Description: Highlights • An eclogite-melt component (slab melt) is present in volcanic rocks throughout the Aleutian arc. • Fluids that drive slab melting are produced by dehydration of serpentinite in the subducting plate. • Slab melting encompasses a large section of mafic oceanic crust unaffected by seawater alteration. • The subducting plate beneath the Aleutian arc is hotter than indicated by most thermal models. Abstract High Mg# andesites and dacites (Mg# = molar Mg/Mg + Fe) from western Aleutian seafloor volcanoes carry high concentrations of Sr (〉1000 ppm) that is unradiogenic (87Sr/86Sr 〈 0.7029) compared to lavas from emergent volcanoes throughout the arc (200–800 ppm Sr, 87Sr/86Sr 〉0.7030). Data patterns in plots of 87Sr/86Sr vs Y/Sr and Nd/Sr imply the existence of an eclogite-melt source component – formed by partial melting of MORB eclogite in the subducting Pacific Plate – which is most clearly expressed in the compositions of western Aleutian andesites and dacites (Nd/Sr and Y/Sr 〈 0.02) and which dominates the source budget for Sr in volcanic rocks throughout the arc. When viewed in combination with inversely correlated εNdεNd and 87Sr/86Sr, these patterns rule out aqueous fluids as an important source of Sr because mixtures of fluids from altered oceanic crust with depleted mantle and sediment produce compositions with 87Sr/86Sr higher than in common Aleutian rocks. The unradiogenic nature of Sr in the western Aleutian andesite–dacite end-member may be understood if H2O required to drive melting of the subducting oceanic crust is transported in fluids containing little Sr. Mass balance demonstrates that such fluids may be produced by dewatering of serpentinite in the mantle section of the subducting plate. If the eclogite-melt source component is present throughout the Aleutian arc, melting of the subducting plate must extend into minimally altered parts of the sheeted dike section or upper gabbros, at depths 〉2 km below the paleo-seafloor. Oxygen isotopes in western Aleutian seafloor lavas, which fall within a narrow range of MORB-like values (δ18O=5.1–5.7δ18O=5.1–5.7), are also consistent with this model. These results indicate that the subducting Pacific lithosphere beneath the Aleutian arc is significantly hotter than indicated my most thermal models.

Description: Highlights • First comprehensive data set of the seamounts from the Walvis Ridge. • The seamounts are 20–40 Myr younger than the age progressive Walvis Ridge basement. • The composition of the seamounts extends from the St. Helena HIMU to EMORB. • The seamounts are derived from a distinct source compared to the Walvis Ridge. • The temporal change from EM I to HIMU could reflect the compositional heterogeneities of the LLSVP. Abstract Volcanic activity at many oceanic volcanoes, ridges and plateaus often reawakens after hiatuses of up to several million years. Compared to the earlier magmatic phases, this late-stage (rejuvenated/post-erosional) volcanism is commonly characterized by a distinct geochemical composition. Late-stage volcanism raises two hitherto unanswered questions: Why does volcanism restart after an extended hiatus and what is the origin of this volcanism? Here we present the first 40Ar/39Ar age and comprehensive trace element and Sr–Nd–Pb–Hf isotopic data from seamounts located on and adjacent to the Walvis Ridge in the South Atlantic ocean basin. The Walvis Ridge is the oldest submarine part of the Tristan-Gough hotspot track and is famous as the original type locality for the enriched mantle one (EM I) end member. Consistent with the bathymetric data, the age data indicates that most of these seamounts are 20–40 Myr younger than the underlying or nearby Walvis Ridge basement. The trace element and isotope data reveal a distinct compositional range from the EM I-type basement. The composition of the seamounts extend from the St. Helena HIMU (high time-integrated 238U/204Pb mantle with radiogenic Pb isotope ratios) end member to an enriched (E) Mid-Ocean-Ridge Basalt (MORB) type composition, reflecting a two-component mixing trend on all isotope diagrams. The EMORB end member could have been generated through mixing of Walvis Ridge EM I with normal (N) MORB source mantle, reflecting interaction of Tristan-Gough (EM I-type) plume melts with the upper mantle. The long volcanic quiescence and the HIMU-like geochemical signature of the seamounts are unusual for classical hotspot related late-stage volcanism, indicating that these seamounts are not related to the Tristan-Gough hotspot volcanism. Two volcanic arrays in southwestern Africa (Gibeon-Dicker Willem and Western Cape province) display similar ages to the late-stage Walvis seamounts and also have HIMU-like compositions, suggesting a larger-scale event at ∼77–49 Ma. We propose that the EM I-like mantle plumes rise from the edges of the African Large Low Shear Velocity Province (LLSVP; Tristan-Gough, Discovery and Shona hotspot), whereas the HIMU-dominated intraplate lavas (St. Helena, Gibeon-Dicker Willem and Western Cape province) and the late-stage Walvis seamounts tap material from internal portions of the African LLSVP, suggesting possible lateral and/or vertical chemical zonation of the African LLSVP.

