Radiocarbon Dating, Memories, and Hopes

DOE R&D Accomplishments Database

Libby, W. F.

1972-10-01

The history of radiocarbon dating from 1939 to the present is reviewed. The basic principles of radiocarbon dating are that cosmic rays make living things radioactive with {sup 14}C to a certain level fixed by the environment and that at death the intake of food stops so no replenishment of the {sup 14}C steadily lost by the immutable decay occurs. Therefore measurement of the degree of decay gives the time lapse since death, i.e., the radiocarbon age. The equipment developed and experiments performed to measure the specific activity of specimens to be dated are described. The results obtained by world-wide experimenters are discussed. These showed that on simultaneity radiocarbon dating is apparently reliable but that absolute dates may be incorrect by as much as 600 to 700 y. The value of radiocarbon dating to archaeologists, geologists, climatologists, and historians is stressed. (LCL)

Predicted net efflux of radiocarbon from the ocean and increase in atmospheric radiocarbon content

NASA Astrophysics Data System (ADS)

Caldeira, Ken; Rau, Greg H.; Duffy, Philip B.

Prior to changes introduced by man, production of radiocarbon (14C) in the stratosphere nearly balanced the flux of 14C from the atmosphere to the ocean and land biosphere, which in turn nearly balanced radioactive decay in these 14C reservoirs. This balance has been altered by land-use changes, fossil-fuel burning, and atmospheric nuclear detonations. Here, we use a model of the global carbon cycle to quantify these radiocarbon fluxes and make predictions about their magnitude in the future. Atmospheric nuclear detonations increased atmospheric 14C content by about 80% by the mid-1960's. Since that time, the 14C content of the atmosphere has been diminishing as this bomb radiocarbon has been entering the oceans and terrestrial biosphere. However, we predict that atmospheric 14C content will reach a minimum and start to increase within the next few years if fossil-fuel burning continues according to a “business-as-usual” scenario, even though fossil fuels are devoid of 14C. This will happen because fossil-fuel carbon diminishes the net flux of 14C from the atmosphere to the oceans and land biosphere, forcing 14C to accumulate in the atmosphere. Furthermore, the net flux of both bomb and natural 14C into the ocean are predicted to continue to slow and then, in the middle of the next century, to reverse, so that there will be a net flux of 14C from the ocean to the atmosphere. The predicted reversal of net 14C fluxes into the ocean is a further example of human impacts on the global carbon cycle.

On the radiocarbon record in banded corals: exchange parameters and net transport of /sup 14/CO/sub 2/ between atmosphere and surface ocean

DOE Office of Scientific and Technical Information (OSTI.GOV)

Druffel, E.M.; Suess, H.E.

1983-02-20

We have made radiocarbon measurements of banded hermatypic corals from Florida, Belize, and the Galapagos Islands. Interpretation is presented here of these previously reported results. These measurements represent the /sup 14/C//sup 12/C ratios in dissolved inorganic carbon (DIOC) in the surface ocean waters of the Gulf Stream and the Peru Current at the time of coral ring formation. A depletion in radiocarbon concentration was observed incoral rings that grew from A.D. 1900--1952. It was caused by dilution of existing /sup 14/C levels with dead CO/sub 2/ from fossil fuel burning (the Suess effect, or S/sub e/). A similar trend wasmore » observed in the distribution of bomb-produced /sup 14/C in corals that had grown during the years following A.D. 1952. The concentration of bomb-produced radiocarbon was much higher in corals from temperate regions (Florida, Belize, Hawaiian Islands) than in corals from tropical regions (Galapagos Islands and Canton Island). The apparent radiocarbon ages of the surface waters in temperate and tropical oceans during the preanthropogenic period range from about 280 to 520 years B.P. (-40 to -69%). At all investigated locations, it is likely that waters at subsurface depths have the same apparent radiocarbon age of about 670 years B.P. From the change of oceanic ..delta../sup 14/C in the surface during post-bomb times, the approximate annual rate of net input of /sup 14/CO/sub 2/ to the ocean waters is calculated to be about 8% of the prevailing /sup 14/C difference between atmosphere and ocean. From this input and from preanthropogenic ..delta../sup 14/C values found at each location, it can be seen that vertical mixing of water in the Peru Current is about 3 times greater than that in the Gulf Stream.« less

Cosmic ray event in 994 C.E. recorded in radiocarbon from Danish oak

NASA Astrophysics Data System (ADS)

Fogtmann-Schulz, A.; Østbø, S. M.; Nielsen, S. G. B.; Olsen, J.; Karoff, C.; Knudsen, M. F.

2017-08-01

We present measurements of radiocarbon in annual tree rings from the time period 980-1006 Common Era (C.E.), hereby covering the cosmic ray event in 994 C.E. The new radiocarbon record from Danish oak is based on both earlywood and latewood fractions of the tree rings, which makes it possible to study seasonal variations in 14C production. The measurements show a rapid increase of ˜10‰ from 993 to 994 C.E. in latewood, followed by a modest decline and relatively high values over the ensuing ˜10 years. This rapid increase occurs from 994 to 995 C.E. in earlywood, suggesting that the cosmic ray event most likely occurred during the period between April and June 994 C.E. Our new record from Danish oak shows strong agreement with existing Δ14C records from Japan, thus supporting the hypothesis that the 994 C.E. cosmic ray event was uniform throughout the Northern Hemisphere and therefore can be used as an astrochronological tie point to anchor floating chronologies of ancient history.

Radiocarbon dating of terrestrial carbonates

USGS Publications Warehouse

Pigati, Jeffrey S.; Rink, W. Jack; Thompson, Jeroen

2014-01-01

Terrestrial carbonates encompass a wide range of materials that potentially could be used for radiocarbon (14C) dating. Biogenic carbonates, including shells and tests of terrestrial and aquatic gastropods, bivalves, ostracodes, and foraminifera, are preserved in a variety of late Quaternary deposits and may be suitable for 14C dating. Primary calcareous deposits (marls, tufa, speleothems) and secondary carbonates (rhizoliths, fracture fill, soil carbonate) may also be targeted for dating when conditions are favorable. This chapter discusses issues that are commonly encountered in 14C dating of terrestrial carbonates, including isotopic disequilibrium and open-system behavior, as well as methods used to determine the reliability of ages derived from these materials. Recent methodological advancements that may improve the accuracy and precision of 14C ages of terrestrial carbonates are also highlighted.

Forensic applications of 14C bomb-pulse dating

NASA Astrophysics Data System (ADS)

Zoppi, U.; Skopec, Z.; Skopec, J.; Jones, G.; Fink, D.; Hua, Q.; Jacobsen, G.; Tuniz, C.; Williams, A.

2004-08-01

After a brief review of the basics of 14C bomb-pulse dating, this paper presents two unique forensic applications. Particular attention is dedicated to the use of the 14C bomb-pulse to establish the time of harvest of illicit drugs such as heroin and opium. Preliminary measurements of 14C concentrations in milligram samples taken from seized drugs are presented. 14C bomb-pulse dating can determine whether drug distribution originates from stockpiles or recent manufacture, and support the action of law enforcement authorities against criminal organisations involved in drug trafficking. In addition, we describe the dating of wine vintages for a number of authenticated single label vintage red wines from the Barossa Valley - South Australia. Our results show that radiocarbon dating can be used to accurately determine wine vintages and therefore reveal the addition of unrelated materials of natural and synthetic origin.

RADIOCARBON ANALYSIS OF PM 2.5 AMBIENT AEROSOL

EPA Science Inventory

The radiocarbon (14C) content of an ambient aerosol sample can be directly related to the fraction of the sample's total carbon mass contributed by natural (biogenic) sources. Such knowledge is difficult to determine by other means, and important for devising ambient PM contro...

Complexities in the Use of Bomb-Curve Radiocarbon to Determine Time Since Death of Human Skeletal Remains

DOE Office of Scientific and Technical Information (OSTI.GOV)

Ubelaker, D H; Buchholz, B A

2005-04-26

Atmospheric testing of nuclear weapons during the 1950s and early 1960s doubled the level of radiocarbon ({sup 14}C) in the atmosphere. From the peak in 1963, the level of {sup 14}CO{sub 2} has decreased exponentially with a mean life of about 16 years, not due to radioactive decay, but due to mixing with large marine and terrestrial carbon reservoirs. Since radiocarbon is incorporated into all living things, the bomb-pulse is an isotopic chronometer of the past half century. The absence of bomb radiocarbon in skeletonized human remains generally indicates a date of death before 1950. Comparison of the radiocarbon valuesmore » with the post 1950 bomb-curve may also help elucidate when in the post 1950 era, the individual was still alive. Such interpretation however, must consider the age at death of the individual and the type of tissue sampled.« less

Extraneous carbon assessment in ultra-microscale radiocarbon analysis using benzene polycarboxylic acids (BPCA)

NASA Astrophysics Data System (ADS)

Hanke, Ulrich M.; McIntyre, Cameron P.; Schmidt, Michael W. I.; Wacker, Lukas; Eglinton, Timothy I.

2016-04-01

Measurements of the natural abundance of radiocarbon (14C) concentrations in inorganic and organic carbon-containing materials can be used to investigate their date of origin. Particularly, the biogeochemical cycling of specific compounds in the environment may be investigated applying molecular marker analyses. However, the isolation of specific molecules from environmental matrices requires a complex processing procedure resulting in small sample sizes that often contain less than 30 μg C. Such small samples are sensitive to extraneous carbon (Cex) that is introduced during the purification of the compounds (Shah and Pearson, 2007). We present a thorough radiocarbon blank assessment for benzene polycarboxylic acids (BPCA), a proxy for combustion products that are formed during the oxidative degradation of condensed polyaromatic structures (Wiedemeier et al, in press). The extraneous carbon assessment includes reference material for (1) chemical extraction, (2) preparative liquid chromatography (3) wet chemical oxidation which are subsequently measured with gas ion source AMS (Accelerator Mass Spectrometer, 5-100 μg C). We always use pairs of reference materials, radiocarbon depleted (14Cfossil) and modern (14Cmodern) to determine the fraction modern (F14C) of Cex.Our results include detailed information about the quantification of Cex in radiocarbon molecular marker analysis using BPCA. Error propagation calculations indicate that ultra-microscale samples (20-30 μg) are feasible with uncertainties of less than 10 %. Calculations of the constant contamination reveal important information about the source (F14C) and mass (μg) of Cex (Wacker and Christl, 2011) for each sub procedure. An external correction of compound specific radiocarbon data is essential for robust results that allow for a high degree of confidence in the 14C results. References Shah and Pearson, 2007. Ultra-microscale (5-25μg C) analysis of individual lipids by 14C AMS: Assessment and

Accumulation of Sellafield-derived radiocarbon ((14)C) in Irish Sea and West of Scotland intertidal shells and sediments.

PubMed

Tierney, Kieran M; Muir, Graham K P; Cook, Gordon T; MacKinnon, Gillian; Howe, John A; Heymans, Johanna J; Xu, Sheng

2016-01-01

The nuclear energy industry produces radioactive waste at various stages of the fuel cycle. In the United Kingdom, spent fuel is reprocessed at the Sellafield facility in Cumbria on the North West coast of England. Waste generated at the site comprises a wide range of radionuclides including radiocarbon ((14)C) which is disposed of in various forms including highly soluble inorganic carbon within the low level liquid radioactive effluent, via pipelines into the Irish Sea. This (14)C is rapidly incorporated into the dissolved inorganic carbon (DIC) reservoir and marine calcifying organisms, e.g. molluscs, readily utilise DIC for shell formation. This study investigated a number of sites located in Irish Sea and West of Scotland intertidal zones. Results indicate (14)C enrichment above ambient background levels in shell material at least as far as Port Appin, 265 km north of Sellafield. Of the commonly found species (blue mussel (Mytilus edulis), common cockle (Cerastoderma edule) and common periwinkle (Littorina littorea)), mussels were found to be the most highly enriched in (14)C due to the surface environment they inhabit and their feeding behaviour. Whole mussel shell activities appear to have been decreasing in response to reduced discharge activities since the early 2000s but in contrast, there is evidence of continuing enrichment of the carbonate sediment component due to in-situ shell erosion, as well as indications of particle transport of fine (14)C-enriched material close to Sellafield. Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.

Radiocarbon application in environmental science and archaeology in Croatia

NASA Astrophysics Data System (ADS)

Krajcar Bronić, I.; Obelić, B.; Horvatinčić, N.; Barešić, J.; Sironić, A.; Minichreiter, K.

2010-07-01

Radiocarbon is a cosmogenic radioisotope equally distributed throughout the troposphere and biosphere. This fact enables its most common application—radiocarbon dating. Natural equilibrium of radiocarbon has been disturbed by diverse anthropogenic activities during the last ˜150 years, enabling also the use of 14C in various environmental applications. Here we present three types of studies by using 14C that were performed in the Zagreb Radiocarbon Laboratory. 14C in atmospheric CO 2 has been monitored at several sites with various anthropogenic influences and the difference between the clean-air sites, the industrial city and the vicinity of a nuclear power plant has been established. 14C has been applied in geochronology of karst areas, especially in dating of tufa, speleothems and lake sediments, as well as in studies of geochemical carbon cycle. 14C has been used in various archaeological studies, among which the dating of the early Neolithic settlements in Croatia is presented. In these studies 14C was measured by radiometric techniques, i.e., by gas proportional counting and more recently by liquid scintillation counting (LSC). Two sample preparation techniques for LSC measurement were used: benzene synthesis for archaeological dating and other applications that require better precision, and direct absorption of CO 2 for monitoring purposes. The presented results show that various studies by using 14C can be successfully performed by the LSC technique, providing a large enough sample (>1 g of carbon).

Grass material as process standard for compound-specific radiocarbon analysis

NASA Astrophysics Data System (ADS)

Cisneros-Dozal, Malu; Xu, Xiaomei; Bryant, Charlotte; Pearson, Emma; Dungait, Jennifer

2015-04-01

Compound-specific radiocarbon analysis (CSRA) is a powerful tool to study the carbon cycle and/or as a dating technique in paleoclimate reconstructions. The radiocarbon value of individual compounds can provide insight into turnover times, organic matter sources and in specific cases can be used to establish chronologies when traditional dating materials (e.g. macrofossils, pollen, charcoal) are not available. The isolation of compounds (or group of compounds) from parent material (e.g. soil, plant) for radiocarbon analysis can, however, introduce carbon contamination through chemical separation steps and preparative capillary gas chromatography (PCGC). In addition, the compounds of interest are often in low abundance which amplifies the contamination effect. The extraneous carbon can be of modern 14C age and/or 14C -free and its amount and 14C value must be determined for a given system/isolation procedure in order to report accurate 14C values. This can be achieved by using adequate standard materials but, by contrast with traditional radiocarbon dating, there are not established reference standards for CSRA work, in part because the type of standard material depends on the compounds of interest and the isolation procedure. Here we evaluate the use of n-alkanes extracted from single-year growth grass as modern process standard material for CSRA using PCGC isolation. The grass material has a known 14C value of 1.224 ± 0.006 fraction modern (FM) and the individual n-alkanes are expected to have a similar 14C value. In order to correct for the addition of extraneous carbon during PCGC isolation of the n-alkanes, we used commercially available compounds of modern 14C content and 14C -free (adipic acid, FM= 0.0015 ± 0.0001 and docosane, FM=1.059 ± 0.003) to evaluate our PCGC procedure. The corrected 14C values of the isolated n-alkanes extracted from the modern grass are within one sigma of the grass bulk 14C value for n-C29 and within two sigma for n-C23-C27, C31

Quantity of dates trumps quality of dates for dense Bayesian radiocarbon sediment chronologies - Gas ion source 14C dating instructed by simultaneous Bayesian accumulation rate modeling

NASA Astrophysics Data System (ADS)

Rosenheim, B. E.; Firesinger, D.; Roberts, M. L.; Burton, J. R.; Khan, N.; Moyer, R. P.

2016-12-01

Radiocarbon (14C) sediment core chronologies benefit from a high density of dates, even when precision of individual dates is sacrificed. This is demonstrated by a combined approach of rapid 14C analysis of CO2 gas generated from carbonates and organic material coupled with Bayesian statistical modeling. Analysis of 14C is facilitated by the gas ion source on the Continuous Flow Accelerator Mass Spectrometry (CFAMS) system at the Woods Hole Oceanographic Institution's National Ocean Sciences Accelerator Mass Spectrometry facility. This instrument is capable of producing a 14C determination of +/- 100 14C y precision every 4-5 minutes, with limited sample handling (dissolution of carbonates and/or combustion of organic carbon in evacuated containers). Rapid analysis allows over-preparation of samples to include replicates at each depth and/or comparison of different sample types at particular depths in a sediment or peat core. Analysis priority is given to depths that have the least chronologic precision as determined by Bayesian modeling of the chronology of calibrated ages. Use of such a statistical approach to determine the order in which samples are run ensures that the chronology constantly improves so long as material is available for the analysis of chronologic weak points. Ultimately, accuracy of the chronology is determined by the material that is actually being dated, and our combined approach allows testing of different constituents of the organic carbon pool and the carbonate minerals within a core. We will present preliminary results from a deep-sea sediment core abundant in deep-sea foraminifera as well as coastal wetland peat cores to demonstrate statistical improvements in sediment- and peat-core chronologies obtained by increasing the quantity and decreasing the quality of individual dates.

Marine radiocarbon reservoir age simulations for the past 50,000 years

NASA Astrophysics Data System (ADS)

Butzin, M.; Köhler, P.; Lohmann, G.

2017-08-01

Radiocarbon (14C) dating calibration for the last glacial period largely relies on cross-dated marine 14C records. However, marine reservoirs are isotopically depleted with respect to the atmosphere and therefore have to be corrected by the Marine Radiocarbon Ages of surface waters (MRAs), whose temporal variabilities are largely unknown. Here we present simulations of the spatial and temporal variability in MRAs using a three-dimensional ocean circulation model covering the past 50,000 years. Our simulations are compared to reconstructions of past surface ocean Δ14C. Running the model with different climatic boundary conditions, we find that low-latitude to midlatitude MRAs have varied between 400 and 1200 14C years, with values of about 780 14C years at the Last Glacial Maximum. Reservoir ages exceeding 2000 14C years are simulated in the polar oceans. Our simulation results can be used as first-order approximation of the MRA variability in future radiocarbon calibration efforts.

Changes in the radiocarbon reservoir age in Lake Xingyun, Southwestern China during the Holocene.

PubMed

Zhou, Aifeng; He, Yuxin; Wu, Duo; Zhang, Xiaonan; Zhang, Can; Liu, Zhonghui; Yu, Junqing

2015-01-01

Chronology is a necessary component of paleoclimatology. Radiocarbon dating plays a central role in determining the ages of geological samples younger than ca. 50 ka BP. However, there are many limitations for its application, including radiocarbon reservoir effects, which may cause incorrect chronology in many lakes. Here we demonstrate temporal changes in the radiocarbon reservoir age of Lake Xingyun, Southwestern China, where radiocarbon ages based on bulk organic matter have been reported in previous studies. Our new radiocarbon ages, determined from terrestrial plant macrofossils suggest that the radiocarbon reservoir age changed from 960 to 2200 years during the last 8500 cal a BP years. These changes to the reservoir effect were associated with inputs from either pre-aged organic carbon or 14C-depleted hard water in Lake Xingyun caused by hydrological change in the lake system. The radiocarbon reservoir age may in return be a good indicator for the carbon source in lake ecosystems and depositional environment.

Holocene age of the Yuha burial: Direct radiocarbon determinations by accelerator mass spectrometry

USGS Publications Warehouse

Stafford, Thomas W.; Jull, A.J.T.; Zabel, T.H.; Donahue, D.J.; Duhamel, R.C.; Brendel, K.; Haynes, C.V.; Bischoff, J.L.; Payen, L.A.; Taylor, R.E.

1984-01-01

The view that human populations may not have arrived in the Western Hemisphere before about 12,000 radiocarbon yr BP1,2 has been challenged by claims of much greater antiquity for a small number of archaeological sites and human skeleton samples. One such site is the Homo sapiens sapiens cairn burial excavated in 1971 from the Yuha desert, Imperial County, California3-5. Radiocarbon analysis of caliche coating one of the bones of the skeleton yielded a radiocarbon age of 21,500??1,000 yr BP4, while radiocarbon and uranium series analyses of caliche coating a cairn boulder yielded ages of 22,125??400 and 19,000??3,000 yr BP, respectively5. The late Pleistocene age assignment to the Yuha burial has been challenged by comparing the cultural context of the burial with other cairn burials in the same region6, on the basis of the site's geomorphological context and from radiocarbon analyses of soil caliches. 7,8 In rebuttal, arguments in defence of the original age assignment have been presented9,10 as well as an amino acid racemization analysis on the Yuha skeleton indicating an age of 23,600??2,600 yr BP11. The tandem accelerator mass spectrometer at the University of Arizona has now been used to measure the ratio of 14C/13C in several organic and inorganic fractions of post-cranial bone from the Yuha H. sapiens sapiens skeleton. Isotope ratios from six chemical fractions all yielded radiocarbon ages for the skeleton of less than 4,000 yr BP. These results indicate that the Yuha skeleton is of Holocene age, in agreement with the cultural context of the burial, and in disagreement with the previously assigned Pleistocene age of 19,000-23,000 yr. ?? 1984 Nature Publishing Group.

Radiocarbon and stable isotopes in Palmyra corals during the past century

NASA Astrophysics Data System (ADS)

Druffel-Rodriguez, Kevin C.; Vetter, Desiree; Griffin, Sheila; Druffel, Ellen R. M.; Dunbar, Robert B.; Mucciarone, David A.; Ziolkowski, Lori A.; Sanchez-Cabeza, Joan-Albert

2012-04-01

Annual samples from two Palmyra Atoll corals (Porites lutea) that lived during the past 110 years were analyzed for radiocarbon (Δ14C) and δ18O. The Δ14C values decreased 7.6‰ from 1896 to 1953, similar to other coral records from the tropical and subtropical Pacific. Δ14C values rose from ˜-60‰ to ˜+110‰ by 1980 due to the input of bomb radiocarbon from the atmosphere. Elevated Δ14C 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 δ18O and δ13C values and a correlation between them. The Δ14C results were more resistant to alteration, except when contamination was from the bomb era (>1956).

Decadally resolved Lateglacial radiocarbon evidence from New Zealand kauri

NASA Astrophysics Data System (ADS)

Hogg, Alan; Southon, John; Turney, Chris; Palmer, Jonathan; Bronk Ramsey, Christopher; Fenwick, Pavla; Boswijk, Gretel; Büntgen, Ulf; Friedrich, Michael; Helle, Gerhard; Hughen, Konrad; Jones, Richard; Kromer, Bernd; Noronha, Alexandra; Reinig, Frederick; Reynard, Linda; Staff, Richard; Wacker, Lukas

2017-04-01

The Last Glacial-Interglacial Transition (LGIT; 15,000 - 11,000 cal BP) was characterised by complex spatiotemporal patterns of climate change, with numerous studies requiring accurate chronological control to decipher leads from lags in global palaeoclimatic, -environmental and archaeological records. However, close scrutiny of the few available tree-ring chronologies and radiocarbon-dated sequences composing the IntCal13 radiocarbon (14C) calibration curve, indicates significant weakness in 14C calibration across key periods of the LGIT. Here, we present a decadally-resolved atmospheric 14C record derived from New Zealand kauri spanning Greenland Stadial 1 (GS-1; 12,900 - 11,650 cal BP). Two floating kauri 14C time series, curve-matched to IntCal13, serve as a radiocarbon backbone through GS-1. Floating Northern Hemisphere (NH) 14C datasets are matched against the new kauri data, forming a robust NH 14C time series to 14,200 cal BP. Our results show that IntCal13 is questionable from 12,200 - 11,900 cal BP and the 10,400 BP 14C plateau is approximately five decades too short. By precisely aligning Southern and Northern Hemisphere tree-ring 14C records with marine 14C sequences, we document two relatively short periods of North Atlantic Meridional Overturning Circulation (AMOC) collapse during GS-1. Hence, sustained North Atlantic cooling across GS-1 was not driven by a prolonged AMOC reduction but was probably due to an equatorward migration of the Polar Front.

Local variance of atmospheric 14C concentrations around Fukushima Dai-ichi Nuclear Power Plant from 2010 to 2012.

PubMed

Chen, Biying; Xu, Sheng; Cook, Gordon T; Freeman, Stewart P H T; Hou, Xiaolin; Liu, Cong-Qiang; Naysmith, Philip; Yamaguchi, Katsuhiko

2017-01-01

Radiocarbon ( 14 C) has been measured in single tree ring samples collected from the southwest of the Fukushima Dai-ichi Nuclear Power Plant. Our data indicate south-westwards dispersion of radiocarbon and the highest 14 C activity observed so far in the local environment during the 2011 accident. The abnormally high 14 C activity in the late wood of 2011 ring may imply an unknown source of radiocarbon nearby after the accident. The influence of 14 C shrank from 30 km during normal reactor operation to 14 km for the accident in the northwest of FDNPP, but remains unclear in the southwest.

A complete terrestrial radiocarbon record for 11.2 to 52.8 kyr B.P.

PubMed

Bronk Ramsey, Christopher; Staff, Richard A; Bryant, Charlotte L; Brock, Fiona; Kitagawa, Hiroyuki; van der Plicht, Johannes; Schlolaut, Gordon; Marshall, Michael H; Brauer, Achim; Lamb, Henry F; Payne, Rebecca L; Tarasov, Pavel E; Haraguchi, Tsuyoshi; Gotanda, Katsuya; Yonenobu, Hitoshi; Yokoyama, Yusuke; Tada, Ryuji; Nakagawa, Takeshi

2012-10-19

Radiocarbon ((14)C) provides a way to date material that contains carbon with an age up to ~50,000 years and is also an important tracer of the global carbon cycle. However, the lack of a comprehensive record reflecting atmospheric (14)C prior to 12.5 thousand years before the present (kyr B.P.) has limited the application of radiocarbon dating of samples from the Last Glacial period. Here, we report (14)C results from Lake Suigetsu, Japan (35°35'N, 135°53'E), which provide a comprehensive record of terrestrial radiocarbon to the present limit of the (14)C method. The time scale we present in this work allows direct comparison of Lake Suigetsu paleoclimatic data with other terrestrial climatic records and gives information on the connection between global atmospheric and regional marine radiocarbon levels.

Late Holocene Radiocarbon Variability in Northwest Atlantic Slope Waters

DOE Office of Scientific and Technical Information (OSTI.GOV)

Sherwood, O; Edinger, E; Guilderson, T P

2008-08-15

Deep-sea gorgonian corals secrete a 2-part skeleton of calcite, derived from dissolved inorganic carbon at depth, and gorgonin, derived from recently fixed and exported particulate organic matter. Radiocarbon contents of the calcite and gorgonin provide direct measures of seawater radiocarbon at depth and in the overlying surface waters, respectively. Using specimens collected from Northwest Atlantic slope waters, we generated radiocarbon records for surface and upper intermediate water layers spanning the pre- and post bomb-{sup 14}C eras. In Labrador Slope Water (LSW), convective mixing homogenizes the pre-bomb {Delta}{sup 14}C signature (-67 {+-} 4{per_thousand}) to at least 1000 m depth. Surface watermore » bomb-{sup 14}C signals were lagged and damped (peaking at {approx} +45{per_thousand} in the early 1980s) relative to other regions of the northwest Atlantic, and intermediate water signals were damped further. Off southwest Nova Scotia, the vertical gradient in {Delta}{sup 14}C is much stronger. In surface water, pre-bomb {Delta}{sup 14}C averaged -75 {+-} 5{per_thousand}. At 250-475 m depth, prebomb {Delta}{sup 14}C oscillated quasi-decadally between -80 and -100{per_thousand}, likely reflecting interannual variability in the presence of Labrador Slope Water vs. Warm Slope Water (WSW). Finally, subfossil corals reveal no systematic changes in vertical {Delta}{sup 14}C gradients over the last 1200 years.« less

Ramped PyrOx 14C With a Twist: Improving Radiocarbon Chronologies on Highly Detrital Marginal Antarctic Sediments

NASA Astrophysics Data System (ADS)

Subt, C.; Yoon, H.; Yoo, K. C.; Lee, J. I.; Domack, E. W.; Rosenheim, B. E.

2016-02-01

Highly detrital sediments can be difficult to date when the detritus includes material similar to that from which dates are sought. For radiocarbon dating, samples with a high degree of pre-aged detrital carbon contamination necessitate measurement of a very small portion of the sample to remove that contamination from the targeted component, even when using advanced techniques such as Ramped PyrOx (RP) 14C dating. Here we present three case studies of alternative RP approaches, producing accurate and precise chronologies for highly detrital sediments near the Larsen C ice shelf, near the Drygalski Ice Tongue in Ross Sea, and in Lapeyrère Bay, Anvers Island. For sediments where the proportion of organic carbon that was modern at the time of deposition is too small for a traditional AMS analysis after RP treatment, we have developed an innovative multiple RP analyses approach to minimize the cost in precision from using smaller temperature intervals, while maximizing the benefit in accuracy. Resulting sub ice-shelf chronologies show vastly improved dates down-core, significantly younger than the equivalent 14C chronology from the bulk acid insoluble organic (AIO) carbon with increasing ages down-core. By comparison, bulk AIO 14C dates in the study areas are not only older, but are subject to age reversals and nearly constant ages that make sedimentation rates impossible to resolve. Using our new approaches, we can reduce pre-aged carbon contamination in Lapeyrère Bay, and date sediments within layers of siliceous mud and ooze in the Ross Sea, and near the Larsen C ice shelf. Improved accuracy for 14C dates of highly detrital sediments can sometimes require the incorporation of a larger blank correction to account for multiple analyses, decreasing the precision. Application of this method refines ages of hard-to-date sediments, removing limits on what to include in a regional approach to chronicle ice shelf collapse.

Determination of microbial carbon sources and cycling during remediation of petroleum hydrocarbon impacted soil using natural abundance (14)C analysis of PLFA.

PubMed

Cowie, Benjamin R; Greenberg, Bruce M; Slater, Gregory F

2010-04-01

In a petroleum impacted land-farm soil in Sarnia, Ontario, compound-specific natural abundance radiocarbon analysis identified biodegradation by the soil microbial community as a major pathway for hydrocarbon removal in a novel remediation system. During remediation of contaminated soils by a plant growth promoting rhizobacteria enhanced phytoremediation system (PEPS), the measured Delta(14)C of phospholipid fatty acid (PLFA) biomarkers ranged from -793 per thousand to -897 per thousand, directly demonstrating microbial uptake and utilization of petroleum hydrocarbons (Delta(14)C(PHC) = -1000 per thousand). Isotopic mass balance indicated that more than 80% of microbial PLFA carbon was derived from petroleum hydrocarbons (PHC) and a maximum of 20% was obtained from metabolism of more modern carbon sources. These PLFA from the contaminated soils were the most (14)C-depleted biomarkers ever measured for an in situ environmental system, and this study demonstrated that the microbial community in this soil was subsisting primarily on petroleum hydrocarbons. In contrast, the microbial community in a nearby uncontaminated control soil maintained a more modern Delta(14)C signature than total organic carbon (Delta(14)C(PLFA) = +36 per thousand to -147 per thousand, Delta(14)C(TOC) = -148 per thousand), indicating preferential consumption of the most modern plant-derived fraction of soil organic carbon. Measurements of delta(13)C and Delta(14)C of soil CO(2) additionally demonstrated that mineralization of PHC contributed to soil CO(2) at the contaminated site. The CO(2) in the uncontaminated control soil exhibited substantially more modern Delta(14)C values, and lower soil CO(2) concentrations than the contaminated soils, suggesting increased rates of soil respiration in the contaminated soils. In combination, these results demonstrated that biodegradation in the soil microbial community was a primary pathway of petroleum hydrocarbon removal in the PEPS system. This study

Drivers of soil organic matter vulnerability to climate change, Part II: RothC modelling of carbon dynamics including radiocarbon data

NASA Astrophysics Data System (ADS)

Studer, Mirjam S.; Abiven, Samuel; González Domínguez, Beatriz R.; Hagedorn, Frank; Reisser, Moritz; Walthert, Lorenz; Zimmermann, Stephan; Niklaus, Pascal A.

2016-04-01

It is still largely unknown what drives the vulnerability of soil organic carbon (SOC) stocks to climate change, i.e. the likelihood of a soil to loose its SOC along with the change in environmental conditions. Our objective is to assess the SOC vulnerability of Swiss forest soils and identify its potential drivers: climate (temperature, soil moisture), soil (clay content, pH) and landscape (slope, aspect) properties. Fifty-four sites were selected for balanced spatial and driver magnitudes distribution. We measured the SOC characteristics (content and radiocarbon) and studied the C decomposition by laboratory soil incubations (details in Part I, abstract by B. González Domínguez). In order to assess the current SOC pool distribution and its radiocarbon signatures, we extended the Rothamsted Carbon (RothC) model with radiocarbon (14C) isotope modelling (RothCiso). The RothC model distinguishes four active SOC pools, decomposable and resistant plant material, microbial biomass and humified organic matter, and an inert SOC pool (Jenkinson 1990). The active pools are decomposed and mineralized to CO2 by first order kinetics. The RothCiso assigns all pools a 14C signature, based on the atmospheric 14C concentrations of the past century (plant C inputs) and their turnover. Currently we constrain the model with 14C signatures measured on the 54 fresh and their corresponding archived bulk soil samples, taken 12-24 years before. We were able to reproduce the measured radiocarbon concentrations of the SOC with the RothCiso and first results indicate, that the assumption of an inert SOC pool, that is radiocarbon dead, is not appropriate. In a second step we will compare the SOC mean residence time assessed by the two methodological approaches - incubation (C efflux based) and modelling (C stock based) - and relate it to the environmental drivers mentioned above. With the combination of the two methodological approaches and 14C analysis we hope to gain more insights into

A novel tertiary prep-HPLC method for the isolation of single amino acids for AMS-radiocarbon measurement.

PubMed

Fernandes, Ricardo; Koudelka, Tomas; Tholey, Andreas; Dreves, Alexander

2017-07-15

AMS-radiocarbon measurements of amino acids can potentially provide more reliable radiocarbon dates than bulk collagen analysis. Nonetheless, the applicability of such an approach is often limited by the low-throughput of existing isolation methods and difficulties in determining the contamination introduced during the separation process. A novel tertiary prep-HPLC amino acid isolation method was developed that relies on the combustion of eluted material without requiring any additional chemical steps. Amino acid separation was carried out using a gradient mix of pure water and phosphoric acid with an acetonitrile step in-between runs to remove hydrophobic molecules from the separation column. The amount of contaminant carbon and its 14 C content were determined from two-point measurements of collagen samples of known 14 C content. The amount of foreign carbon due to the isolation process was estimated at 4±1μg and its 14 C content was 0.43±0.01 F 14 C. Radiocarbon values corrected for carbon contamination have only a minor increase in uncertainties. For Holocene samples, this corresponds to an added uncertainty typically smaller than 10 14 Cyears. The developed method can be added to routine AMS measurements without implying significant operational changes and offers a level of measurement uncertainty that is suitable for many archaeological, ecological, environmental, and biological applications. Copyright © 2017. Published by Elsevier B.V.

Santorini eruption radiocarbon dated to 1627-1600 B.C.

PubMed

Friedrich, Walter L; Kromer, Bernd; Friedrich, Michael; Heinemeier, Jan; Pfeiffer, Tom; Talamo, Sahra

2006-04-28

Precise and direct dating of the Minoan eruption of Santorini (Thera) in Greece, a global Bronze Age time marker, has been made possible by the unique find of an olive tree, buried alive in life position by the tephra (pumice and ashes) on Santorini. We applied so-called radiocarbon wiggle-matching to a carbon-14 sequence of tree-ring segments to constrain the eruption date to the range 1627-1600 B.C. with 95.4% probability. Our result is in the range of previous, less precise, and less direct results of several scientific dating methods, but it is a century earlier than the date derived from traditional Egyptian chronologies.

Ancient dissolved methane in inland waters at low concentrations revealed by a new collection method for radiocarbon (^{14}C) analysis

NASA Astrophysics Data System (ADS)

Dean, Joshua F.; Billett, Michael F.; Murray, Callum; Garnett, Mark H.

2017-04-01

Methane (CH4) is a powerful greenhouse gas and is released to the atmosphere from freshwater systems in numerous biomes globally. Radiocarbon (14C) analysis of methane can provide unique information about its age, source and rate of cycling in natural environments. Methane is often released from aquatic sediments in bubbles (ebullition), but dissolved methane is also present in lakes and streams at lower concentrations, and may not be of the same age or source. Obtaining sufficient non-ebullitive aquatic methane for 14C analysis remains a major technical challenge. Previous studies have shown that freshwater methane, in both dissolved and ebullitive form, can be significantly older than other forms of aquatic carbon (C), and it is therefore important to characterise this part of the terrestrial C balance. We present a novel method to capture sufficient amounts of dissolved methane from freshwater environments for 14C analysis by circulating water across a hydrophobic, gas-permeable membrane and collecting the methane in a large collapsible vessel. The results of laboratory and field tests show that reliable dissolved δ13CH4 and 14CH4 samples can be readily collected over short time periods (˜4 to 24 hours), at relatively low cost and from a variety of surface water types. The initial results further support previous findings that dissolved methane can be significantly older than other forms of aquatic C, especially in organic-rich catchments, and is currently unaccounted for in many terrestrial C balances and models. This method is suitable for use in remote locations, and could potentially be used to detect the leakage of unique 14CH4 signatures from point sources into waterways, e.g. coal seam gas and landfill gas.

Analysis of 14C-bearing compounds released by the corrosion of irradiated steel using accelerator mass spectrometry.

PubMed

Cvetković, B Z; Salazar, G; Kunz, D; Szidat, S; Wieland, E

2018-06-25

The combination of ion chromatography (IC) with accelerator mass spectrometry (AMS) was developed to determine the speciation of 14C-(radiocarbon) bearing organic compounds in the femto to pico molar concentration range. The development of this compound-specific radiocarbon analysis (CSRA) of carboxylic acids is reported and the application of the method on a leaching solution from neutron-irradiated steel is demonstrated. The background and the dynamic range of the AMS-based method were quantified. On using 14C-labelled standards, the measurements demonstrate the repeatability of the analytical method and the reproducible recovery of the main target carboxylic acids (i.e., acetate, formate, malonate, and oxalate). The detection limit was determined to be in the mid fmol 14C per L level while the dynamic range of the analytical method covers three orders of magnitude from the low fmol to the mid pmol 14C per L level. Cross contamination was found to be negligible during IC fractionation and was accounted for during eluate processing and 14C detection by AMS. The 14C-bearing carboxylates released from an irradiated steel nut into an alkaline leaching solution were analysed using the CSRA-based analytical method with the aim to check the applicability of the approach and develop appropriate sample preparation. The concentrations of 14C-bearing formate and acetate, the main organic corrosion products, were at a low pmol 14C per L level for convenient dimensions of the alkaline leaching experiment which demonstrates that compound-specific 14C AMS is an extremely sensitive analytical method for analysing 14C-bearing compounds. The content of total organic 14C in solution (TO14C) determined by the direct measurement of an aliquot of the leaching solution agrees well with the sum of the 14C concentrations of the individual carboxylates within the uncertainty of the data. Furthermore, the TO14C content is in good agreement with the calculated value using the corrosion rate

Differential extraction of radiocarbon associated with soil biomass and humus

DOE Office of Scientific and Technical Information (OSTI.GOV)

Tsao, C.W.; Bartha, R.

To detect the humification of organic compounds in soil that bypasses biomass incorporation, selective extraction procedures for radiocarbon from soil biomass and humus were evaluated. Following the incubation of [sup 14]C-glucose and [sup 14]C-benzoate in soil, fumigation--0.5 M K[sub 2]SO[sub 4] extraction and 0.15 M Na[sub 4]P[sub 2]O[sub 7] extraction selectively removed biomass-associated and humus-associated radiocarbon, respectively. Applying the recovery correction of 3.4[times] to biomass and 3.5[times] to humus, radiocarbon balances of 95 to 107% were obtained during a time window following the degradation of these substrates. Negligible overlap between the extractions renders the technique suitable for investigating the fatemore » of organics that, through cometabolism, attain unusual radiocarbon distributions in soil.« less

Radiocarbon dating of open systems with bomb effect

NASA Technical Reports Server (NTRS)

Mckay, C. P.; Long, A.; Friedmann, E. I.

1986-01-01

The application of radiocarbon dating is extended to include systems that are slowly exchanging carbon with the atmosphere. Simple formulae are derived that relate the true age and the exchange rate of carbon to the apparent radiocarbon age. A radiocarbon age determination does not give a unique true age and exchange rate but determines a locus of values bounded by a minimum age and a minimum exchange rate. It is found that for radiocarbon ages as large as 10,000 years it is necessary to correct for the anthropogenic radiocarbon produced in the atmosphere by nuclear weapons testing. A one-term exponential approximation, with an e-folding time of 14.43 years, is used to model this effect and is shown to be accurate to within 3 percent for exchange time constants of 100 years and greater. The approach developed here is not specific to radiocarbon and can be applied to other radioisotopes in open systems.

Determination of 14C age of inorganic and organic carbon in ancient Siberian permafrost

NASA Astrophysics Data System (ADS)

Onstott, T. C.; Liang, R.; Lau, M.; Vishnivetskaya, T. A.; Lloyd, K. G.; Pfiffner, S. M.; Hodgins, G.; Rivkina, E.

2017-12-01

Permafrost represents a large reservoir of ancient carbon that could have an important impact on the global carbon budget during climate warming. Due to the low turnover rate of carbon by microorganisms at subzero temperatures, the persistence of ancient carbon in younger permafrost deposits could also pose challenges for radiocarbon dating of permafrost sediment. We utilized Accelerator Mass Spectrometry to determine the 14C age of inorganic carbon, labile and recalcitrant organic carbon in Siberian permafrost sediment sampled at various depths from 2.9 to 5.6m. The fraction of inorganic carbon (CO2) was collected after acidification using phosphoric acid. The labile (younger) and recalcitrant (old) organic carbon in the subsequent residues were collected after combustion at 400 ºC and 800 ºC, respectively. The percentages of inorganic carbon increased from the youngest (2.9m) to the oldest (5.6m), whereas the fractions for organic carbon varied significantly at different depths. The 14C age determined in the inorganic fraction in the top sample (2.9 m) was 21,760 yr BP and gradually increased to 33,900 yr BP in the relative deeper sediment (3.5 and 5.6 m). Surprisingly, the fraction of "younger" carbon liberated at 400 oC was older than the more recalcitrant and presumably older organic carbon liberated at 800 oC in all cases. Moreover, the 14C age of the younger and older organic carbon fractions did not increase with depth as observed in the carbonate fraction. In particular, the 14C age of the organic carbon in the top sample (38,590-41,700 yr BP) was much older than the deeper samples at depth of 3.5m (18,228-20,158 yr BP) and 5.6m (29,040-38,020 yr BP). It should be noticed that the metabolism of ancient carbon in frozen permafrost may vary at different depths due to the different proportion of necromass and metabolically active microbes. Therefore, additional knowledge about the carbon dynamics of permafrost and more investigation would be required to

Radiocarbon (14C) Constraints On The Fraction Of Refractory Dissolved Organic Carbon In Primary Marine Aerosol From The Northwest Atlantic

NASA Astrophysics Data System (ADS)

Beaupre, S. R.; Kieber, D. J.; Keene, W. C.; Long, M. S.; Frossard, A. A.; Kinsey, J. D.; Duplessis, P.; Chang, R.; Maben, J. R.; Lu, X.; Zhu, Y.; Bisgrove, J.

2017-12-01

Nearly all organic carbon in seawater is dissolved (DOC), with more than 95% considered refractory based on modeled average lifetimes ( 16,000 years) and characteristically old bulk radiocarbon (14C) ages (4000 - 6000 years) that exceed the timescales of overturning circulation. Although this refractory dissolved organic carbon (RDOC) is present throughout the oceans as a major reservoir of the global carbon cycle, its sources and sinks are poorly constrained. Recently, RDOC was proposed to be removed from the oceans through adsorption onto the surfaces of rising bubble plumes produced by breaking waves, ejection into the atmosphere via bubble bursting as a component of primary marine aerosol (PMA), and subsequent oxidation in the atmosphere. To test this mechanism, we used natural abundance 14C (5730 ± 40 yr half-life) to trace the fraction of RDOC in PMA produced in a high capacity generator at two biologically-productive and two oligotrophic hydrographic stations in the Northwest Atlantic Ocean during a research cruise aboard the R/V Endeavor (Sep - Oct 2016). The 14C signatures of PMA separately generated day and night from near-surface (5 m) and deep (2500 m) seawater were compared with corresponding 14C signatures in seawater of near-surface dissolved inorganic carbon (DIC, a proxy for recently produced organic matter), bulk deep DOC (a proxy for RDOC), and near-surface bulk DOC. Results constrain the selectivity of PMA formation from RDOC in natural mixtures of recently produced and refractory DOC. The implications of these results for PMA formation and RDOC biogeochemistry will be discussed.

Low energy cyclotron for radiocarbon dating

DOE Office of Scientific and Technical Information (OSTI.GOV)

Welch, J.J.

1984-12-01

The measurement of naturally occurring radioisotopes whose half lives are less than a few hundred million years but more than a few years provides information about the temporal behavior of geologic and climatic processes, the temporal history of meteoritic bodies as well as the production mechanisms of these radioisotopes. A new extremely sensitive technique for measuring these radioisotopes at tandem Van de Graaff and cyclotron facilities has been very successful though the high cost and limited availability have been discouraging. We have built and tested a low energy cyclotron for radiocarbon dating similar in size to a conventional mass spectrometer.more » These tests clearly show that with the addition of a conventional ion source, the low energy cyclotron can perform the extremely high sensitivity /sup 14/C measurements that are now done at accelerator facilities. We found that no significant background is present when the cyclotron is tuned to accelerate /sup 14/C negative ions and the transmission efficiency is adequate to perform radiocarbon dating on milligram samples of carbon. The internal ion source used did not produce sufficient current to detect /sup 14/C directly at modern concentrations. We show how a conventional carbon negative ion source, located outside the cyclotron magnet, would produce sufficient beam and provide for quick sampling to make radiocarbon dating milligram samples with a modest laboratory instrument feasible.« less

Investigating the Impact of Past and Future CO2 Emissions on the Distribution of Radiocarbon in the Ocean

NASA Astrophysics Data System (ADS)

Khatiwala, S.; Payne, S.; Graven, H. D.; Heimbach, P.

2015-12-01

The ocean is a significant sink for carbon dioxide from fossil fuel burning, absorbing roughly a third of human CO2 emitted over the industrial period. This has implications not only for climate but also for the chemical and isotopic composition of the ocean. Human activities have increased the ocean radiocarbon content through nuclear bomb tests in the 1950s-60s, which released a large amount of radiocarbon (14C) into the atmosphere, but fossil fuel emissions are decreasing the radiocarbon content through the release of 14C-depleted CO2. Here, we use the ECCO-v4 ocean state estimate to examine the changing nature of the air-sea flux of radiocarbon and its spatial distribution in the ocean in response to past and future CO2 emissions, the latter taken from the the Representative Concentration Pathway (RCP) database used in IPCC simulations. In line with previous studies we find that the large air-sea gradient of 14C induced by nuclear bomb testing led to rapid accumulation of radiocarbon in the surface ocean. Surface fluxes of 14C have considerably weakened over the past several decades and in some areas 14C is being returned to the atmosphere. As fossil fuel emissions continue to reduce the atmospheric 14C/C ratio (Δ14C), in most RCP scenarios the total ocean 14C inventory starts decreasing by 2030. With strong emissions, the Δ14C of surface waters is driven to increasingly negative values and in RCP 8.5 by 2100 much of the surface ocean has apparent radiocarbon ages in excess of 2000 years, with subtropical gyres more depleted in 14C than the Southern Ocean. Surface waters become significantly more negative in Δ14C than underlying waters. As a result, turning conventional tracer oceanography on its head, recently ventilated waters are characterized by more negative Δ14C values. Similar patterns can be expected for CFCs in the ocean as atmospheric concentrations decrease over the next several decades. Our results have a number of implications, notably for

Radiocarbon evidence for a smaller oceanic carbon dioxide sink than previously believed

NASA Astrophysics Data System (ADS)

Hesshaimer, Vago; Heimann, Martin; Levin, Ingeborg

1994-07-01

RADIOCARBON produced naturally in the upper atmosphere or arti-ficially during nuclear weapons testing is the main tracer used to validate models of oceanic carbon cycling, in particular the exchange of carbon dioxide with the atmosphere1-3 and the mixing parameters within the ocean itself4-7. Here we test the overall consistency of exchange fluxes between all relevant compartments in a simple model of the global carbon cycle, using measurements of the long-term tropospheric CO2 concentration8 and radiocarbon composition9-12, the bomb 14C inventory in the stratosphere13,14 and a compilation of bomb detonation dates and strengths15. We find that to balance the budget, we must invoke an extra source to account for 25% of the generally accepted uptake of bomb 14C by the oceans3. The strength of this source decreases from 1970 onwards, with a characteristic timescale similar to that of the ocean uptake. Significant radiocarbon transport from the remote high stratosphere and significantly reduced uptake of bomb 14C by the biosphere can both be ruled out by observational constraints. We therefore conclude that the global oceanic bomb 14C inventory should be revised downwards. A smaller oceanic bomb 14C inventory also implies a smaller oceanic radiocarbon penetration depth16, which in turn implies that the oceans take up 25% less anthropogenic CO2 than had previously been believed.

Optical Measurement of Radiocarbon below Unity Fraction Modern by Linear Absorption Spectroscopy.

PubMed

Fleisher, Adam J; Long, David A; Liu, Qingnan; Gameson, Lyn; Hodges, Joseph T

2017-09-21

High-precision measurements of radiocarbon ( 14 C) near or below a fraction modern 14 C of 1 (F 14 C ≤ 1) are challenging and costly. An accurate, ultrasensitive linear absorption approach to detecting 14 C would provide a simple and robust benchtop alternative to off-site accelerator mass spectrometry facilities. Here we report the quantitative measurement of 14 C in gas-phase samples of CO 2 with F 14 C < 1 using cavity ring-down spectroscopy in the linear absorption regime. Repeated analysis of CO 2 derived from the combustion of either biogenic or petrogenic sources revealed a robust ability to differentiate samples with F 14 C < 1. With a combined uncertainty of 14 C/ 12 C = 130 fmol/mol (F 14 C = 0.11), initial performance of the calibration-free instrument is sufficient to investigate a variety of applications in radiocarbon measurement science including the study of biofuels and bioplastics, illicitly traded specimens, bomb dating, and atmospheric transport.

Radiocarbon Dating

DOE Office of Scientific and Technical Information (OSTI.GOV)

Buchholz, B A

Radiocarbon dating can be used to determine the age of objects that contain components that were once alive. In the case of human remains, a radiocarbon date can distinguish between a crime scene and an archeological site. Documents, museum artifacts and art objects can be dated to determine if their age is correct for the historical context. A radiocarbon date does not confirm authenticity, but it can help identify a forgery.

Results of Radiocarbon Dating of Holocene Deposits from the Sea of Azov

NASA Astrophysics Data System (ADS)

Matishov, G. G.; Kovaleva, G. V.; Arslanov, Kh. A.; Dyuzhova, K. V.; Polshin, V. V.; Zolotareva, A. E.

2018-04-01

New data on the absolute age of Quaternary bottom deposits from the Sea of Azov based on the results of radiocarbon analysis (14C) are presented. Overall, 67 radiocarbon dating of bottom deposits of New and Ancient Azov Ages were obtained. The thickness of sediments of the New Azov Age and their distribution over different areas of the Sea of Azov was determined during the study; the results obtained were compared with the reference data available. An integrated approach to the study of deposits, based on the combination of the biostratigraphy methods and the results of absolute age dating, was applied.

Surface water processes in the Indonesian throughflow as documented by a high-resolution coral Δ14C record

NASA Astrophysics Data System (ADS)

Fallon, Stewart J.; Guilderson, Thomas P.

2008-09-01

To explore the seasonal to decadal variability in surface water masses that contribute to the Indonesian throughflow, we have generated a 115-year bimonthly coral-based radiocarbon time series from a coral in the Makassar Straits. In the pre-bomb (pre-1955) era from 1890 to 1954, the radiocarbon time series occasionally displays a small seasonal signal (10-15‰). After 1954 the radiocarbon record increases rapidly, in response to the increased atmospheric 14C content caused by nuclear weapons testing. From 1957 to 1986 the record displays clear seasonal variability from 15 to 60‰ and the post-bomb peak (163 per mil) occurred in 1974. The seasonal cycle of radiocarbon can be attributed to variations of surface waters passing through the South Makassar Strait. Southern Makassar is under the influence of the Northwest Monsoon, which is responsible for the high austral summer radiocarbon (North Pacific waters) and the Southeast Monsoon that flushes back a mixture of low (South Pacific and upwelling altered) radiocarbon water from the Banda Sea. The coral record also shows a significant 14C peak in 1955 due to the bomb-14C water advected into this region from nuclear weapons tests in the Marshall Islands in 1954.

Bomb-curve radiocarbon measurement of recent biologic tissues and applications to wildlife forensics and stable isotope (paleo)ecology

NASA Astrophysics Data System (ADS)

Uno, Kevin T.; Quade, Jay; Fisher, Daniel C.; Wittemyer, George; Douglas-Hamilton, Iain; Andanje, Samuel; Omondi, Patrick; Litoroh, Moses; Cerling, Thure E.

2013-07-01

Above-ground thermonuclear weapons testing from 1952 through 1962 nearly doubled the concentration of radiocarbon (14C) in the atmosphere. As a result, organic material formed during or after this period may be radiocarbon-dated using the abrupt rise and steady fall of the atmospheric 14C concentration known as the bomb-curve. We test the accuracy of accelerator mass spectrometry radiocarbon dating of 29 herbivore and plant tissues collected on known dates between 1905 and 2008 in East Africa. Herbivore samples include teeth, tusks, soft tissue, hair, and horn. Tissues formed after 1955 are dated to within 0.3-1.3 y of formation, depending on the tissue type, whereas tissues older than ca. 1955 have high age uncertainties (>17 y) due to the Suess effect. 14C dating of tissues has applications to stable isotope (paleo)ecology and wildlife forensics. We use data from 41 additional samples to determine growth rates of tusks, molars, and hair, which improve interpretations of serial stable isotope data for (paleo)ecological studies. 14C dating can also be used to calculate the time interval represented in periodic histological structures in dental tissues (i.e., perikymata), which in turn may be used as chronometers in fossil teeth. Bomb-curve 14C dating of confiscated animal tissues (e.g., ivory statues) can be used to determine whether trade of the item is legal, because many Convention of International Trade of Endangered Species restrictions are based on the age of the tissue, and thus can serve as a powerful forensic tool to combat illegal trade in animal parts.

Bomb-curve radiocarbon measurement of recent biologic tissues and applications to wildlife forensics and stable isotope (paleo)ecology.

PubMed

Uno, Kevin T; Quade, Jay; Fisher, Daniel C; Wittemyer, George; Douglas-Hamilton, Iain; Andanje, Samuel; Omondi, Patrick; Litoroh, Moses; Cerling, Thure E

2013-07-16

Above-ground thermonuclear weapons testing from 1952 through 1962 nearly doubled the concentration of radiocarbon ((14)C) in the atmosphere. As a result, organic material formed during or after this period may be radiocarbon-dated using the abrupt rise and steady fall of the atmospheric (14)C concentration known as the bomb-curve. We test the accuracy of accelerator mass spectrometry radiocarbon dating of 29 herbivore and plant tissues collected on known dates between 1905 and 2008 in East Africa. Herbivore samples include teeth, tusks, soft tissue, hair, and horn. Tissues formed after 1955 are dated to within 0.3-1.3 y of formation, depending on the tissue type, whereas tissues older than ca. 1955 have high age uncertainties (>17 y) due to the Suess effect. (14)C dating of tissues has applications to stable isotope (paleo)ecology and wildlife forensics. We use data from 41 additional samples to determine growth rates of tusks, molars, and hair, which improve interpretations of serial stable isotope data for (paleo)ecological studies. (14)C dating can also be used to calculate the time interval represented in periodic histological structures in dental tissues (i.e., perikymata), which in turn may be used as chronometers in fossil teeth. Bomb-curve (14)C dating of confiscated animal tissues (e.g., ivory statues) can be used to determine whether trade of the item is legal, because many Convention of International Trade of Endangered Species restrictions are based on the age of the tissue, and thus can serve as a powerful forensic tool to combat illegal trade in animal parts.

