A study of the total atmospheric sulfur dioxide load using ground-based measurements and the satellite derived Sulfur Dioxide Index

We present characteristics of the sulfur dioxide (SO₂) loading over Thessaloniki, Greece, and seven other selected sites around the world using SO₂ total column measurements from Brewer spectrophotometers together with satellite estimates of the Version 8 TOMS Sulfur Dioxide Index (SOI) over the same locations, retrieved from Nimbus 7 TOMS (1979–1993), Earth Probe TOMS (1996–2003) and OMI/Aura (2004–2006). Traditionally, the SOI has been used to quantify the SO₂ quantities emitted during great volcanic eruptions. Here, we investigate whether the SOI can give an indication of the total SO₂ load for areas and periods away from eruptive volcanic activity by studying its relative changes as a correlative measure to the SO₂ total column. We examined time series from Thessaloniki and another seven urban and non-urban stations, five in the European Union (Arosa, De Bilt, Hohenpeissenberg, Madrid, Rome) and two in India (Kodaikanal, New Delhi). Based on the Brewer data, Thessaloniki shows high SO₂ total columns for a European Union city but values are still low if compared to highly affected regions like those in India. For the time period 1983–2006 the SO₂ levels above Thessaloniki have generally decreased with a rate of 0.028 Dobson Units (DU) per annum, presumably due to the European Union's strict sulfur control policies. The seasonal variability of the SO₂ total column exhibits a double peak structure with two maxima, one during winter and the second during summer. The winter peak can be attributed to central heating while the summer peak is due to synoptic transport from sources west of the city and sources in the north of Greece. A moderate correlation was found between the seasonal levels of Brewer total SO₂ and SOI for Thessaloniki, Greece (R = 0.710–0.763) and Madrid, Spain (R = 0.691) which shows that under specific conditions the SOI might act as an indicator of the SO₂ total load.     

Study on the distribution characteristics and ecological risk of heavy metal elements in coal gangue taken from 25 mining areas of China

Environmental Science and Pollution Research - The long-term, high-yield production of coal has resulted in the large-scale accumulation of coal gangue on the ground surface, which causes serious...     

An investigation of widespread ozone damage to the soybean crop in the upper Midwest determined from ground-based and satellite measurements

Elevated concentrations of ground-level ozone (O₃) are frequently measured over farmland regions in many parts of the world. While numerous experimental studies show that O₃ can significantly decrease crop productivity, independent verifications of yield losses at current ambient O₃ concentrations in rural locations are sparse. In this study, soybean crop yield data during a 5-year period over the Midwest of the United States were combined with ground and satellite O₃ measurements to provide evidence that yield losses on the order of 10% could be estimated through the use of a multiple linear regression model. Yield loss trends based on both conventional ground-based instrumentation and satellite-derived tropospheric O₃ measurements were statistically significant and were consistent with results obtained from open-top chamber experiments and an open-air experimental facility (SoyFACE, Soybean Free Air Concentration Enrichment) in central Illinois. Our analysis suggests that such losses are a relatively new phenomenon due to the increase in background tropospheric O₃ levels over recent decades. Extrapolation of these findings supports previous studies that estimate the global economic loss to the farming community of more than $10 billion annually.     

Climatology of PM2.5 organic carbon concentrations from a review of ground-based atmospheric measurements by evolved gas analysis

In this work we have compared ground-based measurements of organic carbon (OC) in the fine aerosol (PM2.5) fraction that are reported in peer-reviewed publications as part of both short campaigns and continuous monitoring networks. The comparison provides a quantitative review of global OC measurements for the purpose of establishing the extent to which organic aerosol concentrations are known with sufficient geographic and historical resolution to constrain global climate models. Only North America has sufficient measurements to provide meaningful spatial and temporal trends, although available measurements from China and Japan indicate that the Asian region is the most polluted with OC concentrations of approximately 10 μg m^?3. These measurements have a low spatial resolution, with most sites located in highly urban areas within a small geographic region. OC concentrations in North America are approximately 1 μg m^?3 and are better characterized spatially, temporally, and historically by continuous monitoring networks established decades ago. OC concentration shows a weakly increasing trend in some regions from 1997 to 2006, although in most regions it has remained effectively constant over the last ten years. Eastern U.S. sites show maximum OC in the winter and western U.S. sites show maximum OC in the summer. There is no correlation at U.S. sites between OC concentration and sulfate, nitrate, or ammonium ions, with R² < 0.1 in each case.     

