Evaluation of CO exposure in active smokers while smoking using breath analysis technique

The current study evaluated the personal CO exposure of active smokers while smoking under controlled conditions, decay rate of CO in the body following active smoking, and CO accumulation in the body from repeated active smoking using a novel device for the direct measurement of alveolar breath CO. Prior to this evaluation, the proposed alveolar CO measurement device was successfully evaluated as regards the effect of humidity, CO recovery, carryover effect, and in comparison with the bag sampling method. The breath concentrations prior to and after a single cigarette were measured using a repeated measure design. Under the controlled conditions employed in the present study, active smoking was found to cause a significant body burden of CO. The post-exposure breath CO level was 1.6-2.0 times higher than the background breath level, depending on the subject and cigarette brand. In addition, the pre- and post-exposure breath concentrations were both significantly different among the subjects, yet the ratios of post-exposure to pre-exposure breath concentrations did not differ significantly between the different cigarette brands. The time-series alveolar breath concentrations measured following active smoking showed that the post-exposure alveolar CO concentrations decreased slowly even in the early phase of the decay curves, indicating a mono-compartment uptake and elimination model for the human body. The half-lives estimated in the present study (301, 315, and 385 min) were longer than or comparable to those in previous studies. The breath measurements prior to and after repeated active smoking exhibited a significant increasing trend for both the pre- and post-exposure concentrations. The changes in the pre- and post-exposure breath CO concentrations with repeated smoking ranged from 7% to 23% and from 10% to 15%, respectively, with half-hour intervals between cigarettes, and from 4% to 11% and from 6% to 8%, respectively, with hour intervals between cigarettes. Accordingly, most of the current results indicated that CO was accumulated in the human body with repeated active smoking.     

A nonlinear version of the Coburn,Forster and Kane model of blood carboxyhemoglobin

We provide an integrated form of the preferred nonlinear form of the Coburn, Forster and Kane (1965, J. clin. Invest. 41, 1899–1910) model. The new technique guarantees numerical accuracy, yet substantially reduces the computational burden.     

Quality Science in the Courtroom: U.S. EPA Data Quality and Peer Review Policies and Procedures Compared to the Daubert Factors

Protection of the environment is critically dependent on the quality of data used in decision making. Whether the decisions are part of the scientific process or relate to application of the laws governing people and their living conditions, good quality data are required/needed by two disciplines with distinct differences. This paper examines some differences between science and the law, provides a brief history of science in law, discusses the effects of law on science, compares United States Environmental Protection Agency (U.S. EPA) guidance and U.S. Supreme Court credible science criteria. This paper further speculates on the future use of science data by the courts.     

Quality Science in the Courtroom: U.S. EPA Data Quality and Peer Review Policies and Procedures Compared to the Daubert Factors

Protection of the environment is critically dependent on the quality of data used in decision making. Whether the decisions are part of the scientific process or relate to application of the laws governing people and their living conditions, good quality data are required/needed by two disciplines with distinct differences. This paper examines some differences between science and the law, provides a brief history of science in law, discusses the effects of law on science, compares United States Environmental Protection Agency (U.S. EPA) guidance and U.S. Supreme Court credible science criteria. This paper further speculates on the future use of science data by the courts.     

The U.S. Experience in Promoting Sustainable Chemistry (9 pp)

- Sustainable chemistry - Section editors: Klaus Günter Steinhäuser, Steffi Richter, Petra Greiner, Jutta Penning, Michael AngrickBackground, Aim and Scope Recent developments in European chemicals policy, including the Registration, Evaluation and Authorization of Chemicals (REACH) proposal, provide a unique opportunity to examine the U.S. experience in promoting sustainable chemistry as well as the strengths and weaknesses of existing policies. Indeed, the problems of industrial chemicals and limitations in current regulatory approaches to address chemical risks are strikingly similar on both sides of the Atlantic. We provide an overview of the U.S. regulatory system for chemicals management and its relationship to efforts promoting sustainable chemistry. We examine federal and state and examine lessons learned from this system that can be applied to developing more integrated, sustainable approaches to chemicals management.Main Features There is truly no one U.S. chemicals policy, but rather a series of different un-integrated policies at the federal, regional, state and local levels. While centerpiece U.S. Chemicals Policy, the Toxic Substances Control Act of 1976, has resulted in the development of a comprehensive, efficient rapid screening process for new chemicals, agency action to manage existing chemicals has been very limited. The agency, however, has engaged in a number of successful, though highly underfunded, voluntary data collection, pollution prevention, and sustainable design programs that have been important motivators for sustainable chemistry. Policy innovation in the establishment of numerous state level initiatives on persistent and bioaccumulative toxics, chemical restrictions and toxics use reduction have resulted in pressure on the federal government to augment its efforts.Results and Conclusions It is clear that data collection on chemical risks and phase-outs of the most egregious chemicals alone will not achieve the goals of sustainable chemistry. These alone will also not internalize the cultural and institutional changes needed to ensure that design and implementation of safer chemicals, processes, and products are the focus of the future. Thus, a more holistic approach of ‘carrots and sticks’ – that involves not just chemical producers but those who use and purchase chemicals is necessary. Some important lessons of the US experience in chemicals management include: (1) the need for good information on chemicals flows, toxic risks, and safer substances.; (2) the need for comprehensive planning processes for chemical substitution and reduction to avoid risk trade-offs and ensure product quality; (3) the need for technical and research support to firms for innovation in safer chemistry; and (4) the need for rapid screening processes and tools for comparison of alternative chemicals, materials, and products.     