Description: Highlights • Melt inclusions from southern Payenia have highly variable element enrichment • Magmas formed by mixing of asthenospheric high Nb/U and lithospheric low Nb/U melts • Low Nb/U type inclusions are similar in composition to alkaline lamprophyres • Low Nb/U melts were formed by fractionation of high Nb/U melts in the SCLM • The percolative fractional crystallization involved cpx, rutile and apatite Abstract We present major and trace element compositions of melt inclusions from three alkali basalts from the Río Colorado volcanic field in the Payenia backarc province, Argentina. Modeling of diffusion profiles around the inclusions showed that most inclusions equilibrated 〈14 days after formation, indicating a short crustal residence time for the magmas and nearly direct ascent through the crust. Despite overlapping host rock isotopic compositions, the inclusions show a large variation in their degree of enrichment, and display trends that we interpret as mixing between asthenospheric OIB-type low K2O-high Nb/U melts and enriched high K2O-low Nb/U lithospheric mantle melts similar in composition to alkaline lamprophyres. The low Nb/U magmas are excessively enriched in the elements Cs, Rb, Ba, Th, U, K, Pb and Cl relative to Nb, Ta and REEs. The enriched low Nb/U components are interpreted to have formed by percolative fractional crystallization of asthenospheric high Nb/U melts in the lithospheric mantle involving crystallization of clinopyroxene, apatite and rutile. The residual fluid-rich melts either mixed directly with new batches of high Nb/U melts or metasomatized and veined the lithospheric mantle which later re-melted during continued volcanism. The major element compositions of the high K2O-low Nb/U components are distinct for the whole rocks and melt inclusions, and most enriched inclusions have lower SiO2 and higher TiO2 contents indicating derivation by melting of amphibole-bearing veins. In contrast, most wr low Nb/U basalts have higher SiO2 and lower TiO2 and were most likely formed by melting of pyroxenitic veins or peridotitic metasomatized lithospheric mantle.

Description: Highlights • First data on the composition of deep crust and primitive rocks of high-Ti magmatic series of Manihiki Plateau • High potential mantle temperature for Manihiki sources (〉1460oC) suggests a lower mantle plume origin • EM1 signature in high-Ti Manihiki basalts could originate from recycled lower continental crust or re-fertilized SCLM • The presence of refractory mantle in the Manihiki plume explains 30% lower crustal thickness compared to OJP • Manihiki and OJP could have been formed from a geochemically zoned plume or from two spatially separated mantle plumes Abstract Geochemical studies revealed two major (high- and low-Ti) magmatic series composing the Manihiki Plateau in the Western Pacific. Here we report new geochemical data (major and trace element and Sr-Nd-Pb isotope compositions) of the Manihiki rocks. The rocks belong to the previously rarely sampled high-Ti Manihiki series and represent a section of deep crust of the plateau. The rocks were collected by remotely operated vehicle ROV Kiel 6000 during R/V SONNE SO225 expedition from a tectonic block at a stretched and faulted boundary between the Northern and Western Manihiki sub-plateaus. Additional data is presented on samples obtained by dredging during the same cruise. Judging from the age of stratigraphically higher lavas, most samples must be ≥125 Ma old. They comprise fully crystalline microdolerites, aphyric and Ol-Px-Pl-phyric basalts and breccias metamorphosed under greenschist to amphibolite facies with peak metamorphic temperatures of 636–677 °C and pressures of 2.0–2.7 kbar. A single sample of hornblende gabbro was also recovered and likely represents a late stage intrusion. Despite strong metamorphism, the samples from the ROV profile reveal only minor to moderate chemical alteration and their initial compositions are well preserved. The rocks are relatively primitive with MgO up to 13 wt%, range from enriched to depleted in LREE (LaN/SmN = 0.7–1.1), exhibit variable but mostly depleted Nb contents (Nb/Nb* = 0.8–1.3) and display only a narrow range in isotope compositions with strong EM1 characteristics (εNd (t) = 1.8–3.6, 206Pb/204Pb (t) = 17.9–18.1, 207Pb/204Pb (t) = 15.49–15.53, 208Pb/204Pb (t) = 38.08–38.42). The parental magmas are interpreted to originate from a thermochemical plume with a potential mantle temperature 〉1460 °C. The trace element and isotope EM1 signature of the high-Ti rocks reflects the presence of recycled lower continental crust material or re-fertilized subcontinental lithospheric mantle in the plume source. A highly refractory mantle was the primary source of the low-Ti basalts and could also contribute to the origin of high-Ti basalts. On average a more depleted mantle source for the Manihiki rocks can explain ~30% lower crustal thickness of this plateau compared to Ontong Java Plateau, which was mainly formed by melting of similarly hot but more fertile mantle. The presently available data suggest that the sources of Ontong Java and Manihiki Plateaus were compositionally different and could represent two large domains of a single plume or two contemporaneous but separate plumes.

