Inger K Seierstad

A synchronized dating of three Greenland ice cores throughout the Holocene

As part of the effort to create the new Greenland Ice Core Chronology 2005 (GICC05) a synchronized stratigraphical timescale for the Holocene parts of the DYE- 3, GRIP and NGRIP ice cores is made by using volcanic reference horizons in electri- cal conductivity measurements to match the cores. The main annual layer counting is carried out on the most suited records only, exploit- ing that the three ice cores have been drilled at locations with different climatic con- ditions and differences in ice flow. However, supplemental counting on data from all cores has been performed between each set of reference horizons in order to verify the valid- ity of the match. After the verification, the main dating is transferred to all records us- ing the volcanic reference horizons as tie points. An assessment of the mean annual layer thickness in each core section confirms that the new synchronized dating is consistent for all three cores. The data used for the main annual layer counting of the past 7900 years are the DYE- 3, GRIP and NGRIP stable isotope records. As the high accumulation rate at the DYE- 3 drill site makes the seasonal cycle in the DYE-3 stable isotopes very resistant to firn diffusion, an effort has been made to extend the DYE-3 Holocene record. The new syn- chronized dating relies heavily on this record of �75,000 stable isotope samples. The dat- ing of the early Holocene consists of an already established part of GICC05 for GRIP and NGRIP which has now been transferred to the DYE-3 core. GICC05 dates the Younger Dryas termination, as defined from deuterium excess, to 11,703 b2k; 130 years earlier than the previous GRIP dating.

The duration of the Bølling-Allerød period (Greenland Interstadial 1) in the GRIP ice core

Abstract A new dating of the Bølling-Allerød period (Greenland Interstadial event 1) in the GRIP ice core is presented. Newly measured profiles of δD and δ18O, as well as existing profiles of Ca2+, NH4 +, dust and NO3–, have been used for the dating. As seasonal variations can be observed in all six components, it was possible to simultaneously count annual layers in the profiles in order to obtain a multi-parameter dating. The new data presented in this study include a total of 36.85 m of stable-isotope profiles of 1 cm resolution from five sections of the Bølling-Allerød period in the GRIP ice core. The annual-layer counting suggests a duration of the complete Bølling-Allerød period, as revealed in the GRIP ice core, of 1627 ± 52 years. This estimate contrasts with an earlier finding from the same GRIP ice core, where the Bølling-Allerød was found to span 2168 years (Hammer, in press). This estimate was based on layer counting, using dust concentrations only.

Greenland records of aerosol source and atmospheric lifetime changes from the Eemian to the Holocene

The Northern Hemisphere experienced dramatic changes during the last glacial, featuring vast ice sheets and abrupt climate events, while high northern latitudes during the last interglacial (Eemian) were warmer than today. Here we use high-resolution aerosol records from the Greenland NEEM ice core to reconstruct the environmental alterations in aerosol source regions accompanying these changes. Separating source and transport effects, we find strongly reduced terrestrial biogenic emissions during glacial times reflecting net loss of vegetated area in North America. Rapid climate changes during the glacial have little effect on terrestrial biogenic aerosol emissions. A strong increase in terrestrial dust emissions during the coldest intervals indicates higher aridity and dust storm activity in East Asian deserts. Glacial sea salt aerosol emissions in the North Atlantic region increase only moderately (50%), likely due to sea ice expansion. Lower aerosol concentrations in Eemian ice compared to the Holocene are mainly due to shortened atmospheric residence time, while emissions changed little.Past climate changes in Greenland ice were accompanied by large aerosol concentration changes. Here, the authors show that by correcting for transport effects, reliable source changes for biogenic aerosol from North America, sea salt aerosol from the North Atlantic, and dust from East Asian deserts can be derived.