Philipp A. Brandl

Oxygen isotopes in the Azores islands: Crustal assimilation recorded in olivine

Oxygen isotope ratios of olivine have become a widely used tool for the study of magmatic systems, especially in the interpretation of source heterogeneities in mantle plume–derived ocean island basalts. The underlying assumption is that fresh minerals provide a better guide to magma δ 18 O than bulk rock analyses and that olivine is also likely to be a major phenocryst phase in primitive magmas. However, distinctions between source compositions and the effects of subsequent magma evolution have not always been thoroughly scrutinized. For the Azores samples investigated here, we can demonstrate that the δ 18 O variation (+4.84‰ to +5.25‰ Vienna standard mean ocean water) observed in the olivine phenocryst population is closely linked to evolution in the host magmas during ascent to the surface. We observe a linear, positive correlation between forsterite (Fo) content and δ 18 O in all of the individual island lava suites. This forces us to conclude that the low oxygen isotope ratios result from combined assimilation and fractional crystallization processes, the assimilant being hydrothermally (temperature > 250 °C) altered, lower oceanic crust. Linear regression of the measured δ 18 O olivine values to Fo 89 suggests a homogeneous mantle source with δ 18 O =

Insights into mantle composition and mantle melting beneath mid‐ocean ridges from postspreading volcanism on the fossil Galapagos Rise

New major and trace element and Sr, Nd, and Pb isotope data, together with 39Ar-40Ar ages for lavas from the extinct Galapagos Rise spreading center in the eastern Pacific reveal the evolution in magma compositions erupted during slowdown and after the end of active spreading at a mid-ocean ridge. Lavas erupted at 9.2 Ma, immediately prior to the end of spreading are incompatible element depleted mid-ocean ridge tholeiitic basalts, whereas progressively younger (7.5 to 5.7 Ma) postspreading lavas are increasingly alkalic, have higher concentrations of incompatible elements, higher La/Yb, K/Ti, 87Sr/86Sr, and lower 143Nd/144Nd ratios and were produced by smaller degrees of mantle melting. The large, correlated variations in trace element and isotope compositions can only be explained by melting of heterogenous mantle, in which incompatible trace element enriched lithologies preferentially contribute to smaller degree mantle melts. The effects of variable degrees of melting of heterogeneous mantle on lava compositions must be taken into account when using mid-ocean ridge basalt (MORB) to infer the conditions of melting beneath active spreading ridges. For example, the stronger “garnet signature” inferred from Sm/Nd and 143Nd/144Nd ratios for postspreading lavas from the Galapagos Rise results from a larger contribution from enriched lithologies with high La/Yb and Sm/Yb, rather than from a greater proportion of melting in the stability field of garnet peridotite. Correlations between ridge depth and Sm/Yb and fractionation-corrected Na concentrations in MORB worldwide could result from variations in mantle fertility and/or variations in the average degree of melting, rather than from large variations in mantle temperature. If more fertile mantle lithologies are preferentially melted beneath active spreading ridges, then the upper mantle may be significantly more “depleted” than is generally inferred from the compositions of MORB.

Magmatic Evolution and Source Variations at the Nifonea Ridge (New Hebrides Island Arc)

The Nifonea submarine volcano rises 1000 m above the seafloor of the Vate Trough back-arc basin behind the New Hebrides island arc. This large volcanic edifice has a caldera of ∼8 km diameter and is connected to two ∼20 km long volcanic rift zones in the back-arc basin. We present new chemical and isotope data for volcanic glasses and whole-rocks from both the volcano and its rift zones. Lavas from Nifonea volcano show an evolution towards more incompatible element enrichment, with the most enriched lavas being the youngest eruption products on the caldera floor. These are products of significant fractional crystallization, show minor contamination by hydrothermal fluids (<0·3%) and reflect mixing of melts derived from depleted upper mantle and melts from an enriched source similar to those occurring in the North Fiji Basin. The enrichment in Nb of these lavas is comparable with that of some lavas from the New Hebrides island arc (e.g. Mota Lava island), where these coexist with typical island arc basalts. The lavas erupted along the rift zones in the Vate Trough back-arc basin are relatively depleted in incompatible elements, indicating melting of depleted upper mantle with a minor addition of a sediment-derived fluid. Our observations suggest that the mantle beneath Vate Trough is heterogeneous on a small scale (<20 km) and that the occurrence of these enriched and fertile mantle portions has a stronger control on melting processes than the influx from the subducting slab, as all samples were recovered at a similar distance from the trench.

Primitive andesites from the Taupo Volcanic Zone formed by magma mixing

Andesites with Mg# >45 erupted at subduction zones form either by partial melting of metasomatized mantle or by mixing and assimilation processes during melt ascent. Primitive whole rock basaltic andesites from the Pukeonake vent in the Tongariro Volcanic Centre in New Zealand’s Taupo Volcanic Zone contain olivine, clino- and orthopyroxene, and plagioclase xeno- and antecrysts in a partly glassy matrix. Glass pools interstitial between minerals and glass inclusions in clinopyroxene, orthopyroxene and plagioclase as well as matrix glasses are rhyolitic to dacitic indicating that the melts were more evolved than their andesitic bulk host rock analyses indicate. Olivine xenocrysts have high Fo contents up to 94%, δ18O(SMOW) of +5.1‰, and contain Cr-spinel inclusions, all of which imply an origin in equilibrium with primitive mantle-derived melts. Mineral zoning in olivine, clinopyroxene and plagioclase suggest that fractional crystallization occurred. Elevated O isotope ratios in clinopyroxene and glass indicate that the lavas assimilated sedimentary rocks during stagnation in the crust. Thus, the Pukeonake andesites formed by a combination of fractional crystallization, assimilation of crustal rocks, and mixing of dacite liquid with mantle-derived minerals in a complex crustal magma system. The disequilibrium textures and O isotope compositions of the minerals indicate mixing processes on timescales of less than a year prior to eruption. Similar processes may occur in other subduction zones and require careful study of the lavas to determine the origin of andesite magmas in arc volcanoes situated on continental crust.

