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With the advent of spaceborne spectroradiometers in a geostationary constellation, measuring high spectral resolution ultraviolet–visible (UV-VIS) and selected near-/shortwave-infrared (NIR/SWIR) radiances can enable the probing of the life cycle of key atmospheric trace gases and aerosols at higher temporal resolutions over the globe. The UV-VIS measurements are important for retrieving several key trace gases (e.g., O3, SO2, NO2, and HCHO) and particularly for deriving aerosol characteristics (e.g., aerosol absorption and vertical profile). This study examines the merit of simultaneous retrievals of trace gases and aerosols using a ground-based spectroradiometer covering the UV-NIR to monitor their physicochemical processes and to obtain reliable aerosol information for various applications. During the 2019 pre-monsoon season over northern Thailand, we deployed a ground-based SMART–s (Spectral Measurements for Atmospheric Radiative Transfer–spectroradiometer) instrument, which is an extended-range Pandora with reliable radiometric calibration in the 330–820 nm range, to retrieve remotely sensed chemical and aerosol properties for the first time near biomass burning sources. The high spectral resolution (∼ 1.0 nm full width half maximum with ∼ 3.7 × oversampling) of sun and sky measurements from SMART–s provides several key trace gases (e.g., O3, NO2, and H2O) and aerosol properties covering the UV where significant light absorption occurs by the carbonaceous particles. During the measurement period, highly correlated total column amounts of NO2 and aerosol optical thickness (τaer) retrieved from SMART–s (correlation coefficient, R=0.74) indicated their common emissions from biomass burning events. The SMART–s retrievals of the spectral single scattering albedo (ω0) of smoke aerosols showed an abrupt decrease in the UV, which is an important parameter dictating photochemical processes in the atmosphere. The values of ω0 and column precipitable water vapor (H2O) gradually increase with the mixing of biomass burning smoke particles and higher water vapor concentrations when approaching the monsoon season. The retrieved ω0 and weighted mean radius of fine-mode aerosols from SMART–s showed positive correlations with the H2O (R=0.81 for ω0 at 330 nm and 0.56 for the volume-weighted mean radius), whereas the real part of the refractive index of fine-mode aerosol (nf) showed negative correlations (R=-0.61 at 330 nm), which suggest that aerosol aging processes including hygroscopic growth (e.g., humidification and cloud processing) can be a major factor affecting the temporal trends of aerosol optical properties. Retrieved nf and ω0 were closer to those of the water droplet (i.e., nf of about 1.33 and ω0 of about 1.0) under lower amounts of NO2 during the measurement period; considering that the NO2 amounts in the smoke may indicate the aging of the plume after emission due to its short lifetime, the tendency is also consistent with active hygroscopic processes of the aerosols over this area. Retrieved UV aerosol properties from SMART–s generally support the assumed smoke aerosol models (i.e., the spectral shape of aerosol absorption) used in NASA's current satellite algorithms, and their spectral ω0 retrievals from ground and satellites showed good agreements (R = 0.73–0.79). However, temporal and spectral variabilities in the aerosol absorption properties in the UV emphasize the importance of a realistic optical model of aerosols for further improvements in satellite retrievals.

In order to improve our understanding of air quality in Southeast Asia, the anthropogenic emissions inventory must be well represented. In this work, we apply different anthropogenic emission inventories in the Weather Research and Forecasting Model with Chemistry (WRF-Chem) version 3.3 using Model for Ozone and Related Chemical Tracers (MOZART) gas-phase chemistry and Global Ozone Chemistry Aerosol Radiation and Transport (GOCART) aerosols to examine the differences in predicted carbon monoxide (CO) and ozone (O3) surface mixing ratios for Southeast Asia in March and December 2008. The anthropogenic emission inventories include the Reanalysis of the TROpospheric chemical composition (RETRO), the Intercontinental Chemical Transport Experiment-Phase B (INTEX-B), the MACCity emissions (adapted from the Monitoring Atmospheric Composition and Climate and megacity Zoom for the Environment projects), the Southeast Asia Composition, Cloud, Climate Coupling Regional Study (SEAC4RS) emissions, and a combination of MACCity and SEAC4RS emissions. Biomass-burning emissions are from the Fire Inventory from the National Center for Atmospheric Research (NCAR) (FINNv1) model. WRF-Chem reasonably predicts the 2 m temperature, 10 m wind, and precipitation. In general, surface CO is underpredicted by WRF-Chem while surface O3 is overpredicted. The NO2 tropospheric column predicted by WRF-Chem has the same magnitude as observations, but tends to underpredict the NO2 column over the equatorial ocean and near Indonesia. Simulations using different anthropogenic emissions produce only a slight variability of O3 and CO mixing ratios, while biomass-burning emissions add more variability. The different anthropogenic emissions differ by up to 30% in CO emissions, but O3 and CO mixing ratios averaged over the land areas of the model domain differ by ~4.5% and ~8%, respectively, among the simulations. Biomass-burning emissions create a substantial increase for both O3 and CO by ~29% and ~16%, respectively, when comparing the March biomass-burning period to the December period with low biomass-burning emissions. The simulations show that none of the anthropogenic emission inventories are better than the others for predicting O3 surface mixing ratios. However, the simulations with different anthropogenic emission inventories do differ in their predictions of CO surface mixing ratios producing variations of ~30% for March and 10–20% for December at Thai surface monitoring sites.

There have been a very limited number of systematic studies on PM 2.5 compositions and their source contribution in Southeast Asia. This study aims to explore the characteristics of PM 2.5 composition collected in Chiang Mai (Thailand) during La Niña and El Niño years and to apportion their sources during smoke haze and non-haze periods. The average PM 2.5 concentration of smoke haze episode in 2019 (El Niño) was much higher than in 2017 (La Niña). The ratios of organic carbon (OC) to elemental carbon (EC), as well as K (biomass burning (BB) tracer) to PM 2.5 , were higher during smoke haze episodes in 2019 than in 2017 indicating a significant influence from BB. The ratios of secondary organic carbon (SOC) levels to primary organic carbon (POC) levels during smoke haze episodes were higher than those in non-haze period, which indicated greater SOC contributions or more photo-oxidation of precursors in haze episodes with high ambient temperatures. However, the ratios of soil markers (Ca and Mg) during non-haze period were high implying that soil source contributed more to PM 2.5 concentrations when there less BB occurred. The positive Matrix Factorization (PMF) model revealed that the source of BB, characterized by high K fractions, was the largest contributor during smoke haze episodes accounting for 50% (2017) and 79% (2019). Climate conditions influence meteorological patterns, particularly during incidences of extreme weather such as droughts, which affect the scale and frequency of open burning and thus air pollution levels., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022. Published by Elsevier B.V.)

