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  2. Ioxynil - Wikipedia

    en.wikipedia.org/wiki/Ioxynil

    Ioxynil is a post-emergent [4] selective nitrile herbicide. It is used in Australia, New Zealand [5] and Japan [6] to control broadleaf weeds via the inhibition of photosynthesis. It is used notably on onion crops, [7] among others, normally at 300–900 g/Ha. [8] It was introduced in 1966.

  3. Halosulfuron-methyl - Wikipedia

    en.wikipedia.org/wiki/Halosulfuron-methyl

    Halosulfuron-methyl is a sulfonylurea post-emergence herbicide used to control some annual and perennial broad-leaved weeds and sedges (such as nutsedge/nutgrass) in a range of crops (particularly rice), established landscape woody ornamentals and turfgrass. [citation needed] It is marketed under several tradenames including Sedgehammer [2] and ...

  4. Category:Post-emergent herbicides - Wikipedia

    en.wikipedia.org/wiki/Category:Post-emergent...

    Pages in category "Post-emergent herbicides" The following 4 pages are in this category, out of 4 total. This list may not reflect recent changes. A. Alloxydim; Q.

  5. Mesotrione - Wikipedia

    en.wikipedia.org/wiki/Mesotrione

    The triketone herbicides were found to be effective on a wide range of commercially-important weed species and to have both pre- and post-emergence activity. [9] Mesotrione was chosen for development (by Zeneca Agrochemicals under the code number ZA1296) because it controls a wide range of broad-leaved weeds that compete with maize and can also suppress some annual grass weeds that may be ...

  6. Are Weeds Actually Bad For Your Lawn? - AOL

    www.aol.com/weeds-actually-bad-lawn-030000903.html

    Post-emergent herbicides can be used more selectively, but also pose environmental risks, including toxicity to birds, bees, and mammals that consume or contact them.

  7. Bromoxynil - Wikipedia

    en.wikipedia.org/wiki/Bromoxynil

    Under aerobic conditions in soils or pure cultures, products of bromoxynil degradation often retain the original bromine groups. The herbicide, and one of its common degradation products (3,5-dibromo-4-hydroxybenzoic acid) have been shown to undergo metabolic reductive dehalogenation by the microorganism Desulfitobacterium chlororespirans. [6]