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Sample records for airborne carbon 14c

  1. 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

  2. Cholestyramine-enhanced fecal elimination of carbon-14 in rats after administration of ammonium (/sup 14/C)perfluorooctanoate or potassium (/sup 14/C)perfluorooctanesulfonate

    SciTech Connect

    Johnson, J.D.; Gibson, S.J.; Ober, R.E.

    1984-12-01

    After a single intravenous dose of ammonium (/sup 14/C)perfluorooctanoate (( /sup 14/C)PFO, 13.3 mg/kg) or of potassium (/sup 14/C)perfluorooctanesulfonate (( /sup 14/C)PFOS, 3.4 mg/kg) to rats, cholestyramine fed daily as a 4% mixture in feed was shown to increase the total carbon-14 eliminated via feces and to decrease liver concentration of carbon-14. Rats were fed cholestyramine in feed for 14 days after administration of (/sup 14/C)PFO and for 21 days after administration of (/sup 14/C)PFOS. Control rats were administered radiolabeled fluorochemical but were not treated with cholestyramine. Cholestyramine treatment increased mean cumulative carbon-14 elimination in feces by 9.8-fold for rats administered (/sup 14/C)PFO and by 9.5-fold for rats administered (/sup 14/C)PFOS. After (/sup 14/C)PFO, a mean of 4% of the dose of carbon-14 was in liver of cholestyramine-treated rats at 14 days versus 7.6% in control rats; after (/sup 14/C)PFOS, 11.3% of the dose was in liver at 21 days versus 40.3% in control rats. After administration of either radiolabeled compound, plasma and red blood cell carbon-14 concentrations, which were relatively lower than liver concentrations, were also significantly reduced by cholestyramine treatment.

  3. Tracing terrestrial carbon: a novel application of ∆14C in a humic lake

    NASA Astrophysics Data System (ADS)

    Keaveney, Evelyn; Reimer, Paula J.; Foy, Robert H.

    2016-04-01

    Lakes play an important yet underrated role in global carbon cycles. Terrestrial carbon (C) is buried and/or remineralised in significant quantities, and lake function may also be affected by catchment inputs with potential feedbacks for regional and global C cycling. Changing deposition chemistry, land use and climate induced impacts on hydrology will affect soil biogeochemistry, terrestrial C export, and hence lake ecology. Autochthonous production in lakes is based on dissolved inorganic C (DIC). DIC in alkaline lakes is partially derived from weathering of carbonaceous bedrock, a proportion of which is 14C-free. The low 14C activity yields an artificial age offset leading samples to appear hundreds to thousands of years older than their actual age. Dissolved organic carbon (DOC) and particulate organic carbon (POC) can contain terrestrial inputs. The terrestrial inputs can be labile or detrital and their age depends to a first order on their depth in catchment soil/peat stocks. We present a pilot study that uses the radiocarbon (∆14C) method to determine the source of carbon buried in the surface sediment of Lower Lough Erne, a humic, alkaline lake in northwest Ireland. ∆14C, δ13C and δ15N values were measured from phytoplankton and other biota, dissolved inorganic, dissolved organic and particulate organic carbon. A novel radiocarbon method, Stepped Combustion1 was used to estimate the degree of the burial of terrestrial carbon in surface sediment, collected in 2011. The ∆14C values of the low temperature fractions were comparable to algal ∆14C, while the high temperature fractions were 14C-depleted (older than bulk sediment). The ∆14C end-member model indicated that ~64% of carbon in surface sediment was derived from detrital terrestrial carbon. The same proportion of detrital/labile carbon was found in surface sediment of Upper Lough Erne in 2014, despite the differences in lake type and collection date. The use of ∆14C in conjunction with

  4. Laboratory Experiments to Evaluate Diffusion of 14C into Nevada Test Site Carbonate Aquifer Matrix

    SciTech Connect

    Ronald L. Hershey; William Howcroft; Paul W. Reimus

    2003-03-01

    Determination of groundwater flow velocities at the Nevada Test Site is important since groundwater is the principal transport medium of underground radionuclides. However, 14C-based groundwater velocities in the carbonate aquifers of the Nevada Test Site are several orders of magnitude slower than velocities derived from the Underground Test Area regional numerical model. This discrepancy has been attributed to the loss or retardation of 14C from groundwater into the surrounding aquifer matrix making 14C-based groundwater ages appear much older. Laboratory experiments were used to investigate the retardation of 14C in the carbonate aquifers at the Nevada Test Site. Three sets of experiments were conducted evaluating the diffusion of 14C into the carbonate aquifer matrix, adsorption and/or isotopic exchange onto the pore surfaces of the carbonate matrix, and adsorption and/or isotopic exchange onto the fracture surfaces of the carbonate aquifer. Experimental results a nd published aquifer matrix and fracture porosities from the Lower Carbonate Aquifer were applied to a 14C retardation model. The model produced an extremely wide range of retardation factors because of the wide range of published aquifer matrix and fracture porosities (over three orders of magnitude). Large retardation factors suggest that groundwater with very little measured 14C activity may actually be very young if matrix porosity is large relative to the fracture porosity. Groundwater samples collected from highly fractured aquifers with large effective fracture porosities may have relatively small correction factors, while samples from aquifers with a few widely spaced fractures may have very large correction factors. These retardation factors were then used to calculate groundwater velocities from a proposed flow path at the Nevada Test Site. The upper end of the range of 14C correction factors estimated groundwater velocities that appear to be at least an order of magnitude too high compared

  5. Characteristics of 14C and 13C of carbonate aerosols in dust storm events in China

    NASA Astrophysics Data System (ADS)

    Chen, Bing; Jie, Dongmei; Shi, Meinan; Gao, Pan; Shen, Zhenxing; Uchida, Masao; Zhou, Liping; Liu, Kexin; Hu, Ke; Kitagawa, Hiroyuki

    2015-10-01

    In contrast with its decrease in western China deserts, the dust storm event in eastern China, Korea, and Japan shows an increase in frequency. Although the drylands in northeastern China have been recognized as an important dust source, the relative contributions of dust transport from the drylands and deserts are inconclusive, thus the quantification of dust storm sources in downwind area remains a challenge. We measured the 14C and 13C contents in carbonates of dust samples from six sites in China, which were collected for the duration of dust storm events in drylands, deserts, and urban areas. The δ13C of the dryland dust samples considerably varied in a range of - 9.7 to - 5.0‰, which partly overlapped the desert dust carbonate δ13C ranges. The 14C content of the dryland dust carbonates showed a narrow range of 60.9 ± 4.0 (as an average and 1 SD of five samples) percent modern carbon (pMC), indicating the enrichment of modern carbonate. Dust samples in desert regions contained relatively aged carbonates with the depleting 14C showing of 28.8 ± 3.3 pMC. After the long-range transport of the western China desert dust plume, the carbonates collected at the southern China remained the depletion of 14C (33.5 ± 5.3 pMC) as in the desert regions. On the other hand, the samples of dust storm events at the urban areas of eastern China showed an enrichment of 14C contents (46.2 ± 5.0 pMC, n = 7), which might be explained by the stronger contribution of modern-carbonate-rich dryland dust.

  6. 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.

  7. 14C Activity and Global Carbon Cycle Changes over the Past 50,000 Years

    NASA Astrophysics Data System (ADS)

    Hughen, K.; Lehman, S.; Southon, J.; Overpeck, J.; Marchal, O.; Herring, C.; Turnbull, J.

    2004-01-01

    A series of 14C measurements in Ocean Drilling Program cores from the tropical Cariaco Basin, which have been correlated to the annual-layer counted chronology for the Greenland Ice Sheet Project 2 (GISP2) ice core, provides a high-resolution calibration of the radiocarbon time scale back to 50,000 years before the present. Independent radiometric dating of events correlated to GISP2 suggests that the calibration is accurate. Reconstructed 14C activities varied substantially during the last glacial period, including sharp peaks synchronous with the Laschamp and Mono Lake geomagnetic field intensity minimal and cosmogenic nuclide peaks in ice cores and marine sediments. Simulations with a geochemical box model suggest that much of the variability can be explained by geomagnetically modulated changes in 14C production rate together with plausible changes in deep-ocean ventilation and the global carbon cycle during glaciation.

  8. Modelling of dead carbon fraction in speleothems: a step towards reliable speleothem 14C-chronologies

    NASA Astrophysics Data System (ADS)

    Lechleitner, Franziska A.; Jamieson, Robert A.; McIntyre, Cameron; Baldini, Lisa M.; Baldini, James U. L.; Eglinton, Timothy I.

    2015-04-01

    Over the past two decades, speleothems have become one of the most versatile and promising archives for the study of past continental climate. Very precise absolute dating is often possible using the U-Th method, resulting in paleoclimate records of exceptional resolution and accuracy. However, not all speleothems are amenable to this dating method for a variety of reasons (e.g. low U concentrations, high detrital Th etc). This has lead researchers to exclude many otherwise suitable speleothems and cave sites from further investigation. 14C-dating of speleothems has so far not been applicable, due to the 'dead carbon' problem. As drip water percolates through the karst, dissolving CaCO3, a variable amount of 14C-dead carbon is added to the solution. This results in a temporally variable and site-specific reservoir effect, ultimately undermining the development of speleothem 14C -chronologies. However, a number of recent studies have shown a clear link between karst hydrology and associated proxies (e.g., Mg/Ca and δ13C) and this 'dead carbon fraction' (DCF). We take advantage of this relationship to model DCF and its changes using Mg/Ca, δ13C and 14C data from published speleothem records. Using one record for calibration purposes, we build a transfer function for the DCF in relation to δ13C and Mg/Ca, which we then apply to other 14C records. Initial model results are promising; we are able to reconstruct general long-term average DCF within uncertainties of the calculated DCF from the U-Th chronology. Large shifts in DCF related to hydrology are also often detected. In a second step, we apply the model to a speleothem from southern Poland, which so far could not be dated, due to very low U-concentrations. To construct a 14C chronology, the stalagmite was sampled at 5 mm intervals. CaCO3 powders were graphitized and measured by Accelerator Mass Spectrometry (MICADAS) at ETH Zurich. Additional high-resolution (0.1 mm/sample) 14C measurements were performed on

  9. Stepped-combustion 14C dating of bomb carbon in lake sediment

    USGS Publications Warehouse

    McGeehin, J.; Burr, G.S.; Hodgins, G.; Bennett, S.J.; Robbins, J.A.; Morehead, N.; Markewich, H.

    2004-01-01

    In this study, we applied a stepped-combustion approach to dating post-bomb lake sediment from north-central Mississippi. Samples were combusted at a low temperature (400 ??C) and then at 900 ??C. The CO2 was collected separately for both combustions and analyzed. The goal of this work was to develop a methodology to improve the accuracy of 14C dating of sediment by combusting at a lower temperature and reducing the amount of reworked carbon bound to clay minerals in the sample material. The 14C fraction modern results for the low and high temperature fractions of these sediments were compared with well-defined 137Cs determinations made on sediment taken from the same cores. Comparison of "bomb curves" for 14C and 137Cs indicate that low temperature combustion of sediment improved the accuracy of 14C dating of the sediment. However, fraction modern results for the low temperature fractions were depressed compared to atmospheric values for the same time frame, possibly the result of carbon mixing and the low sedimentation rate in the lake system.

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

    SciTech Connect

    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 sink 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 to

  11. Flux of carbon from 14C-enriched leaf litter throughout a forest soil mesocosm

    SciTech Connect

    Froberg, Mats J.; Hanson, Paul J; Trumbore, Susan E.; Swanston, Christopher W.; Todd Jr, Donald E

    2009-01-01

    The role of DOC for the build-up of soil organic carbon pools is still not well known, but it is thought to play a role in the transport of carbon to a greater depth where it becomes more stable. The aim of this study was to elucidate within-year dynamics of carbon transport from litter to the O (Oe and Oa) and A horizons. Mesocosms with constructed soil profiles were used to study dynamics of C transport from 14C-enriched (about 1000 ) leaf litter to the Oe/Oa and A horizons as well as the mineralization of leaf litter. The mesocosms were placed in the field for 17 months during which time fluxes and 14C content of DOC and CO2 were measured. Changes in 14C in leaf litter and bulk soil C pools were also recorded. Significant simultaneous release and immobilization of DOC occurring in both the O and A horizons was hypothesized. Contrary to our hypothesis, DOC released from the labeled Oi horizon was not retained within the Oe/Oa layer. DOC originating in the unlabeled Oe/Oa layer was also released for transport. Extensive retention of DOC occurred in the A horizon. DOC leaching from A horizon consisted of a mix of DOC from different sources, with a main fraction originating in the A horizon and a smaller fraction leached from the overlaying horizons. The C and 14C budget for the litter layer also indicated a surprisingly large amount of carbon with ambient Δ14C-signature to be respired from this layer. Data for this site also suggested significant contributions from throughfall to dissolved organic carbon (DOC) transport into and respiration from the litter layer. The results from this study showed that DOC retentionwas low in the O horizon and therefore not important for the O horizon carbon budget. In the A horizon DOC retention was extensive, but annual DOC input was small compared to C stocks and therefore not important for changes in soil C on an annual timescale.

  12. 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.

  13. Concentrations and 14C age of nonstructural carbon in California oaks

    NASA Astrophysics Data System (ADS)

    Czimczik, C. I.; Druffel-Rodriguez, K.; Trumbore, S. E.

    2008-12-01

    Plants store photosynthetic assimilates as nonstructural carbon (NSC), mainly glucose, fructose, sucrose, and starch. NSC fuels processes such as respiration and growth. Research suggests that NSC represents a significant fraction of a plant's annual C budget, but temporal dynamics of NSC are poorly understood. We used concentration and radiocarbon (14C) measurements of NSC to investigate how temporal dynamics of NSC vary with life strategy and throughout a species' range. In Mediterranean environments, oaks have developed two strategies (evergreen and deciduous) to cope with drought. Within California, the uncertainty of annual winter rain increases from north to south. We compared two evergreen and deciduous species: Coastal and Interior live oak (Quercus agrifolia and wislizenii) and Valley and Blue oak (Q. lobata and douglasii). Samples (4 mm cores to 20 cm depth at dbh) were taken in 2008 before leaf-out and fall at five sites which represent an inland to coast temperature gradient from high to low summer temperatures as well as a north- south precipitation gradient. Sugars were isolated by shaking in methanol-water and quantified using a spectrometric micro-plate technique. Starch was isolated by boiling in ethanol followed by HCl digestion and quantified manometrically. 14C contents were measured by AMS. Preliminary findings indicate that in live oaks, winter sugar concentrations are constant throughout the tree and across sites, while 14C concentrations increase towards a tree's center. This suggests that the NSC pool oaks is not well mixed. Future work will elucidate whether plants can access these older NSC stores.

  14. Factors Affecting 14C Ages of Lacustrine Carbonates: Timing and Duration of the Last Highstand Lake in the Lahontan Basin

    USGS Publications Warehouse

    Benson, L.

    1993-01-01

    Two processes contribute to inaccurate 14C age estimates of carbonates precipitated within the Lahontan basin, NevadaCalifornia: low initial 14C/C ratios in lake water (reservoir effect) and addition of modern carbon to calcium carbonate after its precipitation. The mast reliable set of 14C ages on carbonates from elevations > 1310 m in the Pyramid and Walker Lake subbasins indicate that lakes in all seven Lahontan subbasins coalesced ???14,200 14C yr B.P. forming Lake Lahontan. Lake Lahontan achieved its 1330-m highstand elevation by ???13,800 14 C yr B.P. and receded to 1310 m by ???13,700 14C yr B.P. Calculations, based on measured carbonate-accumulation rates, of the amount of time Lake Lahontan exceeded 1310 and 1330 m (500 and 50 yr) are consistent with this chronology. The timing of the Lake Lahontan highstand is of interest because of the linkage of highstand climates with proximity to the polar jet stream. The brevity of the Lahontan highstand is interpreted to indicate that the core of the southern branch of the polar jet stream remained only briefly over the Lahontan basin.

  15. Accuracy and precision of 14C-based source apportionment of organic and elemental carbon in aerosols using the Swiss_4S protocol

    NASA Astrophysics Data System (ADS)

    Mouteva, G. O.; Fahrni, S. M.; Santos, G. M.; Randerson, J. T.; Zhang, Y.-L.; Szidat, S.; Czimczik, C. I.

    2015-09-01

    Aerosol source apportionment remains a critical challenge for understanding the transport and aging of aerosols, as well as for developing successful air pollution mitigation strategies. The contributions of fossil and non-fossil sources to organic carbon (OC) and elemental carbon (EC) in carbonaceous aerosols can be quantified by measuring the radiocarbon (14C) content of each carbon fraction. However, the use of 14C in studying OC and EC has been limited by technical challenges related to the physical separation of the two fractions and small sample sizes. There is no common procedure for OC/EC 14C analysis, and uncertainty studies have largely focused on the precision of yields. Here, we quantified the uncertainty in 14C measurement of aerosols associated with the isolation and analysis of each carbon fraction with the Swiss_4S thermal-optical analysis (TOA) protocol. We used an OC/EC analyzer (Sunset Laboratory Inc., OR, USA) coupled to a vacuum line to separate the two components. Each fraction was thermally desorbed and converted to carbon dioxide (CO2) in pure oxygen (O2). On average, 91 % of the evolving CO2 was then cryogenically trapped on the vacuum line, reduced to filamentous graphite, and measured for its 14C content via accelerator mass spectrometry (AMS). To test the accuracy of our setup, we quantified the total amount of extraneous carbon introduced during the TOA sample processing and graphitization as the sum of modern and fossil (14C-depleted) carbon introduced during the analysis of fossil reference materials (adipic acid for OC and coal for EC) and contemporary standards (oxalic acid for OC and rice char for EC) as a function of sample size. We further tested our methodology by analyzing five ambient airborne particulate matter (PM2.5) samples with a range of OC and EC concentrations and 14C contents in an interlaboratory comparison. The total modern and fossil carbon blanks of our setup were 0.8 ± 0.4 and 0.67 ± 0.34 μg C, respectively

  16. Accuracy and precision of 14C-based source apportionment of organic and elemental carbon in aerosols using the Swiss_4S protocol

    NASA Astrophysics Data System (ADS)

    Mouteva, G. O.; Fahrni, S. M.; Santos, G. M.; Randerson, J. T.; Zhang, Y. L.; Szidat, S.; Czimczik, C. I.

    2015-04-01

    Aerosol source apportionment remains a critical challenge for understanding the transport and aging of aerosols, as well as for developing successful air pollution mitigation strategies. The contributions of fossil and non-fossil sources to organic carbon (OC) and elemental carbon (EC) in carbonaceous aerosols can be quantified by measuring the radiocarbon (14C) content of each carbon fraction. However, the use of 14C in studying OC and EC has been limited by technical challenges related to the physical separation of the two fractions and small sample sizes. There is no common procedure for OC/EC 14C analysis, and uncertainty studies have largely focused on the precision of yields. Here, we quantified the uncertainty in 14C measurement of aerosols associated with the isolation and analysis of each carbon fraction with the Swiss_4S thermal-optical analysis (TOA) protocol. We used an OC/EC analyzer (Sunset Laboratory Inc., OR, USA) coupled to vacuum line to separate the two components. Each fraction was thermally desorbed and converted to carbon dioxide (CO2) in pure oxygen (O2). On average 91% of the evolving CO2 was then cryogenically trapped on the vacuum line, reduced to filamentous graphite, and measured for its 14C content via accelerator mass spectrometry (AMS). To test the accuracy of our set-up, we quantified the total amount of extraneous carbon introduced during the TOA sample processing and graphitization as the sum of modern and fossil (14C-depleted) carbon introduced during the analysis of fossil reference materials (adipic acid for OC and coal for EC) and contemporary standards (oxalic acid for OC and rice char for EC) as a function of sample size. We further tested our methodology by analyzing five ambient airborne particulate matter (PM2.5) samples with a range of OC and EC concentrations and 14C contents in an interlaboratory comparison. The total modern and fossil carbon blanks of our set-up were 0.8 ± 0.4 and 0.67 ± 0.34 μg C, respectively

  17. Release of (14)C-labelled carbon nanotubes from polycarbonate composites.

    PubMed

    Rhiem, Stefan; Barthel, Anne-Kathrin; Meyer-Plath, Asmus; Hennig, Michael P; Wachtendorf, Volker; Sturm, Heinz; Schäffer, Andreas; Maes, Hanna M

    2016-08-01

    Waste disposal of carbon nanotube (CNT) containing products is expected to be the most important pathway for release of CNTs into the environment. In the present work, the use of radiolabelled CNTs ((14)C-CNT) for polycarbonate polymer nanocomposites with 1 wt% (14)C-CNT content allowed for the first time to quantify and differentiate the CNT release according to the type of impact along the materials' ageing history. After an initial exposure of the nanocomposite by solar-like irradiation, further environmental impacts were applied to composite material. They aimed at mimicking disposal site conditions that may induce further ageing effects and CNT release. This study included shaking in water, rapid temperature changes, soaking in humic acid solution as well as waste water effluent, and, finally, gentle mechanical abrasion. All ageing impacts were applied sequentially, both on pristine (control) and on solar-irradiated nanocomposites. All experiments were accompanied by absolute quantification of radioactive release as well as chemical and morphological analyses of the nanocomposite surfaces using infra-red (IR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). The morphological analysis showed that spectral irradiation can uncover CNT networks on the outer nanocomposite surface layers by polymer degradation. After having subjected the solar-irradiated nanocomposite to all studied disposal site effect, the total radioactive release was quantified to amount to 64 mg CNT/m(2), whereas only 0.8 mg CNT/m(2) were found for the un-irradiated control sample. Solar degradation of polymers was thus found to significantly increase the propensity of the studied polymer nanocomposites to release CNTs during ageing effects at the product's end-of-life typical for disposal sites. PMID:27194367

  18. Introducing the global carbon cycle to middle school students with a 14C research project

    NASA Astrophysics Data System (ADS)

    Brodman Larson, L.; Phillips, C. L.; LaFranchi, B. W.

