scholarly journals Seasonal variation in atmospheric pollutants transport in central Chile: dynamics and consequences

2021 ◽  
Vol 21 (8) ◽  
pp. 6431-6454
Author(s):  
Rémy Lapere ◽  
Laurent Menut ◽  
Sylvain Mailler ◽  
Nicolás Huneeus

Abstract. Central Chile faces atmospheric pollution issues all year long as a result of elevated concentrations of fine particulate matter during the cold months and tropospheric ozone during the warm season. In addition to public health issues, environmental problems regarding vegetation growth and water supply, as well as meteorological feedback, are at stake. Sharp spatial gradients in regional emissions, along with a complex geographical situation, make for variable and heterogeneous dynamics in the localization and long-range transport of pollutants, with seasonal differences. Based on chemistry–transport modeling with Weather Research Forecasting (WRF)–CHIMERE, this work studies the following for one winter period and one summer period: (i) the contribution of emissions from the city of Santiago to air pollution in central Chile, and (ii) the reciprocal contribution of regional pollutants transported into the Santiago basin. The underlying 3-dimensional advection patterns are investigated. We find that, on average for the winter period, 5 to 10 µg m−3 of fine particulate matter in Santiago come from regional transport, corresponding to between 13 % and 15 % of average concentrations. In turn, emissions from Santiago contribute between 5 % and 10 % of fine particulate matter pollution as far as 500 km to the north and 500 km to the south. Wintertime transport occurs mostly close to the surface. In summertime, exported precursors from Santiago, in combination with mountain–valley circulation dynamics, are found to account for most of the ozone formation in the adjacent Andes cordillera and to create a persistent plume of ozone of more than 50 ppb (parts per billion), extending along 80 km horizontally and 1.5 km vertically, and located slightly north of Santiago, several hundred meters above the ground. This work constitutes the first description of the mechanism underlying the latter phenomenon. Emissions of precursors from the capital city also affect daily maxima of surface ozone hundreds of kilometers away. In parallel, cutting emissions of precursors in the Santiago basin results in an increase in surface ozone mixing ratios in its western area.

2021 ◽  
Author(s):  
Rémy Lapere ◽  
Laurent Menut ◽  
Sylvain Mailler ◽  
Nicolás Huneeus

Abstract. Central Chile faces atmospheric pollution issues all year long, in relation with elevated concentrations of fine particulate matter during the cold months and tropospheric ozone during the warm season. In addition to public health issues, environmental problems regarding vegetation growth and water supply, as well as meteorological feedback are at stake. Sharp spatial gradients in regional emissions along with a complex geographical situation make for variable and heterogeneous dynamics in the localization and long-range transport of pollutants, with seasonal differences. Based on chemistry-transport modeling with WRF-CHIMERE, this work studies for one winter period and one summer period: (i) the contribution of emissions from the Santiago Metropolitan Area to air pollution in central Chile, (ii) the reciprocal contribution of regional pollutants transported into the Santiago basin. The underlying 3-dimensional advection patterns are investigated. We find that on average for the winter period 5 μg m−3 to 10 μg m−3 of fine particulate matter in Santiago come from regional transport, corresponding to 13 % to 15 % of average concentrations. In turn, emissions from the Metropolitan Area contribute to 5 % to 10 % of fine particulate matter pollution as far as 4° north and 4° south. Wintertime transport occurs mostly close to the surface. In summertime, exported precursors from Santiago, in combination with mountain-valley circulation dynamics, are found to account for most of ozone formation in the adjacent Andes cordillera and to create a persistent plume of ozone of more than 50 ppb, extending along 80 km horizontally and 1.5 km vertically, and located several hundred meters above ground, slightly north of Santiago. This work constitutes the first description of such an ozone bubble formation mechanism. Emissions of precursors from the capital city also affect daily maxima of surface ozone hundreds of kilometers away. In parallel, cutting emissions of precursors in the Santiago basin results in an increase of surface ozone mixing ratios in its western area.


