scholarly journals Boreal fire records in Northern Hemisphere ice cores: A review

2016 ◽  
Author(s):  
Michel Legrand ◽  
Joseph McConnell ◽  
Hubertus Fischer ◽  
Eric W. Wolff ◽  
Susanne Preunkert ◽  
...  
Keyword(s):  
High Resolution ◽  
Organic Carbon ◽  
Black Carbon ◽  
Biomass Burning ◽  
Forest Fires ◽  
Greenland Ice Sheet ◽  
Ice Cores ◽  
High Elevation ◽  
Fire Activity

Abstract. Here we review different attempts made since the early 1990s to reconstruct past forest fire activity using chemical signals recorded in ice cores extracted from the Greenland ice sheet and at a few mid-northern latitude, high-elevation glaciers. We first examined the quality of various inorganic (ammonium, nitrate, potassium) and organic (black carbon, various organic carbon compounds including levoglucosan and numerous carboxylic acids) species proposed as fire proxies in ice, particularly in Greenland. We discuss limitations in their use with respect to the considered time period (recent versus pre-industrial times), their atmospheric lifetime, and the relative importance of other non-biomass burning sources. Different high-resolution records obtained at several Greenland drill sites and covering various timescales, including the last century and Holocene, are discussed. We explore the extent to which atmospheric transport can modulate the record of boreal fires from Canada as recorded in Greenland ice. Ammonium, organic fractions (black carbon as well as organic carbon), and organic compounds like formate and vanillic acid are found to be good proxies for tracing past boreal fires in Greenland ice. We show that use of other species – potassium, nitrate, and carboxylates (except formate) – is complicated by either post-depositional effects or existence of large non-biomass-burning sources. The quality of levoglucosan with respect to other proxies is not addressed here because of the present lack of high-resolution profiles for this species, which does not allow for a fair comparison. Several Greenland ice records of ammonium consistently indicate changing fire activity in Canada in response to past climatic conditions that occurred during the last millennium and since the last large climatic transition. Based on this critical review, we make recommendations for further study to increase reliability of the reconstructed history of forest fires occurring in a given region.

scholarly journals Boreal fire records in Northern Hemisphere ice cores: a review

2016 ◽  
Vol 12 (10) ◽  
pp. 2033-2059 ◽  
Author(s):  
Michel Legrand ◽  
Joseph McConnell ◽  
Hubertus Fischer ◽  
Eric W. Wolff ◽  
Susanne Preunkert ◽  
...  
Keyword(s):  
High Resolution ◽  
Organic Carbon ◽  
Biomass Burning ◽  
Forest Fires ◽  
Greenland Ice Sheet ◽  
Ice Cores ◽  
High Elevation ◽  
Potassium Nitrate ◽  
Fire Activity

Abstract. Here, we review different attempts made since the early 1990s to reconstruct past forest fire activity using chemical signals recorded in ice cores extracted from the Greenland ice sheet and a few mid-northern latitude, high-elevation glaciers. We first examined the quality of various inorganic (ammonium, nitrate, potassium) and organic (black carbon, various organic carbon compounds including levoglucosan and numerous carboxylic acids) species proposed as fire proxies in ice, particularly in Greenland. We discuss limitations in their use during recent vs. pre-industrial times, atmospheric lifetimes, and the relative importance of other non-biomass-burning sources. Different high-resolution records from several Greenland drill sites and covering various timescales, including the last century and Holocene, are discussed. We explore the extent to which atmospheric transport can modulate the record of boreal fires from Canada as recorded in Greenland ice. Ammonium, organic fractions (black and organic carbon), and specific organic compounds such as formate and vanillic acid are found to be good proxies for tracing past boreal fires in Greenland ice. We show that use of other species – potassium, nitrate, and carboxylates (except formate) – is complicated by either post-depositional effects or existence of large non-biomass-burning sources. The quality of levoglucosan with respect to other proxies is not addressed here because of a lack of high-resolution profiles for this species, preventing a fair comparison. Several Greenland ice records of ammonium consistently indicate changing fire activity in Canada in response to past climatic conditions that occurred during the last millennium and since the last large climatic transition. Based on this review, we make recommendations for further study to increase reliability of the reconstructed history of forest fires occurring in a given region.

