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1.
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.  相似文献   

2.
Diurnal and annual variations of CO2, O3, SO2, black carbon and condensation nuclei and their source areas were studied by utilizing air parcel trajectories and tropospheric concentration measurements at a boreal GAW site in Pallas, Finland. The average growth trend of CO2 was about 2.5 ppm yr−1 according to a 4-yr measurement period starting in October 1996. The annual cycle of CO2 showed concentration difference of about 19 ppm between the summer minimum and winter maximum. The diurnal cycle was most pronounced during July and August. The variation between daily minimum and maximum was about 5 ppm. There was a diurnal cycle in aerosol concentrations during spring and summer. Diurnal variation in ozone concentrations was weak. According to trajectory analysis the site was equally affected by continental and marine air masses. During summer the contribution of continental air increased, although the southernmost influences decreased. During daytime in summer the source areas of CO2 were mainly located in the northern parts of the Central Europe, while during winter the sources were more evenly distributed. Ozone showed similar source areas during summer, while during winter, unlike CO2, high concentrations were observed in air arriving from the sea. Sulfur dioxide sources were more northern (Kola peninsula and further east) and CO2 sources west-weighted in comparison to sources of black carbon. Source areas of black carbon were similar to source areas of aerosols during winter. Aerosol source area distributions showed signs of marine sources during spring and summer.  相似文献   

3.
Free tropospheric measurements of ozone, peroxyacetylnitrate andprecursors (CO, NMHC) that were made within the framework of the EUROTRACsub-project TOR (Tropospheric Ozone Research) between 1990 and 1995 at theGAW station Izana, Tenerife (28°18N, 16°30W) arediscussed. The average annual cycles reveal the importance of transport fromnorthern mid-latitudes and the role of photo-chemistry. According toair-mass trajectories, which were supplied to us from AEROCE(Atmosphere/Ocean Chemistry Experiment), transport from northernmid-latitudes is associated with high precursor concentrations in winter,whereas ozone concentrations in winter are not much influenced by transportpatterns, suggesting a rather uniform distribution over the northern part ofthe Northern Hemisphere around mean value of 43 ± 5 ppb. In summer,high ozone concentrations of up to 90 ppb are often encountered duringtransport from north, while the levels of precursors are much lower than inwinter, because of photochemical destruction. Trajectories from southerlylatitudes and the Sahara usually have the lowest ozone concentrationsassociated with them.  相似文献   

4.
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.  相似文献   

5.
Daily measurements of atmospheric sulfur dioxide (SO2) concentrations were performed from March 1989 to January 1991 at Amsterdam Island (37°50 S–77°30 E), a remote site located in the southern Indian Ocean. Long-range transport of continental air masses was studied using Radon (222Rn) as continental tracer. Average monthly SO2 concentrations range from less than 0.2 to 3.9 nmol m-3 (annual average = 0.7 nmol m-3) and present a seasonal cycle with a minimum in winter and a maximum in summer, similar to that described for atmospheric DMS concentrations measured during the same period. Clear diel correlation between atmospheric DMS and SO2 concentrations is also observed during summer. A photochemical box model using measured atmospheric DMS concentrations as input data reproduces the seasonal variations in the measured atmospheric SO2 concentrations within ±30%. Comparing between computed and measured SO2 concentrations allowed us to estimate a yield of SO2 from DMS oxidation of about 70%.  相似文献   

6.
Characterization of aerosol optical properties, such as aerosol optical depth, Angstrom exponent, and volume size distribution at the semiarid site of Tombstone Arizona (31°23′N, 110°05′W, 1408 m) will be presented for one annual cycle. In this region, extensive observations of selected optical parameters such as aerosol optical depth (AOD) have been made in the past and reported on in the literature. Less is known about other optical characteristics that are important in climate modeling and remote sensing. New observational techniques and inversion methods allow for the expansion of the earlier information. Observations have been taken with a state of the art sun photometer for a 1-year period and their analysis will be presented here. Monthly mean AODs at 500 nm were found to be in the range of 0.03–0.12; the monthly mean Angstrom exponent ranged from 0.9 to 1.6, being higher in spring and summer and lower in late fall and winter. Volume size distributions exhibit clear dominance of smaller particles, with a gradual increase in size from winter to spring and into summer. Annual variation of the radii of the smaller and the larger particles ranged between 0.05–0.4 and 4–8 μm, respectively. Radiance measurements at 940 nm were used to estimate precipitable water. The retrieved values compared within limits of uncertainty with independently derived estimates from the National Center for Environmental Prediction (NCEP) regional weather forecast model. An interesting outcome from this study was the consistency found in aerosol optical depths as observed in this study and those derived about two decades ago.  相似文献   

