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1.
The rainwater composition in the vicinity of Mainz, FRG, has been investigated with special emphasis on insoluble constituents. The number size distribution was determined in the range from 0.1 m up to 100 m radius. For particles with r>0.5 m radius the shape of the size distribution of insoluble particles in rain follows the shape of the average urban and rural aerosol. In this particular size range no major size selective removal processes could be seen. For r<0.5 m the number size distribution tends to flatten compared to the average aerosol. This might be the indication of a size selective removal process (Greenfield Gap).  相似文献   

2.
Airborne measurements made during August 1985 over Greenland and its environs show that both accumulation-mode (0.1 m D2.0 m) and giant (D2 m) particles were present in relatively high concentrations in arctic haze layers and that the accumulation-mode particles dominated light scattering. Particles with diameters (D) between 1 and 4 m consisted predominately of mixed materials, small and dense inclusions, and probably organic compounds containing sulfur. Many of the particles from 0.1 to 1 m in diameter were also of mixed composition, with sulfuric acid, ammonium sulfate and organics probably the dominant constituents.  相似文献   

3.
A method for determining the distribution of supermicrometer nitrate between size-segregated sea-salt and soil derived particles is presented. The analysis is based on field data from six measurements at a coastal site in southern Finland, and on a theoretical treatment taking into account the transfer of gaseous species onto particle surfaces and their subsequent reaction. Significant amounts of nitrate were found in both the particle types, with the fraction of nitrate associated with soil particles varying from 20–50% in the 1–2 m size to near 90% in particles larger than 10 m. Overall, the nitrate accumulation followed closely the relative abundances of these two particle types. Two overlapping modes in supermicron nitrate mass size distributions could be identified. The lower mode, associated with sea-salt, was located between the surface-area and volume distribution of sodium peaking at about 2–3 m of EAD. The upper mode peaked at 3–5 m and followed more closely the surface-area distribution of calcium in all samples. At our site, the accumulation of nitrate into both particle types was shown to be limited by an effective surface reaction rate rather than by gas-phase diffusion. This rate was estimated to be considerably larger for sea-salt particles. Strong evidence in support of the saturation of nitrate in sea-salt particles were obtained.  相似文献   

4.
Radiative Heat Transfer and Hydrostatic Stability in Nocturnal Fog   总被引：1，自引：0，他引：1  
We have performed a one-dimensional and transient radiative heat transfer analysis in order to investigate interaction between atmospheric radiation and convective instability within a nocturnal fog. The radiation element method using the Ray Emission Model (REM2), which is a generalized numerical method, in conjunction with a line-by-line (LBL) method, is employed to attain high spectral resolution calculations for anisotropically scattering fog. The results show that the convective instability has a strong dependence on radiative properties of the fog. For the condition of a 20-m droplet diameter and liquid water content of 0.1 × 10–3 kg m–3;, the temperature profile within the fog becomes S shaped, and a convective instability layer forms in the middle or lower level of the fog. However, for the same water content and a 40-m diameter droplet, no strong convective instability layer forms, whereas for a 10-m diameter droplet a strong convective instability is observed.  相似文献   

5.
Results from measurements of the composition and size distribution of aerosol particles advected into central Alaska are reported. It is argued that the aerosol predominant in number, but not necessarily in mass, consists of submicron droplets of sulfuric acid. The major aerosol by mass in arctic air is a removal-resistant accumulation mode (radius 0.3 m) probably to large extent originating from pollution sources 103 km upstream (mostly in central Eurasia) from the site in Alaska. The accumulation mode aerosol disappears when arctic air masses are replaced with relatively warmer air masses flowing in from the northern Pacific. The latter air mass systems have been strongly scavenged by clouds and precipitation associated with the Aleutian low pressure system and with forced orographic uplifting over the Alaska Mountain Range; nevertheless the Pacific air masses contain substantial (i.e., 500–1000 cm-3) quantities of small (several hundredths of a micron in radius) particles. Arctic-derived air masses are enriched in large (i.e, 0.3 ) particles compared to Pacific Marine air masses, whereas the opposite trend is found for smaller, Aitken, particles. The smaller particles are found in greatest abundance in warmer air mass systems, presumably because of the relatively brief time since such air masses were last exposed to sunlight with attendant production of small particles from the gas phase.  相似文献   

