Black Carbon Concentrations in Snow at Tronsen Meadow in Central Washington from 2012 to 2013: Temporal and Spatial Variations and the Role of Local Forest Fire Activity

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 100m 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

Mass and Number Size Distributions of rBC in Snow and Firn Samples From Pine Island Glacier, West Antarctica

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) \u3e 500 nm to the total rBC mass (36%), while small particles (DBC \u3c 100 nm) are abundant but contribute \u3c8% to total rBC mass. We observed a primary mass median diameter of 162 ± 40 nm, smaller than reported for snow in other regions of the globe but similar to East Antarctica rBC size distributions. In addition, we observed other modes at 673, 1,040, and \u3e1,810 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 \u3c DBC \u3c 500 nm (small particles) and 500 nm \u3c DBC \u3c 2,000 nm (large particles), respectively, while number of particles in the dry season is 3.5 and 2 times that of the wet season for the same size ranges. Millimeter thick melt layers have been observed in some samples, although they did not change the observed median diameter. This study provides the first detailed rBC mass and number size distribution from West Antarctica

Refractory black carbon (rBC) variability in a 47-year West Antarctic snow and firn core

Black carbon (BC) is an important climate-forcing agent that affects snow albedo. In this work, we present a record of refractory black carbon (rBC) variability, measured from a 20m deep snow and firn core drilled in West Antarctica (79°55’34.600” S, 94°21’13.3”W, 2122m above sea level) during the 2014–2015 austral summer. This is the highest elevation rBC record from West Antarctica. The core was analyzed using the Single Particle Soot Photometer (SP2) coupled to a CETAC Marin-5 nebulizer. Results show a well-defined seasonality with geometric mean concentrations of 0.015 μg L-1 for the wet season (austral summer–fall) and 0.057 μg L-1 for the dry season (austral winter–spring). The core was dated to 47 years (1968–2015) using rBC seasonality as the main parameter, along with sodium (Na), sulfur (S) and strontium (Sr) variations. The annual rBC concentration geometric mean was 0.03 μg L-1, the lowest of all rBC cores in Antarctica referenced in this work, while the annual rBC flux was 6.25 μgm-2 a-1, the lowest flux in West Antarctica rBC records. No long-term trend was observed. Snow albedo reductions at the site due to BC were simulated using SNICAR online and found to be insignificant (-0.48 %) compared to clean snow. Fire spot inventory and BC emission estimates from the Southern Hemisphere suggest Australia and Southern Hemisphere South America as the most probable emission sources of BC to the drilling site, whereas HYSPLIT model particle transport simulations from 1968 to 2015 support Australia and New Zealand as rBC sources, with limited contributions from South America. Spectral analysis (REDFIT method) of the BC record showed cycles related to the Antarctic Oscillation (AAO) and to El Niño–Southern Oscillation (ENSO), but cycles in common with the Amundsen Sea Low (ASL) were not detected. Correlation of rBC records in Antarctica with snow accumulation, elevation and distance to the sea suggests rBC transport to East Antarctica is different from transport to West Antarctica

Black Carbon Concentrations from a Tibetan Plateau Ice Core Spanning 1843–1982: Recent Increases due to Emissions and Glacier Melt

Black carbon (BC) deposited on snow and glacier surfaces can reduce albedo and lead to accelerated melt. An ice core recovered from Guoqu glacier on Mt. Geladaindong and analyzed using a Single Particle Soot Photometer provides the first long-term 5 (1843–1982) record of BC concentrations from the Central Tibetan Plateau. The highest concentrations are observed from 1975–1982, which corresponds to a 2.0-fold and 2.4-fold increase in average and median values, respectively, relative to 1843–1940. BC concentrations post-1940 are also elevated relative to the earlier portion of the record. Causes for the higher BC concentrations include increased regional BC emissions and subsequent deposition, and melt induced enrichment of BC, with the melt potentially accelerated due to the presence of BC at the glacier surface. A qualitative comparison of the BC and Fe (used as a dust proxy) records suggests that if changes in the concentrations of absorbing impurities at the glacier surface have influenced recent glacial melt, the melt may be due to the presence of BC rather than dust. Guoqu 15 glacier has received no net ice accumulation since the 1980s, and is a potential example of a glacier where an increase in the equilibrium line altitude is exposing buried high impurity layers. That BC concentrations in the uppermost layers of the Geladaindong ice core are not substantially higher relative to deeper in the ice core suggests that some of the BC that must have been deposited on Guoqu glacier via wet or dry 20 deposition between 1983 and 2005 has been removed from the surface of the glacier, potentially via supraglacial or englacial meltwater

