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Abstract Twice in the Cryogenian Period (720–635 Ma), during the Sturtian and Marinoan glaciations, ice sheets extended to equatorial latitudes for millions of years. These climate extremes have been interpreted to record the Snowball climate state, in which all of Earth’s oceans were covered with ice. During a Snowball Earth, the hydrological cycle would have been curtailed and silicate weathering greatly reduced. In this scenario, deep ocean chemistry should have evolved toward mantle values through hydrothermal exchange at mid-ocean ridges. Specifically, seawater strontium isotopes (87Sr/86Sr) are predicted to exhibit unradiogenic mantle-like values. However, cap carbonates that overlie the Cryogenian glacial deposits have yielded radiogenic 87Sr/86Sr values similar to those of seawater prior to glaciation, inconsistent with the central geochemical prediction of the Snowball Earth hypothesis. Here we report the discovery of 87Sr/86Sr values of 0.7034 in marine carbonate and authigenic barite that rest directly above Sturtian glacial deposits in Dhofar, Oman. These values record either a local unradiogenic source or Snowball Earth deep-water values that have not been previously identified. If it is a global signal, these new data and geochemical modeling support an extreme Snowball Earth scenario with near-complete ice cover and define one of the largest geochemical perturbations to seawater in Earth history. 

Abstract Lavas erupted at hotspot volcanoes provide evidence of mantle heterogeneity. Samoan Island lavas with high⁸⁷Sr/⁸⁶Sr (>0.706) typify a mantle source incorporating ancient subducted sediments. To further characterize this source, we target a single high⁸⁷Sr/⁸⁶Sr lava from Savai’i Island, Samoa for detailed analyses of⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd isotopes and major and trace elements on individual magmatic clinopyroxenes. We show the clinopyroxenes exhibit a remarkable range of⁸⁷Sr/⁸⁶Sr—including the highest observed in an oceanic hotspot lava—encompassing ~30% of the oceanic mantle’s total variability. These new isotopic data, data from other Samoan lavas, and magma mixing calculations are consistent with clinopyroxene⁸⁷Sr/⁸⁶Sr variability resulting from magma mixing between a high silica, high⁸⁷Sr/⁸⁶Sr (up to 0.7316) magma, and a low silica, low⁸⁷Sr/⁸⁶Sr magma. Results provide insight into the composition of magmas derived from a sediment-infiltrated mantle source and document the fate of sediment recycled into Earth’s mantle. 

Abstract The Earth's upper mantle is isotopically heterogeneous over large lengthscales, but the lower limit of these heterogeneities is not well quantified. Grain scale trace elemental variability has been observed in mantle peridotites, which suggests that isotopic heterogeneity may be preserved as well. Recent advances in isotope ratio mass spectrometry enable isotopic analysis of very small samples (e.g., nanograms or less of analyte) while maintaining the precision necessary for meaningful interpretation. Here we examine four peridotite xenoliths—hosted in lavas from Savai'i (Samoa hotspot) and Tahiti (Societies hotspot) islands—that exhibit grain scale trace element heterogeneity likely related to trapped fluid and/or melt inclusions. To evaluate whether this heterogeneity is also reflected in grain scale isotopic heterogeneity, we separated clinopyroxene, orthopyroxene, and (in the most geochemically enriched xenolith) olivine for single‐grain⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd analyses. We find, in some xenoliths, extreme intra‐xenolith isotopic heterogeneity. For example, in one xenolith, different mineral grains range in⁸⁷Sr/⁸⁶Sr from 0.70987 to 0.71321, with corresponding variability in¹⁴³Nd/¹⁴⁴Nd from 0.512331 to 0.512462. However, not all peridotite xenoliths which display trace elemental heterogeneity exhibit isotopic heterogeneity. Based on coupled isotopic and trace element data (i.e., a negatively‐sloping trend in⁸⁷Sr/⁸⁶Sr vs. Ti/Eu), we suggest that carbonatitic metasomatism is responsible for creating the intra‐xenolith isotopic heterogeneities which we observe. This carbonatitic component falls off the array defined in⁸⁷Sr/⁸⁶Sr‐¹⁴³Nd/¹⁴⁴Nd space by Samoa hotspot basalts, which suggests a second, distinct EM2 (enriched mantle II) component is present in the Samoa hotspot that is not readily recognized in erupted products, but is instead seen only in mantle peridotite xenoliths. 

Abstract The Icelandic hotspot has erupted basaltic magma with the highest mantle‐derived³He/⁴He over a period spanning much of the Cenozoic, from the early‐Cenozoic Baffin Island‐West Greenland flood basalt province (49.8R_A), to mid‐Miocene lavas in northwest Iceland (40.2 to 47.5R_A), to Pleistocene lavas in Iceland's neovolcanic zone (34.3R_A). The Baffin Island lavas transited through and potentially assimilated variable amounts of Precambrian continental basement. We use geochemical indicators sensitive to continental crust assimilation (Nb/Th, Ce/Pb, MgO) to identify the least crustally contaminated lavas. Four lavas, identified as “least crustally contaminated,” have high MgO (>15 wt.%), and Nb/Th and Ce/Pb that fall within the mantle range (Nb/Th = 15.6 ± 2.6, Ce/Pb = 24.3 ± 4.3). These lavas have⁸⁷Sr/⁸⁶Sr = 0.703008–0.703021,¹⁴³Nd/¹⁴⁴Nd = 0.513094–0.513128,¹⁷⁶Hf/¹⁷⁷Hf = 0.283265–0.283284,²⁰⁶Pb/²⁰⁴Pb = 17.7560–17.9375,³He/⁴He up to 39.9R_A, and mantle‐like δ¹⁸O of 5.03–5.21‰. The radiogenic isotopic compositions of the least crustally contaminated lavas are more geochemically depleted than Iceland high‐³He/⁴He lavas, a shift that cannot be explained by continental crust assimilation in the Baffin suite. Thus, we argue for the presence oftwogeochemically distinct high‐³He/⁴He components within the Iceland plume. Additionally, the least crustally contaminated primary melts from Baffin Island‐West Greenland have higher mantle potential temperatures (1510 to 1630 °C) than Siqueiros mid‐ocean ridge basalts (1300 to 1410 °C), which attests to a hot, buoyant plume origin for early Iceland plume lavas. These observations support the contention that the geochemically heterogeneous high‐³He/⁴He domain is dense, located in the deep mantle, and sampled by only the hottest plumes.