Non-haze Periods Research Articles

Effect of agricultural waste burning season on PM2.5-bound polycyclic aromatic hydrocarbon (PAH) levels in Northern Thailand

Smoke from agricultural waste burning causes hazardous haze pollution in Southeast Asian countries every year. Besides traces of a few toxic gases several persistent organic pollutants, natural, and anthropogenic emissions are released, resulting in adverse health effects. The study focuses on identification of sources of PM2.5-bound polycyclic aromatic hydrocarbons (PAHs) during the non-haze and haze seasons and investigates the concentration and toxicity of fine particulate matter, especially in the middle of biomass burning period. Totally, 12 fine particulate PAH congeners were selected and analysed at air quality observatory sites located in nine administrative provinces of Northern Thailand during four different sampling periods from 7th December 2012 to 27th March 2015. Nisbet and Lagoy's toxicity equivalent concentration (TEQ) equation revealed that the B[a]PEquivalent value for 2014–2015 roughly surpassed the value of 2012–2013 by a factor of 17. This can be attributed to the significant rise in five-to six-ring PAHs levels in the past two years. Diagnostic binary ratios and linear regression analysis highlight the roles of vehicular exhausts and biomass burning as two major contributors of PM2.5-bound PAHs. Interestingly, principal component analysis (PCA) reveals similar loading patterns for PC1 during the non-haze and haze periods, indicating that agricultural waste burning cannot be considered as the sole contributor of particulate PAHs in Northern Thailand.

Influence of haze pollution on water-soluble chemical species in PM2.5 and size-resolved particles at an urban site during fall

To investigate the influence of haze on the chemical composition and formation processes of ambient aerosol particles, PM2.5 and size-segregated aerosol particles were collected daily during fall at an urban site of Gwangju, Korea. During the study period, the total concentration of secondary ionic species (SIS) contributed an average of 43.9% to the PM2.5, whereas the contribution of SIS to the PM2.5 during the haze period was 62.3%. The NO3− and SO42− concentrations in PM2.5 during the haze period were highly elevated, being 13.4 and 5.0 times higher than those during non-haze period, respectively. The PM, NO3−, SO42−, oxalate, water-soluble organic carbon (WSOC), and humic-like substances (HULIS) had tri-modal size distributions peaks at 0.32, 1.0, and 5.2μm during the non-haze and haze periods. However, during the non-haze period they exhibited dominant size distributions at the condensation mode peaking at 0.32μm, while on October 21 when the heaviest haze event occurred, they had predominant droplet mode size distributions peaking at 1.00μm. Moreover, strong correlations of WSOC and HULIS with SO42−, oxalate, and K+ at particle sizes of <1.8μm indicate that secondary processes and emissions from biomass burning could be responsible for WSOC and HULIS formations. It was found that the factors affecting haze formation could be the local stable synoptic conditions, including the weak surface winds and high surface pressures, the long-range transportation of haze from eastern China and upwind regions of the Korean peninsula, as well as the locally emitted and produced aerosol particles.

Seasonal variation of particle-induced oxidative potential of airborne particulate matter in Beijing.

An in vitro plasmid scission assay (PSA), the cell apoptosis assay, and ICP-MS were employed to study the oxidative potentials and trace element compositions of the airborne particulate matter (PM) in Beijing during a one year-long field campaign from June 2010 to June 2011. The cell damages induced by PM reveled by the cell apoptosis assay showed a similar variation pattern to the DNA damages obtained by PSA, verifying the feasibility of the PSA in analyzing the oxidative capacity of PM samples. The PSA experiments showed that the particle-induced DNA damage was highest in summer, followed by spring, winter and autumn in descending order. The percentages of the oxidative damages to plasmid DNA induced by the water-soluble fractions of PM under the particle doses from 10 to 250μg/ml were generally lower than 45%, with some values peaking at above 50%. The peak values were frequently present in late spring (i.e. April and May) and early summer (i.e. June) but they were scarcely observed in other seasons. These peak values were mostly associated with haze days or the days with low wind speed (less than 4m/s), indicating that the PM samples during haze had higher oxidative potential than those during non-haze periods. The oxidative potential induced by the water-soluble fraction of the PM displayed a significant positive correlation with the concentrations of the water-soluble elements Cd, Cs, Pb, Rb, Zn, Be and Bi, demonstrating that the particle-induced oxidative potentials were mainly sourced from these elements. The exposure risk represented by the mass concentration of these elements in unit volume of atmosphere was higher in summer and winter, and lower in autumn and spring. The haze day PM samples not only had higher level of oxidative potentials but also had higher concentrations of water-soluble elements.