Influence of regional precipitation patterns on stable isotopes in ice cores from the central Himalayas

Several ice cores have been recovered from the Dasuopu (DSP) Glacier and the East Rongbuk (ER) Glacier in the central Himalayas since the 1990s. Although the distance between the DSP and the ER ice core drilling sites is only 125 km, the stable isotopic record (18O or D) of the DSP core is interpreted in previous studies as a temperature proxy, while the ER core is interpreted as a precipitation proxy. Thus, the climatological significance of the stable isotopic records of these Himalayan ice cores remains a subject of debate. Based on analysis of regional precipitation patterns over the region, we find that remarkable discrepancy in precipitation seasonality between the two sites may account for their disparate isotopic interpretations. At the ER core site, the Indian summer monsoon (ISM) precipitation is dominating due to topographic blocking of the moisture from westerlies by the high ridges of Mt. Qomolangma (Everest), which results in a negative correlation between the ER 18O or D record and precipitation amount along the southern slope of the central Himalayas in response to the “amount effect”. At the DSP core site, in comparison with the ISM precipitation, the wintertime precipitation associated with the westerlies is likely more important owing to its local favorable topographic conditions for interacting with the western disturbances. Therefore, the DSP stable isotopic record may be primarily controlled by the westerlies. Our results have important implications for interpreting the stable isotopic ice core records recovered from different climatological regimes of the Himalayas

The Post-Wildfire Impact of Burn Severity and Age on Black Carbon Snow Deposition and Implications for Snow Water Resources, Cascade Range, Washington

Wildfires in the snow zone affect ablation by removing forest canopy, which enhances surface solar irradiance, and depositing light absorbing particles [LAPs, such as black carbon (BC)] on the snowpack, reducing snow albedo. How variations in BC deposition affects post-wildfire snowmelt timing is poorly known and highly relevant to water resources. We present a field-based analysis of BC variability across five sites of varying burn age and burn severity in the Cascade Range, Washington State, United States. Single particle soot photometer (SP2) analyses of BC snow concentrations were used to assess the impact of BC on snow albedo, and radiative transfer modeling was used to estimate the radiative effect of BC on snowmelt. Results were compared to Snowpack Telemetry (SNOTEL) data from one site that burned in 2012 and another in a proximal unburned forest. We show that post-wildfire forests provide a significant source of BC to the snowpack, and this effect increases by an order of magnitude in regions of high versus low burn severity, and decreased by two orders of magnitude over a decade. There is a shift in the timing of snowmelt, with snow disappearance occurring on average 19 ± 9 days earlier post-wildfire (2013–19) relative to pre-wildfire (1983–2012). This study improves understanding of the connection between wildfire activity and snowmelt, which is of high relevance as climate change models project further decreases in snowpack and increases in wildfire activity in the Washington Cascades

Seasonal and elevational variations of black carbon and dust in snow and ice in the Solu-Khumbu, Nepal and estimated radiative forcings

