In urban areas like Chicago, daily life extends above ground level due to the prevalence of high-rise buildings where residents and commuters live and work. This study examines the variation in fine particulate matter (PM2.5) concentrations across building stories. PM2.5 levels were measured using PurpleAir sensors, installed between 8 April and 7 May 2023, on floors one, four, six, and nine of an office building in Chicago. Additionally, data were collected from a public outdoor PurpleAir sensor on the fourteenth floor of a condominium located 800 m away. The results show that outdoor PM2.5 concentrations peak at 14 m height, and then decline by 0.11 μg/m3 per meter elevation, especially noticeable from midnight to 8 a.m. under stable atmospheric conditions. Indoor PM2.5 concentrations increase steadily by 0.02 μg/m3 per meter elevation, particularly during peak work hours, likely caused by greater infiltration rates at higher floors. Both outdoor and indoor concentrations peak around noon. We find that indoor and outdoor PM2.5 are positively correlated, with indoor levels consistently remaining lower than outside levels. These findings align with previous research suggesting decreasing outdoor air pollution concentrations with increasing height. The study informs decision-making by community members and policymakers regarding air pollution exposure in urban settings.
Residual impacts of a wildland urban interface fire on urban particulate matter and dust: a study from the Marshall Fire
The impacts of wildfires along the wildland urban interface (WUI) on atmospheric particulate concentrations and composition are an understudied source of air pollution exposure. To assess the residual impacts of the 2021 Marshall Fire (Colorado), a wildfire that predominantly burned homes and other human-made materials, on homes within the fire perimeter that escaped the fire, we performed a combination of fine particulate matter (PM2.5) filter sampling and chemical analysis, indoor dust collection and chemical analysis, community scale PurpleAir PM2.5 analysis, and indoor particle number concentration measurements. Following the fire, the chemical speciation of dust collected in smoke-affected homes in the burned zone showed elevated concentrations of the biomass burning marker levoglucosan (medianlevo = 4147 ng g−1), EPA priority toxic polycyclic aromatic hydrocarbons (median Σ16PAH = 1859.3 ng g−1), and metals (median Σ20Metals = 34.6 mg g−1) when compared to samples collected in homes outside of the burn zone 6 months after the fire. As indoor dust particles are often resuspended and can become airborne, the enhanced concentration of hazardous metals and organics within dust samples may pose a threat to human health. Indoor airborne particulate organic carbon (median = 1.91 μg m−3), particulate elemental carbon (median = .02 μg m−3), and quantified semi-volatile organic species in PM2.5 were found in concentrations comparable to ambient air in urban areas across the USA. Particle number and size distribution analysis at a heavily instrumented supersite home located immediately next to the burned area showed indoor particulates in low concentrations (below 10 μg m−3) across various sizes of PM (12 nm–20 μm), but were elevated by resuspension from human activity, including cleaning.
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- Award ID(s):
- 2218009
- PAR ID:
- 10420409
- Date Published:
- Journal Name:
- Air Quality, Atmosphere & Health
- ISSN:
- 1873-9318
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract The Thomas Fire began on December 4, 2017 and burned 281,893 acres over a 40‐day period in Ventura and Santa Barbara Counties, making it one of California's most destructive wildfires to date. A major rainstorm then caused a flash flood event, which led to the containment of the fire. Both airborne ash from the fire and the runoff from the flash flood entered into the Santa Barbara Basin (SBB). Here, we present the results from aerosol, river, and seawater studies of black carbon and metal delivery to the SBB associated with the fire and subsequent flash flood. On day 11 of the Thomas Fire, aerosols sampled under the smoke plume were associated with high levels of PM2.5, levoglucosan, and black carbon (average: 49 μg/m3, 1.05 μg/m3, and 14.93 μg/m3, respectively) and aerosol metal concentrations were consistent with a forest fire signature. Metal concentrations in SBB surface seawater were higher closer to the coastal perimeter of the fire (including 2.22 nM Fe) than further off the coast, suggesting a dependence on continental proximity rather than fire inputs. On days 37–40 of the fire, before, during, and after the flash flood in the Ventura River, dissolved organic carbon, dissolved black carbon, and dissolved metal concentrations were positively correlated with discharge allowing us to estimate the input of fire products into the coastal ocean. We estimated rapid aerosol delivery during the fire event to be the larger share of fire‐derived metal transport compared to runoff from the Ventura River during the flood event.
