Description: Hydrothermal circulation at slow-spreading ridges is important for cooling the newly formed lithosphere, but the depth to which it occurs is uncertain. Magmas which stagnate and partially crystallize during their rise from the mantle provide a means to constrain the depth of circulation because assimilation of hydrothermal fluids or hydrothermally altered country rock will raise their chlorine (Cl) contents. Here we present Cl concentrations in combination with chemical thermobarometry data on glassy basaltic rocks and melt inclusions from the Southern Mid-Atlantic Ridge (SMAR; ~ 3 cm year−1 full spreading rate) and the Gakkel Ridge (max. 1.5 cm year−1 full spreading rate) in order to define the depth and extent of chlorine contamination. Basaltic glasses show Cl-contents ranging from ca. 50–430 ppm and ca. 40–700 ppm for the SMAR and Gakkel Ridge, respectively, whereas SMAR melt inclusions contain between 20 and 460 ppm Cl. Compared to elements of similar mantle incompatibility (e.g. K, Nb), Cl-excess (Cl/Nb or Cl/K higher than normal mantle values) of up to 250 ppm in glasses and melt inclusions are found in 75% of the samples from both ridges. Cl-excess is interpreted to indicate assimilation of hydrothermal brines (as opposed to bulk altered rock or seawater) based on the large range of Cl/K ratios in samples showing a limited spread in H2O contents. Resorption and disequilibrium textures of olivine, plagioclase and clinopyroxene phenocrysts and an abundance of xenocrysts and gabbroic fragments in the SMAR lavas suggest multiple generations of crystallization and assimilation of hydrothermally altered rocks that contain these brines. Calculated pressures of last equilibration based on the major element compositions of melts cannot provide reliable estimates of the depths at which this crystallization/assimilation occurred as the assimilation negates the assumption of crystallization under equilibrium conditions implicit in such calculations. Clinopyroxene–melt thermobarometry on rare clinopyroxene phenocrysts present in the SMAR magmas yield lower crustal crystallization/assimilation depths (10–13 km in the segment containing clinopyroxene). The Cl-excesses in SMAR melt inclusions indicate that assimilation occurred before crystallization, while also homogeneous Cl in melts from Gakkel Ridge indicate Cl addition during magma chamber processes. Combined, these observations imply that hydrothermal circulation reaches the lower crust at slow-spreading ridges, and thereby promotes cooling of the lower crust. The generally lower Cl-excess at slow-spreading ridges (compared to fast-spreading ridges) is probably related to them having few if any permanent magma chambers. Magmas therefore do not fractionate as extensively in the crust, providing less heat for assimilation (on average, slow-spreading ridge magmas have higher Mg#), and hydrothermal systems are ephemeral, leading to lower total degrees of crustal alteration and more variation in the amount of Cl contamination. Hydrothermal plumes and vent fields have samples in close vicinity that display Cl-excess, mostly of 〉 25 ppm, which thus can aid as a guide for the exploration of (active or extinct) hydrothermal vent fields on the axis.

Description: We present major and trace element as well as Sr, Nd, and Hf isotope data on a suite of 87 plutonic rock samples from 27 felsic crustal intrusions in seven blocks of the Oman ophiolite. The rock compositions of the sample suite including associated more mafic rocks range from 48 to 79 wt% SiO2, i.e. from gabbros to tonalites. The samples are grouped into a Ti-rich and relatively light rare earth element (LREE)-enriched P1 group [(Ce/Yb)N 〉 0.7] resembling the early V1 lavas, and a Ti-poor and LREE-depleted P2 group [(Ce/Yb)N 〈 0.7] resembling the late-stage V2 lavas. Based on the geochemical differences and in agreement with previous structural and petrographic models, we define phase 1 (P1) and phase 2 (P2) plutonic rocks. Felsic magmas in both groups formed by extensive fractional crystallization of olivine, clinopyroxene, plagioclase, apatite, and Ti-magnetite from mafic melts. The incompatible element compositions of P1 rocks overlap with those from mid-ocean ridges but have higher Ba/Nb and Th/Nb trending towards the P2 rock compositions and indicating an influence of a subducting slab. The P2 rocks formed from a more depleted mantle source but show a more pronounced slab signature. These rocks also occur in the southern blocks (with the exception of the Tayin block) of the Oman ophiolite implying that the entire ophiolite formed above a subducting slab. Initial Nd and Hf isotope compositions suggest an Indian-MORB-type mantle source for the Oman ophiolite magmas. Isotope compositions and high Th/Nb in some P2 rocks indicate mixing of a melt from subducted sediment into this mantle.

Description: 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.

Description: 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 São 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 São 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.