Particulate matter pollution in the coal-producing regions of the Appalachian Mountains: Integrated ground-based measurements and satellite analysis

This study integrates the relationship between measured surface concentrations of particulate matter 10 μm or less in diameter (PM₁₀), satellite-derived aerosol optical depth (AOD), and meteorology in Roda, Virginia, during 2008. A multiple regression model was developed to predict the concentrations of particles 2.5 μm or less in diameter (PM_2.5) at an additional location in the Appalachia region, Bristol, TN. The model was developed by combining AOD retrievals from Moderate Resolution Imaging Spectro-radiometer (MODIS) sensor on board the EOS Terra and Aqua Satellites with the surface meteorological observations. The multiple regression model predicted PM_2.5 (r² = 0.62), and the two-variable (AOD-PM_2.5) model predicted PM_2.5 (r² = 0.4). The developed model was validated using particulate matter recordings and meteorology observations from another location in the Appalachia region, Hazard, Kentucky. The model was extrapolated to the Roda, VA, sampling site to predict PM_2.5 mass concentrations. We used 10 km x 10 km resolution MODIS 550 nm AOD to predict ground level PM_2.5. For the relevant period in 2008, in Roda, VA, the predicted PM_2.5 mass concentration is 9.11 ± 5.16 μg m^-3 (mean ± 1SD).

Implications: This is the first study that couples ground-based Particulate Matter measurements with satellite retrievals to predict surface air pollution at Roda, Virginia. Roda is representative of the Appalachian communities that are commonly located in narrow valleys, or “hollows,” where homes are placed directly along the roads in a region of active mountaintop mining operations. Our study suggests that proximity to heavy coal truck traffic subjects these communities to chronic exposure to coal dust and leads us to conclude that there is an urgent need for new regulations to address the primary sources of this particulate matter.     

城郊乡村生活垃圾衍生燃料热解特性研究

将城郊乡村生活垃圾加工成粒径6.0 mm左右的垃圾衍生燃料(RDF),采用热重(TG)分析和红外光谱等研究其热解特性.结果表明:(1)在RDF挥发分阶段和生物质挥发分阶段,助燃添加剂处于活泼分解阶段,加入了30％(质量分数)秸秆、玉米芯等生物质作助燃添加剂后的RDF(以下简写为混合RDF)分子碎片正发生内部氢重排,总体挥发分产物较多,并且有明显的二次裂解,失重提高到4.85 mg,失重率约提高12％.在RDF与生物质重叠的碳固定阶段,助燃添加剂失重率有一定提高,热重微分(DTG)峰值速率增加,为RDF碳固定阶段的进一步热解提供了良好的支持.(2)快加热产气速率均大于慢加热.(3)热解终温越高,越有利气体析出.(4)RDF的热解固体产率随着热解终温的升高而降低,在850℃时为31.9％;热解气体产率随着热解终温升高而迅速升高,在850℃时可达49.8％.(5)根据红外光谱图,城郊乡村生活垃圾加工成的RDF中所含的氯元素基本上以HCl形式释放.(6)一级动力学反应可以准确地描述物料热解过程.     

不同温度下制备花生壳生物炭的结构性质差异

热解温度是影响生物炭结构性质的重要因素。在200~700 ℃温度范围内,以花生壳为生物质原材料制备生物炭,并对生物炭的理化性质及结构组成进行表征,以期了解花生壳生物炭特征及其随热解温度变化的规律。结果表明,生物炭的产率随着温度的升高而减少,灰分和pH随着温度升高而增加。生物炭的C含量随着温度升高而增加,H元素含量却随着温度升高而减少。H/C随着温度的增加而减少。红外光谱分析表明,随着温度的升高生物炭的烷基基团减少,芳香化程度逐渐升高。500 ℃制备生物炭的K2Cr2O7和KMnO4氧化碳损失量最低,分别为18.6%和1.70%。X射线衍射分析表明,随着温度的升高,生物炭中草酸钙矿物分解消失,碳酸钙矿物形成。     

Effect of biomass burning and regional background aerosols on CCN activity derived from airborne in-situ measurements