First continuous high-resolution aerosol record from the East Greenland Ice Core Project (EGRIP), covering the last 15,000 years

2020 ◽  
Author(s):  
Camilla Marie Jensen ◽  
Tobias Erhardt ◽  
Giulia Sinnl ◽  
Hubertus Fischer
Keyword(s):  
High Resolution ◽  
Biomass Burning ◽  
Forest Fires ◽  
Ice Core ◽  
Greenland Ice Sheet ◽  
Ice Cores ◽  
Background Level ◽  
Volcanic Eruptions ◽  
Atmospheric Conditions ◽  
Data Set

<p>Ice sheets are reliable archives of atmospheric impurities such as aerosols and gasses of both natural and anthropogenic origin. Impurity records from Greenland ice cores reveal much information about previous atmospheric conditions and long-range transport in the Northern hemisphere going back more than a hundred thousand years.</p><p>Here we present the data from the upper 1,411 m from the EGRIP ice core, measuring conductivity, dust, sodium, calcium, ammonium, and nitrate. These records contain information about ocean sources, transport of terrestrial dust, soil and vegetation emissions as well as biomass burning, volcanic eruptions, etc., covering approximately the past 15,000 years. This newly obtained data set is unique as it provides the first high-resolution information about several thousands of years of the mid-Holocene period in Greenland that none of the previous impurity records from the other deep Greenland ice cores had managed to cover before due to brittle ice. This will contribute to further understanding of the atmospheric conditions for the pre-industrial period.</p><p>The ammonium record contains peaks significantly higher than the background level. These peaks are caused by biomass burning or forest fires emitting plumes of ammonia large enough so that they can extend to the free troposphere and be efficiently transported all the way to the Greenland ice sheet. Here we present preliminary results of the wild fire frequency covering the entire Holocene, where the wild fires are defined as outliers in the ammonium record of annual means.</p>

scholarly journals Fire in ice: two millennia of Northern Hemisphere fire history from the Greenland NEEM ice core

2014 ◽  
Vol 10 (1) ◽  
pp. 809-857 ◽  
Author(s):  
P. Zennaro ◽  
N. Kehrwald ◽  
J. R. McConnell ◽  
S. Schüpbach ◽  
O. Maselli ◽  
...  
Keyword(s):  
Black Carbon ◽  
Biomass Burning ◽  
Fire History ◽  
Global Climate ◽  
Ice Cores ◽  
Dominant Factor ◽  
The Past ◽  
Past 2000 Years ◽  
Isotopic Analyses ◽  
Fire Activity

Abstract. Biomass burning is a major source of greenhouse gases and influences regional to global climate. Pre-industrial fire-history records from black carbon, charcoal and other proxies provide baseline estimates of biomass burning at local to global scales, but there remains a need for broad-scale fire proxies that span millennia in order to understand the role of fire in the carbon cycle and climate system. We use the specific biomarker levoglucosan, and multi-source black carbon and ammonium concentrations to reconstruct fire activity from the North Greenland Eemian (NEEM) ice cores (77.49° N; 51.2° W, 2480 m a.s.l.) over the past 2000 years. Increases in boreal fire activity (1000–1300 CE and 1500–1700 CE) over multi-decadal timescales coincide with the most extensive central and northern Asian droughts of the past two millennia. The NEEM biomass burning tracers coincide with temperature changes throughout much of the past 2000 years except for during the extreme droughts, when precipitation changes are the dominant factor. Many of these multi-annual droughts are caused by monsoon failures, thus suggesting a connection between low and high latitude climate processes. North America is a primary source of biomass burning aerosols due to its relative proximity to the NEEM camp. During major fire events, however, isotopic analyses of dust, back-trajectories and links with levoglucosan peaks and regional drought reconstructions suggest that Siberia is also an important source of pyrogenic aerosols to Greenland.

scholarly journals An 800 year high-resolution black carbon ice-core record from Lomonosovfonna, Svalbard