Description: Over the last decade there has been renewed interest in determining the water contents of basaltic magmas. A commonly applied method is analysis of H2O from melt inclusions in olivine. However, it is also well known that these can rapidly lose (or gain) H2O by diffusion. An alternative is to measure the H2O contents of clinopyroxene phenocrysts and use a partition coefficient (D) to estimate the original H2O content of the host magma. This approach is not without complications and several recent studies have attempted to assess the effects of diffusive loss of H2O from magmatic clinopyroxenes. In the ideal case, these crystals should be taken from rapidly cooled tephra or lapilli but such materials are not always available. In order to further assess the potential of using 5-10mm clinopyroxenes from lavas we undertook a detailed, multi-analytical investigation of clinopyroxenes from an ankaramite flow on Pico Island in the Azores. We conclude that these can be trusted to preserve (probably minimum) magmatic H2O contents if the H2O concentrations of multiple clinopyroxenes from a single sample form a linear correlation with the AlIV content that demonstrates a coupled substitution with little or no H2O loss. Conversely, if H2O contents decrease from core to rim whereas AlIV contents remain relatively constant then it is likely that those clinopyroxenes lost H2O during differentiation and/or cooling. We suspect that the olivine melt inclusions we analysed from Pico and São Miguel Islands also underwent diffusive loss of H2O. Using these criteria, we present clinopyroxene-derived magmatic H2O estimates for Corvo, Flores Faial, Pico and São Miguel Islands that range from 0.28 to 2.2wt%. When combined with published data these show that H2O contents often extend to higher values on the islands than along the adjacent mid-Atlantic ridge. These localised, elevated H2O contents can explain why the islands are emergent despite being situated away from the ridge and perhaps also the asymmetric nature of the bathymetry of the archipelago. It is possible that this H2O was recycled from material subducted very early on in Earth's history.

Description: Highlights • Four of the seven seamounts northeast of the Galápagos Platform are drowned islands • The ages of the seamounts range from 5.2 Ma to 0.5 Ma • Seamount morphology changes from conical to elongate at ~1.5 Ma • The locus of volcanism appears to migrate eastward at the rate of Nazca plate motion Abstract We present new geochemical and 40Ar/39Ar analyses from seven seamounts located off the northeastern margin of the shallow Galápagos Platform. Initial volcanism at 5.2 Ma created a small island (Pico) over the current location of the hotspot with geochemically enriched lavas. There is no further record of magmatism in the study area until 3.8 to 2.5 Ma, during which four roughly conical volcanoes (Sunray, Grande, Fitzroy, and Beagle) formed through eruption of lavas derived from a depleted mantle source. Sunray, Fitzroy, and Grande were islands that existed for ~3 m.y. ending with the submergence of Fitzroy at ~0.5 Ma. The youngest seamounts, Largo and Iguana, do not appear to have been subaerial and were active at 1.3 Ma and 0.5 Ma, respectively, with the style of edifice changing from the previous large cones to E-W elongate, composite structures. The progression of magmatism suggests that Pico erupted near 91.5°W near the location of the Galápagos plume while the others formed well east of the plume center. If the locations of initial volcanism are calculated using the eastward velocity of the Nazca plate, there appears to be a progression of younger volcanism toward the east, opposite what would be expected from a fixed mantle plume source. The rate that initial volcanism moves eastward is close to the plate velocity. A combination of higher temperature and geochemical enrichment of the thickened lithosphere of the Galápagos platform could have provided a viscosity gradient at the boundary between the thick lithosphere and the thinner oceanic lithosphere to the northeast. As this boundary moved eastward with the Nazca plate, it progressively triggered shear-driven mantle upwelling and volcanism.

