Real-time measurements of ammonia, acidic trace gases and water-soluble inorganic aerosol species at a rural site in the Amazon Basin

被引:148
作者
Trebs, I
Meixner, FX
Slanina, J
Otjes, R
Jongejan, P
Andreae, MO
机构
[1] Max Planck Inst Chem, Biogeochem Dept, D-55020 Mainz, Germany
[2] Energy Res Ctr Netherlands, Dept Air Qual, NL-1755 ZG Petten, Netherlands
关键词
D O I
10.5194/acp-4-967-2004
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We measured the mixing ratios of ammonia (NH3), nitric acid (HNO3), nitrous acid (HONO), hydrochloric acid (HCl), sulfur dioxide (SO2) and the corresponding water-soluble inorganic aerosol species, ammonium (NH4+), nitrate (NO3-), nitrite (NO2-), chloride (Cl-) and sulfate (SO42-), and their diel and seasonal variations at a pasture site in the Amazon Basin (Rondonia, Brazil). This study was conducted within the framework of LBA-SMOCC ( Large Scale Biosphere Atmosphere Experiment in Amazonia-Smoke Aerosols, Clouds, Rainfall and Climate: Aerosols from Biomass Burning Perturb Global and Regional Climate). Sampling was performed from 12 September to 14 November 2002, extending from the dry season ( extensive biomass burning activity), through the transition period to the wet season ( background conditions). Measurements were made continuously using a wet-annular denuder ( WAD) in combination with a Steam-Jet Aerosol Collector (SJAC) followed by suitable on-line analysis. A detailed description and verification of the inlet system for simultaneous sampling of soluble gases and aerosol compounds is presented. Overall measurement uncertainties of the ambient mixing ratios usually remained below 15%. The limit of detection (LOD) was determined for each single data point measured during the field experiment. Median LOD values (3sigma-definition) were less than or equal to0.015 ppb for acidic trace gases and aerosol anions and less than or equal to0.118 ppb for NH3 and aerosol NH4+. Mixing ratios of acidic trace gases remained below 1 ppb throughout the measurement period, while NH3 levels were an order of magnitude higher. Accordingly, mixing ratios of NH4+ exceeded those of other inorganic aerosol contributors by a factor of 4 to 10. During the wet season, mixing ratios decreased by nearly a factor of 3 for all compounds compared to those observed when intensive biomass burning took place. Additionally, N-containing gas and aerosol species featured pronounced diel variations. This is attributed to strong relative humidity and temperature variations between day and night as well as to changing photochemistry and stability conditions of the planetary boundary layer. HONO exhibited a characteristic diel cycle with high mixing ratios at nighttime and was not completely depleted by photolysis during daylight hours.
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页码:967 / 987
页数:21
相关论文
共 113 条
[71]   MEASUREMENT OF GASEOUS NITRIC-ACID BY A LASER-PHOTOLYSIS FRAGMENT-FLUORESCENCE (LPFF) METHOD IN THE BLACK-FOREST AND AT THE NORTH-SEA COAST [J].
PAPENBROCK, T ;
STUHL, F .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1991, 25 (10) :2223-2228
[72]   A LASER-PHOTOLYSIS FRAGMENT-FLUORESCENCE (LPFF) METHOD FOR THE DETECTION OF GASEOUS NITRIC-ACID IN AMBIENT AIR [J].
PAPENBROCK, T ;
STUHL, F .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1990, 10 (04) :451-469
[73]   MEASUREMENTS OF HNO3 AND NO3- PARTICULATES AT A RURAL SITE IN THE COLORADO MOUNTAINS [J].
PARRISH, DD ;
NORTON, RB ;
BOLLINGER, MJ ;
LIU, SC ;
MURPHY, PC ;
ALBRITTON, DL ;
FEHSENFELD, FC ;
HUEBERT, BJ .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1986, 91 (D5) :5379-5393
[74]   DETECTION OF NITROUS-ACID IN THE ATMOSPHERE BY DIFFERENTIAL OPTICAL-ABSORPTION [J].
PERNER, D ;
PLATT, U .
GEOPHYSICAL RESEARCH LETTERS, 1979, 6 (12) :917-920
[75]   UPTAKE OF NITROUS-ACID AND NITROGEN-OXIDES BY NYLON SURFACES - IMPLICATIONS FOR NITRIC-ACID MEASUREMENT [J].
PERRINO, C ;
DESANTIS, F ;
FEBO, A .
ATMOSPHERIC ENVIRONMENT, 1988, 22 (09) :1925-1930
[76]   A DIFFUSION SCRUBBER FOR THE COLLECTION OF GASEOUS NITRIC-ACID [J].
PHILIPS, DA ;
DASGUPTA, PK .
SEPARATION SCIENCE AND TECHNOLOGY, 1987, 22 (04) :1255-1267
[77]   THE EQUILIBRIUM OF AMMONIUM-CHLORIDE AEROSOL WITH GASEOUS HYDROCHLORIC-ACID AND AMMONIA UNDER TROPOSPHERIC CONDITIONS [J].
PIO, CA ;
HARRISON, RM .
ATMOSPHERIC ENVIRONMENT, 1987, 21 (05) :1243-1246
[78]   DIFFERENTIAL OPTICAL-ABSORPTION SPECTROMETER FOR MEASURING ATMOSPHERIC TRACE GASES [J].
PLANE, JMC ;
NIEN, CF .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1992, 63 (03) :1867-1876
[79]   MASS-TRANSFER AT THE AIR-WATER-INTERFACE - MASS ACCOMMODATION COEFFICIENTS OF SO2, HNO3, NO2 AND NH3 [J].
PONCHE, JL ;
GEORGE, C ;
MIRABEL, P .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1993, 16 (01) :1-21
[80]   Measurements of nitric acid and ammonium salts in lower Bavaria [J].
Possanzini, M ;
De Santis, F ;
Di Palo, V .
ATMOSPHERIC ENVIRONMENT, 1999, 33 (22) :3597-3602