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Sarcopyrenia
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Sarcopyrenia is a of lichenicolous (-dwelling) . It has 11 species. It is the only genus in Sarcopyreniaceae, a family in the order . Sarcopyreniaceae is one of the few families composed entirely of lichenicolous fungi. These tiny fungi produce small, black, flask-shaped () typically less than half a millimetre across, containing extremely narrow, thread-like . While they initially grow on , their fruiting bodies often outlast their hosts and end up sitting on bare rock, making their exact relationship with lichens somewhat unclear.


Taxonomy
Sarcopyrenia was circumscribed by Finnish lichenologist William Nylander in 1858, with Sarcopyrenia gibba assigned as the . Nylander's Latin emphasised the genus's barely visible , prominent enclosed in a thick outer structure (), and a distinctive double-layered opening. He characterised the as colourless and cylindrical, and noted the absence of . The type species was described from in Algeria, with black, hemispherical fruiting bodies about 0.5 mm across.


Description
In species of Sarcopyrenia the lichen body (), when it is developed at all, is an ill-defined film that is olive-grey and either scaly or made of tiny granules. It partners with a (the ) and often seems to form as the host lichen beneath it breaks down; a separate border () is seldom seen, but when present it is white to pale grey.

The sexual are : small, black, flask-like structures with a single pore (an ostiole) at the top. They are carbon-rich and brittle, smooth to slightly warty, and tend to occur singly rather than in clusters. Young perithecia can begin partly buried in the thallus, but as the surrounding tissue deteriorates they end up sitting on the surface. The wall of the perithecium (the ) is built in three layers of angular cells: an outer, coal-black layer; a middle layer that ranges from colourless to darkened; and a thinner inner layer of smaller, side-compressed cells.

Inside the perithecium the spore-bearing tissue includes fine threads () that disappear early, while short bristles lining the pore () are present. The gel around the spores does not change colour in iodine tests, and the spore sacs () are cylindrical to slightly club-shaped, short-stalked, thin-walled, and do not show the special "double-wall" opening () or beaked tip () seen in some other ascomycetes. Each ascus carries eight colourless spores arranged in two rows. The spores are thin-walled and very narrow—ranging from thread-like to dumb-bell-shaped, sometimes gently S-shaped—with slightly swollen tips; they may be one-celled or with a cross-wall, and lack any gelatinous sheath or appendages. Asexual reproductive structures () have not been observed, and standard thin-layer chromatography has not detected secondary .

Sarcopyrenia species are usually treated as lichen-dwelling fungi (lichenicolous), although some authors have reported an associated simple (a photobiont). Colonies appear to begin as parasites of crustose lichens, but the fruiting bodies often outlast the host and end up on bare rock, leaving their mode of nutrition uncertain.


Species
Host data is from Diederich, Lawrey, and Ertz's 2018 review of lichenicolous fungi.
  • Sarcopyrenia acutispora – on Bagliettoa calciseda
  • Sarcopyrenia bacillosa – on saxicolous lichens
  • Sarcopyrenia bacillospora – on and
  • Sarcopyrenia baetica – on cf. erysibe
  • Sarcopyrenia beckhausiana – on saxicolous lichens (mostly from family )
  • Sarcopyrenia calcarea
  • Sarcopyrenia cylindrospora – mostly on
  • Sarcopyrenia gibba – on saxicolous lichens
  • Sarcopyrenia lichinellae – on Lichinella stipatula
  • Sarcopyrenia pluriseptata – on Pyrenodesmia variabilis
  • Sarcopyrenia sigmoideospora – on

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