Inter-Urban Comparison of Ambient Volatile Organic Compound Concentrations in U.S. Cities

Airborne particulate matter from three ferrous foundries was sampled in granulometric fractions and analyzed by scanning electron microscopy with energy dispersive X-ray analysis (SEM-EDXA), X-ray photoelectron spectroscopy (XPS) and secondary ion mass spectrometry (SIMS) to determine morphology and qualitative bulk and surface chemical compositions. Cluster and principal components analyses (PCA) were used as an aid for interpretation of results. A clear pattern of composition as a function of size emerges; in particular, trace metals accumulate in fine particles and volatile species on the surface of these. Chemical composition changes are also related to daily schedules where applicable: trace metals appear during pouring operations, silicon is generated during mold making and unmolding. Cluster and PCA greatly ease examination of data and offer pictorial representations of results; in particular, the chemical composition versus particle size relationship is very neatly illustrated by PCA graphs.     

A status report on the U.S. national dioxin study

In 1983, the US Environmental Protection Agency (EPA) embarked on an extensive investigation of the presence and extent of contamination of the national environment by CDDs/CDFs. This status report is a prelude to a final report to be delivered to the US Congress in December, 1985.     

Nutrient dynamics as indicators of karst processes: comparison of the Chalk aquifer (Normandy, France) and the Edwards aquifer (Texas, U.S.A.)

Karst aquifers display a range of geologic and geomorphic characteristics in a wide range of climatic and land-use settings; identification of transport dynamics representative of karst aquifers in general could help advance our understanding of these complex systems. To this end, nutrient, turbidity, and major ion dynamics in response to storms were compared at multiple sites in two karst aquifers with contrasting characteristics and settings: the Chalk aquifer (Eure Department, Normandy, France) and the Barton Springs segment of the Edwards Aquifer (Texas, U.S.A.). The Chalk aquifer is typified by high matrix porosity, thick surficial deposits (up to 30 m thick), and agricultural land use; the Barton Springs segment is typified by low matrix porosity, outcropping limestone, and urban land use. Following one to three storms, from 5 to 16 samples from springs and wells were analyzed for major ions, and specific conductance and turbidity were monitored continuously. Comparison of the chemographs indicated some generalized responses, including an increase in turbidity and potassium concentrations and a decrease in major ion and nitrate concentrations with infiltrating storm runoff. Factor analysis of major ions and turbidity revealed strikingly similar behavior of the chemical variables for the two aquifers: The first two factors, explaining more than 75% of the variability, illustrate that dynamics of most major ions (including nitrate) are opposed to those of turbidity and of potassium. The results demonstrate that potassium and nitrate are effective tracers of infiltrating storm runoff and resident ground water, respectively, and the similar results for these two highly contrasting aquifers suggest that the dynamics identified might be applicable to karst systems in general.     

Electricity from fossil fuels without CO2 emissions: assessing the costs of carbon dioxide capture and sequestration in U.S. electricity markets.

