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1.
Deposition of atmospheric mineral particles in the North Pacific Ocean   总被引：5，自引：0，他引：5  
Total deposition of atmospheric mineral particles (wet plus dry) has been measured during consecutive two-week sampling intervals from January, 1981 to March, 1982 at four island stations (Midway, Oahu, Enewetak, and Fanning) of the SEAREX Asian Dust Study Network in the North Pacific. The total deposition of mineral aerosol during the period from February to June is higher than that during the period from July to January at most of the stations. A systematic geographical trend is apparent in the dust flux, with greater fluxes at higher latitudes. The deposition values are correlated with the atmospheric mineral particle concentrations at these stations. The mineral particles are transported from arid regions in Asia to the North Pacific, and the annual dust deposition to the ocean appears to be dominated by sporadic dust events of short duration. Wet deposition dominates the removal of dust particles from the atmosphere over the North Pacific. The total deposition of atmospheric mineral material to the central North Pacific is estimated to be 20×1012 g yr-1.  相似文献   

2.
Wet-only, dry-only, bulk deposition and deposition of sedimentary particles and gases deposited after the last rain (DAR) were collected weekly at La Castanya station in the Montseny mountains (NE Spain, 41°46′N, 2°21′E) from February 2009 to July 2010. These samples were analysed for pH, alkalinity, and the concentrations of major ions (Cl?, NO3 ?, SO4 2?, Na+, K+, Ca2+, Mg2+, NH4 +). Significant differences were observed between bulk and wet-only precipitation, with an enrichment of ions associated to coarse particles in bulk deposition. The comparison between wet and dry fluxes revealed that the removal of compounds at Montseny occurred mainly by wet deposition, which accounted for 74 % of total deposition. The dry flux was characterised by the predominance of K+, Ca2+ and Mg2+, which are related to coarse particles. Bulk collection methods at Montseny were considered representative of total atmospheric deposition, since bulk deposition plus DAR accounted for 97 % of total deposition measured with wet and dry-only collection devices. Thus, bulk deposition collectors can be recommended for deposition networks at remote sites (lacking electricity connection) in environments, where coarse particles are a predominant fraction of the aerosol mass.  相似文献   

3.

The present study comprehensively reports the simultaneous measurement of wet deposition of total inorganic nitrogen (TIN; which is the sum of the NH4+-N and NO3?-N) at three different sites in Nr emission hotspot of Indo-Gangetic plain (IGP) over a year-long temporal scale from October 2017 to September 2018. At rural Meetli (MTL) site, urban Baraut (BRT) site and industrial Loni (LNI) site, the annual wet deposition of NH4+-N was estimated as 21.87, 19.48 and 7.43 kg N ha?1 yr?1, respectively; the annual wet deposition NO3?-N was estimated as 12.96, 12.17 and 4.44 kg N ha?1 yr?1, respectively; and the annual wet deposition of TIN was estimated as 34.83, 31.64 and 11.87 kg N ha?1 yr?1, respectively. NH4+-N was dominantly contributing species in annual, monsoon and non-monsoon-time wet deposition of TIN at all sites. The spatial gradient (variability) in percent contribution of NH4+ to total annual volume-weighted mean (VWM) concentration of all analyte ions was observed as MTL (43.23%)?>?BRT (37.90%)?>?LNI (30%). On the other hand, the spatial gradient in percent contribution of NO3? to total annual VWM concentration of all analyte ions was observed as MTL (7.45%)?>?BRT (6.89%)?>?LNI (5.32%). The extremely narrow range of NH4+-N/NO3?-N ratios (ranging from 1.60 at BRT site to 1.69 at LNI site) showed the approximately equal relative abundance of oxidized and reduced nitrogen (N) deposition across all sites. Inferences from enrichment factor analysis, principal component analysis and Pearson’s correlation coefficient analysis suggested that across all sites, virtually all NH4+-N and NO3?-N depositions were originated anthropogenically. The annual wet deposition of TIN measured in this study showed?≥?6865%,?≥?6228% and?≥?2274% increment than the natural N deposition rate at MTL, BRT and LNI site, respectively. These empirically measured annual wet depositions of TIN also emanated theoretical transgression of critical N load threshold across all sites therefore signifying probable undermining of long-term elastic stability and resilience of ecosystems against stressor in the study domain.

