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1.
Environ Toxicol Chem ; 29(2): 265-274, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20821444

ABSTRACT

The present study investigated cross-media transport between both the sediment and the water column and between the water column and the atmosphere, to understand the role of each compartment as a source or a sink of polycyclic aromatic hydrocarbons (PAH) in southern California, USA, coastal waters. Concentrations of PAH were measured in the atmosphere, water column, and sediment at four water-quality-impaired sites in southern California: Ballona Creek Estuary, Los Angeles Harbor, Upper Newport Bay, and San Diego Bay. These concentrations were used to calculate site-specific sediment-water and atmosphere-water exchange fluxes. The net sediment-water exchange of total PAH (t-PAH) was positive, indicating that sediments were a source to the overlying water column. Furthermore, the net atmosphere-water exchange (gas exchange + dry particle deposition) of t-PAH was typically positive also, indicating the water column was a net source of PAH to the surrounding atmosphere through gas exchange. However, in all cases, the magnitude of the diffusive flux of PAH out of the sediments and into the water column far exceeded input or output of PAH through air/water exchange processes. These results demonstrate the potential importance of contaminated sediments as a source of PAH to the water column in coastal waters of southern California.


Subject(s)
Air Pollutants/analysis , Geologic Sediments/analysis , Polycyclic Aromatic Hydrocarbons/analysis , Seawater/chemistry , Water Pollutants, Chemical/analysis
2.
Environ Toxicol Chem ; 25(9): 2334-41, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16986787

ABSTRACT

Emissions of trace metals to the atmosphere and subsequent deposition, either directly to a waterbody surface or indirectly to the watershed as washoff during rainfall, represents a potential source of contamination to surface waters near urban centers. The present study provides measurements of atmospheric concentrations of particle-bound trace metals, and it estimates the dry deposition mass loading of trace metals in coastal watersheds in the Los Angeles, California, USA, air basin. Coarse-particle atmospheric concentrations of metals were measured seasonally using a Noll Rotary Impactor at six urban sites and one nonurban site. Dry deposition fluxes were calculated by summing the product of air concentration and the theoretical deposition velocity for each particle size fraction. Mean fluxes at urban sites ranged from 3.2 to 9.1, 11 to 34, 3.8 to 8.8, 8.3 to 29, and 69 to 228 microg/m2/d for chromium, copper, nickel, lead, and zinc, respectively. Mean concentrations and fluxes were significantly higher at urban sites compared with the nonurban site, although differences between urban and nonurban sites were reduced when sampling took place within 5 d after rainfall. Dry deposition to watershed land surfaces was substantial, representing a potentially large source of trace metals based on comparisons with load estimates from stormwater runoff.


Subject(s)
Air Pollutants/analysis , Air Pollutants/chemistry , Air Pollution/analysis , Metals/analysis , Water Pollutants, Chemical/analysis , Dust , Los Angeles , Time Factors , Water Pollution, Chemical/analysis
3.
J Air Waste Manag Assoc ; 55(10): 1418-30, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16295266

ABSTRACT

Real-time concentrations of black carbon, particle-bound polycyclic aromatic hydrocarbons, nitrogen dioxide, and fine particulate counts, as well as integrated and real-time fine particulate matter (PM2.5) mass concentrations were measured inside school buses during long commutes on Los Angeles Unified School District bus routes, at bus stops along the routes, at the bus loading/unloading zone in front of the selected school, and at nearby urban "background" sites. Across all of the pollutants, mean concentrations during bus commutes were higher than in any other microenvironment. Mean exposures (mean concentration times time spent in a particular microenvironment) in bus commutes were between 50 and 200 times greater than those for the loading/unloading microenvironment, and 20-40 times higher than those for the bus stops, depending on the pollutant. Although the analyzed school bus commutes represented only 10% of a child's day, on average they contributed one-third of a child's 24-hr overall black carbon exposure during a school day. For species closely related to vehicle exhaust, the within- cabin exposures were generally dominated by the effect of surrounding traffic when windows were open and by the bus's own exhaust when windows were closed. Low-emitting buses generally exhibited high concentrations only when traveling behind a diesel vehicle, whereas high-emitting buses exhibited high concentrations both when following other diesel vehicles and when idling without another diesel vehicle in front of the bus. To reduce school bus commute exposures, we recommend minimizing commute times, avoiding caravanning with other school buses, using the cleanest buses for the longest bus routes, maintaining conventional diesel buses to eliminate visible emissions, and transitioning to cleaner fuels and advanced particulate control technologies as soon as possible.


