Hydrogen Peroxide, Organic Peroxides and Higher Carbonyl Compounds Determined during the BERLIOZ Campaign

Gas-phase H₂O₂, organic peroxides and carbonyl compoundswere determined at various sites from Mid-July to early August 1998 during the BERLIOZ campaign in Germany. The sites were located northwest of Berlin and were chosen to determine pollutants downwind of the city emissions during a summer smog episode. Hydrogen peroxide (H₂O₂),methyl hydroperoxide (MHP, CH₃OOH) and occasionally hydroxymethyl hydroperoxide (HMHP, HOCH₂OOH) were quantified in air samples by commercial fluorimetric methods and classical HPLC with post-column derivatisation by horseradish peroxidase/p-hydroxyphenyl acetic acid and fluorimetric detection. Carbonyl compounds were determined in ambient air by a novel method based onO-pentafluorobenzyl hydroxylamine as derivatisation agent.Mixing ratio profiles of the hydroperoxides and the carbonyl compounds are reported for the intensive phase of the campaign, 20–21 July, 1998. Peroxides showed pronounced diurnal variations with peak mixing ratios in the early afternoon. At times, a second maximum was observed in the late afternoon. The major part of the H₂O₂ was formed throughrecombination reactions of HO₂ radicals, but there is some evidencethat H₂O₂ is also formed from ozonolysis ofanthropogenic and/or biogenic alkenes. Diurnal variations of mixing ratios of various carbonyl compounds are reported: alkanals (C₂ to C₁₀,isobutanal), unsaturated carbonyl compounds (methacrolein, methylvinylketone, acrolein), hydroxycarbonyl (glycolaldehyde, hydroxyacetone) and dicarbonyl compounds (glyoxal, methylglyoxal, biacetyl), aromatic compounds (benzaldehyde, o- and m-tolylaldehyde) and pinonaldehyde.     

Distributions of ozone and related trace gases at an urban site in western India

Continuous in-situ measurements of surface ozone (O₃), carbon monoxide (CO) and oxides of nitrogen (NOx) were conducted at Udaipur city in India during April 2010 to March 2011. We have analyzed the data to investigate both diurnal and seasonal variations in the mixing ratios of trace gases. The diurnal distribution of O₃ showed highest values in the afternoon hours and lower values from evening till early morning. The mixing ratios of CO and NOx showed a sharp peak in the morning hours but lowest in the afternoon hours. The daily mean data of O₃, CO and NOx varied in the ranges of 5–51 ppbv, 145–795 ppbv and 3–25 ppbv, respectively. The mixing ratios of O₃ were highest of 28 ppbv and lowest 19 ppbv during the pre-monsoon and monsoon seasons, respectively. While the mixing ratios of both CO and NOx showed highest and lowest values during the winter and monsoon seasons, respectively. The diurnal pattern of O₃ is mainly controlled by the variations in photochemistry and planetary boundary layer (PBL) depth. On the other hand, the seasonality of O₃, CO and NOx were governed by the long-range transport associated mainly with the summer and winter monsoon circulations over the Indian subcontinent. The back trajectory data indicate that the seasonal variations in trace gases were caused mainly by the shift in long-range transport pattern. In monsoon season, flow of marine air and negligible presence of biomass burning in India resulted in lowest O₃, CO and NOx values. The mixing ratios of CO and NOx show tight correlations during winter and pre-monsoon seasons, while poor correlation in the monsoon season. The emission ratio of ?CO/?NOx showed large seasonal variability but values were lower than those measured over the Indo Gangetic Plains (IGP). The mixing ratios of CO and NOx decreased with the increase in wind speed, while O₃ tended to increase with the wind speed. Effects of other meteorological parameters in the distributions of trace gases were also noticed.     