Radiocarbon dating of twentieth century works of art

NASA Astrophysics Data System (ADS)

Petrucci, F.; Caforio, L.; Fedi, M.; Mandò, P. A.; Peccenini, E.; Pellicori, V.; Rylands, P.; Schwartzbaum, P.; Taccetti, F.

2016-11-01

The atmospheric tests of nuclear weapons caused a sudden increase in the radiocarbon concentration in the atmosphere from 1955, reaching its maximum value in 1963-1965. Once the nuclear tests in the atmosphere were halted, the 14C concentration started to decrease. This behavior of the radiocarbon concentration is called the "Bomb Peak", and it has successfully been used as a tool for high-precision radiocarbon measurements, in forensic sciences and biology. In the art field, the possibility of dating canvas, wood and paper, widely used as supports for paintings, may be an invaluable tool in modern art studies.

Intracavity optogalvanic spectroscopy. An analytical technique for 14C analysis with subattomole sensitivity.

PubMed

Murnick, Daniel E; Dogru, Ozgur; Ilkmen, Erhan

2008-07-01

We show a new ultrasensitive laser-based analytical technique, intracavity optogalvanic spectroscopy, allowing extremely high sensitivity for detection of (14)C-labeled carbon dioxide. Capable of replacing large accelerator mass spectrometers, the technique quantifies attomoles of (14)C in submicrogram samples. Based on the specificity of narrow laser resonances coupled with the sensitivity provided by standing waves in an optical cavity and detection via impedance variations, limits of detection near 10(-15) (14)C/(12)C ratios are obtained. Using a 15-W (14)CO2 laser, a linear calibration with samples from 10(-15) to >1.5 x 10(-12) in (14)C/(12)C ratios, as determined by accelerator mass spectrometry, is demonstrated. Possible applications include microdosing studies in drug development, individualized subtherapeutic tests of drug metabolism, carbon dating and real time monitoring of atmospheric radiocarbon. The method can also be applied to detection of other trace entities.

14C Analysis of Protein Extracts from Bacillus Spores

PubMed Central

Cappucio, Jenny A.; Sarachine Falso, Miranda J.; Kashgarian, Michaele; Buchholz, Bruce A.

2014-01-01

Investigators of bioagent incidents or interdicted materials need validated, independent analytical methods that will allow them to distinguish between recently made bioagent samples versus material drawn from the archives of a historical program. Heterotrophic bacteria convert the carbon in their food sources, growth substrate or culture media, into the biomolecules they need. The F14C (fraction modern radiocarbon) of a variety of media, Bacillus spores, and separated proteins from Bacillus spores was measured by accelerator mass spectrometry (AMS). AMS precisely measures F14C values of biological materials and has been used to date the synthesis of biomaterials over the bomb pulse era (1955 to present). The F14C of Bacillus spores reflects the radiocarbon content of the media in which they were grown. In a survey of commercial media we found that the F14C value indicated that carbon sources for the media were alive within about a year of the date of manufacture and generally of terrestrial origin. Hence, bacteria and their products can be dated using their 14C signature. Bacillus spore samples were generated onsite with defined media and carbon free purification and also obtained from archived material. Using mechanical lysis and a variety of washes with carbon free acids and bases, contaminant carbon was removed from soluble proteins to enable accurate 14C bomb-pulse dating. Since media is contemporary, 14C bomb-pulse dating of isolated soluble proteins can be used to distinguish between historical archives of bioagents and those produced from recent media. PMID:24814329

14C Analysis of protein extracts from Bacillus spores.

PubMed

Cappuccio, Jenny A; Falso, Miranda J Sarachine; Kashgarian, Michaele; Buchholz, Bruce A

2014-07-01

Investigators of bioagent incidents or interdicted materials need validated, independent analytical methods that will allow them to distinguish between recently made bioagent samples versus material drawn from the archives of a historical program. Heterotrophic bacteria convert the carbon in their food sources, growth substrate or culture media, into the biomolecules they need. The F(14)C (fraction modern radiocarbon) of a variety of media, Bacillus spores, and separated proteins from Bacillus spores was measured by accelerator mass spectrometry (AMS). AMS precisely measures F(14)C values of biological materials and has been used to date the synthesis of biomaterials over the bomb pulse era (1955 to present). The F(14)C of Bacillus spores reflects the radiocarbon content of the media in which they were grown. In a survey of commercial media we found that the F(14)C value indicated that carbon sources for the media were alive within about a year of the date of manufacture and generally of terrestrial origin. Hence, bacteria and their products can be dated using their (14)C signature. Bacillus spore samples were generated onsite with defined media and carbon free purification and also obtained from archived material. Using mechanical lysis and a variety of washes with carbon free acids and bases, contaminant carbon was removed from soluble proteins to enable accurate (14)C bomb-pulse dating. Since media is contemporary, (14)C bomb-pulse dating of isolated soluble proteins can be used to distinguish between historical archives of bioagents and those produced from recent media. Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Synthetic Constraint of Ecosystem C Models Using Radiocarbon and Net Primary Production (NPP) in New Zealand Grazing Land

NASA Astrophysics Data System (ADS)

Baisden, W. T.

2011-12-01

Time-series radiocarbon measurements have substantial ability to constrain the size and residence time of the soil C pools commonly represented in ecosystem models. Radiocarbon remains unique in the ability to constrain the large stabilized C pool with decadal residence times. Radiocarbon also contributes usefully to constraining the size and turnover rate of the passive pool, but typically struggles to constrain pools with residence times less than a few years. Overall, the number of pools and associated turnover rates that can be constrained depends upon the number of time-series samples available, the appropriateness of chemical or physical fractions to isolate unequivocal pools, and the utility of additional C flux data to provide additional constraints. In New Zealand pasture soils, we demonstrate the ability to constrain decadal turnover times with in a few years for the stabilized pool and reasonably constrain the passive fraction. Good constraint is obtained with two time-series samples spaced 10 or more years apart after 1970. Three or more time-series samples further improve the level of constraint. Work within this context shows that a two-pool model does explain soil radiocarbon data for the most detailed profiles available (11 time-series samples), and identifies clear and consistent differences in rates of C turnover and passive fraction in Andisols vs Non-Andisols. Furthermore, samples from multiple horizons can commonly be combined, yielding consistent residence times and passive fraction estimates that are stable with, or increase with, depth in different sites. Radiocarbon generally fails to quantify rapid C turnover, however. Given that the strength of radiocarbon is estimating the size and turnover of the stabilized (decadal) and passive (millennial) pools, the magnitude of fast cycling pool(s) can be estimated by subtracting the radiocarbon-based estimates of turnover within stabilized and passive pools from total estimates of NPP. In grazing

Anomalous elevated radiocarbon measurements of PM2.5

NASA Astrophysics Data System (ADS)

Buchholz, Bruce A.; Fallon, Stewart J.; Zermeño, Paula; Bench, Graham; Schichtel, Bret A.

2013-01-01

Two-component models are often used to determine the contributions made by fossil fuel and natural sources of carbon in airborne particulate matter (PM). The models reduce thousands of actual sources to two end members based on isotopic signature. Combustion of fossil fuels produces PM free of carbon-14 (14C). Wood or charcoal smoke, restaurant fryer emissions, and natural emissions from plants produce PM with the contemporary concentration of 14C approximately 1.2 × 10-1214C/C. Such data can be used to estimate the relative contributions of fossil fuels and biogenic aerosols to the total aerosol loading and radiocarbon analysis is becoming a popular source apportionment method. Emissions from incinerators combusting medical or biological wastes containing tracer 14C can skew the 14C/C ratio of PM, however, so critical analysis of sampling sites for possible sources of elevated PM needs to be completed prior to embarking on sampling campaigns. Results are presented for two ambient monitoring sites in different areas of the United States where 14C contamination is apparent. Our experience suggests that such contamination is uncommon but is also not rare (∼10%) for PM sampling sites.

Measuring Carbon-based Contaminant Mineralization Using Combined CO2 Flux and Radiocarbon Analyses.

PubMed

Boyd, Thomas J; Montgomery, Michael T; Cuenca, Richard H; Hagimoto, Yutaka

2016-10-21

A method is described which uses the absence of radiocarbon in industrial chemicals and fuels made from petroleum feedstocks which frequently contaminate the environment. This radiocarbon signal - or rather the absence of signal - is evenly distributed throughout a contaminant source pool (unlike an added tracer) and is not impacted by biological, chemical or physical processes (e.g., the 14 C radioactive decay rate is immutable). If the fossil-derived contaminant is fully degraded to CO2, a harmless end-product, that CO2 will contain no radiocarbon. CO2 derived from natural organic matter (NOM) degradation will reflect the NOM radiocarbon content (usually <30,000 years old). Given a known radiocarbon content for NOM (a site background), a two end-member mixing model can be used to determine the CO2 derived from a fossil source in a given soil gas or groundwater sample. Coupling the percent CO2 derived from the contaminant with the CO2 respiration rate provides an estimate for the total amount of contaminant degraded per unit time. Finally, determining a zone of influence (ZOI) representing the volume from which site CO2 is collected allows determining the contaminant degradation per unit time and volume. Along with estimates for total contaminant mass, this can ultimately be used to calculate time-to-remediate or otherwise used by site managers for decision-making.

Measuring Carbon-based Contaminant Mineralization Using Combined CO2 Flux and Radiocarbon Analyses

PubMed Central

Boyd, Thomas J.; Montgomery, Michael T.; Cuenca, Richard H.; Hagimoto, Yutaka

2016-01-01

A method is described which uses the absence of radiocarbon in industrial chemicals and fuels made from petroleum feedstocks which frequently contaminate the environment. This radiocarbon signal — or rather the absence of signal — is evenly distributed throughout a contaminant source pool (unlike an added tracer) and is not impacted by biological, chemical or physical processes (e.g., the 14C radioactive decay rate is immutable). If the fossil-derived contaminant is fully degraded to CO2, a harmless end-product, that CO2 will contain no radiocarbon. CO2 derived from natural organic matter (NOM) degradation will reflect the NOM radiocarbon content (usually <30,000 years old). Given a known radiocarbon content for NOM (a site background), a two end-member mixing model can be used to determine the CO2 derived from a fossil source in a given soil gas or groundwater sample. Coupling the percent CO2 derived from the contaminant with the CO2 respiration rate provides an estimate for the total amount of contaminant degraded per unit time. Finally, determining a zone of influence (ZOI) representing the volume from which site CO2 is collected allows determining the contaminant degradation per unit time and volume. Along with estimates for total contaminant mass, this can ultimately be used to calculate time-to-remediate or otherwise used by site managers for decision-making. PMID:27805601

Age validation of quillback rockfish (Sebastes maliger) using bomb radiocarbon

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kerr, L A; Andrews, A H; Munk, K

2005-01-05

Rockfishes (Sebastes spp.) support one of the most economically important fisheries of the Pacific Northwest and it is essential for sustainable management that age estimation procedures be validated for these species. Atmospheric testing of thermonuclear devices during the 1950s and 1960s created a global radiocarbon ({sup 14}C) signal in the ocean environment that scientists have identified as a useful tracer and chronological marker in natural systems. In this study, we first demonstrated that fewer samples are necessary for age validation using the bomb-generated {sup 14}C signal by emphasizing the utility of the time-specific marker created by the initial rise ofmore » bomb-{sup 14}C. Second, the bomb-generated {sup 14}C signal retained in fish otoliths was used to validate the age and age estimation methodology of the quillback rockfish (Sebastes maliger) in the waters of southeast Alaska. Radiocarbon values from the first year's growth of quillback rockfish otoliths were plotted against estimated birth year producing a {sup 14}C time series spanning 1950 to 1985. The initial rise of bomb-{sup 14}C from pre-bomb levels ({approx} -90 {per_thousand}) occurred in 1959 {+-} 1 year and {sup 14}C levels rose relatively rapidly to peak {Delta}{sup 14}C values in 1967 (+105.4 {per_thousand}), with a subsequent declining trend through the end of the record in 1985 (+15.4 {per_thousand}). The agreement between the year of initial rise of {sup 14}C levels from the quillback rockfish record and the chronometer determined for the waters of southeast Alaska from yelloweye rockfish (S. ruberrimus) otoliths validated the ageing methodology for the quillback rockfish. The concordance of the entire quillback rockfish {sup 14}C record with the yelloweye rockfish time series demonstrated the effectiveness of this age validation technique, confirmed the longevity of the quillback rockfish up to a minimum of 43 years, and strongly supports higher age estimates of up to 90 years.« less

RADIOCARBON 14C MEASUREMENTS ON ATMOSPHERIC SAMPLES OF PARTICULATE MATTER (& VOLATILE ORGANIC COMPOUNDS)

EPA Science Inventory

Following a brief history of radiocarbon work at EPA since the 1980's, the presentation focuses on recent non-winter measurements for PM-2.5 in the Southeastern U.S. (Houston, TX; Nashville, TN; and particularly, Tampa, FL) and what the measurements suggest about the importance o...

Bomb-curve radiocarbon measurement of recent biologic tissues and applications to wildlife forensics and stable isotope (paleo)ecology

PubMed Central

Uno, Kevin T.; Quade, Jay; Fisher, Daniel C.; Wittemyer, George; Douglas-Hamilton, Iain; Andanje, Samuel; Omondi, Patrick; Litoroh, Moses; Cerling, Thure E.

2013-01-01

Above-ground thermonuclear weapons testing from 1952 through 1962 nearly doubled the concentration of radiocarbon (14C) in the atmosphere. As a result, organic material formed during or after this period may be radiocarbon-dated using the abrupt rise and steady fall of the atmospheric 14C concentration known as the bomb-curve. We test the accuracy of accelerator mass spectrometry radiocarbon dating of 29 herbivore and plant tissues collected on known dates between 1905 and 2008 in East Africa. Herbivore samples include teeth, tusks, soft tissue, hair, and horn. Tissues formed after 1955 are dated to within 0.3–1.3 y of formation, depending on the tissue type, whereas tissues older than ca. 1955 have high age uncertainties (>17 y) due to the Suess effect. 14C dating of tissues has applications to stable isotope (paleo)ecology and wildlife forensics. We use data from 41 additional samples to determine growth rates of tusks, molars, and hair, which improve interpretations of serial stable isotope data for (paleo)ecological studies. 14C dating can also be used to calculate the time interval represented in periodic histological structures in dental tissues (i.e., perikymata), which in turn may be used as chronometers in fossil teeth. Bomb-curve 14C dating of confiscated animal tissues (e.g., ivory statues) can be used to determine whether trade of the item is legal, because many Convention of International Trade of Endangered Species restrictions are based on the age of the tissue, and thus can serve as a powerful forensic tool to combat illegal trade in animal parts. PMID:23818577

Age estimation in forensic sciences: application of combined aspartic acid racemization and radiocarbon analysis.

PubMed

Alkass, Kanar; Buchholz, Bruce A; Ohtani, Susumu; Yamamoto, Toshiharu; Druid, Henrik; Spalding, Kirsty L

2010-05-01

Age determination of unknown human bodies is important in the setting of a crime investigation or a mass disaster because the age at death, birth date, and year of death as well as gender can guide investigators to the correct identity among a large number of possible matches. Traditional morphological methods used by anthropologists to determine age are often imprecise, whereas chemical analysis of tooth dentin, such as aspartic acid racemization, has shown reproducible and more precise results. In this study, we analyzed teeth from Swedish individuals using both aspartic acid racemization and radiocarbon methodologies. The rationale behind using radiocarbon analysis is that aboveground testing of nuclear weapons during the cold war (1955-1963) caused an extreme increase in global levels of carbon-14 ((14)C), which has been carefully recorded over time. Forty-four teeth from 41 individuals were analyzed using aspartic acid racemization analysis of tooth crown dentin or radiocarbon analysis of enamel, and 10 of these were split and subjected to both radiocarbon and racemization analysis. Combined analysis showed that the two methods correlated well (R(2) = 0.66, p < 0.05). Radiocarbon analysis showed an excellent precision with an overall absolute error of 1.0 +/- 0.6 years. Aspartic acid racemization also showed a good precision with an overall absolute error of 5.4 +/- 4.2 years. Whereas radiocarbon analysis gives an estimated year of birth, racemization analysis indicates the chronological age of the individual at the time of death. We show how these methods in combination can also assist in the estimation of date of death of an unidentified victim. This strategy can be of significant assistance in forensic casework involving dead victim identification.

Cold Reversal on Kodiak Island, Alaska, Correlated with the European Younger Dryas by Using Variations of Atmospheric C-14 Content

NASA Technical Reports Server (NTRS)

Hajdas, Irka; Bonani, Georges; Boden, Per; Peteet, Dorothy M.; Mann, Daniel H.

1999-01-01

High-resolution AMS (accelerator-mass-spectrometer) radiocarbon dating was performed on late-glacial macrofossils in lake sediments from Kodiak Island, Alaska, and on shells in marine sediments from southwest Sweden. In both records, a dramatic drop in radiocarbon ages equivalent to a rise in the atmospheric C-14 by approximately 70%. coincides with the beginning of the cold period at 11000 yr B.P. (C-14 age). Thus our results show that a close correlation between climatic records around the globe is possible by using a global signature of changes in atmospheric C-14 content.

The radiocarbon budget for Mono Lake: an unsolved mystery

USGS Publications Warehouse

Broecker, W.S.; Wanninkhof, R.; Mathieu, G.; Peng, T.-H.; Stine, S.; Robinson, S.; Herczeg, A.; Stuiver, M.

1988-01-01

Since 1957 the 14C C ratio of the dissolved inorganic carbon in Mono Lake has risen by about 60???. The magnitude of this increase is about four times larger than that expected from the invasion of bomb-produced 14C from the atmosphere. We have eliminated the following explanations: (1) measurement error, (2) an unusually high physical exchange rate for non-reactive gases, (3) inorganic enhancement of the CO2 exchange rate, and (4) biological enhancement of the CO2 exchange rate. Clandestine disposal of waste radiocarbon remains a dark-horse explanation. In the course of our investigations we have uncovered evidence for at least one episodic input of radiocarbon-free carbon to the lake over the last 1000 years. We speculate that this injection was related to a hydrothermal event resulting from sublacustrine volcanic activity. ?? 1988.

Measurements and modeling of contemporary radiocarbon in the stratosphere

NASA Astrophysics Data System (ADS)

Kanu, A. M.; Comfort, L. L.; Guilderson, T. P.; Cameron-Smith, P. J.; Bergmann, D. J.; Atlas, E. L.; Schauffler, S.; Boering, K. A.

2016-02-01

Measurements of the 14C content of carbon dioxide in air collected by high-altitude balloon flights in 2003-2005 reveal the contemporary radiocarbon distribution in the northern midlatitude stratosphere, four decades after the Limited Test Ban Treaty restricted atmospheric testing of nuclear weapons. Comparisons with results from a 3-D chemical-transport model show that the 14CO2 distribution is now largely governed by the altitude/latitude dependence of the natural cosmogenic production rate, stratospheric transport, and propagation into the stratosphere of the decreasing radiocarbon trend in tropospheric CO2 due to fossil fuel combustion. From the observed correlation of 14CO2 with N2O mixing ratios, an annual global mean net flux of 14CO2 to the troposphere of 1.6(±0.4) × 1017‰ mol CO2 yr-1 and a global production rate of 2.2(±0.6) × 1026 atoms 14C yr-1 are empirically derived. The results also indicate that contemporary 14CO2 observations provide highly sensitive diagnostics for stratospheric transport and residence times in models.

Coral radiocarbon constraints on the source of the Indonesian throughflow

DOE Office of Scientific and Technical Information (OSTI.GOV)

Moore, M.D.; Schrag, D.P.; Kashgarian, M.

1997-06-01

Radiocarbon variability in {ital Porites} spp. corals from Guam and the Makassar Strait (Indonesian Seaway) was used to identify the source waters contributing to the Indonesian throughflow. Time series with bimonthly resolution were constructed using accelerator mass spectrometry. The seasonal variability ranges from 15 to 60{per_thousand}, with large interannual variability. {Delta}{sup 14}C values from Indonesia and Guam have a nearly identical range. Annual mean {Delta}{sup 14}C values from Indonesia are 50 to 60{per_thousand} higher than in corals from Canton in the South Equatorial Current [{ital Druffel}, 1987]. These observations support a year-round North Pacific source for the Indonesian throughflow andmore » imply negligible contribution by South Equatorial Current water. The large seasonality in {Delta}{sup 14}C values from both sites emphasizes the dynamic behavior of radiocarbon in the surface ocean and suggests that {Delta}{sup 14}C time series of similar resolution can help constrain seasonal and interannual changes in ocean circulation in the Pacific over the last several decades.{copyright} 1997 American Geophysical Union« less

Radiocarbon dating and compositional analysis of pre-Columbian human bones

NASA Astrophysics Data System (ADS)

Andrade, E.; Solís, C.; Canto, C. E.; de Lucio, O. G.; Chavez, E.; Rocha, M. F.; Villanueva, O.; Torreblanca, C. A.

2014-08-01

Analysis of ancient human bones found in "El Cóporo", an archaeological site in Guanajuato, Mexico; were performed using a multi techniques scheme: 14C radiocarbon dating, IBA (Ion Beam Analysis), SEM-EDS (Scanning Electron Microscope Energy Dispersive X-ray Spectroscopy). We measured the elemental composition of the bones, especially some with a superficial black pigmentation. Soil samples collected from the burial place were also analyzed. The 14C dating was performed with a new High Voltage Europe 1 MV Tandentron Accelerator Mass Spectrometer (AMS) recently installed in the IFUNAM (Instituto de Física, Universidad Nacional Autónoma de México). The radiocarbon dating allowed us to determine the date of death of the individual in a period between the year 890 and 975 AD, which is consistent with the late period of the Cóporo civilization. The element sample analysis of bones with the surface black pigmentation show higher levels of Fe, Mn and Ba compared when bone's black surface was mechanically removed. These three elements were found in soil samples from the skeleton burial place. These results indicate more likely that the bone black coloration is due to a postmortem alteration occurring in the burial environment.

Radiocarbon and stable-isotope geochemistry of organic and inorganic carbon in Lake Superior

NASA Astrophysics Data System (ADS)

Zigah, Prosper K.; Minor, Elizabeth C.; Werne, Josef P.

2012-03-01

We present a lake-wide investigation of Lake Superior carbon and organic matter biogeochemistry using radiocarbon, stable isotope, and carbon concentrations. Dissolved inorganic carbon (DIC) abundance in the lake was 121-122 Tg C, with offshore concentration andδ13C values being laterally homogenous and tightly coupled to the physical and thermal regime and biochemical processes. Offshore Δ14C of DIC (50-65‰) exhibited lateral homogeneity and was more 14C enriched than co-occurring atmospheric CO2 (˜38‰); nearshore Δ14C of DIC (36-38‰) was similar to atmospheric CO2. Dissolved organic carbon (DOC) abundance was 14.2-16.4 Tg C. DOC's concentration and δ13C were homogenous in June (mixed lake), but varied laterally during August (stratification) possibly due to spatial differences in lake productivity. Throughout sampling, DOC had modern radiocarbon values (14-58‰) indicating a semilabile nature with a turnover time of ≤60 years. Lake particulate organic carbon (POC, 0.9-1.3 Tg C) was consistently 13C depleted relative to DOC. The δ15N of epilimnetic particulate organic nitrogen shifted to more negative values during stratification possibly indicating greater use of nitrate (rather than ammonium) by phytoplankton in August. POC's radiocarbon was spatially heterogeneous (Δ14C range: 58‰ to -303‰), and generally 14C depleted relative to DOC and DIC. POC 14C depletion could not be accounted for by black carbon in the lake but, because of its spatial and temporal distribution, is attributed to sediment resuspension. The presence of old POC within the epilimnion of the open lake indicates possible benthic-pelagic coupling in the lake's organic carbon cycle; the ultimate fate of this old POC bears further investigation.

Assessing Soil Organic C Stability at the Continental Scale: An Analysis of Soil C and Radiocarbon Profiles Across the NEON Sites

NASA Astrophysics Data System (ADS)

Heckman, K. A.; Gallo, A.; Hatten, J. A.; Swanston, C.; McKnight, D. M.; Strahm, B. D.; Sanclements, M.

2017-12-01

Soil carbon stocks have become recognized as increasingly important in the context of climate change and global C cycle modeling. As modelers seek to identify key parameters affecting the size and stability of belowground C stocks, attention has been drawn to the mineral matrix and the soil physiochemical factors influenced by it. Though clay content has often been utilized as a convenient and key explanatory variable for soil C dynamics, its utility has recently come under scrutiny as new paradigms of soil organic matter stabilization have been developed. We utilized soil cores from a range of National Ecological Observatory Network (NEON) experimental plots to examine the influence of physicochemical parameters on soil C stocks and turnover, and their relative importance in comparison to climatic variables. Soils were cored at NEON sites, sampled by genetic horizon, and density separated into light fractions (particulate organics neither occluded within aggregates nor associated with mineral surfaces), occluded fractions (particulate organics occluded within aggregates), and heavy fractions (organics associated with mineral surfaces). Bulk soils and density fractions were measured for % C and radiocarbon abundance (as a measure of C stability). Carbon and radiocarbon abundances were examined among fractions and in the context of climatic variables (temperature, precipitation, elevation) and soil physiochemical variables (% clay and pH). No direct relationships between temperature and soil C or radiocarbon abundances were found. As a whole, soil radiocarbon abundance in density fractions decreased in the order of light>heavy>occluded, highlighting the importance of both surface sorption and aggregation to the preservation of organics. Radiocarbon abundance was correlated with pH, with variance also grouping by dominate vegetation type. Soil order was also identified as an important proxy variable for C and radiocarbon abundance. Preliminary results suggest that

Exploring global carbon turnover and radiocarbon cycling in terrestrial biosphere models

NASA Astrophysics Data System (ADS)

Graven, H. D.; Warren, H.

2017-12-01

The uptake of carbon into terrestrial ecosystems through net primary productivity (NPP) and the turnover of that carbon through various pathways are the fundamental drivers of changing carbon stocks on land, in addition to human-induced and natural disturbances. Terrestrial biosphere models use different formulations for carbon uptake and release, resulting in a range of values in NPP of 40-70 PgC/yr and biomass turnover times of about 25-40 years for the preindustrial period in current-generation models from CMIP5. Biases in carbon uptake and turnover impact simulated carbon uptake and storage in the historical period and later in the century under changing climate and CO2 concentration, however evaluating global-scale NPP and carbon turnover is challenging. Scaling up of plot-scale measurements involves uncertainty due to the large heterogeneity across ecosystems and biomass types, some of which are not well-observed. We are developing the modelling of radiocarbon in terrestrial biosphere models, with a particular focus on decadal 14C dynamics after the nuclear weapons testing in the 1950s-60s, including the impact of carbon flux trends and variability on 14C cycling. We use an estimate of the total inventory of excess 14C in the biosphere constructed by Naegler and Levin (2009) using a 14C budget approach incorporating estimates of total 14C produced by the weapons tests and atmospheric and oceanic 14C observations. By simulating radiocarbon in simple biosphere box models using carbon fluxes from the CMIP5 models, we find that carbon turnover is too rapid in many of the simple models - the models appear to take up too much 14C and release it too quickly. Therefore many CMIP5 models may also simulate carbon turnover that is too rapid. A caveat is that the simple box models we use may not adequately represent carbon dynamics in the full-scale models. Explicit simulation of radiocarbon in terrestrial biosphere models would allow more robust evaluation of biosphere

Historic binnacle of 14C/12C concentration in Mexico City

NASA Astrophysics Data System (ADS)

Flores, J. A.; Solís, C.; Huerta, A.; Ortiz, M. E.; Rodríguez-Ceja, M. G.; Villanueva, J.; Chávez, E.

The radiocarbon concentration is reduced in urban areas, generally due to high CO2 emissions derived from fossil fuels. In this paper, new Δ14C measurements in cellulose extracted from the growth rings of two trees over a 43-year period are presented. The first is in a zone with clean air (El Nayar, Durango, Mexico) and the second is from the Greater Mexico City area (Chapultepec). Data from El Nayar is consistent with that reported for Zone 2 of the Northern Hemisphere while that from the urban area shows a significant decrease in Δ14C. Our results are compared with data from other cities (Nagoya, Japan and Valladolid, Spain).

The curved 14C vs. δ13C relationship in dissolved inorganic carbon: A useful tool for groundwater age- and geochemical interpretations

USGS Publications Warehouse

Han, Liang-Feng; Plummer, Niel; Aggarwal, Pradeep

2014-01-01

Determination of the 14C content of dissolved inorganic carbon (DIC) is useful for dating of groundwater. However, in addition to radioactive decay, the 14C content in DIC (14CDIC) can be affected by many geochemical and physical processes and numerous models have been proposed to refine radiocarbon ages of DIC in groundwater systems. Changes in the δ13C content of DIC (δ13CDIC) often can be used to deduce the processes that affect the carbon isotopic composition of DIC and the 14C value during the chemical evolution of groundwater. This paper shows that a curved relationship of 14CDIC vs. δ13CDIC will be observed for groundwater systems if (1) the change in δ13C value in DIC is caused by a first-order or pseudo-first-order process, e.g. isotopic exchange between DIC and solid carbonate, (2) the reaction/process progresses with the ageing of the groundwater, i.e. with decay of 14C in DIC, and (3) the magnitude of the rate of change in δ13C of DIC is comparable with that of 14C decay. In this paper, we use a lumped parameter method to derive a model based on the curved relationship between 14CDICand δ13CDIC. The derived model, if used for isotopic exchange between DIC and solid carbonate, is identical to that derived by Gonfiantini and Zuppi (2003). The curved relationship of 14CDIC vs. δ13CDIC can be applied to interpret the age of the DIC in groundwater. Results of age calculations using the method discussed in this paper are compared with those obtained by using other methods that calculate the age of DIC based on adjusted initial radiocarbon values for individual samples. This paper shows that in addition to groundwater age interpretation, the lumped parameter method presented here also provides a useful tool for geochemical interpretations, e.g. estimation of apparent rates of geochemical reactions and revealing the complexity of the geochemical environment.

Tips and traps in the 14C bio-AMS preparation laboratory

NASA Astrophysics Data System (ADS)

Buchholz, Bruce A.; Freeman, Stewart P. H. T.; Haack, Kurt W.; Vogel, John S.

2000-10-01

Maintaining a contamination free sample preparation lab for biological 14C AMS requires the same or more diligence as a radiocarbon dating prep lab. Isotope ratios of materials routinely range over 4-8 orders of magnitude in a single experiment, dosing solutions contain thousands of DPM and gels used to separate proteins possess 14C ratios of 1 amol 14C/mg C. Radiocarbon contamination is a legacy of earlier tracer work in most biological laboratories, even if they were never hot labs. Removable surface contamination can be found and monitored using swipes. Contamination can be found on any surface routinely touched: door knobs, light switches, drawer handles, water faucets. In general, all surfaces routinely touched need to be covered with paper, foil or plastic that can be changed frequently. Shared air supplies can also present problems by distributing hot aerosols throughout a building. Aerosols can be monitored for 14C content using graphitized coal or fullerene soot mixed with metal powder as an absorber. The monitors can be set out in work spaces for 1-2 weeks and measured by AMS with regular samples. Frequent air changes help minimize aerosol contamination in many cases. Cross-contamination of samples can be minimized by using disposable plastic or glassware in the prep lab, isolating samples from the air when possible and using positive displacement pipettors.

RADIOCARBON MEASUREMENTS ON PM-2.5 AMBIENT AEROSOL

EPA Science Inventory

Radiocarbon (14C) measurements provide an estimate of the fraction of carbon in a sample that is biogenic. The methodology has been extensively used in past wintertime studies to quantify the contribution of wood smoke to ambient aerosol. In summertime such measurements can p...

Measurements and modeling of contemporary radiocarbon in the stratosphere

DOE PAGES

Kanu, A. M.; Comfort, L. L.; Guilderson, T. P.; ...

2016-01-29

Measurements of the 14C content of carbon dioxide in air collected by high-altitude balloon flights in 2003–2005 reveal the contemporary radiocarbon distribution in the northern midlatitude stratosphere, four decades after the Limited Test Ban Treaty restricted atmospheric testing of nuclear weapons. Comparisons with results from a 3-D chemical-transport model show that the 14CO 2 distribution is now largely governed by the altitude/latitude dependence of the natural cosmogenic production rate, stratospheric transport, and propagation into the stratosphere of the decreasing radiocarbon trend in tropospheric CO 2 due to fossil fuel combustion. From the observed correlation of 14CO 2 with N 2Omore » mixing ratios, an annual global mean net flux of 14CO 2 to the troposphere of 1.6(±0.4) × 10 17‰ mol CO 2 yr –1 and a global production rate of 2.2(±0.6) × 10 26 atoms 14C yr –1 are empirically derived. Furthermore, the results also indicate that contemporary 14CO 2 observations provide highly sensitive diagnostics for stratospheric transport and residence times in models.« less

A graphical method to evaluate predominant geochemical processes occurring in groundwater systems for radiocarbon dating

USGS Publications Warehouse

Han, Liang-Feng; Plummer, Niel; Aggarwal, Pradeep

2012-01-01

A graphical method is described for identifying geochemical reactions needed in the interpretation of radiocarbon age in groundwater systems. Graphs are constructed by plotting the measured 14C, δ13C, and concentration of dissolved inorganic carbon and are interpreted according to specific criteria to recognize water samples that are consistent with a wide range of processes, including geochemical reactions, carbon isotopic exchange, 14C decay, and mixing of waters. The graphs are used to provide a qualitative estimate of radiocarbon age, to deduce the hydrochemical complexity of a groundwater system, and to compare samples from different groundwater systems. Graphs of chemical and isotopic data from a series of previously-published groundwater studies are used to demonstrate the utility of the approach. Ultimately, the information derived from the graphs is used to improve geochemical models for adjustment of radiocarbon ages in groundwater systems.

Constraining global air-sea gas exchange for CO2 with recent bomb 14C measurements

NASA Astrophysics Data System (ADS)

Sweeney, Colm; Gloor, Emanuel; Jacobson, Andrew R.; Key, Robert M.; McKinley, Galen; Sarmiento, Jorge L.; Wanninkhof, Rik

2007-06-01

The 14CO2 released into the stratosphere during bomb testing in the early 1960s provides a global constraint on air-sea gas exchange of soluble atmospheric gases like CO2. Using the most complete database of dissolved inorganic radiocarbon, DI14C, available to date and a suite of ocean general circulation models in an inverse mode we recalculate the ocean inventory of bomb-produced DI14C in the global ocean and confirm that there is a 25% decrease from previous estimates using older DI14C data sets. Additionally, we find a 33% lower globally averaged gas transfer velocity for CO2 compared to previous estimates (Wanninkhof, 1992) using the NCEP/NCAR Reanalysis 1 1954-2000 where the global mean winds are 6.9 m s-1. Unlike some earlier ocean radiocarbon studies, the implied gas transfer velocity finally closes the gap between small-scale deliberate tracer studies and global-scale estimates. Additionally, the total inventory of bomb-produced radiocarbon in the ocean is now in agreement with global budgets based on radiocarbon measurements made in the stratosphere and troposphere. Using the implied relationship between wind speed and gas transfer velocity ks = 0.27(Sc/660)-0.5 and standard partial pressure difference climatology of CO2 we obtain an net air-sea flux estimate of 1.3 ± 0.5 PgCyr-1 for 1995. After accounting for the carbon transferred from rivers to the deep ocean, our estimate of oceanic uptake (1.8 ± 0.5 PgCyr-1) compares well with estimates based on ocean inventories, ocean transport inversions using ocean concentration data, and model simulations.

New radiocarbon measurement methods in the Hertelendi Laboratory, Hungary

NASA Astrophysics Data System (ADS)

Janovics, Róbert; Major, István; Rinyu, László; Veres, Mihály; Molnár, Mihály

2013-04-01

In this paper we present two very different and novel methods for C-14 measurement from dissolved inorganic carbonate (DIC) of water samples. A new LSC sample preparation method for liquid scintillation C-14 measurements was implemented in the ATOMKI. The first method uses direct absorption into a special absorbent (Carbosorb E®) and a following liquid scintillation measurement. Typical sample size is 20-40 litre of water. The developed CO2 absorption method is fast, and simple. The C-14 activities is measured by an ultra low background LSC (TRI-CARB 3170 TR/SL, Perkin Elmer) including quenching parameter (tSIE).The corresponding limit of C-14 dating is 31200 year. Several tests were executed with old borehole CO2 gas without significant content of C-14 and also performed on samples of known C-14 activities between 29 and 7000 pMC, previously measured by GPC. The combined uncertainty of the described determination is about 2 % in the case of recent carbon. It is a very cost-effective and easy to use method based on a novel and simple static absorption process for the CO2 extracted from groundwater. The other very sensitive method is based on accelerator mass spectrometry (AMS) using gas ion source. This method does not require graphite generation and a small volume of water sample (1-20mL) is enough for the radiocarbon measurement. The procedure is very similar to pre-treatment of carbonate contained sample preparation for stable isotope measurement with gasbench technique. We applied a MICADAS type accelerator mass spectrometry (AMS) with gas ion source for C-14 analysis. The radiocarbon content of water was sat free with phosphoric acid and then the headspace gas was rinsed vials. The whole measurement needs only 20 min of each sample. The precision of measurement is better than 1% for modern samples. The preparation is vastly reduced compared to the other AMS methods and principally allows fully automated measurements of groundwater samples with an auto

Performance report for the low energy compact radiocarbon accelerator mass spectrometer at Uppsala University

NASA Astrophysics Data System (ADS)

Salehpour, M.; Håkansson, K.; Possnert, G.; Wacker, L.; Synal, H.-A.

2016-03-01

A range of ion beam analysis activities are ongoing at Uppsala University, including Accelerator Mass Spectrometry (AMS). Various isotopes are used for AMS but the isotope with the widest variety of applications is radiocarbon. Up until recently, only the 5 MV Pelletron tandem accelerator had been used at our site for radiocarbon AMS, ordinarily using 12 MeV 14,13,12C3+ ions. Recently a new radiocarbon AMS system, the Green-MICADAS, developed at the ion physics group at ETH Zurich, was installed. The system has a number of outstanding features which will be described. The system operates at a terminal voltage of 175 kV and uses helium stripper gas, extracting singly charged carbon ions. The low- and high energy mass spectrometers in the system are stigmatic dipole permanent magnets (0.42 and 0.97 T) requiring no electrical power nor cooling water. The system measures both the 14C/12C and the 13C/12C ratios on-line. Performance of the system is presented for both standard mg samples as well as μg-sized samples.

Analysis and Characterization of Organic Carbon in Early Holocene Wetland Paleosols using Ramped Pyrolysis 14C and Biomarkers

NASA Astrophysics Data System (ADS)

Vetter, L.; Schreiner, K. M.; Fernandez, A.; Rosenheim, B. E.; Tornqvist, T. E.

2014-12-01

Radiocarbon analyses are a key tool for quantifying the dynamics of carbon cycling and storage in both modern soils and Quaternary paleosols. Frequently, bulk 14C dates of paleosol organic carbon provide ages older than the time of soil burial, and 14C dates of geochemical fractions such as alkali and acid extracts (operationally defined as humic acids) can provide anomalously old ages when compared to coeval plant macrofossil dates. Ramped pyrolysis radiocarbon analysis of sedimentary organic material has been employed as a tool for investigating 14C age spectra in sediments with multiple organic carbon sources. Here we combine ramped pyrolysis 14C analysis and biomarker analysis (lignin-phenols and other cupric oxide products) to provide information on the source and diagenetic state of the paleosol organic carbon. We apply these techniques to immature early Holocene brackish wetland entisols from three sediment cores in southeastern Louisiana, along with overlying basal peats. Surprisingly, we find narrow 14C age spectra across all thermal aliquots from both paleosols and peats. The weighted bulk 14C ages from paleosols and overlying peats are within analytical error, and are comparable to independently analyzed 14C AMS dates from charcoal fragments and other plant macrofossils from each peat bed. Our results suggest high turnover rates of carbon in soils relative to input of exogenous carbon sources. These data raise broader questions about processes within the active soil and during pedogenesis and burial of paleosols that can effectively homogenize radiocarbon content in soils across the thermochemical spectrum. The concurrence of paleosol and peat 14C ages also suggests that, in the absence of peats with identifiable plant macrofossils, ramped pyrolysis 14C analyses of paleosols may be used to provide ages for sea-level indicators.

Age estimation in forensic sciences: Application of combined aspartic acid racemization and radiocarbon analysis

DOE Office of Scientific and Technical Information (OSTI.GOV)

Alkass, K; Buchholz, B A; Ohtani, S

Age determination of unknown human bodies is important in the setting of a crime investigation or a mass disaster, since the age at death, birth date and year of death, as well as gender, can guide investigators to the correct identity among a large number of possible matches. Traditional morphological methods used by anthropologists to determine age are often imprecise, whereas chemical analysis of tooth dentin, such as aspartic acid racemization has shown reproducible and more precise results. In this paper we analyze teeth from Swedish individuals using both aspartic acid racemization and radiocarbon methodologies. The rationale behind using radiocarbonmore » analysis is that above-ground testing of nuclear weapons during the cold war (1955-1963) caused an extreme increase in global levels of carbon-14 ({sup 14}C) which have been carefully recorded over time. Forty-four teeth from 41 individuals were analyzed using aspartic acid racemization analysis of tooth crown dentin or radiocarbon analysis of enamel and ten of these were split and subjected to both radiocarbon and racemization analysis. Combined analysis showed that the two methods correlated well (R2=0.66, p < 0.05). Radiocarbon analysis showed an excellent precision with an overall absolute error of 0.6 {+-} 04 years. Aspartic acid racemization also showed a good precision with an overall absolute error of 5.4 {+-} 4.2 years. Whereas radiocarbon analysis gives an estimated year of birth, racemization analysis indicates the chronological age of the individual at the time of death. We show how these methods in combination can also assist in the estimation of date of death of an unidentified victim. This strategy can be of significant assistance in forensic casework involving dead victim identification.« less

Radiocarbon signal of a low and intermediate level radioactive waste disposal facility in nearby trees.

PubMed

Janovics, R; Kelemen, D I; Kern, Z; Kapitány, S; Veres, M; Jull, A J T; Molnár, M

2016-03-01

Tree ring series were collected from the vicinity of a Hungarian radioactive waste treatment and disposal facility and from a distant control background site, which is not influenced by the radiocarbon discharge of the disposal facility but it represents the natural regional (14)C level. The (14)C concentration of the cellulose content of tree rings was measured by AMS. Data of the tree ring series from the disposal facility was compared to the control site for each year. The results were also compared to the (14)C data of the atmospheric (14)C monitoring stations at the disposal facility and to international background measurements. On the basis of the results, the excess radiocarbon of the disposal facility can unambiguously be detected in the tree from the repository site. Copyright © 2016 Elsevier Ltd. All rights reserved.

Collagen Fingerprinting: A New Screening Technique for Radiocarbon Dating Ancient Bone.

PubMed

Harvey, Virginia L; Egerton, Victoria M; Chamberlain, Andrew T; Manning, Phillip L; Buckley, Michael

2016-01-01

Collagen is the dominant organic component of bone and is intimately locked within the hydroxyapatite structure of this ubiquitous biomaterial that dominates archaeological and palaeontological assemblages. Radiocarbon analysis of extracted collagen is one of the most common approaches to dating bone from late Pleistocene or Holocene deposits, but dating is relatively expensive compared to other biochemical techniques. Numerous analytical methods have previously been investigated for the purpose of screening out samples that are unlikely to yield reliable dates including histological analysis, UV-stimulated fluorescence and, most commonly, the measurement of percentage nitrogen (%N) and ratio of carbon to nitrogen (C:N). Here we propose the use of collagen fingerprinting (also known as Zooarchaeology by Mass Spectrometry, or ZooMS, when applied to species identification) as an alternative screening method for radiocarbon dating, due to its ability to provide information on collagen presence and quality, alongside species identification. The method was tested on a series of sub-fossil bone specimens from cave systems on Cayman Brac (Cayman Islands), chosen due to the observable range in diagenetic alteration, and in particular, the extent of mineralisation. Six (14)C dates, of 18 initial attempts, were obtained from remains of extinct hutia, Capromys sp. (Rodentia; Capromyidae), recovered from five distinct caves on Cayman Brac, and ranging from 393 ± 25 to 1588 ± 26 radiocarbon years before present (yr BP). All of the bone samples that yielded radiocarbon dates generated excellent collagen fingerprints, and conversely those that gave poor fingerprints also failed dating. Additionally, two successfully fingerprinted bone samples were screened out from a set of 81. Both subsequently generated (14)C dates, demonstrating successful utilisation of ZooMS as an alternative screening mechanism to identify bone samples that are suitable for 1(4)C analysis.

Collagen Fingerprinting: A New Screening Technique for Radiocarbon Dating Ancient Bone

PubMed Central

Harvey, Virginia L.; Egerton, Victoria M.; Chamberlain, Andrew T.; Manning, Phillip L.; Buckley, Michael

2016-01-01

Collagen is the dominant organic component of bone and is intimately locked within the hydroxyapatite structure of this ubiquitous biomaterial that dominates archaeological and palaeontological assemblages. Radiocarbon analysis of extracted collagen is one of the most common approaches to dating bone from late Pleistocene or Holocene deposits, but dating is relatively expensive compared to other biochemical techniques. Numerous analytical methods have previously been investigated for the purpose of screening out samples that are unlikely to yield reliable dates including histological analysis, UV-stimulated fluorescence and, most commonly, the measurement of percentage nitrogen (%N) and ratio of carbon to nitrogen (C:N). Here we propose the use of collagen fingerprinting (also known as Zooarchaeology by Mass Spectrometry, or ZooMS, when applied to species identification) as an alternative screening method for radiocarbon dating, due to its ability to provide information on collagen presence and quality, alongside species identification. The method was tested on a series of sub-fossil bone specimens from cave systems on Cayman Brac (Cayman Islands), chosen due to the observable range in diagenetic alteration, and in particular, the extent of mineralisation. Six 14C dates, of 18 initial attempts, were obtained from remains of extinct hutia, Capromys sp. (Rodentia; Capromyidae), recovered from five distinct caves on Cayman Brac, and ranging from 393 ± 25 to 1588 ± 26 radiocarbon years before present (yr BP). All of the bone samples that yielded radiocarbon dates generated excellent collagen fingerprints, and conversely those that gave poor fingerprints also failed dating. Additionally, two successfully fingerprinted bone samples were screened out from a set of 81. Both subsequently generated 14C dates, demonstrating successful utilisation of ZooMS as an alternative screening mechanism to identify bone samples that are suitable for 14C analysis. PMID:26938469

Radiocarbon Depression in Aquatic Foodwebs of the Colorado River, USA: Coupling Between Carbonate Weathering and the Biosphere

NASA Astrophysics Data System (ADS)

Sickman, J. O.; Huang, W.; Lucero, D.; Anderson, M.

2012-12-01

The 14C isotopic composition of living organisms is generally considered to be in isotopic equilibrium with atmosphere CO2. During the course of investigations of aquatic foodwebs of the Colorado River, we measured substantial radiocarbon depression of organisms within planktonic and benthic foodwebs of Copper Basin Reservoir, a short residence-time water body at the intake to the Colorado River Aqueduct. All trophic levels had depressed radiocarbon content with inferred "age" of ca. 1,200 radiocarbon years (range: 0.85 to 0.87 fraction modern carbon (fmc)). Additional measurements of the radiocarbon content of dissolved organic carbon (DOC) and dissolved inorganic carbon (DIC) were made in other major rivers in California (New (near Salton Sea), Santa Ana (near Riverside), San Joaquin (near Fresno) and Salinas (near San Luis Obispo)). In the New River (which is composed primarily of irrigation tailwater derived from the Colorado River), the radiocarbon values for DIC closely matched those found in biota of the Copper Basin Reservoir (0.85 to 0.87 fmc), but radiocarbon values for DOC were slightly higher (0.91 to 0.95 fmc). In the other California rivers, radiocarbon concentrations in DIC were generally below modern and lower than corresponding levels in DOC; in the case of the Santa Ana River, DOC was older than DIC as a result of wastewater inputs from upstream treatment plants. Together these data suggest that the carbonate equilibrium of California rivers is influenced by weathering of carbonate minerals which produces HCO3- with no 14C. We hypothesize that this dead carbon can move into aquatic foodwebs via algae and phytoplankton uptake during photosynthesis, depressing the 14C content of aquatic foodwebs below that of the atmosphere. Based on a simple two-component mixing model incorporating carbonate weathering and atmospheric CO2, we estimate that 15-17% of the carbon in the aquatic foodweb of Copper Basin is derived directly from mineral weathering of

RADIOCARBON MEASUREMENT OF THE BIOGENIC CONTRIBUTION TO SUMMERTIME PM 2.5 AMBIENT AEROSOL IN NASHVILLE, TN

EPA Science Inventory

Radiocarbon (14C) measurements performed on PM-2.5 samples collected near Nashville, TN from June 21 to July 13, 1999, showed high levels of modern carbon, ranging from 56 to 80% of the total carbon in the samples. Radiocarbon measurements performed on dichloromethane extracts of...

A Brief Review of the Application of 14C in Terrestrial Carbon Cycle Studies

DOE Office of Scientific and Technical Information (OSTI.GOV)

Guilderson, T; Mcfarlane, K

2009-10-22

An over-arching goal of the DOE TCP program is to understand the mechanistic controls over the fate, transport, and residence time of carbon in the terrestrial biosphere. Many of the modern process and modeling studies focus on seasonal to interannual variability. However, much of the carbon on the landscape and in soils is in separate reservoirs with turnover times that are multi-decadal to millennial. It is the controls on these longer term pools or reservoirs that is a critical unknown in the face of rising GHGs and climate change and uncertainties of the terrestrial biosphere as a future global sinkmore » or source of atmospheric CO{sub 2} [eg., Friedlingstein et al., 2006; Govindasamy et al., 2005; Thompson et al., 2004]. Radiocarbon measurements, in combination with other data, can provide insight into, and constraints on, terrestrial carbon cycling. Radiocarbon (t{sub 1/2} 5730yrs) is produced naturally in the stratosphere when secondary neutrons generated by cosmic rays collide with {sup 14}N atoms [Libby 1946; Arnold and Libby, 1949]. Upon formation, {sup 14}C is rapidly oxidized to CO and then to CO{sub 2}, and is incorporated into the carbon cycle. Due to anthropogenic activities, the amount of {sup 14}C in the atmosphere doubled in the mid/late 1950s and early 1960s from its preindustrial value of {sup 14}C/{sup 12}C ratio of 1.18 x 10{sup -12} [eg., Nydal and Lovseth, 1983]. Following the atmospheric weapons test ban in 1963, the {sup 14}C/{sup 12}C ratio, has decreased due to the net isotopic exchange between the ocean and terrestrial biosphere [eg., Levin and Hessheimer, 2000] and a dilution effect due to the burning of {sup 14}C-free fossil fuel carbon, the 'Suess Effect' [Suess, 1955]. In the carbon cycle literature, radiocarbon measurements are generally reported as {Delta}{sup 14}C, which includes a correction for mass dependent fractionation [Stuiver and Polach, 1977]. In the context of carbon cycle studies radiocarbon measurements can be used

Suitability of biogenic carbonate of Lithospermum fruits for 14C dating

NASA Astrophysics Data System (ADS)

Pustovoytov, Konstantin; Riehl, Simone

2006-05-01

Lithospermum (Boraginaceae) belongs to a small group of plant taxa that accumulate biogenic carbonate in their fruits. In this genus, carbonate incrustations form in the cells of the epidermis and sclerenchyma of the pericarp. Fossil Lithospermum fruits (nutlets) with well-preserved calcified tissues commonly occur in Quaternary sediments and cultural layers. We tested the suitability of biogenic carbonate of Lithospermum fruits for radiocarbon dating using a total of 15 AMS measurement results from four modern and 11 fossil samples. The 14C data from modern samples suggest that Lithospermum utilises only atmospheric carbon to synthesise calcite in the nutlets. In general, the ages determined through 14C dating of fossil fruitscorresponded well with the absolute-age intervals for archaeological sites over the last 5000 yr. Biogenic carbonate of Lithospermum fruits, like that of Celtis, represents a new source of chronological information for late Quaternary studies.

C-14 content of ten meteorites measured by tandem accelerator mass spectrometry

NASA Technical Reports Server (NTRS)

Brown, R. M.; Andrews, H. R.; Ball, G. C.; Burn, N.; Imahori, Y.; Milton, J. C. D.; Fireman, E. L.

1984-01-01

Measurements of C-14 in three North American and seven Antarctic meteorites show in most cases that this cosmogenic isotope, which is tightly bound, was separated from absorbed atmospheric radiocarbon by stepwise heating extractions. The present upper limit to age determination by the accelerator method varies from 50,000 to 70,000 years, depending on the mass and carbon content of the sample. The natural limit caused by cosmic ray production of C-14 in silicate rocks at 2000 m elevation is estimated to be 55,000 + or - 5000 years. An estimation is also made of the 'weathering ages' of the Antarctic meteorites from the specific activity of loosely bound CO2 which is thought to be absorbed from the terrestrial atmosphere. Accelerator measurements are found to agree with previous low level counting measurements, but are more sensitive and precise.

Microflora distributions in paleosols: a method for calculating the validity of radiocarbon-dated surfaces

DOE Office of Scientific and Technical Information (OSTI.GOV)

Mahaney, W.C.; Boyer, M.G.

1986-08-01

Microflora (bacteria and fungi) distributions in several paleosols from Mount Kenya, East Africa, provide important information about contamination of buried soil horizons dated by radiocarbon. High counts of bacteria and fungi in buried soils provide evidence for contamination by plant root effects or ground water movement. Profiles with decreasing counts versus depth appear to produce internally consistent and accurate radiocarbon dates. Profiles with disjunct or bimodal distributions of microflora at various depths produce internally inconsistent chronological sequences of radiocarbon-dated buried surfaces. Preliminary results suggest that numbers up to 5 x 10/sup 2/ g/sup -1/ for bacteria in buried A horizonsmore » do not appear to affect the validity of /sup 14/C dates. Beyond this threshold value, contamination appears to produce younger dates, the difference between true age and /sup 14/C age increasing with the amount of microflora contamination.« less

A simplified In Situ cosmogenic 14C extraction system

USGS Publications Warehouse

Pigati, J.S.; Lifton, N.A.; Timothy, Jull A.J.; Quade, Jay

2010-01-01

We describe the design, construction, and testing of a new, simplified in situ radiocarbon extraction system at the University of Arizona. Blank levels for the new system are low ((234 ?? 11) ?? 103 atoms (1 ??; n = 7)) and stable. The precision of a given measurement depends on the concentration of 14C, but is typically <5% for concentrations of 100 ?? 103 atoms g-1 or more. The new system is relatively small and easy to construct, costs significantly less than the original in situ 14C extraction system at Arizona, and lends itself to future automation. ?? 2010 by the Arizona Board of Regents on behalf of the University of Arizona.

Blade-order-dependent radiocarbon variability in brown seaweed (Undaria pinnatifida) reflected a cold Oyashio water intrusion event in an embayment of the Sanriku coast, northeastern Japan

NASA Astrophysics Data System (ADS)

Satoh, N.; Fukuda, H.; Miyairi, Y.; Yokoyama, Y.; Nagata, T.