Gaseous polycyclic aromatic hydrocarbons were measured in northern Thailand. No previous studies have provided data on gaseous PAHs until now, so this study determined the gaseous PAHs during two sampling periods for comparison, and then they were used to assess the correlation with meteorological conditions, other pollutants, and their sources. The total concentrations of 8-PAHs (i.e., NAP, ACY, ACE, FLU, PHE, ANT, FLA, and PYR) were 125 ± 22 ng m -3 and 111 ± 21 ng m -3 , with NAP being the most pronounced at 67 ± 18 ng m -3 and 56 ± 17 ng m -3 , for morning and afternoon, respectively. High temperatures increase the concentrations of four-ring PAHs, whereas humidity and pressure increase the concentrations of two- and three-ring PAHs. Moreover, gaseous PAHs were estimated to contain more toxic derivatives such as nitro-PAH, which ranged from 0.02 ng m -3 (8-Nitrofluoranthene) to 10.46 ng m -3 (1-Nitronaphthalene). Therefore, they could be one of the causes of local people's health problems that have not been reported previously. Strong correlations of gaseous PAHs with ozone indicated that photochemical oxidation influenced four-ring PAHs. According to the Pearson correlation, diagnostic ratios, and principal component analysis, mixed sources including coal combustion, biomass burning, and vehicle emissions were the main sources of these pollutants.

The potential reach of point-of-care (POC) diagnostics into daily routines for exposure to reactive oxygen species (ROS) and Cu in aerosolized particulate matter (PM) demands that microfluidic paper-based analytical devices (μPADs) take into consideration the simple detection of these toxic PM components. Here, we propose μPADs with a dual-detection system for simultaneous ROS and Cu(II) detection. For colorimetric ROS detection, the glutathione (GSH) assay with a folding design to delay the reaction yielded complete ROS and GSH oxidation, and improved homogeneity of color development relative to using the lateral flow pattern. For electrochemical Cu(II) determination, 1,10-phenanthroline/Nafion modified graphene screen-printed electrodes showed ability to detect Cu(II) down to pg level being low enough to be applied to PM analysis. No intra- and inter-interference affecting both systems were found. The proposed μPADs obtained LODs for 1,4-naphthoquinone (1,4-NQ), used as the ROS representative, and Cu(II) of 8.3 ng and 3.6 pg, respectively and linear working ranges of 20 to 500 ng for ROS and 1 × 10 -2 to 2 × 10 2 ng for Cu(II). Recovery of the method was between 81.4 and 108.3% for ROS and 80.5-105.3% for Cu(II). Finally, the sensors were utilized for simultaneous ROS and Cu(II) determination in PM samples and the results statistically agreed with those using the conventional methods at 95% confidence., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.)

Stable isotope ratios of nitrogen and oxygen ( 15 N/ 14 N and 18 O/ 16 O) of nitrate (NO 3 - ) are excellent tracers for developing systematic understanding of sources, conversions, and deposition of reactive atmospheric nitrogen (N r ) in the environment. Despite recent analytical advances, standardized sampling of NO 3 - ) isotopes in precipitation is still lacking. To advance atmospheric studies on N r species, we propose best-practice guidelines for accurate and precise sampling and analysis of NO 3 - isotopes in precipitation based on the experience obtained from an international research project coordinated by the International Atomic Energy Agency (IAEA). The precipitation sampling and preservation strategies yielded a good agreement between the NO 3 - concentrations measured at the laboratories of 16 countries and at the IAEA. Compared to conventional methods (e.g., bacterial denitrification), we confirmed the accurate performance of the lower cost Ti(III) reduction method for isotope analyses ( 15 N and 18 O) of NO 3 - in precipitation samples. These isotopic data depict different origins and oxidation pathways of inorganic nitrogen. This work emphasized the capability of NO 3 - isotopes to assess the origin and atmospheric oxidation of N r and outlined a pathway to improve laboratory capability and expertise at a global scale. The incorporation of other isotopes like 17 O in N r is recommended in future studies.

Fluoroquinolones (FQs) are among the antibiotics whose widespread use in farm-raised animals results in potentially harmful residues in the end products. Additionally, most Thai farmers use antibiotics. Amoxicillin and enrofloxacin were commonly used by pig farms, and hens were given enrofloxacin to prevent immunization side effects. Moreover, antibiotic overuse has harmed food safety in the long term, and the use of low-dose antibiotics causes bacterial resistance. Herein, an indirect competitive enzyme-linked immunosorbent assay (icELISA) was used to make a fast, easy, sensitive, and cost-effective method for monitoring FQs residues. After immunizing hens with mixed multi-hapten ciprofloxacin-bovine serum albumin (CPFX-BSA) with norfloxacin-bovine serum albumin (NFX-BSA), the IgY antibody purified from egg yolk was used for the detection of FQs residues in chicken and pork samples. The efficiency of the IgY antibody showed excellent sensitivity, with 50% inhibitory concentration (IC 50 ) of enrofloxacin at 0.05 µg/mL, far below the MRLs defined by the EU for muscle samples, which was not to exceed 100 µg/kg. The recovery range for chicken muscle samples spiked with ENFX concentrations of 1.00-0.01 µg/mL was 86.65-112.71%, similar to pork samples, which were 84.24-117.22.2%. This method has a lot of potential for analyzing fluoroquinolones in complex samples quickly, easily, and at a low cost on-site. The IgY-based ic ELISA was developed to detect ciprofloxacin (CPFX), norfloxacin (NFX), and enrofloxacin (ENFX) residues; it confirms that IgY could be a promising choice for the detection of antibiotic residues in food samples.

Polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs) were ubiquitous, persistent chemical compounds attached to particulate matter in the atmosphere. We aimed to study the characteristics of these pollutants in atmospheric PM 2.5 of three Asian countries, including Taiwan (Taipei), Thailand (Chiang Mai), and Vietnam (Hanoi). We carried out a source apportionment analysis to determine significant PCDD/F contributors in these areas. Multiple media model was conducted to access the health impact assessment. The PM 2.5 concentration in Taipei (n = 7), Chiang Mai (n = 20), and Hanoi (n = 10) were 18.4 ± 6.21 μg/m 3 , 133 ± 49.5 μg/m 3 , and 88.1 ± 12.6 µg/m 3 , respectively. The PCDD/Fs level in Hanoi was 92.4 ± 67.3 fg I-TEQ/m 3, and in Taipei and Chiang Mai was 5.01 ± 2.39 fg I-TEQ/m 3 and 14.4 ± 13.1 fg I-TEQ/m 3 , respectively, which showed that the higher PM 2.5 concentration was not necessary to follow with higher PCDD/Fs level. In all three cities, the effect of traffic on ambient PCDD/F level was significant (23-25 %). However, we also observed the specific sources of PCDD/Fs in each city during the sampling periods, namely long-range transport (Taipei, 55 %), Biomass/open burning (Chiang Mai, 77 %), and industrial activities (Hanoi, 34 %). In the carcinogenic risk estimation, the highest median total carcinogenic risk was in Hanoi (5.87 × 10 -6 ), followed by Chiang Mai (1.06x10 -6 ), and Taipei (2.95 × 10 -7 ). Although diet was the major absorption pathway, the food contributor of exposure differed among the three areas due to the difference in food consumption composition., (Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Radon exposure is the second leading cause of lung cancer, after smoking. In upper northern Thailand (UNT), lung cancer incidence was frequently reported by Thailand National Cancer Institute. Besides smoking, radon exposure may also influence the high lung cancer incidence in this region. Indoor radon concentrations were measured in 192 houses in eight provinces of UNT. Indoor radon concentrations ranged from 11 to 405 Bq m -3 and estimated annual effective dose ranged from 0.44 to 12.18 mSv y -1 . There were significant differences in indoor radon concentrations between the houses of lung cancer cases and healthy controls (p = 0.033). We estimated that 26% of lung cancer deaths in males and 28% in females were attributable to indoor radon exposure in this region. Other factors influencing indoor radon levels included house characteristics and ventilation. The open window-to-wall ratio was negatively associated with indoor radon levels (B = -0.69, 95% CI -1.37, -0.02) while the bedroom location in the house and building material showed no association. Indoor radon hence induced the fractal proportion of lung cancer deaths in UNT., (© 2022. The Author(s).)

Size-fractionated particulate matters (SPMs) in a range of 9.0 to 0.43 μm, classified based on aerodynamic diameter (d ae ) as fine PMs (0.43 μm ≤ d ae  < 2.1 μm) and coarse PMs (2.1 μm ≤ d ae  < 9.0 μm) were collected by cascade impactors (7 fractions) during smoke haze (SH) and non-smoke haze (NSH) seasons in urban and rural areas of Chiang Mai, Thailand. Their polycyclic aromatic hydrocarbons (PAHs) compositions were determined for respiratory health risk assessment. During SH episode, concentrations of SPMs and PAHs in the rural area were approximately two times higher than in the urban area and about 62-68% of the SPMs were fine particles. Conversely, during NSH season the concentrations in the urban area were higher due to traffic emission. The finest particle sizes (0.65-0.43 μm) contained the highest PAHs concentrations among the other PM sizes. Benzo[b]fluoranthene was a main PAH component found during SH season suggesting biomass burning is a major pollutant source. High molecular weight (5-6 rings) PAHs with high carcinogenicity were likely to concentrate in fine particles. Distribution patterns of SPMs and PAHs during SH season were bimodal with the highest peak at a fine size range (0.65-0.43 μm) and a small peak at a coarse size range (5.8-4.7 μm). Respiratory health risk was estimated based on toxicity equivalent concentrations of PAHs bound-SPMs and inhalation cancer risk (ICR). Relatively high ICR values (1.14 × 10 -4 (rural) and 6.80 × 10 -5 (urban)) were found during SH season in both areas, in which fine particles played an important role. It revealed that high concentration of fine particles in ambient air is related to high respiratory health risk due to high content of carcinogenic substances., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

This study aims to investigate ion composition of PM 2.5 in various sites and seasons and to identify the main sources on spatial and temporal basis. PM 2.5 compositions of two urban and two rural areas in Northern Thailand in 2019 were investigated to distinguish urban traffic and rural open burning sources. During the burning season, average PM 2.5 concentrations in rural areas (104 ± 45 μg m -3 ) were slightly higher than those in urban areas (94 ± 39 μg m -3 ). Source identification of PM 2.5 by cluster analysis during burning season in urban sites and one rural site revealed mixed sources of aged aerosols from biomass burning, traffic and transboundary pollution, characterized by (NH 4 ) 2 SO 4 and KNO 3 . Only PM 2.5 in one rural area (Chiang Dao), where intense open burning activities observed, contained significant KCl level in addition to other compounds. KCl is being used as a tracer for fresh aerosols from biomass burning as opposes to KNO 3 for aged aerosols. It was found that KNO 3 proportion in total ions increased with PM 2.5 concentrations both in urban and rural areas, indicating prominent open burning influences in regional scale. Source identification in other seasons was more distinguishable between urban and rural areas, and more varied depending on local emissions. Urban PM 2.5 sources were secondary inorganic aerosols from traffic gas conversion in contrast with rural PM 2.5 which were mainly from biomass burning., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Exposure to insecticides may result in various health problems. This study investigated the association between haematological parameters and exposure to a mixture of organophosphate (OP) and neonicotinoid (NEO) insecticides among male farmworkers in Fang district, Chiang Mai province, northern Thailand. Concentrations of urinary dialkylphosphates, non-specific metabolites of OPs, and NEOs and their metabolites and haematological parameters were measured in 143 male farmworkers. The Bayesian kernel machine regression model was employed to evaluate the associations. Exposure to a mixture of insecticides was significantly associated with the mean corpuscular haemoglobin concentration (MCHC) when the concentrations of all the compounds and their metabolites were at the 60th percentile or higher compared with the 50th percentile. Furthermore, exposure to clothianidin (CLO) showed a decreasing association with MCHC when all the other insecticides were at their mean concentrations. CLO was the most likely compound to reduce MCHC, and this was confirmed by sensitivity analysis. These findings suggest that exposure to NEO insecticides, especially CLO, affects the haematological status relating to haemoglobin parameters.

Several studies indicated organophosphate (OP) and neonicotinoid (NEO) insecticides are endocrine disruptors; however, data are scarce. This cross-sectional study recruited 143 male farmworkers aged 18-40 years in Fang district, Chiang Mai province, northern Thailand. OP exposure was assessed by measuring urinary dialkylphosphate (DAPs) using a gas-chromatography flame photometric detector. Urinary NEOs, their metabolites (NEO/m) and serum steroid hormones were measured using liquid chromatography-tandem mass spectrometry. Characteristics of participants were determined by face-to-face interviews. DAPs and five NEO/m were detected in more than 60% of samples. The concentration of diethylphosphate was highest among DAP metabolites (geometric mean concentration (GM: 23.9 ng/mL) and the concentration of imidacloprid (IMI) was highest among NEO/m (GM: 17.4 ng/mL). Linear regression models showed that the IMI level was positively associated with testosterone, dehydrocorticosterone (DHC) and dehydroepiandrosterone (DHEA) levels. Imidacloprid-olefin and DHEA levels were positively associated. Thiamethoxam (THX) were inversely associated with DHC and deoxycorticosterone levels. Clothianidin (CLO), THX and N-desmethyl-acetamiprid levels were positively associated with the androstenedione level. CLO and THX levels were inversely associated with the cortisone level. In conclusion, the association between NEO insecticides exposure and adrenal androgens, glucocorticoids and mineralocorticoids, suggest potential steroidogenesis activities. Our findings warrant further investigation.

