The ALOMAR Rayleigh/Mie/Raman lidar: objectives, configuration, and performance     

U. von Zahn  G. von Cossart  J. Fiedler  K. H. Fricke  G. Nelke  G. Baumgarten  D. Rees  A. Hauchecorne  K. Adolfsen 《Annales Geophysicae》2000,18(7):815-833

We report on the development and current capabilities of the ALOMAR Rayleigh/Mie/Raman lidar. This instrument is one of the core instruments of the international ALOMAR facility, located near Andenes in Norway at 69°N and 16°E. The major task of the instrument is to perform advanced studies of the Arctic middle atmosphere over altitudes between about 15 to 90 km on a climatological basis. These studies address questions about the thermal structure of the Arctic middle atmosphere, the dynamical processes acting therein, and of aerosols in the form of stratospheric background aerosol, polar stratospheric clouds, noctilucent clouds, and injected aerosols of volcanic or anthropogenic origin. Furthermore, the lidar is meant to work together with other remote sensing instruments, both ground- and satellite-based, and with balloon- and rocket-borne instruments performing in situ observations. The instrument is basically a twin lidar, using two independent power lasers and two tiltable receiving telescopes. The power lasers are Nd:YAG lasers emitting at wavelengths 1064, 532, and 355 nm and producing 30 pulses per second each. The power lasers are highly stabilized in both their wavelengths and the directions of their laser beams. The laser beams are emitted into the atmosphere fully coaxial with the line-of-sight of the receiving telescopes. The latter use primary mirrors of 1.8 m diameter and are tiltable within 30° off zenith. Their fields-of-view have 180 rad angular diameter. Spectral separation, filtering, and detection of the received photons are made on an optical bench which carries, among a multitude of other optical components, three double Fabry-Perot interferometers (two for 532 and one for 355 nm) and one single Fabry-Perot interferometer (for 1064 nm). A number of separate detector channels also allow registration of photons which are produced by rotational-vibrational and rotational Raman scatter on N₂ and N₂+O₂ molecules, respectively. Currently, up to 36 detector channels simultaneously record the photons collected by the telescopes. The internal and external instrument operations are automated so that this very complex instrument can be operated by a single engineer. Currently the lidar is heavily used for measurements of temperature profiles, of cloud particle properties such as their altitude, particle densities and size distributions, and of stratospheric winds. Due to its very effective spectral and spatial filtering, the lidar has unique capabilities to work in full sunlight. Under these conditions it can measure temperatures up to 65 km altitude and determine particle size distributions of overhead noctilucent clouds. Due to its very high mechanical and optical stability, it can also employed efficiently under marginal weather conditions when data on the middle atmosphere can be collected only through small breaks in the tropospheric cloud layers.  相似文献   

The role of sodium bicarbonate in the nucleation of noctilucent clouds     

J. M. C. Plane 《Annales Geophysicae》2000,18(7):807-814

It is proposed that a component of meteoric smoke, sodium bicarbonate (NaHCO₃), provides particularly effective condensation nuclei for noctilucent clouds. This assertion is based on three conditions being met. The first is that NaHCO₃ is present at sufficient concentration (10⁴ cm^–3) in the upper mesosphere between 80 and 90 km. It is demonstrated that there is strong evidence for this based on recent laboratory measurements coupled with atmospheric modelling. The second condition is that the thermodynamics of NaHCO₃(H₂O)_n cluster formation allow spontaneous nucleation to occur under mesospheric conditions at temperatures below 140 K. The Gibbs free energy changes for forming clusters with n = 1 and 2 were computed from quantum calculations using hybrid density functional/Hartree-Fock (B3LYP) theory and a large basis set with added polarization and diffuse functions. The results were then extrapolated to higher n using an established dependence of the free energy on cluster size and the free energy for the sublimation of H₂O to bulk ice. A 1-dimensional model of sodium chemistry was then employed to show that spontaneous nucleation to form ice particles (n > 100) should occur between 84 and 89 km in the high-latitude summer mesosphere. The third condition is that other metallic components of meteoric smoke are less effective condensation nuclei, so that the total number of potential nuclei is small relative to the amount of available H₂O. Quantum calculations indicate that this is probably the case for major constituents such as Fe(OH)₂, FeO₃ and MgCO₃.  相似文献   