Airborne in-situ measurements were analyzed to investigate the effects of biomass burning and regional background aerosols on cloud condensation nuclei (CCN) activity in the Pacific Dust Experiment (PACDEX) during April and May 2007. Airmass trajectories with both horizontal and vertical motions were provided to identify the aerosol sources. In the biomass burning cases, the elevated aerosol layers were clearly observed at dry conditions because of the convection of airmass in the source region. The relative aging of aerosols was supported by the ratios of BC to particles with size ranging from 0.1 to 1.0 μm (N_0.1–1.0) and BC to carbon monoxide. Compared to aerosols in the precedent plume of biomass burning, aged particles in the latter plume were more activated to CCN at 0.4% (CCN_0.4%) than 0.1% supersaturation (CCN_0.1%) due to aerosols chemical modification during the aging process. On the other hand, significant difference of CCN_0.4% and CCN_0.1% at regional background aerosols over the Pacific Ocean was due to the activated particles below 1 μm in diameter. Although higher concentrations of aged particles were observed over the eastern Pacific Ocean, activated aerosols to cloud droplet was comparatively similar in the western Pacific Ocean because of the similar concentrations of N_0.1–1.0 in both cases.     

Adsorption characteristics of Cu(II) from aqueous solution onto biochar derived from swine manure

The purpose of this study was to investigate adsorption characteristic of swine manure biochars pyrolyzed at 400 °C and 700 °C for the removal of Cu(II) ions from aqueous solutions. The biochars were characterized using BET surface area, Fourier transform infrared spectroscopy (FTIR), zeta potential, scanning electron microscopy/energy dispersive spectrometer (SEM–EDS), and X-ray diffraction (XRD). The adsorption of Cu(II) ions by batch method was carried out and the optimum conditions were investigated. The adsorption processes of these biochars are well described by a pseudo-second-order kinetic model, and the adsorption isotherm closely fitted the Sips model. Thermodynamic analysis suggested that the adsorption was endothermic. The maximum Cu(II) adsorption capacities of biochars derived from fresh and composted swine manure at 400 °C were 17.71 and 21.94 mg g^?1, respectively, which were higher than those at 700 °C. XRD patterns indicated that the silicate and phosphate particles within the biochars served as adsorption sites for Cu(II). The removal of Cu(II) ions from industrial effluent indicated that the fresh swine manure biochar pyrolyzed at 400 °C can be considered as an effective adsorbent.     

Temporal characteristics from continuous measurements of PM2.5 and speciation at the Taipei Aerosol Supersite from 2002 to 2008

This study uses monitoring data collected at the Taipei Aerosol Supersite from March 2002 to February 2008 to analyze characteristics such as seasonal fluctuations, diurnal variations, and photochemical-related variations of PM_2.5 chemical compositions. The results indicate that the average of PM_2.5 mass concentration in Taipei during this period is 30.3 ± 16.0 μg m^?3. The highest average concentration of PM_2.5 components is that of sulfate, which accounts for 21.1% of the PM_2.5 mass, followed by organic carbon (OC) at 15.9%, nitrate at 5.8%, and elemental carbon (EC) at 5.4%. Concentrations of EC, OC, and nitrate have distinctive but similar seasonal fluctuations, which is highest in spring and lowest in fall. Sulfate concentration has less seasonal fluctuations, and the highest value appears during the fall. Similarly, concentrations of EC, OC, and nitrate have notable diurnal variations; however, the diurnal variation of sulfate concentration is not very apparent. These observation data show that EC, OC, and nitrate in PM_2.5 in the Taipei metropolis come mainly from local emissions, while sulfate comes mainly from the regional transport of pollutants. This is likely because Taiwan is located on the lee zone of the Asian prevailing winds from fall to spring; its air quality is frequently affected by the transport of air pollutants from Mainland China. In addition, the extent of increase in aerosols is much higher than that of CO, indicating the formation of secondary aerosol when photochemical activity is strong. Based on six years of observation data, this study explores three potential scenarios to set up Taiwan's PM_2.5 air quality standard (AQS). The analysis indicates that the optimum standard for 24-h air quality of PM_2.5 should be around 50 μg m^?3.     