2018 ◽  
Author(s):  
Dimitri Osmont ◽  
Isabel A. Wendl ◽  
Loïc Schmidely ◽  
Michael Sigl ◽  
Carmen P. Vega ◽  
...  
Keyword(s):  
High Resolution ◽  
Black Carbon ◽  
20Th Century ◽  
Biomass Burning ◽  
Ice Core ◽  
Ice Cores ◽  
The Arctic ◽  
Snow Albedo ◽  
Decadal Scale

Abstract. Produced by the incomplete combustion of fossil fuel and biomass, black carbon (BC) contributes to Arctic warming by reducing snow albedo and thus triggering a snow-albedo feedback leading to increased snow melting. Therefore, it is of high importance to assess past BC emissions to better understand and constrain their role. However, only few long-term BC records are available from the Arctic, mainly originating from Greenland ice cores. Here, we present the first long-term and high-resolution refractory black carbon (rBC) record from Svalbard, derived from the analysis of two ice cores drilled at the Lomonosovfonna ice field in 2009 (LF-09) and 2011 (LF-11) and covering 800 years of atmospheric emissions. Our results show that rBC concentrations strongly increased from 1860 on due to anthropogenic emissions and reached two maxima, at the end of the 19th century and in the middle of the 20th century. No increase in rBC concentrations during the last decades was observed, which is corroborated by atmospheric measurements elsewhere in the Arctic but contradicts a previous study from another ice core from Svalbard. While melting may affect BC concentrations during periods of high temperatures, rBC concentrations remain well-preserved prior to the 20th century due to lower temperatures inducing little melt. Therefore, the preindustrial rBC record (before 1800), along with ammonium (NH4+), formate (HCOO−) and specific organic markers (vanillic acid (VA) and p-hydroxybenzoic acid (p-HBA)), was used as a proxy for biomass burning. Despite numerous single events, no long-term trend was observed over the time period 1222–1800 for rBC and NH4+. In contrast, formate, VA and p-HBA experience multi-decadal peaks reflecting periods of enhanced biomass burning. Most of the background variations and single peak events are corroborated by other ice-core records from Greenland and Siberia. We suggest that the paleofire record from the LF ice core primarily reflects biomass burning episodes from Northern Eurasia, induced by decadal-scale climatic variations.

Forty years later: High resolution continuous flow analysis of the Dye3 ice core

2021 ◽  
Author(s):  
Helle Astrid Kjær ◽  
Margaret Harlan ◽  
Paul Vallelonga ◽  
Anders Svensson ◽  
Thomas Blunier ◽  
...  
Keyword(s):  
High Resolution ◽  
Forest Fires ◽  
Continuous Flow ◽  
Ice Core ◽  
Flow Analysis ◽  
Ice Sheet ◽  
Greenland Ice Sheet ◽  
Ice Cores ◽  
The Core ◽  
Continuous Flow Analysis

<div><span><span>The Dye-3 ice core was drilled to bedrock at the Southern part of the central Greenland ice sheet (65°11'N, 43°50'W) in 1979-1981. The southern location is characterized by high accumulation rates compared to more central locations of the ice sheet. Since its drilling, numerous analyses of the core have been performed, and the ice has since been in freezer storage both in the USA and in Denmark.</span></span></div><div><span>In October and November 2019, the remaining ice, two mostly complete sections covering the depths of 1753–1820m and 1865–1918m of the Dye-3 core, were melted during a continuous flow analysis (CFA) campaign at the Physics of Ice, Climate, and Earth (PICE) group at the University of Copenhagen. The data represents both Holocene, Younger Dryas and Glacial sections (GS 5 to 12).</span></div><div> </div><div><span><span>The measured data consist chemistry and impurities contained in the ice, isotopes, as well as analysis of methane and other atmospheric gases. </span></span></div><div><span><span>The chemistry measurements include NH</span></span><span><span><sub>4</sub></span></span><span><span><sup>+</sup></span></span><span><span>, Ca</span></span><span><span><sup>2+</sup></span></span><span><span>, and Na</span></span><span><span><sup>+</sup></span></span><span><span> ions, which besides being influenced by transport, provide information about forest fires, wind-blown dust, and sea ice, respectively, as well as acidity, which aids in the identification of volcanic events contained in the core. The quantity and grain size distribution of insoluble particles was analyzed by means of an Abakus laser particle counter.</span></span></div><div> </div><div><span>We compare the new high-resolution CFA record of dye3 with previous analysis and thus evaluate the progress made over 40 years. Further we compare overlapping time periods with other central Greenland ice cores and discuss spatial patterns in relation to the presented climate proxies.</span></div>

