A perspective on iron (Fe) in the atmosphere: air quality, climate, and the ocean.

As scientists engage in research motivated by climate change and the impacts of pollution on air, water, and human health, we increasingly recognize the need for the scientific community to improve communication and knowledge exchange across disciplines to address pressing and outstanding research questions holistically. Our professional paths have crossed because our research activities focus on the chemical reactivity of Fe-containing minerals in air and water, and at the air-sea interface. (Photo)chemical reactions driven by Fe can take place at the surface of the particles/droplets or within the condensed phase. The extent and rates of these reactions are influenced by water content and biogeochemical activity ubiquitous in these systems. One of these reactions is the production of reactive oxygen species (ROS) that cause damage to respiratory organs. Another is that the reactivity of Fe and organics in aerosol particles alter surficial physicochemical properties that impact aerosol-radiation and aerosol-cloud interactions. Also, upon deposition, aerosol particles influence ocean biogeochemical processes because micronutrients such as Fe or toxic elements such as copper become bioavailable. We provide a perspective on these topics and future research directions on the reactivity of Fe in atmospheric aerosol systems, from sources to short- and long-term impacts at the sinks with emphasis on needs to enhance the predictive power of atmospheric and ocean models.

Improving Estimates of PM2.5 Concentration and Chemical Composition by Application of High Spectral Resolution Lidar (HSRL) and Creating Aerosol Types from Chemistry (CATCH) Algorithm.

Improved characterization of ambient PM2.5 mass concentration and chemical speciation is a topic of interest in air quality and climate sciences. Over the past decades, considerable efforts have been made to improve ground-level PM2.5 using remotely sensed data. Here we present two new approaches for estimating atmospheric PM2.5 and chemical composition based on the High Spectral Resolution Lidar (HSRL)-retrieved aerosol extinction values and types and Creating Aerosol Types from Chemistry (CATCH)-derived aerosol chemical composition. The first methodology (CMAQ-HSRL-CH) improves EPA's Community Multiscale Air Quality (CMAQ) predictions by applying variable scaling factors derived using remotely-sensed information about aerosol vertical distribution and types and the CATCH algorithm. The second methodology (HSRL-CH) does not require regional model runs and can provide atmospheric PM2.5 mass concentration and chemical speciation using only the remotely sensed data and the CATCH algorithm. The resulting PM2.5 concentrations and chemical speciation derived for NASA DISCOVER-AQ (Deriving Information on Surface Conditions from COlumn and VERtically Resolved Observations Relevant to Air Quality) Baltimore-Washington, D.C. Corridor (BWC) Campaign (2011) are compared to surface measurements from EPA's Air Quality Systems (AQS) network. The analysis shows that the CMAQ-HSRL-CH method leads to considerable improvement of CMAQ's predicted PM2.5 concentrations (R2 value increased from 0.37 to 0.63, the root mean square error (RMSE) was reduced from 11.9 to 7.2 µg m-3, and the normalized mean bias (NMB) was lowered from -46.0 to 4.6%). The HSRL-CH method showed statistics (R2=0.75, RMSE=8.6 µgm-3, and NMB=24.0%), which were better than the CMAQ prediction of PM2.5 alone and analogous to CMAQ-HSRL-CH. In addition to mass concentration, HSRL-CH can also provide aerosol chemical composition without specific model simulations. We expect that the HSRL-CH method will be able to make reliable estimates of PM2.5 concentration and chemical composition where HSRL data are available.

Surface ocean microbiota determine cloud precursors.

One pathway by which the oceans influence climate is via the emission of sea spray that may subsequently influence cloud properties. Sea spray emissions are known to be dependent on atmospheric and oceanic physicochemical parameters, but the potential role of ocean biology on sea spray fluxes remains poorly characterized. Here we show a consistent significant relationship between seawater nanophytoplankton cell abundances and sea-spray derived Cloud Condensation Nuclei (CCN) number fluxes, generated using water from three different oceanic regions. This sensitivity of CCN number fluxes to ocean biology is currently unaccounted for in climate models yet our measurements indicate that it influences fluxes by more than one order of magnitude over the range of phytoplankton investigated.

Observations of new particle formation, modal growth rates, and direct emissions of sub-10 nm particles in an urban environment.

