Long-term monitoring of cloud water chemistry at Whiteface Mountain: the emergence of a new chemical regime

• Published in: Atmospheric chemistry and physics Vol. 23; no. 2; pp. 1619 - 1639
• Main Authors: Lawrence, Christopher E, Casson, Paul, Brandt, Richard, Schwab, James J, Dukett, James E, Snyder, Phil, Yerger, Elizabeth, Kelting, Daniel, VandenBoer, Trevor C, Lance, Sara
• Format: Journal Article
• Language: English
• Published: Katlenburg-Lindau Copernicus GmbH 27.01.2023; Copernicus Publications
• Subjects: Acid deposition; Acidity; Aerosols; Air quality; Aluminum; Ammonium; Ammonium compounds; Analytical chemistry; Anions; Atmospheric chemistry; Atmospheric sciences; Automation; Calcium; Carbon; Cations; Chemistry; Cloud droplet concentration; Cloud droplets; Cloud water; Clouds; Data analysis; Droplets; Ecosystems; Emissions; Environmental impact; Laboratories; Magnesium; Monitoring; Mountains; Nitrates; Nitrogen; Observatories; Organic acids; Organic carbon; Organic compounds; pH effects; Pollutant deposition; Rain; Rain water; Rain-water (Water-supply); Reactive nitrogen species; Sulfates; Sulfur; Sulfur dioxide; Sulfur dioxide emissions; Sulfuric acid; Sulphur; Sulphur dioxide; Sulphuric acid; Total organic carbon; Trends; Vapor phases; Water chemistry; Water monitoring; Water quality; Watershed management; New York; Whiteface Mountain; Adirondack Mountains; United States > US
• DOI: 10.5194/acp-23-1619-2023
• ISSN: 1680-7324; 1680-7316

Atmospheric aqueous chemistry can have profound effects on our environment. The importance of chemistry within the atmospheric aqueous phase started gaining widespread attention in the 1970s as there was growing concern over the negative impacts on ecosystem health from acid deposition. Research at mountaintop observatories including Whiteface Mountain (WFM) showed that gas phase sulfur dioxide emissions react in cloud droplets to form sulfuric acid, which also impacted air quality by increasing aerosol mass loadings. The current study updates the long-term trends in cloud water composition at WFM for the period 1994–2021, with special consideration given to samples that have traditionally been excluded from analysis due to inorganic charge imbalance. We emphasize three major findings: (1) a growing abundance of total organic carbon (TOC), with annual median concentrations more than doubling since measurements began in 2009, (2) a growing imbalance between the measured inorganic cations and anions, consistent with independent rain water observations, implying that a substantial fraction of anions are no longer being measured with the historical suite of measurements, and (3) a growing number of samples exhibiting greater ammonium concentrations than sulfate plus nitrate concentrations, which now routinely describes over one-third of samples. Organic acids are identified as the most likely candidates for the missing anions, since the measured inorganic ion imbalance correlates strongly with measured TOC concentrations. An “inferred cloud droplet pH” is introduced to estimate the pH of the vast majority of cloud droplets as they reside in the atmosphere using a simple method to account for the expected mixing state of calcium and magnesium containing particles. While the inferred cloud droplet pH closely matches the measured bulk cloud water pH during the early years of the cloud water monitoring program, a growing discrepancy is found over the latter half of the record. We interpret these observations as indicating a growing fraction of cloud droplet acidity that is no longer accounted for by the measured sulfate, nitrate and ammonium concentrations. Altogether, these observations indicate that the chemical system at WFM has shifted away from a system dominated by sulfate to a system controlled by base cations, reactive nitrogen species and organic compounds. Further research is required to understand the effects on air quality, climate and ecosystem health.