TOWARD AN UNDERSTANDING OF THE GLOBAL ATMOSPHERIC DISTRIBUTION OF PERSISTENT ORGANIC POLLUTANTS - THE USE OF SEMIPERMEABLE-MEMBRANE DEVICESAS TIME-INTEGRATED PASSIVE SAMPLERS

Citation
Wa. Ockenden et al., TOWARD AN UNDERSTANDING OF THE GLOBAL ATMOSPHERIC DISTRIBUTION OF PERSISTENT ORGANIC POLLUTANTS - THE USE OF SEMIPERMEABLE-MEMBRANE DEVICESAS TIME-INTEGRATED PASSIVE SAMPLERS, Environmental science & technology, 32(18), 1998, pp. 2795-2803
Citations number
36
Categorie Soggetti
Environmental Sciences","Engineering, Environmental
ISSN journal
0013936X
Volume
32
Issue
18
Year of publication
1998
Pages
2795 - 2803
Database
ISI
SICI code
0013-936X(1998)32:18<2795:TAUOTG>2.0.ZU;2-#
Abstract
Triolein-containing semipermeable membrane devices (SPMDs) were deploy ed as passive air samplers alongside conventional air samplers at two sites, and derived atmospheric concentrations from each were compared. Excellent comparability was noted between sampling systems. SPMDs wer e also deployed for 2 years at 10 sites across a latitudinal transect from the south of the U.K. (ca. 50 degrees N) to the north of Norway ( ca. 70 degrees N) to passively sample air. Time-integrated, simultaneo us data were obtained, which were used to test the global fractionatio n hypothesis in the Northern Hemisphere. Extracts were analyzed for a suite of PCB congeners and alpha- and gamma-HCH. A latitudinal change in PCB profiles was seen. The absolute atmospheric concentration of th e tetra-chlorinated PCBs was relatively uniform over the study area (c a. 1.9 pg m(-3)), but their relative concentration increased with incr easing latitude or decreasing temperature (12% of total PCB concentrat ions in the south of the U.K. as compared with 35% at the northern-mos t station). The concentration of the penta-chlorinated PCBs decreased from 6 pg m(-3) at the southern U.K. site to 1.5 pg m(-3) in the north of Norway, but their relative concentration was uniform (33% total PC B) over the transect. Absolute and relative concentrations of heavier PCBs decreased with increasing latitude and decreasing temperature. Th ese data indicate that a temperature-controlled fractionation of PCBs is occurring in the atmosphere. Data were available for soil PCB conce ntrations at or near seven of the air sampling sites. Fugacity quotien ts suggested that across the study area the air/soil system is at or n ear to equilibrium for PCBs. Concentrations of the alpha-HCH isomer se questered by the SPMDs increased from south to north while the sequest ered gamma-HCH concentrations decreased. The ratio of alpha/gamma-HCH increased by a factor of approximately 20 from the south to the north of the study area, These data are consistent with the selective weathe ring of these compounds during their long-range atmospheric transport from southerly source regions to remote northern locations.