Formation of andesite melts and Ca‐rich plagioclase in the submarine Monowai volcanic system, Kermadec arc

Andesites are typical rocks of island arcs and may either form by fractional crystallization processes or by mixing between a mafic and a felsic magma. Here we present new petrographic and geochemical data from lavas of the submarine Monowai volcanic system in the northern Kermadec island arc that display a continuous range in composition from basalt to andesite. Using petrology, major, trace, and volatile element data, we show that basaltic magmas mostly evolve to andesitic magmas by fractional crystallization. Our thermobarometric calculations indicate that the formation of the large caldera is related to eruption of basaltic-andesitic to andesitic magmas from a magma reservoir in the deeper crust. Small variations in trace element ratios between the caldera and the large active cone imply a homogeneous mantle source. Contrastingly, resurgent dome melts of the caldera stagnated at shallower depths are more depleted and show a stronger subduction input than the other edifices. The Monowai basaltic glasses contain less than 1 wt % H2O and follow typical tholeiitic fractionation trends. High-An plagioclase crystals observed in the Monowai lavas likely reflect mixing of H2O-saturated melt batches with hot and dry tholeiitic, decompression melt batches. The result is a relatively H2O-poor mafic magma at Monowai implying that partial melting of the mantle wedge is only partly due to the volatile flux and that adiabatic melting may play a significant role in the formation of the parental melts of the Monowai volcanic system and possibly other arc volcanoes.

Melting and Mantle Sources in the Azores

The Azores archipelago is geochemically distinct amongst the oceanic intraplate volcanoes in that it has trace element and radiogenic Sr–Nd–Pb–Hf isotope signatures that cover much of the global variation observed in Ocean Island Basalts. Thus, it is the prime example of an intraplate melting anomaly preserving the compositional heterogeneity of the Earth’s mantle. Here, we review the trace element and radiogenic isotope geochemistry of the Azores islands and few submarine samples analysed and published over the past decades and summarise these findings and conclusions. The volcanoes of all islands erupted lavas of the alkaline series and their compositions broadly range from basalts to trachytes (see also Chapter “ Petrology of the Azores Islands” by Larrea et al.). Temperatures and pressures of melting imply that melting in the Azores occurs as a result of both slightly increased temperatures in the mantle (~35 °C) and addition of volatile elements into the mantle source. Basalts from the island of Sao Miguel show a stronger enrichment in highly incompatible elements like K and the Light Rare Earth Elements than the other islands further to the west. The older and easternmost island Santa Maria has lavas that are more silica-undersaturated than the rocks occurring on the younger islands. Each of the eastern islands shows a different and distinct radiogenic isotope composition and much of this variability can be explained by variably enriched recycled components of different age in their source regions. Amongst the global array, the lavas from eastern Sao Miguel are uniquely enriched in that they display radiogenic 206Pb/204Pb, 208Pb/204Pb and 87Sr/86Sr isotope ratios best explained by a distinct source in the mantle. The implication of the preservation of such unique, enriched sources in the mantle may indicate that stirring processes in the Azores mantle are not efficiently homogenising heterogeneities over the timescales of recycling of 0.1–1 Ga and possibly even up to 2.5 Ga. One possible explanation is the low buoyancy flux of the Azores mantle when compared to other intraplate settings. The preservation of these source signatures in the lavas on the easternmost Azores islands are the result of smaller degrees of partial melting due to a thicker lithosphere. This likely prevents a homogenisation during magma ascent compared to the western islands, preferentially sampling deep, low degree partial melts from the more fertile mantle sources. The geochemical signatures of the two islands west of the Mid-Atlantic Ridge (Corvo and Flores) imply a source enrichment and degrees of partial melting similar to those east of the ridge. Melting underneath the western islands is the result of a source that must be related to the Azores melting anomaly but has been modified by shallow level processes such as assimilation of oceanic crustal material.

Expedition 351 methods

R.J. Arculus, O. Ishizuka, K. Bogus, M.H. Aljahdali, A.N. Bandini-Maeder, A.P. Barth, P.A. Brandl, R. do Monte Guerra, L. Drab, M.C. Gurnis, M. Hamada, R.L. Hickey-Vargas, F. Jiang, K. Kanayama, S. Kender, Y. Kusano, H. Li, L.C. Loudin, M. Maffione, K.M. Marsaglia, A. McCarthy, S. Meffre, A. Morris, M. Neuhaus, I.P. Savov, C.A. Sena Da Silva, F.J. Tepley III, C. van der Land, G.M. Yogodzinski, and Z. Zhang2