Geodiversidad mineralógica y petrológica del diapiro de Pinoso y su interés como patrimonio geológico

El diapiro de Pinoso, también denominado Cerro o Cabeҫo de la Sal, está situado al W de la provincia de Alicante, (38º24’ N- 01º02”O), de forma elíptica con eje mayor (NW-SE) de 7,5 km y altura máxima de 893 m, 350 m por encima de la superficie erosiva colindante. Constituido por materiales de facies Keuper, presenta un núcleo de halita que ha sido objeto de explotación, tanto por minería subterránea como por evaporación (extracción y comercialización de sal manantial). También, a principios del siglo XX, aguas procedentes del Cabeҫo fueron utilizadas en un balneario, previo calentamiento del agua. Desde 1973 se explota por disolución y la salmuera extraída es llevada a Torrevieja mediante un salmueroducto y allí pasa a formar parte del proceso de evaporación de explotación de las salinas. La variedad de las litologías presentes en él, así como su riqueza en patrimonio mineral mueble, algunos de los cuales son minerales autigénicos característicos de las facies Keuper, confieren al Cabeҫo de la Sal un notable valor como Patrimonio Geológico, este carácter patrimonial se ve aumentado por los rasgos geomorfológicos asociados al exokarst en materiales yesíferos hipergénicos que genera formas erosivas cualitativa y cuantitativamente muy importantes.

Lithologic, mineral, chemical and isotopic compositions of altered rocks with increasing distance across the eastern flank of the Juan de Fuca Ridge, ODP Leg 168 data

During ODP Leg 168, 10 sites were drilled across the eastern flank of the Juan de Fuca Ridge (JdFR), to examine the conditions of fluid-rock interaction in three distinct hydrothermal regimes (referred to as the Hydrothermal Transition (HT), Buried Basement (BB) and Rough Basement (RB) transects), extending over a ~120 km linear transect perpendicular to the spreading ridge. This was carried out in an attempt to constrain the conditions and processes that control the location, style and magnitude of low temperature (<150°C) fluid-rock interaction within this setting. This paper presents new data on the petrology, mineral chemistry and whole rock strontium and oxygen isotopic compositions of basalts from the eastern flank of the JdFR, in order to investigate the extent, style and sequence of low-temperature hydrothermal alteration and to establish how the hydrothermal regime evolved with time. Throughout the flank, a progressive sequence of low-temperature hydrothermal alteration has been identified, marked by changes in the dominant secondary mineral assemblage, changing from: chlorite+chlorite/smectite; to iron oyxhydroxide+celadonite; to saponite+/-pyrite; culminating at present with Ca- to CaMg(+/-Fe,Mn)-carbonate. The changes in secondary mineralogy have been used to infer a series of systematic shifts in the conditions of alteration that occurred as the basement moved off-axis and was progressively buried by sediment. In general, hydrothermal alteration of the uppermost oceanic crust commenced under open, oxidative conditions, with interaction between unmodified to slightly modified seawater and basaltic crust, to a regime in which circulation of a strongly modified seawater-derived fluid was more restricted, and alteration occurred under non-oxidative conditions. Across the flank, petrological observations and microprobe analyses indicate that the observed ranges in secondary mineral composition are directly related to changes in the geochemical and textural characteristics of the basement, as well as to interaction between fluids and phases from the four stages of alteration. This is suggestive of an increase in fluid-rock increased with time. Whole rock 87Sr/86Sr and d18O analyses of basalts from across the eastern flank of the JdFR reinforce petrological observations, with 87Sr/86Sr and d18O values slightly elevated above accepted pristine MORB values for this region. These results are consistent with an increase in the amount of fluid-rock interaction with time. Across the flank, enrichment in the 87Sr/86Sr and d18O relative to MORB, is influenced by a number of factors, including: local and regional variations in the crustal lithology and structure; the age of the crust; the extent of bulk rock alteration; and theoretically, the relative abundance of different isotopically-enriched secondary mineral phases in the crust.