Phytoplankton and cloudiness in the Southern Ocean

The effect of ocean biological productivity on marine clouds is explored over a large phytoplankton bloom in the Southern Ocean with the use of remotely sensed data. Cloud droplet number concentration over the bloom was twice what it was away from the bloom, and cloud effective radius was reduced by 30%. The resulting change in the short-wave radiative flux at the top of the atmosphere was -15 watts per square meter, comparable to the aerosol indirect effect over highly polluted regions. This observed impact of phytoplankton on clouds is attributed to changes in the size distribution and chemical composition of cloud condensation nuclei. We propose that secondary organic aerosol, formed from the oxidation of phytoplankton-produced isoprene, can affect chemical composition of marine cloud condensation nuclei and influence cloud droplet number. Model simulations support this hypothesis, indicating that 100% of the observed changes in cloud properties can be attributed to the isoprene secondary organic aerosol.     

Condensation nucleus discriminator making optical measurements on fog: a tool for environmental research

An instrument providing a new, rapid, and accurate method of determining the number and critical radii of condensation nuclei with radii under 200 angstroms is described. Based on the principle of the cloud chamber, the instrument measures transient changes in the attenuation and scattering of a monochromatic light beam by the growing fog droplets. From data obtained the absolute number concentration and radii of condensation nuclei can be calculated. Preliminary studies of aerosol formation in beta-irradiated mixtures of air and sulfur dioxide showed that carbon monoxide and methane inhibit the formation of nuclei; relative rate constants can be deduced. Some applications of this instrument for environmental and basic research are pointed out.     

Natural Versus Anthropogenic Factors Affecting Low-Level Cloud Albedo over the North Atlantic

Cloud albedo plays a key role in regulating Earth's climate. Cloud albedo depends on column-integrated liquid water content and the density of cloud condensation nuclei, which consists primarily of submicrometer-sized aerosol sulfate particles. A comparison of two independent satellite data sets suggests that, although anthropogenic sulfate emissions may enhance cloud albedo immediately adjacent to the east coast of the United States, over the central North Atlantic Ocean the variability in albedo can be largely accounted for by natural marine and atmospheric processes that probably have remained relatively constant since the beginning of the industrial revolution.     

Size matters more than chemistry for cloud-nucleating ability of aerosol particles

Size-resolved cloud condensation nuclei (CCN) spectra measured for various aerosol types at a non-urban site in Germany showed that CCN concentrations are mainly determined by the aerosol number size distribution. Distinct variations of CCN activation with particle chemical composition were observed but played a secondary role. When the temporal variation of chemical effects on CCN activation is neglected, variation in the size distribution alone explains 84 to 96% of the variation in CCN concentrations. Understanding that particles' ability to act as CCN is largely controlled by aerosol size rather than composition greatly facilitates the treatment of aerosol effects on cloud physics in regional and global models.     

Biomass burning in the tropics: impact on atmospheric chemistry and biogeochemical cycles

Biomass burning is widespread, especially in the tropics. It serves to clear land for shifting cultivation, to convert forests to agricultural and pastoral lands, and to remove dry vegetation in order to promote agricultural productivity and the growth of higher yield grasses. Furthermore, much agricultural waste and fuel wood is being combusted, particularly in developing countries. Biomass containing 2 to 5 petagrams of carbon is burned annually (1 petagram = 10(15) grams), producing large amounts of trace gases and aerosol particles that play important roles in atmospheric chemistry and climate. Emissions of carbon monoxide and methane by biomass burning affect the oxidation efficiency of the atmosphere by reacting with hydroxyl radicals, and emissions of nitric oxide and hydrocarbons lead to high ozone concentrations in the tropics during the dry season. Large quantities of smoke particles are produced as well, and these can serve as cloud condensation nuclei. These particles may thus substantially influence cloud microphysical and optical properties, an effect that could have repercussions for the radiation budget and the hydrological cycle in the tropics. Widespread burning may also disturb biogeochemical cycles, especially that of nitrogen. About 50 percent of the nitrogen in the biomass fuel can be released as molecular nitrogen. This pyrdenitrification process causes a sizable loss of fixed nitrogen in tropical ecosystems, in the range of 10 to 20 teragrams per year (1 teragram = 10(12) grams).     

