scholarly journals Ages and ablation and accumulation rates from 14C measurements on Antarctic ice

1995 ◽  
Vol 21 ◽  
pp. 139-143 ◽  
Author(s):  
J.J. Van Roijen ◽  
K. van der Borg ◽  
A.F.M. De Jong ◽  
J. Oerlemans

Shallow ice cores from an Antarctic blue-ice area at Scharffenbergbotnen were l4C-analyzed using a dry-extraction technique and accelerator mass spectrometry. The in situ production was determined from the 14CO component and used to deduce the natural 14CO2 component. The ages were measured at 10 000 ± 3000 BP. The accumulation and ablation rates determined from the in situ production are 7–20 and 10 cm a−1. respectively, showing agreement with field observations. The derived ages and air-yield data show a nearby origin for the surface ice.

1995 ◽  
Vol 21 ◽  
pp. 139-143 ◽  
Author(s):  
J.J. Van Roijen ◽  
K. van der Borg ◽  
A.F.M. De Jong ◽  
J. Oerlemans

Shallow ice cores from an Antarctic blue-ice area at Scharffenbergbotnen were l4C-analyzed using a dry-extraction technique and accelerator mass spectrometry. The in situ production was determined from the 14CO component and used to deduce the natural 14CO2 component. The ages were measured at 10 000 ± 3000 BP. The accumulation and ablation rates determined from the in situ production are 7–20 and 10 cm a−1. respectively, showing agreement with field observations. The derived ages and air-yield data show a nearby origin for the surface ice.


Radiocarbon ◽  
1992 ◽  
Vol 34 (3) ◽  
pp. 431-435 ◽  
Author(s):  
A. T. Wilson ◽  
D. J. Donahue

In the “sublimation technique,” carbon dioxide entrapped in ice is recovered by sublimation, converted to graphite and ratio of 14C/13C in the CO2 determined by AMS measurements. We describe here several experiments performed to check the validity of such measurements and to study the effect of cosmogenically produced in-situ14C on the measurements.


Radiocarbon ◽  
1986 ◽  
Vol 28 (2A) ◽  
pp. 556-560 ◽  
Author(s):  
N J Conard ◽  
David Elmore ◽  
P W Kubik ◽  
H E Gove ◽  
L E Tubbs ◽  
...  

A method of chemical separation and purification of chloride from relatively small samples (500 to 2100g) of glacial ice is presented. With this procedure the first successful measurements of pre-bomb levels of 36Cl in Greenland ice have been made. Emphasis is placed on methods of reducing sulfur, which causes interference in the accelerator mass spectrometry, and in maximizing the yield. Data regarding the selection of materials for sample holders and the use of metal powders for extending the lifetime of the sample are also presented.


2012 ◽  
Vol 78 (15) ◽  
pp. 5070-5076 ◽  
Author(s):  
Marek Stibal ◽  
Jacob Bælum ◽  
William E. Holben ◽  
Sebastian R. Sørensen ◽  
Anders Jensen ◽  
...  

ABSTRACTThe Greenland ice sheet (GrIS) receives organic carbon (OC) of anthropogenic origin, including pesticides, from the atmosphere and/or local sources, and the fate of these compounds in the ice is currently unknown. The ability of supraglacial heterotrophic microbes to mineralize different types of OC is likely a significant factor determining the fate of anthropogenic OC on the ice sheet. Here we determine the potential of the microbial community from the surface of the GrIS to mineralize the widely used herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). Surface ice cores were collected and incubated for up to 529 days in microcosms simulatingin situconditions. Mineralization of side chain- and ring-labeled [14C]2,4-D was measured in the samples, and quantitative PCR targeting thetfdAgenes in total DNA extracted from the ice after the experiment was performed. We show that the supraglacial microbial community on the GrIS contains microbes that are capable of degrading 2,4-D and that they are likely present in very low numbers. They can mineralize 2,4-D at a rate of up to 1 nmol per m2per day, equivalent to ∼26 ng C m−2day−1. Thus, the GrIS should not be considered a mere reservoir of all atmospheric contaminants, as it is likely that some deposited compounds will be removed from the system via biodegradation processes before their potential release due to the accelerated melting of the ice sheet.