2015-12-01

Radiocarbon in dissolved inorganic carbon (DIC) in seawater varies greatly, both geographically and with depth. This "reservoir effect" is thought to be reflected in the radiocarbon content (Δ14C) of marine organisms, via DIC fixation by primary producers and subsequent trophic transfer. The Δ14C of marine organismal soft tissues might thus provide unique information about their habitats, diets, migration and other environmental histories. However, the effectiveness of this approach has yet to be extensively explored, with data on Δ14C variability in soft tissues of marine organisms being markedly limited. Here we examined whether Δ14C values of individual pinnate blades (leaf-like structures) of brown seaweed (Undaria pinnatifida) reflect the Δ14C of DIC in the water current prevailing at the time of blade formation. The study was conducted in Otsuchi Bay located in the Sanriku coastal region, northeastern Japan, where 14C-depleted cold Oyashio current and warm Tsugaru current (high Δ14C) converge, affecting the physiology and growth of marine organisms growing there. U. pinnatifida individuals cultured in the bay (length of saprophytes, 140-215 cm) were harvested in April 2014 and Δ14C of blades were determined by accelerator mass spectrometry. Younger blades formed after the Oyashio water intrusion had significantly lower Δ14C values compared to older blades formed before the event. The Δ14C values of younger and older blades were generally consistent with the Δ14C of DIC in Oyashio (-60.5 ‰) and Tsugaru (24.9 ‰) waters, respectively. Thus, despite possible turnover of organic carbon in seaweed soft tissues, blade-order-dependent Δ14C variability appeared to strongly reflect the Oyashio intrusion event (radiocarbon shift) in the bay.

Large Variations of Atmospheric 14C Associated With Dansgaard-Oeschger Cycles 10- 13

NASA Astrophysics Data System (ADS)

Weyhenmeyer, C. E.; Burns, S. J.; Fleitmann, D.; Mangini, A.; Matter, A.; Guilderson, T.; Reimer, P. J.

2006-12-01

A 1.7 m long stalagmite from Moomi Cave, Socotra Island in the Indian Ocean provides a continuous, high- resolution record of climate change between 53 and 41 kyr BP. In the northern high-latitude regions, this time period is characterized by several rapid climate change events, corresponding to Dansgaard-Oeschger (D/O) cycles 10-13. It has been suggested that these D/O cycles may be global events but high-resolution data from the low-latitude regions are scarce. As a result, the driving and feedback mechanisms of these rapid changes remain poorly understood. The presented stalagmite data of U/Th, stable isotopes (del 18O, del 13C) and radiocarbon (14C) provide unique information regarding the nature and timing of rapid climate changes in the tropics. A depth-age model for the Moomi Cave stalagmite was developed from 25 high-precision U/Th measurements, providing a solid chronology for this record. Oxygen isotope measurements of the stalagmite calcite reveal several large variations that are believed to reflect changes in the amount of precipitation, rather than temperature. A comparison to the Greenland Ice Core records shows a remarkable similarity to D/O cycles 10- 13 with warmer periods in the high-latitude regions being associated with increased precipitation in the tropics and vice versa. The stalagmite radiocarbon (14C) values from over 100 individual measurements reveal an almost identical cyclic pattern, tracing all four D/O cycles. Assuming no changes in the carbonate chemistry of the precipitating fluid, the radiocarbon values of the stalagmite calcite directly reflect changes in global atmospheric 14C concentrations. There are three possible explanations for these cyclic variations of 14C values: 1) changes in the carbonate chemistry of the drip water resulting in changes of the dead carbon fraction (DCF); 2) changes in the solar activity and/or Earth's magnetic field resulting in direct variations of atmospheric 14C concentrations; and 3) changes in

YALE NATURAL RADIOCARBON MEASUREMENTS. PART VI

DOE Office of Scientific and Technical Information (OSTI.GOV)

Stuiver, M.; Deevey, E.S.

1961-01-01

Most of the measurements made since publication of Yale V are included; some measurements, such as a series collected in Greenland, are withneld pending additional information or field work that will make better interpretations possible. In addition to radiocarbon dates of geologic and/or archaeologic interest, recent assays are given of C/sup 14/ in lake waters and other lacustrine materials, now normalized for C/sup 13/ content. The newly accepted convention is followed in expressing normalized C/sup 14/ values as DELTA = delta C/sup 14/ (2 delta C/sup 13/ + 50)STAl + ( delta C/sup 14//1000)! where DELTA is the per milmore » deviation of the C/sup 14/ if the sample from any contemporary standard (whether organic or a carbonate) after correction of sample and/or standard for real age, for the Suess effect, for normal isotopic fractionation, and for deviations of C/sup 14/ content of the age- and pollution- corrected l9th-century wood standard from that of 95% of the NBS oxalic acid standard; delta C/sup 14/ is the measured deviation from 95% of the NBS standard, and delta C/sup 13/ is the deviation from the NBS limestone standard, both in per mil. These assays are variously affected by artificial C/sup 14/ resulting from nuclear tests. (auth)« less

Atmospheric radiocarbon as a Southern Ocean wind proxy over the last 1000 years

NASA Astrophysics Data System (ADS)

Rodgers, K. B.; Mikaloff Fletcher, S.; Galbraith, E.; Sarmiento, J. L.; Gnanadesikan, A.; Slater, R. D.; Naegler, T.

2009-04-01

Measurements of radiocarbon in tree rings over the last 1000 years indicate that there was a pre-industrial latitudinal gradient of atmospheric radiocarbon of 3.9-4.5 per mail and that this gradient had temporal variability of order 6 per mil. Here we test the idea that the mean gradient as well as variability in he gradient is dominated by the strength of the winds over the Southern Ocean. This is done using an ocean model and an atmospheric transport model. The ocean model is used to derive fluxes of 12CO2 and 14CO2 at the sea surface, and these fluxes are used as a lower boundary condition for the transport model. For the mean state, strong winds in the Southern Ocean drive significant upwelling of radiocarbon-depleted Circumpolar Deep Water (CDW), leading to a net flux of 14CO2 relative to 12CO2 into the ocean. This serves to maintain a hemispheric gradient in pre-anthropogenic atmospheric delta-c14. For perturbations, increased/decreased Southern Ocean winds drive increased/decreased uptake of 14CO2 relative to 12CO2, thus increasing/decreasing the hemispheric gradient in atmospheric delta-c14. The tree ring data is interpreted to reveal a decrease in the strength of the Southern Ocean winds at the transition between the Little Ice Age and the Medieval Warm Period.

The radiocarbon reservoir age of the Chukchi Sea, Arctic Ocean

NASA Astrophysics Data System (ADS)

Pearce, C.; Gyllencreutz, R.; West, G.; O'Regan, M.; Jakobsson, M.

2017-12-01

Radiocarbon (14C) dating is the standard method for obtaining the age of marine sediments of Holocene and late Pleistocene age. For accurate calibrations, however, this tool relies on precise knowledge of the local radiocarbon reservoir age of the surface ocean, i.e. the regional difference (ΔR) from the average global marine calibration dataset. This parameter has become impossible to measure from modern mollusk samples because of 14C contamination from extensive testing of thermo-nuclear bombs in the second half of the twentieth century. The local reservoir age can thus only be calculated from the radiocarbon age of samples collected before AD 1950 or from sediment records containing absolute age markers, derived from e.g. tephrochronology or paleomagnetism. Knowledge of the marine reservoir age in the Arctic Ocean is extremely sparse, and relies on work by only a few studies. No information exists for the entire East Siberian Sea, and the Chukchi Sea is represented solely by sites along the Alaskan coast. Here we present new radiocarbon measurements on historical mollusk collections from the East Siberian and Chukchi margins. Our results show a clear and consistent signal of "old" Pacific Water in the Chukchi Sea with ΔR values around 450 years. Towards the East Siberian Sea the values drop as Pacific Water has decreased influence further away from the Bering Strait. Complementing the modern data, we also provide constraints on the reservoir age during the late Holocene. These are based on tephrochronology and high resolution analyses of paleomagnetic secular variation from a sediment archive from Herald Canyon, Chukchi Sea.

Field Degassing as a New Sampling Method for 14C Analyses in Old Groundwater

DOE Office of Scientific and Technical Information (OSTI.GOV)

Yokochi, Reika; Bernier, Ryan; Purtschert, Roland

Radiocarbon ( 14C) activity in groundwater can be used to determine subsurface residence time up to ~40 kyr, providing crucial information on dynamic properties of groundwater and on paleoclimate. However, commonly applied sampling methods for dissolved inorganic carbon (DIC- 14C) are prone to low level of modern atmospheric contamination, resulting in underestimation of groundwater ages that cluster around 30–40 kyr. We extract CO 2 gas from groundwater using a device originally developed for studies of noble gas radionuclides. Carbon is collected in the gas phase, eliminating the possibility of fostering microbial activities and aqueous chemical reactions during sample storage. Thismore » method collects CO 2- 14C and radiokrypton ( 81Kr and 85Kr) samples simultaneously. The presence of any shorter-lived 85Kr is used to evaluate the degree of atmospheric contamination during sampling or mixing of young groundwater. Most groundwater samples showed lower CO 2- 14C activities than those of DIC- 14C, presumably due to the absence of atmospheric contamination. Samples with 81Kr age exceeding 150 kyr have no detectable CO 2- 14C except where mixing sources of young groundwater is suspected. Furthermore these field data serve as confirmations for the reliability of the newly presented sample collection and CO 2- 14C method, and for the outstanding roles of radiokrypton isotopes in characterizing old groundwater.« less

Field Degassing as a New Sampling Method for 14C Analyses in Old Groundwater

DOE PAGES

Yokochi, Reika; Bernier, Ryan; Purtschert, Roland; ...

2017-09-07

Radiocarbon ( 14C) activity in groundwater can be used to determine subsurface residence time up to ~40 kyr, providing crucial information on dynamic properties of groundwater and on paleoclimate. However, commonly applied sampling methods for dissolved inorganic carbon (DIC- 14C) are prone to low level of modern atmospheric contamination, resulting in underestimation of groundwater ages that cluster around 30–40 kyr. We extract CO 2 gas from groundwater using a device originally developed for studies of noble gas radionuclides. Carbon is collected in the gas phase, eliminating the possibility of fostering microbial activities and aqueous chemical reactions during sample storage. Thismore » method collects CO 2- 14C and radiokrypton ( 81Kr and 85Kr) samples simultaneously. The presence of any shorter-lived 85Kr is used to evaluate the degree of atmospheric contamination during sampling or mixing of young groundwater. Most groundwater samples showed lower CO 2- 14C activities than those of DIC- 14C, presumably due to the absence of atmospheric contamination. Samples with 81Kr age exceeding 150 kyr have no detectable CO 2- 14C except where mixing sources of young groundwater is suspected. Furthermore these field data serve as confirmations for the reliability of the newly presented sample collection and CO 2- 14C method, and for the outstanding roles of radiokrypton isotopes in characterizing old groundwater.« less

Radiocarbon ages of pre-bomb clams and the hard-water effect in Lakes Michigan and Huron

USGS Publications Warehouse

Rea, David K.; Colman, Steven M.

1995-01-01

Five radiocarbon ages, all determined by accelerator mass spectrometry, have been obtained for two pre-bomb bivalves from Lake Michigan and one from Lake Huron. After correcting those ages for the fractionation of14C in calcite and for the radioactively inert CO2 in the atmosphere, we find residual ages, caused by the hard water effect, of about 250 years for Lake Michigan and 440 years for Lake Huron.

No evidence for a deglacial intermediate water Δ14C anomaly in the SW Atlantic

NASA Astrophysics Data System (ADS)

Sortor, R. N.; Lund, D. C.

2010-12-01

Reconstructions of Δ14C from the eastern tropical Pacific show that severe depletions in 14C occurred at intermediate depths during the last deglaciation (Marchitto et al. 2007; Stott et al. 2009). Marchitto et al. (2007) suggested that old radiocarbon from an isolated abyssal reservoir was injected via the Southern Ocean, and that this anomaly was then carried by Antarctic Intermediate Water (AAIW) to the tropical Pacific. However, a core from the southeastern Pacific Ocean near Chile, which is in the direct path of modern-day AAIW, does not exhibit the excursion and therefore casts doubts upon the AAIW mechanism (De Pol-Holz et al. 2010). Here we evaluate whether or not a deglacial 14C anomaly similar to that in the eastern tropical Pacific occurred at intermediate depths in the South Atlantic. We reconstructed Δ14C using planktonic and benthic foraminifera from core KNR159-5-36GGC on the Brazil Margin (27○31’S and 46○28’W, 1268 m depth). In the modern ocean, the hydrography near this core site is heavily influenced by AAIW (Oppo & Horowitz, 2000). Benthic Δ14C values were determined using raw benthic 14C ages and calendar-calibrated planktonic ages. The deglacial benthic Δ14C trend at this site is similar to the atmospheric Δ14C trend, and is consistent with U/Th-dated corals from intermediate depths on the Brazil Margin (Mangini et al. 2010). The amplitude and timing of Δ14C changes in the foraminiferal and coral records are especially congruous during the Mystery Interval. We find no evidence in the southwestern Atlantic of a ~300‰ decrease in intermediate water Δ14C beginning at 18 kyr BP. Changes in reservoir age of ~1000 years are required to create a Baja-like Δ14C anomaly off Brazil, an implausible increase for a subtropical gyre location. Furthermore, the resulting sedimentation rates would be up to ~145 cm/kyr during the deglaciation, an order of magnitude higher than the average sedimentation rate for 36GGC. When our results are

Vertebral bomb radiocarbon suggests extreme longevity in white sharks.

PubMed

Hamady, Li Ling; Natanson, Lisa J; Skomal, Gregory B; Thorrold, Simon R

2014-01-01

Conservation and management efforts for white sharks (Carcharodon carcharias) remain hampered by a lack of basic demographic information including age and growth rates. Sharks are typically aged by counting growth bands sequentially deposited in their vertebrae, but the assumption of annual deposition of these band pairs requires testing. We compared radiocarbon (Δ(14)C) values in vertebrae from four female and four male white sharks from the northwestern Atlantic Ocean (NWA) with reference chronologies documenting the marine uptake of (14)C produced by atmospheric testing of thermonuclear devices to generate the first radiocarbon age estimates for adult white sharks. Age estimates were up to 40 years old for the largest female (fork length [FL]: 526 cm) and 73 years old for the largest male (FL: 493 cm). Our results dramatically extend the maximum age and longevity of white sharks compared to earlier studies, hint at possible sexual dimorphism in growth rates, and raise concerns that white shark populations are considerably more sensitive to human-induced mortality than previously thought.

Vertebral Bomb Radiocarbon Suggests Extreme Longevity in White Sharks

PubMed Central

Hamady, Li Ling; Natanson, Lisa J.; Skomal, Gregory B.; Thorrold, Simon R.

2014-01-01

Conservation and management efforts for white sharks (Carcharodon carcharias) remain hampered by a lack of basic demographic information including age and growth rates. Sharks are typically aged by counting growth bands sequentially deposited in their vertebrae, but the assumption of annual deposition of these band pairs requires testing. We compared radiocarbon (Δ14C) values in vertebrae from four female and four male white sharks from the northwestern Atlantic Ocean (NWA) with reference chronologies documenting the marine uptake of 14C produced by atmospheric testing of thermonuclear devices to generate the first radiocarbon age estimates for adult white sharks. Age estimates were up to 40 years old for the largest female (fork length [FL]: 526 cm) and 73 years old for the largest male (FL: 493 cm). Our results dramatically extend the maximum age and longevity of white sharks compared to earlier studies, hint at possible sexual dimorphism in growth rates, and raise concerns that white shark populations are considerably more sensitive to human-induced mortality than previously thought. PMID:24416189

Synthesizing the Use of Carbon Isotope (14C and 13C) Approaches to Understand Rates and Pathways for Permafrost C Mobilization and Mineralization

NASA Astrophysics Data System (ADS)

Estop-Aragones, C.; Olefeldt, D.; Schuur, E.

2015-12-01

To better understand the permafrost carbon (C) feedback it is important to synthesize our current knowledge, and knowledge gaps, of how permafrost thaw can cause in situ mineralization or downstream mobilization of aged soil organic carbon (SOC) and the rate of this release. This potential loss of old SOC may occur via gaseous flux of CO2 and CH4 exchanged between soil and the atmosphere and via waterborne flux as DOC, POC (and their subsequent decomposition and release to the atmosphere). Carbon isotope (14C and 13C) approaches have been used to estimate both rates and pathways for permafrost C mobilization and mineralization. Radiocarbon (14C) has been used to estimate the contribution of aged C to overall respiration or waterborne C export. We aim to contrast results from radiocarbon studies, in order to assess differences between ecosystems (contrasting wet and dry ecosystems), thaw histories (active layer deepening or thermokarst landforms), greenhouse gas considered (CO2 and CH4) and seasons. We propose to also contrast methodologies used for assessing the contribution of aged C to overall C balance, and include studies using 13C data. Biological fractionation of 13C during both uptake and decomposition has been taken advantage of both in order to aid the interpretation of 14C data and on its own to assess sources and mineralization pathways. For example, 13C data has been used to differentiate between CH4 production pathways, and the relative contribution of anaerobic CO2 production to overall respiration. Overall, carbon isotope research is proving highly valuable for our understanding of permafrost C dynamics following thaw, and there is a current need to synthesize the available literature.

Do site-specific radiocarbon measurements reflect localized distributions of 14C in biota inhabiting a wetland with point contamination sources?

PubMed

Yankovich, T; King-Sharp, K J; Benz, M L; Carr, J; Killey, R W D; Beresford, N A; Wood, M D

2013-12-01

Duke Swamp is a wetland ecosystem that receives (14)C via a groundwater pathway originating from a waste management area on Atomic Energy Canada Limited's Chalk River Laboratories site. This groundwater reaches the surface of the swamp, resulting in relatively high (14)C levels over an area of 146 m(2). The objective of this study was to quantify (14)C concentrations in flora and fauna inhabiting areas of Duke Swamp over the gradient of (14)C activity concentrations in moss to determine whether (14)C specific activities in receptor biota reflect the localized nature of the groundwater source in the swamp. Representative receptor plants and animals, and corresponding air and soil samples were collected at six sites in Duke Swamp with (14)C specific activities in air that ranged from 1140 to 45,900 Bq/kg C. In general, it was found that specific activities of (14)C in biota tissues reflected those measured in environmental media collected from the same sampling site. The findings demonstrate that mosses could be used in monitoring programs to ensure protection of biota in areas with elevated (14)C, negating the need to capture and euthanize higher organisms. Copyright © 2013 Elsevier Ltd. All rights reserved.

Pyrolysis-combustion 14C dating of soil organic matter

USGS Publications Warehouse

Wang, Hongfang; Hackley, Keith C.; Panno, S.V.; Coleman, D.D.; Liu, J.C.-L.; Brown, J.

2003-01-01

Radiocarbon (14C) dating of total soil organic matter (SOM) often yields results inconsistent with the stratigraphic sequence. The onerous chemical extractions for SOM fractions do not always produce satisfactory 14C dates. In an effort to develop an alternative method, the pyrolysis-combustion technique was investigated to partition SOM into pyrolysis volatile (Py-V) and pyrolysis residue (Py-R) fractions. The Py-V fractions obtained from a thick glacigenic loess succession in Illinois yielded 14C dates much younger but more reasonable than the counterpart Py-R fractions for the soil residence time. Carbon isotopic composition (??13C) was heavier in the Py-V fractions, suggesting a greater abundance of carbohydrate- and protein-related constituents, and ??13C was lighter in the Py-R fractions, suggesting more lignin- and lipid-related constituents. The combination of 14C dates and ??13C values indicates that the Py-V fractions are less biodegradation resistant and the Py-R fractions are more biodegradation resistant. The pyrolysis-combustion method provides a less cumbersome approach for 14C dating of SOM fractions. With further study, this method may become a useful tool for analyzing unlithified terrestrial sediments when macrofossils are absent. ?? 2003 University of Washington. Published by Elsevier Inc. All rights reserved.

Insights into soil carbon dynamics across climatic and geologic gradients from time-series and fraction-specific radiocarbon analysis

NASA Astrophysics Data System (ADS)

van der Voort, Tessa Sophia; Hagedorn, Frank; Zell, Claudia; McIntyre, Cameron; Eglinton, Tim

2016-04-01

Understanding the interaction between soil organic matter (SOM) and climatic, geologic and ecological factors is essential for the understanding of potential susceptibility and vulnerability to climate and land use change. Radiocarbon constitutes a powerful tool for unraveling SOM dynamics and is increasingly used in studies of carbon turnover. The complex and inherently heterogeneous nature of SOM renders it challenging to assess the processes that govern SOM stability by solely looking at the bulk signature on a plot-scale level. This project combines bulk radiocarbon measurements on a regional-scale spanning wide climatic and geologic gradients with a more in-depth approach for a subset of locations. For this subset, time-series and carbon pool-specific radiocarbon data has been acquired for both topsoil and deeper soils. These well-studied sites are part of the Long-Term Forest Ecosystem Research (LWF) program of the Swiss Federal Institute for Forest, Snow and Landscape research (WSL). Statistical analysis was performed to examine relationships of radiocarbon signatures with variables such as temperature, precipitation and elevation. Bomb-curve modeling was applied determine carbon turnover using time-series data. Results indicate that (1) there is no significant correlation between Δ14C signature and environmental conditions except a weak positive correlation with mean annual temperature, (2) vertical gradients in Δ14C signatures in surface and deeper soils are highly similar despite covering disparate soil-types and climatic systems, and (3) radiocarbon signatures vary significantly between time-series samples and carbon pools. Overall, this study provides a uniquely comprehensive dataset that allows for a better understanding of links between carbon dynamics and environmental settings, as well as for pool-specific and long-term trends in carbon (de)stabilization.

Radiocarbon Releases from the 2011 Fukushima Nuclear Accident

PubMed Central

Xu, Sheng; Cook, Gordon T.; Cresswell, Alan J.; Dunbar, Elaine; Freeman, Stewart P. H. T.; Hou, Xiaolin; Jacobsson, Piotr; Kinch, Helen R.; Naysmith, Philip; Sanderson, David C. W.; Tripney, Brian G.

2016-01-01

Radiocarbon activities were measured in annual tree rings for the years 2009 to 2015 from Japanese cedar trees (Cryptomeria japonica) collected at six sites ranging from 2.5–38 km northwest and north of the Fukushima Dai-ichi nuclear power plant. The 14C specific activity varied from 280.4 Bq kg−1 C in 2010 to 226.0 Bq kg−1 C in 2015. The elevated 14C activities in the 2009 and 2010 rings confirmed 14C discharges during routine reactor operations, whereas those activities that were indistinguishable from background in 2012–2015 coincided with the permanent shutdown of the reactors after the accident in 2011. High-resolution 14C analysis of the 2011 ring indicated 14C releases during the Fukushima accident. The resulted 14C activity decreased with increasing distance from the plant. The maximum 14C activity released during the period of the accident was measured 42.4 Bq kg−1 C above the natural ambient 14C background. Our findings indicate that, unlike other Fukushima-derived radionuclides, the 14C released during the accident is indistinguishable from ambient background beyond the local environment (~30 km from the plant). Furthermore, the resulting dose to the local population from the excess 14C activities is negligible compared to the dose from natural/nuclear weapons sources. PMID:27841312

Radiocarbon Releases from the 2011 Fukushima Nuclear Accident

NASA Astrophysics Data System (ADS)

Xu, Sheng; Cook, Gordon T.; Cresswell, Alan J.; Dunbar, Elaine; Freeman, Stewart P. H. T.; Hou, Xiaolin; Jacobsson, Piotr; Kinch, Helen R.; Naysmith, Philip; Sanderson, David C. W.; Tripney, Brian G.

2016-11-01

Radiocarbon activities were measured in annual tree rings for the years 2009 to 2015 from Japanese cedar trees (Cryptomeria japonica) collected at six sites ranging from 2.5-38 km northwest and north of the Fukushima Dai-ichi nuclear power plant. The 14C specific activity varied from 280.4 Bq kg-1 C in 2010 to 226.0 Bq kg-1 C in 2015. The elevated 14C activities in the 2009 and 2010 rings confirmed 14C discharges during routine reactor operations, whereas those activities that were indistinguishable from background in 2012-2015 coincided with the permanent shutdown of the reactors after the accident in 2011. High-resolution 14C analysis of the 2011 ring indicated 14C releases during the Fukushima accident. The resulted 14C activity decreased with increasing distance from the plant. The maximum 14C activity released during the period of the accident was measured 42.4 Bq kg-1 C above the natural ambient 14C background. Our findings indicate that, unlike other Fukushima-derived radionuclides, the 14C released during the accident is indistinguishable from ambient background beyond the local environment (~30 km from the plant). Furthermore, the resulting dose to the local population from the excess 14C activities is negligible compared to the dose from natural/nuclear weapons sources.

Re-Emergence of Excess Bomb Radiocarbon in Upwelling Waters with High-Latitude Origins

NASA Astrophysics Data System (ADS)

Lindsay, C. M.; Lehman, S.

2016-02-01

The quantity of radiocarbon (14C) in the atmosphere was nearly doubled by nuclear weapons testing in the 1960s. Since then, the terrestrial biosphere and the ocean have absorbed most of the excess 14C from the atmosphere, although atmospheric radiocarbon activity (∆14C) continues to decline due to ongoing emissions of 14C-free CO2 from combustion of fossil fuels. The large transient decline in atmospheric ∆14C combined with gas exchange at the surface and spatially variable time scales of ocean mixing have led to large ∆14C gradients in the surface ocean between upwelling- and downwelling-dominated regions. These gradients continue to evolve over time. We examine the rate of change of surface ocean ∆14C between CLIVAR (2000-2011) and WOCE era (1990s) or other slightly earlier (1980s) datasets and find spatial patterns that reveal mixing between 14C-enriched mode waters, 14C-depleted deep waters and surface waters that are well-equilibrated with the atmosphere. The ∆14C of mode water reaching equatorial upwelling regions has increased between the WOCE and CLIVAR time periods, and the greater contribution of 14C to the low-latitude surface ocean appears to have significantly offset the ∆14C decline otherwise imparted by air-sea gas exchange with the atmosphere. Consequently, ∆14C gradients between low-latitude upwelling regions and gyre centers have weakened proportionally more than between gyre centers and regions where pre-industrial water still upwells, such as the Southern Ocean. Properly accounting for the re-emergence of water with post-industrial characteristics is important to constrain earth system models that seek to explain DIC, pH and other anthropogenically perturbed tracers in the surface ocean. Because of the history of ∆14C in the atmosphere, ocean ∆14C is a useful tracer for this purpose.

Towards a global understanding of vertical soil carbon dynamics: meta-analysis of soil 14C data

NASA Astrophysics Data System (ADS)

hatte, C.; Balesdent, J.; Guiot, J.

2012-12-01

Soil represents the largest terrestrial storage mechanism for atmospheric carbon from photosynthesis, with estimates ranging from 1600 Pg C within the top 1 meter to 2350 Pg C for the top 3 meters. These values are at least 2.5 times greater than atmospheric C pools. Small changes in soil organic carbon storage could result in feedback to atmospheric CO2 and the sensitivity of soil organic matter to changes in temperature, and precipitation remains a critical area of research with respect to the global carbon cycle. As an intermediate storage mechanism for organic material through time, the vertical profile of carbon generally shows an age continuum with depth. Radiocarbon provides critical information for understanding carbon exchanges between soils and atmosphere, and within soil layers. Natural and "bomb" radiocarbon has been used to demonstrate the importance and nature of the soil carbon response to climatic and human impacts on decadal to millennial timescales. Radiocarbon signatures of bulk, or chemically or physically fractionated soil, or even of specific organic compounds, offer one of the only ways to infer terrestrial carbon turnover times or test ecosystem carbon models. We compiled data from the literature on radiocarbon distribution on soil profiles and characterized each study according to the following categories: soil type, analyzed organic fraction, location (latitude, longitude, elevation), climate (temperature, precipitation), land use and sampling year. Based on the compiled data, soil carbon 14C profiles were reconstructed for each of the 226 sites. We report here partial results obtained by statistical analyses of portion of this database, i.e. bulk and bulk-like organic matter and sampling year posterior to 1980. We highlight here 14C vertical pattern in relationship with external parameters (climate, location and land use).

Rapid increase in cosmogenic 14C in AD 775 measured in New Zealand kauri trees indicates short-lived increase in 14C production spanning both hemispheres

NASA Astrophysics Data System (ADS)

Güttler, D.; Adolphi, F.; Beer, J.; Bleicher, N.; Boswijk, G.; Christl, M.; Hogg, A.; Palmer, J.; Vockenhuber, C.; Wacker, L.; Wunder, J.

2015-02-01

In 2012, Miyake et al. reported a sudden and strong increase of the atmospheric radiocarbon (14C) content in Japanese cedar trees of 1.2% between AD 774 and 775. While their findings were quickly confirmed by a German oak chronology for the Northern Hemisphere (NH), the question remained if the effect was seen in both hemispheres. Here we present the first annually resolved Southern Hemisphere (SH) 14C record spanning the interval AD 760-787, using New Zealand kauri (Agathis australis) chronology wood. An almost identical distinct increase compared to Northern Hemisphere data was observed, suggesting a cosmic event with globally uniform impact as a potential cause for the increase. Deploying a carbon cycle box model a worldwide averaged net 14C production of 2.2 ×108 14C atoms cm-2 was estimated, which is 3.7 times higher than the average annual 14C production. The immediate appearance of the event in tree rings on both hemispheres suggests a short duration event of significantly less than 1 yr.

The remarkable metrological history of 14C dating: From ancient Egyptian artifacts to particles of soot and grains of pollen

NASA Astrophysics Data System (ADS)

Currie, L. A.

2003-01-01

Radiocarbon dating would not have been possible if 14C had not had the “wrong” half-life—a fact that delayed its discovery [1]. Following the discovery of this 5730 year radionuclide in laboratory experiments by Ruben and Kamen, it became clear to W. F. Libby that 14C should exist in nature, and that it could serve as a quantitative means for dating artifacts and events marking the history of civilization. The search for natural radiocarbon was a metrological challenge; the level in the living biosphere [ca. 230 Bq/kg] lay far beyond the then current state of the measurement art. This article traces the metrological history of radiocarbon, from the initial breakthrough devised by Libby, to minor (evolutionary) and major (revolutionary) advances that have brought 14C measurement from a crude, bulk [8 g carbon] dating tool, to a refined probe for dating tiny amounts of precious artifacts, and for “molecular dating” at the 10 μg to 100 μg level. The metrological advances led to opportunities and surprises, such as the non-monotonic dendrochronological calibration curve and the “bomb effect,” that spawned new multidisciplinary areas of application, ranging from cosmic ray physics to oceanography to the reconstruction of environmental history.

Closed tubes preparation of graphite for high-precision AMS radiocarbon analysis

NASA Astrophysics Data System (ADS)

Hajdas, I.; Michczynska, D.; Bonani, G.; Maurer, M.; Wacker, L.

2009-04-01

Radiocarbon dating is an established tool applied in Geochronology. Technical developments of Accelerator Mass Spectrometry AMS, which allow measurements of samples containing less than 1 mg of carbon, opened opportunities for new applications. Moreover, high resolution records of the past changes require high-resolution chronologies i.e. sampling for 14C dating. In result, the field of applications is rapidly expanding and number of radiocarbon analysis is growing rapidly. Nowadays dedicated 14C AMS machines have great capacity for analysis but in order to keep up with the demand for analysis and provide the results as fast as possible a very efficient way of sample preparation is required. Sample preparation for 14C AMS analysis consists of two steps: separation of relevant carbon from the sample material (removing contamination) and preparation of graphite for AMS analysis. The last step usually involves reaction of CO2 with H2, in the presence of metal catalyst (Fe or Co) of specific mesh size heated to 550-625°C, as originally suggested by Vogel et al. (1984). Various graphitization systems have been built in order to fulfil the requirement of sample quality needed for high-precision radiocarbon data. In the early 90ties another method has been proposed (Vogel 1992) and applied by few laboratories mainly for environmental or biomedical samples. This method uses TiH2 as a source of H2 and can be easily and flexibly applied to produce graphite. Sample of CO2 is frozen in to the tube containing pre-conditioned Zn/TiH2 and Fe catalyst. Torch sealed tubes are then placed in the stepwise heated oven at 500/550°C and left to react for several hours. The greatest problem is the lack of control of the reaction completeness and considerable fractionation. However, recently reported results (Xu et al. 2007) suggest that high precision dating using graphite produced in closed tubes might be possible. We will present results of radiocarbon dating of the set of standards

Radiocarbon dating late Quaternary loess deposits using small terrestrial gastropod shells

USGS Publications Warehouse

Pigati, Jeff S.; McGeehin, John P.; Muhs, Daniel R.; Bettis, E. Arthur

2013-01-01

Constraining the ages and mass accumulation rates of late Quaternary loess deposits is often difficult because of the paucity of organic material typically available for 14C dating and the inherent limitations of luminescence techniques. Radiocarbon dating of small terrestrial gastropod shells may provide an alternative to these methods as fossil shells are common in loess and contain ∼12% carbon by weight. Terrestrial gastropod assemblages in loess have been used extensively to reconstruct past environmental conditions but have been largely ignored for dating purposes. Here, we present the results of a multi-faceted approach to understanding the potential for using small terrestrial gastropod shells to date loess deposits in North America. First, we compare highly resolved 14C ages of well-preserved wood and gastropod shells (Succineidae) recovered from a Holocene loess section in Alaska. Radiocarbon ages derived from the shells are nearly identical to wood and plant macrofossil ages throughout the section, which suggests that the shells behaved as closed systems with respect to carbon for at least the last 10 ka (thousands of calibrated 14C years before present). Second, we apply 14C dating of gastropod shells to late Pleistocene loess deposits in the Great Plains using stratigraphy and independent chronologies for comparison. The new shell ages require less interpretation than humic acid radiocarbon ages that are commonly used in loess studies, provide additional stratigraphic coverage to previous dating efforts, and are in correct stratigraphic order more often than their luminescence counterparts. Third, we show that Succineidae shells recovered from historic loess in the Matanuska River Valley, Alaska captured the 20th century 14C bomb spike, which suggests that the shells can be used to date late Holocene and historic-aged loess. Finally, results from Nebraska and western Iowa suggest that, similar to other materials, shell ages approaching ∼40 ka should

Radiocarbon-based assessment of fossil fuel-derived contaminant associations in sediments.

PubMed

White, Helen K; Reddy, Christopher M; Eglinton, Timothy I

2008-08-01

Hydrophobic organic contaminants (HOCs) are associated with natural organic matter (OM) in the environment via mechanisms such as sorption or chemical binding. The latter interactions are difficult to quantitatively constrain, as HOCs can reside in different OM pools outside of conventional analytical windows. Here, we exploited natural abundance variations in radiocarbon (14C) to trace various fossil fuel-derived HOCs (14C-free) within chemically defined fractions of contemporary OM (modern 14C content) in 13 samples including marine and freshwater sediments and one dust and one soil sample. Samples were sequentially treated by solvent extraction followed by saponification. Radiocarbon analysis of the bulk sample and resulting residues was then performed. Fossil fuel-derived HOCs released by these treatments were quantified from an isotope mass balance approach as well as by gas chromatography-mass spectrometry. For the majority of samples (n = 13), 98-100% of the total HOC pool was solvent extractable. Nonextracted HOCs are only significant (29% of total HOC pool)in one sample containing p,p-2,2-bis(chlorophenyl)-1,1,1-trichloroethane and its metabolites. The infrequency of significant incorporation of HOCs into nonextracted OM residues suggests that most HOCs are mobile and bioavailable in the environment and, as such, have a greater potential to exert adverse effects.

Radiocarbon Records of Fossil Fuel Emissions From Urban Trees in the Greater Salt Lake Valley From Mid-Century to Present.

NASA Astrophysics Data System (ADS)

Chritz, K.; Buchert, M.; Walker, J. C.; Mendoza, D.; Pataki, D. E.; Xu, X.; Lin, J. C.

2017-12-01

Generating long term records of fossil fuel emissions of urban environments is complicated by the fact that direct observations of emissions and urban atmospheric CO2 concentrations were only collected in the recent past. Radiocarbon (14C) in tree rings from urban trees can provide archives of fossil fuel emissions that may track population growth over time, as higher population density is typically correlated with increased vehicular traffic and associated CO2 emissions, which are radiocarbon dead. We present radiocarbon measurements (n=125) from five roadside green ash trees (Fraxinus pennsylvanica) located in three cities of northern Utah - Salt Lake City (urban, 2016 population: 193,744), Logan City (agricultural, 2016 population: 49,110) and Heber (rural, 2016 population: 14,969). Urban trees were cored in four cardinal directions and ring widths were measured and counted to establish a chronology. One ring from every third year in a single core from each tree was removed and holocellulose was extracted from bulk wood of individual rings for 14C analysis. Fraction CO2 from fossil fuel burning (CO2-ff) was calculated using a simple mass-balance calculation from measured 14C values and remote background atmospheric 14CO2 values for NH Zone 2. The data from all three cities indicate a general trend of increasing CO2-ff uptake by the trees from 1980s to present, as expected with increased population growth and vehicular traffic. However, records in all three cities show unique elevated CO2-ff prior to the 1980s, assuming similar climate patterns through time, diverging from historic population size. We employed atmospheric simulations from the STILT (Stochastic Time-Inverted Lagrangian Transport) models for each of these trees to create footprints to determine source areas for CO2. These footprints reveal that atmospheric sampling areas can be large for certain trees, and other sources of 14C dead carbon, such as coal and natural gas from industrial emissions

Revised direct radiocarbon dating of the Vindija G1 Upper Paleolithic Neandertals.

PubMed

Higham, Tom; Ramsey, Christopher Bronk; Karavanić, Ivor; Smith, Fred H; Trinkaus, Erik

2006-01-17

The 1998/1999 direct dating of two Neandertal specimens from level G(1) of Vindija Cave in Croatia to approximately 28,000 and approximately 29,000 radiocarbon ((14)C) years ago has led to interpretations concerning the late survival of Neandertals in south-central Europe, patterns of interaction between Neandertals and in-dispersing early modern humans in Europe, and complex biocultural scenarios for the earlier phases of the Upper Paleolithic. Given improvements, particularly in sample pretreatment techniques for bone radiocarbon samples, especially ultrafiltration of collagen samples, these Vindija G(1) Neandertal fossils are redated to approximately 32,000-33,000 (14)C years ago and possibly earlier. These results and the recent redating of a number of purportedly old modern human skeletal remains in Europe to younger time periods highlight the importance of fine chronological control when studying this biocultural time period and the tenuous nature of monolithic scenarios for the establishment of modern humans and earlier phases of the Upper Paleolithic in Europe.

Determination of the Prebomb Southern (Antartic) Ocean Radiocarbon in Organic Matter

DOE Office of Scientific and Technical Information (OSTI.GOV)

Guilderson, T P

2001-02-26

The Southern Hemisphere is an important and unique region of the world's oceans for water-mass formation and mixing, upwelling, nutrient utilization, and carbon export. In fact, one of the primary interests of the oceanographic community is to decipher the climatic record of these processes in the source or sink terms for Southern Ocean surface waters in the CO{sub 2} balance of the atmosphere. Current coupled ocean-atmosphere modeling efforts to trace the input of CO{sub 2} into the ocean imply a strong sink of anthropogenic CO{sub 2} in the southern ocean. However, because of its relative inaccessibility and the difficulty inmore » directly measuring CO{sub 2} fluxes in the Southern Ocean, these results are controversial at best. An accepted diagnostic of the exchange of CO{sub 2} between the atmosphere and ocean is the prebomb distribution of radiocarbon in the ocean and its time-history since atmospheric nuclear testing. Such histories of {sup 14}C in the surface waters of the Southern Ocean do not currently exist, primarily because there are few continuous biological archives (e.g., in corals) such as those that have been used to monitor the {sup 14}C history of the tropics and subtropics. One of the possible long-term archives is the scallop Adamussium collbecki. Although not independently confirmed, relatively crude growth rate estimates of A. collbecki indicate that it has the potential to provide continuous 100 year time-series. We are exploring the suitability of this potential archive.« less

Identification and synchronization of the common cosmic-ray signal in the IntCal13 14C calibration and the Greenland ice-core 10Be records

NASA Astrophysics Data System (ADS)

Muscheler, Raimund; Adolphi, Florian; Bronk Ramsey, Christopher; Rasmussen, Sune; Hughen, Konrad; Cooper, Alan; Turney, Chris

2017-04-01

The production rates of cosmogenic radionuclides (such as 10Be and 14C) are modulated by the solar and geomagnetic shielding of galactic cosmic rays. In addition, 14C and 10Be are influenced by the carbon cycle and the atmospheric transport and deposition, respectively. Isolating and identifying the common production signal allows us to synchronize ice core 10Be and tree ring 14C records during the Holocene (Adolphi and Muscheler, 2016), thereby connecting ice core climate records with 14C-dated records. Extending this comparison further back in time is challenging due to deteriorating quality of the 14C calibration record, IntCal13, (Reimer et al., 2013) and possible unidentified climate influences on the ice-core 10Be records. Nevertheless, by focusing on the most prominent production-rate features this comparison can be extended far back into the last glacial where, for example, the linkage of tree-ring based Kauri 14C data and the Greenland ice-core time scale (GICC05) suggested unresolved data and/or time scale differences around the period of the Laschamp geomagnetic field minimum at about 42000 yrs BP (Muscheler et al., 2014). Here we show that the data underlying the IntCal13 14C record and the ice-core 10Be records exhibit common variability that allows us to tentatively link the ice core GICC05 time scale to the radiocarbon time scale for almost the complete radiocarbon dating range. The observed time scale differences could be related to uncertainties in both the U/Th-based dating of the IntCal13 calibration data set and the GICC05 time scale, and we show that the two can be reconciled within the uncertainties of the ice-core layer counting. This direct comparison between IntCal13 and 10Be also suggests that the 14C differences shown in (Muscheler et al., 2014) around the Laschamp geomagnetic field minimum can be reduced by moderate adjustments to the GICC05 time scale. References: Adolphi, F., and Muscheler, R., 2016, Synchronizing the Greenland ice

Biogenic contribution to PM-2.5 ambient aerosol from radiocarbon measurements

NASA Astrophysics Data System (ADS)

Lewis, C.; Klouda, G.; Ellenson, W.

2003-04-01

Knowledge of the relative contributions of biogenic versus anthropogenic sources to ambient aerosol is of great interest in the formulation of strategies to achieve nationally mandated air quality standards. Radiocarbon (14C) measurements provide a means to quantify the biogenic fraction of any carbon-containing sample of ambient aerosol. In the absence of an impact from biomass burning (e.g., during summertime) such measurements can provide an estimate of the contribution of biogenic secondary organic aerosol, from biogenic volatile organic compound precursors. Radiocarbon results for 11.5-h PM-2.5 samples collected near Nashville, Tennessee, USA, during summer 1999 will be presented. On average the measured biogenic fraction was surprisingly large (more than half), with the average biogenic fraction for night samples being only slightly smaller than for day samples. Discussion will include (a) description of the radiocarbon methodology, (b) use of radiocarbon measurements on local vegetation and fuel samples as calibration data, (c) concurrent measurements of organic carbon and elemental carbon ambient concentrations, (d) assessment of organic aerosol sampling artifact through use of organic vapor denuders, variable face velocities, and filter extraction, and (e) comparison with published radiocarbon results obtained in Houston, Texas in a similar study. Disclaimer: This work has been funded wholly or in part by the United States Environmental Protection Agency under Interagency Agreement No. 13937923 to the National Institute of Standards and Technology, and Contract No. 68-D5-0049 to ManTech Environmental Tecnology, Inc. It has been subjected to Agency review and approved for publication.

Radiocarbon chronology of Black Sea sediments

NASA Astrophysics Data System (ADS)

Jones, Glenn A.; Gagnon, Alan R.

1994-03-01

Accelerator Mass Spectrometer (AMS) radiocarbon analyses have been made on 102 samples from 12 sediment cores and 23 samples from two water column profiles. These materials, collected during the first leg of the 1988 joint U.S.-Turkish Black Sea Expedition, provide the most comprehensive radiocarbon chronology of Black Sea sediments yet attempted. Radiocarbon analyses from carefully collected box cores and a mollusc shell collected live in 1931 suggest the prebomb surface waters had a Δ 14C value of -55% (460 years) and that the maximum detrital correction for radiocarbon ages of Unit I sediments is 580 years for the organic carbon and 260 years for the carbonate fractions. Evidence does not support the 1430-2000 years pre-bomb surface water and/or detrital corrections argued for in past studies. The best estimates for the age of the beginning of the final invasion of the coccolithophore Emiliania huxleyi (Unit 1/2 boundary of Ross and DEGENS, 1974, The Black Sea—geology, chemistry and biology, pp. 183-199) and the age of the first invasion of E. huxeleyi (Unit I/II boundary of HAYet al., 1991, Deep-Sea Research, 38, S1211-S1235) are 1635 ± 60 and 2720 ± 160 years BP, respectively. Sapropel formation began at approximately 7540 ± 130 years BP at all depths in the basin, a pattern in disagreement with those predicted by existing time-evolution models of sapropel formation for this basin. Our data suggest that the oxic-anoxic interface has remained relatively stable throughout the Holocene, is controlled largely by the physical oceanography of the basin, and has not evolved as assumed by previous workers.

Reconciling radiocarbon and ice core timescales over the Holocene - Cosmogenic radionuclides as synchronization tools

NASA Astrophysics Data System (ADS)

Muscheler, R.; Adolphi, F.; Mekhaldi, F.

2015-12-01

The atmospheric production rates of cosmogenic radionuclides, such as 14C and 10Be, vary globally due to external processes, namely the solar and geomagnetic modulation of the galactic cosmic ray flux as well as solar proton events. This signature is recorded in various archives such as ice cores (10Be) and tree-rings (14C). Hence, cosmogenic radionuclides offer a means to continuously assess timescale differences between two of the most widely used timescales in paleoclimatology - the radiocarbon and the ice core timescales. Short lived solar proton events additionally provide distinct marker horizons that allow synchronization of discrete horizons at annual precision. We will present a cosmogenic radionuclide based synchronization of the Greenland ice core timescale (GICC05, Svensson et al., 2008) and the radiocarbon timescale (IntCal13, Reimer et al., 2013) over the Holocene. This synchronization allows radiocarbon dated and ice core paleoclimate records to be compared on a common timescale at down to sub-decadal precision. We will compare these results to independent discrete isochrones obtained from tephrochronology and solar proton events. In addition, we will discuss implications for the accuracy and uncertainty estimates of GICC05 over the Holocene. Reimer, P. J., Bard, E., Bayliss, A., Beck, J. W., Blackwell, P. G., Bronk Ramsey, C., Buck, C. E., Cheng, H., Edwards, R. L., Friedrich, M., Grootes, P. M., Guilderson, T. P., Haflidason, H., Hajdas, I., Hatté, C., Heaton, T. J., Hoffmann, D. L., Hogg, A. G., Hughen, K. A., Kaiser, K. F., Kromer, B., Manning, S. W., Niu, M., Reimer, R. W., Richards, D. A., Scott, E. M., Southon, J. R., Staff, R. A., Turney, C. S. M., and van der Plicht, J.: IntCal13 and Marine13 Radiocarbon Age Calibration Curves 0-50,000 Years cal BP, Radiocarbon, 55, 1869-1887, 10.2458/azu_js_rc.55.16947, 2013. Svensson, A., Andersen, K. K., Bigler, M., Clausen, H. B., Dahl-Jensen, D., Davies, S. M., Johnsen, S. J., Muscheler, R., Parrenin

Rapid analysis method for the determination of 14C specific activity in irradiated graphite

PubMed Central

Remeikis, Vidmantas; Lagzdina, Elena; Garbaras, Andrius; Gudelis, Arūnas; Garankin, Jevgenij; Juodis, Laurynas; Duškesas, Grigorijus; Lingis, Danielius; Abdulajev, Vladimir; Plukis, Artūras

2018-01-01

14C is one of the limiting radionuclides used in the categorization of radioactive graphite waste; this categorization is crucial in selecting the appropriate graphite treatment/disposal method. We propose a rapid analysis method for 14C specific activity determination in small graphite samples in the 1–100 μg range. The method applies an oxidation procedure to the sample, which extracts 14C from the different carbonaceous matrices in a controlled manner. Because this method enables fast online measurement and 14C specific activity evaluation, it can be especially useful for characterizing 14C in irradiated graphite when dismantling graphite moderator and reflector parts, or when sorting radioactive graphite waste from decommissioned nuclear power plants. The proposed rapid method is based on graphite combustion and the subsequent measurement of both CO2 and 14C, using a commercial elemental analyser and the semiconductor detector, respectively. The method was verified using the liquid scintillation counting (LSC) technique. The uncertainty of this rapid method is within the acceptable range for radioactive waste characterization purposes. The 14C specific activity determination procedure proposed in this study takes approximately ten minutes, comparing favorably to the more complicated and time consuming LSC method. This method can be potentially used to radiologically characterize radioactive waste or used in biomedical applications when dealing with the specific activity determination of 14C in the sample. PMID:29370233

Rapid analysis method for the determination of 14C specific activity in irradiated graphite.

PubMed

Remeikis, Vidmantas; Lagzdina, Elena; Garbaras, Andrius; Gudelis, Arūnas; Garankin, Jevgenij; Plukienė, Rita; Juodis, Laurynas; Duškesas, Grigorijus; Lingis, Danielius; Abdulajev, Vladimir; Plukis, Artūras

2018-01-01

14C is one of the limiting radionuclides used in the categorization of radioactive graphite waste; this categorization is crucial in selecting the appropriate graphite treatment/disposal method. We propose a rapid analysis method for 14C specific activity determination in small graphite samples in the 1-100 μg range. The method applies an oxidation procedure to the sample, which extracts 14C from the different carbonaceous matrices in a controlled manner. Because this method enables fast online measurement and 14C specific activity evaluation, it can be especially useful for characterizing 14C in irradiated graphite when dismantling graphite moderator and reflector parts, or when sorting radioactive graphite waste from decommissioned nuclear power plants. The proposed rapid method is based on graphite combustion and the subsequent measurement of both CO2 and 14C, using a commercial elemental analyser and the semiconductor detector, respectively. The method was verified using the liquid scintillation counting (LSC) technique. The uncertainty of this rapid method is within the acceptable range for radioactive waste characterization purposes. The 14C specific activity determination procedure proposed in this study takes approximately ten minutes, comparing favorably to the more complicated and time consuming LSC method. This method can be potentially used to radiologically characterize radioactive waste or used in biomedical applications when dealing with the specific activity determination of 14C in the sample.

Application of Bomb Radiocarbon Chronologies to Shortfin Mako (Isurus oxyrinchus)

DOE Office of Scientific and Technical Information (OSTI.GOV)

Ardizzone, D; Cailliet, G M; Natanson, L J

performed and the number of samples for MIA analysis was insufficient for some months. Hence, unequivocal validation of shortfin mako age estimates has yet to be accomplished. Atmospheric testing of thermonuclear devices in the 1950s and 1960s effectively doubled the natural atmospheric radiocarbon ({sup 14}C). The elevated {sup 14}C levels were first recorded in 1957-58, with a peak around 1963. As a consequence, {sup 14}C entered the ocean through gas exchange with the atmosphere at the ocean surface and in terrestrial runoff. Despite variable oceanographic conditions, a worldwide rise of the bomb {sup 14}C signal entered the ocean mixed layer as dissolved inorganic carbon (DIC) in 1957-58. The large amounts of {sup 14}C released from the bomb tests produced a signature that can be followed through time, throughout the marine food web, and into deeper waters. The marked increase of radiocarbon levels was first measured in the DIC of seawater and in biogenic marine carbonates of hermatypic corals in Florida. Subsequently, this record was documented in corals from other regions and in the thallus of rhodoliths. The accumulation of radiocarbon in the hard parts of most marine organisms in the mixed layer (such as fish otoliths and bivalves) was synchronous with the coral time-series. This technique has been used to validate age estimates and longevity of numerous bony fishes to date, as well as to establish bomb radiocarbon chronologies from different oceans. In the first application of this technique to lamnoid sharks, validated annual band-pair deposition in vertebral growth bands for the porbeagle (Lamna nasus) aged up to 26 years. Radiocarbon values from samples obtained from 15 porbeagle caught in the western North Atlantic Ocean (some of which were known-age) produced a chronology similar in magnitude to the reference carbonate chronology for that region. The observed phase shift of about 3 years was attributed to different sources of carbon between vertebrae and those

A simple method to determine mineralization of (14) C-labeled compounds in soil.

PubMed

Myung, Kyung; Madary, Michael W; Satchivi, Norbert M

2014-06-01

Degradation of organic compounds in soil is often determined by measuring the decrease of the parent compound and analyzing the occurrence of its metabolites. However, determining carbon species as end products of parent compound dissipation requires using labeled materials that allow more accurate determination of the environmental fate of the compound of interest. The current conventional closed system widely used to monitor degradation of (14) C-labeled compounds in soil is complex and expensive and requires a specialized apparatus and facility. In the present study, the authors describe a simple system that facilitates measurement of mineralization of (14) C-labeled compounds applied to soil samples. In the system, soda lime pellets to trap mineralized (14) C-carbon species, including carbon dioxide, were placed in a cup, which was then inserted above the treated soil sample in a tube. Mineralization of [(14) C]2,4-D applied to soil samples in the simple system was compared with that in the conventional system. The simple system provided an equivalent detection of (14) C-carbon species mineralized from the parent compound. The results demonstrate that this cost- and space-effective simple system is suitable for examining degradation and mineralization of (14) C-labeled compounds in soil and could potentially be used to investigate their mineralization in other biological matrices. © 2014 SETAC.

Insights into soil carbon dynamics across climatic and geologic gradients from temporally-resolved radiocarbon measurements

NASA Astrophysics Data System (ADS)

van der Voort, T. S.; Hagedorn, F.; Mannu, U.; Walthert, L.; McIntyre, C.; Eglinton, T. I.

2016-12-01

Soil carbon constitutes the largest terrestrial reservoir of organic carbon, and therefore quantifying soil organic matter dynamics (carbon turnover, stocks and fluxes) across spatial gradients is essential for an understanding of the carbon cycle and the impacts of global change. In particular, links between soil carbon dynamics and different climatic and compositional factors remains poorly understood. Radiocarbon constitutes a powerful tool for unraveling soil carbon dynamics. Temporally-resolved radiocarbon measurements, which take advantage of "bomb-radiocarbon"-driven changes in atmospheric 14C, enable further constraints to be placed on C turnover times. These in turn can yield more precise flux estimates for both upper and deeper soil horizons. This project combines bulk radiocarbon measurements on a suite of soil profiles spanning strong climatic (MAT 1.3-9.2°C, MAP 600 to 2100 mm m-2y-1) and geologic gradients with a more in-depth approach for a subset of locations. For this subset, temporal and carbon-fraction specific radiocarbon data has been acquired for both topsoil and deeper soils. These well-studied sites are part of the Long-Term Forest Ecosystem Research (LWF) program of the Swiss Federal Institute for Forest, Snow and Landscape research (WSL). Resulting temporally-resolved turnover estimates are coupled to carbon stocks, fluxes across this wide range of forest ecosystems and are examined in the context of environmental drivers (temperature, precipitation, primary production and soil moisture) as well as composition (sand, silt and clay content). Statistical analysis on the region-scale - correlating radiocarbon signature with climatic variables such as temperature, precipitation, primary production and elevation - indicates that composition rather than climate is a key driver of ­­Δ14C signatures. Estimates of carbon turnover, stocks and fluxes derived from temporally-resolved measurements highlight the pivotal role of soil moisture as a

A 150 year record of annual Bristlecone Pine 14C from the second millennium BC

NASA Astrophysics Data System (ADS)

Pearson, Charlotte; Salzer, Matthew; Brewer, Peter; Hodgins, Gregory; Jull, A. J. Timothy; Lange, Todd; Cruz, Richard; Brown, David; Boswijk, Gretel

2017-04-01

The Interdisciplinary Chronology of Civilizations Project (ICCP) at the University of Arizona (UA) aims to resolve longstanding chronological issues for Aegean and Near Eastern archaeology. A central component of this work is the production of annual resolution sequences of 14C from securely anchored tree-ring chronologies. Contemporary growth rings from Northern and Southern Hemisphere locations will be tested against a dataset of consecutive annual resolution 14C measurements from tree-rings of securely dated North American bristlecone pine (Pinus longaeva D.K. Bailey). These data will be used in a number of ways: to investigate potential issues with the current IntCal dataset due to interpolation, smoothing, or the inclusion of annual scale rapid changes in 14C; to identify 14C off-sets; to evaluate whether annual determinations of 14C present sufficient advantages for dating to justify the substantial costs involved in creating an annual resolution calibration curve; to explore whether the degree of reproducibility between species and growth locations justifies the construction of regional curves or allows us to pioneer 'annual resolution wigglematching' to anchor substantial floating tree-ring chronologies from Mediterranean archaeological contexts, and; if new rapid changes in 14C (aka 'spikes') are discovered, to use these to achieve this same goal. The initial focus of the project is the first and second millennium BC. From this period we present 150 annual 14C determinations from bristlecone pine and explore preliminary findings based on comparisons with the existing IntCal dataset, decadal data from the Mediterranean, and some contemporary years from Irish Oak (Quercus spp.) and New Zealand Kauri (Agathis australis (D. Don) Lindl.). This work, in combination with results from another UA project team (see abstract by Jull et al.) helps confirm the potential of the bristlecone pine archive for high resolution radiocarbon research.