Size distributions of n-alkanes, fatty acids and fatty alcohols in springtime aerosols from New Delhi, India

Size-segregated aerosol samples were collected in New Delhi, India from March 6 to April 6, 2012. Homologous series of n-alkanes (C19C33), n-fatty acids (C12C30) and n-alcohols (C16C32) were measured using gas chromatography/mass spectrometry. Results showed a high-variation in the concentrations and size distributions of these chemicals during non-haze, haze, and dust storm days. In general, n-alkanes, n-fatty acids and n-alcohols presented a bimodal distribution, peaking at 0.7–1.1 μm and 4.7–5.8 μm for fine modes and coarse modes, respectively. Overall, the particulate matter mainly existed in the coarse mode (≥2.1 μm), accounting for 64.8–68.5% of total aerosol mass. During the haze period, large-scale biomass burning emitted substantial fine hydrophilic smoke particles into the atmosphere, which leads to relatively larger GMDs (geometric mean diameter) of n-alkanes in the fine mode than those during the dust storms and non-haze periods. Additionally, the springtime dust storms transported a large quantity of coarse particles from surrounding or local areas into the atmosphere, enhancing organic aerosol concentration and inducing a remarkable size shift towards the coarse mode, which are consistent with the larger GMDs of most organic compounds especially in total and coarse modes. Our results suggest that fossil fuel combustion (e.g., vehicular and industrial exhaust), biomass burning, residential cooking, and microbial activities could be the major sources of lipid compounds in the urban atmosphere in New Delhi.

Identification of concentrations and sources of PM2.5-bound PAHs in North China during haze episodes in 2013

An analysis of 12 polycyclic aromatic hydrocarbons (PAHs) in PM2.5 (particulate matter with a diameter smaller than 2.5 microns) samples collected at Yucheng, Shandong, in June 2013 was conducted to determine the concentrations, composition, sources, and associated cancer risk. The results revealed that the average PAH concentration was higher during haze episodes (28.28 ± 8.35 ng m−3) when compared to non-haze episodes (23.68 ± 4.17 ng m−3), and diagnostic ratio and principal component analyses indicate that the predominant sources of PAHs were from fossil fuel and coal combustion, likely from vehicle emissions and industrial sources and biomass burning. Coal combustion and biomass burning contributed significantly more during haze episodes, whereas liquid fossil fuel combustion (e.g. petroleum) was the dominant contributor during the non-haze periods. In addition, back-trajectory calculations revealed that the long-distance transport of air masses from regions with industrial pollution and biomass burning contributed significantly to the concentrations of PAHs in the region. The concentration of high molecular weight PAHs (HMW-PAHs) increased from 62.3 % under non-haze conditions to 67.9 % during the haze periods. The benzo[a]pyrene-equivalent carcinogenic potency value during haze episodes was higher (7.09 ng m−3) than that during non-haze (5.64 ng m−3) periods and adults over 30 years old in the Shandong province are at an increased risk of cancer from PAHs.

Fractionation of airborne particulate-bound elements in haze-fog episode and associated health risks in a megacity of southeast China

Haze caused by high particulate matter loadings is an important environmental issue. PM2.5 was collected in Nanjing, China, during a severe haze–fog event and clear periods. The particulate-bound elements were chemically fractionated using sequential extractions. The average PM2.5 concentration was 3.4 times higher during haze–fog (96–518 μg/m3) than non-haze fog periods (49–142 μg/m3). Nearly all elements showed significantly higher concentrations during haze–fog than non-haze fog periods. Zn, As, Pb, Cd, Mo and Cu were considered to have higher bioavailability and enrichment degree in the atmosphere. Highly bioavailable fractions of elements were associated with high temperatures. The integrated carcinogenic risk for two possible scenarios to individuals exposed to metals was higher than the accepted criterion of 10−6, whereas noncarcinogenic risk was lower than the safe level of 1. Residents of a city burdened with haze will incur health risks caused by exposure to airborne metals.