    2012-12-01

    Global Climate Change (GCC) is currently not part of the California Science Standards for 7th grade. Required course elements, however, such as the carbon cycle, photosynthesis, and cellular respiration could be linked to global climate change. Here we present a lesson plan developed in collaboration with scientists from Lawrence Livermore National Laboratory, to involve 7th grade students in monitoring of fossil fuel emissions in the Richmond/San Pablo area of California. -The lesson plan is a Greenhouse Gas/Global Climate Change Unit, with an embedded research project in which students will collect plant samples from various locals for analysis of 14C, to determine if there is a correlation between location and how much CO2 is coming from fossil fuel combustion. Main learning objectives are for students to: 1) understand how fossil fuel emissions impact the global carbon cycle, 2) understand how scientists estimate fossil CO2 emissions, and 3) engage in hypothesis development and testing. This project also engages students in active science learning and helps to develop responsibility, two key factors for adolescentsWe expect to see a correlation between proximity to freeways and levels of fossil fuel emissions. This unit will introduce important GCC concepts to students at a younger age, and increase their knowledge about fossil fuel emissions in their local environment, as well as the regional and global impacts of fossil emissions.

  19. Testing the 14C ages and conservative behavior of dissolved 14C in a carbonate aquifer in Yucca Flat, Nevada (USA), using 36Cl from groundwater and packrat middens

    NASA Astrophysics Data System (ADS)

    Kwicklis, Edward; Farnham, Irene

    2014-09-01

    Corrected groundwater 14C ages from the carbonate aquifer in Yucca Flat at the former Nevada Test Site (now the Nevada National Security Site), USA, were evaluated by comparing temporal variations of groundwater 36Cl/Cl estimated with these 14C ages with published records of meteoric 36Cl/Cl variations preserved in packrat middens (piles of plant fragments, fecal matter and urine). Good agreement between these records indicates that the groundwater 14C ages are reasonable and that 14C is moving with chloride without sorbing to the carbonate rock matrix or fracture coatings, despite opposing evidence from laboratory experiments. The groundwater 14C ages are consistent with other hydrologic evidence that indicates significant basin infiltration ceased 8,000 to 10,000 years ago, and that recharge to the carbonate aquifer is from paleowater draining through overlying tuff confining units along major faults. This interpretation is supported by the relative age differences as well as hydraulic head differences between the alluvial and volcanic aquifers and the carbonate aquifer. The carbonate aquifer 14C ages suggest that groundwater velocities throughout much of Yucca Flat are about 2 m/yr, consistent with the long-held conceptual model that blocking ridges of low-permeability rock hydrologically isolate the carbonate aquifer in Yucca Flat from the outlying regional carbonate flow system.

  20. Strong carbon release from the deep ocean induced a major atmospheric 14C drop over Heinrich Stadial 1

    NASA Astrophysics Data System (ADS)

    Sarnthein, M.; Grootes, P. M.; Schneider, B.

    2012-12-01

    Using the modern global distributions of apparent 14C ventilation ages and DIC we established a transfer function to trace past changes in the carbon storage of ocean waters >2000 m water depth. On this basis we concluded that the LGM carbon inventory was approximately 730-980 Gt larger than during pre-industrial times. This amount compares well with an estimated glacial transfer of 530-700 Gt from both the atmosphere and terrestrial biosphere in addition to a major DIC relocation from ocean intermediate waters. We consider that the LGM atmosphere contained 190 ppm CO2 (~375 Gt C) with a 14C concentration 1.4 times higher than that of the standard modern atmosphere (fMC) (Reimer et al. 2009). The LGM deep ocean had an average reservoir age of 2100 yr, which means that its 14C concentration was 0.77 times that of the LGM atmosphere, 1.08 times that of the modern atmosphere (fMC). During the subsequent early deglac¬ial Heinrich Stadial 1, a large portion of this 14C depleted carbon was released to the atmosphere and terrestrial biosphere (Monnin et al. 2001; Ciais et al. 2012). Our estimates suggest that the ocean-atmosphere exchange, producing this deglacial transfer of deep-ocean carbon, was sufficient to account for a 190-permil drop in atmospheric 14C. Thus an alleged major 'mystery' of last deglacial times, the source of 14C-depleted additional atmospheric carbon, appears solved. -- Ciais, P., Tagliabue, A., Cuntz, M., Bopp, L., et al. (2012), Large inert carbon pool in the terrestrial biosphere during the Last Glacial Maximum. Nature Geoscience 5, 74-79. Monnin, E., et al. (2001), Atmospheric CO2 concentrations over the last glacial termination. Science 291, 112-114. Reimer, P., et al. (2009), INTCAL09 and MARINE09 radiocarbon age calibration curves, 0-50,000 years cal. BP. Radiocarbon 51, 1111-1150.

  1. Carbon cycle dynamics and solar activity embedded in a high-resolution 14C speleothem record from Belize, Central America

    NASA Astrophysics Data System (ADS)

    Lechleitner, Franziska A.; Breitenbach, Sebastian F. M.; McIntyre, Cameron; Asmerom, Yemane; Prufer, Keith M.; Polyak, Victor; Culleton, Brendan J.; Kennett, Douglas J.; Eglinton, Timothy I.; Baldini, James U. L.

    2015-04-01

    Speleothem 14C has recently emerged as a potentially powerful proxy for climate reconstruction. Several studies have highlighted the link between karst hydrology and speleothem 14C content, and a number of possible causes for this relationship have been proposed, such as dripwater flow dynamics in the karst and changes in soil organic matter (SOM) turnover time (e.g. Griffiths et al., 2012). Here we present a high resolution 14C record for a stalagmite (YOK-I) from Yok Balum cave in southern Belize, Central America. YOK-I grew continuously over the last 2000 years, and has been dated very precisely with the U-Th method (40 dates, mean uncertainty < 10 years). The excellent chronological control for this stalagmite allows us to calculate 14C activity (a14C) at the time of speleothem deposition (a14Cinit), as well as the dead carbon fraction (DCF), predominantly a measure of the reservoir effect introduced by limestone dissolution in the karst (Genty et al., 2001). Both records show striking similarities to atmospheric a14C (IntCal13) and reconstructions of solar activity and 14C production rate. We infer close coupling between cave environment and atmosphere, with minimal signal dampening, an observation supported by monitoring data (Ridley et al., in press). DCF fluctuates between approximately 10% and 16% over the entire record, with distinctly lower DCF values and higher a14Cinit during a period of reduced rainfall between ca. 700-1100 AD (linked to the Classic Maya Collapse). This behavior is consistent with observations made elsewhere, and suggests that DCF responds to karst hydrological variability, specifically open-closed system transitions. YOK-I a14Cinit typically lags atmospheric values by 10-100 cal years. A shorter lag appears to be linked to periods of drought, suggesting a response of SOM dynamics above the cave to rainfall reduction. Specifically, drought is inferred to lead to reduced bioproductivity and soil carbon turnover, lowering contributions

  2. Radiocarbon ( 14C) measurements to quantify sources of atmospheric carbon monoxide in urban air

    NASA Astrophysics Data System (ADS)

    Klouda, George A.; Connolly, Michael V.

    Atmospheric air samples were collected during the winter of 1989-1990 in Albuquerque, NM, U.S.A., for radiocarbon ( 14C) analysis of carbon monoxide (CO). An experimental sample design was prepared to target periods when the concentration of CO exceeds the 9 μl l-1 (volume fraction), 8 h National Ambient Air Quality Standard (NAAQS) and during periods of attainment. Sampling sites, time of day, sampling duration, and meteorology were carefully considered so that source impacts be optimal. A balanced sampling factorial design was used to yield maximum information from the constraints imposed; the number of samples was limited by the number of sample canisters available, time and resources. Radiocarbon measurements of urban CO, " clean-air" CO background from Niwot Ridge, Colorado, average (wood) logs and oxygenated-gasolines were used in a three-source model to calculate the contribution of wood burning to the total atmospheric CO burden in Albuquerque. Results show that the estimated fractional contribution of residential wood combustion (Θ' Rwc) ranged from 0 to 0.30 of CO concentrations corrected for " clean-air" background. For these same samples, the respective CO concentrations attributed to wood burning range from 0 to 0.90 μmol mol -1 (mole fraction), well below the NAAQS. In all cases, fossil CO is the predominant source of ambient CO concentrations ranging from 0.96 to 6.34 μmol mol -1 A final comment is made on the potential of fossil CO measurements as an indirect tracer of atmospheric benzene, relevant to exposure risk estimates of motor vehicle emissions and occupational health and safety standards.

  3. Coprecipitation of (14)C and Sr with carbonate precipitates: The importance of reaction kinetics and recrystallization pathways.

    PubMed

    Hodkin, David J; Stewart, Douglas I; Graham, James T; Burke, Ian T

    2016-08-15

    This study investigated the simultaneous removal of Sr(2+) and (14)CO3(2-) from pH>12 Ca(OH)2 solution by the precipitation of calcium carbonate. Initial Ca(2+):CO3(2-) ratios ranged from 10:1 to 10:100 (mM:mM). Maximum removal of (14)C and Sr(2+) both occurred in the system containing 10mM Ca(2+) and 1mM CO3(2-) (99.7% and 98.6% removal respectively). A kinetic model is provided that describes (14)C and Sr removal in terms of mineral dissolution and precipitation reactions. The removal of (14)C was achieved during the depletion of the initial TIC in solution, and was subsequently significantly affected by recrystallization of the calcite precipitate from an elongate to isotropic morphology. This liberated >46% of the (14)C back to solution. Sr(2+) removal occurred as Ca(2+) became depleted in solution and was not significantly affected by the recrystallization process. The proposed reaction could form the basis for low cost remediation scheme for (90)Sr and (14)C in radioactively contaminated waters (<$0.25 reagent cost per m(3) treated). PMID:27104491

  4. Δ14C of Dissolved Inorganic Carbon in Surface Seawater from a Time-Series Site off Southern California

    NASA Astrophysics Data System (ADS)

    Hinger, E. N.; Dos Santos, G. M.; Griffin, S. M.; Druffel, E. R.

    2006-12-01

    To better understand the variability of carbon cycling in coastal seawater, we studied the carbon isotope abundances of dissolved inorganic carbon (DIC) in surface seawater at a time series site off the Newport Beach Pier in Orange County, California. A suite of samples was collected daily from October 16 to November 11, 2004. Δ14C values averaged 34±2‰, similar to values obtained for surface seawater from sites off the coast of CA. Fresh water input from the Santa Ana River caused lower than average Δ14C values. Since this initial set of measurements, a time-series site has been maintained from November 2004 to the present. Surface seawater has been collected every 15 days and analyzed for AMS- 14C, 13C/12C stable isotopes, salinity, and total inorganic carbon concentrations. These data will be presented along with meteorological data from the coastal Orange County region (precipitation, water temperature and Santa Ana River discharge) and discuss the factors important for varying the concentration and isotopic signatures of the dissolved inorganic carbon in seawater at our coastal site

  5. Carbon and 14C distribution in tropical and subtropical agricultural soils

    NASA Astrophysics Data System (ADS)

    Prastowo, Erwin; Grootes, Pieter; Nadeau, Marie

    2016-04-01

    Paddy soil management affects, through the alternating anoxic and oxic conditions it creates, the transport and stabilisation of soil organic matter (SOM). Irrigation water may percolate more organic materials - dissolved (DOM) and colloidal - into the subsoil during anoxic conditions. Yet a developed ploughpan tends to prevent C from going deeper in the subsoil and partly decouple C distribution in top and sub soil. We investigate the influence of different soil type and environment. We observed the C and 14C distribution in paddy and non-paddy soil profiles in three different soil types from four different climatic regions of tropical Indonesia, and subtropical China. Locations were Sukabumi (Andosol, ca. 850 m a.s.l), Bogor (clayey Alisol, ca. 240 m a.s.l), and Ngawi (Vertisol, ca. 70 m a.s.l) in Jawa, Indonesia, and Cixi (Alisol(sandy), ca. 4 - 6 m a.s.l) in Zhejiang Province, China. We compared rice paddies with selected neighbouring non-paddy fields and employed AMS 14C as a tool to study C dynamics from bulk, alkali soluble-humic, and insoluble humin samples, and macrofossils (plant remains, charcoal). Our data suggest that vegetation type determines the quantity and quality of biomass introduced as litter and root material in top and subsoil, and thus contributes to the soil C content and profile, which fits the 14C signal distribution, as well as 13C in Ngawi with C4 sugar cane as upland crop. 14C concentrations for the mobile humic acid fraction were generally higher than for bulk samples from the same depth, except when recent plant and root debris led to high 14C levels in near-surface samples. The difference in sampling, - averaged layer for bulk sample and 1-cm layer thickness for point sample - shows gradients in C and 14C across the layers, which could be a reason for discrepancies between the two. High 14C concentrations - in Andosol Sukabumi up to 111 pMC - exceed the atmospheric 14CO2concentration in the sampling year in 2012 (˜ 103 pMC) and

  6. Lung retention and binding of (/sup 14/C)-1-nitropyrene when inhaled by F344 rats as a pure aerosol or adsorbed to carbon black particles

    SciTech Connect

    Wolff, R.K.; Sun, J.D.; Barr, E.B.; Rothenberg, S.J.; Yeh, H.C.

    1989-01-01

    1-Nitropyrene (NP), as found in the environment, is more typically associated with carbonaceous particles than found as an aerosol of the pure compound. To determine whether (and why) an association with particles resulted in prolonged lung retention of NP, rats were exposed to 14C-NP as a pure aerosol or adsorbed on carbon black particles. Total 14C retained in the lung was greater at all times from 0.5 h to 30 d after exposure to 14C-NP adsorbed to carbon black particles than after exposure to pure 14C-NP (p less than .05). The fraction of total 14C in lung bound to carbon black particles decreased steadily with time after exposure, indicating in vivo removal of NP from the particles. At 0.5 h after exposure, the fraction of the estimated deposited 14C that was covalently bound to lung macromolecules was twofold greater for NP adsorbed on carbon black than for pure NP. Covalently bound 14C in lungs increased with time after exposure to 14C-NP adsorbed to carbon black, reaching levels of approximately 1% of the deposited radioactivity at 7-30 d after exposure, whereas levels of covalently bound 14C declined with time after exposure to pure NP. Thus, at 30 d after exposure, the amount of 14C covalently bound to lung macromolecules was approximately 10-fold greater (p less than .05) in rats that inhaled 14C-NP adsorbed on carbon black particles than in rats that inhaled pure 14C-NP aerosols. These results suggest that association of NP with carbon black particles augments the interaction of reactive metabolites of NP with target macromolecules. This phenomenon is thought to be related to the slow release of NP from carbon black particles, and may augment the biological effects of inhaled NP when adsorbed on carbon black or similar particles in the environment.

  7. Recent AMS measurements of {sup 14}C in soil organic matter: Understanding controls of carbon storage and turnover in soils

    SciTech Connect

    Trumbore, S.E.; Torn, M.S.; Chadwick, O.A.

    1996-10-01

    Radiocarbon measurements are one of the best tools available for determining the rates of carbon and turnover of in soil organic matter. AMS measurements of radiocarbon are essential they allow measurement of {sup 14}C in archived soils with very low carbon content, in physically or chemically fractionated soil organic matter, in dissolved organic carbon leached from soils, as well as in CO{sub 2} and CH{sub 4} produced during decomposition. We report recent results demonstrating the importance of applying AMS soil radiocarbon measurements to questions of soil C dynamics. We used the increase in {open_quote}bomb{close_quote} {sup 14}C between archived an modem soil profiles sampled along an elevation transect in the Sierra Nevada mountains, California, to determine the role of temperature in determining the rate of turnover of fast-cycling soil organic matter. To study the role of soil mineralogy in determining how carbon is stabilized in {open_quote}passive{close_quote} soil organic matter pools, we compare soil mineralogy and C and {sup 14}C storage in soils along a chronosequence in the Hawaiian islands. Implications for the global C cycle will be discussed.

  8. 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.

  9. 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.

  10. [Quantifying rice (Oryza sativa L.) photo-assimilated carbon input into soil organic carbon pools following continuous 14C labeling].

    PubMed

    Nie, San-An; Zhou, Ping; Ge, Ti-Da; Tong, Cheng-Li; Xiao, He-Ai; Wu, Jin-Shui; Zhang, Yang-Zhu

    2012-04-01

    The microcosm experiment was carried out to quantify the input and distribution of photo-assimilated C into soil C pools by using a 14C continuous labeling technique. Destructive samplings of rice (Oryza sativa) were conducted after labeling for 80 days. The allocation of 14C-labeled photosynthates in plants and soil C pools such as dissolved organic C (DOC) and microbial biomass C (MBC) in rice-planted soil were examined over the 14C labeling span. The amounts of rice shoot and root biomass C was ranged from 1.86 to 5.60 g x pot(-1), 0.46 to 0.78 g x pot(-1) in different tested paddy soils after labeling for 80 days, respectively. The amount of 14C in the soil organic C (14C-SOC) was also dependent on the soils, ranged from 114.3 to 348.2 mg x kg(-1), accounting for 5.09% to 6.62% of the rice biomass 14C, respectively. The amounts of 14C in the dissolved organic C (14C-DOC) and in the microbial biomass C(14C-MBC), as proportions of 14C-SOC, were 2.21%-3.54% and 9.72% -17.2%, respectively. The 14C-DOC, 14C-MBC, and 14C-SOC as proportions of total DOC, MBC, and SOC, respectively, were 6.72% -14.64%, 1.70% -7.67%, and 0.73% -1.99%, respectively. Moreover, the distribution and transformation of root-derived C had a greater influence on the dynamics of DOC and MBC than on the dynamics of SOC. Further studies are required to ascertain the functional significance of soil microorganisms (such as C-sequestering bacteria and photosynthetic bacteria) in the paddy system. PMID:22720588

  11. 14C in cropland soil of a long-term field trial - experimental variability and implications for estimating carbon turnover

    NASA Astrophysics Data System (ADS)

    Leifeld, J.; Mayer, J.

    2015-07-01

    Because of their controlled nature, the presence of independent replicates, and their known management history, long-term field experiments are key to the understanding of factors controlling soil carbon. Together with isotope measurements, they provide profound insight into soil carbon dynamics. For soil radiocarbon, an important tracer for understanding these dynamics, experimental variability across replicates is usually not accounted for; hence, a relevant source of uncertainty for quantifying turnover rates is missing. Here, for the first time, radiocarbon measurements of five independent field replicates, and for different layers, of soil from the 66-year-old controlled field experiment ZOFE in Zurich, Switzerland, are used to address this issue. 14C variability was the same across three different treatments and for three different soil layers between the surface and 90 cm depths. On average, experimental variability in 14C content was 12 times the analytical error but still, on a relative basis, smaller than variability in soil carbon concentration. Despite a relative homogeneous variability across the field and along the soil profile, the curved nature of the relationship between radiocarbon content and modelled carbon mean residence time implies that the absolute error of calculated soil carbon turnover time increases with soil depth. In our field experiment findings on topsoil carbon turnover variability would, if applied to subsoil, tend to underweight turnover variability even if experimental variability in the subsoil isotope concentration is the same. Together, experimental variability in radiocarbon is an important component in an overall uncertainty assessment of soil carbon turnover.

