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S S Talmage

Publications and source records attributed to S S Talmage.

5 recordsLinked to original sources

Derivation of aquatic screening benchmarks for 1,2-dibromoethane.

Ethylene dibromide (1,2-dibromoethane or EDB) was primarily used in the United States as an additive in leaded gasoline and as a soil and grain fumigant for worm and insect control until it was banned in 1983. Historical releases of EDB have resulted in detectable EDB in groundwater and drinking wells, and recently concentrations up to 16 microg/L were detected in ground water at two fuel spill plumes in the vicinity of the Massachusetts Military Reservation Base on Cape Cod, Massachusetts. Because the ground water in this area is used to flood cranberry bogs for the purposes of harvesting, the U.S. Air Force sponsored the development of aquatic screening benchmarks for EDB. Acute toxicity tests with Pimephales promelas (fathead minnow), Daphnia magna, and Ceriodaphnia dubia were conducted to provide data needed for development of screening benchmarks. Using a closed test-system to prevent volatilization of EDB, the 48-h LC50S (concentration that kills 50% of the test organisms) for P. promelas, D. magna, and C. dubia were 4.3 mg/L, 6.5 mg/L, and 3.6 mg/L, respectively. The screening benchmark for aquatic organisms, derived as the Tier II chronic water quality criteria, is 0.031 mg EDB/L. The sediment screening benchmark, based on equilibrium partitioning, is 2.45 mg EDB/kg of organic carbon in the sediment. The screening benchmarks developed here are an important component of an ecological risk assessment, during which perhaps hundreds of chemicals must be evaluated for their potential to cause ecological harm.

Animals↗

Nitroaromatic munition compounds: environmental effects and screening values.

Available data on the occurrence, transport, transformation, and toxicity of eight nitroaromatic munition compounds and their degradation products, TNT, TNB, DNB, DNA, 2-ADNT, RDX, HMX, and tetryl were used to identify potential fate in the environment and to calculate screening benchmarks or safe environmental levels for aquatic and terrestrial organisms. Results of monitoring studies revealed that some of these compounds persist at sites where they were produced or processed. Most of the compounds are present in soil, sediment, and surface water or groundwater at military sites. Soil adsorption coefficients indicate that these chemicals are only moderately adsorbed to soil and may leach to groundwater. Most of these compounds are transformed by abiotic or biotic mechanisms in environmental media. Primary transformation mechanisms involve photolysis (TNT, RDX, HMX, tetryl), hydrolysis (tetryl), and microbial degradation (TNT, TNB, DNB, DNA, 2-ADNT, and HMX). Microbial degradation for both nitro and nitramine aromatic compounds involves rapid reduction of nitro groups to amino groups, but further metabolism is slow. With the exception of DNB, complete mineralization did not usually occur under the conditions of the studies. RDX was resistant to microbial degradation. Available ecotoxicological data on acute and chronic studies with freshwater fish and invertebrates were summarized, and water quality criteria or ecotoxicological screening benchmarks were developed. Depending on the available data, criteria/benchmarks were calculated according to USEPA Tier I or Tier II guidelines. The munitions chemicals are moderately to highly toxic to freshwater organisms, with chronic screening values < 1 mg/L. For some chemicals, these low values are caused by inherent toxicity; in other cases, they result from the conservative methods used in the absence of data. For nonionic organic munitions chemicals, sediment quality benchmarks were calculated (based on Kow values and the final chronic value) according to USEPA guidelines. Available data indicate that none of the compounds is expected to bioconcentrate. In the same manner in which reference doses for humans are based on studies with laboratory animals, reference doses or screening benchmarks for wildlife may also be calculated by extrapolation among mammalian species. Chronic NOAELs for the compounds of interest were determined from available laboratory studies. Endpoints selected for wildlife species were those that diminish population growth or survival. Equivalent NOAELs for wildlife were calculated by scaling the test data on the basis of differences in body weight. Data on food and water intake for seven selected wildlife species--short-tailed shrew, white-footed mouse, meadow vole, cottontail rabbit, mink, red fox, and whitetail deer--were used to calculate NOAELs for oral intake. In the case of TNB, a comparison of toxicity data from studies conducted with both the white-footed mouse and the laboratory rat indicates that the white-footed mouse may be more resistant to the toxic effects of chemicals than the laboratory rat and may further indicate the lesser sensitivity of wildlife species to chemical insult. Chronic NOAEL values for the test species based on the laboratory studies indicate that, by the oral route of exposure, TNB and RDX are not highly toxic to mammalian species. However, as seen with TNB, values are less conservative when chronic studies are available or when studies were conducted with wildlife species. Insufficient data were located to calculate NOAELs for avian species. In the absence of criteria or guidelines for terrestrial plants, invertebrates, and soil heterotrophic processes, LOECs were used as screening benchmarks for effect levels in the environment. In most cases, too few data were available to derive a screening benchmark or to have a high degree of confidence in the benchmarks that were derived. (ABSTRACT TRUNCATED)

