The delivery of low-abundance, bioactive trace elements to the surface ocean by aerosol mineral dust is a major planetary control over marine primary production and hence the global carbon cycle. Variations in atmospheric dust have established links to global climate over geologic timescales and to regional biogeographic shifts over seasonal timescales. Constraining atmospheric dust variability is thus of high value to understanding oceanographic systems, especially vast, constitutively low-nutrient subtropical gyre ecosystems and high-nutrient/low-chlorophyll ecosystems where availability of the trace element iron is a dominant ecological control. Here we leverage the MERRA-2 reanalysis product to examine over four decades of surface-level atmospheric mineral dust variability in a domain of the subtropical North Pacific centered at ocean Station ALOHA. This study region has been sampled regularly since the mid-1980s and was the site of the Hawaii Aerosol Time-Series (HATS) project in 2022-2023. Two nearly semi-annual dust pulses evident in the long-term data are described and constrained. We look for evidence of shifts in total and seasonal atmospheric dust abundances and in the onset timing of the dominant spring/summer pulse, finding year-to-year variations but little evidence for long-term trends. We observe significant and complex monthly relationships between the Pacific Decadal Oscillation (PDO) index and both dust and precipitation, offering new insights into the role of timing for increased or diminished dust delivery. We observe that 2022 was among the dustiest years for the study domain in the preceding two decades and, by contrast, that 2023 exhibited a significant early-spring lull in dust.

Chromium (Cr) has shown promise as a paleoceanographic proxy due to the redox-driven control of dissolved Cr concentrations ([Cr]) and stable isotope composition (δ53Cr). However, substantial uncertainties in the biogeochemical Cr cycle have limited its paleoproxy application to date. To improve the mechanistic understanding of Cr cycling in the modern ocean and strengthen its potential proxy applications, we present new data from regeneration incubations, bottom and sediment pore waters, and a compilation of intermediate and deep water data. While Cr removal and biological export from the surface ocean is associated with organic carbon export, the deep water release of dissolved Cr from sinking particles is not directly dependent on organic carbon respiration, as indicated by differing trends between Cr, oxygen utilization and the regeneration of organic-associated macronutrients (e.g. N, P). Pore water and bottom water data demonstrate that benthic Cr fluxes are locally important and may be significant globally. The pore water dissolved Cr flux at our CaCO3-rich site is likely driven by the re-release of Cr scavenged from the water column by sinking particles, with minor contributions from lithogenic phases. We argue this is consistent with the highest open ocean [Cr] to date being found in the water column below oxygen minimum zones, likely reflecting the release of scavenged Cr in deep waters or surface sediments. Chromium released from suspended particles and surface sediments follows the global δ53Cr–[Cr] array, supporting the proposed role of biological export and regeneration in shaping global Cr and δ53Cr distributions. Global intermediate and deep water [Cr], δ53Cr and Cr:macronutrient relationships are thus shaped by a synergy of circulation patterns, water mass mixing, a deep Cr regeneration cycle, and benthic Cr sources. A biogenic control on global Cr distributions indicates that sedimentary Cr records may reflect biogenic as well as O2-dependent processes, while more research is needed to assess sediment Cr record fidelity based on an active diagenetic cycle.