7.
Twenty-first century climate model projections show an amplification of the annual cycle in tropical precipitation with increased strength in both wet and dry seasons, but uncertainty is large and few studies have examined transition seasons. Here we analyze coupled climate model projections of global land monsoons and show a redistribution of precipitation from spring to summer in northern (North America, West Africa and Southeast Asia) and southern (South America, Southern Africa) regions. The annual cycle changes are global in scale. Two mechanisms, remote (based on tropospheric stability) and local (based on low level and surface moisture), are evaluated through the annual cycle. Increases in tropospheric stability persist from winter into spring and are reinforced by a reduction in surface moisture conditions, suggesting that in spring both remote and local mechanisms act to inhibit convection. This enhanced spring convective barrier leads to reduced early season rainfall; however, once sufficient increases in moisture (by transport) are achieved, decreases in tropospheric stability result in increased precipitation during the late rainy season. Further examination of this mechanism is needed in observations and models, as the projected changes would have substantial implications for agriculture, water management, and disaster preparedness.  相似文献   

8.
Summary The variations and trends in annual and seasonal air temperatures in Greece were examined on the basis of ground measurements for 25 stations during the period 1951–1993, and satellite measurements for the south eastern Mediterranean during the period 1979–1991. Data were smoothed using a 5-year running mean and were thereafter examined by regression analysis to define trends in the long duration time series. Data were also examined to detect abrupt changes and trends in the long duration annual, winter and summer series of mean maximum, mean minimum and mean temperatures. An overall cooling trend was detected for the majority of stations in winter over the entire period; the same cooling trend was also recognised for the annual and summer mean values, although a reverse warming trend was detected around the mid-70s at several stations. Satellite measurements indicate a slight warming trend, although this is not statistically significant. Considering the results of the regression analysis and the statistical tests applied to the 25 stations, it may be concluded that annual mean temperatures are dominated by an overall cooling trend, with the exception of stations in urban areas where urbanisation effects may have resulted in a warming trend. Summer temperatures, however, exhibit a warming trend roughly after 1975 at most stations.With 5 Figures  相似文献   

9.
Condensation nucleus (CN) concentrations have been measured at Mawson (67.6°S, 62.9°E) since mid 1981. Weekly median concentrations have an annual cycle with a maximum of around 300 to 400 cm-3 in summer and a minimum of a few tens of particles per cm-3 in winter. In this respect Mawson behaves very much like an Antarctic continental location. Preliminary measurements of the size distribution of CN particles taken over a nine month period suggest a seasonal change in typical particle radius from around 0.01 m in winter to around 0.04 m in summer. Diurnal variation in the CN concentration is generally very weak and does not show any systematic relation to the pronounced diurnal variation in wind-speed at Mawson.Department of Science, Antarctic Division  相似文献   

10.
Results of regular measurements during 1992–1995 of hydrocarbons and carbonyl compounds for a number of rural European monitoring sites are presented. The measurements are part of the EMEP programme for VOC measurements in Europe. In addition, several years of regular measurements are included from the Norwegian stations Birkenes at the south coast, and Zeppelin Mountain on Spitsbergen in the Arctic. The sampling frequency has been about twice per week throughout the years, implying that a substantial amount of measurement data are available. Almost all the chemical analyses have been performed by one laboratory, the EMEP Chemical Co-ordinating Centre located at NILU, which avoids problems of intercomparison and intercalibration among different laboratories. For the measured concentrations both seasonal and geographical variations are shown and discussed. The diurnal cycles of the hydrocarbon concentrations were studied in detail at one site, where the grab samples by EMEP where compared with a parallel continuous sampler, operated by EMPA, Switzerland. Hydrocarbons linked to natural gas and fuel evaporation become well mixed into the Arctic in the winter, whereas combustion products show a latitudinal gradient. The sum of oxygenated species constitutes about 5–15% of the sum of C2–C5 hydrocarbons in winter. In summer they are almost equal in magnitude, consistent with an increasing oxidation of hydrocarbons.  相似文献   

