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Ozopore
An ozopore is the opening of a defensive gland present in some arthropods, notably in millipedes of the order PolydesmidaOzopore.
External Anatomy of Polydesmida. polydesmida.info
and in , the eight-legged arachnids also known as "daddy long-legs". The glands themselves are known as ozadenes, also called "scent glands", "repugnatorial glands", "odoriferous glands" or "stink glands" by various authors. The name is derived from ''ozo'' "smell" and ''porus'' "por ...
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Ozophore
An ozophore is an elevated cone present in the harvestman ("daddy long-legs") suborder Cyphophthalmi. It carries the openings, called ozopores, of the defensive glandsPinto-da-Rocha ''et al.'' 2007: 22f that are present in many harvestmen. The name is derived from Ancient Greek Ancient Greek includes the forms of the Greek language used in ancient Greece and the ancient world from around 1500 BC to 300 BC. It is often roughly divided into the following periods: Mycenaean Greek (), Dark Ages (), the Archaic p ... ''ozo'' "smell" and ''phorein'' "to bear". Footnotes References * (eds.) (2007): Harvestmen - The Biology of Opiliones. ''Harvard University Press'' Harvestmen Arachnid anatomy {{Opiliones-stub ...
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Benzoquinone
Benzoquinone (C6H4O2) is a quinone with a single benzene ring. There are 2 (out of 3 hypothetical) benzoquinones: * 1,4-Benzoquinone, most commonly, right image (also ''para''-benzoquinone, ''p''-benzoquinone, ''para''-quinone, or just quinone) * 1,2-Benzoquinone, less commonly, left image (also ''ortho''-benzoquinone, ''o''-benzoquinone, ''ortho''-quinone) *1,3-benzoquinone "does not exist, because its structure would be nonplanar and highly strained", though derivatives are known. An alkylated ''p''-benzoquinone has been found in the rhizomes of '' Iris kemaonensis''. See also * Arene substitution pattern Arene substitution patterns are part of organic chemistry IUPAC nomenclature and pinpoint the position of substituents other than hydrogen in relation to each other on an aromatic hydrocarbon. ''Ortho'', ''meta'', and ''para'' substitution * I ... References {{Chemistry index ...
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Arthropod Anatomy
Arthropods (, (gen. ποδός)) are invertebrate animals with an exoskeleton, a segmented body, and paired jointed appendages. Arthropods form the phylum Arthropoda. They are distinguished by their jointed limbs and cuticle made of chitin, often mineralised with calcium carbonate. The arthropod body plan consists of segments, each with a pair of appendages. Arthropods are bilaterally symmetrical and their body possesses an external skeleton. In order to keep growing, they must go through stages of moulting, a process by which they shed their exoskeleton to reveal a new one. Some species have wings. They are an extremely diverse group, with up to 10 million species. The haemocoel, an arthropod's internal cavity, through which its haemolymph – analogue of blood – circulates, accommodates its interior organs; it has an open circulatory system. Like their exteriors, the internal organs of arthropods are generally built of repeated segments. Their nervous system is "ladder ...
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Julida
Julida is an order of millipedes. Members are mostly small and cylindrical, typically ranging from in length. Eyes may be present or absent, and in mature males of many species, the first pair of legs is modified into hook-like structures. Additionally, both pairs of legs on the 7th body segment of males are modified into gonopods. Distribution Julida contains predominantly temperate species ranging from North America to Panama, Europe, Asia north of the Himalayas, Asir region, Saudi Arabia, and Southeast Asia. Classification The order Julida contains approximately 750 species, divided into the following superfamilies and families: ;Blaniuloidea C. L. Koch, 1847 * Blaniulidae C. L. Koch, 1847 * Galliobatidae Brolemann, 1921 *Okeanobatidae Verhoeff, 1942 * Zosteractinidae Loomis, 1943 ;Juloidea Leach, 1814 * Julidae Leach, 1814 * Rhopaloiulidae Attems, 1926 * Trichoblaniulidae Verhoeff, 1911 * Trichonemasomatidae Enghoff, 1991 ;Nemasomatoidea Bollman, 1893 * Chelojulidae Eng ...
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Glomerida
Glomerida is an order of pill-millipedes found primarily in the Northern Hemisphere. They superficially resemble pill-bugs or woodlice, and can enroll into a protective ball. They have twelve body segments, 17 to 19 pairs of legs, and males have enlarged rear legs involved in mating. The order includes about 30 genera and at least 280 species, including ''Glomeris marginata'', the common European pill-millipede. The order contains members in Europe, South-east Asia and the Americas from California to Guatemala. Although historically considered closely related with the similar sphaerotheriidans that also enroll, some DNA evidence suggest they may be more closely related to glomeridesmidans, a poorly known order that does not enroll. Description Glomeridans are small, oval-shaped millipedes reaching up to long. Like the Sphaerotheriida (so-called Giant Pill-millipedes), they are capable of enrolling into a ball ("volvation"), a trait also shared with the unrelated pillbugs (Onis ...
