Non-haze Periods Research Articles

Mitigation of indoor human exposure to airborne particles of outdoor origin in an urban environment during haze and non-haze periods

During the 2019 smoke haze episode in Singapore, elevated levels of fine particulate matter (PM2.5) were observed, deteriorating both ambient and indoor air quality (IAQ). We investigated the mitigation of indoor human exposure to PM2.5 of outdoor origin under diverse exposure scenarios with and without filtration of PM2.5 during both hazy and non-hazy days. The key objective of our study was to make a comparative evaluation of the effectiveness of portable air cleaners (PACs) and air conditioning (AC) systems equipped with particle filters in improving IAQ and to assess related long-term carcinogenic and non-carcinogenic health risks. We conducted real-time measurements of PM2.5, black carbon mass concentrations and particle number concentrations in both indoor and outdoor areas, quantified the relative concentrations of the water-soluble fraction of toxic trace elements in PM2.5 for health risk assessment, and estimated the levels of thermal comfort. In addition, we calculated the total estimated cost of indoor air pollution control. Our findings suggest that indoor air cleaners are more effective at mitigating human exposure to airborne particles and reducing health risk with less consumption of electricity and better cost-effectiveness compared to AC. This information would be beneficial for public health interventions during major air pollution events.

Impact of transport of fine and ultrafine particles from open biomass burning on air quality during 2019 Bangkok haze episode

Transboundary and domestic aerosol transport during 2018–2019 affecting Bangkok air quality has been investigated. Physicochemical characteristics of size-segregated ambient particles down to nano-particles collected during 2017 non-haze and 2018–2019 haze periods were analyzed. The average PM2.5 concentrations at KU and KMUTNB sites in Bangkok, Thailand during the haze periods were about 4 times higher than in non-haze periods. The highest average organic carbon and elemental carbon concentrations were 4.6 ± 2.1 µg/m3 and 1.0 ± 0.4 µg/m3, respectively, in PM0.5–1.0 range at KU site. The values of OC/EC and char-EC/soot-EC ratios in accumulation mode particles suggested the significant influence of biomass burning, while the nuclei and coarse mode particles were from mixed sources. PAH concentrations during 2018–2019 haze period at KU and KMUTNB were 3.4 ± 0.9 ng/m3 and 1.8 ± 0.2 ng/m3, respectively. The PAH diagnostic ratio of PM2.5 also suggested the main contributions were from biomass combustion. This is supported by the 48-hrs backward trajectory simulation. The higher PM2.5 concentrations during 2018–2019 haze period are also associated with the meteorological conditions that induce thermal inversions and weak winds in the morning and evening. Average values of benzo(a)pyrene toxic equivalency quotient during haze period were about 3–6 times higher than during non-haze period. This should raise a concern of potential human health risk in Bangkok and vicinity exposing to fine and ultrafine particulate matters in addition to regular exposure to traffic emission.

Comparative Analysis of Pollution Characteristics of Carbonaceous Aerosol Components in the Atmosphere Between Urban and Suburban Areas

To compare the pollution characteristics of carbonaceous aerosol components in the atmosphere between urban and suburban areas, Chengdu City and Renshou County were selected as study areas from which 88 samples of PM2.5 during haze and non-haze periods were collected and analyzed. Quantification of mass concentrations of PM2.5, carbonaceous aerosol components[organic carbon (OC), elemental carbon (EC), and secondary organic carbon (SOC)], along with correlation analysis of OC and EC, and principal component analysis (PCA) of carbon components were carried out. The results show that pollutant concentrations during the haze period were higher than those during the non-haze period. The OC and EC for Chengdu City and Renshou County were positively correlated, with their correlation coefficients during the non-haze period higher than those during the haze period. The ratios of SOC/PM2.5 in Renshou County were higher than those in Chengdu City during the haze period. This indicates that secondary aerosols play a more important role in haze formation in Renshou than in Chengdu City. In contrast, the proportion of secondary aerosols during the non-haze period in Chengdu City was significantly higher, indicating that direct emissions are still the main cause of air pollution in Chengdu City. PCA results showed that PM2.5 formation in both Chengdu City and Renshou County was mainly due to coal burning, vehicle operation, and biomass burning.

