Sheep dip

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Plunge dipping sheep Sheep dipping.jpg
Plunge dipping sheep

Sheep dip is a liquid formulation of insecticide and fungicide that shepherds and farmers use to protect their sheep from infestation against external parasites such as itch mite (Psoroptes ovis), blow-fly, ticks and lice.

Contents

History

Sheep dipping is the immersion of sheep in water containing insecticides and fungicide.

The world's first sheep dip was invented and produced by George Wilson of Coldstream, Scotland, in 1830. That dip was based on arsenic powder and was exported by package steamer from nearby Berwick-upon-Tweed. [1] One of the most successful brands of dip to be brought to market was Cooper's Dip, which was developed in 1852 by the veterinary surgeon and industrialist William Cooper of Berkhamsted, England. [2]

Design

Sheep dip is available as wettable powders, pastes, solutions, or suspensions which are used to prepare diluted solutions or suspensions. The term is used both for the formulation itself, and the trough in which the sheep is completely immersed.

There are two broad classes of sheep dip: organophosphorus compounds, from which chemical warfare agents were later developed, and synthetic pyrethroids.[ citation needed ] Organophosphorus compounds are very toxic to humans exposed even to very low doses, as they travel easily through the skin, and are cumulatively toxic. [3]

Plunge sheep dips may be permanent in-ground structures, often of concrete, or mobile transportable steel structures. Invented after the permanent plunge dip was the rotating, power spray dip. These dips are redundant in the major sheep breeding countries, as the backliners and jetting provide a better alternative.

Negative health and environmental effects

Sheep dips have been found to cause soil contamination and water pollution. [4] They contain chemical insecticides that are highly toxic to aquatic plants and animals. [5] For this reason, it is important that the dip and dipped sheep are well managed to avoid spreading the chemicals and causing water pollution.

Some chemicals used in sheep dips are known to have been harmful. A sheep dip based on organo-phosphates has resulted in neurological conditions known as "OP poisoning". [6]

See also

Related Research Articles

Pyrethrum was a genus of several Old World plants now classified in either Chrysanthemum or Tanacetum which are cultivated as ornamentals for their showy flower heads. Pyrethrum continues to be used as a common name for plants formerly included in the genus Pyrethrum. Pyrethrum is also the name of a natural insecticide made from the dried flower heads of Chrysanthemum cinerariifolium and Chrysanthemum coccineum. The insecticidal compounds present in these species are pyrethrins.

<span class="mw-page-title-main">Parathion</span> Chemical compound

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.

<span class="mw-page-title-main">Chlorfenvinphos</span> Chemical compound

Chlorfenvinphos is an organophosphorus compound that was widely used as an insecticide and an acaricide. The molecule itself can be described as an enol ester derived from dichloroacetophenone and diethylphosphonic acid. Chlorfenvinphos has been included in many products since its first use in 1963. However, because of its toxic effect as a cholinesterase inhibitor it has been banned in several countries, including the United States and the European Union. Its use in the United States was cancelled in 1991.

<span class="mw-page-title-main">Organophosphate</span> Organic compounds with the structure O=P(OR)3

In organic chemistry, organophosphates are a class of organophosphorus compounds with the general structure O=P(OR)3, a central phosphate molecule with alkyl or aromatic substituents. They can be considered as esters of phosphoric acid. Organophosphates are best known for their use as pesticides.

Demeton-S-methyl is an organic compound with the molecular formula C6H15O3PS2. It was used as an organothiophosphate acaricide and organothiophosphate insecticide. It is flammable. With prolonged storage, Demeton-S-methyl becomes more toxic due to formation of a sulfonium derivative which has greater affinity to the human form of the acetylcholinesterase enzyme, and this may present a hazard in agricultural use.

<span class="mw-page-title-main">Fenthion</span> Chemical compound

Fenthion is an organothiophosphate insecticide, avicide, and acaricide. Like most other organophosphates, its mode of action is via cholinesterase inhibition. Due to its relatively low toxicity towards humans and mammals, fenthion is listed as moderately toxic compound in U.S. Environmental Protection Agency and World Health Organization toxicity class.

<span class="mw-page-title-main">Azinphos-methyl</span> Chemical compound

Azinphos-methyl (Guthion) is a broad spectrum organophosphate insecticide manufactured by Bayer CropScience, Gowan Co., and Makhteshim Agan. Like other pesticides in this class, it owes its insecticidal properties to the fact that it is an acetylcholinesterase inhibitor. It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act, and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities.

