In:
Geophysical Research Letters, American Geophysical Union (AGU), Vol. 21, No. 12 ( 1994-06-15), p. 1161-1164
Abstract:
The isotopic composition of chlorine sampled from the atmosphere has been measured for the first time. Eight aerosol samples collected on bulk filters at Bermuda are enriched in 37 Cl relative to sea water. Stable chlorine isotopic compositions are reported in units of per mil as δ 37 Cl which is defined as 1000 × [( R sample / R sea water ) ‐ 1] where R is the ratio of 37 Cl to 35 Cl. The δ 37 Cl of the aerosols range from +0.42 to +2.53 per mil and strongly correlate with chlorine deficit (based upon sea salt sodium) and non‐sea salt sulfate. The data trend is consistent with the fractional distillation (loss) of HCl from an acidified aerosol governed by a fractionation factor of 0.9972. Subsequent experiments support the hypothesis that HCl evaporation was most likely the primary mechanism of chlorine volatilization in the sampled aerosols. Furthermore, the data indicate that marine aerosols perturbed by anthropogenic NOx and SO 2 are an important source of isotopically light chlorine in the free troposphere.
Type of Medium:
Online Resource
ISSN:
0094-8276
,
1944-8007
Language:
English
Publisher:
American Geophysical Union (AGU)
Publication Date:
1994
detail.hit.zdb_id:
2021599-X
detail.hit.zdb_id:
7403-2
SSG:
16,13