Physicochemical and toxicological characteristics of nanoparticles in aerosols in southern Thailand during recent haze episodes in lower southeast Asia

Transboundary haze from biomass burning is one of the most important air pollutions in Southeast Asia. The most recent serious haze episode occurred in 2015. Southern Thailand was affected by the haze during September to October when the particulate matter concentration hit a record high. We investigated physical and chemical characteristics of aerosols, including concentration and aerosol size distribution down to sub-micron sizes during haze episodes in 2013 and 2015 and, for reference, an insignificant haze period in 2017. The highest total suspended particulates and PM10 levels in Hat Yai city were 340.1 and 322.5 µg/m3. The mass fractions were nanoparticles (< 100 nm) 3.1%-14.8% and fine particles (< 1 µm) 54.6%-59.1%. Polycyclic aromatic hydrocarbon size distributions in haze periods peaked at 0.75 µm and the concentrations are 2-30 times higher than the normal period. High molecular weight (4-6 ring) PAHs during the haze episode contribute to about 56.7%-88.0% for nanoparticles. The average values of benzo(a)pyrene toxic equivalency quotient were 3.34±2.54ng/m3 in the 2015 haze period but only 0.89±0.17 ng/m3 in 2017. It is clear that particles smaller than 1 µm, were highly toxic. Nanoparticles contributed 19.4%-26.0% of total BaP-TEQ, whereas the mass fraction is 13.1%-14.8%. Thus the nanoparticles were more carcinogenic and can cause greater health effect than larger particles. The fraction of BaP-TEQ for nanoparticles during 2017 non-haze period was nearly the same, while the mass fraction was lower. This indicates that nanoparticles are the significant source of carcinogenic aerosols both during haze and non-haze periods.

El Niño driven haze over the Southern Malaysian Peninsula and Borneo

The Southeast Asian (SEA) region is no stranger to forest fires - the region has been suffering from severe air pollution (known locally as ‘haze’) as a result of these fires, for decades. The fires in SEA region are caused by a combination of natural (the El Niño weather pattern) and manmade (slash-and-burn and land clearing for plantations) factors. These fires cause the emissions of toxic aerosols and pollutants that can affect millions of people in the region. Thus, this study aims to identify the impact of the SEA haze on the Southern region of the Malaysian Peninsula and Borneo region of East Malaysia using the entire air quality observation data at surface level in 2015. Overall, the concentration of PM10 was about two-fold higher during the haze period compared to non-haze period. The concentrations of CO, flux of CO and flux of BC were aligned with PM10 during the entire observation period. The wind field and cluster of trajectory indicated that the Southern Malaysian Peninsula and Borneo were influenced mainly from the wildfires and the combustion of peat soil in the Indonesian Borneo. This study finds that wildfires from Borneo impacted the Southern Malaysian Borneo more seriously than that from Sumatra region.

Personal level exposure and hazard potential of particulate matter during haze and non-haze periods in Singapore.

Severe haze episodes originating from biomass burning are common in Southeast Asia. However, there is a paucity of data on the personal exposure and characteristics of Particulate Matter (PM) present in ambient air during haze and non-haze periods. Aims of this study were to monitor 24h ambulatory exposure to PM among school children in Singapore; characterize haze and non-haze PM for their physicochemical properties, cytotoxicity and inflammatory potential, using bronchial epithelial cell culture model (BEAS-2B). Forty-six children had ambulatory PM exposure monitored using portable Aethalometer and their hourly activity recorded. The mean (±SE) PM exposure on a typical school day was 3343 (±174.4) ng/m3/min. Higher PM exposure was observed during haze periods and during commuting to and from the school. Characterization of PM collected showed a drastic increase in the proportion of ultrafine particle (UFP) in haze PM. These PM fraction showed higher level of sulphur, potassium and trace metals in comparison to those collected during non-haze periods. Dose dependent increases in abiotic reactive oxygen species generation, activation of NF-κB and cytotoxicity were observed for both haze and non-haze PM. Generally, haze PM induced significantly higher release of IL-6, IL-8 and TNFα by BEAS-2B cells in comparison to non-haze PM. In summary, this study provides experimental evidence for higher PM exposure during haze period which has the potential to elicit oxidative stress and pro-inflammatory cytokine release from airway epithelial cells.