Comparisons of WRF/Chem simulated O3 concentrations in Mexico City with ground-based RAMA measurements during the MILAGRO period

This work compares the WRF/Chem (Weather Research and Forecasting – Chemistry) simulated O₃ concentrations in the Mexico City Metropolitan Area (MCMA) with measurements from the ground-based RAMA network during the MILAGRO (Megacity Initiative: Local and Global Research Observations) period. The model resolves the observations reasonably well in terms of diurnal cycle and mean magnitude as reflected by high correlation coefficients and low root-mean-square errors. Stations located in the center of the MCMA generally exhibit higher correlation coefficients and lower model biases than those stations located in the peripheral of the MCMA. Large temporal variations in the observed and simulated O₃ concentrations are noted from station to station during the MILAGRO period. Sensitivity analyses of O₃ concentrations to changes in NO_x and VOC emissions rates suggest that O₃ production in the MCMA is VOC-sensitive, and VOC-emissions reduction appears to be an effective strategy for reducing high surface O₃ concentrations in the MCMA.     

The contribution of traffic and solvent use to the total NMVOC emission in a German city derived from measurements and CMB modelling

In order to quantify the contribution of solvent use and road traffic to the total non-methane volatile organic compound (NMVOC) emissions in Germany, the composition of air in the city of Wuppertal was investigated during three campaigns at different locations. The measurements covered NMVOCs in the range of C₃–C₁₀ hydrocarbons and C₁–C₆ oxygenated compounds. An assessment of the contribution from different emission sources to the observed NMVOC concentrations was attempted with the chemical mass balance (CMB) modelling technique. Emission profiles for traffic were obtained from measurements performed in a traffic tunnel, at a downtown street intersection and during drives through the city and on motorways. Solvent emission profiles were investigated in the vicinity of different factories and workshops using solvents in Wuppertal. Apportionment analyses were performed for several receptor points located down-wind from the city centre, in residential, dense traffic and industrial areas.The results of the present work show that traffic emission rather than solvent use determines the ambient NMVOC composition. The maximum contribution of solvent use to the NMVOC emission estimated on the basis of experimentally obtained results amounts to about 23% in the whole area of Wuppertal. It can be concluded that the contribution of solvent use to the NMVOC concentrations also in other German cities falls in the range of few to about 20%, assuming that Wuppertal can be considered as a typical German urban area with certain proportions of domestic, traffic and various industrial activities. These results are in strong disagreement with the German Emission Inventory, which states, that in the reference year 2003 about 51% of the total NMVOC emissions originate from solvent use and only 14% from traffic.     

Ground-based measurements and modeling of solar UV-B radiation in Lhasa,Tibet

We present results from measurements by a NILU-UV Irradiance Meter of solar UV-B radiation in Lhasa, Tibet for the period from 7 July 1999 to 17 November 2002. The measured maximum UV-B dose rate was 1.50 W/m² during the winter, and 3.96 W/m², during the summer. The clear-sky values were below 3.00 W/m². Comparisons between measured and calculated UV-B dose rates on clear-sky days in Lhasa show good agreement. Comparisons of UV-B radiation levels in Lhasa (Tibet), Oslo (Norway), and Dar-Es-Salaam (Tanzania) show that the UV-B dose rates during the summer in Lhasa are higher than the maximum value in Dar-Es-Salaam, which is at the sea level in the equatorial region, and 60% higher than in Oslo, which is at the sea level but 60 degrees North. We conclude that the UV-B dose rates during the summer on the Tibetan plateau are among the highest levels in habituated regions of the world. Maximum measured daily-integrated UV-B doses in Lhasa range from about 10 kJ/m² in the winter to about 65 kJ/m² in the summer.     

Comparison of emissions estimates derived from atmospheric measurements with national estimates of HFCs,PFCs and SF6

This paper assesses the feasibility of using atmospheric measurement of fluorinated greenhouse gases (HFCs, PFCs and SF6) for the review and verification of greenhouse gas inventories provided by national governments. For this purpose, available data were compiled. It was found that atmospheric measurements of these gases are available and provide an indication of global annual emissions with sufficient certainty to reach the following conclusions: Within the uncertainty of the method, it was found that emissions of HFC-23, a by-product of HCFC-22 production, as obtained from atmospheric measurements did not decrease as fast, as the countries have reported. In contrast, SF6 concentrations in the atmosphere suggest higher emissions than reported by countries. Regional emission estimates from atmospheric measurements are still in a more pioneering state and cannot be compared to national estimates. Intensified efforts to measure HFCs, PFCs and SF6 in the atmosphere are recommended.     

