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  2. Rodenticide - Wikipedia

    en.wikipedia.org/wiki/Rodenticide

    Rodenticides are chemicals made and sold for the purpose of killing rodents. While commonly referred to as " rat poison ", rodenticides are also used to kill mice , woodchucks , chipmunks , porcupines , nutria , beavers , [ 1 ] and voles .

  3. American kestrel - Wikipedia

    en.wikipedia.org/wiki/American_kestrel

    Several other colloquial names for the kestrel are also in use, including grasshopper hawk, due to its diet, and killy hawk, due to its distinct call. [9] As noted in the introduction, DNA analysis shows the American kestrel to actually be genetically more closely related to the larger American falcons [2] [3] than to the true kestrels. However ...

  4. Pyrinuron - Wikipedia

    en.wikipedia.org/wiki/Pyrinuron

    Pyrinuron (Pyriminil, Vacor) is a chemical compound formerly used as a rodenticide. [1] Commercial distribution was voluntarily suspended in 1979 and it is not approved by the Environmental Protection Agency for use in the United States. [2]

  5. San Joaquin kit fox - Wikipedia

    en.wikipedia.org/wiki/San_Joaquin_Kit_Fox

    The San Joaquin kit fox (Vulpes macrotis mutica) is an endangered species of fox that was formerly very common in the San Joaquin Valley and much of Central California.As an opportunistic hunter, the San Joaquin kit fox primarily preys on kangaroo rats but also targets white-footed mice, pocket mice, ground squirrels, rabbits, and ground-nesting birds.

  6. Difenacoum - Wikipedia

    en.wikipedia.org/wiki/Difenacoum

    Because other species of mammals and birds may prey upon affected rodents, or directly ingest rodenticide bait, there is a risk of primary, secondary or tertiary exposure; examples are described in a 2012 publication on veterinary toxicology. [3]

  7. Chlorophacinone - Wikipedia

    en.wikipedia.org/wiki/Chlorophacinone

    The rodenticide was found to metabolized in the liver. Metabolism is mediated by cytochrome P450 isozymes and ring hydroxylation also appears to be an important biotransformation step. Hydroxylation occurs on the phenyl and indandionyl rings, [ 13 ] these metabolites can then further undergo conjugation with glucuronic acid prior to entering ...

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