Chemical speciation of water-soluble ionic components in PM2.5 derived from peatland fires in Sumatra Island

We conducted a field study to characterize water-soluble ionic species in PM2.5 from peatland fires using ground-based samplings at fire sources and receptor sites in the Riau Province, Sumatra, Indonesia. We determined the concentrations of PM2.5 mass, water-soluble ions, and some chemical elements. Through PM2.5 field samplings at three peatland fire sources, we have shown that the mass fractions of typical peatland fire water-soluble ionic components tend to differ between peatland fire sources. Thus, our results indicate that PM2.5 source profiles of water-soluble ionic components for peatland fire must be selected with extreme caution if applied to a receptor model. From the viewpoint of ionic composition of each peatland fire sample, Cl− and NH4+ were consistently dominant anions and cations, respectively, for all peatland fire samples, i.e., NH4Cl was a consistently dominant component. Through field samplings of the ambient PM2.5 in Pekanbaru during peatland fire-induced haze and non-haze periods, we found differences in PM2.5 mass and total water-soluble ionic component concentrations between haze and non-haze samples. Four components, C2O42−, NO3−, SO42−, and NH4+, showed highly elevated levels during haze periods. Since these four ions are recognized as the major secondarily formed aerosol components, the increased total concentrations of water-soluble ionic components during haze periods can mainly be derived from the gas-to-aerosol conversion process. The ionic compositions of haze samples at receptor sites are obviously different from those at peatland fire source samples. In particular, NH4Cl, which is characteristic of peatland fire PM2.5 sources, is low at sites during haze periods.

Economic losses due to health hazards caused by haze event in Johor Bahru, Malaysia

This study assessed the health risk analysis of haze pollution in Pasir Gudang and Larkin. The relationship between health risk and economic effect due to air pollution exposure in Johor is still poorly understood. Therefore, the objective of this study was to analyse the relationship between air pollution and health. Then, the economic impact due to smoke haze on associated outpatients was calculated. Daily morbidity data from 2014 to 2016 for three haze-related illnesses were collected from two health clinics. Data on air quality were obtained at two Continuous Air Quality Monitoring (CAQM) stations in Johor. Health risks for all age categories in the haze periods were higher than those in non-haze periods. The outpatient morbidity cases in health clinics increased with the rising occurrence of smoke haze in Johor Bahru. The average annual economic losses due to the outpatient health impact of haze were valued at RM83,233 and RM107,486 for Pasir Gudang and Larkin, respectively.

Characteristics of Indoor and Outdoor Fine Phthalates during Different Seasons and Haze Periods in Beijing

ABSTRACT We studied the concentrations, seasonal distributions, sources, exposures, and health risks of phthalates in indoor and outdoor PM2.5 in Beijing. The results showed that phthalate concentrations during haze periods were significantly higher than during non-haze periods both indoors and outdoors, with higher concentrations for the former, which reached a maximum of 1995.56 ng m–3. Phthalates are mainly derived from the use of indoor plasticized products, the outdoor plastic products industry, and other sources of fuel emissions. Lifelong exposure to fine (2-ethylhexyl) phthalate (DEHP) through inhalation and dermal absorption was calculated, and the results indicated a risk of cancer, with DEHP carcinogenic risk levels of 4.09 × 10–6 and 10.50 × 10–6 for adults and children, respectively. The highest DEHP carcinogenic risk group was 1–2-year-old children, and the risk decreased afterward with age.

Analysis of Compositional Variation and Source Characteristics of Water-Soluble Ions in PM2.5 during Several Winter-Haze Pollution Episodes in Shenyang, China