  12. Simulation of carbon cycling, including dissolved organic carbon transport, in forest soil locally enriched with 14C

    SciTech Connect

    Tipping, Ed; Chamberlain, Paul M.; Froberg, Mats J.; Hanson, Paul J; Jardine, Philip M

    2012-01-01

    The DyDOC model was used to simulate organic matter decomposition and dissolved organic matter (DOM) transport in deciduous forest soils at the Oak Ridge Reservation (ORR) in Tennessee, USA. The model application relied on extensive data from the Enriched Background Isotope study (EBIS), which made use of a local atmospheric enrichment of radiocarbon to establish a large-scale manipulation experiment with different inputs of 14C from both above-ground and below-ground litter. The aim of the modelling was to test if the processes that constitute DyDOC can explain the available observations for C dynamics in the ORR. More specifically we used the model to investigate the origins of DOM, its dynamics within the soil profile, and how it contributes to the formation of stable carbon in the mineral soil. The model was first configured to account for water transport through the soil, then observed pools and fluxes of carbon and 14C data were used to fit the model parameters that describe the rates of the metabolic transformations. The soils were described by a thin O-horizon, a 15 cm thick A-horizon and a 45-cm thick B-horizon. Within the thin O-horizon, litter is either converted to CO2 or to a second organic matter pool, which is converted to CO2 at a different rate, both pools being able to produce DOM. The best model performance was obtained by assuming that adsorption of downwardly transported DOM in horizons A and B, followed by further conversion to stable forms, produces mineral-associated carbon pools, while root litter is the source of non-mineral associated carbon, with relatively short residence times. In the simulated steady-state, most carbon entering the O-horizon leaves quickly as CO2, but 17% (46 gC m-2 a-1) is lost as DOC in percolating water. The DOM comprises mainly hydrophobic material, 40% being derived from litter and 60% from older organic matter pools (residence time ~ 10 years). Most of the DOM is converted to CO2 in the mineral soil, over

  13. Tracing source, mixing and uptaking processes of carbon in an epikarst spring-pond system in southeastern Guizhou of China by carbon isotopes (13C-14C)

    NASA Astrophysics Data System (ADS)

    Zhao, M.; Chen, B.; Liu, Z.; Li, H. C.; Yang, R.

    2015-12-01

    δ13C and Δ14C of dissolved inorganic carbon (DIC), particulate organic carbon (POC) and aquatic plants from a karst spring and two spring-fed ponds in Laqiao, Maolan County, Guizhou Province in January, July and October of 2013 were measured to understand the roles of aquatic photosynthesis through DIC uptake in karst surface waters. The mean Δ14C and δ13C values of DIC for the spring pool, midstream and downstream ponds are -60.6±26.3‰ and -13.53±1.97‰, -62.8±62.9‰ and -11.72±2.72‰, and -54.2±56.5‰ and -9.40±2.03‰, respectively. Both Δ14C and δ13C show seasonal variations, with lower Δ14C values but heavier δ13C values in dry season and vice versa in summer rainy season. This observation indicates that (1) the main carbon source of the spring DIC is from limestone bedrock dissolution and soil CO2 with higher contribution in summer due to higher productivity; and (2) 13C and 14C have different behaviors during DIC uptake by aquatic plants and during CO2 exchange between DIC and the atmospheric CO2. Biological uptake of CO2 will not affect the Δ14C of DIC, but lead to δ13CDIC enrichment. CO2 exchange between DIC and the atmospheric CO2 should elevate both the Δ14C and δ13C of DIC. In Laqiao spring-pond system, it seems that the effect of biological uptake on the Δ14C and δ13C of DIC is much stronger than that of CO2 exchange with the atmosphere. The mean Δ14C values of POC from the spring pool, midstream and downstream ponds are -308.1 ±64.3‰, -164.4±84.4‰ and -195.1±108.5‰, respectively, indicating mixture of aquatic algae and detrital particle (clay and dust). More aquatic algae were formed in the stream ponds especially in the summer. SEM results of the POC samples support this conclusion. Furthermore, the Δ14C values of the submerged aquatic plants range from -200.0‰ to -51.3 ‰ and were similar to those of the DIC, indicating that the aquatic plants used DIC for photosynthesis. The Δ14C value of an emergent plant

  14. 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).

  15. Estimation of groundwater residence time using environmental radioisotopes (14C,T) in carbonate aquifers, southern Poland.

    PubMed

    Samborska, Katarzyna; Różkowski, Andrzej; Małoszewski, Piotr

    2013-01-01

    Triassic carbonate aquifers in the Upper Silesia region, affected by intense withdrawal, have been investigated by means of isotopic analyses of (14)C, δ(13)C, δ(2)H, δ(18)O and (3)H. The isotopic examinations were carried out in the 1970s and in the early 1980s, and it was the first application of tracers to estimate age and vulnerability for the contamination of groundwater in this region. Similar isotopic analyses were conducted in 2007 and 2008 with the same Triassic carbonate formation. The isotopic examinations were performed within the confined part of the carbonate formation, wherein aquifers are covered by semi-permeable deposits. The direct recharge of the aquifer occurs in the outcrop areas, but it mainly takes place due to percolation of the water through aquitards and erosional windows. The Triassic aquifer has been intensively drained by wells and by lead-zinc mines. Nowadays, the declining water demand and closure of some mines have induced a significant increase in the water table level. The detailed analysis of the results, including the radiocarbon age corrections and the comparison of radioisotope activities, has made it possible to estimate the range of residence time within the carbonate Triassic aquifer. This range from several tens to several tens of thousands indicates that the recharge of aquifers might have occurred between modern times and the Pleistocene. The apparent age of the water estimated on the basis of (14)C activity was corrected considering the carbon isotope exchange and the diffusion between mobile water in fractures and stagnant water in micropores. The obtained corrected period of recharge corresponds to the result of investigations of noble gases, which were carried out in the 1990s. In almost half of the cases, groundwater is a mixture of young and old water. The mixing processes occur mainly in areas of heavy exploitation of the aquifer. PMID:22607326

  16. The14C 'bomb' pulse in selected European stalagmites as a tracer of soil carbon cycling dynamics

    NASA Astrophysics Data System (ADS)

    Rudzka, D.; McDermott, F.

    2012-04-01

    The decomposition of soil organic matter (SOM) is temperature dependant, but its response to a future warmer climate remains equivocal. Enhanced rates of decomposition of SOM under increased global temperatures might cause higher CO2 emissions to the atmosphere, and could constitute a strong positive feedback. The magnitude of this feedback however remains poorly understood primarily because of the difficulty in quantifying the temperature sensitivity of stored, recalcitrant carbon that comprises the bulk (>90%) of SOM in most soils. In this study we investigated the effects of climate on soil carbon using the 'bomb' radiocarbon systematics of selected modern European speleothems. The 'bomb' 14C spike was used as a tracer of the accumulation and decomposition of SOM under different climatic settings. New time-series radiocarbon measurements were carried out, and the attenuation of the 'bomb' 14C spike was studied in three stalagmites and in one soda straw stalactite. The results were used to examine the quality of soil organic matter and carbon dynamics on decadal timescales under a range of soil conditions and different climatic regimes. These new data were combined with published results to further examine soil carbon transfer dynamics, and to explore the sensitivity of labile and recalcitrant organic matter decomposition to different climatic conditions. The initial radiocarbon activity from each speleothem was modelled using a three pool soil carbon inverse model (applying a Monte Carlo method) in order to investigate the soil carbon residence time and its turnover above the cave site. Sites that are characterised by high mean annual air temperatures (MAAT) and a high soil carbon storage capacity (e.g. overlain by thick soil cover with dense, well developed vegetation, such as La Garma, N. Spain and Sofular, Turkey) display the highest damping effect, and the oldest mean soil carbon ages (MSCA), with residence times of c. half a millennium. This suggests that

  17. Bayesian calibration of a soil organic carbon model using Δ14C measurements of soil organic carbon and heterotrophic respiration as joint constraints

    NASA Astrophysics Data System (ADS)

    Ahrens, B.; Reichstein, M.; Borken, W.; Muhr, J.; Trumbore, S. E.; Wutzler, T.

    2014-04-01

    Soils of temperate forests store significant amounts of organic matter and are considered to be net sinks of atmospheric CO2. Soil organic carbon (SOC) turnover has been studied using the Δ14C values of bulk SOC or different SOC fractions as observational constraints in SOC models. Further, the Δ14C values of CO2 that evolved during the incubation of soil and roots have been widely used together with Δ14C of total soil respiration to partition soil respiration into heterotrophic respiration (HR) and rhizosphere respiration. However, these data have not been used as joint observational constraints to determine SOC turnover times. Thus, we focus on (1) how different combinations of observational constraints help to narrow estimates of turnover times and other parameters of a simple two-pool model, the Introductory Carbon Balance Model (ICBM); (2) whether relaxing the steady-state assumption in a multiple constraints approach allows the source/sink strength of the soil to be determined while estimating turnover times at the same time. To this end ICBM was adapted to model SOC and SO14C in parallel with litterfall and the Δ14C of litterfall as driving variables. The Δ14C of the atmosphere with its prominent bomb peak was used as a proxy for the Δ14C of litterfall. Data from three spruce-dominated temperate forests in Germany and the USA (Coulissenhieb II, Solling D0 and Howland Tower site) were used to estimate the parameters of ICBM via Bayesian calibration. Key findings are as follows: (1) the joint use of all four observational constraints (SOC stock and its Δ14C, HR flux and its Δ14C) helped to considerably narrow turnover times of the young pool (primarily by Δ14C of HR) and the old pool (primarily by Δ14C of SOC). Furthermore, the joint use of all observational constraints made it possible to constrain the humification factor in ICBM, which describes the fraction of the annual outflux from the young pool that enters the old pool. The Bayesian parameter

  18. The next chapter of direct phytolith 14C dating: debunking the myth of occluded photosynthetic carbon exclusivity

    NASA Astrophysics Data System (ADS)

    Santos, G.; Harutyunyan, A.; Alexandre, A. E.; Reyerson, P. E.; Gallagher, K. L.; Isabelle, B. D.

    2014-12-01

    Radiocarbon dating of carbon (C) encapsulated in phytoliths (phytC) is currently used in many Earth Science disciplines for absolute chronologies and paleoclimatic reconstructions; however, the usefulness of phytC has been hampered by inadequate extraction methods[1] and uncertainties regarding its origin as purely photosynthetic [2,3,4]. An early investigation measuring isotopes from Gramineae spp. grown in free-air C enrichment experiments (FACE), showed that part of of its phytC is from a non-photosynthetic source, thus indicating a dual origin[5]. To demonstrate that non-photosynthetic sources within phytC could be from soil C stocks, we measured 14C-AMS phytC extracted from a set of Sorghum bicolor growing on known 14C and d13C bulk substrates and hydroponic solutions. The phytolith concentrates and a silica blank were extracted at UCI, CEREGE and Wisconsin using an improved protocol [1,2]. We also measured CO2 fluxes and isotopic signatures of microbial respiration, percentage of biomass and phytolith extracts produced, and isotopic signatures of the local air and bulk-plant during the growing season of 2012. This allowed comparison of the belowground substrate and nutrient C contributions to phytC 14C results. Meanwhile, NanoSIMS analyses of phytolith polished sections was used to locate phytC in the phytolith siliceous structure [6]. These results will be shown and discussed. [1] Corbineau et al. 2013 R. Paleobot. Palyn. 197: 179 [2] Santos et al. 2010 T. Radiocarbon 52:113 [3] Santos et al. 2012a Biogeosci. 9:1873 [4] Santos et al. 2012b Biogeosci. Discussion 9:C6114 [5] Reyerson et al. 2013 AGU Fall meeting 2013 (Abstract ID: 1803125). [6] Alexandre, et al., submitted.

  19. Bayesian calibration of a soil organic carbon model using Δ14C measurements of soil organic carbon and heterotrophic respiration as joint constraints

    NASA Astrophysics Data System (ADS)

    Ahrens, B.; Reichstein, M.; Borken, W.; Muhr, J.; Trumbore, S. E.; Wutzler, T.

    2013-08-01

    Soils of temperate forests store significant amounts of organic matter and are considered to be net sinks of atmospheric CO2. Soil organic carbon (SOC) turnover has been studied using the Δ14C values of bulk SOC or different SOC fractions as observational constraints in SOC models. Further, the Δ14C values of CO2 evolved during the incubation of soil and roots have been widely used together with Δ14C of total soil respiration to partition soil respiration into heterotrophic respiration (HR) and rhizosphere respiration. However, these data have not been used as joint observational constraints to determine SOC turnover times. Thus, we focus on: (1) how different combinations of observational constraints help to narrow estimates of turnover times and other parameters of a simple two-pool model, ICBM; (2) if a multiple constraints approach allows determining whether the soil has been storing or losing SOC. To this end ICBM was adapted to model SOC and SO14C in parallel with litterfall and the Δ14C of litterfall as driving variables. The Δ14C of the atmosphere with its prominent bomb peak was used as a proxy for the Δ14C of litterfall. Data from three spruce dominated temperate forests in Germany and the USA (Coulissenhieb II, Solling D0 and Howland Tower site) were used to estimate the parameters of ICBM via Bayesian calibration. Key findings are: (1) the joint use of all 4 observational constraints (SOC stock and its Δ14C, HR flux and its Δ14C) helped to considerably narrow turnover times of the young pool (primarily by Δ14C of HR) and the old pool (primarily by Δ14C of SOC). Furthermore, the joint use all observational constraints allowed constraining the humification factor in ICBM, which describes the fraction of the annual outflux from the young pool that enters the old pool. The Bayesian parameter estimation yielded the following turnover times (mean ± standard deviation) for SOC in the young pool: Coulissenhieb II 1.7 ± 0.5 yr, Solling D0 5.7 ± 0

  20. Ancient carbon from a melting glacier gives high 14C age in living pioneer invertebrates

    PubMed Central

    Hågvar, Sigmund; Ohlson, Mikael

    2013-01-01

    Glaciers are retreating and predatory invertebrates rapidly colonize deglaciated, barren ground. The paradox of establishing predators before plants and herbivores has been explained by wind-driven input of invertebrate prey. Here we present an alternative explanation and a novel glacier foreland food web by showing that pioneer predators eat locally produced midges containing 21,000 years old ancient carbon released by the melting glacier. Ancient carbon was assimilated by aquatic midge larvae, and terrestrial adults achieved a radiocarbon age of 1040 years. Terrestrial spiders, harvestmen and beetles feeding on adult midges had radiocarbon ages of 340–1100 years. Water beetles assumed to eat midge larvae reached radiocarbon ages of 1100–1200 years. Because both aquatic and terrestrial pioneer communities use ancient carbon, the term “primary succession” is questionable in glacier forelands. If our “old” invertebrates had been collected as subfossils and radiocarbon dated, their age would have been overestimated by up to 1100 years. PMID:24084623

  1. Biochar, activated carbon, and carbon nanotubes have different effects on fate of 14C-catechol and microbial community in soil

    NASA Astrophysics Data System (ADS)

    Shan, Jun; Ji, Rong; Yu, Yongjie; Xie, Zubin; Yan, Xiaoyuan

    2015-10-01

    This study investigated the effects of biochar, activated carbon (AC)-, and single-walled and multi-walled carbon nanotubes (SWCNTs and MWCNTs) in various concentrations (0, 0.2, 20, and 2,000 mg/kg dry soil) on the fate of 14C-catechol and microbial community in soil. The results showed that biochar had no effect on the mineralization of 14C-catechol, whereas AC at all amendment rates and SWCNTs at 2,000 mg/kg significantly reduced mineralization. Particularly, MWCNTs at 0.2 mg/kg significantly stimulated mineralization compared with the control soil. The inhibitory effects of AC and SWCNTs on the mineralization were attributed to the inhibited soil microbial activities and the shifts in microbial communities, as suggested by the reduced microbial biomass C and the separated phylogenetic distance. In contrast, the stimulatory effects of MWCNTs on the mineralization were attributed to the selective stimulation of specific catechol-degraders by MWCNTs at 0.2 mg/kg. Only MWCNTs amendments and AC at 2,000 mg/kg significantly changed the distribution of 14C residues within the fractions of humic substances. Our findings suggest biochar, AC, SWCNTs and MWCNTs have different effects on the fate of 14C-catechol and microbial community in soil.

  2. Biochar, activated carbon, and carbon nanotubes have different effects on fate of 14C-catechol and microbial community in soil

    PubMed Central

    Shan, Jun; Ji, Rong; Yu, Yongjie; Xie, Zubin; Yan, Xiaoyuan

    2015-01-01

    This study investigated the effects of biochar, activated carbon (AC)-, and single-walled and multi-walled carbon nanotubes (SWCNTs and MWCNTs) in various concentrations (0, 0.2, 20, and 2,000 mg/kg dry soil) on the fate of 14C-catechol and microbial community in soil. The results showed that biochar had no effect on the mineralization of 14C-catechol, whereas AC at all amendment rates and SWCNTs at 2,000 mg/kg significantly reduced mineralization. Particularly, MWCNTs at 0.2 mg/kg significantly stimulated mineralization compared with the control soil. The inhibitory effects of AC and SWCNTs on the mineralization were attributed to the inhibited soil microbial activities and the shifts in microbial communities, as suggested by the reduced microbial biomass C and the separated phylogenetic distance. In contrast, the stimulatory effects of MWCNTs on the mineralization were attributed to the selective stimulation of specific catechol-degraders by MWCNTs at 0.2 mg/kg. Only MWCNTs amendments and AC at 2,000 mg/kg significantly changed the distribution of 14C residues within the fractions of humic substances. Our findings suggest biochar, AC, SWCNTs and MWCNTs have different effects on the fate of 14C-catechol and microbial community in soil. PMID:26515132

  3. Soil Carbon Vulnerability in Arctic Coastal Tundra: Seasonal and Spatial Variations in 14C-CO2

    NASA Astrophysics Data System (ADS)

    Smith, L. J.; Torn, M. S.; Conrad, M. E.; Curtis, J. B.; Hahn, M. S.

    2013-12-01

    One reason permafrost soils contain large, old soil organic carbon stores is slow decomposition rates due to cold and waterlogged conditions. If climate change causes high latitude soils to warm and dry, carbon emissions from permafrost soils could be an important atmospheric greenhouse gas source. The vulnerability of global Arctic soil carbon stocks to increased decomposition due to thaw is hard to assess, due to environmental heterogeneity, complex controls on microbial processes, uncertain carbon stocks and flux rates, and poorly understood soil carbon stabilization mechanisms. To address these knowledge gaps, we are using radiocarbon measurements to estimate carbon turnover times in polygonal tundra in Barrow, Alaska. Specifically, we ask: (1) how do old versus recently fixed soil carbon pools contribute to total decomposition, (2) how does this vary seasonally, and (3) how does it vary across a permafrost degradation gradient? Old radiocarbon ages of soil organic matter in perennially frozen soils and deep portions of the seasonally thawed active layer reflect slow historic decomposition rates, and changes in the radiocarbon content of respired CO2 indicate relative mineralization rates of this old, stored carbon. At four time points from June-October 2013, we sample soil organic matter and respired CO2 from low-centered, transitional, and high-centered polygons characteristic of a permafrost degradation cycle. We measure the radiocarbon content of CO2 in surface fluxes and soil pore space from 3 depths in the soil profile, and concurrently incubate active layer soils to resolve the 14C-CO2 signatures of individual soil layers. Preliminary data from 2012 suggest that old soil carbon stores are vulnerable to decomposition. CO2 ages increase with depth in the profile from modern radiocarbon ages to as old as 3115 BP, and high incubation flux rates indicate availability to microbes. As part of the Next Generation Ecosystem Experiment (NGEE-Arctic), we now study

  4. 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.; 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.

  5. The evolution of a tropical rainforest/grassland mosaic in southeastern Brazil since 28,000 14C yr BP based on carbon isotopes and pollen records

    NASA Astrophysics Data System (ADS)

    Ruiz Pessenda, Luiz Carlos; De Oliveira, Paulo Eduardo; Mofatto, Milene; de Medeiros, Vanda Brito; Francischetti Garcia, Ricardo José; Aravena, Ramon; Bendassoli, José Albertino; Zuniga Leite, Acácio; Saad, Antonio Roberto; Lincoln Etchebehere, Mario

    2009-05-01

    The lack of paleoecological records from the montane Atlantic Rainforest of coastal Brazil, a hotspot of biological diversity, has been a major obstacle to our understanding of the vegetational changes since the last glacial cycle. We present carbon isotope and pollen records to assess the impact of the glaciation on the native vegetation of the Serra do Mar rainforest in São Paulo, Brazil. From ca. 28,000 to ˜ 22,000 14C yr BP, a subtropical forest with conifer trees is indicative of cool and humid conditions. In agreement carbon isotopic data on soil organic matter suggest the presence of C 3 plants and perhaps C 4 plants from ˜ 28,000 to ˜ 19,000 14C yr BP. The significant increase in the sedimentation rate and algal spores from ˜ 19,450 to ˜ 19,000 14C yr BP indicates increasing humidity, associated to an erosion process between ˜ 19,000 and ˜ 15,600 14C yr BP. From ˜ 15,600 14C yr BP to present there is a substantial increase in arboreal elements and herbs, indicating more humid and warmer climate. From ˜ 19,000 to ˜ 1000 14C yr BP, δ 13C values indicated the predominance of C 3 plants. These results are in agreement with studies in speleothems of caves, which suggest humid conditions during the last glacial maximum.

