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Measurements were conducted to determine the carbonyl sulfide levels in ancient air preserved in the Greenland ice sheet using samples from the GISP2D and GISP2B ice cores from Summit, Greenland. The GISP2D is a fluid-drilled core and the GISP2B is a dry-drilled core. This data set includes four CSV files. Most of the measurements are from the GISP2D ice core and 3 out of the 4 data files associated with this submission include data from the GISP2D. Both dry and wet extraction methods were used to extract the ice core air. All dry extraction-based GISP2D data are presented in one file. The wet extraction-based data are split between 3 data files: 1) GISP2B data, 2) shallow GISP2D data, 3) deep GISP2D data. The shallow and deep wet extraction-based GISP2D data are presented in 2 separate files despite including some overlapping depths because the measurements were conducted over different time periods. All data are depth-coded and presented "as measured" with associated 1 sigma uncertainties after having gone through a preliminary quality control and having been finalized in terms of calibration. Note that the wet extraction-based measurements require a solubility correction before they can be compared with the dry extraction-based measurements from the same depths. 

Abstract. Carbonyl sulfide (COS) is the most abundant sulfur gas in the atmosphere with links to terrestrial and oceanic productivity. We measured COS in ice core air from an intermediate-depth ice core from the South Pole using both dry and wet extraction methods, recovering a 52 500-year record. We find evidence for COS production in the firn, altering the atmospheric signal preserved in the ice core. Mean sea salt aerosol concentrations from the same depth are a good proxy for the COS production, which disproportionately impacts the measurements from glacial period ice with high sea salt aerosol concentrations. The COS measurements are corrected using sea salt sodium (ssNa) as a proxy for the excess COS resulting from the production. The ssNa-corrected COS record displays substantially less COS in the glacial period atmosphere than the Holocene and a 2 to 4-fold COS rise during the deglaciation synchronous with the associated climate signal. The deglacial COS rise was primarily source driven. Oceanic emissions in the form of COS, carbon disulfide (CS2), and dimethylsulfide (DMS) are collectively the largest natural source of atmospheric COS. A large increase in ocean COS emissions during the deglaciation suggests enhancements in emissions of ocean sulfur gases via processes that involve ocean productivity, although we cannot quantify individual contributions from each gas. 

The atmospheric history of molecular hydrogen (H 2 ) from 1852 to 2003 was reconstructed from measurements of firn air collected at Megadunes, Antarctica. The reconstruction shows that H 2 levels in the southern hemisphere were roughly constant near 330 parts per billion (ppb; nmol H 2 mol −1 air) during the mid to late 1800s. Over the twentieth century, H 2 levels rose by about 70% to 550 ppb. The reconstruction shows good agreement with the H 2 atmospheric history based on firn air measurements from the South Pole. The broad trends in atmospheric H 2 over the twentieth century can be explained by increased methane oxidation and anthropogenic emissions. The H 2 rise shows no evidence of deceleration during the last quarter of the twentieth century despite an expected reduction in automotive emissions following more stringent regulations. During the late twentieth century, atmospheric CO levels decreased due to a reduction in automotive emissions. It is surprising that atmospheric H 2 did not respond similarly as automotive exhaust is thought to be the dominant source of anthropogenic H 2. The monotonic late twentieth century rise in H 2 levels is consistent with late twentieth-century flask air measurements from high southern latitudes. An additional unknown source of H 2 is needed to explain twentieth-century trends in atmospheric H 2 and to resolve the discrepancy between bottom-up and top-down estimates of the anthropogenic source term. The firn air–based atmospheric history of H 2 provides a baseline from which to assess human impact on the H 2 cycle over the last 150 y and validate models that will be used to project future trends in atmospheric composition as H 2 becomes a more common energy source. 

Biomass burning drives changes in greenhouse gases, climate-forcing aerosols, and global atmospheric chemistry. There is controversy about the magnitude and timing of changes in biomass burning emissions on millennial time scales from preindustrial to present and about the relative importance of climate change and human activities as the underlying cause. Biomass burning is one of two notable sources of ethane in the preindustrial atmosphere. Here, we present ice core ethane measurements from Antarctica and Greenland that contain information about changes in biomass burning emissions since 1000 CE (Common Era). The biomass burning emissions of ethane during the Medieval Period (1000–1500 CE) were higher than present day and declined sharply to a minimum during the cooler Little Ice Age (1600–1800 CE). Assuming that preindustrial atmospheric reactivity and transport were the same as in the modern atmosphere, we estimate that biomass burning emissions decreased by 30 to 45% from the Medieval Period to the Little Ice Age. The timing and magnitude of this decline in biomass burning emissions is consistent with that inferred from ice core methane stable carbon isotope ratios but inconsistent with histories based on sedimentary charcoal and ice core carbon monoxide measurements. This study demonstrates that biomass burning emissions have exceeded modern levels in the past and may be highly sensitive to changes in climate. 