scholarly journals Fire in ice: two millennia of boreal forest fire history from the Greenland NEEM ice core

2014 ◽  
Vol 10 (5) ◽  
pp. 1905-1924 ◽  
Author(s):  
P. Zennaro ◽  
N. Kehrwald ◽  
J. R. McConnell ◽  
S. Schüpbach ◽  
O. J. Maselli ◽  
...  
Keyword(s):  
Black Carbon ◽  
Biomass Burning ◽  
High Latitude ◽  
Fire History ◽  
Global Climate ◽  
Ice Cores ◽  
Back Trajectories ◽  
The Past ◽  
Isotopic Analyses ◽  
Fire Activity

Abstract. Biomass burning is a major source of greenhouse gases and influences regional to global climate. Pre-industrial fire-history records from black carbon, charcoal and other proxies provide baseline estimates of biomass burning at local to global scales spanning millennia, and are thus useful to examine the role of fire in the carbon cycle and climate system. Here we use the specific biomarker levoglucosan together with black carbon and ammonium concentrations from the North Greenland Eemian (NEEM) ice cores (77.49° N, 51.2° W; 2480 m a.s.l) over the past 2000 years to infer changes in boreal fire activity. Increases in boreal fire activity over the periods 1000–1300 CE and decreases during 700–900 CE coincide with high-latitude NH temperature changes. Levoglucosan concentrations in the NEEM ice cores peak between 1500 and 1700 CE, and most levoglucosan spikes coincide with the most extensive central and northern Asian droughts of the past millennium. Many of these multi-annual droughts are caused by Asian monsoon failures, thus suggesting a connection between low- and high-latitude climate processes. North America is a primary source of biomass burning aerosols due to its relative proximity to the Greenland Ice Cap. During major fire events, however, isotopic analyses of dust, back trajectories and links with levoglucosan peaks and regional drought reconstructions suggest that Siberia is also an important source of pyrogenic aerosols to Greenland.

scholarly journals An 800-year high-resolution black carbon ice core record from Lomonosovfonna, Svalbard

2018 ◽  
Vol 18 (17) ◽  
pp. 12777-12795 ◽  
Author(s):  
Dimitri Osmont ◽  
Isabel A. Wendl ◽  
Loïc Schmidely ◽  
Michael Sigl ◽  
Carmen P. Vega ◽  
...  
Keyword(s):  
High Resolution ◽  
Black Carbon ◽  
20Th Century ◽  
Biomass Burning ◽  
Ice Core ◽  
Ice Cores ◽  
The Arctic ◽  
Snow Albedo ◽  
Decadal Scale

Abstract. Produced by the incomplete combustion of fossil fuel and biomass, black carbon (BC) contributes to Arctic warming by reducing snow albedo and thus triggering a snow-albedo feedback leading to increased snowmelt. Therefore, it is of high importance to assess past BC emissions to better understand and constrain their role. However, only a few long-term BC records are available from the Arctic, mainly originating from Greenland ice cores. Here, we present the first long-term and high-resolution refractory black carbon (rBC) record from Svalbard, derived from the analysis of two ice cores drilled at the Lomonosovfonna ice field in 2009 (LF-09) and 2011 (LF-11) and covering 800 years of atmospheric emissions. Our results show that rBC concentrations strongly increased from 1860 on due to anthropogenic emissions and reached two maxima, at the end of the 19th century and in the middle of the 20th century. No increase in rBC concentrations during the last decades was observed, which is corroborated by atmospheric measurements elsewhere in the Arctic but contradicts a previous study from another ice core from Svalbard. While melting may affect BC concentrations during periods of high temperatures, rBC concentrations remain well preserved prior to the 20th century due to lower temperatures inducing little melt. Therefore, the preindustrial rBC record (before 1800), along with ammonium (NH4+), formate (HCOO−) and specific organic markers (vanillic acid, VA, and p-hydroxybenzoic acid, p-HBA), was used as a proxy for biomass burning. Despite numerous single events, no long-term trend was observed over the time period 1222–1800 for rBC and NH4+. In contrast, formate, VA, and p-HBA experience multi-decadal peaks reflecting periods of enhanced biomass burning. Most of the background variations and single peak events are corroborated by other ice core records from Greenland and Siberia. We suggest that the paleofire record from the LF ice core primarily reflects biomass burning episodes from northern Eurasia, induced by decadal-scale climatic variations.

