Canoparmelia Rarotongensis
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Canoparmelia Rarotongensis
''Canoparmelia rarotongensis'' is a species of foliose lichen in the family Parmeliaceae. Found in Rarotonga (Cook Islands), it was formally described as a new species in 2000 by Simone Louwhoff and John Elix. The type specimen was collected by the second author from the Muri Lagoon (on the eastern coast of Rarotonga), where it was found growing on hibiscus along the foreshore. It is named for its type locality. The main physical characteristic that distinguishes it from others in its genus is its conspicuous isidia, which are consistently inflated and branched. Description This lichen has a moderately attached, thin and flexible thallus that can grow up to wide. The are unevenly shaped and connected in the centre, but separate near the tips, measuring 2–4 mm wide. The edges of the lobes are smooth and occasionally wavy, appearing flat, without any . The top surface is a dusty grey-green colour, unevenly cracked in the centre with visible isidia, which are inflated a ...
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John Alan Elix
John Alan (Jack) Elix (born 1941) emeritus professor in chemistry at the Australian National University, is an organic chemist who has contributed in many fields: lichenology, lichen chemotaxonomy, plant physiology and biodiversity and natural product chemistry. He has authored 2282 species names, and 67 genera in the field of mycology. Education His first degree, B.Sc., and his Ph.D were both in organic chemistry from the University of Adelaide. This was followed by post-doctoral years at the University of Cambridge and then a D.Sc. in natural products chemistry from the Australian National University. Career Elix spent a post doctoral year in 1966 at Cambridge, returning to Australia in 1967 to a lectureship in chemistry at the ANU. He retired as professor of chemistry in 2002, becoming professor emeritus. By 1975 he had already published several papers on the organic chemistry of lichens, and ultimately leading to work on the evolution, taxonomy and phylogeny of liche ...
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Apothecia
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). Classification The ascocarp is classified according to its placement (in ways not fundamental to the basic taxonomy). It is called ''epigeous'' if it grows above ground, as with the morels, while underground ascocarps, such as truffles, are termed ''hypogeous''. The structure enclosing the hymenium is divided into the types described below (apothecium, cleistothecium, etc.) and this character ''is'' important for the taxonomic classification of the fungus. Apothecia can be relatively large and fleshy, whereas the others are microscopic—about the size of flecks of ...
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Lichens Described In 2000
A lichen ( , ) is a composite organism that arises from algae or cyanobacteria living among filaments of multiple fungi species in a mutualistic relationship.Introduction to Lichens – An Alliance between Kingdoms
. University of California Museum of Paleontology.
Lichens have properties different from those of their component organisms. They come in many colors, sizes, and forms and are sometimes plant-like, but are not s. They may have tiny, leafless branches (); flat leaf-like structures (
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Lichen Species
A lichen ( , ) is a composite organism that arises from algae or cyanobacteria living among filaments of multiple fungi species in a mutualistic relationship.Introduction to Lichens – An Alliance between Kingdoms
. University of California Museum of Paleontology.
Lichens have properties different from those of their component organisms. They come in many colors, sizes, and forms and are sometimes plant-like, but are not s. They may have tiny, leafless branches (); flat leaf-like structures (

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Spot Test (lichen)
A spot test in lichenology is a spot analysis used to help identify lichens. It is performed by placing a drop of a chemical on different parts of the lichen and noting the colour change (or lack thereof) associated with application of the chemical. The tests are routinely encountered in dichotomous keys for lichen species, and they take advantage of the wide array of lichen products produced by lichens and their uniqueness among taxa. As such, spot tests reveal the presence or absence of chemicals in various parts of a lichen. They were first proposed by the botanist William Nylander in 1866. Three common spot tests use either 10% aqueous KOH solution (K test), saturated aqueous solution of bleaching powder or calcium hypochlorite (C test), or 5% alcoholic ''p''-phenylenediamine solution (P test). The colour changes occur due to presence of particular secondary metabolites in the lichen. There are several other less frequently used spot tests of more limited use that are employed ...
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Canoparmelia
''Canoparmelia'' is a genus of lichen-forming fungi in the family Parmeliaceae. The widespread genus contains about 35 species. ''Canoparmelia'', a segregate of the parmelioid lichen genus ''Pseudoparmelia'', was circumscribed by John Elix and Mason Hale in 1986. Description ''Canoparmelia'' lichens have grey or rarely yellow-green thalli containing the secondary chemicals atranorin and chloroatranorin, or rarely usnic acid, in the cortex. The thallus is made of more or less rotund lobes that are 3.0–5.0 mm wide and lack cilia; the medulla is white. The underside of the thallus is black or brown with naked brown margins and simple rhizines of the same colour. ''Canoparmelia'' produces small ellipsoid ascospores that measure 10–14 by 6–8 μm. The conidia are fusiform (spindle-shaped) or bifusiform, measuring 7–10 μm long. Species *'' Canoparmelia alabamensis'' *'' Canoparmelia albomaculata'' – Brazil *'' Canoparmelia amabilis'' *'' Canoparmelia antedel ...
