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1.
Haze and fog are both low visibility events, but with different physical properties. Haze is caused by the increase of aerosol loading or the hygroscopic growth of aerosol at high relative humidity, whereas visibility degradation in fog is due to the light scattering of fog droplets, which are transited from aerosols via activation. Based on the difference of physical properties between haze and fog, this study presents a novel method to distinguish haze and fog using real time measurements of PM2.5, visibility, and relative humidity. In this method, a criterion can be developed based on the local historical data of particle number size distributions and aerosol hygroscopicity. Low visibility events can be classified into haze and fog according to this criterion.  相似文献   

2.
In-situ measurements of number density, size distribution, and mass loading of near-surface aerosols were carried out at Kharagpur, a site on the eastern part of Indo-Gangetic Plains during the winter month of December 2004. The data have been used to investigate wintertime characteristics of aerosols and their effects on the occurrence of haze. The aerosol number density is found to be of the order of 109 m?3 and mass loading is ~265±70 μg m?3 (5–8 times that reported from south Indian sites). The diurnal patterns and day-to-day variations in aerosol number density and mass loading are closely associated with atmospheric boundary layer height. During haze events, the number density of submicron particles is found to be 2–5 times higher than that during non-hazy period. This could be attributed to the enhanced concentration of anthropogenic aerosols, low atmospheric boundary layer height/ventilation coefficient and airflow convergence.  相似文献   

3.
During a study of the growth of cloud drops by condensation the evolution of cloud drop size spectra with height above cloud base was determined for maritime aerosols, and for continental aerosols containing aerosol particles of mixed composition. Air parcel models were used in which the parcel was either completely closed to mass and heat transfer (strictly adiabatic models), or open to heat transfer and to partial or complete mass transfer (entrainment models). It was found that adiabatic models and models which consider the entraining of air devoid of aerosol particles predict drop size distributions which are considerably narrower than those observed in non-precipitating cumulus clouds, and have only a single maximum. On the other hand, relative broad drop size distributions and distributions with a double maximum — as they are observed in atmospheric clouds — are predicted if the entrainment of both air and aerosol particles are considered in the condensation model. Our results support the findings ofWarner (1973) which were obtained for a purely maritime aerosol.  相似文献   

4.
Summary An analytical method for determining the size distribution of polydisperse submicron aerosols are described. It is shown that we can determine approximately the size distribution function analyzingZ(Q) (dependence of the aerosol concentration at the exit of a diffusion battery upon the flow rate) by a iterative technique using response matrixes. Numerical experiments were carried out to evaluate the practical application and limitations of this technique, and the technique was found to be useful itZ(Q) may be determined within the errors of about ±5 percents. Practical measurements of atmospheric submicron aerosols were made on the university campus and some examples of the size distributions of aerosols determined by this method were shown.  相似文献   

5.
Recent results from the real time analysis of individual aerosol particles by laser mass spectrometry have revived interest in the inverted micelle structure for aerosols containing organic molecules; indeed for many aerosols the organic content is high enough, for example 50% by mass in the tropical upper troposphere, that it is likely to be the only viable structure. It is pointed out that atmospheric aerosols would have had many advantages as prebiotic chemical reactors, having the potential to address several key problems in a way arising naturally from the probable geophysical and chemical environment on the prebiotic planet. Bacterial and viral size can be predicted for these structures by an equation combining atmospheric aerodynamics and gravity, and which is therefore applicable to other astronomical objects which are candidates for supporting life. Experimental tests and mathematical modelling of the early stages of the chemical evolution of aerosols should be possible.  相似文献   

6.
Summary The paper focuses on the applicability of simple optimizing methods to determining the aerosol structure based on the measured values of the spectral optical thickness of aerosol δ(λ). The necessary conditions leading to a stable solution are assessed. By applying the particle distribution function in the form of summations of modified gamma functions we obtain the simple form of δ(λ). It is not suitable for proving Gaussian functions. The application of approximate methods to determine the aerosol structure from spectral optical thickness of atmospheric aerosol is based on measurements of the direct spectral solar radiation flux density which formed a part of the radiation experiment conducted in Zingst (Germany) on the coast of the Baltic Sea in 1987. on leave from the Astronomical Institute, Slovak Academy of Sciences  相似文献   

