Ramonia

The genus was circumscribed by Ernst Stizenberger in 1862, with Ramonia valenzueliana as the type species. In the protologue, Stizenberger distinguished Ramonia from the preceding genus Urceolaria chiefly by its polysporous asci and its spores (with spores divided by multiple septa into a row of cells). Modern molecular phylogenetics work has suggested that the traditional circumscription of Ramonia is closely tied to that of Thelopsis. In a three-locus phylogenetic study using nrLSU, mtSSU, and RPB2 sequences, Damien Ertz and coauthors found that Thelopsis was polyphyletic, and that R. valenzueliana was recovered as the sister species of T. melathelia. On that basis, they transferred the latter species to Ramonia as Ramonia melathelia. The authors also argued that Ramonia, as then understood, appears morphologically heterogeneous. They suggested that such as a wrinkled ascomatal surface, a darker , and ascospores with a thick gelatinous sheath may help indicate closer relationships within the group, but concluded that broader sampling is still needed to clarify the limits of Ramonia and its relationship to Thelopsis. The genus name Ramonia honours Ramón Dionisio José de la Sagra (1798–1871), who was a Spanish anarchist, politician, writer, and botanist who founded the world's first anarchist journal, El Porvenir (Spanish for "The Future"). ==Description==

Ramonia species form a thin, crust-like thallus (vegetative body) that spreads indefinitely over the surface, sometimes sinking into the substrate so that little is visible externally. No distinct border zone () develops at the edge of the thallus. The photosynthetic partner () is from the green algal genus Trentepohlia, whose cells are roughly spherical, 6–10 μm wide, and packed closely together or arranged in short chains. The fruiting bodies are apothecia (open, disc-bearing structures) that begin partly embedded in the thallus and later push through the surface to sit directly on it. They are urn-shaped (), with a strongly inrolled rim () that curves over the spore-producing surface and nearly closes it, leaving only a small central pore. The beneath is concave and pale pink to pale grey. The exciple eventually splits along radial lines. In cross-section it is cup-shaped, hyaline to brown, and built from diamond-shaped or nearly spherical, tissue-like () cells 3–7 μm wide, with short inward-pointing hairs () lining its inner edge. The spore-bearing layer (hymenium) is colourless and stains blue with iodine (KI+ blue). The paraphyses (sterile filaments between the asci) are unbranched, sometimes with swollen tips. The asci (spore-producing cells) are narrowly cylindrical to club-shaped and contain (2–)8 to many spores; they are of the Gyalecta-type, with a thin, iodine-positive wall and a poorly developed, non-amyloid plug ([). The ascospores range from (undivided) to transversely septate or (divided by both cross-walls and longitudinal walls into a brick-like pattern), and are oblong to spindle-shaped or ellipsoidal, colourless, thin-walled, and surrounded by a gelatinous outer layer (perispore). No asexual fruiting structures (conidiomata) are known. No secondary metabolites have been detected. ==Species==

• Ramonia absconsa • Ramonia athallina • Ramonia calcicola • Ramonia cupellina • Ramonia elixii – Tanzania • Ramonia elongata • Ramonia eungellae • Ramonia extensa • Ramonia himelbrantii – Russia • Ramonia leptospora • Ramonia longispora • Ramonia melathelia • Ramonia micrococca • Ramonia microspora • Ramonia minima • Ramonia nepalensis • Ramonia rappii • Ramonia subantarctica • Ramonia subsphaeroides • Ramonia valenzueliana • Ramonia variespora • Ramonia vermispora • Ramonia xylophila ==References==