Electromechanical drilling of a 300 m core in a dry hole at Summit, Greenland

During the EUROCORE project in 1989 at Summit, Central Greenland, a 304.8-m long ice core of 105mm diameter was retrieved with an electromechanical drill. A dry drilling technique was used in order to minimise contamination of the ice. A special drill head with a small chipping depth was designed to assure minimal fracturing of the core. The quality was excellent to the depth of 180m, but then deteriorated due to increasing brittleness of the ice. Down to 280m we were able to maintain the mean length of unbroken core pieces above 0.1m by reducing the pitch from 7 to 2mm. The sticking of the consequently finer chips to the drill barrels was reduced by treating the barrels repeatedly with a silicone-based wax solution. Hole enlargement cutters near the upper end of the drill head prevented the drill from becoming stuck due to borehole closure

Atmospheric abundance and global emissions of perfluorocarbons CF4, C2F6 and C3F8 since 1800 inferred from ice core, firn, air archive and in situ measurements

Perfluorocarbons (PFCs) are very potent and long-lived greenhouse gases in the atmosphere, released predominantly during aluminium production and semiconductor manufacture. They have been targeted for emission controls under the United Nations Framework Convention on Climate Change. Here we present the first continuous records of the atmospheric abundance of CF4 (PFC-14), C2F6 (PFC-116) and C3F8 (PFC-218) from 1800 to 2014. The records are derived from high-precision measurements of PFCs in air extracted from polar firn or ice at six sites (DE08, DE08-2, DSSW20K, EDML, NEEM and South Pole) and air archive tanks and atmospheric air sampled from both hemispheres. We take account of the age characteristics of the firn and ice core air samples and demonstrate excellent consistency between the ice core, firn and atmospheric measurements. We present an inversion for global emissions from 1900 to 2014. We also formulate the inversion to directly infer emission factors for PFC emissions due to aluminium production prior to the 1980s. We show that 19th century atmospheric levels, before significant anthropogenic influence, were stable at 34.1 ± 0.3 ppt for CF4 and below detection limits of 0.002 and 0.01 ppt for C2F6 and C3F8, respectively. We find a significant peak in CF4 and C2F6 emissions around 1940, most likely due to the high demand for aluminium during World War II, for example for construction of aircraft, but these emissions were nevertheless much lower than in recent years. The PFC emission factors for aluminium production in the early 20th century were significantly higher than today but have decreased since then due to improvements and better control of the smelting process. Mitigation efforts have led to decreases in emissions from peaks in 1980 (CF4) or early-to-mid-2000s (C2F6 and C3F8) despite the continued increase in global aluminium production; however, these decreases in emissions appear to have recently halted. We see a temporary reduction of around 15 % in CF4 emissions in 2009, presumably associated with the impact of the global financial crisis on aluminium and semiconductor production

Newly detected ozone-depleting substances in the atmosphere

Ozone-depleting substances emitted through human activitiescause large-scale damage to the stratospheric ozone layer, and influence global climate. Consequently, the production of many of these substances has been phased out; prominent examples are the chlorofluorocarbons (CFCs), and their intermediate replacements, the hydrochlorofluorocarbons (HCFCs). So far, seven types of CFC and six types of HCFC have been shown to contribute to stratospheric ozone destruction 1,2. Here, we report the detection and quantification of a further three CFCs and one HCFC. We analysed the composition of unpolluted air samples collected in Tasmania between 1978 and 2012, and extracted from deep firn snow in Greenland in 2008, using gas chromatography with mass spectrometric detection. Using the firn data, we show that all four compounds started to emerge in the atmosphere in the 1960s. Two of the compounds continue to accumulate in the atmosphere. We estimate that, before 2012, emissions of all four compounds combined amounted to more than 74,000 tonnes. This is small compared with peak emissions of other CFCs in the 1980s of more than one million tonnes each year 2. However, the reported emissions are clearly contrary to the intentions behind the Montreal Protocol, and raise questions about the sources of these gases

Dome C age scale EDC1 for ice core EDC99

A tentative age scale (EDC1) for the last 45 kyr is established for the new 788 m EPICA Dome C ice core using a simple ice flow model. The age of volcanic eruptions, the end of the Younger Dryas event, and the estimated depth and age of elevated 10Be, about 41 kyr ago were used to calibrate the model parameters. The uncertainty of EDC1 is estimated to ±10 yr for 0 to 700 yr BP, up to ±200 yr back to 10 kyr BP, and up to ±2 kyr back to 41 kyr BP. The age of the air in the bubbles is calculated with a firn densification model. In the Holocene the air is about 2000 yr younger than the ice and about 5500 yr during the last glacial maximum

The transformation of snow to ice and the occlusion of gases

The gases enclosed in the bubbles of glacier ice represent samples of the atmosphere approximately from the time of bubble formation. The age of this air is different from the surrounding ice. Also, the age cannot be given by a simple value but is described by an age distribution. This age distribution is determined by the mixing in the permeable firn layer and the air trapping rate at the firn-ice transition. At present it is possible to estimate the age distribution, using model calculations, in special cases. More data. especially on the spatial variability of the air permeability and diffusivity in the firn, are needed to permit modeling of more general cases. Tracer experiments would be a further possibility to assess the age of the air in the bubbles of ice. Due to physical and chemical processes, the concentrations of the gases in the bubbles may differ from the atmospheric concentrations. Apparently the gas compositions in bubbles of very cold glaciers (no surface melting during summer) do not differ from samples of the atmosphere