Air pollution creates high Fe solubility in pyrogenic aerosols, raising the flux of biologically essential Fe to the oceans.

This work reports on the current status of the global modeling of iron (Fe) deposition fluxes and atmospheric concentrations and the analyses of the differences between models, as well as between models and observations. A total of four global 3-D chemistry transport (CTMs) and general circulation (GCMs) models participated in this intercomparison, in the framework of the United Nations Joint Group of Experts on the Scientific Aspects of Marine Environmental Protection (GESAMP) Working Group 38, The Atmospheric Input of Chemicals to the Ocean. The global total Fe (TFe) emission strength in the models is equal to ∼ 72 Tg Fe yr⁻¹ (38–134 Tg Fe yr⁻¹) from mineral dust sources and around 2.1 Tg Fe yr⁻¹ (1.8–2.7 Tg Fe yr⁻¹) from combustion processes (the sum of anthropogenic combustion/biomass burning and wildfires). The mean global labile Fe (LFe) source strength in the models, considering both the primary emissions and the atmospheric processing, is calculated to be 0.7 (±0.3) Tg Fe yr⁻¹, accounting for both mineral dust and combustion aerosols. The mean global deposition fluxes into the global ocean are estimated to be in the range of 10–30 and 0.2–0.4 Tg Fe yr⁻¹ for TFe and LFe, respectively, which roughly corresponds to a respective 15 and 0.3 Tg Fe yr⁻¹ for the multi-model ensemble model mean. The model intercomparison analysis indicates that the representation of the atmospheric Fe cycle varies among models, in terms of both the magnitude of natural and combustion Fe emissions as well as the complexity of atmospheric processing parameterizations of Fe-containing aerosols. The model comparison with aerosol Fe observations over oceanic regions indicates that most models overestimate surface level TFe mass concentrations near dust source regions and tend to underestimate the low concentrations observed in remote ocean regions. All models are able to simulate the tendency of higher Fe concentrations near and downwind from the dust source regions, with the mean normalized bias for the Northern Hemisphere ( ∼ 14), larger than that of the Southern Hemisphere ( ∼ 2.4) for the ensemble model mean. This model intercomparison and model–observation comparison study reveals two critical issues in LFe simulations that require further exploration: (1) the Fe-containing aerosol size distribution and (2) the relative contribution of dust and combustion sources of Fe to labile Fe in atmospheric aerosols over the remote oceanic regions.

Changing atmospheric acidity alters the delivery of nutrients to the ocean and affects marine productivity and ecology.

Large ash plumes emitted by the 2019–2020 Australian wildfires were associated with a widespread phytoplankton bloom in the iron‐limited Pacific sector of the Southern Ocean. In this study, we used satellite observations and aerosol reanalysis products to study the regional phytoplankton community response to wildfire emissions. The bloom was stimulated by pyrogenic iron fertilization and coincided with elevated cellular pigment concentrations, increased photochemical efficiency, and apparent community structural shifts. Physiological anomalies were consistent with previously observed phytoplankton responses to iron stress relief and persisted for up to 9 months. Supported by a regional iron budget, we conclude that the bloom was sustained by iron recycling and episodic inputs of pyrogenic and dust‐borne mineral iron. The continuous regeneration of iron was likely facilitated by the bloom's large size, mitigating edge dilution effects, as well as enhanced bioavailability of pyrogenic and mineral iron due to atmospheric and chemical processing during long‐range transport.