Extraction of in situ cosmogenic 14C from olivine

USGS Publications Warehouse

Pigati, J.S.; Lifton, N.A.; Timothy, Jull A.J.; Quade, Jay

2010-01-01

Chemical pretreatment and extraction techniques have been developed previously to extract in situ cosmogenic radiocarbon (in situ 14C) from quartz and carbonate. These minerals can be found in most environments on Earth, but are usually absent from mafic terrains. To fill this gap, we conducted numerous experiments aimed at extracting in situ 14C from olivine ((Fe,Mg)2SiO4). We were able to extract a stable and reproducible in situ 14C component from olivine using stepped heating and a lithium metaborate (LiBO2) flux, following treatment with dilute HNO3 over a variety of experimental conditions. However, measured concentrations for samples from the Tabernacle Hill basalt flow (17.3 ?? 0.3 ka4) in central Utah and the McCarty's basalt flow (3.0 ?? 0.2 ka) in western New Mexico were significantly lower than expected based on exposure of olivine in our samples to cosmic rays at each site. The source of the discrepancy is not clear. We speculate that in situ 14C atoms may not have been released from Mg-rich crystal lattices (the olivine composition at both sites was ~Fo65Fa35). Alternatively, a portion of the 14C atoms released from the olivine grains may have become trapped in synthetic spinel-like minerals that were created in the olivine-flux mixture during the extraction process, or were simply retained in the mixture itself. Regardless, the magnitude of the discrepancy appears to be inversely proportional to the Fe/(Fe+Mg) ratio of the olivine separates. If we apply a simple correction factor based on the chemical composition of the separates, then corrected in situ 14C concentrations are similar to theoretical values at both sites. At this time, we do not know if this agreement is fortuitous or real. Future research should include measurement of in situ 14C concentrations in olivine from known-age basalt flows with different chemical compositions (i.e. more Fe-rich) to determine if this correction is robust for all olivine-bearing rocks. ?? 2010 by the Arizona

RADIOCARBON DATING: A CASE AGAINST THE PROPOSED LINK BETWEEN RIVER MOLLUSKS AND SOIL HUMUS

DOE Office of Scientific and Technical Information (OSTI.GOV)

Broecker, W.

The C/sup 14/ link between river mollusks and soil humus is discussed. It is stated that the explanation that the C/sup 13/ deficiency should be attributed to the uptake of soil CO/sub 2/ by ground water (oxidation of humus in the soil, rather than after it has been transported into streams) and the C/sup 14/ deficiency to the solution of limestone is far more plausible. It was concluded that any relation between the radiocarbon concentrations in soil humus and fresh water mollusks is almost certainly coincidental. (P.C.H.)

Evidence for Biomass Burning from 14C and 13C/12C Measurements at T-0 and T-1 during MILAGRO.

NASA Astrophysics Data System (ADS)

Gaffney, J. S.; Marley, N. A.; Tackett, M. J.; Sturchio, N. C.; Heraty, L. J.; Martinez, N.; Hardy, K.; Guilderson, T.

2007-12-01

Both stable carbon isotopic and radiocarbon characterizations of aerosols can yield important information regarding the sources of carbonaceous aerosols in urban and regional environments. Biomass derived materials are labeled due to their recent photochemical activity in radiocarbon and vary depending upon the photochemical pathway (either C-4 or C-3) in stable carbon-13 content. C-4 being enriched over C-3. During the MILAGRO campaign, quartz filter samples were taken at 12 hour intervals from 5 am to 5 pm (day) and from 5 pm to 5 am (night) during the month of March 2006. These samples were taken at the two super-sites, T-0 (Instituto Mexicano de Petroleo in Mexico City) and T-1 (Universidad Technologica de Tecamac, State of Mexico). The total carbon content was analyzed for stable carbon isotopic composition as well as for radiocarbon. Stable isotope mass spectroscopy was used to determine the carbon-13 to carbon-12 isotopic ratios on carbon dioxide. The carbon dioxide was then converted to graphite for analysis by accelerator mass spectrometry at the Center for Accelerator Mass Spectrometry at Lawrence Livermore National Laboratory. Results are presented for the carbon-13 content relative to the PDB standard and radiocarbon is given relative to recent carbon. The results for total radiocarbon content show that the carbonaceous aerosol content in Mexico City has more than half of the carbon coming from biomass derived sources. These can include inflow of biomass burning aerosols into the T-0 site as well as the input from local burning of biofuels and trash containing biomass derived materials (paper, boxes, etc.). Data also indicate that at the T-1 site biomass burning of C-4 grasses appears to be significant in that the carbon-13 values observed are enriched. Also at T-1 the radiocarbon levels are also found to be slightly higher indicating regional biomass burning as a significant contributor to aerosol carbon in the 0.1 to 1.0 micron size fraction. Some day

Improving 14C dating precision in dynamic, brackish waters by one order of magnitude: 87Sr/86Sr isotopes as a quantitative proxy for 14C reservoir age.

NASA Astrophysics Data System (ADS)

Lougheed, B.; Davies, G.; Filipsson, H. L.; van der Lubbe, J.; Snowball, I.

2016-12-01

Accurate geochronologies are crucial for reconstructing the sensitivity of brackish and estuarine environments to external impacts. A common geochronological method used for such studies is radiocarbon (14C) dating, but its application in brackish environments is severely limited by an inability to quantify spatiotemporal variations in 14C reservoir age, or R(t), due to dynamic interplay between river runoff and marine water in these environments. Additionally, old carbon effects and species-specific behavioural processes also influence 14C ages. Using the world's largest brackish water body (the estuarine Baltic Sea) as a test-bed, combined with a comprehensive approach that objectively excludes both old carbon and species-specific effects, we demonstrate that it is possible to use 87Sr/86Sr ratios to quantify R(t) in ubiquitous mollusc shell material, leading to an almost one order of magnitude increase in Baltic Sea 14C geochronological precision over the current state-of-the-art. We propose that this novel proxy method can be developed for other brackish water bodies worldwide, thereby improving geochronological control in these climate sensitive, near-coastal environments.

Carbonates in leaching reactions in context of 14C dating

NASA Astrophysics Data System (ADS)

Michalska, Danuta; Czernik, Justyna

2015-10-01

Lime mortars as a mixture of binder and aggregate may contain carbon of various origins. If the mortars are made of totally burnt lime, radiocarbon dating of binder yields the real age of building construction. The presence of carbonaceous aggregate has a significant influence on the 14C measurements results and depending on the type of aggregate and fraction they may cause overaging. Another problem, especially in case of hydraulic mortars that continue to be chemically active for a very long time, is the recrystallization usually connected with rejuvenation of the results but also, depending on local geological structures, with so called reservoir effect yielding apparent ages. An attempt in separating the binder from other carbonaceous components successfully was made for samples from Israel by Nawrocka-Michalska et al. (2007). The same preparation procedure, after taking into account the petrographic composition, was used for samples coming from Poland, Nawrocka et al. (2009). To verify the procedure used previously for non-hydraulic samples determination an experimental tests on carbonaceous mortars with crushed bricks from Novae in Bulgaria were made. Additionally, to identify different carbonaceous structures and their morphology, a cathodoluminescence and scanning electron microscope with electron dispersive spectrometer were applied. The crushed bricks and brick dust used in mortars production process have been interpreted as an alternative use to other pozzolanic materials. The reaction between lime and pozzolanic additives take place easily and affects the rate and course of carbonates decomposition in orthophosphric acid, during the samples pretreatment for dating. The composition of the Bulgarian samples together with influence of climate conditions on mortar carbonates do not allow for making straightforward conclusions in chronology context, but gives some new guidelines in terms of hydraulic mortars application for dating. This work has mainly

Resampling soil profiles can constrain large-scale changes in the C cycle: obtaining robust information from radiocarbon measurements

NASA Astrophysics Data System (ADS)

Baisden, W. T.; Prior, C.; Lambie, S.; Tate, K.; Bruhn, F.; Parfitt, R.; Schipper, L.; Wilde, R. H.; Ross, C.

2006-12-01

, 1 kg C m-2 or more may be reactive on decadal timescales, supporting evidence of soil C losses from throughout the soil profiles. Information from resampled soil profiles can be combined with additional contemporary measurements to test hypotheses about mechanisms for soil C changes. For example, Δ14C in excess of 200‰ in water extractable dissolved organic C (DOC) from surface soil horizons supports the hypothesis that decadal movement of DOC represents an important translocation of soil C. These preliminary results demonstrate that resampling whole soil profiles can support substantial progress in C cycle science, ranging from updating operational C accounting systems to the frontiers of research. Resampling can be complementary or superior to fixed-depth interval sampling of surface soil layers. Resampling must however be undertaken with relative urgency to maximize the potential interpretive power of bomb-derived radiocarbon.

Associated terrestrial and marine fossils in the late-glacial Presumpscot Formation, southern Maine, USA, and the marine reservoir effect on radiocarbon ages

NASA Astrophysics Data System (ADS)

Thompson, Woodrow B.; Griggs, Carol B.; Miller, Norton G.; Nelson, Robert E.; Weddle, Thomas K.; Kilian, Taylor M.

2011-05-01

Excavations in the late-glacial Presumpscot Formation at Portland, Maine, uncovered tree remains and other terrestrial organics associated with marine invertebrate shells in a landslide deposit. Buds of Populus balsamifera (balsam poplar) occurred with twigs of Picea glauca (white spruce) in the Presumpscot clay. Tree rings in Picea logs indicate that the trees all died during winter dormancy in the same year. Ring widths show patterns of variation indicating responses to environmental changes. Fossil mosses and insects represent a variety of species and wet to dry microsites. The late-glacial environment at the site was similar to that of today's Maine coast. Radiocarbon ages of 14 tree samples are 11,907 ± 31 to 11,650 ± 50 14C yr BP. Wiggle matching of dated tree-ring segments to radiocarbon calibration data sets dates the landslide occurrence at ca. 13,520 + 95/-20 cal yr BP. Ages of shells juxtaposed with the logs are 12,850 ± 65 14C yr BP ( Mytilus edulis) and 12,800 ± 55 14C yr BP ( Balanus sp.), indicating a marine reservoir age of about 1000 yr. Using this value to correct previously published radiocarbon ages reduces the discrepancy between the Maine deglaciation chronology and the varve-based chronology elsewhere in New England.

Biodegradation of [(sup14)C]Benzo[a]pyrene Added in Crude Oil to Uncontaminated Soil

PubMed Central

Kanaly, R.; Bartha, R.; Fogel, S.; Findlay, M.

1997-01-01

To investigate the possible cometabolic biodegradation of benzo[a]pyrene (BaP), crude oil spiked with [7-(sup14)C]BaP and unlabeled BaP was added to soil with no known pollution history, to give 34 g of oil and 67 mg of BaP/kg of dry soil. The oil-soil mixture was amended with mineral nutrients and incubated in an airtight container with continuous forced aeration. Total CO(inf2) and (sup14)CO(inf2) in the off-gas were trapped and quantified. Soil samples were Soxhlet extracted with dichloromethane at seven time points during the 150-day incubation period, and the extracted soil was subjected to further fractionation in order to recover reversibly and irreversibly bound radiocarbon. Radiocarbon recovery was 100% (plusmn) 3% for each time point. During the first 50 days of incubation, no (sup14)CO(inf2) was evolved, but over the next 100 days, 50% of the BaP radiocarbon was evolved as (sup14)CO(inf2). At 150 days, only 5% of the intact BaP and 23% of the crude oil remained. Of the remaining radiolabel, 20% was found in solvent-extractable metabolites and 25% was incorporated into soil organic matter. Only 1/10 of this could be solubilized by chemical hydrolysis. An abiotic control experiment exhibited binding of only 2% of the BaP, indicating the microbial nature of the BaP transformations. We report that in soil containing suitable cosubstrates, BaP can be completely degraded. PMID:16535735

Annual variability in the radiocarbon age and source of dissolved CO2 in a peatland stream.

PubMed

Garnett, Mark H; Dinsmore, Kerry J; Billett, Michael F

2012-06-15

Radiocarbon dating has the capacity to significantly improve our understanding of the aquatic carbon cycle. In this study we used a new passive sampler to measure the radiocarbon ((14)C) and stable carbon (δ(13)C) isotopic composition of dissolved CO(2) for the first time in a peatland stream throughout a complete year (May 2010-June 2011). The in-stream sampling system collected time-integrated samples of CO(2) continuously over approximately 1 month periods. The rate of CO(2) trapping was proportional to independently measured streamwater CO(2) concentrations, demonstrating that passive samplers can be used to estimate the time-averaged dissolved CO(2) concentration of streamwater. While there was little variation and no clear trend in δ(13)CO(2) values (suggesting a consistent CO(2) source), we found a clear temporal pattern in the (14)C concentration of dissolved CO(2). The (14)C age of CO(2) varied from 707±35 to 1210±39 years BP, with the youngest CO(2) in the autumn and oldest in spring/early summer. Mean stream discharge and (14)C content of dissolved CO(2) were positively correlated. We suggest that the observed pattern in the (14)C content of dissolved CO(2) reflects changes in its origin, with older carbon derived from deeper parts of the peat profile contributing proportionally more gaseous carbon during periods of low stream flow. Copyright © 2012 Elsevier B.V. All rights reserved.

The role of inter-comparisons in radiocarbon quality assurance

NASA Astrophysics Data System (ADS)

Scott, Marian; Cook, Gordon; Naysmith, Philip

2016-04-01

Radiocarbon dating is used widely in many geochronology projects as a basis for the creation and testing of chronological constructs. Radiocarbon measurements are by their nature complex and the degree of sample pre-treatment varies considerably depending on the material. Within the UK and Europe, there are a number of well-established laboratories and increasingly, scientists are not just commissioning new dates, but also using statistical modelling of assemblages of dates, perhaps measured in different laboratories, to provide formal date estimates for their investigations. The issue of comparability of measurements (and thus bias, accuracy and precision of measurement) from the diverse laboratories is one which has been the focus of some attention both within the 14C community and the wider user communities for some time. As a result of this but also as part of laboratory benchmarking and quality assurance, the 14C community has undertaken a wide-scale, far-reaching and evolving programme of inter-comparisons, to the benefit of laboratories and users alike. This paper presents the results from the most recent exercise SIRI. The objectives of SIRI included, through choice of material, to contribute to the discussion concerning laboratory offsets and error multipliers in the context of IntCal (the International Calibration Programme) and to gain a better understanding of differences in background derived from a range of infinite age material types.

Evaluation of soil C-14 data for estimating inert organic matter in the RothC model

DOE Office of Scientific and Technical Information (OSTI.GOV)

Rethemeyer, J.; Grootes, P.M.; Brodowski, S.

2007-07-01

Changes in soil organic carbon stocks were simulated with the Rothamsted carbon (RothC) model. We evaluated the calculation of a major input variable, the amount of inert organic matter (IOM), using measurable data. Three different approaches for quantifying IOM were applied to soils with mainly recent organic matter and with carbon contribution from fossil fuels: 1) IOM estimation via total soil organic carbon (SOC); 2) through bulk soil radiocarbon and a mass balance; and 3) by quantifying the portion of black carbon via a specific marker. The results were highly variable in the soil containing lignite-derived carbon and ranged frommore » 8% to 52% inert carbon of total SOC, while nearly similar amounts of 5% to 8% were determined in the soil with mainly recent organic matter. We simulated carbon dynamics in both soils using the 3 approaches for quantifying IOM in combination with carbon inputs derived from measured crop yields. In the soil with recent organic matter, all approaches gave a nearly similar good agreement between measured and modeled data, while in the soil with a fossil carbon admixture, only the C-14 approach was successful in matching the measured data. Although C-14 was useful for initializing RothC, care should be taken when interpreting SOC dynamics in soils containing carbon from fossil fuels, since these reflect the contribution from both natural and anthropogenic carbon sources.« less

A comparison of the Greenland ice-core and IntCal timescales through the Laschamp geomagnetic excursion, utilising new 14C data from Tenaghi Philippon, Greece

NASA Astrophysics Data System (ADS)

Staff, Richard; Hardiman, Mark; Bronk Ramsey, Christopher; Hare, Vincent; Koutsodendris, Andreas; Pross, Jörg

2017-04-01

Cosmogenic radionuclides, such as 10Be and 14C, share a common production signal, with their formation in the Earth's upper atmosphere modulated by changes to the geomagnetic field, as well as variations in the intensity of the solar wind. Here, we present 54 14C measurements from a terrestrial fen peat core extracted from the site of Tenaghi Philippon, NE Greece, contiguously spanning the time period between 48,000 and 39,000 cal. BP. Utilising the most pronounced cosmogenic production peak of the last 100,000 years - that associated with the Laschamp geomagnetic excursion circa 41,000 years ago - we exploit this common production signal, comparing Greenland 10Be with our Tenaghi Philippon 14C record, thereby providing a means to assess the concordance between the radiocarbon (IntCal) and Greenland ice-core (GICC05) timescales themselves for this, the oldest portion of the radiocarbon technique.

Accessing the application of in situ cosmogenic 14C to surface exposure dating of amorphous SiO2

NASA Astrophysics Data System (ADS)

Cesta, J. M.; Goehring, B. M.; Ward, D. J.

2017-12-01

We assess the feasibility and utility of in situ cosmogenic 14C as a geochronometer for landforms composed of amorphous SiO2 through the comparison of 14C surface exposure ages to independently determined eruption ages on Obsidian Dome, California. Landforms composed of amorphous SiO2 phases are difficult to date by conventional cosmogenic nuclide methods due to several complications that may arise (e.g., inability to remove meteoric contamination). The onset of an increased understanding of production rates and analytical measurement of in situ 14C in SiO2 provides an opportunity to address this limitation. Obsidian Dome is a 600-year-old phreatomagmatic dome of the Mono-Inyo Craters located in Inyo County, California, and consists of vesicular pumice, obsidian, and rhyolite. Exposure ages from eight obsidian and banded pumice and obsidian surface samples range from 3947 ± 678 to 914 ± 134 years, all significantly older than the accepted radiocarbon age of 650-550 years. δ13C values for the samples range between +2.65‰ and +1.34‰ and show a negative correlation with CO2 yield. The `too old' exposure ages coupled with this negative correlation between δ13C and CO2 yield suggests the incorporation of an atmospheric component of 14C. Measurement of 14C concentrations in shielded, subsurface samples will assist in isolating the atmospheric 14C component and aid in correcting the surface exposure ages.

Insights from 14C into C loss pathways in degraded peatlands

NASA Astrophysics Data System (ADS)

Evans, Martin; Evans, Chris; Allott, Tim; Stimson, Andrew; Goulsbra, Claire

2016-04-01

Peatlands are important global stores of terrestrial carbon. Lowered water tables due to changing climate and direct or indirect human intervention produce a deeper aerobic zone and have the potential to enhance loss of stored carbon from the peat profile. The quasi continuous accumulation of organic matter in active peatlands means that the age of fluvial dissolved organic carbon exported from peatland systems is related to the source depth in the peat profile. Consequently 14C analysis of DOC in waters draining peatlands has the potential not only to tell us about the source of fluvial carbon and the stability of the peatland but also about the dominant hydrological pathways in the peatland system. This paper will present new radiocarbon determinations from peatland streams draining the heavily eroded peatlands of the southern Pennine uplands in the UK. These blanket peatland systems are highly degraded, with extensive bare peat and gully erosion resulting from air pollution during the industrial revolution, overgrazing, wildfire and climatic changes. Deep and extensive gullying has significantly modified the hydrology of these systems leading to local and more widespread drawdown of water table. 14C data from DOC in drainage waters are presented from two catchments; one with extensive gully erosion and the other with a combination of gully erosion and sheet erosion of the peat. At the gully eroded site DOC in drainage waters is as old as 160 BP but at the site with extensive sheet erosion dates of up to 1069 BP are amongst the oldest recorded from blanket peatland globally These data indicate significant degradation of stored carbon from the eroding peatlands. Initial comparisons of the 14C data with modelled water table for the catchments and depth-age curves for catchment peats suggests that erosion of the peat surface, allowing decomposition of exposed older organic material is a potential mechanism producing aged carbon from the eroded catchment. This

Improved radiocarbon analyses of modern human hair to determine the year-of-death by cross-flow nanofiltered amino acids: common contaminants, implications for isotopic analysis, and recommendations.

PubMed

Santos, Guaciara M; De La Torre, Hector A Martinez; Boudin, Mathieu; Bonafini, Marco; Saverwyns, Steven

2015-10-15

In forensic investigation, radiocarbon ((14)C) measurements of human tissues (i.e., nails and hair) can help determine the year-of-death. However, the frequent use of cosmetics can bias hair (14)C results as well as stable isotope values. Evidence shows that hair exogenous impurities percolate beyond the cuticle layer, and therefore conventional pretreatments are ineffective in removing them. We conducted isotopic analysis ((14)C, δ(13)C, δ(15)N and C/N) of conventionally treated and cross-flow nanofiltered amino acid (CFNAA)-treated samples (scalp- and body-hair) from a single female subject using fingernails as a reference. The subject studied frequently applies a permanent dark-brown dye kit to her scalp-hair and uses other care products for daily cleansing. We also performed pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) analyses of CFNAA-treated scalp-hair to identify contaminant remnants that could possibly interfere with isotopic analyses. The conventionally treated scalp- and body-hair showed (14)C offsets of ~21‰ and ~9‰, respectively. These offsets confirm the contamination by petrochemicals in modern human hair. A single CFNAA extraction reduced those offsets by ~34%. No significant improvement was observed when sequential extractions were performed, as it appears that the procedure introduced some foreign contaminants. A chromatogram of the CFNAA scalp-hair pyrolysis products showed the presence of petroleum and plant/animal compound residues, which can bias isotopic analyses. We have demonstrated that CFNAA extractions can partially remove cosmetic contaminants embedded in human hair. We conclude that fingernails are still the best source of keratin protein for year-of-death determinations and isotopic analysis, with body-hair and/or scalp-hair coupled with CFNAA extraction a close second. Copyright © 2015 John Wiley & Sons, Ltd.

Chlorophyll a-specific Δ14C, δ13C and δ15N values in stream periphyton: implications for aquatic food web studies

NASA Astrophysics Data System (ADS)

Ishikawa, N. F.; Yamane, M.; Suga, H.; Ogawa, N. O.; Yokoyama, Y.; Ohkouchi, N.

2015-11-01

Periphytic algae attached to a streambed substrate (periphyton) are an important primary producer in stream ecosystems. We determined the isotopic composition of chlorophyll a in periphyton collected from a stream flowing on limestone bedrock in the Seri River, central Japan. Stable isotope ratios of carbon (δ13C) and nitrogen (δ15N) and natural radiocarbon abundances (Δ14C) were measured in chlorophyll a (δ13Cchl, δ15Nchl and Δ14Cchl) and bulk (δ13Cbulk, δ15Nbulk and Δ14Cbulk) for periphyton, a pure aquatic primary producer (Cladophora sp.) and a terrestrial primary producer (Quercus glauca). Periphyton δ13Cbulk and δ13Cchl values did not necessarily correspond to δ13Cbulk for an algal-grazing specialist (Epeorus latifolium). Periphyton Δ14Cchl values (-258 ‰ in April and -190 ‰ in October) were slightly lower than Δ14Cbulk values (-228 ‰ in April and -179 ‰ in October) but were close to the Δ14C value for dissolved inorganic carbon (DIC; -217 ± 31 ‰), which is a mixture of weathered carbonates (Δ14C = -1000 ‰), CO2 derived from aquatic and terrestrial organic matters (variable Δ14C) and dissolved atmospheric CO2 (Δ14C approximately +30 ‰ in 2013). Δ14Cchl values were also close to Δ14Cbulk for E. latifolium (-215 ‰ in April and -199 ‰ in October) and Cladophora sp. (-210 ‰), whereas the Δ14Cbulk value for Q. glauca (+27 ‰) was closer to Δ14C for atmospheric CO2. Although the bulk isotopic composition of periphyton is recognised as a surrogate for the photosynthetic algal community, natural periphyton is a mixture of aquatic and terrestrial organic materials. Our results indicate that the bulk periphyton matrix at the study site consists of 89 to 95 % algal carbon (derived from 14C-depleted DIC) and 5 to 11 % terrestrial organic carbon (derived from 14C-enriched atmospheric CO2).

Radiocarbon variability in the western equatorial Pacific inferred from a high-resolution coral record from Nauru Island

DOE Office of Scientific and Technical Information (OSTI.GOV)

Guilderson, T.P.; Schrag, D.P.; Kashgarian, M.

1998-10-01

We have generated a high resolution coral {Delta}{sup 14}C record spanning the last 50 years to document the seasonal and interannual redistribution of surface waters in the western tropical Pacific. Prebomb (1947{endash}1956) {Delta}{sup 14}C values average {minus}63{per_thousand} and have a total range of 30{per_thousand}. Values begin to increase in 1957, reaching a maximum of 137{per_thousand} in mid-1983. Large interannual variability of up to 80{per_thousand} closely follows the El Ni{tilde n}o-Southern Oscillation (ENSO). During each ENSO warm phase, {Delta}{sup 14}C values begin to increase, reflecting the reduction of low-{sup 14}C water upwelling in the east and the invasion of subtropical watermore » into the western equatorial tropical Pacific. Maximum {Delta}{sup 14}C values are in phase or lag the corresponding sea surface temperature maxima in the eastern tropical Pacific, whereas the rapid return to more negative {Delta}{sup 14}C is in phase with eastern Pacific ENSO indices. The highest-amplitude excursions occur during the 1965/1966 and 1972/1973 events, when the {sup 14}C contrast is highest between the eastern Pacific and subtropics. The 1982/1983 El Ni{tilde n}o, although a larger ENSO event, has a lower {Delta}{sup 14}C amplitude, reflecting the penetration of bomb radiocarbon into the equatorial undercurrent and the reduced contrast in {Delta}{sup 14}C between thermocline and subtropical surface waters at that time. This coral record demonstrates the potential for using similar radiocarbon time series for documenting variability in Pacific shallow circulation over interannual and decadal timescales. {copyright} 1998 American Geophysical Union« less

Summary findings of the fourth international radiocarbon intercomparison (FIRI)(1998-2001)

NASA Astrophysics Data System (ADS)

Boaretto, Elisabetta; Bryant, Charlotte; Carmi, Israel; Cook, Gordon; Gulliksen, Steinar; Harkness, Doug; Heinemeier, Jan; McClure, John; McGee, Edward; Naysmith, Philip; Possnert, Goran; Scott, Marian; van der Plicht, Hans; van Strydonck, Mark

2002-10-01

Interlaboratory comparisons have been widely used in applied radiocarbon science. These are an important part of ongoing quality assurance (QA) programmes, which are vital to the appropriate interpretation of the evidence provided by the 14C record in Quaternary applications (including climate change and environmental reconstruction). International comparisons of laboratory performance are an essential component of the quality assurance process in radiocarbon dating. If the user community is to have confidence in radiocarbon results, it needs to be assured that laboratories world wide are producing measurements that are reliable and in accordance with good practice. The findings from the most recent (completed in 2001) and extensive (more than 90 participating laboratories) radiocarbon intercomparison (FIRI) are reported here. This study was designed (i) to assess comparability, or otherwise, of the results from different laboratories and (ii) to quantify the extent and possible causes of any interlaboratory variation. The results demonstrate that there are no significant differences amongst the main measurement techniques (gas proportional counting, liquid scintillation counting and accelerator mass spectrometry (AMS)) but there is evidence of small laboratory offsets relative to known age samples for some laboratories. There is also evidence in some cases of underestimation of measurement precision. Approximately 10% of all results were classified as extreme (outliers) and these results were generated by 14% of the laboratories. Overall, the evidence supports the fact that radiocarbon laboratories are generally accurate and precise but that, notwithstanding internal QA procedures, some problems still occur, which can best be detected by participation in independent intercomparisons such as FIRI, where the results allow individual laboratories to assess their performance and to take remedial measures where necessary. The results from FIRI are significant in that

Chlorophyll a specific Δ14C, δ13C and δ15N values in stream periphyton: implications for aquatic food web studies

NASA Astrophysics Data System (ADS)

Ishikawa, N. F.; Yamane, M.; Suga, H.; Ogawa, N. O.; Yokoyama, Y.; Ohkouchi, N.

2015-07-01

We determined the isotopic composition of chlorophyll a in periphytic algae attached to a streambed substrate (periphyton). The samples were collected from a stream flowing on limestone bedrock in the Seri River, central Japan. Stable isotope ratios of carbon (δ13C) and nitrogen (δ15N) and natural radiocarbon abundances (Δ14C) were measured in chlorophyll a (δ13Cchl, δ15Nchl and Δ14Cchl) and bulk (δ13Cbulk, δ15Nbulk and Δ14Cbulk) for periphyton, pure aquatic primary producer (Cladophora sp.) and terrestrial primary producer (Quercus glauca). Periphyton δ13Cbulk and δ13Cchl values did not necessarily correspond to δ13Cbulk for an algal-grazing specialist (Mayfly larva, Epeorus latifolium), suggesting that periphyton δ13C values do not faithfully trace carbon transfer between primary producers and primary consumers. Periphyton Δ14Cchl values (-258 ‰ in April and -190 ‰ in October) were slightly lower than Δ14Cbulk values (-228 ‰ in April and -179 ‰ in October), but were close to the Δ14C value for dissolved inorganic carbon (DIC) (-217 ± 31 ‰), which is a mixture of weathered carbonates (Δ14C = -1000 ‰) and dissolved atmospheric CO2 (Δ14C approximately +30 ‰ in 2013). Δ14Cchl values were also close to Δ14Cbulk for E. latifolium (-215 ‰ in April and -199 ‰ in October) and Cladophora sp. (-210 ‰), whereas the Δ14Cbulk value for Q. glauca (+27 ‰) was closer to Δ14C for atmospheric CO2. Although the bulk isotopic composition of periphyton is recognised as a surrogate for the photosynthetic algal community, natural periphyton is a mixture of aquatic and terrestrial organic materials. Our results indicate that the bulk periphyton matrix at the study site consists of 89 to 95 % algal carbon (derived from 14C-depleted DIC) and 5 to 11 % terrestrial organic carbon (derived from 14C-enriched atmospheric CO2).

A generic biokinetic model for carbon-14 labelled compounds

NASA Astrophysics Data System (ADS)

Manger, Ryan Paul

Carbon-14, a radioactive nuclide, is used in many industrial applications. Due to its wide range of uses in industry, many workers are at risk of accidental internal exposure to 14C. Being a low energy beta emitter, 14C is not a significant external radiation hazard, but the internal consequences posed by 14C are important, especially because of its long half life of 5730 years [46]. The current biokinetic model recommended by the International Commission on Radiological Protection (ICRP) is a conservative estimate of how radiocarbon is treated by the human body. The ICRP generic radiocarbon model consists of a single compartment representing the entire human body. This compartment has a biological half life of 40 days yielding an effective dose coefficient of 5.8x10-10 Sv B q-1 [44, 45, 49, 53, 54]. This overestimates the dose of all radiocarbon compounds that have been studied [96]. An improved model has been developed that includes and alimentary tract, a urinary bladder, CO2 model, and an "Other" compartment used to model systemic tissues. The model can be adapted to replicate any excretion curve and excretion pattern. In addition, the effective dose coefficient produced by the updated model is near the mean effective dose coefficient of carbon compounds that have been considered in this research. The major areas of improvement are: more anatomically significant, a less conservative dose coefficient, and the ability to manipulate the model for known excretion data. Due to the wide variety of carbon compounds, it is suggested that specific biokinetic models be implemented for known radiocarbon substances. If the source of radiocarbon is dietary, then the physiologically based model proposed by Whillans [102] that splits all ingested radiocarbon compounds into carbohydrates, fats, and proteins should be used.

Stable and radiocarbon isotopic composition of dissolved organic matter in the Gulf of Mexico

NASA Astrophysics Data System (ADS)

Walker, B. D.; Druffel, E. R. M.; Kolasinski, J.; Roberts, B. J.; Xu, X.; Rosenheim, B. E.

2017-08-01

Dissolved organic carbon (DOC) is of primary importance to marine ecosystems and the global carbon cycle. Stable carbon (δ13C) and radiocarbon (Δ14C) isotopic measurements are powerful tools for evaluating DOC sources and cycling. However, the isotopic signature of DOC in the Gulf of Mexico (GOM) remains almost completely unknown. Here we present the first DOC Δ14C and δ13C depth profiles from the GOM. Our results suggest the Mississippi River exports large amounts of DOC with an anthropogenic "bomb" Δ14C signature. Riverine DOC is removed and recycled offshore, and some marine production of DOC is observed in the river plume. Offshore profiles show that DOC has higher Δ14C than its Caribbean feed waters, indicative of a modern deep DOC source in the GOM basin. Finally, high DOC with negative δ13C and Δ14C values were observed near the Macondo Wellhead, suggesting a transformation of Deepwater Horizon hydrocarbons into a persistent population of DOC.

Centuries of marine radiocarbon reservoir age variation within archaeological Mesodesma Donacium shells from Southern Peru

USGS Publications Warehouse

Jones, K.B.; Hodgins, G.W.L.; Etayo-Cadavid, M. F.; Andrus, C.F.T.; Sandweiss, D.H.

2010-01-01

Mollusk shells provide brief (<5 yr per shell) records of past marine conditions, including marine radiocarbon reservoir age (R) and upwelling. We report 21 14C ages and R calculations on small (~2 mg) samples from 2 Mesodesma donacium (surf clam) shells. These shells were excavated from a semi-subterranean house floor stratum 14C dated to 7625 ?? 35 BP at site QJ-280, Quebrada Jaguay, southern Peru. The ranges in marine 14C ages (and thus R) from the 2 shells are 530 and 170 14C yr; R from individual aragonite samples spans 130 ?? 60 to 730 ?? 170 14C yr. This intrashell 14C variability suggests that 14C dating of small (time-slice much less than 1 yr) marine samples from a variable-R (i.e. variable-upwelling) environment may introduce centuries of chronometric uncertainty. ?? 2010 by the Arizona Board of Regents on behalf of the University of Arizona.

Blank corrections for ramped pyrolysis radiocarbon dating of sedimentary and soil organic carbon.

PubMed

Fernandez, Alvaro; Santos, Guaciara M; Williams, Elizabeth K; Pendergraft, Matthew A; Vetter, Lael; Rosenheim, Brad E

2014-12-16

Ramped pyrolysis (RP) targets distinct components of soil and sedimentary organic carbon based on their thermochemical stabilities and allows the determination of the full spectrum of radiocarbon ((14)C) ages present in a soil or sediment sample. Extending the method into realms where more precise ages are needed or where smaller samples need to be measured involves better understanding of the blank contamination associated with the method. Here, we use a compiled data set of RP measurements of samples of known age to evaluate the mass of the carbon blank and its associated (14)C signature, and to assess the performance of the RP system. We estimate blank contamination during RP using two methods, the modern-dead and the isotope dilution method. Our results indicate that during one complete RP run samples are contaminated by 8.8 ± 4.4 μg (time-dependent) of modern carbon (MC, fM ∼ 1) and 4.1 ± 5.5 μg (time-independent) of dead carbon (DC, fM ∼ 0). We find that the modern-dead method provides more accurate estimates of uncertainties in blank contamination; therefore, the isotope dilution method should be used with caution when the variability of the blank is high. Additionally, we show that RP can routinely produce accurate (14)C dates with precisions ∼100 (14)C years for materials deposited in the last 10,000 years and ∼300 (14)C years for carbon with (14)C ages of up to 20,000 years.

Source apportionment of elevated wintertime PAHs by compound-specific radiocarbon analysis

NASA Astrophysics Data System (ADS)

Sheesley, R. J.; Kruså, M.; Krecl, P.; Johansson, C.; Gustafsson, Ã.-.

2009-05-01

Natural abundance radiocarbon analysis facilitates distinct source apportionment between contemporary biomass/biofuel (14C "alive") versus fossil fuel (14C "dead") combustion. Here, the first compound-specific radiocarbon analysis (CSRA) of atmospheric polycyclic aromatic hydrocarbons (PAHs) was demonstrated for a set of samples collected in Lycksele, Sweden a small town with frequent episodes of severe atmospheric pollution in the winter. Renewed interest in using residential wood combustion (RWC) means that this type of seasonal pollution is of increasing concern in many areas. Five individual/paired PAH isolates from three pooled fortnight-long filter collections were analyzed by CSRA: phenanthrene, fluoranthene, pyrene, benzo[b+k]fluoranthene and indeno[cd]pyrene plus benzo[ghi]perylene; phenanthrene was the only compound also analyzed in the gas phase. The measured Δ14C for PAHs spanned from -138.3‰ to 58.0‰. A simple isotopic mass balance model was applied to estimate the fraction biomass (fbiomass) contribution, which was constrained to 71-87% for the individual PAHs. Indeno[cd]pyrene plus benzo[ghi]perylene had an fbiomass of 71%, while fluoranthene and phenanthrene (gas phase) had the highest biomass contribution at 87%. The total organic carbon (TOC, defined as carbon remaining after removal of inorganic carbon) fbiomass was estimated to be 77%, which falls within the range for PAHs. This CSRA data of atmospheric PAHs established that RWC is the dominating source of atmospheric PAHs to this region of the boreal zone with some variations among RWC contributions to specific PAHs.

Comparison of Radiocarbon Ages of Sediments, Plants, and Shells From Coastal Lakes in North Florida

NASA Astrophysics Data System (ADS)

Wang, Y.; Das, O.; Liu, J.; Xu, X.; Roy, R.; Donoghue, J. F.; Means, G. H.

2017-12-01

Coastal lakes sediments are valuable archives of paleo-hurricanes and environmental changes during the late Quaternary provided that they can be accurately dated. Here, we report new radiocarbon (14C) dates derived from various organic and inorganic substrates, including bulk sediment organic matter, plants, shells, particulate organic matter (POM) and dissolved organic matter (DOM), from three coastal lakes in Florida, and compare these ages to evaluate the "reservoir effect" on 14C dating of both organic and inorganic carbon in these lakes. Bulk sediment organic matter yielded consistently older 14C ages than contemporaneous plants and shell fragments, indicating significant radiocarbon deficiencies in sedimentary organic matter in these coastal lakes, caused by influx of old organic carbon from terrestrial sources (such as soils and ancient peat deposits) in the watershed. Several reversals are observed in the 14C ages of bulk sediment organic matter in sediment cores from these lakes, indicating that input of aged organic matter from terrestrial sources into these lakes can vary considerably over time. DOM and POM samples collected at different times also yielded variable 14C signatures, further confirming the temporal variability in the contribution of old organic carbon from terrestrial sources to the lakes. The 14C age discrepancy between bulk sediment organic matter and co-occurring plant fragments or shells varies from less than one hundred years to nearly three thousand years in sediment cores examined in this study. The results show that 14C ages obtained from bulk sediment organic matter in these coastal lakes are unreliable. Analyses of both modern and fossil shells from one of the lakes suggest that the 14C reservoir effect on inorganic carbon in the lake is small and thus freshwater shells (if preserved in the sediment cores) may serve as a good substrate for 14C dating in the absence of plant fragments. However, unidentifiable shell fragments

Constraining the sources and cycling of dissolved organic carbon in a large oligotrophic lake using radiocarbon analyses

NASA Astrophysics Data System (ADS)

Zigah, Prosper K.; Minor, Elizabeth C.; McNichol, Ann P.; Xu, Li; Werne, Josef P.

2017-07-01

We measured the concentrations and isotopic compositions of solid phase extracted (SPE) dissolved organic carbon (DOC) and high molecular weight (HMW) DOC and their constituent organic components in order to better constrain the sources and cycling of DOC in a large oligotrophic lacustrine system (Lake Superior, North America). SPE DOC constituted a significant proportion (41-71%) of the lake DOC relative to HMW DOC (10-13%). Substantial contribution of 14C-depleted components to both SPE DOC (Δ14C = 25-43‰) and HMW DOC (Δ14C = 22-32‰) was evident during spring mixing, and depressed their radiocarbon values relative to the lake dissolved inorganic carbon (DIC; Δ14C ∼ 59‰). There was preferential removal of 14C-depleted (older) and thermally recalcitrant components from HMW DOC and SPE DOC in the summer. Contemporary photoautotrophic addition to HMW DOC was observed during summer stratification in contrast to SPE DOC, which decreased in concentration during stratification. Serial thermal oxidation radiocarbon analysis revealed a diversity of sources (both contemporary and older) within the SPE DOC, and also showed distinct components within the HMW DOC. The thermally labile components of HMW DOC were 14C-enriched and are attributed to heteropolysaccharides (HPS), peptides/amide and amino sugars (AMS) relative to the thermally recalcitrant components reflecting the presence of older material, perhaps carboxylic-rich alicyclic molecules (CRAM). The solvent extractable lipid-like fraction of HMW DOC was very 14C-depleted (as old as 1270-2320 14C years) relative to the carbohydrate-like and protein-like substances isolated by acid hydrolysis of HMW DOC. Our data constrain relative influences of contemporary DOC and old DOC, and DOC cycling in a modern freshwater ecosystem.

Mortar radiocarbon dating: preliminary accuracy evaluation of a novel methodology.

PubMed

Marzaioli, Fabio; Lubritto, Carmine; Nonni, Sara; Passariello, Isabella; Capano, Manuela; Terrasi, Filippo

2011-03-15

Mortars represent a class of building and art materials that are widespread at archeological sites from the Neolithic period on. After about 50 years of experimentation, the possibility to evaluate their absolute chronology by means of radiocarbon ((14)C) remains still uncertain. With the use of a simplified mortar production process in the laboratory environment, this study shows the overall feasibility of a novel physical pretreatment for the isolation of the atmospheric (14)CO(2) (i.e., binder) signal absorbed by the mortars during their setting. This methodology is based on the assumption that an ultrasonic attack in liquid phase isolates a suspension of binder carbonates from bulk mortars. Isotopic ((13)C and (14)C), % C, X-ray diffractometry (XRD), and scanning electron microscopy (SEM) analyses were performed to characterize the proposed methodology. The applied protocol allows suppression of the fossil carbon (C) contamination originating from the incomplete burning of the limestone during the quick lime production, providing unbiased dating for "laboratory" mortars produced operating at historically adopted burning temperatures.

Pre- and post-bomb radiocarbon in fish otoliths

NASA Astrophysics Data System (ADS)

Kalish, John M.

1993-02-01

Measurements of radiocarbon in seawater dissolved inorganic carbon (DIC), or suitable proxies such as hermatypic corals, are a valuable source of information on carbon flux and ocean circulation. However, knowledge of the global distribution of both pre- and post-bomb radiocarbon is limited due to the sources of these data. Suitable hermatypic corals are restricted to shallow tropical and subtropical waters and oceanographic collections of seawater are prohibitively expensive. What is needed is a proxy for ocean radiocarbon that can be collected at most latitudes and depths, and which can be reliably aged. Here I report accelerator mass spectrometry analyses of radiocarbon from selected regions of fish otoliths and show that such measurements are suitable for determining both pre- and post-bomb radiocarbon in all oceans and at most depths. Radiocarbon data obtained from otoliths can extend our knowledge of carbon flux in the oceans and atmosphere and help to develop further understanding of the fate of atmospheric CO 2 and ocean circulation. The data presented here represent the first pre- and post-bomb time series of radiocarbon levels from temperate waters. Furthermore, I demonstrate that the dramatic increase in radiocarbon in the atmosphere and oceans, attributable to the atmospheric testing of thermonuclear bombs during the 1950's and 1960's, provides a chemical mark on fish otoliths that is suitable for the validation of age in fishes.

A review of single-sample-based models and other approaches for radiocarbon dating of dissolved inorganic carbon in groundwater

USGS Publications Warehouse

Han, L. F; Plummer, Niel

2016-01-01

underlying assumptions on which the various models and approaches are based can result in a wide range of estimates of 14C0 and limit the usefulness of radiocarbon as a dating tool for groundwater. In each of the three generalized approaches (single-sample-based models, statistical approach, and geochemical mass-balance approach), successful application depends on scrutiny of the isotopic (14C and 13C) and chemical data to conceptualize the reactions and processes that affect the 14C content of DIC in aquifers. The recently developed graphical analysis method is shown to aid in determining which approach is most appropriate for the isotopic and chemical data from a groundwater system.

New and revised 14C dates for Hawaiian surface lava flows: Paleomagnetic and geomagnetic implications

USGS Publications Warehouse

Pressline, N.; Trusdell, F.A.; Gubbins, David

2009-01-01

Radiocarbon dates have been obtained for 30 charcoal samples corresponding to 27 surface lava flows from the Mauna Loa and Kilauea volcanoes on the Island of Hawaii. The submitted charcoal was a mixture of fresh and archived material. Preparation and analysis was undertaken at the NERC Radiocarbon Laboratory in Glasgow, Scotland, and the associated SUERC Accelerator Mass Spectrometry facility. The resulting dates range from 390 years B.P. to 12,910 years B.P. with corresponding error bars an order of magnitude smaller than previously obtained using the gas-counting method. The new and revised 14C data set can aid hazard and risk assessment on the island. The data presented here also have implications for geomagnetic modelling, which at present is limited by large dating errors. Copyright 2009 by the American Geophysical Union.

Radiocarbon constraints on the extent and evolution of the South Pacific glacial carbon pool

PubMed Central

Ronge, T. A.; Tiedemann, R.; Lamy, F.; Köhler, P.; Alloway, B. V.; De Pol-Holz, R.; Pahnke, K.; Southon, J.; Wacker, L.

2016-01-01

During the last deglaciation, the opposing patterns of atmospheric CO2 and radiocarbon activities (Δ14C) suggest the release of 14C-depleted CO2 from old carbon reservoirs. Although evidences point to the deep Pacific as a major reservoir of this 14C-depleted carbon, its extent and evolution still need to be constrained. Here we use sediment cores retrieved along a South Pacific transect to reconstruct the spatio-temporal evolution of Δ14C over the last 30,000 years. In ∼2,500–3,600 m water depth, we find 14C-depleted deep waters with a maximum glacial offset to atmospheric 14C (ΔΔ14C=−1,000‰). Using a box model, we test the hypothesis that these low values might have been caused by an interaction of aging and hydrothermal CO2 influx. We observe a rejuvenation of circumpolar deep waters synchronous and potentially contributing to the initial deglacial rise in atmospheric CO2. These findings constrain parts of the glacial carbon pool to the deep South Pacific. PMID:27157845

The radiocarbon signature of microorganisms in the mesopelagic ocean.

PubMed

Hansman, Roberta L; Griffin, Sheila; Watson, Jordan T; Druffel, Ellen R M; Ingalls, Anitra E; Pearson, Ann; Aluwihare, Lihini I

2009-04-21

Several lines of evidence indicate that microorganisms in the meso- and bathypelagic ocean are metabolically active and respiring carbon. In addition, growing evidence suggests that archaea are fixing inorganic carbon in this environment. However, direct quantification of the contribution from deep ocean carbon sources to community production in the dark ocean remains a challenge. In this study, carbon flow through the microbial community at 2 depths in the mesopelagic zone of the North Pacific Subtropical Gyre was examined by exploiting the unique radiocarbon signatures (Delta(14)C) of the 3 major carbon sources in this environment. The radiocarbon content of nucleic acids, a biomarker for viable cells, isolated from size-fractionated particles (0.2-0.5 microm and >0.5 microm) showed the direct incorporation of carbon delivered by rapidly sinking particles. Most significantly, at the 2 mesopelagic depths examined (670 m and 915 m), carbon derived from in situ autotrophic fixation supported a significant fraction of the free-living microbial community (0.2-0.5 microm size fraction), but the contribution of chemoautotrophy varied markedly between the 2 depths. Results further showed that utilization of the ocean's largest reduced carbon reservoir, (14)C-depleted, dissolved organic carbon, was negligible in this environment. This isotopic portrait of carbon assimilation by the in situ, free-living microbial community, integrated over >50,000 L of seawater, implies that recent, photosynthetic carbon is not always the major carbon source supporting microbial community production in the mesopelagic realm.

Impacts of C-uptake by plants on the spatial distribution of 14C accumulated in vegetation around a nuclear facility-Application of a sophisticated land surface 14C model to the Rokkasho reprocessing plant, Japan.

PubMed

Ota, Masakazu; Katata, Genki; Nagai, Haruyasu; Terada, Hiroaki

2016-10-01

The impacts of carbon uptake by plants on the spatial distribution of radiocarbon ( 14 C) accumulated in vegetation around a nuclear facility were investigated by numerical simulations using a sophisticated land surface 14 C model (SOLVEG-II). In the simulation, SOLVEG-II was combined with a mesoscale meteorological model and an atmospheric dispersion model. The model combination was applied to simulate the transfer of 14 CO 2 and to assess the radiological impact of 14 C accumulation in rice grains during test operations of the Rokkasho reprocessing plant (RRP), Japan, in 2007. The calculated 14 C-specific activities in rice grains agreed with the observed activities in paddy fields around the RRP within a factor of four. The annual effective dose delivered from 14 C in the rice grain was estimated to be less than 0.7 μSv, only 0.07% of the annual effective dose limit of 1 mSv for the public. Numerical experiments of hypothetical continuous atmospheric 14 CO 2 release from the RRP showed that the 14 C-specific activities of rice plants at harvest differed from the annual mean activities in the air. The difference was attributed to seasonal variations in the atmospheric 14 CO 2 concentration and the growth of the rice plant. Accumulation of 14 C in the rice plant significantly increased when 14 CO 2 releases were limited during daytime hours, compared with the results observed during the nighttime. These results indicated that plant growth stages and diurnal photosynthesis should be considered in predictions of the ingestion dose of 14 C for long-term chronic releases and short-term diurnal releases of 14 CO 2 , respectively. Copyright © 2016 Elsevier Ltd. All rights reserved.

On radiocarbon and plutonium leakage to groundwater in the vicinity of a shallow-land radioactive waste repository.

PubMed

Gudelis, A; Gvozdaite, R; Kubareviciene, V; Druteikiene, R; Lukosevicius, S; Sutas, A

2010-06-01

A shallow-land radioactive waste repository operated in boggy forest environment from 1963 to 1989. During the operation period, a considerable amount of technogenic radionuclides, in solidified state, was disposed into the vault established in the geological structure at the depth of up to 3m. Environmental monitoring activities started after the closure of the repository in 1989. Recent investigations revealed transfer of radiocarbon and plutonium to the groundwater in the prevailing flow direction. Activity concentration of (239,240)Pu in non-filtered fraction of the groundwater from observation well no. 4 determined by alpha-spectrometry was 6.4 x 10(-5) Bq l(-1) in 2005, and 3.2 x 10(-4) Bq l(-1) in 2006. Further analysis of colloid-facilitated transport of plutonium is planned. Variation of (14)C activity concentration in the same well was monitored in 2006. It varied from 0.2+/-0.1 Bq l(-1) in October to 2.8+/-0.6 Bq l(-1) in June and July. Results imply further research into radiocarbon transfer to atmosphere and selected plant species. Copyright (c) 2008 Elsevier Ltd. All rights reserved.

Geographic and temporal trends in proboscidean and human radiocarbon histories during the late Pleistocene

NASA Astrophysics Data System (ADS)

Ugan, Andrew; Byers, David

2007-12-01

The causes of large animal extinctions at the end of the Pleistocene remain a hotly debated topic focused primarily on the effects of human over hunting and climate change. Here we examine multiple, large radiocarbon data sets for humans and extinct proboscideans and explore how variation in their temporal and geographic distributions were related prior to proboscidean extinction. These data include 4532 archaeological determinations from Europe and Siberia and 1177 mammoth and mastodont determinations from Europe, Siberia, and North America. All span the period from 45,000 to 12,000 calendar years BP. We show that while the geographic ranges of dated human occupations and proboscidean remains overlap across the terminal Pleistocene of the Old World, the two groups remain largely segregated and increases in the frequency of human occupations do not coincide with declines in proboscidean remains. Prior to the Last Glacial Maximum (LGM; ca 21,000 years BP), archaeological 14C determinations increase slightly in frequency worldwide while the frequency of dated proboscidean remains varies depending on taxon and location. After the LGM, both sympatric and allopatric groups of humans and proboscideans increase sharply as climatic conditions ameliorate. Post-LGM radiocarbon frequencies among proboscideans peak at different times, also depending upon taxon and location. Woolly mammoths in Beringia reach a maximum and then decline beginning between 16,000 and 15,500 years BP, woolly mammoths in Europe and Siberia ca 14,500 and 13,500 BP, and Columbian mammoth and American mastodont only after 13,000 BP. Declines among woolly mammoths appear to coincide with the restructuring of biotic communities following the Pleistocene-Holocene transition.

Status report on the Zagreb Radiocarbon Laboratory - AMS and LSC results of VIRI intercomparison samples

NASA Astrophysics Data System (ADS)

Sironić, Andreja; Krajcar Bronić, Ines; Horvatinčić, Nada; Barešić, Jadranka; Obelić, Bogomil; Felja, Igor

2013-01-01

A new line for preparation of the graphite samples for 14C dating by Accelerator Mass Spectrometry (AMS) in the Zagreb Radiocarbon Laboratory has been validated by preparing graphite from various materials distributed within the Fifth International Radiocarbon Intercomparison (VIRI) study. 14C activity of prepared graphite was measured at the SUERC AMS facility. The results are statistically evaluated by means of the z-score and u-score values. The mean z-score value of 28 prepared VIRI samples is (0.06 ± 0.23) showing excellent agreement with the consensus VIRI values. Only one sample resulted in the u-score value above the limit of acceptability (defined for the confidence interval of 99%) and this was probably caused by a random contamination of the graphitization rig. After the rig had been moved to the new adapted and isolated room, all u-score values laid within the acceptable limits. Our LSC results of VIRI intercomparison samples are also presented and they are all accepted according to the u-score values.

Assessing open-system behavior of 14C in terrestrial gastropod shells

USGS Publications Warehouse

Rech, Jason A.; Pigati, Jeffrey S.; Lehmann, Sophie B.; McGimpsey, Chelsea N.; Grimley, David A.; Nekola, Jeffrey C.

2011-01-01

In order to assess open-system behavior of radiocarbon in fossil gastropod shells, we measured the 14C activity on 10 aliquots of shell material recovered from Illinoian (~190-130 ka) and pre-Illinoian (~800 ka) loess and lacustrine deposits in the Midwestern USA. Eight of the 10 aliquots yielded measurable 14C activities that ranged from 0.25 to 0.53 percent modern carbon (pMC), corresponding to apparent 14C ages between 48.2 and 42.1 ka. This small level of open-system behavior is common in many materials that are used for 14C dating (e.g. charcoal), and typically sets the upper practical limit of the technique. Two aliquots of gastropod shells from the Illinoian-aged Petersburg Silt (Petersburg Section) in central Illinois, USA, however, yielded elevated 14C activities of 1.26 and 1.71 pMC, which correspond to apparent 14C ages of 35.1 and 32.7 ka. Together, these results suggest that while many fossil gastropods shells may not suffer from major (>1%) open-system problems, this is not always the case. We then examined the mineralogy, trace element chemistry, and physical characteristics of a suite of fossil and modern gastropod shells to identify the source of contamination in the Petersburg shells and assess the effectiveness of these screening techniques at identifying samples suitable for 14C dating. Mineralogical (XRD) and trace element analyses were inconclusive, which suggests that these techniques are not suitable for assessing open-system behavior in terrestrial gastropod shells. Analysis with scanning electron microscopy (SEM), however, identified secondary mineralization (calcium carbonate) primarily within the inner whorls of the Petersburg shells. This indicates that SEM examination, or possibly standard microscope examination, of the interior of gastropod shells should be used when selecting fossil gastropod shells for 14C dating.