11.
基于2008年9月—2010年9月河北固城生态与农业气象试验站多轴差分吸收光谱仪 (multi-axis differential optical absorption spectroscopy, MAX-DOAS) 获得的太阳散射光谱观测,反演计算该地区NO2对流层柱浓度,分析其季节、日变化特征以及不同来源输送的影响,并与同期NO2地面观测资料和卫星产品进行对比分析。发现固城站NO2对流层柱浓度冬高 (5.14×1016 cm-2) 夏低 (1.28×1016 cm-2);日变化形态在四季均呈现中午低、傍晚高的特征,且冬季最明显。与北京城市区域同期的观测相比,冬季固城站观测值略低,而在春、夏季则偏低较显著。地面风玫瑰图分析显示,来自SW, SSW, NE方向及ENE方向的污染输送对其贡献最大。与地面、卫星NO2观测的对比表明,MAX-DOAS反演的NO2柱浓度与地面观测浓度具有一致的季节和日变化特征,卫星反演的NO2对流层柱浓度产品在华北平原农村地区存在系统性低估。  相似文献   

12.
从描述南、北半球间大气经向质量传输的角度人手,考察IPCC第4次评估报告提供的8个AMIP大气环流模式对越赤道质量通量输送的模拟性能。结果表明:NCAR、MPI和UKMO模式模拟出的越赤道整层大气质量通量与观测大体相一致;MIROC3模拟的整层大气质量通量年循环与观测结果相去甚远,尤其在夏季模拟出较强的虚假向北大气质量输送;IAP模拟的整层大气质量通量年循环方向与观测结果在7个月份中相反;把垂直大气分为4层.各模式对700 hPa以下(I_1)和300-70 hPa(I_3)两层质量通量的模拟能力普遍较好;对700-300 hPa层(I_2)质量通量模拟结果偏差较大;除MIROC3外,其余模式基本能够模拟出70-10 hPa(I_4)大气质量通量的季节变化.显然,不仅南、北半球间大气存在质量交换,越过其他纬度同样存在着经向大气质量输送,无论冬季、夏季还是年平均,各模式对越过其他纬度(60°S-60°N)经向大气质量输送的模拟结果与观测差异明显。整体权衡,UKMO_HADGEMl在模拟越赤道大气质量通量方面表现突出,MPI_ECHAM5模式优势较明显;NCAR、GISS和GFDL 3个模式在某些压力层内具有较好的模拟水平;MIROC模式对整层、700-300 hPa层的模拟能力较低,而对700 hPa以下层和300-70 hPa层的模拟水平较高;IAP_FGOALS和CNRM模式在模拟越赤道大气质量通量方面存在一定的不足.  相似文献   

13.
Summary Atmospheric ozone concentrations have been monitored at a subalpine forest ecosystem site, 3180m above mean sea level (msl), and at a 2680m msl forest-steppe ecotone site 15km to the southeast. Ozone concentrations were monitored at three heights above the ground on a 30m tower at the higher elevation site, and on a 10m tower in a large meadow downwind of this site.The research reported here concentrates on the data for the first six months of 1990–1994. The diel amplitude of ozone concentrations is very small in winter, increasing as the seasons advance to June. Following snowmelt in late May or June, the nighttime minima decrease under the forest canopy. The highest monthly mean ozone concentrations occur in April or May, depending on the year. Episodal high concentrations were recorded during spring months when upper level atmospheric low pressure troughs and cut-off low centers occurred. These contributions peak in May, and add about 10% to normal May background ozone concentrations, varying widely from year to year. Spectral representations of ozone concentrations, illustrate the suppression of the diel peak during spring months, when stratospheric-tropospheric intrusion patterns show no significant diel cycle.With 9 Figures  相似文献   

