We present a brief discussion of sample preparation procedures at the Keck Carbon Cycle Accelerator Mass Spectrometer (KCCAMS), University of California, Irvine, and a systematic investigation of the use of Mg(ClO4)2 as an absorptive water trap, replacing the standard dry ice/ethanol cold finger in graphite sample preparation. We compare high-precision AMS measurement results from oxalic acid I and USGS coal samples using Mg(ClO4)2 under different conditions. The results obtained were also compared with those achieved using the conventional water removal technique. Final results demonstrate that the use of Mg(ClO4)2 as an alternative water trap seems very convenient and reliable, provided the Mg(ClO4)2 is replaced frequently.
ABSTRACT.A new radiocarbon accelerator mass spectrometry (AMS) laboratory for carbon cycle studies has been established at the University of California, Irvine. The 0.5MV AMS system was installed in mid-2002 and has operated routinely since October of that year. This paper briefly describes the spectrometer and summarizes lessons learned during the first year of operation. In the process of setting up the system, we identified and largely suppressed a previously unreported 14 C AMS background: charge exchange tails from 14 N beams derived from nitrogen-containing molecular ions produced near the entrance of the accelerator.
ABSTRACT. Primary and secondary standards are essential in radiocarbon analyses for the purpose of reporting and comparing data among laboratories, as well as for internal laboratory data quality control. ANU sucrose is one of the IAEA-certified 14 C standards (C-6) with a consensus value of 1.5061 ± 0.0011 fraction modern (Fm). All of our measurements of ANU sucrose (n = 351) as a secondary standard over the last 7 yr result in an average value of 1.5016 ± 0.0005 Fm (2- standard error). After applying the same outlier tests used for IAEA reference standards, a weighted average value of 1.5016 ± 0.0002 Fm (n = 294) was calculated. This value is significantly lower than the IAEA C-6 consensus value (t test with unequal variance; p=0.023). In contrast, our measurements of other secondary standards over the same time period are in excellent agreement with their respective consensus values. Since ANU is the only secondary standard measured in our lab that does not agree with the consensus values, and we have measured a larger number analyses compared to what went into the definition of the consensus value, we suggest that the consensus value of ANU sucrose might be too high by ~0.0045 ± 0.0011 Fm. Given that some labs routinely use ANU sucrose as a primary standard, our results suggest that revisiting the consensus value of ANU sucrose may be necessary.
Radiocarbon (Δ14C) measurements of monthly samples from a Galapagos surface coral are among the first data sets from the new Keck Carbon Cycle Accelerator Mass Spectrometry laboratory at the University of California, Irvine. An average Δ14C value of −62 is obtained for 144 measurements of samples from monthly coral bands that lived from about AD 1760–1771 (±6 yr). High Δ14C values were found during January through March, when upwelling was weak or absent at the Galapagos Islands. Low Δ14C values were obtained mid-year during strong upwelling. The average seasonal variability of Δ14C was 15–25, which is greater than that at other tropical and subtropical locations in the Pacific Ocean because of intense seasonal upwelling at this site. Periods of sustained high Δ14C values were found during 1762–1763 and 1766. A spectral analysis revealed that the spectral density for the Δ14C data displays most of its variance at the 5-yr cycle, which is reflective of El Niño periodicity during the 20th century.
Annual samples from two Palmyra Atoll corals (Porites lutea) that lived during the past 110 years were analyzed for radiocarbon (D 14 C) and d 18 O. The D 14 C values decreased 7.6& from 1896 to 1953, similar to other coral records from the tropical and subtropical Pacific. D 14 C values rose from $À60& to $+110& by 1980 due to the input of bomb radiocarbon from the atmosphere. Elevated D 14 C values were observed for the mid-to late-1950s, suggesting early input of bomb radiocarbon, possibly from the largest Marshall Islands bomb tests in 1954. Secondary aragonite precipitation was identified in a portion of one core using scanning electron microscopy and X-radiography, and was responsible for high d 18 O and d 13 C values and a correlation between them. The D 14 C results were more resistant to alteration, except when contamination was from the bomb era (>1956).
We report ∆14C measurements of cellulose extracted from near monthly tree ring growth for the 1960s of a white oak that grew in western Oregon, USA. Comparison with ∆14C measurements of atmospheric CO2 reveals that the tree ring ∆14C values were equal to or lower than those in atmospheric CO2 at the time of ring formation. We suggest that the low tree ring ∆14C values during the period 1962–1963 were caused by the presence of an atmospheric front or blocking between subpolar and temperate air masses that delayed the arrival of the bomb signal at the tree’s site.
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