Ultrafine particles with diameters less than 100 nm suspended in the air are a topic of interest in air quality and climate sciences. Sub-10 nm particles are of additional interest due to their health effects and contribution to particle growth processes. Ambient measurements were carried out at North Carolina State University in Raleigh, NC between April to June 2019 and November 2019 to May 2020 to investigate the temporal variability of size distribution and number concentration of ultrafine particles. A mobile lab was deployed between March and May 2020 to characterize the spatial distribution of sub-10 nm particle number concentration. New particle formation and growth events were observed regularly. Also observed were direct emissions of sub-10 nm particles. Analysis against meteorological variables, gas-phase species, and particle concentrations show that the sub-10nm particles dominated number concentration during periods of low planetary boundary layer height, low solar radiation, and northeast winds. The spatial patterns observed during mobile deployments suggest that multiple temporally stable and spatially confined point sources of sub-10 nm particles are present within the city. These sources likely include the campus utility plants and the Raleigh-Durham International Airport. Additionally, the timing of data collection allowed for investigation of variations in the urban aerosol number size distribution due to reduced economic activity during the COVID-19 pandemic.

Spatial and temporal variations of PM2.5 mass closure and inorganic PM2.5 in the Southeastern U.S.

Fine particulate matter (i.e., PM2.5) has gained extensive attention owing to its adverse effects. The impacts of PM2.5 may vary in time and space due to the spatiotemporal variations of PM2.5 number size distribution and chemical compositions. This research analyzed the latest PM2.5 chemical compositions measurements with an aim to better understand the dynamic changes of PM2.5 in response to emission reductions due to the new regulations. The particulate measurements from the Southeastern Aerosol Research and Characterization (SEARCH) network between 2001 and 2016 were analyzed for the spatiotemporal variations of PM2.5 and inorganic PM2.5 (iPM2.5 = SO42- + NH4+ + NO3-) chemical compositions in the Southeastern United States (U.S.). It was discovered that PM2.5 and iPM2.5 mass concentrations exhibited significant downward trends in 2001-2016. Both PM2.5 and iPM2.5 mass concentrations were higher at urban and inland sites than rural/suburban and coastal sites. The higher iPM2.5 concentrations at agricultural sites were attributed to the influences of ammonia (NH3) emissions from animal feeding operations (AFOs). The iPM2.5 was the dominant contributor to PM2.5 in 2001-2016 at the coastal sites, whereas organic carbon matter (OCM) was the major contributor to PM2.5 after 2011 at the inland sites. Our data analysis suggests that significant decrease of PM2.5 concentrations is attributed to the reductions in nitrogen oxides (NOx) and sulfur dioxide (SO2) emissions in 2001-2016. Findings from this research provide insights into the development of effective PM2.5 control strategies and assessment of air pollutants exposure.

Pyrogenic iron: The missing link to high iron solubility in aerosols.

Atmospheric deposition is a source of potentially bioavailable iron (Fe) and thus can partially control biological productivity in large parts of the ocean. However, the explanation of observed high aerosol Fe solubility compared to that in soil particles is still controversial, as several hypotheses have been proposed to explain this observation. Here, a statistical analysis of aerosol Fe solubility estimated from four models and observations compiled from multiple field campaigns suggests that pyrogenic aerosols are the main sources of aerosols with high Fe solubility at low concentration. Additionally, we find that field data over the Southern Ocean display a much wider range in aerosol Fe solubility compared to the models, which indicate an underestimation of labile Fe concentrations by a factor of 15. These findings suggest that pyrogenic Fe-containing aerosols are important sources of atmospheric bioavailable Fe to the open ocean and crucial for predicting anthropogenic perturbations to marine productivity.

Phytoplankton and cloudiness in the Southern Ocean.

The effect of ocean biological productivity on marine clouds is explored over a large phytoplankton bloom in the Southern Ocean with the use of remotely sensed data. Cloud droplet number concentration over the bloom was twice what it was away from the bloom, and cloud effective radius was reduced by 30%. The resulting change in the short-wave radiative flux at the top of the atmosphere was -15 watts per square meter, comparable to the aerosol indirect effect over highly polluted regions. This observed impact of phytoplankton on clouds is attributed to changes in the size distribution and chemical composition of cloud condensation nuclei. We propose that secondary organic aerosol, formed from the oxidation of phytoplankton-produced isoprene, can affect chemical composition of marine cloud condensation nuclei and influence cloud droplet number. Model simulations support this hypothesis, indicating that 100% of the observed changes in cloud properties can be attributed to the isoprene secondary organic aerosol.