14.
近60a来洞庭湖区气温的变化特征   总被引：2，自引：1，他引：1  
以洞庭湖区24个气象站1952-2010年的平均气温资料为基础,利用气候倾向率、Mann-Kendall突变检验法和小波分析等方法,分析了洞庭湖区的气温变化特征.结果表明:洞庭湖区年平均、冬季、春季和秋季气温均呈显著上升趋势,增温速率尤以冬季和春季为甚.除夏季外,年平均和其他各季气温在1990s,先后发生增温性突变.高温日数呈上升趋势,但显著性不明显,低温日数下降趋势非常显著.除夏季外,年平均和各季异常冷年,基本出现在1950s至1970s,异常暖年,均出现在1998年以后.除夏季外,各季气温均存在准9a周期.  相似文献   

15.
Outputs from a high-resolution data assimilation system,the global Hybrid Coordinate Ocean Model and Navy Coupled Ocean Data Assimilation （HYCOM＋NCODA） 1/12° analysis,were analyzed for the period September 2008 to February 2012.The objectives were to evaluate the performance of the system in simulating ocean circulation in the tropical northwestern Pacific and to examine the seasonal to interannual variations of the western boundary currents.The HYCOM assimilation compares well with altimetry observations and mooring current measurements.The mean structures and standard deviations of velocities of the North Equatorial Current （NEC）,Mindanao Current （MC） and Kuroshio Current （KC） also compare well with previous observations.Seasonal to interannual variations of the NEC transport volume are closely correlated with the MC transport volume,instead of that of the KC.The NEC and MC transport volumes mainly show well-defined annual cycles,with their maxima in spring and minima in fall,and are closely related to the circulation changes in the Mindanao Dome （MD） region.In seasons of transport maxima,the MD region experiences negative SSH anomalies and a cyclonic gyre anomaly,and in seasons of transport minima the situation is reversed.The sea surface NEC bifurcation latitude （NBL） in the HYCOM assimilation also agrees well with altimetry observations.In 2009,the NBL shows an annual cycle similar to previous studies,reaching its southernmost position in summer and its northernmost position in winter.In 2010 and 2011,the NBL variations are dominantly influenced by La Ni（n）a events.The dynamics responsible for the seasonal to interannual variations of the NEC-MC-KC current system are also discussed.  相似文献   

16.
Photochemical box modelling was undertaken to investigate OH and HO2 radical chemistry during summer and winter field campaigns in the urban city-centre of Birmingham in the UK. The model employed the most recent version of the Master Chemical Mechanism (v3.1) and was constrained to 15-minute average measurements of long-lived species determined in situ at the site. The model was used to predict OH and HO2 concentrations for comparison with measurements made by the fluorescence assay by gas expansion technique. Whilst there was generally good agreement between the modelled and measured OH concentrations, particularly during summer, there was sometimes a significant model under-prediction during daylight hours, which significantly skews the overall model: measured agreement. There were less measured data available for HO2, but the agreement between model and measurement for the days where measurements existed were less good than for OH, with one or two exceptions. The modelled:measured ratios between the hours of 11:00–15:00 h for OH were 0.58 and 0.50 for summer and winter respectively. For HO2, the same ratios were 0.56 in the summer and 0.49 in the winter. Sensitivity studies were conducted to attempt to understand the model-measurement discrepancy. The predicted radical concentrations were particularly sensitive to changes in NOX concentrations. Constraining the model to the observed HO2 concentrations made the OH predictions worse. These results highlight the fact that there are many complexities in urban areas and that more highly-instrumented campaigns are required in the future to further our understanding.  相似文献   