From 18 February to 13 March 2014 and from 17 December 2016 to 27 January 2017, an online analyzer for monitoring aerosols and gases (MARGA) and an online single particle aerosol mass spectrometer (SPAMS) were used to measure and analyze the concentrations and sources of water-soluble (WS) ions in PM10, PM2.5, and gases (NH3, HNO3, HCl), in Shenyang City, China. During the field campaign, nine haze episodes (or smog episodes, total 582 h) were identified, with 960 identified as non-haze periods. The average mass concentrations of PM2.5 and total water-soluble ions (TWSIs) in PM2.5 during haze episodes were 131 μg·m−3 and 77.2 μg·m−3, 2.3 times and 1.9 times the values in non-haze periods, respectively. The average mass concentration of TWSIs in PM2.5 was 55.9 μg·m−3 (accounting for 55.9% of PM2.5 mass loading), 37.6% of which was sulfate, 31.7% nitrate, 20.0% ammonium, 6.6% chloride, 1.9% potassium, 1.4% calcium, and 0.8% magnesium throughout the campaign. Concentrations of sulfate, nitrate, and ammonium (SNA) secondary pollution ions increased rapidly during haze episodes to as much as 2.2 times, 3.0 times, and 2.4 times higher than during non-haze periods, respectively. Diurnal variations during non-haze periods were significant, while complex pollution was insignificant. Based on changes in the backward trajectories and concentrations of WS ions, the hazy episodes were divided into three types: complex, coal-burning, and automobile exhaust pollution. All complex episodes had high concentrations and greater contributions of ammonium nitrate from complex and automobile exhaust pollution, while the contribution of ammonium sulfate from coal-burning pollution was greater than that of ammonium nitrate. The correlation coefficients among SNA species were very high in complex pollution, with nitrate and sulfate the main forms present. The results of principal component analysis (PCA) were related to emissions from burning coal for heating and from long-range transmission in winter. In the case of exhaust pollution, NO3− accounted for the highest percentage of PM2.5, and NH4+ was more closely related to NO3− than to SO42−. Coal-burning pollution was the most common type of pollution in Shenyang. The contribution of sulfate was higher than that of nitrate. Based on PCA, the contribution of coal-burning emissions varied from 36.7% to 53.6% due to industry, soil sources, and other factors.

Hazy Weather-Induced Variation in Environmental Behavior of PCDD/Fs and PBDEs in Winter Atmosphere of A North China Megacity.

Haze is a serious pollution problem during the wintertime in North China. In this study, we investigated how the periodic cycle of winter haze events affect the environmental behaviors of two typical persistent organic pollutants, namely, polychlorinated dibenzo- p-dioxins and dibenzofurans (PCDD/Fs) and polybrominated diphenyl ethers (PBDEs), in the atmosphere of a typical megacity, Beijing. The average atmospheric concentrations of the total di- to octa-CDD/Fs (∑PCDD/Fs: 378.0 pg/m3) and the total mono- to nona-BDEs (∑9hPBDEs: 166.5 pg/m3) during haze episodes increased by 3.6-fold and 1.9-fold compared with those during the nonhaze periods, respectively; and their concentrations both linearly increased with PM2.5 levels and decreased as a power function of the atmospheric boundary layer height. The elevated concentrations could be clearly attributed to the vertically sinking motion of airflow in the midlower troposphere. When a haze event occurred, the partitioning rate of PCDD/Fs and PBDEs into particles was reduced; the largest fraction of the particle-bound ∑PCDD/Fs was shifted from ultrafine particles to accumulation mode particles; and a steady-state model (Li-Ma-Yang model) satisfactorily described the gas-particle partitioning of the PCDD/F and PBDE homologues. The inhalation exposure risk evaluation indicated that special attention should be paid to the increased cancer risk induced by the elevated inhalation intake of PCDD/Fs during haze episodes.

Annual Southeast Asia haze increases respiratory admissions: A 2-year large single institution experience.

The Southeast Asia (SEA) haze is an annual problem and at its worst could produce respirable particles of concentrations up to 500 μg/m3 which is five times the level considered as 'unhealthy'. However, there are limited reports examining the direct clinical impact of the annual haze. This study examines the effects of the SEA haze on respiratory admissions. Data from all respiratory admissions in Universiti Kebangsaan Malaysia Medical Centre (UKMMC) from 1st January 2014 to 31st December 2015 were collected retrospectively from chart and electronic database. A total of 16 weeks of haze period had been formally dated by the Department of Environment using the definition of weather phenomenon leading to atmospheric visibility of less than 10 km. Multivariable regression analyses were performed to estimate rate ratios and 95% CI. There were 1968 subjects admitted for respiratory admissions in UKMMC during the study period. Incidence rates per week were significantly different between the two groups with 27.6 ± 9.2 cases per week during the haze versus 15.7 ± 6.7 cases per week during the non-haze period (P < 0.01). A total of 4% versus 2% was admitted to the intensive care unit in the haze and the non-haze groups, respectively (P = 0.02). The mean ± SD lengths of stay was 12.1 ± 5.2 days; the haze group had a longer stay (18.2 ± 9.7 days) compared to the non-haze groups (9.7 ± 3.9) (P < 0.001). The annual SEA haze is associated with increased respiratory admissions.

