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Abstract To deconvolve contributions from the four overlapping hotspots that form the “hotspot highway” on the Pacific plate—Samoa, Rarotonga, Arago-Rurutu, and Macdonald—we geochemically characterize and/or date (by the 40Ar/39Ar method) a suite of lavas sampled from the eastern region of the Samoan hotspot and the region “downstream” of the Samoan hotspot track. We find that Papatua seamount, located ~60 km south of the axis of the Samoan hotspot track, has lavas with both a HIMU (high μ = 238U/204Pb) composition (206Pb/204Pb = 20.0), previously linked to one of the Cook-Austral hotspots, and an enriched mantle I (EM1) composition, which we interpret to be rejuvenated and Samoan in origin. We show that these EM1 rejuvenated lavas at Papatua are geochemically similar to rejuvenated volcanism on Samoan volcanoes and suggest that flexural uplift, caused by tectonic forces associated with the nearby Tonga trench, triggered a new episode of melting of Samoan mantle material that had previously flattened and spread laterally along the base of the Pacific plate under Papatua, resulting in volcanism that capped the previous HIMU edifice. We argue that this process generated Samoan rejuvenated volcanism on the older Cook-Austral volcano of Papatua. We also study Waterwitch seamount, located ~820 km WNW of the Samoan hotspot, and provide an age (10.49 ± 0.09 Ma) that places it on the Samoan hotspot trend, showing that it is genetically Samoan and not related to the Cook-Austral hotspots as previously suggested. Consequently, with the possible exception of the HIMU stage of Papatua seamount, there are currently no known Arago-Rurutu plume-derived lava flows sampled along the swath of Pacific seafloor that stretches between Rose seamount (~25 Ma) and East Niulakita seamount (~45 Ma), located 1400 km to the west. The “missing” ~20-million-year segment of the Arago-Rurutu hotspot track may have been subducted into the northern Tonga trench, or perhaps was covered by subsequent volcanism from the overlapping Samoan hotspot, and has thus eluded sampling. Finally, we explore tectonic reactivation as a cause for anomalously young volcanism present within the western end of the Samoan hotspot track. 

Sanitary sewer overflows (SSOs) are a common problem across the United States. An estimated number of 23 000–75 000 SSOs occurred in 2004, discharging between 11 and 38 billion liters of untreated wastewater to receiving waters. SSOs release many contaminants, including engineered nanomaterials (ENMs), to receiving water bodies. Measuring ENM concentrations in environmental samples remains a key challenge in environmental nanotechnology and requires the distinction between natural and engineered particles. This distinction between natural and engineered particles is often hampered by the similarities in the intrinsic properties of natural and engineered particles, such as particle size, composition, density, and surface chemistry, and by the limitations of the available nanometrology tools. To overcome these challenges, we applied a multi-method approach to measure the concentrations and properties of TiO 2 engineered particles ( e.g. , ENMs and pigments) including: 1) multi element-single particle-inductively coupled plasma-mass spectrometry (ME-SP-ICP-MS) to identify elemental associations and to determine elemental ratios in natural particles, 2) calculation of total elemental concentrations and ratios from total metal concentrations measured following total sample digestion to estimate engineered particle concentrations, and 3) transmission electron microscopy (TEM) to characterize engineered particle size and morphology. ME-SP-ICP-MS analysis revealed that natural TiO 2 particles are often associated with at least one of the following elements: Al, Fe, Ce, Si, La, Zr, Nb, Pb, Ba, Th, Ta, W and U, and that elemental ratios of Ti to these elements, except Pb, are typical of riverine particulates and the average crustal ratios. High TiO 2 engineered particle concentrations up to 100 μg L −1 were found in SSO-impacted surface waters. TEM analysis demonstrated the presence of regular-shape TiO 2 particles in SSO-impacted surface waters. This study provides a comprehensive approach for measuring TiO 2 engineered particle concentrations in surface waters. The quantitative data produced in this work can be used as input for modeling studies and pave the way for routine monitoring of ENMs in environmental systems, validation of ENM fate models, and more accurate ENM exposure and risk assessment. 

Rare high-³He/⁴He signatures in ocean island basalts (OIB) erupted at volcanic hotspots derive from deep-seated domains preserved in Earth’s interior. Only high-³He/⁴He OIB exhibit anomalous¹⁸²W—an isotopic signature inherited during the earliest history of Earth—supporting an ancient origin of high³He/⁴He. However, it is not understood why some OIB host anomalous¹⁸²W while others do not. We provide geochemical data for the highest-³He/⁴He lavas from Iceland (up to 42.9 times atmospheric) with anomalous¹⁸²W and examine how Sr-Nd-Hf-Pb isotopic variations—useful for tracing subducted, recycled crust—relate to high³He/⁴He and anomalous¹⁸²W. These data, together with data on global OIB, show that the highest-³He/⁴He and the largest-magnitude¹⁸²W anomalies are found only in geochemically depleted mantle domains—with high¹⁴³Nd/¹⁴⁴Nd and low²⁰⁶Pb/²⁰⁴Pb—lacking strong signatures of recycled materials. In contrast, OIB with the strongest signatures associated with recycled materials have low³He/⁴He and lack anomalous¹⁸²W. These observations provide important clues regarding the survival of the ancient He and W signatures in Earth’s mantle. We show that high-³He/⁴He mantle domains with anomalous¹⁸²W have low W and⁴He concentrations compared to recycled materials and are therefore highly susceptible to being overprinted with low³He/⁴He and normal (not anomalous)¹⁸²W characteristic of subducted crust. Thus, high³He/⁴He and anomalous¹⁸²W are preserved exclusively in mantle domains least modified by recycled crust. This model places the long-term preservation of ancient high³He/⁴He and anomalous¹⁸²W in the geodynamic context of crustal subduction and recycling and informs on survival of other early-formed heterogeneities in Earth’s interior. 

Abstract The ratio of boron to calcium (B/Ca) in a subset of foraminifera has been shown to covary with seawater carbonate chemistry, making this geochemical signature a promising proxy for carbon cycle science. Some studies suggest complications with the B/Ca proxy in photosymbiont‐bearing planktonic foraminifera, while relatively few studies have investigated B/Ca in species that lack large dinoflagellate symbionts. For the first time, we use a sediment trap time series to evaluate B/Ca of subtropical and subpolar planktonic foraminifera species that are asymbiotic (Globigerina bulloidesandNeogloboquadrina incompta) and a species that hosts small intrashell photosymbionts (Neogloboquadrina dutertrei). We find that B/Ca measurements across size fractions indicate overall little to no size‐dependent uptake of boron that has previously been reported in some symbiont‐bearing foraminifera.Neogloboquadrina incomptaandN.dutertreiB/Ca are strongly correlated with calcite saturation, pH, and carbonate ion concentration, which is in good agreement with the limited number of published core top results. WhileG.bulloidesB/Ca trends with seasonal fluctuations in carbonate chemistry, during discrete periods considerable B/Ca offsets occur when a crypticG.bulloidesspecies is known to be seasonally present within the region. We confirm presence and significant B/Ca offset between cryptic species by individual LA‐ICP‐MS analyses. This finding calls into question the use of traditional morphological classification to lump what might be genetically distinct species for geochemical analyses. Our overall results highlight the utility ofG.bulloides,N.incompta, andN.dutertreiB/Ca while bringing to light new considerations regarding divergent geochemistry of cryptic species.