2014 ◽  
Vol 2014 ◽  
pp. 1-12 ◽  
Author(s):  
Richard Toro Araya ◽  
Robert Flocchini ◽  
Rául G. E. Morales Segura ◽  
Manuel A. Leiva Guzmán

Measurements of carbonaceous aerosols in South American cities are limited, and most existing data are of short term and limited to only a few locations. For 6 years (2002–2007), concentrations of fine particulate matter and organic and elemental carbon were measured continuously in the capital of Chile. The contribution of carbonaceous aerosols to the primary and secondary fractions was estimated at three different sampling sites and in the warm and cool seasons. The results demonstrate that there are significant differences in the levels in both the cold (March to August) and warm (September to February) seasons at all sites studied. The percent contribution of total carbonaceous aerosol fine particulate matter was greater in the cool season (53 ± 41%) than in the warm season (44 ± 18%). On average, the secondary organic carbon in the city corresponded to 29% of the total organic carbon. In cold periods, this proportion may reach an average of 38%. A comparison of the results with the air quality standards for fine particulate matter indicates that the total carbonaceous fraction alone exceeds the World Health Organization standard (10 µg/m3) and the United States Environmental Protection Agency standard (15 µg/m3) for fine particulate matter.


2012 ◽  
Vol 12 (14) ◽  
pp. 6335-6355 ◽  
Author(s):  
U. Im ◽  
M. Kanakidou

Abstract. Megacities are large urban agglomerations with intensive anthropogenic emissions that have significant impacts on local and regional air quality. In the present mesoscale modeling study, the impacts of anthropogenic emissions from the Greater Istanbul Area (GIA) and the Greater Athens Area (GAA) on the air quality in GIA, GAA and the entire East Mediterranean are quantified for typical wintertime (December 2008) and summertime (July 2008) conditions. They are compared to those of the regional anthropogenic and biogenic emissions that are also calculated. Finally, the efficiency of potential country-based emissions mitigation in improving air quality is investigated. The results show that relative contributions from both cities to surface ozone (O3) and aerosol levels in the cities' extended areas are generally higher in winter than in summer. Anthropogenic emissions from GIA depress surface O3 in the GIA by ~ 60% in winter and ~ 20% in summer while those from GAA reduce the surface O3 in the GAA by 30% in winter and by 8% in summer. GIA and GAA anthropogenic emissions contribute to the fine particulate matter (PM2.5) levels inside the cities themselves by up to 75% in winter and by 50% (GIA) and ~ 40% (GAA), in summer. GIA anthropogenic emissions have larger impacts on the domain-mean surface O3 (up to 1%) and PM2.5 (4%) levels compared to GAA anthropogenic emissions (<1% for O3 and ≤2% for PM2.5) in both seasons. Impacts of regional anthropogenic emissions on the domain-mean surface pollutant levels (up to 17% for summertime O3 and 52% for wintertime fine particulate matter, PM2.5) are much higher than those from Istanbul and Athens together (~ 1% for O3 and ~ 6% for PM2.5, respectively). Regional biogenic emissions are found to limit the production of secondary inorganic aerosol species in summer up to 13% (non-sea-salt sulfate (nss-SO42−) in rural Athens) due to their impact on oxidant levels while they have negligible impact in winter. Finally, the responses to country-based anthropogenic emission mitigation scenarios inside the studied region show increases in O3 mixing ratios in the urban areas of GIA and GAA, higher in winter (~ 13% for GIA and 2% for GAA) than in summer (~ 7% for GIA and <1% for GAA). On the opposite PM2.5 concentrations decrease by up to 30% in GIA and by 20% in GAA with the highest improvements computed for winter. The emission reduction strategy also leads to domain-wide decreases in most primary pollutants like carbon monoxide (CO) or nitrogen oxides (NOx) for both seasons. The results show the importance of long range transport of pollutants for the air quality in the East Mediterranean. Thus, improvements of air quality in the East Mediterranean require coordinated efforts inside the region and beyond.


