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Proceedings of the International Cyanide Detection Testing Workshop

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Blennies, which were net-caught and exposed<br />

to cyanide. Both <strong>the</strong> test and <strong>the</strong> control<br />

fi sh (not exposed to cyanide) were found to<br />

exhibit cyanide levels <strong>of</strong> about 300 mg/L<br />

(ppm). Hence, <strong>the</strong> addition <strong>of</strong> lead carbonate<br />

to <strong>the</strong> solution prior to ISE testing did not<br />

eliminate <strong>the</strong> anomalously high readings.<br />

A second experiment evaluated whe<strong>the</strong>r<br />

<strong>the</strong> high readings might be due to iodide<br />

interference with <strong>the</strong> ISE. Again, <strong>the</strong><br />

experiment was inconclusive. In a third<br />

experiment, test fi sh (4 Caribbean Blue<br />

Chromis, 1 Atlantic Wrasse, and 3 Goldfi sh)<br />

were exposed to cyanide concentrations<br />

ranging from 1.3 to 3.9 ppm CN - for times<br />

ranging from one minute (for <strong>the</strong> 4 chromis)<br />

to 14 minutes (for a goldfi sh). Readings for<br />

control fi sh (1 wrasse and 2 goldfi sh) not<br />

exposed to cyanide produced higher mV<br />

readings than fi sh exposed to cyanide.<br />

Recent analyses by Ms. Benita Manipula<br />

using <strong>the</strong> Soundararajan procedure and<br />

cyanide measurements obtained using an<br />

Industrial Test Systems (ITS) colorimetric<br />

<strong>Cyanide</strong> Reagent Strip TM (<strong>Cyanide</strong> Test Kit<br />

484003) have also experienced diffi culty in<br />

obtaining reliable measurements <strong>of</strong> cyanide<br />

concentrations in comparison to known<br />

concentrations <strong>of</strong> cyanide ion in sodium<br />

hydroxide solution (lacking slurry). The<br />

problem does not appear to be related to<br />

<strong>the</strong> reliability <strong>of</strong> <strong>the</strong> ITS cyanide test strips,<br />

since <strong>the</strong>y have been demonstrated to be<br />

sensitive (down to 0.02 mg/L) and reliable<br />

for measuring cyanide ion concentrations in<br />

water (Battelle 2005).<br />

The most likely explanation for <strong>the</strong>se results<br />

is that organics in <strong>the</strong> digested tissue solutions<br />

containing sodium hydroxide produced <strong>the</strong><br />

anomalous readings both with <strong>the</strong> ISE and<br />

<strong>the</strong> ITS test strips. Dr. Frant suggested that<br />

<strong>the</strong>se could be volatile mercaptans from<br />

47<br />

sulfur-containing proteins. Fur<strong>the</strong>r research<br />

is needed to see whe<strong>the</strong>r it is possible to<br />

measure cyanide ion concentrations in<br />

solutions obtained from marine fi sh using<br />

<strong>the</strong> Soundararajan tissue digestion method. It<br />

does not appear likely that <strong>the</strong> Soundararajan<br />

procedure can be applied as a fi eld test (Rubec<br />

and Soundararajan 1991, Rubec and Manipula<br />

2008).<br />

Cyantesmo Screening Test<br />

The workshop committee agreed that it<br />

might be possible to digest fi sh samples in<br />

sulfuric acid in a closed container to release<br />

hydrogen cyanide (HCN) from <strong>the</strong> digested<br />

sample into <strong>the</strong> atmosphere <strong>of</strong> <strong>the</strong> container.<br />

Test strips mounted in <strong>the</strong> container (such as<br />

near <strong>the</strong> lid <strong>of</strong> a jar) might be able to provide<br />

a colorimetric indication for <strong>the</strong> presence <strong>of</strong><br />

cyanide ion. This approach would need fur<strong>the</strong>r<br />

research and fi eld evaluations. It is likely to<br />

only work near <strong>the</strong> point <strong>of</strong> collection in <strong>the</strong><br />

exporting countries; where cyanide ion is<br />

most likely to be present in <strong>the</strong> fi sh at higher<br />

concentrations.<br />

Actually, <strong>the</strong>re are several testing protocols<br />

based on this idea. The American Society<br />

<strong>of</strong> <strong>Testing</strong> and Materials (ASTM) published<br />

a screening method (D-5049) for screening<br />

cyanides in waste (ASTM 1990). The protocol<br />

involves adding 5 grams <strong>of</strong> organic sample<br />

to a sealed vial also containing concentrated<br />

sulfuric acid. Hydrogen cyanide released<br />

from <strong>the</strong> sample causes a color change<br />

with Cyantesmo paper suspended over <strong>the</strong><br />

sample.<br />

A similar screening protocol (Figure 1) is used<br />

by <strong>the</strong> U.S. Food and Drug Administration<br />

(FDA) to analyze various foodstuffs for <strong>the</strong><br />

presence <strong>of</strong> cyanide-including meat and<br />

vegetables (Flurer et al. 2005). It has been<br />

used to detect cyanide with tuna samples<br />

(both frozen and canned) spiked with cyanide.

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