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4.
Total sulfur deposition was determined above a Norway spruce forest, in Hungary. Two methods were applied, on one hand dry + wet deposition measurements and on the other, throughfall and stemflow deposition estimations have been carried out. Results show: total depositions are 3.3 and 3.2 g S m–2 yr–1 determined by dry + wet and throughfall deposition methods, respectively. The share of the dry deposition in the total S-load is 73%. The agreement between the results of the two different methods is good and suggests the needlessness of complicated dry + wet flux measurements, i.e. the total and dry deposition of sulfur compounds to forests can be determined by simple throughfall and wet deposition measurements.  相似文献   

5.
Concentrations of manganese in 56 rain events in Wilmington, NC, USA rainwater from April 1, 2005 to March 31, 2006 were 11 ± 3 nM for dissolved Mn and 1.2 ± 0.4 nM for particulate Mn. Concentrations of both forms of Mn were higher in terrestrial storms relative to marine events. This observation along with the positive correlation of Mn with pollutant indicators suggests anthropogenic inputs to rain at this location, as has been observed at other locations. The ratio of Mnpart/Mndiss was threefold larger in summer relative to winter rain, which matched the increase of particulate to dissolved Fe in rainwater suggesting influence of Saharan dust during the summer. Like Fe in rain, Mn undergoes photoreduction in rainwater, which has also been shown to be important in Mn cycling in seawater. The flux of Mn removed from the atmosphere via wet deposition is 1.5 × 10−5 moles m−2 yr−1 at this location, which is approximately twice the flux reported from two rainwater studies conducted in the early 1980s on Bermuda. Atmospheric input of Mn to the oceans is important because Mn like Fe is an essential and potentially limiting nutrient. Experiments mixing authentic rainwater and seawater demonstrate that rainwater dissolved Mn does not rapidly precipitate in seawater suggesting wet deposition is an important source of soluble, stable Mn to surface seawater.  相似文献   

6.
The inorganic chemical composition (major ions and trace metals) of bulk deposition samples collected monthly with bulk collectors at seven Atlantic Coastal European cities (Galicia, Northwest of Spain) during wet season (September 2011 to March 2012) has been assessed and compared. Trace metals (Al, As, Ba, Co, Cr, Cu, Fe, Mn, Ni, Pb, Sr, V and Zn) were analysed in soluble fraction and non-soluble fraction (after acid extraction) of the bulk deposition by inductively coupled plasma-mass spectrometry. Major inorganic ions (Cl?, NO3 ?, SO4 2?, Na+, K+, Ca2+, Mg2+ and NH4 +) were analysed in the soluble fraction of the bulk deposition by capillary zone electrophoresis. Univariate analysis (ANOVA and Multiple Range Test) according to the location of each sampling site was performed. Results also suggest a great influence of cleaner Atlantic air masses. After partition coefficients and enrichment factor estimation, similar sources could be assigned for the ionic and metal composition of bulk deposition at seven urban sites.  相似文献   

