Airborne minerals and related aerosol particles:: Effects on climate and the environment

被引:372
作者
Buseck, PR [1 ]
Pósfai, M
机构
[1] Arizona State Univ, Dept Geog, Tempe, AZ 85287 USA
[2] Arizona State Univ, Dept Chem Biochem, Tempe, AZ 85287 USA
关键词
D O I
10.1073/pnas.96.7.3372
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Aerosol particles are ubiquitous in the troposphere and exert an important influence on global climate and the environment. They affect climate through scattering, transmission, and absorption of radiation as well as by acting as nuclei for cloud formation. A significant fraction of the aerosol particle burden consists of minerals, and most of the remainder-whether natural or anthropogenic-consists of materials that can be studied by the same methods as are used for fine-grained minerals. Our emphasis is on the study and character of the individual particles. Sulfate particles are the main cooling agents among aerosols; we found that in the remote oceanic atmosphere a significant fraction is aggregated with soot, a material that can diminish the cooling effect of sulfate. Our results suggest oxidization of SO2 may have occurred on soot surfaces, implying that even in the remote marine troposphere soot provided nuclei for heterogeneous sulfate formation. Sea salt is the dominant aerosol species (by mass) above the oceans. In addition to being important light scatterers and contributors to cloud condensation nuclei, sea-salt particles also provide large surface areas for heterogeneous atmospheric reactions, Minerals comprise the dominant mass fraction of the atmospheric aerosol burden. As all geologists know, they are a highly heterogeneous mixture. However, among atmospheric scientists they are commonly treated as a fairly uniform group, and one whose interaction with radiation is widely assumed to be unpredictable. Given their abundances, large total surface areas, and reactivities, their role in influencing climate will require increased attention as climate models are refined.
引用
收藏
页码:3372 / 3379
页数:8
相关论文
共 99 条
[1]
Airborne particulate matter [J].
Abelson, PH .
SCIENCE, 1998, 281 (5383) :1609-1609
[2]
ABSORPTION OF VISIBLE RADIATION IN ATMOSPHERE CONTAINING MIXTURES OF ABSORBING AND NON-ABSORBING PARTICLES [J].
ACKERMAN, TP ;
TOON, OB .
APPLIED OPTICS, 1981, 20 (20) :3661-3668
[3]
Characterization of the Bermuda tropospheric aerosol by combined individual-particle and bulk-aerosol analysis [J].
Anderson, JR ;
Buseck, PR ;
Patterson, TL ;
Arimoto, R .
ATMOSPHERIC ENVIRONMENT, 1996, 30 (02) :319-338
[4]
CHARACTERIZATION OF INDIVIDUAL FINE-FRACTION PARTICLES FROM THE ARCTIC AEROSOL AT SPITSBERGEN, MAY-JUNE 1987 [J].
ANDERSON, JR ;
BUSECK, PR ;
SAUCY, DA ;
PACYNA, JM .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1992, 26 (09) :1747-1762
[5]
ANDERSON JR, 1998, ADV MINERALOGY, V3, P301
[6]
Andreae M.O., 1995, World Survey of Climatology, vol. 16, V16, P341, DOI 10.1016/S0168-6321(06)80033-7
[7]
INTERNAL MIXTURE OF SEA SALT, SILICATES, AND EXCESS SULFATE IN MARINE AEROSOLS [J].
ANDREAE, MO ;
CHARLSON, RJ ;
BRUYNSEELS, F ;
STORMS, H ;
VANGRIEKEN, R ;
MAENHAUT, W .
SCIENCE, 1986, 232 (4758) :1620-1623
[8]
Raising dust in the greenhouse [J].
Andreae, MO .
NATURE, 1996, 380 (6573) :389-390
[9]
Atmospheric aerosols: Biogeochemical sources and role in atmospheric chemistry [J].
Andreae, MO ;
Crutzen, PJ .
SCIENCE, 1997, 276 (5315) :1052-1058
[10]