6.
Thermal and optical techniques were used at Barrow, Alaska during AGASP II (3/20/86–4/7/86) to measure in-situ variability of major aerosol components present in Arctic Haze. The experiment provided continuous data on the concentration, size distribution and relative proportions of sulfate species and refractory aerosol for particle diameters of 0.15 to 5 m. Filter samples were also taken for determination of aerosol optical absorption due to soot (EC-elemental carbon). Although pronounced haze events were absence during this period the haze aerosol present varied in concentration between 2 and 6 g/m3 but showed little change in relative constituents. Apart from local influences, the optical data indicated a persistent fine-mode sulfate aerosol with a NH4 +/SO4 – molar ratio of about 0.4 and a refractory component of somewhat less than 10% by mass. A preliminary comparison of soot estimates determined from the light absorption data with the size distributions of refractory aerosol observed independently by the optical particle counter showed good agreement during the sample period. In the absence of local pollution, values of single scatter albedo derived from light scattering and light absorption showed similar variation about the average value of 0.86 found by us during flights north of Barrow three years earlier during AGASP I.  相似文献   

7.
Measurements at Barrow during the second Arctic Gas and Aerosol Sampling Program (AGASP-II), conducted in April 1986, showed no rapid long-range transport from lower-latitude source regions to Barrow, and only limited vertical transport from above the boundary layer to the surface. New aerosol size distribution measurements in the 0.005–0.1 m diameter size range using a Nuclepore-filter diffusion battery apparatus showed a median diameter of about 0.01 m during times of high condensation nucleus (CN) concentrations. Aerosol black carbon concentrations exceeding 400 ng m–3 were detected at the surface and were more strongly correlated with CN concentrations than with aerosol scattering extinction (sp), suggesting that aerosol carbon was generally associated with small particles rather than large particles. Measurements at Barrow during AGASP-I, conducted in March–April 1983, showed a series of aerosol events detected at the ground that were caused by rapid long-range transport paths to the vicinity of Barrow from Eurasia. These events were strongly correlated with aerosol loading in the vertical column (optical depth).  相似文献   

8.
Use of an airborne quartz crystal microbalance cascade impactor instrument together with a correlation spectrometer has allowed the flux of particles and their size distribution to be determined at Mount Erebus. The plume contributes 21±3 metric tomnes/day of aerosol particles to the Antarctic upper troposphere. The aerosol particles consist of larger (5–25 m) particles of elemental sulfur and silica, a middle sized group of iron oxides and smaller particles (less than 1 m) of complex liquids. Unlike many volcanic plumes, the Erebus plume has only a small amount of sulfate particles. The concentrations of particles in the Erebus plumes was 70–370 m/m3. Limited sampling of the Antarctic atmosphere at 8 km altitude but hundreds of km away from Erebus obtained a few large particles of sulfur and silicates, suggesting a similarity with the Erebus plume. The fallout of these particles occurs slowly over a broad area of the Antarctic continent.  相似文献   

9.
Data collected during the french VOVES-1977 experiment are used for the determination of the functionsA() andB() of the stability parameter . It is found that, although pertaining to different geographic conditions, they lead to the same kind of dependency ofA andB upon as found previously considered data. The influence of baroclinicity onA andB is also studied and it is found in that, statistically, consideration of this parameter does not lead either to a decrease of the large scatter of experimental points or to a significant improvement of the similarity theory. It is also shown that a satisfactory estimation of the surface geostrophic wind can be made from the network of meteorological stations, to compute such functions.  相似文献   

10.
During April 1986, as part of an international arctic air chemistry study (AGASP-2), ground level observations of aerosol trace elements, oxides of sulphur and nitrogen and particle number size distribution were made at Alert Canada (82.5N, 62.3W). Pollution haze was evident as indicated by daily aerosol number (size > 0.15 m diameter) and SO4 = concentrations in the range 125 – 260 cm–3 and 1.6 – 4.5 g m–3, respectively. Haze and associated acidic gases tended to increase throughout the period. SO2 and peroxyacetylnitrate (PAN) mixing ratios were in the range 140 – 480 and 370 – 590 ppt(v), respectively. About 88% of the total end-product nitrogen was in the form of PAN. In air dried to 2% relative humidity by warming to room temperature, the aerosol mass size distribution had a major mode at 0.3 m diameter and a minor one at 2.5 m. Aerosol mass below 1.5 m was well correlated with SO4 =, K+ and PAN. There was a steady increase in the oxidized fraction of total airborne sulphur and nitrogen oxide throughout April as the sun rose above the horizon and remained above. The mean oxidation rate of SO2 between Eurasia and Alert was estimated as 0.25 – 0.5% h–1. The molar ratio of total nitrogen oxide to total sulphur oxide in the arctic atmosphere (0.67±0.17) was comparable to that in European emissions. A remarkably strong inverse correlation of filterable Br and O3 led to the conclusion that O3 destruction and filterable Br production below the Arctic surface radiation inversion is associated with tropospheric photochemical reactions involving naturally occurring gaseous bromine compounds.  相似文献   

