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    <marc:controlfield tag="003">CaOODSP</marc:controlfield>
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    <marc:controlfield tag="007">cr |||||||||||</marc:controlfield>
    <marc:controlfield tag="008">171027s1996    onca|||fo    f000 0 eng d</marc:controlfield>
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      <marc:subfield code="a">CaOODSP</marc:subfield>
      <marc:subfield code="b">eng</marc:subfield>
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      <marc:subfield code="a">eng</marc:subfield>
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      <marc:subfield code="a">En13-5/96-171E-PDF</marc:subfield>
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      <marc:subfield code="a">Microbial transformation of the new antifouling compound Irgarol 1051 </marc:subfield>
      <marc:subfield code="h">[electronic resource] / </marc:subfield>
      <marc:subfield code="c">by D. Liu  ... [et al.].</marc:subfield>
    </marc:datafield>
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      <marc:subfield code="a">Burlington, Ont. : </marc:subfield>
      <marc:subfield code="b">National Water Research Institute, </marc:subfield>
      <marc:subfield code="c">[1996].</marc:subfield>
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      <marc:subfield code="a">[26] p. : </marc:subfield>
      <marc:subfield code="b">ill. </marc:subfield>
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      <marc:subfield code="a">NWRI contribution ; </marc:subfield>
      <marc:subfield code="v">96-171</marc:subfield>
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      <marc:subfield code="a">Digitized edition from print [produced by Environment and Climate Change Canada].</marc:subfield>
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      <marc:subfield code="a">Includes bibliographical references.</marc:subfield>
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      <marc:subfield code="a">"Irgarol 1051, 2-methylthio-4-tert-butylamino-6-cyclopropylamino-s-triazine, is a newly developed herbicidal for use in the copper-based antifouling paints. It is intended to replace the widely used antifouling agent tributyltin (TBT) which has been banned internationally since 1990, primarily due to its severe impact on the aquatic ecosystem. ... This study shows that the white rot fungus Phaiterochaete chrysosporium was capable of biotransforming Irgarol 1051 via partial N-dealkylation. Metabolic dealkylation occurs at the cyclopropylamino group resulting in metabolite M1 (2-methylthio-4-tert-butylamino-6-amino-s-triazine). No evidence of the heterocyclic ring cleavage of Irgarol 1051 was observed, thus implying a possibility of its degradation products accumulation in the environment. This is the first report of metabolites of Irgarol 1051"--Management perspective.</marc:subfield>
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      <marc:subfield code="a">Abstracts in English and French.</marc:subfield>
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      <marc:subfield code="2">gccst</marc:subfield>
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      <marc:subfield code="2">gccst</marc:subfield>
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      <marc:subfield code="2">gccst </marc:subfield>
      <marc:subfield code="a">Toxic substances</marc:subfield>
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      <marc:subfield code="2">gccst</marc:subfield>
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      <marc:subfield code="a">Liu, Dickson, </marc:subfield>
      <marc:subfield code="d">1935-</marc:subfield>
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      <marc:subfield code="a">Canada. </marc:subfield>
      <marc:subfield code="b">Environment Canada.</marc:subfield>
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      <marc:subfield code="a">National Water Research Institute (Canada)</marc:subfield>
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      <marc:subfield code="a">NWRI contribution ;</marc:subfield>
      <marc:subfield code="v">no. 96-171</marc:subfield>
      <marc:subfield code="w">(CaOODSP)9.844121</marc:subfield>
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      <marc:subfield code="q">PDF</marc:subfield>
      <marc:subfield code="s">1.64 MB</marc:subfield>
      <marc:subfield code="u">https://publications.gc.ca/collections/collection_2017/eccc/En13-5-96-171-eng.pdf</marc:subfield>
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