The role of sea spray in cleansing air pollution over ocean via cloud processes

Particulate air pollution has been shown to strongly suppress precipitation from convective clouds over land. New observations show that precipitation from similar polluted clouds over oceans is much less affected, because large sea salt nuclei override the precipitation suppression effect of the large number of small pollution nuclei. Raindrops initiated by the sea salt grow by collecting small cloud droplets that form on the pollution particles, thereby cleansing the air. Therefore, sea salt helps cleanse the atmosphere of the air pollution via cloud processes. This implies that over oceans, the climatic aerosol indirect effects are significantly smaller than current estimates.     

Cloud condensation nuclei on the atlantic seaboard of the United States

Concentrations of cloud condensation nuclei measured along the East Coast from Virginia to Long Island ranged from 1000 to 3500 per cubic centimeter as compared to 100 per cubic centimeter in clean maritime air and 300 per cubic centimeter in continental air. The global anthropogenic production rate of cloud condensation nuclei may be comparable to the natural production rate; in some industrial areas cloud condensation nuclei are dominated by anthropogenic sources.     

Flood or drought: how do aerosols affect precipitation?

Aerosols serve as cloud condensation nuclei (CCN) and thus have a substantial effect on cloud properties and the initiation of precipitation. Large concentrations of human-made aerosols have been reported to both decrease and increase rainfall as a result of their radiative and CCN activities. At one extreme, pristine tropical clouds with low CCN concentrations rain out too quickly to mature into long-lived clouds. On the other hand, heavily polluted clouds evaporate much of their water before precipitation can occur, if they can form at all given the reduced surface heating resulting from the aerosol haze layer. We propose a conceptual model that explains this apparent dichotomy.     

Particle formation by ion nucleation in the upper troposphere and lower stratosphere

Unexpectedly high concentrations of ultrafine particles were observed over a wide range of latitudes in the upper troposphere and lower stratosphere. Particle number concentrations and size distributions simulated by a numerical model of ion-induced nucleation, constrained by measured thermodynamic data and observed atmospheric key species, were consistent with the observations. These findings indicate that, at typical upper troposphere and lower stratosphere conditions, particles are formed by this nucleation process and grow to measurable sizes with sufficient sun exposure and low preexisting aerosol surface area. Ion-induced nucleation is thus a globally important source of aerosol particles, potentially affecting cloud formation and radiative transfer.     

Effects of aerosol from biomass burning on the global radiation budget

An analysis is made of the likely contribution of smoke particles from biomass burning to the global radiation balance. These particles act to reflect solar radiation directly; they also can act as cloud condensation nuclei, increasing the reflectivity of clouds. Together these effects, although uncertain, may add up globally to a cooling effect as large as 2 watts per square meter, comparable to the estimated contribution of sulfate aerosols. Anthropogenic increases of smoke emission thus may have helped weaken the net greenhouse warming from anthropogenic trace gases.     

河北省气溶胶与云微物理结构的飞机探测个例分析

通过对2008年4月21日河北省正定1次飞机探测气溶胶垂直分布和云微物理结构的资料进行分析,结果表明：探测的气溶胶数浓度为10^2～10^3个／cm^3,平均直径为0．19～0．70μm;云滴数浓度为10^0～10^2／cm^3,云滴平均直径为4～15μm。边界层是气溶胶和云凝结核（CCN）最密集处,云区为1176～2465m,云底云滴数浓度低,蒸发释放核膜态粒子使得气溶胶进入云层后数浓度减少幅度较小,另云滴对CCN有消耗作用。气溶胶平均谱基本为双峰型,高层云区云滴增加促使气溶胶由核膜态向积聚模态、粗模态转变。云滴谱较复杂,具有单峰型和双峰型,云顸平均谱最宽。     

