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The names on the list are the ISO common name for the active ingredient which is formulated into the branded product sold to end-users. [1] The University of Hertfordshire maintains a database of the chemical and biological properties of these materials, [2] including their brand names and the countries and dates where and when they have been ...
One major complication to the use of herbicides for weed control is the ability of plants to evolve herbicide resistance, rendering the herbicides ineffective against target plants. Out of 31 known herbicide modes of action, weeds have evolved resistance to 21. 268 plant species are known to have evolved herbicide resistance at least once. [ 59 ]
Pages in category "Herbicides" The following 136 pages are in this category, out of 136 total. This list may not reflect recent changes. ...
Oxyfluorfen is a diphenyl ether herbicide and acts via inhibition of protoporphyrinogen oxidase, (destroying chlorophill production and cell membranes), [3] making its HRAC resistance class Group G (Aus), [5] Group E (Global) and 14 (numerical). [6] Oxyfluorfen suffers from poor translocation, despite rapid shoot and foliar uptake.
In the same report, it added the "yield loss plus increased herbicide cost may result in an average estimated loss of $28 per acre" if atrazine were unavailable to corn farmers. [4] In 2006, the EPA concluded that the triazine herbicides posed "no harm that would result to the general U.S. population, infants, children or other... consumers." [5]
The Herbicide Resistance Action Committee (HRAC) classifies herbicides by their mode of action (MoA) to provide a uniform way for farmers and growers to identify the agents they use and better manage pesticide resistance around the world. [1] [2] It is run by CropLife International [3] in conjunction with the Weed Science Society of America ...
The best known phenoxy herbicides are (4-chloro-2-methylphenoxy)acetic acid , 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). [2] Analogues of each of these three compounds, with an extra methyl group attached next to the carboxylic acid, were subsequently commercialised as mecoprop, dichlorprop and fenoprop.
The names on the list are the ISO common names. A complete list of pesticide common names is published by the BCPC. [1] The University of Hertfordshire maintains a database of the chemical and biological properties of these materials, [2] including their brand names and the countries and dates where and when they have been introduced. [3]
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