Observational insights into the compound environmental effect for 2-methyltetrols formation under humid ambient conditions.

Laboratory experiments suggest acid-catalyzed aqueous-phase production can promote the formation of isoprene SOA, i.e., 2-methyltetrols. In this study we use ambient observations of the 2-methyltetrols along with other chemical measurements, as well as meteorological factors to investigate the relative importance of environmental influence for isoprene epoxydiols (IEPOX) SOA formation under atmospheric humidity conditions. The 2-Methyltetrols revealed good relationships with temperature and total solar radiation, but were weakly correlated with aerosol acidity and SO42-. EC-scaled 2-methyltetrols were observed to vary in a narrow pH range (1.5-2.0), indicating aerosol acidity was not a limiting factor for 2-methyltetrols formation. High values of 2-methyltetrols were consistently observed at high total solar radiation, the strong dependence of total solar radiation demonstrated that photochemical processes dominated 2-methyltetrols formation in humid environments. Although 2-methyltetrols can be enhanced by acid-catalyzed aqueous-phase reactions, it is not sufficient to compensate the synchronously weakened photochemical activity influence, leading to an obvious net decrease in the formation of 2-methyltetrols in the ambient. Moreover, aerosol droplet acidity was reduced under high liquid water content (LWC) condition, subsequently diminishing the enhancement of SOA formation by acidity. Overall, our results highlight that the environmental impact factors are highly variable and interplay, influencing the production of 2-methyltetrols, and suggest that the formation pathway of 2-methyltetrols is insensitive to aerosol acidity but dominated by photochemical production process in humid environments.

Chemical speciation, including polycyclic aromatic hydrocarbons (PAHs), and toxicity of particles emitted from meat cooking operations.

We assessed the chemical properties and oxidative stress of particulate matter (PM) emissions from underfired charbroiled meat operations with and without the use of aftertreatment control technologies. Cooking emissions concentrations showed a strong dependence on the control technology utilized, with all emission rates showing decreases with the control technologies compared to the baseline testing. The organic acids profile was dominated by the saturated nonanoic, myristic, palmitic, and stearic acids, and the unsaturated oleic, elaidic, and palmitoleic acids. Cholesterol was also found in relatively high concentrations. Lower and medium-weight polycyclic aromatic hydrocarbons (PAHs) were the dominant species for all cooking experiments. Heavier PAHs were also detected in high concentrations, especially in the particle-phase. For the nitrated PAH emissions (nitro-PAHs), low molecular weight compounds dominated the cooking emissions. Under the present experimental conditions, the heterocyclic aromatic amines (HAAs) showed very low concentrations, which suggests these species are rarely formed in meat cooking PM. The most efficient control technology for reducing the majority of the toxic pollutants was the electrostatic precipitator, which resulted in total emissions reductions on the order of 95%, 79%, 90%, 96%, 90%, and 94%, respectively, for particle-phase PAHs, gas-phase PAHs, particle-phase nitro-PAHs, gas-phase nitro-PAHs, particle-phase HAAs, and gas-phase HAAs compared to the baseline testing. Our experiment showed that cooking aerosol contained higher levels of prooxidants in the particle-phase and the corresponding vapors contained higher levels of electrophiles. Overall, the use of control technologies reduced the redox and electrophilic activities of cooking PM.

Biomarkers as indicators of fungal biomass in the atmosphere of São Paulo, Brazil.

The biogenic aerosol contribution to atmospheric particulate matter (PM) mass concentration is usually neglected due to the difficulty in identifying its components, although it can be significant. In the Metropolitan Area of São Paulo (MASP)-Brazil, several studies have been performed to identify sources for PM, revealing vehicular emissions and soil re-suspension as the main identified sources. The organic fraction has been related primarily to biomass burning (BB) and fuel combustion, although there is significant presence of green areas in the city which render biogenic emissions as an additional source of organic carbon (OC). The objectives of this work are to (i) characterise the composition of the PM10 (ii) estimate the relative mass contribution of fungal spores to PM concentrations with sizes smaller than 10µm (PM10) in MASP and (iii) assess the main sources of PM10. To achieve these objectives, we measured markers of biogenic sources and BB, during the fall-winter transition, which along with other constituents, such as ions, organic/elemental carbon, elemental composition and fungal spore concentrations, help assess the PM10 sources. We used receptor models to identify distinct source-related PM10 fractions and conversion factors to convert biomarker concentrations to fungal mass. Our results show the mean contributions of fungal aerosol to PM10 and OC mass were 2% and 8%, respectively, indicating the importance of fungal spores to the aerosol burden in the urban atmosphere. Using specific rotation factor analysis, we identified the following factors contributing to PM: soil re-suspension, biogenic aerosol, secondary inorganic aerosol, vehicular emissions and BB/isoprene-related secondary organic aerosol (I-SOA). BB/I-SOA was the main source representing 28% of the PM10 mass, while biogenic aerosol explained a significant (11%) fraction of the PM10 mass as well. Our findings suggest that primary biogenic aerosol is an important fraction of PM10 mass, yet not considered in most studies.