7.
Agriculture crop residue burning in tropics is an important source of atmospheric aerosols and monitoring their long-range transport is an important element in climate change studies. Synchronous measurements using micro-pulsed lidar, MICROTOPS-II sun photometer, multi-filter rotating shadow band radiometer (MFRSR) on aerosol optical depth and ground reaching solar irradiance were carried at an urban location in central region of India. Aerosol backscatter profiles obtained from micro-pulse lidar showed elevated aerosol layers up to ～3 km on certain days during October 2007. Satellite data observations on aerosol properties suggested transport of particles from agriculture crop residue burning in Indo-Gangetic Plains over large regions. Radiative forcing of aerosols estimated from SBDART model with input information on aerosol chemical properties, aerosol optical depth and single scattering albedo and broadband solar irradiance measurements using MFRSR showed good correlation (R=0.98).  相似文献   

8.
The Solar Occultation For Ice Experiment (SOFIE) was launched onboard the Aeronomy of Ice in the Mesosphere (AIM) spacecraft to measure polar mesospheric clouds (PMCs) and their environment. This work describes methods for identifying PMCs in SOFIE observations and determining mass density, particle shape, particle effective radius, and the parameters of a Gaussian size distribution. Results using SOFIE measurements from the northern summer of 2007 are compared with concurrent observations by the ALOMAR lidar in northern Norway. Ice particle properties determined from SOFIE are in good agreement with the lidar results, considering the differences in instrument characteristics.  相似文献   

9.
Aerosol particle size distribution and chemical properties are important in studies related to human health and climate. The present study describes an analysis of aerosol mass loading, Aerosol Optical Depth (AOD), black carbon aerosol mass concentration and carbon monoxide over tropical urban region of Hyderabad, India, during March 2006, coinciding with active forest fires season over India. Aerosol optical depth, particulate matter mass loading and carbon monoxide were observed to be high on days with air mass coming from north of the study area. Spatial occurrence of forest fires was analysed using MODIS daytime data and DMSP-OLS nighttime data sets. Aerosol optical depth measured using Microtops-II sunphotometer correlated well with MODIS derived AOD values. Results of the study suggested that synoptic meteorological conditions play an important role in the observed aerosol properties over the study area during the forest fire season.  相似文献   

10.
--Atmospheric aerosols were sampled from aircraft at various levels over Rihand in northern India during the monsoon season of 1974 and at surface levels at Calcutta, Delhi, Varanasi and Jodhpur during different seasons of 1970 and 1971. Millipore filter assembly was used for this purpose. Chloride nuclei, total aerosol and ice nuclei concentrations were evaluated from millipore filters. At Rihand/Varanasi, during the monsoon, the chloride size spectrum was broader and the distribution bimodal at cloud base level while the spectra were narrower and the distributions unimodal at other levels. At Rihand, chloride mass and larger giant chloride number were considerably higher, total aerosol higher while ice nuclei concentrations were lower on the days with moderate rain as compared to those with light rain. Calcutta (maritime) showed maximum while Varanasi (well-inland) showed minimum chloride number concentrations. As compared with Calcutta, Delhi (continental) had lower chloride and total aerosol, and markedly higher ice nuclei concentrations. Varanasi (high rainfall region) showed all the values, except for small-sized chlorides, notably higher with respect to Jodhpur (low rainfall region). Ice nuclei concentration was lowest in winter and highest in summer at Delhi. Variations of the aerosols during different parts of the day/night are also discussed.  相似文献   

11.
Cunnold  D. M.  Gray  C. R.  Merritt  D. C. 《Pure and Applied Geophysics》1973,106(1):1264-1271
Summary Recent satellite experiments have measured the radiance of the earth at ultraviolet wavelengths and the data thus obtained has been used to determine atmospheric ozone concentrations. It is pointed out in this paper that in the presence of significant concentrations of aerosols at high altitudes, it is not possible from observations of backscattered ultraviolet radiation to separate the effects of aerosols from those attributable to ozone.The earth's daytime horizon was scanned on several occasions between 1963 and 1967 from an altitude of 80 km. For at least one of the flights analyzed we interpret the data to indicate the existence of an aerosol layer at 50 km. This observation, in combination with related observations of other experimenters, implies a limitation on the ability of the backscattered ultraviolet technique to determine ozone concentrations, particularly at altitudes in the region between 35 and 50 km. This limitation may be overcome by altering the viewing geometry and making observations of the earth's horizon. Data thus obtained may be used to deduce the concentrations of both ozone and aerosols.  相似文献   

