Avicide
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Avicide
An avicide is any substance (normally a chemical) used to kill birds. Commonly used avicides include strychnine (also used as rodenticide and predacide), DRC-1339 (3-chloro-4-methylaniline hydrochloride, Starlicide) and CPTH (3-chloro-p-toluidine, the free base of Starlicide), Avitrol (4-aminopyridine) and chloralose (also used as rodenticide). In the past, highly concentrated formulations of parathion in diesel oil were sprayed by aircraft over birds' nesting colonies. Avicides are banned in many countries because of their ecological impact, which is poorly studied. They are still used in the United States, Canada, Australia and New Zealand. The practice is criticized by animal rights advocates and those who kill birds with guns and traps. Pigeon fanciers sometimes poison problematic birds of prey, even in countries like Russia and Ukraine where avicides are illegal.Wegler, R.: Chemie der Pflanzenschutz- und Schädlingsbekämpfungsmittel, Band 1, Springer, 1970 (german) Se ...
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Strychnine
Strychnine (, , US chiefly ) is a highly toxic, colorless, bitter, crystalline alkaloid used as a pesticide, particularly for killing small vertebrates such as birds and rodents. Strychnine, when inhaled, swallowed, or absorbed through the eyes or mouth, causes poisoning which results in muscular convulsions and eventually death through asphyxia. While it is no longer used medicinally, it was used historically in small doses to strengthen muscle contractions, such as a heart and bowel stimulant and performance-enhancing drug. The most common source is from the seeds of the ''Strychnos nux-vomica'' tree. Biosynthesis Strychnine is a terpene indole alkaloid belonging to the ''Strychnos'' family of '' Corynanthe'' alkaloids, and it is derived from tryptamine and secologanin. The biosynthesis of strychine was solved in 2022. The enzyme, strictosidine synthase, catalyzes the condensation of tryptamine and secologanin, followed by a Pictet-Spengler reaction to form strictosidine ...
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DRC-1339
Starlicide or gull toxicant is a chemical avicide that is highly toxic to European starlings (thus the name) and gulls, but less toxic to other birds or to mammals such as humans and pets. Synonyms The name Starlicide originated as a registered trademark of the animal feed manufacturer Ralston-Purina in St. Louis, Missouri. Starlicide is a small molecule in which a central benzene ring is modified by amine, chloro and methyl substituents in a specific pattern. Because special names exist for benzene rings modified with one or two of these functional groups, several synonymous chemical names may be encountered: 3-chloro-4-methylaniline or 3-chloro-4-methylbenzenamine, 2-chloro-4-aminotoluene, or 3-chloro-''p''-toluidine. Numbered groups (2-chloro, 4-amino) also may be named out of order; the numbers of such groups equal the number of carbon atoms in the benzene ring separating them from the group implied in the special name. Preparations of this chemical may be named as a hydr ...
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CPTH
Starlicide or gull toxicant is a chemical avicide that is highly toxic to European starlings (thus the name) and gulls, but less toxic to other birds or to mammals such as humans and pets. Synonyms The name Starlicide originated as a registered trademark of the animal feed manufacturer Ralston-Purina in St. Louis, Missouri. Starlicide is a small molecule in which a central benzene ring is modified by amine, chloro and methyl substituents in a specific pattern. Because special names exist for benzene rings modified with one or two of these functional groups, several synonymous chemical names may be encountered: 3-chloro-4-methylaniline or 3-chloro-4-methylbenzenamine, 2-chloro-4-aminotoluene, or 3-chloro-''p''-toluidine. Numbered groups (2-chloro, 4-amino) also may be named out of order; the numbers of such groups equal the number of carbon atoms in the benzene ring separating them from the group implied in the special name. Preparations of this chemical may be named as a hydr ...