  6. New 230Th/U and 14C ages from Lake Lahontan carbonates, Nevada, USA, and a discussion of the origin of initial thorium

    NASA Astrophysics Data System (ADS)

    Lin, J. C.; Broecker, W. S.; Anderson, R. F.; Hemming, S.; Rubenstone, J. L.; Bonani, G.

    1996-08-01

    Five sets of coeval lacustrine carbonate samples from Pleistocene Lake Lahontan in western Nevada were dated by both the AMS 14C and 230Th/U isochron methods. All five groups of samples were analyzed for U-Th isotopes by alpha spectrometry and one of the groups was additionally measured by thermal and secondary ionization mass spectrometry (TIMS and SIMS) for comparison. The 14C ages were corrected to calendar years using the calibration curve recommended by Bard et al. (1992) . Without local reservoir correction on the 14C ages, mean 230Th/U isochron ages of some sets are apparently older than their calendar-corrected 14C ages by up to 2300 years. Modern carbon contamination of these carbonate samples through recrystallization or deposition of secondary calcite is likely to be responsible for part of the age discrepancies. We explored additional biases associated with the isochron ages, maybe produced by the presence of initial Th coprecipitated from the lake water. It can be shown that if dissolved (hydrogenous) Th is directly incorporated into the pure carbonates, then the three-component mixing among (1) detrital Th, (2) hydrogenous Th adsorbed on detritus, and (3) hydrogenous Th incorporated by the carbonate can introduce a positive age bias. We have developed an approach to estimate the magnitude of this bias of the Lake Lahontan carbonates. The preliminary estimates suggest a positive age bias of 1000 to 2000 years for two sets of the samples.

  7. Sources of Respired Carbon in a Northern Minnesota Ombrotrophic Spruce Bog: Preliminary 14C Results from the SPRUCE Site.

    NASA Astrophysics Data System (ADS)

    Guilderson, T. P.; McNicol, G.; Machin, A.; Hanson, P. J.; McFarlane, K. J.; Osuna, J. L.; Pett-Ridge, J.; Singleton, M. J.

    2014-12-01

    A significant uncertainty in future land-surface carbon budgets is the response of wetlands to climate change. A corollary and related question is the future net climate (radiative) forcing impact from wetlands. Active wetlands emit both CO2 and CH4 to the atmosphere. CH4 is, over a few decades, a much more potent greenhouse gas than CO2. CO2 has a longer atmospheric lifetime and a longer 'tail' to its radiative influence. Whether wetlands are a net source or sink of atmospheric carbon under future climate change will depend on ecosystem response to rising temperatures and elevated CO2. The largest uncertainty in future wetland C-budgets, and their climate forcing is the stability of the large below-ground carbon stocks, often in the form of peat, and the partitioning of CO2 and CH4 released via ecosystem respiration. In advance of a long-term experimental warming and elevated CO2 manipulation at the DOE Spruce and Peatland Responses Under Climatic and Environmental Change (SPRUCE) site in the Marcell Experimental Forest, we have characterized the source of respired carbon used for both the production of CO2 and CH4. Samples were collected in early June, late July, and will be collected in early September from three large (~1.1 m2, ~0.5m3) chambers from the control plot, and two of the experimental plots selected for heating (+9°C, +4.5°C). Early June fluxes from the three chambers were ~5500 mgC-m-2-d-1 and ~16 mgC-m-2-d-1 for CO2 and CH4 respectively. Radiocarbon analysis of CO2 and CH4 indicate that the source for the respired carbon is for the most part recent, with most 14C values between 30 and 40‰ - i.e., carbon that was photosynthetically fixed in the last few years. In concert with rising air and ground temperatures fluxes in late July increased to ~6500 mgC-m-2-d-1 and ~86 mgC-m-2-d-1. Although deep-heating was initiated in mid to late June we hypothesize that the July respiration signal is dominated by the regular seasonal cycle of natural warming

  8. Carbon cycling in primary production bottle incubations: inferences from grazing experiments and photosynthetic studies using 14C and 18O in the Arabian Sea

    NASA Astrophysics Data System (ADS)

    Laws, Edward A.; Landry, Michael R.; Barber, Richard T.; Campbell, Lisa; Dickson, Mary-Lynn; Marra, John

    Estimates of photosynthesis based on the incorporation of 14C-labeled inorganic carbon into particulate carbon were compared to estimates of gross photosynthesis based on net O 2 production and the production of 18O2 from H218O during the US Joint Global Ocean Flux Study (US JGOFS) Arabian Sea process cruises. For samples incubated below the surface and at optical depths<3, the 14C uptake : gross photosynthesis ratio averaged 0.45±0.1. This result is in accord with theoretical considerations of the combined effects of the Mehler reaction, photorespiration, dark respiration, excretion, and grazing effects on the two estimates of photosynthesis. The 14C uptake : gross photosynthesis ratio was distinctly higher (0.62) for samples incubated at the surface. This result is likely due to UV light effects, since the O 2 and 14C incubations were done in quartz and polysulfone bottles, respectively. The 14C uptake : gross photosynthesis ratio was lower (0.31) for bottles incubated at optical depths>3. This result probably reflects an increase in the ratio of dark respiration to net photosynthesis in the vicinity of the compensation light level.

  9. Constraints on the Origin of Sedimentary Organic Carbon in the Beaufort Sea from Coupled Molecular 13C and 14C Measurements

    NASA Astrophysics Data System (ADS)

    Drenzek, N.; Montlucon, D.; Yunker, M.; MacDonald, R.; Eglinton, T.

    2005-12-01

    The type and flux of organic carbon (OC) delivered from the continents to the sea can both influence, and be influenced by, climate change on regional and global scales. In order to develop a more complete view of OC delivery in the climatically sensitive Arctic region, we measured the stable carbon and radiocarbon isotopic signatures of individual lipid biomarkers and products of kerogen pyrolysis from the surficial sediments of several sites on the Mackenzie Shelf and adjacent slope of the Beaufort Sea. Even carbon numbered fatty acids exhibit a trend of increasing radiocarbon age with increasing chain length, from modern values for shorter homologues (nC18 or below) to several thousand years old for their longer counterparts (nC24 or greater). Such depleted Δ14C values for longer-chain fatty acids likely reflect supply of vascular plant OC that has been `pre-' on the continents for several millennia prior to delivery to the Beaufort Sea. Their concomitant stable carbon isotopic compositions support a C3 land plant source. The molecular distributions and corresponding δ13C and Δ14C signatures of solvent-extractable alkanes point to at least two sources: higher plant leaf waxes and a 14C-`dead' component likely derived from erosion of organic-rich sedimentary rocks exposed within the Mackenzie River drainage basin. The stable carbon and radiocarbon compositions of straight chain n-hydrocarbon pyrolysis products from the corresponding demineralized sediments suggest their vascular plant-derived precursor structures also spent several millennia in continental reservoirs before being delivered to the Beaufort Sea. On a bulk level, the trend in sedimentary organic carbon contents, C/N ratios, and δ13C values point to an overall decrease in the terrigenous input (mainly from the Mackenzie river) with distance offshore, whereas bulk Δ14C measurements exhibit no trend suggesting a somewhat constant pre-aged component. A dual molecular isotopic mass balance approach

  10. Airborne Oceanographic Lidar (AOL) (Global Carbon Cycle)

    NASA Technical Reports Server (NTRS)

    2003-01-01

    This bimonthly contractor progress report covers the operation, maintenance and data management of the Airborne Oceanographic Lidar and the Airborne Topographic Mapper. Monthly activities included: mission planning, sensor operation and calibration, data processing, data analysis, network development and maintenance and instrument maintenance engineering and fabrication.

  11. New {sup 230}Th/U and {sup 14}C ages from Lake Lahontan carbonates, Nevada, USA, and a discussion of the origin of initial thorium

    SciTech Connect

    Lin, J.C.; Broecker, W.S.; Anderson, R.F.

    1996-08-01

    Five sets of coeval lacustrine carbonate samples from Pleistocene Lake Lahontan in western Nevada were dated by both the AMS {sup 14}C and {sup 230}Th/U isochron methods. All five groups of samples were analyzed for U-Th isotopes by alpha spectrometry and one of the groups was additionally measured by thermal and secondary ionization mass spectrometry (TIMS and SIMS) for comparison. The {sup 14}C ages were corrected to calendar years using the calibration curve recommended by Bard et al. (1992). Without local reservoir correction on the {sup 14}C ages mean {sup 230}Th/U isochron ages of some sets are apparently older than their calendar-corrected {sup 14}C ages by up to 2300 years. Modern carbon contamination of these carbonate samples through recrystallization or deposition of secondary calcite is likely to be responsible for part of the age discrepancies. We explored additional biases associated with the isochron ages, maybe produced by the presence of initial Th coprecipitated from the lake water. It can be shown that if dissolved (hydrogenous) Th is directly incorporated into the pure carbonates, then the three-component mixing among (1) detrital Th, (2) hydrogenous Th adsorbed on detritus, and (3) hydrogenous Th incorporated by the carbonate can introduce a positive age bias. We have developed an approach to estimate the magnitude of this bias of the Lake Lahontan carbonates. The preliminary estimates suggest a positive age bias of 1000 to 2000 years for two sets of the samples. 49 refs., 10 figs., 9 tabs.

  12. Translocation of Radioactive Carbon after the Application of 14C-Alanine and 14CO2 to Sunflower Leaves 1

    PubMed Central

    Chopowick, R. E.; Forward, D. F.

    1974-01-01

    14C-(UL)-l-Alanine was applied to the surface of mature leaves at the second node of sunflower (Helianthus annuus L. cv Commander) plants, under illumination. The alanine was absorbed during a 4-hour period, and some of it was metabolized by the absorbing tissue. After a lag period of about 15 minutes from first application, distribution of 14C through the plant proceeded in much the same pattern as when 14CO2 is assimilated by similar leaves. Most, if not all, of the 14C exported from the absorbing regions was in sucrose. Only minute amounts appeared in alanine or other amino acids in surrounding parts of the leaf blade or in the petiole, although these were strongly labeled in the tissue absorbing 14C-alanine. When 14CO2 was supplied for 15 minutes to leaves of different ages, amino acids were lightly labeled in the leaf blade. Mature green leaves exported only sucrose. Yellowing leaves on 60-day-old plants exported a variety of substances including amino acids. PMID:16658645

  13. Inverse modelling of the 14C bomb pulse in stalagmites to constrain the dynamics of soil carbon cycling at selected European cave sites

    NASA Astrophysics Data System (ADS)

    Rudzka-Phillips, D.; McDermott, F.; Jackson, A.; Fleitmann, D.

    2013-07-01

    The decomposition of soil organic matter (SOM) is temperature dependent, but its response to a future warmer climate remains equivocal. Enhanced rates of decomposition of SOM under increased global temperatures might cause higher CO2 emissions to the atmosphere, and could therefore constitute a strong positive feedback. The magnitude of this feedback however remains poorly understood, primarily because of the difficulty in quantifying the temperature sensitivity of stored, recalcitrant carbon that comprises the bulk (>90%) of SOM in most soils. In this study we investigated the effects of climatic conditions on soil carbon dynamics using the attenuation of the 14C 'bomb' pulse as recorded in selected modern European speleothems. These new data were combined with published results to further examine soil carbon dynamics, and to explore the sensitivity of labile and recalcitrant organic matter decomposition to different climatic conditions. Temporal changes in 14C activity inferred from each speleothem was modelled using a three pool soil carbon inverse model (applying a Monte Carlo method) to constrain soil carbon turnover rates at each site. Speleothems from sites that are characterised by semi-arid conditions, sparse vegetation, thin soil cover and high mean annual air temperatures (MAATs), exhibit weak attenuation of atmospheric 14C 'bomb' peak (a low damping effect, D in the range: 55-77%) and low modelled mean respired carbon ages (MRCA), indicating that decomposition is dominated by young, recently fixed soil carbon. By contrast, humid and high MAAT sites that are characterised by a thick soil cover and dense, well developed vegetation, display the highest damping effect (D = c. 90%), and the highest MRCA values (in the range from 350 ± 126 years to 571 ± 128 years). This suggests that carbon incorporated into these stalagmites originates predominantly from decomposition of old, recalcitrant organic matter. SOM turnover rates cannot be ascribed to a single

  14. Investigation of carbon distribution with {sup 14}C as tracer for carbon dioxide (CO{sub 2}) sequestration through NH{sub 4}HCO{sub 3} production

    SciTech Connect

    Zhongxian Cheng; Youhua Ma; Xin Li; Wei-Ping Pan

    2007-12-15

    This work studies carbon fate using the {sup 14}C tracer technique in ecosystems when synthesized fertilizer is applied. The concept of aqueous ammonia solution scrubbing CO{sub 2} from flue gas is used in the fertilizer synthesis. Products after the capture are ammonium bicarbonate (ABC, NH{sub 4}HCO{sub 3}) or long-term effect ammonium bicarbonate (LEABC, NH{sub 4}HCO{sub 3}), an economic source of nitrogen fertilizer. The ABC or LEABC is used as a 'carrier' to transport CO{sub 2} from the atmosphere to the crops and soil. An indoor greenhouse was built, and wheat was chosen as the plant to study in this ecosystem. The investigated ecosystem consists of plant (wheat), soils with three different pH values (alkaline, neutral, and acidic), and three types of underground water (different Ca{sup 2+} and Mg{sup 2+} concentrations). After biological assimilation and metabolism in wheat receiving ABC or LEABC, it was found that a considerable amount (up to 10%) of the carbon source was absorbed by the wheat with increased biomass production. The majority of the unused carbon source (up to 76%) percolated into the soil as carbonates, such as environmentally benign calcium carbonate (CaCO{sub 3}). Generally speaking, alkaline soil has a higher capability to capture and store carbon. For the same soil, there is no apparent difference in carbon capturing capability between ABC and LEABC. These findings answer the question of how carbon is distributed after synthesized ABC or LEABC is applied into the ecosystem. In addition, a separate postexperiment on carbon forms that existed in the soil was made. It was found that up to 88% of the trapped carbon existed in the form of insoluble salts (i.e., CaCO{sub 3}) in alkaline soils. This indicates that alkaline soil has a greater potential for storing carbon after the use of the synthesized ABC or LEABC from exhausted CO{sub 2}. 21 refs., 6 figs., 5 tabs.

  15. Revised 14C dating of ice wedge growth in interior Alaska (USA) to MIS 2 reveals cold paleoclimate and carbon recycling in ancient permafrost terrain

    NASA Astrophysics Data System (ADS)

    Lachniet, Matthew S.; Lawson, Daniel E.; Sloat, Alison R.

    2012-09-01

    Establishing firm radiocarbon chronologies for Quaternary permafrost sequences remains a challenge because of the persistence of old carbon in younger deposits. To investigate carbon dynamics and establish ice wedge formation ages in Interior Alaska, we dated a late Pleistocene ice wedge, formerly assigned to Marine Isotope Stage (MIS) 3, and host sediments near Fairbanks, Alaska, with 24 radiocarbon analyses on wood, particulate organic carbon (POC), air-bubble CO2, and dissolved organic carbon (DOC). Our new CO2 and DOC ages are up to 11,170 yr younger than ice wedge POC ages, indicating that POC is detrital in origin. We conclude an ice wedge formation age between 28 and 22 cal ka BP during cold stadial conditions of MIS 2 and solar insolation minimum, possibly associated with Heinrich event 2 or the last glacial maximum. A DOC age for an ice lens in a thaw unconformity above the ice wedge returned a maximum age of 21,470 ± 200 cal yr BP. Our variable 14C data indicate recycling of older carbon in ancient permafrost terrain, resulting in radiocarbon ages significantly older than the period of ice-wedge activity. Release of ancient carbon with climatic warming will therefore affect the global 14C budget.

  16. 14C chronology of the oldest Scandinavian church in use. An AMS/PIXE study of lime lump carbonate in the mortar

    NASA Astrophysics Data System (ADS)

    Lindroos, Alf; Ranta, Heikki; Heinemeier, Jan; Lill, Jan-Olof

    2014-07-01

    Mortar dating was applied to newly revealed, original mortar in the church of Dalby in Scania, southern Sweden which is considered to be the oldest still standing church in Scandinavia. Small white lime lumps were sampled by chipping from the supporting pillars in the interior of the church. Special emphasis was in sampling lime lumps because the church is situated in the Scania limestone area and aggregate limestone contamination was anticipated in the bulk mortars. Earlier studies have, however, shown that lime lumps do not contain aggregate material but only possible limestone rests from incomplete calcination. The sampled material was prepared for radiocarbon AMS dating. The carbonate in the lime lumps was hydrolyzed according to the sequential leaching technique developed for the Århus 14C laboratory in Denmark. Prior to the hydrolysis the lime lumps were examined for dead-carbon contamination using a stereo microscope and cathodoluminescence. The lime lumps displayed heterogeneous carbonate luminescence. This is, however, common and it was not considered a problem because carbonate growth in changing pH/Eh conditions often leads to changing luminescence colors. Two lumps had little dead carbon contamination and an early second millennium 14C signature. One lump, however, seemed to be heavily contaminated with dead carbon. Since the sample passed the microscopic screening, the leftovers of the lump was subjected to PIXE analysis and compared with the other two lumps. The well-defined, early 2nd millennium 14C age of the lime lumps of this particular church is an important contribution to the discussion on stone church chronology in Scandinavia.

  17. 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

  18. 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.

  19. 14C-dead living biomass: evidence for microbial assimilation of ancient organic carbon during shale weathering.

    PubMed

    Petsch, S T; Eglington, T I; Edwards, K J

    2001-05-11

    Prokaryotes have been cultured from a modern weathering profile developed on a approximately 365-million-year-old black shale that use macromolecular shale organic matter as their sole organic carbon source. Using natural-abundance carbon-14 analysis of membrane lipids, we show that 74 to 94% of lipid carbon in these cultures derives from assimilation of carbon-14-free organic carbon from the shale. These results reveal that microorganisms enriched from shale weathering profiles are able to use a macromolecular and putatively refractory pool of ancient organic matter. This activity may facilitate the oxidation of sedimentary organic matter to inorganic carbon when sedimentary rocks are exposed by erosion. Thus, microorganisms may play a more active role in the geochemical carbon cycle than previously recognized, with profound implications for controls on the abundance of oxygen and carbon dioxide in Earth's atmosphere over geologic time. PMID:11283356

  20. 14C in cropland soil of a long-term field trial - in-field variability and implications for estimating carbon turnover

    NASA Astrophysics Data System (ADS)

    Leifeld, J.; Mayer, J.

    2015-03-01

    Because of their controlled nature, the presence of independent replicates, and their known management history long-term field experiments are key to the understanding of factors controlling soil carbon. Together with isotope measurements, they provide profound insight into soil carbon dynamics. For soil radiocarbon, an important tracer for understanding these dynamics, in-field variability across replicates is usually not accounted for, hence, a relevant source of uncertainty for quantifying turnover rates is missing. Here, for the first time, radiocarbon measurements of independent field replicates, and for different layers, of soil from the 60 years old controlled field experiment ZOFE in Zurich, Switzerland, is used to address this issue. 14C variability was the same across three different treatments and for three different soil layers between surface and 90 cm depths. On average, in-field variability in 14C content was 12 times the analytical error but still, on a relative basis, smaller than that of in-field soil carbon concentration variability. Despite a relative homogeneous variability across the field and along the soil profile, the curved nature of the relationship between radiocarbon content and modelled carbon mean residence time suggests that the absolute error, without consideration of in-field variability, introduced to soil carbon turnover time calculations increases with soil depth. In our field experiment findings on topsoil carbon turnover variability would, if applied to subsoil, tend to underweight turnover variability even if in-field variability of the subsoil isotope concentration is not higher. Together, in-field variability in radiocarbon is an important component in an overall uncertainty assessment of soil carbon turnover.

  1. Airborne Measurement of Ecosystem Carbon Dynamics over Heterogeneous Landscapes

    NASA Astrophysics Data System (ADS)

    Wade, T. J.; Hill, T. C.; Clement, R.; Moncrieff, J.; Disney, M.; Nichol, C. J.; Williams, M. D.