scholarly journals Black carbon variability since preindustrial times in Eastern part of Europe reconstructed from Mt Elbrus, Caucasus ice cores

2016 ◽  
Author(s):  
Saehee Lim ◽  
Xavier Faïn ◽  
Patrick Ginot ◽  
Vladimir Mikhalenko ◽  
Stanislav Kutuzov ◽  
...  
Keyword(s):  
Black Carbon ◽  
20Th Century ◽  
Biomass Burning ◽  
Mass Concentration ◽  
Ice Core ◽  
Ice Cores ◽  
Anthropogenic Emissions ◽  
Ice Core Record ◽  
Summer Time ◽  
Mass Concentrations

Abstract. Black carbon (BC), emitted by fossil fuel combustion and biomass burning, is the second largest man-made contributor to global warming after carbon dioxide (Bond et al., 2013). However, limited information exists on its past emissions and atmospheric variability. In this study, we present the first high-resolution record of refractory BC (rBC, including mass concentration and size) reconstructed from ice cores drilled at a high-altitude Eastern European site in Mt. Elbrus (ELB), Caucasus (5115 m a.s.l.). The ELB ice core record, covering the period 1825–2013, reflects the atmospheric load of rBC particles at the ELB site transported from the European continent with a larger rBC input from sources located in the Eastern part of Europe. In the first half of the 20th century, European anthropogenic emissions resulted in a 1.5-fold increase in the ice core rBC mass concentrations as respect to its level in the preindustrial era (before 1850). The rBC mass concentrations increased by a 5-fold in 1960–1980, followed by a decrease until ~ 2000. Over the last decade, the rBC signal for summer time slightly increased. We have compared the signal with the atmospheric BC load simulated using past BC emissions (ACCMIP and MACCity inventories) and taken into account the contribution of different geographical region to rBC distribution and deposition at the ELB site. Interestingly, the observed rBC variability in the ELB ice core record since the 1960s is not in perfect agreement with the simulated atmospheric BC load. Similar features between the ice core rBC record and the best scenarios for the atmospheric BC load support that anthropogenic BC increase in the 20th century is reflected in the ELB ice core record. However, the peak in BC mass concentration observed in ~ 1970 in the ice core is estimated to occur a decade later from past inventories. BC emission inventories for the period 1960s–1970s may be underestimating European anthropogenic emissions. Furthermore, for summer time snow layers of the last 2000s, the slightly increasing trend of rBC deposition likely reflects recent changes in anthropogenic and biomass burning BC emissions in the Eastern part of Europe. Our study highlights that the past changes in BC emissions of Eastern Europe need to be considered in assessing on-going air quality regulation.

scholarly journals Molecular Composition and Photochemical Evolution of Water Soluble Organic Carbon (WSOC) Extracted from Field Biomass Burning Aerosols using High Resolution Mass Spectrometry

2019 ◽  
Author(s):  
Jing Cai ◽  
Xiangying Zeng ◽  
Guorui Zhi ◽  
Sasho Gligorovski ◽  
Guoying Sheng ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
High Resolution ◽  
Organic Carbon ◽  
Biomass Burning ◽  
High Resolution Mass Spectrometry ◽  
Water Soluble ◽  
Oxygenated Compounds ◽  
Water Soluble Organic Carbon ◽  
Soluble Organic Carbon ◽  
Resolution Mass

