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Total toxic residue

The Total toxic residue analytical method is provided for plant, soil and water samples. [Pg.542]

All of the compounds (pyraflufen-ethyl and its metabolites) are converted to E-2 and quantified as the total toxic residue of pyraflufen-ethyl. The conversion to E-2 is carried out by oxidative decomposition with concentrated sulfuric acid. The reaction mixture is extracted with a solvent and subjected to simple cleanup, followed by GC/NPD analysis. This method is rapid and simple compared with the Multi-residue analytical method , and has wide applicability to different varieties of the samples, such as plant materials, soils and water, with only minor adjustment of the analytical method. [Pg.542]

One shortcoming in many field studies is a failure to address adequately exposure to toxic transformation products. In efforts to manage time and cost constraints, the concentrations of parent materials and transformation products are often added together to produce a total toxic residue amount. However, it is more appropriate to evaluate individual transformation products as their toxicity may be significantly increased (e.g. active oxons) or decreased (e.g. dehalogenation or dealkylation products) relative to the parent compound. [Pg.940]

Total toxic residue analytical method (for rice plant)... [Pg.1202]

In the Total toxic residue analytical method , careful handling is recommended for concentrating steps to prevent the loss of volatile 2-TFBA and 2-TFBA Me-ester. [Pg.1206]

At the Florida field site, we evaluated the significance of tillage-induced extrinsic variability in bromide (Br) and aldicarbfs total toxic residues (TTR) variability. [Pg.106]

Determination of the Total Toxic Aldlcarb Residue In Water", Union Carbide Corporation, 1980. [Pg.260]

By the fifth hour, I was mending the physical zombie is not there anymore. I can ignore the crawling. At the ten hour point I am still dilated, and teeth rubby, and hypoxic. Something is still poisonous. Sleep not satisfactory. Restless, with strange mental interpretations. The next day, I am clear and totally without residues. This a,0-DMS is probably the most potent indolic psychedelic yet uncovered, at least via the oral route. Any higher dose would require a babysitter, and I must remember that there is a big toxic component that is part of this trip."... [Pg.50]

The 1997 consultation addressed the topic of safety factors, which is vitally important for die protection of public health. Setting MRLs is in fact based on a series of assumptions. One assumption is that humans are at least as sensitive as the most sensitive laboratory animal to a potentially toxic residue. Another assumption is diat all the residues covered by the MRLs are as toxic as the parent substance. A third assumption is that residues free from the human gastrointestinal tract are all totally bioavailable. A fourth assumption is the safety factor used to infer an ADI from a NOEL, including the additional safety factor, generally with a value of 2, to establish a provisional ADI until further information is available to convert this into a definite ADI. Other assumptions are the overestimation of consumer exposure to drug residues and the reduction of MRL values to take account of normal conditions under which the veterinary drugs are administered. [Pg.319]

DW Woodham, RG Reeves, RR Edwards. Total toxic aldicarb residues in weeds, grasses, and wildlife from the Texas high plains following a soil treatment with the insecticide. J Agric Food Chem 21 604-607, 1973. [Pg.713]

The procedure involves converting oxon to thion toxicity equivalents by multiplying the oxon value by its relative toxicity (ED of thion r ED,.q of oxon) in Table I. The ED. value is the aermal dose in ug/cnr of total body surface which produces 50% inhibition of red cell ChE activity 72 hours after application. The total thion and oxon level is then divided by the thion toxicity equivalents and the factor is multiplied by the safe level established for thion in Table I. This procedure was conducted for the dislodgeable residues of parathion-paraoxon, methidathion-methidathion oxon, and azinphosmethyl-azinphosmethyl oxon. The safe levels for the total disloggeable residues were determined to be 0.06, 0.2 and 1.6 ug/cm, respectively, for... [Pg.26]

Leslie, H.A., J.L.M. Hermens, and M.H.S. Kraak. 2004. Baseline toxicity of a chlorobenzene mixture and total body residues measured and estimated with solid-phase microextraction. Environ. Toxicol. Chem. 23 2017-2021. [Pg.92]