Characterization of C2−C4 NMHCs distributions at a high altitude tropical site in India

Air samples were collected covering a full diurnal cycle during each month of the year 2002 at a mountaintop of Mt. Abu (24.6^∘ N, 72.7^∘ E, 1680 amsl). These samples were analyzed for C₂−C₄ NMHCs using a gas chromatograph (GC) equipped with flame ionization detector (FID). The seasonally averaged diurnal distributions of these NMHCs do not show significant variations in the summer season. While sharp peaks in the diurnal variation of some species during evening hours are additional features apart from higher levels in all NMHCs in the winter season. The seasonal variations in relatively long lived species (e.g. ethane, propane and acetylene) are observed to be more pronounced compared to those in reactive species (e.g. ethene, propene and butanes). The seasonal changes in transport patterns seem to be more dominant factor at this site for the observed variations in NMHCs than changes in OH radical concentration. The annual mean mixing ratios of ethane, ethene, propane, propene, i-butane, acetylene, and n-butane are 1.22 ± 0.58, 0.34 ± 0.24, 0.46 ± 0.20, 0.17 ± 0.14, 0.21 ± 0.18, 0.41 ± 0.43, and 0.31 ± 0.35 ppbv, respectively. Only few pairs of NMHCs are observed to show good correlations, mainly due to transport of air masses with different degree of photochemical processing. A comparison of this measurement with data reported for other remote sites of the globe indicates lower levels of light NMHCs in the tropical sites. The annual mean mixing ratios of various C₂−C₄ NMHCs at Mt. Abu are lower by factors ranging between 3 to 9 compared to a nearest urban site of Ahmedabad. The annual mean propylene (propene) equivalent concentrations of about 1.12 and 8.62 ppbC were calculated for Mt. Abu and Ahmedabad, respectively.     

A study of ozone in the Colorado mountains

The seasonal and diurnal variations of ozone mixing ratios have been observed at Niwot Ridge. Colorado. The ozone mixing ratios have been correlated with the NO _x (NO+NO₂) mixing ratios measured concurrently at the site. The seasonal and diurnal variations in O₃ can be reasonably well understood by considering photochemistry and transport. In the winter there is no apparent systematic diurnal variation in the O₃ mixing ratio because there is little diurnal change of transport and a slow photochemistry. In the summer, the O₃ levels at the site are suppressed at night due to the presence of a nocturnal inversion layer that isolated ozone near the surface, where it is destroyed. Ozone is observed to increase in the summer during the day. The increases in ozone correlate with increasing NO _x levels, as well as with the levels of other compounds of anthropogenic origin. We interpret this correlation as in-situ or in-transit photochemical production of ozone from these precursors that are transported to our site. The levels of ozone recorded approach 100 ppbv at NO _x mixing ratios of approximately 3 ppbv. Calculations made using a simple clean tropospheric chemical model are consistent with the NO _x -related trend observed for the daytime ozone mixing ratio. However, the chemistry, which does not include nonmethane hydrocarbon photochemistry, underestimates the observed O₃ production.     

Study of a high SO2 event observed over an urban site in western India

Continuous measurements of SO₂, NO_x and O₃ along with sampling based measurements of CO, CH₄, NMHCs and CO₂ were carried out during May, 2010 at Ahmedabad. The diurnal variations of SO₂ in ambient air exhibited elevated values during the night and lower levels during the sunlit hours. The mean concentration of SO₂ during the study period was 0.95 ± 0.88 ppbv. However, the ambient SO₂ exceeded 17 ppbv in the night of 20 May, 2010. On the same day, tropospheric columnar SO₂ from OMI showed almost 350% increase corroborating the surface observations over an extended height regime. This was also the highest columnar value of SO₂ during the summer of 2010. Columnar loadings were also found to be high for formaldehyde, precipitable water vapor and aerosol optical depth on 20 May. Elevated concentrations were also recorded for other trace gases like NO₂ and O₃. Analysis of related data of trace gases indicated characteristics of fresh emissions with dominant contributions from mobile sources during the study period. However, SO₂/NO₂ ratio of 0.36 during the event period on 20th May connotes non-local influences. Analyses of meteorological parameters suggest combined impacts of transport and inversion causing higher levels of SO₂ and other pollutants during 20?C21 May. Episodes of such enhancements may perturb chemical and radiative balance of the atmosphere.     