2020 ◽  
Vol 20 (21) ◽  
pp. 13455-13466
Author(s):  
Zhihao Shi ◽  
Lin Huang ◽  
Jingyi Li ◽  
Qi Ying ◽  
Hongliang Zhang ◽  
...  

Abstract. Meteorological conditions play important roles in the formation of ozone (O3) and fine particulate matter (PM2.5). China has been suffering from serious regional air pollution problems, characterized by high concentrations of surface O3 and PM2.5. In this study, the Community Multiscale Air Quality (CMAQ) model was used to quantify the sensitivity of surface O3 and PM2.5 to key meteorological parameters in different regions of China. Six meteorological parameters were perturbed to create different meteorological conditions, including temperature (T), wind speed (WS), absolute humidity (AH), planetary boundary layer height (PBLH), cloud liquid water content (CLW) and precipitation (PCP). Air quality simulations under the perturbed meteorological conditions were conducted in China in January and July of 2013. The changes in O3 and PM2.5 concentrations due to individual meteorological parameters were then quantified. T has a great influence on the daily maximum 8 h average O3 (O3-8 h) concentrations, which leads to O3-8 h increases by 1.7 in January in Chongqing and 1.1 ppb K−1 in July in Beijing. WS, AH, and PBLH have a smaller but notable influence on O3-8 h with maximum change rates of 0.3 ppb %−1, −0.15 ppb %−1, and 0.14 ppb %−1, respectively. T, WS, AH, and PBLH have important effects on PM2.5 formation of both in January and July. In general, PM2.5 sensitivities are negative to T, WS, and PBLH and positive to AH in most regions of China. The sensitivities in January are much larger than in July. PM2.5 sensitivity to T, WS, PBLH, and AH in January can be up to −5 µg m−3 K−1, −3 µg m−3 %−1, −1 µg m−3 %−1, and +0.6 µg m−3 %−1, respectively, and in July it can be up to −2 µg m−3 K−1, −0.4 µg m−3 %−1, −0.14 µg m−3 %−1, and +0.3 µg m−3 %−1, respectively. Other meteorological factors (CLW and PCP) have negligible effects on O3-8 h (less than 0.01 ppb %−1) and PM2.5 (less than 0.01 µg m−3 %−1). The results suggest that surface O3 and PM2.5 concentrations can change significantly due to changes in meteorological parameters, and it is necessary to consider these effects when developing emission control strategies in different regions of China.


Author(s):  
Ming-Ta Tsai ◽  
Yu-Ni Ho ◽  
Charng-Yen Chiang ◽  
Po-Chun Chuang ◽  
Hsiu-Yung Pan ◽  
...  

Pneumonia, one of the important causes of death in children, may be induced or aggravated by particulate matter (PM). Limited research has examined the association between PM and its constituents and pediatric pneumonia-related emergency department (ED) visits. Measurements of PM2.5, PM10, and four PM2.5 constituents, including elemental carbon (EC), organic carbon (OC), nitrate, and sulfate, were extracted from 2007 to 2010 from one core station and two satellite stations in Kaohsiung City, Taiwan. Furthermore, the medical records of patients under 17 years old who had visited the ED in a medical center and had a diagnosis of pneumonia were collected. We used a time-stratified, case-crossover study design to estimate the effect of PM. The single-pollutant model demonstrated interquartile range increase in PM2.5, PM10, nitrate, OC, and EC on lag 3, which increased the risk of pediatric pneumonia by 18.2% (95% confidence interval (Cl), 8.8‒28.4%), 13.1% (95% CI, 5.1‒21.7%), 29.7% (95% CI, 16.4‒44.5%), 16.8% (95% CI, 4.6‒30.4%), and 14.4% (95% Cl, 6.5‒22.9%), respectively. After PM2.5, PM10, and OC were adjusted for, nitrate and EC remained significant in two-pollutant models. Subgroup analyses revealed that nitrate had a greater effect on children during the warm season (April to September, interaction p = 0.035). In conclusion, pediatric pneumonia ED visit was related to PM2.5 and its constituents. Moreover, PM2.5 constituents, nitrate and EC, were more closely associated with ED visits for pediatric pneumonia, and children seemed to be more susceptible to nitrate during the warm season.