Risk assessment of bioaccessible trace elements in smoke haze aerosols versus urban aerosols using simulated lung fluids

Abstract Smoke-haze episodes, caused by uncontrolled peat and forest fires, occur almost every year in the South-East Asian region with increased concentrations of PM2.5 (airborne particulate matter (PM) with diameter ≤ 2.5 μm). Particulate-bound trace elements (TrElems), especially carcinogenic and toxic elements, were measured during smoke haze as well as non-haze periods in 2014 as they are considered to be indicators of potential health effects. The bioaccessibilities of 13 TrElems were investigated using two types of simulated lung fluids (SLFs), Gamble's solution and artificial lysosomal fluid (ALF), instead of the commonly used leaching agent (water). The dissolution kinetics was also examined for these TrElems. Many TrElems showed higher solubility in SLFs, and were more soluble in ALF compared to the Gamble's solution. Cu, Mn and Cd were observed to be the most soluble trace elements in ALF, while in Gamble's solution the most soluble trace elements were Cu, Mn and Zn. The dissolution rates were highly variable among the elements. Health risk assessment was conducted based on the measured concentrations of TrElems and their corresponding toxicities for three possible scenarios involving interactions between carcinogenic and toxic TrElems and SLFs, using the United States Environmental Protection Agency (USEPA) human health risk assessment model. The cumulative cancer risks exceeded the acceptable level (1 in a million i.e. 1 × 10−6). However, the estimation of health quotient (HQ) indicated no significant chronic toxic health effects. The risk assessment results revealed that the assessment of bioaccessibility of particulate-bound TrElems using water as the leaching agent may underestimate the health risk.

Hospital out-and-in-patients as Functions of Trace Gaseous Species and Other Meteorological Parameters in Chiang-Mai, Thailand

The aims of this study were to investigate the impact of meteorological parameters and trace gas concentrations on daily hospital walk-ins and admissions in Chiang-Mai province, Thailand, during 2007-2013. Advanced statistical models, including t-tests, Analysis of Variance (ANOVA), Multiple Linear Regression Analysis (MLRA) and Incremental Lifetime Particulate Matter Exposure (ILPE), were constructed using meteorological data from the Pollution Control Department (PCD), Ministry of Natural Resources and Environment (MNRE), Thailand, and the Thai Meteorological Department at Chiang-Mai Province Air Quality Observatory Site (TMCS) as well as the number of walk-in and admitted patients at Nakornping Hospital, Chiang-Mai (NHCM). The results showed that all trace gaseous species and PM_(10) were significantly higher during the ＂haze episode＂ than during the ＂non-haze period.＂ The FTIR spectra highlight the relatively homogeneous organic functional compositions of PM_(2.5) collected from urban, suburban and rural observatory sites, indicating that agricultural waste burning plays an important role in air quality during the ＂haze episode.＂ The effect of age on susceptibility to respiratory diseases was investigated by separating the dataset into four groups (i.e., ＜ 15 years, 15-59 years, 60-74 years and ≥ 75 years). The ANOVA results revealed a significant increase in hospital walk-ins and admissions for both genders in the ＜ 15 years group (p ＜ 0.005). MLRA revealed the significantly highest impacts of CO on hospital walk-ins for both genders. The predicted ILPE of PM_(10) showed the highest values for both genders during the ＂haze-episode＂ in 2007, with average values of 3.338 ± 0.576 g and 1.838 ± 0.317 g for male and female outdoor workers, respectively, over an exposure duration of 25 years.

In situ acidity and pH of size-fractionated aerosols during a recent smoke-haze episode in Southeast Asia.