Evidence for liquid-phase cirrus cloud formation from volcanic aerosols: climatic implications

Supercooled droplets in cirrus uncinus cell heads between -40 degrees and -50 degrees C are identified from Project FIRE [First ISCCP (International Satellite Cloud Climatology Project) Regional Experiment] polarization lidar measurements. Although short-lived, complexes of these small liquid cells seem to have contributed importantly to the formation of the cirrus. Freezing-point depression effects in solution droplets, apparently resulting from relatively large cloud condensation nuclei of volcanic origin, can be used to explain this rare phenomenon. An unrecognized volcano-cirrus cloud climate feedback mechanism is implied by these findings.     

Organic aerosol growth mechanisms and their climate-forcing implications

Surface- and volume-limited chemical reactions on and in atmospheric aerosol particles cause growth while changing organic composition by 13 to 24% per day. Many of these particles contain carbonaceous components from mineral dust and combustion emissions in Africa, Asia, and North America and reveal reaction rates that are three times slower than those typically used in climate models. These slower rates for converting from volatile or hydrophobic to condensed and hygroscopic organic compounds increase carbonaceous particle burdens in climate models by 70%, producing organic aerosol climate forcings of as much as -0.8 watt per square meter cooling and +0.3 watt per square meter warming.     

阴天条件下河北地区大气气溶胶粒子分布特征分析

利用2007年春季在河北省中南部地区2架次飞机探测资料,分析了该地区阴天情况下大气气溶胶粒子浓度和谱的分布特征。结果表明,南支槽和华北低涡天气系统下气溶胶粒子浓度随高度的增加总的趋势是减小的,但如果高空有卷层云存在时,出现随高度增加而增加的现象。逆温层底存在气溶胶和云滴的明显累积。受复杂天气系统的影响,气溶胶粒子谱由于上升气流或乱流的扰动,呈多峰型分布。     

How Does a Raindrop Grow?: Precipitation in natural clouds may develop from ice crystals or from large hygroscopic aerosols

On the basis of presently available data, combined with present-day knowledge of the physics and chemistry of cloud particle development, it is possible to make the following generalizations about the mode of precipitation in natural clouds. 1) The all-water mechanism begins to operate as soon as a parcel of cloud air is formed and continues to operate throughout the life of the cloud. The ice-crystal mechanism, on the other hand, can begin to operate only after the top of the cloud has reached levels where ice nuclei can be effective (about -15 degrees C). Some clouds never reach this height; any precipitation from them must be through the all-water mechanism. In cold climates and at high levels in the atmosphere, the cloud bases may be very close to this critical temperature. In the tropics, approximately 25,000 feet separate the bases of low clouds from the natural ice level. 2) The number of large hygroscopic nuclei in maritime air over tropical oceans is entirely adequate to rain-out any cloud with a base below about 10,000 feet, provided the cloud duration and cloud depth is sufficient for the precipitation process to operate. Extensive trajectories over land will decrease the number of sea-salt particles, both because of sedimentation and removal in rain. Measurements show an order-of-magnitude decrease in the number of large particles as maritime air moves from the Gulf of Mexico to the vicinity of St. Louis, during the summer months. Measurements in Arizona and New Mexico show even smaller chloride concentrations, presumably because of the long overland trajectories required in reaching these areas. The maritime particles lost in overland trajectories apparently are more than replaced by particles of land origin. The latter are usually of mixed composition and are less favorable for the formation of outsized solution droplets. 3) Ice nuclei, required for the formation of ice crystals and for droplet freezing, are rather rare at temperatures higher than about -10 degrees C. This, of course, accounts for the fact that natural clouds undergo extensive undercooling. Because of the scarcity of suitable nuclei, precipitation through the ice phase usually is not found in clouds warmer than about -15 degrees to -20 degrees C. Natural cirrus clouds might provide ice nuclei for precipitation at somewhat higher temperatures, but this possibility has not been extensively studied. 4) Precipitation in tropical clouds invariably first develops through the all-water mechanism; points discussed in paragraphs 1, 2, and 3 above all work toward this end. Tropical clouds which reach to heights above about 25,000 feet also develop precipitation through snow pellets. The data for mid-latitude clouds are conflicting. Some measurements suggest that summer clouds in the central United States and in the semiarid Southwest develop rain largely through the all-water process; existing theories support such a suggestion. However, flight measurements indicate that there is considerably more ice and snow in the clouds than can be accounted for by present theory; as a consequence, one must be careful in ruling out the ice mechanism in these areas. It appears to me, however, that the ice particles in these clouds are best accounted for through the hypothesis of freezing of drops which have grown to fairly large size through diffusion of vapor. Thus, the ice would be only incidental to the precipitation development. Winter clouds in the central United States and almost all of the clouds of northern United States and Canada appear to precipitate largely through the ice-crystal mechanism. The relatively cold cloud bases and the continental sources of air masses in these regions appear to retard the warm-rain mechanism to the point where the ice mechanism dominates. But here again, a great deal of research must be completed before a firm conclusion can be drawn (18).     

