MINERALOGY AND GEOCHEMISTRY OF THE CARBONATES IN THE CALATAYUD BASIN (ZARAGOZA, SPAIN)

Citation
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
Citations number
43
Categorie Soggetti
Geochemitry & Geophysics
Journal title
ISSN journal
00092541
Volume
130
Issue
1-2
Year of publication
1996
Pages
123 - 136
Database
ISI
SICI code
0009-2541(1996)130:1-2<123:MAGOTC>2.0.ZU;2-N
Abstract
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.