Protein amino acids as markers for biological sources in urban aerosols

Biological aerosol particles are recently gaining increased attention, but global estimates of their emissions are unclear. Traditional organic tracers for biological particles have not been able to capture the diversity of biological sources such as residential wood burning. Here, we have analyzed protein content in air particulate matter over a year in a suburban area near Shibuya, in order to identify contributions from biological sources. Aerosols were separated into five size fractions using a high-volume cascade impactor. Amino acid profiles were obtained from acid hydrolysates by high-performance liquid chromatography and were subsequently used in a receptor model for source apportionment. Results show that protein content ranged from 0.5 to 2 % throughout the year in all size fractions. We observed contributions from seasonally variable emission sources such as pollen and fallen leaves in coarse particles, larger than 7 µm, at elevated concentrations during spring and winter. We also found contributions from pollen and fallen leaves in the smallest size fraction, lower than 1.1 µm, after spring. This finding indicates that sources are broken up to smaller particles in the urban environment. Overall, our findings demonstrate that protein content can be used as marker for biological aerosol particles, and that protein amino acid composition can distinguish multiple sources.     

Indoor particle dynamics in a school office: determination of particle concentrations,deposition rates and penetration factors under naturally ventilated conditions

Recently, the problem of indoor particulate matter pollution has received much attention. An increasing number of epidemiological studies show that the concentration of atmospheric particulate matter has a significant effect on human health, even at very low concentrations. Most of these investigations have relied upon outdoor particle concentrations as surrogates of human exposures. However, considering that the concentration distribution of the indoor particulate matter is largely dependent on the extent to which these particles penetrate the building and on the degree of suspension in the indoor air, human exposures to particles of outdoor origin may not be equal to outdoor particle concentration levels. Therefore, it is critical to understand the relationship between the particle concentrations found outdoors and those found in indoor micro-environments. In this study, experiments were conducted using a naturally ventilated office located in Qingdao, China. The indoor and outdoor particle concentrations were measured at the same time using an optical counter with four size ranges. The particle size distribution ranged from 0.3 to 2.5 μm, and the experimental period was from April to September, 2016. Based on the experimental data, the dynamic and mass balance model based on time was used to estimate the penetration rate and deposition rate at air exchange rates of 0.03–0.25 h^?1. The values of the penetration rate and deposition velocity of indoor particles were determined to range from 0.45 to 0.82 h^?1 and 1.71 to 2.82 m/h, respectively. In addition, the particulate pollution exposure in the indoor environment was analyzed to estimate the exposure hazard from indoor particulate matter pollution, which is important for human exposure to particles and associated health effects. The conclusions from this study can serve to provide a better understanding the dynamics and behaviors of airborne particle entering into buildings. And they will also highlight effective methods to reduce exposure to particles in office buildings.     

Dry deposition and particle size distributions of nitrate and sulfate in ambient air

This study reports the dry deposition pollutants of anion species (NO₃ ^‐ and SO₄ ^‐2) in the Ping Tung City of Southern Taiwan. Several deposition properties are discussed in this paper. It included dry deposition flux, anion species size distribution and deposition velocities. Noll Rotary Impactor (NRI) and Microorifice Uniform Deposit Impactor (MOUDI) were used to collect ambient air coarse and fine particulate. Dry deposition plate was applied to collect particle deposition flux. Dionex 2000i/SP Ion Chromatography equipped with 4 mm AG4A‐SC and AS4A‐SC column was employed to analyze the anion species. The eluent solution is 1.8 mM sodium carbonate/1.7 mM sodium bicarbonate. The measured dry deposition flux of nitrate ranged from 0.63 to 3.96 mg/m²‐day and averaged 2.12 mg/m²‐day, while the measured dry deposition of sulfate ranged from 1.17 to 9.53 mg/m²‐day and averaged 3.92 mg/m²‐day. The particle size distribution of nitrate has bimodal particle size distributions. However, the sulfate displayed uniform particle size distribution for all four sampling sites. Mean cumulative fraction (F%) of nitrate in the particle size range below 1, 2.5, 10 and 25 μm, in sequence, were 34.6%, 60.9%, 91.0% and 97.6%, respectively. However, the mean F% of sulfate in the particle size range below 1, 2.5, 10 and 25 um, in sequence, were 57.3%, 82.6%, 90.3% and 98.0%, respectively. The sulfate has more F% in the submicron particles. The mean MMD _o of nitrate and sulfate are 2.35 and 0.87 μm, respectively. The mean dry deposition velocities of nitrate and sulfate are 0.45 and 0.38 cm/sec, respectively.     