The characterization of aerosol acidity has received increased attention in recent years due to its influence on atmospheric visibility, climate change and human health. Distribution of water soluble inorganic (WSI) ions in 12 different size fractions of aerosols was investigated under two different atmospheric conditions (smoke-haze and non-haze periods) in 2012 using the Micro-Orifice Uniform Deposit Impactor (MOUDI) and nano-MOUDI for the first time in Singapore. To estimate the in situ acidity ([H(+)]Ins) and in situ aerosol pH (pHIS), the Aerosol Inorganic Model version-IV under deliquescent mode of airborne particles was used at prevailing ambient temperature and relative humidity. The study revealed an increase in the levels of airborne particulate matter (PM) mass and concentrations of WSI ions for all size fractions during the smoke-haze period, which was caused by the trans-boundary transport of biomass burning-impacted air masses from Indonesia. A bimodal distribution was observed for concentrations of SO4(2-), NO3(-), Cl(-), K(+) and Na(+), whereas concentrations of NH4(+), Ca(2+) and Mg(2+) showed a single mode distribution. The concentration of WSI ions in PM1.8 during the smoke-haze period increased by 3.8 (for SO4(2-)) to 10.5 (for K(+)) times more than those observed during the non-haze period. The pHIS were observed to be lower during the smoke-haze period than that during the non-haze period for all size fractions of PM, indicating that atmospheric aerosols were more acidic due to the influence of biomass burning emissions. The particles in the accumulation mode were more acidic than those in the coarse mode.

Characterization and estimation of human airway deposition of size-resolved particulate-bound trace elements during a recent haze episode in Southeast Asia.

Toxic elements present in airborne particulate matter (PM) are associated with human health effects; however, their toxic characteristics depend on the source of their origins and their concentrations in ambient air. Twenty four elements (Al, B, Ba, Be, Bi, Ca, Cd, Co, Cr, Cu, Fe, Ga, K, Li, Mg, Mn, Na, Ni, Pb, Se, Sr, Te, Tl, and Zn) in 12 different size fractions of PM ranging from 10nm to 10μm were characterized in Singapore during two different atmospheric conditions (smoke haze and non-haze periods) in 2012 for the first time. In addition, their possible sources were identified based on backward air trajectory analysis and principal component analysis (PCA). The health implications of inhalable particles were assessed using a human airway deposition model, the Multiple-Path Particle Dosimetry model (MPPD). The results concerning particle-bound trace elements are interpreted in terms of coarse (PM2.5-10), fine (PM2.5), ultrafine (PM0.01-0.1, 0.01μm < Dp < 0.10μm), and nano (PM0.01-0.056, 0.01μm < Dp < 0.056μm) particles. The ratios of elemental concentrations measured between the smoke haze episode and the non-haze period in coarse, fine, ultrafine, and nano particles varied from 1.2 (Bi) to 6.6 (Co). Both the PCA and backward trajectory analysis revealed that trans-boundary biomass-burning emissions from Indonesia were primarily responsible for enhanced concentrations of particulate-bound elements during the smoke haze episode. The particle depositions in the respiratory system were higher during the smoke haze episode compared to the non-haze period. The study finds that ultrafine and nano particles present in the atmosphere have higher tendencies to be deposited into the deeper parts of the respiratory system, compared to coarse and fine particles.

Influence of trans-boundary biomass burning impacted air masses on submicron particle number concentrations and size distributions

Submicron particle number concentration (PNC) and particle size distribution (PSD) in the size range of 5.6–560 nm were investigated in Singapore from 27 June 2009 through 6 September 2009. Slightly hazy conditions lasted in Singapore from 6 to 10 August. Backward air trajectories indicated that the haze was due to the transport of biomass burning impacted air masses originating from wild forest and peat fires in Sumatra, Indonesia. Three distinct peaks in the morning (08:00–10:00), afternoon (13:00–15:00) and evening (16:00–20:00) were observed on a typical normal day. However, during the haze period no distinct morning and afternoon peaks were observed and the PNC (39,775 ± 3741 cm−3) increased by 1.5 times when compared to that during non-haze periods (26,462 ± 6017). The morning and afternoon peaks on the normal day were associated with the local rush hour traffic while the afternoon peak was induced by new particle formation (NPF). Diurnal profiles of PNCs and PSDs showed that primary particle peak diameters were large during the haze (60 nm) period when compared to that during the non-haze period (45.3 nm). NPF events observed in the afternoon period on normal days were suppressed during the haze periods due to heavy particle loading in atmosphere caused by biomass burning impacted air masses.

