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Fominiella Tenerifensis
''Fominiella'' is a genus of lichen-forming fungi in the family Teloschistaceae. It contains two species with a thin, film like and inconspicuous thallus. Taxonomy The genus ''Fominiella'' was proposed in 2017 by the lichenologists Sergey Kondratyuk, Dalip Kumar Upreti, and Jae-Seoun Hur. Their molecular phylogenetic analysis revealed several monophyletic branches in the phylogenetic tree of the family Teloschistaceae. One of these new branches was occupied by a species known only from the Canary Islands, which was named ''Fominiella tenerifensis'' and assigned as the type species of the genus. The species then known as ''Caloplaca skii'' was also included in the genus on the basis of DNA analysis. The genus name honours the Ukrainian botanist Aleksandr Vasiljevich Fomin, who specialised in cryptogams. ''Fominiella'' is in the subfamily Xanthorioideae of the family Teloschistaceae. It is somewhat similar to two other genera in that subfamily that also have very reduced thalli: ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Fominiella Skii
''Fominiella'' is a genus of lichen-forming fungi in the family Teloschistaceae. It contains two species with a thin, film like and inconspicuous thallus. Taxonomy The genus ''Fominiella'' was proposed in 2017 by the lichenologists Sergey Kondratyuk, Dalip Kumar Upreti, and Jae-Seoun Hur. Their molecular phylogenetic analysis revealed several monophyletic branches in the phylogenetic tree of the family Teloschistaceae. One of these new branches was occupied by a species known only from the Canary Islands, which was named ''Fominiella tenerifensis'' and assigned as the type species of the genus. The species then known as ''Caloplaca skii'' was also included in the genus on the basis of DNA analysis. The genus name honours the Ukrainian botanist Aleksandr Vasiljevich Fomin, who specialised in cryptogams. ''Fominiella'' is in the subfamily Xanthorioideae of the family Teloschistaceae. It is somewhat similar to two other genera in that subfamily that also have very reduced thalli: ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Xanthocarpia
''Xanthocarpia'' is a genus of mostly crustose lichens in the family Teloschistaceae. It has 12 species with a largely Northern Hemisphere distribution. Taxonomy The genus was originally circumscription (taxonomy), circumscribed in 1859 by Abramo Bartolommeo Massalongo and Giuseppe De Notaris, with ''Xanthocarpia ochracea'' as the type species. This species has tetralocular ascospores (i.e. divided into 4 chambers). Description ''Xanthocarpia'' has a thallus that is either crust-like (crustose lichen, crustose) or like a shield or plate attached on the lower surface at a single central point (peltate). In some cases, the thallus is absent; in all cases, a cortex (botany), cortex is absent. The lichen contains anthraquinones compounds. ''Xanthocarpia'' species often have apothecia, which are coloured yellow to orange. These apothecia are zeorine, meaning that the proper exciple (the ring-shaped layer surrounding the hymenium) is enclosed in the thalline exciple. Pycnidia can be p ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Lichen Genera
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 ( |
Teloschistales Genera
The Teloschistales are an order of mostly lichen-forming fungi belonging to the class Lecanoromycetes in the division Ascomycota. According to one 2008 estimate, the order contains 5 families, 66 genera, and 1954 species. The predominant photobiont partners for the Teloschistales are green algae The green algae (singular: green alga) are a group consisting of the Prasinodermophyta and its unnamed sister which contains the Chlorophyta and Charophyta/Streptophyta. The land plants (Embryophytes) have emerged deep in the Charophyte alga as ... from the genera '' Trebouxia'' and '' Asterochloris''. Families * Brigantiaeaceae * Letrouitiaceae * Megalosporaceae * Teloschistaceae References Lichen orders Lecanoromycetes orders Taxa described in 1986 Taxa named by David Leslie Hawksworth {{Teloschistales-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Teloschistales
The Teloschistales are an order of mostly lichen-forming fungi belonging to the class Lecanoromycetes in the division Ascomycota. According to one 2008 estimate, the order contains 5 families, 66 genera, and 1954 species. The predominant photobiont partners for the Teloschistales are green algae from the genera ''Trebouxia'' and '' Asterochloris''. Families *Brigantiaeaceae *Letrouitiaceae *Megalosporaceae *Teloschistaceae The Teloschistaceae are a large family of mostly lichen-forming fungi belonging to the class Lecanoromycetes in the division Ascomycota. The family, estimated to contain over 1800 species, was extensively revised in 2013, including the creati ... References Lichen orders Lecanoromycetes orders Taxa described in 1986 Taxa named by David Leslie Hawksworth {{Teloschistales-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Teloschistin
Fallacinol (teloschistin) is an organic compound in the structural class of chemicals known as anthraquinones. It is found in some lichens, particularly in the family Teloschistaceae, as well as a couple of plants and non lichen-forming fungi. In 1936, Japanese chemists isolated a pigment named fallacin from the lichen ''Oxneria fallax'', which was later refined and assigned a tentative structural formula; by 1949, Indian chemists had isolated a substance from ''Teloschistes flavicans'' with an identical structural formula to fallacin. Later research further separated fallacin into two distinct pigments, fallacin-A (later called fallacinal) and fallacin-B (fallacinol). The latter compound is also known as teloschistin due to its structural match with the substance isolated earlier. History In 1936, Japanese chemists Mitizo Asano and Sinobu Fuziwara reported on their chemical investigations into the colour pigments of the lichen ''Xanthoria fallax'' (now known as ''Oxneria fallax'' ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Fallacinal
