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Rasberry Crazy Ant
The Rasberry crazy ant or tawny crazy ant (''Nylanderia fulva'') is an ant originating in South America. Like the longhorn crazy ant (''Paratrechina longicornis''), this species is called "crazy ant" because of its quick, unpredictable movements (the related '' N. pubens'' is known as the "Caribbean crazy ant"). It is sometimes called the "Rasberry crazy ant" in Texas after the exterminator Tom Rasberry, who noticed that the ants were increasing in numbers in 2002. Scientists have reorganised the genera taxonomy within this clade of ants, and now it is identified as ''Nylanderia fulva''. In 2014, it was discovered that the ant produces and covers itself with formic acid as an antidote to the fire ant's venom. It is the first known example of an insect being able to neutralize another insect's venom, an ability speculated to have evolved in South America where the two species share the same native range. Colonies have multiple queens, which also contributes to their survival.< ...
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Longhorn Crazy Ant
The longhorn crazy ant (''Paratrechina longicornis''), also known as the black crazy ant, is a species of small Formicine ant. These ants are commonly called "crazy ants" because instead of following straight lines, they dash around erratically. They have a broad distribution, including much of the tropics and subtropics, and are also found in buildings in more temperate regions, making them one of the most widespread ant species in the world. This species, as well as all others in the ant subfamily Formicinae, cannot sting. However, this species can fire/shoot a formic acid spray from its abdomen when under attack by other insects or attacking other insects. When the longhorn crazy ant (''Paratrechina longicornis'') bends its abdomen while aiming at an enemy insect, it is typically shooting its hard-to-see acid. These ants can be touched safely, similar to the ghost ants. Description The worker longhorn crazy ant is about long with a brownish-black head, thorax, petiole, and ...
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The New York Times
''The New York Times'' (''NYT'') is an American daily newspaper based in New York City. ''The New York Times'' covers domestic, national, and international news, and publishes opinion pieces, investigative reports, and reviews. As one of the longest-running newspapers in the United States, the ''Times'' serves as one of the country's Newspaper of record, newspapers of record. , ''The New York Times'' had 9.13 million total and 8.83 million online subscribers, both by significant margins the List of newspapers in the United States, highest numbers for any newspaper in the United States; the total also included 296,330 print subscribers, making the ''Times'' the second-largest newspaper by print circulation in the United States, following ''The Wall Street Journal'', also based in New York City. ''The New York Times'' is published by the New York Times Company; since 1896, the company has been chaired by the Ochs-Sulzberger family, whose current chairman and the paper's publ ...
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Lipophilicity
Lipophilicity (from Greek λίπος "fat" and φίλος "friendly") is the ability of a chemical compound to dissolve in fats, oils, lipids, and non-polar solvents such as hexane or toluene. Such compounds are called lipophilic (translated as "fat-loving" or "fat-liking"). Such non-polar solvents are themselves lipophilic, and the adage "like dissolves like" generally holds true. Thus lipophilic substances tend to dissolve in other lipophilic substances, whereas hydrophilic ("water-loving") substances tend to dissolve in water and other hydrophilic substances. Lipophilicity, hydrophobicity, and non-polarity may describe the same tendency towards participation in the London dispersion force, as the terms are often used interchangeably. However, the terms "lipophilic" and "hydrophobic" are not synonymous, as can be seen with silicones and fluorocarbons, which are hydrophobic but not lipophilic. __TOC__ Surfactants Hydrocarbon-based surfactants are compounds that are amph ...
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Protonate
In chemistry, protonation (or hydronation) is the adding of a proton (or hydron, or hydrogen cation), usually denoted by H+, to an atom, molecule, or ion, forming a conjugate acid. (The complementary process, when a proton is removed from a Brønsted–Lowry acid, is deprotonation.) Some examples include * The protonation of water by sulfuric acid: *: H2SO4 + H2O H3O+ + * The protonation of isobutene in the formation of a carbocation: *: (CH3)2C=CH2 + HBF4 (CH3)3C+ + * The protonation of ammonia in the formation of ammonium chloride from ammonia and hydrogen chloride: *: NH3( g) + HCl( g) → NH4Cl( s) Protonation is a fundamental chemical reaction and is a step in many stoichiometric and catalytic processes. Some ions and molecules can undergo more than one protonation and are labeled polybasic, which is true of many biological macromolecules. Protonation and deprotonation (removal of a proton) occur in most acid–base reactions; they are the core of most acid–base reacti ...
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Denaturation (biochemistry)
In biochemistry, denaturation is a process in which proteins or nucleic acids lose folded structure present in their native state due to various factors, including application of some external stress or compound, such as a strong acid or base, a concentrated inorganic salt, an organic solvent (e.g., alcohol or chloroform), agitation, radiation, or heat. If proteins in a living cell are denatured, this results in disruption of cell activity and possibly cell death. Protein denaturation is also a consequence of cell death. Denatured proteins can exhibit a wide range of characteristics, from conformational change and loss of solubility or dissociation of cofactors to aggregation due to the exposure of hydrophobic groups. The loss of solubility as a result of denaturation is called ''coagulation''. Denatured proteins, e.g., metalloenzymes, lose their 3D structure or metal cofactor, and therefore, cannot function. Proper protein folding is key to whether a globular or memb ...