Air quality measurements from the Fresno Supersite

The Fresno Supersite intends to 1) evaluate non-routine monitoring methods, establishing their comparability with existing methods and their applicability to air quality planning, exposure assessment, and health effects studies; 2) provide a better understanding of aerosol characteristics, behavior, and sources to assist regulatory agencies in developing standards and strategies that protect public health; and 3) support studies that evaluate relationships between aerosol properties, co-factors, and observed health end-points. Supersite observables include in-situ, continuous, short-duration measurements of 1) PM2.5, PM10, and coarse (PM10 minus PM2.5) mass; 2) PM2.5 SO4(-2), NO3-, carbon, light absorption, and light extinction; 3) numbers of particles in discrete size bins ranging from 0.01 to approximately 10 microns; 4) criteria pollutant gases (O3, CO, NOx); 5) reactive gases (NO2, NOy, HNO3, peroxyacetyl nitrate [PAN], NH3); and 6) single particle characterization by time-of-flight mass spectrometry. Field sampling and laboratory analysis are applied for gaseous and particulate organic compounds (light hydrocarbons, heavy hydrocarbons, carbonyls, polycyclic aromatic hydrocarbons [PAH], and other semi-volatiles), and PM2.5 mass, elements, ions, and carbon. Observables common to other Supersites are 1) daily PM2.5 24-hr average mass with Federal Reference Method (FRM) samplers; 2) continuous hourly and 5-min average PM2.5 and PM10 mass with beta attenuation monitors (BAM) and tapered element oscillating microbalances (TEOM); 3) PM2.5 chemical speciation with a U.S. Environmental Protection Agency (EPA) speciation monitor and protocol; 4) coarse particle mass by dichotomous sampler and difference between PM10 and PM2.5 BAM and TEOM measurements; 5) coarse particle chemical composition; and 6) high sensitivity and time resolution scalar and vector wind speed, wind direction, temperature, relative humidity, barometric pressure, and solar radiation. The Fresno Supersite is coordinated with health and toxicological studies that will use these data in establishing relationships with asthma, other respiratory disease, and cardiovascular changes in human and animal subjects.     

Concentrations and characteristics of organochlorine pesticides in aquatic biota from Qiantang River in China

The Qiantang River is a typical river flowing through an agricultural area in China. It was studied in 2006 for its aquatic biota quality by determining 13 organochlorine pesticides (OCPs) in the edible parts of crabs, clams, shrimp, fish, aquatic plants, as well as water and sediments collected from seven sites along its upper reaches all the way downstream. The levels of all insecticides were in the range of 17+/-13 (water plants), 35+/-36 (shrimp), 32+/-14 (crabs), 39+/-21 (clams), 47+/-35 (fish) ng/g wet weight (ww) and in the range of 2936+/-2356 (water plants), 5827+/-6013 (shrimp), 2102+/-966 (crabs), 1859+/-1018 (clams), 3624+/-11331 (fish) ng/g lipid. DDT and its metabolites were the predominant contaminants in most biota. A linear relationship was observed between the log bio-concentration factor (BCF) and log octanol-water partition coefficients (Kow) for fish, clams and shrimp. Composition analyses in various environmental media indicated a recent usage of lindane and dicofol into the river.     

Bioaccumulative characteristics of hexabromocyclododecanes in freshwater species from an electronic waste recycling area in China

Hexabromocyclododecanes (HBCDs) are now emerging ubiquitous contaminants due to their wide usage, persistence and toxicities. To investigate the bioaccumulative characteristics of HBCDs, sediments, Winkle (Littorina littorea), crucian carp (Carassius carassius) and loach (Misgurnus anguillicaudatus) were collected from two streams near an E-waste dismantling site in China, and HBCD exposure test was then conducted on Chinese rare minnow. The concentration of HBCDs was 14 ng g⁻¹ dry weight in sediments, 186, 377 and 1791 ng g⁻¹ lipid weight in winkle, crucian carp and loach, respectively. γ-HBCD was found to be the dominant diastereoisomer in the sediments (63% of total HBCDs). However, α-HBCD was selectively accumulated in the biotic samples and contributed to 77%, 63% and 63% of total HBCDs in winkle, crucian carp and loach, respectively. Moreover, an enrichment of (−)-enantiomers of α- and γ-HBCD were found in the winkle. The reverse results were observed in the crucian carp and loach. Similar observations of diastereoisomeric and enantiomeric composition were obtained in Chinese rare minnow with those found in the crucian carp and loach. These results indicate that the freshwater species from the streams are contaminated by HBCDs. α-HBCD can be selectively accumulated in organisms and the accumulative characteristics are enantioselective among species.     