Analysis of 14C and 13C in teeth provides precise birth dating and clues to geographical origin

PubMed Central

K, Alkass; BA, Buchholz; H, Druid; KL, Spalding

2011-01-01

The identification of human bodies in situations when there are no clues as to the person’s identity from circumstantial data, poses a difficult problem to investigators. The determination of age and sex of the body can be crucial in order to limit the search to individuals that are a possible match. We analyzed the proportion of bomb pulse derived carbon-14 (14C) incorporated in the enamel of teeth from individuals from different geographical locations. The ‘bomb pulse’ refers to a significant increase in 14C levels in the atmosphere caused by above ground test detonations of nuclear weapons during the cold war (1955-1963). By comparing 14C levels in enamel with 14C atmospheric levels systematically recorded over time, high precision birth dating of modern biological material is possible. Above ground nuclear bomb testing was largely restricted to a couple of locations in the northern hemisphere, producing differences in atmospheric 14C levels at various geographical regions, particularly in the early phase. Therefore, we examined the precision of 14C birth dating of enamel as a function of time of formation and geographical location. We also investigated the use of the stable isotope 13C as an indicator of geographical origin of an individual. Dental enamel was isolated from 95 teeth extracted from 84 individuals to study the precision of the 14C method along the bomb spike. For teeth formed before 1955 (N = 17), all but one tooth showed negative Δ14C values. Analysis of enamel from teeth formed during the rising part of the bomb-spike (1955-1963, N = 12) and after the peak (>1963, N = 66) resulted in an average absolute date of birth estimation error of 1.9 ±1.4 and 1.3 ± 1.0 years, respectively. Geographical location of an individual had no adverse effect on the precision of year of birth estimation using radiocarbon dating. In 46 teeth, measurement of 13C was also performed. Scandinavian teeth showed a substantially greater depression in average δ13C

Analysis of 14C and 13C in teeth provides precise birth dating and clues to geographical origin.

PubMed

Alkass, K; Buchholz, B A; Druid, H; Spalding, K L

2011-06-15

The identification of human bodies in situations when there are no clues as to the person's identity from circumstantial data, poses a difficult problem to the investigators. The determination of age and sex of the body can be crucial in order to limit the search to individuals that are a possible match. We analyzed the proportion of bomb pulse derived carbon-14 ((14)C) incorporated in the enamel of teeth from individuals from different geographical locations. The 'bomb pulse' refers to a significant increase in (14)C levels in the atmosphere caused by above ground test detonations of nuclear weapons during the cold war (1955-1963). By comparing (14)C levels in enamel with (14)C atmospheric levels systematically recorded over time, high precision birth dating of modern biological material is possible. Above ground nuclear bomb testing was largely restricted to a couple of locations in the northern hemisphere, producing differences in atmospheric (14)C levels at various geographical regions, particularly in the early phase. Therefore, we examined the precision of (14)C birth dating of enamel as a function of time of formation and geographical location. We also investigated the use of the stable isotope (13)C as an indicator of geographical origin of an individual. Dental enamel was isolated from 95 teeth extracted from 84 individuals to study the precision of the (14)C method along the bomb spike. For teeth formed before 1955 (N=17), all but one tooth showed negative Δ(14)C values. Analysis of enamel from teeth formed during the rising part of the bomb-spike (1955-1963, N=12) and after the peak (>1963, N=66) resulted in an average absolute date of birth estimation error of 1.9±1.4 and 1.3±1.0 years, respectively. Geographical location of an individual had no adverse effect on the precision of year of birth estimation using radiocarbon dating. In 46 teeth, measurement of (13)C was also performed. Scandinavian teeth showed a substantially greater depression in

Solar activity around AD 775 from aurorae and radiocarbon

NASA Astrophysics Data System (ADS)

Neuhäuser, R.; Neuhäuser, D. L.

2015-04-01

A large variation in 14C around AD 775 has been considered to be caused by one or more solar super-flares within one year. We critically review all known aurora reports from Europe as well as the Near, Middle, and Far East from AD 731 to 825 and find 39 likely true aurorae plus four more potential aurorae and 24 other reports about halos, meteors, thunderstorms etc., which were previously misinterpreted as aurorae or misdated; we assign probabilities for all events according to five aurora criteria. We find very likely true aurorae in AD 743, 745, 762, 765, 772, 773, 793, 796, 807, and 817. There were two aurorae in the early 770s observed near Amida (now Diyarbak\\i r in Turkey near the Turkish-Syrian border), which were not only red, but also green-yellow - being at a relatively low geomagnetic latitude, they indicate a relatively strong solar storm. However, it cannot be argued that those aurorae (geomagnetic latitude 43 to 50°, considering five different reconstructions of the geomagnetic pole) could be connected to one or more solar super-flares causing the 14C increase around AD 775: There are several reports about low- to mid-latitude aurorae at 32 to 44° geomagnetic latitude in China and Iraq; some of them were likely observed (quasi-)simultaneously in two of three areas (Europe, Byzantium/Arabia, East Asia), one lasted several nights, and some indicate a particularly strong geomagnetic storm (red colour and dynamics), namely in AD 745, 762, 793, 807, and 817 - always without 14C peaks. We use 39 likely true aurorae as well as historic reports about sunspots together with the radiocarbon content from tree rings to reconstruct the solar activity: From AD {˜ 733} to {˜ 823}, we see at least nine Schwabe cycles; instead of one of those cycles, there could be two short, weak cycles - reflecting the rapid increase to a high 14C level since AD 775, which lies at the end of a strong cycle. In order to show the end of the dearth of naked-eye sunspots, we

Increase of radiocarbon concentration in tree rings from Kujawy (SE Poland) around AD 774-775

NASA Astrophysics Data System (ADS)

Rakowski, Andrzej Z.; Krąpiec, Marek; Huels, Mathias; Pawlyta, Jacek; Dreves, Alexander; Meadows, John

2015-10-01

Evidence of a rapid increase in atmospheric radiocarbon (14C) content in AD 774-775 was presented by Miyake et al. (2012), who observed an increase of about 12‰ in the 14C content in annual tree rings from Japanese cedar. Usoskin et al. (2013) report a similar 14C spike in German oak, and attribute it to exceptional solar activity. If this phenomenon is global in character, such rapid changes in 14C concentration may affect the accuracy of calibrated dates, as the existing calibration curve is composed mainly of decadal samples. Single-year samples of dendro-chronologically dated tree rings of deciduous oak (Quercus robur) from Kujawy, a village near Krakow (SE Poland), spanning the years AD 765-796, were collected and their 14C content was measured using the AMS system in the Leibniz Laboratory. The results clearly show a rapid increase of 9.2 ± 2.1‰ in the 14C concentration in tree rings between AD 774 and AD 775, with maximum Δ14C = 4.1 ± 2.3‰ noted in AD 776.

Source apportionment of elevated wintertime PAHs by compound-specific radiocarbon analysis

NASA Astrophysics Data System (ADS)

Sheesley, R. J.; Kruså, M.; Krecl, P.; Johansson, C.; Gustafsson, Ã.-.

2008-12-01

Natural abundance radiocarbon analysis facilitates distinct source apportionment between contemporary biomass/biofuel (14C "alive") versus fossil fuel (14C "dead") combustion. Here, the first compound-specific radiocarbon analysis (CSRA) of atmospheric polycylic aromatic hydrocarbons (PAHs) was demonstrated for a set of samples collected in Lycksele, Sweden a small town with frequent episodes of severe atmospheric pollution in the winter. Renewed interest in residential wood combustion means than this type of seasonal pollution is of increasing concern in many areas. Five individual/paired PAH isolates from three pooled fortnight-long filter collections were analyzed by CSRA: phenanthrene, fluoranthene, pyrene, benzo[b+k]fluoranthene and indeno[cd]pyrene plus benzo[ghi]perylene; phenanthrene was the only compound also analyzed in the gas phase. The measured Δ14C for PAHs spanned from -138.3‰ to 58.0‰. A simple isotopic mass balance model was applied to estimate the fraction biomass (fbiomass) contribution that was constrained to a range of 71% for indeno[cd]pyrene+benzo[ghi]perylene to 87% for the gas phase phenanthrene and particulate fluoranthene, respectively. Indeno[cd]pyrene plus benzo[ghi]perylene, known to be enhanced in gasoline-powered motor vehicle exhaust compared to diesel exhaust, had the lowest contribution of biomass combustion of the measured PAHs by 9%. The total organic carbon (TOC, defined as carbon remaining after removal of inorganic carbon) fbiomass was estimated to be 77%, which falls within the range for PAHs. This CSRA data of atmospheric PAHs demonstrate the non-uniformity of biomass combustion contribution to different PAHs even in a location with limited local emission sources and illustrates that regulatory efforts would not evenly reduce all PAHs.

Sun, Ocean, Nuclear Bombs, and Fossil Fuels: Radiocarbon Variations and Implications for High-Resolution Dating

NASA Astrophysics Data System (ADS)

Dutta, Koushik

2016-06-01

Radiocarbon, or 14C, is a radiometric dating method ideally suited for providing a chronological framework in archaeology and geosciences for timescales spanning the last 50,000 years. 14C is easily detectable in most common natural organic materials and has a half-life (5,730±40 years) relevant to these timescales. 14C produced from large-scale detonations of nuclear bombs between the 1950s and the early 1960s can be used for dating modern organic materials formed after the 1950s. Often these studies demand high-resolution chronology to resolve ages within a few decades to less than a few years. Despite developments in modern, high-precision 14C analytical methods, the applicability of 14C in high-resolution chronology is limited by short-term variations in atmospheric 14C in the past. This article reviews the roles of the principal natural drivers (e.g., solar magnetic activity and ocean circulation) and the anthropogenic perturbations (e.g., fossil fuel CO2 and 14C from nuclear and thermonuclear bombs) that are responsible for short-term 14C variations in the environment. Methods and challenges of high-resolution 14C dating are discussed.

Changes in14c activity over time during vacuum distillation of carbon from rock pore water

USGS Publications Warehouse

Davidson, G.R.; Yang, I.C.

1999-01-01

The radiocarbon activity of carbon collected by vacuum distillation from a single partially saturated tuff began to decline after approximately 60% of the water and carbon had been extracted. Disproportionate changes in 14C activity and ??13C during distillation rule out simple isotopic fractionation as a causative explanation. Additional phenomena such as matrix diffusion and ion exclusion in micropores may play a role in altering the isotopic value of extracted carbon, but neither can fully account for the observed changes. The most plausible explanation is that distillation recovers carbon from an adsorbed phase that is depleted in 14C relative to DIC in the bulk pore water. ?? 1999 by the Arizona Board of Regents on behalf of the University of Arizona.

An effective method of UV-oxidation of dissolved organic carbon in natural waters for radiocarbon analysis by accelerator mass spectrometry

NASA Astrophysics Data System (ADS)

Xue, Yuejun; Ge, Tiantian; Wang, Xuchen

2015-12-01

Radiocarbon (14C) measurement of dissolved organic carbon (DOC) is a very powerful tool to study the sources, transformation and cycling of carbon in the ocean. The technique, however, remains great challenges for complete and successful oxidation of sufficient DOC with low blanks for high precision carbon isotopic ratio analysis, largely due to the overwhelming proportion of salts and low DOC concentrations in the ocean. In this paper, we report an effective UV-Oxidation method for oxidizing DOC in natural waters for radiocarbon analysis by accelerator mass spectrometry (AMS). The UV-oxidation system and method show 95%±4% oxidation efficiency and high reproducibility for DOC in both river and seawater samples. The blanks associated with the method was also low (about 3 µg C) that is critical for 14C analysis. As a great advantage of the method, multiple water samples can be oxidized at the same time so it reduces the sample processing time substantially compared with other UV-oxidation method currently being used in other laboratories. We have used the system and method for 14C studies of DOC in rivers, estuaries, and oceanic environments and have received promise results.

Radiocarbon Based Ages and Growth Rates: Hawaiian Deep Sea Corals

DOE Office of Scientific and Technical Information (OSTI.GOV)

Roark, E B; Guilderson, T P; Dunbar, R B

2006-01-13

The radial growth rates and ages of three different groups of Hawaiian deep-sea 'corals' were determined using radiocarbon measurements. Specimens of Corallium secundum, Gerardia sp., and Leiopathes glaberrima, were collected from 450 {+-} 40 m at the Makapuu deep-sea coral bed using a submersible (PISCES V). Specimens of Antipathes dichotoma were collected at 50 m off Lahaina, Maui. The primary source of carbon to the calcitic C. secundum skeleton is in situ dissolved inorganic carbon (DIC). Using bomb {sup 14}C time markers we calculate radial growth rates of {approx} 170 {micro}m y{sup -1} and ages of 68-75 years on specimensmore » as tall as 28 cm of C. secundum. Gerardia sp., A. dichotoma, and L. glaberrima have proteinaceous skeletons and labile particulate organic carbon (POC) is their primary source of architectural carbon. Using {sup 14}C we calculate a radial growth rate of 15 {micro}m y{sup -1} and an age of 807 {+-} 30 years for a live collected Gerardia sp., showing that these organisms are extremely long lived. Inner and outer {sup 14}C measurements on four sub-fossil Gerardia spp. samples produce similar growth rate estimates (range 14-45 {micro}m y{sup -1}) and ages (range 450-2742 years) as observed for the live collected sample. Similarly, with a growth rate of < 10 {micro}m y{sup -1} and an age of {approx}2377 years, L. glaberrima at the Makapuu coral bed, is also extremely long lived. In contrast, the shallow-collected A. dichotoma samples yield growth rates ranging from 130 to 1,140 {micro}m y{sup -1}. These results show that Hawaiian deep-sea corals grow more slowly and are older than previously thought.« less

Atmosphere-ocean gas exchange based on radiocarbon data

NASA Astrophysics Data System (ADS)

Byalko, Alexey

2014-05-01

In recent decades, the intensity of global atmospheric convection has accelerated faster than climate warming; it is possible to judge this process from indirect data. Increasing ocean salinity contrasts provide evidence that evaporation has intensified [1]; sea surface wind velocities and wave heights have increased [2]. The CO2 gas exchange between the atmosphere and ocean must also simultaneously increase. Monthly measurements of atmospheric CO2 concentration have been published since 1958 [3], but directly measuring its fluxes from the atmosphere to the ocean and back is hardly possible. We show they can be reconstructed from 14C isotope concentration data. In the past century, two processes influenced the atmospheric 14C concentration in opposite directions: burning fossil fuels and testing nuclear weapons in the atmosphere. We compare the gas exchange theory with measurements of radiocarbon content in the atmosphere [4—6], which allows assessing the gas exchange quantitatively for the ocean to atmosphere and atmosphere to ocean fluxes separately for period 1960—2010 [7]. References 1. Durack P. J. and Wijffels S. E., J. Climate 23, 4342 (2010). 2. Young I. R., Sieger S., and Babanin A.V., Science 332, 451 (2011). 3. NOAA Earth System Research Laboratory Data: ftp://ftp.cmdl.noaa.gov/ccg/co2/trends/co2_mm_mlo.txt. 4. Nydal R., Lövseth K. // J. Geophys. Res. 1983. V. 88. P. 3579. 5. Levin I., Kromer B. // Radiocarbon. 1997. V. 39. P. 205. 6. Miller J.B., Lehman S.J., Montzka S.A., et al. // J. Geophys. Res. 2012. V. 117. D08302. 7. Byalko A.V. Doklady Physics, 2013. V. 58, 267-271.

Δ14CO2 from dark respiration in plants and its impact on the estimation of atmospheric fossil fuel CO2.

PubMed

Xiong, Xiaohu; Zhou, Weijian; Cheng, Peng; Wu, Shugang; Niu, Zhenchuan; Du, Hua; Lu, Xuefeng; Fu, Yunchong; Burr, George S

2017-04-01

Radiocarbon ( 14 C) has been widely used for quantification of fossil fuel CO 2 (CO 2ff ) in the atmosphere and for ecosystem source partitioning studies. The strength of the technique lies in the intrinsic differences between the 14 C signature of fossil fuels and other sources. In past studies, the 14 C content of CO 2 derived from plants has been equated with the 14 C content of the atmosphere. Carbon isotopic fractionation mechanisms vary among plants however, and experimental study on fractionation associated with dark respiration is lacking. Here we present accelerator mass spectrometry (AMS) radiocarbon results of CO 2 respired from 21 plants using a lab-incubation method and associated bulk organic matter. From the respired CO 2 we determine Δ 14 C res values, and from the bulk organic matter we determine Δ 14 C bom values. A significant difference between Δ 14 C res and Δ 14 C bom (P < 0.01) was observed for all investigated plants, ranging from -42.3‰ to 10.1‰. The results show that Δ 14 C res values are in agreement with mean atmospheric Δ 14 CO 2 for several days leading up to the sampling date, but are significantly different from corresponding bulk organic Δ 14 C values. We find that although dark respiration is unlikely to significantly influence the estimation of CO 2ff , an additional bias associated with the respiration rate during a plant's growth period should be considered when using Δ 14 C in plants to quantify atmospheric CO 2ff . Copyright © 2017 Elsevier Ltd. All rights reserved.

Comparison of Soil Organic Matter Dynamics at Four Temperate Deciduous Forests with Physical Fractionation and Radiocarbon Measurements

NASA Astrophysics Data System (ADS)

McFarlane, K. J.; Torn, M. S.; Hanson, P. J.; Swanston, C.; Guilderson, T. P.; Porras, R. C.

2009-12-01

Forest soils represent a significant pool for C sequestration and storage, but the factors controlling soil C cycling are not well constrained. We used density fractionation and radiocarbon measurements to assess differences in soil C cycling amongst four eastern deciduous forests that are part of the AmeriFlux Network and vary in climate, soil type, parent material, and soil ecology. We collected mineral soil from 0-5 cm and 5-15 cm depth at Harvard Forest (HAF) in central Massachusetts, Bartlett Experimental Forest (BEF) in New Hampshire, the University of Michigan Biological Station (UMBS), and Baskett Wildlife Recreation and Education Area in the Missouri Ozarks (MOZ). Deeper soil samples have been collected (to 75 cm in some cases) for future analysis. We fractionated soil samples by density into free light (unprotected SOM), occluded light (physically protected SOM), and dense (mineral-protected) fractions using sodium polytungstate (1.65 g ml-1), measured C concentration and radiocarbon in bulk soil and fractions, and used a three-pool steady-state model to determine radiocarbon-based turnover times for fractions. The northeastern sites, HAF and BEF, had higher bulk soil C (65 and 40 g C kg soil-1, respectively) than did MOZ or UMBS (20 and 10 g C kg soil-1). Bulk soil radiocarbon values (Δ14C) decreased with depth and were lower at northeastern sites than Midwestern sites (36, 8, 113, and 65 ‰ for 0-5 cm at HF, BEF, MOZ, and UMBS, respectively). Soil C distribution amongst fractions was similar at HAF, BEF, and MOZ with the unprotected free light fraction containing about 40% of bulk soil C for 0-5 cm and 20% of bulk soil C for 5-15 cm. At these three sites, the physically protected occluded light fraction contained about 10% of bulk soil C, with the mineral-protected dense fraction containing the remaining 50-70%. In contrast, UMBS, the site with the sandiest soil, had a greater portion of bulk soil C recovered in the unprotected free light fraction and

Radiocarbon constraints on the glacial ocean circulation and its impact on atmospheric CO2

PubMed Central

Skinner, L. C.; Primeau, F.; Freeman, E.; de la Fuente, M.; Goodwin, P. A.; Gottschalk, J.; Huang, E.; McCave, I. N.; Noble, T. L.; Scrivner, A. E.

2017-01-01

While the ocean’s large-scale overturning circulation is thought to have been significantly different under the climatic conditions of the Last Glacial Maximum (LGM), the exact nature of the glacial circulation and its implications for global carbon cycling continue to be debated. Here we use a global array of ocean–atmosphere radiocarbon disequilibrium estimates to demonstrate a ∼689±53 14C-yr increase in the average residence time of carbon in the deep ocean at the LGM. A predominantly southern-sourced abyssal overturning limb that was more isolated from its shallower northern counterparts is interpreted to have extended from the Southern Ocean, producing a widespread radiocarbon age maximum at mid-depths and depriving the deep ocean of a fast escape route for accumulating respired carbon. While the exact magnitude of the resulting carbon cycle impacts remains to be confirmed, the radiocarbon data suggest an increase in the efficiency of the biological carbon pump that could have accounted for as much as half of the glacial–interglacial CO2 change. PMID:28703126

Radiocarbon constraints on the glacial ocean circulation and its impact on atmospheric CO2

NASA Astrophysics Data System (ADS)

Skinner, L. C.; Primeau, F.; Freeman, E.; de La Fuente, M.; Goodwin, P. A.; Gottschalk, J.; Huang, E.; McCave, I. N.; Noble, T. L.; Scrivner, A. E.

2017-07-01

While the ocean's large-scale overturning circulation is thought to have been significantly different under the climatic conditions of the Last Glacial Maximum (LGM), the exact nature of the glacial circulation and its implications for global carbon cycling continue to be debated. Here we use a global array of ocean-atmosphere radiocarbon disequilibrium estimates to demonstrate a ~689+/-53 14C-yr increase in the average residence time of carbon in the deep ocean at the LGM. A predominantly southern-sourced abyssal overturning limb that was more isolated from its shallower northern counterparts is interpreted to have extended from the Southern Ocean, producing a widespread radiocarbon age maximum at mid-depths and depriving the deep ocean of a fast escape route for accumulating respired carbon. While the exact magnitude of the resulting carbon cycle impacts remains to be confirmed, the radiocarbon data suggest an increase in the efficiency of the biological carbon pump that could have accounted for as much as half of the glacial-interglacial CO2 change.

Direct dating of archaeological pottery by compound-specific 14C analysis of preserved lipids.

PubMed

Stott, Andrew W; Berstan, Robert; Evershed, Richard P; Bronk-Ramsey, Christopher; Hedges, Robert E M; Humm, Martin J

2003-10-01

A methodology is described demonstrating the utility of the compound-specific 14C technique as a direct means of dating archaeological pottery. The method uses automated preparative capillary gas chromatography employing wide-bore capillary columns to isolate individual compounds from lipid extracts of archaeological potsherds in high purity (>95%) and amounts (>200 microg) sufficient for radiocarbon dating using accelerator mass spectrometry (AMS). A protocol was developed and tested on n-alkanes and n-carboxylic acids possessing a broad range of 14C ages. Analytical blanks and controls allowed background 14C measurements to be assessed and potential sources of errors to be detected, i.e., contamination with modern or dead 14C, isotopic fraction effects, etc. A "Russian doll" method was developed to transfer isolated target compounds onto tin powder/capsules prior to combustion and AMS analyses. The major advantage of the compound-specific technique is that 14C dates obtained for individual compounds can be directly linked to the commodities processed in the vessels during their use, e.g., animal fats. The compound-specific 14C dating protocol was validated on a suite of ancient pottery whose predicted ages spanned a 5000-year date range. Initial results indicate that meaningful correlations can be obtained between the predicted date of pottery and that of the preserved lipids. These findings constitute an important step forward to the direct dating of archaeological pottery.

Use of Ramped PyrOx 14C dating to simultaneously determine the organic carbon age and carbonate material age of Antarctic marginal sediments

NASA Astrophysics Data System (ADS)

Reese, D.; DeCesare, M.; Subt, C.; Bart, P. J.; Wellner, J. S.; Rosenheim, B. E.

2016-12-01

Chronicling deglaciation rates and style in Antarctic margin sediment is difficult because of low preservation/deposition of carbonate foraminiferal tests as well as incorporation of pre-aged organic carbon from carbonaceous rocks. When carbonates for radiocarbon dating are absent, acid-insoluble organic matter (AIOM) 14C dates are often used as an alternative and providing reliable chronologies in some locations. Results obtained by this method can cause difficulties such as false age reversals and ambiguity due to contamination with pre-aged carbon (Rosenheim et. al., 2008; Subt et al., 2016). Ramped PyrOx 14C dating has exploited the higher thermochemical stability of pre-aged carbon to separate carbon dating to the time of sediment deposition, and recently has produced chronologies similar to foraminifera-based chronologies (Subt et al., 2016). Samples for Ramped PyrOx 14C dating have generally been treated with acid to remove carbonates, and thus some acid soluble organic matter. In an effort to minimize the alteration of the organic matter, we apply Ramped PyrOx 14C dating to samples that have been both treated with 1N HCl and left untreated. Untreated samples display a characteristic large, sharp peak at higher temperatures than pyrolysis of organic matter that we interpret as carbonate decomposition. These carbonate decomposition peaks are characteristically sharp and occur at higher temperatures than the maximum evolution of CO2 from the organic matter in the sample. We isolated these peaks for comparison between known carbonate ages from picked foraminifera and low-temperature Ramped PyrOx splits from acid treated samples. We will discuss the treatment of the suite of 14C ages with reconciliation of two dating methods in mind. Ultimately, this approach offers promise for a single treatment of Antarctic margin sediments that provides chronologies from both carbonate and organic material.

Marine radiocarbon reservoir corrections (∆R) for Chesapeake Bay and the Middle Atlantic Coast of North America

NASA Astrophysics Data System (ADS)

Rick, Torben C.; Henkes, Gregory A.; Lowery, Darrin L.; Colman, Steven M.; Culleton, Brendan J.

2012-01-01

Radiocarbon dates from known age, pre-bomb eastern oyster (Crassostrea virginica) shells provide local marine reservoir corrections (∆R) for Chesapeake Bay and the Middle Atlantic coastal area of eastern North America. These data suggest subregional variability in ∆R, ranging from 148 ± 46 14C yr on the Potomac River to - 109 ± 38 14C yr at Swan Point, Maryland. The ∆R weighted mean for the Chesapeake's Western Shore (129 ± 22 14C yr) is substantially higher than the Eastern Shore (- 88 ± 23 14C yr), with outer Atlantic Coast samples falling between these values (106 ± 46 and 2 ± 46 14C yr). These differences may result from a combination of factors, including 14C-depleted freshwater that enters the bay from some if its drainages, 14C-depleted seawater that enters the bay at its mouth, and/or biological carbon recycling. We advocate using different subregional ∆R corrections when calibrating 14C dates on aquatic specimens from the Chesapeake Bay and coastal Middle Atlantic region of North America.

Radiocarbon dating of archaeological samples (sambaqui) using CO(2) absorption and liquid scintillation spectrometry of low background radiation.

PubMed

Mendonça, Maria Lúcia T G; Godoy, José M; da Cruz, Rosana P; Perez, Rhoneds A R

2006-01-01

Sambaqui means, in the Tupi language, a hill of shells. The sambaquis are archaeological sites with remains of pre-historical Brazilian occupation. Since the sambaqui sites in the Rio de Janeiro state region are older than 10,000 years, the applicability of CO(2) absorption on Carbo-sorb and (14)C determination by counting on a low background liquid scintillation counter was tested. In the present work, sambaqui shells were treated with H(3)PO(4) in a closed vessel in order to generate CO(2). The produced CO(2) was absorbed on Carbo-sorb. On saturation about 0.6g of carbon, as CO(2), was mixed with commercial liquid scintillation cocktail (Permafluor), and the (14)C activity determined by counting on a low background counter, Packard Tricarb 3170 TR/SL, for a period of 1000 mins to enable detection of a radiocarbon age of 22,400 BP. But only samples with ages up to 3500 BP were submitted to the method because the samples had been collected in the municipality of Guapimirim, in archaeological sambaqui-type sites belonging to this age range. The same samples were sent to the (14)C Laboratory of the Centro de Energia Nuclear na Agricultura (CENA/USP) where similar results were obtained.

Assessing open-system behavior of 14C in terrestrial gastropod shells

USGS Publications Warehouse

Rech, J.A.; Pigati, J.S.; Lehmann, S.B.; McGimpsey, C.N.; Grimley, D.A.; Nekola, J.C.

2011-01-01

In order to assess open-system behavior of radiocarbon in fossil gastropod shells, we measured the 14C activity on 10 aliquots of shell material recovered from Illinoian (~190-130 ka) and pre-Illinoian (~800 ka) loess and lacustrine deposits in the Midwestern USA. Eight of the 10 aliquots yielded measurable 14C activities that ranged from 0.25 to 0.53 percent modern carbon (pMC), corresponding to apparent 14C ages between 48.2 and 42.1 ka. This small level of open-system behavior is common in many materials that are used for 14C dating (e.g. charcoal), and typically sets the upper practical limit of the technique. Two aliquots of gastropod shells from the Illinoian-aged Petersburg Silt (Petersburg Section) in central Illinois, USA, however, yielded elevated 14C activities of 1.26 and 1.71 pMC, which correspond to apparent 14C ages of 35.1 and 32.7 ka. Together, these results suggest that while many fossil gastropods shells may not suffer from major (>1%) open-system problems, this is not always the case. We then examined the mineralogy, trace element chemistry, and physical characteristics of a suite of fossil and modern gastropod shells to identify the source of contamination in the Petersburg shells and assess the effectiveness of these screening techniques at identifying samples suitable for 14C dating. Mineralogical (XRD) and trace element analyses were inconclusive, which suggests that these techniques are not suitable for assessing open-system behavior in terrestrial gastropod shells. Analysis with scanning electron microscopy (SEM), however, identified secondary mineralization (calcium carbonate) primarily within the inner whorls of the Petersburg shells. This indicates that SEM examination, or possibly standard microscope examination, of the interior of gastropod shells should be used when selecting fossil gastropod shells for 14C dating. ?? 2011 by the Arizona Board of Regents on behalf of the University of Arizona.

Opportunities in low-level radiocarbon microtracing: applications and new technology

PubMed Central

Vuong, Le Thuy; Song, Qi; Lee, Hee Joo; Roffel, Ad F; Shin, Seok-Ho; Shin, Young G; Dueker, Stephen R

2016-01-01

14C-radiolabeled (radiocarbon) drug studies are central to defining the disposition of therapeutics in clinical development. Concerns over radiation, however, have dissuaded investigators from conducting these studies as often as their utility may merit. Accelerator mass spectrometry (AMS), originally designed for carbon dating and geochronology, has changed the outlook for in-human radiolabeled testing. The high sensitivity of AMS affords human clinical testing with vastly reduced radiative (microtracing) and chemical exposures (microdosing). Early iterations of AMS were unsuitable for routine biomedical use due to the instruments’ large size and associated per sample costs. The situation is changing with advances in the core and peripheral instrumentation. We review the important milestones in applied AMS research and recent advances in the core technology platform. We also look ahead to an entirely new class of 14C detection systems that use lasers to measure carbon dioxide in small gas cells. PMID:28031933

Methane sources in gas hydrate-bearing cold seeps: Evidence from radiocarbon and stable isotopes

USGS Publications Warehouse

Pohlman, J.W.; Bauer, J.E.; Canuel, E.A.; Grabowski, K.S.; Knies, D.L.; Mitchell, C.S.; Whiticar, Michael J.; Coffin, R.B.

2009-01-01

Fossil methane from the large and dynamic marine gas hydrate reservoir has the potential to influence oceanic and atmospheric carbon pools. However, natural radiocarbon (14C) measurements of gas hydrate methane have been extremely limited, and their use as a source and process indicator has not yet been systematically established. In this study, gas hydrate-bound and dissolved methane recovered from six geologically and geographically distinct high-gas-flux cold seeps was found to be 98 to 100% fossil based on its 14C content. Given this prevalence of fossil methane and the small contribution of gas hydrate (??? 1%) to the present-day atmospheric methane flux, non-fossil contributions of gas hydrate methane to the atmosphere are not likely to be quantitatively significant. This conclusion is consistent with contemporary atmospheric methane budget calculations. In combination with ??13C- and ??D-methane measurements, we also determine the extent to which the low, but detectable, amounts of 14C (~ 1-2% modern carbon, pMC) in methane from two cold seeps might reflect in situ production from near-seafloor sediment organic carbon (SOC). A 14C mass balance approach using fossil methane and 14C-enriched SOC suggests that as much as 8 to 29% of hydrate-associated methane carbon may originate from SOC contained within the upper 6??m of sediment. These findings validate the assumption of a predominantly fossil carbon source for marine gas hydrate, but also indicate that structural gas hydrate from at least certain cold seeps contains a component of methane produced during decomposition of non-fossil organic matter in near-surface sediment.

The Remarkable Metrological History of Radiocarbon Dating [II].

PubMed

Currie, Lloyd A

2004-01-01

This article traces the metrological history of radiocarbon, from the initial breakthrough devised by Libby, to minor (evolutionary) and major (revolutionary) advances that have brought (14)C measurement from a crude, bulk [8 g carbon] dating tool, to a refined probe for dating tiny amounts of precious artifacts, and for "molecular dating" at the 10 µg to 100 µg level. The metrological advances led to opportunities and surprises, such as the non-monotonic dendrochronological calibration curve and the "bomb effect," that gave rise to new multidisciplinary areas of application, ranging from archaeology and anthropology to cosmic ray physics to oceanography to apportionment of anthropogenic pollutants to the reconstruction of environmental history. Beyond the specific topic of natural (14)C, it is hoped that this account may serve as a metaphor for young scientists, illustrating that just when a scientific discipline may appear to be approaching maturity, unanticipated metrological advances in their own chosen fields, and unanticipated anthropogenic or natural chemical events in the environment, can spawn new areas of research having exciting theoretical and practical implications.

The Remarkable Metrological History of Radiocarbon Dating [II

PubMed Central

Currie, Lloyd A.

2004-01-01

This article traces the metrological history of radiocarbon, from the initial breakthrough devised by Libby, to minor (evolutionary) and major (revolutionary) advances that have brought 14C measurement from a crude, bulk [8 g carbon] dating tool, to a refined probe for dating tiny amounts of precious artifacts, and for “molecular dating” at the 10 µg to 100 µg level. The metrological advances led to opportunities and surprises, such as the non-monotonic dendrochronological calibration curve and the “bomb effect,” that gave rise to new multidisciplinary areas of application, ranging from archaeology and anthropology to cosmic ray physics to oceanography to apportionment of anthropogenic pollutants to the reconstruction of environmental history. Beyond the specific topic of natural 14C, it is hoped that this account may serve as a metaphor for young scientists, illustrating that just when a scientific discipline may appear to be approaching maturity, unanticipated metrological advances in their own chosen fields, and unanticipated anthropogenic or natural chemical events in the environment, can spawn new areas of research having exciting theoretical and practical implications. PMID:27366605

A simple radiocarbon dating method for determining the age and growth rate of deep-sea sponges

NASA Astrophysics Data System (ADS)

Fallon, S. J.; James, K.; Norman, R.; Kelly, M.; Ellwood, M. J.

2010-04-01

The ability to reliably age siliceous sponges is explored using radiocarbon dating of several hexactinellid sponge specimens including Rossella racovitzaeracovitzae Topsent, 1901 ( C. Hexactinellida: O. Lyssacinosida: F. Rossellidae), collected from the Ross Sea, Antarctica. The optimal pretreatment was found to consist of both sequential acid digestion and pre-roasting at temperatures >400 °C. Subsequent combustion at 900 °C liberated the proteinaceous material within the spicule matrix and once the reservoir age of the surrounding water was accounted for, a linear extension rate was calculated to be around 2.9 mm yr -1, aging the sponge at ˜440 years old.

Determination of radiocarbon reservoir age of Lake Van by mineral magnetic and geochemical analysis

NASA Astrophysics Data System (ADS)

Makaroglu, Ozlem; Namik Cagatay, M.; Pesonen, Lauri J.; Orbay, Naci

2017-04-01

Lake Van is the largest soda lake in the world, located on the east Anatolian Plateau in Turkey. Its varved sediments provide an excellent archive of high-resolution paleoclimate record for the Near East. Varve counting and radiocarbon methods are therefore important dating techniques for investigating the Lake Van sedimentary paleoclimate record. In here we present detailed magnetic and geochemical record of Lake Van. We have studied 4.56 m (core VP0801) and 4.70 m (core VP0807) long cores recovered from 80 m and 65 m water depths located in SE and SW of Lake Van, respectively. Here, we have benefited from magnetic properties with associated remanent magnetization of the sediments from Lake Van to correlate the cores which contain of tephra layers. The cores cover the last 8.4 ka and lithologically include three laminated sedimentary units. From top to the bottom, the units were dated 4.2 ka BP-present, 5.4-4.2 ka BP and older than 5.4 ka BP. We identified tephra layers previously dated by varve counting, and used the varve ages to obtain age models for the cores. We also obtained a total of eight Accelerator Mass Spectrometry (AMS) 14C dates from total organic carbon (TOC) in the two cores, close to the tephra layers. Comparison of the varve ages of the AMS 14C dated samples with their corresponding AMS 14C dates indicates large differences, suggesting significant reservoir ages that range from 2.8 to 2.5 ka for 3.0-2.4 varve ka BP and from 2.8 to 3.3 ka for 8.0-5.9 varve ka BP. The results suggest that the reservoir age of the organic matter increases with the varve age of the sediments. This increase is mainly related to the rate of supply of "dead" carbon from the old carbonate rocks in the watershed of Lake Van, which was relatively higher during 8.4-5.9 ka than during 3.0-2.4 ka BP because of the higher atmospheric precipitation and higher rate of biochemical weathering during the former period.

Indian Ocean radiocarbon: Data from the INDIGO 1, 2, and 3 cruises

DOE Office of Scientific and Technical Information (OSTI.GOV)

Sepanski, R.J.

1991-01-01

This document presents {sup 14}C activities (expressed in the internationally adopted {Delta}{sup 14}C scale) from water samples taken at various locations and depths in the Indian and Southern oceans through the Indien Gaz Ocean (INDIGO) project. These data were collected as part of the INDIGO 1, INDIGO 2, and INDIGO 3 cruises, which took place during the years 1985, 1986, and 1987, respectively. These data have been used to estimate the penetration of anthropogenic CO{sub 2} in the Indian and Southern oceans. The document also presents supporting data for potential temperature, salinity, density (sigma-theta), {delta}{sup 13}C, and total CO{sub 2}.more » All radiocarbon measurements have been examined statistically for quality of sample counts and stability of counting efficiency and background. In addition, all data have been reviewed by the Carbon Dioxide Information Analysis Center and assessed for gross accuracy and consistency (absence of obvious outliers and other anomalous values). These data are available free of charge as a numeric data package (NDP) from the Carbon Dioxide Information Analysis Center. The NDP consists of this document and a magnetic tape containing machine-readable files. This document provides sample listing of the Indian Ocean radiocarbon data as they appear on the magnetic tape, as well as a complete listing of these data in tabular form. This document also offers retrieval program listings, furnishes information on sampling methods and data selection, defines limitations and restrictions of the data, and provides reprints of pertinent literature. 13 refs., 4 tabs.« less

Radiocarbon dating of magnetic and non magnetic soil fractions as a method to estimate the heterotrophic component of soil respiration in a primary forest of Ghana.

NASA Astrophysics Data System (ADS)

Chiti, T.; Certini, G.; Marzaioli, F.; Valentini, R.

2012-04-01

by the physical protection in aggregates. Surprisingly, the non magnetic fraction is not influenced at all by the bomb C (negative delta 14) already at a depth of 5-15 cm and, even, at 15-30 cm all the four fractions have pre-bomb C, which means relatively high radiocarbon age. The finest fractions are the main contributors to the Rh flux, particularly the magnetic fraction (<0-5 mm) which show also the higher C concentration among all fractions, opposite to the non-magnetic one that is poorer in C. The Rh flux, estimated from the mean residence time of the fractions and their C amount, allowed to get a more precise estimate with respect to a previous one performed at the same site with radiocarbon analyses on bulk soils. The Rh flux from soil is hard to be estimate based on radiocarbon analysis of the bulk soil alone, and only by means of a SOC fractionation the Rh flux can be estimated quite accurately. This alternative approach for estimating the Rh component of CO2 from soils of tropical areas is currently being applied in 10 tropical forest sites in western and central Africa in the context of the ERC Africa GHG project, and together with measurements of the C inputs annually entering the soil will allow determining the sink-source capacity of primary forest soils.

High-precision 14C and 40Ar/39Ar dating of the Campanian Ignimbrite (Y-5) reconciles the time-scales of climatic-cultural processes at 40 ka.

PubMed

Giaccio, Biagio; Hajdas, Irka; Isaia, Roberto; Deino, Alan; Nomade, Sebastien

2017-04-06

The Late Pleistocene Campanian Ignimbrite (CI) super-eruption (Southern Italy) is the largest known volcanic event in the Mediterranean area. The CI tephra is widely dispersed through western Eurasia and occurs in close stratigraphic association with significant palaeoclimatic and Palaeolithic cultural events. Here we present new high-precision 14 C (34.29 ± 0.09 14 C kyr BP, 1σ) and 40 Ar/ 39 Ar (39.85 ± 0.14 ka, 95% confidence level) dating results for the age of the CI eruption, which substantially improve upon or augment previous age determinations and permit fuller exploitation of the chronological potential of the CI tephra marker. These results provide a robust pair of 14 C and 40 Ar/ 39 Ar ages for refining both the radiocarbon calibration curve and the Late Pleistocene time-scale at ca. 40 ka. In addition, these new age constraints provide compelling chronological evidence for the significance of the combined influence of the CI eruption and Heinrich Event 4 on European climate and potentially evolutionary processes of the Early Upper Palaeolithic.

High-precision 14C and 40Ar/39Ar dating of the Campanian Ignimbrite (Y-5) reconciles the time-scales of climatic-cultural processes at 40 ka

PubMed Central

Giaccio, Biagio; Hajdas, Irka; Isaia, Roberto; Deino, Alan; Nomade, Sebastien

2017-01-01

The Late Pleistocene Campanian Ignimbrite (CI) super-eruption (Southern Italy) is the largest known volcanic event in the Mediterranean area. The CI tephra is widely dispersed through western Eurasia and occurs in close stratigraphic association with significant palaeoclimatic and Palaeolithic cultural events. Here we present new high-precision 14C (34.29 ± 0.09 14C kyr BP, 1σ) and 40Ar/39Ar (39.85 ± 0.14 ka, 95% confidence level) dating results for the age of the CI eruption, which substantially improve upon or augment previous age determinations and permit fuller exploitation of the chronological potential of the CI tephra marker. These results provide a robust pair of 14C and 40Ar/39Ar ages for refining both the radiocarbon calibration curve and the Late Pleistocene time-scale at ca. 40 ka. In addition, these new age constraints provide compelling chronological evidence for the significance of the combined influence of the CI eruption and Heinrich Event 4 on European climate and potentially evolutionary processes of the Early Upper Palaeolithic. PMID:28383570

Authentication of Chinese vintage liquors using bomb-pulse 14C

NASA Astrophysics Data System (ADS)

Cheng, Peng; Zhou, Weijian; Burr, G. S.; Fu, Yunchong; Fan, Yukun; Wu, Shugang

2016-12-01

The older a bottle of Chinese vintage liquor is, the higher the price it commands. Driven by the potential for higher profits, some newly-founded distilleries openly sell liquor whose storage ages are exaggerated. In China, the market for vintage liquor has become fraught with uncertainty and a pressing need has arisen to establish an effective method to authenticate the age of vintage liquors. A radiocarbon (14C) dating method is described here that can verify cellar-stored years of Chinese liquors distilled within the last fifty years. Two different flavored Chinese liquors produced in “the golden triangular region” in the Upper Yangtze River region in southwest China, with known cellar-stored years, were analyzed to benchmark the technique. Strong flavored liquors are found to be consistent with local atmospheric Δ14C values. A small offset of 2-3 years between predicted vintage years of soy-sauce flavored liquors and strong flavored liquors is found to be associated with the fermentation cycle of certain varieties. The technique can measure cellar-stored years of a wide range of liquors including those with fundamentally different aromas. This demonstrates the strength of our method in identifying suspect Chinese vintage liquors.

Radiocarbon Evidence That Millennial and Fast-Cycling Soil Carbon are Equally Sensitive to Warming

NASA Astrophysics Data System (ADS)

Vaughn, L. S.; Torn, M. S.; Porras, R. C.

2017-12-01

Within the century, the Arctic is expected to shift from a sink to a source of atmospheric CO2 due to climate-induced increases in soil carbon mineralization. The magnitude of this effect remains uncertain, due in large part to unknown temperature sensitivities of organic matter decomposition. In particular, the distribution of temperature sensitivities across soil carbon pools remains unknown. New experimental approaches are needed, because studies that fit multi-pool models to CO2 flux measurements may be sensitive to model assumptions, statistical effects, and non-steady-state changes in substrate availability or microbial activity. In this study, we developed a new methodology using natural abundance radiocarbon to evaluate temperature sensitivities across soil carbon pools. In two incubation experiments with soils from Barrow, AK, we (1) evaluated soil carbon age and decomposability, (2) disentangled the effects of temperature and substrate depletion on carbon mineralization, and (3) compared the temperature sensitivities of fast- and slow-cycling soil carbon pools. From a long-term incubation, both respired CO2 and the remaining soil organic matter were highly depleted in radiocarbon. At 20 cm depth, median Δ14C values were -167‰ in respired CO2 and -377‰ in soil organic matter, corresponding to turnover times of 1800 and 4800 years, respectively. Such negative Δ14C values indicate both storage and decomposition of old, stabilized carbon, while radiocarbon differences between the mineralized and non-mineralized fractions suggest that decomposability varies along a turnover time gradient. Applying a new analytical method combining CO2 flux and Δ14C, we found that fast- and slow-cycling carbon pools were equally sensitive to temperature, with a Q10 of 2 irrespective of turnover time. We conclude that in these Arctic soils, ancient soil carbon is vulnerable to warming under thawed, aerobic conditions. In contrast to many previous studies, we found no

50 Years And 400 Radiocarbon Measurements Since 1959: What Has The “Bomb Spike” Taught Us About Soil C Dynamics In New Zealand Soils?

NASA Astrophysics Data System (ADS)

Baisden, W. T.; Parfitt, R. L.; Ross, C.

2009-12-01

In 1959, Athol Rafter began a substantial programme of monitoring the flow of 14C produced by atmospheric thermonuclear tests through New Zealand’s atmosphere, biosphere and soil. The programme produced important publications, but also leaves a legacy of unpublished data critical for understanding soil C dynamics. A database of ~400 soil radiocarbon measurements spanning 50 years has now been compiled. Among the most compelling data is a comparison of soil carbon dynamics in deforested dairy pastures under similar climate in the Tokomaru silt loam (non-Andisol) versus the Egmont black loam (Andisol), originally sampled in 1962-3, 1965 and 1969. After adding soil profiles sampled to similar depths in 2008, we can use a relatively simple 2-box model to calculate that the residence time of soil C (upper ~8 cm) in the Tokomaru soil is ~9 years compared to ~15 years for the Egmont soil. This difference represents nearly a doubling of soil C residence time, and roughly explains the doubling of the soil C stock. With three measurements in the 1960s, the data is of sufficient resolution to estimate the parameters for an “inert” or “passive pool” comprising approximately 15% of soil C, and having a residence time of 600 years in the Tokomaru soil versus 3000 years in the Egmont surface soil. The Tokomaru/Egmont comparison is necessarily illustrative since the 1960s samplings were not replicated extensively, but provides globally unique data illustrating the nature of C movement through soil. Moreover, the Tokomaru/Egmont comparison supports evidence that C dynamics does differ in Andisols versus other soils. Additional lines of evidence include emerging theories of soil organic matter stabilisation processes, rates of soil organic matter change following land-use change, and chemistry data. The contrasting soil C dynamics in these different soils appear to have implications for land-use change and management schemes that could be eligible for “C credits”. More

Comparison of sampling methods for radiocarbon dating of carbonyls in air samples via accelerator mass spectrometry

NASA Astrophysics Data System (ADS)

Schindler, Matthias; Kretschmer, Wolfgang; Scharf, Andreas; Tschekalinskij, Alexander

2016-05-01

Three new methods to sample and prepare various carbonyl compounds for radiocarbon measurements were developed and tested. Two of these procedures utilized the Strecker synthetic method to form amino acids from carbonyl compounds with either sodium cyanide or trimethylsilyl cyanide. The third procedure used semicarbazide to form crystalline carbazones with the carbonyl compounds. The resulting amino acids and semicarbazones were then separated and purified using thin layer chromatography. The separated compounds were then combusted to CO2 and reduced to graphite to determine 14C content by accelerator mass spectrometry (AMS). All of these methods were also compared with the standard carbonyl compound sampling method wherein a compound is derivatized with 2,4-dinitrophenylhydrazine and then separated by high-performance liquid chromatography (HPLC).

Discordant 14C ages from buried tidal-marsh soils in the Cascadia subduction zone, southern Oregon coast

USGS Publications Warehouse

Nelson, A.R.

1992-01-01

Peaty, tidal-marsh soils interbedded with estuarine mud in late Holocene stratigraphic sequences near Coos Bay, Oregon, may have been submerged and buried during great (M > 8) subduction earthquakes, smaller localized earthquakes, or by nontectonic processes. Radiocarbon dating might help distinguish among these alternatives by showing that soils at different sites were submerged at different times along this part of the Cascadia subduction zone. But comparison of conventional 14C ages for different materials from the same buried soils shows that they contain materials that differ in age by many hundreds of years. Errors in calibrated soil ages represent about the same length of time as recurrence times for submergence events (150-500 yr)-this similarity precludes using conventional 14C ages to distinguish buried soils along the southern Oregon coast. Accelerator mass spectrometer 14C ages of carefully selected macrofossils from the tops of peaty soils should provide more precise estimates of the times of submergence events. ?? 1992.

Multimolecular tracers of terrestrial carbon transfer across the pan-Arctic: 14C characteristics of sedimentary carbon components and their environmental controls

NASA Astrophysics Data System (ADS)

Feng, Xiaojuan; Gustafsson, Örjan; Holmes, R. Max; Vonk, Jorien E.; van Dongen, Bart E.; Semiletov, Igor P.; Dudarev, Oleg V.; Yunker, Mark B.; Macdonald, Robie W.; Wacker, Lukas; Montluçon, Daniel B.; Eglinton, Timothy I.

2015-11-01

Distinguishing the sources, ages, and fate of various terrestrial organic carbon (OC) pools mobilized from heterogeneous Arctic landscapes is key to assessing climatic impacts on the fluvial release of carbon from permafrost. Through molecular 14C measurements, including novel analyses of suberin- and/or cutin-derived diacids (DAs) and hydroxy fatty acids (FAs), we compared the radiocarbon characteristics of a comprehensive suite of terrestrial markers (including plant wax lipids, cutin, suberin, lignin, and hydroxy phenols) in the sedimentary particles from nine major arctic and subarctic rivers in order to establish a benchmark assessment of the mobilization patterns of terrestrial OC pools across the pan-Arctic. Terrestrial lipids, including suberin-derived longer-chain DAs (C24,26,28), plant wax FAs (C24,26,28), and n-alkanes (C27,29,31), incorporated significant inputs of aged carbon, presumably from deeper soil horizons. Mobilization and translocation of these "old" terrestrial carbon components was dependent on nonlinear processes associated with permafrost distributions. By contrast, shorter-chain (C16,18) DAs and lignin phenols (as well as hydroxy phenols in rivers outside eastern Eurasian Arctic) were much more enriched in 14C, suggesting incorporation of relatively young carbon supplied by runoff processes from recent vegetation debris and surface layers. Furthermore, the radiocarbon content of terrestrial markers is heavily influenced by specific OC sources and degradation status. Overall, multitracer molecular 14C analysis sheds new light on the mobilization of terrestrial OC from arctic watersheds. Our findings of distinct ages for various terrestrial carbon components may aid in elucidating fate of different terrestrial OC pools in the face of increasing arctic permafrost thaw.

Radiocarbon dating casts doubt on the late chronology of the Middle to Upper Palaeolithic transition in southern Iberia.

PubMed

Wood, Rachel E; Barroso-Ruíz, Cecilio; Caparrós, Miguel; Jordá Pardo, Jesús F; Galván Santos, Bertila; Higham, Thomas F G

2013-02-19

It is commonly accepted that some of the latest dates for Neanderthal fossils and Mousterian industries are found south of the Ebro valley in Iberia at ca. 36 ka calBP (calibrated radiocarbon date ranges). In contrast, to the north of the valley the Mousterian disappears shortly before the Proto-Aurignacian appears at ca. 42 ka calBP. The latter is most likely produced by anatomically modern humans. However, two-thirds of dates from the south are radiocarbon dates, a technique that is particularly sensitive to carbon contaminants of a younger age that can be difficult to remove using routine pretreatment protocols. We have attempted to test the reliability of chronologies of 11 southern Iberian Middle and early Upper Paleolithic sites. Only two, Jarama VI and Zafarraya, were found to contain material that could be reliably dated. In both sites, Middle Paleolithic contexts were previously dated by radiocarbon to less than 42 ka calBP. Using ultrafiltration to purify faunal bone collagen before radiocarbon dating, we obtain ages at least 10 ka (14)C years older, close to or beyond the limit of the radiocarbon method for the Mousterian at Jarama VI and Neanderthal fossils at Zafarraya. Unless rigorous pretreatment protocols have been used, radiocarbon dates should be assumed to be inaccurate until proven otherwise in this region. Evidence for the late survival of Neanderthals in southern Iberia is limited to one possible site, Cueva Antón, and alternative models of human occupation of the region should be considered.

Radiocarbon dating casts doubt on the late chronology of the Middle to Upper Palaeolithic transition in southern Iberia

PubMed Central

Wood, Rachel E.; Barroso-Ruíz, Cecilio; Caparrós, Miguel; Jordá Pardo, Jesús F.; Galván Santos, Bertila; Higham, Thomas F. G.

2013-01-01

It is commonly accepted that some of the latest dates for Neanderthal fossils and Mousterian industries are found south of the Ebro valley in Iberia at ca. 36 ka calBP (calibrated radiocarbon date ranges). In contrast, to the north of the valley the Mousterian disappears shortly before the Proto-Aurignacian appears at ca. 42 ka calBP. The latter is most likely produced by anatomically modern humans. However, two-thirds of dates from the south are radiocarbon dates, a technique that is particularly sensitive to carbon contaminants of a younger age that can be difficult to remove using routine pretreatment protocols. We have attempted to test the reliability of chronologies of 11 southern Iberian Middle and early Upper Paleolithic sites. Only two, Jarama VI and Zafarraya, were found to contain material that could be reliably dated. In both sites, Middle Paleolithic contexts were previously dated by radiocarbon to less than 42 ka calBP. Using ultrafiltration to purify faunal bone collagen before radiocarbon dating, we obtain ages at least 10 ka 14C years older, close to or beyond the limit of the radiocarbon method for the Mousterian at Jarama VI and Neanderthal fossils at Zafarraya. Unless rigorous pretreatment protocols have been used, radiocarbon dates should be assumed to be inaccurate until proven otherwise in this region. Evidence for the late survival of Neanderthals in southern Iberia is limited to one possible site, Cueva Antón, and alternative models of human occupation of the region should be considered. PMID:23382220

Difference in radiocarbon ages of carbonized material from the inner and outer surfaces of pottery from a wetland archaeological site.

PubMed

Miyata, Yoshiki; Minami, Masayo; Onbe, Shin; Sakamoto, Minoru; Matsuzaki, Hiroyuki; Nakamura, Toshio; Imamura, Mineo

2011-01-01

AMS (Accelerator Mass Spectrometry) radiocarbon dates for eight potsherds from a single piece of pottery from a wetland archaeological site indicated that charred material from the inner pottery surfaces (5052 ± 12 BP; N = 5) is about 90 (14)C years older than that from the outer surfaces (4961 ± 22 BP; N = 7). We considered three possible causes of this difference: the old wood effect, reservoir effects, and diagenesis. We concluded that differences in the radiocarbon ages between materials from the inner and outer surfaces of the same pot were caused either by the freshwater reservoir effect or by diagenesis. Moreover, we found that the radiocarbon ages of carbonized material on outer surfaces (soot) of pottery from other wetland archaeological sites were the same as the ages of material on inner surfaces (charred food) of the same pot within error, suggesting absence of freshwater reservoir effect or diagenesis.

An analysis of carbon and radiocarbon profiles across a range ecosystems types

NASA Astrophysics Data System (ADS)

Heckman, K. A.; Gallo, A.; Hatten, J. A.; Swanston, C.; Strahm, B. D.; Sanclements, M.

