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Pesticide Subject

The document lists common technical grade pesticides and recommended classihcations together with a listing of active ingredients believed to be obsolete or discontinued for use as pesticides, pesticides subject to the prior informed consent procedure, limitations to trade because of the Persistent Organic Pollutants (POPs) convention (UN 2001), and gaseous or volatile fumigants not classified under these recommendations. [Pg.15]

CONSENSUS REPORTS EPA FIFRA 1988 pesticide subject to registration or re-reg istration. EPA Genetic Toxicology Program. [Pg.155]

CONSENSUS REPORTS lARC Cancer Review Group 3 IMEMDT 7,56,87 Animal Inadequate Evidence IMEMDT 15,103,77. Reported in EPA TSCA Inventory. Copper and its compounds are on the Community Right-To-Know List. EPA FIFRA 1988 pesticide subject to registration or reregistration. [Pg.199]

CONSENSUS REPORTS Reported in EPA TSCA Inventory. EPA FIFRA 1988 pesticide subject to registration or registration. NCI Carcinogenesis Studies (derm), clear evidence mouse (derm), equivocal evidence rat SAFETY PROFILE A poison by ingestion. A moderate skin irritant. Questionable carcinogen with experimental Carcinogenic data reported. When heated to decomposition it emits acrid smoke and irritating vapors. [Pg.382]

This paper briefly examines the basis of spectrophotometry as a diagnostic method. It summarizes current and future applications of the method for detecting pesticides subject to enhanced degradation in soil. [Pg.241]

Pesticide subject to registration or re-registration acrolein, acrylaldehyde, acrylic aldehyde, allyl aldehyde, ethylene aldehyde... [Pg.468]

Milk and its products can be subjected to a variety of tests to determine composition, microbial quaUty, adequacy of pasteurization, contamination with antibiotics and pesticides (qv), and radioactivity (18). [Pg.363]

Discovery. The traditional approach to new pesticide discovery was to make iatuitive changes ia the substitueats oa a promising primary chemical stmcture. Initially, materials from any source were subjected to screening for biological activity as iasecticides, herbicides, or fungicides. [Pg.143]

Although most nonionic organic chemicals are subject to low energy bonding mechanisms, sorption of phenyl- and other substituted-urea pesticides such as diuron to sod or sod components has been attributed to a variety of mechanisms, depending on the sorbent. The mechanisms include hydrophobic interactions, cation bridging, van der Waals forces, and charge-transfer complexes. [Pg.221]

Pesticides can be transported away from the site of appHcation either in the atmosphere or in water. The process of volatili2ation that transfers the pesticide from the site of appHcation to the atmosphere has been discussed in detail (46). The off-site transport and deposition can be at scales ranging from local to global. Once the pesticide is in the atmosphere, it is subject to chemical and photochemical processes, wet deposition in rain or fog, and dry deposition. [Pg.222]

For carckiogen pesticides (70,71), animal testkigs are subject to maximum tolerated doses (M I L)). M I D is the maximum amount of a substance that can be administered to an experimental animal without causkig extreme health consequences, such as death, to occur but while continuing to produce some measurable toxic effects. Current regulatory theory holds that carckiogen effects do not have a threshold and caimot be related to reference doses. [Pg.235]

A professional society for persons in the environmental health field that conducts continuing education programs, placement sendees, awards programs, and compiles statistics on such subjects as air, water and land quality, food, pesticides, hazardous waste and toxic substances. [Pg.279]

Heterocyclic chemistry is of the utmost practical and theoretical importance. Heterocyclic compounds are in use as pharmaceuticals, dyes, pesticides, herbicides, plastics, and for many other purposes the industries producing and researching into these products provide employment for a large fraction of all chemists. On the theoretical side, heterocyclic chemistry has provided a host of interesting concepts and structures. Yet, the subject is often deprived of the importance it deserves it is said that it is possible to complete work at graduate schools of some universities without having attended a lecture course dealing specifically with heterocyclic chemistry. [Pg.483]

The only study located regarding immunological effects in humans after dermal exposure to endosulfan was an account of the results of patch tests on the backs of 14 farm workers with work-related dermatitis and 8 controls who were not exposed to pesticides (Schuman and Dobson 1985). Skin sensitization was not observed in any of the subjects following a 48-hour, closed-patch exposure to an unspecified amount of 0.1 % endosulfan in petrolatum. [Pg.117]

Many pesticides are not as novel as they may seem. Some, such as the pyre-throid and neonicotinoid insecticides, are modeled on natural insecticides. Synthetic pyrethroids are related to the natural pyrethrins (see Chapter 12), whereas the neo-nicotinoids share structural features with nicotine. In both cases, the synthetic compounds have the same mode of action as the natural products they resemble. Also, the synthetic pyrethroids are subject to similar mechanisms of metabolic detoxication as natural pyrethrins (Chapter 12). More widely, many detoxication mechanisms are relatively nonspecific, operating against a wide range of compounds that... [Pg.3]

Tables 2.6 and 2.7 give examples of the modes of action of pollutants in animals and in plants/fungi, respectively. It is noteworthy that many of the chemicals represented are pesticides. Pesticides are designed to be toxic to target species. On the other hand, manufacturers seek to minimize toxicity to humans, beneficial organisms and, more generally, nontarget species. Selective toxicity is an important issue. Regardful of the potential risks associated with the release of bioactive compounds into the environment, regulatory authorities usually require evidence of the mode of toxic action before pesticides can be marketed. Other industrial chemicals are not subject to such strict regulatory requirements, and their mode of action is frequently unknown. Tables 2.6 and 2.7 give examples of the modes of action of pollutants in animals and in plants/fungi, respectively. It is noteworthy that many of the chemicals represented are pesticides. Pesticides are designed to be toxic to target species. On the other hand, manufacturers seek to minimize toxicity to humans, beneficial organisms and, more generally, nontarget species. Selective toxicity is an important issue. Regardful of the potential risks associated with the release of bioactive compounds into the environment, regulatory authorities usually require evidence of the mode of toxic action before pesticides can be marketed. Other industrial chemicals are not subject to such strict regulatory requirements, and their mode of action is frequently unknown.
It is only very recently that organic componnds synthesized by humans have begun to exert a selection pressure upon natural populations, with the consequent emergence of resistant strains. Pesticides are a prime example and will be the principal subject of the present section. It should be mentioned, however, that other types of biocides (e.g., antibiotics and disinfectants) can produce a similar response in microbial populations that are exposed to them. [Pg.93]

The other major mechanism of pyrethroid resistance found in some field strains of Heliothis virescens was enhanced detoxication due to a high rate of oxidative detoxication, mediated by a form of cytochrome P450 (McCaffery 1998). Some strains, such as PEG 87, which was subjected to a high level of field and laboratory selection, possessed both mechanisms. Other example of pyrethroid resistance due to enhanced detoxication may be found in the literature on pesticides. [Pg.238]


See other pages where Pesticide Subject is mentioned: [Pg.160]    [Pg.49]    [Pg.662]    [Pg.386]    [Pg.177]    [Pg.669]    [Pg.160]    [Pg.49]    [Pg.662]    [Pg.386]    [Pg.177]    [Pg.669]    [Pg.146]    [Pg.148]    [Pg.150]    [Pg.108]    [Pg.458]    [Pg.468]    [Pg.27]    [Pg.28]    [Pg.34]    [Pg.81]    [Pg.49]    [Pg.131]    [Pg.3]    [Pg.5]    [Pg.211]    [Pg.476]    [Pg.195]    [Pg.1]    [Pg.8]   
See also in sourсe #XX -- [ Pg.495 ]




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