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Soil residue definition

The crop residue definition includes parent flucarbazone-sodium and the A/-desmethyl flucarba-zone metabolite (I). The soil and water residue definitions include parent flucarbazone-sodium and the sulfonic acid, sulfonamide and A/,0-dimethyl triazoli-none (NODT) metabolites... [Pg.490]

The polar character of neonicotinoids makes them, in general, potentially mobile in soil. Acetamiprid and nitenpyram have short soil persistence. Imidacloprid and thi-amethoxam, however, are sufficiently persistent in soil to be used for soil treatment. The definition of soil residues for the various neonicotinoid compounds except for imidacloprid are the parent compound and it metabolites. The metabolites of acetamiprid are lM-1-2, lM-1-4 and lC-0 (Figure 6). The metabolites of nitenpyram are 2-[N-(6-chloro-3-pyridyl-methyl)-A-ethyl]amino-2-methyliminoacetic acid (CPMA) and A-(6-chloro-3-pyridylmethyl)-Ai-ethyl-A -methylformamidine] (CPMF). [Pg.1138]

Oxime carbamates are generally applied either directly to the tilled soil or sprayed on crops. One of the advantages of oxime carbamates is their short persistence on plants. They are readily degraded into their metabolites shortly after application. However, some of these metabolites have insecticidal properties even more potent than those of the parent compound. For example, the oxidative product of aldicarb is aldicarb sulfoxide, which is observed to be 10-20 times more active as a cholinesterase inhibitor than aldicarb. Other oxime carbamates (e.g., methomyl) have degradates which show no insecticidal activity, have low to negligible ecotoxicity and mammalian toxicity relative to the parent, and are normally nondetectable in crops. Therefore, the residue definition may include the parent oxime carbamate (e.g., methomyl) or parent and metabolites (e.g., aldicarb and its sulfoxide and sulfone metabolites). The tolerance or maximum residue limit (MRL) of pesticides on any food commodity is based on the highest residue concentration detected on mature crops at harvest or the LOQ of the method submitted for enforcement purposes if no detectable residues are found. For example, the tolerances of methomyl in US food commodities range from 0.1 to 6 mg kg for food items and up to 40 mg kg for feed items. ... [Pg.1153]

Regulatory position The residue definition consists of tebuconazole alone for crops, soil, and water... [Pg.1233]

The residue definition for plant samples is acetamiprid only. In soil, it includes acetamiprid and three of its... [Pg.1242]

In addition to the residual soils, transported soils are also found in the tropics, though in terms of coverage, but not necessarily in the order of significance, they are less in extent than the residual soils. Transported soils by definition are soils that are formed from materials formed elsewhere and which have moved to the present site where they constitute the unconsolidated superficial layer. The physical processes through the operation of their agents of transportation i.e. mainly gravity and water have dislodged, eroded and transported soil particles to their present location. [Pg.4]

Clomeprop, naproanilide, propanil and pentanochlor are unstable to sunlight in/on the soil surface. The definition of residues in soil samples is summarized below. [Pg.336]

Agricultural waste. To prevent overregulation of farms and promote waste recycling, solid wastes generated by crop or animal farming are excluded from the definition of hazardous waste provided that the wastes are returned to the ground as fertilizers or soil conditioners. Examples of such wastes are crop residues and manures. [Pg.495]

An important benefit of the isotopic approach is that below-ground biomass values are not required. The 13C natural abundance isotopic carbon budget approach is based on C3 plants having lower 13C value than C4 plants (Ehleringer 1991 Clay et al. 2006) and that the signatures can be tracked by placing C3 plant residue into a soil derived from C4 plants or vice versa. In these calculations, several definitions are needed. These definitions include... [Pg.204]

The humic/organic matter coatings of different solid phases (i. e., SPm /SP0M), such as soils, sediments, suspended solids, colloids, and biocolloids/biosolids, interact with organic pollutants in aqueous systems in various ways. Adsorption is an important interaction mode. The reversibility and/or irreversibility of the adsorption processes is of major importance. The question whether the bound residues of pollutants are to be considered definitely inactivated has been the focus of extensive research. This question was posed as follows. Have the adsorbed pollutants become common components incorporated into the humic polymer coating of solid phases (i. e., being absorbed), or are they only momentarily inactivated in reversibly bound forms thus representing a possible source of pollution by a time-delayed release of toxic units ... [Pg.158]

The term bound residue was adopted by the International Union of Pure and Applied Chemistry (lUPAC) in 1984. According to this definition and that of the European Commission (adopted in 1991), nonextractable residues in soil are... [Pg.123]

Fuhr F, Ophoff H, Burauel P. Wanner U, Haider K (1998) Modification of definition of bound residues. In Fuhr F, Phoff H (eds) Pesticide bound residues in soils. Wiley-VCH, Weinheim, pp 175-176... [Pg.389]

These definitions were essentially the same as those put forward by Berzelius. Mulder considered, however, that, besides humus substances, products from the decomposition of organic residues, such as leucine, butyric acid, valeric acid, and formic and ethanoic acids, could exist in soil. These observations are of interest because of the information that has emerged in the past half-century about growth inhibitors and stimulators from low-molecular-weight extracts from SOM and composts. [Pg.7]

In operationally defined speciation the physical or chemical fractionation procedure applied to the sample defines the fraction isolated for measurement. For example, selective sequential extraction procedures are used to isolate metals associated with the water/acid soluble , exchangeable , reducible , oxidisable and residual fractions in a sediment. The reducible, oxidisable and residual fractions, for example, are often equated with the metals associated, bound or adsorbed in the iron/manganese oxyhydroxide, organic matter/sulfide and silicate phases, respectively. While this is often a convenient concept it must be emphasised that these associations are nominal and can be misleading. It is, therefore, sounder to regard the isolated fractions as defined by the operational procedure. Physical procedures such as the division of a solid sample into particle-size fractions or the isolation of a soil solution by filtration, centrifugation or dialysis are also examples of operational speciation. Indeed even the distinction between soluble and insoluble species in aquatic systems can be considered as operational speciation as it is based on the somewhat arbitrary definition of soluble as the ability to pass a 0.45/Am filter. [Pg.4]

SOM is composed of a continuum of organic resources from fresh plant residues to stabilized organic matter (OM) or humus (Stevenson, 1994). Although this definition of SOM includes intact plant litter, in this review we will often distinguish between decomposition of litter on the soil surface and decomposition/stabilization of OM within the mineral soil. Within the mineral soil, SOM is often divided into four categories the light fraction, microbial biomass (discussed above), dissolved organic matter (DOM), and stable humic substances. [Pg.4118]


See other pages where Soil residue definition is mentioned: [Pg.336]    [Pg.25]    [Pg.471]    [Pg.65]    [Pg.152]    [Pg.52]    [Pg.27]    [Pg.78]    [Pg.14]    [Pg.124]    [Pg.70]    [Pg.306]    [Pg.42]    [Pg.48]    [Pg.6]    [Pg.28]    [Pg.43]    [Pg.45]    [Pg.197]    [Pg.177]    [Pg.506]    [Pg.120]    [Pg.254]   
See also in sourсe #XX -- [ Pg.336 ]




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Soil residues

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