Description: Oceanic basalts reflect the heterogeneities in the earth's mantle, which can be explained by five mantle end members. The HIMU end member, characterized by high time-integrated μ (238U/204Pb), is defined by the composition of lavas from the ocean islands of St. Helena, South Atlantic Ocean and Mangaia and Tubuai (Cook-Austral Islands), South Pacific Ocean. It is widely considered to be derived from a mantle reservoir that is rarely sampled and not generally involved in mixing with the other mantle components. On the other hand, the FOZO end member, located at the FOcal ZOne of oceanic volcanic rock arrays on isotope diagrams, is considered to be a widespread common component with slightly less radiogenic 206Pb/204Pb and intermediate Sr-Nd-Hf isotopic compositions. Here we present new major and trace element, Sr-Nd-Pb-Hf isotope and geochronological data from the Walvis Ridge and Richardson Seamount in the South Atlantic Ocean and the Manihiki Plateau and Eastern Chatham Rise in the southwest Pacific Ocean. Our new data, combined with literature data, document a more widespread (nearly global) distribution of the HIMU end member than previously postulated. Our survey shows that HIMU is generally associated with low-volume alkaline, carbonatitic and/or kimberlitic intraplate volcanism, consistent with derivation from low degrees of melting of CO2-rich sources. The majority of end member HIMU locations can be directly related to hotspot settings. The restricted trace element and isotopic composition (St. Helena type HIMU), but near-global distribution, point to a deep-seated, widespread reservoir, which most likely formed in the Archean. In this context we re-evaluate the origin of a widespread HIMU reservoir in an Archean geodynamic setting. We point out that the classic ocean crust recycling model cannot be applied in a plume-lid dominated tectonic setting, and instead propose that delamination of carbonatite- metasomatized subcontinental lithospheric mantle could be a suitable HIMU source.

Description: Highlights • First comprehensive dataset of spinel inclusions in high-Mg olivine from Kamchatka • Oxidation state of parental magmas of Kamchatka ranging from ΔQFM+0.7 to +3.7 • ΔQFM correlates with Ba/La and La/Nb for back-arc magmas of Kamchatka • Decoupling of Cr# and TiO2 in primitive Cr-Spinel suggests slab melt contribution Abstract The Kamchatka volcanic arc (Russia) is one of well-studied but complex tectonic margins on Earth, with an extensive geologic history stretching as far back as the Late Cretaceous. Unlike many other subduction zones, primitive basalts with Mg# 〉 65 are abundant in Kamchatka, thereby allowing characterization of the mantle source through compositional analyses of near-liquidus minerals in the rocks. In this paper, we present a comprehensive dataset on the composition of Cr-spinel inclusions in olivine for all main Late Quaternary volcanic zones in Kamchatka, comprising of analyses of 1604 spinel inclusions and their host-olivine from 104 samples representing 30 volcanoes and volcanic fields. The studied rocks are basalts, basaltic andesites and high-Mg andesites, which cover the whole compositional range the Late Quaternary primitive volcanic rocks in Kamchatka. The composition of spinel shows large variability. Spinel inclusions with the lowest Cr# and Fe3+/Fe2+ ratios were found in basalts from Sredinny Range and Northern Kamchatka, whereas the most Cr-rich and oxidized spinel inclusions occur in basalts and high-Mg andesites from the Central Kamchatka Depression. Intermediate Cr-spinel compositions characterize the Eastern Volcanic Belt of Kamchatka. The compositions of olivine-spinel pairs were used to quantify the oxidation state of parental Kamchatka magmas and the degree of partial mantle melting. The redox conditions recorded in spinel compositions range from ΔQFM = +0.7 to +3.7. ΔQFM for samples from the Sredinny Range and Northern Kamchatka correlates with a number of proxies of the involvement of slab-derived components incorporated in the composition of their host-rocks (e.g., La/Nb and Ba/La), which suggests a coupling between the mantle oxidation and metasomatism by slab-derived fluids or melts. These correlations were not observed for frontal Kamchatka volcanoes with the highest estimated ΔQFM, which possibly indicates a buffering of the mantle oxidation state by sulfur. The estimated degrees of partial mantle melting range from 8 to 〉20% for Kamchatka volcanoes. Spinel from the Central Kamchatka Depression has the highest Cr# and could crystallize from magmas generated from the most depleted sources. In contrast to the Eastern Volcanic Belt, spinel Cr# and the inferred degrees of melting in the Central Kamchatka Depression do not correlate with spinel TiO2 content. The apparent decoupling between the proxies of mantle depletion in the CKD spinel is interpreted to reflect refertilization of the CKD mantle by oxidized Ti-rich slab- or mantle lithosphere-derived melts near the northern edge of the subducting Pacific Plate. This study demonstrates that the composition of Cr-spinel in volcanic rocks in combination with bulk-rock compositions can be a powerful tool to map regional variations of the mantle source depletion, oxidation state, and involvement of various slab derived components in island-arc magmatism.

