Abstract
Elevated water vapor (H(2)O(v)) mole fractions were occassionally observed downwind of Indianapolis, IN, and the Washington, D.C.-Baltimore, MD, area during airborne mass balance experiments conducted during winter months between 2012 and 2015. On days when an urban H(2)O(v) excess signal was observed, H(2)O(v) emissions estimates range between 1.6 × 10(4) and 1.7 × 10(5) kg s(-1), and account for up to 8.4% of the total (background + urban excess) advected flow of atmospheric boundary layer H(2)O(v) from the urban study sites. Estimates of H(2)O(v) emissions from combustion sources and electricity generation facility cooling towers are 1-2 orders of magnitude smaller than the urban H(2)O(v) emission rates estimated from observations. Instances of urban H(2)O(v) enhancement could be a result of differences in snowmelt and evaporation rates within the urban area, due in part to larger wintertime anthropogenic heat flux and land cover differences, relative to surrounding rural areas. More study is needed to understand why the urban H(2)O(v) excess signal is observed on some days, and not others. Radiative transfer modeling indicates that the observed urban enhancements in H(2)O(v) and other greenhouse gas mole fractions contribute only 0.1°C day(-1) to the urban heat island at the surface. This integrated warming through the boundary layer is offset by longwave cooling by H(2)O(v) at the top of the boundary layer. While the radiative impacts of urban H(2)O(v) emissions do not meaningfully influence urban heat island intensity, urban H(2)O(v) emissions may have the potential to alter downwind aerosol and cloud properties.