    2009-12-01

    Terrestrial carbon sinks are currently believed to account for the removal and storage of approximately 25% of anthropogenic carbon emissions from the atmosphere. The processes involved are numerous and complex and many feedbacks are at play. The ability to study the dynamics of different ecosystems at scales meaningful to climatic forcing is essential for understanding the key processes involved and identifying crucial sensitivities and thresholds. Airborne platforms with the requisite instrumentation offer the opportunity to directly measure biological processes and atmospheric structures at scales that are not achievable by ground measurements alone. The current generation of small research aircraft such as the University of Edinburgh’s Diamond HK36TTC ECO Dimona present excellent platforms for measurement of both the atmosphere and terrestrial surface. In this study we present results from airborne CO2/H2O flux measuring campaigns in contrasting climatic systems to quantify spatial patterns in ecosystem photosynthesis. Several airborne campaigns were undertaken in Arctic Finland, as part of the Arctic Biosphere Atmosphere Coupling at Multiple Scales (ABACUS) project (2008), and mainland UK as part of the UK Population Biology Network (UKPopNet) 2009 project, to explore the variability in surface CO2 flux across spatial scales larger than captured using conventional ground based eddy covariance. We discuss the application of our aircraft platform as a tool to address the challenge of understanding carbon dynamics within landscapes of heterogeneous vegetation class, terrain and hydrology using complementary datasets acquired from airborne eddy covariance and remote sensing.

  2. Detecting Airborne Mercury by Use of Polymer/Carbon Films

    NASA Technical Reports Server (NTRS)

    Shevade, Abhijit; Ryan, Margaret; Homer, Margie; Kisor, Adam; Jewell, April; Yen, Shiao-Pin; Manatt, Kenneth; Blanco, Mario; Goddard, William

    2009-01-01

    Films made of certain polymer/carbon composites have been found to be potentially useful as sensing films for detecting airborne elemental mercury at concentrations on the order of tens of parts per billion or more. That is to say, when the polymer/carbon composite films are exposed to air containing mercury vapor, their electrical resistances decrease by measurable amounts. Because airborne mercury is a health hazard, it is desirable to detect it with great sensitivity, especially in enclosed environments in which there is a risk of a mercury leak from lamps or other equipment. The present effort to develop polymerbased mercury-vapor sensors complements the work reported in NASA Tech Briefs Detecting Airborne Mercury by Use of Palladium Chloride (NPO- 44955), Vol. 33, No. 7 (July 2009), page 48 and De tecting Airborne Mer cury by Use of Gold Nanowires (NPO-44787), Vol. 33, No. 7 (July 2009), page 49. Like those previously reported efforts, the present effort is motivated partly by a need to enable operation and/or regeneration of sensors under relatively mild conditions more specifically, at temperatures closer to room temperature than to the elevated temperatures (greater than 100 C ) needed for regeneration of sensors based on noble-metal films. The present polymer/carbon films are made from two polymers, denoted EYN1 and EYN2 (see Figure 1), both of which are derivatives of poly-4-vinyl pyridine with amine functional groups. Composites of these polymers with 10 to 15 weight percent of carbon were prepared and solution-deposited onto the JPL ElectronicNose sensor substrates for testing. Preliminary test results showed that the resulting sensor films gave measurable indications of airborne mercury at concentrations on the order of tens of parts per billion (ppb) or more. The operating temperature range for the sensing films was 28 to 40 C and that the sensor films regenerated spontaneously, without heating above operating temperature (see Figure 2).

  3. On the isolation of elemental carbon for micro-molar 14C accelerator mass spectrometry; evaluation of alternative isolation procedures, and accuracy assurance using a hybrid isotopic particulate carbon reference material

    NASA Astrophysics Data System (ADS)

    Currie, L. A.; Kessler, J. D.

    2005-05-01

    The primary objective of the research reported here has been the development of an hybrid reference material (RM) to serve as a test of accuracy for elemental carbon (EC) isotopic (14C) speciation measurements. Such measurements are critically important for the quantitative apportionment of fossil and biomass sources of ''soot'' (EC), the tracer of fire that has profound effects on health, atmospheric visibility, and climate. Previous studies of 14C-EC measurement quality, carried out with NIST SRM 1649a (Urban Dust), showed a range of results, but since the ''truth'' was not known for this natural matrix RM, one had to rely on isotopic-chemical consistency evidence (14C in PAH, EC) of measurement validity (Currie et al., 2002). Components of the new Hybrid RM (DiesApple), however, have known 14C and EC composition, and they are nearly orthogonal (isotopically and chemically). NIST SRM 2975 (Forklift Diesel Soot) has little or no 14C, and its major compositional component is EC. SRM 1515 (Apple Leaves) has the 14C content of biomass-C, and it has little or no EC. Thus, the hybrid RM can serve as an absolute isotopic test for the absence of EC-mimicking pyrolysis-C from SRM 1515 in the EC isolate of the hybrid RM, together with testing for conservation of its dominant soot fraction through the isolation procedure.

  4. Biophysical influence of airborne carbon nanomaterials on natural pulmonary surfactant.

    PubMed

    Valle, Russell P; Wu, Tony; Zuo, Yi Y

    2015-05-26

    Inhalation of nanoparticles (NP), including lightweight airborne carbonaceous nanomaterials (CNM), poses a direct and systemic health threat to those who handle them. Inhaled NP penetrate deep pulmonary structures in which they first interact with the pulmonary surfactant (PS) lining at the alveolar air-water interface. In spite of many research efforts, there is a gap of knowledge between in vitro biophysical study and in vivo inhalation toxicology since all existing biophysical models handle NP-PS interactions in the liquid phase. This technical limitation, inherent in current in vitro methodologies, makes it impossible to simulate how airborne NP deposit at the PS film and interact with it. Existing in vitro NP-PS studies using liquid-suspended particles have been shown to artificially inflate the no-observed adverse effect level of NP exposure when compared to in vivo inhalation studies and international occupational exposure limits (OELs). Here, we developed an in vitro methodology called the constrained drop surfactometer (CDS) to quantitatively study PS inhibition by airborne CNM. We show that airborne multiwalled carbon nanotubes and graphene nanoplatelets induce a concentration-dependent PS inhibition under physiologically relevant conditions. The CNM aerosol concentrations controlled in the CDS are comparable to those defined in international OELs. Development of the CDS has the potential to advance our understanding of how submicron airborne nanomaterials affect the PS lining of the lung. PMID:25929264

  5. Large fluxes and rapid turnover of mineral-associated carbon across topographic gradients in a humid tropical forest: insights from paired 14C analysis

    DOE PAGESBeta

    Hall, S. J.; McNicol, G.; Natake, T.; Silver, W. L.

    2015-01-16

    It has been proposed that the large soil carbon (C) stocks of humid tropical forests result predominantly from C stabilization by reactive minerals, whereas oxygen (O2) limitation of decomposition has received much less attention. We examined the importance of these factors in explaining patterns of C stocks and turnover in the Luquillo Experimental Forest, Puerto Rico, using radiocarbon (14C) measurements of contemporary and archived samples. Samples from ridge, slope, and valley positions spanned three soil orders (Ultisol, Oxisol, Inceptisol) representative of humid tropical forests, and differed in texture, reactive metal content, O2 availability, and root biomass. Mineral-associated C comprised themore » large majority (87 ± 2%, n = 30) of total soil C. Turnover of most mineral-associated C (74 ± 4%) was rapid (9 to 29 years, mean and SE 20 ± 2 years) in 25 of 30 soil samples across surface horizons (0–10 and 10–20 cm depths) and all topographic positions, independent of variation in reactive metal concentrations and clay content. Passive C with centennial – millennial turnover was much less abundant (26%), even at 10–20 cm depths. Carbon turnover times and concentrations significantly increased with concentrations of reduced iron (Fe(II)) across all samples, suggesting that O2 availability may have limited the decomposition of mineral associated C over decadal scales. Steady-state inputs of mineral-associated C were similar among the three topographic positions, and could represent 10–30% of annual litterfall production (estimated by doubling aboveground litterfall). Observed trends in mineral-associated Δ14C over time could not be fit using the single pool model used in many other studies, which generated contradictory relationships between turnover and Δ14C as compared with a more realistic constrained two-pool model. The large C fluxes in surface and near-surface soils implied by our data suggest that other studies using single-pool Δ14C

  6. Large fluxes and rapid turnover of mineral-associated carbon across topographic gradients in a humid tropical forest: insights from paired 14C analysis

    DOE PAGESBeta

    Hall, S. J.; McNicol, G.; Natake, T.; Silver, W. L.

    2015-04-29

    It has been proposed that the large soil carbon (C) stocks of humid tropical forests result predominantly from C stabilization by reactive minerals, whereas oxygen (O2) limitation of decomposition has received much less attention. We examined the importance of these factors in explaining patterns of C stocks and turnover in the Luquillo Experimental Forest, Puerto Rico, using radiocarbon (14C) measurements of contemporary and archived samples. Samples from ridge, slope, and valley positions spanned three soil orders (Ultisol, Oxisol, Inceptisol) representative of humid tropical forests, and differed in texture, reactive metal content, O2 availability, and root biomass. Mineral-associated C comprised themore » large majority (87 ± 2%, n = 30) of total soil C. Turnover of most mineral-associated C (66 ± 2%) was rapid (11 to 26 years; mean and SE: 18 ± 3 years) in 25 of 30 soil samples across surface horizons (0–10 and 10–20 cm depths) and all topographic positions, independent of variation in reactive metal concentrations and clay content. Passive C with centennial–millennial turnover was typically much less abundant (34 ± 3%), even at 10–20 cm depths. Carbon turnover times and concentrations significantly increased with concentrations of reduced iron (Fe(II)) across all samples, suggesting that O2 availability may have limited the decomposition of mineral-associated C over decadal scales. Steady-state inputs of mineral-associated C were statistically similar among the three topographic positions, and could represent 10–25% of annual litter production. Observed trends in mineral-associated Δ14C over time could not be fit using the single-pool model used in many other studies, which generated contradictory relationships between turnover and Δ14C as compared with a more realistic two-pool model. The large C fluxes in surface and near-surface soils documented here are supported by findings from paired 14C studies in other types of ecosystems, and

  7. Large fluxes and rapid turnover of mineral-associated carbon across topographic gradients in a humid tropical forest: insights from paired 14C analysis

    NASA Astrophysics Data System (ADS)

    Hall, S. J.; McNicol, G.; Natake, T.; Silver, W. L.

    2015-04-01

    It has been proposed that the large soil carbon (C) stocks of humid tropical forests result predominantly from C stabilization by reactive minerals, whereas oxygen (O2) limitation of decomposition has received much less attention. We examined the importance of these factors in explaining patterns of C stocks and turnover in the Luquillo Experimental Forest, Puerto Rico, using radiocarbon (14C) measurements of contemporary and archived samples. Samples from ridge, slope, and valley positions spanned three soil orders (Ultisol, Oxisol, Inceptisol) representative of humid tropical forests, and differed in texture, reactive metal content, O2 availability, and root biomass. Mineral-associated C comprised the large majority (87 ± 2%, n = 30) of total soil C. Turnover of most mineral-associated C (66 ± 2%) was rapid (11 to 26 years; mean and SE: 18 ± 3 years) in 25 of 30 soil samples across surface horizons (0-10 and 10-20 cm depths) and all topographic positions, independent of variation in reactive metal concentrations and clay content. Passive C with centennial-millennial turnover was typically much less abundant (34 ± 3%), even at 10-20 cm depths. Carbon turnover times and concentrations significantly increased with concentrations of reduced iron (Fe(II)) across all samples, suggesting that O2 availability may have limited the decomposition of mineral-associated C over decadal scales. Steady-state inputs of mineral-associated C were statistically similar among the three topographic positions, and could represent 10-25% of annual litter production. Observed trends in mineral-associated Δ14C over time could not be fit using the single-pool model used in many other studies, which generated contradictory relationships between turnover and Δ14C as compared with a more realistic two-pool model. The large C fluxes in surface and near-surface soils documented here are supported by findings from paired 14C studies in other types of ecosystems, and suggest that most

  8. sup 14 C ages of hydrothermal petroleum and carbonate in Guaymas Basin, Gulf of California: implications for oil generation, expulsion, and migration

    SciTech Connect

    Peter, J.M.; Peltonen, P.; Scott, S.D. ); Simoneit, B.R.T.; Kawka, O.E. )

    1991-03-01

    {sup 14}C dates have been obtained by accelerator mass spectrometry and by conventional techniques from hydrothermally derived petroleum, calcite, and vent water from the southern trough of Guaymas Basin, Gulf of California. The ages for petroleum range from 4240 to 5705 B.P., whereas those for calcite range from 7340 to 33,168 B.P. The CO{sub 2} in a sample of hydrothermal vent fluid (24% end member) yielded an apparent age of 14,820 B.P., which is within the calcite age range. These are not true ages, but rather they reflect the age of carbon within these materials. The data indicate that the conversion of sedimentary organic matter to petroleum occurs very rapidly and that the petroleum is mobilized from sedimentary organic matter in the upper 30 m of the sediment column ({le}500 m thick) underlying the sea-floor deposits. The large difference in ages between the petroleum and most of the calcites indicates that the carbon source in the calcites is more complex. The inorganic carbon pool probably originates from the dissolution of older detrital carbonates and autochthonous biogenic carbonates in the shallow sediments, and/or the decarboxylation of organic matter at greater depth, with a magmatic component of dead carbon.

  9. Soil Carbon and Microbial Dynamics during Long-term Incubation involving 13C and 14C Measurements.

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Grasslands in the conterminous United States include about 212 of which about ~48 million hectares (Mha) of pasture and 164 Mha of rangeland. Rates of soil organic carbon (SOC) sequestration can range from none to approaching 1 metric ton (mt) SOC/year. Climate and management influence potential i...

  10. ARM Airborne Continuous carbon dioxide measurements

    DOE Data Explorer

    Biraud, Sebastien

    2013-03-26

    The heart of the AOS CO2 Airborne Rack Mounted Analyzer System is the AOS Manifold. The AOS Manifold is a nickel coated aluminum analyzer and gas processor designed around two identical nickel-plated gas cells, one for reference gas and one for sample gas. The sample and reference cells are uniquely designed to provide optimal flushing efficiency. These cells are situated between a black-body radiation source and a photo-diode detection system. The AOS manifold also houses flow meters, pressure sensors and control valves. The exhaust from the analyzer flows into a buffer volume which allows for precise pressure control of the analyzer. The final piece of the analyzer is the demodulator board which is used to convert the DC signal generated by the analyzer into an AC response. The resulting output from the demodulator board is an averaged count of CO2 over a specified hertz cycle reported in volts and a corresponding temperature reading. The system computer is responsible for the input of commands and therefore works to control the unit functions such as flow rate, pressure, and valve control.The remainder of the system consists of compressors, reference gases, air drier, electrical cables, and the necessary connecting plumbing to provide a dry sample air stream and reference air streams to the AOS manifold.

  11. On the isolation of elemental carbon (EC) for micro-molar 14C accelerator mass spectrometry: development of a hybrid reference material for 14C-EC accuracy assurance, and a critical evaluation of the thermal optical kinetic (TOK) EC isolation procedure

    NASA Astrophysics Data System (ADS)

    Currie, L. A.; Kessler, J. D.

    2005-10-01

    The primary objective of the research reported here has been the development of a hybrid reference material (RM) to serve as a test of accuracy for elemental carbon (EC) isotopic (14C) speciation measurements. Such measurements are vital for the quantitative apportionment of fossil and biomass sources of "soot" (EC), the tracer of fire that has profound effects on health, atmospheric visibility, and climate. Previous studies of 14C-EC measurement quality, carried out with NIST SRM 1649a (Urban Dust), showed a range of results, but since the "truth" was not known for this natural matrix RM, one had to rely on isotopic-chemical consistency evidence (14C in PAH, EC) of measurement validity (Currie et al., 2002). Components of the new Hybrid RM (DiesApple), however, have known 14C and EC composition, and they are nearly orthogonal (isotopically and chemically). NIST SRM 2975 (Forklift Diesel Soot) has little or no 14C, and its major compositional component is EC; SRM 1515 (Apple Leaves) has the 14C content of biomass-C, and it has little or no EC. Thus, the Hybrid RM can serve as an absolute isotopic test for the absence of EC-mimicking pyrolysis-C (char) from SRM 1515 in the EC isolate of the Hybrid RM, as well as a test for conservation of its dominant soot fraction throughout the isolation procedure.

    The secondary objective was to employ the Hybrid RM for the comparative evaluation of the thermal optical kinetic (TOK) and thermal optical transmission (TOT) methods for the isolation of EC for micro-molar carbon accelerator mass spectrometry (AMS). As part of this process, the relatively new TOK method was subjected to a critical evaluation and significant development. Key findings of our study are: (1) both methods exhibited biomass-C "leakage"; for TOT, the EC fraction isolated for AMS contained about 8% of the original biomass-C; for TOK, the refractory carbon (RC) isolated contained about 3% of the original biomass-C.; (2) the

  12. Tritium and radioactive carbon (14C) analyses of gas collected from unsaturated sediments next to a low-level radioactive-waste burial site south of Beatty, Nevada, April 1994 and July 1995

    USGS Publications Warehouse

    Prudic, David E.; Striegl, Robert G.

    1995-01-01

    Tritium activities in water vapor and radioactive carbon (14C) activities in carbon dioxide were determined in gas samples pumped from small-diameter air ports installed in a test hole within the unsaturated sediments next to a commercial burial site for low-level radioactive waste south of Beatty, Nevada. In April 1994, gas samples were collected from test hole UZB-2, which was drilled about 350 feet south of the southwest corner of the fence enclosing the burial site. The test hole is part of a study to determine the depth to which atmospheric air circulates through the unsaturated sediments at the desert site. Laboratory results completed in May 1995 show activities of tritium and 14C were greater than expected, with measured tritium in the water vapor as high as 762 tritium units at a depth of 79 feet and measured 14C in carbon dioxide as high as 1,700 percent modern carbon at a depth of 18 feet. In July 1995, the uppermost five air ports in test hole UZB-2 were resampled. In addition, water vapor was collected for tritium analyses at a distant test hole, and water vapor for tritium analyses and carbon dioxide for 14C analyses were collected from three depths at the research shaft about 200 feet north of test hole UZB-2, and at two shallow probes (depth of 5.5 feet) next to the fence enclosing the burial site. Analyses of samples collected in the upper 112 feet from test hole UZB-2 in July 1995 show the same distribution of tritium and 14C as analyses of samples collected in April 1994, except that activities were somewhat greater in July. The greatest activities of tritium and 14C were measured from a shallow probe next to the fence with activities of 29,400 tritium units and 517,000 percent modern carbon, respectively.

  13. METHOD FOR SEPARATING VOLATILE ORGANIC CARBON FROM 0.1 M3 OF AIR TO IDENTIFY SOURCES OF OZONE PRECURSORS VIA ISOTOPE (14C) MEASUREMENTS

    EPA Science Inventory

    Atmospheric non-methane volatile organic compounds (VOCS) are known to play an important role in urban ozone formation during the summer. o respond to the need for a direct measure of VOC source contributions from biogenic (14C/12C=10-12) and fossil fuel (14C/12C=O) emissions, a ...

  14. Organic Carbon Delivery to a High Arctic Watershed over the Late Holocene: Insights from Plant Biomarkers and Compound Specific δ13C and Δ14C Measurements

    NASA Astrophysics Data System (ADS)

    Schreiner, K. M.; Bianchi, T. S.; Eglinton, T. I.; Allison, M. A.

