M. Stein et al., STRONTIUM ISOTOPIC, CHEMICAL, AND SEDIMENTOLOGICAL EVIDENCE FOR THE EVOLUTION OF LAKE-LISAN AND THE DEAD-SEA, Geochimica et cosmochimica acta, 61(18), 1997, pp. 3975-3992
Precise strontium isotope ratios, combined with chemical analyses and
sedimentological information, are used to monitor the water sources an
d the evolution of the Dead Sea and its late Pleistocene precursor, La
ke Lisan (70-18 kyr B.P.). The materials analyzed include bulk aragoni
te, water-leached soluble salts, and residual aragonite and gypsum fro
m the Lisan Formation in the Perazim Valley (near the SW shore of the
Dead Sea). The residual aragonite and the associated soluble salts dis
play systematic fluctuations in Sr-87/Sr-86 ratios between 0.70803 and
0.70806 and from 0.70805 to 0.70807, respectively. In individual solu
ble salt-residual aragonite pairs, the soluble salt displays a higher
Sr-87/Sr-86 ratio. Gypsum samples yield Sr-87/Sr-86 ratios similar to
the soluble salts from adjacent layers in the section. This shows that
, in individual samples, the source of Sr in aragonite was distinct fr
om that in soluble salts and the gypsum. The sterility of the Lisan se
diments, their strictly nonbioturbated fine lamination, and their high
content of chloride salts indicate that Lake Lisan was a saline, or e
ven hypersaline water body. In the absence of alternative sources of H
CO3- and SO42- the abundance of primary aragonite and gypsum in the Li
san column reflects an import of very large volumes of freshwater into
the otherwise saline lake, resulting in a density stratification of t
his water body. The history of the upper water layer and that of the l
ower brine is reflected in the chemical and strontium isotope composit
ion of the aragonite and in that of the associated soluble salts and i
n the gypsum samples, respectively. Whereas the bicarbonate and much o
f the Ca2+ required for aragonite crystallization were supplied by the
freshwater, the complementary Ca2+ (and Sr2+) were added by the lower
brine. The upper water layer of Lake Lisan acted as a SO42- capacitor
during the lake's rise periods. It was removed therefrom, as prominen
t gypsum beds, upon climatic-induced (drier period) mixing or even com
plete overturn of the lake. The evolution of Lake Lisan took place bet
ween two distinct modes. The first was characterized by an extensive s
upply of freshwater and resulted in a rise of the lake's level, a (den
sity) layered structure, and precipitation of aragonite. The second mo
de was marked by a diminishing freshwater input, resulting in mixing o
r complete overturn of its water, and precipitation of gypsum. These t
wo modes reflect the climatic evolution of the region in the late Plei
stocene which fluctuated between drier and wetter periods. The transit
ion to the Holocene is accompanied by the dry up of Lake Lisan and its
contraction to the present Dead Sea. Copyright (C) 1997 Elsevier Scie
nce Ltd.