Measurements of Cl-36 were performed in modern annual precipitation from ma
ny world-wide distributed stations. The measured deposition fluxes were on
the average half an order of magnitude larger than fluxes calculated from t
he cosmic-ray-induced atmospheric production. These discrepancies were tent
atively explained by recycling of bomb Cl-36 from the biosphere as methyl c
hloride (CH3Cl) into the troposphere, destruction of CH3Cl by OH reactions
and subsequent tropospheric deposition of Cl-36. Simulations were performed
for natural atmospheric production, bomb fall-out and recycling of Cl-36.
The simulations including recycling were qualitatively able to explain the
excess in deposition fluxes, especially for tropical regions. (C) 2000 Else
vier Science B.V. All rights reserved.