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The Paradox Basin in the Colorado Plateau (USA) has some of the most iconic records of paleofluid flow, including sandstone bleaching and ore mineralization, and hydrocarbon, CO2, and He reservoirs, yet the sources of fluids responsible for these extensive fluid-rock reactions are highly debated. This study, for the first time, characterizes fluids within the basin to constrain the sources and emergent behavior of paleofluid flow resulting in the iconic rock records. Major ion and isotopic (δ18Owater; δDwater; δ18OSO4; δ34SSO4; δ34SH2S; 87Sr/86Sr) signatures of formation waters were used to evaluate the distribution and sources of fluids and water-rock interactions by comparison with the rock record. There are two sources of salinity in basinal fluids: (1) diagenetically altered highly evaporated paleo-seawater-derived brines associated with the Pennsylvanian Paradox Formation evaporites; and (2) dissolution of evaporites by topographically driven meteoric circulation. Fresh to brackish groundwater in the shallow Cretaceous Burro Canyon Formation contains low Cu and high SO4 concentrations and shows oxidation of sulfides by meteoric water, while U concentrations are higher than within other formation waters. Deeper brines in the Pennsylvanian Honaker Trail Formation were derived from evaporated paleo-seawater mixed with meteoric water that oxidized sulfides and dissolved gypsum and have high 87Sr/86Sr indicating interaction with radiogenic siliciclastic minerals. Upward migration of reduced (hydrocarbon- and H2S-bearing) saline fluids from the Pennsylvanian Paradox Formation along faults likely bleached sandstones in shallower sediments and provided a reduced trap for later Cu and U deposition. The distribution of existing fluids in the Paradox Basin provides important constraints to understand the rock record over geological time. 

Abstract The composition of Earth's mantle, continental crust, and oceanic crust continuously evolve in response to the dynamic forces of plate tectonics and mantle convection. The classical view of terrestrial geochemistry, where mid‐ocean ridges sample mantle previously depleted by continental crust extraction, broadly explains the composition of the oceanic and continental crust but is potentially inconsistent with observed slab subduction to the lower mantle and oceanic crust accumulation in the deep mantle. We develop a box model to explore the key processes controlling crust‐mantle chemical evolution. The model mimics behaviors observed in thermochemical convection simulations including subducted oceanic crust separating and accumulating in the deep mantle. We demonstrate that oceanic crust accumulation strongly depletes the mantle independently of continental crust extraction. Slab stalling depths and continental crust recycling rates also affect the extent and location of mantle depletion. We constrain model regimes that reproduce oceanic and continental crust compositions using Markov chain Monte Carlo sampling. Some regimes deplete the lower mantle more than the upper mantle, contradicting the assumption of a more enriched lower mantle. All regimes require oceanic crust accumulation in the mantle. Though a small fraction of the mantle mass, accumulated oceanic crust can sequester trace element budgets exceeding the continental crust, depleting the mantle more than continental crust extraction alone. Oceanic crust accumulation may therefore be as important as continental crust extraction in depleting the mantle, contradicting the paradigmatic complementarity of depleted mantle and continental crust. Instead, depleted mantle is complementary to continental crust plus sequestered oceanic crust. 

Abstract Halogens are primarily located within surface reservoirs of the Earth; as such they have proven to be effective tracers for the identification of subducted volatiles within the mantle. Subducting lithologies exhibit a wide variety of halogen compositions, yet the mantle maintains a fairly uniform signature, suggesting halogens may be homogenized during subduction to the mantle or during eruption. Here we present halogen (Cl, Br, and I), K, noble gas, and major and trace element data on olivines from three seamounts along the Hawaiian‐Emperor seamount chain to determine if the deep mantle source has retained evidence of halogen heterogeneities introduced through subduction. High Ni contents indicate that the Hawaiian‐Emperor mantle source contains a recycled oceanic crust component in the form of pyroxenite, which increases from the 46% in the oldest (Detroit) to 70% in the younger seamount (Koko). Detroit seamount retains mid‐ocean ridge basalts (MORB)‐like Br/Cl and I/Cl, while the Br/Cl and I/Cl of Suiko and Koko seamounts are higher than MORB and similar to altered oceanic crust and dehydrated serpentinite. Helium isotopes show a similar evolution, from MORB‐like values at Detroit seamount toward higher values at Suiko and Koko seamounts. The correlation between pyroxenite contributions, Br/Cl, I/Cl, and³He/⁴He indicates that subducted material has been incorporated into the primordial undegassed Hawaiian mantle plume source. The identification of recycled oceanic crustal signatures in both the trace elements and halogens indicates that subduction and dehydration of altered oceanic crust may exert control on the cycling of volatile elements to the deep mantle.