Abstract

Abstract. This is the second study in a three-part study designed to demonstrate dynamic entanglements among gaseous organic compounds (VOCs), particulate matter (PM), and their subsequent potential biological effects. We study these entanglements in increasingly complex VOC and PM mixtures in urban-like conditions in a large outdoor chamber, both in the dark and in sunlight. To the traditional chemical and physical characterizations of gas and PM, we added new measurements of gas-only- and PM-only-biological effects, using cultured human lung cells as model living receptors. These biological effects are assessed here as increases in cellular damage or expressed irritation (i.e., cellular toxic effects) from cells exposed to chamber air relative to cells exposed to clean air. Our exposure systems permit side-by-side, gas-only- and PM-only-exposures from the same air stream containing both gases and PM in equilibria, i.e., there are no extractive operations prior to cell exposure for either gases or PM. In Part 1 (Ebersviller et al., 2012a), we demonstrated the existence of PM "effect modification" (NAS, 2004) for the case of a single gas-phase toxicant and an inherently non-toxic PM (mineral oil aerosol, MOA). That is, in the presence of the single gas-phase toxicant in the dark, the initially non-toxic PM became toxic to lung cells in the PM-only-biological exposure system. In this Part 2 study, we used sunlit-reactive systems to create a large variety of gas-phase toxicants from a complex mixture of oxides of nitrogen and 54 VOCs representative of those measured in US city air. In these mostly day-long experiments, we have designated the period in the dark just after injection (but before sunrise) as the "Fresh" condition and the period in the dark after sunset as the "Aged" condition. These two conditions were used to expose cells and to collect chemical characterization samples. We used the same inherently non-toxic PM from the Part 1 study as the target PM for "effect modification". Fortunately, in the absence of "seed particles", the complex highly-reactive VOC system used does not create any secondary aerosol in situ. All PM present in these tests were, therefore, introduced by injection of MOA to serve as PM-to-be-modified by the gaseous environment. PM addition was only done during dark periods, either before or after the daylight period. The purpose of this design is to test if a non-toxic PM becomes toxic in initially unreacted ("Fresh"), or in reacted ("Aged") complex VOC conditions. To have a complete design, we also tested the effects of clean air and the same VOC conditions, but without introducing any PM. Thus, there were six exposure treatment conditions that were evaluated with the side-by-side, gas-only- and PM-only-effects exposure systems; five separate chamber experiments were performed: two with clean air and three with the complex VOC/NOx mixture. For all of these experiments and exposures, chemical composition data and matching biological effects results for two end-points were compared. Chemical measurements demonstrate the temporal evolution of oxidized species, with a corresponding increase in toxicity observed from exposed cells. The largest increase in gas-phase toxicity was observed in the two "Aged" VOC exposures. The largest increase in particle-phase toxicity was observed in the "Aged" VOC exposure with the addition of PM after sunset. These results are a clear demonstration that the findings from Part 1 can be extended to the complex urban oxidized environment. This further demonstrates that the atmosphere itself cannot be ignored as a source of toxic species when establishing the risks associated with exposure to PM. Because gases and PM are transported and deposited differently within the atmosphere and lungs, these results have significant consequences. In the next (and final) part of the study, testing is further applied to systems with real diesel exhaust, including primary PM from a vehicle operated with different types of diesel fuel.

Highlights

  • In its most-recent document summarizing the state of the science related to particulate matter (PM), the US National Research Council (NRC) stated that “a finding that the effect of particles depends on the concentration of another pollutant that is, “effect modification” would have implications for setting National Ambient Air Quality Standards (NAAQS) independently for the various criteria pollutants” (NAS, 2004)

  • Its use will not create any secondary PM into the observation of the PM effects. This experimental design for the atmospheric chemistry environment results in a complex and highly realistic, but not totally quantifiable, set of gas-phase potential toxicants that are available for both gas-only exposures, and for potential uptake by test PM we introduce to the chamber to test PM “effect modification.”

  • The results are organized into sections related to: 1. the temporal changes in the gas-phase nitrogen oxides (NOx), O3, and VOC concentrations as revealed by the gas monitors, the GCMS, and flame ionization detector (FID) measurements; 2. the temporal creation of secondary carbonyl species, some of which were further oxidized, as revealed by direct GCMS sampling and GCMS of PFBHA-derivatised samples; 3. the demonstration of a lack of secondary PM formation from the daytime oxidation of the SynUrb54 VOCs; the quantification of mineral oil aerosol (MOA) size distributions and mass concentrations following the injection of MOA into the chamber during dark periods; www.atmos-chem-phys.net/12/12293/2012/

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Summary

Introduction

In its most-recent document summarizing the state of the science related to PM, the US National Research Council (NRC) stated that “a finding that the effect of particles depends on the concentration of another pollutant that is, “effect modification” would have implications for setting National Ambient Air Quality Standards (NAAQS) independently for the various criteria pollutants” (NAS, 2004).In Part 1 (Ebersviller et al, 2012a), we demonstrated the existence of PM “effect modification” for the case of a single gas-phase toxicant and an inherently non-toxic PM (mineral oil aerosol, MOA). The non-toxic PM (MOA) was added to clean air and both biological exposures were performed, which resulted in no response from cells to either gases or PM. For the gas with lower volatility, it appears that much of the gasphase mass was removed to the PM, but in the higher volatility gas, it was less clear how the toxicant partitioned These results showed that a gas from the environment surrounding an initially non-toxic PM could modify the PM so that it became toxic to lung cells due to atmospheric processes only. This is the “effect modification” that the NRC posed would have implications for research and regulation of PM

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