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1.
Sci Total Environ ; 819: 152053, 2022 May 01.
Article in English | MEDLINE | ID: mdl-34856270

ABSTRACT

Contaminants are ubiquitous in the environment, often reaching aquatic systems. Combinations of forestry use pesticides have been detected in both water and aquatic organism tissue samples in coastal systems. Yet, most toxicological studies focus on the effects of these pesticides individually, at high doses, and over acute time periods, which, while key for establishing toxicity and safe limits, are rarely environmentally realistic. We examined chronic (90 days) exposure by the soft-shell clam, Mya arenaria, to environmentally relevant concentrations of four pesticides registered for use in forestry (atrazine, 5 µg/L; hexazinone, 0.3 µg/L; indaziflam, 5 µg/L; and bifenthrin, 1.5 µg/g organic carbon (OC)). Pesticides were tested individually and in combination, except bifenthrin, which was tested only in combination with the other three. We measured shell growth and condition index every 30 days, as well as feeding rates, mortality, and chemical concentrations in tissue from a subset of clams at the end of the experiment to measure contaminant uptake. Indaziflam caused a high mortality rate (max. 36%), followed by atrazine (max. 27%), both individually as well as in combination with other pesticides. Additionally, indaziflam concentrations in tissue (61.70-152.56 ng/g) were higher than those of atrazine (26.48-48.56 ng/g), despite equal dosing concentrations, indicating higher tissue accumulation. Furthermore, clams exposed to indaziflam and hexazinone experienced reduced condition index and clearance rates individually and in combination with other compounds; however, the two combined did not result in significant mortality. These two compounds, even at environmentally relevant concentrations, affected a non-target organism and, in the case of the herbicide indaziflam, accumulated in clam tissue and appeared more toxic than other tested pesticides. These findings underscore the need for more comprehensive studies combining multiple compounds at relevant concentrations to understand their impacts on aquatic ecosystems.


Subject(s)
Mya , Pesticides , Water Pollutants, Chemical , Animals , Ecosystem , Forestry , Pesticides/analysis , Pesticides/toxicity , Water Pollutants, Chemical/analysis
2.
Toxics ; 9(3)2021 Mar 02.
Article in English | MEDLINE | ID: mdl-33801358

ABSTRACT

Terrestrial land use activities present cross-ecosystem threats to riverine and marine species and processes. Specifically, pesticide runoff can disrupt hormonal, reproductive, and developmental processes in aquatic organisms, yet non-point source pollution is difficult to trace and quantify. In Oregon, U.S.A., state and federal forestry pesticide regulations, designed to meet regulatory water quality requirements, differ in buffer size and pesticide applications. We deployed passive water samplers and collected riverine and estuarine bivalves Margaritifera falcata, Mya arenaria, and Crassostrea gigas from Oregon Coast watersheds to examine forestry-specific pesticide contamination. We used non-metric multidimensional scaling and regression to relate concentrations and types of pesticide contamination across watersheds to ownership and management metrics. In bivalve samples collected from eight coastal watersheds, we measured twelve unique pesticides (two herbicides; three fungicides; and seven insecticides). Pesticides were detected in 38% of bivalve samples; and frequency and maximum concentrations varied by season, species, and watershed with indaziflam (herbicide) the only current-use forestry pesticide detected. Using passive water samplers, we measured four current-use herbicides corresponding with planned herbicide applications; hexazinone and atrazine were most frequently detected. Details about types and levels of exposure provide insight into effectiveness of current forest management practices in controlling transport of forest-use pesticides.

3.
Environ Toxicol Chem ; 39(8): 1590-1598, 2020 08.
Article in English | MEDLINE | ID: mdl-32430919

ABSTRACT

Microplastics are ubiquitous in our environment and are found in rivers, streams, oceans, and even tap water. Riverine microplastics are relatively understudied compared with those in marine ecosystems. In Oregon (USA), we sampled 8 sites along 4 freshwater rivers spanning rural to urban areas to quantify microplastics. Plankton tow samples from sites along the Columbia, Willamette, Deschutes, and Rogue Rivers were analyzed using traditional light microscopy for initial microplastic counts. Application of Nile Red dye to validate microplastics improved microplastic identification, particularly for particles (Wilcox test; p = 0.001). Nile Red-corrected microfiber abundance was correlated with human population within 5 km of the sample site (R² = 0.554), although no such relationship was observed between microparticles and population (R² = 0.183). We found that plastics were present in all samples from all sites, despite the range from undeveloped, remote stretches of river in rural areas to metropolitan sites within Portland (OR, USA), demonstrating the pervasive presence of plastic pollution in freshwater ecosystems. Environ Toxicol Chem 2020;39:1590-1598. © 2020 SETAC.


Subject(s)
Cost-Benefit Analysis , Environmental Monitoring/economics , Environmental Monitoring/methods , Microplastics/analysis , Rivers/chemistry , Cities , Environmental Pollution/analysis , Fresh Water/chemistry , Geography , Oregon , Water Pollutants, Chemical/analysis
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