R. Sequeira, ON THE LARGE-SCALE IMPACT OF ARID DUST ON PRECIPITATION CHEMISTRY OF THE CONTINENTAL NORTHERN-HEMISPHERE, Atmospheric environment. Part A, General topics, 27(10), 1993, pp. 1553-1565
Airborne calcium is an indicator of a major alkaline component, calcit
e, when associated with soil-derived dust. Hence, a study of the distr
ibution of calcium in aerosol and precipitation is as important as sul
phate, and ammonium nitrate for a balanced understanding of the distri
bution of background acidity in precipitation. The large-scale distrib
ution of the concentration of dissolved continental calcium in north h
emispheric precipitation has been examined critically in relation to t
he geographical distribution of the arid zones and loessial belts-insi
de and outside the desert margins. Some unfamiliar but potential aeoli
an impacts are also discussed. The two distributions are closely tied,
once long-distance transports are explained. Available data point to
the vast arid region to the east and north of the Caspian Sea in the s
outhwestern part of the Asian C.I.S. (Commonwealth of Independent Stat
es) to be housing the most energetic and frequent dust-producers in th
e Northern Hemisphere. Some of the weakest and less frequent sources s
eem to lie in the region of southwestern U.S.A. Intermediate positions
are occupied by the central Asian deserts and the vast Saharan belt.
Some large-scale implications of these data to neutralization of preci
pitation acidity are suggested. It is apparent that the usual distribu
tion of calcium concentration is bracketed by the range 0.5-8 mg l-1 w
ith anomalous maxima in individual samples exceeding 10 mg l-1, someti
mes reaching a little over 40 mg l-1. Such high maxima are attributed
mainly to calcareous silt particles of loessial origin. The sudden tem
poral decrease in the annual average calcium concentration from 1.4 pp
m to approximately 0.5 ppm between the mid-1950s to the early 1980s is
almost identical for the eastern U.S.A. and northern Europe. Temporal
decrease in soil aridity and/or identical recent changes in precipita
tion sampling strategy in the U.S.A. and Scandinavia may have caused t
his change.