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Proceedings of the International Cyanide Detection Testing Workshop

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<strong>of</strong> degradation on <strong>the</strong> scale <strong>of</strong> a reef. For<br />

example, Mouse et al. (Mouse, Pet-Soede<br />

et al., 2000) state that blast fi shing accounts<br />

for a loss in live coral cover <strong>of</strong> 3.75 m 2 per<br />

100 m 2 <strong>of</strong> reef each year (Pet and Pet-Soede,<br />

1999), which is about 75 times more than one<br />

estimate <strong>of</strong> cyanide impact, and still about 5–6<br />

times more than <strong>the</strong> ‘worst-case’ estimate for<br />

<strong>the</strong> loss <strong>of</strong> coral cover due to cyanide fi shing<br />

for food fi sh.<br />

O<strong>the</strong>r Toxins Used to Catch Fish<br />

<strong>Cyanide</strong> is <strong>the</strong> most widely used chemical in<br />

marine fi sh capture. However, o<strong>the</strong>r poisons<br />

are utilized as well. Clove oil (or eugenol in<br />

its purifi ed form) is a moderately well-known<br />

anes<strong>the</strong>tic for small fi shes and crustaceans<br />

(eg. Soto and Burhanuddin, 1995; Munday<br />

and Wilson, 1997; Erdman and Pet, 1999).<br />

Quinaldine is ano<strong>the</strong>r narcotic associated<br />

with <strong>the</strong> ornamental industry. It is reported<br />

to be less dangerous than cyanide, but<br />

capable <strong>of</strong> killing fi sh during collection when<br />

concentrations are high or exposure time is<br />

long (Randall, 1987). Bleach, formalin, and<br />

gasoline were reported to be used occasionally<br />

to catch aquarium fi sh in Puerto Rico in <strong>the</strong><br />

early 1990s (Sadovy, 1992), but <strong>the</strong> extent to<br />

which <strong>the</strong>y are used elsewhere is not known.<br />

There are no data available that quantify <strong>the</strong><br />

extent <strong>of</strong> use <strong>of</strong> <strong>the</strong>se chemicals.<br />

Non-Toxic Fish Collection<br />

An alternative to fi shing with toxic substances<br />

such as cyanide is to catch fi sh with small nets<br />

or to use hook and line. Numerous regional<br />

organizations train collectors in how to use<br />

<strong>the</strong>se non-destructive methods. Despite <strong>the</strong><br />

training, collectors have been slow to switch<br />

to using nets because <strong>the</strong>y can earn more<br />

using cyanide. In some cases it is possible<br />

to pay <strong>the</strong> collector a premium price for fi sh<br />

caught in a non-destructive manner (Barber<br />

and Pratt, 1997).<br />

100<br />

Existing <strong>Cyanide</strong> <strong>Detection</strong> Tests<br />

Because <strong>of</strong> <strong>the</strong> fact that cyanide can damage<br />

<strong>the</strong> marine environment and potentially<br />

decrease <strong>the</strong> mortality <strong>of</strong> fi sh sold in <strong>the</strong><br />

commercial trade, <strong>the</strong> use <strong>of</strong> cyanide to<br />

capture fi sh is illegal in nearly all countries<br />

where it is commonly used. In order to enforce<br />

<strong>the</strong> law and monitor <strong>the</strong> presence <strong>of</strong> cyanide<br />

in fi sh, <strong>the</strong> <strong>International</strong> Marinelife Alliance-<br />

Philippines (IMA) and <strong>the</strong> Philippine Bureau<br />

<strong>of</strong> Fisheries and Aquatic Resources (BFAR)<br />

have developed a cyanide detection test (CDT)<br />

to determine <strong>the</strong> presence <strong>of</strong> cyanide in livecaught<br />

fi sh. The American Analytical <strong>Testing</strong><br />

Laboratory supported <strong>the</strong> development <strong>of</strong><br />

<strong>the</strong> test (Mak, Yanase et al., 2005).<br />

The fi rst CDT laboratory was established<br />

at BFAR headquarters in Manila in 1992<br />

and now includes six laboratories and three<br />

monitoring inspection stations. The IMA<br />

CDT uses ion selective electrodes (ISEs) to<br />

detect <strong>the</strong> concentration <strong>of</strong> cyanide in <strong>the</strong><br />

distillate (Mak, Yanase et al., 2005, see Table<br />

1). In brief, internal organs <strong>of</strong> a fi sh, where<br />

cyanide is rapidly absorbed, are homogenized<br />

with water in a blender. Then <strong>the</strong> homogenate<br />

is strongly acidified in a 1-hour reflux<br />

distillation. If cyanide is present in <strong>the</strong> sample,<br />

it is liberated as hydrogen cyanide (HCN) and<br />

absorbed into a sodium hydroxide solution.<br />

Finally, <strong>the</strong> presence <strong>of</strong> cyanide in absorbing<br />

solution is detected using ISE. Each CDT lab<br />

is capable <strong>of</strong> running at least 20 tests per day.<br />

Each test takes a total <strong>of</strong> 1.5 hours including<br />

<strong>the</strong> procedures described as above. After <strong>the</strong><br />

test, <strong>the</strong> result is given back to <strong>the</strong> owner<br />

<strong>of</strong> <strong>the</strong> source <strong>of</strong> <strong>the</strong> sample in <strong>the</strong> form <strong>of</strong><br />

certification (Barber and Pratt, 1997; Mak,<br />

Yanase et al., 2005).<br />

Possibilities to Improve <strong>Cyanide</strong> <strong>Detection</strong><br />

Tests<br />

Recently, researchers from <strong>the</strong> University<br />

<strong>of</strong> Hong Kong simulated and reviewed <strong>the</strong>

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