Abstract

ABSTRACT Aerosols create large uncertainty in the planetary energy balance due to both direct and indirect radiative forcing. Understanding aerosol seasonal patterns is essential for accurate climate change prediction, but mountain regions are often difficult for climate models to resolve. Therefore, long-term observations collected at high elevations are particularly useful. In-situ surface aerosol optical measurements were analyzed for the years 2011–2016 at a mountain site located in western Colorado and tied to potential sources based on relationships among the aerosol properties. The peak values for the scattering and absorption coefficients were observed during the summer, suggesting greater aerosol loading (likely due to wildfires), whereas the lowest values were observed during the winter, indicating cleaner conditions (due to less influence from the boundary layer). The scattering Angstrom exponent, a property that provides information about size distributions, revealed the predominance of coarse-mode particles during the spring, which is consistent with the presence of dust. The aerosols observed during the summer, however, were mostly composed of fine-mode particles. This increase in the fine fraction points to combustion, likely wildfires during the dry season (Hallar, 2015), as a source, which is further supported by the absorption Angstrom exponent dropping to its lowest value (close to 1) during the summer after exhibiting a slightly higher value (~1.3) during the spring. Schmeisser et al. (2017) suggests that, for in-situ aerosol, absorption Angstrom exponents larger than 1.5 may be indicative of dust if they are associated with low (< 1.3) scattering Angstrom exponents. The increase in combustion aerosols during the summer accompanied by high values for the single scattering albedo suggests that these aerosols underwent processing in the atmosphere before reaching Storm Peak Laboratory. These results are important for improving visibility and predicting future aerosol concentrations in the western U.S.

Highlights

  • Atmospheric aerosols change rapidly over short time intervals, making future concentrations difficult to predict (Laj et al, 2009)

  • The absorption data follows a similar pattern to the scattering data, with the highest monthly values found during the summer season and lowest values during the winter months

  • A strong wildfire signal was observed in the summer at Storm Peak Laboratory (SPL), yet these events were not associated with a significant decrease in single-scattering albedo (SSA)

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Summary

Introduction

Atmospheric aerosols change rapidly over short time intervals, making future concentrations difficult to predict (Laj et al, 2009). Aerosols absorb and scatter radiation and have a direct effect on the planetary energy balance. These effects can be quantified by calculating direct radiative forcing from measured aerosol optical properties. The current estimate from the Intergovernmental Panel on Climate Change of direct aerosol radiative forcing is –0.35 ± 0.5 W m–2 (Stocker et al, 2013). The large uncertainty associated with this value is a consequence of rapidly changing aerosol distributions with respect to time and location (Stocker et al, 2013), model uncertainties (Reddington et al, 2017), and varied aerosol composition (Jacobson, 2001)

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