Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Herbicide mechanisms

The growth inhibitory mechanism of the thiocarbamate herbicides, eg, EPTC, butylate, cycloate, diaHate, and triaHate, is not well defined. Cell elongation, rather than cell division, appears to be inhibited (183), although mitotic entry may be inhibited by diaHate (184). Thiocarbamates have a greater effect on shoot than toot tissue (163,184). The weU-documented inhibition of Hpid synthesis by thiocarbamates certainly contributes to the observed inhibitions of cell division and elongation. These compounds may also inhibit gibbereUic acid synthesis (185). [Pg.46]

Chemical, cultural, and mechanical weed control practices have been relatively successful ia reducing yield losses from weeds (448). However, herbicide-resistant weed populations, soil erosion, pesticide persistence ia the environment, and other problems associated with technologies used (ca 1993) to control weeds have raised concerns for the long-term efficacy and sustainability of herbicide-dependent crop production practices (449). These concerns, coupled with ever-increasing demands for food and fiber, contribute to the need for innovative weed management strategies (450). [Pg.55]

Nonchemical or traditional practices, such as weed seed removal, optimal crop seeding rates, crop selection, enhanced crop competitiveness, crop rotation, and mechanical weed control are all important components of an effective weed management program (458,459). In the context of modern intensive chemical herbicide appHcation, nonchemical practices may even represent an innovative approach to weed management and should receive careful consideration. [Pg.55]

Hydrophobic interactions and trapping of molecules in a molecular sieve formed by humic materials have been hypothesized as retention mechanisms for prometryn. It has been shown that fluridone, fluazifop, and bipyridyhum herbicides penetrate into interlamellar spaces of smectites and can become trapped. [Pg.221]

The second most important (3%) use of sodium chlorate in 1990 was as an intermediate in the production of other chlorates and of perchlorates. The use of sodium chlorate as in agricultural appHcation amounted to about 7000 metric tons in 1990. The agricultural use of sodium chlorate is as a herbicide, as a defoHant for cotton (qv). Magnesium chlorate is used as a desiccant for soybeans to remove the leaves prior to mechanical picking (see Desiccants). [Pg.501]

Baler, manual package in feed, mechanized closing — Baler hag 23 X 30 585 X 760 2-140 Glued 12, 5-lh (2.3 kg) hags herbicide 45 721 —325 mesh... [Pg.1960]

We showed that these mesoporous silica materials, with variable pore sizes and susceptible surface areas for functionalization, can be utilized as good separation devices and immobilization for biomolecules, where the ones are sequestered and released depending on their size and charge, within the channels. Mesoporous silica with large-pore-size stmctures, are best suited for this purpose, since more molecules can be immobilized and the large porosity of the materials provide better access for the substrates to the immobilized molecules. The mechanism of bimolecular adsorption in the mesopore channels was suggested to be ionic interaction. On the first stage on the way of creation of chemical sensors on the basis of functionalized mesoporous silica materials for selective determination of herbicide in an environment was conducted research of sorption activity number of such materials in relation to 2,4-D. [Pg.311]

Problem 16.17 1 The herbicide oxyfluorfen can be prepared by reaction between a phenol and an aryl fluoride. Propose a mechanism. [Pg.574]

To control weeds, approximately 90% of U.S. agricultural acreage is treated with nonchemical, mechanical weed controls, such as mechanical cultivation and rotary hoes (15), whereas only about 25% receives treatment with herbicides (13). [Pg.314]

Mechanism of action can be an important factor determining selectivity. In the extreme case, one group of organisms has a site of action that is not present in another group. Thus, most of the insecticides that are neurotoxic have very little phytotoxicity indeed, some of them (e.g., the OPs dimethoate, disyston, and demeton-5 -methyl) are good systemic insecticides. Most herbicides that act upon photosynthesis (e.g., triaz-ines and substituted ureas) have very low toxicity to animals (Table 2.7). The resistance of certain strains of insects to insecticides is due to their possessing a mutant form of the site of action, which is insensitive to the pesticide. Examples include certain strains of housefly with knockdown resistance (mutant form of Na+ channel that is insensitive to DDT and pyrethroids) and strains of several species of insects that are resistant to OPs because they have mutant forms of acetylcholinesterase. These... [Pg.59]

These high levels were sporadic and transitory. However, some of them were high enough to have caused phytotoxicity, and more work needs to be done to establish whether herbicides are having adverse effects upon populations of aquatic plants in areas highlighted in this study. It should also be borne in mind that there may have been additive or synergistic effects caused by the combinations of herbicides found in these samples. For example, urea herbicides such as diuron and chlortoluron act upon photosynthesis by a common mechanism, so it seems likely that any effects upon aquatic plants will be additive. Similarly, simazine and atrazine share a common mechanism of action. [Pg.263]

In addition to these mechanisms, the degradation of thiocarbamates may be carried out in Rhodococcus erythropolis NI86/21 by a herbicide-inducible nonheme haloperoxidase (de Schrijver et al. 1997). [Pg.323]

Chlorinated anilines are produced by the hydrolysis of a range of acetanilide, urea, and carbamate herbicides, and are therefore widely distributed in agricultural soils. Mechanisms for their loss... [Pg.489]

Nitrophenols are phytotoxic, and dinoseb (6-iec-butyl-2,4-dinitrophenol) has been used as a herbicide, while nitrophenols have been detected in rainwater and plausible mechanisms for their abiotic formation have been proposed (Kohler and Heeb 2003 Vione et al. 2005). The pathway for the degradation of phenols with a single nitro group depends on the position of the substituents, while... [Pg.514]


See other pages where Herbicide mechanisms is mentioned: [Pg.253]    [Pg.39]    [Pg.44]    [Pg.44]    [Pg.44]    [Pg.44]    [Pg.46]    [Pg.47]    [Pg.48]    [Pg.52]    [Pg.53]    [Pg.53]    [Pg.55]    [Pg.221]    [Pg.221]    [Pg.327]    [Pg.24]    [Pg.309]    [Pg.283]    [Pg.285]    [Pg.87]    [Pg.118]    [Pg.120]    [Pg.137]    [Pg.314]    [Pg.144]    [Pg.263]    [Pg.107]    [Pg.588]    [Pg.672]   
See also in sourсe #XX -- [ Pg.271 ]




SEARCH



Crop selectivity mechanisms sulfonylurea herbicides

Herbicides resistance mechanisms

Herbicides, mechanism of action

Mechanism of herbicidal action

Mechanisms of Herbicide Safener Action

© 2024 chempedia.info