Particle Size Distributions of Oxidative Potential of Lung-Deposited Particles: Assessing Contributions from Quinones and Water-Soluble Metals

Redox-active species in ambient particulate matter (PM) cause adverse health effects through the production of reactive oxygen species (ROS) in the human respiratory tract. However, respiratory deposition of these species and their relative contributions to oxidative potential (OP) have not been described. Size-segregated aerosols were collected during haze and nonhaze periods using a micro-orifice uniform deposit impactor sampler at an urban site in Shanghai to address this issue. Samples were analyzed for redox-active species content and PM OP. The average dithiothreitol (DTT) activity of haze samples was approximately 2.4-fold higher than that of nonhaze samples and significantly correlated with quinone and water-soluble metal concentrations. The size-specific distribution data revealed that both water-soluble OPvDTT (volume-normalized OP quantified by DTT assay) and OPmDTT (mass-normalized OP) were unimodal, peaking at 0.56-1 and 0.1-0.32 μm, respectively, due to contributions from accumulation-mode quinones and water-soluble metals. We further estimated that transition metals (mainly copper and manganese) contributed 55 ± 13% of the DTT activity while quinones accounted for only 8 ± 3%. Multiple-path particle dosimetry calculations estimated that OP deposition in the pulmonary region was mainly from accumulation-mode transition metals despite quinones having the highest DTT activity. This behavior is primarily attributed to the efficiency of deposition of transition metals in the pulmonary region being approximately 1.2-fold greater than that of quinones. These results reveal that accumulation-mode transition metals are significant contributors to the OP of deposited water-soluble particles in the pulmonary region of the lung.

Local and transboundary factors' impacts on trace gases and aerosol during haze episode in 2015 El Niño in Malaysia

Southeast Asian haze is a semi-natural phenomenon that chokes the region each year during the dry monsoon season. Smoke-haze episodes caused by the vegetation and peat fires in Indonesia severely affected large parts of Malaysia during the 2015 El Niño phenomenon. This study aimed to evaluate the factors that influenced the concentrations of aerosol and trace gases during the 2015 haze and non-haze period on a semi-urban site in the southern part of Malaysian peninsula that facing Sumatra (Muar, Site A), and on an urban site near to Kuala Lumpur, influenced by the city centre (Cheras, Site B). Local land use data and the cluster of air mass weighted backward trajectory were used to identify the potential factors from local sources and the transboundary region, respectively. The annual median concentrations of PM10 for semi-urban and urban sites were 45.0μg/m3 and 47.0μg/m3, respectively for the study period (Jan–Dec 2015) from the hourly observation dataset. The highest PM10 concentrations during the haze were 358μg/m3 and 415μg/m3 for the two sites, respectively, representing absolutely unhealthy air. However, the trace gases were within the safe threshold. The average concentrations of PM10 and carbon monoxide were two fold higher during the haze than the non-haze episodes on both sites. Nitrogen dioxide was more influenced by haze compared with sulphur dioxide and ozone. The results of the land use change suggest that the local factor can also partially affect the air pollution on the urban area (Site B) but more visible in 2015. The results of the backward trajectory and the wildfire radiative power showed that the smoke-haze episodes that affected Malaysia in 2015 were mainly initiated in the Indonesian Sumatra and Kalimantan regions. This study provides a very useful information towards the impacted region during El Niño haze episode.

Characteristics and source apportionment of fine haze aerosol in Beijing during the winter of 2013