Light-absorbing organic carbon (or brown carbon, BrC) has been recognized as a critical driver in regional-to-global climate change on account of its significant contribution to light absorption. BrC sources vary from primary combustion processes (burning of biomass, biofuel, and fossil fuel) to secondary formation in the atmosphere. This paper investigated the light-absorbing properties of BrC such as site-specific mass absorption cross-section (MAC BrC ), absorption Ångström exponent (AAE BrC ), and the absorbing component of the refractive index (k BrC ) by using light absorption measurements from a 7-wavelength aethalometer over an urban environment of Chiang Mai, Thailand in northern peninsular Southeast Asia (PSEA), from March to April 2016. The contribution of BrC to total aerosol absorption (mean ± SD) was 46 ± 9%, 29 ± 7%, 24 ± 6%, 20 ± 4%, and 15 ± 3% at 370, 470, 520, 590, and 660 nm, respectively, highlighting the significant influence of BrC absorption on the radiative imbalance over northern PSEA. Strong and significant associations between BrC light absorption and biomass-burning (BB) organic tracers highlighted the influence of primary BB emissions. The median MAC BrC and k BrC values at 370 nm were 2.4 m 2  g -1 and 0.12, respectively. The fractional contribution of solar radiation absorbed by BrC relative to BC (mean ± SD) in the 370-950 nm range was estimated to be 34 ± 7%, which can significantly influence the regional radiation budget and consequently atmospheric photochemistry. This study provides valuable information to understand BrC absorption over northern PSEA and can be used in model simulations to reassess the regional climatic impact with greater accuracy., Competing Interests: Declaration of competing interest The authors declare that there is no conflict of interest regarding financial funding and the publication of this paper., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Amyloid beta peptides (A β 1-42) have been found to be associated with the cause of Alzheimer's disease (AD) and dementia. Currently, methods for detecting A β 1-42 are complicated and expensive. The present study is aimed at developing an indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) to detect A β 1-42 by using a polyclonal antibody from alpaca, an application used in urine samples. The serum was collected from the alpaca after immunizing it with A β 1-42 at 500  μ g/injection 5 times. The ic-ELISA was developed and showed a half-maximal inhibitory concentration (IC 50 ) of 103.20 ng/ml. The limit of detection (LOD) was 0.39 ng/100  μ l. The cross-reactivity was tested with A β 1-40 and 8 synthesized peptides that had sequence similarities to parts of A β 1-42. The cross-reactivity of A β 1-40 and peptide 1 (DAEFRHDSGYE) was 55% and 69.4%, respectively. The ic-ELISA was applied to analyze A β 1-42 in the urine and precipitated protein urine samples. This method can be used for detecting a normal level of total soluble A β (approximately 1 ng in 5 mg of precipitated urine protein) and can be used for detecting the early stages of AD. It is considered to be an easy and inexpensive method for monitoring and diagnosing AD., Competing Interests: The authors declare no conflicts of interest., (Copyright © 2020 Anurak Wongta et al.)

Carcinogenic polycyclic aromatic hydrocarbons (cPAHs) in ambient PM 2.5 and a specific molecular marker of biomass burning, levoglucosan, are used to investigate the influence on public health of biomass burning. In this work, we present an effective method for one-time analysis of cPAHs and levoglucosan by GC-MS without derivatization. The method was applied for the analysis of PM 2.5 samples (64.3 ± 17.6 μg m -3 , n = 57) collected during a smoke haze period in Chiang Mai, Thailand. Levoglucosan was analyzed by using both the developed method (GC-MS) and a reference method (HPAEC-PAD) for comparison. Its average concentration obtained from GC-MS (0.31 ± 0.21 μg m -3 ) was about 4 times less than the concentration obtained from the reference method (1.22 ± 0.76 μg m -3 ). Therefore, a correcting factor (CF = 4) was used as a multiplying factor, to obtain a comparative value (1.23 ± 0.86 μg m -3 ). The average concentration of cPAHs found in PM 2.5 samples was 5.88 ± 1.97 ng m -3 with the highest value of 10.86 ng m -3 indicating medium to high cancer risk due to PAHs exposure when referring to values of toxicity equivalence and inhalation cancer risk. Diagnostic ratios of BaA/(BaA + CHR) (0.48 ± 0.04) and IND/(IND + BPER) (0.58 ± 0.04) and strong correlations between PM 2.5 , levoglucosan and cPAHs concentrations implied that the major source of air pollution in the study period was biomass burning. PM 2.5 concentration as a pollution indicator was labelled as BB-low, BB-medium, BB-high or BB-extreme; <50, 50-75, 75-100 and > 100 μg m -3 , respectively. The levoglucosan and cPAHs concentration during BB-extreme pollution was 4.3 times and 2.34 times, respectively, that during BB-low pollution, and the correlation coefficient (r) between the concentrations of levoglucosan and cPAHs was as high as 0.987, indicating that the more intense the burning of biomass, the higher the carcinogenic risk in the urban air., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Black carbon (BC) has been demonstrated to pose significant negative impacts on climate and human health. Equivalent BC (EBC) measurements were conducted using a 7-wavelength aethalometer, from March to May 2016, over an urban atmosphere, viz., Chiang Mai (98.957°E, 18.795°N, 373 m above sea level), Thailand in northern peninsular Southeast Asia. Daily variations in aerosol light absorption were mainly governed by open fire activities in the region. The mean mass-specific absorption cross-section (MAC) value of EBC at 880 nm was estimated to be 9.3 m 2  g -1 . The median EBC mass concentration was the highest in March (3.3 μg m -3 ) due to biomass-burning (comprised of forest fire and agricultural burning) emissions accompanied by urban air pollution within the planetary boundary layer under favorable meteorological conditions. Daily mean absorption Ångström exponent (AAE 470/950 ) varied between 1.3 and 1.7 and could be due to variations in EBC emission sources and atmospheric mixing processes. EBC source apportionment results revealed that biomass-burning contributed significantly more to total EBC concentrations (34-92%) as compared to fossil-fuel (traffic emissions). Health risk estimates of EBC in relation to different health outcomes were assessed in terms of passive cigarette equivalence, highlighting the considerable health effects associated with exposure to EBC levels. As a necessary action, the reduction of EBC emissions would promote considerable climate and health co-benefits., Competing Interests: Declaration of competing interest The authors declare that there is no conflict of interest regarding financial funding and the publication of this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

