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An extended‐range Single Particle Soot Photometer (SP2) coupled to a Marin‐5 nebulizer was used to measure the refractory black carbon (rBC) mass and number size distributions in 1,004 samples from a West Antarctica snow/firn core. The SP2 was calibrated using Aquadag and a Centrifugal Particle Mass Analyzer for BC particles ranging from 0.5 to 800 fg. Our results indicate a significant contribution of rare, large particles of mass‐equivalent diameter (DBC) > 500 nm to the total rBC mass (36%), while small particles (DBC 1,810 nm (uncontained mode). We compared two sets of samples from different seasons (wet vs. dry) and observed that dry season concentrations are 3.4 and 2 times that of the wet season in the ranges of 80 nm

Remote sensing of light-absorbing particles (LAPs), or dark colored impurities, such as black carbon (BC) and dust on snow, is a key remaining challenge in cryospheric surface characterization and application to snow, ice, and climate models. We present a quantitative data set of in situ snow reflectance, measured and modeled albedo, and BC and trace element concentrations from clean to heavily fossil fuel emission contaminated snow near South Pole, Antarctica. Over 380 snow reflectance spectra (350-2500 nm) and 28 surface snow samples were collected at seven distinct sites in the austral summer season of 2014-2015. Snow samples were analyzed for BC concentration via a single particle soot photometer and for trace element concentration via an inductively coupled plasma mass spectrometer. Snow impurity concentrations ranged from 0.14 to 7000 part per billion (ppb) BC, 9.5 to 1200 ppb sulfur, 0.19 to 660 ppb iron, 0.013 to 1.9 ppb chromium, 0.13 to 120 ppb copper, 0.63 to 6.3 ppb zinc, 0.45 to 82 parts per trillion (ppt) arsenic, 0.0028 to 6.1 ppb cadmium, 0.062 to 22 ppb barium, and 0.0044 to 6.2 ppb lead. Broadband visible to shortwave infrared albedo ranged from 0.85 in pristine snow to 0.62 in contaminated snow. LAP radiative forcing, the enhanced surface absorption due to BC and trace elements, spanned from less than 1 W m(exp. -2) for clean snow to approximately 70 W m(exp. -2) for snow with high BC and trace element content. Measured snow reflectance differed from modeled snow albedo due to specific impurity-dependent absorption features, which we recommend be further studied and improved in snow albedo models.

A multiple linear regression (MLR) chemical mass balance model was applied to data collected during an air quality field experiment in Yakima, WA during January, 2013to determine the relative contribution of residential wood combustion (RWC) and vehicle emissions to ambient pollutant levels. Acetonitrile was used as a chemical tracer for wood burning and nitrogen oxides (NOx) as a chemical tracer for mobile sources. RWC was found to be a substantial source of gas phase air toxics in winter time. The MLR model found RWC primarily responsible for emissions of formaldehyde (73%), acetaldehyde (69%), and black carbon (55%) and mobile sources primarily responsible for emissions of carbon monoxide (CO) (83%), toluene (81%), C2 – alkylbenzenes (81%), and benzene (64%). When compared with the EPA's 2011 winter emissions inventory, the MLR results suggest that the contribution of RWC to CO emissions was underestimated in the inventory by a factor of 2. Emission ratios to NOx from the MLR model agreed to within 25% with wintertime emission ratios predicted from the Motor Vehicle Emissions Simulator (MOVES) 2010b emission model for Yakima County for all pollutants modeled except for CO, C2 – alkylbenzenes, and black carbon. The MLR model results suggest that MOVES was over predicting mobile source emissions of CO relative to NOx by a factor of 1.33 and black carbon relative to NOx by about a factor of 3.

Characterizing black carbon (BC) concentrations in the seasonal snowpack is of interest because BC deposition on snow can reduce albedo and accelerate melt. In Washington State, USA snowmelt from the seasonal snowpack provides an important source of water resources, but minimal work has been done characterizing BC concentrations in snow in this region. BC concentrations in snow were monitored over two winters (2012 and 2013) at Tronsen Meadow, located near Blewett Pass in the eastern Cascade Mountains in Central Washington, to characterize spatial and temporal variations in BC concentrations, and the processes affecting BC concentrations in the snowpack. BC concentrations were measured using a Single Particle Soot Photometer. Snowpit BC concentrations at spatial scales ranging from centimeter to 100 m scales were fairly homogenous during the accumulation season, with greater spatial variability during the melt season due to variable melt patterns. BC concentrations in snow increased in late winter-spring due to an increase in atmospheric BC concentrations and trapping of BC on the snow surface during melt. However, during a period of intense melt in 2013 BC concentrations decreased, likely caused by meltwater scavenging. In summer 2012 the Table Mountain forest fire burned adjacent to the study site, and BC concentrations in the snowpack in 2013 were far higher than in previous years, with charred trees postfire the likely source of the elevated BC.

Understanding past atmospheric dust variability is necessary to put modern atmospheric dust into historical context and assess the impacts of dust on the climate. In Asia, meteorological data of atmospheric dust is temporally limited, beginning only in the 1950s. High-resolution ice cores provide the ideal archive for reconstructing preinstrumental atmospheric dust concentrations. Using a ~500 year (1477–1982 A.D.) annually resolved calcium (Ca) dust proxy from a Tibetan Plateau (TP) ice core, we demonstrate the lowest atmospheric dust concentrations in the past ~500 years during the latter twentieth century. Declines in late nineteenth to twentieth century Ca concentrations significantly correspond with regional zonal wind trends from two reanalysis models, suggesting that the Ca record provides a proxy for the westerlies. Twentieth century warming and attendant atmospheric pressure reductions over northern Asia have potentially reduced temperature/pressure gradients resulting in lower zonal wind velocities and associated dust entrainment/transport in the past ~500 years over the TP.

