4.7 Article

Titanium isotopic compositions of bulk rocks and mineral separates from the Kos magmatic suite: Insights into fractional crystallization and magma mixing processes

Journal

CHEMICAL GEOLOGY
Volume 578, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.chemgeo.2021.120303

Keywords

Titanium isotopes; Mineral separates; Magmatic differentiation; Magma mixing; Plagioclase; Volcanism

Funding

  1. Swiss National Science foundation [181172]
  2. NASA [NNX17AE86G, NNX17AE87G, 80NSSC17K0744, 80NSSC20K0821]
  3. NSF [EAR-2001098]
  4. National Centre for Competence in Research PlanetS - Swiss National Science Foundation (SNSF)

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Terrestrial and extraterrestrial rocks show significant variations in their mass-dependent Ti isotopic compositions, with basaltic rocks being lighter than evolved lithologies. The measured Ti isotopic compositions in mineral separates and bulk rocks from a volcanic system in Greece reveal two different Ti isotope trends driven by fractional crystallization and mixing between basaltic and rhyolitic magmas. The differences in Ti isotopic compositions in different minerals reflect their equilibrium nature.
Terrestrial and extraterrestrial rocks exhibit significant variations in their mass-dependent Ti isotopic compositions, with basalts being isotopically lighter than evolved lithologies. The observed trend from light to heavy Ti isotopic compositions from more primitive to more differentiated rocks agrees with theoretical predictions that light Ti isotopes are sequestered in Fe-Ti oxides. However, there are lingering questions about the exact extent of this fractionation and whether it is influenced by the nature of oxides and silicate melt. To improve on this matter, we measured the Ti isotopic compositions of mineral separates and bulk rocks from the calc-alkaline Kos volcano-plutonic system, Aegean arc, Greece. Bulk rock Ti isotopic compositions (849Ti) increase with differentiation of the magmatic system, from 849Ti of +0.042 +/- 0.033%o in basalt to +0.654 +/- 0.034%o in rhyolite. We document two different Ti isotope trends produced by (i) fractional crystallization, and (ii) mixing between a basaltic melt and an evolved (rhyolitic) magma. Trend (i) can be explained by a melt-cumulate Ti isotopic fraction factor alpha of 0.9998 (i.e., the bulk cumulate is on average 0.20%o lighter than the melt). The mineral separates reveal variable 849Ti values, with magnetite having the lightest 49Ti/47Ti isotopic composition, biotite being intermediate and neso- and tectosilicates (i.e., olivine, plagioclase and quartz) heaviest. Comparing the TiO2 concentrations of the low-Ti minerals olivine, plagioclase and quartz determined with LA-ICP-MS and isotope dilution shows that the 849Ti values measured in these minerals reflect their isotopic compositions, and contamination by inclusions is minimal. The difference in 849Ti between different minerals is smallest in a basalt (A49Tiolivine-magnetite = +0.426) and largest in two rhyolites (A49Tiquartz-magnetite = +1.083; both +/- 0.046%o). Our data agree with theoretical predictions that Fe-Ti oxides have a light 849Ti signature, and neso/tectosilicate minerals are heavy. Furthermore, the measured difference in 849Ti between magnetite-olivine, magnetiteplagioclase and magnetite-quartz agree to first order with theoretically predicted inter-mineral Ti isotopic fractionation factors, thus suggesting that the measured inter-mineral Ti isotopic variations are equilibrium in nature.

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