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Oxidized organic aerosol (OOA) is a major component of ambient particulate matter, substantially impacting climate, human health, and ecosystems. OOA is readily produced in the presence of sunlight, and requires days of photooxidation to reach the levels observed in the atmosphere. High concentrations of OOA are thus expected in the summer; however, our current mechanistic understanding fails to explain elevated OOA during wintertime periods of low photochemical activity that coincide with periods of intense biomass burning. As a result, atmospheric models underpredict OOA concentrations by a factor of 3 to 5. Here we show that fresh emissions from biomass burning exposed to NO2 and O3 (precursors to the NO3 radical) rapidly form OOA in the laboratory over a few hours and without any sunlight. The extent of oxidation is sensitive to relative humidity. The resulting OOA chemical composition is consistent with the observed OOA in field studies in major urban areas. Additionally, this dark chemical processing leads to significant enhancements in secondary nitrate aerosol, of which 50 to 60% is estimated to be organic. Simulations that include this understanding of dark chemical processing show that over 70% of organic aerosol from biomass burning is substantially influenced by dark oxidation. This rapid and extensive dark oxidation elevates the importance of nocturnal chemistry and biomass burning as a global source of OOA.
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Poluentes Atmosféricos/química , Poluição do Ar/estatística & dados numéricos , Biomassa , Material Particulado/química , Aerossóis/química , Cidades , Modelos Teóricos , Dióxido de Nitrogênio/análise , Dióxido de Nitrogênio/química , Oxirredução , Oxigênio/químicaRESUMO
Polycyclic aromatic hydrocarbons (PAHs) represent one of the major toxic pollutants associated with PM2.5 with significant human health and climate effects. Because of local and long-range transport of atmospheric PAHs to receptor sites, higher global attentions have been focused to improve PAHs pollution emission management. In this study, PM2.5 samples were collected at three urban sites located in the capital of Iran, Tehran, during the heating and non-heating periods (H-period and NH-period). The US EPA 16 priority PAHs were analyzed and the data were processed to the following detailed aims: (i) investigate the H-period and NH-period variations of PM2.5 and PM2.5-bound PAHs concentrations; (ii) identify the PAHs sources and the source locations during the two periods; (iii) carry out a source-specific excess cancer risk (ECR) assessment highlighting the potential source locations contributing to the ECR using a hybrid approach. Total PAHs (TPAHs) showed significantly higher concentrations (1.56-1.89 times) during the H-period. Among the identified PAHs compounds, statistically significant periodical differences (p-value < 0.05) were observed only between eight PAHs species (Nap, BaA, Chr, BbF, BkF, BaP, IcdP, and DahA) at all three sampling sites which can be due to the significant differences of PAHs emission sources during H and NH-periods. High molecular weight (HMW) PAHs accounted for 52.7% and 46.8% on average of TPAHs during the H-period and NH-period, respectively. Positive matrix factorization (PMF) led to identifying four main PAHs sources including industrial emissions, petrogenic emissions, biomass burning and natural gas emissions, and vehicle exhaust emissions. Industrial and petrogenic emissions exhibited the highest contribution (19.8%, 27.2%, respectively) during the NH-period, while vehicle exhaust and biomass burning-natural gas emissions showed the largest contribution (40.7%, 29.6%, respectively) during the H-period. Concentration weighted trajectory (CWT) on factor contributions was used for tracking the potential locations of the identified sources. In addition to local sources, long-range transport contributed to a significant fraction of TPHAs in Tehran both during the H- and NH-periods. Source-specific carcinogenic risks assessment apportioned vehicle exhaust (44.2%, 2.52 × 10-4) and biomass burning-natural gas emissions (33.9%, 8.31 × 10-5) as the main cancer risk contributors during the H-period and NH-period, respectively. CWT maps pointed out the different distribution patterns associated with the cancer risk from the identified sources. This will allow better risk management through the identification of priority PAHs sources.