Particle size distribution and pollutants in road-deposited sediments in different areas of Zhenjiang,China

An understanding of road-deposited sediment (RDS) characteristics on an impervious surface is essential to estimate pollutant washoff characteristics and to minimise the impacts of pollutants on the water environment. A total of 62 RDS samples were collected from four different land-use types (commercial, residential, intense traffic and riverside park) in Zhenjiang City, China. The samples were fractionated into seven grain-size classes and analysed for particle size distribution and concentrations of pollutants. The samples are found to consist predominantly of fine particles (60–80%, <250 μm). The maximum mean concentrations of zinc, lead and copper were 686.93, 589.19 and 158.16 mg/kg, respectively, with the highest metal concentrations found in samples from the intense traffic area. The maximum mean contents of organic matter (12.55%), nitrogen (6.31 mg/g) and phosphorus (5.15 mg/g) were found in samples from the commercial area. The concentrations of heavy metals were highest in the smallest particle size fraction analysed (63 μm). The organic matter and nitrogen content generally increased with decreasing particle sizes in the <500-μm particle size range. The results also revealed that most of the total nitrogen (TN) is attached to the finer sediments and that to effectively reduce TN loads in particulates, treatment facilities must be able to remove the finer particles (down to 125 μm for TN).     

Faster phototransformation of the formate (terrestrial) versus methanesulphonate (marine) markers of airborne particles: implications for modelling climate change

Atmospheric particulate matter is altering climate. For instance marine biogenic particles are cooling climate. Organic markers are major tools to elucidate the sources of atmospheric particulate matter. Formate is commonly used as a marker of continental aerosols, whereas methanesulphonate is used as tracer of biogenic marine aerosols. However, transformation processes during aerosol transport may modify their relative concentrations and, in turn, introduce a bias in the assessment of particle sources. Actually very little is known about the transformation of formate and methanesulphonate in aerosols. Therefore, we irradiated formate and methanesulphonate in the presence of nitrate and haematite. Nitrate and haematite are aerosol photosensitisers, producing reactive species that degrade organic compounds. The time evolution of formate and methanesulphonate was monitored by ion chromatography. Our results show that formate is transformed from 1.6 to 4.1 times faster than methanesulphonate. This trend is partly due to higher reactivity with the hydroxyl radical and partly due to additional reaction with other transients such as nitrogen dioxide. Such results strongly suggest faster formate transformation during particle transport. Therefore, when formate and methanesulphonate are used as particle tracers, an overestimation of marine biogenic versus continental particle sources is expected. This bias has major implications for climate prediction models, because marine biogenic particles have a cooling effect on climate.     

Lead-210 and Beryllium-7 in the Aerosol Particles Around Taiwan Off-Shore Areas

Abstract

Distributions of ²¹⁰Pb and ⁷Be in the aerosol particles of different size fractions were measured around Taiwan offshore areas from October, 1994 to October, 1995. the size distribution and abundance of the aerosol particles showed both spatial and temporal variations. the particle concentrations off northwestern Taiwan were more than twice as those off northeastern Taiwan both in November and March, and the values were much higher in November than in March for both areas. the measured particle concentrations, except for one sample with an unusually high value, ranged from 10 to 83 μOgm ^?3 in the study areas. the ²¹⁰Pb concentrations in the aerosol particles filtered from the air mass varied between 20 × 10^?3 and 72 × 10^?3 dpm m^?3 (1dpm = 0.45 pCi). the ²¹⁰Pb concentrations in the area off southwestern Taiwan appeared somewhat higher than in other areas and were probably contributed by the land air from Taiwan which contains higher ²¹⁰Pb in winter. the ²¹⁰Pb concentrations off northern Taiwan were low in November when the aerosol concentrations were high, but they were high in March when the aerosol concentrations were low.

