Meridianelia | |
---|---|
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Fungi |
Division: | Ascomycota |
Class: | Lecanoromycetes |
Order: | Umbilicariales |
Family: | Elixiaceae |
Genus: | Meridianelia Kantvilas & Lumbsch (2009) |
Species: | M. maccarthyana |
Binomial name | |
Meridianelia maccarthyana Kantvilas & Lumbsch (2009) | |
Holotype: near Lake Fenton, Tasmania [1] |
Meridianelia is a fungal genus in the family Elixiaceae. [2] [3] It consists of the single species Meridianelia maccarthyana, a corticolous (bark-dwelling), crustose lichen. This lichen forms greyish-white, crust-like growths on tree bark in subalpine woodlands of Tasmania, Australia. Discovered in 2003 and scientifically described in 2009, Meridianelia is classified in the small fungal family Elixiaceae based on its genetic and structural characteristics. The genus is notable for its unique reproductive structures and its apparent rarity, having been found in only a few locations despite growing in a relatively common type of forest.
The genus Meridianelia was circumscribed in 2009 by the lichenologists Gintaras Kantvilas and H. Thorsten Lumbsch based on collections from Tasmania, Australia. The type specimen (holotype) of Meridianelia maccarthyana was collected by Kantvilas on December 17, 2003. It was found 1 km southeast of Lake Fenton, Tasmania, at an elevation of 950 m (3,120 ft). The specimen was collected from the trunk of Eucalyptus coccifera in subalpine woodland. The genus name Meridianelia is derived from the Latin meridianus (meaning 'southern'), referring to its geographic distribution in Tasmania. It also alludes to the similarity of this lichen to members of the genus Trapelia . The species epithet honours the Australian lichenologist Patrick McCarthy. [1]
Phylogenetic analysis of mitochondrial small subunit rDNA sequences showed that Meridianelia clusters strongly with Elixia flexella , one of the few representatives of the small fungal family Elixiaceae. This supported the placement of Meridianelia in Elixiaceae. [1] The placement was further corroborated with the description of the third Elixiaceae species in 2010, Elixia cretica , which, together with E. flexella, formed a clade sister to Meridianelia. [4] However, in some later (2018) phylogenetic analyses, the authors note that the current arrangement "was not significantly supported by any analyses", and that "Elixia monophyly was not supported, as Meridianelia grouped with accessions of E. flexella and Elixia sp. and excluded Elixia cretica." [5]
While superficially similar to Trapelia in some morphological features, Meridianelia differs significantly in its ascus structure. The asci in Meridianelia have a prominent, weakly amyloid tholus with an intensely amyloid cap, characteristic of the Elixia -type ascus. This ascus structure, along with other anatomical and molecular evidence, justified the creation of a new genus separate from Elixia and Trapelia. [1]
The addition of Meridianelia to Elixiaceae necessitated a recircumscription of the family to accommodate the morphological differences between the two genera. The family is now defined as lichenised ascomycetes with a crustose thallus containing a coccoid green photobiont , hemiangiocarpous apothecia, eight-spored Elixia-type asci, simple hyaline ascospores, and either aliphatic acids or no lichen substances. [1]
Meridianelia is a lichen genus characterised by a crust-like, thin outer layer (thallus) that forms spreading colonies up to 10–20 cm wide. The thallus is dull greyish white, somewhat glossy, and 120–200 μm thick. Initially smooth, it develops small wart-like structures ( verrucae ) 0.5–1 mm wide, and may become worn, eroded, or develop powdery reproductive structures (soredia) over time. Like all lichens, Meridianelia is a symbiotic organism, containing a green algal partner (photobiont) with round to oval cells, 9–20 by 9–16 μm, typically clustered in bundles within the thallus. [1]
The lichen's reproductive structures (apothecia) are disc-shaped and partially immersed in the thallus. These discs are roundish to irregularly angular, 0.3–1 mm wide, and generally clustered in groups of 2–3 (occasionally up to 5). The surface of the disc starts deeply concave, becoming flat to wavy, dark grey, and covered with a thick whitish powder-like coating ( pruina ). The apothecium is surrounded by a very thin layer of fungal tissue ( excipulum ), measuring up to about 10 μm thick, pale greyish green, composed of interwoven thread-like structures (hyphae). [1]
Inside the apothecium is a colourless reproductive layer (hymenium), 160–200 μm thick, containing scattered oil droplets and topped by a grey-green layer 30–50 μm thick. Within this layer are spore-producing sacs (asci) and sterile filaments (paraphyses). The asci are elongated and club-shaped, 130–170 by 17–25 μm, containing 8 spores each. They have a specialised structure at the tip for releasing spores, resembling those found in the related genus Elixia. The paraphyses are very delicate, highly branched, and intertwined, 0.8–1 μm thick, with narrowed tips. [1]