Description: Spatial geochemical zonation is being increasingly recognized in Pacific and Atlantic hotspot tracks and is believed to reflect zonation within plumes upwelling from the margins of the Large Low Shear Velocity Provinces (LLSVPs) at the base of Earth’s mantle. We present new 40Ar/39Ar age data for the Discovery Rise (South Atlantic Ocean) that show an age progression in the direction of plate motion from 23Ma in the southwest to 40Ma in the northeast of the Rise, consistent with formation of the Rise above a mantle plume. The lavas have incompatible element and Sr–Nd–Pb–Hf radiogenic isotope characteristics similar to the enriched DUPAL anomaly occurring in the southern hemisphere. The northern chain of seamounts is compositionally similar to the adjacent Gough subtrack of the bilaterally-zoned Tristan–Gough hotspot track, whereas the southern chain has some of the most extreme DUPAL compositions found in South Atlantic intraplate lavas thus far. The nearby southern Mid-Atlantic Ridge, believed to interact with the Discovery hotspot, shows a similar spatial geochemical distribution, consistent with the Discovery hotspot being zoned over its entire 40Ma history. Our study implies a deep origin for the DUPAL anomaly, suggesting recycling of subcontinental lithospheric mantle (±lower crust) and oceanic crust through the lower mantle. The presence of an additional (Southern Discovery) DUPAL-like component, in addition to the Tristan and Gough/Northern Discovery components, in long-term zoned South Atlantic hotspots, points to the presence of a third lower mantle reservoir and thus is not consistent with the simple model that bilaterally-zoned plumes sample a chemically distinct LLSVP and the ambient mantle outside of the LLSVP.

Description: Shallow (elevated) portions of mid-ocean ridges with enriched geochemical compositions near hotspots document the interaction of hot geochemically enriched plume mantle with shallow depleted upper mantle. Whereas the spatial variations in geochemical composition of ocean crust along the ridge axis in areas where plume-ridge interaction is taking place have been studied globally, only restricted information exists concerning temporal variations in geochemistry of ocean crust formed through plume-ridge interaction. Here we present a detailed geochemical study of 0-1.5 Ma ocean crust sampled from the Western Galápagos Spreading Center (WGSC) axis to 50 km north of the axis, an area that is presently experiencing a high influx of mantle material from the Galápagos Hotspot. The tholeiitic to basaltic andesitic fresh glass and few bulk rock samples have incompatible element abundances and Sr-Nd-Pb isotopic compositions intermediate between depleted normal mid-ocean-ridge basalt (N-MORB) from 〉95.5°W along the WGSC and enriched lavas from the Galápagos Archipelago, displaying enriched (E-)MORB type compositions. Only limited and no systematic geochemical variations are observed with distance from the ridge axis for 〈1.0 Ma old WGSC crust, whereas 1.0-1.5 Ma old crust trends to more enriched isotopic compositions in 87Sr/86Sr, 143Nd/144Nd, 207Pb/204Pb and 208Pb/204Pb isotope ratios. On isotope correlation diagrams, the data set displays correlations between depleted MORB and two enriched components. Neither the geographically referenced geochemical domains of the Galápagos Archipelago nor the end members used for principle component analysis can successfully describe the observed mixing relations. Notably an off-axis volcanic cone at site DR63 has the appropriate composition to serve as the enriched component for the younger WGSC and could represent a portion of the northern part of the Galápagos plume not sampled south of the WGSC. Similar compositions to samples from volcanic cone DR63 have been found in the northern part of the 11-14 Ma Galápagos hotspot track offshore Costa Rica, indicating that this composition is derived from the northern portion of the Galápagos plume. The older WGSC requires involvement of an enriched mantle two (EMII) type source, not recognized thus far in the Galápagos system, and is interpreted to reflect entrained material either from small-scale heterogeneities within the upper mantle or from the mantle transition zone. Overall the source material for the 0-1.5 Ma WGSC ocean crust appears to represent mixing of depleted upper mantle with Northern Galápagos Plume material of relatively uniform composition in relatively constant proportions.