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null (Ed.)Urban air pollution poses a major threat to human health. Understanding where and when urban air pollutant concentrations peak is essential for effective air quality management and sustainable urban development. To this end, we implement a mobile monitoring methodology to determine the spatiotemporal distribution of particulate matter (PM) and black carbon (BC) throughout Philadelphia, Pennsylvania and use hot spot analysis and heatmaps to determine times and locations where pollutant concentrations are highest. Over the course of 12 days between June 27 and July 29, 2019, we measured air pollution concentrations continuously across two 150 mile (241.4 km) long routes. Average daily mean concentrations were 11.55 ± 5.34 μg/m 3 (PM 1 ), 13.48 ± 5.59 μg/m 3 (PM 2.5 ), 16.13 ± 5.80 μg/m 3 (PM 10 ), and 1.56 ± 0.39 μg/m 3 (BC). We find that fine PM size fractions (PM 2.5 ) constitute approximately 84% of PM 10 and that BC comprises 11.6% of observed PM 2.5 . Air pollution hotspots across three size fractions of PM (PM 1 , PM 2.5 , and PM 10 ) and BC had similar distributions throughout Philadelphia, but were most prevalent in the North Delaware, River Wards, and North planning districts. A plurality of detected hotspots found throughout the data collection period (30.19%) occurred between the hours of 8:00 AM–9:00 AM.more » « less
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Indoor dust can be a major source of heavy metals, nutrients, and bacterial contamination in residential environments and may cause serious health problems. The goal of this research is to characterize chemical and bacterial contaminants of indoor, settled house dust in the Houston Metropolitan region. To achieve this, a total of 31 indoor dust samples were collected, along with household survey data, which were subsequently analyzed for elemental and bacterial concentrations. Microscopic and geospatial analysis was conducted to characterize and map potential hotspots of contamination. Interestingly Cd, Cr, Cu, Pb, and Zn concentrations of all 31 indoor dust samples were significantly enriched and exceeded soil background concentrations. Furthermore, As, Cd, Pb, and Zn concentrations in the dust samples were significantly correlated to the enteric bacterial load concentrations. Human health assessment revealed that cancer risk values via ingestion for Cd, Cr, and Ni were greater than the acceptable range. Of our 31 dust sample isolates, three Gram-negative and 16 Gram-positive pathogenic bacteria were identified, capable of causing a wide range of diseases. Our results demonstrate that both chemical and bacterial characterization of indoor dust coupled with spatial mapping is essential to assess and monitor human and ecological health risks.more » « less
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Organosulfates (OSs) are the most abundant class of organosulfur compounds (OrgS) in atmospheric fine particulate matter (PM2.5). Globally, isoprene‐derived OSs (iOSs) are the most abundantly reported OSs. The methyltetrol sulfates (MTSs), formed from multiphase chemical reactions of isoprene‐derived epoxidiols (IEPOX) with acidic sulfate aerosols, are the predominant iOSs. A recent study revealed that the heterogeneous hydroxyl radical (•OH) oxidation of fine particulate MTSs yields several highly oxygenated and functionalized OSs previously attributed to non‐IEPOX pathways. By using hydrophilic interaction liquid chromatography interfaced to electrospray ionization high‐resolution quadrupole time‐of‐flight mass spectrometry (HILIC/ESI‐HRQTOFMS), iOSs were quantitatively characterized in PM2.5 collected from 20 ground sites within the Interagency Monitoring of Protected Visual Environments (IMPROVE) network during the 2016 summer and winter seasons. Total water‐soluble sulfur (TWS‐S) and sulfur in the form of inorganic sulfate (Sinorg) were determined by inductively coupled plasmaoptical emission spectroscopy (ICP‐OES) and ion chromatography (IC), respectively. The difference between TWS‐S and Sinorg was used as an upper bound estimate of water‐soluble OrgS concentration. Significantly higher OrgS concentrations, coincident with elevated iOS concentrations, were observed only in summer. On average, iOSs (130 ± 60, up to 240 ng m‐3) explained 29% (± 7%) of OrgS and 5% (± 2%) of organic matter (OM = 1.8*OC) in summertime PM2.5 collected from the eastern U.S. For the western U.S., iOSs (11 ± 6 ng m‐3) account for 6% (± 5%) of OrgS and 0.7% (± 0.4%) of OM. This study provides critical insights into the abundance, prevalence, spatial variability of iOSs across the U.S.more » « less
- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1007/s11869-023-01376-3
