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NASA Scientific and Technical Aerospace Reports

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20040070705 <strong>NASA</strong> Ames Research Center, Moffett Field, CA, USA<br />

Environment Partitioning <strong>and</strong> Reactivity of Polybrominated Diphenylethers<br />

Hua, Inez; Iraci, Laura T.; Jafvert, Chad; Bezares-Cruz, Juan; March 1, 2004; 1 pp.; In English; American <strong>and</strong> Canadian<br />

Geophysical Union Meeting, 17-21 May 2004, Montreal, Canada<br />

Contract(s)/Grant(s): RTOP 622-67-21-10; No Copyright; Avail: Other Sources; Abstract Only<br />

Polybrominated diphenyl ethers (PBDEs) are an important class of flame retardants. Annual global dem<strong>and</strong> for these<br />

compounds was over 67,000 metric tons in 2001. PBDEs have recently been extensively investigated as environmental<br />

contaminants because they have been detected in air, sediment, <strong>and</strong> tissue samples from urban <strong>and</strong> remote areas. Important<br />

issues include quantifying PBDE partitioning in various environmental compartments, <strong>and</strong> elucidating transformation<br />

pathways. The partitioning of PBDE congeners to aerosols was estimated for 16 sites in the USA, Canada, <strong>and</strong> Mexico. The<br />

aerosol particles were PM2.5, the total suspended particle (TSP) concentration varied between 3.0 - 55.4 micro g/cubic meter,<br />

<strong>and</strong> the organic fraction ranged from 11 - 41%; these data are published values for each site. It is estimated that the largest<br />

fraction of each PBDE associated with the aerosol particles occurs in Mexico City, <strong>and</strong> the smallest fraction in Colorado<br />

Plateau. Although the organic fraction in Mexico City is about 60% of that observed in the Colorado Plateau, the TSP is larger<br />

by a factor of about 18.5, <strong>and</strong> it is the difference in TSP that strongly influences the fraction of particle-bound PBDE in this<br />

case. PBDE partitioning to PM2.5 particles also varies seasonally because of temperature variations. For the less brominated<br />

congeners the percentage that is particle-bound is relatively low, regardless of air temperature. In contrast, the heavier<br />

congeners exhibit a significant temperature dependence: as the temperature decreases (fall, winter) the percentage of PBDE<br />

that is particle-bound increases. The partitioning calculations complement experimental data indicating that<br />

decabromodiphenyl ether (DBDE) dissolved in hexane transforms very rapidly when irradiated with solar light. DBDE is the<br />

most highly brominated PBDE congener (10 bromine atoms) <strong>and</strong> occurs in the commercial formulation which is subject to<br />

the largest global dem<strong>and</strong>.<br />

Author<br />

Bromine; Congeners; Contaminants; Diphenyl Compounds; Ethers; Reactivity; Global Air Pollution<br />

20040070706 <strong>NASA</strong> Ames Research Center, Moffett Field, CA, USA<br />

Brown Cloud Pollution <strong>and</strong> Smog Ozone Transport 6,000 km to the Tropical Atlantic: Mechanism <strong>and</strong> Sensing<br />

Chatfield, Robert B.; Thompson, Anne M.; Guan, Hong; Witte, Jacquelyn C.; Hudson, Robert D.; [2004]; 1 pp.; In English;<br />

Quadrennial Ozone Symposium 2004, 1-8 Jun. 2004, Kos, Greece; No Copyright; Avail: Other Sources; Abstract Only<br />

We have found repeated illustrations in the maps of Total Tropospheric Ozone (TTO) of apparent transport of ozone from<br />

the Indian Ocean to the Equatorial Atlantic Ocean. Most interesting are examples that coincide with the INDOEX observations<br />

of late northern winter. Three soundings with the SHADOZ (Southern Hemisphere Additional Ozonesondes) network help<br />

confirm <strong>and</strong> quantify degree of influence of pollution, lightning, <strong>and</strong> stratospheric sources, suggesting that perhaps 40% of<br />

increased Atlantic ozone could be Asian pollution during periods of maximum identified in the TTO maps. This analysis also<br />

indicates a mechanism for such extended transport. We outline recurrent periods of apparent ozone transport from Indian to<br />

Atlantic Ocean regions outside the late-winter period. Clearly brown-cloud aerosol affects tropospheric ozone, both limiting<br />

its chemical production <strong>and</strong> also potentially obscuring its detection by the TOMS instrument. Introductory statistical studies<br />

will be presented, evaluating the role of tropopause meteorology, aerosol, <strong>and</strong> other factors in the modifying the relationship<br />

between true tropospheric ozone measured by SHADOZ <strong>and</strong> the TTO product, with suggestions for extending the product.<br />

Author<br />

Ozone; Pollution Transport; Smog; Air Pollution; Gas Transport<br />

20040070986 Health Effects Inst., Boston, MA, USA<br />

Peroxides <strong>and</strong> Macrophages in the Toxicity of Fine Particulate Matter in Rats<br />

Laksin, D. L.; Morio, L.; Hooper, K.; Li, T. H.; Buckley, B.; Dec. 2003; In English<br />

Report No.(s): PB2004-103505; No Copyright; Avail: National <strong>Technical</strong> Information Service (NTIS)<br />

This study was conducted to determine: (1) whether tissue injury induced by aerosols is medicated by cytotoxic hydrogen<br />

peroxide carried into the lower lung by fine particles <strong>and</strong> (2) whether exposure of rats to fine particulate matter (PM) leads<br />

to accumulation of activated macrophages in the lung.<br />

NTIS<br />

Exposure; Hydrogen Peroxide; Injuries; Lungs; Toxins <strong>and</strong> Antitoxins<br />

138

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