2013 Southeast Asian Smoke Haze: Fractionation of Particulate-Bound Elements and Associated Health Risk

Recurring biomass burning-induced smoke haze is a serious regional air pollution problem in Southeast Asia (SEA). The June 2013 haze episode was one of the worst air pollution events in SEA. Size segregated particulate samples (2.5-1.0 μm; 1.0-0.5 μm; 0.5- 0.2 μm; and <0.2 μm) were collected during the June 2013 haze episode. PM2.5 concentrations were elevated (up to 329 μg/m(3)) during the haze episode, compared to those during the nonhaze period (11-21 μg/m(3)). Chemical fractionation of particulate-bound trace elements (B, Ca, K, Fe, Al, Ni, Zn, Mg, Se, Cu, Cr, As, Mn, Pb, Co, and Cd) was done using sequential extraction procedures. There was a 10-fold increase in the concentration of K, an inorganic tracer of biomass burning. A major fraction (>60%) of the elements was present in oxidizable and residual fractions while the bioavailable (exchangeable) fraction accounted for up to 20% for most of the elements except K and Mn. Deposition of inhaled potentially toxic trace elements in various regions of the human respiratory system was estimated using a Multiple-Path Particle Dosimetry model. The particle depositions in the respiratory system tend to be more severe during hazy days than those during nonhazy days. A prolonged exposure to finer particles can thus cause adverse health outcomes during hazy days. Health risk estimates revealed that the excessive lifetime carcinogenic risk to individuals exposed to biomass burning-impacted aerosols (18 ± 1 × 10(-6)) increased significantly (P < 0.05) compared to those who exposed to urban air (12 ± 2 × 10(-6)).

Black carbon aerosols in urban central China

The first ever (to our knowledge), year-round measurements of Black Carbon (BC) aerosols in Hefei, an urban site of central China, from June 2012 to May 2013 are performed. The aim of this paper is to evaluate the black carbon in Hefei in terms of seasonal, monthly and diurnal variations, including their source identification. The annual mean BC mass concentration MBC is found to be 3.5±2.5μgm−3 in Hefei, while the aerosol optical depth shows a yearly average value of ~0.6. The seasonality of MBC depicts minimum values in the summer, moderate levels in the spring and fall, and maximum in the winter. The monthly average values of MBC vary threefold, ranging from the lowest average value of 2.0±1.0μgm−3 in July to the highest 6.0±2.6μgm−3 during January. Diurnal variations exhibit two BC peaks, corresponding to the morning and evening rush hours. Higher median BC concentrations are observed during haze episodes compared with non-haze periods, although low MBC is sometimes observed for high visibility, which is probably indicative of the aerosol scattering dominating diminished visibility. Based on trajectory analyses, the haze BC pollutions are mostly classified into three types from local areas, long-range transport from the Yangtze Delta, and transport from the North China Plain. The median MBC values for haze groups attributed to biomass burning from MODIS wildfire maps are higher than related groups that are not, which is indicative of the significant enhancement of BC aerosols due to agricultural biomass burning. The study suggests that aerosol absorption contributes more to the observed haze episodes in fall compared to other seasons.

Airborne submicron particulate (PM1) pollution in Shanghai, China: Chemical variability, formation/dissociation of associated semi-volatile components and the impacts on visibility

Hourly mass concentrations of water-soluble ions in PM1 and gasses (NH3, HNO3, HCl) were on-line measured with a Monitor for AeRosols and Gases Analyzer (MARGA) in Shanghai from Oct. 1 to Nov. 16, 2012. During the field campaign, 7 haze episodes (total 157h) were identified. 845h were identified as non-haze periods, excluding fog events and wet precipitation. The average mass concentration of PM1 and total water-soluble ions (TWSI) in PM1 in haze episodes were 78.9±29.9μg/m3 and 47.2±17.2μg/m3, 3.11 times (from 1.49 to 4.06 times) and 3.28 times (1.96 to 4.34 times) as those in non-haze periods, respectively. TWSI accounted for 60.4±18.8% of PM1 mass loading in the whole campaign. With the ascending PM1 mass concentration from 2.5 to 125.0μg/m3 from non-haze periods to haze episodes, average contribution of TWSI to PM1 mass loading decreased from 86.1% to 54.2%, while different species altered. Contribution of NO3− increased from 14.0% to 26.8%, while SO42− decreased from 39.5% to 15.0% and NH4+ remained around 13.7%. Relationship of visibility with PM1 and TWSI was addressed in specific RH ranges. It was found that hourly TWSI mass concentration showed better correlation with visibility. Formation/dissociation of semi-volatiles (NH4NO3 and NH4Cl) was also investigated and demonstrated. NH4NO3 and NH4Cl tended to partition into gas phase in non-haze periods. Particularly, strong dissociation from 11:00 LT to 17:00 LT was observed. In haze episodes, HNO3 and HCl tended to react with NH3 to form particulate matters. Interestingly, we found that formation/dissociation of NH4NO3 and NH4Cl exerted great impacts on visibility. Excluding the strong dissociation hours (11:00 LT to 17:00 LT) in correlation analysis of PM1 and visibility, correlation coefficients (R2) increased from 0.5762 to 0.7738 at RH<50%. No significant difference was observed in other RH ranges. In addition, Strong NH3 and HNO3 reaction resulted in the enhancement of NH4NO3 mass fraction, therefore increased associated water content in PM1 under high RH condition and contributed to visibility degradation.