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Chloralose
Chloralose (also known as α-chloralose) is an avicide, and a rodenticide used to kill mice in temperatures below 15 °C. It is also widely used in neuroscience and veterinary medicine as an anesthetic and sedative. Either alone or in combination, such as with urethane, it is used for long-lasting, but light anesthesia. Chemically, it is a chlorinated acetal derivative of glucose. It is listed in Annex I of Directive 67/548/EEC with the classification ''Harmful'' (Xn) Chloralose exerts barbiturate-like actions on synaptic transmission in the brain, including potent effects at inhibitory γ-aminobutyric acid type A receptors (GABAAR). A structural isomer of chloralose, β-chloralose (also called parachloralose in older literature), is inactive as a GABAAR modulator and also as a general anesthetic. Chloralose is often abused for its avicide properties. In the United Kingdom The United Kingdom of Great Britain and Northern Ireland, commonly known as the United Kin ...
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Bird Kill
Bird kill is a localized event resulting in the death of large numbers of birds at the same time. Scientific explanations Large die offs of animals are not unusual in nature, and happen for a variety of reasons including bad weather, disease, and poisonings, with pollution and climate change adding to the stresses on wildlife. According to the USGS National Wildlife Health Center in the US, 175 mass deaths events exceeding 1,000 birds has occurred over the past 10 years. Russian scientist Afanasiy Ilich Tobonov researched mass animal deaths in the 1990s and concluded that the mass deaths of birds and wildlife in the Sakha Republic were noted only along the flight paths of space rockets. Examples * In 2004 thousands of tiny birds fell from the sky over Chinese president Hu Jintao's birthplace Taizhou, Jiangsu. The event was seen as a worrying omen for his rule to come. * 15 January 2009, in New York City. A large flock of Canada geese was struck by US Airways Flight 1549, dis ...
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Chemical
A chemical substance is a form of matter having constant chemical composition and characteristic properties. Some references add that chemical substance cannot be separated into its constituent elements by physical separation methods, i.e., without breaking chemical bonds. Chemical substances can be simple substances (substances consisting of a single chemical element), chemical compounds, or alloys. Chemical substances are often called 'pure' to set them apart from mixtures. A common example of a chemical substance is pure water; it has the same properties and the same ratio of hydrogen to oxygen whether it is isolated from a river or made in a laboratory. Other chemical substances commonly encountered in pure form are diamond (carbon), gold, table salt (sodium chloride) and refined sugar (sucrose). However, in practice, no substance is entirely pure, and chemical purity is specified according to the intended use of the chemical. Chemical substances exist as solids, liquids, ...
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Bird
Birds are a group of warm-blooded vertebrates constituting the class Aves (), characterised by feathers, toothless beaked jaws, the laying of hard-shelled eggs, a high metabolic rate, a four-chambered heart, and a strong yet lightweight skeleton. Birds live worldwide and range in size from the bee hummingbird to the ostrich. There are about ten thousand living species, more than half of which are passerine, or "perching" birds. Birds have whose development varies according to species; the only known groups without wings are the extinct moa and elephant birds. Wings, which are modified forelimbs, gave birds the ability to fly, although further evolution has led to the loss of flight in some birds, including ratites, penguins, and diverse endemic island species. The digestive and respiratory systems of birds are also uniquely adapted for flight. Some bird species of aquatic environments, particularly seabirds and some waterbirds, have further evolved for swimming. B ...
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Parathion
Parathion, also called parathion-ethyl or diethyl parathion and locally known as "Folidol", is an organophosphate insecticide and acaricide. It was originally developed by IG Farben in the 1940s. It is highly toxic to non-target organisms, including humans, so its use has been banned or restricted in most countries. The basic structure is shared by parathion methyl. History Parathion was developed by Gerhard Schrader for the German trust IG Farben in the 1940s. After World War II and the collapse of IG Farben due to the war crime trials, the Western allies seized the patent, and parathion was marketed worldwide by different companies and under different brand names. The most common German brand was E605 (banned in Germany after 2002); this was not a food-additive "E number" as used in the EU today. "E" stands for ''Entwicklungsnummer'' (German for "development number"). It is an irreversible acetylcholinesterase inhibitor. Safety concerns have later led to the development o ...
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