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Neoplasias , Hidrocarbonetos Policíclicos Aromáticos , Calefação , Humanos , Irã (Geográfico) , Oriente Médio , Material ParticuladoRESUMO
The response of respiratory infections to source-specific particulate matter (PM) is an area of active research. Using source-specific PM2.5 concentrations at six urban sites in New York State, a case-crossover design, and conditional logistic regression, we examined the association between source-specific PM and the rate of hospitalizations and emergency department (ED) visits for influenza or culture-negative pneumonia from 2005 to 2016. There were at most N = 14â¯764 influenza hospitalizations, N = 57â¯522 influenza ED visits, N = 274â¯226 culture-negative pneumonia hospitalizations, and N = 113â¯997 culture-negative pneumonia ED visits included in our analyses. We separately estimated the rate of respiratory infection associated with increased concentrations of source-specific PM2.5, including secondary sulfate (SS), secondary nitrate (SN), biomass burning (BB), pyrolyzed organic carbon (OP), road dust (RD), residual oil (RO), diesel (DIE), and spark ignition vehicle emissions (GAS). Increased rates of ED visits for influenza were associated with interquartile range increases in concentrations of GAS (excess rate [ER] = 9.2%; 95% CI: 4.3%, 14.3%) and DIE (ER = 3.9%; 95% CI: 1.1%, 6.8%) for lag days 0-3. There were similar associations between BB, SS, OP, and RO, and ED visits or hospitalizations for influenza, but not culture-negative pneumonia hospitalizations or ED visits. Short-term increases in PM2.5 from traffic and other combustion sources appear to be a potential risk factor for increased rates of influenza hospitalizations and ED visits.
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Poluentes Atmosféricos , Poluição do Ar , Hospitalização , Infecções Respiratórias , Adulto , Serviço Hospitalar de Emergência , Humanos , New York , Material ParticuladoRESUMO
Prior work found increased rates for emergency department (ED) visits for asthma and hospitalizations for chronic obstructive pulmonary disease per unit mass of PM2.5 across New York State (NYS) during 2014-2016 after significant reductions in ambient PM2.5 concentrations had occurred following implementation of various policy actions and major economic disruptions. The associations of source-specific PM2.5 concentrations with these respiratory diseases were assessed with a time-stratified case-cossover design and logistic regression models to identify the changes in the PM2.5 that have led to the apparently increased toxicity per unit mass. The rates of ED visits and hospitalizations for asthma and COPD associated with increases in source-specific PM2.5 concentrations in the prior 1, 4, and 7 days were estimated for 6 urban sites in New York State. Overall, there were similar numbers of significantly increased (nâ¯=â¯9) and decreased rates (nâ¯=â¯8) of respiratory events (asthma and COPD hospitalizations and ED visits) associated with increased source-specific PM2.5 concentrations in the previous 1, 4, and 7 days. Associations of source-specific PM2.5 concentrations with excess rates of hospitalizations for COPD for spark- and compression ignition vehicles increased in the 2014-2016 period, but the values were not statistically significant. Other source types showed inconsistent patterns of excess rates. For asthma ED visits, only biomass burning and road dust showed consistent positive associations with road dust having significant values for most lag times. Secondary nitrate also showed significant positive associations with asthma ED visits in the AFTER period compared to no associations in the prior periods. These results suggest that the relationships of asthma and COPD exacerbation with source-specific PM2.5 are not well defined and further work will be needed to determine the causes of the apparent increases in the per unit mass toxicity of PM2.5 in New York State in the 2014-16 period.
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Poluição do Ar , Serviço Hospitalar de Emergência , Exposição Ambiental/estatística & dados numéricos , Poluentes Atmosféricos , Hospitalização , Humanos , Masculino , New York , Material ParticuladoRESUMO
BACKGROUND: Previous studies have reported that fine particle (PM2.5) concentrations triggered ST elevation myocardial infarctions (STEMI). In Rochester, NY, multiple air quality policies and economic changes/influences from 2008 to 2013 led to decreased concentrations of PM2.5 and its major constituents (SO42-, NO3-, elemental and primary organic carbon). This study examined whether the rate of STEMI associated with increased ambient gaseous and PM component concentrations was different AFTER these air quality policies and economic changes (2014-2016), compared to DURING (2008-2013) and BEFORE these polices and changes (2005-2007). METHODS: Using 921 STEMIs treated at the University of Rochester Medical Center (2005-2016) and a case-crossover design, we examined whether the rate of STEMI associated with increased PM2.5, ultrafine particles (UFP, < 100 nm), accumulation mode particles (AMP, 100-500 nm), black carbon, SO2, CO, and O3 concentrations in the previous 1-72 h was modified by the time period related to these pollutant source changes (BEFORE, DURING, AFTER). RESULTS: Each interquartile range (3702 particles/cm3) increase in UFP concentration in the previous 1 h was associated with a 12% (95% CI = 3%, 22%) increase in the rate of STEMI. The effect size was larger in the AFTER period (26%) than the DURING (5%) or BEFORE periods (9%). There were similar patterns for black carbon and SO2. CONCLUSIONS: An increased rate of STEMI associated with UFP and other pollutant concentrations was higher in the AFTER period compared to the BEFORE and DURING periods. This may be due to changes in PM composition (e.g. higher secondary organic carbon and particle bound reactive oxygen species) following these air quality policies and economic changes.
