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

A 200 Year Sub-Annual Record of Sulfate in West Antarctica, from Sixteen Ice Cores

Sixteen high-resolution ice-core records from West Antarctica and South Pole are used to examine the spatial and temporal distribution of sulfate for the last 200 years. The preservation of seasonal layers throughout the length of each record results in a dating accuracy of better than 1 year based on known global-scale volcanic events. A dual transport source for West Antarctic sea-salt (ss) SO42- and excess (xs) SO42- is observed: lower-tropospheric for areas below 1000m elevation and mid-/upper-tropospheric/stratospheric for areas located above 1000m. Our XsSO(4)(2-) records with volcanic peaks removed do not display any evidence of an anthropogenic impact on West Antarctic SO42- concentrations but do reveal that a major climate transition takes place over West Antarctica at similar to 1940. Global-scale volcanic eruptions appear as significant peaks in the robust-spline residual xsSO(4)(2-) records from sites located above 1000 m elevation but do not appear in the residual records from sites located below 1000 m

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

Radiative Forcing by Dust and Black Carbon on the Juneau Icefield, Alaska

Here we present the first known data set on black carbon (BC) and mineral dust concentrations in snow from the Juneau Icefield (JIF) in southeastern Alaska, where glacier melt rates are among the highest on Earth. In May 2016, concentrations of BC (0.4–3.1 μg/L) and dust (0.2–34 mg/L) were relatively low and decreased toward the interior of the JIF. The associated radiative forcing (RF) averaged 4 W/m2. In July, after 10 weeks of exposure, the aged snow surface had substantially higher concentrations of BC (2.1–14.8 μg/L) and dust (11–72 mg/L) that were not spatially distributed by elevation or distance from the coast. RF by dust and BC ranged from 70 to 130 W/m2 (87 W/m2 average) across the JIF in July, and RF was dominated by dust. The associated median snow water equivalent reduction in the July samples is estimated at 10–18 mm/day, potentially advancing melt on the scale of days to weeks. Aging of the snow surface in summer likely resulted in a positive feedback of melt consolidation, enhanced solar absorption and melting, and further concentration of surface particles. Regional projections of warming temperatures and increased rain at the expense of snow make it likely that summer season darkening will become a more important contributor to the high melt rates on the JIF. Further studies are needed to elucidate the spatiotemporal occurrence of various light‐absorbing particles on the JIF, and models of ice field wastage should incorporate their associated RF

Recent increase in black carbon concentrations from a Mt. Everest ice core spanning 1860–2000 AD

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/95622/1/grl27751.pd

The spectral and chemical measurement of pollutants on snow near South Pole, Antarctica

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 \u3c1 W m­–2 for clean snow to ~70 W m­–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 High-Resolution Record of Atmospheric Dust Composition and Variability Since Ad 1650 from a Mount Everest Ice Core

A Mount Everest ice core analyzed at high resolution for 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, Co) and spanning the period A. D. 1650- 2002 is used to investigate the sources of and variations in atmospheric dust through time. The chemical composition of dust varies seasonally, and peak dust concentrations occur during the winter-spring months. Significant correlations between the Everest dust record and dust observations at stations suggest that the Everest record is representative of regional variations in atmospheric dust loading. Back-trajectory analysis in addition to a significant correlation of Everest dust concentrations and the Total Ozone Mapping Spectrometer (TOMS) aerosol index indicates that the dominant winter sources of dust are the Arabian Peninsula, Thar Desert, and northern Sahara. Factors that contribute to dust generation at the surface include soil moisture and temperature, and the long-range transport of dust aerosols appears to be sensitive to the strength of 500-mb zonal winds. There are periods of high dust concentration throughout the 350-yr Mount Everest dust record; however, there is an increase in these periods since the early 1800s. The record was examined for recent increases in dust emissions associated with anthropogenic activities, but no recent dust variations can be conclusively attributed to anthropogenic inputs of dust

A 200 Year Sulfate Record from Sixteen Antarctic Ice Cores and Associations With Southern Ocean Sea-Ice Extent

Chemistry data from 16, 50-115 m deep, sub-annually dated ice cores are used to investigate spatial and temporal concentration variability of sea-salt (ss) SO42- and excess (xs) SO42- over West Antarctica and the South Pole for the last 200 years. Low-elevation ice-core sites in western West Antarctica contain higher concentrations Of SO42- as a result of cyclogenesis over the Ross Ice Shelf and proximity to the Ross Sea Polynya. Linear correlation analysis of 15 West Antarctic ice-core SO42- time series demonstrates that at several sites concentrations Of ssSO(4)(2-) are higher when sea-ice (SIE) extent is greater, and the inverse for XSS04. Concentrations Of XSS04 from the South Pole site (East Antarctica) are associated with SIE from the Weddell region, and West Antarctic XSSO42- concentrations are associated with SIE from the Bellingshausen-Amundsen-Ross region. The only notable rise of the last 200 years in xsSO(4)(2-), around 1940, is not related to SIE fluctuations and is most likely a result of increased xsSO(4)(2-) production in the mid-low latitudes and/or an increase in transport efficiency from the mid-low latitudes to central West Antarctica. These high-resolution records show that the source types and source areas Of ssSO(4)(2-) and xsSO(4)(2-) delivered to eastern and western West Antarctica and the South Pole differ from site to site but can best be resolved using records from spatial ice-core arrays such as the International Trans-Antarctic Scientific Expedition (ITASE)

Dramatic loss of glacier accumulation area on the Tibetan Plateau revealed by ice core tritium and mercury records

Two ice cores were retrieved from high elevations (~5800 m a.s.l.) at Mt. Nyainqêntanglha and Mt. Geladaindong in the southern and central Tibetan Plateau region. The combined tracer analysis of tritium (3H), 210Pb and mercury, along with other chemical records, provided multiple lines of evidence supporting that the two coring sites had not received net ice accumulation since at least the 1950s and 1980s, respectively. These results implied an annual ice loss rate of more than several hundred millimeter water equivalent over the past 30–60 years. Both mass balance modeling at the sites and in situ data from the nearby glaciers confirmed a continuously negative mass balance (or mass loss) in the region due to dramatic warming in recent decades. Along with a recent report on Naimona\u27nyi Glacier in the Himalayas, the findings suggest that the loss of accumulation area of glacier is a possibility from the southern to central Tibetan Plateau at high elevations, probably up to about 5800 m a.s.l. This mass loss raises concerns over the rapid rate of glacier ice loss and associated changes in surface glacier runoff, water availability, and sea levels

Climate Variability in West Antarctica Derived from Annual Accumulation-Rate Records from ITASE Firn/Ice Cores

Thirteen annually resolved accumulation-rate records covering the last similar to 200 years from the Pine Island-Thwaites and Ross drainage systems and the South Pole are used to examine climate variability over West Antarctica. Accumulation is controlled spatially by the topography of the ice sheet, and temporally by changes in moisture transport and cyclonic activity. A comparison of mean accumulation since 1970 at each site to the long-term mean indicates an increase in accumulation for sites located in the western sector of the Pine Island-Thwaites drainage system. Accumulation is negatively associated with the Southern Oscillation Index (Sol) for sites near the ice divide, and periods of sustained negative Sol (1940-42, 1991-95) correspond to above-mean accumulation at most sites. Correlations of the accumulation-rate records with sea-level pressure (SLP) and the SOI suggest that accumulation near the ice divide and in the Ross drainage system may be associated with the midlatitudes. The post-1970 increase in accumulation coupled with strong SLP-accumulation-rate correlations near the coast suggests recent intensification of cyclonic activity in the Pine Island-Thwaites drainage system