The electrocoagulation (EC) technique is an alternative method of isolating natural products with the advantage of minimizing the amounts of organic solvents required for this process, which are often harmful to the environment. In this research, the EC and the conventional solvent extraction methods were used in the isolation of Stemona alkaloids from the aerial parts of Stemona aphylla. A comparison was made between the amounts of the isolated alkaloids and the solvents used. The isolated alkaloids were evaluated for their larvicidal, ovicidal and oviposition-deterrent activities against the dengue vector, Aedes aegypti. The morphology and histopatology of the alkaloid treated larvae were also investigated. Two Stemona alkaloids, (2'S)-hydroxystemofoline and stemofoline, were isolated from both the EC and the conventional method. The amounts of (2'S)-hydroxystemofoline from the EC method was about the same as that obtained from the conventional method. However, the amounts of stemofoline obtained from the EC method were about two times larger than those obtained from the conventional method. Importantly, the EC method required six times less total organic solvents. The larvicidal activity assays of (2'S)-hydroxystemofoline and stemofoline showed that these were highly effective against Aedes aegypti larvae with LC 50 values of 3.91 μg/ml and 4.35 μg/ml, respectively. Whereas, the crude EC extract (LC 50  = 11.86 μg/ml) showed greater larvicidal activity than the crude extract obtained from the conventional extraction method (LC 50  = 53.40 μg/ml). The morphological observations of the (2'S)-hydroxystemofoline and the stemofoline treated larvae revealed that the anal gills were the sites of aberrations. A histopathological study showed that larvae treated with these alkaloids had cytopathological alterations to the epithelial cells of the midgut. At a concentration 40 μg/ml (2'S)-hydroxystemofoline showed 100% ovicidal activity on 24 h old eggs while stemofoline showed 97.2%. Furthermore, the oviposition-deterrent effects of (2'S)-hydroxystemofoline and stemofoline, at a concentration of 80 μg/ml were 99.5% and 97.2%, respectively., (Copyright © 2019 Elsevier Inc. All rights reserved.)

An open-system combustion chamber was designed and constructed for simulation of burning of various biomass types to estimate emission factors of pollutant gases, fine particulate matters and their composition to find out significant tracers. Rice straw (RS), maize residues (MR) and forest leaf litters (FLL) from mixed deciduous forest (MDF) and dry dipterocarp forest (DDF) were collected from various places in Northern Thailand based on land-use types. Approximately 1 kg of air-dried biomass sample was burned in the chamber, PM 2.5 were collected. CO 2 dominated during the flaming state while CO is predominant in the smoldering state. The highest EF PM2.5 was obtained from MDF burning (4.38 ± 2.99 g kg -1 ), while the lowest value was from MR burning (2.15 ± 0.95 g kg -1 ). Among water soluble ions, K + (biomass burning (BB) tracer) was the most abundant species in PM 2.5 followed by Cl - and SO 4 2- . The average EF K + from the burning of agricultural biomass was significantly higher than the burning of FLL. Scatter plot of K + /SO 4 2- versus K + /Cl - can be used to distinguish between agricultural crop residues and FLL burning. Levoglucosan (BB tracer) was a dominant species among anhydrosugars and also a major component found in FLL burning. The ratios of levoglucosan/K + and levoglucosan/mannosan obtained from forest and agricultural waste burnings were significantly different, therefore they can be used for BB source identification., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

In recent years, biochar has received a significant amount of attention for its potential beneficial applications in various fields due to its bio-physico-chemical properties. The spent coffee ground biochar was prepared by slow pyrolysis for adsorption of 16-polycyclic aromatic hydrocarbons (PAHs) in ambient air. New materials and extraction methods were developed for PAHs analysis, particularly for low molecular weight (2-4 rings) PAHs, which are likely to evaporate at room temperature. Production and characterization of biochar and its extraction parameters after PAHs adsorption were investigated and optimized. The biochar production at 500 °C provided adequate quality for PAHs adsorption with a 35% yield. An effective clean-up method for biochar was proposed. A new method of PAHs extraction from biochar was developed using 25 mL of a mixture of dichloromethane and 2-propanol (4:1) for 30 min at low temperatures (5-10 °C). A test on the efficiency of the extraction method was carried out and recoveries of 85-104% of PAHs were obtained. The lab-made biochar was also tested for its potential in ambient PAHs sampling and compared with a commercial sorbent (XAD-2). The results revealed that almost the same concentrations of ambient PAHs (ng/m 3 ) were absorbed by both sorbent types, particularly with regard to the 4 ring-PAHs.

Severe air pollution in the form of smoke haze in the northern part of Southeast Asia (SEA) occurs annually in the dry season due to huge open area burning. Molecular markers of biomass burning were investigated by characterization of fine particles (PM 2.5 ) collected in the dry season (23 February-28 April 2016). The average PM 2.5 , organic carbon (OC) and elemental carbon (EC) concentrations were 64.3 ± 17.6 μg m -3 , 23.6 ± 8.1 μg m -3 and 2.85 ± 0.98 μg m -3 , respectively. SO 4 2- was the dominant species (8.73 ± 2.88 μg m -3 ) of water-soluble ion, followed by NH 4 + (3.32 ± 1.01 μg m -3 ) and NO 3 - (2.70 ± 0.51 μg m -3 ). High concentrations of the biomass burning tracers K + (1.27 ± 0.38 μg m -3 ) and levoglucosan (1.22 ± 0.75 μg m -3 ) were observed. The ratios of levoglucosan/K + (0.92 ± 0.35) and levoglucosan/mannosan (20.4 ± 4.1) identified forest and agricultural waste burning as major contributors to the aerosol. Strong correlations (r > 0.800) between levoglucosan and OC, K + , anhydrosugar isomer (mannosan and galactosan) and other saccharides (mannose, arabitol and mannitol) verified that combustion of biomass was the major source of organic compounds associated with PM 2.5 aerosols. Oxalate was the most abundant (0.75 ± 0.17 μg m -3 ; 53%) of the carboxylates. The concentration of oxalate was strongly correlated to that of PM 2.5 (r = 0.799) and levoglucosan (r = 0.615), indicating that oxalate originates mainly from primary emissions from biomass burning rather than secondary formation from photochemical processes. Backward trajectories indicated that long-range transport air masses influencing air quality in Northern Thailand originated to the west and southwest., (Copyright © 2018. Published by Elsevier B.V.)