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Poluentes Atmosféricos/efeitos adversos , Poluição do Ar/prevenção & controle , Exposição Ambiental/efeitos adversos , Material Particulado/efeitos adversos , Infarto do Miocárdio com Supradesnível do Segmento ST/epidemiologia , Idoso , Idoso de 80 Anos ou mais , Estudos Cross-Over , Feminino , Gases/efeitos adversos , Humanos , Masculino , Pessoa de Meia-Idade , New York/epidemiologia , Tamanho da Partícula , Infarto do Miocárdio com Supradesnível do Segmento ST/induzido quimicamenteRESUMO
Pellet combustion in residential heating stoves has increased globally during the last decade. Despite their high combustion efficiency, the widespread use of pellet stoves is expected to adversely impact air quality. The atmospheric aging of pellet emissions has received even less attention, focusing mainly on daytime conditions, while the degree to which pellet emissions undergo night-time aging as well as the role of relative humidity remain poorly understood. In this study, environmental simulation chamber experiments were performed to characterize the fresh and aged organic aerosol (OA) emitted by a pellet stove. The fresh pellet stove PM1 (particulate matter with an aerodynamic diameter less than 1 µm) emissions consisted mainly of OA (93 ± 4%, mean ± standard deviation) and black carbon (5 ± 3%). The primary OA (POA) oxygen-to-carbon ratio (O : C) was 0.58 ± 0.04, higher than that of fresh logwood emissions. The fresh OA at a concentration of 70 µg m-3 (after dilution and equilibration in the chamber) consisted of semi-volatile (68%), low and extremely low volatility (16%) and intermediate-volatility (16%) compounds. The oxidation of pellet emissions under dark conditions was investigated by injecting nitrogen dioxide (NO2) and ozone (O3) into the chamber, at different (10-80%) relative humidity (RH) levels. In all dark aging experiments secondary organic aerosol (SOA) formation was observed, increasing the OA levels after a few hours of exposure to NO3 radicals. The change in the aerosol composition and the extent of oxidation depended on RH. For low RH, the SOA mass formed was up to 30% of the initial OA, accompanied by a moderate change in both O : C levels (7-8% increase) and the OA spectrum. Aging under higher RH conditions (60-80%) led to a more oxygenated aerosol (increase in O : C of 11-18%), but only a minor (1-10%) increase in OA mass. The increase in O : C at high RH indicates the importance of heterogeneous aqueous reactions in this system, that oxidize the original OA with a relatively small net change in the OA mass. These results show that the OA in pellet emissions can chemically evolve under low photochemical activity (e.g. the wintertime period) with important enhancement in SOA mass under certain conditions.
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In the past several decades, a variety of efforts have been made in the United States to improve air quality, and ambient particulate matter (PM) concentrations have been used as a metric to evaluate the efficacy of environmental policies. However, ambient PM concentrations result from a combination of source emission rates and meteorological conditions, which also change over time. Dispersion normalization was recently developed to reduce the influence of atmospheric dispersion and proved an effective approach that enhanced diel/seasonal patterns and thus provides improved source apportionment results for speciated PM mass and particle number concentration (PNC) measurements. In this work, dispersion normalization was incorporated in long-term trend analysis of 11-500 nm PNCs derived from particle number size distributions (PNSDs) measured in Rochester, NY from 2005 to 2019. Before dispersion normalization, a consistent reduction was observed across the measured size range during 2005-2012, while after 2012, the decreasing trends slowed down for accumulation mode PNCs (100-500 nm) and reversed for ultrafine particles (UFPs, 11-100 nm). Through dispersion normalization, we showed that these changes were driven by both emission rates and dispersion. Thus, it is important for future studies to assess the effects of the changing meteorological conditions when evaluating policy effectiveness on controlling PM concentrations. Before and after dispersion normalization, an evident increase in nucleation mode particles was observed during 2015-2019. This increase was possibly enabled by a cleaner atmosphere and will pose new challenges for future source apportionment and accountability studies.