Chemical characterization and sources of personal exposure to fine particulate matter (PM2.5) in the megacity of Guangzhou, China.

Concurrent ambient and personal measurements of fine particulate matter (PM2.5) were conducted in eight districts of Guangzhou during the winter of 2011. Personal-to-ambient (P-C) relationships of PM2.5 chemical components were determined and sources of personal PM2.5 exposures were evaluated using principal component analysis and a mixed-effects model. Water-soluble inorganic ions (e.g., SO42-, NO3-, NH4+, C2O42-) and anhydrosugars (e.g., levoglucosan, mannosan) exhibited median personal-to-ambient (P/C) ratios < 1 accompanied by strong P-C correlations, indicating that these constituents in personal PM2.5 were significantly affected by ambient sources. Conversely, elemental carbon (EC) and calcium (Ca2+) showed median P/C ratios greater than unity, illustrating significant impact of local traffic, indoor sources, and/or personal activities on individual's exposure. SO42- displayed very low coefficient of divergence (COD) values coupled with strong P-C correlations, implying a uniform distribution of SO42- in the urban area of Guangzhou. EC, Ca2+, and levoglucosan were otherwise heterogeneously distributed across individuals in different districts. Regional air pollution (50.4 ± 0.9%), traffic-related particles (8.6 ± 0.7%), dust-related particles (5.8 ± 0.7%), and biomass burning emissions (2.0 ± 0.2%) were moderate to high positive sources of personal PM2.5 exposure in Guangzhou. The observed positive and significant contribution of Ca2+ to personal PM2.5 exposure, highlighting indoor sources and/or personal activities, were driving factors determining personal exposure to dust-related particles. Considerable discrepancies (COD values ranging from 0.42 to 0.50) were shown between ambient concentrations and personal exposures, indicating caution should be taken when using ambient concentrations as proxies for personal exposures in epidemiological studies.

Brown and black carbon in Beijing aerosol: Implications for the effects of brown coating on light absorption by black carbon.

Brown carbon (BrC) is increasingly included in climate models as an emerging category of particulate organic compounds that can absorb solar radiation efficiently at specific wavelengths. Water-soluble organic carbon (WSOC) has been commonly used as a surrogate for BrC; however, it only represents a limited fraction of total organic carbon (OC) mass, which could be as low as about 20% in urban atmosphere. Using methanol as the extraction solvent, up to approximately 90% of the OC in Beijing aerosol was isolated and measured for absorption spectra over the ultraviolet-to-visible wavelength range. Compared to methanol-soluble OC (MSOC), WSOC underestimated BrC absorption by about 50% at 365nm. The mass absorption efficiencies measured for BrC in Beijing aerosol were converted to the imaginary refractive indices of BrC and subsequently used to compute BrC coating-induced enhancement of light absorption (Eabs) by black carbon. Eabs attributed to lensing was reduced in the case of BrC coating relative to that caused by purely-scattering coating. However, this reduction was overwhelmed by the effect of BrC shell absorption, indicating that the overall effect of BrC coating was an increase in Eabs. Methanol extraction significantly reduced charring of OC during thermal-optical analysis, leading to a large increase in the measured elemental carbon (EC) mass and an apparent improvement in the consistency of EC measurements by different thermal-optical methods.

Characterization of ambient-generated exposure to fine particles using sulfate as a tracer in the Chinese megacity of Guangzhou.