The decoupling of fossil-fueled electricity production from atmospheric CO2 emissions via CO2 capture and sequestration (CCS) is increasingly regarded as an important means of mitigating climate change at a reasonable cost. Engineering analyses of CO2 mitigation typically compare the cost of electricity for a base generation technology to that for a similar plant with CO2 capture and then compute the carbon emissions mitigated per unit of cost. It can be hard to interpret mitigation cost estimates from this plant-level approach when a consistent base technology cannot be identified. In addition, neither engineering analyses nor general equilibrium models can capture the economics of plant dispatch. A realistic assessment of the costs of carbon sequestration as an emissions abatement strategy in the electric sector therefore requires a systems-level analysis. We discuss various frameworks for computing mitigation costs and introduce a simplified model of electric sector planning. Results from a "bottom-up" engineering-economic analysis for a representative U.S. North American Electric Reliability Council (NERC) region illustrate how the penetration of CCS technologies and the dispatch of generating units vary with the price of carbon emissions and thereby determine the relationship between mitigation cost and emissions reduction.     

Electricity from Fossil Fuels without CO2 Emissions: Assessing the Costs of Carbon Dioxide Capture and Sequestration in U.S. Electricity Markets

ABSTRACT

The decoupling of fossil-fueled electricity production from atmospheric CO₂ emissions via CO₂ capture and sequestration (CCS) is increasingly regarded as an important means of mitigating climate change at a reasonable cost. Engineering analyses of CO₂ mitigation typically compare the cost of electricity for a base generation technology to that for a similar plant with CO₂ capture and then compute the carbon emissions mitigated per unit of cost. It can be hard to interpret mitigation cost estimates from this plant-level approach when a consistent base technology cannot be identified. In addition, neither engineering analyses nor general equilibrium models can capture the economics of plant dispatch. A realistic assessment of the costs of carbon sequestration as an emissions abatement strategy in the electric sector therefore requires a systems-level analysis. We discuss various frameworks for computing mitigation costs and introduce a simplified model of electric sector planning. Results from a “bottom-up” engineering-economic analysis for a representative U.S. North American Electric Reliability Council (NERC) region illustrate how the penetration of CCS technologies and the dispatch of generating units vary with the price of carbon emissions and thereby determine the relationship between mitigation cost and emissions reduction.     

Pesticides in ground water in the united states: Monitoring,modeling, and risks from the U.S. perspective

Abstract

Scientific and regulatory interest in ground water contamination by pesticides increased significantly in 1979. This was prompted by findings of the nematicide 1,2‐dibromo‐3‐chloropropane (DBCP) and the nematicide/insecticide aldicarb (Temik®) in ground water in several states. Since that time, at least 130 pesticides and pesticide metabolites have been detected in ground water in over 150 studies, but detection frequencies are 4–10% nationally. Detection frequencies of pesticides over Health Advisory Levels are generally lower. Screening‐level models and detailed computer simulation models are useful for risk assessments and regulatory decisions. Attenuation Factor, CMLS, PRZM2, GLEAMS, and LEACHM are all useful models.     

Groundwater munition residues and nitrate near Grand Island,Nebraska, U.S.A.

Munition residues from waste disposal on ordnance property have resulted in a defined plume of RDX contaminated groundwater stretching 6.5 km and underlying an area of 6.5 km². A smaller plume of TNT was detected near the plant's boundary. The relative positions of the plumes combined with an historical review of total plant output of RDX and TNT indicates that RDX is much more persistent than TNT. The estimated RDX transport velocity of 0.5 m day⁻¹ closely approximates the calculated Darcian velocity. The RDX plume sinks with recharge at a rate of about 0.5 m yr⁻¹.Nitrate is associated primarily with adjacent upgradient landuse and is not related to plant manufacture of ammonium nitrate. The average δ¹⁵N of the Nitrate was about + 10% and strongly suggests that animal wastes are the predominant source.     

Principles and organization of methods for establishing maximum permissible emissions in the cities of the U.S.S.R.

Principles are presented for standardization and establishment of maximum permissible emissions (MPE) into the atmosphere in accordance with theoretical and experimental investigations of pollutant diffusion from sources of various types, accounting for meteorological and topographical conditions. MPE refers to the amount of pollutants from a single source that together with other neighbouring sources give rise to air pollution concentrations that do not exceed the air quality standard. Due to a lack of confidence in theories it is impossible at present to prove the establishment of MPE and our present technical knowledge supports only a gradual decrease of emissions and determination of temporarily agreed emissions (TAE). For determination of MPE and TAE from multiple urban sources, calculation and analysis of their total concentration field are performed. The physical bases of the methods for standardization of industrial emissions officially adopted in the U.S.S.R. for practical use are presented. It is considered how standardization and establishment of MPE and control on their fulfillment are organized in the U.S.S.R.     

Visibility reductions from soil dust in the Western U.S.

