Daniel J. Letinski

TOXICITY OF PHYSICALLY AND CHEMICALLY DISPERSED OILS UNDER CONTINUOUS AND ENVIRONMENTALLY REALISTIC EXPOSURE CONDITIONS: APPLICABILITY TO DISPERSANT USE DECISIONS IN SPILL RESPONSE PLANNING

ABSTRACT As part of efforts to develop standardized testing protocols under the Chemical Response to Oil Spills Environmental Research Forum (CROSERF) and apply the results to real-world scenarios, three types of oils and two dispersants were tested in both continuous and short-term spiked exposures using the early life-stages of several marine organisms. Test species included embryo-larval stages of Pacific oyster (Crassostrea gigas), two marine mysids (Holmesimysis costata and Mysidopsis bahia), and two marine fishes (turbot, Scophthalmus maximus and inland silverside, Menidia beryllina). Oils were physically dispersed in seawater by vortex mixing in a flask and chemically dispersed using the same approach with COREXIT® 9527 or COREXIT® 9500 applied in a 10:1 oil-to-dispersant ratio to generate maximum exposure concentrations. Continuous exposure tests followed standard testing protocols for 96-hour or 48-hour duration, according to demands of the test species. Spiked exposures reflect continuous diluti...

A novel passive dosing system for determining the toxicity of phenanthrene to early life stages of zebrafish.

Reliable experimental early life stage chronic toxicity data for fish are limited and further data are needed for polyaromatic hydrocarbons to establish environmental quality objectives and compare with toxicity model predictions. Efforts are underway to develop a zebrafish embryo toxicity test guideline to reduce, refine and replace the use of vertebrates in animal testing. An adaptation of this method which includes embryo lethal and sub-lethal developmental endpoints after a 5-day exposure as well as larval survival and growth endpoints during a subsequent 25-day test period is described using phenanthrene as a model test substance. To deliver well controlled exposure concentrations, a passive dosing system consisting of silicone coated vials and silicone O-rings was employed. Acute results indicated that edema and spinal curvature were the most sensitive sub-lethal effects observed and in many cases preceded observed mortality. The 30-day LC/EC10 for larval survival and growth was 40 and 67 μg/L respectively. Concentrations shown to cause adverse effects in this study are in the range of previous studies that have investigated the chronic effects of phenanthrene on fish. Further, results indicate that predicted water quality objectives for phenanthrene derived using the target lipid model are protective of early life stage effects on zebrafish. Based on these results the predicted water quality objectives for phenanthrene derived using the target lipid model (10 μg/L) would be protective of early life stage effects on zebrafish.

Genotoxicity of intermittent co-exposure to benzene and toluene in male CD-1 mice.

Benzene is an important industrial chemical. At certain levels, benzene has been found to produce aplastic anemia, pancytopenia, myeloblastic anemia and genotoxic effects in humans. Metabolism by cytochrome P450 monooxygenases and myeloperoxidase to hydroquinone, phenol, and other metabolites contributes to benzene toxicity. Other xenobiotic substrates for cytochrome P450 can alter benzene metabolism. At high concentrations, toluene has been shown to inhibit benzene metabolism and benzene-induced toxicities. The present study investigated the genotoxicity of exposure to benzene and toluene at lower and intermittent co-exposures. Mice were exposed via whole-body inhalation for 6h/day for 8 days (over a 15-day time period) to air, 50 ppm benzene, 100 ppm toluene, 50 ppm benzene and 50 ppm toluene, or 50 ppm benzene and 100 ppm toluene. Mice exposed to 50 ppm benzene exhibited an increased frequency (2.4-fold) of micronucleated polychromatic erythrocytes (PCE) and increased levels of urinary metabolites (t,t-muconic acid, hydroquinone, and s-phenylmercapturic acid) vs. air-exposed controls. Benzene co-exposure with 100 ppm toluene resulted in similar urinary metabolite levels but a 3.7-fold increase in frequency of micronucleated PCE. Benzene co-exposure with 50 ppm toluene resulted in a similar elevation of micronuclei frequency as with 100 ppm toluene which did not differ significantly from 50 ppm benzene exposure alone. Both co-exposures - 50 ppm benzene with 50 or 100 ppm toluene - resulted in significantly elevated CYP2E1 activities that did not occur following benzene or toluene exposure alone. Whole blood glutathione (GSH) levels were similarly decreased following exposure to 50 ppm benzene and/or 100 ppm toluene, while co-exposure to 50 ppm benzene and 100 ppm toluene significantly decreased GSSG levels and increased the GSH/GSSG ratio. The higher frequency of micronucleated PCE following benzene and toluene co-exposure when compared with mice exposed to benzene or toluene alone suggests that, at the doses used in this study, toluene can enhance benzene-induced clastogenic or aneugenic bone marrow injury. These findings exemplify the importance of studying the effects of binary chemical interactions in animals exposed to lower exposure concentrations of benzene and toluene on benzene metabolism and clastogenicity. The relevance of these data on interactions for humans exposed at low benzene concentrations can be best assessed only when the mechanism of interaction is understood at a quantitative level and incorporated within a biologically based modeling framework.

