Abstract

Late Miocene to Quaternary basalts and associated magnesian basaltic andesites and andesites, locally referred to as “bajaites”, occur in the central part of the Baja California (BC) Peninsula. They form five volcanic fields (Jaraguay, San Borja, San Ignacio, Santa Rosalia, La Purisima) delineating a 600-km-long array parallel to the Gulf of California. They range in age from Late Miocene to Pleistocene, and display very specific geochemical characteristics: SiO 2=50% to 58%, high MgO contents, very low FeO*/MgO ratios usually less than 1.5, highly fractionated rare earth element patterns with low Y and heavy rare earth element, very high Sr (commonly between 2000 and 3000 ppm) and Ba (up to 2300 ppm) contents. The geochemical study and K–Ar dating of ca. 50 samples of these rocks allow us to show that most of their incompatible element ratios, which vary significantly in space and time, reflect source heterogeneities rather than partial melting, fractional crystallisation or crustal contamination effects. Their slab melt imprint increases from northwest to southeast and with time. It is best expressed in the geochemical signatures of Quaternary lavas from La Purisima volcanic field. These features reflect the origin of the “bajaites” by melting of mantle peridotites previously metasomatised by slab melts, in connection with the opening of an asthenospheric window below the Baja California Peninsula during Early and Middle Miocene in northern Baja California, and during Late Miocene in southern Baja California. Melting was initiated by the high thermal regime accompanying ridge subduction or slab tearing/breakoff, and later by Plio-Pleistocene thermal pulses linked to the opening of the Gulf of California. We show that the incongruent melting of metasomatic pargasitic amphibole, leaving a garnet-rich residue, accounts for most of the specific geochemical features of the magnesian andesite suite. This breakdown started at ca. 1000 °C at depths of 70–110 km, and amphibole was probably not entirely consumed during the melting process.

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