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Orcinol
Orcinol is an organic compound with the formula CH3C6H3(OH)2. It occurs in many species of lichens including ''Roccella tinctoria'' and ''Lecanora''. Orcinol has been detected in the "toxic glue" of the ant species ''Camponotus saundersi''. It is a colorless solid. It is related to resorcinol, 1,3-C6H4(OH)2. Synthesis and reactions Orcinol was first prepared by dehydroacetic acid, a conversion that involved ring-opening of the pyrone to a triketone. This early experiment helped establish the rich condensation chemistry of polyketides. It can be obtained by fusing extract of aloes with potash, followed by acidification. It undergoes O-methylation with dimethylsulfate. It is used in the production of the dye orcein and as a reagent in some chemical tests for pentoses, such as Bial's Test. It may be synthesized from toluene; more interesting is its production when acetone dicarboxylic ester is condensed with the aid of sodium. It crystallizes in colorless prisms with one molecul ...
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Orsellinic Acid
Orsellinic acid, more specifically ''o''-orsellinic acid, is a phenolic acid. It is of importance in the biochemistry of lichens, from which it can be extracted. It is a common subunit of depsides. Chemistry It can be prepared by the oxidation of orsellaldehyde. This is also produced when everninic acid and ramalic acid is boiled with barium hydroxide Barium hydroxide is a chemical compound with the chemical formula Ba(OH)2. The monohydrate (''x'' = 1), known as baryta or baryta-water, is one of the principal compounds of barium. This white granular monohydrate is the usual commercial form. .... It forms colorless crystals in the form of needles which on rapid heating melt with decomposition in the neighborhood of 175 °C. [Sep 22, 2021: this citation to J Chromatog 511 needs to be revised because that paper makes no reference to crystals of orsellinic acid nor its melting point. In fact, the text never specifically mentions orsellinic acid: it simply appear ...
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Lichen Product
Lichen products, also known as lichen substances, are organic compounds produced by a lichen. Specifically, they are secondary metabolites. Lichen products are represented in several different chemical classes, including terpenoids, orcinol derivatives, chromones, xanthones, depsides, and depsidones. Over 800 lichen products of known chemical structure have been reported in the scientific literature, and most of these compound are exclusively found in lichens. Examples of lichen products include usnic acid (a dibenzofuran), atranorin (a depside), lichexanthone (a xanthone), salazinic acid (a depsidone), and isolichenan, an α-glucan. Many lichen products have biological activity, and research into these effects is ongoing. Lichen products accumulate on the outer walls of the fungal hyphae, and are quite stable. Crystal deposits can be visualised using scanning electron microscopy. For this reason, even very old herbarium specimens can be analysed. The amount of lichen products i ...
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Lecanoric Acid
Lecanoric acid is a chemical produced by several species of lichen.ubChem - Lecanoric acid"> Lecanoric acid is classified as a polyphenol and a didepside and it functions as an antioxidant. The acid is named after the lichen ''Lecanora''. The acid has also been isolated from ''Usnea subvacata'', ''Parmotrema stuppuem'', ''Parmotrema tinctorum,'' '' Parmotrema grayana,'' Xanthoparmelia arida and Xanthoparmelia lecanorica. A related compound, 5-chlorolecanoric acid, is found in some species of ''Punctelia ''Punctelia'' is a genus of foliose lichens belonging to the large family Parmeliaceae. The genus, which contains about 50 species, was segregated from genus ''Parmelia'' in 1982. Characteristics that define ''Punctelia'' include the presence of ...''. References {{Reflist Polyphenols Benzoic acids Benzoate esters Lichen products ...
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Atranorin
Atranorin is a chemical substance produced by some species of lichen. It is a secondary metabolite belonging to a group of compounds known as depsides. Atranorin has analgesic, anti-inflammatory, antibacterial, antifungal, cytotoxic, antioxidant, antiviral, and immunomodulatory properties. In rare cases, people can react allergic Allergies, also known as allergic diseases, refer a number of conditions caused by the hypersensitivity of the immune system to typically harmless substances in the environment. These diseases include hay fever, food allergies, atopic derma ... to atranorin. References Further reading * * * * Polyphenols Lichen products {{organic-compound-stub ...
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