2016-12-01

Soil carbon stocks have become recognized as increasingly important in the context of climate change and global C cycle modeling. As modelers seek to identify key parameters affecting the size and stability of belowground C stocks, attention has been drawn to the mineral matrix and the soil physiochemical factors influenced by it. Though clay content has often been utilized as a convenient and key explanatory variable for soil C dynamics, its utility has recently come under scrutiny as new paradigms of soil organic matter stabilization have been developed. We utilized soil cores from a range of National Ecological Observatory Network (NEON) experimental plots to examine the influence of mineralogical parameters on soil C stocks and turnover and their relative importance in comparison to climatic variables. Results are presented for a total of 11 NEON sites, spanning Alfisols, Entisols, Mollisols and Spodosols. Soils were sampled by genetic horizon, density separated according to density fractionation: light fractions (particulate organics neither occluded within aggregates nor associated with mineral surfaces), occluded fractions (particulate organics occluded within aggregates), and heavy fractions (organics associated with mineral surfaces). Bulk soils and density fractions were measured for % C and radiocarbon abundance (as a measure of C stability). Carbon and radiocarbon abundances were examined among fractions and in the context of climatic variables (temperature, precipitation, elevation) and soil physiochemical variables (% clay and pH). No direct relationships between temperature and soil C or radiocarbon abundances were found. As a whole, soil radiocarbon abundance in density fractions decreased in the order of light>heavy>occluded, highlighting the importance of both surface sorption and aggregation to the preservation of organics. Radiocarbon concentrations of the heavy fraction (mineral adsorbed) were significantly, though weakly, correlated with pH (r

Incorporation of sup 14 C from ( sup 14 C)phenylalanine into condensed tannin of sorghum grain

DOE Office of Scientific and Technical Information (OSTI.GOV)

Reddy, V.; Butler, L.G.

A procedure is described for obtaining condensed tannin from sorghum (Sorghum bicolor (L.) Moench) seeds metabolically labeled from ({sup 14}C)phenylalanine. The ({sup 14}C)tannin should be useful in determining the metabolic fate of dietary condensed tannin.

Tritium and radiocarbon in the western North Pacific waters: post-Fukushima situation.

PubMed

Kaizer, Jakub; Aoyama, Michio; Kumamoto, Yuichiro; Molnár, Mihály; Palcsu, László; Povinec, Pavel P

2018-04-01

Impact of the Fukushima Dai-ichi Nuclear Power Plant (FNPP1) accident on tritium ( 3 H) and radiocarbon ( 14 C) levels in the water column of the western North Pacific Ocean in winter 2012 is evaluated and compared with radiocesium ( 134,137 Cs) data collected for the same region. Tritium concentrations in surface seawater, varying between 0.4 and 2.0 TU (47.2-236 Bq m -3 ), follow the Fukushima radiocesium trend, however, some differences in the vertical profiles were observed, namely in depths of 50-400 m. No correlation was visible in the case of 14 C, whose surface Δ 14 C levels raised from negative values (about -40‰) in the northern part of transect, to positive values (∼68‰) near the equator. Homogenously mixed 14 C levels in the subsurface layers were observed at all stations. Sixteen surface (from 30 in total) and 6 water profile (from 7) stations were affected by the Fukushima tritium. Surface and vertical profile data together with the calculated water column inventories indicate that the total amount of the FNPP1-derived tritium deposited to the western North Pacific Ocean was 0.7 ± 0.3 PBq. No clear impact of the Fukushima accident on 14 C levels in the western North Pacific was observed. Copyright © 2018 Elsevier Ltd. All rights reserved.

Using 50 years of soil radiocarbon data to identify optimal approaches for estimating soil carbon residence times

NASA Astrophysics Data System (ADS)

Baisden, W. T.; Canessa, S.

2013-01-01

In 1959, Athol Rafter began a substantial programme of systematically monitoring the flow of 14C produced by atmospheric thermonuclear tests through organic matter in New Zealand soils under stable land use. A database of ∼500 soil radiocarbon measurements spanning 50 years has now been compiled, and is used here to identify optimal approaches for soil C-cycle studies. Our results confirm the potential of 14C to determine residence times, by estimating the amount of ‘bomb 14C’ incorporated. High-resolution time series confirm this approach is appropriate, and emphasise that residence times can be calculated routinely with two or more time points as little as 10 years apart. This approach is generally robust to the key assumptions that can create large errors when single time-point 14C measurements are modelled. The three most critical assumptions relate to: (1) the distribution of turnover times, and particularly the proportion of old C (‘passive fraction’), (2) the lag time between photosynthesis and C entering the modelled pool, (3) changes in the rates of C input. When carrying out approaches using robust assumptions on time-series samples, multiple soil layers can be aggregated using a mixing equation. Where good archived samples are available, AMS measurements can develop useful understanding for calibrating models of the soil C cycle at regional to continental scales with sample numbers on the order of hundreds rather than thousands. Sample preparation laboratories and AMS facilities can play an important role in coordinating the efficient delivery of robust calculated residence times for soil carbon.

Changes in groundwater reserves and radiocarbon and chloride content due to a wet period intercalated in an arid climate sequence in a large unconfined aquifer

NASA Astrophysics Data System (ADS)

Custodio, E.; Jódar, J.; Herrera, C.; Custodio-Ayala, J.; Medina, A.

2018-01-01

The concentration of atmospheric tracers in groundwater samples collected from springs and deep wells is, in most cases, the result of a mixture of waters with a wide range of residence times in the ground. Such is the case of an unconfined aquifer recharged over all its surface area. Concentrations greatly differ from the homogeneous residence time case. Data interpretation relies on knowledge of the groundwater flow pattern. To study relatively large systems, the conservative ion chloride and the decaying radiocarbon (14C) are considered. Radiocarbon (14C) activity in groundwater, after correction to discount the non-biogenic contribution, is often taken as an indication of water age, while chloride can be used to quantify recharge. In both cases, the observed tracer content in groundwater is an average value over a wide range which is related to water renewal time in the ground. This is shown considering an unconfined aquifer recharged all over its area under arid conditions, in which a period of greater recharge happened some millennia ago. The mathematical solution is given. As the solution cannot be made general, to show and discuss the changes in water reserve and in chloride and radiocarbon concentration (apparent ages), two scenarios are worked out, which are loosely related to current conditions in Northern Chile. It is shown that tracer concentration and the estimated water age are not directly related to the time since recharge took place. The existence of a previous wetter-than-present period has an important and lasting effect on current aquifer water reserves and chloride concentration, although the effect on radiocarbon activity is less pronounced. Chloride concentrations are smaller than in current recharge and apparent 14C ages do not coincide with the timing, duration and characteristics of the wet period, except in the case in which recharge before and after the wet period is negligible and dead aquifer reserves are non-significant. The use of

Calibration of the C-14 timescale over the past 30,000 years using mass spectrometric U-Th ages from Barbados corals

NASA Technical Reports Server (NTRS)

Bard, Edouard; Hamelin, Bruno; Fairbanks, Richard G.; Zindler, Alan

1990-01-01

Uranium-thorium ages obtained by mass spectrometry from corals raised off the island of Barbados confirm the high precision of this technique over at least the past 30,000 years. Comparison of the U-Th ages with C-14 ages obtained on the Holocene samples shows that the U-Th ages are accurate, because they accord with the dendrochronological calibration. Before 9,000 yr BP, the C-14 ages are systematically younger than the U-Th ages, with a maximum difference of about 3500 yr at about 20,000 yr BP. The U-Th technique thus provides a way of calibrating the radiocarbon timescale beyond the range of dendrochronological calibration.

Estimates of upwelling rates in the Arabian Sea and the equatorial Indian Ocean based on bomb radiocarbon.

PubMed

Bhushan, R; Dutta, K; Somayajulu, B L K

2008-10-01

Radiocarbon measurements were made in the water column of the Arabian Sea and the equatorial Indian Ocean during 1994, 1995 and 1997 to assess the temporal variations in bomb 14C distribution and its inventory in the region with respect to GEOSECS measurements made during 1977-1978. Four GEOSECS stations were reoccupied (three in the Arabian Sea and one in the equatorial Indian Ocean) during this study, with all of them showing increased penetration of bomb 14C along with decrease in its surface water activity. The upwelling rates derived by model simulation of bomb 14C depth profile using the calculated exchange rates ranged from 3 to 9 m a(-1). The western region of the Arabian Sea experiencing high wind-induced upwelling has higher estimated upwelling rates. However, lower upwelling rates obtained for the stations occupied during this study could be due to reduced 14C gradient compared to that during GEOSECS.

Modified procedure for determining (/sup 14/C)CO/sub 2/ produced by respiration in water or sediment samples

DOE Office of Scientific and Technical Information (OSTI.GOV)

Brown, K.A.

Poor recovery of radioactivity when determining (/sup 14/C)CO/sub 2/ respired by microbes can be overcome by substituting 2-ethanolamine for 2-phenylethylamine to absorb (/sup 14/C)CO/sub 2/ in the scintillation solution with 2-ethoxyethanol.

Coral skeletal carbon isotopes (δ13C and Δ14C) record the delivery of terrestrial carbon to the coastal waters of Puerto Rico

USGS Publications Warehouse

Moyer, R.P.; Grottoli, A.G.

2011-01-01

Tropical small mountainous rivers deliver a poorly quantified, but potentially significant, amount of carbon to the world's oceans. However, few historical records of land-ocean carbon transfer exist for any region on Earth. Corals have the potential to provide such records, because they draw on dissolved inorganic carbon (DIC) for calcification. In temperate systems, the stable- (δ13C) and radiocarbon (Δ14C) isotopes of coastal DIC are influenced by the δ13C and Δ14C of the DIC transported from adjacent rivers. A similar pattern should exist in tropical coastal DIC and hence coral skeletons. Here, δ13C and Δ14C measurements were made in a 56-year-old Montastraea faveolata coral growing ~1 km from the mouth of the Rio Fajardo in eastern Puerto Rico. Additionally, the δ13C and Δ14C values of the DIC of the Rio Fajardo and its adjacent coastal waters were measured during two wet and dry seasons. Three major findings were observed: (1) synchronous depletions of both δ13C and Δ14C in the coral skeleton are annually coherent with the timing of peak river discharge, (2) riverine DIC was always more depleted in δ13C and Δ14C than seawater DIC, and (3) the correlation of δ13C and Δ14C was the same in both coral skeleton and the DIC of the river and coastal waters. These results indicate that coral skeletal δ13C and Δ14C are recording the delivery of riverine DIC to the coastal ocean. Thus, coral records could be used to develop proxies of historical land-ocean carbon flux for many tropical regions. Such information could be invaluable for understanding the role of tropical land-ocean carbon flux in the context of land-use change and global climate change.

Coral skeletal carbon isotopes (δ13C and Δ14C) record the delivery of terrestrial carbon to the coastal waters of Puerto Rico

USGS Publications Warehouse

Moyer, R.P.; Grottoli, A.G.

2011-01-01

Tropical small mountainous rivers deliver a poorly quantified, but potentially significant, amount of carbon to the world's oceans. However, few historical records of land-ocean carbon transfer exist for any region on Earth. Corals have the potential to provide such records, because they draw on dissolved inorganic carbon (DIC) for calcification. In temperate systems, the stable- (??13C) and radiocarbon (??14C) isotopes of coastal DIC are influenced by the ??13C and ??14C of the DIC transported from adjacent rivers. A similar pattern should exist in tropical coastal DIC and hence coral skeletons. Here, ??13C and ??14C measurements were made in a 56-year-old Montastraea faveolata coral growing ~1 km from the mouth of the Rio Fajardo in eastern Puerto Rico. Additionally, the ??13C and ??14C values of the DIC of the Rio Fajardo and its adjacent coastal waters were measured during two wet and dry seasons. Three major findings were observed: (1) synchronous depletions of both ??13C and ??14C in the coral skeleton are annually coherent with the timing of peak river discharge, (2) riverine DIC was always more depleted in ??13C and ??14C than seawater DIC, and (3) the correlation of ??13C and ??14C was the same in both coral skeleton and the DIC of the river and coastal waters. These results indicate that coral skeletal ??13C and ??14C are recording the delivery of riverine DIC to the coastal ocean. Thus, coral records could be used to develop proxies of historical land-ocean carbon flux for many tropical regions. Such information could be invaluable for understanding the role of tropical land-ocean carbon flux in the context of land-use change and global climate change. ?? 2011 United States Geological Survey.

Bomb-14C Peak in the North Pacific Recorded in Long-Lived Bivalve Shells (Mercenaria stimpsoni)

NASA Astrophysics Data System (ADS)

Kubota, Kaoru; Shirai, Kotaro; Murakami-Sugihara, Naoko; Seike, Koji; Minami, Masayo; Nakamura, Toshio; Tanabe, Kazushige

2018-04-01

The excess radiocarbon produced by nuclear bomb testing in the atmosphere in the 1950s-1960s (bomb-14C) is used as a tracer in the surface ocean, extending our understanding of geophysics and biogeochemical cycles. However, there is no bomb-14C record for the high-latitude western North Pacific Ocean because of the paucity of long-lived marine calcifying organisms equivalent to reef-building corals. The shells of Stimpson's hard clam, Mercenaria stimpsoni, potentially provide such a record because the clam's lifespan is very long (>100 years). We analyzed 14C in six live-caught M. stimpsoni shells from the western North Pacific (39.4°N, 142°E) and report, for the first time, the bomb-14C record with robust calendar ages based on annual growth increments. The value was constant in 1934-1952 (Δ14C = -66‰), with a sudden increase in 1959, a peak in 1974 (107‰), which was 60‰ lower than that of the Kuroshio Current, a gradual decline after 1974, and a current value of 16-18‰, which is ˜10‰ higher than the atmospheric value. The bomb-14C values are between the Kuroshio Current (the northwestern subtropical gyre) and Oyashio Current (the Western Subarctic Gyre) values, suggesting that the Tsugaru Current, downstream from the Kuroshio Current, mixes with the Oyashio Current after passing through Tsugaru Strait.

At the end of the 14C time scale--the Middle to Upper Paleolithic record of western Eurasia.

PubMed

Jöris, Olaf; Street, Martin

2008-11-01

The dynamics of change underlying the demographic processes that led to the replacement of Neandertals by Anatomically Modern Humans (AMH) and the emergence of what are recognized as Upper Paleolithic technologies and behavior can only be understood with reference to the underlying chronological framework. This paper examines the European chronometric (mainly radiocarbon-based) record for the period between ca. 40 and 30 ka 14C BP and proposes a relatively rapid transition within some 2,500 years. This can be summarized in the following falsifiable hypotheses: (1) final Middle Paleolithic (FMP) "transitional" industries (Uluzzian, Chatelperronian, leaf-point industries) were made by Neandertals and date predominantly to between ca. 41 and 38 ka 14C BP, but not younger than 35/34 ka 14C BP; (2) initial (IUP) and early (EUP) Upper Paleolithic "transitional" industries (Bachokirian, Bohunician, Protoaurignacian, Kostenki 14) will date to between ca. 39/38 and 35 ka 14C BP and document the appearance of AMH in Europe; (3) the earliest Aurignacian (I) appears throughout Europe quasi simultaneously at ca. 35 ka 14C BP. The earliest appearance of figurative art is documented only for a later phase ca. 33.0/32.5-29.2 ka 14C BP. Taken together, the Middle to Upper Paleolithic transition appears to be a cumulative process involving the acquisition of different elements of "behavioral modernity" through several "stages of innovation."

Titan's Radioactive Haze : Production and Fate of Radiocarbon On Titan

NASA Astrophysics Data System (ADS)

Lorenz, R. D.; Jull, A. J. T.; Swindle, T. D.; Lunine, J. I.

Just as cosmic rays interact with nitrogen atoms in the atmosphere of Earth to gener- ate radiocarbon (14C), the same process should occur in Titan`s nitrogen-rich atmo- sphere. Titan`s atmosphere is thick enough that cosmic ray flux, rather than nitrogen column depth, limits the production of 14 C. Absence of a strong magnetic field and the increased distance from the sun suggest production rates of 9 atom/cm2/s, approx- imately 4 times higher than Earth. On Earth the carbon is rapidly oxidised into CO2. The fate and detectability of 14C on Titan depends on the chemical species into which it is incorporated in Titan's reducing atmosphere : as methane it would be hopelessly diluted even in only the atmosphere (ignoring the other, much more massive carbon reservoirs likely to be present on Titan, like hydrocarbon lakes.) However, in the more likely case that the 14C attaches to the haze that rains out onto the surface (as tholin, HCN or acetylene and their polymers - a much smaller carbon reservoir) , haze in the atmosphere or recently deposited on the surface would therefore be quite intrinsically radioactive. Such activity may modify the haze electrical charging and hence its coag- ulation. Measurements with compact instrumentation on future in-situ missions could place useful constraints on the mass deposition rates of photochemical material on the surface and identify locations where surface deposits of such material are `freshest`.

Acceptance Tests for AMS Radiocarbon Measurements at iThemba LABS, Gauteng, South Africa

NASA Astrophysics Data System (ADS)

Mbele, Vela L.; Mullins, Simon M.; Winkler, Stephan R.; Woodborne, Stephan

The accelerator mass spectrometer was commissioned recently at the iThemba LABS 6 MV tandem accelerator. Improvements in the vacuum system, requiring procurement of cryo-pumps and the reducing the tank pressure of the N2 + CO2 insulation gas mixture below the level used for IBA measurements, were necessary. This resulted in the reduction of the nitrogen background and improved the resolution of 14C from 14N background in the ionisation chamber. The nitrogen was leaking to the stripping canal because of inadequate sealing. The analysing magnet was scaled to detect C3+ ions, at 3 MV terminal potential. The first sensible spectra allowed for the pin-pointing of many persistent issues. This resulted in measurements with a precision better than 1 pMC, and current blank levels correspond to 12 half-lives of 14C or ∼68000 years. The radiocarbon sample preparation laboratory has reached production status. A brief outlook of the work towards the implementation of the measurement and chemical preparation protocols for radionuclides 10Be and 26Al is also summarised in the conclusion

14C dates from Tel Rehov: Iron-Age chronology, pharaohs, and Hebrew kings.

PubMed

Bruins, Hendrik J; van der Plicht, Johannes; Mazar, Amihai

2003-04-11

Stratified radiocarbon dates provide an independent chronological link between archaeological layers and historical data. The invasion by Pharaoh Shoshenq I (Shishak) is a key historical synchronism, approximately 925 B.C.E., mentioned in both Egyptian inscriptions and the Hebrew Bible. The list of places raided by Shoshenq, mentioned at Karnak (Egypt), includes Rehov (Israel). The site yielded a consistent series of radiocarbon dates from the 12th to 9th century B.C.E. Our results (i) suggest a revised Iron-Age chronology; (ii) date an archaeological stratum to Shoshenq's campaign; (iii) indicate the similarity of "Solomonic" and "Omride" pottery; and (iv) provide correlation with Greece and Cyprus.

A 3500 14C yr High-Resolution Record of Water-Level Changes in Lake Titicaca, Bolivia/Peru

NASA Astrophysics Data System (ADS)

Abbott, Mark B.; Binford, Michael W.; Brenner, Mark; Kelts, Kerry R.

1997-03-01

Sediment cores collected from the southern basin of Lake Titicaca (Bolivia/Peru) on a transect from 4.6 m above overflow level to 15.1 m below overflow level are used to identify a new century-scale chronology of Holocene lake-level variations. The results indicate that lithologic and geochemical analyses on a transect of cores can be used to identify and date century-scale lake-level changes. Detailed sedimentary analyses of subfacies and radiocarbon dating were conducted on four representative cores. A chronology based on 60 accelerator mass spectrometer radiocarbon measurements constrains the timing of water-level fluctuations. Two methods were used to estimate the 14C reservoir age. Both indicate that it has remained nearly constant at ˜250 14C yr during the late Holocene. Core studies based on lithology and geochemistry establish the timing and magnitude of five periods of low lake level, implying negative moisture balance for the northern Andean altiplano over the last 3500 cal yr. Between 3500 and 3350 cal yr B.P., a transition from massive, inorganic-clay facies to laminated organic-matter-rich silts in each of the four cores signals a water-level rise after a prolonged mid-Holocene dry phase. Evidence of other significant low lake levels occurs 2900-2800, 2400-2200, 2000-1700, and 900-500 cal yr B.P. Several of the low lake levels coincided with cultural changes in the region, including the collapse of the Tiwanaku civilization.

Using radiocarbon to investigate soil respiration impacts on atmospheric CO2

NASA Astrophysics Data System (ADS)

Phillips, C. L.; LaFranchi, B. W.; McFarlane, K. J.; Desai, A. R.

2013-12-01

While soil respiration is believed to represent the largest single source of CO2 emissions on a global scale, there are few tools available to measure soil emissions at large spatial scales. We investigated whether radiocarbon (14C) abundance in CO2 could be used to detect and characterize soil emissions in the atmosphere, taking advantage of the fact that 14C abundance in soil carbon is elevated compared to the background atmosphere, a result of thermonuclear weapons testing during the mid-20th Century (i.e. bomb-C). Working in a temperate hardwood forest in Northern Wisconsin during 2011-12, we made semi-high-frequency measurements of CO2 at nested spatial scales from the soil subsurface to 150 m above ground level. These measurements were used to investigate seasonal patterns in respired C sources, and to evaluate whether variability in soil-respired Δ14C could also be detected in atmospheric measurements. In our ground-level measurements we found large seasonal variation in soil-respired 14CO2 that correlated with soil moisture, which was likely related to root activity. Atmospheric measurements of 14CO2 in the forest canopy (2 to 30m) were used to construct Keeling plots, and these provided larger spatial-scale estimates of respired 14CO2 that largely agreed with the soil-level measurements. In collaboration with the NOAA we also examined temporal patterns of 14CO2 at the Park Falls tall-tower (150m), and found elevated 14CO2 levels during summer months that likely resulted from increased respiration from heterotrophic sources. These results demonstrate that a fingerprint from soil-respired CO2 can be detected in the seasonal patterns of atmospheric 14CO2, even at a regionally-integrating spatial scale far from the soil surface.

Distributions and Transformations of Natural Abundance 14C and 13C in Dissolved and Particulate Lipids in a Major Temperate Estuary

NASA Astrophysics Data System (ADS)

Bauer, J. E.; Canuel, E. A.; McIntosh, H.; Barrett, A.; Ferer, E.; Hossler, K.

2013-12-01

Limited previous studies have shown major differences in the natural 14C and 13C isotopic signatures and radiocarbon ages of different biochemical classes (e.g., proteins, carbohydrates, lipid, etc.) in river, estuarine and marine dissolved and particulate organic matter (DOM and POM, respectively). Of particular note are the much greater radiocarbon ages of lipophilic materials than other compound classes. Possible explanations for these findings include greater-than-expected inputs of fossil and highly aged lipid-containing organic matter to rivers and estuaries, extended sorptive-protection of lipophilic materials from degradation and/or lower overall reactivities of lipids vs. other major biochemical classes. We measured the Delta 14C and del 13C signatures and 14C ages of lipid classes in DOM and POM in a major temperate estuary, Delaware Bay (USA) over two years. Changes in DOM were also followed during large volume dark and light incubations to assess the microbial and photochemical reactivity and processing of DOM and lipids. Neutral lipids in DOM were among the most highly aged (> 30,000 yrs BP) of any materials measured in natural waters to date, and were significantly older than co-occurring polar lipids (~4,000-5,000 yrs BP). In general, DOM lipid ages were significantly greater than POM lipid ages across the river-estuary transect, arguing against sorptive protection as the major factor explaining greater ages of lipid than those of other compound classes. Both dark and light incubations of DOM resulted in losses of very highly aged material (30-50,000 y BP), with the remnant exported lipids being correspondingly younger. The microbial and photochemical alterations were most pronounced for lipids from freshwater reaches of the system (i.e., the Delaware River). These findings suggest that a) dissolved vs. particulate lipids have fundamentally different sources and/or physico-chemical partitioning, b) different lipid classes (e.g., neutral vs. polar

Time in tortoiseshell: a bomb radiocarbon-validated chronology in sea turtle scutes.

PubMed

Van Houtan, Kyle S; Andrews, Allen H; Jones, T Todd; Murakawa, Shawn K K; Hagemann, Molly E

2016-01-13

Some of the most basic questions of sea turtle life history are also the most elusive. Many uncertainties surround lifespan, growth rates, maturity and spatial structure, yet these are critical factors in assessing population status. Here we examine the keratinized hard tissues of the hawksbill (Eretmochelys imbricata) carapace and use bomb radiocarbon dating to estimate growth and maturity. Scutes have an established dietary record, yet the large keratin deposits of hawksbills evoke a reliable chronology. We sectioned, polished and imaged posterior marginal scutes from 36 individual hawksbills representing all life stages, several Pacific populations and spanning eight decades. We counted the apparent growth lines, microsampled along growth contours and calibrated Δ(14)C values to reference coral series. We fit von Bertalanffy growth function (VBGF) models to the results, producing a range of age estimates for each turtle. We find Hawaii hawksbills deposit eight growth lines annually (range 5-14), with model ensembles producing a somatic growth parameter (k) of 0.13 (range 0.1-0.2) and first breeding at 29 years (range 23-36). Recent bomb radiocarbon values also suggest declining trophic status. Together, our results may reflect long-term changes in the benthic community structure of Hawaii reefs, and possibly shed light on the critical population status for Hawaii hawksbills. © 2016 The Author(s).

Time in tortoiseshell: a bomb radiocarbon-validated chronology in sea turtle scutes

PubMed Central

Van Houtan, Kyle S.; Andrews, Allen H.; Jones, T. Todd; Murakawa, Shawn K. K.; Hagemann, Molly E.

2016-01-01

Some of the most basic questions of sea turtle life history are also the most elusive. Many uncertainties surround lifespan, growth rates, maturity and spatial structure, yet these are critical factors in assessing population status. Here we examine the keratinized hard tissues of the hawksbill (Eretmochelys imbricata) carapace and use bomb radiocarbon dating to estimate growth and maturity. Scutes have an established dietary record, yet the large keratin deposits of hawksbills evoke a reliable chronology. We sectioned, polished and imaged posterior marginal scutes from 36 individual hawksbills representing all life stages, several Pacific populations and spanning eight decades. We counted the apparent growth lines, microsampled along growth contours and calibrated Δ14C values to reference coral series. We fit von Bertalanffy growth function (VBGF) models to the results, producing a range of age estimates for each turtle. We find Hawaii hawksbills deposit eight growth lines annually (range 5–14), with model ensembles producing a somatic growth parameter (k) of 0.13 (range 0.1–0.2) and first breeding at 29 years (range 23–36). Recent bomb radiocarbon values also suggest declining trophic status. Together, our results may reflect long-term changes in the benthic community structure of Hawaii reefs, and possibly shed light on the critical population status for Hawaii hawksbills. PMID:26740617

High-precision 14C and 40Ar/39Ar dating of the Campanian Ignimbrite (Y-5) reconciles the time-scales of climatic-cultural processes at 40 ka

NASA Astrophysics Data System (ADS)

Giacco, Biagio; Hajdas, Irka; Isaia, Roberto; Deino, Alan; Nomade, Sebastien

2017-04-01

The Campanian Ignimbrite (CI) super-eruption ( 40 ka, Southern Italy) is the largest known volcanic event of Mediterranean area. The CI tephra is widely dispersed through western Eurasia and occurs in close stratigraphic association with significant Late Pleistocene paleoclimatic and Paleolithic cultural events. This makes the CI tephra one of the most important tool for investigating several scientific issues ranging from volcanology, paleoclimatology to archaeology. Yet despite concerted attempts, the absolute age of the CI eruption is not well constrained. Here we present the first direct radiocarbon age for the CI obtained using accepted modern practices, from multiple 14C analyses of an exceptional large charred tree branch embedded in the lithified Yellow Tuff facies of the CI pyroclastic flow deposits, as well as new high-precision 40Ar/39Ar dating for the CI. These data substantially improve upon previous age determinations and permit fuller exploitation of the chronological potential of the CI tephra marker. Specifically, the results of our study are twofold: they provide (i) a robust pair of 14C and 40Ar/39Ar ages for refining both the radiocarbon calibration curve and the Late Pleistocene time-scale in the narrow, but significant time-span across CI event and (ii) compelling chronological evidence for the significance of the combined influence of the CI eruption and Heinrich Event 4 on European climate and potentially evolutionary processes of the Early Upper Palaeolithic.

BIOGENIC CONTRIBUTION TO PM-2.5 AMBIENT AEROSOL FROM RADIOCARBON MEASUREMENTS

EPA Science Inventory

Knowledge of the relative contributions of biogenic versus anthropogenic sources to ambient aerosol is of great interest in the formulation of strategies to achieve nationally mandated air quality standards. Radiocarbon (Carbon-14) measurements provide a means to quantify the ...

Radiocarbon and stable isotope investigations at the Central Rhineland sites of Gönnersdorf and Andernach-Martinsberg, Germany.

PubMed

Stevens, Rhiannon E; O'Connell, Tamsin C; Hedges, Robert E M; Street, Martin

2009-08-01

The late glacial open-air sites of Gönnersdorf and Andernach-Martinsberg in the German Central Rhineland are well known for their Magdalenian occupation and activities. The latter site also produced evidence for a younger, Final Palaeolithic occupation of the locality by people of the Federmessergruppen. Both sites are particularly well preserved, largely due to their burial beneath volcanic deposits of the late glacial Laacher See eruption. We conducted a program of AMS radiocarbon dating and stable isotope analyses with the aim of improving understanding of the chronological history and ecological setting of the two sites. Previously published radiocarbon dates appeared to indicate that the earliest Magdalenian occupation at Gönnersdorf fell around 12,900 uncalibrated (14)C yr BP, while the earliest occupation at Andernach may have been more than 500 radiocarbon years earlier. The AMS determinations presented here revise this impression and suggest that the onset of occupation at the two sites was in fact simultaneous and prior to the warming of Greenland Interstadial GI 1e. At Gönnersdorf, a chronological hiatus exists between the main Magdalenian faunal assemblage and mega-faunal remains interpreted as collected sub-fossil material. At Andernach-Martinsberg, there is a clear chronological hiatus between the Magdalenian occupation and subsequent Federmessergruppen activities at the site. However, an intermediate radiocarbon date on an atypically preserved horse bone is suggestive of ephemeral human visits to the site between these well demonstrated phases. A date of similar age on an elk bone from Gönnersdorf may indicate broadly contemporaneous human presence at Gönnersdorf too. Stable isotope analysis of faunal remains from Gönnersdorf and Andernach-Martinsberg was conducted with the aim of both reconstructing and comparing local environmental conditions at the two sites, and also potentially identifying subtle variations in the chronological development

Evolution of dissolved inorganic carbon in groundwater recharged by cyclones and groundwater age estimations using the 14C statistical approach

NASA Astrophysics Data System (ADS)

Meredith, K. T.; Han, L. F.; Cendón, D. I.; Crawford, J.; Hankin, S.; Peterson, M.; Hollins, S. E.

2018-01-01

The Canning Basin is the largest sedimentary basin in Western Australia and is located in one of the most cyclone prone regions of Australia. Despite its importance as a future resource, limited groundwater data is available for the Basin. The main aims of this paper are to provide a detailed understanding of the source of groundwater recharge, the chemical evolution of dissolved inorganic carbon (DIC) and provide groundwater age estimations using radiocarbon (14CDIC). To do this we combine hydrochemical and isotopic techniques to investigate the type of precipitation that recharge the aquifer and identify the carbon processes influencing 14CDIC, δ13CDIC, and [DIC]. This enables us to select an appropriate model for calculating radiocarbon ages in groundwater. The aquifer was found to be recharged by precipitation originating from tropical cyclones imparting lower average δ2H and δ18O values in groundwater (-56.9‰ and -7.87‰, respectively). Water recharges the soil zone rapidly after these events and the groundwater undergoes silicate mineral weathering and clay mineral transformation processes. It was also found that partial carbonate dissolution processes occur within the saturated zone under closed system conditions. Additionally, the processes could be lumped into a pseudo-first-order process and the age could be estimated using the 14C statistical approach. In the single-sample-based 14C models, 14C0 is the initial 14CDIC value used in the decay equation that considers only 14C decay rate. A major advantage of using the statistical approach is that both 14C decay and geochemical processes that cause the decrease in 14CDIC are accounted for in the calculation. The 14CDIC values of groundwater were found to increase from 89 pmc in the south east to around 16 pmc along the groundwater flow path towards the coast indicating ages ranging from modern to 5.3 ka. A test of the sensitivity of this method showed that a ∼15% error could be found for the oldest

Dating ivory by determination of 14C, 90Sr and 228/232Th.

PubMed

Schmied, Stefanie A K; Brunnermeier, Matthias J; Schupfner, Robert; Wolfbeis, Otto S

2012-09-10

A method is described to determine the time of death of elephants. This is accomplished by analysis of the radionuclides 14C, 90Sr and 228/232Th in known samples of ivory, and in samples of unknown age. The reliability of this method is considerably increased by multi nuclide analysis. Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.

Associated terrestrial and marine fossils in the late-glacial Presumpscot Formation, southern Maine, USA, and the marine reservoir effect on radiocarbon ages

USGS Publications Warehouse

Thompson, W.B.; Griggs, C.B.; Miller, N.G.; Nelson, R.E.; Weddle, T.K.; Kilian, T.M.

2011-01-01

Excavations in the late-glacial Presumpscot Formation at Portland, Maine, uncovered tree remains and other terrestrial organics associated with marine invertebrate shells in a landslide deposit. Buds of Populus balsamifera (balsam poplar) occurred with twigs of Picea glauca (white spruce) in the Presumpscot clay. Tree rings in Picea logs indicate that the trees all died during winter dormancy in the same year. Ring widths show patterns of variation indicating responses to environmental changes. Fossil mosses and insects represent a variety of species and wet to dry microsites. The late-glacial environment at the site was similar to that of today's Maine coast. Radiocarbon ages of 14 tree samples are 11,907??31 to 11,650??5014C yr BP. Wiggle matching of dated tree-ring segments to radiocarbon calibration data sets dates the landslide occurrence at ca. 13,520+95/??20calyr BP. Ages of shells juxtaposed with the logs are 12,850??6514C yr BP (Mytilus edulis) and 12,800??5514C yr BP (Balanus sp.), indicating a marine reservoir age of about 1000yr. Using this value to correct previously published radiocarbon ages reduces the discrepancy between the Maine deglaciation chronology and the varve-based chronology elsewhere in New England. ?? 2011 University of Washington.

Radiocarbon-based source apportionment of carbonaceous aerosols at a regional background site on Hainan Island, South China.

PubMed

Zhang, Yan-Lin; Li, Jun; Zhang, Gan; Zotter, Peter; Huang, Ru-Jin; Tang, Jian-Hui; Wacker, Lukas; Prévôt, André S H; Szidat, Sönke

2014-01-01

To assign fossil and nonfossil contributions to carbonaceous particles, radiocarbon ((14)C) measurements were performed on organic carbon (OC), elemental carbon (EC), and water-insoluble OC (WINSOC) of aerosol samples from a regional background site in South China under different seasonal conditions. The average contributions of fossil sources to EC, OC and WINSOC were 38 ± 11%, 19 ± 10%, and 17 ± 10%, respectively, indicating generally a dominance of nonfossil emissions. A higher contribution from fossil sources to EC (∼51%) and OC (∼30%) was observed for air-masses transported from Southeast China in fall, associated with large fossil-fuel combustion and vehicle emissions in highly urbanized regions of China. In contrast, an increase of the nonfossil contribution by 5-10% was observed during the periods with enhanced open biomass-burning activities in Southeast Asia or Southeast China. A modified EC tracer method was used to estimate the secondary organic carbon from fossil emissions by determining (14)C-derived fossil WINSOC and fossil EC. This approach indicates a dominating secondary component (70 ± 7%) of fossil OC. Furthermore, contributions of biogenic and biomass-burning emissions to contemporary OC were estimated to be 56 ± 16% and 44 ± 14%, respectively.

RADIOCARBON MEASUREMENTS ON PM 2.5 AMBIENT AEROSOL FROM NASHVILLE, TN

EPA Science Inventory

Radiocarbon (Carbon-14) measurements provide an estimate of the fraction of carbon in a sample that is biogenic. The methodology has been extensively used in past wintertime studies to quantify the contribution of wood smoke to ambient aerosol. In summertime such measurements...

Geochemistry, radiocarbon ages, and paleorecharge conditions along a transect in the central High Plains aquifer, southwestern Kansas, USA

USGS Publications Warehouse

McMahon, P.B.; Böhlke, J.K.; Christenson, S.C.

2004-01-01

Water samples from short-screen monitoring wells installed along a 90-km transect in southwestern Kansas were analyzed for major ions, trace elements, isotopes (H, B, C, N, O, S, Sr), and dissolved gases (He, Ne, N2, Ar, O2, CH4) to evaluate the geochemistry, radiocarbon ages, and paleorecharge conditions in the unconfined central High Plains aquifer. The primary reactions controlling water chemistry were dedolomitization, cation exchange, feldspar weathering, and O2 reduction and denitrification. Radiocarbon ages adjusted for C mass transfers ranged from <2.6 ka (14C) B.P. near the water table to 12.8 ± 0.9 ka (14C) B.P. at the base of the aquifer, indicating the unconfined central High Plains aquifer contained a stratified sequence of ground water spanning Holocene time. A cross-sectional model of steady-state ground-water flow, calibrated using radiocarbon ages, is consistent with recharge rates ranging from 0.8 mm/a in areas overlain by loess to 8 mm/a in areas overlain by dune sand. Paleorecharge temperatures ranged from an average of 15.2 ± 0.7 °C for the most recently recharged waters to 11.6 ± 0.4 °C for the oldest waters. The temperature difference between Early and Late Holocene recharge was estimated to be 2.4 ± 0.7 °C, after taking into account variable recharge elevations. Nitrogen isotope data indicate NO3 in paleorecharge (average concentration=193 μM) was derived from a relatively uniform source such as soil N, whereas NO3 in recent recharge (average concentration=885 μM) contained N from varying proportions of fertilizer, manure, and soil N. Deep water samples contained components of N2 derived from atmospheric, denitrification, and deep natural gas sources. Denitrification rates in the aquifer were slow (5 ± 2× 10−3 μmol N L−1 a−1), indicating this process would require >10 ka to reduce the average NO3 concentration in recent recharge to the Holocene background concentration.

Radiocarbon dating of the human eye lens crystallines reveal proteins without carbon turnover throughout life.

PubMed

Lynnerup, Niels; Kjeldsen, Henrik; Heegaard, Steffen; Jacobsen, Christina; Heinemeier, Jan

2008-01-30

Lens crystallines are special proteins in the eye lens. Because the epithelial basement membrane (lens capsule) completely encloses the lens, desquamation of aging cells is impossible, and due to the complete absence of blood vessels or transport of metabolites in this area, there is no subsequent remodelling of these fibers, nor removal of degraded lens fibers. Human tissue ultimately derives its (14)C content from the atmospheric carbon dioxide. The (14)C content of the lens proteins thus reflects the atmospheric content of (14)C when the lens crystallines were formed. Precise radiocarbon dating is made possible by comparing the (14)C content of the lens crystallines to the so-called bomb pulse, i.e. a plot of the atmospheric (14)C content since the Second World War, when there was a significant increase due to nuclear-bomb testing. Since the change in concentration is significant even on a yearly basis this allows very accurate dating. Our results allow us to conclude that the crystalline formation in the lens nucleus almost entirely takes place around the time of birth, with a very small, and decreasing, continuous formation throughout life. The close relationship may be further expressed as a mathematical model, which takes into account the timing of the crystalline formation. Such a life-long permanence of human tissue has hitherto only been described for dental enamel. In confront to dental enamel it must be held in mind that the eye lens is a soft structure, subjected to almost continuous deformation, due to lens accommodation, yet its most important constituent, the lens crystalline, is never subject to turnover or remodelling once formed. The determination of the (14)C content of various tissues may be used to assess turnover rates and degree of substitution (for example for brain cell DNA). Potential targets may be nervous tissues in terms of senile or pre-senile degradation, as well as other highly specialised structures of the eyes. The precision with

New Radiocarbon Dates on Upper Mid-West Proboscideans: Determining Date Robustness

NASA Astrophysics Data System (ADS)

Hodgins, G.; Widga, C.; Lengyel, S. N.; Saunders, J.; Walker, J. D.

2013-12-01

With the objective of refining the picture of Megafaunal extinction patterns in the upper Midwest in the terminal Pleistocene, we have assembled for radiocarbon dating specimens from more than 80 distinct Mammut and Mammuthus remains from potentially late sites. So far, we have measurements for 65 bones, tusks and teeth, nearly double the extant number of published dates . These new specimens were all from museums rather than excavation sites, and 60% were known to be coated with a consolidant. The predominant consolidant was Butvar B-76, however shellac, Elmer's Glue, Glyptol were also noted in the conservation records, or deduced from knowledge of a particular museum's practices. Given the objective of the project is to identify extinction patterns, coupled with the wide prevalence of consolidants amongst the specimen set, it was imperative that testing be carried out to confirm that radiocarbon laboratory protocols removed the consolidants, so that ultimately the dates can be considered robust. To this end, key specimens were dated three times using different sample preparation protocols. These were 1) a solvent extraction followed by a modified Longin-plus -Base continuous flow collagen extraction method used in the NSF-Arizona AMS facility, 2) the solvent/modified Longin method plus ultrafiltration, and 3) solvent/modified Longin method plus hydroxyproline single amino acid dating. Among the specimens subjected to triplicate testing were some of the youngest late Wisconsin proboscidean specimens from the Upper Midwest Region. The data reveal general agreement between the different protocols, and suggested either limited penetration of consolidants into the specimens, or that the standard laboratory cleaning protocols were sufficient to remove traces from deep within bone, tooth or tusk tissue. The preservation of each specimen, recorded in terms of collagen content, C/N ratio and stable isotope values, indicated that most were actually well preserved, implying

Willard Libby, Radiocarbon, and Carbon Dating

Science.gov Websites

: Radiocarbon from Pile Graphite; Chemical Methods for Its Concentrations, DOE Technical Report Download Adobe Carbon Dating Chronological Methods 8 - Radiocarbon Dating, University of California, Santa Barbara Why

14C/C measurements support Andreev's internode method to determine lichen growth rates in Cladina stygia (Fr.) Ahti

DOE Office of Scientific and Technical Information (OSTI.GOV)

Holt, E; Bench, G

2007-12-05

Growth rates and the ability to date an organism can greatly contribute to understanding its population biology and community dynamics. 1n 1954, Andreev proposed a method to date Cladina, a fruticose lichen, using total thallus length and number of internodes. No research, however, has demonstrated the reliability of this technique or compared its estimates to those derived by other means. In this study, we demonstrate the utility of {sup 14}C/C ratios to determine lichen age and growth rate in Cladina stygia (Fr.) Ahti collected from northwestern Alaska, USA. The average growth rate using {sup 14}C/C ratios was 6.5 mm {center_dot}more » yr{sup -1}, which was not significantly different from growth rates derived by Andreev's internode method (average = 6.2 mm {center_dot} yr{sup -1}); thus, suggesting the reliability of Andreev's simple field method for dating lichens. In addition, we found lichen growth rates appeared to differ with geographic location, yet did not seem related to ambient temperature and total precipitation.« less

Determining the biomass fraction of mixed waste fuels: A comparison of existing industry and {sup 14}C-based methodologies

DOE Office of Scientific and Technical Information (OSTI.GOV)

Muir, G.K.P., E-mail: Graham.Muir@glasgow.ac.uk; Hayward, S.; Tripney, B.G.

2015-01-15

Highlights: • Compares industry standard and {sup 14}C methods for determining bioenergy content of MSW. • Differences quantified through study at an operational energy from waste plant. • Manual sort and selective dissolution are unreliable measures of feedstock bioenergy. • {sup 14}C methods (esp. AMS) improve precision and reliability of bioenergy determination. • Implications for electricity generators and regulators for award of bio-incentives. - Abstract: {sup 14}C analysis of flue gas by accelerator mass spectrometry (AMS) and liquid scintillation counting (LSC) were used to determine the biomass fraction of mixed waste at an operational energy-from-waste (EfW) plant. Results were convertedmore » to bioenergy (% total) using mathematical algorithms and assessed against existing industry methodologies which involve manual sorting and selective dissolution (SD) of feedstock. Simultaneous determinations using flue gas showed excellent agreement: 44.8 ± 2.7% for AMS and 44.6 ± 12.3% for LSC. Comparable bioenergy results were obtained using a feedstock manual sort procedure (41.4%), whilst a procedure based on selective dissolution of representative waste material is reported as 75.5% (no errors quoted). {sup 14}C techniques present significant advantages in data acquisition, precision and reliability for both electricity generator and industry regulator.« less

Radiocarbon dating of dissolved inorganic carbon in groundwater from confined parts of the Upper Floridan aquifer, Florida, USA

USGS Publications Warehouse

Plummer, Niel; Sprinkle, C.L.

2001-01-01

Geochemical reaction models were evaluated to improve radiocarbon dating of dissolved inorganic carbon (DIC) in groundwater from confined parts of the Upper Floridan aquifer in central and northeastern Florida, USA. The predominant geochemical reactions affecting the 14C activity of DIC include (1) dissolution of dolomite and anhydrite with calcite precipitation (dedolomitization), (2) sulfate reduction accompanying microbial degradation of organic carbon, (3) recrystallization of calcite (isotopic exchange), and (4) mixing of fresh water with as much as 7% saline water in some coastal areas. The calculated cumulative net mineral transfers are negligibly small in upgradient parts of the aquifer and increase significantly in downgradient parts of the aquifer, reflecting, at least in part, upward leakage from the Lower Floridan aquifer and circulation that contacted middle confining units in the Floridan aquifer system. The adjusted radiocarbon ages are independent of flow path and represent travel times of water from the recharge area to the sample point in the aquifer. Downgradient from Polk City (adjusted age 1.7 ka) and Keystone Heights (adjusted age 0.4 ka), 14 of the 22 waters have adjusted 14C ages of 20-30 ka, indicating that most of the fresh-water resource in the Upper Floridan aquifer today was recharged during the last glacial period. All of the paleowaters are enriched in 18O and 2H relative to modern infiltration, with maximum enrichment in ??18O of approximately 2.0%o.

An investigation of size-fractionated organic matter from Lake Superior and a tributary stream using radiocarbon, stable isotopes and NMR

NASA Astrophysics Data System (ADS)

Zigah, Prosper K.; Minor, Elizabeth C.; Abdulla, Hussain A. N.; Werne, Josef P.; Hatcher, Patrick G.

2014-02-01

This study investigated the concentration and isotopic composition of different size fractions of organic matter (OM) in Lake Superior and in one of its many tributary streams and rivers (Amity Creek, Duluth, Minnesota, USA). Structural compositional drivers of the Δ14C of high molecular weight (HMW, >1 kDa) dissolved organic carbon (DOC) in the lake were also evaluated. Low molecular weight (LMW, <1 kDa) DOC was the fraction containing the largest proportion (68-88%) of organic carbon (OC) in the lake. Particulate organic carbon (POC, >0.7 μm) was generally 13C-depleted (-29 ± 1.2‰) relative to “bulk” (<0.7 μm) DOC (-26.4 ± 0.7‰), “init” (<0.2 μm) DOC (-26.6 ± 0.8‰), HMW DOC (-26.9 ± 0.3‰) and LMW DOC (-26.5 ± 0.9‰), and had more variable 14C content (Δ14C of -94‰ to 53‰; 735 years BP to modern) than the other size fractions. Init DOC (Δ14C of 17-59‰), HMW DOC (Δ14C of 23-64‰) and LMW DOC (Δ14C of 16-62‰) all reflected contemporary (modern) radiocarbon signatures. Bulk DOC (Δ14C of -19‰ to 57‰; 90 years BP to modern) had modern radiocarbon values in the offshore sites (Δ14C of 2-57‰) with pre-aged samples (Δ14C of -8‰ to -19‰) seen at the nearshore site. HMW DOM was relatively N-poor (C:N of 12-19) compared to particulate organic matter (POM, C:N of 8-10) revealing either a more diagenetically altered state or contrasting sources. 13C NMR data showed that biochemical composition of HMW DOC in Lake Superior was dominated by carbohydrates (53-65%) with only trace aromatic components (2-4%). Structurally complex components such as heteropolysaccharides (HPS), amide/peptides and amino sugars (AMS) constitute 75-84% of HMW DOC whereas carboxylic-rich alicyclic molecules (CRAM) made up 16-25% of HMW DOC in the lake. Combined HPS and AMS, O-alkyl carbohydrate carbon, and total carbohydrate carbon contents were significantly positively correlated to the Δ14C of HMW DOC suggesting they contribute a contemporary 14C

Determination of Glucose Utilization Rates in Cultured Astrocytes and Neurons with [14C]deoxyglucose: Progress, Pitfalls, and Discovery of Intracellular Glucose Compartmentation.

PubMed

Dienel, Gerald A; Cruz, Nancy F; Sokoloff, Louis; Driscoll, Bernard F

2017-01-01

2-Deoxy-D-[ 14 C]glucose ([ 14 C]DG) is commonly used to determine local glucose utilization rates (CMR glc ) in living brain and to estimate CMR glc in cultured brain cells as rates of [ 14 C]DG phosphorylation. Phosphorylation rates of [ 14 C]DG and its metabolizable fluorescent analog, 2-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino)-2-deoxyglucose (2-NBDG), however, do not take into account differences in the kinetics of transport and metabolism of [ 14 C]DG or 2-NBDG and glucose in neuronal and astrocytic cells in cultures or in single cells in brain tissue, and conclusions drawn from these data may, therefore, not be correct. As a first step toward the goal of quantitative determination of CMR glc in astrocytes and neurons in cultures, the steady-state intracellular-to-extracellular concentration ratios (distribution spaces) for glucose and [ 14 C]DG were determined in cultured striatal neurons and astrocytes as functions of extracellular glucose concentration. Unexpectedly, the glucose distribution spaces rose during extreme hypoglycemia, exceeding 1.0 in astrocytes, whereas the [ 14 C]DG distribution space fell at the lowest glucose levels. Calculated CMR glc was greatly overestimated in hypoglycemic and normoglycemic cells because the intracellular glucose concentrations were too high. Determination of the distribution space for [ 14 C]glucose revealed compartmentation of intracellular glucose in astrocytes, and probably, also in neurons. A smaller metabolic pool is readily accessible to hexokinase and communicates with extracellular glucose, whereas the larger pool is sequestered from hexokinase activity. A new experimental approach using double-labeled assays with DG and glucose is suggested to avoid the limitations imposed by glucose compartmentation on metabolic assays.

Nuclear Bombs and Coral: Guam Coral Core Reveals Operation-Specific Radiocarbon Signals from the Pacific Proving Grounds

NASA Astrophysics Data System (ADS)

Andrews, A. H.

2016-12-01

Radiocarbon (14C) analyses on a coral core extracted from the western Central Pacific (Guam) has revealed a series of early peaks in the marine bomb 14C record. The typical marine bomb 14C signal, one that is phase lagged and attenuated relative to atmospheric bomb 14C, is present in the coral core and is consistent with other North Pacific records. However, 14C levels that are well above what can be explained by air-sea diffusion alone punctuate this pattern. This anomaly has been demonstrated to a limited extent in other coral cores of the Indo-Pacific region, but is unmatched relative to the magnitude and temporal resolution recorded in the Guam coral core. Other records have shown an early Δ14C rise on the order of 40-50‰ above pre-bomb levels, with a subsequent decline before continuing the gradual Δ14C rise that is indicative of air-sea diffusion of 14CO2. The Guam coral Δ14C record provided three strong pulses in 1954-55, 1956-57, and 1958-59 that are superimposed on the pre-bomb to initial Δ14C rise from atmospheric bomb 14C. Each of these peaks can be directly linked to testing of thermonuclear devices in the Pacific Proving Grounds at Eniwetok and Bikini Atoll of the Marshall Islands. The measurable lag in reaching Guam can be tied to ocean surface currents and can be traced to other regional Δ14C records from corals, providing a transport timeline to places as distant as the Indonesian throughflow, Okinawa and Palmyra.

Radiocarbon Analysis to Calculate New End-Member Values for Biomass Burning Source Samples Specific to the Bay Area

NASA Astrophysics Data System (ADS)

Yoon, S.; Kirchstetter, T.; Fairley, D.; Sheesley, R. J.; Tang, X.

2017-12-01

Elemental carbon (EC), also known as black carbon or soot, is an important particulate air pollutant that contributes to climate forcing through absorption of solar radiation and to adverse human health impacts through inhalation. Both fossil fuel combustion and biomass burning, via residential firewood burning, agricultural burning, wild fires, and controlled burns, are significant sources of EC. Our ability to successfully control ambient EC concentrations requires understanding the contribution of these different emission sources. Radiocarbon (14C) analysis has been increasingly used as an apportionment tool to distinguish between EC from fossil fuel and biomass combustion sources. However, there are uncertainties associated with this method including: 1) uncertainty associated with the isolation of EC to be used for radiocarbon analysis (e.g., inclusion of organic carbon, blank contamination, recovery of EC, etc.) 2) uncertainty associated with the radiocarbon signature of the end member. The objective of this research project is to utilize laboratory experiments to evaluate some of these uncertainties, particularly for EC sources that significantly impact the San Francisco Bay Area. Source samples of EC only and a mix of EC and organic carbon (OC) were produced for this study to represent known emission sources and to approximate the mixing of EC and OC that would be present in the atmosphere. These samples include a combination of methane flame soot, various wood smoke samples (i.e. cedar, oak, sugar pine, pine at various ages, etc.), meat cooking, and smoldering cellulose smoke. EC fractions were isolated using a Sunset Laboratory's thermal optical transmittance carbon analyzer. For 14C analysis, samples were sent to Woods Hole Oceanographic Institution for isotope analysis using an accelerated mass spectrometry. End member values and uncertainties for the EC isolation utilizing this method will be reported.

Radiocarbon Analysis of Individual Amino Acids: Carbon Blank Quantification for a Small-Sample High-Pressure Liquid Chromatography Purification Method.

PubMed

Bour, Amy L; Walker, Brett D; Broek, Taylor A B; McCarthy, Matthew D

2016-04-05

Compound-specific radiocarbon analysis (CSRA) of amino acids (AAs) is of great interest as a proxy for organic nitrogen (N) cycling rates, dating archeological bone collagen, and investigating processes shaping the biogeochemistry of global N reservoirs. However, recoverable quantities of individual compounds from natural samples are often insufficient for radiocarbon ((14)C) analyses (<50 μg C). Constraining procedural carbon (C) blanks and their isotopic contributions is critical for reporting of accurate CSRA measurements. Here, we report the first detailed quantification of C blanks (including sources, magnitudes, and variability) for a high-pressure liquid chromatography (HPLC) method designed to purify individual AAs from natural samples. We used pairs of AA standards with either modern (M) or dead (D) fraction modern (Fm) values to quantify MC and DC blanks within several chromatographic regions. Blanks were determined for both individual and mixed AA standard injections with peak loadings ranging from 10 to 85 μg C. We found 0.8 ± 0.4 μg of MC and 1.0 ± 0.5 μg of DC were introduced by downstream sample preparation (drying, combustion, and graphitization), which accounted for essentially the entire procedural blank for early eluting AAs. For late-eluting AAs, higher eluent organic content and fraction collected volumes contributed to total blanks of 1.5 ± 0.75 μg of MC and 3.0 ± 1.5 μg of DC. Our final measurement uncertainty for 20 μg of C of most AAs was ±0.02 Fm, although sample size requirements are larger for similar uncertainty in late-eluting AAs. These results demonstrate the first CSRA protocol for many protein AAs with uncertainties comparable to the lowest achieved in prior studies.

Simulation of bombe radiocarbon transient in the Mediterranean Sea using a high-resolution regional model.

NASA Astrophysics Data System (ADS)

Ayache, Mohamed; Dutay, Jean-claude; Mouchet, Anne; Tisnérat-Laborde, Nadine; Houma-Bachari, Fouzia; Louanchi, Ferial; jean-baptiste, Philippe

2016-04-01

The radiocarbon isotope of carbon "14C", which a half-life of 5730 years, is continually formed naturally in the atmosphere by the neutron bombardment of 14N atoms. However, in the 1950s and early1960s, the atmospheric testing of thermonuclear weapons added a large amount of 14C into the atmosphere. The gradual infusion and spread of this "bomb" 14C through the oceans has provided a unique opportunity to gain insight into the specific rates characterizing the carbon cycle and ocean ventilations on such timescales. This numerical study provides, for the first time in the Mediterranean Sea, a simulation of the anthropogenic 14C invasion covers a 70-years period spanning the entire 14C generated by the bomb test, by using a high resolution regional model NEMO-MED12 (1/12° of horizontal resolution). This distribution and evolution of Δ14C of model is compared with recent high resolution 14C measurements obtained from surface water corals (Tisnérat-Laborde et al, 2013). In addition to providing constraints on the air-sea transfer of 14C, our work provides information on the thermohaline circulation and the ventilation of the deep waters to constrain the degree to which the NEMO-MED12 can reproduce correctly the main hydrographic features of the Mediterranean Sea circulation and its variations estimated from corals 14C time series measurements. This study is part of the work carried out to assess the robustness of the NEMO-MED12 model, which will be used to study the evolution of the climate and its effect on the biogeochemical cycles in the Mediterranean Sea, and to improve our ability to predict the future evolution of the Mediterranean Sea under the increasing anthropogenic pressure.

