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Abstract Estimating fire emissions prior to the satellite era is challenging because observations are limited, leading to large uncertainties in the calculated aerosol climate forcing following the preindustrial era. This challenge further limits the ability of climate models to accurately project future climate change. Here, we reconstruct a gridded dataset of global biomass burning emissions from 1750 to 2010 using inverse analysis that leveraged a global array of 31 ice core records of black carbon deposition fluxes, two different historical emission inventories as a priori estimates, and emission-deposition sensitivities simulated by the atmospheric chemical transport model GEOS-Chem. The reconstructed emissions exhibit greater temporal variabilities which are more consistent with paleoclimate proxies. Our ice core constrained emissions reduced the uncertainties in simulated cloud condensation nuclei and aerosol radiative forcing associated with the discrepancy in preindustrial biomass burning emissions. The derived emissions can also be used in studies of ocean and terrestrial biogeochemistry. 

Abstract Rapid warming and human exploitation threaten boreal forests. Understanding links among vegetation, climate, and people in this vast biome requires highly resolved long‐term records that integrate regional inputs. We developed an 850‐year pollen‐based record of supraregional vegetation change using a southern Greenland ice core and atmospheric modeling that identified the boreal and mixed‐conifer forests of eastern Canada as the dominant pollen source regions. Conifer pollen increased ∼1400 CE at the onset of the cooler and drier Little Ice Age. A subsequent decline began ∼1650 CE and a statistically significant pollen change after 1760 CE suggests ecological consequences of the Little Ice Age cooling and initial human exploitation that persisted until recent decades. These supraregional changes are broadly consistent with local records and demonstrate intensification of human impacts on northern forests, suggesting a shift from a climate‐modulated to an increasingly human‐controlled system during recent centuries. 

Black carbon is a paleofire proxy that has been measured from glacial ice, snow, soils and lake sediments, though relatively few comparisons have been made with other fire indicators in sedimentary geoarchives. Microscopic charcoal, quantified from palynological microscope slides and macroscopic charcoal, quantified from wet-sieved deposits, are the most commonly applied methods for paleofire interpretation of Quaternary sediments. This research explores the down-profile patterns across three paleofire proxies (refractory black carbon, microscopic and macroscopic charcoal) and potential paleofire interpretations from a sediment core dating to the last centuries from Speke Gulf, Lake Victoria, and a young soil profile from a kopje located in the surrounding watershed in Serengeti National Park, Tanzania. The results of three paleofire metrics show similar trends within each site, with a positive trend across all metrics and increasing variability with increased measurement values (heteroscedastic). Notably, refractory black carbon (rBC) concentrations are two orders of magnitude higher in lake sediment samples compared to soil samples. rBC is positively correlated with both microscopic and macroscopic charcoal values and the overall profile patterns down the sediment core are similar, with the exception of the rBC increases from 2.5 to 0 cm depth that may result from increased fossil fuel combustion. The Speke Gulf rBC measurements are in an intermediate range between those published from glacial ice and other lake sediments. New rBC records from different ecosystems and temporal scales will provide paleofire insights and potential to interpret source areas and depositional patterns. The exploration of soil archives offers the potential to exploit semi-arid ecosystems and archaeological sites that have no nearby traditional paleoenvironmental study site targets. 

Aerosol radiative forcing is an important but often poorly understood component of regional climate. While glacier ice contains the most detailed archives of past atmospheric aerosol composition and temperature, no well-preserved ice records extending into the last climatic transition have been reported for the historically important European region. Here, we use an Alpine ice core to document changes in European aerosols and climate from the end of the last glacial age (LGA) through the Holocene. The core was drilled on a glacier dome in the French Alps called the Dôme du Goûter (DDG), and it provides a stratigraphically intact record of aerosol and climate extending to at least 12 kyears (ky) before present. Although dating near the base of the glacier is not well constrained, the oldest DDG ice layers reflect glacial conditions in western Europe during the LGA. In addition to changes in atmospheric transport, increased sea-salt and dust deposition in western Europe recorded in the LGA ice suggest enhanced westerly winds and more active dust sources, possibly including North Africa. Deposition of terrestrial biogenic indicators during the cold LGA climate was lower, however, consistent with strongly reduced European vegetation. The DDG record of terrestrial biogenic emissions also suggests a decline of European forests throughout the Holocene, resulting from deterioration of climatic conditions and more recently from establishment of the first agricultural societies. The pronounced changes in atmospheric aerosol recorded in Alpine ice imply large variations in aerosol radiative forcing in western Europe during the last 12 ky. 