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Poluentes Atmosféricos , Poluição do Ar , Monitoramento Ambiental , New York , Tamanho da Partícula , Material Particulado , Emissões de VeículosRESUMO
PM2.5-bound PAHs were analyzed in a total of 135 daily samples collected during four seasons from 2018 to 2019, at three urban sites in Tehran, Iran. This study aims to investigate spatio-temporal variations, source apportionment, potential local and regional sources contributions and lung cancer risks associated with the 16 US EPA priority PAHs. PM2.5 concentrations ranged from 43.8 to 80.3 µg m-3 with the highest concentrations observed in summer. Total PAHs (TPAHs) concentrations ranged between 24.6 and 38.9 ng m-3. Autumn period exhibited the highest average concentration (48.3 ng m-3) followed by winter (29.5 ng m-3), spring (25.9 ng m-3) and summer (16.1 ng m-3). Five PAHs sources were identified by positive matrix factorization (PMF) analysis: diesel exhaust, unburned petroleum-petrogenic, industrial, gasoline exhaust and coal/biomass combustion-natural gas emissions, accounting for 22.3%, 15.6%, 7.5%, 30.9%, and 23.6% of TPAHs, respectively. Site-specific bivariate polar (BP) and conditional bivariate probability function (CBPF) plots were computed to assess PM2.5 and TPAHs local source locations. CBPF pointed out that TPHAs sources are likely of local origin, showing the highest probability close to the sampling sites associated with low wind speed (<5 m s-1). The potential source contribution function (PSCF) and the concentration weighted trajectory (CWT) models were applied to investigate the long-range transport of PM2.5 and TPAHs. In addition to local sources contributions, Eastern areas were highly related to long-distance transport of PM2.5 and the Western areas showed the highest contribution of the total, medium molecular weight (MMW) (4 rings) and high molecular weight (HMW) (5-6 rings) PAHs. The upper bound of incremental lifetime cancer risk (ILCR) via inhalation exposure to PM2.5-bound PAHs was at a moderate risk level (3.14 × 10-4 to 6.17 × 10-4).
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Poluentes Atmosféricos , Neoplasias , Hidrocarbonetos Policíclicos Aromáticos , Poluentes Atmosféricos/análise , China , Monitoramento Ambiental , Humanos , Irã (Geográfico) , Material Particulado/análise , Hidrocarbonetos Policíclicos Aromáticos/análise , Medição de Risco , Estações do Ano , Emissões de Veículos/análiseRESUMO
PURPOSE: Long-term exposure to ambient fine particle (PM2.5) concentrations has been associated with an increased rate or risk of neurodegenerative conditions, but individual PM sources have not been previously examined in relation to neurodegenerative diseases. METHODS: Using the Statewide Planning and Research Cooperative System database, we studied 63,287 hospital admissions with a primary diagnosis of either Alzheimer's disease, dementia, or Parkinson's disease for New York State residents living within 15 miles from six PM2.5 monitoring sites. In addition to PM2.5 concentrations, we studied seven specific PM2.5 sources: secondary sulfate, secondary nitrate, biomass burning, diesel, spark-ignition emissions, pyrolyzed organic rich, and road dust. We estimated the rate of neurodegenerative hospital admissions associated with increased concentration of PM2.5 and individual PM2.5 sources average concentrations in the previous 0-29, 0-179, and 0-364 days. RESULTS: Increases in ambient PM2.5 concentrations were not consistently associated with increased hospital admissions rates. Increased source-specific PM2.5 concentrations were associated with both increased (e.g., secondary sulfates and diesel emissions) and decreased rates (e.g., secondary nitrate and spark-ignition vehicular emissions) of neurodegenerative admissions. CONCLUSIONS: We did not observe clear associations between overall ambient PM2.5 concentrations or source-apportioned ambient PM2.5 contributions and rates of neurologic disease hospitalizations.
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Poluição do Ar , Hospitalização , Doenças Neurodegenerativas , Material Particulado , Adulto , Idoso , Idoso de 80 Anos ou mais , Poluição do Ar/efeitos adversos , Poluição do Ar/análise , Monitoramento Ambiental , Feminino , Hospitalização/estatística & dados numéricos , Humanos , Masculino , Pessoa de Meia-Idade , Doenças Neurodegenerativas/induzido quimicamente , Doenças Neurodegenerativas/terapia , New York/epidemiologia , Material Particulado/análise , Material Particulado/toxicidade , Emissões de Veículos/análise , Emissões de Veículos/toxicidade , Adulto JovemRESUMO
The levels of Cd, Cr, Cu, Fe, Mn, Pb and Zn were determined in floor dusts from mechanical (MRWs) and battery repairing workshops (BRWs) in Yazd, Iran. The study aimed to evaluate the anthropogenic contribution to the presence of heavy metals (HMs), the possible sources and the related risks that could arise from occupational exposure in the studied workplace microenvironments. Among the analyzed heavy metals, Cu, Pb and Zn exhibited enhanced concentrations in the floor dusts. The EF calculations showed an extremely severe enrichment of HMs, especially for Cd, Cu and Pb, while floor dusts were characterized as "extremely polluted" with regards to those metals. In any case, both EF and Igeo values were significantly higher in the BRWs. These results were also supported by NIPI and PLI values, while contour maps of PLI values in both MRWs and BRWs outlined workshops in N-NE part of Yazd as more impacted compared to other spatial locations. Principal component analysis (PCA) and Pearson's correlation outscored workshops activities as the principal sources of heavy metals. The health risk assessment suggested considerable non-carcinogenic risks regarding Pb in the BRWs which exhibited HQing (mean 2.91) and HI (mean 3.03) values higher than safe level. Regarding carcinogenic risks, CR values for both Cd and Cr were below the safe level (1.0 × 10-6). The occupational exposure to Pb was evaluated through the predicted BLL values, where with averages of 3.33 µg/dl and 21.4 µg/dl for MRWs and BRWs workers, respectively, indicated a severe Pb exposure for BRWs workers.