Total personal exposures can differ from the concentrations measured at stationary ambient monitoring sites. To provide further insight into factors affecting exposure to particles, chemical tracers were used to separate total personal exposure into its ambient and non-ambient components. Simultaneous measurements of ambient and personal exposure to fine particles (PM2.5) were conducted in eight districts of Guangzhou, a megacity in South China, during the winter of 2011. Considerable significant correlations (Spearman's Rho, rs) between personal exposures and ambient concentrations of sulfate (SO42-; rs>0.68) were found in contrast to elemental carbon (EC; rs>0.37). The average fraction of personal SO42- to ambient SO42- resulting in an adjusted ambient exposure factor of α=0.72 and a slope of 0.73 was determined from linear regression analysis when there were minimal indoor sources of SO42-. From all data pooled across the districts, the estimated average ambient-generated and non-ambient-generated exposure to PM2.5 were 55.3µg/m3 (SD=23.4µg/m3) and 18.1µg/m3 (SD=29.1µg/m3), respectively. A significant association was found between ambient-generated exposure and ambient PM2.5 concentrations (Pearson's r=0.51, p<0.001). As expected, the non-ambient generated exposure was not related to the ambient concentrations. This study highlights the importance of both ambient and non-ambient components of total personal exposure in the megacity of Guangzhou. Our results support the use of SO42- as a tracer of personal exposure to PM2.5 of ambient origin in environmental and epidemiological studies.

Seasonal variations and source estimation of saccharides in atmospheric particulate matter in Beijing, China.

Saccharides are important constituents of atmospheric particulate matter (PM). In order to better understand the sources and seasonal variations of saccharides in aerosols in Beijing, China, saccharide composition was measured in ambient PM samples collected at an urban site in Beijing. The highest concentrations of total saccharides in Beijing were observed in autumn, while an episode with abnormal high total saccharide levels was observed from 15 to 23 June, 2011, due to extensive agricultural residue burning in northern China during the wheat harvest season. Compared to the other two categories of saccharides, sugars and sugar alcohols, anhydrosugars were the predominant saccharide group, indicating that biomass burning contributions to Beijing urban aerosol were significant. Ambient sugar and sugar alcohol levels in summer and autumn were higher than those in spring and winter, while they were more abundant in PM2.5 during winter time. Levoglucosan was the most abundant saccharide compound in both PM2.5 and PM10, the annual contributions of which to total measured saccharides in PM2.5 and PM10 were 61.5% and 54.1%, respectively. To further investigate the sources of the saccharides in ambient aerosols in Beijing, the PM10 datasets were subjected to positive matrix factorization (PMF) analysis. Based on the objective function to be minimized and the interpretable factors identified by PMF, six factors appeared to be optimal as to the probable origin of saccharides in the atmosphere in Beijing, including biomass burning, soil or dust, isoprene SOA and the direct release of airborne fungal spores and pollen.

The characteristics of Beijing aerosol during two distinct episodes: impacts of biomass burning and fireworks.

The chemical composition of Beijing aerosol was measured during summer and winter. Two distinct episodes were identified. Water-soluble potassium (K(+)) increased significantly during the firework episode in winter with an episode to non-episode ratio of 4.97, whereas the biomass burning (BB) episode in summer was characterized by high episode to non-episode ratios of levoglucosan (6.38) and K(+) (6.90). The BB and firework episodes had only a minor influence on the water-soluble OC (organic carbon) to OC ratio. Based on separate investigations of episode and non-episode periods, it was found that: (i) sulfate correlated strongly with both relative humidity and nitrate during the typical winter period presumably indicating the importance of the aqueous-phase oxidation of sulfur dioxide by nitrogen dioxide, (ii) oxalate and WSOC during both winter and summer in Beijing were mainly due to secondary formation, and (iii) high humidity can significantly enhance the formation potential of WSOC in winter.

Organosulfates in humic-like substance fraction isolated from aerosols at seven locations in East Asia: a study by ultra-high-resolution mass spectrometry.

