Atmospheric semivolatile organochlorine compounds in European high-mountain areas (Central Pyrenees and High Tatras)

被引:76
作者
Van Drooge, BL
Grimalt, JO
Camarero, L
Catalan, J
Stuchlík, E
García, CJT
机构
[1] CSIC, ICER, Dept Environm Chem, Barcelona 08034, Spain
[2] CSIC, CEAB, Ctr Adv Studies, Blanes 17300, Catalonia, Spain
[3] Charles Univ Prague, Dept Hydrol, Prague 12044, Czech Republic
[4] Natl Inst Meteorol, Izana Atmospher Observ, Santa Cruz de La Palma 38071, Tenerife, Spain
关键词
D O I
10.1021/es030108p
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Atmospheric samples from two European high-mountain areas showed similar composition of semivolatile organochlorine compounds (SOC), such as polychlorobiphenyls (PCBs), DDTs, endosulfans, hexachlorobenzene (HCB), and hexachlorocyclohexanes (HCHs). Nearly all compounds were predominantly found in the gas phase and only the less volatile such as some PCBs (e.g., 149, 118, 153, 138, and 180) were found in higher abundance in the particulate phase. HCB, 49-85 pg m(-3), is the dominant SOC. This compound is only found in the gas phase exhibiting uniform concentrations irrespective of season and air mass origin. SOC of present use, like HCHs and endosulfans, were found in higher concentrations in the warm periods, 3246 and 4-10 pg m(-3) in the gas + particulate phases, respectively, reflecting their seasonal pattern of use in many European countries. PCB and 4,4'-DDE, 39-42 and 4-6 pg m(-3) in the gas + particulate phases, respectively, also showed a seasonal trend despite neither the former nor the precursor of the latter (4,4'-DDT) being manufactured with their use drastically restricted since the 1980s. The seasonal differences are mainly due to a higher occurrence of air masses with strong continental inputs in the warm than in the cold periods. In this respect, samples whose air masses traveled at the high troposphere (backward air mass trajectories >6000 m) have been observed to carry considerably smaller PCB and 4,4'-DDE loads (9.3 +/- 2.8 and 0.4 +/- 0.05 pg m(-3), respectively) than overall average.
引用
收藏
页码:3525 / 3532
页数:8
相关论文
共 39 条
[1]  
ARGELL C, 1999, ENVIRON SCI TECHNOL, V33, P1149
[2]  
Barry R. G., 1992, MOUNTAIN WEATHER CLI
[4]   Accumulation of persistent organochlorine compounds in mountains of western Canada [J].
Blais, JM ;
Schindler, DW ;
Muir, DCG ;
Kimpe, LE ;
Donald, DB ;
Rosenberg, B .
NATURE, 1998, 395 (6702) :585-588
[5]   Towards a global historical emission inventory for selected PCB congeners - a mass balance approach 2. Emissions [J].
Breivik, K ;
Sweetman, A ;
Pacyna, JM ;
Jones, KC .
SCIENCE OF THE TOTAL ENVIRONMENT, 2002, 290 (1-3) :199-224
[6]   CONCENTRATIONS AND FLUXES OF ORGANIC-COMPOUNDS IN THE ATMOSPHERE OF THE SWEDISH WEST-COAST [J].
BRORSTROMLUNDEN, E ;
LINDSKOG, A ;
MOWRER, J .
ATMOSPHERIC ENVIRONMENT, 1994, 28 (22) :3605-3615
[7]   EFFECTS OF TEMPERATURE AND WIND DIRECTION ON THE ATMOSPHERIC CONCENTRATIONS OF ALPHA-ENDOSULFAN [J].
BURGOYNE, TW ;
HITES, RA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1993, 27 (05) :910-914
[8]   Atmospheric deposition of organochlorine compounds to remote high mountain lakes of Europe [J].
Carrera, G ;
Fernández, P ;
Grimalt, JO ;
Ventura, M ;
Camarero, L ;
Catalan, J ;
Nickus, U ;
Thies, H ;
Psenner, R .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (12) :2581-2588
[9]   Enhanced sensitivity in the analysis of trace organochlorine compounds by negative-ion mass spectrometry with ammonia as reagent gas [J].
Chaler, R ;
Vilanova, R ;
Santiago-Silva, M ;
Fernandez, P ;
Grimalt, JO .
JOURNAL OF CHROMATOGRAPHY A, 1998, 823 (1-2) :73-79
[10]  
DANIELSEN EF, 1961, J METEOROL, V18, P479, DOI 10.1175/1520-0469(1961)018<0479:TIIAA>2.0.CO