A comprehensive monitoring study, sponsored by the Chemical Manufacturers Association and designed in cooperation with the Environmental Protection Agency (EPA), measured the levels of nonylphenol (NP) and its ethoxylates (NPE) in 30 rivers. The sites, all receiving municipal or industrial wastewater, were selected at random from EPA’s United States river reach database by a statistical procedure. Water column and bottom sediment samples were collected along a perpendicular transect at each site. All samples were assayed for NP and NPE1, and the higher ethoxylates (NPE2 to NPE17) were determined in the water samples. Analysis was by high‐performance liquid chromatography (HPLC) with fluorescence detection of microgram quantities of NPE obtained by extractive steam distillation (NP and NPE1) or a dualcolumn extraction procedure (NPE2 to NPE17). Sample collection and analytical procedures were validated according to rigorous EPA guidelines, and quality assurance standards were met throughout the study. NP and NPE concentrations in river water were mostly (60 to 75% of the samples) below their detection limits (about 0.1 ppb for NP, NPE1, and NPE2; 1.6 ppb for NPE3–17). The highest levels found were about 1 ppb for NP, NPE1, and NPE2, 15 ppb for NPE3–17. A majority of sediment samples contained detectable amounts of NP and NPE1, ranging up to 3000 ppb for NP and 170 ppb for NPE1. Sediment interstitial water concentrations of NP were estimated to be similar to concentrations in the water column.

In vitro assays are widely employed to obtain intrinsic clearance estimates used in toxicokinetic modeling efforts. However, the reliability of these methods is seldom reported. Here we describe the results of an international ring trial designed to evaluate two in vitro assays used to measure intrinsic clearance in rainbow trout. An important application of these assays is to predict the effect of biotransformation on chemical bioaccumulation. Six laboratories performed substrate depletion experiments with cyclohexyl salicylate, fenthion, 4-n-nonylphenol, deltamethrin, methoxychlor, and pyrene using cryopreserved hepatocytes and liver S9 fractions from trout. Variability within and among laboratories was characterized as the percent coefficient of variation (CV) in measured in vitro intrinsic clearance rates (CLIN VITRO, INT; ml/h/mg protein or 106 cells) for each chemical and test system. Mean intralaboratory CVs for each test chemical averaged 18.9% for hepatocytes and 14.1% for S9 fractions, whereas interlaboratory CVs (all chemicals and all tests) averaged 30.1% for hepatocytes and 22.4% for S9 fractions. When CLIN VITRO, INT values were extrapolated to in vivo intrinsic clearance estimates (CLIN VIVO, INT; l/d/kg fish), both assays yielded similar levels of activity (<4-fold difference for all chemicals). Hepatic clearance rates (CLH; l/d/kg fish) calculated using data from both assays exhibited even better agreement. These findings show that both assays are highly reliable and suggest that either may be used to inform chemical bioaccumulation assessments for fish. This study highlights several issues related to the demonstration of assay reliability and may provide a template for evaluating other in vitro biotransformation assays.

N,N-Diethyl-m-toluamide's (DEET) commercial use as an insect repellent and other reported uses are reviewed. Evidence that DEET is reaching the environment mainly from consumer use of DEET-containing insect repellent includes studies reporting higher concentrations of DEET in surface water and wastewater samples during the summer months, the presence of DEET in on-site septic tank effluent at concentrations similar to that reported in wastewater treatment plant (WWTP) influent, and changes in WWTP effluent concentrations before and after the introduction of a DEET replacement in Germany. Its detected concentrations in influent and effluent of WWTP and surface water worldwide are reviewed and correlations between DEET usage and wastewater effluent concentrations are analyzed. The removability during wastewater treatment is also evaluated. A correlation between commercial DEET use in a metropolitan area and concentrations in WWTP effluents was assessed, and 2 different models were used to predict DEET concentrations in rivers and streams throughout the United States. Ecological toxicity data are reviewed for acute studies and for chronic values that are available for Daphnia magna and algae. The ecological risk of DEET usage is evaluated by examining the relationship of the expected dose/response to observed concentrations.

The extensive database of acute and chronic aquatic toxicity data for alkylphenol ethoxylates (APEs) and selected biodegradation intermediates was reviewed and summarized for freshwater and saltwater aquatic microorganisms, algae, invertebrates, and fish inhabiting cold and warm water bodies. Most acute toxicity studies that tested APE‐9 and APE‐10, the most common commercially relevant APEs, reported results that ranged from about 1,000 to 10,000 μg/L. Results from studies testing alkylphenols, intermediate by‐products of APE biodegradation, ranged from about 20 to 3,000 μg/L. Chronic values are a factor of about 2 to 10 lower. Although most studies used one of several common species and standard protocols to assay conventional endpoints, many nontraditional species and toxicological endpoints were also used. This toxicological database encompasses virtually all important types of aquatic habitats and classes of aquatic species. Bioaccumulation data from both laboratory and field studies indicate that alkylphenols have a low to moderate bioaccumulation potential. Fresh weight, nonlipid‐based bioconcentration factors (BCFs) measured in the laboratory ranged from < 1 to 1,250 for fish and 1 to 3,400 for invertebrates, whereas field bioaccumulation factors (BAFs) ranged from 6 to 487, with most values < 100. Overall, these data provide an extensive and useful database to support environmental risk assessment activities.

A 150-day post-metamorphosis (dpm) partial lifecycle study exposing Silurana tropicalis to <0.03 (control), 0.06, 0.13 0.25, 0.5 and 1.0 mg/L perfluorooctanesulfonate (PFOS) was conducted. A subset of specimens from the control and each treatment were evaluated at metamorphic completion. A significant increase in the median metamorphosis time was observed in the 1.0 mg/L PFOS treatment relative to the control. A modest increase in the occurrence, but not severity, of mild follicular hypertrophy was found in thyroid glands from organisms exposed to the 0.62 and 1.1 mg/L PFOS treatments. At 150 dpm, a concentration-dependent increase in whole body PFOS residues was measured ranging from 29.6 to 163.5 mg/kg in the 0.05 and 1.1 mg/L PFOS treatments. Decreased body weight and snout-vent length were noted in specimens exposed to 1.1 mg PFOS/L at the completion of metamorphosis. Body weight was reduced in the 1.1 mg/L PFOS concentration; however, snout-vent length was not affected by PFOS exposure at 150 dpm. An increased proportion of phenotypic males were noted in the 0.62 and 1.1 mg/L PFOS treatments. Abnormal ovary development characterized by size asymmetry, necrosis and formation of excessive fibrous connective tissue was identified in females exposed to 0.29 and 1.1 mg PFOS/L. Asymmetrically misshaped testes were found at 1.1 mg/L PFOS. Results suggested that PFOS is capable of interfering with S. tropicalis growth before metamorphic completion and growth and gonad development during juvenile development.