Microanalysis of large volume silicic magma in continental and oceanic arcs: Melt inclusions in Taupo Volcanic Zone and Kermadec Arc rocks, South West Pacific

2010 ◽  
Vol 190 (1-2) ◽  
pp. 203-218 ◽  
Author(s):  
K.E. Saunders ◽  
J.A. Baker ◽  
R.J. Wysoczanski
2020 ◽  
Vol 61 (2) ◽  
Author(s):  
Georg F Zellmer ◽  
Jun-Ichi Kimura ◽  
Claudine H Stirling ◽  
Gert Lube ◽  
Phil A Shane ◽  
...  

Abstract Mafic magmatism of the rifting Taupo Volcanic Zone (TVZ) of the North Island, New Zealand, is volumetrically minor, but is thought to tap the material that provides the heat source for voluminous rhyolite production through partial melting of the crust, which ultimately results in very large volume explosive eruptions. We have studied the major and trace element chemistry of 14 mafic samples from across the entire TVZ, and the U isotopic composition of whole-rocks, groundmasses and separates of mafic mineral phases from a selection of nine samples (with the remaining five too sparsely phyric for mineral separation). Some minerals yield significant 234U enrichments despite groundmass and whole-rock close to 238U–234U secular equilibrium, pointing to uptake of variably hydrothermally altered antecrystic minerals prior to the eruption of originally sparsely phyric to aphyric mafic magmas. However, incompatible trace element patterns indicate that there are three chemically distinct groups of samples, and that samples may be used to derive primary melt compositions. We employ the latest version of the Arc Basalt Simulator (ABS5) to forward model these compositions, deriving mantle source parameters including mantle fertility, slab liquid flux, mantle volatile content, degree of melting, and P–T conditions of melt segregation. We show that mafic rocks erupted in areas of old, now inactive calderas constitute low-degree, deep melts, whereas those in areas of active caldera-volcanism are high-degree partial melts segregated from a less depleted source at an intermediate depth. Finally, high-Mg basaltic andesites erupted in the SW and NE of the TVZ point to a fertile, shallow mantle source. Our data are consistent with a petrogenetic model in which mantle melting is dominated by decompression, rather than fluid fluxing, and progresses from shallow to deeper levels with time. Melt volumes initially increase to a tipping point, at which large-scale crustal melting and caldera volcanism become prominent, and then decrease owing to progressive depletion of the mantle wedge by melting, resulting in the dearth of heat provided and eventual cessation of very large volume rhyolitic volcanism. ABS5 modelling therefore supports the notion of a direct link between the chemistry of recently erupted mafic magmas and the long-term activity and evolution of rhyolitic volcanism in the TVZ.


2021 ◽  
Author(s):  
Ery Hughes ◽  
Sally Law ◽  
Geoff Kilgour ◽  
Jon Blundy ◽  
Heidy Mader

The Okataina Volcanic Centre (OVC) is the most recently active rhyolitic volcanic centre in the Taupō Volcanic Zone, Aotearoa New Zealand. Although best known for its high rates of explosive rhyolitic volcanism, there are numerous examples of basaltic to basaltic-andesite contributions to OVC eruptions, ranging from minor involvement of basalt in rhyolitic eruptions to the exclusively basaltic 1886 C.E. Plinian eruption of Tarawera. To explore the basaltic component supplying this dominantly rhyolitic area, we analyse the textures and compositions (minerals and melt inclusions) of four basaltic eruptions within the OVC that have similar whole rock chemistry, namely: Terrace Rd, Rotomakariri, Rotokawau, and Tarawera. Data from these basaltic deposits provide constraints on the conditions of magma evolution and ascent in the crust prior to eruption, revealing that at least five different magma types (two basalts, two dacites, one rhyolite) are sampled during basaltic eruptions. The most abundant basaltic magma type is generated by cooling-induced crystallisation of a common, oxidised, basaltic melt at various depths throughout the crust. The volatile content of this melt was increased by protracted fluid-undersaturated crystallisation. All eruptions display abundant evidence for syn-eruptive mixing of the different magma types. Rotomakariri, consisting of a mafic crystal cargo mixed into a dacitic magma is the most extreme example of this process. Despite similar bulk compositions, comparable to other basaltic deposits in the region, these four OVC eruptions are texturally distinct as a consequence of their wide variation in eruption style.