The spores are arranged in a single row within the ascus ( uniseriate ). They are thin-walled, without a gel coating, and round to oval in shape, typically measuring 14–23 by 9–20 μm, often containing a single, large bubble-like structure (vacuole). Chemically, the lichen contains protolichesterinic acid, but does not show any colour changes when tested with common lichen identification chemicals. Another type of reproductive structure common in lichens, pycnidia, has not been observed in this genus. [1]
Meridianelia maccarthyana is known to occur only in Tasmania, Australia. It has been recorded in open subalpine woodland dominated by Eucalyptus coccifera , typically growing on dolerite boulder fields at elevations around 950–1010 metres above sea level. The species forms conspicuous white patches up to 20 cm wide on the lowermost 1–2 metres of eucalypt trunks, as well as on larger individuals of Olearia with loose, papery bark. It has also been found at the margins of Nothofagus cunninghamii -dominated cool temperate rainforest. [1]
Meridianelia maccarthyana prefers sunny conditions and is most frequently found on trees where the understorey is sparse. It is absent in areas where undershrubs form a closed cover. Despite its conspicuous appearance where present, the species has been encountered infrequently, suggesting it may have specific ecological requirements that are not yet fully understood. [1]
Associated lichen species in its habitat include Mycoblastus campbellianus , M. coniophorellus , Ochrolechia species, Pertusaria jamesii , P. pertractata , Pseudoramonia richeae , Ramboldia stuartii , Trapeliopsis granulosa , and Usnea oncodes . Below the "Meridianelia-zone" on eucalypt trunks, there is often a basal cover of bryophytes and species of Cladia and Cladonia . [1]
Ochrolechia is a genus of crustose lichens in the family Ochrolechiaceae. These lichens typically form uneven, often thick, crust-like growths on various surfaces and are characterised by their white to pale grey thalli, which may have a greenish tint. The genus has a long evolutionary history, with fossils dating back to the Paleogene period, about 34 million years ago. Ochrolechia species have disc-like apothecia, which are usually yellowish or brownish-pink and often covered with a fine white powdery coating. The genus is widely distributed and includes both common and rare species, with some found in extreme environments such as arctic and alpine regions. Ochrolechia lichens produce diverse secondary metabolites, including orcinol depsides, depsidones, and xanthones.
Gallaicolichen is a fungal genus that contains the single species Gallaicolichen pacificus, a foliicolous (leaf-dwelling) lichen. Originally discovered in Hawaii in 2007, G. pacificus has since been found in various locations across the Pacific, including Australia, New Caledonia, Vanuatu, the Philippines, and Japan. The lichen forms small, pale greenish-yellow to yellowish-grey patches on leaves, typically in mid-altitude forests and along forest edges. G. pacificus is notable for its unique reproductive structures called peltidiangia, which produce disc-shaped propagules (peltidia) for asexual reproduction. Initially, its taxonomic classification was uncertain, but recent discoveries of specimens with sexual reproductive structures have enabled scientists to confidently place it within the family Porinaceae.
Stromatella bermudana is a saxicolous (rock-dwelling) crustose lichen. It is the only species in Stromatella, a monotypic fungal genus in the family Lichinaceae.
Fuscideaceae is a family of fungi that form symbiotic] relationships with algae to create lichens. These lichens typically have a crust-like appearance and are found worldwide, though they are most common in temperate regions. The family includes five genera and about 55 species, which primarily grow on tree bark, rocks, or occasionally on wood or leaves. Fuscideaceae lichens are characterised by their reproductive structures, cup-like formations called apothecia, which can vary in colour from red to dark brown or black. The family has undergone several changes in its classification over the years, with recent genetic studies placing it within the order Umbilicariales. Fuscideaceae lichens produce various chemical compounds, some of which are unique to this family, and these chemicals are often used to help identify different species.
Graphis marusae is a species of corticolous (bark-dwelling) crustose lichen in the family Graphidaceae. It is found in a relict tropical lowland rainforest in Veracruz, Mexico, growing in exposed understory.
The Tephromelataceae are a family of lichenized fungi in the order Lecanorales. The family was circumscribed by Austrian lichenologist Josef Hafellner in 1984. Tephromelataceae comprises the genera Tephromela, Calvitimela, Mycoblastus and Violella, which together constitute a well-supported monophyletic group.
Roccellinastrum is a genus of lichen-forming fungi in the family Pilocarpaceae. It has seven species.