Subject(s)
Environment , Environmental Exposure , Transportation , Air Pollutants, Occupational/analysis , California , Carbon/analysis , Child , Humans , Nitrogen Dioxide/analysis , Polycyclic Aromatic Hydrocarbons/analysis , Schools
4.
Water Res ; 39(16): 3929-37, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16112162

ABSTRACT

The contribution of atmospheric deposition to emissions of trace metals in stormwater runoff was investigated by quantifying wet and dry deposition fluxes and stormwater discharges within a small, highly impervious urban catchment in Los Angeles. At the beginning of the dry season in spring 2003, dry deposition measurements of chromium, copper, lead, nickel, and zinc were made monthly for 1 year. Stormwater runoff and wet deposition samples also were collected, and loading estimates of total annual deposition (wet+dry) were compared with annual stormwater loads. Wet deposition contributed 1-10% of the total deposition inside the catchment, indicating the dominance of dry deposition in semi-arid regions such as Los Angeles. Based on the ratio of total deposition to stormwater, atmospheric deposition potentially accounted for as much as 57-100% of the total trace metal loads in stormwater within the study area. Despite potential bias attributable to processes that were not quantified in this study (e.g., resuspension out of the catchment or sequestration within the catchment), these results demonstrate atmospheric deposition represents an important source of trace metals in stormwater to waterbodies near urban centers.


Subject(s)
Metals, Heavy/analysis , Water Pollutants/analysis , Air Pollutants , Atmosphere , Cities , Environmental Monitoring , Rain
5.
J Expo Anal Environ Epidemiol ; 15(5): 377-87, 2005 Sep.
Article in English | MEDLINE | ID: mdl-15592444

ABSTRACT

Real-time and integrated measurements of gaseous and particulate pollutants were conducted inside five conventional diesel school buses, a diesel bus with a particulate trap, and a bus powered by compressed natural gas (CNG) to determine the range of children's exposures during school bus commutes and conditions leading to high exposures. Measurements were made during 24 morning and afternoon commutes on two Los Angeles Unified School District bus routes from South to West Los Angeles, with seven additional runs on a rural/suburban route, and three runs to test the effect of window position. For these commutes, the mean concentrations of diesel vehicle-related pollutants ranged from 0.9 to 19 microg/m(3) for black carbon, 23 to 400 ng/m(3) for particle-bound polycyclic aromatic hydrocarbon (PB-PAH), and 64 to 220 microg/m(3) for NO(2). Concentrations of benzene and formaldehyde ranged from 0.1 to 11 microg/m(3) and 0.3 to 5 microg/m(3), respectively. The highest real-time concentrations of black carbon, PB-PAH and NO(2) inside the buses were 52 microg/m(3), 2000 ng/m(3), and 370 microg/m(3), respectively. These pollutants were significantly higher inside conventional diesel buses compared to the CNG bus, although formaldehyde concentrations were higher inside the CNG bus. Mean black carbon, PB-PAH, benzene and formaldehyde concentrations were higher when the windows were closed, compared with partially open, in part, due to intrusion of the bus's own exhaust into the bus cabin, as demonstrated through the use of a tracer gas added to each bus's exhaust. These same pollutants tended to be higher on urban routes compared to the rural/suburban route, and substantially higher inside the bus cabins compared to ambient measurements. Mean concentrations of pollutants with substantial secondary formation, such as PM(2.5), showed smaller differences between open and closed window conditions and between bus routes. Type of bus, traffic congestion levels, and encounters with other diesel vehicles contributed to high exposure variability between runs.


Subject(s)
Air Pollution, Indoor/analysis , Environmental Exposure , Vehicle Emissions/analysis , Child , Child Welfare , Environmental Monitoring , Fossil Fuels , Humans , Los Angeles , Motor Vehicles , Rural Population , Students , Urban Population
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