Animals↗

The sources, fate, and toxicity of chemical warfare agent degradation products.

We include in this review an assessment of the formation, environmental fate, and mammalian and ecotoxicity of CW agent degradation products relevant to environmental and occupational health. These parent CW agents include several vesicants: sulfur mustards [undistilled sulfur mustard (H), sulfur mustard (HD), and an HD/agent T mixture (HT)]; nitrogen mustards [ethylbis(2-chloroethyl)amine (HN1), methylbis(2-chloroethyl)amine (HN2), tris(2-chloroethyl)amine (HN3)], and Lewisite; four nerve agents (O-ethyl S-[2-(diisopropylamino)ethyl] methylphosphonothioate (VX), tabun (GA), sarin (GB), and soman (GD)); and the blood agent cyanogen chloride. The degradation processes considered here include hydrolysis, microbial degradation, oxidation, and photolysis. We also briefly address decontamination but not combustion processes. Because CW agents are generally not considered very persistent, certain degradation products of significant persistence, even those that are not particularly toxic, may indicate previous CW agent presence or that degradation has occurred. Of those products for which there are data on both environmental fate and toxicity, only a few are both environmentally persistent and highly toxic. Major degradation products estimated to be of significant persistence (weeks to years) include thiodiglycol for HD; Lewisite oxide for Lewisite; and ethyl methyl phosphonic acid, methyl phosphonic acid, and possibly S-(2-diisopropylaminoethyl) methylphosphonothioic acid (EA 2192) for VX. Methyl phosphonic acid is also the ultimate hydrolysis product of both GB and GD. The GB product, isopropyl methylphosphonic acid, and a closely related contaminant of GB, diisopropyl methylphosphonate, are also persistent. Of all of these compounds, only Lewisite oxide and EA 2192 possess high mammalian toxicity. Unlike other CW agents, sulfur mustard agents (e.g., HD) are somewhat persistent; therefore, sites or conditions involving potential HD contamination should include an evaluation of both the agent and thiodiglycol.

Animals↗

Chemical warfare agents: estimating oral reference doses.

