Bb. Lazaro et al., MINERALOGY AND GEOCHEMISTRY OF MIOCENE DEPOSITS AT ALCUBIERRE-SIERRA,CENTRAL SECTOR OF THE EBRO BASIN, SPAIN, Clay Minerals, 29(3), 1994, pp. 391-400
Two profiles in Miocene fluvio-lacustrine deposits consist of sandy, m
arly, lutitic and carbonatic levels constituted by variable percentage
s of quartz, calcite and clay minerals as major components, and feldsp
ars, dolomite and occasionally gypsum and anhydrite as minor ones. The
clay minerals are inherited and consist mostly of micas, with minor q
uantities of chlorites, pyrophyllites and kaolinites. The crystalloche
mical parameters of the micas indicate muscovitic compositions and the
ir uniformity through both the different rocks and their silt and clay
fractions suggest the same provenance source area, possibly located n
orthward. Clay minerals concentrate preferentially Li, Sc, V, Cr, Co,
Ni, Cu, Zn, Rb, Cs, Ba, Zr, Hf, Th, U and REE whereas the authigenic c
arbonates concentrate Mn and Sr. The Sc, Cr, Th, Y, Zr and REE values
in clay minerals indicate that the provenance source area of these dep
osits was similar in composition to the average continental upper crus
t, probably as a result of sedimentary recycling processes. Zeolitic l
evels constituted by different proportions of analcime and smectite as
major components outcrop at the top of the profiles. The analcimes sh
ow anhedral to euhedral morphologies, with grain-size ranging between
1 and 20 mum, and Si/Al ratios ranging from 2.2 to 2.5. The smectites
are dioctahedral and beidellitic in composition. The zeolitic levels p
resent significant chemical differences relative to the other ones, su
ch as higher overall REE contents, more pronounced negative Eu anomali
es and higher (LaNb)n, Th/Sc and La/Sc ratios, suggesting a different
provenance source area. Their chondrite-normalized REE patterns reflec
t the possibility that the starting materials were pyroclastic eruptiv
e rocks originating from intracrustal partial melting. The variable an
alcime and smectite percentages are attributed to variations in H+/(Na
+ + K+) and K+/(Na + Ca2+ + Mg2+) activity ratios and silica and water
activities in the pore-waters during diagenetic processes.