Humic-like substances (HULIS) in ambient aerosols collected at seven locations in East Asia were analyzed using electrospray ionization (ESI) coupled with an ultra-high-resolution mass spectrometer (UHRMS). Locations included a 3 km high mountaintop site in Taiwan, rural, suburban, and urban locations in the Pearl River Delta (PRD), South China, and in Taiwan. Organosulfates (OS) in the HULIS fraction were tentatively identified through accurate mass measurements and MS/MS spectra interpretation. In the two mountaintop samples collected in regional background atmosphere, little OS were detected, while a few hundred OS formulas were identified in the six samples taken in Taiwan and PRD. Many of the OS ions were among the most intense peaks in the negative ESI-UHRMS spectra, and their elemental formulas were identical to OS derived from biogenic volatile organic compounds (BVOCs) (e.g., monoterpenes) that have been identified in chamber studies. With OS having less than 6 carbon atoms too hydrophilic to be effectively retained in the HULIS fraction, OS containing 10 carbon atoms were the most abundant, indicating monoterpenes as important precursors of OS in the HULIS fraction. Clear spatial variation in abundance of OS was found among different atmospheric environments, with enhanced coupling of BVOCs with anthropogenic acidic aerosols observed in the PRD samples over the Taiwan samples. The double bond equivalent (DBE) values indicate the majority of OS (>90%) in the HULIS fraction are aliphatic. The elemental compositions of OS compounds containing N atoms (defined as CHONS) indicate that they are probably nitrooxy OS. Some insights into OS formation mechanisms are also gained through examining the presence/absence of perceived reactant-product formula pairs in the mass spectra. The results suggest the dominant epoxide intermediate pathway for formation of OS compounds without N atoms (defined as CHOS) and confirm the more readily hydrolyzed characteristics of the --ONO2 group than the --OSO3 group. There is a lack of evidence for the epoxide pathway to account for the formation of OS in the CHONS subgroup.

Observation of elevated fungal tracers due to biomass burning in the Sichuan Basin at Chengdu City, China.

Fungal material (i.e., spores and fragments) is an important component of atmospheric aerosols. In order to examine the variability of fungal abundance in fine particles (PM(2.5)) during a biomass burning season, an intensive measurement campaign was conducted in the Sichuan Basin at Chengdu, a megacity in southwest China, in spring 2009. The aerosol samples were analyzed for carbonaceous species, including molecular tracers for biomass burning and fungal material, and water soluble ions. The results were interpreted with the help of principle component analysis, fire count maps, and the WRF model. Elevated concentrations of arabitol and mannitol were found with average concentrations of 21.5±16.6 ng m(-3) and 43.9±19.3 ng m(-3), respectively, which were unexpectedly higher than those measured in fine particles in any other study reported previously. Even higher concentrations were observed in cases with simultaneous enhancements in the biomass burning tracers levoglucosan and K(+). In the case of influence by pollution plumes from biomass burning regions, the fungal tracer concentrations reached maximum values of 79.6 ng m(-3) and 121.8 ng m(-3), coinciding with peak levels of levoglucosan and K(+). Statistically significant correlations were found between the simultaneously observed fungal tracers (arabitol and mannitol) and biomass burning tracers (levoglucosan and K(+)), suggesting that these species were emitted by co-located sources, and hence the elevated fungal tracers were likely associated with biomass burning activities.

Stable carbon isotope ratio analysis of anhydrosugars in biomass burning aerosol particles from source samples.

A new method for stable carbon isotope ratio analysis of anhydrosugars from biomass burning aerosol particle source filter samples was developed by employing Thermal Desorption--2 Dimensional Gas Chromatography--Isotope Ratio Mass Spectrometry (TD-2DGC-IRMS). Compound specific isotopic measurements of levoglucosan, mannosan, and galactosan performed by TD-2DGC-IRMS in a standard mixture show good agreement with isotopic measurements of the bulk anhydrosugars, carried out by Elemental Analyzer--Isotope Ratio Mass Spectrometry (EA-IRMS). The established method was applied to determine the isotope ratios of levoglucosan, mannosan, and galactosan from source samples collected during combustion of hard wood, softwood, and crop residues. δ(13)C values of levoglucosan were found to vary between -25.6 and -22.2‰, being higher in the case of softwood. Mannosan and galactosan were detected only in the softwood samples showing isotope ratios of -23.5‰ (mannosan) and -25.7‰ (galactosan). The isotopic composition of holocellulose in the plant material used for combustion experiments was determined with δ(13)C values between -28.5 and -23.7‰. The difference in δ(13)C of levoglucosan in biomass burning aerosol particles compared to the parent fuel holocellulose was found to be -1.89 (±0.37)‰ for the investigated biomass fuels. Compound specific δ(13)C measurements of anhydrosugars should contribute to an improved source apportionment.

Levoglucosan and carbonaceous species in the background aerosol of coastal southeast China: case study on transport of biomass burning smoke from the Philippines.