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Metais Pesados/análise , Saúde Ocupacional , China , Cidades , Poeira/análise , Monitoramento Ambiental , Humanos , Irã (Geográfico) , Medição de Risco , Local de TrabalhoRESUMO
This study investigates the major chemical components, particle-bound water content, acidity (pH), and major potential sources of PM2.5 in major cities (Belluno, Conegliano, Vicenza, Mestre, Padua, and Rovigo) in the eastern end of the Po Valley. The measured PM2.5 mass was reconstructed using a multiple-site hybrid chemical mass closure approach that also accounts for aerosol inorganic water content (AWC) estimated by the ISORROPIA-II model. Annually, organic matter accounted for 31-45% of the PM2.5 at all sites, followed by nitrate (10-19%), crustal material (10-14%), sulfate (8-10%), ammonium (5-9%), elemental carbon (4-7%), other inorganic ions (3-4%), and trace elements (0.2-0.3%). Water represented 7-10% of measured PM2.5. The ambient aerosol pH varied from 1.5 to 4.5 with lower values in summer (average in all sites 2.2 ± 0.3) and higher in winter (3.9 ± 0.3). Six major PM2.5 sources were quantitatively identified with multiple-site positive matrix factorization: secondary sulfate (34% of PM2.5), secondary nitrate (30%), biomass burning (17%), traffic (11%), re-suspended dust (5%), and fossil fuel combustion (3%). Biomass burning accounted for ~90% of total PAHs. Inorganic aerosol acidity was driven primarily by secondary sulfate, fossil fuel combustion (decreasing pH), secondary nitrate, and biomass burning (increasing pH). Secondary nitrate was the primary driver of the inorganic AWC variability. A concentration-weighted trajectory (multiple-site) analysis was used to identify potential source areas for the various factors and modeled aerosol acidity. Eastern and Central Europe were the main source areas of secondary species. Less acidic aerosol was associated with air masses originating from Northern Europe owing to the elevated presence of the nitrate factor. More acidic particles were observed for air masses traversing the Po Valley and the Mediterranean, possibly due to the higher contributions of fossil fuel combustion factor and the loss of nitric acid due to its interaction with coarse sea-salt particles.
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An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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Ten relatively-low-cost ozone monitors (Aeroqual Series 500 with OZL ozone sensor) were deployed to assess the spatial and temporal variability of ambient ozone concentrations across residential areas in the Monroe County, New York from June to October 2017. The monitors were calibrated in the laboratory and then deployed to a local air quality monitoring site where they were compared to the federal equivalent method values. These correlations were used to correct the measured ozone concentrations. The values were also used to develop hourly land use regression models (LUR) based on the deletion/substitution/addition (D/S/A) algorithm that can be used to predict the spatial and temporal concentrations of ozone at any hour of a summertime day and given location in Monroe County. Adjusted R2 values were high (average 0.83) with the highest adjusted R2 for the model between 8 and 9â¯AM (i.e. 1-2â¯h after the peak of primary emissions during the morning rush hours). Spatial predictors with the highest positive effects on ozone estimates were high intensity developed areas, low and medium intensity developed areas, forestsâ¯+â¯shrubs, average elevation, Interstateâ¯+â¯highways, and the annual average vehicular daily traffic counts. These predictors are associated with potential emissions of anthropogenic and biogenic precursors. Maps developed from the models exhibited reasonable spatial and temporal patterns, with low ozone concentrations overnight and the highest concentrations between 11â¯AM and 5â¯PM. The adjusted R2 between the model predictions and the measured values varied between 0.79 and 0.87 (meanâ¯=â¯0.83). The combined use of the network of low-cost monitors and LUR modeling provide useful estimates of intraurban ozone variability and exposure estimates that will be used in future epidemiological studies.