Distribution characteristics of organochlorine pesticides in surface and vertical sediments from the Zha Long Wetland, China

Introduction

The Zha Long Wetland, the first water bird conservation area in China, lies on the northern bank of the Song Nen Plain with an area of 2,100 km². In many areas of the Zha Long Wetland, water pollution has led to a decrease in the wetland??s ecological function, vegetation degradation, a decrease in the number of bird species, and the depletion of fish resources.

Materials and methods

The sediments used in this study were collected from the surface sediment of seven sites and from different depths in three types of marshes in the Zha Long Wetland in northeast China in late October 2006. The levels and distribution patterns of 17 organochlorine pesticides (OCPs; ??-HCH, ??-HCH, ??-HCH, ??-HCH, p,p??-DDE, p,p??-DDD, p,p??-DDT, endosulfan I, endosulfan II, endosulfan sulfate, heptachlor, heptachlor epoxide, aldrin, dieldrin, endrin, endrin aldehyde, and methoxychlor) in surface sediments as well as hexachlorocyclohexane (HCH) and 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane (DDT) in vertical sediments were investigated.

Results and discussion

The concentrations of HCHs, DDTs, endosulfans, heptachlors, aldrin, and methoxychlor in surface sediments ranged from 10.44 to 41.97 ng/g, nd (undetectable levels) to 211.88 ng/g, nd to 69.89 ng/g, nd to 28.10 ng/g, 9.81 to 623.83 ng/g, and from nd to 3.99 ng/g, respectively. The highest levels of OCPs were detected in Tangtugangzi at a total concentration of 727.72 ng/g, where the dominant compound was endrin at a concentration of 483.04 ng/g. In the vertical sediments, the HCHs and DDTs were in the ranges of nd?C136.00 and nd?C214.06 ng/g, respectively.

Conclusions

Different distributions of HCHs, DDTs, and other OCPs indicated that they originated from different contamination sources. Composition analyses in surface sediments indicated recent OCP usage or discharge at some sample sites in the Zha Long Wetland.     

Assessment spatio-temporal coupling coordination relationship between mountain rural ecosystem health and urbanization in Chongqing municipality,China

Environmental Science and Pollution Research - Coercive and constraints mechanism analysis between rural ecosystem health (REH) and urbanization is required to comprehend spatio-temporal coupling...     

Dust characteristics over the North Pacific observed through shipboard measurements during the ACE-Asia experiment

To examine the diversity of chemical and physical properties of aerosol particles, in particular dust, over the North Pacific, aerosols were collected along ∼32°N latitude between 140°E and 170°W longitude aboard the NOAA R/V Ronald H. Brown during the Asian Pacific Regional Aerosol Characterization Experiment (ACE-Asia) in the spring 2001. A total of 11,482 aerosol particles were examined through individual-particle analysis. Results indicate that dust particles over this region were dominated primarily by Si-rich particles, including aluminosilicates that contain Fe. Fe is also present as separate Fe-rich particles. Additional common particle types include Ca- and S-rich particles; many of the later appear to represent soil-derived calcium carbonate and its reaction products whereas the former are predominantly reaction products of sea salt and sulfate. Particles are often aggregates of different types including pollution-derived substances and highly heterogeneous, both internally and externally. Dust particles are non-spherical, having circularities from 1.0 up to 4.5, suggesting the high degree of complexity of particle shape. The majority of dust particles were dominated by particles with median diameters from 0.67 to 1.26 μm. However, dust particles with diameters of 5 μm or even larger do exist associated with those events of dust originated from Asian desert areas. The existence of soot and Fe-rich particles over this region indicates the influence of fossil fuel sources in Asia. Aerosol Fe from both Asian desert and fossil fuel combustion may contribute to the nutrient Fe in the surface waters of the North Pacific basin. Therefore, the transport of Asian dust associated with species of fossil fuel burning in the spring may play an important role in altering the natural composition of aerosols over the North Pacific.