Atmospheric samples were collected during warm and cold weather condit
ions at continental, coastal and marine sites. Source sampling was per
formed at a coal-fired power plant and several volcanic sites. Atmosph
eric gas-phase and particulate boron concentrations were determined by
neutron capture prompt-gamma activation analysis and compared to meas
urements from other studies. Rain and snow samples collected at one co
ntinental site were analysed for soluble and insoluble B. Volcanic dep
osit and ash samples were also analysed for B. The tropospheric burden
s for particulate and gas-phase B were estimated to be 0.6 x 10(10) g
and (6-11) x 10(10) g, respectively, with the latter about a factor of
3 lower than previous estimates. Global anthropogenic particulate and
gas-phase B source estimates were consistent with previous estimates,
and natural particulate and gas-phase B source estimates agreed reaso
nably well with previously reported upper limits. About 65-85 % of tot
al B source strength can be attributed to the oceans, and 8-20% to coa
l, agricultural, fuelwood and refuse burning. Volcanism may contribute
6-15% of the total, but accurate source estimates are difficult. Tota
l global B removal from the atmosphere by wet and dry deposition was e
stimated to be (530-700) x 10(10) gyr-1, a factor of 2 lower than prev
iously reported but in fairly good agreement with the global total B s
ource estimate of (200-530) x 10(10) gyr-1.