11.
A liquid jet of 90 m diameter and variable length has been utilized to determine absorption rates and, hence, mass accommodation coefficients , of atmospheric trace gases. The compounds investigated are HCl (0.01), HNO3 (0.01), N2O5 (0.005), peroxyacetyl nitrate (>0.001), and HONO (0.005). It is concluded that the absorption of these trace gases by liquid atmospheric water is not significantly retarded by interfacial mass transport. The strengths and limitations of the liquid jet technique for measuring mass accommodation coefficients are explored.  相似文献   

12.
Weekly bulk aerosol samples collected at Funafuti, Tuvalu (8°30S, 179°12E), American Samoa (14°15S, 170°35W), and Rarotonga (21°15S, 159°45W), from 1983 through most of 1987 have been analyzed for nitrate and other constituents. The mean nitrate concentration is about 0.11 g m–3 at each of these stations: 0.107±0.011 g m–3 at Funafuti; 0.116±0.008 at American Samoa; and 0.117±0.010 at Rarotonga. Previous measurements of mineral aerosol and trace metal concentrations at American Samoa are among the lowest ever recorded for the near-surface troposphere and indicate that this region is minimally affected by transport of soil material and pollutants from the continents. Consequently, the nitrate concentration of 0.11 g m–3 can be regarded as the natural level for the remote marine boundary layer of the tropical South Pacific Ocean. In contrast, over the tropical North Pacific which is significantly impacted by the transport of material from Asia and North America, the mean nitrate concentrations are about three times higher, 0.29 and 0.36 g m–3 at Midway and Oahu, respectively. The major sources of the nitrate over the tropical South Pacific are still very uncertain. A very significant correlation between the nitrate concentrations at American Samoa and the concentrations of 210Pb suggests that transport from continental sources might be important. This continental source could be lightning, which occurs most frequently over the tropical continents. A near-zero correlation with 7Be indicates that the stratosphere and upper troposphere are probably not the major sources. A significant biogenic source would be consistent with the higher mean nitrate concentrations, 0.16 to 0.17 g m–3, found over the equatorial Pacific at Fanning Island (3°55N, 159°20W) and Nauru (0°32S, 166°57E). The lack of correlation between nitrate and nss sulfate at American Samoa does not necessarily preclude an important role for marine biogenic sources.  相似文献   

13.
On the determination of the height of the Ekman boundary layer   总被引：1，自引：1，他引：1  
The heighth of the Ekman turbulent boundary layer determined by the momentum flux profile is estimated with the aid of considerations of similarity and an analysis of the dynamic equations. Asymptotic formulae have been obtained showing that, with increasing instability,h increases as ¦¦1/2 (where is the non-dimensional stratification parameter); with increasing stability, on the other hand,h decreases as –1/2. For comparison, a simple estimate of the boundary-layer heighth u determined by the velocity profile is given. As is shown, in unstable stratification,h u behaves asymptotically as ¦¦–1, i.e., in a manner entirely different from that ofh .  相似文献   

14.
STAR (System for Transfer of Atmospheric Radiation) was developed to calculate accurately and efficiently the irradiance, the actinic flux, and the radiance in the troposphere. Additionally a very efficient calculation scheme to computer photolysis frequencies for 21 different gases was evolved. STAR includes representative data bases for atmospheric constituents, especially aerosol particles. With this model package a sensitivity study of the influence of different parameter on photolysis frequencies in particular of O3 to Singlet D oxygen atoms, of NO2, and of HCHO was performed. The results show the quantitative effects of the influence of the solar zenith angle, the ozone concentration and vertical profile, the aerosol particles, the surface albedo, the temperature, the pressure, the concentration of NO2, and different types of clouds on the photolysis frequencies.Notation I A(, ) actinic flux - I H(, ) irradiance - L(, , , ) radiance - wavelength - azimuth angle - cosine of zenith angle - s cosine of solar zenith angle - optical depth - s scattering coefficient - c extinction coefficient - o single scattering albedo - p mix mixed phase function - g mix mixed asymmetry factor - J gas photolysis frequency  相似文献   

