Mj. Mayayo et al., MINERALOGY AND GEOCHEMISTRY OF THE CARBONATES IN THE CALATAYUD BASIN (ZARAGOZA, SPAIN), Chemical geology, 130(1-2), 1996, pp. 123-136
The Calatayud Basin is an elongated NW-SE depression in northeastern S
pain. It is filled with continental Miocene sediments resulting from e
rosion of Palaeozoic and Mesozoic rocks of the Castilian and Aragonese
branches of the Iberian Range. Miocene series consist of lutitic, mar
ry, carbonate and evaporitic levels characteristic of a short-lived sa
lt lake or a low-salinity playa-lake depositional environment. The car
bonates detected in the series were calcite, dolomite and magnesite. T
he calcites generally show micritic textures, anhedral to subhedral mo
rphologies and contain from 0 to 1 mole% MgCO3, and so can be consider
ed ''low-Mg calcites''. Their mean isotopic values are delta(18)O = -7
.8 parts per thousand (PDB) and delta(13)C = -7.7 parts per thousand i
ndicating precipitation in isotopic equilibrium with meteoric water an
d an extensive contribution of CO, of organic origin to the total diss
olved C, respectively. The calcites present Mg/Ca, Sr/Ca and Na/Ca mol
ar ratios that suggest precipitation from Na-enriched meteoric water.
Dolomites are non-stoichiometric (44.5-47.7 mole% MgCO3), disordered,
micritic and anhedral to subhedral; their mean isotopic values [delta(
18)O = + 0.4 parts per thousand (PDB) and delta(13)C = -3.8 parts per
thousand] indicate that they precipitated from more evolved water and
with a higher contribution of atmospheric CO2 to the total dissolved C
, respectively, than those of the calcites. Moreover, they present Mg/
Ca, Sr/Ca and Na/Ca molar ratios suggesting precipitation from water w
ith similar composition to seawater. The isotopic composition of magne
site [delta(18)O = + 4.6 parts per thousand (PDB) and delta(13)C = - 4
.0 parts per thousand], together with the higher concentration in Sr a
nd Na, indicates that this phase probably precipitated from more evolv
ed water. The isotopic values and trace-element contents of carbonates
appear to confirm the mineralogical trend from calcite to dolomite an
d to magnesite corresponding to the progressive increase of evaporitic
concentration as the water, in a hydrologically closed system, was su
bjected to more acutely arid conditions.