Mass balance of the atmospheric aerosol in a South African subtropical savanna (Nylsvley, May 1997)

被引:48
作者
Puxbaum, H
Rendl, J
Allabashi, R
Otter, L
Scholes, MC
机构
[1] Vienna Univ Technol, Inst Analyt Chem, A-1060 Vienna, Austria
[2] Univ Witwatersrand, Dept Bot, Johannesburg, South Africa
关键词
D O I
10.1029/2000JD900306
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Aerosol samples were collected at Nylsvley Natural Reserve in northeastern South Africa at the beginning of the dry season, when large-scale fires were absent. Aerosol was collected on quartz fiber filters with open face stack filters in an inlet with an upper cutoff mass median diameter of 30 mu m. The samples were analyzed for soluble ions (Cl-, NO3-, SO42-, oxalate, NH4+, Na+, K+, Ca2+, Mg2+), trace metals and crustal elements (Fe, Mn, Ca, Mg, Pb, Cu, Ag, Cd), "black carbon" (BC), total carbon (TC); and in selected samples for aerosol humidity, for mono- and dicarboxylic acids and other polar organic components, and for cellulose as a tracer for plant debris. Aerosol mass balances for the individual samples were constructed from the sum of following groups: Humidity (determined as weight loss at 100 degrees C with a microthermobalance), ammonium sulfate, Cl- and NO3-, organic material, BC, and soil dust. On the average, the fit between the sum of the determined groups of components and the gravimetrically determined mass was within 6%, whereas deviations ranged for individual samples from -12 to +27% relative to the gravimetrically determined mass. The main component in aerosol was soil dust (36%), followed by organic material (28%), and ammonium sulfate (27%). Humidity was 6%, BC was 2%, and Cl- lard NO3- were 1% of aerosol mass. The low BC/TC ratio of 0.09 indicated little influence from combustion sources. The diurnal trend of the BC/TC ratio of 0.06 during day and 0.14 during night indicated a daytime source for organic components with no BC associated. As there were no industrial or other anthropogenic sources evident, the daytime source of organic components is assumed to be gas-particle conversion from biogenic emissions. Plant debris and organic acids were the major analytically accessible groups; however, together they form only 7.2% of the carbonaceous material. With 0.4% other polar organics and 5.7% BC in this group, 86.7% of the carbonaceous material remains unidentified.
引用
收藏
页码:20697 / 20706
页数:10
相关论文
共 54 条
[31]   OPTICAL AND THERMAL MEASUREMENTS OF BLACK CARBON AEROSOL CONTENT IN DIFFERENT ENVIRONMENTS - VARIATION OF THE SPECIFIC ATTENUATION CROSS-SECTION, SIGMA (SIGMA) [J].
LIOUSSE, C ;
CACHIER, H ;
JENNINGS, SG .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1993, 27 (08) :1203-1211
[32]   Regional atmospheric aerosol composition and sources in the eastern Transvaal, South Africa, and impact of biomass burning [J].
Maenhaut, W ;
Salma, I ;
Cafmeyer, J ;
Annegarn, HJ ;
Andreae, MO .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1996, 101 (D19) :23631-23650
[33]  
MAENHAUT W, 1998, EOS Transactions of the American Geophysical Union, V79, pF155
[34]  
Moore, 1982, PRINCIPLES GEOCHEMIS
[35]   LARGE CONTRIBUTION OF ORGANIC AEROSOLS TO CLOUD-CONDENSATION-NUCLEI CONCENTRATIONS [J].
NOVAKOV, T ;
PENNER, JE .
NATURE, 1993, 365 (6449) :823-826
[36]   Chemical characterization of atmospheric fine particles in Sapporo with determination of water content [J].
Ohta, S ;
Hori, M ;
Yamagata, S ;
Murao, N .
ATMOSPHERIC ENVIRONMENT, 1998, 32 (06) :1021-1025
[37]   A CHEMICAL CHARACTERIZATION OF ATMOSPHERIC AEROSOL IN SAPPORO [J].
OHTA, S ;
OKITA, T .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1990, 24 (04) :815-822
[38]  
PIKETH SJ, 1996, EOS T AGU S, V77, P77
[39]   CONTINUED DEVELOPMENT OF A GENERAL EQUILIBRIUM-MODEL FOR INORGANIC MULTICOMPONENT ATMOSPHERIC AEROSOLS [J].
PILINIS, C ;
SEINFELD, JH .
ATMOSPHERIC ENVIRONMENT, 1987, 21 (11) :2453-2466
[40]  
PUXBAUM H, 1983, MIKROCHIM ACTA, V1, P263