A large concentration of finer particulate matter (PM 2.5 ), the primary air-quality concern in northern peninsular Southeast Asia (PSEA), is believed to be closely related to large amounts of biomass burning (BB) particularly in the dry season. In order to quantitatively estimate the contributions of BB to aerosol radiative effects, we thoroughly investigated the physical, chemical, and optical properties of BB aerosols through the integration of ground-based measurements, satellite retrievals, and modelling tools during the Seven South East Asian Studies/Biomass-burning Aerosols & Stratocumulus Environment: Lifecycles & Interactions Experiment (7-SEAS/BASELInE) campaign in 2014. Clusters were made on the basis of measured BB tracers (Levoglucosan, nss-K + , and NO 3 ) to classify the degree of influence from BB over an urban atmosphere, viz., Chiang Mai (18.795°N, 98.957°E, 354m.s.l.), Thailand in northern PSEA. Cluster-wise contributions of BB to PM - ) to classify the degree of influence from BB over an urban atmosphere, viz., Chiang Mai (18.795°N, 98.957°E, 354m.s.l.), Thailand in northern PSEA. Cluster-wise contributions of BB to PM 2.5 , organic carbon, and elemental carbon were found to be 54-79%, 42-79%, and 39-77%, respectively. Moreover, the cluster-wise aerosol optical index (aerosol optical depth at 500nm≈0.98-2.45), absorption (single scattering albedo ≈0.87-0.85; absorption aerosol optical depth ≈0.15-0.38 at 440nm; absorption Ångström exponent ≈1.43-1.57), and radiative impacts (atmospheric heating rate ≈1.4-3.6Kd -1 ) displayed consistency with the degree of BB. PM 2.5 during Extreme BB (EBB) was ≈4 times higher than during Low BB (LBB), whereas this factor was ≈2.5 for the magnitude of radiative effects. Severe haze (visibility≈4km) due to substantial BB loadings (BB to PM 2.5 ≈79%) with favorable meteorology can significantly impact the local-to-regional air quality and the, daily life of local inhabitants as well as become a respiratory health threat. Additionally, such enhancements in atmospheric heating could potentially influence the regional hydrological cycle and crop productivity over Chiang Mai in northern PSEA., (Copyright © 2018 Elsevier B.V. All rights reserved.)

Organophosphate (OP) pesticides are widely used for crop protection in many countries including Thailand. Aside from causing environmental contamination, they affect human health especially by over-stimulating of the neurotransmission system. OP pesticides, as with other non-persistent pesticides, degrade quickly in the environment as well as are metabolized quite rapidly in humans. Assessing human exposures to these compounds requires analytical methods that are sensitive, robust, and most importantly, suitable for specific laboratory settings. The aim of this study was to develop and validate an analytical method for measuring 11 OP pesticide residues in human plasma and breast milk. Analytes in both plasma and breast milk samples were extracted with acetone and methylene chloride, cleaned-up using aminopropyl solid phase extraction cartridges, and analyzed by gas chromatography with flame photometric detection. The optimized method exhibited good linearity, with the coefficients of determination of 0.996-0.999 and <7% error about the slope. Extraction recoveries from spiked plasma and breast milk samples at low and medium concentrations (0.8-5.0 and 1.6-10ngmL(-1), respectively) ranged from 59.4% (ethion) to 94.0% (chlorpyrifos). Intra-batch and inter-batch precisions ranged from 2.3-18.9% and 5.8-19.5%, respectively. Method detection limits of plasma and breast milk ranged from 0.18-1.36 and 0.09-2.66ngmL(-1), respectively. We analyzed 63 plasma and 30 breastmilk samples collected from farmworkers in Chiang Mai Province to determine the suitability of this method for occupational exposure assessment. Of the 11 pesticides measured, seven were detected in plasma samples and five were detected in breast milk samples. Mass spectrometry was used to confirm results. Overall, this method is rapid and reliable. It offers the laboratories with limited access to mass spectrometry a capacity to investigate levels OP pesticides in plasma and breastmilk in those occupationally exposed for health risk assessment., (Copyright © 2016 Elsevier B.V. All rights reserved.)

Prenatal organophosphate (OP) pesticide exposure has been reported to be associated with adverse birth outcomes and neurodevelopment. However, the mechanisms of toxicity of OP pesticides on human fetal development have not yet been elucidated. Our pilot study birth cohort, the Study of Asian Women and Offspring's Development and Environmental Exposures (SAWASDEE cohort) aimed to evaluate environmental chemical exposures and their relation to birth outcomes and infant neurodevelopment in 52 pregnant farmworkers in Fang district, Chiang Mai province, Thailand. A large array of data was collected multiple times during pregnancy including approximately monthly urine samples for evaluation of pesticide exposure, three blood samples for pesticide-related enzyme measurements and questionnaire data. This study investigated the changes in maternal acetylcholinesterase (AChE) and paraoxonase 1 (PON1) activities and their relation to urinary diakylphosphates (DAPs), class-related metabolites of OP pesticides, during pregnancy. Maternal AChE, butyrylcholinesterase (BChE) and PON1 activities were measured three times during pregnancy and urinary DAP concentrations were measured, on average, 8 times from enrollment during pregnancy until delivery. Among the individuals in the group with low maternal PON1 activity (n=23), newborn head circumference was negatively correlated with log10 maternal ∑DEAP and ∑DAP at enrollment (gestational age=12±3 weeks; β=-1.0 cm, p=0.03 and β=-1.8 cm, p<0.01, respectively) and at 32 weeks pregnancy (β=-1.1cm, p=0.04 and β=-2.6 cm, p=0.01, respectively). Furthermore, among these mothers, newborn birthweight was also negatively associated with log10 maternal ∑DEAP and ∑DAP at enrollment (β=-219.7 g, p=0.05 and β=-371.3g, p=0.02, respectively). Associations between maternal DAP levels and newborn outcomes were not observed in the group of participants with high maternal PON1 activity. Our results support previous findings from US birth cohort studies. This is the first study to report the associations between prenatal OP pesticide exposure and birth outcomes in Thailand., (Copyright © 2015 Elsevier Inc. All rights reserved.)

The interactions between aerosols, clouds, and precipitation remain among the largest sources of uncertainty in the Earth's energy budget. Biomass-burning aerosols are a key feature of the global aerosol system, with significant annually-repeating fires in several parts of the world, including Southeast Asia (SEA). SEA in particular provides a "natural laboratory" for these studies, as smoke travels from source regions downwind in which it is coupled to persistent stratocumulus decks. However, SEA has been under-exploited for these studies. This review summarizes previous related field campaigns in SEA, with a focus on the ongoing Seven South East Asian Studies (7-SEAS) and results from the most recent BASELInE deployment. Progress from remote sensing and modeling studies, along with the challenges faced for these studies, are also discussed. We suggest that improvements to our knowledge of these aerosol/cloud effects require the synergistic use of field measurements with remote sensing and modeling tools., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