Molecular composition and size distribution of sugars, sugar-alcohols and carboxylic acids in airborne particles during a severe urban haze event caused by wheat straw burning

Abstract Molecular compositions and size distributions of water-soluble organic compounds (WSOC, i.e., sugars, sugar-alcohols and carboxylic acids) in particles from urban air of Nanjing, China during a severe haze event caused by field burning of wheat straw were characterized and compared with those in the summer and autumn non-haze periods. During the haze event levoglucosan (4030 ng m−3) was the most abundant compound among the measured WSOC, followed by succinic acid, malic acid, glycerol, arabitol and glucose, being different from those in the non-haze samples, in which sucrose or azelaic acid showed a second highest concentration, although levoglucosan was the highest. The measured WSOC in the haze event were 2–20 times more than those in the non-hazy days. Size distribution results showed that there was no significant change in the compound peaks in coarse mode (>2.1 μm) with respect to the haze and non-haze samples, but a large difference in the fine fraction (

Genotoxicity of total and fractionated extractable organic matter in fine air particulate matter from urban Guangzhou: Comparison between haze and nonhaze episodes

To investigate the genotoxic potencies of extractable organic matter (EOM) in aerosols, fine air particulate matter (PM(2.5)) was collected simultaneously at a roadside (1.2 m above ground) and at a rooftop location (50 m above ground) in urban Guangzhou (China) during a nonhaze period in September 2006 and a haze period in October 2006. Particle-bound organics were extracted and separated into aliphatic, aromatic, and polar fractions. The genotoxicity of total and fractionated extracts were tested by single-cell electrophoresis (comet assay) with human blood lymphocytes. The PM(2.5) concentrations usually exceeded the U.S. National Ambient Air-Quality Standard level (65 microg/m(3)) at both the roadside and the rooftop. During nonhaze days, the roadside samples showed substantially higher PM(2.5) levels (108-130 microg/m(3)) and significantly higher genotoxic effects of total and fractionated EOM (p < 0.05 for >10 m(3) air equivalent/ml) than the rooftop samples. During haze days, however, PM(2.5) levels and genotoxic potencies of rooftop samples were drastically elevated and comparable to those of roadside samples, implying that during haze episodes, most people in the urban area are exposed to PM(2.5) pollution as serious as in the heavily polluted roadside microenvironment. All total EOM samples showed significant (p < 0.05) dose-response effects, and their effects as olive tail moment were less than the sums of the three fractions. Aromatic fractions of EOM exhibited the greatest genotoxic potencies, but polar fractions also contributed substantially to DNA-damaging effects. Polycyclic aromatic hydrocarbons and nitrated derivatives likely are the most important species responsible for the genotoxicity of EOM in PM(2.5).

Particulate Air Pollution from Bushfires: Human Exposure and Possible Health Effects

Toxicological studies have implicated trace metals adsorbed onto airborne particles as possible contributors to respiratory and/or cardiovascular inflammation. In particular, the water-soluble metal content is considered to be a harmful component of airborne particulate matter. In this work, the trace metal characteristics of airborne particulate matter, PM2.5, collected in Singapore from February to March 2005 were investigated with specific reference to their bioavailability. PM2.5 mass concentrations varied between 20.9 μg/m3 and 46.3 μg/m3 with an average mass of 32.8 μg/m3. During the sampling period, there were several bushfires in Singapore that contributed to sporadic increases in the particulate air pollution, accompanied by an acrid smell and asthma-related allergies. The aerosol samples were subjected to analysis of trace elements for determining their total concentrations as well as their water soluble fractions. Our results showed an increase in concentration of several water-soluble trace metals during bushfires compared to their urban background levels in Singapore. In order to measure the human exposure to particulate air pollution, the daily respiratory uptake (DRU) of several trace metals was calculated and compared between haze and nonhaze periods. The DRU values were significantly higher for several metals, including Zn, Cu, and Fe, during bushfires. Electron paramagnetic resonance (EPR) measurements showed that the particulate samples collected during bush fires generate more toxic hydroxyl radicals (OH·) than those in the background air, due to the presence of more soluble iron ions.