7.
The spatial variability and temporal behavior of the vertical flux of ozone have been investigated from turbulence measurements collected on aircraft flight legs in the daytime period during two consecutive summer experimental field programs. The data were obtained during horizontal flight legs conducted over agricultural crops and forested land in three different regions of the eastern United States.Results from individual experimental cases and statistics derived from all cases in each region are presented. Ozone flux generally exhibited a significant height dependency. The strongest negative (downward) fluxes in the lowest-level flight legs were primarily attributed to the uptake of ozone by the surface and vegetative cover. Fluxes were near-zero in the middle of the convective boundary layer (CBL) in the afternoon period. As ozone flux was proportional to concentration, slightly stronger fluxes were found in low-level urban plume segments where ozone concentrations were 10–20 ppb higher than in the surrounding area. The derived deposition velocity showed no such bias as a function of position across the urban plume. Ozone flux differences were not apparent between the more heavily forested sections and the primarily agricultural cropland areas in these regions. During the afternoon period when no clear temporal trend was evident, means from values obtained below 0.15Z i (Z i being the CBL height) were -0.421 and -0.431 ppb m-2 s-1 for ozone flux and 0.81 and 0.82 cm s-1 for the derived mean deposition velocity in the southeastern Pennsylvania and central Ohio areas, respectively. These experimental results for ozone provide support to a dry deposition parameterization module which computes grid-area averaged deposition velocities for use in regional-scale models.On assignment from the National Oceanic and Atmospheric Administration, U.S. Department of Commerce.  相似文献   

8.
Cloud events whose wet deposition is comparable to that shown to trigger negative health symptoms in trees constitute environmentally significant episodes of wet deposition. They accounted for approximately one fourth of all cloud events that traversed the Mt. Mitchell State Park, NC, during the summer field seasons of 1986–1988 and 1993. The environmentally significant episodes of wet deposition most frequently occurred during the month of June. The June occurrence is equivalent to the frequency of acid mist treatments shown to initiate health related decline in Red Spruce. The slightly more than three seasons of data were analyzed for a possible relationship between cloudwater acidity, liquid water content, wind speed and wind direction. The data analysis shows: (i) A scatter plot of the liquid water flux versus the H+ ion flux differentiates between environmentally significant and non-environmentally significant cloud events of wet deposition. (ii) The synoptic and resulting local wind speed and direction are important in determining whether a cloud event will be environmentally significant or not, since they are related to the origin and the approach of the airflow into the Mt. Mitchell site. (iii) A characteristic 850 mb height field associated with the most frequently occurring environmentally significant cloud only event of wet deposition. Further investigation of wet acidic deposition episodes capable of damaging Red Spruce in the Mt. Mitchell State Park  相似文献   

9.
Throughfall (TF) and wet only (WO) deposition along with SO2 and sulfate (SO42−) concentration in air at 4 urban and rural sites in southwestern China were monitored in order to understand the role of different forms of sulfur (S) emission to the S deposition and its effect in China. The sites were located in Chongqing, Hunan, and Guizhou provinces. S deposition at the most polluted site reached 15 g S m− 2 yr− 1. At three of the sites, located in the vicinity of several emission sources, dry S deposition is 2.1–4.2 times that of wet deposition, which is significantly higher than what is found in most other parts of the world.Main components in airborne particles (PM10) are (NH4)2SO4 and CaSO4 at the highly polluted Tie Shan Ping (TSP) site. Dust particles of gypsum (CaSO4) in the air are partly due to direct emission and partly from the reaction of calcium oxides and carbonates with sulfuric acid in the air. To illustrate the importance of sulfate emission to total S deposition we analyzed the source of S deposition based on both measurements and models. Results indicated that direct emission of SO42− particles could account for high proportion in total S deposition at the three most polluted sites.  相似文献   

10.
Concentrations of natural 7Be in air and rainwater were monitored for one year at Hokitika, New Zealand. The mean airborne concentration was 3.1±1.3 mBq m–3, the mean Hokitika, New Zealand. The mean airborne concentration was 3.1±1.3 mBq m–3, the mean concentration in rainwater was 2600±1200 Bq m–3, and the mean total deposition was estimated to be 130±99 Bq m–2 wk–1. Most of the 7Be was wet deposited and the washout ratio was independent of precipitation amount. A significant linear relationship exists between the weekly wet deposition flux and weekly precipitation at this high-rainfall site.  相似文献   