Soil dust can at times contribute significantly to atmospheric turbidity in the western U.S.A. An examination of meteorological surface observations from three sites in the west shows an increase in the number of cases of blowing dust (BD) over the past 30 years, while the mean wind speed associated with BD has decreased in growing, urban areas. Dust is reported more often in developing areas (such as Denver and Tucson) than in less disturbed areas (Winslow, AZ). Dust turbidity models, whose development was stimulated by the 1930s great plains dust bowl catastrophe are applicable to western soils as well and help explain visibility reductions caused by dust. Vehicle generated dust from unpaved roads can limit visibilities to values of one-third or less than the molecular scattering limit. The upper limits to the amounts of dust and visibility reduction to be expected in the west for differing meteorological conditions are calculated. It is estimated that dust devils may occasionally contribute 247 μg m ⁻³ of dust to the lower atmosphere in the west and a possible correlation between dust devils and human activity is noted.     

Persistent organic pollutants (POPs) in the conventional activated sludge treatment process: model predictions against experimental values

The FATE and treatibility estimator (FATE) model, developed by the United States Environmental Protection Agency was used for the prediction of the FATE of 26 persistent organic pollutants (POPs), i.e. 7 PCBs and 19 organochlorine compounds (OCs), during the conventional activated sludge treatment process applied in the waste water treatment plant (WWTP) of Thessaloniki, Greece. The removal rates predicted by the model for the primary and the secondary treatment stages were found to differ substantially from those experimentally measured. When the overall treatment was considered, the differences between measured and model predicted removals were within acceptable limits of confidence. Possible reasons that might cause deviations from experimental values were suggested to be the wastewater content in dissolved organic carbon (DOC), and/or the low concentrations of POPs in untreated wastewater.     

Levels of 2,3,7,8-Tetrachlorodibenzo- -dioxin (2,3,7,8-TCDD) in adipose tissue of U.S. Vietnam veterans seeking medical assistance

2,3,7,8-Tetrachlorodibenzo- -dioxin (2,3,7,8-TCDD) was detected in an earlier study in adipose tissue of U.S. veterans who were exposed to Agent Orange in Vietnam. The levels appear to be directly related to the intensity of exposure¹. We now report on a group of thirteen Vietnam veterans who were screened for 2,3,7,8-TCDD in adipose tissue. All the veterans had sought medical assistance and some had health effects that may be ascribed to exposure to 2,3,7,8-TCDD. Also included are control patients who were taken from the population of the U.S. 2,3,7,8-TCDD was detected in most of the adipose tissue samples at levels ranging from 2 to 14 ppt. No significant differences in the tissue levels of Vietnam veterans and the other persons were found in this preliminary study.     

Lead analysis in urban dust on St. Thomas,U.S. Virgin Islands

The average concentration of Pb in urban dust in central Charlotte Amalie, St. Thomas, U.S. Virgin Islands, was found to be 803 ppm. On the hills in the town the level was higher, over 2000 ppm. The Pb content of dust was found to depend on the distance from the street of the sampling site, but the dependence was less than expected. Urban dust samples taken on the neighbouring island of St. Croix, where there is lower traffic density, showed an average Pb level of 327 ppm.     

Arsenic Background Concentrations in Florida,U.S.A. Surface Soils: Determination and Interpretation

Background concentrations of soil arsenic have been used as an alternative soil cleanup criterion in many states in the U.S. This research addresses issues related to the interpretation of background concentrations of arsenic in near pristine soils in Florida. Total arsenic was measured in 448 taxonomic and geographic representative surface soil samples using USEPA Method 3052 (HCl-HNO₃-HF, microwave digestion) and graphite furnace atomic absorption spectrophotometry analysis procedure. Values were log-normally distributed, with geometric mean and baseline concentration (defined as 95% of the expected range of background concentrations) providing the most satisfactory statistical results. An upper baseline concentration of 6.21 mg As/kg was estimated for undisturbed soils (n = 267) compared to 7.63 mg As/kg for disturbed soils (n = 181). Temporal trend of total soil arsenic concentrations from 1967 to 1989 paralleled decreased usage of arsenic in U.S. agriculture. Soil arsenic background concentrations were generally higher in south Florida than in north and central Florida, and associated with wet soils. Individual high arsenic sites were scattered throughout the state, but the most highly concentrated of these occurred in the Leon-Lee belt along the Ocala uplift district extending to the southwestern flatwoods district. Extrapolation of the data using a single arsenic value regardless of the taxonomic and geographical differences in soil arsenic distribution would underestimate potential arsenic contamination in upland soils.