Slow-stir water solubility measurements of selected alcohols and diesters

Experimental data are presented for 11 C8-C15 aliphatic alcohols and 12 phthalate and adipate diesters using a slow-stir water solubility test method. The slow stirring method provides more reliable water solubility measurements for these liquid substances than previous studies since the formation of emulsions is avoided. Because the solubility of these chemicals spanned a range of more than six orders of magnitude, several different analytical procedures were employed. The water solubility data reported in this work agree well with other recently reported slow-stir measurements and with structure-property model predictions (SPARC and WSKOWWIN).

Influence of toluene co-exposure on the metabolism and genotoxicity of benzene in mice using continuous and intermittent exposures

Benzene exposure in occupational settings often occurs with concurrent exposure to toluene, the methyl-substituted derivative of benzene. Toluene is also readily metabolized by CYP450 isozymes although oxidation primarily occurs in the methyl group. While earlier mouse studies addressing co-exposure to benzene and toluene at high concentrations demonstrated a reduction in benzene-induced genotoxicity, we have previously found, using an intermittent exposure regimen with lower concentrations of benzene (50 ppm) and toluene (100 ppm), that toluene enhances benzene-induced clastogenic or aneugenic bone marrow injury in male CD-1 mice with significantly increased CYP2E1, and depleted GSH and GSSG levels. The follow-up study reported here also used the same daily and total co-exposures but over consecutive days and compared the effects of co-exposure on genotoxicity and metabolism in CD-1 mice both with and without buthionine sulfoximine (BSO) treatment to deplete GSH. In this study the toluene co-exposure doubled the genotoxic response (as determined by the erythrocyte micronucleus test) to benzene alone. Further, GSH depletion caused a reduction in this genotoxicity in both benzene exposed and benzene/toluene co-exposed mice. The results are discussed in terms of the analyses of urinary metabolites from this consecutive day study and the intermittent exposure study as well as levels of CYP2E1, epoxide hydrolase, quinone reductase, alcohol dehydrogenase, and aldehyde dehydrogenase activities. The results suggest that the presence of glutathione is necessary for benzene genotoxicity either as a metabolite conjugate or through an indirect mechanism such as TNF-induced apoptosis.

Health assessment of gasoline and fuel oxygenate vapors: generation and characterization of test materials.

In compliance with the Clean Air Act regulations for fuel and fuel additive registration, the petroleum industry, additive manufacturers, and oxygenate manufacturers have conducted comparative toxicology testing on evaporative emissions of gasoline alone and gasoline containing fuel oxygenates. To mimic real world exposures, a generation method was developed that produced test material similar in composition to the re-fueling vapor from an automotive fuel tank at near maximum in-use temperatures. Gasoline vapor was generated by a single-step distillation from a 1000-gallon glass-lined kettle wherein approximately 15-23% of the starting material was slowly vaporized, separated, condensed and recovered as test article. This fraction was termed vapor condensate (VC) and was prepared for each of the seven test materials, namely: baseline gasoline alone (BGVC), or gasoline plus an ether (G/MTBE, G/ETBE, G/TAME, or G/DIPE), or gasoline plus an alcohol (G/EtOH or G/TBA). The VC test articles were used for the inhalation toxicology studies described in the accompanying series of papers in this journal. These studies included evaluations of subchronic toxicity, neurotoxicity, immunotoxicity, genotoxicity, reproductive and developmental toxicity. Results of these studies will be used for comparative risk assessments of gasoline and gasoline/oxygenate blends by the US Environmental Protection Agency.

Use of passive samplers for improving oil toxicity and spill effects assessment.

Methods that quantify dissolved hydrocarbons are needed to link oil exposures to toxicity. Solid phase microextraction (SPME) fibers can serve this purpose. If fibers are equilibrated with oiled water, dissolved hydrocarbons partition to and are concentrated on the fiber. The absorbed concentration (Cpolymer) can be quantified by thermal desorption using GC/FID. Further, given that the site of toxic action is hypothesized as biota lipid and partitioning of hydrocarbons to lipid and fibers is well correlated, Cpolymer is hypothesized to be a surrogate for toxicity prediction. To test this method, toxicity data for physically and chemically dispersed oils were generated for shrimp, Americamysis bahia, and compared to test exposures characterized by Cpolymer. Results indicated that Cpolymer reliably predicted toxicity across oils and dispersions. To illustrate field application, SPME results are reported for oil spills at the Ohmsett facility. SPME fibers provide a practical tool to improve characterization of oil exposures and predict effects in future lab and field studies.