Gas phase measurements of hydrogen peroxide in Greenland and their meaning for the interpretation of H2O2 records in ice cores

The gas phase concentration of hydrogen peroxide at Summit, Central Greenland, has been measured continuously during June/July 1990 using a coil scrubber technique combined with liquid phase fluorometry. The concentrations ranged between 0.3 ppbv and 3.5 ppbv, which is considerably higher than expected from model calculations and can be explained by low deposition rates. The record shows pronounced diurnal variations with minimum concentrations during night and maximum concentrations in the afternoon. The nocturnal minima can be explained by scavenging of H₂O₂ by hoarfrost. The scavenging mechanisms of H₂O₂ by snow and the redistribution of H₂O₂ during firnification are discussed. There is indirect evidence, that H₂O₂ is uniformly distributed in the ice lattice and that the fractionation between H₂O₂ and H₂O is small during diffusional crystal growth from the vapor phase (co-condensation).     

Tropospheric Ozone at the Swedish Mountain Site Åreskutan: Budget and Trends

Ozone measurements, performed since 1987, at the Swedish TOR/EUROTRACstation Åreskutan (lat. 63.4° N, long. 13.1° E, 1250 m abovesea level) are analyzed. The annual average ozone concentration at the sitehas increased by about 0.4 ppbv (1%) per year during the period1987–1994. The corresponding trends for individual months show adecrease during April–September and an increase during the rest of theyear. The ozone budget at Åreskutan has been investigated using backtrajectories of the air parcels, and the cosmogenic radionuclide⁷Be as a tracer of stratospheric air. From a simple diagnosticmodel, it is estimated that the contribution of stratospheric ozone to theconcentrations measured at Åreskutan is 5 ppbv (or 14% of themeasured values) on average, reaching a maximum of 23 ppbv (50%),during the episodes of direct stratospheric influence. In spring, thestratospheric contribution to ozone budget at Åreskutan is at itsmaximum, and approximately equal to the net photochemical ozone productionin the air mass affecting the site, whereas in winter, it is compensated byozone chemical sink during the transport of air masses from pollutedEuropean regions, to Scandinavia.     

北京城区冬春季过氧化氢浓度变化特征

大气过氧化氢（H₂O₂）是一种重要的光化学产物,也是硫酸盐气溶胶生成及降水酸化过程的关键氧化剂。然而,我国对H₂O₂的观测研究较少,尤其对雾霾期间H₂O₂浓度变化特征认识不足。该文介绍了冬春时段（2016年12月-2017年4月）在北京城区中国气象局的H₂O₂观测结果,并结合同期O₃,PAN,NO_X,PM_2.5等污染物和气象要素观测数据,分析H₂O₂浓度变化特征与影响因素。观测结果表明:观测期间H₂O₂体积混合比（简称为浓度）为（0.65±0.59）×10-9,其中,春季浓度（0.83±0.67）×10-9高于冬季浓度（0.51±0.47）×10-9;H₂O₂平均日变化基本呈现单峰特征,峰值出现在18:00-21:00,比其他地区峰值出现稍晚,并滞后于O₃峰值时间4~7 h;相对湿度对H₂O₂日峰值时间和浓度水平有影响,小于55%时日峰值出现于18:00-24:00,平均峰值浓度1.52×10-9;大于65%时日峰值出现于11:00-16:00,日峰值浓度均小于1×10-9。H₂O₂,O₃和PAN虽然同属光化学产物,但在不同污染状况下浓度水平和变化趋势差异明显;H₂O₂清洁日峰值浓度高于污染日,但11:00-15:00污染日浓度略高于清洁日。     

Hydrogen Peroxide at the Bermuda Atlantic Time Series Station. Part 1: Temporal Variability of Atmospheric Hydrogen Peroxide and Its Influence on Seawater Concentrations

