Surface melt in the ablation zone is dominated by atmospheric temperature and surface albedo. We developed a surface mass-balance model with a dynamic component of glacier ice albedo which includes surface properties, clouds and the angle of the sun. The ice albedo reduction is mainly caused by impurity accumulation of non-biological origin such as dust and black carbon ( BC), which is currently not included in other surface mass-balance models. Simulations show that dust from meltout is the main source of impurity mass at the melting glacier ice surface, and current rates of atmospheric deposition of dust play only a minor role. However, for BC the atmospheric deposition is the main source where ice melt rates are below 1 m, and atmospheric deposition is most likely from intercontinental transport due to the scarce population and lack of forests in Greenland.

Light absorbing impurities (LAI) initiate powerful snow albedo feedbacks, yet due to a scarcity of observations and measurements, LAI radiative forcing is often neglected or poorly constrained in climate and hydrological models. To support physically-based modeling of LAI processes, daily measurements of dust and black carbon (BC) stratigraphy, optical grain size, snow density and spectral albedo were collected over the 2013 ablation season in the Rocky Mountains, CO. Surface impurity concentrations exhibited a wide range of values (0.02- 6.0 mg g(-1) pptw) with 98% of mass being deposited by three episodic dust events in April. Even minor dust loading initiated albedo decline, and the negative relationship between dust concentrations and albedo was log-linear. As melt progressed, individual dust layers coalesced and emerged at the snow surface, with minimal mass loss to meltwater scavenging. The observations show that the convergence of dust layers at the surface reduced albedo to 0.3 and snow depth declined similar to 50% faster than other years with similar depth but less dust. The rapid melt led to an unexpected reduction in both grain size and density in uppermost surface layers. BC concentrations covaried with dust concentrations but were several orders of magnitude lower (< 1- 20 ppb).