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Increased ambient air pollutant concentrations during pregnancy have been associated with reduced birth weight, but the etiologically relevant pregnancy time window(s) is/are unclear. In 76,500 singleton births in Monroe County, NY (2005-2016), who were 37-42 gestational weeks at delivery, we used generalized linear models to regress term birth weight against mean gestational month pollutant concentrations, adjusting for mean temperature, and maternal, infant, and medical service use characteristics. Overall, there were no clear patterns of term birth weight change associated with increased concentrations of any pollutant across gestational months. However, among Hispanic women only, increases in all pollutants, except O3, in multiple gestational months, were associated with decreased term birth weight. Each 3.25 µg/m3 increase in PM2.5 concentration in the 6th gestational month was associated with a -20.4 g (95% CI = -34.0, -6.8) reduction in term birth weight among Hispanic women, but a 4.1 g (95% CI = -2.5, 10.8) increase among non-Hispanic mothers (p for interaction < 0.001). Although ambient air pollutant concentrations during pregnancy were not associated with reduced term birth weight among women of all ethnicities living in Monroe County, this observed association in Hispanic mothers may be a result of less exposure misclassification and bias (due to closer residential proximity to the monitoring site).
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Poluentes Atmosféricos/análise , Peso ao Nascer , Adulto , Feminino , Humanos , Recém-Nascido , Exposição Materna , New York , GravidezRESUMO
BACKGROUND: Previous work reported increased rates of acute cardiovascular hospitalizations associated with increased PM2.5 concentrations in the previous few days across urban centers in New York State from 2005 to 2016. These relative rates were higher after air quality policies and economic changes resulted in decreased PM2.5 concentrations and changes in PM composition (e.g. increased secondary organic carbon), compared to before and during these changes. Changes in PM composition and sources may explain this difference. OBJECTIVES: To estimate the rate of acute cardiovascular hospitalizations associated with increases in source specific PM2.5 concentrations. METHODS: Using source apportioned PM2.5 concentrations at the same NYS urban sites, a time-stratified case-crossover design, and conditional logistic regression models adjusting for ambient temperature and relative humidity, we estimated the rate of these acute cardiovascular hospitalizations associated with increases in mean source specific PM2.5 concentrations in the previous 1, 4, and 7â¯days. RESULTS: Interquartile range (IQR) increases in spark-ignition emissions (GAS) concentrations were associated with increased excess rates of cardiac arrhythmia hospitalizations (2.3%; 95% CIâ¯=â¯0.4%, 4.2%; IQRâ¯=â¯2.56⯵g/m3) and ischemic stroke hospitalizations (3.7%; 95% CIâ¯=â¯1.1%, 6.4%; 2. 73⯵g/m3) over the next day. IQR increases in diesel (DIE) concentrations were associated with increased rates of congestive heart failure hospitalizations (0.7%; 95% CIâ¯=â¯0.2% 1.3%; 0.51⯵g/m3) and ischemic heart disease hospitalizations (0.8%; 95% CIâ¯=â¯0.3%, 1.3%; 0.60⯵g/m3) over the next day, as hypothesized. However, secondary sulfate PM2.5 (SS) was not. Increased acute cardiovascular hospitalization rates were also associated with IQR increases in concentrations of road dust (RD), residual oil (RO), and secondary nitrate (SN) over the previous 1, 4, and 7â¯days, but not other sources. CONCLUSIONS: These findings suggest a role of several sources of PM2.5 in New York State (i.e. traffic emissions, non-traffic emissions such as brake and tire wear, residual oil, and nitrate that may also reflect traffic emissions) in the triggering of acute cardiovascular events.
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Poluentes Atmosféricos/análise , Doenças Cardiovasculares/epidemiologia , Hospitalização/estatística & dados numéricos , Material Particulado/análise , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Poluição do Ar/análise , Cidades/epidemiologia , Monitoramento Ambiental , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , New York/epidemiologia , Nitratos/análise , Sulfatos/análise , Emissões de Veículos/análise , Adulto JovemRESUMO
RATIONALE: Fine particulate matter air pollution of 2.5 µm or less in diameter (PM2.5) has been associated with an increased risk of respiratory disease, but assessments of specific respiratory infections in adults are lacking. OBJECTIVES: To estimate the rate of respiratory infection healthcare encounters in adults associated with acute increases in PM2.5 concentrations. METHODS: Using case-crossover methods, we studied 498,118 adult New York State residents with a primary diagnosis of influenza, bacterial pneumonia, or culture-negative pneumonia upon hospitalization or emergency department (ED) visit (2005-2016). We estimated the relative rate of healthcare encounters associated with increases in PM2.5 in the previous 1-7 days and explored differences before (2005-2007), during (2008-2013), and after (2014-2016) implementation of air quality policies and economic changes. RESULTS: Interquartile range increases in PM2.5 over the previous 7 days were associated with increased excess rates (ERs) of culture-negative pneumonia hospitalizations (2.5%; 95% confidence interval [CI], 1.7-3.2%) and ED visits (2.5%; 95% CI, 1.4-3.6%), and increased ERs of influenza ED visits (3.9%; 95% CI, 2.1-5.6%). Bacterial pneumonia hospitalizations, but not ED visits, were associated with increases in PM2.5 and, though imprecise, were of a similar magnitude to culture-negative pneumonia (Lag Day 6 ER, 2.3%; 95% CI, 0.3-4.3). Increased relative rates of influenza ED visits and culture-negative pneumonia hospitalizations were generally larger in the "after" period (P < 0.025 for both outcomes), compared with the "during" period, despite reductions in overall PM2.5 concentrations. CONCLUSIONS: Increased rates of culture-negative pneumonia and influenza were associated with increased PM2.5 concentrations during the previous week, which persisted despite reductions in PM2.5 from air quality policies and economic changes. Though unexplained, this temporal variation may reflect altered toxicity of different PM2.5 mixtures or increased pathogen virulence.