15.
Summary The performance of evaporation schemes with and approach and their combination within resistance representation of evaporation from bare soil surface is discussed. For this purpose nine schemes, based on different functions of or , on the ratio of the volumetric soil moisture content and its saturated value are used.The quality of the chosen schemes has been evaluated using the results of time integration by the coupled soil moisture and surface temperature prediction model, BARESOIL, using in situ data. A sensitivity analysis was made using two sets of data derived from the volumetric soil moisture content of the top soil layer. One with values below the wilting point (0.17 m3m–3) and the second with values above 0.20m3m–3. Data sets were obtained at the experimental site Rimski anevi, Yugoslavia, from the bare surface of a chernozem soil.With 4 Figures  相似文献   

16.
Zusammenfassung Auf dem Feldberg (1493 m NN) im südlichen Schwarzwald wurden von Januar 1953 bis Mai 1953 und von September 1954 bis Februar 1955 Messungen von Tropfengröße, Wassergehalt und Sichtweite in Wolken durchgeführt. Die Tropfen der einzelnen Spektren haben einen mittleren Durchmesser zwischen 6 und 30 ; die Durchmesser der größten gemessenen Tropfen liegen zwischen 50 und 60 . Der Wassergehalt hat Werte zwischen 0,003 und 1,54 g/m3, wobei über 90% aller Messungen einen Wassergehalt unter 0,50 g/m3 zeigen. Ein einfacher Zusammenhang zwischen Sichtweite, Tropfengröße und Wassergehalt nach derTrabertschen Formel besteht nicht.Eine enge beziehung wurde zwischen der Form der Spektren und dem Niederschlag gefunden. In Zeiten ohne Niederschlag und bei geringfügigem Niederschlag überwiegen schmale ( < 12,0 ), in Zeiten mit länger andauerndem Niederschlag breite Spektren ( > 12,0 ). Eine Ausnahme machen alle Messungen in Hochnebel, die breite Spektren mit zwischen 13 und 17 zeigen, ohne daß Niederschlag fällt.Das gleichzeitige Vorhandensein der drei Phasen Wasserdampf, flüssiges Wasser und Eisteilchen über längere Zeiträume hinweg wurde festgestellt; somit kann die Eiskristall-Niederschlagstheorie vonBergeron und vonFindeisen für den Mechanismus der Niederschlagsbildung nicht im allgemein angenommenen Ausmaß zutreffen. Es erscheint notwendig, die Frage der Wolkenphysik nicht nur thermodynamisch, sondern auch in vermehrtem maß kolloidphysikalisch im Sinne vonSchmauss zu untersuchen.
Summary Measurements of drop size, water content and visibility in clouds have been carried out from January till May 1953 and from September 1954 to February 1955 on the Feldberg (1493 m. a. s. 1.) in the southern Black Forest. The drops of the different spectra have a mean diameter between 6 and 30 ; the diameters of the largest measured drops lie between 50 and 60 . The water content shows values between 0.003 and 1.54g/m3 whereby more than 90 per cent of all measurements lead to a water content below 0.50 g/m3. A simple relation between visibility, drop size and water content according to the formula ofTrabert does not exist.A closed connection between the form of the spectra and the precipitations has been found. In periods without or with only slight precipitation narrow spectra ( < 12.0 ) prevail, in periods with persistent precipitation broad ones ( > 12.0 ). All measurements in elevanted fog make an exception, showing broad spectra with between 13 and 17 without any precipitation.The simultaneous existance of the 3 phases: water vapour, liquid water and ice particles over alonger periods has been stated; the ice crystall precipitation theory ofBergeron andFindeisen for the mechanism of precipitation can therefore not hold in the generally accepted extent. The examination of the problems of cloud physics appears to be necessary, not only in thermodynamical respect, but also in the sense of coloid physics according toSchmauss.
Résumé On a effectué de janvier à mai 1953 et de septembre 1954 à février 1955 au Feldberg (1493 m.) en Forêt-Noire des mesures de grosseur de gouttelettes, de teneur en eau et de visibilité dans les nuages. Les gouttelettes ont und diamètre moyen compris entre 6 et 30 ; les plus grosses mesurent 50 à 60 . La teneur en eau varie de 0,003 à 1,54 g/m3; dans plus de 90% des mesures, elle reste inférieure a 0,5g/m3. Il n'y a pas de relation simple, qui suivrait la formula deTrabert, entre visibilité, grosseur des gouttelettes et teneur en eau.Il existe par contre une relation étroite entre la forme du spectre de fréquence et les précipitations. Lorsque celles-ci sont nulles ou très faibles ce sont les spectres étroit ( < 12,0 ) qui dominent; par précipitations durables, ce sont les spectres larges ( > ). Dans le stratus, sans pluie, les spectres larges ( entre 13 et 17 ) prédominent.On a constaté l'existence simultanée des trois phases solide, liquide et gazeuse pendant d'assez longs intervalles de temps, de sorte que le théorie deBergeron et deFindeisen concernant la genène des précipitations n'a pas la généralité qu'on lui prête. Il apparaît nécessaire d'aborder les problèmes de la physique des nuages non seulement du point de vue thermodynamique, mais aussi de celui de l'état colloïdal au sens deSchmauss.