The specific goal of this project was to develop a more complete and quantitative understanding of natural and anthropogenic drivers of biomass burning over the Common Era. To do so, new high-resolution measurements of a broad range of chemical, elemental, and isotopic species were analyzed on the archived HT95 core using the continuous flow analysis system at the Desert Research Institute in 2023. These new measurements of the Hans Tausen 1995 (HT95) ice core, which was provided by collaborators at the University of Copenhagen, were used along with existing ice-core datasets to underpin atmospheric modeling to understand past emissions of black carbon from biomass burning and anthropogenic activities over the past 250 years (Zhang et al., 2024). The HT95 ice core was collected in 1995 and extends to ~3670 BCE. 

Refractory black carbon (rBC) aerosols in air and precipitation result from incomplete combustion. Prior to 18th century industrialization, the primary emission sources were wildfires and agricultural fires. After industrialization, fossil fuel burning has become an important emission source as well. Because these aerosols are import contributors to Earth’s radiative forcing both in the air and when deposited to bright surfaces such as fresh snow, quantifying past rBC emissions is critical to accurate Earth System Modeling. This data set contains 1750 to 2010 annual rBC depositional fluxes measured in a global array of 31, mostly polar ice cores. They were used (Zhang et al., Nature Communications, 2024) to reconstruct atmospheric rBC emissions using the atmospheric chemical transport GEOS-Chem. Details on the rBC measurement methods and chronology development are provided in the associated references for the individual ice core records. 

The overall objective of this research is to (1) develop high resolution measurements of a range of aerosol-related elements, chemical species, and isotopes in archived Greenland Ice Sheet Project Two (GISP2) ice corresponding to Greenland stadial and interstadial events 5 through 12 from the last Glacial period, and (2) use these measurements -- together with the Goddard Earth Observing System (GEOS)-Chem atmospheric chemistry and other models -- to better understand climate processes and feedbacks underlying rapid climate change events and atmospheric chemistry during the last Glacial with particular focus on biomass burning emissions. Here we report high resolution (approximately annual) and decadal-scale measurements of water stable isotopic ratios, refractory black carbon concentration and particle size, semi-quantitative insoluble particle mass concentration, as well as ammonium, sea-salt sodium and non-sea-salt calcium concentrations measured from 2100 to 2365 meter (m) depth in the GISP2 core. These data ,as well as a modified simple atmospheric transport model, were used initially to evaluate aerosol emissions, transport, and deposition during rapid climate change events GI 5 through GI 12 (Liu et al., 2024). 

Abstract Black carbon emitted by incomplete combustion of fossil fuels and biomass has a net warming effect in the atmosphere and reduces the albedo when deposited on ice and snow; accurate knowledge of past emissions is essential to quantify and model associated global climate forcing. Although bottom-up inventories provide historical Black Carbon emission estimates that are widely used in Earth System Models, they are poorly constrained by observations prior to the late 20th century. Here we use an objective inversion technique based on detailed atmospheric transport and deposition modeling to reconstruct 1850 to 2000 emissions from thirteen Northern Hemisphere ice-core records. We find substantial discrepancies between reconstructed Black Carbon emissions and existing bottom-up inventories which do not fully capture the complex spatial-temporal emission patterns. Our findings imply changes to existing historical Black Carbon radiative forcing estimates are necessary, with potential implications for observation-constrained climate sensitivity.