular chamber, or oculus, refers to the epiplasm that is surrounded by the "bourrelet".
Aquamarina is a fungal genus in the class Dothideomycetes. It is a monotypic genus, containing the single marine species Aquamarina speciosa, originally found in North Carolina, and distributed in the Atlantic Coast of the United States. The bluish-green species fruits exclusively in the lower parts of dying culms of the saltmarsh plant Juncus roemerianus.
The Aliquandostipitaceae are a family of fungi in the Ascomycota, class Dothideomycetes. The family was described by Patrik Inderbitzin in 2001, and the order Jahnulales was created in 2002 to accommodate the family. The distinguishing characteristic for members of the family are the unusually wide hyphae that support the spore-bearing structures, and the presence of ascomata both with and without stalks. The genus Aliquandostipe has a pantropical distribution, having been found in Central America and southeast Asia; Jahnula has a wider distribution. Species in the family are saprobic, and are typically found growing on rotting wood.
The Loramycetaceae are a family of fungi in the Ascomycota, class Leotiomycetes. This is a monotypic taxon, containing the single genus Loramyces; the genus contains two aquatic species, L. juncicola, named by American mycologist William H. Weston in 1929, and L. macrosporus, first described by C.T. Ingold and B. Chapman in 1952.
Tuber oregonense, commonly known as the Oregon white truffle, is a species of edible truffle in the genus Tuber. Described as new to science in 2010, the North American species is found on the western coast of the United States, from northern California to southern British Columbia west of the Cascade Range. A mycorrhizal fungus, it grows in a symbiotic association with Douglas fir. It overlaps in distribution with the closely related T. gibbosum, but they have different growing seasons: T. oregonense typically appears from October through March, while T. gibbosum grows from January to June. The fruit bodies of the fungus are roughly spherical to irregular in shape, and resemble small potatoes up to 5 cm (2 in) in diameter. Inside the truffle is the gleba, which is initially white before it becomes a marbled tan color. The large, often thick-walled, and strongly ornamented spores are produced in large spherical asci. The truffle is highly prized for its taste and aroma. Some individuals have claimed success in cultivating the truffles in Christmas tree farms.
Keissleriella rara is a rare species of fungus in the family Lophiostomataceae. The species fruits exclusively on dead or dying standing culms of the saltmarsh plant Juncus roemerianus. It is known only from the Atlantic Coast of North Carolina.
Massarina carolinensis is a species of fungus in the Lophiostomataceae family. The species is found exclusively on the lower parts of the culms of the saltmarsh Juncus roemerianus on the Atlantic Coast of North Carolina.
Zopfiella ebriosa is an unharmful fungus discovered covering the corks of wine bottles in 1991 in Tarragona, Spain. A member of the division Ascomycota, Zopfiella ebriosa is characterized by small and asymmetrical asci, presence of ostioles, and possession of germ slits.
Cercophora areolata is a member of the Ascomycota division, and is grouped into the Lasiosphaeriaceae family based on morphology. C. areolata is a coprophilous fungus that has been most recently isolated from porcupine dung. Defining features of C. areolata include: 1) ovoid-conical, glabrous ascomata, 2) black, carbonaceous, areolate peridium and 3) clavate-shaped, single-walled asci. From studies on C. areolata, this fungus produces multiple antifungal compounds, which inhibit other competitor fungi.
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Ostropomyces is a genus of fungi in the family Stictidaceae. It has two species, both of which are found in tropical forests in northern Thailand, where they grow as saprotrophs on bark.
Etheirophoraceae is a family of ascomycetous marine based fungi within the order of Torpedosporales in the subclass Hypocreomycetidae and within the class Sordariomycetes. They are saprobic on intertidal wood and bark within marine habitats.
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Polycoccaceae is a family of lichenicolous (lichen-dwelling) fungi in the order Trypetheliales. The family was circumscribed in 2015 by Damien Ertz, Josef Hafellner, and Paul Diederich. Molecular phylogenetic analysis shows Polycoccaceae to have a sister relationship with the family Trypetheliaceae.
Alloarthopyrenia is a monotypic fungal genus in the family Trypetheliaceae. It contains the single species Alloarthopyrenia italica, a little-known fungus that lives as a saprotroph on living tree branches. The fungus is known from material collected in Italy, for which it is named.
Zwackhiomacromyces is a genus of lichenicolous (lichen-dwelling) fungi in the family Xanthopyreniaceae. It has two species. The genus is distinguished by its black, pear-shaped fruiting bodies with large, nipple-shaped ostioles that have a granular surface, and a dark, multi-layered wall made up of hyphal cells forming a pseudoparenchymatous structure. The genus is closely related to the similarly named genus Zwackhiomyces.
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