    2012-12-01

    The Colville River in Alaska is the largest river in North America which has a drainage basin that is exclusively underlain by permafrost, and as such provides a unique signal of historical changes in one of the world's most vulnerable areas to climate changes. Additionally, the Colville flows into Simpson's Lagoon, an area of the Alaskan Beaufort coast protected by a barrier island chain, lessening the impacts of Arctic storms and ice grounding on sediment mixing. Cores collected from the Colville river delta in August of 2010 were found to be composed of muddy, organic-rich, well-laminated sediments. The 2.5 to 3 meter length of each core spans about one to two thousand years of Holocene history, including the entire Anthropocene and much of the late Holocene. Two cores were sampled for this data set - one from close to the river mouth, and one from farther east in Simpson's Lagoon. Samples were taken every 2 cm for the entire length of both cores. In order to determine how the amount of terrestrial organic matter input changed over the Holocene, bulk analyses including percent organic carbon, percent nitrogen, and stable carbon isotopic analysis were performed, and biomarkers including lignin-phenols and fatty acids were measured. It was shown that lignin-phenol input is positively correlated with Alaskan North Slope temperature reconstructions. To determine whether the source of this increased terrestrial organic matter input was from fresh vegetation (for example, shrub encroachment onto tundra areas) or aged soil organic matter (potentially due to permafrost thawing and breakdown), selected samples were analyzed for compound-specific δ13C and Δ14C of fatty acids and lignin-phenols. These analyses show significant changes in carbon storage and in terrestrial carbon delivery to the Lagoon over time. These results represent the first fine-scale organic biomarker study in a high Arctic North American Lagoon, and have many implications for the future of carbon

  15. Different organic carbon status in soil and its influence on the distribution of 14C-labelled xenobiotics in soil fractions

    NASA Astrophysics Data System (ADS)

    Schnitzler, Frauke; Séquaris, Jean-Marie; Berns, Anne E.; Burauel, Peter

    2010-05-01

    Aggregate size fractionation in combination with chemical extraction was used to assess pesticide interactions with soil organic matter under different soil management practices [1]. In this study, surface area measurements (BET-N2) were established as a method to calculate the distribution of organic carbon (OC) and xenobiotics in clay and combined silt+sand fractions. It was shown that concentrations of OC associated with clay can be determined from linear relationships between OC and mineral specific surface area [2]. Two sets of experiments were conducted with undisturbed soil columns under field-like conditions. In the first set, maize straw was incorporated into the topsoil and after three months incubation the 14C-labelled xenobiotics benazolin or benzo[a]pyrene were applied. The second set was treated equally, but without maize addition. The calculated distribution coefficients Kd indicated a stronger sorption of benzo[a]pyrene than benazolin derivates. Furthermore, the binding capacity for the xenobiotics was higher in the clay than in the silt+sand fraction due to the relative high specific surface area in the clay fraction. Incorporation of maize straw led to a significant retention and decrease of mobility of the acidic benazolin. The hydrophobic benzo[a]pyrene was less affected by the addition of organic amendment and remained in the topsoil. [1] Schnitzler, F., Lavorenti, A., Berns, A.E., Drewes, N., Vereecken, H., Burauel, P., 2007. The influence of maize residues on the mobility and binding of benazolin: Investigating physically extracted soil fractions. Environmental Pollution 147, 4-13. [2] Séquaris, J.-M., Guisado, M., Moreno, C., Burauel, P., Narres, H.-D., Vereecken, H., 2010. Organic carbon fractions in an agricultural topsoil assessed by the determination of the soil mineral surface area. Journal of Plant Nutrition and Soil Science, in press

  16. Distribution of carbon-14 and associated radiation dose in rat fetal brain and liver after maternal injection of [{sup 14}C]thymidine

    SciTech Connect

    Takahashi, Sentaro; Kubota, Yoshihisa; Koshimoto, Chihiro; Sato, Hiroshi; Hatashita, Shizuo

    1994-10-01

    Pregnant Sprague-Dawley rats were injected intravenously with [{sup 14}C]thymidine on day 13.5 of gestation, and the concentrations and radiation doses of {sup 14}C in the fetal brain and liver were determined by liquid scintillation counting were 1.01% of the injected dose per gram wet weight at 6 h after injection and decreased to 0.39% g{sup {minus}1} at 48 h after injection. A significant accumulation of {sup 14}C was observed in the fetal liver: 3.8 and 0.51% of the injected dose per gram wet weight at 6 and 48 h after injection, respectively. Autoradiography showed that, especially at earlier periods after injection, there was remarkable concentration of {sup 14}C in the ventricular zone of the brain and the central region of the liver. With increasing time after injection, the distribution of {sup 14}C became relatively uniform. The concentrations of {sup 14}C in the ventricular zone of the fetal brain, determined by autoradiography, were much higher than those in the whole brain as determined by liquid scintillation counting. Cumulative radiation doses for 6-48 h after injection were 1.27 mGy for the whole fetus and 1.45 mGy for the whole brain. In contrast, the cumulative radiation dose for the ventricular zone of the brain which was determined by autoradiography was approximately 2.2 times that for the whole brain. 18 refs., 5 figs., 3 tabs.

  17. ARM Airborne Carbon Measurements VI (ACME VI) Science Plan

    SciTech Connect

    Biraud, S

    2015-12-01

    From October 1 through September 30, 2016, the Atmospheric Radiation Measurement (ARM) Aerial Facility will deploy the Cessna 206 aircraft over the Southern Great Plains (SGP) site, collecting observations of trace-gas mixing ratios over the ARM’s SGP facility. The aircraft payload includes two Atmospheric Observing Systems, Inc., analyzers for continuous measurements of CO2 and a 12-flask sampler for analysis of carbon cycle gases (CO2, CO, CH4, N2O, 13CO2, 14CO2, carbonyl sulfide, and trace hydrocarbon species, including ethane). The aircraft payload also includes instrumentation for solar/infrared radiation measurements. This research is supported by the U.S. Department of Energy’s ARM Climate Research Facility and Terrestrial Ecosystem Science Program and builds upon previous ARM Airborne Carbon Measurements (ARM-ACME) missions. The goal of these measurements is to improve understanding of 1) the carbon exchange at the SGP site, 2) how CO2 and associated water and energy fluxes influence radiative forcing, convective processes and CO2 concentrations over the SGP site, and 3) how greenhouse gases are transported on continental scales.

  18. Simplified analytical methods for the measurement of the synthesis rate of plasma proteins in vivo by the [14C]carbonate method.

    PubMed

    Caine, S; Fleck, A

    1984-09-01

    We describe a method for obtaining the specific activity of 14C in urea, essential in the measurement of the synthesis rate of a plasma protein in vivo, which is simpler than the original procedure. The principle is the measurement of 14CO2 and NH4+ separately, after incubation with urease. A simple alteration gives samples of 13CO2 for mass spectrometry. The 'recoveries' of 14C and 13C in urea were invariably between 90 and 96% and the CV was 3%. PMID:6439102

  19. COCAP - A compact carbon dioxide analyser for airborne platforms

    NASA Astrophysics Data System (ADS)

    Kunz, Martin; Lavrič, Jošt V.; Jeschag, Wieland; Bryzgalov, Maksym; Hök, Bertil; Heimann, Martin

    2014-05-01

    Airborne platforms are a valuable tool for atmospheric trace gas measurements due to their capability of movement in three dimensions, covering spatial scales from metres to thousands of kilometres. Although crewed research aircraft are flexible in payload and range, their use is limited by high initial and operating costs. Small unmanned aerial vehicles (UAV) have the potential for substantial cost reduction, but require lightweight, miniaturized and energy-efficient scientific equipment. We are developing a COmpact Carbon dioxide analyser for Airborne Platforms (COCAP). It contains a non-dispersive infrared CO2sensor with a nominal full scale of 3000 μmol/mol. Sampled air is dried with magnesium perchlorate before it enters the sensor. This enables measurement of the dry air mole fraction of CO2, as recommended by the World Meteorological Organization. During post-processing, the CO2 measurement is corrected for temperature and pressure variations in the gas line. Allan variance analysis shows that we achieve a precision of better than 0.4 μmol/mol for 10 s averaging time. We plan to monitor the analyser's stability during flight by measuring reference air from a miniature gas tank in regular intervals. Besides CO2, COCAP measures relative humidity, temperature and pressure of ambient air. An on-board GPS receiver delivers accurate timestamps and allows georeferencing. Data is both stored on a microSD card and simultaneously transferred over a wireless serial interface to a ground station for real-time review. The target weight for COCAP is less than 1 kg. We deploy COCAP on a commercially available fixed-wing UAV (Bormatec Explorer) with a wingspan of 2.2 metres. The UAV has high payload capacity (2.5 kg) as well as sufficient space in the fuselage (80x80x600 mm3). It is built from a shock-resistant foam material, which allows quick repair of minor damages in the field. In case of severe damage spare parts are readily available. Calculations suggest that the

  20. 14C Analysis via Intracavity Optogalvanic Spectroscopy

    PubMed Central

    Murnick, Daniel; Dogru, Ozgur; Ilkmen, Erhan

    2010-01-01

    A new ultra sensitive laser-based analytical technique, intracavity optogalvanic spectroscopy (ICOGS), allowing extremely high sensitivity for detection of 14C-labeled carbon dioxide has recently been demonstrated. Capable of replacing accelerator mass spectrometers (AMS) for many applications, the technique quantifies zeptomoles of 14C in sub micromole CO2 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 14C/12C ratios have been obtained with theoretical limits much lower. Using a 15 W 14CO2 laser, a linear calibration with samples from 5 × 10−15 to >1.5 × 10−12 in 14C/12C ratios, as determined by AMS, was demonstrated. Calibration becomes non linear over larger concentration ranges due to interactions between CO2 and buffer gas, laser saturation effects and changes in equilibration time constants. The instrument is small (table top), low maintenance and can be coupled to GC or LC input. The method can also be applied to detection of other trace entities. Possible applications include microdosing studies in drug development, individualized sub therapeutic tests of drug metabolism, carbon dating and real time monitoring of atmospheric radiocarbon. PMID:20448803

  1. First Airborne Laser Remote Measurements of Atmospheric Carbon Dioxide

    NASA Astrophysics Data System (ADS)

    Browell, E. V.; Dobbs, M. E.; Dobler, J.; Kooi, S.; Choi, Y.; Harrison, F. W.; Moore, B.; Zaccheo, T. S.

    2008-12-01

    A unique, multi-frequency, single-beam, laser absorption spectrometer (LAS) that operates at 1.57 μm has been developed for a future space-based mission to determine the global distribution of sources and sinks of atmospheric carbon dioxide (CO2). A prototype of the space-based LAS system was developed by ITT, and it has been successfully flight tested in five airborne campaigns conducted in different geographic regions over the last three years. Flight tests were conducted over Oklahoma, Michigan, New Hampshire, and Virginia under a wide range of atmospheric conditions. Remote LAS measurements were compared to high-quality in situ measurements obtained from instrumentation on the same aircraft on spirals under the ground track of the LAS. LAS flights were conducted over a wide range of land and water reflectances and in the presence of scattered clouds. An extensive data set of CO2 measurements has been obtained for evaluating the LAS performance. LAS CO2 measurements with a signal-to-noise in excess of 250 were obtained for a 1-s average over land and for a 10-s average over water. Absolute comparisons of CO2 remote and in situ measurements showed agreement over a range of altitudes to better than 2 percent. LAS oxygen (O2) measurements, which are needed to convert LAS CO2 density measurements to CO2 mixing ratios (XCO2), have been made in the 1.26-μm region in horizontal ground-based experiments and in initial flight tests. Details of flight test campaigns and measured versus modeled results are presented in this paper.

  2. Effects of airborne black carbon pollution on maize

    NASA Astrophysics Data System (ADS)

    Illes, Bernadett; Anda, Angela; Soos, Gabor

    2013-04-01

    The black carbon (BC) changes the radiation balance of the Earth and contributes to global warming. The airborne BC deposited on the surface of plant, changing the radiation balance, water balance and the total dry matter (TDM) content of plant. The objective of our study was to investigate the impact of soot originated from motor vehicle exhaust on maize. The field experiment was carried out in Keszthely Agrometeorological Research Station (Hungary) in three consecutive years (2010, 2011, 2012) of growing season. The test plant was the maize hybrid Sperlona (FAO 340) with short growing season. The BC was chemically "pure", which means that it is free any contaminants (e.g. heavy metals). The BC was coming from the Hankook Tyre Company (Dunaújváros, Hungary), where used that for improve the wear resistance of tires. We used a motorised sprayer of SP 415 type to spray the BC onto the leaf surface. The leaf area index (LAI) was measured each week on the same 12 sample maize in each treatment using an LI 3000A automatic planimeter (LI-COR, Lincoln, NE). Albedo was measured by pyranometers of the CMA-11 type (Kipp & Zonen, Vaisala), what we placed the middle of the plot of 0.3 ha. The effects of BC were studied under two different water supplies: evapotranspirometers of Thornthwaite type were used for "ad libitum" treatment and rainfed treatment in field plots. In 2010 and 2012, a big difference was not observed in the case of LAI in the effects of BC. However, in 2011 there was a significant difference. The LAI of the BC polluted maize was higher (10-15%, P<0.05), than the LAI of the control maize in the rainfed plot and in the ET chambers, respectively. The albedo of the BC contaminated maize decreased (15-30%, P<0.05) in all three years. We also detected that the green plant surface of maize increased on BC contaminated treatment. These results may suggest that the plant is able to absorb the additional carbon source through the leaves. The albedo decreased

  3. Airborne Measurements in Support of the NASA Atmospheric Carbon and Transport - America (ACT-America) Mission

    NASA Technical Reports Server (NTRS)

    Meadows, Byron; Davis, Ken; Barrick, John; Browell, Edward; Chen, Gao; Dobler, Jeremy; Fried, Alan; Lauvaux, Thomas; Lin, Bing; McGill, Matt; Miles, Natasha; Nehrir, Amin; Obland, Michael; O'Dell, Chris; Sweeney, Colm; Yang, Melissa

    2015-01-01

    NASA announced the research opportunity Earth Venture Suborbital -2 (EVS-2) mission in support of the NASA's science strategic goals and objectives in 2013. Penn State University, NASA Langley Research Center (LaRC), and other academic institutions, government agencies, and industrial companies together formulated and proposed the Atmospheric Carbon and Transport -America (ACT -America) suborbital mission, which was subsequently selected for implementation. The airborne measurements that are part of ACT-America will provide a unique set of remote and in-situ measurements of CO2 over North America at spatial and temporal scales not previously available to the science community and this will greatly enhance our understanding of the carbon cycle. ACT -America will consist of five airborne campaigns, covering all four seasons, to measure regional atmospheric carbon distributions and to evaluate the accuracy of atmospheric transport models used to assess carbon sinks and sources under fair and stormy weather conditions. This coordinated mission will measure atmospheric carbon in the three most important regions of the continental US carbon balance: Northeast, Midwest, and South. Data will be collected using 2 airborne platforms (NASA Wallops' C-130 and NASA Langley's B-200) with both in-situ and lidar instruments, along with instrumented ground towers and under flights of the Orbiting Carbon Observatory (OCO-2) satellite. This presentation provides an overview of the ACT-America instruments, with particular emphasis on the airborne CO2and backscatter lidars, and the, rationale, approach, and anticipated results from this mission.

  4. Airborne Measurements in Support of the NASA Atmospheric Carbon and Transport - America (ACT-America) Mission

    NASA Astrophysics Data System (ADS)

    Meadows, B.; Davis, K.; Barrick, J. D. W.; Browell, E. V.; Chen, G.; Dobler, J. T.; Fried, A.; Lauvaux, T.; Lin, B.; McGill, M. J.; Miles, N. L.; Nehrir, A. R.; Obland, M. D.; O'Dell, C.; Sweeney, C.; Yang, M. M.

    2015-12-01

    NASA announced the research opportunity Earth Venture Suborbital - 2 (EVS-2) mission in support of the NASA's science strategic goals and objectives in 2013. Penn State University, NASA Langley Research Center (LaRC), and other academic institutions, government agencies, and industrial companies together formulated and proposed the Atmospheric Carbon and Transport - America (ACT - America) suborbital mission, which was subsequently selected for implementation. The airborne measurements that are part of ACT-America will provide a unique set of remote and in-situ measurements of CO2 over North America at spatial and temporal scales not previously available to the science community and this will greatly enhance our understanding of the carbon cycle. ACT - America will consist of five airborne campaigns, covering all four seasons, to measure regional atmospheric carbon distributions and to evaluate the accuracy of atmospheric transport models used to assess carbon sinks and sources under fair and stormy weather conditions. This coordinated mission will measure atmospheric carbon in the three most important regions of the continental US carbon balance: Northeast, Midwest, and South. Data will be collected using 2 airborne platforms (NASA Wallops' C-130 and NASA Langley's B-200) with both in-situ and lidar instruments, along with instrumented ground towers and under flights of the Orbiting Carbon Observatory (OCO-2) satellite. This presentation provides an overview of the ACT-America instruments, with particular emphasis on the airborne CO2 and backscatter lidars, and the, rationale, approach, and anticipated results from this mission.

  5. Rates and quantities of carbon flux to ectomycorrhizal mycelium following 14C pulse labeling of Pinus sylvestris seedlings: effects of litter patches and interaction with a wood-decomposer fungus.

    PubMed

    Leake, J R; Donnelly, D P; Saunders, E M; Boddy, L; Read, D J

    2001-02-01

    We used a novel digital autoradiographic technique that enabled, for the first time, simultaneous visualization and quantification of spatial and temporal changes in carbon allocation patterns in ectomycorrhizal mycelia. Mycorrhizal plants of Pinus sylvestris L. were grown in microcosms containing non-sterile peat. The time course and spatial distribution of carbon allocation by P. sylvestris to mycelia of its mycorrhizal partners, Paxillus involutus (Batsch) Fr. and Suillus bovinus (L.): Kuntze, were quantified following 14C pulse labeling of the plants. Litter patches were used to investigate the effects of nutrient resource quality on carbon allocation. The wood-decomposer fungus Phanerochaete velutina (D.C.: Pers.) Parmasto was introduced to evaluate competitive and territorial interactions between its mycelial cords and the mycelial system of S. bovinus. Growth of ectomycorrhizal mycelium was stimulated in the litter patches. Nearly 60% of the C transferred from host plant to external mycorrhizal mycelium (> 2 mm from root surfaces) was allocated to mycelium in the patches, which comprised only 12% of the soil area available for mycelial colonization. Mycelia in the litter patch most recently colonized by mycorrhizal mycelium received the largest investment of carbon, amounting to 27 to 50% of the total 14C in external mycorrhizal mycelium. The amount of C transfer to external mycelium of S. bovinus following pulse labeling was reduced from a maximum of 167 nmol in systems with no saprotroph to a maximum of 61 nmol in systems interacting with P. velutina. The 14C content of S. bovinus mycelium reached a maximum 24-36 h after labeling in control microcosms, but allocation did not reach a peak until 56 h after labeling, when S. bovinus interacted with mycelium of P. velutina. The mycelium of S. bovinus contained 9% of the total 14C in the plants (including mycorrhizae) at the end of the experiment, but this was reduced to 4% in the presence of P. velutina. The

  6. ENVIRONMENTAL BIODEGRADABILITY OF [14C] SINGLE-WALLED CARBON NANOTUBESBY TRAMETES VERSICOLOR AND NATURAL MICROBIAL CULTURES FOUND IN NEWBEDFORD HARBOR SEDIMENT AND AERATED WASTEWATER TREATMENT PLANT SLUDGE

    EPA Science Inventory

    Little is known about environmental biodegradability or biotransformations of single-walled carbon nanotubes (SWNT). Because of their strong association with aquatic organic matter, detailed knowledge of the ultimate fate and persistence of SWNT requires investigation of possible...

  7. Synthesis of [(14) C]omarigliptin.

    PubMed

    Ren, Sumei; Gauthier, Donald; Marques, Rosemary; Helmy, Roy; Hesk, David

    2016-08-01

    An efficient synthesis for [(14) C]Omarigliptin (MK-3102) is described. The initial synthesis of a key (14) C-pyrazole moiety did not work due to the lack of stability of (14) C-DMF-DMA reagent. Thus, a new radiolabeled synthon, (14) C-biphenylmethylformate, was synthesized from (14) C-sodium formate in one step in 92% yield and successfully used in construction of the key (14) C-pyrazole moiety. Regioselective N-sulfonation of the pyrazole moiety was achieved through a dehydration-sulfonation-isomerization sequence. [(14) C]MK 3102 was synthesized in five steps from (14) C-biphenylmethylformate with 25% overall yield. PMID:27334864

  8. Airborne radioactivity Survey of part of Saratoga NW quadrangle, Carbon County, Wyoming

    USGS Publications Warehouse

    Henderson, J.R.

    1954-01-01

    The accompanying map shows the results of an airborne radioactivity survey in 133 square miles of Saratoga NW quadrangle, Wyoming. This area is part of a larger survey made in southern Carbon and Sweetwater Counties by the U. S. Geological Survey, November 9-24, 1953. The work was undertaken as part of a cooperative program with the U.S. Atomic Energy Commission.

  9. Tracing sources and deposition processes of organic carbon in river deltas: carbon isotopes (Δ14C and δ13C) coupled to density fractionation in the Rhône River delta (Gulf of Lion, France)

    NASA Astrophysics Data System (ADS)

    Tisnérat-Laborde, Nadine; Toussaint, Flora; Cathalot, Cécile; Rabouille, Christophe

    2013-04-01

    Despite its relatively modest surface area, coastal zones play a crucial role in the biogeochemical cycles of carbon because they receive large inputs of terrestrial organic matter (OM) by rivers, and appear as a large biogeochemical reactor. The terrestrial OM inputs can be buried or mineralized depending of physical and biological processes. Improved understanding of the fate of organic carbon and its distribution in River-dominated ocean margins is necessary to predict evolution of carbon in this system impacted by human disturbances and climate change. The Rhône River is the main source of freshwater and terrigenous particles including organic carbon to the Mediterranean Sea. Previous studies based on bulk 14C analysis of surface sediment of Rhône delta have shown an aging of the OM from the River mouth to the continental shelf. The distribution of OM is stable over several years (without flood) with a decreasing proportion of terrigenous OM with increasing distance of the river. Yet, the processes leading to this distribution are still being investigated: degradation, size or density sorting, petrogenic carbon accumulation… In order to better understand the origin and the distribution of matter, we measured radiocarbon and δ13C in the different fractions of sediments samples obtained by density fractionation. Surface sediment of 4 sites located on a transect offshore (A, K, C and E) was sampled in April 2007, in May 2011 and during one flood event, together with the suspended material discharged by the Rhône River. Sediment aliquot was separated in 4 fractions with sodium polytungstate using the same methods as Wakeham et al. (2009) (<1.6, 1.6-2, 2-2.5 and >2.5 g cm-3) in order to separate different types of OM. Radiocarbon measurements were obtained after physicochemical treatment by Accelerator Mass Spectroscopy at LMC14 and stable carbon isotopes measurements by EA-IRMS Mass Spectrometer (ThermoFiniganDelta+XP) at LSCE. First results indicate that the

  10. (14)C, delta(13)C and total C content in soils around a Brazilian PWR nuclear power plant.