Abstract. For PM2.5 filter samples collected daily at the Chinese Research Academy of Environmental Sciences (Beijing, China) from December of 2013 to February of 2014 (the winter period), chemical characteristics and sources were investigated with an emphasis on haze events in different alert levels. During the 3 months, the average PM2.5 concentration was 89 µg m−3, exceeding the Chinese national standard of 75 µg m−3 in 24 h. The maximum PM2.5 concentration was 307 µg m−3, which characterizes developed-type pollution (PM2.5 / PM10&gt;0.5) in the World Health Organization criteria. PM2.5 was dominated by SO42−, NO3−, and pseudo-carbonaceous compounds with obvious differences in concentrations and proportions between non-haze and haze episodes. The non-negative matrix factorization (NMF) analysis provided reasonable PM2.5 source profiles, by which five sources were identified: soil dust, traffic emission, biomass combustion, industrial emission, and coal combustion accounting for 13, 22, 12, 28, and 25 % of the total, respectively. The dust impact increased with northwesterlies during non-haze periods and decreased under stagnant conditions during haze periods. A blue alert of heavy air pollution was characterized by the greatest contribution from industrial emissions (61 %). During the Chinese Lantern Festival, an orange alert was issued and biomass combustion was found to be the major source owing to firework explosions. Red-alert haze was almost equally contributed by local traffic and transported coal combustion emissions from the vicinity of Beijing (approximately 40 % each) that was distinguished by the highest levels of NO3− and SO42−, respectively. This study also reveals that the severity and source of haze are largely dependent on meteorological conditions.

Short communication: Diagnosis of lung cancer increases during the annual southeast Asian haze periods

There have been few but timely studies examining the role of air pollution in lung cancer and survival. The Southeast Asia haze is a geopolitical problem that has occurred annually since 1997 in countries such as Malaysia, Singapore and Indonesia. To date, there has been no study examining the impact of the annual haze in the presentation of lung cancer. Data on all lung cancers and respiratory admissions to Universiti Kebangsaan Malaysia Medical Centre (UKMMC) from 1st January 2010 to 31th October 2015 were retrospectively collected and categorized as presentation during the haze and non-haze periods defined by the Department of Environment Malaysia. We report a lung cancer incidence rate per week of 4.5 cases during the haze compared to 1.8 cases during the non-haze period (p<0.01). The median survival for subjects presenting during the haze was 5.2 months compared to 8.1 months for the non-haze period (p<0.05). The majority of subjects diagnosed during the haze period initially presented with acute symptoms. Although this study could not suggest a cause and effect relationship of the annual haze with the incidence of lung cancer, this is the first study reporting a local air pollution-related modifiable determinant contributing to the increase in presentation of lung cancer in Southeast Asia.

Size distribution, characterization and risk assessment of particle-bound polycyclic aromatic hydrocarbons during haze periods in Phayao Province, northern Thailand

This study aims to investigate the concentrations and distributions of particulate matters and particle-bound polycyclic aromatic hydrocarbons (p-PAHs) in different inhalable fractions during haze periods in Phayao Province, northern Thailand and identify their possible emission sources through the characteristic ratios of selected PAHs, then determine an estimate of the potential lung cancer risk. The particulate samples were collected during haze periods between February 18 and April 8, 2014 and non-haze period from June 17 to 22, 2014 using an eight-stage cascade impactor. Each filter sample was weighed, ultrasonically extracted with acetonitrile, and then analyzed by SIM-GC-MS to identify 16 PAHs. The experimental results show that the concentrations of ultrafine (d ae < 0.4 μm), fine (0.4 μm < d ae < 2.1 μm), and coarse (d ae > 2.1 μm) particles during haze periods were in the range of 14.98–26.52 μg m−3, 62.57–101.52 μg m−3, and 55.27–89.68 μg m−3, respectively; whereas, their concentrations of 16 PAHs were in the range of 7.82–36.06 ng m−3, 26.66–61.89 ng m−3, and 9.35–30.93 ng m−3, respectively. The p-PAH distribution profiles during the haze periods were bimodal in coarse and accumulation modes, which are closely related to their particle size distributions. The characteristic ratios of BaP/BgP and INP/(BgP+InP) adsorbed on ultrafine and fine particles were 0.81–0.88 and 0.38–0.86 and 0.54–0.57 and 0.44–0.52, respectively. The values of B[a]Peq observed during haze periods varied from 9.57 to 29.05 ng m−3. Estimated lifetime cancer risks during haze periods ranged from 8.324 to 25.27 additional cases per 10,000 people exposed, which is about 10 times higher than that during non-haze period.