A summer and winter apportionment of particulate matter at urban and rural areas in northern France     

F. Ledoux  L. Courcot  D. Courcot  A. Aboukaïs  E. Puskaric   《Atmospheric Research》2006,82(3-4):633

The apportionment of atmospheric aerosols undertaken in Northern France during two sampling campaigns allowed to determine the influence of the atmospheric contribution of a heavy industrialized urban center on the particulate matter composition at a nearby rural site. The concentrations of major components and trace elements sampled by bulk filtration have been determined on June–July 2000 and January–February 2001, and the comparison of these two campaigns shows very well the importance of wind directions. The sources of 10 trace elements (Al, Ba, Cu, Fe, K, Mn, Pb, Sr, Ti and Zn) and 7 major components (Cl⁻, NO₃⁻, SO₄²⁻, NH₄⁺, Na, Mg and Ca) are better identified by studying their elemental contribution at each sampling site according to wind sectors. This kind of study shows that the concentrations recorded at the urban sampling site are always higher than those observed at the rural site as well during the summer campaign (about + 35%) as during the winter campaign (+ 90%), because of the predominance of the W–NW wind sector, corresponding to the influence of the urban and industrialized areas.  相似文献   

The Kuwae (Vanuatu) eruption of<Emphasis Type="SmallCaps"> AD</Emphasis> 1452: potential magnitude and volatile release     

J. B. Witter  S. Self 《Bulletin of Volcanology》2007,69(3):301-318

Sometime during AD 1452, according to new evidence, a large-magnitude, initially phreatomagmatic eruption, destroyed the island of Kuwae (16.83°S, 168.54°E), located in the present-day Republic of Vanuatu. It created a 12×6-km submarine caldera composed of two adjacent basins. Based on estimates of caldera volume, between 30 and 60 km³ DRE of dacite magma was ejected as pyroclastic flow and fall deposits during this event. Annual layers of ice dating from the period AD 1450–1460 contain acidity peaks representing fallout of sulfuric acid onto both the Greenland and Antarctic ice caps. These acidity peaks have been attributed by others to the sedimentation of H₂SO₄ aerosols that originated from sulfur degassing during the Kuwae eruption. Improved dating techniques and new data from nineteen ice cores reveal a single acidity peak attributed to Kuwae lasting from 1453 to 1457. In this study, we present new electron microprobe analyses of the S, Cl, and F contents of matrix glasses and glass inclusions in phenocrysts from tephra ejected during the Kuwae eruption. We establish that the Kuwae event did indeed yield a large release of sulfur gases. From our glass inclusion data and analysis, we calculate that the total atmospheric aerosol loading from the 1452 Kuwae eruption was ≫100 Tg H₂SO₄. Much of the volatile mass released during the eruption was probably contained in a separate, volatile-rich, fluid phase within the pre-eruptive Kuwae magma body. Comparing the volatile release of the Kuwae eruption with other large-magnitude eruptions, places Kuwae as the greatest sulfuric acid aerosol producer in the last seven centuries, larger even than sulfur emissions from the eruption of Tambora (Indonesia) in 1815, and possibly Laki (Iceland) in 1783. The severe and unusual climatic effects reported in the mid- to late-1450s were likely caused by the Kuwae eruption.  相似文献   

Source Sector Contributions to Aerosol Levels in Pakistan          下载免费PDF全文

Muhammad Zeeshaan SHAHID  LIAO Hong  QIU Yu-Lu  Imran SHAHID 《大气和海洋科学快报》2015,8(5)