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Poluição do Ar/legislação & jurisprudência , Custos de Cuidados de Saúde , Política de Saúde/economia , Material Particulado/efeitos adversos , Infecções Respiratórias/epidemiologia , Medição de Risco/métodos , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Poluição do Ar/efeitos adversos , Custos e Análise de Custo , Feminino , Seguimentos , Hospitalização/tendências , Humanos , Incidência , Masculino , Pessoa de Meia-Idade , Infecções Respiratórias/economia , Infecções Respiratórias/etiologia , Estudos Retrospectivos , Fatores de Risco , Fatores Socioeconômicos , Estados Unidos/epidemiologia , Adulto JovemRESUMO
Prior studies reported that exposure to increased concentrations of fine particulate matter (PM2.5) were associated with increased rates of hospitalization and emergency department (ED) visits for asthma and chronic obstructive pulmonary disease (COPD). In this study, rates were examined from 2005 to 2016 using a case-crossover design to ascertain if there have been changes in the rates per unit mass exposure given substantial reductions in PM2.5 concentration and changes in its composition. PM2.5 concentrations were reduced through a combination of policies designed to improve air quality and economic drivers, including the 2008 economic recession and shifts in the relative costs of coal and natural gas. The study period was split into three periods reflecting that much of the emissions changes occurred between 2008 and 2013. Thus, the three periods were defined as: BEFORE (2005 to 2007), DURING (2008-2013), and AFTER (2014-2016). In general, the number of hospitalizations and ED visits declined with the decreased concentration of PM2.5. However, the rate of COPD hospitalizations and asthma ED visits associated with each interquartile range increase in ambient PM2.5 concentration was larger in the AFTER period than the DURING and BEFORE periods. For example, each 6.8⯵g/m3 increase in PM2.5 on the same day was associated with 0.4% (0.0%, 0.8%), 0.3% (-0.2%, 0.7%), and 2.7% (1.9%, 3.5) increases in the rate of asthma emergency department visits in the BEFORE, DURING, and AFTER periods, respectively, suggesting the same mass concentration of PM2.5 was more toxic in the AFTER period.
Assuntos
Poluentes Atmosféricos/análise , Asma/epidemiologia , Serviço Hospitalar de Emergência/estatística & dados numéricos , Exposição Ambiental/efeitos adversos , Hospitalização/estatística & dados numéricos , Material Particulado/efeitos adversos , Doença Pulmonar Obstrutiva Crônica/epidemiologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Poluição do Ar , Asma/induzido quimicamente , Feminino , Humanos , Incidência , Masculino , Pessoa de Meia-Idade , New York/epidemiologia , Doença Pulmonar Obstrutiva Crônica/induzido quimicamente , Adulto JovemRESUMO
The performance of a low cost ozone monitor (Aeroqual Series 500 portable gas monitors using a metal oxide sensor for ozone; model OZL) was assessed under field conditions. Ten ozone monitors were calibrated under clean-air laboratory conditions and controlled ozone concentrations of 5 to 100 ppb. Good linearity and response were obtained relative to a research-grade ozone monitor. One monitor was co-located at a regulatory air quality monitoring station that uses a U.S. federal equivalent method (FEM) ozone analyzer. Raw data from the Aeroqual monitor collected over 4 months (June-October) at a 10-minute time-resolution, showed good agreement (r2=0.83) with the FEM values but with an overestimation of ~12%. Data were averaged to different time resolutions; 1 h time averaged concentrations showed the best fit with the FEM results (r2=0.87). Data analyses suggested the potential of interferences due to temperature, relative humidity, nitrogen oxides, and volatile organic compounds. Correction models using temperature, humidity, and nitrogen dioxide (NO2) were tested to relate the monitor concentrations to the FEM values. Temperature and humidity were two readily available variables. The model (#3) that added NO2 did not provide a substantial improvement in the fit. Thus, the models with only temperature and humidity can be easily developed by any user. The best model explained 91% of the variance and showed statistically significant improvement of the goodness of fits as well as decreased influence of the interfering variables on the diurnal and weekly patterns. The correction models were also able to lower the effect of seasonal temperature changes, allowing the use of the monitors over long-term sampling campaigns. Thus, the Aeroqual ozone monitor can return "FEM-like" concentrations after appropriate corrections. Data provided by a network of monitors could provide intra-urban spatial variations in ozone concentrations and provide more accurate human exposure assessments by reducing exposure misclassification.