Abstract An intermediate-depth (1751 m) ice core was drilled at the South Pole between 2014 and 2016 using the newly designed US Intermediate Depth Drill. The South Pole ice core is the highest-resolution interior East Antarctic ice core record that extends into the glacial period. The methods used at the South Pole to handle and log the drilled ice, the procedures used to safely retrograde the ice back to the National Science Foundation Ice Core Facility (NSF-ICF), and the methods used to process and sample the ice at the NSF-ICF are described. The South Pole ice core exhibited minimal brittle ice, which was likely due to site characteristics and, to a lesser extent, to drill technology and core handling procedures. 

Abstract A large volcanic sulfate increase observed in ice core records around 1450 C.E. has been attributed in previous studies to a volcanic eruption from the submarine Kuwae caldera in Vanuatu. Both EPMA–WDS (electron microprobe analysis using a wavelength dispersive spectrometer) and SEM–EDS (scanning electron microscopy analysis using an energy dispersive spectrometer) analyses of five microscopic volcanic ash (cryptotephra) particles extracted from the ice interval associated with a rise in sulfate ca. 1458 C.E. in the South Pole ice core (SPICEcore) indicate that the tephra deposits are chemically distinct from those erupted from the Kuwae caldera. Recognizing that the sulfate peak is not associated with the Kuwae volcano, and likely not a large stratospheric tropical eruption, requires revision of the stratospheric sulfate injection mass that is used for parameterization of paleoclimate models. Future work is needed to confirm that a volcanic eruption from Mt. Reclus is one of the possible sources of the 1458 C.E. sulfate anomaly in Antarctic ice cores. 

Abstract Biomass burning is an important component of the Earth system in terms of global biogeochemistry, atmospheric composition, climate, terrestrial ecology, and land use. This study examines published ice core trace gas measurements of acetylene, ethane, and methane, which have been used as proxies for paleofire emissions. We investigate the consistency of these records for the past 1,000 years in terms of (1) temporal trends in global fire emissions and (2) quantitative estimates for changes in global burning (dry matter burned per year). Three‐dimensional transport and box models were used to construct emissions scenarios for the trace gases consistent with each ice core record. Burning histories were inferred from trace gas emissions by accounting for biome‐specific emission factors for each trace gas. The temporal trends in fire inferred from the trace gases are in reasonable agreement, with a large decline in biomass burning emissions from the Medieval Period (MP: 1000–1500 CE) to the Little Ice Age (LIA: 1650–1750 CE). However, the three trace gas ice core records do not yield a consistent fire history, even assuming dramatic (and unrealistic) changes in the spatial distribution of fire and biomes. Substantial changes in other factors such as meteorological transport or atmospheric photochemical lifetimes appear to be required to reconcile the trace gas records. 

Abstract. The South Pole Ice Core (SPICEcore) was drilled in 2014–2016 to provide adetailed multi-proxy archive of paleoclimate conditions in East Antarcticaduring the Holocene and late Pleistocene. Interpretation of these recordsrequires an accurate depth–age relationship. Here, we present the SPICEcore (SP19) timescale for the age of the ice of SPICEcore. SP19 is synchronized to theWD2014 chronology from the West Antarctic Ice Sheet Divide (WAIS Divide) icecore using stratigraphic matching of 251 volcanic events. These eventsindicate an age of 54 302±519 BP (years before 1950) at thebottom of SPICEcore. Annual layers identified in sodium and magnesium ionsto 11 341 BP were used to interpolate between stratigraphic volcanic tiepoints, yielding an annually resolved chronology through the Holocene.Estimated timescale uncertainty during the Holocene is less than 18 yearsrelative to WD2014, with the exception of the interval between 1800 to 3100BP when uncertainty estimates reach ±25 years due to widely spacedvolcanic tie points. Prior to the Holocene, uncertainties remain within 124 years relative to WD2014. Results show an average Holocene accumulation rateof 7.4 cm yr−1 (water equivalent). The time variability of accumulation rateis consistent with expectations for steady-state ice flow through the modernspatial pattern of accumulation rate. Time variations in nitrateconcentration, nitrate seasonal amplitude and δ15N of N2 in turn are as expected for the accumulation rate variations. The highlyvariable yet well-constrained Holocene accumulation history at the site canhelp improve scientific understanding of deposition-sensitive climateproxies such as δ15N of N2 and photolyzed chemicalcompounds.