Author(s):  
Mei Zheng ◽  
Caiqing Yan ◽  
Tong Zhu

Fine particulate matter has been a major concern in China as it is closely linked to issues such as haze, health and climate impacts. Since China released its new national air quality standard for fine particulate matter (PM 2.5 ) in 2012, great efforts have been put into reducing its concentration and meeting the standard. Significant improvement has been seen in recent years, especially in Beijing, the capital city of China. This paper reviews how China understands its sources of fine particulate matter, the major contributor to haze, and the most recent findings by researchers. It covers the characteristics of PM 2.5 in China, the major methods to understand its sources such as emission inventory and measurement networks, the major research programmes in air quality research, and the major measures that lead to successful control of fine particulate matter pollution. A great example of linking scientific findings to policy is the control of coal combustion from the residential sector in northern China. This review not only provides an overview of the fine particulate matter pollution problem in China, but also its experience of air quality management, which may benefit other countries facing similar issues. This article is part of a discussion meeting issue ‘Air quality, past present and future’.


2020 ◽  
Author(s):  
Zhihao Shi ◽  
Lin Huang ◽  
Jingyi Li ◽  
Qi Ying ◽  
Hongliang Zhang ◽  
...  

Abstract. Meteorological conditions play important roles in the formation of ozone (O3) and fine particulate matter (PM2.5). China has been suffering from serious regional air pollution problems, characterized by high concentrations of surface O3 and PM2.5. In this study, the Community Multiscale Air Quality (CMAQ) model was used to quantify the sensitivity of surface O3 and PM2.5 to key meteorological parameters in different regions of China. Six meteorological parameters were perturbed to create different meteorological conditions, including temperature (T), wind speed (WS), absolute humidity (AH), planetary boundary layer height (PBLH), cloud liquid water content (CLW) and precipitation (PCP). Air quality simulations under the perturbed meteorological conditions were conducted in China in January and July of 2013. The changes in O3 and PM2.5 concentrations due to individual meteorological parameters were then quantified. T has the greatest impact on the daily maximum 8-h average O3 (O3-8 h) concentrations, which leads to O3-8 h increases by 1.7 ppb K−1 in January in Chongqing and 1.1 ppb K−1 in July in Beijing. WS, AH, and PBLH have a smaller but notable influence on O3-8 h with maximum change rates of 0.3, −0.15, and 0.14 ppb %−1, respectively. T, WS, AH, and PBLH have important effects on PM2.5 formation of in both January and July. In general, PM2.5 sensitivities are negative to T, WS, and PBLH and positive to AH in most regions of China. The sensitivities in January are much larger than in July. PM2.5 sensitivity to T, WS, PBLH, and AH in January can be up to −5 μg m−3 K−1, −3 μg m3 %−1, −1 g m−3, and +0.6 μg m−3 %−1, respectively, and in July can be up to −2 μg m−3 K−1, −0.4 μg m−3 %−1, −0.14 μg m−3 %−1, and +0.3 μg m−3 %−1, respectively. Other meteorological factors (CLW and PCP) have negligible effects on O3-8 h (less than 0.01 ppb %−1) and PM2.5 (less than 0.01 μg m−3 %−1). The results suggest that surface O3 and PM2.5 concentrations can change significantly due to changes in meteorological parameters and it is necessary to consider these effects when developing emission control strategies in different regions of China.


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