Toxicity of binary mixtures of Cu, Cr and As to the earthworm Eisenia andrei.

Chromated copper arsenate (CCA) mixtures were used in the past for wood preservation, leading to large scale soil contamination. This study aimed at contributing to the risk assessment of CCA-contaminated soils by assessing the toxicity of binary mixtures of copper, chromium and arsenic to the earthworm Eisenia andrei in OECD artificial soil. Mixture effects were related to reference models of Concentration Addition (CA) and Independent Action (IA) using the MIXTOX model, with effects being related to total and available (H2O and 0.01 M CaCl2 extractable) concentrations in the soil. Since only in mixtures with arsenic dose-related mortality occurred (LC50 92.5 mg/kg dry soil), it was not possible to analyze the mixture effects on earthworm survival with the MIXTOX model. EC50s for effects of Cu, Cr and As on earthworm reproduction, based on total soil concentrations, were 154, 449 and 9.1 mg/kg dry soil, respectively. Effects of mixtures were mainly antagonistic when related to the CA model but additive related to the IA model. This was the case when mixture effects were based on total and H2O-extractable concentrations; when based on CaCl2-extractable concentrations effects mainly were additive related to the CA model except for the Cr-As mixture which acted antagonistically. These results suggest that the CCA components do interact leading to a reduced toxicity when present in a mixture.

An uptake and elimination kinetics approach to assess the bioavailability of chromium, copper, and arsenic to earthworms (Eisenia andrei) in contaminated field soils.

The aim of this study was to determine the bioavailability of metals in field soils contaminated with chromated copper arsenate (CCA) mixtures. The uptake and elimination kinetics of chromium, copper, and arsenic were assessed in the earthworm Eisenia andrei exposed to soils from a gradient of CCA wood preservative contamination near Hartola, Finland. In soils contaminated with 1480-1590 mg Cr/kg dry soil, 642-791 mg Cu/kg dry soil, and 850-2810 mg Ag/kg dry soil, uptake and elimination kinetics patterns were similar for Cr and Cu. Both metals were rapidly taken up and rapidly excreted by Eisenia andrei with equilibrium reached within 1 day. The metalloid As, however, showed very slow uptake and elimination in the earthworms and body concentrations did not reach equilibrium within 21 days. Bioaccumulation factors (BAF) were low for Cu and Cr (< 0.1), but high for As at 0.54-1.8. The potential risk of CCA exposure for the terrestrial ecosystem therefore is mainly due to As.

Ecological risks of an old wood impregnation mill: application of the Triad approach.

Although many studies deal with the distribution and mobility of chromated copper arsenate (CCA) metals in soil, the ecotoxicity of CCA-contaminated soils is rarely studied. The Triad approach was applied to determine the ecological risks posed by a CCA mixture at a decommissioned wood impregnation mill in southern Finland. A combination of (1) chemical analyses; (2) toxicity tests with plants (aquatic: Lemna minor; terrestrial: Lactuca sativa), earthworms (Lumbricus rubellus), and enchytraeids (Enchytraeus albidus) conducted on contaminated soils, their aqueous extracts, and well water collected from the site; and (3) determination of the abundance of enchytraeids and nematodes and the bioaccumulation of metals in plants (horsetail) collected from the field were used to assess the actual risk. Although metal concentrations were low, L. minor growth appeared to be reduced by As contamination of the well water. In soil, metals were heterogeneously distributed with total concentrations of 14.8 to 4360 mg As/kg, 15.2 to 1740 mg Cr/kg, and 4.83 to 790 mg Cu/kg. In several samples, concentrations were above Finnish regulatory guideline values and exceeded the half maximal effective concentration (EC50) or 50% lethal concentration (LC50) values for the toxicity of the individual metals to earthworms and enchytraeids, indicating hazards to the ecosystem. (Bio)availability of metals was high, as indicated by weak electrolyte extractions and body residues in L. rubellus and E. albidus exposed in bioassays. Earthworm survival correlated significantly with body metal concentrations, but not with soil total metal concentrations. Enchytraeid responses in the soil bioassays were less sensitive to CCA metal exposure. Plant growth was affected by CCA pollution, with L. sativa root elongation correlating significantly with total and available As concentrations and L. minor development being significantly reduced in H2O extracts of the most contaminated soil sample. Abundance of enchytraeids and nematodes in the field was much lower than in nonpolluted Finnish soils but did not significantly correlate with CCA contamination. Arsenic accumulation in horsetail did not correlate with As concentrations in soil. Overall, the results of the 3 lines of evidence of the Triad approach indicate possible increased risks to the ecosystem at the most contaminated sites of the CCA treatment area.

Atrazine and terbutryn degradation in deposits from groundwater environment within the boreal region in Lahti, Finland.

The degradation of pesticides atrazine and terbutryn was investigated under aerobic and anaerobic conditions in the northern boreal region subsurface deposits and sterilized controls from the depths of 6.3-21.0 m below the surface and 1.2-16.9 m below the groundwater table. During 1.3-1.7 years of laboratory incubation, atrazine degradation under aerobic conditions varied from rapid (half-live 38 days) to no degradation. Anaerobically, atrazine half-lives were 430-829 days. Organic matter, nitrogen, and lead in deposits correlated positively with the atrazine concentration in groundwater. Aerobic and anaerobic terbutryn half-lives were 193-644 and 266-400 days, respectively. Microbial aerobic atrazine and terbutryn degradation was confirmed in the deep deposits near the water table. Under aerobic conditions, the high amounts of Cr, Mn, Ni, and Zn in deposits decreased the chemical degradation of terbutryn.