Fallacinal is an organic compound in the structural class of chemicals known as anthraquinones. It is found in many species of the lichen family Teloschistaceae. History In 1936, Japanese chemists Mitizo Asano and Sinobu Fuziwara reported on their investigations into the colour pigments of the lichen ''Xanthoria fallax'' (now known as ''Oxneria fallax''), found growing on the bark of mulberry trees. They isolated a biological pigment, pigment they named fallacin. A few years later Asano and Yosio Arata further purified the crude material from this lichen, ultimately obtaining an orange-yellow compound with a molecular formula of C16H12O6. Using information from additional chemical tests, they proposed a tentative structural formula for fallacin. In 1949, T. R. Seshadri and S. Subramanian described their work with the Indian lichen ''Teloschistes flavicans'', in which they isolated an orange substance they named teloschistin, and which had a structural formula identical to that of ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Parietinic Acid
Parietinic acid is an organic compound in the structural class of chemicals known as anthraquinones. It is found in many species of the lichen family Teloschistaceae. The substance was first reported in the literature by the German chemist Walter Eschrich in 1958. Occurrence Originally isolated from the lichen ''Xanthoria parietina'', it has since been identified in many lichens of the family Teloschistaceae. In 1970, Johan Santesson proposed a possible biogenetic relationship between the anthraqunone compounds commonly found in ''Caloplaca''. According to this scheme, emodin is methylated to give parietin, which then undergoes three successive oxidations, sequentially forming fallacinol, fallacinal, and then parietinic acid. A is a set of biosynthetically related compounds produced by a lichen. In 2002, Ulrik Søchting and Patrik Frödén identified chemosyndrome A, the most common chemosyndrome in the genus ''Teloschistes'' and in the entire family Teloschistaceae, whic ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Emodin
Emodin (6-methyl-1,3,8-trihydroxyanthraquinone) is a chemical compound, of the anthraquinone family, that can be isolated from rhubarb, buckthorn, and Japanese knotweed (''Reynoutria japonica'' syn. ''Polygonum cuspidatum''). Emodin is particularly abundant in the roots of the Chinese rhubarb (Rheum palmatum), knotweed and knotgrass (Polygonum cuspidatum and multiflorum) as well as Hawaii ‘au‘auko‘i cassia seeds or coffee weed (Semen cassia). It is specifically isolated from Rheum palmatum L. It is also produced by many species of fungi, including members of the genera ''Aspergillus'', ''Pyrenochaeta'', and ''Pestalotiopsis'', inter alia. The common name is derived from ''Rheum emodi'', a taxonomic synonym of ''Rheum australe'', (Himalayan rhubarb) and synonyms include emodol, frangula emodin, rheum emodin, 3-methyl-1,6,8-trihydroxyanthraquinone, Schüttgelb (Schuttgelb), and Persian Berry Lake. Pharmacology Emodin is an active component of several plants used in Traditiona ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
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 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Secondary Metabolite
Secondary metabolites, also called specialised metabolites, toxins, secondary products, or natural products, are organic compounds produced by any lifeform, e.g. bacteria, fungi, animals, or plants, which are not directly involved in the normal growth, development, or reproduction of the organism. Instead, they generally mediate ecological interactions, which may produce a selective advantage for the organism by increasing its survivability or fecundity. Specific secondary metabolites are often restricted to a narrow set of species within a phylogenetic group. Secondary metabolites often play an important role in plant defense against herbivory and other interspecies defenses. Humans use secondary metabolites as medicines, flavourings, pigments, and recreational drugs. The term secondary metabolite was first coined by Albrecht Kossel, a 1910 Nobel Prize laureate for medicine and physiology in 1910. 30 years later a Polish botanist Friedrich Czapek described secondary metabolit ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Parietin
Parietin is the predominant cortical pigment of lichens in the genus '' Caloplaca'', a secondary product of the lichen ''Xanthoria parietina'', and a pigment found in the roots of Curled Dock (''Rumex crispus''). It has an orangy-yellow color and absorbs blue light. It is also known as physcion. It has also been shown to protect lichens against UV-B light, at high altitudes in Alpine regions. The UV-B light stimulates production of parietin and the parietin protects the lichens from damage. Lichens in arctic regions such as Svarlbard retain this capability though they do not encounter damaging levels of UV-B, a capability that could help protect the lichens in case of Ozone layer thinning. It has also shown anti-fungal activity against barley powdery mildew and cucumber powdery mildew, more efficiently in the latter case than treatments with fenarimol and polyoxin B. It reacts with KOH to form a deep, reddish-magenta compound. Effect on human cancer cells Also found in rhu ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
