Petrographic and Geochemical Evidence for a Complex Magmatic Plumbing System beneath Bagana Volcano, Papua New Guinea

Author:

Brown Joshua R1ORCID,Buisman Iris2,Castellanos Melendez Maria P3,Dikaung John B4,Steenssens Léa Dumon5,Edmonds Marie2,Ellis Ben S3,Hartley Margaret E1ORCID,Itikarai Ima4,Mulina Kila4,Neave David A1ORCID,Nicoli Gautier6,Salem Lois C2,Vukmanovic Zoja7,McCormick Kilbride Brendan T1

Affiliation:

1. Department of Earth and Environmental Sciences, University of Manchester , Oxford Road, Manchester M13 9PL , UK

2. Department of Earth Sciences, University of Cambridge , Downing Street, Cambridge CB2 3EQ , UK

3. Institute of Geochemistry and Petrology, ETH Zürich , NW Clausiusstrasse 25, Zürich 8092 , Switzerland

4. Rabaul Volcanological Observatory , R557+J9M, Rabaul , Papua New Guinea

5. Institute of Earth Sciences, University of Iceland , Sturlugata 7, Reykjavík 102 , Iceland

6. Yorkshire Wildlife Trust , Unit 23 Gargrave Rd, Skipton BD23 1UD , UK

7. School of Environmental Sciences, University of East Anglia , Research Park, Norwich NR4 7TJ , UK

Abstract

Abstract Bagana is a persistently active stratovolcano located on Bougainville Island, Papua New Guinea. Characteristic activity consists of prolonged lava effusion over months to years, with occasional shifts to explosive vulcanian or sub Plinian eruptions that threaten surrounding communities. Satellite observations have shown that Bagana is a major SO2 emitter, particularly during eruptive intervals. Despite persistent and potentially hazardous activity, no previous geophysical, petrological, or geochemical studies have constrained the magma storage conditions and reservoir processes at Bagana. To address this knowledge gap, we present new bulk rock major, trace element, and radiogenic isotope data, plus mineral phase major element compositions, for Bagana lavas erupted in 2005 and 2012 and ash erupted in 2016. We use our new data to understand the magmatic processes controlling the typical effusive activity and provide the first estimates of magma storage conditions beneath Bagana. The basaltic andesite bulk rock compositions (56–58 wt% SiO2) of our Bagana lavas reflect accumulation of a plagioclase + clinopyroxene + amphibole + magnetite + orthopyroxene crystal cargo by andesitic-dacitic (57–66 wt% SiO2) carrier melts. Constraints from clinopyroxene and amphibole thermobarometry, amphibole hygrometry, and experimental petrology suggest that the high-An plagioclase + clinopyroxene + amphibole + magnetite assemblage crystallizes from basaltic-basaltic andesite parental magmas with >4 wt% H2O, over a temperature interval of ~1100–900°C, at pressures of ~130–570 MPa, corresponding to ~5–21 km depth. Continued crystallization in the magma storage region at ~5–21 km depth produces andesitic to dacitic residual melts, which segregate and ascend towards the surface. These ascending melts entrain a diverse crystal cargo through interaction with melt-rich and mushy magma bodies. Degassing of carrier melts during ascent results in crystallization of low-An plagioclase and the formation of amphibole breakdown rims. The radiogenic isotope and trace element compositions of Bagana lavas suggest that parental magmas feeding the system derive from an enriched mantle source modified by both slab fluids and subducted sediments. Our findings suggest that the prolonged lava effusion and persistently high gas emissions that characterise Bagana’s activity in recent decades are sustained by a steady state regime of near-continuous ascent and degassing of magmas from the crustal plumbing system. Our characterisation of the Bagana magmatic plumbing system during effusive activity provides a valuable framework for interpreting ongoing monitoring data, and for identifying any differences in magmatic processes during any future shift to explosive activity.

Funder

Alfred P. Sloan Foundation

Deep Carbon Observatory Deep Earth Carbon Degassing Program

University of Manchester

Centre for the Observation and Modelling of Earthquakes, Volcanoes and Tectonics

Clare College

University of Cambridge

NERC IRF

Publisher

Oxford University Press (OUP)

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