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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.

The disturbed stratigraphy of the ice in the lowest 10% of the Greenland GRIP ice core has been previously demonstrated using gas measurements (δ18O of O2 and CH4) on a few meters depth scale. However, rapid ice isotopic variations (on the scale of 20 cm) are experienced in the bottom of the GRIP ice core with complex chemical signatures that make them difficult to reconcile with a disturbed stratigraphy of the ice. This is the case for event 5e1, first described as a dramatic cooling 120 kyr BP. We analyzed at a 5 cm resolution the isotopic composition of the air from 2 m of the GRIP bottom ice core covering event 5e1. The δ15N measurements, combined with a basic firn modeling, lead to the solid conclusion that the rapid event 5e1 is not a climatic event. Rapid variations of δ18O of O2 (δ18Oatm) are in agreement with a disturbed ice stratigraphy. However, the double peak shape of the δ18Oatm, recalling chemical data at the same depth, requires processes of diffusion after the mixing or even postcoring, placing limits to the interpretation of some classical paleoclimatic proxies in small scale mixed ice (

The assassination of Julius Caesar in 44 BCE triggered a power struggle that ultimately ended the Roman Republic and, eventually, the Ptolemaic Kingdom, leading to the rise of the Roman Empire. Climate proxies and written documents indicate that this struggle occurred during a period of unusually inclement weather, famine, and disease in the Mediterranean region; historians have previously speculated that a large volcanic eruption of unknown origin was the most likely cause. Here we show using well-dated volcanic fallout records in six Arctic ice cores that one of the largest volcanic eruptions of the past 2,500 y occurred in early 43 BCE, with distinct geochemistry of tephra deposited during the event identifying the Okmok volcano in Alaska as the source. Climate proxy records show that 43 and 42 BCE were among the coldest years of recent millennia in the Northern Hemisphere at the start of one of the coldest decades. Earth system modeling suggests that radiative forcing from this massive, high-latitude eruption led to pronounced changes in hydroclimate, including seasonal temperatures in specific Mediterranean regions as much as 7 °C below normal during the 2 y period following the eruption and unusually wet conditions. While it is difficult to establish direct causal linkages to thinly documented historical events, the wet and very cold conditions from this massive eruption on the opposite side of Earth probably resulted in crop failures, famine, and disease, exacerbating social unrest and contributing to political realignments throughout the Mediterranean region at this critical juncture of Western civilization.

This study reports the chemical composition of particles present along Greenland’s North Greenland Eemian Ice Drilling (NEEM) ice core, back to 110,000 years before present. Insoluble and soluble particles larger than 0.45 μm were extracted from the ice core by ice sublimation, and their chemical composition was analyzed using scanning electron microscope and energy dispersive X-ray spectroscopy and micro-Raman spectroscopy. We show that the dominant insoluble components are silicates, whereas NaCl, Na₂SO₄, CaSO ₄, and CaCO₃ represent major soluble salts. For the first time, particles of CaMg(CO₃)₂ and Ca(NO₃)₂ 4H₂O are identified in a Greenland ice core. The chemical speciation of salts varies with past climatic conditions. Whereas the fraction of Na salts (NaCl + Na₂SO₄) exceeds that of Ca salts (CaSO₄+ CaCO₃) during the Holocene (0.6–11.7 kyr B.P.), the two fractions are similar during the Bølling-Allerød period (12.9–14.6 kyr B.P.). During cold climate such as over the Younger Dryas (12.0–12.6 kyr B.P.) and the Last Glacial Maximum (15.0–26.9 kyr B.P.), the fraction of Ca salts exceeds that of Na salts, showing that the most abundant ion generally controls the salt budget in each period. High-resolution analyses reveal changing particle compositions: those in Holocene ice show seasonal changes, and those in LGM ice show a difference between cloudy bands and clear layers, which again can be largely explained by the availability of ionic components in the atmospheric aerosol body of air masses reaching Greenland.

A continuous high-resolution record of digital images has been obtained from the North Greenland Ice Core Project (NorthGRIP) ice core (75.1°N, 42.3°W) in the depth interval from 1330 m to the bedrock at 3085 m. The ice core stratigraphy is clearly visible throughout the glacial period with the most frequent and brightest visible layers appearing during the coldest events. Down to a depth of 2600 m the horizontal layering is very regular; below this depth, small irregularities in the layering start to appear, and below 2800 m the visual stratigraphy becomes more uncertain, perhaps because of penetration into climatically warmer ice. Comparison of the visual stratigraphy with high-resolution continuous records of chemical impurities and dust reveals a high degree of correlation, which indicates that the visible layers are caused by these impurities. A new approach is used to automatically determine annual layer thicknesses from the visual stratigraphy record by carrying out a frequency analysis of the most prominent visible layers in the profile. The result gives strong support for the NorthGRIP timescale model.

The disturbed stratigraphy of the ice in the lowest 10% of the Greenland GRIP ice core prevents direct access to climatic information older than 110 kyr. This is especially regretful since this period covers the previous interglacial corresponding to marine isotopic stage 5e (MIS 5e, 130–120 kyr B.P.). Here we present a tentative reconstruction of the disturbed GRIP chronology based on the succession of globally well mixed gas parameters. The GRIP δ18Oice chronological sequence is obtained by comparing a new set of δ18O of atmospheric O2 and CH4 measurements from the bottom section of the GRIP core with their counterpart in the Vostok Antarctic profiles. This comparison clearly identifies ice from the penultimate glacial maximum (MIS 6, 190–130 kyr B.P.) in the GRIP core. Further it allows rough reconstruction of the last interglacial period and of the last glacial inception in Greenland which appears to lay its Antarctic counterpart. Our data suggest that while Antarctica is already entering into a glaciation, Greenland is still experiencing a warm maximum during MIS 5e.