MEASUREMENTS OF REDUCED SULFUR-COMPOUNDS IN AN INDUSTRIALIZED TROPICAL REGION - CUBATAO (BRAZIL)

Citation
W. Jaeschke et al., MEASUREMENTS OF REDUCED SULFUR-COMPOUNDS IN AN INDUSTRIALIZED TROPICAL REGION - CUBATAO (BRAZIL), International journal of environmental analytical chemistry, 54(4), 1994, pp. 315-337
Citations number
36
Categorie Soggetti
Environmental Sciences","Chemistry Analytical
ISSN journal
03067319
Volume
54
Issue
4
Year of publication
1994
Pages
315 - 337
Database
ISI
SICI code
0306-7319(1994)54:4<315:MORSIA>2.0.ZU;2-#
Abstract
Ambient concentrations of SO2, H2S, COS and CS2 has been determined at various sites in the highly industrialized area of Cubatao (Brazil) a nd in adjacent ecosystems during the years 1990 to 1993. Sulphate has been analyzed in rain samples collected at three sites in the Serra do Mar. The sites are called Vale do Mogi (heavily polluted), Paranapiac aba (moderately polluted), and Vale do Piloes (less polluted). Gas exc hange of reduced sulphur compounds between biosphere and atmosphere ha s been examined with the aid of ambient air enclosures. The investigat ed sulphur sources (and sinks) were the estuaries South of Cubatao, a reservoir north of Cubatao, and vegetated soils at Vale do Mogi, Paran apiacaba, and Vale do Piloes. The content of reduced sulphur compounds was determined in surface water samples from lakes, rivers, and estua ries in the area under investigation. We sulphate deposition and ambie nt SO2 concentrations revealed a similar hierarchy of Vale do Mogi, Pa ranapiacaba, and Vale do Piloes confirming the assumed pollution level s. In addition all investigated sites showed considerably elevated amb ient concentrations of H2S, COS, and CS2 when exposed to industrial em issions. Emissions from biogenic sources are dominant over the Billing s reservoir and over the estuaries. Flux measurements showed emissions of DMS and CH3SH from vegetated soils. Deposition or uptake were obse rved with respect to H2S, COS, and CS2 mainly due to high ambient conc entrations of these gases. DMS, COS, and CH3SH were present in most of the water samples analysed. Maximum DMS concentrations have been dete cted in anoxic freshwater and estuarine water.