Based on the ⁷Be monitoring records of 20 years on the aerosol particles of the island by the Taiwan Radiation Monitoring Center, the mean settling rate averaged 0.91, 0.79 and 0.68 cm s^?1, respectively, in northern, central and southern Taiwan. with these values and the ²¹⁰Pb concentrations in the aerosols, the ²¹⁰Pb flux was determined to be between 0.58 and 2.30 dpm cm^?2y^?1, with an average of 1.19 dpm cm^?2y^?1. Excluding the highest value due to its extremely high ²¹⁰Pb and aerosol concentrations, the average is reduced to 1.05 dpm cm^?2y^?1. the activity median diameters (AMD) for ²¹⁰Pb in the study areas were between 0.69 and < 0.49 μM with a mean of 0.5 öm based on ²¹⁰Pb distributions in different particle size fractions. Thus, ²¹⁰Pb was preferentially adsorbed on to the submicron particles. ⁷Be in the study areas showed a good correlation with ²¹⁰Pb in total activity although the two nucides had different sources.     

Fluxes and Transport of Organic Carbon and Trace Metals in the Tropical Tsengwen Estuary,Southwestern Taiwan

Distributions of organic carbon and trace metals were investigated in the tropical Tsengwen river end-member and in the estuary to better understand thoroughly the riverine fluxes and estuarine transports of constituents into the sea. Experimental results indicated that riverine fluxes of organic carbon and trace metals possessed a highly temporal variability, attributed primarily to temporal variation in river water discharge and suspended load. More than 70% of annual fluxes of dissolved constituents and >90% of particulate constituents arose from river floods caused by summer typhoons. the flushing time of fresh water in the estuary varied from a half month in the dry season to a half day in the flood period. Dissolved organic carbon (DOC) and nutrienttype metals (Cd, Cu, Zn) were conservatively transported through the estuary. Dissolved particle-reactive metals (Mn, Pb), however, were apparently transported non-conservatively through the estuary. Particulate organic carbon (POC) and trace metals (PTM) were transported non-conservatively by following the transport mode of total suspended matter (TSM) in the estuary. DOC slightly dominates the transport of organic carbon while particle-reactive PTM predominates the transport of trace metals through the estuary. Total organic carbon (TOC) in estuarine sediment was progressively enriched with ¹³C downstream, as derived by mixing the overlying TSM between terrestrial and marine end-members. Distributions of trace metals in sediment were subsequently controlled by sedimentary TOC and particle size. Based on results presented here, we believe that enrichments of trace metals in the estuary are attributed primarily to the natural processes of transport and sedimentation of fluvial TSM     

Influences of suspended particles on the runoff of pesticides from an agricultural field at Askim, SE-Norway

Field and laboratory experiments were conducted to study the loss of particles from agricultural fields, and the role of suspended particles in carrying pesticides in surface runoff and drainage water. Propiconazole, a widely used fungicide was applied to experimental fields located at Askim, SE-Norway. Samples from surface runoff and drainage water were collected and analyzed for sediment mass, pesticides, particulate and dissolved organic carbon through a whole year. The surface soil and the runoff material were characterized by its particle size distribution, organic carbon content in size fractions and its ability to bind propiconazole. The results show that (1) particle runoff mostly occurred during the rainfall event shortly after harrowing in autumn. The highest particle concentration observed in the surface runoff water was 4600 mg l(-1), and in the drainage water 1130 mg l(-1); (2) the erosion of surface soil is size selective. The runoff sediment contained finer particle/aggregates rich in organic matter compared to its original surface soil; (3) the distribution coefficient (Kd) of propiconazole was significantly higher in the runoff sediment than in the parent soil. According to our calculation, particle-bound propiconazole can represent up to 23% of the total amount of propiconazole in a water sample with a sediment concentration of 7600 mg l(-1), which will significantly influence the transport behavior of the pesticide.     