Diurnal and seasonal variations in atmospheric hydrogen peroxideconcentrations wereinvestigated during a summer and winter cruise aboard the R.V. `Endeavor' atthe BermudaAtlantic Time Series Station. Rainwater peroxide concentrations in Augustdisplayed dielvariability while no temporal H₂O₂ pattern was evidentin March rain. Averageconcentrations in March were also significantly lower than August whichindicates photochemicalprocesses are involved in controlling hydrogen peroxide concentrations inmarine rainwaterfalling over the open ocean. The range of gas phase hydrogen peroxideconcentrations wasbetween 1 and 6 ppbv and also exhibited a strong diurnal pattern during bothAugust and Marchwith concentration maxima in the early evening. The influence of atmosphericdeposition onsurface seawater hydrogen peroxide levels was also evaluated. Hydrogenperoxide depth profileswere measured on four separate occasions before and after rain events duringthe Augustsampling period. The input of rainfall hydrogen peroxide was observedthroughout the 25 metermixed layer with surface concentrations two fold larger in the morning aftera rain event. Theintegrated increase in hydrogen peroxide after the rain from 0 to 90 meterswas 1,720 molalmost all of which could be accounted for by the peroxide added from rain.The data presentedin this study represent the first detailed, simultaneous measurements ofhydrogen peroxide inmarine air, rain and surface seawater.     

Observation of hydrogen peroxide concentrations in a Japanese red pine forest

In order to study the concentrations of hydrogen peroxide (H₂O₂) and the factors controlling its concentrations, we monitored concentrations of H₂O₂ and other gases such as sulfur dioxide, ozone, and NO _x as well as meteorological factors such as air temperature, relative humidity, and wind direction/speed during eight measurement periods from 2000 to 2002 in a Japanese red pine forest in Japan. The H₂O₂ concentrations ranged from below 0.01 to 1.64 ppb, and analysis of the diurnal variation in H₂O₂ concentration showed high concentrations around noon, and low concentrations in the morning and late afternoon. The H₂O₂ concentrations were high in early summer, when O₃ concentration, temperature, and solar radiation were high, and were low in fall, when O₃ concentration, temperature, and solar radiation were low. We propose that O₃ concentration affects the production of H₂O₂ in the monitored region during the period under study, but that high H₂O₂ concentrations were sometimes caused by the transport of polluted air from urban regions. H₂O₂ concentrations decreased remarkably when SO₂ concentrations increased by transported volcanic emission on Miyake Island. In the absence of the effects of SO₂, H₂O₂ concentrations increased with increasing O₃ concentration and temperature.     

Measurements of atmospheric hydroperoxides at a rural site in central Japan

Measurements of hydroperoxides (H₂O₂ and MHP) at ground level were made from 2012 to 2015 in Imizu City, Toyama Prefecture in central Japan. H₂O₂ and MHP concentrations ranged from 0.01 to 3.5 ppb and from below the level of detection (< 0.01 ppb) to 1.4 ppb, respectively. The concentrations of H₂O₂ and MHP were high in the summer and low in the winter. The H₂O₂ concentration was at its maximum in July and August, whereas the concentration of O₃ in the daytime was highest in May and June. The ratio of [H₂O₂]/[SO₂] presented clear seasonal variations. Many cases showed the condition of [H₂O₂] < [SO₂], called oxidant limitation especially in the cold months. Hydroperoxide concentrations in the rainwater were also high in the summer. The concentrations of MHP were much lower than those of H₂O₂ in the rain water. High concentrations of H₂O₂ (> 2.5 ppb) were detected in the summer during the inflow of air pollution. The concentrations of H₂O₂ were significantly high in July and August of 2013. The H₂O₂ was well correlated with the O₃ in July and August whereas there was no correlation between O₃ and H₂O₂ in May and June. There was a negative correlation between NO_X and H₂O₂.     