Identifying sources of dissolved organic carbon in agriculturally dominated rivers using radiocarbon age dating: Sacramento-San Joaquin River Basin, California

USGS Publications Warehouse

Sickman, James O.; DiGiorgio, Carol L.; Davisson, M. Lee; Lucero, Delores M.; Bergamaschi, Brian A.

2010-01-01

We used radiocarbon measurements of dissolved organic carbon (DOC) to resolve sources of riverine carbon within agriculturally dominated landscapes in California. During 2003 and 2004, average Δ14C for DOC was −254‰ in agricultural drains in the Sacramento–San Joaquin Delta, −218‰ in the San Joaquin River, −175‰ in the California State Water Project and −152‰ in the Sacramento River. The age of bulk DOC transiting the rivers of California’s Central Valley is the oldest reported for large rivers and suggests wide-spread loss of soil organic matter caused by agriculture and urbanization. Using DAX 8 adsorbent, we isolated and measured 14C concentrations in hydrophobic acid fractions (HPOA); river samples showed evidence of bomb-pulse carbon with average Δ14C of 91 and 76‰ for the San Joaquin and Sacramento Rivers, respectively, with older HPOA, −204‰, observed in agricultural drains. An operationally defined non-HPOA fraction of DOC was observed in the San Joaquin River with seasonally computed Δ14C values of between −275 and −687‰; the source of this aged material was hypothesized to be physically protected organic-matter in high clay-content soils and agrochemicals (i.e., radiocarbon-dead material) applied to farmlands. Mixing models suggest that the Sacramento River contributes about 50% of the DOC load in the California State Water Project, and agricultural drains contribute approximately one-third of the load. In contrast to studies showing stabilization of soil carbon pools within one or two decades following land conversion, sustained loss of soil organic matter, occurring many decades after the initial agricultural-land conversion, was observed in California’s Central Valley.

Radiocarbon behaviour in seawater and the brown algae Fucus serratus in the vicinity of the COGEMA La Hague spent fuel reprocessing plant (Goury)--France.

PubMed

Douville, Eric; Fiévet, Bruno; Germain, Pierre; Fournier, Marc

2004-01-01

Extensive studies of the radiocarbon (14C) distribution and transfer in the marine environment of the North-Cotentin peninsula and along the English Channel have been carried out. The main aims of these studies have been to estimate the spatial and temporal variation of the 14C concentration in seawater and to calculate 14C concentration factors for some biological species. Such information will be helpful in order to calculate precisely radiation doses to humans. First results obtained in the vicinity of the COGEMA La Hague nuclear plant (Goury) indicate a 14C labelling of the dissolved inorganic carbon (DIC) in seawater (8.0-26.2 Bq.m(-3)) and a tight relationship between the 14C in the liquid releases from the plant and the 14C concentrations in DIC. The particulate organic carbon (POC) is also labelled. The concentration factor calculations for the brown algae (Fucus serratus) sampled from Goury, and also along the English Channel, give 14C values around 3000 Bq.kg(-1) fresh weight / Bq.L(-1).

Characterizing The Microbial Lability And Isotopic (14C, 13C) Signatures Of Marine Organic Matter With A Novel Culture Vessel System

NASA Astrophysics Data System (ADS)

Beaupre, S. R.; Mahmoudi, N.; Pearson, A.

2016-02-01

The rate at which non-living organic matter is respired in the ocean is an unconstrained and important property of the marine carbon cycle. Studies of inherent mineralization rates are complicated by the fact that marine organic matter is a mixture of compounds that vary in reactivity and concentration. While natural radiocarbon ages (14C, half-life = 5730 yr) have served as proxies for lability, they have not been used extensively to characterize that fraction of marine organic matter that is biologically accessible. To address this problem, we developed a novel batch culture system to monitor the time-dependent production rates and isotopic signatures of CO2 released during microbial degradation of natural organic matter. The system simulated a nepheloid layer by maintaining a slurry of decarbonated sediment and minimal media (M9) in a custom 2-liter culture vessel. The natural microbial community was allowed to develop within the sediment, and respired CO2 was continuously sparged from the medium with helium and oxygen, quantified in real time with an infrared gas analyzer, and isolated as a series of contiguous fractions for subsequent isotopic (∆14C, d13C) characterization. Control experiments indicated the accumulation of just 4.5 mg of background carbon per hour of continuous gas flow, which constituted ≤ 10 % of the respired carbon mass in each fraction. Since ∆14C values are conserved during molecular transformations, this low-blank system enables the detection of subtle shifts in the "age" of organic matter respired during the course of a culture experiment. Analyses of sediments from Falmouth, MA revealed both a variable CO2 production rate and an increase in post-bomb ∆14C values during a 10-day incubation. This suggests that the microbial lability of organic matter at this site decreased non-linearly with apparent 14C age, and that the least labile fraction observed was not more than 50 years old. These results underscore the complex

Radiocarbon and stable carbon isotope compositions of chemically fractionated soil organic matter in a temperate-zone forest.

PubMed

Koarashi, Jun; Iida, Takao; Asano, Tomohiro

2005-01-01

To better understand the role of soil organic matter in terrestrial carbon cycle, carbon isotope compositions in soil samples from a temperate-zone forest were measured for bulk, acid-insoluble and base-insoluble organic matter fractions separated by a chemical fractionation method. The measurements also made it possible to estimate indirectly radiocarbon ((14)C) abundances of acid- and base-soluble organic matter fractions, through a mass balance of carbon among the fractions. The depth profiles of (14)C abundances showed that (1) bomb-derived (14)C has penetrated the first 16cm mineral soil at least; (2) Delta(14)C values of acid-soluble organic matter fraction are considerably higher than those of other fractions; and (3) a significant amount of the bomb-derived (14)C has been preserved as the base-soluble organic matter around litter-mineral soil boundary. In contrast, no or little bomb-derived (14)C was observed for the base-insoluble fraction in all sampling depths, indicating that this recalcitrant fraction, accounting for approximately 15% of total carbon in this temperate-zone forest soil, plays a role as a long-term sink in the carbon cycle. These results suggest that bulk soil organic matter cannot provide a representative indicator as a source or a sink of carbon in soil, particularly on annual to decadal timescales.

Estimation of the fossil fuel component in atmospheric CO2 based on radiocarbon measurements at the Beromünster tall tower, Switzerland

NASA Astrophysics Data System (ADS)

Berhanu, Tesfaye A.; Szidat, Sönke; Brunner, Dominik; Satar, Ece; Schanda, Rüdiger; Nyfeler, Peter; Battaglia, Michael; Steinbacher, Martin; Hammer, Samuel; Leuenberger, Markus

2017-09-01

Fossil fuel CO2 (CO2ff) is the major contributor of anthropogenic CO2 in the atmosphere, and accurate quantification is essential to better understand the carbon cycle. Since October 2012, we have been continuously measuring the mixing ratios of CO, CO2, CH4, and H2O at five different heights at the Beromünster tall tower, Switzerland. Air samples for radiocarbon (Δ14CO2) analysis have also been collected from the highest sampling inlet (212.5 m) of the tower on a biweekly basis. A correction was applied for 14CO2 emissions from nearby nuclear power plants (NPPs), which have been simulated with the Lagrangian transport model FLEXPART-COSMO. The 14CO2 emissions from NPPs offset the depletion in 14C by fossil fuel emissions, resulting in an underestimation of the fossil fuel component in atmospheric CO2 by about 16 %. An average observed ratio (RCO) of 13.4 ± 1.3 mmol mol-1 was calculated from the enhancements in CO mixing ratios relative to the clean-air reference site Jungfraujoch (ΔCO) and the radiocarbon-based fossil fuel CO2 mole fractions. The wintertime RCO estimate of 12.5 ± 3.3 is about 30 % higher than the wintertime ratio between in situ measured CO and CO2 enhancements at Beromünster over the Jungfraujoch background (8.7 mmol mol-1) corrected for non-fossil contributions due to strong biospheric contribution despite the strong correlation between ΔCO and ΔCO2 in winter. By combining the ratio derived using the radiocarbon measurements and the in situ measured CO mixing ratios, a high-resolution time series of CO2ff was calculated exhibiting a clear seasonality driven by seasonal variability in emissions and vertical mixing. By subtracting the fossil fuel component and the large-scale background, we have determined the regional biospheric CO2 component that is characterized by seasonal variations ranging between -15 and +30 ppm. A pronounced diurnal variation was observed during summer modulated by biospheric exchange and vertical mixing, while no

87Sr/86Sr as a quantitative geochemical proxy for 14C reservoir age in dynamic, brackish waters: assessing applicability and quantifying uncertainties.

NASA Astrophysics Data System (ADS)

Lougheed, Bryan; van der Lubbe, Jeroen; Davies, Gareth

2016-04-01

Accurate geochronologies are crucial for reconstructing the sensitivity of brackish and estuarine environments to rapidly changing past external impacts. A common geochronological method used for such studies is radiocarbon (14C) dating, but its application in brackish environments is severely limited by an inability to quantify spatiotemporal variations in 14C reservoir age, or R(t), due to dynamic interplay between river runoff and marine water. Additionally, old carbon effects and species-specific behavioural processes also influence 14C ages. Using the world's largest brackish water body (the estuarine Baltic Sea) as a test-bed, combined with a comprehensive approach that objectively excludes both old carbon and species-specific effects, we demonstrate that it is possible to use 87Sr/86Sr ratios to quantify R(t) in ubiquitous mollusc shell material, leading to almost one order of magnitude increase in Baltic Sea 14C geochronological precision over the current state-of-the-art. We propose that this novel proxy method can be developed for other brackish water bodies worldwide, thereby improving geochronological control in these climate sensitive, near-coastal environments.

Radiocarbon Production by Thunderstorms

NASA Astrophysics Data System (ADS)

Babich, L. P.

2017-11-01

In view of the neutron flux enhancements observed in thunderstorms, a contribution of thunderstorm neutrons to atmospheric radiocarbon (isotope 614C) production is analyzed in connection with the archaeometry. Herein, estimates of neutron fluence per lightning electromagnetic pulse in regions with severe thunderstorm activity, at which a local rate of the 614C production is comparable to the observed rates, are shown to be consistent with the measured magnitudes of thunderstorm neutron fluence. At present, available observations of atmospheric neutron and parent gamma ray flashes correlated with thunderstorms do not allow making final conclusions about thunderstorm contributions to 614C production. For this, numerous studies of high-energy phenomena in thunderstorms are required, especially in the tropical belt where the thunderstorm activity is especially severe and where the 614C production by galactic cosmic rays is almost independent of the solar activity disturbing the Earth's magnetic field shielding the Earth from cosmic rays.

The transfer of bomb radiocarbon and anthropogenic lead to the deep North Atlantic Ocean observed from a deep sea coral

NASA Astrophysics Data System (ADS)

Lee, Jong-Mi; Eltgroth, Selene F.; Boyle, Edward A.; Adkins, Jess F.

2017-01-01

Deep-ocean, Δ14C, Pb concentrations, and Pb isotopes were reconstructed from a deep-sea coral Enallopsammia rostrata from 1410 m depth off of Bermuda. Our high-resolution time series is created from closely spaced radial cross sections, with samples taken from the center of concentric coral growth bands that we show to be the oldest portion of the section. Prebomb radiocarbon ages from the coral demonstrate that the vertical growth rate of the coral is linear, and the age of the coral is estimated to be 560-630 yr old based on the growth rate. Using this age model to reconstruct Δ14C in deep seawater, we first detect bomb radiocarbon at the coral growth site around 1980, and show that Δ14C increased from - 80 ± 1 ‰ (average 1930-1979) to a plateau at - 39 ± 3 ‰ (1999-2001). Pb/Ca of the coral ranges between 1.1-4.5 nmol/mol during the 16th and 17th centuries, and Pb isotope ratios (206Pb/207Pb = 1.21, 208Pb/207Pb = 2.495) in this period agree with pre-anthropogenic values found in the pelagic sediments of the North Atlantic Ocean basin. Coral Pb/Ca is slightly elevated to 6.2 ± 0.9 nmol /mol between the 1740s and the 1850s and then increases to 25.1 ± 0.2 nmol /mol in the 1990s. The increase in coral Pb/Ca is accompanied by a decrease in coral 206Pb/207Pb and 208Pb/207Pb, indicating that the increase was caused by the infiltration of anthropogenic Pb to the coral growth site. Comparing our data to the surface coral Δ14C and Pb records from Bermuda reveals a time scale of tracer transport from the surface ocean to the coral growth site. Some characteristic features, e.g., the bomb-derived Δ14C increase, appear in the deep ocean approximately 25 yr later than the surface, but the overall increase of Δ14C and Pb in the deep ocean is smaller and slower than the surface, showing the importance of mixing during the transport of these tracers.

Residence time revisited: The role of radiocarbon in reactive transport modeling

NASA Astrophysics Data System (ADS)

Lawrence, C. R.; Druhan, J. L.; Schulz, M. S.

2016-12-01

In recent years, our changing understanding of the dominant controls on soil carbon (C) storage and stability has cast a greater emphasis on the importance of physical and hydrological processes. These shifts in our understanding of C cycling have fostered increasingly commonplace measurements of soil physical and hydrological parameters in soil C studies (e.g. specific surface area, quantitative mineralogy, porosity) that reflect the importance of microbial accessibility to soil C. As a result, we are now poised to reassess the applicability of our approaches for conceptualizing and modeling soil C dynamics, particularly with regard to our representation of soil C pools. The goal of this work is to explore how the quantity and turnover of C, as approximated by radiocarbon measurements, is mechanistically linked to the physical and hydrologic parameters of soils. We utilize a reactive transport (RT) approach to link hydrologic transport, geochemical transformations and microbial activity influencing the magnitude and residence time of different carbon pools under variably saturated conditions. A newly developed version of the CrunchTope software is used to explicitly simulate the coupled transport, transformation, fractionation and decay of the three isotopes of carbon (12C, 13C and 14C) through a mechanistic framework. We constrain this model with a high-resolution dataset of soil carbon content, stable isotope composition and radiocarbon ages as well as physical and hydrologic data measured from a chronosequence of soils located near Santa Cruz, California. The Santa Cruz dataset is highly amenable to this task in that it demonstrates both seasonal and millennial variations in soil C distributions and associated soil properties. We present data from a series of simulations examining the sensitivity of C stocks, fluxes and mean residence times to transient processes spanning a range of temporal scales, including redox conditions, fluid flow and the distribution of

Annually resolved atmospheric radiocarbon records reconstructed from tree-rings

NASA Astrophysics Data System (ADS)

Wacker, Lukas; Bleicher, Niels; Büntgen, Ulf; Friedrich, Michael; Friedrich, Ronny; Diego Galván, Juan; Hajdas, Irka; Jull, Anthony John; Kromer, Bernd; Miyake, Fusa; Nievergelt, Daniel; Reinig, Frederick; Sookdeo, Adam; Synal, Hans-Arno; Tegel, Willy; Wesphal, Torsten

2017-04-01

The IntCal13 calibration curve is mainly based on data measured by decay counting with a resolution of 10 years. Thus high frequency changes like the 11-year solar cycles or cosmic ray events [1] are not visible, or at least not to their full extent. New accelerator mass spectrometry (AMS) systems today are capable of measuring at least as precisely as decay counters [2], with the advantage of using 1000 times less material. The low amount of material required enables more efficient sample preparation. Thus, an annually resolved re-measurement of the tree-ring based calibration curve can now be envisioned. We will demonstrate with several examples the multitude of benefits resulting from annually resolved radiocarbon records from tree-rings. They will not only allow for more precise radiocarbon dating but also contain valuable new astrophysical information. The examples shown will additionally indicate that it can be critical to compare AMS measurements with a calibration curve that is mainly based on decay counting. We often see small offsets between the two measurement techniques, while the reason is yet unknown. [1] Miyake F, Nagaya K, Masuda K, Nakamura T. 2012. A signature of cosmic-ray increase in AD 774-775 from tree rings in Japan. Nature 486(7402):240-2. [2] Wacker L, Bonani G, Friedrich M, Hajdas I, Kromer B, Nemec M, Ruff M, Suter M, Synal H-A, Vockenhuber C. 2010. MICADAS: Routine and high-precision radiocarbon dating. Radiocarbon 52(2):252-62.

Concordance of Collagen-Based Radiocarbon and Aspartic-Acid Racemization Ages

PubMed Central

Bada, Jeffrey L.; Schroeder, Roy A.; Protsch, Reiner; Berger, Rainer

1974-01-01

By determining the extent of racemization of aspartic acid in a well-dated bone, it is possible to calculate the in situ first-order rate constant for the interconversion of the L and D enantiomers of aspartic acid. Collagen-based radiocarbon-dated bones are shown to be suitable samples for use in “calibrating” the racemization reaction. Once the aspartic-acid racemization reaction has been “calibrated” for a site, the reaction can be used to date other bones from the deposit. Ages deduced by this method are in good agreement with radiocarbon ages. These results provide evidence that the aspartic-acid racemization reaction is an important chronological tool for dating bones either too old or too small for radiocarbon dating. As an example of the potential application of the technique for dating fossil man, a piece of Rhodesian Man from Broken Hill, Zambia, was analyzed and tentatively assigned an age of about 110,000 years. PMID:4522802

Investigations of (Delta)14C, (delta)13C, and (delta)15N in vertebrae of white shark (Carcharodon carcharias) from the eastern North Pacific Ocean

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kerr, L A; Andrews, A H; Cailliet, G M

The white shark (Carcharodon carcharias) has a complex life history that is characterized by large scale movements and a highly variable diet. Estimates of age and growth for the white shark from the eastern North Pacific Ocean indicate they have a slow growth rate and a relatively high longevity. Age, growth, and longevity estimates useful for stock assessment and fishery models, however, require some form of validation. By counting vertebral growth band pairs, ages can be estimated, but because not all sharks deposit annual growth bands and many are not easily discernable, it is necessary to validate growth band periodicitymore » with an independent method. Radiocarbon ({sup 14}C) age validation uses the discrete {sup 14}C signal produced from thermonuclear testing in the 1950s and 1960s that is retained in skeletal structures as a time-specific marker. Growth band pairs in vertebrae, estimated as annual and spanning the 1930s to 1990s, were analyzed for {Delta}{sup 14}C and stable carbon and nitrogen isotopes ({delta}{sup 13}C and {delta}{sup 15}N). The aim of this study was to evaluate the utility of {sup 14}C age validation for a wide-ranging species with a complex life history and to use stable isotope measurements in vertebrae as a means of resolving complexity introduced into the {sup 14}C chronology by ontogenetic shifts in diet and habitat. Stable isotopes provided useful trophic position information; however, validation of age estimates was confounded by what may have been some combination of the dietary source of carbon to the vertebrae, large-scale movement patterns, and steep {sup 14}C gradients with depth in the eastern North Pacific Ocean.« less

Radiocarbon Dating of the Human Eye Lens Crystallines Reveal Proteins without Carbon Turnover throughout Life

PubMed Central

Lynnerup, Niels; Kjeldsen, Henrik; Heegaard, Steffen; Jacobsen, Christina; Heinemeier, Jan

2008-01-01

Background Lens crystallines are special proteins in the eye lens. Because the epithelial basement membrane (lens capsule) completely encloses the lens, desquamation of aging cells is impossible, and due to the complete absence of blood vessels or transport of metabolites in this area, there is no subsequent remodelling of these fibers, nor removal of degraded lens fibers. Human tissue ultimately derives its 14C content from the atmospheric carbon dioxide. The 14C content of the lens proteins thus reflects the atmospheric content of 14C when the lens crystallines were formed. Precise radiocarbon dating is made possible by comparing the 14C content of the lens crystallines to the so-called bomb pulse, i.e. a plot of the atmospheric 14C content since the Second World War, when there was a significant increase due to nuclear-bomb testing. Since the change in concentration is significant even on a yearly basis this allows very accurate dating. Methodology/Principal Findings Our results allow us to conclude that the crystalline formation in the lens nucleus almost entirely takes place around the time of birth, with a very small, and decreasing, continuous formation throughout life. The close relationship may be further expressed as a mathematical model, which takes into account the timing of the crystalline formation. Conclusions/Significance Such a life-long permanence of human tissue has hitherto only been described for dental enamel. In confront to dental enamel it must be held in mind that the eye lens is a soft structure, subjected to almost continuous deformation, due to lens accommodation, yet its most important constituent, the lens crystalline, is never subject to turnover or remodelling once formed. The determination of the 14C content of various tissues may be used to assess turnover rates and degree of substitution (for example for brain cell DNA). Potential targets may be nervous tissues in terms of senile or pre-senile degradation, as well as other highly

A reevaluation of the Pallett Creek earthquake chronology based on new AMS radiocarbon dates, San Andreas fault, California

NASA Astrophysics Data System (ADS)

Scharer, Katherine M.; Biasi, Glenn P.; Weldon, Ray J., II

2011-12-01

The Pallett Creek paleoseismic record occupies a keystone position in most attempts to develop rupture histories for the southern San Andreas fault. Previous estimates of earthquake ages at Pallett Creek were determined by decay counting radiocarbon methods. That method requires large samples which can lead to unaccounted sources of uncertainty in radiocarbon ages because of the heterogeneous composition of organic layers. In contrast, accelerator mass spectrometry (AMS) radiocarbon dates may be obtained from small samples that have known carbon sources and also allow for a more complete sampling of the section. We present 65 new AMS radiocarbon dates that span nine ground-rupturing earthquakes at Pallett Creek. Overall, the AMS dates are similar to and reveal no dramatic bias in the conventional dates. For many layers, however, individual charcoal samples were younger than the conventional dates, leading to earthquake ages that are overall slightly younger than previously reported. New earthquake ages are determined by Bayesian refinement of the layer ages based on stratigraphic ordering and sedimentological constraints. The new chronology is more regular than previously published records in large part due to new samples constraining the age of event R. The closed interval from event C to 1857 has a mean recurrence of 135 years (σ = 83.2 years) and a quasiperiodic coefficient of variation (COV) of 0.61. We show that the new dates and resultant earthquake chronology have a stronger effect on COV than the specific membership of this long series and dating precision improvements from sedimentation rates.

Determination of transfer rate and nature of the residue(s) in milk from {sup 14}C-atrazine cows

DOE Office of Scientific and Technical Information (OSTI.GOV)

Thalacker, F.W.; Ash, S.G.; Simoneaux, B.J.

1996-10-01

In order to determine the rate of transfer and the nature of the atrazine residues present in milk, lactating dairy cattle were treated with atrazine at three concentrations, 0.764 ppm, 0.0747 ppm and 0.0085 ppm (dry weight of food consumed). The concentrations were selected to bridge the gap between the concentration used for EPA metabolism studies (10 ppm) and the potential exposure level of dairy cattle to atrazine and its chlorotriazine metabolites through feed. The cattle were dosed following the morning milking for nine consecutive days with a single capsule bolus of {sup 14}C-atrazine. Milk was collected twice daily andmore » aliquots of each milking and the individual cow`s daily pool of milk were analyzed by liquid scinitllation counting (LSC). The concentrations of {sup 14}C-residues in the milk plateaued on approximately day 3 and the mean {sup 14}C-atrazine levels in milk were 11.2 ppb, 1.13 ppb and 0.152 ppb for the high, middle and low dosed animals, respectively. The transfer of radioactive level of exposure to {sup 14}C-atrazine. The nature of the residues in milk were determined by extracting milk samples and analysis by HPLC, TLC or Aminex chromatography. Diaminchlorotriazine was the only chlorinated metabolite in the milk, constituting approximately 65% to 75% of the total radioactive residues (TRR).« less

Radiocarbon Dating the Anthropocene

NASA Astrophysics Data System (ADS)

Chaput, M. A.; Gajewski, K. J.

2015-12-01

The Anthropocene has no agreed start date since current suggestions for its beginning range from Pre-Industrial times to the Industrial Revolution, and from the mid-twentieth century to the future. To set the boundary of the Anthropocene in geological time, we must first understand when, how and to what extent humans began altering the Earth system. One aspect of this involves reconstructing the effects of prehistoric human activity on the physical landscape. However, for global reconstructions of land use and land cover change to be more accurately interpreted in the context of human interaction with the landscape, large-scale spatio-temporal demographic changes in prehistoric populations must be known. Estimates of the relative number of prehistoric humans in different regions of the world and at different moments in time are needed. To this end, we analyze a dataset of radiocarbon dates from the Canadian Archaeological Radiocarbon Database (CARD), the Palaeolithic Database of Europe and the AustArch Database of Australia, as well as published dates from South America. This is the first time such a large quantity of dates (approximately 60,000) has been mapped and studied at a global scale. Initial results from the analysis of temporal frequency distributions of calibrated radiocarbon dates, assumed to be proportional to population density, will be discussed. The utility of radiocarbon dates in studies of the Anthropocene will be evaluated and potential links between population density and changes in atmospheric greenhouse gas concentrations, climate, migration patterning and fire frequency coincidence will be considered.

Structure of C 14 and B 14 from the C 14 , 15 ( d , He 3 ) B 13 , 14 reactions

DOE Office of Scientific and Technical Information (OSTI.GOV)

Bedoor, S.; Wuosmaa, A. H.; Albers, M.

We have studied the C-14,C-15(d,He-3)B-13,B-14 proton-removing reactions in inverse kinematics. The (d,He-3) reaction probes the proton occupation of the target ground state, and also provides spectroscopic information about the final states in B-13,B-14. The experiments were performed using C-14,C-15 beams from the ATLAS accelerator at Argonne National Laboratory. The reaction products were analyzed with the HELIOS device. Angular distributions were obtained for transitions from both reactions. The C-14-beam data reveal transitions to excited states in B-13 that suggest configurations with protons outside the pi(0p(3/2)) orbital, and some possibility of proton cross-shell 0p-1s0d excitations, in the C-14 ground state. The C-15-beammore » data confirm the existence of a broad 2(-) excited state in B-14. The experimental data are compared to the results of shell-model calculations.« less

Marine04 Marine radiocarbon age calibration, 26 ? 0 ka BP

DOE Office of Scientific and Technical Information (OSTI.GOV)

Hughen, K; Baille, M; Bard, E

2004-11-01

New radiocarbon calibration curves, IntCal04 and Marine04, have been constructed and internationally ratified to replace the terrestrial and marine components of IntCal98. The new calibration datasets extend an additional 2000 years, from 0-26 ka cal BP (Before Present, 0 cal BP = AD 1950), and provide much higher resolution, greater precision and more detailed structure than IntCal98. For the Marine04 curve, dendrochronologically dated tree-ring samples, converted with a box-diffusion model to marine mixed-layer ages, cover the period from 0-10.5 ka cal BP. Beyond 10.5 ka cal BP, high-resolution marine data become available from foraminifera in varved sediments and U/Th-dated corals.more » The marine records are corrected with site-specific {sup 14}C reservoir age information to provide a single global marine mixed-layer calibration from 10.5-26.0 ka cal BP. A substantial enhancement relative to IntCal98 is the introduction of a random walk model, which takes into account the uncertainty in both the calendar age and the radiocarbon age to calculate the underlying calibration curve. The marine datasets and calibration curve for marine samples from the surface mixed layer (Marine04) are discussed here. The tree-ring datasets, sources of uncertainty, and regional offsets are presented in detail in a companion paper by Reimer et al.« less

Analysis of past recurrent methane seep activity using radiocarbon dating of Calyptogena spp. shells in the eastern Nankai subduction zone, Japan

NASA Astrophysics Data System (ADS)

Yagasaki, Kazuhiro; Ashi, Juichiro; Yokoyama, Yusuke; Miyairi, Yosuke; Kuramoto, Shin'ichi

2016-04-01

Fault activity around subduction zones have been widely studied and monitored through drilling of oceanic plates, studying piston cores, use of monitoring equipment or through visual analysis using submersible vehicles. Yet the understanding of how small scale faults near shallow regions of the seabed behave in relation to cold seep vent activity is still vague, especially determining when they were active in the past. In tectonically active margins such as the Nankai and Tokai regions off Japan, dense methane hydrate reservoirs have been identified. Cold seeps releasing methane rich hydrocarbon fluids are common here, supporting a wide variety of biological species that hold a symbiotic relationship with the chemosynthetic bacteria. In 1998 a large dead Calyptogena spp. bivalve colony (over 400m2 in size) was discovered off Tokai, Japan. It is unusual for a bivalve colony this size to mostly be dead, raising questions as to what caused their death. In this study we document the radiocarbon 14C age of these bivalve shells to attempt analysing the possible methane seep bahaviour in the past. The measured 14C age ranged in three age groups of 1396±36-1448±34, 1912±31-1938±35 and 5975±34. The 14C age of shells that were alive upon collection and the dissolved inorganic carbon (DIC) in seawater show little difference (˜100 14C age) indicating that shells are not heavily affected by the dead carbon effect from cold seeps that is of biogenic or thermogenic origin, which can make the age to become considerably older than the actual age. Thus the novel calibration model used was based on the seawater DIC collected above the Calyptogena spp. colony site (1133±31), which resulted in the dead shells to be clustered around 1900 Cal AD. This proves to be interesting as the predicted epicenter of the Ansei-Tokai earthquake (M 8.4) in 1854 is extremely close to the bibalve colony site. Using geological data obtained using visual analysis and sub-seafloor structural

Determination of Natural 14C Abundances in Dissolved Organic Carbon in Organic-Rich Marine Sediment Porewaters by Thermal Sulfate Reduction

NASA Astrophysics Data System (ADS)

Johnson, L.; Komada, T.

2010-12-01

The abundances of natural 14C in dissolved organic carbon (DOC) in the marine environment hold clues regarding the processes that influence the biogeochemical cycling of this large carbon reservoir. At present, UV irradiation is the widely accepted method for oxidizing seawater DOC for determination of their 14C abundances. This technique yields precise and accurate values with low blanks, but it requires a dedicated vacuum line, and hence can be difficult to implement. As an alternative technique that can be conducted on a standard preparatory vacuum line, we modified and tested a thermal sulfate reduction method that was previously developed to determine δ13C values of marine DOC (Fry B. et al., 1996. Analysis of marine DOC using a dry combustion method. Mar. Chem., 54: 191-201.) to determine the 14C abundances of DOC in marine sediment porewaters. In this method, the sample is dried in a 100 ml round-bottom Pyrex flask in the presence of excess oxidant (K2SO4) and acid (H3PO4), and combusted at 550 deg.C. The combustion products are cryogenically processed to collect and quantify CO2 using standard procedures. Materials we have oxidized to date range from 6-24 ml in volume, and 95-1500 μgC in size. The oxidation efficiency of this method was tested by processing known amounts of reagent-grade dextrose and sucrose (as examples of labile organic matter), tannic acid and humic acid (as examples of complex natural organic matter), and porewater DOC extracted from organic-rich nearshore sediments. The carbon yields for all of these materials averaged 99±4% (n=18). The 14C abundances of standard materials IAEA C-6 and IAEA C-5 processed by this method using >1mgC aliquots were within error of certified values. The size and the isotopic value of the blank were determined by a standard dilution technique using IAEA C-6 and IAEA C-5 that ranged in size from 150 to 1500 μgC (n=4 and 2, respectively). This yielded a blank size of 6.7±0.7 μgC, and a blank isotopic

Cross-checking groundwater age by 4He and 14C dating in a granite, Tono area, central Japan

NASA Astrophysics Data System (ADS)

Hasegawa, Takuma; Nakata, Kotaro; Tomioka, Yuichi; Goto, Kazuyuki; Kashiwaya, Koki; Hama, Katsuhiro; Iwatsuki, Teruki; Kunimaru, Takanori; Takeda, Masaki

2016-11-01

Groundwater dating was performed simultaneously by the 4He and 14C methods in granite of the Tono area in central Japan. Groundwater was sampled at 30 packed-off sections of six 1000-m boreholes. 4He concentrations increased and 14C concentrations decreased along a groundwater flow path on a topographic gradient. 4He ages were calculated by using the in situ 4He production rate derived from the porosity, density, and U and Th content of the rock, neglecting external flux. 14C ages were calculated with a noncorrected model in which the initial 14C content was 100 percent of the modern radiocarbon level (Co = 100 pmC), a statistical model using the average 14C content of tritium-bearing samples (Co = 46.4 pmC), and a δ13C model based on the isotopic mass balance. Although the absolute 14C ages calculated by the models were different, the relative 14C ages were almost identical. The relative 14C ages were considered reliable because dissolved inorganic carbon has no significant geochemical reactions in granite. The relation between the 4He ages and the noncorrected 14C ages was [4He age] = 1.15 [14C age] + 7200 (R2 = 0.81), except in the discharge area. The slope of this relation was equivalent to unity, which indicates that the 4He accumulation rate is confirmed by the relative 14C ages. Moreover, the accumulated 3He/4He ratio was equivalent to that derived from the 6Li(α,n)3H reaction in granite. These results show that the accumulated He is of crustal origin, produced in situ without external flux, except in the discharge area. The intercept value of 7200 a implies that the 14C concentrations were diluted due to geochemical reactions. Tritium-bearing samples supported this result. Simultaneous measurements make it feasible to estimate the accumulation rate of 4He and initial dilution of 14C, which cannot be done with a single method. Cross-checking groundwater dating has the potential to provide more reliable groundwater ages. The circulation time of the

RADIOCARBON SOURCE APPORTIONMENT IN A BIOFUELS ERA

EPA Science Inventory

Biofuels (gasohol and biodiesel) introduce radiocarbon into the U.S. mobile source fuel supply where it was previously absent. Initial measurements of radiocarbon in the PM_2.5 combustion emissions from engines using gasohol indicate that this may have less effect on r...

Interface dissolution control of the 14C profile in marine sediment

USGS Publications Warehouse

Keir, R.S.; Michel, R.L.

1993-01-01

The process of carbonate dissolution at the sediment-water interface has two possible endmember boundary conditions. Either the carbonate particles dissolve mostly before they are incorporated into the sediment by bioturbation (interface dissolution), or the vertical mixing is rapid relative to their extermination rate (homogeneous dissolution). In this study, a detailed radiocarbon profile was determined in deep equatorial Pacific sediment that receives a high rate of carbonate supply. In addition, a box model of sediment mixing was used to simulate radiocarbon, carbonate content and excess thorium profiles that result from either boundary process following a dissolution increase. Results from homogeneous dissolution imply a strong, very recent erosional event, while interface dissolution suggests that moderately increased dissolution began about 10,000 years ago. In order to achieve the observed mixed layer radiocarbon age, increased homogeneous dissolution would concentrate a greater amount of clay and 230Th than is observed, while for interface dissolution the predicted concentrations are too small. These results together with small discontinuities beneath the mixed layer in 230Th profiles suggest a two-stage increase in interface dissolution in the deep Pacific, the first occurring near the beginning of the Holocene and the second more recently, roughly 5000 years ago. ?? 1993.

Contribution of deep sourced carbon from hydrocarbon seeps to sedimentary organic carbon: Evidence from Δ14C and δ13C isotopes

NASA Astrophysics Data System (ADS)

Feng, D.; Peckmann, J.; Peng, Y.; Liang, Q.; Roberts, H. H.; Chen, D.

2017-12-01

Sulfate-driven anaerobic oxidation of methane (AOM) limits the release of methane from marine sediments and promotes the formation of carbonates close to the seafloor along continental margins. It has been established that hydrocarbon seeps are a source of dissolved inorganic and organic carbon to marine environments. However, questions remain about the contribution of deep sourced carbon from hydrocarbon seeps to the sedimentary organic carbon pool. For a number of hydrocarbon seeps from the South China Sea and the Gulf of Mexico, the portion of modern carbon was determined based on natural radiocarbon abundances (Δ14C) and stable carbon isotope (δ13Corganic carbon) compositions of the non-carbonate fractions extracted from authigenic carbonates. Samples from both areas show a mixing trend between ideal planktonic organic carbon (δ13C = -22‰ VPDB and 90% modern carbon) and the ambient methane. The δ13Corganic carbon values of non-carbonate fractions from three ancient seep deposits (northern Italy, Miocene; western Washington State, USA, Eocene to Oligocene) confirm that the proxy can be used to constrain the record of sulfate-driven AOM through most of Earth history by measuring the δ13C values of organic carbon. This study reveals the potential of using δ13C values of organic carbon to discern seep and non-seep environments. This new approach is particularly promising when authigenic carbonate is not present in ancient sedimentary environments. Acknowledgments: The authors thank BOEM and NOAA for their years' support of the deep-sea dives. Funding was provided by the NSF of China (Grants: 41422602 and 41373085).

Revised age of deglaciation of Lake Emma based on new radiocarbon and macrofossil analyses

USGS Publications Warehouse

Elias, S.A.; Carrara, P.E.; Toolin, L.J.; Jull, A.J.T.

1991-01-01

Previous radiocarbon ages of detrital moss fragments in basal organic sediments of Lake Emma indicated that extensive deglaciation of the San Juan Mountains occurred prior to 14,900 yr B.P. (Carrara et al., 1984). Paleoecological analyses of insect and plant macrofossils from these basal sediments cast doubt on the reliability of the radiocarbon ages. Subsequent accelerator radiocarbon dates of insect fossils and wood fragments indicate an early Holocene age, rather than a late Pleistocene age, for the basal sediments of Lake Emma. These new radiocarbon ages suggest that by at least 10,000 yr B.P. deglaciation of the San Juan Mountains was complete. The insect and plant macrofossils from the basal organic sediments indicate a higher-than-present treeline during the early Holocene. The insect assemblages consisted of about 30% bark beetles, which contrasts markedly with the composition of insects from modern lake sediments and modern specimens collected in the Lake Emma cirque, in which bark beetles comprise only about 3% of the assemblages. In addition, in the fossil assemblages there were a number of flightless insect species (not subject to upslope transport by wind) indicative of coniferous forest environments. These insects were likewise absent in the modern assemblage. ?? 1991.

Agriculture, population growth, and statistical analysis of the radiocarbon record.

PubMed

Zahid, H Jabran; Robinson, Erick; Kelly, Robert L

2016-01-26

The human population has grown significantly since the onset of the Holocene about 12,000 y ago. Despite decades of research, the factors determining prehistoric population growth remain uncertain. Here, we examine measurements of the rate of growth of the prehistoric human population based on statistical analysis of the radiocarbon record. We find that, during most of the Holocene, human populations worldwide grew at a long-term annual rate of 0.04%. Statistical analysis of the radiocarbon record shows that transitioning farming societies experienced the same rate of growth as contemporaneous foraging societies. The same rate of growth measured for populations dwelling in a range of environments and practicing a variety of subsistence strategies suggests that the global climate and/or endogenous biological factors, not adaptability to local environment or subsistence practices, regulated the long-term growth of the human population during most of the Holocene. Our results demonstrate that statistical analyses of large ensembles of radiocarbon dates are robust and valuable for quantitatively investigating the demography of prehistoric human populations worldwide.

Development of radiocarbon-based methods to investigate atmospheric fossil carbon pollution

NASA Astrophysics Data System (ADS)

Major, István; Vodila, Gergely; Furu, Enikő; Kertész, Zsófia; Haszpra, László; Hajdas, Irka; Molnár, Mihály

2013-04-01

Gaseous and solid state carbon containing compounds significantly affect global climate change based on current atmospheric research results. Major part of the anthropogenic changes of the atmospheric carbon dioxide can be attributed to the combustion of fossil fuels and 95% of their emission is realised in the industrially active areas of the northern hemisphere. Anthropogenic carbonaceous aerosol particles play also a key role in the atmosphere modifying indirectly climate change and the quality of the environment and affecting directly human health. Since September 2008, the CO2 concentration of the air and its specific radiocarbon content (14C) has been monitored in the city of Debrecen (Hungary) and in a rural background site, Hegyhátsál (Hungary). To obtain a more representative view regarding anthropogenic contribution of the atmospheric carbon species, our measurement programme was enhanced by including the investigation of atmospheric aerosols in 2010. An aerosol cascade sampler for continuous monitoring was installed close to the atmospheric CO2 sampling station in the inner city of Debrecen. For 14C measurements, special sample preparation system and method was developed for the tiny total carbon content of the aerosol samples collected synchronously with the carbon dioxide observations. The radiocarbon measurement of the aerosol samples was performed by a high-sensitivity accelerator mass spectrometer (AMS) dedicated to environmental samples (EnvironMICADAS) developed together with ETH Zürich. The δ13C values of the samples were measured by the Dual Inlet system of a Delta PLUS XP Isotope Ratio Mass Spectrometer from the tiny CO2 amount aimed to reserve. The atmospheric fossil CO2 and fossil PM2.5 concentration variations show high similarity in the air of Debrecen city. During the winter heating period, due to the meteorological conditions (frequent thermal inversion, decreasing rate of mixing and upwelling), significantly higher total PM2

Root-Uptake of C-14 Acetic Acid by Various Plants and C-14 Dynamics Surrounding the Experimental Tessera

DOE Office of Scientific and Technical Information (OSTI.GOV)

Ogiyama, S.; Takeda, H.; Uchida, S.

Carbon-14 (C-14, t{sub 1/2} = 5.73x10{sup 3} yrs) from radioactive waste is one of the most important radioactive nuclides for environmental assessment in the context of geological disposal, and understanding the transfer of radioactive elements to plants is essential for public health safety. In order to obtain fundamental knowledge, culture experiments using marigold (Tagetes patula L.), tall fescue (Festuca arundinacea S.), paddy rice (Oryza sativa L.), radish (Raphanus sativus L.), and carrot (Daucus carota L.) plants were conducted to examine root-uptake and dynamics of C-14 in the laboratory. The C-14 radioactivity in each plant part (e.g. shoot, root, edible part,more » etc.), medium (e.g. culture solution, sand, etc.), and air was determined. The distribution of C-14 in the plants was visualized using autoradiography. For a comparison, autoradiography was also done using Na-22. Results of the present study indicated that C-14 labeled CO{sub 2} gas was released from the culture solution to the atmosphere. Clear autoradiography images were observed in plants for the shoots and lower roots which were soaked in the culture solution. The upper roots which were not soaked in the culture solution were not clearly imaged. In the radiotracer experiment using Na-22, a clear image was observed for the whole carrot seedling, even including the upper root, on the autoradiography. However, the amounts of C-14 acetic acid absorbed by all the plants through their roots were considered to be very small. Inorganic carbon transformed from C-14 acetic acid would be taken up by plants through the roots, and some fraction of C-14 would be assimilated into the shoots by photosynthesis. (authors)« less

In situ cosmogenic radiocarbon production and 2-D ice flow line modeling for an Antarctic blue ice area

NASA Astrophysics Data System (ADS)

Buizert, Christo; Petrenko, Vasilii V.; Kavanaugh, Jeffrey L.; Cuffey, Kurt M.; Lifton, Nathaniel A.; Brook, Edward J.; Severinghaus, Jeffrey P.

2012-06-01

Radiocarbon measurements at ice margin sites and blue ice areas can potentially be used for ice dating, ablation rate estimates and paleoclimatic reconstructions. Part of the measured signal comes from in situ cosmogenic 14C production in ice, and this component must be well understood before useful information can be extracted from 14C data. We combine cosmic ray scaling and production estimates with a two-dimensional ice flow line model to study cosmogenic 14C production at Taylor Glacier, Antarctica. We find (1) that 14C production through thermal neutron capture by nitrogen in air bubbles is negligible; (2) that including ice flow patterns caused by basal topography can lead to a surface 14C activity that differs by up to 25% from the activity calculated using an ablation-only approximation, which is used in all prior work; and (3) that at high ablation margin sites, solar modulation of the cosmic ray flux may change the strength of the dominant spallogenic production by up to 10%. As part of this effort we model two-dimensional ice flow along the central flow line of Taylor Glacier. We present two methods for parameterizing vertical strain rates, and assess which method is more reliable for Taylor Glacier. Finally, we present a sensitivity study from which we conclude that uncertainties in published cosmogenic production rates are the largest source of potential error. The results presented here can inform ongoing and future 14C and ice flow studies at ice margin sites, including important paleoclimatic applications such as the reconstruction of paleoatmospheric 14C content of methane.

Radial ooids from Great Salt Lake (Utah) as paleoenvironmental archives: Insights from radiocarbon chronology and stable isotopes

NASA Astrophysics Data System (ADS)

Paradis, O. P.; Corsetti, F. A.; Bardsley, A.; Hammond, D. E.; Xu, X.; Walker, J. C.

2017-12-01

Ooids (laminated, carbonate coated grains) are ubiquitous in the geologic record in marine and lacustrine settings, and thus remain a common target for geochemical analysis to understand modern and ancient aqueous environments. However, the processes governing ooid formation remain unclear. Recently, radiocarbon dating has revealed that modern marine ooids grow slowly (Beaupre et al. 2015), and laboratory experiments have highlighted the importance of sediment transport and abrasion on net growth rates and ooid size (Trower et al. 2017). Ooid cortex structure includes micritic, tangential and/or radially oriented fabrics. Most modern marine ooids have tangential or micritic cortices, whereas many ancient ooids have radial cortices—thus, there is a need to understand how radial ooids in ancient rocks might inform us about their depositional environment. The Great Salt Lake (GSL), Utah, provides a unique environment to assess the growth rate of primary radial aragonitic ooids. Ooids collected near Antelope Island in the south arm of GSL were sieved, the 355-500 µm fraction was sequentially leached, and 14C of the evolved gas was analyzed to provide a time series of growth. The oldest inorganic carbon of this size fraction has an apparent 14C age of 6600 yr BP, with subsequent growth spanning over 6,000 years. Closed-basin lakes are particularly susceptible to a "reservoir effect" which results in anomalously old apparent radiocarbon ages. The 14C age of the modern dissolved inorganic carbon (DIC) of the south arm was measured to be 295 yr BP, a reservoir age comparable to estimates from lacustrine cave carbonates (McGee et al. 2012). Net growth rate of south arm ooids ranges between 0.01-0.025 µm per year. The δ13C of the outermost cortex suggests that the ooids resemble the modern DIC in the south arm water, suggesting ooids precipitate in equilibrium with lake water. Finer-scale structure in the δ13C of the ooid cortex through time suggests lake level changed

Evaluating microbial carbon sources in Athabasca oil sands tailings ponds using natural abundance stable and radiocarbon isotopes

NASA Astrophysics Data System (ADS)

Ahad, J. M.; Pakdel, H.

2013-12-01

Natural abundance stable (δ13C) and radiocarbon (Δ14C) isotopes of phospholipid fatty acids (PLFAs) were used to evaluate the carbon sources utilized by the active microbial populations in surface sediments from Athabasca oil sands tailings ponds. The absence of algal-specific PLFAs at three of the four sites investigated, in conjunction with δ13C signatures for PLFAs that were generally within ~3‰ of that reported for oil sands bitumen (~ -30‰), indicated that the microbial communities growing on petroleum constituents were dominated by aerobic heterotrophs. The Δ14C values of PLFAs ranged from -906 to -586‰ and pointed to a significant uptake of fossil carbon (up to ~90% of microbial carbon derived from petroleum), particularly in PLFAs (e.g., cy17:0 and cy19:0) often associated with petroleum hydrocarbon degrading bacteria. The comparatively higher levels of 14C in other, less specific PLFAs (e.g., 16:0) indicated the preferential uptake of younger organic matter by the general microbial population (~50-80% of microbial carbon derived from petroleum). Since the main carbon pools in tailings sediment were essentially 'radiocarbon dead' (i.e., no detectable 14C), the principal source for this modern carbon is considered to be the Athabasca River, which provides the bulk of the water used in the bitumen extraction process. The preferential uptake of the minor amount of young and presumably more biodegradable material present in systems otherwise dominated by recalcitrant petroleum constituents has important implications for remediation strategies. On the one hand, it implies that mining-related organic contaminants could persist in the environment long after tailings pond reclamation has begun. Alternatively, it may be that the young, labile organic matter provided by the Athabasca River plays an important role in stimulating or supporting the microbial utilization of petroleum carbon in oil sands tailings ponds via co-metabolism or priming processes

Status report: Implementation of gas measurements at the MAMS 14C AMS facility in Mannheim, Germany

NASA Astrophysics Data System (ADS)

Hoffmann, Helene; Friedrich, Ronny; Kromer, Bernd; Fahrni, Simon

2017-11-01

By implementing a Gas Interface System (GIS), CO2 gas measurements for radiocarbon dating of small environmental samples (<100 μgC) have been established at the MICADAS (Mini Carbon Dating System) AMS instrument in Mannheim, Germany. The system performance has been optimized and tested with respect to stability and ion yield by repeated blank and standard measurements for sample sizes down to 3 μgC. The highest 12C- low-energy (LE) ion currents, typically reaching 8-15 μA, could be achieved for a mixing ratio of 4% CO2 in Helium, resulting in relative counting errors of 1-2% for samples larger than 10 μgC and 3-7% for sample sizes below 10 μgC. The average count rate was ca. 500 counts per microgram C for OxII standard material. The blank is on the order of 35,000-40,000 radiocarbon years, which is comparable to similar systems. The complete setup thus enables reliable dating for most environmental samples (>3 μgC).

The feasibility of bomb radiocarbon analysis to support an age-at-length relationship for red abalone, Haliotis rufescens Swainson in northern California

DOE Office of Scientific and Technical Information (OSTI.GOV)

Leaf, R T; Andrews, A H; Cailliet, G M

2009-01-07

Analysis of bomb generated radiocarbon ({sup 14}C) changes in a red abalone, Haliotis rufescens Swainson shell was used to investigate age-at-length relationships derived from data from a previous multi-year, multi-site tag-recapture study. Shell carbonate was extracted from four successive growth trajectory locations in a single shell with a length of 251 mm MSL. Extraction locations were based on VBGF predictions and chosen to span the initial rise of the {sup 14}C-bomb pulse that is known to have occurred in surface ocean waters during 1958 {+-} 1 y in the northeast Pacific. The close temporal correspondence of the red abalone samplemore » series to regional {Delta}{sup 14}C records demonstrated the utility of the technique for validating age-at-length relationships for the red abalone. The findings provided support for a mean VBGF derived age of 32 y (range 30 to 33 y) for the specimen; however, the analysis of {sup 14}C data indicated that the specimen could be older.« less

Carbon Isotopes Profiles of Human Whole Blood, Plasma, Red Blood Cells, Urine and Feces for Biological/Biomedical 14C-Accelerator Mass Spectrometry Applications

PubMed Central

Kim, Seung-Hyun; Chuang, Jennifer C.; Kelly, Peter B.; Clifford, Andrew J.

2011-01-01

Radiocarbon (14C) is an ideal tracer for in vivo human ADME (absorption, distribution, metabolism, elimination) and PBPK (physiological-based pharmacokinetic) studies. Living plants preferentially incorporate atmospheric 14CO2, vs 13CO2, vs 12CO2, which result in unique signature. Furthermore, plants and the food chains they support also have unique carbon isotope signatures. Humans, at the top of the food chain, consequently acquire isotopic concentrations in the tissues and body fluids depending on their dietary habits. In preparation of ADME and PBPK studies, 12 healthy subjects were recruited. The human baseline (specific to each individual and their diet) total carbon (TC) and carbon isotope 13C (δ13C) and 14C (Fm) were quantified in whole blood (WB), plasma, washed red blood cell (RBC), urine, and feces. TC (mg of C/100μL) in WB, plasma, RBC, urine, and feces were 11.0, 4.37, 7.57, 0.53, and 1.90, respectively. TC in WB, RBC, and feces was higher in men over women, P < 0.05. Mean δ13C were ranked low to high as follows, feces < WB = plasma = RBC = urine, P < 0.0001. δ13C was not affected by gender. Our analytic method shifted δ13C by only ± 1.0 ‰ ensuring our Fm measurements were accurate and precise. Mean Fm were ranked low to high as follows, plasma = urine < WB = RBC = feces, P < 0.05. Fm in feces was higher for men over women, P < 0.05. Only in WB, 14C levels (Fm) and TC were correlated with one another (r = 0.746, P < 0.01). Considering the lag time to incorporate atmospheric 14C into plant foods (vegetarian) and or then into animal foods (non-vegetarian), the measured Fm of WB in our population (recruited April 2009) was 1.0468 ± 0.0022 (mean±SD), the Fm of WB matched the (extrapolated) atmospheric Fm of 1.0477 in 2008. This study is important in presenting a procedure to determine a baseline for a study group for human ADME and PBPK studies using 14C as a tracer. PMID:21452856

Millennial-scale variability in the local radiocarbon reservoir age of the Florida Keys reef tract during the Holocene

NASA Astrophysics Data System (ADS)

Ashe, E.; Toth, L. T.; Cheng, H.; Edwards, R. L.; Richey, J. N.

2016-12-01

The oceanic passage between the Florida Keys and Cuba, known as the Straits of Florida, provides a critical connection between the tropics and northern Atlantic. Changes in the character of water masses transported through this region may ultimately have important impacts on high-latitude climate variability. Although recent studies have documented significant changes in the density of regional surface waters over millennial timescales, little is known about the contribution of local- to regional-scale changes in circulation to surface-water variability. Local variability in the radiocarbon age, ΔR, of surface waters can be used to trace changes in local water-column mixing and/or changes in regional source water over a variety of spatial and temporal scales. We reconstructed "snapshots" of ΔR variability across the Florida Keys reef tract during the last 10,000 years by dating 68 unaltered corals collected from Holocene reef cores with both U-series and radiocarbon techniques. We combined the snapshots of ΔR into a semi-empirical model to develop a robust statistical reconstruction of millennial-scale variability in ΔR on the Florida Keys reef tract. Our model demonstrates that ΔR varied significantly during the Holocene, with relatively high values during the early Holocene and around 3000 years BP and relatively low values around 7000 years BP and at present. We compare the trends in ΔR to existing paleoceanographic reconstructions to evaluate the relative contribution of local upwelling versus changes in source water to the region as a whole in driving local radiocarbon variability, and discuss the importance of these results to our understanding of regional-scale oceanographic and climatic variability during the Holocene. We also discuss the implications of our results for radiocarbon dating of marine samples from south Florida and present a model of ΔR versus 14C age that can be used to improve the accuracy of radiocarbon calibrations from this region.

Source Apportionment of Elemental Carbon in Beijing, China: Insights from Radiocarbon and Organic Marker Measurements.

PubMed

Zhang, Yan-Lin; Schnelle-Kreis, Jürgen; Abbaszade, Gülcin; Zimmermann, Ralf; Zotter, Peter; Shen, Rong-rong; Schäfer, Klaus; Shao, Longyi; Prévôt, André S H; Szidat, Sönke

2015-07-21

Elemental carbon (EC) or black carbon (BC) in the atmosphere has a strong influence on both climate and human health. In this study, radiocarbon ((14)C) based source apportionment is used to distinguish between fossil fuel and biomass burning sources of EC isolated from aerosol filter samples collected in Beijing from June 2010 to May 2011. The (14)C results demonstrate that EC is consistently dominated by fossil-fuel combustion throughout the whole year with a mean contribution of 79% ± 6% (ranging from 70% to 91%), though EC has a higher mean and peak concentrations in the cold season. The seasonal molecular pattern of hopanes (i.e., a class of organic markers mainly emitted during the combustion of different fossil fuels) indicates that traffic-related emissions are the most important fossil source in the warm period and coal combustion emissions are significantly increased in the cold season. By combining (14)C based source apportionment results and picene (i.e., an organic marker for coal emissions) concentrations, relative contributions from coal (mainly from residential bituminous coal) and vehicle to EC in the cold period were estimated as 25 ± 4% and 50 ± 7%, respectively, whereas the coal combustion contribution was negligible or very small in the warm period.

