RESUMO
Agricultural landscapes, including paddies, play an important role in maintaining biodiversity, but this biodiversity has been under the threat of toxic agro-chemicals. Our knowledge about how aquatic communities react to, and recover from, pesticides, particularly in relation to their residues, is deficient, despite the importance of such information for realistic environmental impact assessment of pesticides. The cumulative ecological impacts on aquatic paddy communities and their recovery processes after two successive annual applications of two systemic insecticides, imidacloprid and fipronil, were monitored between mid-May and mid-September each year. The abundance of benthic organisms during both years was significantly lower in both insecticide-treated fields than in the controls. Large-impacts of fipronil on aquatic arthropods were found after the two years. Growth of medaka fish, both adults and their juveniles, was affected by the application of the two insecticides. A Principal Response Curve analysis (PRC) showed the escalation and prolongation of changes in aquatic community composition by the successive annual treatments of each insecticide over two years. Residues of fipronil in soil, which are more persistent than those of imidacloprid, had a high level of impact on aquatic communities over time. For some taxonomic groups, particularly for water surface-dwelling and water-borne arthropods, the second annual treatment had far greater impacts than the initial treatment, indicating that impacts of these insecticides under normal use patterns cannot be accurately assessed during short-term monitoring studies, i.e., lasting less than one year. It is concluded that realistic prediction and assessment of pesticide effects at the community level should also include the long-term ecological risks of their residues whenever these persist in paddies over a year.
Assuntos
Imidazóis/toxicidade , Inseticidas/toxicidade , Nitrocompostos/toxicidade , Pirazóis/toxicidade , Poluentes Químicos da Água/toxicidade , Agricultura , Animais , Organismos Aquáticos/classificação , Organismos Aquáticos/efeitos dos fármacos , Organismos Aquáticos/crescimento & desenvolvimento , Ecossistema , Meio Ambiente , Monitoramento Ambiental , Neonicotinoides , OryzaRESUMO
Chlorpyrifos [O,O-diethyl O-(3,5,6-trichloro-2-pyridyl) phosphorothioate] is the most widely used soil-applied termiticide in Australia. It is relatively stable, has low water solubility, is absorbed by organic matter, and has a high affinity for soil with low partitioning potential from soil matter to soil water. The purpose of this degradation study is to determine the effect of soil alkalinity on the longevity of termite protection when chlorpyrifos is applied as a termiticide in a range of Australian soils, particularly high-pH substrates. The study also examines the effects of initial soil concentration on the degradation of chlorpyrifos in the range of soils. At an initial soil concentration of 1000 mg kg(-)(1) for termite control, the degradation rate of chlorpyrifos is very strongly retarded in soils tested when compared with lower soil concentrations of 100 and 10 mg kg(-)(1) in the same soils. The degradation data correlated with a logarithmic model of decay, and it was thus possible to produce half-lives and predict likely periods of termite control. Average half-lives for all soils for the three concentrations were 385, 155, and 41 days, respectively. Soil pH had no effect on the rate of degradation at all concentrations tested.
Assuntos
Clorpirifos/farmacocinética , Inseticidas/farmacocinética , Poluentes do Solo/análise , Animais , Austrália , Biodegradação Ambiental , Clorpirifos/química , Concentração de Íons de Hidrogênio , Inseticidas/química , IsópterosRESUMO
The fate and transport of endosulfan (6,7,8,9,10,10-hexachloro-1,5, 5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin 3-oxide) applied to cotton (Gossypium hirsutum L.) fields were studied throughout three consecutive years on two selected locations in New South Wales (Australia). Rates of dissipation from foliage and soil, volatilization from the field, and transport of residues in irrigation and/or storm runoff waters were measured in order to estimate a total field balance. Dissipation of endosulfan from both foliage and soil is best explained by a two-phase process rather than by a first-order decay. Half-lives of total endosulfan toxic residues (alpha- and beta-endosulfan and the sulfate product) in the first phase were 1.6 d in foliage and 7.1 d in soil, and could be explained by the rapid volatilization of the parent isomers in the first 5 d (up to 70% of endosulfan volatilizes). In the second phase, half-lives were 9.5 d in foliage and 82 d in soil, mostly due to the persistence of the sulfate product. Concentration of endosulfan residues in runoff water varied from 45 to 2.5 microg L(-1) depending on the residue levels present on field soil at the time of the irrigation or storm events. These in turn are related to the total amounts applied, the cotton canopy cover at application, and the time since last spraying. Most of the endosulfan in runoff was found in the water phase (80%), suggesting it was bound to colloidal matter. Total endosulfan residues in runoff for a whole season accounted for no more than 2% of the pesticide applied on-field.
Assuntos
Endossulfano/análise , Hidrocarbonetos Clorados , Inseticidas/análise , Poluentes do Solo/análise , Poluentes da Água/análise , Agricultura , Endossulfano/química , Monitoramento Ambiental , Gossypium , Inseticidas/química , Resíduos de Praguicidas/análise , Volatilização , Movimentos da ÁguaRESUMO
Although the use of endosulfan to control cotton pests has declined, this insecticide still has widespread application in agriculture and can contaminate riverine systems as runoff from soil or by aerial deposition. The degradation of endosulfan in pure water at different pH values of 5, 7 and 9 and in river water from the Namoi and the Hawkesbury rivers of New South Wales (NSW), Australia, was studied in the laboratory. Endosulfan transformation into endosulfan sulfate in river water using artificial mesocosms was also investigated. The results show endosulfan is stable at pH 5, with increasing rates of disappearance at pH 7 and pH 9 by chemical hydrolysis. Incubation of endosulfan with river water at pH 8.3 resulted in the disappearance of endosulfan and the formation of endosulfan diol due to the alkaline pH as well as formation of endosulfan sulfate. Although the degradation of endosulfan by Anabaena, a blue-green alga, did not result in the transformation of endosulfan to endosulfan sulfate, we conclude that other microorganisms catalyzed the formation of the sulfate. Significant conversions of endosulfan into endosulfan sulfate were also reported from associated field studies using artificial mesocoms containing irrigation water from rivers inhabitated by micro-macro fauna. From these results, we conclude that the presence of endosulfan sulfate in river water cannot be used to distinguish contamination by runoff from soil from contamination by aerial drift or redeposition.