Ocellularia upretii is a species of corticolous (bark-dwelling) lichen in the family Graphidaceae. It is found in India.
Elixia cretica is a rare species of corticolous (bark-dwelling), crustose lichen in the family Elixiaceae. It is only known to occur in a single location in the mountains of the Greek island of Crete.
Aspiciliopsis is a genus of lichen-forming fungi in the family Trapeliaceae. It has two species, both of which occur in the Southern Hemisphere.
Megalospora austropacifica is a species of corticolous (bark-dwelling), crustose lichen in the family Megalosporaceae. It is found on the islands of Taveuni and Viti Levu in Fiji. It has a yellowish grey to whitish grey, glossy thallus that is thick and may appear slightly wrinkled or smooth, often with irregular cracks and small papillae containing conidiomata, but lacking isidia and soredia. Its apothecia are circular, up to 4.5 mm in diameter, with the disc evolving from concave to slightly convex and coloured from orange-brown to red-brown, surrounded by a thick, prominent margin.
Eilifdahlia sergeyana is a species of saxicolous (rock-dwelling), crustose lichen in the family Teloschistaceae. It is endemic to Kangaroo Island in South Australia. The lichen thallus has an uneven and scaly texture, forming patches up to 40 mm wide in dull greenish-grey or brownish-grey. Its fruiting bodies (apothecia) are orange to yellow, with a biatorine structure, and range from 0.5 to 1 mm wide. These apothecia have a matte surface and a cup-shaped margin containing golden-yellow crystals. The paraphyses within are slender and branched, and the asci contain ellipsoid spores.
Baeomyces heteromorphus is a species of terricolous (ground-dwelling) lichen in the family Baeomycetaceae. It has an Australasian distribution. Characteristics of the lichen include its greenish-grey thallus, the pink to brownish discs of its apothecia, translucent spores lacking internal partitions (septa), and the presence of the secondary metabolites norstictic acid and connorstictic acid.
Melanotopelia is a genus of lichen-forming fungi in the family Graphidaceae. It has four species of corticolous (bark-dwelling), crustose lichens. This genus includes species characterised by dark pigmentation in their exciple, non-amyloid ascospores, and specific secondary metabolites.
Rhizocarpon torquatum is a species of saxicolous (rock-dwelling), crustose lichen in the family Rhizocarpaceae. This species is recognised by its pale, thick, smooth, areolate thallus that contains hypostictic acid as a major metabolite, and its large apothecia that are distinctively adorned with a whitish inner collar in immature stages.
Tapellaria intermedia is a little-known species of foliicolous (leaf-dwelling) crustose lichen in the family Pilocarpaceae. It occurs in Bolivia.
Ochrolechia gowardii is a species of corticolous (bark-dwelling), crustose lichen in the family Ochrolechiaceae. First described in 1991 by the Canadian lichenologist Irwin M. Brodo, this lichen is characterised by its very thin, yellowish-white body (thallus) that partially embeds into tree bark. O. gowardii has small, powdery structures (soralia) that produce asexual reproductive granules, and its disc-like fruiting bodies (apothecia) with pale yellow-orange to light orange centres. O. gowardii can be found in parts of northwestern North America and Scandinavia, typically growing on subalpine fir or Norway spruce trees.
Austroparmeliella is a genus of lichen-forming fungi in the family Pannariaceae. It consists of five species, all of which are found in the Southern Hemisphere.
Ramboldia gowardiana is a species of corticolous (bark-dwelling), crustose lichen in the family Ramboldiaceae. First discovered in 2003 in Montana, United States, it typically appears as a grayish or greenish crust on tree bark, particularly on conifers like pines and firs. The lichen is characterised by its small, bright red to orange-red reproductive structures (apothecia) visible on its surface. R. gowardiana is found in dry, temperate forests from Alaska to California, often at elevations between 300 and 1,400 meters. Initially classified in a different genus, it was reclassified as Ramboldia in 2008 based on genetic studies. This lichen is part of the biodiversity of the Pacific Northwest region of North America.
Megaloblastenia is a genus of crustose lichen-forming fungi in the family Megalosporaceae, comprising three species. Proposed by Dutch lichenologist Harrie Sipman in 1983, the genus is characterised by its thick, ecorticate thallus ranging from pale whitish-grey to yellowish, and its disc-like fruiting bodies (apothecia) that can be biatorine or lecideine. Megaloblastenia lichens form a symbiotic relationship with Dictyochloropsis algae, produce hyaline, bicellular ascospores with polaribilocular structure, and contain chemical compounds such as zeorin, pannarin, or usnic acid. Found in Australasia and South America, these lichens typically grow as epiphytes on trees in moist forests within temperate to tropical oceanic climates.