12.
Elongated aerosol particle removal on fibrous filters has been investigated. It was shown that particle agglomerates are removed much more efficiently compared to the regularly shaped single particles with identical electrical mobility diameter at two filtration velocities tested. The experimental results were compared with the classical filtration theory and it was shown that the theoretical predictions, which are based on the assumption that the particles are spherical, are significantly different compared to an agglomerate filtration efficiency value. In order to account for a particle shape non-regularity, dominating nanoparticle removal mechanisms were firstly evaluated for a regular particle of certain size and then adjusted by fitting coefficients k1 (for diffusion component) and k2 (for interception). These coefficients were determined by fitting the theoretical values that gives the best coincidence with the measured data points. As was further demonstrated theoretically, the coefficient k1 is identical to the ratio of the actual particle surface area to the surface area of the spherical particle of the equivalent diameter. On the other hand, the coefficient k2 was found to be equal to the ratio of the projection of a given particle on a plane perpendicular to a streamline, to that of the spherical particle of the equivalent diameter. The reported findings would allow undertaking more accurate evaluation of the removal efficiency of non-regular aerosol particle, which is especially important for industrial applications where non-regular aerosols are frequently met.  相似文献   

13.
Two year measurements of aerosol concentration and size distribution (0.25 μm < d < 30 μm) in the atmospheric surface layer, collected in L’Aquila (Italy) with an optical particle counter, are reported and analysed for the different modes of the particle size distribution. A different seasonal behaviour is shown for fine mode aerosols (largely produced by anthropogenic combustion), coarse mode and large-sized aerosols, whose abundance is regulated not only by anthropogenic local production, but also by remote natural sources (via large scale atmospheric transport) and by local sources of primary biogenic aerosols. The observed total abundance of large particles with diameter larger than 10 μm is compared with a statistical counting of primary biogenic particles, made with an independent technique. Results of these two observational approaches are analysed and compared to each other, with the help of a box model driven by observed meteorological parameters and validated with measurements of fine and coarse mode aerosols and of an atmospheric primary pollutant of anthropogenic origin (NOx). Except in winter months, primary biogenic particles in the L’Aquila measurement site are shown to dominate the atmospheric boundary layer population of large aerosol particles with diameter larger than 10 μm (about 80 % of the total during summer months), with a pronounced seasonal cycle, contrary to fine mode aerosols of anthropogenic origin. In order to explain these findings, the main mechanisms controlling the abundance and variability of particulate matter tracers in the atmospheric surface layer are analysed with the numerical box-model.  相似文献   

14.
ENSO对平流层气溶胶分布的影响   总被引：1，自引：0，他引：1       下载免费PDF全文
本文采用ONI(Oceanic Nino Index)和HALOE(Halogen Occultation Experiment)气溶胶面积密度资料,从其滞后相关性入手分析了ENSO循环对平流层气溶胶的影响,通过对滞后于El Nino和La Nina时气溶胶含量的比较探讨了ENSO强迫的影响程度,并用剩余环流及其输送量...  相似文献   

15.
Solar, sky, and aureole radiance data from Kensington, Australia, and Lagos, Nigeria, are analysed. The values of the aerosol optical thickness at Lagos are comparable to measured values elsewhere in the subregion (Abidjan) under light haze. The values at Kensington are close to those of the “background aerosol.” Identical and anomalous values of aerosol optical thickness occurred at 1.67 μm at both stations as less than 15% of the values can be accounted for by aerosols. The high optical depths are therefore explained in terms of absorption, possibly mainly by CO2 (59–65%) and, to a lesser extent, by H2O (20–26%). Following correction for molecular multiple scattering, the aerosol scattering phase function increases substantially at 0.5 μm in Kensington and decreases considerably at 0.76 μm in Lagos when compared to the uncorrected function, confirming the relative fineness of the Kensington aerosol. The Lagos aerosol size distribution for moderately dusty air is reasonably bimodally log-normal with modal radiusr m=0.49 μm (1.36 μm) for the moder≤1 μm (r>1 μm). The Kensington aerosol resembles one withr m=0.05 μm forr<1 μm. There the Born approximation appears appropriate, and the weighted mean square radiusp 2=0.13 μm2. In the near forward direction the aerosol scattering phase funciton for Lagos resembles Deirmendjian’s simulations for a silicate-L haze and, for Kensington, a silicate-H haze.  相似文献   

