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The Mount Johns (MJ) ice core (79°55′ S; 94°23′ W) was drilled near the Pine Island Glacier ice divide on the West Antarctic Ice Sheet during the 2008-2009 austral summer, to a depth of 92.26 m. The upper 45m of the record covers approximately 125 years (1883-2008), showing marked seasonal variability. Trace element concentrations in 2137 samples were determined using inductively coupled plasma mass spectrometry. In this study, we reconstruct mineral dust and sea salt aerosol transport and investigate the influence of climate variables on the elemental concentrations at the MJ site. The ice core record reflects changes in emissions as well as atmospheric circulation and transport processes. Our trajectory analysis shows distinct seasonality, with strong westerly transport in the winter months and secondary northeasterly transport in the summer. During summer months, the trajectories present slow-moving (short) transport and are more locally influenced than in other seasons. Finally, our reanalysis correlations with trace element suggest that marine-derived trace element concentrations are strongly influenced by sea ice concentration and sea surface temperature anomalies. The results show that seasonal elemental concentration maxima in sea salt elements correlate well with the sea ice concentration winter maxima in the west Amundsen and Ross seas. Lastly, we observed an increased concentration of marine aerosols when sea surface temperature decreased. [ABSTRACT FROM AUTHOR]

An ice core, 92.26 m in length, was collected near the ice divide of the West Antarctica ice sheet during the 2008/2009 austral summer. This paper described the fieldwork at the Mount Johns site (79°55'S; 94°23'W) and presented the first results of the upper 45.00 m record covering approximately 125 years (1883 - 2008), dated by annual layer counting and volcanic reference horizons. Trace element concentrations in 2,137 samples were determined using inductively coupled plasma mass spectrometry. The concentrations obtained for Al, Ba, Ca, Fe, K, Mg, Mn, Na, Sr and Ti are controlled by climate variations, the transport distance, and the natural sources of these aerosols. Natural dust contributions, mainly derived from the arid areas of Patagonia and Australia, are important sources for aluminum, barium, iron, manganese and titanium. Marine aerosols from sea ice and transported by air masses are important sources of sodium and magnesium. Calcium, potassium and strontium showed considerable inputs of both continental dust and marine aerosols. [ABSTRACT FROM AUTHOR]

Arsenic variability records are preserved in snow and ice cores and can be utilized to reconstruct air pollution history. The Mount Johns ice core (79°55′S; 94°23′W and 91.2 m depth) was collected from the West Antarctic Ice Sheet in the 2008/09 austral summer. Here, we report the As concentration variability as determined by 2137 samples from the upper 45 m of this core using ICP-SFMS (CCI, University of Maine, USA). The record covers approximately 125 years (1883–2008) showing a mean concentration of 4.32 pg g −1 . The arsenic concentration in the core follows global copper mining evolution, particularly in Chile (the largest producer of Cu). From 1940 to 1990, copper-mining production increased along with arsenic concentrations in the MJ core, from 1.92 pg g −1 (before 1900) to 7.94 pg g −1 (1950). In the last two decades, environmental regulations for As emissions have been implemented, forcing smelters to treat their gases to conform to national and international environmental standards. In Chile, decontamination plants required by the government started operating from 1993 to 2000. Thereafter, Chilean copper production more than doubled while As emission levels declined, and the same reduction was observed in the Mount Johns ice core. After 1999, arsenic concentrations in our samples decreased to levels comparable to the period before 1900. [ABSTRACT FROM AUTHOR]

Shallow firn cores, in addition to a near-basal ice core, were recovered in 2018 from the Quelccaya ice cap (5470 m a.s.l) in the Cordillera Vilcanota, Peru, and in 2017 from the Nevado Illimani glacier (6350 m a.s.l) in the Cordillera Real, Bolivia. The two sites are ~450 km apart. Despite meltwater percolation resulting from warming, particle-based trace element records (e.g. Fe, Mg, K) in the Quelccaya and Illimani shallow cores retain well-preserved signals. The firn core chronologies, established independently by annual layer counting, show a convincing overlap indicating the two records contain comparable signals and therefore capture similar regional scale climatology. Trace element records at a ~1–4 cm resolution provide past records of anthropogenic emissions, dust sources, volcanic emissions, evaporite salts and marine-sourced air masses. Using novel ultra-high-resolution (120 μm) laser technology, we identify annual layer thicknesses ranging from 0.3 to 0.8 cm in a section of 2000-year-old radiocarbon-dated near-basal ice which compared to the previous annual layer estimates suggests that Quelccaya ice cores drilled to bedrock may be older than previously suggested by depth-age models. With the information collected from this study in combination with past studies, we emphasize the importance of collecting new surface-to-bedrock ice cores from at least the Quelccaya ice cap, in particular, due to its projected disappearance as soon as the 2050s. [ABSTRACT FROM AUTHOR]