11.
Chemical compositions of precipitation samples collected from a remote and high elevation site (Nam Co Station, 30°46.44??N, 90°59.31??E, 4730?m?a.s.l.) in central Tibetan Plateau (TP, hereafter) from August 2005 to August 2009 are investigated. During the study period, Ca2+ and HCO 3 - have the highest concentrations among ions and are the dominant cation and anion in precipitation, taking 27.46?% and 30.84?% to the total ions respectively. Empirical Orthogonal Functions (EOFs) analyses reveal that crustal aerosol inputs significantly contributed to the loading of Ca2+, Mg2+, SO 4 2- and HCO 3 - in precipitation, while lake salt plays a major source of K+ and Cl-. Seasonal variations of ionic wet deposition fluxes show high values during monsoon seasons due to large precipitation amount. Among the cations, annual Ca2+ flux is the largest (86.26?eq hm?2), Na+ and NH 4 + fluxes are following. Among anions, HCO 3 - has the highest flux (98.66?eq hm?2) while that of NO 3 - is the lowest. Annual wet deposition of nitrogen has varied considerably with the average value of 0.70?kg?ha?1 a?1 at Nam Co Station. About 80?% of total nitrogen flux occurs during the monsoon seasons when precipitation is concentrated, in which NH 4 + and NO 3 - contributed to 61?% and 39?% of the total nitrogen deposition. Thus, our ionic concentrations and wet deposition fluxes in precipitation can provide a useful dataset to assess atmospheric environment and its impacts on ecosystem in the inland TP.  相似文献   

12.
In 1978–1980 nine aircraft flights to an altitude of up to 15 km were made over western Europe. Sulfur dioxide was measured with a sensitive chemiluminescence method consisting of separate sampling and analysis stages and application of a wet chemical filter procedure (detection limit: 8 pptv SO2).The measurements performed in the upper troposphere and lower stratosphere lead to some unexpected results: (a) the meteorological conditions at the tropopause level have an important influence on the observed SO2 mixing ratio; (b) between the 500 mb and the actual tropopause level the SO2 mixing ratio is found to be <100 pptv, and weak vertical gradients of SO2 suggest only a small flux of tropospheric SO2 into the stratosphere; (c) increasing SO2 mixing ratios within the first kilometers of the stratosphere give strong support to a stratospheric source of SO2.In the light of improved one-dimensional models considering the vertical distribution of stratospheric sulfur compounds (Crutzen, 1981; Turco et al. 1981) it can be shown that the oxidation of organic sulfur compounds (e.g., OCS, CS2) seems to be a stratospheric source of SO2. Furthermore, the flux calculations based on the SO2 mixing ratios measured at the tropopause level indicate that the contribution of tropospheric (man-made) SO2 to the stratospheric aerosol layer is of only minor importance.  相似文献   

13.
Changes in the frequency of precipitation as a result of a changing climate, as well as anthropogenic induced deposition of nitrogen (N), both have the potential to alter grassland productivity and diversity. Central U.S. weather patterns are dominated by three major air mass trajectories including regional sources from the Gulf of Mexico (marine tropical, Mt), the Pacific Northwest (mild pacific, mP), and the Desert Southwest (continental tropical, Ct). In this work, the Hybrid Single Particle Lagrangian Integrated Trajectory model was used to determine trends in the proportion of precipitation events from these air mass sources from 1983 to 2006 relative to Konza Prairie Biological Station (KPBS), KS. The annual volume-weighted mean (VWM) concentrations and wet deposition of a variety of precipitation dissolved solutes were linked to source regions north or south of KPBS. The proportion of precipitation events from Mt significantly increased, while the proportion of events from Ct and mP decreased significantly over the study period. The annual VWM concentrations of most solutes were typically higher from precipitation sourced to the north of KPBS. However, wet deposition of four ecologically relevant solutes (NH4+, NO3?, H+, and SO4?2) was higher from events from the southern region, likely due to higher precipitation amounts. The proportion of reduced N increased significantly over the study period but was not affected by source region despite the higher use of fertilizers for agriculture in the northern source region. Given the location of this site relative to three dominant air mass paths, future shifts in these patterns will likely impact wet nutrient deposition.  相似文献   

