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Hydrothermal seafloor massive sulfide deposition at ocean spreading centers modifies the flux of iron from vents while producing an archive of these processes in both active and fossil hydrothermal complexes. Despite hopes of stable iron isotopes tracing mineral formation and iron cycling at these sites, the competing fractionations accompanying various mineralization processes have presented an obstacle to confidently interpreting iron isotopic datasets. We have developed a triple iron isotope proxy that can resolve some of these previously indistinguishable mineral formation histories, and applied it to a suite of samples from the Trans-Atlantic Geotraverse (TAG) active hydrothermal mound on the Mid-Atlantic Ridge. We show that massive pyrite-dominated sulfides formed near the TAG mound surface retain primary kinetic isotope signatures indicative of their rapid formation, likely from an iron monosulfide intermediate. Pyrite-anhydrite breccias retain mixed isotopic signatures of reworked primary massive sulfides together with secondary pyrite, grown in confined conditions, in some cases in equilibrium with subsurface hydrothermal fluid. We also suggest that iron oxyhydroxide-rich chert precipitation across parts of the mound surface trapped isotopically evolved fluid within the mound, and a later generation of sulfides precipitated from this evolved fluid. Metalliferous sediments from a core recovered near the base of the TAG mound mostly fall along a primary mass fractionation law defined by mound sulfides. This is consistent with a dominant contribution of collapsed mound debris and/or black smoker sulfide fallout to the seafloor near the base of the TAG mound. However, the triple iron isotopic composition of surface sediment from this core suggests it may also contain iron oxyhydroxide fallout from the dispersing non-buoyant plume that had already undergone extensive sulfide precipitation. Triple iron isotope studies of non-buoyant plume sediments may be used to quantify the mineral fate of iron vented to the oceans, estimate variations in iron to sulfide ratios of primary vent fluids, and resolve the relative importance of low and high temperature hydrothermal flow to basin-scale iron-rich plumes in the global oceans. 

Iodine intersects with the marine biogeochemical cycles of several major elements and can influence air quality through reactions with tropospheric ozone. Iodine is also an element of interest in paleoclimatology, whereby iodine-to-calcium ratios in marine carbonates are widely used as a proxy for past ocean redox state. While inorganic iodine in seawater is found predominantly in its reduced and oxidized anionic forms, iodide (I⁻) and iodate (IO₃⁻), the rates, mechanisms and intermediate species by which iodine cycles between these inorganic pools are poorly understood. Here, we address these issues by characterizing the speciation, composition and cycling of iodine in the upper 1,000 m of the water column at Station ALOHA in the subtropical North Pacific Ocean. We first obtained high-precision profiles of iodine speciation using isotope dilution and anion exchange chromatography, with measurements performed using inductively coupled plasma mass spectrometry (ICP-MS). These profiles indicate an apparent iodine deficit in surface waters approaching 8% of the predicted total, which we ascribe partly to the existence of dissolved organic iodine that is not resolved during chromatography. To test this, we passed large volumes of seawater through solid phase extraction columns and analyzed the eluent using high-performance liquid chromatography ICP-MS. These analyses reveal a significant pool of dissolved organic iodine in open ocean seawater, the concentration and complexity of which diminish with increasing water depth. Finally, we analyzed the rates of IO₃⁻formation using shipboard incubations of surface seawater amended with¹²⁹I⁻. These experiments suggest that intermediate iodine species oxidize to IO₃⁻much faster than I⁻does, and that rates of IO₃⁻formation are dependent on the presence of particles, but not light levels. Our study documents the dynamics of iodine cycling in the subtropical ocean, highlighting the critical role of intermediates in mediating redox transformations between the major inorganic iodine species. 

Abstract Fluids mediate the transport of subducted slab material and play a crucial role in the generation of arc magmas. However, the source of subduction-derived fluids remains debated. The Kamchatka arc is an ideal subduction zone to identify the source of fluids because the arc magmas are comparably mafic, their source appears to be essentially free of subducted sediment-derived components, and subducted Hawaii-Emperor Seamount Chain (HESC) is thought to contribute a substantial fluid flux to the Kamchatka magmas. Here we show that Tl isotope ratios are unique tracers of HESC contribution to Kamchatka arc magma sources. In conjunction with trace element ratios and literature data, we trace the progressive dehydration and melting of subducted HESC across the Kamchatka arc. In succession, serpentine (<100 km depth), lawsonite (100–250 km depth) and phengite (>250 km depth) break down and produce fluids that contribute to arc magmatism at the Eastern Volcanic Front (EVF), Central Kamchatka Depression (CKD), and Sredinny Ridge (SR), respectively. However, given the Tl-poor nature of serpentine and lawsonite fluids, simultaneous melting of subducted HESC is required to explain the HESC-like Tl isotope signatures observed in EVF and CKD lavas. In the absence of eclogitic crust melting processes in this region of the Kamchatka arc, we propose that progressive dehydration and melting of a HESC-dominated mélange offers the most compelling interpretation of the combined isotope and trace element data. 

Abstract Iron (Fe) availability impacts marine primary productivity, potentially influencing the efficiency of the biological carbon pump. Stable Fe isotope analysis has emerged as a tool to understand how Fe is sourced and cycled in the water column; however its application to sediment records is complicated by overlapping isotope signatures of different sources and uncertainties in establishing chronologies. To overcome these challenges, we integrate Fe and osmium isotope measurements with multi‐element geochemical analysis and statistical modeling. We apply this approach to reconstruct the history of Fe delivery to the South Pacific from three pelagic clay sequences spanning 93 million years. Our analysis reveals five principal Fe sources—dust, distal background, two distinct hydrothermal inputs, and a magnesium‐rich volcanic ash. Initially, hydrothermal inputs dominated Fe deposition, but as the sites migrated away from their respective mid‐ocean ridges, other sources became prominent. Notably, from 66 to 40 million years ago (Ma), distal background Fe was the primary source before a shift to increasing dust dominance around 30 Ma. This transition implies that Fe in South Pacific seawater has been dust‐dominated since ≈30 Ma, despite extremely low dust deposition rates today. We speculate that the shift to episodic and low Fe fluxes in the South Pacific and Southern Ocean over the Cenozoic helped shape an ecological niche that favored phytoplankton that adapted to these conditions, such as diatoms. Our analysis highlights how Fe delivery to the ocean is driven by large‐scale tectonic and climatic shifts, while also influencing climate through its integral role in marine phytoplankton and Earth's biogeochemical cycles.