    PubMed

    Dias, Cíntia Melazo; Telles, Everaldo C; Santos, Roberto Ventura; Stenström, Kristina; Nícoli, Iêda Gomes; da Silveira Corrêa, Rosangela; Skog, Göran

    2009-04-01

    Nuclear power plants release (14)C during routine operation mainly as airborne gaseous effluents. Because of the long half-life (5730 years) and biological importance of this radionuclide (it is incorporated in plant tissue by photosynthesis), several countries have monitoring programs in order to quantify and control these emissions. This paper compares the activity of (14)C in soils taken within 1km from a Brazilian nuclear power plant with soils taken within a reference area located 50km away from the reactor site. Analyses of total carbon, delta(13)C and (137)Cs were also performed in order to understand the local soil dynamics. Except for one of the profiles, the isotopic composition of soil organic carbon reflected the actual forest vegetation present in both areas. The (137)Cs data show that the soils from the base of hills are probably allocthonous. The (14)C measurements showed that there is no accumulation due to the operation of the nuclear facility, although excess (14)C was found in the litter taken in the area close to power plant. This indicates that the anthropogenic signal observed in the litter fall has not been transferred yet to the soil. This study is part of an extensive research programme in which other samples including air, vegetation and gaseous effluents (taken in the vent stack of the Brazilian nuclear power reactors Angra I and II) were also analyzed. The present paper aimed to evaluate how (14)C emissions from the nuclear power plant are transferred and stored by soils present in the surroundings of the reactor site. This is the first study concerning anthropogenic (14)C in soils in Brazil. PMID:19216012

  11. Near Surface Leakage Monitoring for the Verification and Accounting of Geologic Carbon Sequestration Using a Field Ready {sup 14}C Isotopic Analyzer

    SciTech Connect

    Marino, Bruno

    2014-04-14

    Results for the development of a field ready multi-isotopic analyzer for {sup 12}CO{sub 2}, {sup 13}CO{sub 2} and {sup 14}CO{sub 2} and applications for carbon capture and storage (CCS) containment performance are described. A design goal of the field platform was to provide isotopic data with a high data rate, a standardized reference baseline and acceptable precision (e.g., ~ ±50 per mil D{sup 14}CO{sub 2}) for detection and quantification of fossil-fuel CO{sub 2} CCS leakage scenarios. The instrument platform was not designed to replace high precision accelerator mass spectrometry. An additional goal was to combine project scale isotopic data and associated fluxes with unique financial instruments linking CCS containment performance to a publicly traded security providing project revenue to stakeholders. While the primary goals of the project were attained additional work is needed for the instrument platform and deployment within a full scale CCS site that was not available during the project timeframe.

  12. 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. PMID:24814329

  13. 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

  14. Airborne radioactivity surveys of parts of Savery SW and Savery SE quadrangles, Carbon County, Wyoming

    USGS Publications Warehouse

    Henderson, J.R.

    1954-01-01

    The accompanying map shows the results of an airborne radioactivity survey in 222 square miles of Savery SW and Savery SE quadrangles, Wyoming. This area is part of a larger survey made in southern Carbon and Sweetwater Counties by the U. S. Geological Survey, November 9-24, 1953. The work was undertaken as part of a cooperative program with the U.S. Atomic Energy Commission.

  15. Airborne radioactivity survey of parts of Savery NW and Savery NE quadrangles, Carbon County, Wyoming

    USGS Publications Warehouse

    Henderson, J.R.

    1954-01-01

    The accompanying map shows the results of an airborne radioactivity survey in 266 square miles of Savery NW and Savery NE quadrangles, Wyoming. This area is part of a larger survey made in southern Carbon and Sweetwater Counties by the U. S. Geological Survey, November 9-24, 1953. The work was undertaken as part of a cooperative program with the U.S. Atomic Energy Commission.

  16. A Novel Airborne Carbon Isotope Analyzer for Methane and Carbon Dioxide Source Fingerprinting

    NASA Astrophysics Data System (ADS)

    Berman, E. S.; Huang, Y. W.; Owano, T. G.; Leifer, I.

    2014-12-01

    Recent field studies on major sources of the important greenhouse gas methane (CH4) indicate significant underestimation of methane release from fossil fuel industrial (FFI) and animal husbandry sources, among others. In addition, uncertainties still exist with respect to carbon dioxide (CO2) measurements, especially source fingerprinting. CO2 isotopic analysis provides a valuable in situ measurement approach to fingerprint CH4 and CO2as associated with combustion sources, leakage from geologic reservoirs, or biogenic sources. As a result, these measurements can characterize strong combustion source plumes, such as power plant emissions, and discriminate these emissions from other sources. As part of the COMEX (CO2 and MEthane eXperiment) campaign, a novel CO2 isotopic analyzer was installed and collected data aboard the CIRPAS Twin Otter aircraft. Developing methods to derive CH4 and CO2 budgets from remote sensing data is the goal of the summer 2014 COMEX campaign, which combines hyperspectral imaging (HSI) and non-imaging spectroscopy (NIS) with in situ airborne and surface data. COMEX leverages the synergy between high spatial resolution HSI and moderate spatial resolution NIS. The carbon dioxide isotope analyzer developed by Los Gatos Research (LGR) uses LGR's patented Off-Axis ICOS (Integrated Cavity Output Spectroscopy) technology and incorporates proprietary internal thermal control for high sensitivity and optimal instrument stability. This analyzer measures CO2 concentration as well as δ13C, δ18O, and δ17O from CO2 at natural abundance (100-3000 ppm). The laboratory accuracy is ±1.2 ppm (1σ) in CO2 from 370-1000 ppm, with a long-term (1000 s) precision of ±0.012 ppm. The long-term precision for both δ13C and δ18O is 0.04 ‰, and for δ17O is 0.06 ‰. The analyzer was field-tested as part of the COWGAS campaign, a pre-cursor campaign to COMEX in March 2014, where it successfully discriminated plumes related to combustion processes associated with

  17. Double-Pulse Two-Micron IPDA Lidar Simulation for Airborne Carbon Dioxide Measurements

    NASA Technical Reports Server (NTRS)

    Refaat, Tamer F.; Singh, Upendra N.; Yu, Jirong; Petros, Mulugeta

    2015-01-01

    An advanced double-pulsed 2-micron integrated path differential absorption lidar has been developed at NASA Langley Research Center for measuring atmospheric carbon dioxide. The instrument utilizes a state-of-the-art 2-micron laser transmitter with tunable on-line wavelength and advanced receiver. Instrument modeling and airborne simulations are presented in this paper. Focusing on random errors, results demonstrate instrument capabilities of performing precise carbon dioxide differential optical depth measurement with less than 3% random error for single-shot operation from up to 11 km altitude. This study is useful for defining CO2 measurement weighting, instrument setting, validation and sensitivity trade-offs.

  18. Forensic applications of 14C at CIRCE

    NASA Astrophysics Data System (ADS)

    Marzaioli, F.; Fiumano, V.; Capano, M.; Passariello, I.; Cesare, N. De.; Terrasi, F.

    2011-12-01

    The decreasing trend of the radiocarbon pulse produced during the atmospheric tests of nuclear weapons (bomb-carbon) coupled with high sensitivity accelerator mass spectrometry (AMS) measurements, drastically increased the precision of radiocarbon age determinations since the second part of the sixties, allowing the application of radiocarbon AMS to a wide range of studies previously not directly involving conventional radiocarbon dating (i.e. food authenticity, forensic, biochemistry). In the framework of authenticity evaluation of artworks, high precision radiocarbon ( 14C) AMS measurements (Δ R/ R < 0.3%) reduce the conventional uncertainty of the dating to few decades, allowing precise age estimation of materials containing carbon (C). The Centre for Isotopic Research on Cultural and Environmental heritage (CIRCE) during its activity on AMS 14C dating achieved high precision measurements opening the opportunity to these kinds of applications. This paper presents the main results obtained from radiocarbon measurements on a set of bone samples analyzed for the determination of the post-mortem interval in the framework of an unsolved case investigated by the Rome prosecutor office. The chronological characterization of the wooden support of the "Acerenza portrait" is also presented with the aim to evaluate its age and to further investigate the possibility to attribute this artwork to Leonardo da Vinci. Bomb- 14C dating on the lipid and collagen fractions of bones allows the evaluation of the year of the death of the individuals by means of ad hoc calibration data sheet with the typical few years precision and difference between collagen apparent age and the year of death appeared in agreement with the age of one individual estimated by dating of tooth collagen. Conventional radiocarbon dating on both wood and wood extracted cellulose leads to an estimation of the portrait wood board age (2σ) of 1459-1524 AD (57% relative probability), 1571-1631 AD interval (42

  19. Comparison between carbon monoxide measurements from spaceborne and airborne platforms

    NASA Technical Reports Server (NTRS)

    Connors, V. S.; Cahoon, D. R.; Reichle, H. G., Jr.; Scheel, H. E.

    1991-01-01

    The measurements of air pollution from satellites (MAPS) experiment measured the distribution of middle tropospheric carbon monoxide (CO) from the Space Shuttle during October 1984. A critical area of the experiment is the assessment of experimental error of the MAPS data. This error is determined by the comparison between the space-based CO data and concurrent, direct CO measurements taken aboard aircraft. Because of the variability in the CO measurements near land sources, a strategy for comparing the tropospheric CO measurements over the remote oceans is presented.

  20. Flux Of Carbon from an Airborne Laboratory (FOCAL): Synergy of airborne and surface measures of carbon emission and isotopologue content from tundra landscape in Alaska

    NASA Astrophysics Data System (ADS)

    Dobosy, R.; Dumas, E.; Sayres, D. S.; Kochendorfer, J.

    2013-12-01

    Arctic tundra, recognized as a potential major source of new atmospheric carbon, is characterized by low topographic relief and small-scale heterogeneity consisting of small lakes and intervening tundra vegetation. This fits well the flux-fragment method (FFM) of analysis of data from low-flying aircraft. The FFM draws on 1)airborne eddy-covariance flux measurements, 2)a classified surface-characteristics map (e.g. open water vs tundra), 3)a footprint model, and 4)companion surface-based eddy-covariance flux measurements. The FOCAL, a collaboration among Harvard University's Anderson Group, NOAA's Atmospheric Turbulence and Diffusion Division (ATDD), and Aurora Flight Sciences, Inc., made coordinated flights in 2013 August with a collaborating surface site. The FOCAL gathers not only flux data for CH4 and CO2 but also the corresponding carbon-isotopologue content of these gases. The surface site provides a continuous sample of carbon flux from interstitial tundra over time throughout the period of the campaign. The FFM draws samples from the aircraft data over many instances of tundra and also open water. From this we will determine how representative the surface site is of the larger area (100 km linear scale), and how much the open water differs from the tundra as a source of carbon.

  1. A universal airborne LiDAR approach for tropical forest carbon mapping.

    PubMed

    Asner, Gregory P; Mascaro, Joseph; Muller-Landau, Helene C; Vieilledent, Ghislain; Vaudry, Romuald; Rasamoelina, Maminiaina; Hall, Jefferson S; van Breugel, Michiel

    2012-04-01

    Airborne light detection and ranging (LiDAR) is fast turning the corner from demonstration technology to a key tool for assessing carbon stocks in tropical forests. With its ability to penetrate tropical forest canopies and detect three-dimensional forest structure, LiDAR may prove to be a major component of international strategies to measure and account for carbon emissions from and uptake by tropical forests. To date, however, basic ecological information such as height-diameter allometry and stand-level wood density have not been mechanistically incorporated into methods for mapping forest carbon at regional and global scales. A better incorporation of these structural patterns in forests may reduce the considerable time needed to calibrate airborne data with ground-based forest inventory plots, which presently necessitate exhaustive measurements of tree diameters and heights, as well as tree identifications for wood density estimation. Here, we develop a new approach that can facilitate rapid LiDAR calibration with minimal field data. Throughout four tropical regions (Panama, Peru, Madagascar, and Hawaii), we were able to predict aboveground carbon density estimated in field inventory plots using a single universal LiDAR model (r ( 2 ) = 0.80, RMSE = 27.6 Mg C ha(-1)). This model is comparable in predictive power to locally calibrated models, but relies on limited inputs of basal area and wood density information for a given region, rather than on traditional plot inventories. With this approach, we propose to radically decrease the time required to calibrate airborne LiDAR data and thus increase the output of high-resolution carbon maps, supporting tropical forest conservation and climate mitigation policy. PMID:22033763

  2. Brown Carbon: Results From Ground and Airborne Studies

    NASA Astrophysics Data System (ADS)

    Weber, R. J.; Forrister, H.; Liu, J.; Nenes, A.

    2015-12-01

    Brown carbon (BrC) is directly measured with high sensitivity by isolating it from black carbon in aerosol extracts and using long path wave-guide spectrophotometry. Ambient measurements by this approach show that BrC is pervasive and can be found in almost all locations, ranging from urban environments to remote continental sites and upper reaches of the free troposphere. Biomass burning appears to be the major source in many urban and rural locations, but other sources of incomplete combustion, such as vehicle emissions in urban environments also play a role. Secondary aerosols not associated with combustion sources may also contribute, but are likely of lesser importance. Studies of ambient wildfire smoke plumes show that BrC levels decrease as it ages, with a half-life of approximately 10 hours. However, a small fraction of the emitted BrC is stable and may account for much of the BrC observed throughout the atmosphere due to widely dispersed and ubiquitous smoke. A radiative transfer model indicates that this background BrC reduced US continental TOA forcing by 20 percent. Human health studies point to similar chemical components linked to BrC (i.e., HULIS), of this same ubiquitous smoke, as a significant source of adverse cardiorespiratory effects. This talk will summarize findings on BrC sources, transformations and estimates of environmental effects based on bulk measurements.

  3. Metabolism of (2-14C)acetate and its use in assessing hepatic Krebs cycle activity and gluconeogenesis

    SciTech Connect

    Schumann, W.C.; Magnusson, I.; Chandramouli, V.; Kumaran, K.; Wahren, J.; Landau, B.R. )

    1991-04-15

    To examine the fate of the carbons of acetate and to evaluate the usefulness of labeled acetate in assessing intrahepatic metabolic processes during gluconeogenesis, (2-14C)acetate, (2-14C)ethanol, and (1-14C)ethanol were infused into normal subjects fasted 60 h and given phenyl acetate. Distributions of 14C in the carbons of blood glucose and glutamate from urinary phenylacetylglutamine were determined. With (2-14C)acetate and (2-14C)ethanol, carbon 1 of glucose had about twice as much 14C as carbon 3. Carbon 2 of glutamate had about twice as much 14C as carbon 1 and one-half to one-third as much as carbon 4. There was only a small amount in carbon 5. These distributions are incompatible with the metabolism of (2-14C)acetate being primarily in liver. Therefore, (2-14C)acetate cannot be used to study Krebs cycle metabolism in liver and in relationship to gluconeogenesis, as has been done. The distributions can be explained by: (a) fixation of 14CO2 from (2-14C)acetate in the formation of the 14C-labeled glucose and glutamate in liver and (b) the formation of 14C-labeled glutamate in a second site, proposed to be muscle. (1,3-14C)Acetone formation from the (2-14C)acetate does not contribute to the distributions, as evidenced by the absence of 14C in carbons 2-4 of glutamate after (1-14C)ethanol administration.

  4. Domestic airborne black carbon and exhaled nitric oxide in children in NYC

    PubMed Central

    Cornell, Alexandra G.; Chillrud, Steven N.; Mellins, Robert B.; Acosta, Luis M.; Miller, Rachel L.; Quinn, James W.; Yan, Beizhan; Divjan, Adnan; Olmedo, Omar E.; Lopez-Pintado, Sara; Kinney, Patrick L.; Perera, Frederica P.; Jacobson, Judith S.; Goldstein, Inge F.; Rundle, Andrew G.; Perzanowski, Matthew S.

    2012-01-01

    Differential exposure to combustion by-products and allergens may partially explain the marked disparity in asthma prevalence (3%–18%) among New York City neighborhoods. Subclinical changes in airway inflammation can be measured by fractional exhaled nitric oxide (FeNO). FeNO could be used to test independent effects of these environmental exposures on airway inflammation. Seven and eight year-old children from neighborhoods with lower (range 3–9%, n=119) and higher (range 11–18%, n=121) asthma prevalence participated in an asthma case-control study. During home visits, FeNO was measured, and samples of bed dust (allergens) and air (black carbon) were collected. Neighborhood built-environment characteristics were assessed for the 500m surrounding participants’ homes. Airborne black carbon concentrations in homes correlated with neighborhood asthma prevalence (P<0.001) and neighborhood densities of truck routes (P<0.001) and buildings burning residual oil (P<0.001). FeNO concentrations were higher among asthmatics with compared to asthmatics without frequent wheeze (≥4 times/year) (P=0.002). FeNO concentrations correlated with domestic black carbon among children without seroatopy (P=0.012) and with dust mite allergen among children with seroatopy (P=0.020). The association between airborne black carbon in homes and both neighborhood asthma prevalence and FeNO suggest that further public health interventions on truck emissions standards and residual oil use are warranted. PMID:22377682

  5. DEVELOPMENT & APPLICATION OF RADIOCARBON (14C)/ORGANIC DENUDER METHODS

    EPA Science Inventory

    The radiocarbon (14C) content of a sample measures the fraction of the sample's carbon originating from non-fossil-fuel (biogenic) sources. The most important of these sources are biomass burning (mostly winter, but wildfires can contribute in other seasons as well) and secondar...

  6. Improving Aboveground Carbon Estimates in Dryland Ecosystems with Airborne LiDAR and Satellite Laser Altimetry

    NASA Astrophysics Data System (ADS)

    Glenn, N. F.; Shrestha, R.; Li, A.; Spaete, L.

    2014-12-01

    Numerous studies have demonstrated the utility of ground and airborne LiDAR data to quantify ecosystem structure. In addition, data from satellite-based laser altimetry (e.g. ICESat's GLAS instrument) have been used to estimate vegetation heights, aboveground carbon, and topography in forested areas. With the upcoming ICESAT-2 satellite scheduled to launch in 2017, we have the potential to map vegetation characteristics and dynamics in other ecosystems, including semiarid and low-height ecosystems, at global and regional scales. The ICESat-2 satellite will include the Advanced Topographic Laser Altimeter System (ATLAS) with a configuration of 6 laser beams with 532 nm wavelength and photon counting detectors. We will demonstrate the potential of ICESat-2 to provide estimates of vegetation structure and topography in a dryland ecosystem by simulating the configuration of the ATLAS mission. We will also examine how airborne LiDAR can be used together with ICESat-2 and other satellite data to achieve estimates of aboveground carbon. We will explore how these data may be used for future monitoring and quantification of spatial and temporal changes in aboveground carbon and topography.

  7. Taking Stock of Circumboreal Forest Carbon With Ground Measurements, Airborne and Spaceborne LiDAR

    NASA Technical Reports Server (NTRS)

    Neigh, Christopher S. R.; Nelson, Ross F.; Ranson, K. Jon; Margolis, Hank A.; Montesano, Paul M.; Sun, Guoqing; Kharuk, Viacheslav; Naesset, Erik; Wulder, Michael A.; Andersen, Hans-Erik

    2013-01-01

    The boreal forest accounts for one-third of global forests, but remains largely inaccessible to ground-based measurements and monitoring. It contains large quantities of carbon in its vegetation and soils, and research suggests that it will be subject to increasingly severe climate-driven disturbance. We employ a suite of ground-, airborne- and space-based measurement techniques to derive the first satellite LiDAR-based estimates of aboveground carbon for the entire circumboreal forest biome. Incorporating these inventory techniques with uncertainty analysis, we estimate total aboveground carbon of 38 +/- 3.1 Pg. This boreal forest carbon is mostly concentrated from 50 to 55degN in eastern Canada and from 55 to 60degN in eastern Eurasia. Both of these regions are expected to warm >3 C by 2100, and monitoring the effects of warming on these stocks is important to understanding its future carbon balance. Our maps establish a baseline for future quantification of circumboreal carbon and the described technique should provide a robust method for future monitoring of the spatial and temporal changes of the aboveground carbon content.