Clouds of venus: particle size distribution measurements

Data from the Pioneer Venus cloud particle size spectrometer experiment has revealed the Venus cloud system to be a complicated mixture of particles of various chemical composition distinguishable by their multimodal size distributions. The appearance, disappearance, growth, and decay of certain size modes has aided the preliminary identification of both sulfuric acid and free sulfur cloud regions. The discovery of large particles > 30 micrometers, significant particle mass loading, and size spectral features suggest that precipitation is likely produced; a peculiar aerosol structure beneath the lowest cloud layer could be residue from a recent shower.     

Venus clouds: a dirty hydrochloric Acid model

The spectral and polarization data for Venus are consistent with micrometer-sized aerosol cloud particles of hydrochloric acid with soluble and insoluble iron compounds, whose source could be volcanic or crustal dust. The yellow color of the clouds could be due to absorption bands in the near ultraviolet involving ferric iron and chlorine complexes. The ultraviolet features could arise from variations in the concentrations of iron and hydrochloric acid in the cloud particles.     

Clouds of venus: a preliminary assessment of microstructure

The multimodal microstructure of the Venus cloud system has been examined. In addition to confirmed H(2)SO(4) droplets and suspected elemental sulfur, a highly concentrated aerosol population has been observed extending above, within, and below the cloud system. These aerosols appear to cycle through the cloud droplets, but can never be removed by the weak precipitation mechanisms present. All cloud particles are likely laced with aerosol contaminants. Sedimentation and decomposition of H(2)SO(4) in the droplets of the lower cloud region contribute more than 7 watts per square meter of heat flux equaling one-fourth of the solar net flux at 50 kilometers.     

Dissipation of marine stratiform clouds and collapse of the marine boundary layer due to the depletion of cloud condensation nuclei by clouds

When the production of cloud condensation nuclei in the stratocumulus-topped marine boundary layer is low enough, droplet collisions can reduce concentrations of cloud droplet numbers to extremely low values. At low droplet concentrations a cloud layer can become so optically thin that cloud-top radiative cooling cannot drive vertical mixing. Under these conditions, model simulations indicate that the stratocumulus-topped marine boundary layer collapses to a shallow fog layer. Through this mechanism, marine stratiform clouds may limit their own lifetimes.     

Cloud condensation nuclei from a simulated forest fire

Measurements made downwind of a simulated forest fire showed that the concentration of cloud condensation nuclei active at a supersaturation of 1 percent was increased by a factor of about 2.5. Smaller increases were observed at lower supersaturations.