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1. The multiple depleted mantle components in the Hawaiian-Emperor chain

   https://doi.org/10.1016/j.chemgeo.2019.119324  

   Harrison, L ; Weis, D ; Garcia, M.O. ( January 2020 , Chemical geology)

   null (Ed.)

   Oceanic island basalts are targeted for geochemical study because they provide a direct window into mantle composition and a wealth of information on the dynamics and timescales associated with Earth mixing. Previous studies mainly focused on the shield volcanic stage of oceanic islands and the more fusible, enriched mantle components that are easily distinguished in those basalts. Mantle depleted compositions are typically more difficult to resolve unless large amounts of this material participated in mantle melting (e.g., mid-ocean ridges), or unique processes allow for their compositions to be erupted undiluted, such as very small degrees of melting of a source with minimal fusible enriched components (e.g., rejuvenated basalts) or as xenoliths (e.g., abyssal peridotites). Mantle depleted components, defined here as material with low time-integrated Rb/Sr (low 87Sr/86Sr) and high time-integrated Sm/Nd and Lu/Hf ratios (high 143Nd/144Nd and 176Hf/177Hf) relative to primitive mantle, derive from a potentially very large volume reservoir (up to 80% of the mantle), and therefore need adequate characterization in order estimate the composition of the Earth and mantle-derived melts. This review focuses on mantle depleted compositions in oceanic island basalts using the Hawaiian-Emperor chain as a case study. The Hawaiian-Emperor chain is the ∼6000 km long geological record of the deeply sourced Hawaiian mantle plume, active for>81 Myr. Hawaiian volcanism evolves through four volcanic stages as a volcano traverses the Hawaiian plume: alkalic preshield, tholeiitic shield (80–90% volcano volume), alkalic postshield (∼1%), and silica undersaturated rejuvenated (< 0.1%). We report Pb-Sr-Nd-Hf isotope compositions and trace element concentrations of three rejuvenated Northwest Hawaiian Ridge basalts and compare them to an exhaustive compiled dataset of basalts from the Hawaiian Islands to the Emperor Seamounts. The Northwest Hawaiian Ridge (NWHR) includes 51 volcanoes spanning ∼42 m.y. between the bend in the Hawaiian-Emperor chain and the Hawaiian Islands where there is no high-precision isotopic data published on the rejuvenated-stage over ∼47% of the chain. NWHR and Hawaiian Island rejuvenated basalts are geochemically similar, indicating a consistent source for rejuvenated volcanism over ∼12.5 million years. In contrast, shield-stage basalts from the oldest Emperor Seamounts are more depleted in isotopic composition (i.e., higher 176Hf/177Hf, and 143Nd/144Nd with lower 87Sr/86Sr and 208Pb*/206Pb*) and trace element concentrations (i.e., much lower concentrations of highly incompatible elements) than all other depleted Hawaiian basalts younger than the bend, including NWHR rejuvenated basalts. The strongly depleted source for the oldest Emperor Seamounts (> 70 Ma) was likely related to interaction with the Kula-Pacific-Izanagi mid-ocean ridge spreading system active near the Hawaiian plume in the Late Cretaceous. In contrast, the incompatible trace element ratios of NWHR rejuvenated basalts require a distinct source in the Hawaiian mantle plume that was imprinted by ancient (> 1 Ga) partial melting, likely ancient recycled oceanic lithosphere. This review of the geochemistry of Hawaiian depleted components documents the need for the sampling of multiple distinctive depleted compositions, each preferentially melted during specific periods of Hawaiian plume activity. This suggests that the composition of depleted components can evolve during the lifetime of the mantle plume, as observed for enriched components in the Hawaiian mantle plume. Changes in the composition of depleted components are dominantly controlled by the upper mantle tectonic configurations at the time of eruption (i.e., proximity to a mid-ocean ridge), as this effect overwhelms the signal imparted by potentially sampling different lower mantle components through time. 