Influences of Suspended Particles on the Runoff of Pesticides from an Agricultural Field at Askim, SE-Norway

Field and laboratory experiments were conducted to study the loss of particles from agricultural fields, and the role of suspended particles in carrying pesticides in surface runoff and drainage water. Propiconazole, a widely used fungicide was applied to experimental fields located at Askim, SE-Norway. Samples from surface runoff and drainage water were collected and analyzed for sediment mass, pesticides, particulate and dissolved organic carbon through a whole year. The surface soil and the runoff material were characterized by its particle size distribution, organic carbon content in size fractions and its ability to bind propiconazole. The results show that (1) particle runoff mostly occurred during the rainfall event shortly after harrowing in autumn. The highest particle concentration observed in the surface runoff water was 4600 mg l^–1, and in the drainage water 1130 mg l^–1; (2) the erosion of surface soil is size selective. The runoff sediment contained finer particle/aggregates rich in organic matter compared to its original surface soil; (3) the distribution coefficient (K _d) of propiconazole was significantly higher in the runoff sediment than in the parent soil. According to our calculation, particle-bound propiconazole can represent up to 23% of the total amount of propiconazole in a water sample with a sediment concentration of 7600 mg l^–1, which will significantly influence the transport behavior of the pesticide.     

复合生态处理系统颗粒构成差异及其效应分析

研究了复合生态处理系统中不同单元颗粒物的构成差异，探讨了颗粒构成对其去除机制、粒径分布和去除规律的影响．结果表明，水环境对系统后端颗粒构成产生的影响明显高于对系统前端的影响．颗粒构的成差异决定无机颗粒沉降，有机颗粒分解、藻类被捕食、颗粒截滤依次在颗粒物的去除中占主导地位．不同水环境中，颗粒构成和去除机制的差异导致不同单元颗粒物去除规律的相应变化．     

武汉市秋冬季室内外空气颗粒物以及有机碳、元素碳的污染特征

为了解秋冬季室内外空气颗粒物PM10、PM2.5以及其有机碳和元素碳的污染特征,于2009年10月及12月对武汉大学医学部学生宿舍室内、外PM10、PM2.5进行了两周连续采样。结果表明：秋季室内PM10和PM2.5的平均浓度分别为121.8和91.3μg/m3,室外为153.9和104.2μg/m3;冬季室内PM10...     

用扫描电镜分析表征大气气溶胶单颗粒

1　IntroductionAtmosphericaerosolsarecomplexmixture,originatedfromavarietyofsources.Mostoftheanalyticaltechniquesusedforitscharacterizationarebulkmethodsthatgenerateonesetofdatapersample,describingtheoverallcompositionofthesample .Toworkoutusefulinformationonpollu tionsources,itrequiresdataofagreatnumberofsamplesandmultivariatedataanalysismethodsusuallyareneeded .Ontheotherhand ,scanningelectronmicroscope energydispersiveX rayanaly sissystem (SEM EDX)isabletoprovideanalyticaldataforeachsing…     

Variability of biochemical composition and size distributions of seston in the euphotic zone of the Bay of Biscay: implications for microplankton trophic structure

Particle-size distributions and several biochemical components of seston were studied from October 1986 to December 1987 in surface waters of the Bay of Biscay. Variance partitioning of hydrographic and seston parameters indicates that, although seasonal variability related to the thermal cycle was important, most of the differences in seston concentration were caused by spatial components of variance. Changes in the vertical structure of the water column appeared to be the principal source of variability. Phytoplankton blooms in spring and fall and the effects of the coastal upwelling and the thermocline during summer were traced using seston concentration and biochemical composition. The different seston measurements were scaled according to their correlations with total concentration and particle size. Photosynthetic pigment biomass was related to both large and small partieles. However, concentrations of particulate proteins, lipids and carbohydrates were more related to small particles. Although not specifically analysed, low concentrations of inorganic particles and detritus can be expected in the study area, thus most of the particulate organic matter was associated with small, non-pigmented organisms, particularly in surface waters during the period of thermal stratification. The variability in concentrations of total seston and particulate organic matter was mainly due to variations in particulate proteins, lipids and carbohydrates; pigment concentrations were of secondary importance. Expressed as the ratio chlorophyll a: particulate protein-nitrogen, phytoplankton constituted an important fraction of the microplankton biomass only during spring blooms, when it averaged 75% of the particulate protein-nitrogen. In constrast, <30% of protein-nitrogen was related to chlorophyll a during the summer. These results suggest that an oligotrophic structure based on the microbial-loop prevails in microplankton assemblages of surface waters for most of the year.     