Urban air pollution in Pakistan is a serious challenge and it causes significant damage to human health and ecosystems. This paper presents a modelling study using the Weather Research and Forecasting Model coupled with Chemistry(WRF-Chem) to simulate the spatial distributions and temporal variations of aerosol concentrations over Pakistan, focusing on contributions of domestic emission sectors(transport, industry, residential, and energy) to mass concentrations of sulfate(SO2–4), nitrate(NO–3), ammonium(NH+4), black carbon(BC), and organic carbon(OC) during the months of January, April, July, and October in 2010. Sensitivity studies indicate that, averaged over January, April, July, and October of 2010, energy and industry sectors have the largest contributions to SO2–4 concentrations, each of which contributes about 10%?20% to SO2– 4over the polluted eastern Pakistan. The contributions from residential and transport sectors to NO–3 concentrations reach 40%?50% in central Pakistan. The residential sector has the highest contribution of 50%–80% to BC and OC loading in northeastern and southern Pakistan. Examination of sector contributions to aerosol levels in Lahore, the most polluted city in Pakistan, suggests that reductions in emissions in the residential sector should be an efficient measure for improving particulate matter air quality in this region.  相似文献   

A global satellite view of the seasonal distribution of mineral dust and its correlation with atmospheric circulation     

《Dynamics of Atmospheres and Oceans》2014

Aerosols make a considerable contribution to the climate system through their radiative and cloud condensation nuclei effects, which underlines the need for understanding the origin of aerosols and their transport pathways. Seasonal distribution of mineral dust around the globe and its correlation with atmospheric circulation is investigated using satellite data, and meteorological data from ECMWF. The most important sources of dust are located in North Africa, the Middle East and Southwest Asia with an observed summer maximum, and East Asia with a spring peak. Maximum dust activity over North Africa and the Middle East in summer is attributed to dry convection associated with the summertime low-pressure system, while unstable weather and dry conditions are responsible for the spring peak in dust emission in East Asia. Intercontinental transport of mineral dust by atmospheric circulation has been observed, including trans-Atlantic transport of North African dust, trans-Pacific transport of Asian dust, and transport of dust from the Middle East across the Indian Ocean. The extent of African dust over the Atlantic Ocean and its latitudinal variation with season is related to the large-scale atmospheric circulation, including seasonal changes in the position of the intertropical convergence zone (ITCZ) and variation of wind patterns. North African aerosols extend over longer distances across the North Atlantic in summer because of greater dust emission, an intensified easterly low level jet (LLJ) and strengthening of the Azores-Bermuda anticyclonic circulation. Transport of East Asian aerosol is facilitated by the existence of a LLJ that extends from East Asia to the west coast of North America.  相似文献   

Modeling Study of the Effect of Anthropogenic Aerosols on Late Spring Drought in South China     

HU Ning  LIU Xiaohong 《Acta Meteorologica Sinica》2013,27(5):701-715

In this study,the mechanisms underlying the decadal variability of late spring precipitation in South China are investigated by using the latest Community Earth System Model version 1 （CESM1）.We aim to unravel the effects of different climate forcing agents such as aerosols and greenhouse gases （GHGs） on the decadal variation of precipitation,based on transient experiments from pre-industry （for year 1850） to present-day （for year 2000）.Our results reveal that：（1） CESM1 can reproduce the climatological features of atmospheric circulation and precipitation for the late spring in South China; （2） only simulations including the forcing of anthropogenic aerosols can reproduce the observed decreasing trend of late spring precipitation from 1950-2000 in South China; （3） aerosols affect the decadal change of precipitation mainly by altering the large-scale atmospheric circulation,and to a less extent by increasing the lower-tropospheric stability to inhibit the convective precipitation; and （4） in comparison,other climate forcing agents such as GHGs have much smaller effects on the decadal change of spring precipitation in South China.  相似文献   

The Tambora eruption in 1815 provides a test on possible global climatic and chemical perturbations in the past     

R. K. R. Vupputuri 《Natural Hazards》1984,5(1):1-16

A coupled one-dimensional radiative-convective-photochemical diffusion model, which takes into account the influence of ocean inertia on global radiative perturbations is used to investigate the possible climatic and other atmospheric effects of a major volcanic eruption, thought to be similar in magnitude to that of the Tambora eruption, Indonesia, which took place in 1815. A volcanic cloud was introduced in the model stratosphere between 20–25 km and the global average peak aerosol optical thickness was assumed to be 0.25. Both the aerosol optical thickness and aerosol composition, which determine the optical properties, were allowed to vary in the model atmosphere during the life cycle of the volcanic cloud. The results indicate that the global average surface temperature decreases steadily from the date of eruption (7–12 April 1815) with maximum cooling of 1° K occurring in the spring of 1816. The calculations also show significant warming of the stratosphere, with temperature increasing up to 15° K at 25 km in less than six months after the date of eruption. The important effects of the Tambora eruption on stratospheric ozone and UV-B radiation at the surface are also mentioned.  相似文献   