RESUMO
The Po Valley is one of the most important hot spots in Europe for air pollution. Morphological features and anthropogenic pressures lead to frequent breaching of air quality standards and to high-pollution episodes in an ~46 × 103-km2-wide alluvial lowland. Therefore, it is increasingly important to study the air quality in a wide geographical scale to better implement possible and successful mitigation measures. The Veneto region lies in the eastern part of the Po Valley and the elemental composition of PM has been mainly studied in the Venice area, whereas scarce data are available for the remaining territory of the region. In this study, the elemental composition of PM2.5 was investigated over 1 year (2012-2013) at six major cities of the Veneto region. Samples were analyzed for 16 elements (Ca, Al, Fe, S, K, Mg, Ti, Mn, Zn, Ba, As, Ni, Pb, Sb, V, and Cu), and results were processed to investigate spatial and seasonal variations, the influence of meteorological factors, and the most probable sources by using a procedure based on (i) elemental ratios (Cu/Sb, Cu/Zn, Cu/Pb, Mn/V, V/Ni, and Zn/Pb), (ii) cluster analysis on wind data, and (iii) conditional probability function (CPF). The percentage of elements in PM2.5 ranged between 11 and 20%, and Ca and S were the most abundant elements in the region. Typical seasonal variations and similar trends were exhibited by each element, especially in the lowland. Some elements such as Zn, K, Mn, Pb, and Sb were found at high concentrations during the cold period. However, no similar dispersion processes were observed throughout the region, and their concentrations were mostly depending on individual local sources. In the alpine and foothill parts of the region, lower concentrations were recorded with respect to the Po Valley cities, which resulted enriched of most of the elements considered in this study. The cluster analysis on wind data and the CPF of the ratio-related sources demonstrated that a widespread pollution condition exists in the region, apart from the coastal area. However, specific directions (e.g., a link with high-traffic roads, industrial areas, and airports) resulted the most probable explanation for each ratio-related source. In addition, the Veneto region hosts one of the most important Mediterranean ports for the cruise sector (Venice harbor), and its impact was previously demonstrated in the historical city center. In this study, the impact of Venice shipping emissions was estimated to be 3.5% of PM2.5 in some particular days.
Assuntos
Poluentes Atmosféricos/análise , Monitoramento Ambiental/métodos , Metais Pesados/análise , Metais Leves/análise , Material Particulado/química , Cidades , Análise por Conglomerados , Itália , Limite de Detecção , Estações do Ano , Enxofre/análise , VentoRESUMO
Significant changes in emission sources have occurred in the northeastern United States over the past decade, due in part to the implementation of emissions standards, the introduction and addition of abatement technologies for road transport, changes in fuel sulfur content for road and non-road transport, as well as economic impacts of a major recession and differential fuel prices. These changes in emission scenarios likely affected the concentrations of airborne submicron particles. This study investigated the characteristics of 11-500nm particle number concentrations and their size spectra in Rochester, NY during the past 15years (2002 to 2016). The modal structure, diurnal, weekly and monthly patterns of particle number concentrations are analyzed. Long-term trends are quantified using seasonal-trend decomposition procedures based on "Loess", Mann-Kendall regression with Theil-Sen slope and piecewise regression. Particle concentrations underwent significant (p<0.05) downward trends. An annual decrease of -323particles/cm3/y (-4.6%/y) was estimated for the total particle number concentration using Theil-Sen analysis. The trends were driven mainly by the decrease in particles in the 11-50nm range (-181particles/cm3/y; -4.7%/y). Slope changes were investigated annually and seasonally. Piecewise regression found different slopes for different portions of the overall period with the strongest declines between 2005 and 2011/2013, followed by small upward trends between 2013 and 2016 for most size bins, possibly representing increased vehicular traffic after the recovery from the 2008 recession.