Arsenic distribution and bioaccessibility across particle fractions in historically contaminated soils

Incidental soil ingestion is a common contaminant exposure pathway for humans, notably children. It is widely accepted that the inclusion of total soil metal concentrations greatly overestimates the risk through soil ingestion for people due to contaminant bioavailability constraints. The assumption also assumes that the contaminant distribution and the bioaccessible fraction is consistent across all particle sizes. In this study, we investigated the distribution of arsenic across five particle size fractions as well as arsenic bioaccessibility in the <250-, <100-, <10- and 2.5-μm soil particle fractions in 50 contaminated soils. The distribution of arsenic was generally uniform across the larger particle size fractions but increased markedly in the <2.5-μm soil particle fraction. The marked increase in arsenic concentration in the <2.5-μm fraction was associated with a marked increase in the iron content. Arsenic bioaccessibility, in contrast, increased with decreasing particle size. The mean arsenic bioaccessibility increased from 25 ± 16% in the <250-μm soil particle fraction to 42 ± 23% in the <10-μm soil particle fraction. These results indicate that the assumption of static arsenic bioaccessibility values across particle size fractions should be reconsidered if the ingested material is enriched with small particle fractions such as those found in household dust.     

Trace metal distribution in different chemical fractions of marine sediments along the eastern Aegean shelf

The major objective of this study was to carry out sequential chemical extraction for the partitioning of particulate trace metals in sediment samples, collected along the eastern Aegean shelf during cruises July‐August 1994, in the framework of a National Marine Measurement and Monitoring Programme for the Aegean Sea.

Five metals, Cd, Pb, Cu, Zn and Cr were examined in each of sediment samples. Three chemical fractions of the sediments were separated and concentrations of the trace metals were determined by AAS techniques. The three different leaches used were hydroxylamine hydrochloride‐acetic acid, hydrogen peroxide and nitric‐perchloric acids.

Metals were concentrated mainly in the fraction extracted by nitric‐perchloric acids. Lead in the first fraction were found in the sediments of Northern part of Aegean, where the concentration of organic material was high.

The total concentrations of Cd, Cu, Zn, Cr were higher in Izmir Bay than the other sampling points. The distribution of Pb concentrations was the highest in Edremit Bay and Izmir Bay.     

Elemental concentrations in air, water, and aquatic biota in two rural provinces in northern Vietnam

The present study on environmental pollution in northern Vietnam investigates elemental concentrations in fine particulate matter (PM_2.5), freshwater, and aquatic biota at two sites with differing levels of industrial activities. An Thin is situated 47 km east of Hanoi in the neighbourhood of a coal combustion power plant, whereas the reference site, Duy Minh, is situated in the agricultural province of Ha Nam, 40 km south of Hanoi. Elemental concentrations were analysed using energy-dispersive X-ray fluorescence, total reflection X-ray fluorescence, and graphite furnace atomic absorption spectro-metry. All investigated elements in fine particles (PM_2.5) had significantly higher concentrations in An Thin, thus identifying the air at this site as polluted. In contrast to the aerosol samples, elemental concentrations as well as quantitative differences between the sampling sites were low in freshwater and biota, indicating that the impact of atmospheric deposition was limited.     

