The Payenia region of Argentina (34.5–38°S) is a large Pliocene‐Quaternary volcanic province of basaltic compositions in the Andean Cordillera foothills representing the northernmost extent of back‐arc volcanism in the Andean Southern Volcanic Zone (SVZ). Although the chemical diversity of the Payenia basalts has been characterized previously, the processes and sources responsible for such variation remain controversial. Here, we report new whole‐rock major and trace element concentrations, Sr‐, Nd‐, Hf‐, and Pb‐isotope ratios and high‐precision olivine oxygen‐isotope ratios in a suite of 35 alkaline basalts from Payenia. These lavas have major and trace elements that define a compositional range from arc‐influenced to intraplate signature. Variable crustal contamination and/or recent slab‐derived inputs inadequately account for elemental and isotopic systematics and spatial compositional variations of Payenia lavas. We present a simple forward model indicating that early metasomatism and subsequent melting of the metasomatized subcontinental lithospheric mantle (SCLM) has significantly contributed to the Payenia lava compositional range. Isotopic ingrowth calculations of radiogenic Sr, Nd, Hf, and Pb suggest that the SCLM metasomatism occurred at 50–150 Ma, consistent with the timing of the breakup of Gondwana and the development of the proto‐Pacific Andean arc. Variations in δ18Oolivinevalues from modeled melts indicate that the metasomatism and melting within the SCLM can fractionate oxygen isotopes even when the metasomatizing melt has MORB‐like δ18O values, providing a different explanation for the low‐δ18O signatures observed in continental arc settings.
Carbonatite volcanism remains poorly understood compared to silicic volcanism due to the scarcity of carbonatite volcanoes worldwide and because volcanic H2O and CO2—major components in carbonatite volcanic systems—are not well preserved in the rock record. To further our understanding of carbonatite genesis, we utilize the non‐traditional thallium (Tl) isotope system in Khanneshin carbonatites in Afghanistan. These carbonatites contain 250–30,000 ng/g Tl and have ε205Tl values (−4.6 to +4.6) that span much of the terrestrial igneous range. We observe that δ18OVSMOW(+8.6‰ to +23.5‰) correlates positively with δ13CVPDB(−4.6‰ to +3.5‰) and ε205Tl up to δ18O = 15‰. Rayleigh fractionation of calcite from an immiscible CO2‐H2O fluid with a mantle‐like starting composition can explain the δ18O and δ13C—but not ε205Tl—trends. Biotite fractionates Tl isotopes in other magmatic settings, so we hypothesize that a Tl‐rich hydrous brine caused potassic metasomatism (i.e., biotite fenitization) of wall rock that increased the ε205Tl of the residual magma‐fluid reservoir. Our results imply that, in carbonatitic volcanic systems, simultaneous igneous differentiation and potassic metasomatism increase ε205Tl, δ18O, δ13C, and light rare earth element concentrations in residual fluids. Our fractionation models suggest that the Tl isotopic compositions of the primary magmas were among the isotopically lightest (less than or equal to ε205Tl = −4.6) material derived from the mantle for which Tl isotopic constraints exist. If so, the ultimate source of Tl in Khanneshin lavas—and perhaps carbonatites elsewhere—may be recycled ocean crust.
more » « less- NSF-PAR ID:
- 10453247
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Geochemistry, Geophysics, Geosystems
- Volume:
- 22
- Issue:
- 3
- ISSN:
- 1525-2027
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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