Application of the target lipid model for deriving predicted no‐effect concentrations for wastewater organisms

The target lipid model (TLM) was applied to literature data from 10 microbial toxicity assays to provide a quantitative effects assessment framework for wastewater treatment plant organisms. For the nonpolar organic chemicals considered, linear relationships between the logarithm of the median effect concentrations (EC50) and log(K(OW)) conformed to the TLM for all endpoints with the exception of nitrification inhibition. Additional experimental data for the nitrification inhibition endpoint were generated for 16 narcotic chemicals using a procedure that allowed testing of volatile substances. Results obtained from the present study demonstrated that the nitrification inhibition endpoint was not adequately described by the TLM consistent with previous literature data. Acute to chronic ratios (ACRs) defined as the ratio of the EC50 to the 10% effect concentration (EC10) were available for two of the endpoints investigated and ranged from 1.1 to 2.3 for the Tetrahymena growth assay and from 2.4 to 24.1 for the nitrification inhibition endpoint. No inhibitory effects for any of the microbial endpoints investigated were observed for compounds with log(K(OW)) >5. The critical target lipid body burdens (C(L)(*)) were calculated for the nine microbial toxicity endpoints conforming to the TLM and ranged from 252 to 2,250 micromol/g octanol. The Microtox light inhibition (C(L)(*) = 252 micromol/g octanol) and Tetrahymena pyriformis growth (C(L)(*) = 254 micromol/g octanol) assays were found to be the most sensitive endpoints. The predicted no-effect concentration (PNEC) derived using the HC5 (hazardous concentration to 5% of test organisms) statistical extrapolation procedure was calculated using TLM parameters for substances with log(K(OW)) from 0 to 5. Results from this analysis demonstrate PNECs for narcotic compounds are protective of wastewater organisms excluding nitrifying bacteria. Further model improvement is needed if protection of nitrifying bacteria in wastewater treatment systems is required.

A re‐evaluation of PETROTOX for predicting acute and chronic toxicity of petroleum substances

The PETROTOX model was developed to perform aquatic hazard assessment of petroleum substances based on substance composition. The model relies on the hydrocarbon block method, which is widely used for conducting petroleum substance risk assessments providing further justification for evaluating model performance. Previous work described this model and provided a preliminary calibration and validation using acute toxicity data for limited petroleum substance. The objective of the present study was to re-evaluate PETROTOX using expanded data covering both acute and chronic toxicity endpoints on invertebrates, algae, and fish for a wider range of petroleum substances. The results indicated that recalibration of 2 model parameters was required, namely, the algal critical target lipid body burden and the log octanol-water partition coefficient (KOW ) limit, used to account for reduced bioavailability of hydrophobic constituents. Acute predictions from the updated model were compared with observed toxicity data and found to generally be within a factor of 3 for algae and invertebrates but overestimated fish toxicity. Chronic predictions were generally within a factor of 5 of empirical data. Furthermore, PETROTOX predicted acute and chronic hazard classifications that were consistent or conservative in 93 and 84% of comparisons, respectively. The PETROTOX model is considered suitable for the purpose of characterizing petroleum substance hazard in substance classification and risk assessments. Environ Toxicol Chem 2017;36:2245-2252.

Assessing Aromatic-Hydrocarbon Toxicity to Fish Early Life Stages Using Passive-Dosing Methods and Target-Lipid and Chemical-Activity Models

Aromatic hydrocarbons (AH) are known to impair fish early life stages (ELS). However, poorly defined exposures often confound ELS-test interpretation. Passive dosing (PD) overcomes these challenges by delivering consistent, controlled exposures. The objectives of this study were to apply PD to obtain 5 d acute embryo lethality and developmental data and 30 d chronic embryo-larval survival and growth-effects data using zebrafish with different AHs; to analyze study and literature toxicity data using target-lipid (TLM) and chemical-activity (CA) models; and to extend PD to a mixture and test the assumption of AH additivity. PD maintained targeted exposures over a concentration range of 6 orders of magnitude. AH toxicity increased with log Kow up to pyrene (5.2). Pericardial edema was the most sensitive sublethal effect that often preceded embryo mortality, although some AHs did not produce developmental effects at concentrations causing mortality. Cumulative embryo-larval mortality was more sensitive than larval growth, with acute-to-chronic ratios of <10. More-hydrophobic AHs did not exhibit toxicity at aqueous saturation. The relationship and utility of the TLM-CA models for characterizing fish ELS toxicity is discussed. Application of these models indicated that concentration addition provided a conservative basis for predicting ELS effects for the mixture investigated.