典型农耕区黑土和沼泽土团聚体颗粒中重金属的分布特征解析

了解重金属在土壤中的富集特征是其风险评价和土壤修复的基础。分别以黑龙江省典型的农耕黑土和沼泽土为研究对象,采用干筛法获得〉4000、4000～2000、2000～1000、1000～250、250～53和〈53衄16个粒级的土壤团聚体颗粒组。利用等离子质谱（ICP-MS）测定了本土和各级团聚体颗粒中Cr、Cd、As和Pb的含量,并对其颗粒组分布特征及对有机碳的响应进行了解析。研究表明,2种土壤中的重金属Cr、Cd和Pb的富集因子均大于1,而As则存在明显的流失。除了黑土中的As和Pb外,其他重金属随着团聚体粒径的增加而呈现富集减弱的趋势。其中,cr和cd主要趋向分布在粉．黏团聚体（〈53wn）颗粒中;Pb在黑土中易赋存于1000～2000μm大团聚体中,在沼泽土中则富集于53～250μm的微团聚体中;As不但趋向被吸附在53～250μm的微团聚体中,而且在黑土中也容易被吸附在〉l000μm的大团聚体中。金属质量负载计算表明,大粒径颗粒组对土壤中重金属含量的总体贡献较大。土壤中有机碳含量均随着团聚体粒径减小而升高,cr和Cd分布与颗粒有机碳含量正相关,黑土中As的分布与颗粒中有机碳含量负相关而在沼泽土中呈弱正相关,Pb的分布则与有机碳含量均无明显的相关性。     

Ambient air particulates and particulate-bound mercury Hg(p) concentrations: dry deposition study over a Traffic,Airport, Park (T.A.P.) areas during years of 2011–2012

The main purpose of this study was to monitor ambient air particles and particulate-bound mercury Hg(p) in total suspended particulate (TSP) concentrations and dry deposition at the Hung Kuang (Traffic), Taichung airport and Westing Park sampling sites during the daytime and nighttime, from 2011 to 2012. In addition, the calculated/measured dry deposition flux ratios of ambient air particles and particulate-bound mercury Hg(p) were also studied with Baklanov & Sorensen and the Williams models. For a particle size of 10 μm, the Baklanov & Sorensen model yielded better predictions of dry deposition of ambient air particulates and particulate-bound mercury Hg(p) at the Hung Kuang (Traffic), Taichung airport and Westing Park sampling site during the daytime and nighttime sampling periods. However, for particulates with sizes 20–23 μm, the results obtained in the study reveal that the Williams model provided better prediction results for ambient air particulates and particulate-bound mercury Hg(p) at all sampling sites in this study.

     

Water-soluble inorganic ions in airborne particulates from the nano to coarse mode: a case study of aerosol episodes in southern region of Taiwan

In 2004, airborne particulate matter (PM) was collected for several aerosol episodes occurring in the southern region of Taiwan. The particulate samples were taken using both a MOUDI (Micro-orifice Uniform Deposit Impactor) and a nano-MOUDI sampler. These particulate samples were analyzed for major water-soluble ionic species with an emphasis to characterize the mass concentrations and distributions of these ions in the ambient ultrafine (PM_0.1, diameter <0.1 μm) and nano mode (PM_nano, diameter <0.056 μm) particles. Particles collected at the sampling site (the Da-Liao station) on the whole exhibited a typical tri-modal size distribution on mass concentration. The mass concentration ratios of PM_nano/PM_2.5, PM_0.1/PM_2.5, and PM₁/PM_2.5 on average were 1.8, 2.9, and 71.0%, respectively. The peak mass concentration appeared in the submicron particle mode (0.1 μm < diameter <1.0 μm). Mass fractions (percentages) of the three major water-soluble ions (nitrate, sulfate, and ammonium) as a group in PM_nano, PM_0.1, PM₁, and PM_2.5 were 18.4, 21.7, 50.0, and 50.7%, respectively. Overall, results from this study supported the notion that secondary aerosols played a significant role in the formation of ambient submicron particulates (PM_0.1−1). Particles smaller than 0.1 μm were essentially basic, whereas those greater than 2.5 μm were neutral or slightly acidic. The neutralization ratio (NR) was close to unity for airborne particles with diameters ranging from 0.18 to 1 μm. The NRs of these airborne particles were found strongly correlated with their sizes, at least for samples taken during the aerosol episodes under study. Insofar as this study is exploratory in nature, as only a small number of particulate samples were used, there appears to be a need for further research into the chemical composition, source contribution, and formation of the nano and ultrafine mode airborne particulates.