INTRODUCTION: Levoglucosan and carbonaceous species in the background aerosol of coastal southeast China were measured at Jianfengling (JFL), a background mountain site in a National Reserve Park on Hainan Island, and at Hok Tsui (HT), a rural site on the southern coast of Hong Kong from April to May of 2004 during an intensive field study. METHODS: We integrated the information from field study, satellite and backward trajectory model to examine the long-range transport of biomass burning smoke from the Philippines and assess its impact on background aerosol in coastal southeast China. RESULTS AND DISCUSSION: The average levoglucosan concentrations were 42 and 30 ng m(-3) at JFL and HT, respectively, while the organic and elemental carbon concentrations were 3.1 and 0.4 µg C m(-3) respectively at JFL, and 4.1 and 1.3 µg C m(-3) respectively at HT. Elevated levoglucosan concentrations of 85-106 ng m(-3) (250-340% extra loadings) at JFL and 57 ng m(-3) (170% extra loading) at HT were observed during transport events in which air masses originated from the Philippines. Fire hot spot counts and aerosol index derived from satellite data showed that the spread of biomass burning smoke from the Philippines resulted in large-scale dense aerosol clouds in the adjacent South China Sea and the western Pacific Ocean. The observed high ratio of two biomass-burning tracers (levoglucosan to mannosan) at JFL (7-36) and HT (27) indicated that the biomass smoke originating from the Philippines had significant contributions from open-field burning of agricultural residues, such as rice straw. The pollution plumes were transported to southeast China resulting in elevated concentrations of carbonaceous aerosol and levoglucosan in particular. Using a simplified receptor-based approach, biomass smoke aerosol was estimated to account for 16-28% of OC in the background atmosphere of Hainan and 4.9% of OC at the rural site of Hong Kong during these episode cases, indicating that biomass burning smoke generated in the Philippines could have a significant contribution to background ambient aerosol of southeast coastal China.

Observations of ozone and carbon monoxide at Mei-Feng mountain site (2269 m a.s.l.) in Central Taiwan: seasonal variations and influence of Asian continental outflow.

Continuous measurements of ozone (O(3)) and carbon monoxide (CO) were carried out at Mei-Feng (24.05°N, 120.10°E, 2269 m above sea level), a remote mountain site in central Taiwan, to investigate the influence of long-range transported air pollution on O(3) and CO variations in the subtropical Pacific region. Data collected from March 2009 to September 2010 revealed average mixing ratios of 37±14 ppb for O(3) and 188±82 ppb for CO at this remote site. Diurnal variations for both O(3) and CO were observed as well in all seasons. The higher levels for O(3) and CO in the afternoon were attributed to transport of boundary layer pollution to the site during daytime upslope flow. Monthly means of both O(3) and CO showed maxima in spring and in the continental air masses from Southeast Asia, coastal China, and Korea/Japan. On the contrary, the lower O(3) and CO levels found in summer were due to the marine air masses originating from the Philippine Sea and Pacific Ocean. The relationship between O(3) and CO was analyzed, using nighttime data to minimize any local influence. The results showed a fairly good correlation between O(3) and CO from March to September. The contribution of CO from the Asian outflow reached a maximum in spring (88 ppb) and had a minimum in summer (27 ppb). The photochemical buildup of O(3) resulting from anthropogenic emissions in continental Asia was estimated to be 15 ppb in spring, while its production was insignificant, with an average of 4 ppb, in summer. A positive correlation between O(3) and CO plus high ozone levels in springtime suggested that the enhancements of O(3) were likely due to O(3) which was photochemically produced over this region.

Change of air quality and its impact on atmospheric visibility in central-western Pearl River Delta.

Ambient air quality data, including atmospheric visibility, of Foshan city, a highly polluted city in the Pearl River Delta (PRD), and data obtained by the On-line Air Pollutant Exhaust Monitoring Network (OAPEMN), recently established by the National Emission Monitoring and Control Network for major industrial enterprises, were analyzed and are reported here for the first time, revealing the change in air pollution patterns and its impact on visibility degradation in the last decade. Reduced visibility of less than 8 km (after elimination of rainy and foggy periods) was found 22% of the time from 1998 to 2008, accompanied by elevated levels of pollutants, especially SO2 and PM10, in comparison with that of other developed cities. However, PM10 showed a steady decreasing trend (0.004 mg m⁻³) year⁻¹) during 2001-2008, in contrast to the noticeable increase in ambient NO2 concentrations from ~0.020 mg m⁻³ before 2005 to above 0.050 mg m⁻³ afterward. Multiple regression analysis revealed that the percentage of reduced visibility strongly correlated with PM10 concentration, suggesting that visibility degradation was directly proportional to the loading of particles. Moreover, the fairly significant correlation between reduced visibility and NO2 concentration also implied that the impact of primary emissions of NO2 and enhanced secondary pollutants, formed via photochemical processes in the atmosphere, could not be ignored. The decreased PM10levels were obviously the predominant factor for the improvement in visibility (5.0% per 0.01 mg m⁻³) and were likely due to the implementation of stricter air pollution control measures for industrial exhaust, which also resulted in reduced SO2 pollution levels in the recent 2 years. In particular, the OAPEMN records showed an overall enhanced SO2 removal by 64% in major industrial sectors. The continuous increase in road traffic and lack of efficient NO(x) control strategies in the PRD region, however, caused an increase in ambient NO2 concentrations.