Occurrence of microorganic pollutants in the atmosphere of Singapore during haze and non-haze periods

Occurrence of microorganic pollutants in the atmosphere of Singapore during haze and non-haze periods

Contributions to CO concentrations from biomass burning and traffic during haze episodes in Singapore

Prediction of ambient carbon monoxide (CO) due to haze in the presence of transportation sources at a busy expressway site in Singapore was made using street Canyon and Gaussian line source modules of a regional-scale Indic Airviro dispersion model for the haze episodes that occurred in the years 1994 and 1997. The fleet average emission factors for each vehicle category were estimated from US EPA MOBILE 5 A guidelines as a function of speed, vehicle deterioration rates and model years. One hour CO concentrations during the non-haze period for the year 1995 were first simulated and compared with measured readings to test the accuracy of the proposed approach. The calibrated model was then used to compute hourly CO values for the 1994 and 1997 haze episodes. The difference between the modeled CO values with and without haze provided CO contribution due to haze. An analysis of CO values estimated through modeling with experimental measurements made during haze periods confirmed this unique approach to establish concentration of CO due to haze in the presence of transportation sources.

Air quality in Malaysia: impacts, management issues and future challenges.

Observations have been made on the long-term trends of major air pollutants in Malaysia including nitrogen dioxide, carbon monoxide, the ozone and total suspended particulate matter (particularly PM10), and sulfur dioxide, emitted from industrial and urban areas from early 1970s until late 1998. The data show that the status of atmospheric environment in Malaysia, in particular in highly industrialized areas such as Klang Valley, was determined both by local and transboundary emissions and could be described as haze and non-haze periods. During the non-haze periods, vehicular emissions accounted for more than 70% of the total emissions in the urban areas and have demonstrated two peaks in the diurnal variations of the aforementioned air pollutants, except ozone. The morning 'rush-hour' peak was mainly due to vehicle emissions, while the late evening peak was mainly attributed to meteorological conditions, particularly atmospheric stability and wind speed. Total suspended particulate matter was the main pollutant with its concentrations at few sites often exceeding the Recommended Malaysia Air Quality Guidelines. The levels of other pollutants were generally within the guidelines. Since 1980, six major haze episodes were officially reported in Malaysia: April 1983, August 1990, June 1991, October 1991, August to October 1994, and July to October 1997. The 1997 haze episode was the worst ever experienced by the country. Short-term observations using continuous monitoring systems during the haze episodes during these periods clearly showed that suspended particulate matter (PM10) was the main cause of haze and was transboundary in nature. Large forest fires in parts of Sumatra and Kalimantan during the haze period, clearly evident in satellite images, were identified as the probable key sources of the widespread heavy haze that extended across Southeast Asia from Indonesia to Singapore, Malaysia and Brunei. The results of several studies have also provided strong evidence that biomass burning is the dominating source of particulate matter. The severity and extent of 1997's haze pollution was unprecedented, affecting some 300 million people across the region. The amount of economic costs suffered by Southeast Asian countries during this environmental disaster was enormous and is yet to be fully determined. Among the important sectors severely affected were air and land transport, shipping, construction, tourism and agro-based industries. The economic cost of the haze-related damage to Malaysia presented in this study include short-term health costs, production losses, tourism-related losses and the cost of avertive action. Although the cost reported here is likely to be underestimated, they are nevertheless significant (roughly RM1 billion). The general air quality of Malaysia since 1970 has deteriorated. Studies have shown that should no effective countermeasures be introduced, the emissions of sulfur dioxide, nitrogen oxides, particulate matter, hydrocarbons and carbon monoxide in the year 2005 would increase by 1.4, 2.12, 1.47 and 2.27 times, respectively, from the 1992 levels.