Rice production is one of the major non-point sources of pesticide pollution in Japan because more than half of all arable land is paddy fields, from which pesticides can easily be transported to rivers. Public concerns regarding the adverse effects of pesticides in runoff on aquatic ecosystems and drinking water are increasing. In 2003, the Ministry of the Environment of Japan imposed a new pesticide registration scheme concerning ecological risk in an aquatic environment based on concepts adopted in the EU and the USA. In this scheme, the acute effect concentration in the assessment species (i.e., fish, Daphnia, or algae) is compared with the predicted environmental concentration calculated using environmental models based on the standard scenario of the pesticide use.
1)Recently, mathematical models (e.g., PADDY 2,3) and PCPF-1 4-6) ) have been developed to simulate the transport and fate of paddy rice pesticides in Japan; however, these models do not consider metabolites derived from the parent compound by hydrolysis, photolysis, or microbial degradation. The RICEWQ model, developed in the EU and the USA, is the only one that considers metabolites under paddy conditions.
7)The metabolites of some pesticides, such as organophosphorus insecticides, may be more toxic to aquatic organisms than the parent compound. Therefore, for ecological risk assessment it is necessary to evaluate the exposure of aquatic organisms not only to the parent compound but also to its metabolites. PADDY 2,3) is used to predict pesticide behavior in paddies. The objective of this study was to develop and evaluate an improved PADDY-based model that includes photoisomerization and metabolic pathways for the herbicide pyriminobacmethyl [methyl 2-(4,6-dimethoxy-2-pyrimidinyloxy)-6-(E,Z)-(1-methoxyiminoethyl)benzoate], which is used for selective control of early water grass. To validate the model, values calculated by the improved model were compared with measured values from paddy lysimeter and field experiments.
Theory, Materials, and Methods
ChemicalsPyriminobac-methyl herbicide consists of a mixture of its (E)-isomer (I) and (Z)-isomer (II) as active ingredients, with an (E)/(Z) ratio of ca. 5/1 in a technical grade of the active ingredient. The photo-transformation of this compound is the Improved PADDY model including photoisomerization and metabolic pathways for predicting pesticide behavior in paddy fields:Application to the herbicide pyriminobac-methyl Kumiai Chemical Ind. Co., Ltd., Tamari, Kakegawa, Shizuoka 436-0011, Japan (Received May 16, 2009; Accepted September 17, 2009) An improved simulation model for predicting pesticide behavior in paddy fields based on PADDY was developed to include photoisomerization and metabolic pathways and applied to the herbicide pyriminobac-methyl. Isomerization of pyriminobac-methyl in paddy water by sunlight was modeled as a reversible first-order reaction between the (E)-and (Z)-isomers in response to UV-B irradiation. The formation and degradation of its main metabolites in flooded so...