Fog and rain water chemistry at Mt. Fuji: A case study during the September 2002 campaign

Measurements of fog and rain water chemistry at the summit of Mt. Fuji, the highest peak in Japan, as well as at Tarobo, the ESE slope of Mt. Fuji in September 2002. The pH of fog and rain water sampled at Mt. Fuji varied over a range of 4.0–6.8. Acidic fogs (pH < 5.0) were observed at the summit when the air mass came from the industrial regions on the Asian continent. The ratio of [SO₄²⁻]/[NO₃⁻] in the fog water was lower at Tarobo than at the summit. High concentrations of Na⁺ and Cl⁻ were determined in the rain water sampled at the summit, possibly because of the long-range transport of sea-salt particles raised by a typhoon through the middle troposphere. The vertical transport of sea-salt particles would influence the cloud microphysical properties in the middle troposphere. Significant loss of Mg²⁺ was seen in the rain water at the summit. The concentrations of peroxides in the fog and rain water were relatively large (10–105 μM). The potential capacity for SO₂ oxidation seems to be strong from summer to early autumn at Mt. Fuji. The fog water peroxide concentrations displayed diurnal variability. The peroxide concentrations in the nighttime were significantly higher than those in the daytime.     

Hydroperoxides in the marine troposphere over the Atlantic Ocean

Hydrogen peroxide (H₂O₂) and organic hydroperoxides (ROOH) were measured on board of theRV Polarstern during its cruise across the Atlantic Ocean from 20 October to 12 November 1990 (54° N to 51° S latitude) by the enzyme fluorometric method. The H₂O₂ mixing ratio varied from below the detection limit of about 0.12 ppbv up to 3.89 ppbv, showing a latitudinal dependence with generally higher values around the equator and decreasing values poleward. The shape of the latitudinal H₂O₂ distribution agrees well with an analytical steady state expression for H₂O₂ using the measured H₂O and O₃ distribution and a wind dependent H₂O₂ deposition rate. The ROOH mixing ratio varied from below the detection limit of about 0.08 ppbv up to 1.25 ppbv with qualitatively the same latitudinal dependence as H₂O₂. The observed ratio ROOH/(ROOH + H₂O₂) varied between 0.17 and 0.98 showing higher values at the lowest H₂O₂ mixing ratios at high latitudes. The measured H₂O₂ mixing ratio shows a significant diurnal variation with a maximum around 14:00 local time, explicable by a superposition of the photochemical H₂O₂ production with a constant H₂O₂ deposition rate. Four independent estimations of the average effective H₂O₂ deposition rate inferred from the H₂O₂ decrease in the night, from the midday H₂O₂ production deficit (as derived from comparison with a photochemical model and from the daily ozone loss), and from the offset in the latitudinal H₂O₂ distribution, were consistent. An episode of maximum H₂O₂ concentration suggests the possibility of its formation in clouds.     

Diurnal and seasonal variations of meteorology and aerosol concentrations in the foothills of the nepal himalayas (Nagarkot: 1,900 m asl)

A 10-months long monitoring experiment to investigate the diurnal and seasonal variation of aerosol size distribution at Nagarkot (1,900 m asl) in the Kathmadu Valley was carried out as part of a study on katabatic and anabatic influence on pollution dispersion mechanisms. Seasonal means show total aerosol number concentration was highest during post-monsoon season (775 ± 417 cm^?3) followed by pre-monsoon (644 ± 429 cm^?3) and monsoon (293 ± 205 cm^?3) periods. Fine particle concentration (0.25 μm ≤ D_P ≤ 2.5 μm) dominated in all seasons, however, contribution by coarse particles (3.0 μm ≤ D_P ≤ 10.0 μm) is more significant in the monsoon season with contributions from particles larger than 10.0 μm being negligible. Our results show a regular diurnal pattern of aerosol concentration in the valley with a morning and an evening peak. The daily twin peaks are attributed to calm conditions followed by transitional growth and break down of the valley boundary layer below. The peaks are generally associated with enhancement of the coarse particle fraction. The evening peak is generally higher than the morning peak, and is caused by fresh evening pollution from the valley associated with increased local activities coupled with recirculation of these trapped pollutants. Relatively clean air masses from neighbouring valleys contribute to the smaller morning peak. Gap flows through the western passes of the Kathmandu Valley, which sweep away the valley pollutants towards the eastern passes modulated by the mountain - valley wind system, are mainly responsible for the dominant pollutant circulation patterns exhibited within the valley.     

