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dc.contributor.author
Kaspari, Susan
dc.contributor.author
Painter, Thomas H.
dc.contributor.author
Gysel, Martin
dc.contributor.author
Skiles, S.M.
dc.contributor.author
Schwikowski, Margit
dc.date.accessioned
2018-09-25T11:17:21Z
dc.date.available
2017-06-11T12:28:47Z
dc.date.available
2018-09-25T11:17:21Z
dc.date.issued
2014
dc.identifier.issn
1680-7324
dc.identifier.issn
1680-7375
dc.identifier.other
10.5194/acp-14-8089-2014
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/89360
dc.identifier.doi
10.3929/ethz-b-000089360
dc.description.abstract
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 < 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 < 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.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
Copernicus
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/3.0/
dc.title
Seasonal and elevational variations of black carbon and dust in snow and ice in the Solu-Khumbu, Nepal and estimated radiative forcings
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 3.0 Unported
dc.date.published
2014-08-13
ethz.journal.title
Atmospheric Chemistry and Physics
ethz.journal.volume
14
en_US
ethz.journal.issue
15
en_US
ethz.journal.abbreviated
Atmos. Chem. Phys.
ethz.pages.start
8089
en_US
ethz.pages.end
8103
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.nebis
004294181
ethz.publication.place
Göttingen
en_US
ethz.publication.status
published
en_US
ethz.date.deposited
2017-06-11T12:29:37Z
ethz.source
ECIT
ethz.identifier.importid
imp5936524e0ad2a59552
ethz.ecitpid
pub:140609
ethz.eth
no
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2017-07-14T16:24:43Z
ethz.rosetta.lastUpdated
2023-02-06T15:55:02Z
ethz.rosetta.exportRequired
true
ethz.rosetta.versionExported
true
ethz.COinS
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