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2. Decoupled Trace Element and Isotope Compositions Recorded in Orthopyroxene and Clinopyroxene in Composite Pyroxenite Veins from the Xiugugabu Ophiolite (SW Tibet)

   https://doi.org/10.1093/petrology/egac046  

   Zhang, Zhen-Yu ; Liu, Chuan-Zhou ; Liang, Yan ; Zhang, Chang ; Liu, Tong ; Zhang, Wei-Qi ; Ji, Wen-Bin ( June 2022 , Journal of Petrology)

   Abstract Pyroxenite veins and dikes are commonly observed in the mantle section of ophiolites. Because of their mantle occurrence, these pyroxenites are free from crustal contamination and offer a unique opportunity for studying mantle compositions and melt–rock interaction processes. We conducted an integrated petrological and geochemical study of a suite of composite orthopyroxenite, websterite, and pyroxene-bearing dunite veins from the Xiugugabu ophiolite located on the western segment of Yarlung–Zangbo Suture Zone. The dunite is separated from the host peridotite by a layer of pyroxenite, forming a composite vein system. Systematic variations in major, minor, and trace element compositions in minerals across the composite veins are observed. Two generations of orthopyroxenes in the pyroxenites are characterized by high Mg#, low TiO2 concentrations, and depleted patterns of incompatible trace elements. Clinopyroxenes in the pyroxenites are characterized by high Mg#, low contents of TiO2 and Na2O, spooned shaped REE patterns, and a negative Zr anomaly. Through major and trace element modeling, we showed that both orthopyroxene and clinopyroxene were in equilibrium with melts with different compositions. This hypothesis is further confirmed by distinct initial Nd and Hf isotope ratios in the two pyroxenes. A model for the formation of composite pyroxenite veins is developed, whereby hydrous and silica-rich melts percolate along the margins of a dunite channel. The orthopyroxenite was formed by the reaction between a hydrous, silica-rich melt and the surrounding peridotite. The websterite is formed by reactive crystallization of a hybrid melt produced by mixing silica-rich melt and the melt formed by remelting of previously depleted peridotite in the deeper part of the mantle column. The extremely enriched Nd–Hf isotope compositions of the pyroxenite veins (εNd = −20.3 to +11.5 and εHf = −13.2 to +25.3, 125 million years ago) can be explained by the addition of ancient, recycled sediments to the mantle source in a supra-subduction setting. Based on the low-Cr# spinel in the Xiugugabu dunites (Cr# = 19–50) and the depleted nature of the parental melt of the Xiugugabu pyroxenites, we deduced that the formation of pyroxenites postdate the formation of the Xiugugabu ophiolite at ~125–130 Ma. Collectively, results from this study have provided support to the hypothesis that the Xiugugabu ophiolite experience a two-stage evolution, i.e., firstly formed in a mid-ocean ridge setting and subsequently modified in a supra subduction zone. 

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3. Magmatic Response to Subduction Initiation: Part 1. Fore‐arc Basalts of the Izu‐Bonin Arc From IODP Expedition 352

   https://doi.org/10.1029/2018GC007731  

   Shervais, John W. ; Reagan, Mark ; Haugen, Emily ; Almeev, Renat R. ; Pearce, Julian A. ; Prytulak, Julie ; Ryan, Jeffrey G. ; Whattam, Scott A. ; Godard, Marguerite ; Chapman, Timothy ; et al ( January 2019 , Geochemistry, Geophysics, Geosystems)

   The Izu‐Bonin‐Mariana (IBM) fore arc preserves igneous rock assemblages that formed during subduction initiation circa 52 Ma. International Ocean Discovery Program (IODP) Expedition 352 cored four sites in the fore arc near the Ogasawara Plateau in order to document the magmatic response to subduction initiation and the physical, petrologic, and chemical stratigraphy of a nascent subduction zone. Two of these sites (U1440 and U1441) are underlain by fore‐arc basalt (FAB). FABs have mid‐ocean ridge basalt (MORB)‐like compositions, however, FAB are consistently lower in the high‐field strength elements (TiO₂, P₂O₅, Zr) and Ni compared to MORB, with Na₂O at the low end of the MORB field and FeO* at the high end. Almost all FABs are light rare earth element depleted, with low total REE, and have low ratios of highly incompatible to less incompatible elements (Ti/V, Zr/Y, Ce/Yb, and Zr/Sm) relative to MORB. Chemostratigraphic trends in Hole U1440B are consistent with the uppermost lavas forming off axis, whereas the lower lavas formed beneath a spreading center axis. Axial magma of U1440B becomes more fractionated upsection; overlying off‐axis magmas return to more primitive compositions. Melt models require a two‐stage process, with early garnet field melts extracted prior to later spinel field melts, with up to 23% melting to form the most depleted compositions. Mantle equilibration temperatures are higher than normal MORB (1,400 °C–1,480 °C) at relatively low pressures (1–2 GPa), which may reflect an influence of the Manus plume during subduction initiation. Our data support previous models of FAB origin by decompression melting but imply a source more depleted than normal MORB source mantle.