Variations in surface ozone and NOx at Kannur: a tropical, coastal site in India

Continuous measurements of surface ozone (O₃), NOx (NO + NO₂) and meteorological parameters have been made in Kannur (11.9?°N, 75.4?°E, 5?m asl), India from November 2009 to October 2010. It was observed that O₃ and NOx showed distinct diurnal and seasonal variabilities at this site. The annual average diurnal profile of O₃ showed a peak of (30.3?±?10.4) ppbv in the late afternoon and a minimum of (3.2?±?0.7) ppbv in the early morning. The maximum value of O₃ mixing ratio was observed in winter (44?±?3.1) ppbv and minimum during monsoon (18.46?±?3.5) ppbv. The rate of production of O₃ was found to be higher in December (10.1?ppbv/h) and lower in July (1.8?ppbv/h) during the time interval 0800?C1000?h. A correlation coefficient of 0.52 for the relationship between O₃ and [NO₂]/[NO] reveals the role of NO₂ photolysis that generates O₃ at this site. The correlation between O₃ and meteorological parameters indicate the influence of seasonal changes on O₃ production. Investigations were further extended to explore the week day weekend variations in O₃ mixing ratio at an urban site reveals the enhancement of O₃. The variations of O₃ mixing ratio with seasonal air mass flows were elucidated with the aid of backward air trajectories. This study also indicates how vapor phase organic species present in the ambient air at this location may influence the complex chemistry involving (VOCs) that enhances the production of O₃ at this location.     

旋转正压大气中的非线性Schrödinger方程和大气阻塞

本文利用WKB方法导出了旋转正压大气中的非线性Rossby波所满足的立方Schrödinger方程,指出在1≤m≤2的情况下,非线性Schrödinger方程具有包络孤立波解,同时我们还对大气中的包络Rossby孤立波的流场进行了计算,结果得到了阻塞高压和切断低压等结构,并且这些阻塞系统能够维持五天以上。     

有霾和无霾时宁波市大气混合层高度的日变化特征

根据2007—2013年宁波市每日8次地面观测气象资料,运用罗氏法和统计分析法计算大气混合层高度,分析其在霾日和非霾日的不同日变化特征。结果表明宁波市霾日与非霾日混合层高度均呈白天高,夜晚低的日变化特征,夏季两者差值的日变化波动最明显,波峰时间比其他季节晚3 h。混合层高度日变化趋势与风速、气温、能见度趋于一致,霾等级越重,混合层高度越低。霾日与非霾日的气温差值除冬季呈正变温外,其他季节呈负变温,冬季14时差值最小,夜间加大,春夏季凌晨差值最小,14时最大,秋季波动不明显;风速差值除冬季夜间为正值外,其余季节为负值,秋冬季差值最小、夏季最大。大气处于不稳定状态时,混合层高度随着稳定度增加而逐渐处于稳定状态时,随着稳定度增加而降低,中性大气是宁波易致霾的大气层结。霾日与非霾日大气稳定度表现不一致,中午霾日中性大气占多数,非霾日则是不稳定大气;夜间霾日稳定—弱稳定大气和中性大气所占比例相当,非霾日稳定—弱稳定大气占多数。另外,PM_(2.5)浓度在霾日和非霾日均为白天低、夜间高的日变化特征,但霾日波动大,波峰时间晚于非霾日2 h,峰值浓度也高于非霾日2.7倍;早晨或下午到上半夜是霾日的PM_(2.5)浓度两个上升时段,上午为下降时段;非霾日的两个浓度缓升(降)时段分别出现凌晨和下午(上午和前半夜)。研究成果有助于预报员了解大气混合层高度及其对霾的可能影响,从而提高霾预报预警能力。     

Continuous observations of water-soluble ions in PM2.5 at Mount Tai (1534 m a.s.l.) in central-eastern China

