We have determined the production yields for radionuclides in Al2O3, SiO2, S, Ar, K2SO4, CaCO3, Fe, Ni and Cu targets, which were irradiated with slow negative muons at the Paul Scherrer Institute in Villigen (Switzerland). The fluences of the stopped negative muons were determined by measuring the muonic X-rays. The concentrations of the long-lived and short-lived radionuclides were measured with accelerator mass spectrometry (AMS) and γ-spectroscopy, respectively. Special emphasis was put on the radionuclides 10Be, 14C and 26Al produced in quartz targets, 26Al in Al2O3 and S targets, 36Cl in K2SO4 and CaCO3 targets, and 53Mn in Fe2O3 targets. These targets were selected because they are also the naturally occurring target minerals for cosmic ray interactions in typical rocks. We also present results of calculations for depth-dependent production rates of radionuclides produced after cosmic ray μ− capture, as well as cosmic ray-induced production rates of geologically relevant radionuclides produced by the nucleonic component, by μ− capture, by fast muons and by neutron capture. 相似文献
Natural production of the radionuclide chlorine-36 (36Cl) has provided a valuable tracer for groundwater studies. The nuclear industry, especially the testing of thermonuclear
weapons, has also produced large amounts of 36Cl that can be detected in many samples of groundwater. In order to be most useful in hydrologic studies, the natural production
prior to 1952 should be distinguished from more recent artificial sources. The object of this study was to reconstruct the
probable preanthropogenic levels of 36Cl in groundwater in the United States. Although significant local variations exist, they are superimposed on a broad regional
pattern of 36Cl/Cl ratios in the United States. Owing to the influence of atmospherically transported ocean salt, natural ratios of 36Cl/total Cl are lowest near the coast and increase to a maximum in the central Rocky Mountains of the United States.
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We have measured the concentration of in situ produced cosmogenic 10Be and 26Al from bare bedrock surfaces on summit flats in four western U.S. mountain ranges. The maximum mean bare-bedrock erosion rate from these alpine environments is 7.6 ± 3.9 m My−1. Individual measurements vary between 2 and 19 m My−1. These erosion rates are similar to previous cosmogenic radionuclide (CRN) erosion rates measured in other environments, except for those from extremely arid regions. This indicates that bare bedrock is not weathered into transportable material more rapidly in alpine environments than in other environments, even though frost weathering should be intense in these areas. Our CRN-deduced point measurements of bedrock erosion are slower than typical basin-averaged denudation rates ( 50 m My−1). If our measured CRN erosion rates are accurate indicators of the rate at which summit flats are lowered by erosion, then relief in the mountain ranges examined here is probably increasing.
We develop a model of outcrop erosion to investigate the magnitude of errors associated with applying the steady-state erosion model to episodically eroding outcrops. Our simulations show that interpreting measurements with the steady-state erosion model can yield erosion rates which are either greater or less than the actual long-term mean erosion rate. While errors resulting from episodic erosion are potentially greater than both measurement and production rate errors for single samples, the mean value of many steady-state erosion rate measurements provides a much better estimate of the long-term erosion rate. 相似文献