Vermilacinia Paleoderma
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Vermilacinia Paleoderma
''Vermilacinia paleoderma'' is a pale yellow-green fruticose lichen that occurs commonly along the fog zone of the Pacific Coast of Northern Vizcaíno Desert region of Baja Californica and occasionally in the Chaparral Islands of California.Spjut, R. W. 1996. ''Niebla'' and ''Vermilacinia'' (Ramalinaceae) from California and Baja California. Sida Miscellany 14 Distinguishing features ''Vermilacinia paleoderma'' is distinguished by its thallus divided into relatively long tubular-prismatic branches—to 6 cm long in contrast to 4 cm long in ''V. combeoides''—that arise from a common base, the branches generally of longitudinal spiraled cortical ribs with recessed crater-like depression between the ribs; the craters frequently separated by transverse pastry-like creases, which gives the overall prismatic appearance to the branches. Primary branches vary from less than 5 to more than 20, simple or often divided well above base into equal secondary branches, or with ma ...
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Fruticose Lichen
A fruticose lichen is a form of lichen fungi that is characterized by a coral-like shrubby or bushy growth structure. It is formed from a symbiotic relationship of a photobiont such as green algae or less commonly cyanobacteria and one, two or more mycobionts. Fruticose lichens are not a monophyletic and holophyletic lineage, but is a form encountered in many classes. Fruticose lichens have a complex vegetation structure, and are characterized by an ascending, bushy or pendulous appearance. As with other lichens, many fruticose lichens can endure high degrees of desiccation. They grow slowly and often occur in habitats such as on tree barks, on rock surfaces and on soils in the Arctic and mountain regions. Characteristics Fruticose lichens are lichens composed of a shrubby or bushy thallus and a holdfast. The thallus is the vegetative body of a lichen that does not have true leaves, stems, or roots. The thallus colour is affected by the algae in the lichen, compounds created by t ...
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Depside
A depside is a type of polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond. Depsides are most often found in lichens, but have also been isolated from higher plants, including species of the Ericaceae, Lamiaceae, Papaveraceae and Myrtaceae. Certain depsides have antibiotic, anti- HIV, antioxidant, and anti-proliferative activity ''in vitro''. As inhibitors of prostaglandin synthesis and leukotriene B4 biosynthesis, some depsides have ''in vitro'' anti-inflammatory activity. A depsidase is a type of enzyme that cuts depside bonds. One such enzyme is tannase. Examples Gyrophoric acid, found in the lichen '' Cryptothecia rubrocincta'', is a depside. Merochlorophaeic acid, isolated from lichens of the genus '' Cladonia'', is an inhibitor of prostaglandin synthesis. Some depsides are described as anti-HIV. See also *Salsalate homodimer formed from self-condensation of salicylic acid Salicylic acid is an organic compound with the ...
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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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Ramalinaceae
The Ramalinaceae are a family of lichenized fungi in the order Lecanorales. The family name is synonymous with the name ''Bacidiaceae''. Species of this family have a widespread distribution. Genera *''Aciculopsora'' *''Adelolecia'' *'' Arthrosporum'' *''Bacidia'' *'' Bacidina'' *'' Bacidiopsora'' *'' Badimia'' *''Bibbya'' *'' Biatora'' *''Bilimbia'' *'' Catinaria'' *'' Cenozosia'' *'' Cliostomum'' *'' Compsocladium'' *''Coppinsidea'' *'' Crocynia'' *'' Echidnocymbium'' *'' Frutidella'' *'' Heppsora'' *'' Herteliana'' *'' Japewia'' *''Jarmania'' *''Krogia'' *''Lecania'' *'' Lopezaria'' *'' Lueckingia'' *'' Myelorrhiza'' *'' Phyllopsora'' *'' Physcidia'' *''Ramalina'' *'' Ramalinopsis'' *'' Rolfidium'' *'' Schadonia'' *''Scutula'' *'' Stirtoniella'' *'' Thamnolecania'' *'' Tibellia'' *''Toninia'' *'' Toniniopsis'' *'' Triclinum'' – synonymous with ''Squamacidia'' Brako *''Vermilacinia ''Vermilacinia'', a genus of lichenized fungi in the family Ramalinaceae, is a yellow-gree ...
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Depsidone
Depsidones (+ "depside" + "one") are chemical compounds that are sometimes found as secondary metabolites in lichens. They are esters that are both depsides and cyclic ethers. An example is norstictic acid Norstictic acid is a depsidone produced as a secondary metabolite Secondary metabolites, also called specialised metabolites, toxins, secondary products, or natural products, are organic compounds produced by any lifeform, e.g. bacteria, fun .... References {{reflist Biochemistry Carboxylate esters ...
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Triterpene
Triterpenes are a class of chemical compounds composed of three terpene units with the molecular formula C30H48; they may also be thought of as consisting of six isoprene units. Animals, plants and fungi all produce triterpenes, including squalene, the precursor to all steroids. Structures Triterpenes exist in a great variety of structures. Nearly 200 different skeletons have been identified. These skeletons may be broadly divided according to the number of rings present. In general pentacyclic structures (5 rings) tend to dominate. Squalene is biosynthesized through the head-to-head condensation of two farnesyl pyrophosphate units. This coupling converts a pair of C15 components into a C30 product. Squalene serves as precursor for the formation of many triterpenoids, including bacterial hopanoids and eukaryotic sterols. Triterpenoids By definition triterpenoids are triterpenes that possess heteroatoms, usually oxygen. The terms ''triterpene'' and ''triterpenoid'' oft ...
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Sekikaic Acid
Sekikaic acid is an organic compound in the structural class of chemicals known as depsides. It is found in some lichens. First isolated from '' Ramalina sekika'', it is a fairly common lichen product in ''Ramalina'' and ''Cladonia'', both genera of lichen-forming fungi. The species epithet of the powdery lichen '' Lepraria sekikaica'' refers to the presence of this substance—a rarity in genus ''Lepraria''. Properties In its purified form, sekikaic acid exists as colourless rectangular prisms or rhombic plates. Its molecular formula is C22H2608. It has a melting point of . An ethanolic solution of sekikaic acid reacts with iron(III) chloride to produce a violet colour. Its ultraviolet spectrum has three peaks of maximum absorption (λmax) at 219, 263, and 303  nm. Sekikaic acid has been demonstrated to have several biological activities in laboratory experiments. These include antioxidant activity, inhibition of the enzymes α-glucosidase and α-amylase, hypoglycemic ac ...
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Lichen Substance
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 prod ...
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Terpenoid
The terpenoids, also known as isoprenoids, are a class of naturally occurring organic chemicals derived from the 5-carbon compound isoprene and its derivatives called terpenes, diterpenes, etc. While sometimes used interchangeably with "terpenes", terpenoids contain additional functional groups, usually containing oxygen. When combined with the hydrocarbon terpenes, terpenoids comprise about 80,000 compounds. They are the largest class of plant secondary metabolites, representing about 60% of known natural products. Many terpenoids have substantial pharmacological bioactivity and are therefore of interest to medicinal chemists. Plant terpenoids are used for their aromatic qualities and play a role in traditional herbal remedies. Terpenoids contribute to the scent of eucalyptus, the flavors of cinnamon, cloves, and ginger, the yellow color in sunflowers, and the red color in tomatoes. Well-known terpenoids include citral, menthol, camphor, salvinorin A in the plant '' Salvia di ...
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