In this study, the enzyme-linked immunosorbent assays (ELISA) were modified to detect 3-PBA in plasma (including the adducted form) and urine among a large group of consumers and farmers in an agricultural area. The samples were collected on the same day in the morning from 100 consumers (50 females, 50 males) and 100 farmers (50 females, 50 males) in the Fang district, Chiang Mai province, northern Thailand. The ELISA was very sensitive having an IC50 value of 26.7 and 15.3 ng/mL, a limit of quantitation of 5 and 2.5 ng/mL and a limit of detection of 1.08 and 1.94 ng/mL for plasma and urine, respectively. These methods had low (< 5%) intra- and inter-assay coefficients of variation. The extraction technique satisfactorily eliminated the matrix effect from samples before ELISA analysis, yielding good recoveries (85.9-99.4% and 87.3-98.0%, respectively). For the volunteer study, the detection rate for plasma 3-PBA was 24% in consumers and 42% in farmers, but the median and range values were similar (median 5.87 ng/mL, range 5.16-8.44 ng/mL in consumers and 6.27 ng/mL, range 4.29-9.57 ng/mL in farmers). The rate of detection in the urine was similar (76% and 69%, in consumers and in farmers), yet the median concentration was significantly higher in farmers (8.86 μg/g creatinine in consumers vs 16.1 μg/g creatinine in farmers) and the range also much wider in farmers (1.62-80.5 μg/g creatinine in consumers and 0.80-256.2 μg/g creatinine in farmers). There was no correlation between plasma 3-PBA and urinary 3-PBA concentrations in the study presumably because plasma 3-PBA is a measure of cumulative exposures while urinary 3-PBA reflects acute exposures. In addition, metabolism and excretion of pyrethroids varies by individual. Nevertheless, this study demonstrated that these volunteers were exposed to pyrethroids. To our knowledge, this is the first report that compared plasma 3-PBA and urinary 3-PBA in a large group of volunteers. The ELISA method provided higher sample throughput with lower cost as compared to the instrumental analysis.

Biomass samples including agricultural waste (rice straw and maize residue) and forest leaf litter were collected from Chiang Mai Province, Thailand for the burning experiment in the self-designed stainless steel chamber to simulate the emissions of PM10. The burning of leaf litter emitted the highest PM10 (1.52±0.65 g kg(-1)). The PM10-bound ions emitted from the burning of rice straw and maize residue showed the same trend, which was K(+)>Cl(-)>SO4(2-)>NH4(+)>NO3(-). However, the emissions from maize residue burning were ~1.5-2.0 times higher than those from the rice straw burning. The ion content emitted from leaf litter burning was almost the same for all ion species. Noticeably, K(+) and Cl(-) concentrations were ~2-4 times lower than those emitted from agricultural waste burning. It can be deduced that K(+) and Cl(-) were highly emitted from agricultural waste burning due to the use of fertilizer and herbicides in the field, respectively. Based on emission values obtained from the chamber, the pollutant emission rate from open burning was calculated. Burned areas in Chiang Mai Province were 3510 and 866 km(2) in 2010 and 2011, respectively. Forest burning was 71-88%, while agricultural land burning accounted for 12-29% (rice field: crop field=1:3) of total burned area. Therefore, emissions of PM10 from open burning in Chiang Mai were 3051 ton (2010) and 705 ton (2011). Major ions emitted from agricultural waste burning were found to be K(+) and Cl(-), while those from forest burning were SO4(2-) and K(+)., (Copyright © 2013 Elsevier Ltd. All rights reserved.)

Petroleum sludge is a hazardous waste that contains various organic compounds including polycyclic aromatic hydrocarbons (PAHs) which have carcinogenic-mutagenic and toxic characteristics. This study focuses on the thermal treatment (indirect heating) of petroleum sludge cake for PAH degradation at 250, 450, and 650 degrees C using Ca(OH)2 + NaHCO3 as an additive. The treatment was conducted in a rotary drum electric heater. All experiments were carried out in triplicate. Concentrations of the 16 priority PAHs in gas (absorbed on Amberlite XAD-4 adsorbent), particulate (on quartz filter) and residue phases were determined using gas chromatography-mass spectrometry (GC-MS). The samples were extracted with acetonitrile by ultra-sonication prior to GC-MS analysis. The use of additive was beneficial and a temperature of 450 degrees C was suitable for PAH degradation. Low levels of PAH emissions, particularly carcinogenic PAH and toxic equivalent concentration (sigma TEC), were observed in gas, particulate and residue phases after treatment.

The aim of this study was to identify a plasma biomarker of exposure to pyrethroid insecticides. A major metabolite, 3-phenoxybenzoic acid (3-PBA), can be detected in urine but urinary 3-PBA cannot be used to assess the active dose. The 3-PBA-adduct represents a much more persistent class of biomarkers than metabolites excreted into urine, having half lives up to several weeks or months. We developed an enzyme-linked immunosorbent assay (ELISA) for total 3-PBA including adduct formed after alkaline hydrolysis, liquid-liquid extraction (LLE) and solid phase extraction (SPE) of the sample. The developed ELISA had an IC 50 value of 26.7 ng/mL. The intra- and inter-assay coefficients of variation (%CV) were lower than 5% and were within the optimum condition variance (OCV) range. The LLE cleanup technique satisfactorily eliminated the matrix effect from plasma samples before SPE and ELISA analysis yielding good recoveries (85.9-99.4%) with a limit of quantitation (LOQ, 5 ng/mL) that was 30- to 47-fold more sensitive than previous studies. Moreover, the developed method could separate more than 80% of 3-PBA from adduct form. The method was successfully applied to the detection of the target in real samples obtained from consumers (n=50) and farmers (n=50). To our knowledge, this is the first ELISA method for detecting 3-PBA in human plasma and applied to a field study.

1,1-Dichloro-2,2-bis(p-chlorophenyl) ethylene (p,p'-DDE) is the major metabolite of insecticide 2,2-bis(p-chlorophenyl)-1,1,1-trichloroethane (p,p'-DDT) and a persistent organic pollutant (POPs) with concerns regarding its bioaccumulation and persistence in the environment and food chain. In the present study, an indirect competitive enzyme-linked immunosorbant assay (ic-ELISA) specific for the detection of p,p'-DDE is described. In hapten synthesis, 2,2'-bis(4-chlorophenyl)ethanol and glutaric anhydride were used as precursor and spacer arm, respectively. The hapten was then conjugated to bovine serum albumin (BSA) as immunogen for mouse immunization and also conjugated to ovalbumin as coating antigen for ELISA. The developed ic-ELISA was used for detecting p,p'-DDE in human milk samples and validated against the results from conventional gas chromatography-electron capture detection (GC-ECD). Coefficients of variation (%CV) of ELISA were 5.7-10.4% for intra-assay and 10.6-19.6% for interassay variations. The Pearson correlation coefficient of p,p'-DDE concentrations between ic-ELISA and GC-ECD was r = 0.766, which was in an acceptable range. The results indicate that the developed assay could be an alternative analytical tool for monitoring p,p'-DDE in lipimic matrices such as human milk.