16.
Sun-photometer measurements at Hefei, an urban site located in central East China, were examined to investigate the variations of aerosol loading and optical properties. It is found that aerosol optical thickness (AOT) keeps higher in winter/spring and gets relatively lower in summer/autumn. The large AOT in winter is caused by anthropogenic sulfate/nitrate aerosols, while in spring dust particles elevate the background aerosol loading and the excessive fine-mode particles eventually lead to severe pollution. There is a dramatic decline of AOT during summer, with monthly averaged AOT reaching the maximum in June and soon the minimum in August. Meanwhile, aerosol size decreases consistently and single scattering albedo (SSA) reaches its minimum in July. During summertime large-sized particles play a key role to change the air from clean to mild-pollution situation, while the presence of massive small-sized particles makes the air being even more polluted. These complicated summer patterns are possibly related to the three key processes that are active in the high temperature/humidity environment concentrating on sulfate/nitrate aerosols, i.e., gas-to-particle transformation, hygroscopic growth, and wet scavenging. Regardless of season, the increase of SSA with increasing AOT occurs across the visible and near-infrared bands, suggesting the dominant negative/cooling effect with the elevated aerosol loading. The SSA spectra under varying AOT monotonically decrease with wavelength. The relatively large slope arises in summer, reinforcing the dominance of sulfate/nitrate aerosols that induce severe pollution in summer season around this city.  相似文献   

17.
Solar irradiance, skylight, and aureole intensities were measured early in spring 1981 in Kensington, Australia. The aerosol optical thickness, the aureole intensities, and the scattering phase function at 5° suggest that scattering was due to aerosols of very small sizes. The estimates of the weighted aerosol mean square radius,p 2, seem to lead to the same conclusion.  相似文献   

18.
The use of predictive models for the understanding and management of sediment and contaminant transport generally requires knowledge of particle size and settling velocity. Particle size is often obtained by direct measurements, and the settling velocities are usually predicted using the Stokes' law (or a modification thereof) for single‐grained spherical particles. Such measurements and estimates are not satisfactory measures for cohesive sediments, which exist as agglomerated particles called flocs and whose behaviour is significantly different from that of the single‐grained particles. Direct measurement of settling velocity and size using optical methods in settling columns has also been employed to improve these predictions; however, the subjectivity in determining which particles are in focus results in unreliable size data. An out‐of‐focus particle will generally possess a larger size than in reality. This paper evaluates a laser‐assisted particle sizing/settling velocity determination technique's ability to eliminate the subjectivity and improve particle‐sizing accuracy during settling column experiments. Although the diffraction of light by the translucent standard beads (used for evaluating the technique's accuracy for determining particle size) posed a problem, the results suggest that this technique has potential for assisting researchers to obtain the most accurate settling particle size data possible. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

19.
The physical and chemical characterization of aerosols from three large cities, Karachi and Islamabad, Pakistan, and New York City (NYC), USA, was investigated. A scanning electron microscope equipped with an energy dispersive spectrometer (EDS) was used to determine particle morphology and elemental composition of the samples. A Bruker Spirit system in combination with a Sahara detector provided both computer controlled Automated Chemical Classification (ACC) and digital mapping features for analysis purposes. The use of these two features to characterize the elemental composition, particle size, and to determine specific classes or source types is described in this paper. Filters were analyzed for the following elements; Na, Mg, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Br, Sr, Y, Zr, Mo, Pd, Ag, Cd, In, Sn, Sb, Ba, La, Au, Hg, Tl, Pb, and U. The EDS work was qualitative not quantitative. Seven source types (mobile, cement, soil, steel mill, fossil fuel, sea salt and biological) contributed to particulate matter in the ambient air of both cities in Pakistan, whereas there were eight source types (diesel, road dust, automobile, iron, residual fuel oil, sea salt, ammonium sulfate and ammonium nitrate) for NYC. For all three urban centers, vehicular traffic emissions were the main contributor to particle number. Diesel emissions from trucks and buses were relatively more prominent in NYC aerosols, while gasoline emission from automotive exhaust was dominant in the two cities of Pakistan. The cement/limestone component from local cement industries was very evident in both particle surface characteristics and number for both Karachi and Islamabad, but not in NYC air. Sea salt aerosols were seen in the two coastal cities, Karachi and NYC. It was also witnessed in Islamabad aerosols and was attributable to the mining of rock salt at the world's richest salt mine, Khewra, situated upwind from the city.  相似文献   

20.
Summary In order to interpret scattered light measurements a comparison with theoretical values is necessary. It is demonstrated by means of an example the possibility to obtain a first view on the measurement results. From calculated values of various aerosol size distribution models as well as from measurements were computed: 1) the angular quotients of scattered light intensity (i.e., quotients of intensity at two scattering angles and the same wavelength) and 2) the wavelength quotients (i.e., quotients of intensity at two wavelengths and the same scattering angle). The comparison between measured and theoretical values informs us of the exponent of the aerosol size distribution and its boundary radius.Finally, it is shown that maesurements of polarization may be explained by a similar method.  相似文献   

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