Mit 9 Textabbildungen.

Hinsichtlich der Wiedergabe von Tabellen und Tropfenspektren stark verkürzte Fassung einer bei der Technischen Hochschule in Karlsruhe eingereichten und genehmigten Dissertation; die hier weggelssene Dokumentation kann zur Einsichtnahme bezogen werden bei den Bibliotheken der Technischen Hochschule Karlsruhe und des Deutschen Wetterdienstes, Offenbach (Main).  相似文献   

17.
Rain and air of Florence have been collected in a continuous way andanalysed by flow analysis spectrofluorimetric methods for formaldehydeand hydrogen peroxide. Diurnal and seasonal variations were observed;the mean/maximum concentrations of all data (as gm–3) are 3.3/23.4 for HCHO and 0.4/4.93 forH2O2. The effect of external sources and ofphotochemical reactions produces periods of positive and negativecorrelations for these compounds. The mean/maximum rain concentration ofall data are 98/443 g l–1 for HCHO and 84/685 g l–1 for H2O2. Concentrationratios rain/air and discrepancies to Henry's Law equilibrium arediscussed.  相似文献   

18.
Cloud water and interstitial aerosol samples collected at Mt. Sonnblick (SBO) were analyzed for sulfate and aerosol carbon to calculate in-cloud scavenging efficiencies. Scavenging efficiencies for sulfate (SO) ranged from 0.52 to 0.99 with an average of 0.80. Aerosol carbon was scavenged less efficiently with an average value (AC) of 0.45 and minimum and maximum values of 0.14 and 0.81, respectively. Both SO and AC showed a marked, but slightly different, dependence on the liquid water content (LWC) of the cloud. At low LWC, SO increased with rising LWC until it reached a relatively constant value of 0.83 above an LWC of 0.3 g/m3. In the case of aerosol carbon, we obtained a more gradual increase of AC up to an LWC of 0.5 g/m3. At higher LWCs, _ remained relatively constant at 0.60. As the differences between SO and A varied across the LWC range observed at SBO, we assume that part of the aerosol carbon was incorporated into the cloud droplets independently from sulfate. This hypothesis is supported by size classified aerosol measurements. The differences in the size distributions of sulfate and total carbon point to a partially external mixture. Thus, the different chemical nature and the differences in the size and mixing state of the aerosol particles are the most likely candidates for the differences in the scavenging behavior.  相似文献   

19.
Recently Wilson and Flesch (Boundary-Layer Meteorology, 84, 411-426, 1997) suggested that the average increment d z to the orientation = arctan(w/u) of the Lagrangian velocity-fluctuation vector can be used to distinguish the better Lagrangian stochastic models within the well-mixed class. Here it is demonstrated that the specification of d z constitutes neither a sufficient or universally applicable criterion to distinguish the better Lagrangian stochastic models within the well-mixed class. The hypothesis made by Wilson and Flesch that Lagrangian stochastic models with /PE irrotational are zero-spin models, having d z=0, is proven  相似文献   

20.
Two types of neutral planetary boundary layer (PBL) are distinguished:truly neutral – developed against a neutrally stratified free flow, and conventionally neutral – developed against a background stable stratification. Atmospheric PBLs treated asneutral are almost always conventionally neutral. Theoretical reasoning and results from large-eddy simulation (LES) show that A and B coefficients of the Rossby-number similarity theory are not constants. The same is true for thecoefficient Ch in the Rossby–Montgomery formula for the neutral boundary-layer depth h = Chu*/|f|, where u* is the friction velocity. Contrary to classical ideas, A, B and Ch depend on the ratio N N/|f| of the free-flow Brunt–V*auml;isäl ä frequency N to the absolute value of the Coriolis parameter |f|. This new development can explain why atmospheric and LES estimates of A, B and Ch appear inconsistent. It results from neglecting the fact that atmospheric data for N 102 were compared with LES data for N = 0, violating an obvious requirement of similarity with respect to N.  相似文献   

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