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Report from the Sub-comittee on the environment and health

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cases, low c<strong>on</strong>centrati<strong>on</strong>s of pesticides have been detected in places<br />

where <str<strong>on</strong>g>the</str<strong>on</strong>g>se substances have not been used for years. This could indicate<br />

that <str<strong>on</strong>g>the</str<strong>on</strong>g> retenti<strong>on</strong> time for <str<strong>on</strong>g>the</str<strong>on</strong>g> pesticides in questi<strong>on</strong> in <str<strong>on</strong>g>the</str<strong>on</strong>g> soil has been<br />

l<strong>on</strong>g in <str<strong>on</strong>g>the</str<strong>on</strong>g>se cases. In a special analysis of <str<strong>on</strong>g>the</str<strong>on</strong>g> chlorophenoxy acids<br />

MCPA, dichlorprop, 2,4-D <strong>and</strong> mechlorprop, all <str<strong>on</strong>g>the</str<strong>on</strong>g> substances were<br />

detected after 3 years in soil water at a depth of <strong>on</strong>e metre in<br />

c<strong>on</strong>centrati<strong>on</strong>s that were in several cases greater than 0.1 microgramme<br />

per litre (Felding 1993). The detecti<strong>on</strong>s of ETU are <str<strong>on</strong>g>from</str<strong>on</strong>g> a trial area<br />

treated many times with dithiocarbamate fungicides, which break down<br />

into ETU (Spliid 1998a).<br />

As a test system between full-scale field analyses <strong>and</strong> simple laboratory<br />

analyses, lysimeter analyses with undisturbed columns of soil can be<br />

used to predict whe<str<strong>on</strong>g>the</str<strong>on</strong>g>r a pesticide or its degradati<strong>on</strong> products can leach<br />

<str<strong>on</strong>g>from</str<strong>on</strong>g> a column of soil. Such lysimeter analyses now form part of <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

documentati<strong>on</strong> material used as <str<strong>on</strong>g>the</str<strong>on</strong>g> basis for approving new pesticides. A<br />

lysimeter can c<strong>on</strong>sist of a block of soil sampled at <str<strong>on</strong>g>the</str<strong>on</strong>g> site in a steel frame<br />

without being disturbed. The lysimeter is moved to <str<strong>on</strong>g>the</str<strong>on</strong>g> test locality,<br />

where crops are grown in it <strong>and</strong> it is treated with <str<strong>on</strong>g>the</str<strong>on</strong>g> pesticide in <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

ordinary way. The naturally or artificially supplied water passing <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

block of soil is collected. Using a radioactively labelled pesticide, <strong>on</strong>e<br />

can determine whe<str<strong>on</strong>g>the</str<strong>on</strong>g>r <str<strong>on</strong>g>the</str<strong>on</strong>g>re is any breakthrough of radioactivity <strong>and</strong><br />

thus of pesticide or degradati<strong>on</strong> products. Where possible, <str<strong>on</strong>g>the</str<strong>on</strong>g> substances<br />

passing <str<strong>on</strong>g>the</str<strong>on</strong>g> soil column are identified by means of chromatographic<br />

methods <strong>and</strong> by comparis<strong>on</strong> with reference substances. A lysimeter<br />

analysis is typically carried out several years after <str<strong>on</strong>g>the</str<strong>on</strong>g> pesticide has been<br />

applied. It can be used to determine <str<strong>on</strong>g>the</str<strong>on</strong>g> risk of a pesticide leaching in<br />

different types of soil, with different cultivati<strong>on</strong> c<strong>on</strong>diti<strong>on</strong>s <strong>and</strong> in<br />

different precipitati<strong>on</strong> situati<strong>on</strong>s, with a surface area <str<strong>on</strong>g>from</str<strong>on</strong>g> 0.25 to 1 m 2 .<br />

To determine <str<strong>on</strong>g>the</str<strong>on</strong>g> mobility in columns of soil in <str<strong>on</strong>g>the</str<strong>on</strong>g> deeper soil layers,<br />

columns with a surface area of, for example, 0.25 m 2 can be sampled in a<br />

steel cylinder <strong>and</strong> taken to <str<strong>on</strong>g>the</str<strong>on</strong>g> laboratory, where <str<strong>on</strong>g>the</str<strong>on</strong>g> temperature <strong>and</strong> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

groundwater’s movements can be simulated <strong>and</strong> c<strong>on</strong>trolled.<br />

Table 4.13<br />

Pesticides <strong>and</strong> metabolites detected in fields with s<strong>and</strong>y soil (Spliid 1998a)<br />

Soil water <strong>and</strong> drain water analyses<br />

Localities with s<strong>and</strong>y soil<br />

Comp<strong>on</strong>ent Detecti<strong>on</strong>s Detecti<strong>on</strong>s Highest value Number of<br />

< 0.1 µg/l > 0.1 µg/l (µg/l) analyses<br />

Atrazine 10 1 0.11 98<br />

Cyanazine n.d. n.d. n.d. 21<br />

Desethylatrazine M<br />

n.d. n.d. n.d. 21<br />

Desisopropylatrazine M<br />

1 1 0.11 21<br />

Dimethoate n.d. n.d. n.d. 21<br />

Hexazin<strong>on</strong>e 1 n.d. 0.02 21<br />

Hydroxy-carbofuran M<br />

n.d. n.d. n.d. 21<br />

Isoprotur<strong>on</strong> 4 1 0.29 75<br />

Metamitr<strong>on</strong> 4 n.d. 0.01 21<br />

Simazine 8 n.d. 0.09 82<br />

Terbuthylazine n.d. n.d. n.d. 21<br />

2,4-D 2 3 1.2 82<br />

2,4-dichlorophenol M<br />

7 5 0.22 54<br />

2,6-dichlorophenol M<br />

1 n.d. 0.05 54<br />

4-chloro-, 2-methylphenol M<br />

n.d. n.d. n.d. 54<br />

Bentaz<strong>on</strong>e 3 2 0.1 21<br />

37

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