Near real-time measurements of PM_2.5 ionic compositions were performed at the summit of the highest mountain in the central-eastern plains in the spring and summer of 2007 in order to characterize aerosol composition and its interaction with clouds. The average concentrations of total water soluble ions were 27.5 and 36.7 μg?m^?3, accounting for 44% and 62% of the PM_2.5 mass concentration in the spring and summer, respectively. A diurnal pattern of SO ₄ ^2- , NH ₄ ⁺ and NO ₃ ^- was observed in both campaigns and attributed to the upslope/downslope transport of air mass and the development of the planetary boundary layer (PBL). The average SO₂ oxidation ratio (SOR) in summer was 57% (±27%), more than twice that in spring 24% (±16%); the fine nitrate oxidation ratio (NOR) was comparable in the two seasons (9?±?6% and 11?±?10% in summer and spring, respectively). This result indicates strong summertime production of sulfate aerosol. A principal component analysis shows that short-range and long-range transport of pollution, cloud processing, and crustal source were the main factors affecting the variability of the measured ions (and other trace gases and aerosols) at Mt. Tai. Strong indications of biomass burning were observed in summer. Cloud scavenging rates showed larger variations for different ions and in different cloud events. The elevated concentrations of the water soluble ions at Mt. Tai indicate serious aerosol pollution over the North China plain of eastern China.     

Temporal variations in surface ozone and its precursors and meteorological effects at an urban site in China

Continuous measurements of ozone and its precursors including NO, NO₂, and CO at an urban site (32°03′N, 118°44′E) in Nanjing, China during the period from January 2000 to February 2003 are presented. The effects of local meteorological conditions and distant transports associated with seasonal changed Asian monsoons on the temporal variations of O₃ and its precursors are studied by statistical, backward trajectory, and episode analyses. The diurnal variation in O₃ shows high concentrations during daytime and low concentrations during late night and early morning, while the precursors show high concentrations during night and early morning and low concentrations during daytime. The diurnal variations in air pollutants are closely related to those in local meteorological conditions. Both temperature and wind speed have significant positive correlations with O₃ and significant negative correlations with the precursors. Relative humidity has a significant negative correlation with O₃ and significant positive correlations with the precursors. The seasonal variation in O₃ shows low concentrations in late autumn and winter and high concentrations in late spring and early summer, while the precursors show high concentrations in late autumn and winter and low concentrations in summer. Local mobile and stationary sources make a great contribution to the precursors, but distant transports also play a very important role in the seasonal variations of the air pollutants. The distant transport associated with the southeastern maritime monsoon contributes substantially to the O₃ because the originally clean maritime air mass is polluted when passing over the highly industrialized and urbanized areas in the Yangtze River Delta. The high frequency of this type of air mass in summer causes the fact that a common seasonal characteristic of surface O₃ in East Asia, summer minimum, is not observed at this site. The distant transports associated with the northern continental monsoons that dominate in autumn and winter are related to the high concentrations of the precursors in these two seasons. This study can contribute to a better understanding of the O₃ pollution in vast inland of China affected by meteorological conditions and the rapid urbanization and industrialization.     

A comparison of the enzyme fluorometric and the peroxyoxalate chemiluminescence methods for measuring H2O2

During September 25 to October 28, 1985, the enzyme fluorometric (Lazrus et al., 1985) and the peroxyoxalate chemiluminescence (Klockow and Jacob, 1986; Jaeschke, 1986) techniques for analyzing H₂O₂ were compared in laboratory studies at the National Center for Atmospheric Research in Boulder, Colorado, U.S.A. and under field conditions at the Whiteface Mt. field station of the Atmospheric Sciences Research Center, Albany, New York, U.S.A. Both methods showed excellent agreement, with a maximum deviation of ±5%. Only at unusually high concentrations of some potential atmospheric species could slight interferences be observed. During the experiments the detection limits were 1.3×10^-8 mol/l (0.44 ppbm) of H₂O₂ for the fluorometric instrument and 4×10^-8 mol/l (1.36 ppbm) of H₂O₂ for the chemiluminescence instrument. For the chemiluminescence technique, the response to methylhydroperoxide was approximately 80-fold less than that to an equivalent concentration of H₂O₂.