Health risk assessments for sites contaminated with chemical warfare agents require a comparison of the potential levels of exposure with a characterization of the toxic potency of each chemical. For noncancer health effects, toxic potency is expressed in terms of Reference Doses (RfD). A RfD is a daily exposure level or dose (usually expressed in units of milligrams of chemical per kilogram body weight per day) for the human population, including sensitive subpopulations, that is likely to be without an appreciable risk of deleterious effects. A daily exposure at or below the RfD is not likely to be associated with health risks, but as the amount of chemical that an individual is exposed to increases above the RfD, the probability that an adverse effect will occur also increases. A RfD is derived by first examining the available human or animal toxicity data to identify a dose or exposure that corresponds to a no-observed-adverse-effect level (NOAEL) or a lowest-observed-adverse-effect level (LOAEL). The NOAEL is the exposure level at which there are no statistically or biologically significant increases in frequency or severity of adverse effects between the exposed population and its appropriate control. Effects may be produced at this level, but they are not considered to be adverse if they do not result in functional impairment or pathological lesions that affect the performance of the whole organism or which reduce an organism's ability to cope with additional challenge. The LOAEL is the lowest exposure level at which there are statistically or biologically significant increases in frequency or severity of adverse effects between the exposed population and its appropriate control. If only a LOAEL is identified by the toxicity data, a NOAEL is estimated by dividing the LOAEL by a factor no greater than 10. This extrapolation factor of 10 or less is termed the LOAEL-to-NOAEL Uncertainty Factor (UFL). The NOAEL is also adjusted by the application of other Uncertainty Factors, including (1) a UFH < or = 10 to ensure that the resulting RfD protects segments of the human population that may be more sensitive to the chemical than the average person; (2) a UFA < or = 10 to extrapolate from the experimental animal species to humans; (3) a UFS < or = 10 to extrapolate from an experimental subchronic exposure study to a potential chronic exposure; and (4) a UFD < or = 10 to ensure that the resulting RfD is protective for all possible adverse effects, particularly those that may not have been adequately evaluated in the available studies. A Modifying Factor (MF), based on a qualitative professional assessment of the data, may also be used to account for other factors (e.g., deficiencies in the critical study) that are not adequately covered by the standard Uncertainty Factors. 1. Agent HD (Sulfur Mustard). RfDe = 7 x 10(-6) mg kg-1 d-1. A LOAEL was identified in a two-generation reproductive toxicity study conducted in rats. A total uncertainty factor of 3000 was applied to account for protection of sensitive subpopulations (10), animal-to-human extrapolation (10), LOAEL-to-NOAEL extrapolation (3), and extrapolation from a subchronic to chronic exposure (10). A LOAEL-to-NOAEL UF of 3, instead of the default value of 10, was used because the critical effect (stomach lesions) was considered to be "mild" in severity and may have been enhanced by the vehicle used (sesame oil in which sulfur mustard is fully soluble) and the route of administration (gavage), which is more likely to result in localized irritant effects. The key study did identify a toxic effect that is consistent with the vesicant properties of sulfur mustard. In none of the other available studies was there any indication of a different effect occurring at a lower exposure level.

Air Pollutants↗

Small mammals as monitors of environmental contaminants.

The merit of using small mammals as monitors of environmental contaminants was assessed using data from the published literature. Information was located on 35 species of small mammals from 7 families used to monitor heavy metals, radionuclides, and organic chemicals at mine sites, industrial areas, hazardous and radioactive waste disposal sites, and agricultural and forested land. To document foodchain transfer of chemicals, concentrations in soil, vegetation, and invertebrates, where available, were included. The most commonly trapped North American species were Peromyscus leucopus, Blarina brevicauda, and Microtus pennsylvanicus. In these species, exposure to chemicals was determined from tissue residue analyses, biochemical assays, and cytogenetic assays. Where enough information was available, suitable target tissues, or biological assays for specific chemicals were noted. In general, there was a relationship between concentrations of contaminants in the soil or food, and concentrations in target tissues of several species. This relationship was most obvious for the nonessential heavy metals, cadmium, lead, and mercury and for fluoride. Kidney was the single best tissue for residue analyses of inorganic contaminants. However, bone should be the tissue of choice for both lead and fluorine. Exposure to lead was also successfully documented using biochemical and histopathological endpoints. Bone was the tissue of choice for exposure to 90Sr, whereas muscle was an appropriate tissue for 137Cs. For organic contaminants, exposure endpoints depended on the chemical(s) of concern. Liver and whole-body residue analyses, as well as enzyme changes, organ histology, genotoxicity, and, in one case, population dynamics, were successfully used to document exposure to these contaminants. Based on information in these studies, each species' suitability as a monitor for a specific contaminant or type of contaminant was evaluated and subsequently ranked. A relationship between contaminant exposure and trophic level emerged. Insectivores (shrews) had the highest levels of contaminants, followed by omnivores (cricetid mice) with intermediate levels, and herbivores (voles) with the lowest levels. A substantial number of these biomonitoring studies using small mammals collectively point to the importance of food habits and habitat of small mammals, and their availability and abundance as factors that should influence species selection for monitoring studies. The type of contaminants under consideration as well as the appropriateness of the endpoints selected are important factors to consider when deciding whether or not to include small mammals in biomonitoring studies.

Animals↗