Evaluating real-time air-quality data as earthquake indicator.

A catastrophic earthquake, namely the 921-earthquake, occurred with a magnitude of M(L)=7.3 in Taiwan on September 21, 1999, causing severe disaster. The evaluation of real-time air-quality data, obtained by the Taiwan Environmental Protection Administration (EPA), revealed a staggering increase in ambient SO(2) concentrations by more than one order of magnitude across the island several hours prior to the earthquake, particularly at background stations. The abrupt increase in SO(2) concentrations likely resulted from seismic-triggered degassing instead of air pollution. An additional case of a large earthquake (M(L)=6.8), occurring on March 31, 2002, was examined to confirm our observations of significantly enhanced SO(2) concentrations in ambient air prior to large earthquakes. The coincidence between large earthquakes and increases in trace gases during the pre-quake period (several hours) indicates the potential of employing air-quality monitoring data to forecast catastrophic earthquakes.

Particle size distributions of organic aerosol constituents during the 2002 Yosemite Aerosol Characterization Study.

The Yosemite Aerosol Characterization Study (YACS) was conducted in the summer of 2002 to investigate sources of regional haze in Yosemite National Park. Organic carbon and molecular source marker species size distributions were investigated during hazy and clear periods. More than 75% of the organic carbon mass was associated with submicron aerosol particles. Most molecular marker species for wood smoke, an important source of particulate matter during the study, were contained in submicron particles, although on some fire influenced days, levoglucosan shifted toward larger sizes. Various wood smoke marker species exhibited slightly different size distributions in the samples, suggesting different, size dependent emission or atmospheric processing rates of these species. Secondary biogenic compounds including pinic and pinonic acids were associated with smaller particles. Pinonaldehyde, however, exhibited a broader distribution, likely due to its higher volatility. Dicarboxylic acids were associated mainly with submicron particles. Hopanes, molecular markers for vehicle emissions, were mostly contained in smaller particles but exhibited some tailing into larger size classes.

Determination of levoglucosan from smoke samples using microchip capillary electrophoresis with pulsed amperometric detection.

Separation and detection of native anhydrous carbohydrates derived from the combustion of biomass using an electrophoretic microchip with pulsed amperometric detection (PAD) is described. Levoglucosan represents the largest single component of the water extractable organics in smoke particles and can be used to trace forest fires or discriminate urban air pollution sources. Detection of levoglucosan and other sugar anhydrides in both source and ambient aerosol samples is typically performed by gas chromatographic (GC) separation with mass spectrometric (MS) detection. This method is cost, time, and labor intensive, typically involving a multistep solvent extraction, chemical derivatization, and finally analysis by GC/MS. However, it provides a rich wealth of chemical information as the result of the combination of a separation method and MS and exhibits good sensitivity. In contrast, microchip capillary electrophoresis offers the possibility of performing simpler, less expensive, and faster analysis. In addition, integrated devices can be fabricated and incorporated with an aerosol collection system to perform semicontinuous, onsite analysis. In the present report, the effect of the separation potential, buffer pH and composition, injection time, and pulsed amperometric detection parameters were studied in an effort to optimize both the separation and detection of anhydrous sugars. Using the optimized conditions, the analysis can be performed in less than a minute, with detection limits ranging from 22 fmol (16.7 microM) for levoglucosan to 336 fmol (258.7 microM) for galactosan. To demonstrate the capabilities of the device, a comparison was made between GC/MS and microchip electrophoresis using an aerosol source sample generated in a wood-burning chamber. A second example utilizing an ambient aerosol sample illustrates a matrix interference necessitating additional method development for application to samples not dominated by wood smoke.