Resources of the ionized atmosphere as an aerosol source     

V.V. Smirnov  A.V. Savchenko 《Atmospheric Research》2006,82(3-4):554

The potential resources on the ion-stimulated syntheses effects of aerosol particles of lower troposphere in test sites in the arctic, mountain, arid and forest areas as the function of irradiation time and gas-precursor concentration were experimentally and theoretically evaluated. The dust-free outdoor air was irradiated with an ionization current of 10^− 6 A by α-rays from isotope ²³⁹Pu. The total output of radiolytic aerosols (RA) with a diameter of 3–1000 nm was found to be 0.05–0.1 molecules per 1 eV of absorbed radiation, while the physical upper limit is 0.25–0.4 molecules/eV. In an interval of exposition time from 6 to 800 s (adsorbed energy is 3 · 10¹²–10¹⁴ eV/cm³) the RA mass concentration at different sites was increased from 1–10 to 50–500 μg/m³. According to the liquid chromatography data the major RA material is the H₂O/HNO₃ solution with acid concentration  25%. The used physical model presents new aerosols as a product from small and intermediate ion association through formation of neutral clusters and describes adequately some of the peculiarities in field experiment data. Introducing SO₂, NH₃, and also hydrochloric, nitric and sulphuric acid vapours with concentration 0.1–1 mg/m³ in the irradiated air stimulated an increase of mass aerosol concentration by a factor of 8–30. The mean size also decreased by a factor of 3–5. These facts allowed us to expect that the chemical composition of radiolytic aerosols generated in outdoor air would noticeably differ after addition of the gas-precursors.  相似文献   

Aerosol characteristics during winter fog at Agra,North India     

P. D. Safai  S. Kewat  G. Pandithurai  P. S. Praveen  K. Ali  S. Tiwari  P. S. P. Rao  K. B. Budhawant  S. K. Saha  P. C. S. Devara 《Journal of Atmospheric Chemistry》2008,61(2):101-118

Simultaneous measurements on physical, chemical and optical properties of aerosols over a tropical semi-arid location, Agra in north India, were undertaken during December 2004. The average concentration of total suspended particulates (TSP) increased by about 1.4 times during intense foggy/hazy days. Concentrations of SO₄ ²⁻, NO₃ ⁻, NH₄ ⁺ and Black Carbon (BC) aerosols increased by 4, 2, 3.5 and 1.7 times, respectively during that period. Aerosols were acidic during intense foggy/hazy days but the fog water showed alkaline nature, mainly due to the neutralizing capacity of NH₄ aerosols. Trajectory analyses showed that air masses were predominantly from NW direction, which might be responsible for transport of BC from distant and surrounding local sources. Diurnal variation of BC on all days showed a morning and an evening peak that were related to domestic cooking and vehicular emissions, apart from boundary layer changes. OPAC (Optical properties of aerosols and clouds) model was used to compute the optical properties of aerosols. Both OPAC-derived and observed aerosol optical depth (AOD) values showed spectral variation with high loadings in the short wavelengths (<1 μm). AOD value at 0.5 μm wavelength was significantly high during intense foggy/hazy days (1.22) than during clear sky or less foggy/hazy days (0.63). OPAC-derived Single scattering albedo (SSA) was 0.84 during the observational period, indicating significant contribution of absorbing aerosols. However, the BC mass fraction to TSP increased by only 1% during intense foggy/hazy days and thereby did not show any impact on SSA during that period. A large increase was observed in the shortwave (SW) atmospheric (ATM) forcing during intense foggy/hazy days (+75.8 W/m²) than that during clear sky or less foggy/hazy days (+38 W/m²), mainly due to increase in absorbing aerosols. Whereas SW forcing at surface (SUF) increased from −40 W/m² during clear sky or less foggy/hazy days to −76 W/m² during intense foggy/hazy days, mainly due to the scattering aerosols like SO₄ ^2-.  相似文献