2021 ◽  
Author(s):  
◽  
Katharine Emma Saunders

<p>The petrogenesis of silicic arc magmas is controversial with end-member models of fractional crystallisation and crustal anatexis having been invoked. A prime example of this is the archetypical continental Taupo Volcanic Zone and the adjacent oceanic Kermadec Arc. Insights into the genesis and timescales of magmatic processes of four continental rhyolitic magmas (Whakamaru, Oruanui, Taupo and Rotorua eruptives) and an oceanic (Healy seamount) rhyodacitic magma are documented through micro-analytical chemical studies of melt inclusions and crystal zonation of plagioclase and quartz. Electron probe microanalysis, laser ablation inductively coupled plasma mass spectrometry and Fourier transform infrared spectroscopy have been used to measure major, trace and volatile element concentrations, respectively, of melt inclusions and crystals. Melt inclusions are high silica (e.g. 74 - 79 wt%) irrespective of arc setting and display a wide range of trace element compositions (e.g. Sr = 17 - 180 ppm). Taupo Volcanic Zone melt inclusions exhibit higher K2O and Ce/Yb relative to Healy melt inclusions reflecting the assimilation of continental lithosphere. Quantitative trace element modelling of melt inclusion compositions: (a) demonstrates that magma genesis occurred through 62 - 76% fractional crystallisation at Healy whereas assimilation of continental lithosphere (greywacke) in addition to 60 - 80% fractional crystallisation is required for the Taupo Volcanic Zone magmas; and (b) suggests the presence of crystal mush bodies beneath silicic magma chambers in both continental and oceanic arc environments. Water concentrations of melt inclusions ranged between 1.4 - 5.1 wt% for the Whakamaru, Taupo and Healy samples. However, the inconsistency in the measured molecular water to hydroxyl concentrations of melt inclusions relative to those determined experimentally for groundmass rhyolitic glasses provide evidence for the degassing of inclusions prior to quenching, by diffusion of hydroxyl groups through the crystal host. Thus, partial pressures of water estimated from the inclusions and inferred depths of the crystallising magma bodies are underestimated. Chemical profiles of mineral zonation, however, indicate a more complex origin of silicic melts than simple fractionation and assimilation. For example, trace element modelling of Whakamaru plagioclase suggests that the three distinct textural plagioclase populations present in Whakamaru samples crystallised from four physiochemically discrete silicic melts. This modelling indicates a strong petrogenetic link between andesitic and silicic magmas from the chemical variation of selected Whakamaru plagioclase crystals possessing high anorthite (45-60 mol %) cores and low anorthite (~ 30 mol %) rim compositions and the interaction of greywacke partial melts. Furthermore, Sr diffusion modelling of core-rim interfaces of the same plagioclase crystals indicate the amalgamation of the magma chamber occurred continuously over the 15,000 years preceding the climactic eruption. Conversely, the major element zonation of Taupo plagioclases implies magma genesis occurred solely through assimilation and fractional crystallisation without the incorporation of evolved crystal mush magmas, indicating a spectrum of magmatic processes are occurring beneath the Taupo Volcanic Zone with each eruption providing only a snapshot of the petrogenesis of the Taupo Volcanic Zone.</p>


2003 ◽  
Vol 206 (3-4) ◽  
pp. 441-457 ◽  
Author(s):  
Bruce L.A Charlier ◽  
David W Peate ◽  
Colin J.N Wilson ◽  
Jacob B Lowenstern ◽  
Michael Storey ◽  
...  

2014 ◽  
Vol 410 (1) ◽  
pp. 71-94 ◽  
Author(s):  
Florence Bégué ◽  
Darren M. Gravley ◽  
Isabelle Chambefort ◽  
Chad D. Deering ◽  
Ben M. Kennedy

Geology ◽  
1989 ◽  
Vol 17 (3) ◽  
pp. 234 ◽  
Author(s):  
Nelia W. Dunbar ◽  
Philip R. Kyle ◽  
Colin J.N. Wilson

2021 ◽  
Author(s):  
◽  
Katharine Emma Saunders

<p>The petrogenesis of silicic arc magmas is controversial with end-member models of fractional crystallisation and crustal anatexis having been invoked. A prime example of this is the archetypical continental Taupo Volcanic Zone and the adjacent oceanic Kermadec Arc. Insights into the genesis and timescales of magmatic processes of four continental rhyolitic magmas (Whakamaru, Oruanui, Taupo and Rotorua eruptives) and an oceanic (Healy seamount) rhyodacitic magma are documented through micro-analytical chemical studies of melt inclusions and crystal zonation of plagioclase and quartz. Electron probe microanalysis, laser ablation inductively coupled plasma mass spectrometry and Fourier transform infrared spectroscopy have been used to measure major, trace and volatile element concentrations, respectively, of melt inclusions and crystals. Melt inclusions are high silica (e.g. 74 - 79 wt%) irrespective of arc setting and display a wide range of trace element compositions (e.g. Sr = 17 - 180 ppm). Taupo Volcanic Zone melt inclusions exhibit higher K2O and Ce/Yb relative to Healy melt inclusions reflecting the assimilation of continental lithosphere. Quantitative trace element modelling of melt inclusion compositions: (a) demonstrates that magma genesis occurred through 62 - 76% fractional crystallisation at Healy whereas assimilation of continental lithosphere (greywacke) in addition to 60 - 80% fractional crystallisation is required for the Taupo Volcanic Zone magmas; and (b) suggests the presence of crystal mush bodies beneath silicic magma chambers in both continental and oceanic arc environments. Water concentrations of melt inclusions ranged between 1.4 - 5.1 wt% for the Whakamaru, Taupo and Healy samples. However, the inconsistency in the measured molecular water to hydroxyl concentrations of melt inclusions relative to those determined experimentally for groundmass rhyolitic glasses provide evidence for the degassing of inclusions prior to quenching, by diffusion of hydroxyl groups through the crystal host. Thus, partial pressures of water estimated from the inclusions and inferred depths of the crystallising magma bodies are underestimated. Chemical profiles of mineral zonation, however, indicate a more complex origin of silicic melts than simple fractionation and assimilation. For example, trace element modelling of Whakamaru plagioclase suggests that the three distinct textural plagioclase populations present in Whakamaru samples crystallised from four physiochemically discrete silicic melts. This modelling indicates a strong petrogenetic link between andesitic and silicic magmas from the chemical variation of selected Whakamaru plagioclase crystals possessing high anorthite (45-60 mol %) cores and low anorthite (~ 30 mol %) rim compositions and the interaction of greywacke partial melts. Furthermore, Sr diffusion modelling of core-rim interfaces of the same plagioclase crystals indicate the amalgamation of the magma chamber occurred continuously over the 15,000 years preceding the climactic eruption. Conversely, the major element zonation of Taupo plagioclases implies magma genesis occurred solely through assimilation and fractional crystallisation without the incorporation of evolved crystal mush magmas, indicating a spectrum of magmatic processes are occurring beneath the Taupo Volcanic Zone with each eruption providing only a snapshot of the petrogenesis of the Taupo Volcanic Zone.</p>


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