Black carbon (BC) and dust deposited on snow and glacier surfaces can reduce the surface albedo, accelerate snow and ice melt, and trigger albedo feedback. Assessing BC and dust concentrations in snow and ice in the Himalaya is of interest because this region borders large BC and dust sources, and seasonal snow and glacier ice in this region are an important source of water resources. Snow and ice samples were collected from crevasse profiles and snow pits at elevations between 5400 and 6400 m a.s.l. from Mera glacier located in the Solu-Khumbu region of Nepal during spring and fall 2009, providing the first observational data of BC concentrations in snow and ice from the southern slope of the Himalaya. The samples were measured for Fe concentrations (used as a dust proxy) via ICP-MS, total impurity content gravimetrically, and BC concentrations using a Single Particle Soot Photometer (SP2). Measured BC concentrations underestimate actual BC concentrations due to changes to the sample during storage and loss of BC particles in the ultrasonic nebulizer; thus, we correct for the underestimated BC mass. BC and Fe concentrations are substantially higher at elevations \u3c 6000 m due to post-depositional processes including melt and sublimation and greater loading in the lower troposphere. Because the largest areal extent of snow and ice resides at elevations \u3c 6000 m, the higher BC and dust concentrations at these elevations can reduce the snow and glacier albedo over large areas, accelerating melt, affecting glacier mass balance and water resources, and contributing to a positive climate forcing. Radiative transfer modeling constrained by measurements at 5400 m at Mera La indicates that BC concentrations in the winter–spring snow/ice horizons are sufficient to reduce albedo by 6–10% relative to clean snow, corresponding to localized instantaneous radiative forcings of 75–120 W m−2. The other bulk impurity concentrations, when treated separately as dust, reduce albedo by 40–42% relative to clean snow and give localized instantaneous radiative forcings of 488 to 525 W m−2. Adding the BC absorption to the other impurities results in additional radiative forcings of 3 W m−2. The BC and Fe concentrations were used to further examine relative absorption of BC and dust. When dust concentrations are high, dust dominates absorption, snow albedo reduction, and radiative forcing, and the impact of BC may be negligible, confirming the radiative transfer modeling. When impurity concentrations are low, the absorption by BC and dust may be comparable; however, due to the low impurity concentrations, albedo reductions are small. While these results suggest that the snow albedo and radiative forcing effect of dust is considerably greater than BC, there are several sources of uncertainty. Further observational studies are needed to address the contribution of BC, dust, and colored organics to albedo reductions and snow and ice melt, and to characterize the time variation of radiative forcing

Snow Accumulation Rate on Qomolangma (Mount Everest), Himalaya: Synchroneity With Sites Across the Tibetan Plateau on 50-100 Year Timescales

Annual-layer thickness data, spanning AD 1534-2001, from an ice core from East Rongbuk Coll on Qomolangma (Mount Everest, Himalaya) yield an age-depth profile that deviates systematically from a constant accumulation-rate analytical model. The profile clearly shows that the mean accumulation rate has changed every 50-100 years. A numerical model was developed to determine the magnitude of these multi-decadal-scale rates. The model was used to obtain a time series of annual accumulation. The mean annual accumulation rate decreased from similar to 0.8 m ice equivalent in the 1500s to similar to 0.3 m in the mid-1800s. From similar to 1880 to similar to 1970 the rate increased. However, it has decreased since similar to 1970. Comparison with six other records from the Himalaya and the Tibetan Plateau shows that the changes in accumulation in East Rongbuk Col are broadly consistent with a regional pattern over much of the Plateau. This suggests that there may be an overarching mechanism controlling precipitation and mass balance over this area. However, a record from Dasuopu, only 125 km northwest of Qomolangma and 700 m higher than East Rongbuk Col, shows a maximum in accumulation during the 1800s, a time during which the East Rongbuk Col and Tibetan Plateau ice-core and tree-ring records show a minimum. This asynchroneity may be due to altitudinal or seasonal differences in monsoon versus westerly moisture sources or complex mountain meteorology

Accelerated Glacier Melt on Snow Dome, Mount Olympus, Washington, USA, due to Deposition of Black Carbon and Mineral Dust from Wildfire

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 ravimetric 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 37–53Wm_2 and 112–149Wm_2, respectively, with the greater forcings in 2011 corresponding to a 29–38mm/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

Contributions of wood smoke and vehicle emissions to ambient concentrations of volatile organic compounds and particulate matter during the Yakima wintertime nitrate study

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 2013 to 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 wintertime. 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 Environmental Protection Agency’s 2011 winter emission 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 overpredicting 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