In the mechanistic models used to predict toxic effects of time-variable exposure to organisms, a distinction can be made between 1-step models and 2-step models (Ashauer et al. 2006). One-step models only consider toxicokinetics, whereas 2-step models consider both toxicokinetics and toxicodynamics. One-step models try to describe the uptake and elimination of a given compound in an organism and relate the calculated internal concentration to the effect occurring. Usually, an average total body residue is calculated, assuming that the concentration at the actual site(s) of action will be linearly related to the total body concentration. In specific cases, it may be necessary to calculate the concentration at the site of action through the use of more refined multicompartment (PBPK) models. [Pg.195]

Most of the work on the individual tolerance concept has focused on organic chemicals. One of the reasons may be that for metals a CBR on a whole body basis has only limited applicability. Due to compartmentalization of metals in the body and the presence of regulation and detoxification mechanisms, it is unlikely that the total body residue is simply related to toxicity (see, e.g., Lock and Janssen 2001 Vijver et al. 2004). The biotic ligand models (BLMs) assume a critical level of metal accumulation at the biotic ligand and do not include a time aspect, although more TD-like approaches have been suggested (Paquin et al. 2002b). [Pg.77]

However, the problem is greater in India as safety procedures and detoxification procedures advocated in developed countries are often not implemented totally. Human exposure to environmental chemicals can arise from inhalation, dermal contact, and ingestion of polluted water or food, especially those containing biomagnified toxic residues. The industrial and economic developments have changed the lifestyle of urban and rural populations considerably. This has also led to increased stress, thereby threatening health in general. [Pg.111]

The following notation will be used the price p of the chemical is a function of the total quantity sold, Q, and an index A, representing the reliability of the chemical this index will be referred to as the accumulation constant of the chemical. The inverse demand curve can therefore be written as p(Q, A). Consumers preferences for chemical persistence mean that marginal utility (and hence price) is increasing in the level of this characteristic, up to some critical point A after this point, concerns for toxic residues and personal safety mean that marginal utility/price decreases. Therefore dp/dA = p >OfoiA< A but < 0 for A > A and p < 0. As usual the price of the chemical decreases with the aggregate quantity sold (i.e. dp/dQ= Pq< 0). [Pg.188]

A typical sterilization process with EtO consists of a preconditioning phase, the actual sterilization run, and a period of poststerilization aeration to remove toxic residues, such as EtO, ethylene glycol (formed out of EtO and ambient humidity), and ethylene chlorohydrme (formed out of EtO and materials containing chlorine, such as PVC). In the medical device industry EtO is the most common sterilization method, used for over 70% of total sterilizations and 50% of all disposable medical devices. [Pg.53]

Fig. 7. Toxicity of chlorine to aquatic organisms, (a) Time-dependent mortaUty (50%) of four example species in various levels of total residual chlorine in the laboratory, where for A, A.losa aestivalis and B, Salmogairdnerii r (correlation coefficient of the curve) = —0.96 and for C, P/euroneetesplatessa and D, Salmo trutta r = —0.98. (b) A summary of chlorine toxicity to freshwater species, indicating overall no-effect thresholds for acute and chronic exposures. Numbers indicate where more than one test yielded the same result. A different summary figure appHes to marine organisms because of differences in the... Fig. 7. Toxicity of chlorine to aquatic organisms, (a) Time-dependent mortaUty (50%) of four example species in various levels of total residual chlorine in the laboratory, where for A, A.losa aestivalis and B, Salmogairdnerii r (correlation coefficient of the curve) = —0.96 and for C, P/euroneetesplatessa and D, Salmo trutta r = —0.98. (b) A summary of chlorine toxicity to freshwater species, indicating overall no-effect thresholds for acute and chronic exposures. Numbers indicate where more than one test yielded the same result. A different summary figure appHes to marine organisms because of differences in the...

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See also in sourсe #XX -- [ Pg.162 ]




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