17.
Formic and acetic acid measured as daily averages in 1993–1994show equal and highly correlated concentrations up to 3 ppb in the summer(May–August). In the winter (October–March) the formicacid/acetic acid ratio was 0.6 and the formic acid concentrations wereusually below 1 ppb. In winter the carboxylic acids correlate withOx, NOy, SO2 and particulatesulphur. The main sources are suggested to be ozonolysis of anthropogenicalkenes and reactions between peroxyacetyl radicals and RO2radicals. In spring–summer the carboxylic acids correlate withO3, Ox, HNO3, PAN,NOy, SO2, particulate sulphur and temperature.In addition to the sources of the winter a contribution from ozonolysis ofbiogenic alkenes is likely. Quite similar formic acid/acetic acid ratios forall wind directions suggest that the source(s) are atmospheric oxidationprocesses distributed over large areas. The highest concentrations occurringfor winds from east to south and the correlation with e.g., particulatesulphur indicate chemical production in polluted air masses during longrange transport.  相似文献   

18.
Ambient particulate sulfate measurements have been intermittently performed at a rural site in Israel over a period of more than two years. Concurrent measurements of ambient pollutants (SO2, NO–NOx, and O3), as well as meteorological data, were also carried out. The daily data included four particulate sulfate samples representing four successive 6 h accumulating periods. The measured concentrations of sulfate ions ranged from a low 2 g m-3 observed during the winter season to a high of >50 g m-3 obtained during the summer. Little correlation was obtained between the sulfate concentration and either O3 or SO2, although sulfate and O3 showed a similar diurnal and annual trend. Based on the data distribution and on a photochemical model, it was concluded that a large part of the particulate sulfate observed at the eastern coast of the Mediterranean Sea must be related to long-range transport from distant sources.  相似文献   

19.
Meridional cross sections of the concentration of light hydrocarbons are reported. They were obtained from 20. April to 10. May, 1980, during the French research flight STRATOZ II, and cover the latitudes between 60° N and 60° S and the altitudes between 800 mb and 200 mb. The mixing ratios of ethane, ethene, acetylene, propane, propene, n-butane, i-butane, n-pentane, and i-pentane range between 2.0 and 0.02 ppb. Globally, a decrease in concentration with increasing altitude and -in most cases-with decreasing latitude is observed. In addition the 2-dimensional concentration fields show structures of different scales. In particular, isolated maxima of high concentrations are found in the upper troposphere. They point to fast vertical transport between the boundary layer and the upper troposphere. In the present case these maxima seem to be correlated with large scale meteorological systems, such as low pressure regions or the Inter Tropical Convergence Zone. It is argued that the NMHC provide a set of tracers well suited to the detection of fast vertical transport.  相似文献   

20.
Long-term measurements of light hydrocarbons(C2–C5 HCs) were performed in the courseof the EUROTRAC sub-project TOR (Tropospheric Ozone Research) in thesouthern part of the Black Forest in southwest Germany. The measurementscover a time period of five years (January 1989–January 1994) and theair samples were analyzed onsite by an automated GC-system. Pronouncedannual cycles with maxima in late winter and minima in late summer wereobserved in the case of the slowly reacting hydrocarbons ethane, propane andacetylene, reflecting the fact that the seasonal variation of these speciesis photochemically driven. For the shorter lived compounds the seasonalvariations are considerably weaker, connected with a stronger scatter of theindividual measurements, which is caused by different distances to theirmain sources for different wind vectors as well as by varying sourcestrengths. From a detailed characterization of the hydrocarbon patterns theinfluence of two different sources could be distinguished. An extrapolationto photochemical age of zero and completion of our data with those from aspeciated VOC inventory yields an estimated [VOC]/NOx sourceratio for Schauinsland of 5 [ppbC/ppb]. Comparable[VOC]/NOx ratios are observed in automobile exhaust gasesunder low speed conditions, which points to the important role of trafficunder conditions, when freshly polluted air masses from a near-by city areadvected to the site. From an investigation of the photochemical age of theadvected air masses it becomes clear that there must exist biogenic sourcesof light olefins in the vicinity of the observatory during the vegetationperiod. For propene and the butenes we are able to estimate a lower limit oftheir contributions in terms of reactivity to the total reactivity( [HC](i) k_OH(i),i=C2-C5) of the measured hydrocarbons. Forlowest pollution levels in summer (acetylene <300 ppt, about 40%of the summer values) this source is found to be responsible for15–20% of the total C2–C5reactivity observed at Schauinsland. On the average, this source accountsfor 5–10% of the total C2–C5reactivity.  相似文献   

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