F. Mees et al., STABLE-ISOTOPE CHEMISTRY OF GAYLUSSITE AND NAHCOLITE FROM THE DEPOSITS OF THE CRATER LAKE AT MALHA, NORTHERN SUDAN, Chemical geology, 146(1-2), 1998, pp. 87-98
Gaylussite (Na2CO3. CaCO3. 5H(2)O) and nahcolite (NaHCO3)( )in deposit
s of the crater lake at Malha are predictably characterized by a stron
g O-18 enrichment that is typical of evaporitic environments, Both min
erals also yield high delta(13)C values, which, in the case of gayluss
ite, are covariant with the delta(18)O values. The fact that the covar
iant trend, which is a feature that is commonly recognized for the dep
osits of closed basins, pertains both to the synsedimentary and pedoge
nic gaylussite deposits of the Malha basin demonstrates that C-13 enri
chment was mainly controlled by inorganic processes. An important biol
ogical control on the carbon isotope composition is also contradicted
by the occurrence of a covariance for synsedimentary gaylussite that m
ainly formed by bottom growth in a well-mixed water mass. Degassing of
carbon dioxide is the most likely cause of C-13 enrichment, although
this implies that CO2 loss is a process that occurs concurrently with
the evaporation of water, without, as could be expected, being driven
by changes in the relative abundance of compounds within the CO2-H2O s
ystem. The lack of a covariance of delta(18)O and delta(13)C for nahco
lite seems to be partly related to bacterial activity, which did play
an important role during lake stages with nahcolite formation, and par
tly to the lack of a further increase of delta(18)O with continued eva
poration at advanced stages of the evaporitic concentration of brines.
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