Occurrence and formation of chloroform at Danish forest sites

被引:42
作者
Haselmann, KF
Ketola, RA
Laturnus, F
Lauritsen, FR
Gron, C
机构
[1] Riso Natl Lab, Dept Plant Biol & Biogeochem, DK-4000 Roskilde, Denmark
[2] Odense Univ, Dept Biochem, DK-5230 Odense, Denmark
[3] VTT Chem Technol, FIN-02044 Espoo, Finland
关键词
chloroform; volatile chlorinated compounds; soil production; air sampling; gas chromatography; coniferous forest;
D O I
10.1016/S1352-2310(99)00279-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ambient air and soil air of spruce forest, beech forest and grassland from Zealand, Denmark, were investigated for volatile chlorinated compounds by adsorbent tube sampling, thermodesorption, cryo-trapping and analysis by high-resolution gas chromatography with electron capture detection. The mean concentration of chloroform in the top soil-air was in the range of 0.4-2.3 ng 1(-1). Compared to ambient air, the chloroform concentration in the topsoil was 6.7, 4.3 and 4.6 times higher for spruce forest, beech forest and grassland, respectively. For tetrachloromethane, 1,1,1-trichloroethane, trichloroethene and tetrachloroethene, the concentrations were in the same order of magnitude (0.04-1.2 ng 1(-1)). However, the concentration ratios between soil air and ambient air were close to unity. Release studies in the topsoil of the spruce forest showed an increase of the chloroform concentration of approximately 4 times the initial soil air concentration after 38 h, while the concentrations of the other volatile chlorinated compounds investigated remained fairly constant. The observed chloroform concentration profiles and release rates may indicate a biogenic formation of chloroform in the upper soil layer of spruce forests, whereas an anthropogenic origin is suggested for the other chlorinated compounds investigated. From the release study and concentration gradient measurements in the spruce forest soil, chloroform release to the atmosphere was calculated for northern temperate regions. The release was in the range of the annual anthropogenic chloroform emissions, and, therefore, the terrestrial environment can be considered as an important contributor to the atmospheric chloroform input. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:187 / 193
页数:7
相关论文
共 32 条
[1]  
[Anonymous], STAT WORLDS FOR 1997
[2]  
[Anonymous], 1998, CHEMODYNAMICS ENV MO
[3]   ORGANOHALOGENS IN NATURE [J].
ASPLUND, G ;
GRIMVALL, A .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1991, 25 (08) :1346-1350
[4]   A CHLOROPEROXIDASE-LIKE CATALYST IN SOIL - DETECTION AND CHARACTERIZATION OF SOME PROPERTIES [J].
ASPLUND, G ;
CHRISTIANSEN, JV ;
GRIMVALL, A .
SOIL BIOLOGY & BIOCHEMISTRY, 1993, 25 (01) :41-46
[5]  
Asplund G, 1995, ENVIRON CHEM, V1, P35
[6]  
ASPLUND G, 1989, HUMIC SUBSTANCES AQU, P475
[7]   C1-HALOCARBONS AND C2-HALOCARBONS IN SOIL-AIR OF FORESTS [J].
FRANK, H ;
FRANK, W ;
THIEL, D .
ATMOSPHERIC ENVIRONMENT, 1989, 23 (06) :1333-1335
[8]  
Frank Hartmut, 1994, Environmental Science and Pollution Research International, V1, P4, DOI 10.1007/BF02986917
[9]   CONCENTRATIONS OF AIRBORNE C1-HALOCARBONS AND C2-HALOCARBONS IN FOREST AREAS IN WEST-GERMANY - RESULTS OF 3 CAMPAIGNS IN 1986, 1987 AND 1988 [J].
FRANK, W ;
FRANK, H .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1990, 24 (07) :1735-1739
[10]  
Grimvall A, 1995, ENVIRON CHEMISTRY, V1, P3