14.
Summary Because of the obvious importance of aerosols for atmospheric modelling, an aerosol module has been developed as part of the European Acid Deposition Model (EURAD). The chemical and physical processes have been restricted to the sulfate-nitrate-ammonia system to study the influence of aerosols on acid deposition. Special consideration is given to the reversible formation process ofNH 4 NO 3 aerosols and the influence of the dissociation constant on the aerosol and gas phase concentrations. This component appears to be important in particular for regions where large ammonia emissions are found as in Europe.Concentration and deposition fields as predicted by EURAD are analysed for a simulation with and without the new aerosol module. Due to their smaller dry deposition velocities in the aerosol phase, the amount of nitrogen species in air is larger and the spatial distribution is considerably different if aerosols are taken into account. On the other hand wet deposition of nitrogen is enhanced due to the presence of easily soluble ammonium nitrate aerosols.A comparison with observations from the EMEP network has been conducted to evaluate the performance of the aerosol module. Modelling with the aerosol phase leads to a much better agreement between modelled and measured concentration fields.With 12 Figures  相似文献   

15.
Deposition of atmospheric particulate PCBs in suburban site of Turkey   总被引：2，自引：1，他引：2  
Dry deposition and air concentration samples were collected from July 2004 to May 2005 at a suburban site in Turkey. A water surface sampler (WSS) was used to measure directly the dry deposition flux of particulate polychlorinated biphenyls (PCBs) while a high volume air sampler (HVAS) was employed to collect air samples. Particulate PCB concentrations accounted for 15% of total PCBs (gas + particle phase) at the site. The overall particulate phase PCB flux ranged from 2 to 160 ng m− 2 d− 1 with an average of 46.3 ± 40.6 ng m− 2 d− 1. Forty one PCB congeners were targeted in the samples while twenty one congeners were found to be higher than detection limits in deposition samples. Fluxes for homolog groups ranged between 0.9 (7-CBs) and 21.0 (3-CBs) ng m− 2 d− 1. Measured dry deposition fluxes were lower than the ones usually reported for urban sites. Average PCB dry deposition velocity, calculated using flux values and concurrently measured atmospheric concentrations, was 1.26 ± 1.86 cm s− 1 depended on size distribution of particles, atmospheric PCB concentrations and meteorological conditions.  相似文献   

16.
Abstract

A 30‐year record (1951–1980) of surface heat fluxes at Ocean Weather Station P in the northeastern Pacific Ocean (50°N, 145°W) was examined for differences in the interdecadal variation between fail and winter. During the latter part of the 1950s and the early 1960s, the winter surface heat flux from the ocean to the atmosphere diminished significantly whereas the fall heat flux increased slightly This difference in the modulation of the winter heat flux from the fall heat flux during this period appears to be caused by the presence of an atmospheric circulation anomaly resembling that of the Pacific/North America (PNA) low‐frequency variability mode during the winter season.  相似文献   

17.
In this study, turbulent heat flux data from two sites within the Baltic Sea are compared with estimates from two models. The main focus is on the latent heat flux. The measuring sites are located on small islands close to the islands of Bornholm and Gotland. Both sites have a wide wind direction sector with undisturbed over-water fetch. Mean parameters and direct fluxes were measured on masts during May to December 1998.The two models used in this study are the regional-scale atmospheric model HIRLAM and the ocean model PROBE-Baltic. It is shown that both models overestimate the sensible and latent heat fluxes. The overestimation can, to a large extent, be explained by errors in the air-water temperature and humidity differences. From comparing observed and modelled data, the estimated 8-month mean errors in temperature and humidity are up to 1 °C and 1 g kg-1, respectively. The mean errors in the sensible and latent heat fluxes for the same period are approximately 15 and 30 W m-2, respectively.Bulk transfer coefficients used for calculating heat and humidity fluxes at the surface were shown to agree rather well with the measurements, at least for the unstable data. For stable stratification, the scatter in data is generally large, and it appears that the bulk formulation chosen overestimates turbulent heat fluxes.  相似文献   