Radiocarbon ◽  
2016 ◽  
Vol 58 (2) ◽  
pp. 419-435 ◽  
Author(s):  
C Welte ◽  
L Wacker ◽  
B Hattendorf ◽  
M Christl ◽  
J Koch ◽  
...  

AbstractConventional radiocarbon analysis of carbonate records with accelerator mass spectrometry (AMS) is time consuming and the achievable spatial resolution is limited, because individual samples have to be taken and need to be converted to graphite for the measurement. A new laser ablation (LA) in situ sampling technique for rapid online 14C analyses of carbonate records by AMS is presented. By focusing a 193-nm ArF excimer laser on carbonate samples, carbon dioxide is generated and can directly be introduced into the gas ion source of an AMS. A dedicated LA cell for AMS was constructed in a way that combines rapid gas exchange with the capacity to carry sample specimen with maximum dimensions of 15×2.5×1.5 cm3. With the presented setup, negative carbon ion currents up to 20 µA were achieved. A low 14C background of 0.011±0.002 F14C was observed on 14C-free marble and different standard and reference materials could be well reproduced within errors. The novel technique allows scanning carbonate samples continuously over several cm per hour with achievable measurement precisions of less than 1% for modern samples. This approach allows acquiring highly spatially resolved 14C records at a far higher rate than with any currently available method.


2013 ◽  
Vol 9 (3) ◽  
pp. 2471-2487
Author(s):  
S. Hou ◽  
J. Chappellaz ◽  
D. Raynaud ◽  
V. Masson-Delmotte ◽  
J. Jouzel ◽  
...  

Abstract. Two ice cores recovered from the Himalayan East Rongbuk (ER) Glacier on the northeast saddle of Mt. Qomolangma (Everest) (28° 01' N, 86° 58' E, 6518 m a.s.l.) give access to a tentative record of past Himalayan atmospheric mixing ratio of CH4 spanning the past 1200 yr. The major part of the record is affected by artefacts probably due to in-situ production. After selecting what may represent the true atmospheric mixing ratio, an average of 749 ± 25 ppbv of CH4 is estimated for the late preindustrial Holocene, which is ~ 36 ± 17 (~ 73 ± 18) ppbv higher than the atmospheric levels recorded respectively in Greenland and Antarctic ice cores. A comparison of these new data with model simulations of the CH4 latitudinal gradient suggests either that the models do not get a correct balance between high and low latitude CH4 sources, or that the filtered CH4 profile from the ER cores remains infected by small artefacts.


2017 ◽  
Vol 32 (11) ◽  
pp. 2153-2163 ◽  
Author(s):  
Evan E. Groopman ◽  
Kenneth S. Grabowski ◽  
Albert J. Fahey ◽  
Levke Kööp

We present a novel method for rapid and high-sensitivity in situ measurements of the rare earth elements (REEs) by combined secondary ion mass spectrometry and single-stage accelerator mass spectrometry (SIMS-SSAMS).


Radiocarbon ◽  
2002 ◽  
Vol 44 (3) ◽  
pp. 691-699 ◽  
Author(s):  
Scott M Fitzpatrick ◽  
Jenna E Boyle

Pearl shell was an important and highly valued resource for producing tools and ornaments in Oceania. One pearl shell artifact type that is quite rare in Micronesia, however, is the crescent-shaped scraper/grater. These artifacts have recently been found in 2 burial caves in Palau, Western Caroline Islands, suggesting they may have played important social and symbolic roles in society. The first direct accelerator mass spectrometry (AMS) dating of this tool type, found in association with an in-situ female burial at the Chelechol ra Orrak site, provides a date of AD 150–270, while associated dates range from 770 BC–AD 180. These dates help contextualize human burials and associated artifacts from one of the earliest and most diverse burial sites in Austronesia.


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