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Source: Landcare Research (1964). Control of poisons. Royal ...

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1080 Reassessment Application October 2006<br />

Appendix C<br />

Cappenberg, T. E. and Prins, R. A. (1974). Interrelations between sulfate-reducing and methane-producing<br />

bacteria in bottom deposits <strong>of</strong> a fresh-water lake. III. experiments with 14 -C labelled substrates. Antonie van<br />

Leeuwenhoek 40, 457-469.<br />

Keywords: bacteria/fluoroacetate/inhibition/toxicity<br />

Abstract: An ecological substrate relationship between sulfate-reducing and methane-producing bacteria in<br />

14-C labeled acetate and lactate as substrates. Fluoroacetate strongly<br />

mud <strong>of</strong> Lake Vechten has been studied in experiments using<br />

inhibited the formation <strong>of</strong> 14CO2 from [U-14C]-acetate and β-fluorolactate gave an inhibition <strong>of</strong> similar magnitude <strong>of</strong> the breakdown <strong>of</strong> [U-14C]-L-lactate to 14CO2<br />

thus confirming earlier results on the specific action <strong>of</strong> these inhibitors.<br />

Carrell, H. L., Glusker, J. P., Villafranca, J. J., Mildvan, A. S., Dummel, R. J., and Kun, E. (1970).<br />

Fluorocitrate inhibition <strong>of</strong> aconitase : relative configuration <strong>of</strong> inhibitory isomer by X-ray crystallography.<br />

Science 170, 1412-1414.<br />

Keywords: product chemistry/mode <strong>of</strong> action<br />

Abstract: The fluorocitrate isomer that is a strong inhibitor and inactivator <strong>of</strong> aconitase has been shown by<br />

x-ray crystallographic studies on the rubidium ammonium salt to have the configurations (1R:2R) or<br />

(1S:2S) 1-fluoro-2-hydroxy-1,2,3-propanetricarboxylic acid. A possible mechanism for the action <strong>of</strong><br />

fluorocitrate is proposed which involves the 1R:2R isomer suggested from biochemical data.<br />

Casper, H. H., McMahon, T. L., and Paulson, G. D. (1984). Sodium fluoroacetate levels in canine tissues.<br />

Proceedings <strong>of</strong> the Annual Meeting <strong>of</strong> the American Association <strong>of</strong> Veterinary Laboratory Diagnosticians<br />

26 (1983 Meeting), 155-160.<br />

Keywords: acute toxicity/non-target species/persistence in animals/sodium<br />

fluoroacetate/fluoroacetate/1080/poisoning/dogs/liver/kidney/secondary poisoning/analysis<br />

Abstract: Sodium fluoroacetate (1080) poisoning in dogs is a continuing problem. A recently developed<br />

assay for 1080 in tissue was applied to tissues from field cases <strong>of</strong> suspected 1080 toxicosis in dogs. The<br />

assay utilizes C14-1080 internal standards and capillary gas chromatography / mass spectrometry to give<br />

clear identification <strong>of</strong> 1080 levels down to 10 ppb tissue equivalent. The 1080 levels in tissues from field<br />

cases <strong>of</strong> 1080 toxicosis ranged from 45 to 5451 ppb for liver (n=11) and 55 to 297 ppb for kidney (n=5).<br />

There were no clear differences in liver 1080 levels for primary poisoning cases vs levels in suspected<br />

secondary poisoning cases. For routine diagnostic use a 1080 analysis must be reliable at the 20 ppb tissue<br />

level.<br />

Casper, H. H., McMahon, T. L., and Paulson, G. D. (1985). Capillary gas chromatographic-mass<br />

spectrometric determination <strong>of</strong> fluoroacetate residues in animal tissues. Journal <strong>of</strong> the Association <strong>of</strong><br />

Official Analytical Chemists 68, 722-725.<br />

Keywords: fluoroacetate/acetate/analysis<br />

Abstract: A method for the quantitative determination <strong>of</strong> fluoroacetate (FAC) (a rodenticide) residues in<br />

animal tissues is described. The procedure involves tungstic acid extraction, partitioning into ethyl acetate,<br />

evaporation <strong>of</strong> ethyl acetate, derivation with pentafluorobenzyl bromide (PFB), and analysis <strong>of</strong> the resulting<br />

derivative (PFB-FAC) by capillary gas chromatography-mass spectrometry (CGC-MS) with specific ion<br />

monitoring (SIM). The tungstic acid system extracted 96.8 +- 4.2% <strong>of</strong> the endogenous 14C-1080 residues<br />

in rat tissues. Recovery <strong>of</strong> FAC during the extraction, purification, and derivatization procedures is<br />

established by use <strong>of</strong> a 14C-FAC spike. 1,2-Dibromobenzene is used as an internal standard for the CGC-<br />

MS analysis. PFB-FAC is identified on the basis <strong>of</strong> comparative retention times and the relative intensities<br />

<strong>of</strong> m/z 257.9 and 181.0. PFB-FAC is quantitated by comparing the response at m/z 257.9 to a PFB-FAC<br />

standard curve. Routine sensitivity <strong>of</strong> the method allows determination <strong>of</strong> 10 ppb fluoroacetate in tissue<br />

Casper, H. H., Mount, M. E., Marsh, R. E., and Schmidt, R. H. (1986). Fluoroacetate residues in ground<br />

squirrel and coyote tissues due to primary or secondary 1080 poisoning. Journal <strong>of</strong> the Association <strong>of</strong><br />

Official Analytical Chemists 69, 441-442.<br />

Keywords: acute toxicity/secondary poisoning/mammals/persistence in animals/1080<br />

Abstract: Fluoroacetate residues in various tissues <strong>of</strong> 1080 poisoned ground squirrels and coyotes are listed.<br />

The tissues (excluding the stomach) <strong>of</strong> squirrels poisoned with an average <strong>of</strong> 0.8mg 1080/kg (low dose)<br />

contained from 182 to 1309 ppb Fluoroacetate. In squirrels poisoned with an average <strong>of</strong> 4.8 mg 1080/kg<br />

(high dose), the tissue residues ranged from 535 to 9754 ppb Fluoroacetate. Tissues from coyotes which<br />

died after consuming 1080 poisoned ground squirrels were also analyzed for fluoroacetate residues.<br />

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