Intraplate Basalt Alkalinity Modulated by a Lithospheric Mantle Filter at the Dunedin Volcano (New Zealand)

Author:

Pontesilli A12,Brenna M2,Ubide T3,Mollo S14,Masotta M5,Caulfield J36,Le Roux P7,Nazzari M1,Scott J M2,Scarlato P1

Affiliation:

1. Istituto Nazionale di Geofisica E Vulcanologia, Via di Vigna Murata 605, Rome 00143, ITALY

2. Department of Geology, University of Otago, PO Box 56, Dunedin 9054, New Zealand

3. School of Earth and Environmental Sciences, The University of Queensland, Brisbane, QLD 4072, Australia

4. Dipartimento di Scienze Della Terra, Sapienza-università di Roma, P.le Aldo Moro 5, Roma 00185, Italy

5. Dipartimento di Scienze Della Terra, Università Degli Studi di Pisa, Via S. Maria 53, Pisa 56126, Italy

6. Central Analytical Research Facility, Institute for Future Environments, Queensland University of Technology, 2 George Street, Brisbane, QLD 4000, Australia

7. Department of Geological Sciences, University of Cape Town, Rondebosch 7701, South Africa

Abstract

Abstract Systematic variations in the crystal cargo and whole-rock isotopic compositions of mantle-derived basalts in the intraplate Dunedin Volcano (New Zealand) indicate the influence of a complex mantle-to-crust polybaric plumbing system. Basaltic rocks define a compositional spectrum from low-alkali basalts through mid-alkali basalts to high-alkali basalts. High-alkali basalts display clinopyroxene crystals with sector (hourglass) and oscillatory zoning (Mg#61–82) as well as Fe-rich green cores (Mg#43–69), whereas low-alkali basalts are characterized by clinopyroxenes with unzoned overgrowths (Mg#69–83) on resorbed mafic cores (Mg#78–88), coexisting with reversely zoned plagioclase crystals (An43–68 to An60–84 from core to rim). Complex magma dynamics are indicated by distinctive compositional variations in clinopyroxene phenocrysts, with Cr-rich zones (Mg#74–87) indicating continuous recharge by more mafic magmas. Crystallization of olivine, clinopyroxene and titanomagnetite occurred within a polybaric plumbing system extending from upper mantle to mid-crustal depths (485–1059 MPa and 1147–1286°C), whereas crystallization of plagioclase with subordinate clinopyroxene and titanomagnetite proceeded towards shallower crustal levels. The compositions of high-alkali basalts and mid-alkali basalts resemble those of ocean island basalts and are characterized by FOZO-HIMU isotopic signatures (87Sr/86Sri = 0.70277–0.70315, 143Nd/144Ndi = 0.51286–0.51294 and 206Pb/204Pb = 19.348–20.265), whereas low-alkali basalts have lower incompatible element abundances and isotopic compositions trending towards EMII (87Sr/86Sri = 0.70327–70397, 143Nd/144Ndi = 0.51282–0.51286 and 206Pb/204Pb = 19.278–19.793). High- and mid-alkali basalt magmas mostly crystallized in the lower crust, whereas low-alkali basalt magma recorded deeper upper mantle clinopyroxene crystallization before eruption. The variable alkaline character and isotope composition may result from interaction of low-alkaline melts derived from the asthenosphere with melts derived from lithospheric mantle, possibly initiated by asthenospheric melt percolation. The transition to more alkaline compositions was induced by variable degrees of melting of metasomatic lithologies in the lithospheric mantle, leading to eruption of predominantly small-volume, high-alkali magmas at the periphery of the volcano. Moreover, the lithosphere imposed a filtering effect on the alkalinity of these intraplate magmas. As a consequence, the eruption of low-alkali basalts with greater asthenospheric input was concentrated at the centre of the volcano, where the plumbing system was more developed.

Funder

University of Otago Research Committee

Publisher

Oxford University Press (OUP)

Subject

Geochemistry and Petrology,Geophysics

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