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Reindeer Lichen
''Cladonia rangiferina'', also known as reindeer cup lichen, reindeer lichen (cf. Sw. ''renlav'') or grey reindeer lichen, is a light-colored fruticose, cup lichen species in the family Cladoniaceae. It grows in both hot and cold climates in well-drained, open environments. Found primarily in areas of alpine tundra, it is extremely cold-hardy. Other common names include reindeer moss, deer moss, and caribou moss, but these names can be misleading since it is, though somewhat moss-like in appearance, not a moss. As the common names suggest, reindeer lichen is an important food for reindeer (caribou), and has economic importance as a result. Synonyms include ''Cladina rangiferina'' and ''Lichen rangiferinus''. Description Thalli are fruticose, and extensively branched, with each branch usually dividing into three or four (sometimes two); the thicker branches are typically in diameter. The color is grayish, whitish or brownish gray. ''C. rangiferina'' forms extensive mats up ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Carl Linnaeus
Carl Linnaeus (; 23 May 1707 – 10 January 1778), also known after his ennoblement in 1761 as Carl von Linné Blunt (2004), p. 171. (), was a Swedish botanist, zoologist, taxonomist, and physician who formalised binomial nomenclature, the modern system of naming organisms. He is known as the "father of modern taxonomy". Many of his writings were in Latin; his name is rendered in Latin as and, after his 1761 ennoblement, as . Linnaeus was born in Råshult, the countryside of Småland, in southern Sweden. He received most of his higher education at Uppsala University and began giving lectures in botany there in 1730. He lived abroad between 1735 and 1738, where he studied and also published the first edition of his ' in the Netherlands. He then returned to Sweden where he became professor of medicine and botany at Uppsala. In the 1740s, he was sent on several journeys through Sweden to find and classify plants and animals. In the 1750s and 1760s, he continued to collect an ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Trebouxia Irregularis
''Trebouxia'' is a unicellular green alga.Silverside, A. J. (2009). Retrieved from http://www.bioref.lastdragon.org/Chlorophyta/''Trebouxia''.html It is a photosynthetic organism that can exist in almost all habitats found in polar, tropical, and temperate regions.Erokhina, L. G., Shatilovich, A. V., Kaminskaya, O. P., & Gilichinskii, D. A. (2004). Spectral Properties of the Green Alga ''Trebouxia'', a Phycobiont of Cryptoendolithic Lichens in the Antarctic Dry Valley. Microbiology,73(4), 420-424. doi:10.1023/b:mici.0000036987.18559Lukesova, A., & Frouz, J. (2007). Soil and Freshwater Micro-Algae as a Food Source for Invertebrates in Extreme Environments. Cellular Origin, Life in Extreme Habitats and Astrobiology Algae and Cyanobacteria in Extreme Environments,265-284. doi:10.1007/978-1-4020-6112-7_14Seckbach, J. (2007). Algae and cyanobacteria in extreme environments. Dordrecht: Springer. doi:https://doi.org/10.1007/978-1-4020-6112-7Seckbach, J. (2002). Symbiosis: Mechanisms and m ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Barbatic Acid
Barbatic acid is an organic compound that is made by some lichens. It is in the structural class known as depsides. It is particularly common in the genera ''Usnea'' (the beard lichens) and ''Cladonia''. History The compound was first isolated in 1880 from the lichen '' Usnea barbata'' by chemists John Stenhouse and Charles Groves. The compound coccellic acid, isolated from '' Cladonia coccifera'', was later shown to be the same compound as barbatic acid. Properties Biosynthetically, barbatic acid is made of two units of orsellinate derivatives that are created by an aromatic synthase enzyme. The repeated action of this enzyme produces an 8-carbon polyketide intermediate that is cyclized. Barbatic acid's IUPAC name is 2-hydroxy-4-(2-hydroxy-4-methoxy-3,6-dimethylbenzoyl)oxy-3,6-dimethylbenzoic acid. Its chemical formula is C19H20O7; it has a molecular mass of 360.36 grams per mole. In its purified crystalline form, it exists as various forms: small rhombic prisms, lo ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Sugiol
Sugiol is a phenolic abietane derivative of ferruginol and can be used as a biomarker for specific families of conifers. The presence of sugiol can be used to identify the ''Cupressaceae'' s.1., ''podocarpaceae'', and A''raucaraiaceae'' families of conifers. The polar terpenoids are among the most resistant molecules to degradation besides n-alkanes and fatty acids, affording them high viability as biomarkers due to their longevity in the sedimentary record. Significant amounts of sugiol has been detected in fossil wood dated to the Eocene and Miocene periods, as well as a sample of ''Protopodocarpoxylon'' dated to the middle Jurassic. Background Sugiol is a naturally occurring phenolic diterpenoid. Diterpenoids are a group of secondary metabolites with 20 carbons. Acyclic diterpenes are uncommon, due to the way that they are assembled, and include important molecules such as phytol. Sugiol has three six-membered rings, one of which is aromatic (ring C), and differs from ferrugi ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Diterpenoid
Diterpenes are a class of chemical compounds composed of four isoprene units, often with the molecular formula C20H32. They are biosynthesized by plants, animals and fungi via the HMG-CoA reductase pathway, with geranylgeranyl pyrophosphate being a primary intermediate. Diterpenes form the basis for biologically important compounds such as retinol, retinal, and phytol. They are known to be antimicrobial and antiinflammatory. Structures As with most terpenes a huge number of potential structures exists, which may be broadly divided according to the number of rings present. Biosynthesis Diterpenes are derived from the addition of one IPP unit to FPP to form geranylgeranyl-pyrophosphate (GGPP). From GGPP, structural diversity is achieved mainly by two classes of enzymes; the diterpene synthases and cytochromes P450. Several diterpenes are produced by plants and cyanobacteria. GGPP is also the precursor for the synthesis of the phytane by the action of the enzyme geranylger ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
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