    

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4. Preserved Nd-Hf-Os isotope variability in replacive channels from the Lanzo ophiolite: Traces of incomplete melt aggregation in the shallow mantle

   A. Sanfilippo ; C.Z. Liu ; V. Salters ; A. Mosconi ; A. Zanetti ; R. Tribuzio ( December 2023 , Chemical geology)

   N/A (Ed.)

   Long-lived radiogenic isotopes of abyssal peridotites, residues of MORB extraction, show that the asthenosphere is intrinsically heterogeneous, which is inherited from ancient melting events and crustal recycling during Earth's history. Yet, Mid Ocean Ridge Basalts (MORB) have a rather uniform average composition, suggesting that the variability of their mantle source is concealed during their ascent. Here we document that mantle heterogeneity is exceptionally well preserved in high permeability mantle conduits from the Lanzo South mantle massif, Western Italian Alps. Nd-Hf-Os isotopes of decametre-scale replacive bodies provide evidence for the existence of two generations of mantle channels. The first generation consists of dunites concordant to the main foliation of host peridotites. The replacive dunites include clinopyroxene with MORB-like incompatible element signature and initial (160 Ma) ƐNd and ƐHf ranging from +4 to +7 and from +10 to +15, respectively. The second generation, made up of pyroxene-poor harzburgites discordant to the main foliation, is geochemically depleted in incompatible elements and its clinopyroxene displays highly radiogenic Hf isotopes (initial ƐHf up to +202). The mantle channel heterogeneity is confirmed by Resingle bondOs isotopes and platinum-groups elements. The MORB-type dunites have high Pt, Pd and, locally, Re, and have 187Os/188Os ratios similar to the host peridotite (0.122–0.128). On the other hand, the depleted bodies have lower Pt, Pd and Re, and 187Os/188Os ratios ranging from those of host peridotites (0.124) to highly unradiogenic values (0.118) in the most refractory sample. The preserved heterogeneity in trace elements, PGE, and Nd-Hf-Os isotopes highlights infiltration of melts from a highly heterogeneous mantle, still partially preserved within these mantle bodies. If applied to present-day Mid Ocean Ridges, our model indicates that the isotopic variability of melts migrating through replacive mantle conduits is by far larger than magmas erupted on the seafloor, which implies that diverse mantle components are mainly delivered and homogenised above the crust-mantle boundary. 

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5. Mixing Loops, Mixing Envelopes, and Scattered Correlations among Trace Elements and Isotope Ratios Produced by Mixing of Melts Derived from a Spatially and Lithologically Heterogenous Mantle

   https://doi.org/10.1093/petrology/egac092  

   Liang, Yan ( September 2022 , Journal of Petrology)

   Abstract Mixing has been widely used in the interpretation of radiogenic isotope ratios and highly incompatible trace element variations in basalts produced by melting of a heterogeneous mantle. The binary mixing model is constructed by considering mass balance of endmember components, which is independent of physical state and spatial distribution of the endmembers in the mantle source. Variations of radiogenic isotope ratios and highly incompatible trace elements in basalts also depend on the size and spatial distribution of chemical and lithological heterogeneities in the mantle source. Here we present a new mixing model and a mixing scheme that take into account of the size, spatial location, and melting history of enriched mantle (EM) and depleted mantle (DM) parcels in the melting column. We show how Sr, Nd, and Hf concentrations and isotope ratios in the aggregated or pooled melt collected at the top of the melting column vary as a function of location of the EM parcel in the melting column. With changing location of the EM parcel in the upwelling melting column, compositions of the pooled melt do not follow a single mixing curve expected by the binary mixing model. Instead, they define a mixing loop that has an enriched branch and a depleted branch joined by two extreme points in composition space. The origin of the mixing loop can be traced back to four types of EM distribution or configuration in the melting column. The shape of the mixing loop depends on the relative melting rate of the EM to that of the DM and the number and spacing of EM parcels in the melting column. Probabilities of sampling the enriched and depleted branches in the pooled melt are proportional to volume fractions of the enriched and depleted materials in the mantle source. Mixing of pooled melts from a bundle of melting columns results in mixing envelopes in the isotope ratio correlation diagrams. The mixing envelope is a useful tool for studying chemical variations in mantle-derived melts. As an application, we consider scattered correlations in 87Sr/86Sr vs. 143Nd/144Nd and 143Nd/144Nd vs. 176Hf/177Hf in mid-ocean ridge basalts. We show that such correlations arise naturally from melting of a spatially heterogeneous mantle. 

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