Abstract. Photochemistry plays an important role in the evolution of atmospheric water soluble organic carbon (WSOC), which dissolves into clouds, fogs and aerosol liquid water. In this study, we examined the molecular composition and evolution of a WSOC mixture extracted from fresh biomass burning aerosols upon photolysis, using direct infusion electrospray ionization high-resolution mass spectrometry (ESI-HRMS) and liquid chromatography coupled with mass spectrometry (LC/ESI-HRMS). For comparison, two typical phenolic compounds (i.e., phenol and guaiacol) emitted from lignin pyrolysis in combination with hydrogen peroxide (H2O2) as a typical OH radical precursor, were exposed to simulated sunlight irradiation. The photochemistry of both, the phenols (photo-oxidation) and WSOC mixture (direct photolysis) can produce a series of highly oxygenated compounds which in turn increases the degree of oxidation of organic composition and acidity of the bulk solution. In particular, the LC/ESI-HRMS technique revealed significant photochemical evolution on the WSOC composition, e.g., the photodegradation of low oxygenated species and the formation of highly oxygenated products. We also tentatively compared the mass spectra of photolytic time-profile extract with each other for a more comprehensive description of the photolytic evolution. The calculated average oxygen-to-carbon (O / C) ratios of oxygenated compounds in bulk extract increases from 0.38 ± 0.02 to 0.44 ± 0.02 (mean±standard deviation) while the intensity (S / N)-weighted average O / C (O / Cw) increases from 0.45 ± 0.03 to 0.53 ± 0.06 as the time of irradiation extends from 0 to 12 h. These findings indicate that the water soluble organic fraction of fresh combustion-derived aerosols have the potential to form more oxidized organic matter, accounting for the highly oxygenated nature of atmospheric organic aerosols.

scholarly journals Biomass burning contribution to black carbon in the Western United States Mountain Ranges

2011 ◽  
Vol 11 (21) ◽  
pp. 11253-11266 ◽  
Author(s):  
Y. H. Mao ◽  
Q. B. Li ◽  
L. Zhang ◽  
Y. Chen ◽  
J. T. Randerson ◽  
...  
Keyword(s):  
United States ◽  
Black Carbon ◽  
Biomass Burning ◽  
Forest Fires ◽  
Transport Model ◽  
Reanalysis Data ◽  
Western United States ◽  
Fire Season ◽  
Carbonaceous Aerosols ◽  
Mountain Ranges

Abstract. Forest fires are an important source to carbonaceous aerosols in the Western United States (WUS). We quantify the relative contribution of biomass burning to black carbon (BC) in the WUS mountain ranges by analyzing surface BC observations for 2006 from the Interagency Monitoring of PROtected Visual Environment (IMPROVE) network using the GEOS-Chem global chemical transport model. Observed surface BC concentrations show broad maxima during late June to early November. Enhanced potassium concentrations and potassium/sulfur ratios observed during the high-BC events indicate a dominant biomass burning influence during the peak fire season. Model surface BC reproduces the observed day-to day and synoptic variabilities in regions downwind of but near urban centers. Major discrepancies are found at elevated mountainous sites during the July-October fire season when simulated BC concentrations are biased low by a factor of two. We attribute these low biases largely to the underestimated (by more than a factor of two) and temporally misplaced biomass burning emissions of BC in the model. Additionally, we find that the biomass burning contribution to surface BC concentrations in the USA likely was underestimated in a previous study using GEOS-Chem (Park et al., 2003), because of the unusually low planetary boundary layer (PBL) heights in the GEOS-3 meteorological reanalysis data used to drive the model. PBL heights from GEOS-4 and GEOS-5 reanalysis data are comparable to those from the North American Regional Reanalysis (NARR). Model simulations show slightly improved agreements with the observations when driven by GEOS-5 reanalysis data, but model results are still biased low. The use of biomass burning emissions with diurnal cycle, synoptic variability, and plume injection has relatively small impact on the simulated surface BC concentrations in the WUS.

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