Radiocarbon dating of silica sinter deposits in shallow drill cores from the Upper Geyser Basin, Yellowstone National Park

USGS Publications Warehouse

Lowenstern, Jacob B.; Hurwitz, Shaul; McGeehin, John

2016-01-01

To explore the timing of hydrothermal activity at the Upper Geyser Basin (UGB) in Yellowstone National Park, we obtained seven new accelerator mass spectrometry (AMS) radiocarbon 14C ages of carbonaceous material trapped within siliceous sinter. Five samples came from depths of 15–152 cm within the Y-1 well, and two samples were from well Y-7 (depths of 24 cm and 122 cm). These two wells, at Black Sand and Biscuit Basins, respectively, were drilled in 1967 as part of a scientific drilling program by the U.S. Geological Survey (White et al., 1975). Even with samples as small as 15 g, we obtained sufficient carbonaceous material (a mixture of thermophilic mats, pollen, and charcoal) for the 14C analyses. Apparent time of deposition ranged from 3775 ± 25 and 2910 ± 30 14C years BP at the top of the cores to about 8000 years BP at the bottom. The dates are consistent with variable rates of sinter formation at individual sites within the UGB over the Holocene. On a basin-wide scale, though, these and other existing 14C dates hint that hydrothermal activity at the UGB may have been continuous throughout the Holocene.

Changes in Soil Carbon Turnover after Five Years of Bioenergy Cropping Systems from a Long-Term Incubation Experiment and Radiocarbon Measurements.

NASA Astrophysics Data System (ADS)

Szymanski, L. M.; Sanford, G. R.; Heckman, K. A.; Jackson, R. D.; Marin-Spiotta, E.

2016-12-01

In the face of climate change, the global production of bioenergy crops has increased in response to policies calling for non-fossil energy sources as a means to mitigate rising atmospheric carbon (C) concentrations. To provide overall C sequestration benefits, identifying biomass crops that can maintain or enhance soil resources is desirable for sustainable bioenergy production. The objective of our study was to compare the effects of four bioenergy cropping systems on SOM dynamics in two agricultural soils: Mollisols at the University of Wisconsin Agricultural Research Station in Arlington, Wisconsin and Alfisols at Kellogg Biological Station in Hickory Corners, Michigan, USA. We used fresh soils collected in 2013 and archived soils collected in 2008 to measure differences among biofuel crops after 5 years of management. Using a 365-day laboratory soil incubation and radiocarbon measurements of bulk soil and respired C, we separated soils into three SOM pools and determined their corresponding turnover times. Total soil C respired from surface soils increased in the order: mixed species perennials > monoculture perennials > monoculture annuals. More C was associated with the active fraction in the sandy loam Alfisol and with the slow-cycling fraction in the silt loam Mollisol. Radiocarbon content of respired CO2 did not differ between corn and switchgrass, but did differ between 2008 and 2013. The respiration of more radiocarbon-depleted C after 5 years of cultivation may be due to an initial flux of young C following tillage in 2008 or to depletion of labile plant inputs with continued harvest. All bioenergy cropping systems lost soil C after 5 years. Monoculture perennial switchgrass systems did not provide significant C sequestration benefits, as expected, compared to monoculture annual corn systems. Bioenergy crop land-use change affects soil C dynamics, with implications for assessing C costs associated with biofuel production.

Use of Stored Carbon Reserves in Growth of Temperate Tree Roots and Leaf Buds: Analyses Using Radiocarbon Measurements and Modeling

DOE Office of Scientific and Technical Information (OSTI.GOV)

Gaudinski, Julia B.; Torn, Margaret S.; Riley, W. J.

2009-01-01

Characterizing the use of C reserves in trees is important for understanding stress responses, impacts of asynchrony between photosynthesis and growth demand, and isotopic exchanges in plant dynamic studies. Using an inadvertent, whole ecosystem radiocarbon (14C) exposure in a temperate deciduous oak forest and numerical modeling, we calculated that the mean age of stored C used to grow leaf buds and new fine root tissue is 0.5-1.0 y. The mean age of stored C used to grow new roots was about 0.7 y across a range of realistic values of 14C inputs to the system. The amount of stored Cmore » used on an annual basis to grow fine roots was between 15 and 55% of total root growth, with the range defined by the assumed 14C input profile. We estimate the annually-averaged mean age of C in new root tissues is 1-5 months. Therefore, accounting for storage C use in isotope root models may be unnecessary in all but the fastest cycling root populations (i.e., mean age <1 y). Consistent with the whole ecosystem labeling results, we found, using "bomb-14C," that the mean C age of new root tissues in three additional forest sites (one deciduous, two coniferous) was less than 2 years. We conclude that in many ecosystem types, growth from stored C is insufficient to impact bomb-14C based estimates of long root lifetimes.« less

Bomb-produced radiocarbon in the western tropical Pacific Ocean: Guam coral reveals operation-specific signals from the Pacific Proving Grounds

NASA Astrophysics Data System (ADS)

Andrews, Allen H.; Asami, Ryuji; Iryu, Yasufumi; Kobayashi, Donald R.; Camacho, Frank

2016-08-01

High-resolution radiocarbon (14C) analyses on a coral core extracted from Guam, a western tropical Pacific island, revealed a series of early bomb-produced 14C spikes. The typical marine bomb 14C signal—phase lagged and attenuated relative to atmospheric records—is present in the coral and is consistent with other regional coral records. However, 14C levels well above what can be attributed to air-sea diffusion alone punctuate this pattern. This anomaly was observed in other Indo-Pacific coral records, but the Guam record is unmatched in magnitude and temporal resolution. The Guam coral Δ14C record provided three spikes in 1954-1955, 1956-1957, and 1958-1959 that are superimposed on a normal 14C record. Relative to mean prebomb levels, the first peak rises an incredible ˜700‰ and remained elevated for ˜1.2 years. A follow up assay with finer resolution increased the peak by ˜300‰. Subsequent spikes were less intense with a rise of ˜35 and ˜70‰. Each can be linked to thermonuclear testing in the Pacific Proving Grounds at Bikini and Enewetak atolls in Operations Castle (1954), Redwing (1956), and Hardtack I (1958). These 14C signals can be explained by vaporization of coral reef material in the nuclear fireball, coupled with neutron activation of atmospheric nitrogen (14C production), and subsequent absorption of 14CO2 to form particulate carbonates of close-in fallout. The lag time in reaching Guam and other coral records abroad was tied to ocean surface currents and modeling provided validation of 14C arrival observations.

Source apportionment of carbonaceous aerosols in a megacity of northwest China: insights from radiocarbon measurement

NASA Astrophysics Data System (ADS)

Ni, Haiyan; Huang, Rujin; Dusek, Ulrike

2017-04-01

Fine particulate matter (PM2.5) samples were collected from 5 July 2008 to 27 June 2009 at Xi'an, a very polluted megacity in Northwest China. The 24 h averaged PM2.5concentrations (ranged from 32 μg m-3 to 339 μg m-3) were 1-14 times higher than the WHO guideline for 24 h PM2.5(25 μg m-3). In this work, we unambiguously quantify fossil (e.g., vehicle emissions, coal burning etc.) and non-fossil (e.g., biomass burning, cooking, biogenic emissions etc.) contributions to organic carbon (OC) and elemental carbon (EC) of PM2.5using radiocarbon (14C) measurement. In addition, we measured PM2.5 major components and source markers, including OC and EC, ions, trace elements, polycyclic aromatic hydrocarbons (PAHs), oxygenated PAHs (o-PAHs), anhydrous sugars and hopanes. The preliminary results of radiocarbon measurements in OC and EC show that the annual mean contributions from fossil-fuel combustion to EC was 76 ± 8% (6 ± 2 μg m-3). The remaining 24 ± 8% (2 ± 1 μg m-3) was attributed to biomass burning, with higher contribution in the cold period (˜33%) compared to the warm period (˜21%), due to enhanced emissions from local biomass burning activities in winter. In contrast with EC, OC was dominated by non-fossil sources, with an annual average of 54 ± 8 % (13 ± 10 μg m-3). Clear seasonal variations were seen in OC concentrations both from fossil fuel (OCff), and from non-fossil sources (OCnf), with maxima in the cold period and minima in the warm period, because of enhanced fossil and non-fossil activities in winter, mainly biomass burning and domestic coal burning. Further source apportionment of OC, including primary/secondary fossil OC, primary/secondary non-fossil OC, will be conducted by combining 14C results with positive matrix factorization (PMF) analysis of organic matter (OM).

Technique for Simultaneous Determination of [35S]Sulfide and [14C]Carbon Dioxide in Anaerobic Aqueous Samples †

PubMed Central

Taylor, Craig D.; Ljungdahl, Per O.; Molongoski, John J.

1981-01-01

A technique for the simultaneous determination of [35S]sulfide and [14C]carbon dioxide produced in anaerobic aqueous samples dual-labeled with [35S]sulfate and a 14C-organic substrate is described. The method involves the passive distillation of sulfide and carbon dioxide from an acidified water sample and their subsequent separation by selective chemical absorption. The recovery of sulfide was 93% for amounts ranging from 0.35 to 50 μmol; recovery of carbon dioxide was 99% in amounts up to 20 μmol. Within these delineated ranges of total sulfide and carbon dioxide, 1 nmol of [35S]sulfide and 7.5 nmol of [14C]carbon dioxide were separated and quantified. Correction factors were formulated for low levels of radioisotopic cross-contamination by sulfide, carbon dioxide, and volatile organic acids. The overall standard error of the method was ±4% for sulfide and ±6% for carbon dioxide. PMID:16345742

Reconstruction of Monsoon Driven South China Sea Surface Ocean Circulation using Coral Δ14C

NASA Astrophysics Data System (ADS)

Goodkin, N.; Bolton, A.; Karnauskas, K. B.; Hughen, K. A.; Griffin, S.; Druffel, E. R. M.

2016-12-01

The need to improve our understanding of annual and decadal climate behavior in the South China Sea is increasingly important, as this region includes the largest population density globally but encompasses few climate records. Here we present a record of annually resolved Δ14C from a coral collected off the coast of Nha Trang, Vietnam (12°12'49.90″N, 109°18'17.51″E), that reveals a significant correlation to regional winter sea level pressure (SLP) and sea surface temperature (SST), and extends back more than 400 years. Coral Δ14C during thermonuclear bomb testing indicates the presence of wet-season (summer) upwelling, demonstrated by low Δ14C values for both baseline and peak values relative to other records in the region (Bolton et al., 2016, Radiocarbon). However, annually resolved pre-bomb Δ14C correlates significantly to regional dry-season (winter) SLP and SST, indicating that annual variability is driven by changes to the East Asian Winter Monsoon (EAWM) and subsequent down-welling at this site. Spectral density is focused at 25, 11.8, 7, 4, and 3.2 years per cycle reflecting a range of influences on surface advection variability including the EAWM (D'Arrigo et al., 2005, GRL) and the El Nino Southern Oscillation (ENSO). Spectral power at all of these frequencies decreases following the Little Ice Age ( 1600-1850?) to today, indicating that wind driven surface advection was more variable when hemispheric temperatures were cooler. Decadal variance in the past 100 years is significantly correlated to variance records of the Arctic Oscillation (AO, Thompson and Wallace, 1989, GRL), suggesting that increasing variance in the EAWM may be tied to increasing variance of the AO during the Little Ice Age and vice versa.

Combined dendrochronological and radiocarbon dating of six Russian icons from the 15th-17th centuries

NASA Astrophysics Data System (ADS)

Dolgikh, A. V.; Matskovsky, V. V.; Voronin, K. V.; Solomina, O. N.

2017-06-01

The results of dendrochronological and radiocarbon dating by means of accelerator mass spectrometry (AMS) of six medieval icons, originating from northern European Russia and painted on wooden panels made from Scots pine, dated to the 15th to 17th centuries are presented. The panels of each icon were studied using dendrochronology. Five to six AMS dates were obtained for four icons. Although five icons were dendro-dated successfully, one failed to be reliably cross-dated with the existing master tree-ring chronologies and it was dated by radiocarbon wiggle-matching. Dendrochronological dating and wiggle-matching of radiocarbon dates allowed us to determine the narrow chronological intervals of icon creation.

Development of a nanofiltration method for bone collagen 14C AMS dating

NASA Astrophysics Data System (ADS)

Boudin, Mathieu; Boeckx, Pascal; Buekenhoudt, Anita; Vandenabeele, Peter; Van Strydonck, Mark

2013-01-01

Radiocarbon dating of bones is usually performed on the collagen fraction. However, this collagen can contain exogenous molecules, including humic substances (HSs) and/or other soil components that may have a different age than the bone. Incomplete removal can result in biased 14C dates. Ultrafiltration of collagen, dissolved as gelatin (molecular weight (MW) ∼100,000 Dalton), has received considerable attention to obtain more reliable dates. Ultrafiltration is an effective method of removal of low-molecular weight contaminants from bone collagen but it does not remove high-molecular weight contaminants, such as cross-linked humic collagen complexes. However, comparative dating studies have raised the question whether this cleaning step itself may introduce contamination with carbon from the filters used. In this study, a nanofiltration method was developed using a ceramic filter to avoid a possible extraneous carbon contamination introduced by the filter. This method should be applicable to various protein materials e.g. collagen, silk, wool, leather and should be able to remove low-molecular and high molecular weight HSs. In this study bone collagen was hot acid hydrolyzed to amino acids and nanofiltrated. A filter with a molecular weight cutoff (MWCO) of 450 Dalton was chosen in order to collect the amino acids in the permeate and the HSs in the retentate. Two pilot studies were set up. Two nanofiltration types were tested in pilot study 1: dead end and cross flow filtration. Humic substance (HS)-solutions with fossil carbon and modern hydrolyzed collagen contaminated with HSs were filtrated and analyzed with spectrofluorescence to determine the HS removal. Cross flow nanofiltration showed the most efficient HS removal. A second pilot study based upon these results was set up wherein only cross flow filtration was performed. 14C measurements of the permeates of hydrolyzed modern collagen contaminated with fossil HSs demonstrate a significant but incomplete

Radiocarbon-based carbon source quantification of anomalous isotopic foraminifera in last glacial sediments in the western North Pacific

NASA Astrophysics Data System (ADS)

Uchida, Masao; Ohkushi, Ken'ichi; Kimoto, Katsunori; Inagaki, Fumio; Ishimura, Toyoho; Tsunogai, Urumu; Tuzino, Taqumi; Shibata, Yasuyuki

2008-04-01

A previous study interpreted extremely 13C-depleted excursions of planktonic and benthic foraminifera in last glacial sediments (17,500 to 25,400 cal years B.P.) of the core retrieved from off Shimokita Peninsula and off Hokkaido, Japan, as evidence for periodic releases of methane, arising from the dissociation of methane hydrate. To better understand the formation process of the 13C-depleted excursions, we conducted high-resolution natural radiocarbon measurements and biogeochemical analyses. We found highly depleted 13C excursions ranging from -10.2‰ to -1.6‰ and -6.8‰ to -1.6‰ in planktonic and benthic foraminifera, respectively. Most of the foraminiferal tests in these horizons were brown, most likely as a result of postdepositional alteration, reflecting the formation of authigenic carbonate on the surface of tests. These alterations were also supported by high levels of Mg-calcite and the acid-leaching test for anomalous foraminifera. To evaluate the carbon sources in the altered foraminifera tests, we quantified the relative contributions of 14C-free methane-derived carbon sources to the formation of authigenic carbonates in foraminifera with depleted 13C excursions using a coupled mass balance isotopic model (14C/C and 13C/12C). The radiocarbon ages of both planktonic and benthic 13C-depleted foraminifera were approximately 600 to 2000 years older than those of normal tests from nearby horizons. The relative contributions of authigenic carbonates derived from the methane oxidizing process reached to ˜22 wt% for planktonic foraminifera and ˜15 wt% for benthic foraminifera. The δ13C values of methane calculated from the mass balance model were between -29‰ and -68‰ for planktonic foraminifera and between -40‰ and -108‰ for benthic foraminifera, consistent with δ13C values reported for thermogenic and abiogenic methane in global methane hydrate reservoirs. These data consistently suggest that methane-related drastic environmental change

Tapping the deglacial secrets of Lake Oneida sediments: Establishing a connection between radiocarbon and paleomagnetics in Fish Creek sediments

NASA Astrophysics Data System (ADS)

Peck, D.; Rosenheim, B. E.; Ridge, J. C.

2017-12-01

Postglacial varved and rhythmically-laminated clays deposited within the Ontario Basin are often associated with the retreat of the Laurentide Ice Sheet immediately preceding the onset of the Younger Dryas. The paleoclimatic significance of the Ontario Basin has made it a popularly studied region. To determine ages that correlate with ice sheet retreat, classical radiocarbon ages were generated. However low total organic carbon (TOC) values found in glaciolacustrine sediments make accuracy of data a concern. Using the magnetic orientation of sediments during deposition, paleomagnetism has presented reliable dates in similar regions across the northeastern United States. While useful, paleomagnetism also comes with limitations, which have left areas of unexplored research. Lake Oneida, last glaciated by the Ontario Lobe, is one of the deepest and most untapped reservoirs of sediment dating back to the retreat of the Laurentide Ice Sheet, due primarily to the difficulty it poses for classical methods. Using samples taken from exposed varved glaciolacustrine sediment exposed by the downcutting of Fish Creek, a fluvial system terminating in eastern Lake Oneida, we compare Ramped Pyrolysis 14C data with paleomagnetic data. Ramped PyrOx 14C data unmask the distribution of ages in the organic matter of these sediments, at least partially separating autochthonous sources of carbon from allochthonous sources that tend to be older in these settings. Our comparison will test whether Ramped PyrOx 14C data match paleomagnetic data well enough to be used as the sole chronometer in sediment cores taken from Lake Oneida cores for which paleomagnetic orientation becomes more difficult to ascertain.

One Isotope, Two Tales: using plant and cosmogenic 14C to constrain Holocene glacier activity on Baffin Island.

NASA Astrophysics Data System (ADS)

Pendleton, S.; Miller, G. H.; Lifton, N. A.; Young, N. E.

2017-12-01

As the cryosphere continues to undergo rapid and accelerating change, it is more important than ever to understand past glacier activity to predict the future of the cryosphere. However, continuous Holocene glacier records are notoriously difficult to reconstruct because an advancing glacier will re-incorporate previous deposits so that moraines typically only record the farthest downvalley glacier expansion. Here we combine dates of ice margin advance from in situ dead vegetation with in situ cosmogenic 14C (in situ 14C) from preserved bedrock surfaces at the same locations to further constrain the timing of ice-free episodes during the Holocene following deglaciation on southern Baffin Island. Radiocarbon ages from recently exposed in situ plants suggest that ice last advanced over sample locations at 9.4, 9.2, 9.0, and 3.7 ka and that they remained ice covered until modern times. Associated in situ 14C inventories are variable, but well above background levels, suggesting some amount of Holocene in situ 14C production. Using plant 14C ages representing the beginning of ice coverage and in situ 14C inventories representative of exposure prior to ice coverage, a simple model of cosmogenic in situ 14C production (accounting for muon production through ice) provides constraints timing and duration of ice-free times at sample locations prior to their most recent burial. Using conservative Holocene ice thicknesses, the locations buried at 9.4, 9.2, and 9.0 ka require, at minimum, 1000 years of pre-burial exposure to match the observed in situ 14C inventory. This suggests these locations were ice free by at least 10 ka and likely earlier. The in situ 14C inventory at the location buried at 3.7 ka limits prior exposure to 2000 years, suggesting that this location experienced more complex Holocene ice cover/burial history. These pilot data show that valuable information regarding periods of exposure is contained within in situ 14C inventories. Additional paired plant and

Constraints on primary and secondary particulate carbon sources using chemical tracer and 14C methods during CalNex-Bakersfield

NASA Astrophysics Data System (ADS)

Sheesley, Rebecca J.; Nallathamby, Punith Dev; Surratt, Jason D.; Lee, Anita; Lewandowski, Michael; Offenberg, John H.; Jaoui, Mohammed; Kleindienst, Tadeusz E.

2017-10-01

The present study investigates primary and secondary sources of organic carbon for Bakersfield, CA, USA as part of the 2010 CalNex study. The method used here involves integrated sampling that is designed to allow for detailed and specific chemical analysis of particulate matter (PM) in the Bakersfield airshed. To achieve this objective, filter samples were taken during thirty-four 23-hr periods between 19 May and 26 June 2010 and analyzed for organic tracers by gas chromatography - mass spectrometry (GC-MS). Contributions to organic carbon (OC) were determined by two organic tracer-based techniques: primary OC by chemical mass balance and secondary OC by a mass fraction method. Radiocarbon (14C) measurements of the total organic carbon were also made to determine the split between the modern and fossil carbon and thereby constrain unknown sources of OC not accounted for by either tracer-based attribution technique. From the analysis, OC contributions from four primary sources and four secondary sources were determined, which comprised three sources of modern carbon and five sources of fossil carbon. The major primary sources of OC were from vegetative detritus (9.8%), diesel (2.3%), gasoline (<1.0%), and lubricating oil impacted motor vehicle exhaust (30%); measured secondary sources resulted from isoprene (1.5%), α-pinene (<1.0%), toluene (<1.0%), and naphthalene (<1.0%, as an upper limit) contributions. The average observed organic carbon (OC) was 6.42 ± 2.33 μgC m-3. The 14C derived apportionment indicated that modern and fossil components were nearly equivalent on average; however, the fossil contribution ranged from 32 to 66% over the five week campaign. With the fossil primary and secondary sources aggregated, only 25% of the fossil organic carbon could not be attributed. Whereas, nearly 80% of the modern carbon could not be attributed to primary and secondary sources accessible to this analysis, which included tracers of biomass burning, vegetative

Constraints on primary and secondary particulate carbon sources using chemical tracer and 14C methods during CalNex-Bakersfield

PubMed Central

Sheesley, Rebecca J.; Nallathamby, Punith Dev; Surratt, Jason D.; Lee, Anita; Lewandowski, Michael; Offenberg, John H.; Jaoui, Mohammed; Kleindienst, Tadeusz E.

2018-01-01

The present study investigates primary and secondary sources of organic carbon for Bakersfield, CA, USA as part of the 2010 CalNex study. The method used here involves integrated sampling that is designed to allow for detailed and specific chemical analysis of particulate matter (PM) in the Bakersfield airshed. To achieve this objective, filter samples were taken during thirty-four 23-hr periods between 19 May and 26 June 2010 and analyzed for organic tracers by gas chromatography – mass spectrometry (GC-MS). Contributions to organic carbon (OC) were determined by two organic tracer-based techniques: primary OC by chemical mass balance and secondary OC by a mass fraction method. Radiocarbon (14C) measurements of the total organic carbon were also made to determine the split between the modern and fossil carbon and thereby constrain unknown sources of OC not accounted for by either tracer-based attribution technique. From the analysis, OC contributions from four primary sources and four secondary sources were determined, which comprised three sources of modern carbon and five sources of fossil carbon. The major primary sources of OC were from vegetative detritus (9.8%), diesel (2.3%), gasoline (<1.0%), and lubricating oil impacted motor vehicle exhaust (30%); measured secondary sources resulted from isoprene (1.5%), α-pinene (<1.0%), toluene (<1.0%), and naphthalene (<1.0%, as an upper limit) contributions. The average observed organic carbon (OC) was 6.42 ± 2.33 μgC m−3. The 14C derived apportionment indicated that modern and fossil components were nearly equivalent on average; however, the fossil contribution ranged from 32-66% over the five week campaign. With the fossil primary and secondary sources aggregated, only 25% of the fossil organic carbon could not be attributed. Whereas, nearly 80% of the modern carbon could not be attributed to primary and secondary sources accessible to this analysis, which included tracers of biomass burning, vegetative

Synthesis and characterization of 3-ketohexadecanoic acid-1-14-C, DL-3-hydroxyhexadecanoic acid-1-14-C, and trans-2-hexadecenoic acid-1-14-C.

PubMed

Jones, J A; Blecher, M

1966-05-01

The chemical synthesis and characterization of three intermediates in the Beta oxidation of palmitic acid-1-(14)C by rat liver mitochondria, namely, 3-ketohexadecanoic acid-1-(14)C, DL-3-hydroxyhexadecanoic acid-1-(14)C, and trans-2-hexadecenoic acid-1-(14)C, are described.

The use of stored carbon reserves in growth of temperate tree roots and leaf buds: Analyses using radiocarbon measurements and modeling

DOE Office of Scientific and Technical Information (OSTI.GOV)

Gaudinski, J.B.; Torn, M.S.; Riley, W.J.

2009-02-01

Characterizing the use of carbon (C) reserves in trees is important for understanding regional and global C cycles, stress responses, asynchrony between photosynthetic activity and growth demand, and isotopic exchanges in studies of tree physiology and ecosystem C cycling. Using an inadvertent, whole-ecosystem radiocarbon ({sup 14}C) release in a temperate deciduous oak forest and numerical modeling, we estimated that the mean age of stored C used to grow both leaf buds and new roots is 0.7 years and about 55% of new-root growth annually comes from stored C. Therefore, the calculated mean age of C used to grow new-root tissuemore » is {approx}0.4 years. In short, new roots contain a lot of stored C but it is young in age. Additionally, the type of structure used to model stored C input is important. Model structures that did not include storage, or that assumed stored and new C mixed well (within root or shoot tissues) before being used for root growth, did not fit the data nearly as well as when a distinct storage pool was used. Consistent with these whole-ecosystem labeling results, the mean age of C in new-root tissues determined using 'bomb-{sup 14}C' in three additional forest sites in North America and Europe (one deciduous, two coniferous) was less than 1-2 years. The effect of stored reserves on estimated ages of fine roots is unlikely to be large in most natural abundance isotope studies. However, models of root C dynamics should take stored reserves into account, particularly for pulse-labeling studies and fast-cycling roots (<1 years).« less

Radiocarbon dating of individual lignin phenols: a new approach for establishing chronology of late quaternary lake sediments.

PubMed

Hou, Juzhi; Huang, Yongsong; Brodsky, Corynn; Alexandre, Marcelo R; McNichol, Ann P; King, John W; Hu, Feng Sheng; Shen, Ji

2010-09-01

The reliability of chronology is a prerequisite for meaningful paleoclimate reconstructions from sedimentary archives. The conventional approach of radiocarbon dating bulk organic carbon in lake sediments is often hampered by the old carbon effect, i.e., the assimilation of ancient dissolved inorganic carbon (DIC) derived from carbonate bedrocks or other sources. Therefore, radiocarbon dating is ideally performed on organic compounds derived from land plants that use atmospheric CO(2) and rapidly delivered to sediments. We demonstrate that lignin phenols isolated from lake sediments using reversed phase high performance liquid chromatography (HPLC) can serve as effective (14)C dating materials for establishing chronology during the late Quaternary. We developed a procedure to purify lignin phenols, building upon a published method. By isolating lignin from standard wood reference substances, we show that our method yields pure lignin phenols and consistent ages as the consensus ages and that our procedure does not introduce radiocarbon contamination. We further demonstrate that lignin phenol ages are compatible with varve counted and macrofossil dated sediment horizons in Steel Lake and Fayetteville Green Lake. Applying the new method to lake sediment cores from Lake Qinghai demonstrates that lignin phenol ages in Lake Qinghai are consistently younger than bulk total organic carbon (TOC) ages which are contaminated by old carbon effect. We also show that the age offset between lignin and bulk organic carbon differs at different Lake Qinghai sedimentary horizons, suggesting a variable hard water effect at different times and that a uniform age correction throughout the core is inappropriate.

Stimulation of Microbially Mediated Arsenic Release in Bangladesh Aquifers by Young Carbon Indicated by Radiocarbon Analysis of Sedimentary Bacterial Lipids.

PubMed

Whaley-Martin, K J; Mailloux, B J; van Geen, A; Bostick, B C; Silvern, R F; Kim, C; Ahmed, K M; Choudhury, I; Slater, G F

2016-07-19

The sources of reduced carbon driving the microbially mediated release of arsenic to shallow groundwater in Bangladesh remain poorly understood. Using radiocarbon analysis of phospholipid fatty acids (PLFAs) and potential carbon pools, the abundance and carbon sources of the active, sediment-associated, in situ bacterial communities inhabiting shallow aquifers (<30 m) at two sites in Araihazar, Bangladesh, were investigated. At both sites, sedimentary organic carbon (SOC) Δ(14)C signatures of -631 ± 54‰ (n = 12) were significantly depleted relative to dissolved inorganic carbon (DIC) of +24 ± 30‰ and dissolved organic carbon (DOC) of -230 ± 100‰. Sediment-associated PLFA Δ(14)C signatures (n = 10) at Site F (-167‰ to +20‰) and Site B (-163‰ to +21‰) were highly consistent and indicated utilization of carbon sources younger than the SOC, likely from the DOC pool. Sediment-associated PLFA Δ(14)C signatures were consistent with previously determined Δ(14)C signatures of microbial DNA sampled from groundwater at Site F indicating that the carbon source for these two components of the subsurface microbial community is consistent and is temporally stable over the two years between studies. These results demonstrate that the utilization of relatively young carbon sources by the subsurface microbial community occurs at sites with varying hydrology. Further they indicate that these young carbon sources drive the metabolism of the more abundant sediment-associated microbial communities that are presumably more capable of Fe reduction and associated release of As. This implies that an introduction of younger carbon to as of yet unaffected sediments (such as those comprising the deeper Pleistocene aquifer) could stimulate microbial communities and result in arsenic release.

Global Peak in Atmospheric Radiocarbon Provides a Potential Definition for the Onset of the Anthropocene Epoch in 1965.

PubMed

Turney, Chris S M; Palmer, Jonathan; Maslin, Mark A; Hogg, Alan; Fogwill, Christopher J; Southon, John; Fenwick, Pavla; Helle, Gerhard; Wilmshurst, Janet M; McGlone, Matt; Bronk Ramsey, Christopher; Thomas, Zoë; Lipson, Mathew; Beaven, Brent; Jones, Richard T; Andrews, Oliver; Hua, Quan

2018-02-19

Anthropogenic activity is now recognised as having profoundly and permanently altered the Earth system, suggesting we have entered a human-dominated geological epoch, the 'Anthropocene'. To formally define the onset of the Anthropocene, a synchronous global signature within geological-forming materials is required. Here we report a series of precisely-dated tree-ring records from Campbell Island (Southern Ocean) that capture peak atmospheric radiocarbon ( 14 C) resulting from Northern Hemisphere-dominated thermonuclear bomb tests during the 1950s and 1960s. The only alien tree on the island, a Sitka spruce (Picea sitchensis), allows us to seasonally-resolve Southern Hemisphere atmospheric 14 C, demonstrating the 'bomb peak' in this remote and pristine location occurred in the last-quarter of 1965 (October-December), coincident with the broader changes associated with the post-World War II 'Great Acceleration' in industrial capacity and consumption. Our findings provide a precisely-resolved potential Global Stratotype Section and Point (GSSP) or 'golden spike', marking the onset of the Anthropocene Epoch.

THE ABSOLUTE AGE OF THE UPPER PALEOLITHIC PERIOD (SOLUTREAN, GRAVETTIAN TYPE) IN THE REGION ADJOINING THE DNESTER RIVER, DETERMINED BY RADIOCARBON DATING (in Russian)

DOE Office of Scientific and Technical Information (OSTI.GOV)

Ivanova, I.K.; Chernysh, A.P.

1963-01-11

Determination of the age of the dwellings of primitive man is of interest both from the point of view of the stratigraphy of quaternary deposits and for solving anthropogenetic problems. For this reason, radiocarbon dating techniques were used for layers containing paleolithic residue of Molodova V, located in a 200-m deep canyon at the right bank of the Dnester River in the Chernowith region. The measurements were carried out at a depth of 3.1 to 3.25 m from the surface. The age of layer VI was calculated at 23,000 plus or minus 800 years which is close to the agemore » reported for the Czechoslovak gravette and from samples from the French Abri plateau. Thus, radiocarbon dating results confirmed earlier findings obtained by topological means concerning the age of the region near the Dnester River. (TTT)« less

The radiocarbon hydroxyl technique

NASA Technical Reports Server (NTRS)

Campbell, Malcolm J.; Sheppard, John C.

1994-01-01

The Radiocarbon Technique depends upon measuring the rate of oxidation of CO in an essentially unperturbed sample of air. The airborne technique is slightly different. Hydroxyl concentrations can be calculated directly; peroxyl concentrations can be obtained by NO doping.

Earliest Human Presence in North America Dated to the Last Glacial Maximum: New Radiocarbon Dates from Bluefish Caves, Canada.

PubMed

Bourgeon, Lauriane; Burke, Ariane; Higham, Thomas

2017-01-01

The timing of the first entry of humans into North America is still hotly debated within the scientific community. Excavations conducted at Bluefish Caves (Yukon Territory) from 1977 to 1987 yielded a series of radiocarbon dates that led archaeologists to propose that the initial dispersal of human groups into Eastern Beringia (Alaska and the Yukon Territory) occurred during the Last Glacial Maximum (LGM). This hypothesis proved highly controversial in the absence of other sites of similar age and concerns about the stratigraphy and anthropogenic signature of the bone assemblages that yielded the dates. The weight of the available archaeological evidence suggests that the first peopling of North America occurred ca. 14,000 cal BP (calibrated years Before Present), i.e., well after the LGM. Here, we report new AMS radiocarbon dates obtained on cut-marked bone samples identified during a comprehensive taphonomic analysis of the Bluefish Caves fauna. Our results demonstrate that humans occupied the site as early as 24,000 cal BP (19,650 ± 130 14C BP). In addition to proving that Bluefish Caves is the oldest known archaeological site in North America, the results offer archaeological support for the "Beringian standstill hypothesis", which proposes that a genetically isolated human population persisted in Beringia during the LGM and dispersed from there to North and South America during the post-LGM period.

Earliest Human Presence in North America Dated to the Last Glacial Maximum: New Radiocarbon Dates from Bluefish Caves, Canada

PubMed Central

Bourgeon, Lauriane; Burke, Ariane; Higham, Thomas

2017-01-01

The timing of the first entry of humans into North America is still hotly debated within the scientific community. Excavations conducted at Bluefish Caves (Yukon Territory) from 1977 to 1987 yielded a series of radiocarbon dates that led archaeologists to propose that the initial dispersal of human groups into Eastern Beringia (Alaska and the Yukon Territory) occurred during the Last Glacial Maximum (LGM). This hypothesis proved highly controversial in the absence of other sites of similar age and concerns about the stratigraphy and anthropogenic signature of the bone assemblages that yielded the dates. The weight of the available archaeological evidence suggests that the first peopling of North America occurred ca. 14,000 cal BP (calibrated years Before Present), i.e., well after the LGM. Here, we report new AMS radiocarbon dates obtained on cut-marked bone samples identified during a comprehensive taphonomic analysis of the Bluefish Caves fauna. Our results demonstrate that humans occupied the site as early as 24,000 cal BP (19,650 ± 130 14C BP). In addition to proving that Bluefish Caves is the oldest known archaeological site in North America, the results offer archaeological support for the “Beringian standstill hypothesis”, which proposes that a genetically isolated human population persisted in Beringia during the LGM and dispersed from there to North and South America during the post-LGM period. PMID:28060931

Improved radiocarbon dating for contaminated archaeological bone collagen, silk, wool and hair samples via cross-flow nanofiltrated amino acids.

PubMed

Boudin, Mathieu; Boeckx, Pascal; Vandenabeele, Peter; Van Strydonck, Mark

2013-09-30

Radiocarbon dating and stable isotope analyses of bone collagen, wool, hair and silk contaminated with extraneous carbon (e.g. humic substances) does not yield reliable results if these materials are pre-treated using conventional methods. A cross-flow nanofiltration method was developed that can be applied to various protein materials like collagen, hair, silk, wool and leather, and should be able to remove low-molecular and high-molecular weight contaminants. To avoid extraneous carbon contamination via the filter a ceramic filter (molecular weight cut-off of 200 Da) was used. The amino acids, released by hot acid hydrolysis of the protein material, were collected in the permeate and contaminants in the retentate (>200 Da). (14)C-dating results for various contaminated archaeological samples were compared for bulk material (pre-treated with the conventional methods) and for cross-flow nanofiltrated amino acids (permeate) originating from the same samples. Contamination and quality control of (14)C dates of bulk and permeate samples were obtained by measuring C:N ratios, fluorescence spectra, and δ(13)C and δ(15)N values of the samples. Cross-flow nanofiltration decreases the C:N ratio which means that contaminants have been removed. Cross-flow nanofiltration clearly improved sample quality and (14)C results. It is a quick and non-labor-intensive technique and can easily be implemented in any (14)C and stable isotope laboratory for routine sample pre-treatment analyses. Copyright © 2013 John Wiley & Sons, Ltd.

A Chronology of Late-Glacial and Holocene Advances of Quelccaya Ice Cap, Peru, Based on 10Be and Radiocarbon Dating

NASA Astrophysics Data System (ADS)

Kelly, M. A.; Lowell, T. V.; Schaefer, J. M.

2007-12-01

The Quelccaya Ice Cap region in the southeastern Peruvian Andes (~13-14°S latitude) is a key location for the development of late-glacial and Holocene terrestrial paleoclimate records in the tropics. We present a chronology of past extents of Quelccaya Ice Cap based on ~thirty internally consistent 10Be dates of boulders on moraines and bedrock as well as twenty radiocarbon dates of organic material associated with moraines. Based on results from both dating methods, we suggest that significant advances of Quelccaya Ice Cap occurred during late-glacial time, at ~12,700-11,400 yr BP, and during Late Holocene time ~400-300 yr BP. Radiocarbon dating of organic material associated with moraines provides maximum and minimum ages for ice advances and recessions, respectively, thus providing an independent check on 10Be dates of boulders on moraines. The opportunity to use both 10Be and radiocarbon dating makes the Quelccaya Ice Cap region a potentially important low-latitude calibration site for production rates of cosmogenic nuclides. Our radiocarbon chronology provides a tighter constraint on maximum ages of late-glacial and Late Holocene ice advances. Upcoming field research will obtain organic material for radiocarbon dating to improve minimum age constrains for late-glacial and Late Holocene ice recessions.

Radiocarbon dating of American pika fecal pellets provides insights into population extirpations and climate refugia.

PubMed

Millar, Constance I; Heckman, Katherine; Swanston, Christopher; Schmidt, Karena; Westfall, Robert D; Delany, Diane L

The American pika (Ochotona princeps) has become a species of concern for its sensitivity to warm temperatures and potential vulnerability to global warming. We explored the value of radiocarbon dating of fecal pellets to address questions of population persistence and timing of site extirpation. Carbon was extracted from pellets collected at 43 locations in the western Great Basin, USA, including three known occupied sites and 40 sites of uncertain status at range margins or where previous studies indicated the species is vulnerable. We resolved calibrated dates with high precision (within several years), most of which fell in the period of the mid-late 20th century bomb curve. The two-sided nature of the bomb curve renders far- and near-side dates of equal probability, which are separated by one to four decades. We document methods for narrowing resolution to one age range, including stratigraphic analysis of vegetation collected from pika haypiles. No evidence was found for biases in atmospheric 14C levels due to fossil-derived or industrial CO2 contamination. Radiocarbon dating indicated that pellets can persist for >59 years; known occupied sites resolved contemporary dates. Using combined evidence from field observations and radiocarbon dating, and the Bodie Mountains as an example, we propose a historical biogeographic scenario for pikas in minor Great Basin mountain ranges adjacent to major cordillera, wherein historical climate variability led to cycles of extirpation and recolonization during alternating cool and warm centuries. Using this model to inform future dynamics for small ranges in biogeographic settings similar to the Bodie Mountains in California, extirpation of pikas appears highly likely under directional warming trends projected for the next century, even while populations in extensive cordillera (e.g., Sierra Nevada, Rocky Mountains, Cascade Range) are likely to remain viable due to extensive, diverse habitat and high connectivity.

AMS 14C analysis of teeth from archaeological sites showing anomalous esr dating results

NASA Astrophysics Data System (ADS)

Grün, Rainer; Abeyratne, Mohan; Head, John; Tuniz, Claudio; Hedges, Robert E. M.

We have carried out AMS radiocarbon analysis on two groups of samples: the first one gave reasonable ESR age estimates and the second one yielded serious age underestinations. All samples were supposedly older than 35 ka, the oldest being around 160 ka. Two pretreatment techniques were used for radiocarbon dating: acid evolution and thermal release. Heating to 600, 750 and 900°C combined with total de-gassing at these temperatures was chosen to obtain age estimates on the organic fraction, secondary carbonates and original carbonate present in the hydroxyapatite mineral phase, respectively. All radiocarbon results present serious age underestimations. The secondary carbonate fraction gives almost modern results indicating an extremely rapid exchange of this component. Owing to this very rapid carbonate exchange it is not likely that the ESR signals used for dating are associated with the secondary carbonates. One tooth from Tabun with independent age estimates of >150 ka was further investigated by the Oxford AMS laboratory, yielding an age estimate of 1930±100 BP on the residual collagen from dentine and 18,000±160 BP on the carbonate component of the enamel bioapatite. We did not, however, find an explanation of why some samples give serious ESR underestimatioils whilst many others provide reasonable results.

Present day and Allerod - Younger Dryas marine 14C reservoir ages of surface waters in the North Atlantic-Norwegian Sea

NASA Astrophysics Data System (ADS)

Mangerud, J.; Bondevik, S.; Gulliksen, S.; Birks, H. H.; Reimer, P.; Hufthammer, A. K.; Hoisaeter, T.

2005-12-01

In order to compare radiocarbon dates on marine and terrestrial samples, the former have to be corrected for a marine reservoir age. We have calculated present day reservoir ages in this area by dating 22 whales collected AD 1860-1901 and 23 molluscs collected AD 1857-1926. Whales feed on pelagic organisms and will provide the reservoir age for the open ocean surface water. However, they travel large distances and integrate the reservoir ages of water masses along their way. Molluscs are stationary and monitor the sea water passing their living site. For the surface water in the N-Atlantic and Norwegian Sea we recommend to use the mean obtained for the two sets, i.e. reservoir ages of 400 +/- 40 and 375 +/- 30 years relative to tree rings of Intcal04 and British oak respectively, for the parts of the Holocene where specific time-dependent reservoir ages are not determined. The reservoir ages relative to British oak best reflects regional processes and we therefore prefer those, whereas IntCal04 ages are much more precisely determined, but dominated by trees from NW-USA in this time period. The reservoir ages for Allerod-Younger Dryas (YD) are obtained by dating parallel samples of terrestrial plant fragments and marine shells from sediment cores from the outermost western coast of Norway. The marine mud contains both plant fragments blown or washed in from adjacent land and in situ marine shells. In the earliest period (13,800-14,500 cal yrs BP) the reservoir age is 300-400 years, similar to present day values. This suggests that the exchange of CO2 between the atmosphere and the surface ocean was comparable to the present. During a short interval 13,200-13,500 cal yrs BP we found higher reservoir ages of 500-600 years coinciding with lower organic carbon content in our cores, and an inter-Allerod fluctuation seen in marine records. During the early YD the reservoir ages increased gradually from 400 to 650 years, causing a 700-14C year-long plateau, centred at 11

Radiocarbon constraints on fossil thinolite tufa formation in the Mono Basin, CA, USA

NASA Astrophysics Data System (ADS)

Leroy, S. L.; Zimmerman, S. R.; Hemming, S. R.; Stine, S.; Guilderson, T. P.

2009-12-01

Mono Lake is a terminal lake located at the western edge of the Great Basin, and is famous for its tufa towers. Thinolite, which is thought to be a CaCO3 pseudomorph of ikaite, is found around the Mono Basin in many fossil tufa towers, particularly at elevations above 2000 meters. The subaqueous parent mineral ikaite forms at low temperatures (< 6 °C) (Bischoff et al., 1993) and requires specific water chemistry. Previous radiocarbon dating of fossil tufa towers around the Mono Basin has yielded a rather small range of ages for the highest elevation towers, between 11.8 and 14.1 14C kyr BP (no corrections for reservoir effects have been made). A thinolite fan collected from outcrops in Mill Creek, just north of the current Mono Lake yielded an age of 10,690 ± 45 14C yr BP (12,750 ± 80 cal yr BP), consistent with a ca. 1000 year reservoir age and coincidence with thinolite crystals found in a core from the northwestern embayment of Mono Lake (Davis, 1999, QR), and thus correlating with the Younger Dryas cooling event as exhibited in the GISP2 δ18O record. While most of the thinolite textures are found at high elevations, we sampled a mound at 1955 meters (near the current shoreline, north of the lake and just east of Black Point) that has many concentric layers, some containing thinolite textures. Although tufa mounds can form very rapidly, the location at low elevation and the presence of at least 19 distinct layers led us to consider that this mound might represent a long term record of Mono Lake’s chemistry. The new data confirm that the mound formed over a long period within the last glacial cycle, with ages ranging beyond the current limits of measurement (>34 kyr) to as young as 15.5 14C kyr BP. In general there is a consistent stratigraphic trend of ages within the mound, but the thinolite ages are anomalously young and one thinolite sample shows a large age reversal. The best estimate of the age of the precipitation of this tufa mound is given by the

New radiocarbon dates on the cereals from Wadi Kubbaniya

DOE Office of Scientific and Technical Information (OSTI.GOV)

Wendorf, F.; Schild, R.; Close, A.E.

1984-01-01

In 1978, three carbonized grains of barley and a carbonized grain of einkorn wheat were found in a buried hearth at a Late Paleolithic site at Wadi Kubbaniya in Egypt. In 1981, two large clusters of barley seeds, which were identified as six-row barley and thus domestic, were found at a nearby site of comparable age. Numerous grinding stones, presumed to have been used for processing the cereals, were found in these and other sites, often deeply buried, and 30 radiocarbon dates placed the occupations between 18,500 and 17,000 radiocarbon years ago. These finds led us to suggest an earlymore » origin of food production, with implications for the initial development of complex societies. Several barley seeds were analyzed by electron spin resonance spectroscopy to determine the maximal temperature to which they had been subjected before burial. Six barley seeds and three small pieces of wood charcoal were dated directly by using a tandem accelerator mass spectrometer.« less

Optimization of simultaneous tritium–radiocarbon internal gas proportional counting

DOE Office of Scientific and Technical Information (OSTI.GOV)

Bonicalzi, R. M.; Aalseth, C. E.; Day, A. R.

Specific environmental applications can benefit from dual tritium and radiocarbon measurements in a single compound. Assuming typical environmental levels, it is often the low tritium activity relative to the higher radiocarbon activity that limits the dual measurement. In this paper, we explore the parameter space for a combined tritium and radiocarbon measurement using a methane sample mixed with an argon fill gas in low-background proportional counters of a specific design. We present an optimized methane percentage, detector fill pressure, and analysis energy windows to maximize measurement sensitivity while minimizing count time. The final optimized method uses a 9-atm fill ofmore » P35 (35% methane, 65% argon), and a tritium analysis window from 1.5 to 10.3 keV, which stops short of the tritium beta decay endpoint energy of 18.6 keV. This method optimizes tritium counting efficiency while minimizing radiocarbon beta decay interference.« less

Intercomparison of radiocarbon bomb pulse and 210Pb age models. A study in a peat bog core from North Poland

NASA Astrophysics Data System (ADS)

Piotrowska, Natalia; De Vleeschouwer, François; Sikorski, Jarosław; Pawlyta, Jacek; Fagel, Nathalie; Le Roux, Gaël; Pazdur, Anna

2010-04-01

Radiocarbon and 210Pb were measured on the uppermost 40 cm of a Wardenaar peat core retrieved from a Baltic raised bog at Słowińskie Błota (Pomerania, North Poland). This site is the subject of ongoing multiproxy studies covering the last 1300 years. Radiocarbon age model was constructed on the basis of 14 AMS dates obtained on selected Sphagnum spp. fragments, with use of P_Sequence tool. We present here a comparison of this model with the age model obtained using CRS model classically applied to 210Pb measurements.

Ocean science: Radiocarbon variability in the western North Atlantic during the last deglaciation

USGS Publications Warehouse

Robinson, L.F.; Adkins, J.F.; Keigwin, L.D.; Southon, J.; Fernandez, D.P.; Wang, S.-L.; Scheirer, D.S.

2005-01-01

We present a detailed history of glacial to Holocene radiocarbon in the deep western North Atlantic from deep-sea corals and paired benthic-planktonic foraminifera. The deglaciation is marked by switches between radiocarbon-enriched and -depleted waters, leading to large radiocarbon gradients in the water column. These changes played an important role in modulating atmospheric radiocarbon. The deep-ocean record supports the notion of a bipolar seesaw with increased Northern-source deep-water formation linked to Northern Hemisphere warming and the reverse. In contrast, the more frequent radiocarbon variations in the intermediate/deep ocean are associated with roughly synchronous changes at the poles.

Age validation and growth of bluenose Hyperoglyphe antarctica using the bomb chronometer method of radiocarbon ageing.

PubMed

Horn, P L; Neil, H L; Paul, L J; Marriott, P

2010-11-01

Age validation of bluenose Hyperoglyphe antarctica was sought using the independent bomb chronometer procedure. Radiocarbon ((14) C) levels were measured in core micro-samples from 12 otoliths that had been aged using a zone count method. The core (14) C measurement for each fish was compared with the value on a surface water reference curve for the calculated birth year of the fish. There was good agreement, indicating that the line-count ageing method described here is not substantially biased. A second micro-sample was also taken near the edge of nine of the otolith cross-sections to help define a bomb-carbon curve for waters deeper than 200-300 m. There appears to be a 10 to 15 year lag in the time it takes the (14) C to reach the waters where adult H. antarctica are concentrated. The maximum estimated age of this species was 76 years, and females grow significantly larger than males. Von Bertalanffy growth curves were estimated, and although they fit the available data reasonably well, the lack of aged juvenile fish results in the K and t(0) parameters being biologically meaningless. Consequently, curves that are likely to better represent population growth were estimated by forcing t(0) to be -0·5. © 2010 NIWA. Journal of Fish Biology © 2010 The Fisheries Society of the British Isles.

Comparison of the gravimetric, phenol red, and 14C-PEG-3350 methods to determine water absorption in the rat single-pass intestinal perfusion model.

PubMed

Sutton, S C; Rinaldi, M T; Vukovinsky, K E

2001-01-01

This study was undertaken to determine whether the gravimetric method provided an accurate measure of water flux correction and to compare the gravimetric method with methods that employ nonabsorbed markers (eg, phenol red and 14C-PEG-3350). Phenol red,14C-PEG-3350, and 4-[2-[[2-(6-amino-3-pyridinyl)-2-hydroxyethyl]amino]ethoxy]-, methyl ester, (R)-benzene acetic acid (Compound I) were co-perfused in situ through the jejunum of 9 anesthetized rats (single-pass intestinal perfusion [SPIP]). Water absorption was determined from the phenol red,14C-PEG-3350, and gravimetric methods. The absorption rate constant (ka) for Compound I was calculated. Both phenol red and 14C-PEG-3350 were appreciably absorbed, underestimating the extent of water flux in the SPIP model. The average +/- SD water flux microg/h/cm) for the 3 methods were 68.9 +/- 28.2 (gravimetric), 26.8 +/- 49.2 (phenol red), and 34.9 +/- 21.9 (14C-PEG-3350). The (average +/- SD) ka for Compound I (uncorrected for water flux) was 0.024 +/- 0.005 min(-1). For the corrected, gravimetric method, the average +/- SD was 0.031 +/- 0.001 min(-1). The gravimetric method for correcting water flux was as accurate as the 2 "nonabsorbed" marker methods.

Large-scale Patterns of 14C Age of Bulk Organic Carbon and Various Molecular Components in Grassland Soils

NASA Astrophysics Data System (ADS)

Jia, J.; Liu, Z.; Cao, Z.; Chen, L.; He, J. S.; Haghipour, N.; Wacker, L.; Eglinton, T. I.; Feng, X.

2017-12-01

Unraveling the fate of organic carbon (OC) in soils is essential to understanding the impact of global changes on the global carbon cycle. Previous studies have shown that while various soil OC components have different decomposability, chemically labile OC can have old 14C ages. However, few studies have compared the 14C age of various soil OC components on a large scale, which may provide important information on the link between the age or turnover of soil OC components to their sources, molecular structures as well as environmental variables. In this project, a suite of soil profiles were sampled along a large-scale transect of temperate and alpine grasslands across the Tibetan and Mongolian Plateaus in China with contrasting climatic, vegetation and soil properties. Bulk OC and source-specific compounds (including fatty acids (FAs), diacids (DAs) and lignin phenols) were radiocarbon-dated to investigate the age and turnover dynamics of different OC pools and the mechanisms controlling their stability. Our results show that lignin phenols displayed a large 14C variability. Short-chain (C16, 18) FAs sourced from vascular plants as well as microorganisms were younger than plant-derived long-chain FAs and DAs, indicating that short-chain FAs were easier to be decomposed or newly synthesized. In the temperate grasslands, long-chain DAs were younger than FAs, while the opposite trend was observed in the alpine grasslands. Preliminary correlation analysis suggests that the age of short-chain FAs were mainly influenced by clay contents and climate, while reactive minerals, clay or silt particles were important factors in the stabilization of long-chain FAs, DAs and lignin phenols. Overall, our study provided a unique 14 C dataset of soil OC components in grasslands, which will provide important constraints on soil carbon turnover in future investigations.

Strong regional atmospheric 14C signature of respired CO 2 observed from a tall tower over the midwestern United States

DOE Office of Scientific and Technical Information (OSTI.GOV)

LaFranchi, B. W.; McFarlane, K. J.; Miller, J. B.

Radiocarbon in CO 2 ( 14CO 2) measurements can aid in discriminating between fast (<1 year) and slower (>5–10 years) cycling of C between the atmosphere and the terrestrial biosphere due to the 14C disequilibrium between atmospheric and terrestrial C. However, 14CO 2 in the atmosphere is typically much more strongly impacted by fossil fuel emissions of CO 2, and, thus, observations often provide little additional constraints on respiratory flux estimates at regional scales. Here we describe a data set of 14CO 2 observations from a tall tower in northern Wisconsin (USA) where fossil fuel influence is far enough removedmore » that during the summer months, the biospheric component of the 14CO 2 budget dominates. We find that the terrestrial biosphere is responsible for a significant contribution to 14CO 2 that is 2–3 times higher than predicted by the Carnegie-Ames-Stanford approach terrestrial ecosystem model for observations made in 2010. This likely includes a substantial contribution from the North American boreal ecoregion, but transported biospheric emissions from outside the model domain cannot be ruled out. The 14CO 2 enhancement also appears somewhat decreased in observations made over subsequent years, suggesting that 2010 may be anomalous. Furthermore, with these caveats acknowledged, we discuss the implications of the observation/model comparison in terms of possible systematic biases in the model versus short-term anomalies in the observations. Going forward, this isotopic signal could be exploited as an important indicator to better constrain both the long-term carbon balance of terrestrial ecosystems and the short-term impact of disturbance-based loss of carbon to the atmosphere.« less

Strong regional atmospheric 14C signature of respired CO 2 observed from a tall tower over the midwestern United States

DOE PAGES

LaFranchi, B. W.; McFarlane, K. J.; Miller, J. B.; ...

2016-08-31

Radiocarbon in CO 2 ( 14CO 2) measurements can aid in discriminating between fast (<1 year) and slower (>5–10 years) cycling of C between the atmosphere and the terrestrial biosphere due to the 14C disequilibrium between atmospheric and terrestrial C. However, 14CO 2 in the atmosphere is typically much more strongly impacted by fossil fuel emissions of CO 2, and, thus, observations often provide little additional constraints on respiratory flux estimates at regional scales. Here we describe a data set of 14CO 2 observations from a tall tower in northern Wisconsin (USA) where fossil fuel influence is far enough removedmore » that during the summer months, the biospheric component of the 14CO 2 budget dominates. We find that the terrestrial biosphere is responsible for a significant contribution to 14CO 2 that is 2–3 times higher than predicted by the Carnegie-Ames-Stanford approach terrestrial ecosystem model for observations made in 2010. This likely includes a substantial contribution from the North American boreal ecoregion, but transported biospheric emissions from outside the model domain cannot be ruled out. The 14CO 2 enhancement also appears somewhat decreased in observations made over subsequent years, suggesting that 2010 may be anomalous. Furthermore, with these caveats acknowledged, we discuss the implications of the observation/model comparison in terms of possible systematic biases in the model versus short-term anomalies in the observations. Going forward, this isotopic signal could be exploited as an important indicator to better constrain both the long-term carbon balance of terrestrial ecosystems and the short-term impact of disturbance-based loss of carbon to the atmosphere.« less