<span class="mw-page-title-main">Phosmet</span> Organophosphate non-systemic insecticide

Phosmet is a phthalimide-derived, non-systemic, organophosphate insecticide used on plants and animals. It is mainly used on apple trees for control of codling moth, though it is also used on a wide range of fruit crops, ornamentals, and vines for the control of aphids, suckers, mites, and fruit flies.

<span class="mw-page-title-main">Dimethoate</span> Chemical compound

Dimethoate is a widely used organophosphate insecticide and acaricide. It was patented and introduced in the 1950s by American Cyanamid. Like other organophosphates, dimethoate is an acetylcholinesterase inhibitor which disables cholinesterase, an enzyme essential for central nervous system function. It acts both by contact and through ingestion. It is readily absorbed and distributed throughout plant tissues, and is degraded relatively rapidly. One of the breakdown products of dimethoate is omethoate, a potent cholinesterase inhibitor, is ten times more toxic than its parent compound.

<span class="mw-page-title-main">Chlorethoxyfos</span> Chemical compound

Chlorethoxyfos is an organophosphate acetylcholinesterase inhibitor used as an insecticide. It is registered for the control of corn rootworms, wireworms, cutworms, seed corn maggot, white grubs and symphylans on corn. The insecticide is sold under the trade name Fortress by E.I. du Pont de Nemours & Company.

This is an index of articles relating to pesticides.

<span class="mw-page-title-main">Emamectin</span> Chemical compound

Emamectin is the 4″-deoxy-4″-methylamino derivative of abamectin, a 16-membered macrocyclic lactone produced by the fermentation of the soil actinomycete Streptomyces avermitilis. It is generally prepared as the salt with benzoic acid, emamectin benzoate, which is a white or faintly yellow powder. Emamectin is widely used in the US and Canada as an insecticide because of its chloride channel activation properties.

<span class="mw-page-title-main">Terbufos</span> Chemical compound

Terbufos is a chemical compound used in insecticides and nematicides. It is part of the chemical family of organophosphates. It is a clear, colourless to pale yellow or reddish-brown liquid and sold commercially as granulate.

<span class="mw-page-title-main">Triamiphos</span> Chemical compound

Triamiphos (chemical formula: C12H19N6OP) is an organophosphate used as a pesticide and fungicide. It is used to control powdery mildews on apples and ornamentals. It was discontinued by the US manufacturer in 1998.

<span class="mw-page-title-main">Triazofos</span> Chemical compound

Triazofos is a chemical compound used in acaricides, insecticides, and nematicides.

<span class="mw-page-title-main">Trichloronate</span> Chemical compound

Trichloronate is a highly toxic organophosphate insecticide. It is used against vegetable fly larvae and soil pests.

<span class="mw-page-title-main">Ethiofencarb</span> Chemical compound

Ethiofencarb is a carbamate insecticide which is useful in controlling aphids on hard and soft fruits and some vegetables. It is not as dangerous as organophosphorous pesticides, but is considered highly toxic to humans in the UK, moderately toxic under US EPA classification, and highly toxic to aquatic life.

<span class="mw-page-title-main">Hexaethyl tetraphosphate</span> Chemical compound

Hexaethyl tetraphosphate (also known as HETP) is the organophosphorus compound with the chemical formula [(C2H5O)3P2O3]2O. The compound has not been isolated in pure form but appears to be a colorless liquid at room temperature. Commercial samples appear brown due to impurities. It is a constituent of the insecticide Bladan. In the 1940s, it was about as significant an insecticide as DDT and was referred to as "another of DDT's rivals for fame" in a 1948 book.

Flag dipping refers to the movement of a flag as a signal.

References

  1. W. E. Howden - The Oldest Pet Food Shop in Britain Retrieved 2010-12-10
  2. "The famous dip the helped cure the scourge of Sheep". Dacorum Heritage Trust. Archived from the original on 3 March 2016. Retrieved 18 March 2016.
  3. Booker, Christopher (10 March 2002). "Ministers hushed up report on the dangers of sheep dip". The Daily Telegraph .
  4. "Managing old sheep dip and footbath sites: a guideline for landowners" (PDF). January 2003. Archived from the original (PDF) on 2010-05-23. Retrieved 2010-05-22.
  5. "Manage water on land: guidance for land managers". environment-agency.gov.uk. Archived from the original on 2013-12-03.
  6. Tom Levitt (20 April 2015). "Revealed: government knew of farm poisoning risk but failed to act". The Guardian . London. Retrieved 29 November 2017.