18.
The deposition fluxes of inorganic compounds dissolved in fog and rain were quantified for two different ecosystems in Europe. The fogwater deposition fluxes were measured by employing the eddy covariance method. The site in Switzerland that lies within an agricultural area surrounded by the Jura mountains and the Alps is often exposed to radiation fog. At the German mountain forest ecosystem, on the other hand, advection fog occurs most frequently. At the Swiss site, fogwater deposition fluxes of the dominant components SO42− (0.027 mg S m−2 day−1), NO3− (0.030 mg N m−2 day−1) and NH4+ (0.060 mg N m−2 day−1) were estimated to be <5% of the measured wet deposition (0.85, 0.70 and 1.34 mg m−2 day−1, respectively). The corresponding fluxes at the forest site (0.62, 0.82 and 1.16 mg m−2 day−1, respectively) were of the same order of magnitude as wet deposition (1.04, 1.01 and 1.36 mg m−2 day−1), illustrating the importance of fog (or occult) deposition. Trajectory analyses at the forest site indicate significantly higher fogwater concentrations of all major ions if air originated from the east (i.e. the Czech Republic), which is in close agreement with earlier studies.  相似文献   

19.
北京325米气象塔上CO2梯度观测数据质量控制与评价   总被引：2，自引：1，他引：1  
近些年涡度相关系统在城市通量研究中得到了广泛应用,因城市下垫面的特殊性和复杂性,以及系统观测原理和仪器精度存在着局限性,使得结果存在10%以上偏差,故必须对原始观测数据进行质量控制和评价。本文对北京325 m气象塔七层高度上的CO2(二氧化碳)、能量等通量进行了长期观测,研究了涡度相关技术在城市环境通量观测中的适用性,设计出了一套适合于复杂城市下垫面上的涡度相关系统资料前处理和质量控制方案,并对比了不同修正方案效果。分析结果表明,城市下垫面环境中计算CO2通量的最优周期为30 min;二次坐标旋转法优于平面拟合法;频率响应修正后的感热通量提高5.21%,潜热通量和CO2通量均提高9.42%。空气密度脉动修正Liu法(Liu,2005)优于WPL法(Webb et al.,1980);湍流谱在惯性副区满足-2/3次方定律,协方差谱满足-4/3次方定律。经过这套前处理和质量控制方案,原始数据中有79%能够用于基础研究,该质量控制与评价体系可为复杂城市下垫面通量研究提供参考。  相似文献   

20.
Ammonia has a short residence time in the atmosphere and rapidly neutralizes acid gases that occur near its source, requiring a rapid measurement system for ammonia and particulate ammonium concentrations to better understand their sources, temporal variation of ammonia emissions, and the formation of secondary ammonium aerosols. A semi-continuous measurement system, consisting of a diffusion scrubber, a particle growth chamber, an air-liquid separator, and a fluorescent detector, was developed to determine both gaseous ammonia (NH3) and particulate ammonium (NH 4 + ) in PM2.5 in the ambient atmosphere of Gwangju, South Korea, during the months of March, April, July, and September of 2007. During the sampling periods, the average concentrations of ammonia and ammonium were found to be 2.33?±?1.29 μg/m3 and 1.89?±?0.99 μg/m3, respectively. Although the average gaseous ammonia concentration was highest in March, the particulate ammonium concentration was higher during the warmer season, reaching 2.08?±?1.07 μg/m3 and 2.32?±?0.94 μg/m3 in April and July, respectively, while only 1.68?±?0.61 μg/m3 in March and 1.24?±?0.99 μg/m3 in September. It is proposed that the higher availability of acid species during the warmer months produced a significant amount of particulate ammonium sulfate. Diurnal fluctuation of ammonia and ammonium during the warmer months showed that their peak time occurred at approximately 10:00 am. Both ammonia and ammonium concentrations were better correlated during the warmer months than during the cooler months. Further, the data suggest that the ammonia and ammonium were measured under well dispersed conditions, and multiple sources contributed to the ammonia at the sampling site.  相似文献   

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