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Heterocyclic Compound
A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). Heterocyclic organic chemistry is the branch of organic chemistry dealing with the synthesis, properties, and applications of organic heterocycles. Examples of heterocyclic compounds include all of the nucleic acids, the majority of drugs, most biomass (cellulose and related materials), and many natural and synthetic dyes. More than half of known compounds are heterocycles. 59% of US FDA-approved drugs contain nitrogen heterocycles. Classification The study of organic heterocyclic chemistry focuses especially on organic unsaturated derivatives, and the preponderance of work and applications involves unstrained organic 5- and 6-membered rings. Included are pyridine, thiophene, pyrrole, and furan. Another large class of organic heterocycles refers to those fused to benzene rings. For example, the fused benzene derivatives of py ...
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Ionic Liquid
An ionic liquid (IL) is a salt (chemistry), salt in the liquid state at ambient conditions. In some contexts, the term has been restricted to salts whose melting point is below a specific temperature, such as . While ordinary liquids such as water and gasoline are predominantly made of electric charge, electrically neutral molecules, ionic liquids are largely made of ions. These substances are variously called liquid electrolytes, ionic melts, ionic fluids, fused salts, liquid salts, or ionic glasses. Ionic liquids have many potential applications. They are powerful solvents and can be used as electrolytes. Salts that are liquid at near-ambient temperature are important for electric battery applications, and have been considered as sealants due to their very low vapor pressure. Any salt that melts without pyrolysis, decomposing or vaporizing usually yields an ionic liquid. Sodium chloride (NaCl), for example, melts at into a liquid that consists largely of sodium cations () and ...
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Competition (biology)
Competition is an Biological interaction, interaction between organisms or species in which both require one or more Resource (biological), resources that are in Limiting factor, limited supply (such as food, water, or Territory (animal), territory). Competition lowers the Fitness (biology), fitness of both organisms involved since the presence of one of the organisms always reduces the amount of the resource available to the other. In the study of community ecology, competition within and between members of a species is an important biological interaction. Competition is one of many interacting Biotic component, biotic and Abiotic component, abiotic factors that affect Community (ecology), community structure, species diversity, and population dynamics (shifts in a population over time). There are three major Mechanism (biology), mechanisms of competition: interference, exploitation, and apparent competition (in order from most direct to least direct). Interference and exploitat ...
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Solenopsin
Solenopsin is a lipophilic alkaloid with the molecular formula C17H35N found in the venom of fire ants (''Solenopsis''). It is considered the primary toxin in the venom and may be the component responsible for the cardiorespiratory failure in people who experience excessive fire ant stings. Structurally solenopsins are a piperidine ring with a methyl group substitution at position 2 and a long hydrophobic chain at position 6. They are typically oily at room temperature, water-insoluble, and present an absorbance peak at 232 nanometers. Fire ant venom contains other chemically related piperidines which make purification of solenopsin from ants difficult. Therefore, solenopsin and related compounds have been the target of organic synthesis from which pure compounds can be produced for individual study. Originally synthesized in 1993, several groups have designed novel and creative methods of synthesizing enantiopure solenopsin and other alkaloidal components of ant venom. To ...
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Alkaloid
Alkaloids are a broad class of natural product, naturally occurring organic compounds that contain at least one nitrogen atom. Some synthetic compounds of similar structure may also be termed alkaloids. Alkaloids are produced by a large variety of organisms including bacteria, fungus, fungi, Medicinal plant, plants, and animals. They can be purified from crude extracts of these organisms by acid-base extraction, or solvent extractions followed by silica-gel column chromatography. Alkaloids have a wide range of pharmacology, pharmacological activities including antimalarial medication, antimalarial (e.g. quinine), asthma, antiasthma (e.g. ephedrine), chemotherapy, anticancer (e.g. omacetaxine mepesuccinate, homoharringtonine), cholinomimetic (e.g. galantamine), vasodilation, vasodilatory (e.g. vincamine), Antiarrhythmic agent, antiarrhythmic (e.g. quinidine), analgesic (e.g. morphine), antibacterial (e.g. chelerythrine), and anti-diabetic, antihyperglycemic activities (e.g. berb ...
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Acidopore
The acidopore is a component of ant anatomy; a round orifice located on the abdomen encircled by hairs which typifies the subfamily Formicinae. The conical structure connects to the posterior end of an ant's gaster where formic acid Formic acid (), systematically named methanoic acid, is the simplest carboxylic acid. It has the chemical formula HCOOH and structure . This acid is an important intermediate in chemical synthesis and occurs naturally, most notably in some an ... and other hydrocarbons are formed, collectively comprising the venom. Ants are able to disinfect fungus-infected brood by taking up acidopore venom into their mouth by self-grooming and applying it by brood grooming. This structure is unique to, but not present in all members of the ant subfamily Formicinae. It is termed an acidopore because it is the pore, or hole, from which formic acid is sprayed. See also * Ant venom References Insect anatomy Myrmecology {{ant-stub ...
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Formicinae
The Formicinae are a subfamily within the Formicidae containing ants of moderate evolutionary development. Formicines retain some primitive features, such as the presence of cocoons around pupae, the presence of ocelli in workers, and little tendency toward reduction of palp or antennal segmentation in most species, except subterranean groups. Extreme modification of mandibles is rare, except in the genera '' Myrmoteras'' and '' Polyergus''. However, some members show considerable evolutionary advancement in behaviors such as slave-making and symbiosis with root-feeding hemipterans. Finally, all formicines have very reduced stings and enlarged venom reservoirs, with the venom gland, specialized (uniquely among ants) for the production of formic acid. All members of the Formicinae "have a one-segmented petiole in the form of a vertical scale". Identification Formicine ants have a single node-like or scale-like petiole (postpetiole entirely lacking) and the apex of th ...
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