Publications by authors named "Robert C Finkel"

The Greenland Ice Sheet (GIS) contains the equivalent of 7.4 metres of global sea-level rise. Its stability in our warming climate is therefore a pressing concern.

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Greenland ice cores reveal that mean annual temperatures during the Younger Dryas (YD) cold interval--about 12.9 to 11.7 thousand years ago (ka)--and the ~150-year-long cold reversal that occurred 8.

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Millennial-scale cold reversals in the high latitudes of both hemispheres interrupted the last transition from full glacial to interglacial climate conditions. The presence of the Younger Dryas stadial (approximately 12.9 to approximately 11.

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Understanding the timings of interhemispheric climate changes during the Holocene, along with their causes, remains a major problem of climate science. Here, we present a high-resolution 10Be chronology of glacier fluctuations in New Zealand's Southern Alps over the past 7000 years, including at least five events during the last millennium. The extents of glacier advances decreased from the middle to the late Holocene, in contrast with the Northern Hemisphere pattern.

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The local last glacial maximum in the tropical Andes was earlier and less extensive than previously thought, based on 106 cosmogenic ages (from beryllium-10 dating) from moraines in Peru and Bolivia. Glaciers reached their greatest extent in the last glacial cycle approximately 34,000 years before the present and were retreating by approximately 21,000 years before the present, implying that tropical controls on ice volumes were asynchronous with those in the Northern Hemisphere. Our estimates of snowline depression reflect about half the temperature change indicated by previous widely cited figures, which helps resolve the discrepancy between estimates of terrestrial and marine temperature depression during the last glacial cycle.

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A method using accelerator mass spectrometry (AMS) has been developed for quantifying attomoles of beryllium (Be) in biological samples. This method provides the sensitivity to trace Be in biological samples at very low doses with the purpose of identifying the molecular targets involved in chronic beryllium disease. Proof of the method was tested by administering 0.

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