Human exposure to methyl parathion can be assessed by measuring the concentration of its metabolite paranitrophenol (PNP) in urine. Our biologic monitoring study in Chiang Mai, Thailand, measured PNP and dialkylphosphate metabolites (i.e., dimethylphosphate [DMP] and dimethylthiophosphate [DMTP]) of methyl parathion in urine samples collected from 136 farmers (age 20 to 65 years) and 306 school children (age 10 to 15 years) in 2006. Participants came from two topographically different areas: one was colder and mountainous, whereas the other was alluvial with climate fluctuations depending on the monsoon season. Both children and farmers were recruited from each area. Despite methyl parathion's prohibited use in agriculture in 2004, we detected PNP in >90% of all samples analyzed. We applied a nonparametric correlation test (PNP vs. DMP and DMTP) to determine whether the PNP found in most of the samples tested resulted from exposures to methyl parathion. DMP (Spearman's rho = 0.601 [p = 0.001] for farmers and Spearman's rho = 0.263 [p <0.001] for children) and DMTP (Spearman's rho = 0.296 [p = 0.003] for farmers and Spearman's rho = 0.304 [p<0.001] for children) were positively correlated with PNP, suggesting a common source for the three analytes, presumably methyl parathion or related environmental degradates. Although we found a modest correlation between the metabolites, our findings suggest that despite the prohibition, at least a portion (approximately 25% to 60%) of the PNP detected among farmers and children in Thailand may be attributed to exposure from continued methyl parathion use.

Daily PM10 concentrations were measured at four sampling stations located in Chiang Mai and Lamphun provinces, Thailand. The sampling scheme was conducted during June 2005 to June 2006; every 3 days for 24 h in each sampling period. The result revealed that all stations shared the same pattern, in which the PM10 (particulate matters with diameter of less than 10 microm) concentration increased at the beginning of dry season (December) and reached its peak in March before decreasing by the end of April. The maximum PM10 concentration for each sampling station was in the range of 140-182 microg/m(3) which was 1.1-1.5 times higher than the Thai ambient air quality standard of 120 microg/m(3). This distinctly high concentration of PM10 in the dry season (Dec. 05-Mar. 06) was recognized as a unique seasonal pattern for the northern part of Thailand. PM10 concentration had a medium level of negative correlation (r = -0.696 to -0.635) with the visibility data. Comparing the maximum PM10 concentration detected at each sampling station to the permitted PM10 level of the national air quality standard, the warning visibility values for the PM10 pollution-watch system were determined as 10 km for Chiang Mai Province and 5 km for Lamphun Province. From the analysis of PM10 constituents, no component exceeded the national air quality standard. The total concentrations of PM10-bond polycyclic aromatic hydrocarbons (PAHs) are calculated in terms of total toxicity equivalent concentrations (TTECs) using the toxicity equivalent factors (TEFs) method. TTECs in Chiang Mai and Lamphun ambient air was found at a level comparable to those observed in Nagasaki, Bangkok and Rome and at a lower level than those reported at Copenhagen. The annual number of lung cancer cases for Chiang Mai and Lamphun Provinces was estimated at two cases/year which was lower than the number of cases in Bangkok (27 cases/year). The principal component analysis/absolute principal component scores (PCA/APCS) model and multiple regression analysis were applied to the PM10 and its constituents data. The results pointed to the vegetative burning as the largest PM10 contributor in Chiang Mai and Lamphun ambient air. Vegetative burning, natural gas burning & coke ovens, and secondary particle accounted for 46-82%, 12-49%, and 3-19% of the PM10 concentrations, respectively. However, natural gas burning & coke ovens as well as vehicle exhaust also deserved careful attention due to their large contributions to PAHs concentration. In the wet season and transition periods, 42-60% of the total PAHs concentrations originated from vehicle exhaust while 16-37% and 14-38% of them were apportioned to natural gas burning & coke ovens and vegetative burning, respectively. In the dry period, natural gas burning & coke ovens, vehicle exhaust, and vegetative burning accounted for 47-59%, 20-25%, and 19-28% of total PAHs concentrations. The close agreement between the measured and predicted concentrations data (R(2) > 0.8) assured enough capability of PCA/APCS receptor model to be used for the PM10 and PAHs source apportionment.

We evaluated exposure to pesticides among secondary school students aged 12-13 years old in Chiang Mai Province, Thailand. Pesticide-specific urinary metabolites were used as biomarkers of exposure for a variety of pesticides, including organophosphorus insecticides, synthetic pyrethroid insecticides and selected herbicides. We employed a simple solid-phase extraction with analysis using isotope dilution high-performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS). A total of 207 urine samples from Thai students were analyzed for 18 specific pesticide metabolites. We found 14 metabolites in the urine samples tested; seven of them were detected with a frequency > or=17%. The most frequently detected metabolites were 2-[(dimethoxyphosphorothioyl) sulfanyl] succinic acid (malathion dicarboxylic acid), para-nitrophenol (PNP), 3,5,6-trichloro-2-pyridinol (TPCY; metabolite of chlorpyrifos), 2,4-dichlorophenoxyacetic acid (2,4-D), cis- and trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylic acids (c-DCCA and t-DCCA; metabolite of permethrin) and 3-phenoxybenzoic acid (3-PBA; metabolite of pyrethroids). The students were classified into 4 groups according to their parental occupations: farmers (N=60), merchants and traders (N=39), government and company employees (N=52), and laborers (N=56). Children of farmers had significantly higher urinary concentrations of pyrethroid insecticide metabolites than did other children (p<0.05). Similarly, children of agricultural families had significantly higher pyrethroid metabolite concentrations. Males had significantly higher values of PNP (Mann-Whitney test, p=0.009); however, no other sex-related differences were observed. Because parental occupation and agricultural activities seemed to have little influence on pesticide levels, dietary sources were the likely contributors to the metabolite levels observed.

Our research goal was to assess exposure to currently used pesticides among small-scale male farmers residing in two topographically different areas in Chiang Mai Province, Thailand. Farmers (N=136) were recruited from Pong Yaeng subdistrict (N=67) and Inthakhin subdistrict (N=69). Each farmer provided a morning urine void for the analysis of 30 urinary metabolites of insecticides, herbicides, and fungicides. Farmers in Pong Yaeng had significantly higher urinary concentrations of metabolites of organophosphorus insecticides and ethylene bisdithiocarbamates, while farmers from Inthakhin had significantly higher concentrations of malathion, 2,4-D, alachlor, and parathion or EPN metabolites. Based upon the metabolites measured in the urine of the farmers, chlorpyrifos and pyrethroid insecticides seemed to be commonly used across both communities; no significant differences in metabolite concentrations of these insecticides were observed between the two farmer groups. The presence of methamidaphos in the urine of farmers suggests that, despite a ban on its use, methamidaphos continues to be used in the communities. A similar finding with metabolites of methyl parathion must be further investigated. Overall, our results suggest that while each community may use different pesticides, Thai farmers are exposed to a wide variety of pesticides with a broad range in exposure magnitude. Furthermore, age, field size, crop production type, and the use of protective equipment were found to be potential factors influencing the degree of exposure.