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Naphthoquinone
Naphthoquinones constitute a class of organic compounds structurally related to naphthalene. Two isomers are common for the parent naphthoquinones: * 1,2-Naphthoquinone * 1,4-Naphthoquinone Natural products * Alkannin * Hexahydroxy-1,4-naphthalenedione * Juglone * Lapachol * Lawsone * Menatetrenone * 2-Methoxy-1,4-naphthoquinone, a compound found in ''Impatiens'' species * Nigrosporin B * 2,3,5,6,8-Pentahydroxy-1,4-naphthalenedione * Phylloquinone * Plumbagin * 2,3,5,7-Tetrahydroxy-1,4-naphthalenedione * Vitamin K and related compounds Synthetic naphthoquinones * Menadione (2-Methyl-1,4-naphthoquinone), a vitamin K mimic * 5,8-Dihydroxy-1,4-naphthoquinone and dihydroxynaphthoquinones * Atovaquone * Buparvaquone, an antiprotozoal drug used in veterinary medicine * Diazonaphthoquinone Diazonaphthoquinone (DNQ) is a diazo derivative of naphthoquinone. Upon exposure to light, DNQ converts to a derivative that is susceptible to etching. In this way, DNQ has become a ...
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Phalangiidae
The Phalangiidae are a family of harvestmen with about 380 known species. The best known is ''Phalangium opilio''. '' Dicranopalpus ramosus'' is an invasive species in Europe. It is not to be confused with the harvestman family Phalangodidae, which belongs to the suborder Laniatores. Name The name of the type genus is derived from Ancient Greek ''phalangion'' "harvestman". (2007): Phalangiidae Latreille, 1802. In: Pinto-da-Rocha ''et al.'' 2007: 123ff Systematics * Dicranopalpinae :* '' Amilenus'' Martens, 1969 (1 species; central Europe) :* '' Dicranopalpus'' Doleschall, 1852 (12 species; Europe, South America) :* '' Lanthanopilio'' Cokendolpher & Cokendolpher, 1984 (1 species) * Oligolophinae Banks, 1893 :* '' Lacinius'' Thorell, 1876 (17 species; China, Europe, North America) :* '' Mitopiella'' Banks, 1930 (1 species; Borneo) :* '' Mitopus'' Thorell, 1876 (9 species; Eurasia, North America) :* '' Odiellus'' Roewer, 1923 (17 species; Eurasia, North Africa, North America ...
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Alcohol (chemistry)
In chemistry, an alcohol is a type of organic compound that carries at least one hydroxyl () functional group bound to a saturated carbon atom. The term ''alcohol'' originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. An important class of alcohols, of which methanol and ethanol are the simplest examples, includes all compounds which conform to the general formula . Simple monoalcohols that are the subject of this article include primary (), secondary () and tertiary () alcohols. The suffix ''-ol'' appears in the IUPAC chemical name of all substances where the hydroxyl group is the functional group with the highest priority. When a higher priority group is present in the compound, the prefix ''hydroxy-'' is used in its IUPAC name. The suffix ''-ol'' in non-IUPAC names (such as paracetamol or cholesterol) also typically indicates that the substance is an alcohol. However, some ...
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Ketone
In organic chemistry, a ketone is a functional group with the structure R–C(=O)–R', where R and R' can be a variety of carbon-containing substituents. Ketones contain a carbonyl group –C(=O)– (which contains a carbon-oxygen double bond C=O). The simplest ketone is acetone (where R and R' is methyl), with the formula . Many ketones are of great importance in biology and in industry. Examples include many sugars (ketoses), many steroids (e.g., testosterone), and the solvent acetone. Nomenclature and etymology The word ''ketone'' is derived from ''Aketon'', an old German word for ''acetone''. According to the rules of IUPAC nomenclature, ketone names are derived by changing the suffix ''-ane'' of the parent alkane to ''-anone''. Typically, the position of the carbonyl group is denoted by a number, but traditional nonsystematic names are still generally used for the most important ketones, for example acetone and benzophenone. These nonsystematic names are considered reta ...
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Open Chain Compound
In chemistry, an open-chain compound (also spelled as open chain compound) or acyclic compound (Greek prefix "α", ''without'' and "κύκλος", ''cycle'') is a compound with a linear structure, rather than a cyclic one. An open-chain compound having no side chains is called a straight-chain compound (also spelled as straight chain compound). Many of the simple molecules of organic chemistry, such as the alkanes and alkenes, have both linear and ring isomers, that is, both acyclic and cyclic, with the latter often classified as aromatic. For those with 4 or more carbons, the linear forms can have straight-chain or branched-chain isomers. The lowercase prefix ''n-'' denotes the straight-chain isomer; for example, ''n''-butane is straight-chain butane, whereas ''i''-butane is isobutane. Cycloalkanes are isomers of alkenes, not of alkanes, because the ring's closure involves a C-C bond. Having no rings (aromatic or otherwise), all open-chain compounds are aliphatic. Typically in ...
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