Characteristics and source apportionment of PM2.5 during persistent extreme haze events in Chengdu, southwest China

Based on detailed data from Chengdu Plain (CP) from 6 January to 16 January, two typical haze episodes were analyzed to clarify the haze formation mechanism in winter. Weather conditions, chemical compositions, secondary pollutant transformation, optical properties of aerosols, the potential source contribution function (PSCF) and source apportionment were studied. The planetary boundary layer (PBL) height decreased distinctly during the haze episodes and restrained air pollutant vertical dispersion. As the haze worsened, the value of PBL × PM2.5 increased notably. The [NO3−]/[SO42−] ratio was 0.61, 0.76 and 0.88 during a non-haze period, episode 1 and episode 2, respectively, indicating that the mobile source of the air pollution is increasingly predominant in Chengdu. Water vapor also played a vital role in the formation of haze by accelerating the chemical transformation of secondary pollutants, leading to the hygroscopic growth of aerosols. The PSCF and backward trajectories of the air masses indicated that the pollution mainly came from the south. The secondary inorganic aerosols, vehicle emissions, coal combustion, biomass burning, industry, and dust contributed 34.1%, 24.1%, 12.7%, 12.3%, 7.6%, and 7.2% to PM2.5 masses in episode 1 and 28.9%, 23.1%, 9.4%, 9.5%, 20.3% and 7.5% in episode 2.

Volatile organic compounds (VOCs) during non-haze and haze days in Shanghai: characterization and secondary organic aerosol (SOA) formation.

To better understand the characterization and secondary organic aerosol (SOA) formation of volatile organic compounds (VOCs) during non-haze and haze days, ambient VOCs were continuously measured by a vehicle-mounted online thermal desorption system coupled with a gas chromatography-mass spectrometry (TD-GC/MS) system in Shanghai, China. The average concentrations of VOCs in haze episodes (193.2μgm-3) were almost 50% higher than in non-haze periods (130.8μgm-3). VOC concentrations exhibited a bi-modal pattern in the morning and evening rush hour periods on both non-haze and haze days. The ratios of toluene to benzene (T/B) and m,p-xylene to ethylbenzene (X/E) indicated that VOCs were aged air mass transported from nearby areas. The estimated SOA yields were 12.6±5.3 and 16.7±6.7μgm-3 for non-haze and haze days, respectively, accounting for 9.6 and 8.7% of the corresponding PM2.5 concentrations, which were slightly underestimated. VOCs-sensitivity (VOCs-S) based on a PM2.5-dependent model was used to investigate the variation between VOCs and PM2.5 concentrations in the morning rush hour. It was found that VOCs were more sensitive to PM2.5 on clean days than during periods of heavy particulate pollution. VOCs-sensitivity was significantly correlated with the ratio of specific PM2.5 to background PM2.5, with a simulated equation of y=0.84x-0.62 (r 2=0.93, p<0.001). Our findings suggest that strategies to mitigate VOC emissions and further alleviate haze episodes in Shanghai based on reducing gasoline vehicle-related sources would be very efficient.

Characterization of rainwater chemical composition after a Southeast Asia haze event: insight of transboundary pollutant transport during the northeast monsoon.

Open biomass burning in Peninsula Malaysia, Sumatra, and parts of the Indochinese region is a major source of transboundary haze pollution in the Southeast Asia. To study the influence of haze on rainwater chemistry, a short-term investigation was carried out during the occurrence of a severe haze episode from March to April 2014. Rainwater samples were collected after a prolonged drought and analyzed for heavy metals and major ion concentrations using inductively coupled plasma mass spectroscopy (ICP-MS) and ion chromatography (IC), respectively. The chemical composition and morphology of the solid particulates suspended in rainwater were examined using a scanning electron microscope coupled with energy-dispersive X-ray spectroscopy (SEM-EDS). The dataset was further interpreted using enrichment factors (EF), statistical analysis, and a back trajectory (BT) model to find the possible sources of the particulates and pollutants. The results show a drop in rainwater pH from near neutral (pH 6.54) to acidic (<pH 4.00) during the haze to non-haze transitional period, suggesting that the deposition rate of sulfate and nitrate in the atmosphere via the precipitation process was relatively lower compared to the mineral components. Zinc, nitrate, and calcium, which were the predominant elements in the first rainwater samples. Besides, the results of the SEM-EDS indicated that the zinc was possibly originated from anthropogenic activities which are consistent with the results obtained from EF. The BT model showed that pollutants transported from the mainland of Indo-China and the marine region in the South China Sea were responsible for the high pollution event in the study area. These findings can be useful in identifying contributions of pollutants from single or multiple sources in rainwater samples during haze episodes.