Assessing the potential for black carbon (BC) and dust deposition to reduce albedo and accelerate glacier melt is of interest in Washington because snow and glacier melt are an important source of water resources, and glaciers are retreating. In August 2012 on Snow Dome, Mount Olympus, Washington, we measured snow surface spectral albedo and collected surface snow samples and a 7 m ice core. The snow and ice samples were analyzed for iron (Fe, used as a dust proxy) via inductively coupled plasma sector field mass spectrometry, total impurity content gravimetrically, BC using a single-particle soot photometer (SP2), and charcoal through microscopy. In the 2012 summer surface snow, BC (54 ± 50 µg/L), Fe (367±236 µg/L) and gravimetric impurity (35 ± 18 mg/L) concentrations were spatially variable, and measured broadband albedo varied between 0.67–0.74. BC and dust concentrations in the ice core 2011 summer horizon were a magnitude higher (BC = 3120 µg/L, Fe = 22000 µg/L, and gravimetric impurity = 1870 mg/L), corresponding to a modeled broadband albedo of 0.45 based on the measured BC and gravimetric impurity concentrations. The Big Hump forest fire is the likely source for the higher concentrations. Modeling constrained by measurements indicates that the all-sky 12 h daily mean radiative forcings in summer 2012 and 2011 range between 37–53 W m−2 and 112–149 W m−2, respectively, with the greater forcings in 2011 corresponding to a 29–38 mm/d enhancement in snowmelt. The timing of the forest fire impurity deposition is coincident with an increase in observed discharge in the Hoh River, highlighting the potential for BC and dust deposition on glaciers from forest fires to accelerate melt.

A Mt. Everest ice core spanning 1860–2000 AD and analyzed at high resolution for black carbon (BC) using a Single Particle Soot Photometer (SP2) demonstrates strong seasonality, with peak concentrations during the winter-spring, and low concentrations during the summer monsoon season. BC concentrations from 1975–2000 relative to 1860–1975 have increased approximately threefold, indicating that BC from anthropogenic sources is being transported to high elevation regions of the Himalaya. The timing of the increase in BC is consistent with BC emission inventory data from South Asia and the Middle East, however since 1990 the ice core BC record does not indicate continually increasing BC concentrations. The Everest BC and dust records provide information about absorbing impurities that can contribute to glacier melt by reducing the albedo of snow and ice. There is no increasing trend in dust concentrations since 1860, and estimated surface radiative forcing due to BC in snow exceeds that of dust in snow. This suggests that a reduction in BC emissions may be an effective means to reduce the effect of absorbing impurities on snow albedo and melt, which affects Himalayan glaciers and the availability of water resources in major Asian rivers.

record (1935–2005). Statistical analysis of major ion time series suggests that atmospheric soluble dust species dominate the chemical signature and that background dust levels conceal marine ion species deposition. The soluble dust time series have interspecies relations and common structure (empirical orthogonal function (EOF) 1), suggesting a similar soluble dust source or transport route. Annual and seasonal correlations between the EOF 1 time series and National Centers for Environmental Prediction/National Center for Atmospheric Research reanalysis climate variables (1948–2004) suggest that the Mt. Geladaindong ice core record provides a proxy for local and regional surface pressure. An approximately threefold decrease of soluble dust concentrations in the middle to late 1970s, accompanied by regional increases in pressure and temperature and decreases in wind velocity, coincides with the major 1976–1977 shift of the Pacific Decadal Oscillation (PDO) from a negative to a positive state. This is the first ice core evidence of a potential teleconnection between central Asian atmospheric soluble dust loading and the PDO. Analysis of temporally longer ice cores from Mt. Geladaindong may enhance understanding of the relationship between the PDO and central Asian atmospheric circulation and subsequent atmospheric soluble dust loading.

[1] High-resolution major and trace elements (Sr, Cs, Ba, La, Ce, Pr, Nd, Sm, Eu, Tb, Dy, Ho, Er, Tm, Yb, Lu, Bi, U, Tl, Al, S, Ca, Ti, V, Cr, Mn, Fe, and Co) quantified in a Mount Everest ice core (6518 m above sea level) spanning the period 1650–2002 AD provides the first Asian record of trace element concentrations from the pre-industrial era, and the first continuous high-resolution Asian record from which natural baseline concentrations and subsequent changes due to anthropogenic activities can be examined. Modern concentrations of most elements remain within the pre-industrial range; however, Bi, U, and Cs concentrations and their enrichment factors (EF) have increased since the ∼1950s, and S and Ca concentrations and their EFs have increased since the late 1980s. A comparison of the Bi, U, Cs, S, and Ca data with other ice core records and production data indicates that the increase in atmospheric concentrations of trace elements is widespread, but that enrichment varies regionally. Likely sources for the recent enrichment of these elements include mining, metal smelting, oil and coal combustion, and end uses for Bi, and mining and refinement for U and Cs. The source of the synchronous enrichment of Ca and S is less certain, but may be related to land use and environmental change.

[1] A highly resolved Mt. Everest ice core reveals a decrease in marine and increase in continental air masses related to relatively high summer surface pressure over Mongolia, and reduction in northward incursions of the summer South Asian monsoon since ∼1400 AD. Previously published proxy records from lower sites south of the Himalayas indicate strengthening of the monsoon since this time. These regional differences are consistent with a south–north seesaw in convective activity in the Asian monsoon region, and reflect a southward shift in the mean summer position of the monsoon trough since ∼1400 AD. The change in monsoonal circulation at 1400 AD is synchronous with a reduction in solar irradiance and the onset of the LIA. This demonstrates a hemispheric scale circulation reorganization at this time, and the potential for future large shifts in monsoonal circulation.