  8. Low-level 14C measurements and Accelerator Mass Spectrometry

    SciTech Connect

    Litherland, A.E.; Beukens, R.P.; Zhao, X.-L.; Kieser, W.E.; Gove, H.E.

    2005-09-08

    Accelerator Mass Spectrometry (AMS) and isotope enrichment were used in 1991 to estimate that the 14C content of methane in natural gas was {<=}1.6x10-18 of the total carbon. The low content of 14C in underground hydrocarbons was verified later in the remarkable results from the Borexino test scintillation counter for solar neutrino studies. Since then studies of the 14C background problem have demonstrated that much of the background originally observed in the AMS measurements can, in principle, be eliminated. However, many difficulties and other backgrounds are to be faced as the limit for AMS is pushed still further towards possibly a ratio of < 10-21. These will be discussed.

  9. 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.

  10. Calculation of the compounded uncertainty of 14C AMS measurements

    NASA Astrophysics Data System (ADS)

    Nadeau, Marie-Josée; Grootes, Pieter M.

    2013-01-01

    The correct method to calculate conventional 14C ages from the carbon isotopic ratios was summarised 35 years ago by Stuiver and Polach (1977) and is now accepted as the only method to calculate 14C ages. There is, however, no consensus regarding the treatment of AMS data, mainly of the uncertainty of the final result. The estimation and treatment of machine background, process blank, and/or in situ contamination is not uniform between laboratories, leading to differences in 14C results, mainly for older ages. As Donahue (1987) and Currie (1994), among others, mentioned, some laboratories find it important to use the scatter of several measurements as uncertainty while others prefer to use Poisson statistics. The contribution of the scatter of the standards, machine background, process blank, and in situ contamination to the uncertainty of the final 14C result is also treated in different ways. In the early years of AMS, several laboratories found it important to describe their calculation process in details. In recent years, this practise has declined. We present an overview of the calculation process for 14C AMS measurements looking at calculation practises published from the beginning of AMS until present.

  11. Pyrolysis-combustion 14C dating of soil organic matter

    NASA Astrophysics Data System (ADS)

    Wang, Hong; Hackley, Keith C.; Panno, Samuel V.; Coleman, Dennis D.; Liu, Jack Chao-li; Brown, Johnie

    2003-11-01

    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 (δ 13C) was heavier in the Py-V fractions, suggesting a greater abundance of carbohydrate- and protein-related constituents, and δ 13C was lighter in the Py-R fractions, suggesting more lignin- and lipid-related constituents. The combination of 14C dates and δ 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.

  12. Measurement of fecal /sup 14/C excretion

    SciTech Connect

    Kumaran, K.A.; Wiener, N.S.; Katz, J.B.

    1982-11-01

    Simultaneous measurements of fecal /sup 14/C and expired /sup 14/CO/sub 2/ in the breath are necessary to evaluate patients with various ileal abnormalities and bile salt malabsorption. Following the oral ingestion of the labeled bile acid, glycine-(I-/sup 14/C)cholic acid, detection of increased fecal /sup 14/C without abnormal expiration of /sup 14/CO/sub 2/ identifies patients with ileal resection. This contrasts with the normal fecal /sup 14/C content and abnormal expired /sup 14/CO/sub 2/ found in patients with bacterial overgrowth. Fecal /sup 14/C content was determined by utilizing Van Slyke combustion of the specimen and trapping the liberated /sup 14/CO/sub 2/ with Scintisorb C. The method is simple, rapid, and accurate, and expands the diagnostic usefulness of the bile salt absorption test.

  13. Detection of airborne carbon nanotubes based on the reactivity of the embedded catalyst.

    PubMed

    Neubauer, N; Kasper, G

    2015-01-01

    A previously described method for detecting catalyst particles in workplace air((1,2)) was applied to airborne carbon nanotubes (CNT). It infers the CNT concentration indirectly from the catalytic activity of metallic nanoparticles embedded as part of the CNT production process. Essentially, one samples airborne CNT onto a filter enclosed in a tiny chemical reactor and then initiates a gas-phase catalytic reaction on the sample. The change in concentration of one of the reactants is then determined by an IR sensor as measure of activity. The method requires a one-point calibration with a CNT sample of known mass. The suitability of the method was tested with nickel containing (25 or 38% by weight), well-characterized multi-walled CNT aerosols generated freshly in the lab for each experiment. Two chemical reactions were investigated, of which the oxidation of CO to CO2 at 470°C was found to be more effective, because nearly 100% of the nickel was exposed at that temperature by burning off the carbon, giving a linear relationship between CO conversion and nickel mass. Based on the investigated aerosols, a lower detection limit of 1 μg of sampled nickel was estimated. This translates into sampling times ranging from minutes to about one working day, depending on airborne CNT concentration and catalyst content, as well as sampling flow rate. The time for the subsequent chemical analysis is on the order of minutes, regardless of the time required to accumulate the sample and can be done on site. PMID:25271474

  14. Double-Pulse Two-micron LPDA Lidar Simulation for Airborne Carbon Dioxide Measurements

    NASA Astrophysics Data System (ADS)

    Refaat, Tamer F.; Singh, Upendra N.; Yu, Jirong; Petros, Mulugeta

    2016-06-01

    An advanced double-pulse 2-μm integrated path differential absorption lidar has been developed at NASA Langley Research Center for measuring atmospheric carbon dioxide. The instrument utilizes a state-of-the-art 2-μm laser transmitter with tunable on-line wavelength and advanced receiver. Instrument modeling and airborne simulations are presented in this paper. Focusing on random errors, results demonstrate instrument capabilities of performing precise carbon dioxide differential optical depth measurement with less than 3% random error for single-shot operation up to 11 km altitude. This study is useful for defining CO2 measurement weighting function for adaptive targeting, instrument setting, validation and sensitivity trade-offs.

  15. Airborne Carbon Dioxide Laser Absorption Spectrometer for IPDA Measurements of Tropospheric CO2: Recent Results

    NASA Technical Reports Server (NTRS)

    Spiers, Gary D.; Menzies, Robert T.

    2008-01-01

    The National Research Council's decadal survey on Earth Science and Applications from Space[1] recommended the Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) mission for launch in 2013-2016 as a logical follow-on to the Orbiting Carbon Observatory (OCO) which is scheduled for launch in late 2008 [2]. The use of a laser absorption measurement technique provides the required ability to make day and night measurements of CO2 over all latitudes and seasons. As a demonstrator for an approach to meeting the instrument needs for the ASCENDS mission we have developed the airborne Carbon Dioxide Laser Absorption Spectrometer (CO2LAS) which uses the Integrated Path Differential Absorption (IPDA) Spectrometer [3] technique operating in the 2 micron wavelength region.. During 2006 a short engineering checkout flight of the CO2LAS was conducted and the results presented previously [4]. Several short flight campaigns were conducted during 2007 and we report results from these campaigns.

  16. Verification of engineering assumptions in modeling of airborne release of Carbon-14

    SciTech Connect

    Simonson, S.A.; Yim, Man-Sung

    1996-10-01

    The effects of atmospheric pressure variation on the flow velocity, water vapor transport, and oxygen depletion within a hypothetical low-level engineered waste facility were recently modeled with a set of engineering assumptions. The model that resulted from these activates is termed {open_quotes}GETAR{close_quote} for gas evolution, transport and reaction. Results of transport calculations show that the pumping effect of barometric pressure changes is the dominant mechanism for inducing the release of carbon-14 in a facility with a monitoring well. Coupled with this calculation, are recent results that indicate that a greater fraction of the carbon-14 within a hypothetical waste facility would be available for biodegradation and release via an airborne pathway rather than into groundwater.

  17. 14C-carbaryl residues in hazelnut.

    PubMed

    Yücel, Ulkü; Ilim, Murat; Aslan, Nazife

    2006-01-01

    A hazelnut ocak (shrub growing form) in the field in Black Sea region of Turkey was treated with commercial carbaryl insecticide spiked with 14C-carbaryl. Three months later, the harvested hazelnuts were separated into husk, shell, and kernel components, then homogenized and analyzed. The total and unextractable (bound) 14C-residues were determined by combustion and the extractable 14C-residues were obtained by extracting the samples with methanol. Concentrated extracts were first analyzed by thin layer chromatography (TLC). The extracts were also subjected to a series of liquid-liquid extraction procedures for clean-up and the final extracts were analyzed by high performance liquid chromatography (HPLC). Crude hazelnut oil was also extracted with hexane and analyzed for total 14C-residue. A total of 1.3% of applied radioactivity was recovered from the total nut harvested, with 0.04%, 0.06%, and 1.2% present in shell, kernel, and husk, respectively. The results show that the inedible husk and shell contained 95.7% 14C, whereas the edible kernel contained 4.3% of the total 14C recovered. The terminal 14C-residue in hazelnut kernel and oil did not contain carbaryl and/or its metabolite naphthol. PMID:16785168

  18. Exposure assessment to airborne endotoxin, dust, ammonia, hydrogen sulfide and carbon dioxide in open style swine houses.

    PubMed

    Chang, C W; Chung, H; Huang, C F; Su, H J

    2001-08-01

    Information is limited for the exposure levels of airborne hazardous substances in swine feed buildings that are not completely enclosed. Open-style breeding, growing and finishing swine houses in six farms in subtropical Taiwan were studied for the airborne concentrations of endotoxin, dust, ammonia, hydrogen sulfide and carbon dioxide. The air in the farrowing and nursery stalls as partially enclosed was also simultaneously evaluated. Three selected gases and airborne dusts were quantified respectively by using Drager diffusion tubes and a filter-weighing method. Endotoxin was analyzed by the Limulus amoebocyte lysate assay. Average concentration of airborne total endotoxin among piggeries was between 36.8 and 298 EU/m(3), while that for respirable endotoxin was 14.1-129 EU/m(3). Mean concentration of total dust was between 0.15 and 0.34 mg/m(3), with average level of respirable dust of 0.14 mg/m(3). The respective concentrations of NH3, CO2 and H2S were less than 5 ppm, 600-895 ppm and less than 0.2 ppm. Airborne concentrations of total dust and endotoxin in the nursery house were higher than in the other types of swine houses. The finishing house presented the highest exposure risk to NH3, CO2 and H2S. Employees working in the finishing stalls were also exposed to the highest airborne levels of respirable endotoxin and dust. On the other hand, the air of the breeding units was the least contaminated in terms of airborne endotoxin, dust, NH3, CO2 and H2S. The airborne concentrations of substances measured in the present study were all lower than most of published studies conducted in mainly enclosed swine buildings. Distinct characteristics, including maintaining swine houses in an open status and frequent spraying water inside the stalls, significantly reduce accumulation of gases and airborne particulates. PMID:11513795

  19. Peat Depth Assessment Using Airborne Geophysical Data for Carbon Stock Modelling

    NASA Astrophysics Data System (ADS)

    Keaney, Antoinette; McKinley, Jennifer; Ruffell, Alastair; Robinson, Martin; Graham, Conor; Hodgson, Jim; Desissa, Mohammednur

    2013-04-01

    The Kyoto Agreement demands that all signatory countries have an inventory of their carbon stock, plus possible future changes to this store. This is particularly important for Ireland, where some 16% of the surface is covered by peat bog. Estimates of soil carbon stores are a key component of the required annual returns made by the Irish and UK governments to the Intergovernmental Panel on Climate Change. Saturated peat attenuates gamma-radiation from underlying rocks. This effect can be used to estimate the thickness of peat, within certain limits. This project examines this relationship between peat depth and gamma-radiation using airborne geophysical data generated by the Tellus Survey and newly acquired data collected as part of the EU-funded Tellus Border project, together encompassing Northern Ireland and the border area of the Republic of Ireland. Selected peat bog sites are used to ground truth and evaluate the use of airborne geophysical (radiometric and electromagnetic) data and validate modelled estimates of soil carbon, peat volume and depth to bedrock. Data from two test line sites are presented: one in Bundoran, County Donegal and a second line in Sliabh Beagh, County Monaghan. The plane flew over these areas at different times of the year and at a series of different elevations allowing the data to be assessed temporally with different soil/peat saturation levels. On the ground these flight test lines cover varying surface land use zones allowing future extrapolation of data from the sites. This research applies spatial statistical techniques, including uncertainty estimation in geostatistical prediction and simulation, to investigate and model the use of airborne geophysical data to examine the relationship between reduced radioactivity and peat depth. Ground truthing at test line locations and selected peat bog sites involves use of ground penetrating radar, terrestrial LiDAR, peat depth probing, magnetometry, resistivity, handheld gamma

  20. 14C content in aerosols in Mexico City

    NASA Astrophysics Data System (ADS)

    Gómez, V.; Solís, C.; Chávez, E.; Andrade, E.; Ortiz, M. E.; Huerta, A.; Aragón, J.; Rodríguez-Ceja, M.; Martínez, M. A.; Ortiz, E.

    2016-03-01

    14C-AMS of total carbon was determined in aerosols (PM10 fraction), collected in Mexico City during two weeks from 21 November to 3 December 2012. Other tracers such as total carbon (TC), organic carbon (OC), elemental carbon (EC) and trace element contents were also determined. F14C values varied from 0.39 to 0.48 with an average of 0.43. These values are slightly lower than those previously obtained for PM2.5 in 2003 and 2006 and reflect a high contribution of fossil CO2 to the carbonaceous matter in aerosols from Mexico City. In contrast, from 2006 to 2012 PM10 increased; EC, Ca, Ti and Fe concentrations remained constant, while OC, TC and K concentrations decreased. The use of potassium as an indicator of biomass burning showed that this source was negligible during this campaign. Combined analytical approaches allowed us to distinguish temporal variations of anthropogenic and natural inputs to the F14C.

  1. Uptake and distribution of 14C during and following exposure to [14C]methyl isocyanate.

    PubMed

    Ferguson, J S; Kennedy, A L; Stock, M F; Brown, W E; Alarie, Y

    1988-06-15

    Guinea pigs were exposed to [14C]methyl isocyanate (14CH3-NCO, 14C MIC) for periods of 1 to 6 hr at concentrations of 0.5 to 15 ppm. Arterial blood samples taken during exposure revealed immediate and rapid uptake of 14C. Clearance of 14C was then gradual over a period of 3 days. Similarly 14C was present in urine and bile immediately following exposure, and clearance paralleled that observed in blood. Guinea pigs fitted with a tracheal cannula and exposed while under anesthesia showed a reduced 14C uptake in blood indicating that most of the 14C MIC uptake in normal guinea pigs occurred from retention of this agent in the upper respiratory tract passages. In exposed guinea pigs 14C was distributed to all examined tissues. In pregnant female mice similarly exposed to 14C MIC, 14C was observed in all tissues examined following exposure including the uterus, placenta, and fetus. While the form of 14C distributed in blood and tissues has not yet been identified, these findings may help to explain the toxicity of MIC or MIC reaction products on organs other than the respiratory tract, as noted by several investigators. PMID:3376108

  2. Mapping Above- and Below-Ground Carbon Pools in Boreal Forests: The Case for Airborne Lidar.

    PubMed

    Kristensen, Terje; Næsset, Erik; Ohlson, Mikael; Bolstad, Paul V; Kolka, Randall

    2015-01-01

    A large and growing body of evidence has demonstrated that airborne scanning light detection and ranging (lidar) systems can be an effective tool in measuring and monitoring above-ground forest tree biomass. However, the potential of lidar as an all-round tool for assisting in assessment of carbon (C) stocks in soil and non-tree vegetation components of the forest ecosystem has been given much less attention. Here we combine the use airborne small footprint scanning lidar with fine-scale spatial C data relating to vegetation and the soil surface to describe and contrast the size and spatial distribution of C pools within and among multilayered Norway spruce (Picea abies) stands. Predictor variables from lidar derived metrics delivered precise models of above- and below-ground tree C, which comprised the largest C pool in our study stands. We also found evidence that lidar canopy data correlated well with the variation in field layer C stock, consisting mainly of ericaceous dwarf shrubs and herbaceous plants. However, lidar metrics derived directly from understory echoes did not yield significant models. Furthermore, our results indicate that the variation in both the mosses and soil organic layer C stock plots appears less influenced by differences in stand structure properties than topographical gradients. By using topographical models from lidar ground returns we were able to establish a strong correlation between lidar data and the organic layer C stock at a stand level. Increasing the topographical resolution from plot averages (~2000 m2) towards individual grid cells (1 m2) did not yield consistent models. Our study demonstrates a connection between the size and distribution of different forest C pools and models derived from airborne lidar data, providing a foundation for future research concerning the use of lidar for assessing and monitoring boreal forest C. PMID:26426532

  3. Mapping Above- and Below-Ground Carbon Pools in Boreal Forests: The Case for Airborne Lidar

    PubMed Central

    Kristensen, Terje; Næsset, Erik; Ohlson, Mikael; Bolstad, Paul V.; Kolka, Randall

    2015-01-01

    A large and growing body of evidence has demonstrated that airborne scanning light detection and ranging (lidar) systems can be an effective tool in measuring and monitoring above-ground forest tree biomass. However, the potential of lidar as an all-round tool for assisting in assessment of carbon (C) stocks in soil and non-tree vegetation components of the forest ecosystem has been given much less attention. Here we combine the use airborne small footprint scanning lidar with fine-scale spatial C data relating to vegetation and the soil surface to describe and contrast the size and spatial distribution of C pools within and among multilayered Norway spruce (Picea abies) stands. Predictor variables from lidar derived metrics delivered precise models of above- and below-ground tree C, which comprised the largest C pool in our study stands. We also found evidence that lidar canopy data correlated well with the variation in field layer C stock, consisting mainly of ericaceous dwarf shrubs and herbaceous plants. However, lidar metrics derived directly from understory echoes did not yield significant models. Furthermore, our results indicate that the variation in both the mosses and soil organic layer C stock plots appears less influenced by differences in stand structure properties than topographical gradients. By using topographical models from lidar ground returns we were able to establish a strong correlation between lidar data and the organic layer C stock at a stand level. Increasing the topographical resolution from plot averages (~2000 m2) towards individual grid cells (1 m2) did not yield consistent models. Our study demonstrates a connection between the size and distribution of different forest C pools and models derived from airborne lidar data, providing a foundation for future research concerning the use of lidar for assessing and monitoring boreal forest C. PMID:26426532

  4. Development of an Airborne System for Direct Validation of Regional Carbon Flux Estimates

    NASA Astrophysics Data System (ADS)

    Wolfe, G.; Kawa, S. R.; Hanisco, T. F.; Newman, P. A.

    2015-12-01

    Global distributions of greenhouse gas (GHG) sources and sinks, principally CO2 and CH4, and characterization of the processes that control them, comprise a key uncertainty in projections of future climate. A broad spectrum of tools is currently used to characterize these processes. Top-down inversions of orbital GHG column observations (e.g. ACOS/GOSAT and OCO-2) provide a global perspective, but little information is available to validate these estimates. Indirect (boundary-layer budget) or direct (tower-based eddy covariance) surface flux measurements can provide bottom-up constraints, but the former is typically focused on large point and area emission sources while the latter relies on sparse networks with limited spatial coverage. Aircraft are an ideal platform to bridge the flux representation scale from kilometers (as measured from towers) to the tens or hundreds of kilometers relevant to satellite observations and global models. In light of current measurement gaps and the emerging need for direct validation of GHG surface flux estimates, NASA is developing a sophisticated facility for airborne eddy covariance observations of carbon dioxide, methane, water vapor and other trace gases. Three components comprise the core measurement system: i) the NASA Wallops Sherpa, which is ideal for airborne eddy covariance due to its substantial payload and the ability to fly low and slow, ii) commercial GHG sensors optimized for airborne flux measurements, and iii) a custom gust-probe system for high-fidelity measurements of vertical wind velocity. These systems will be discussed in detail, along with future plans for deployment and application of measurements to improving GHG flux estimates on local, regional and global scales.

  5. Relating urban airborne particle concentrations to shipping using carbon based elemental emission ratios

    NASA Astrophysics Data System (ADS)

    Johnson, Graham R.; Juwono, Alamsyah M.; Friend, Adrian J.; Cheung, Hing-Cho; Stelcer, Eduard; Cohen, David; Ayoko, Godwin A.; Morawska, Lidia

    2014-10-01

    This study demonstrates a novel method for testing the hypothesis that variations in primary and secondary particle number concentration (PNC) in urban air are related to residual fuel oil combustion at a coastal port lying 30 km upwind, by examining the correlation between PNC and airborne particle composition signatures chosen for their sensitivity to the elemental contaminants present in residual fuel oil. Residual fuel oil combustion indicators were chosen by comparing the sensitivity of a range of concentration ratios to airborne emissions originating from the port. The most responsive were combinations of vanadium and sulphur concentration ([S], [V]) expressed as ratios with respect to black carbon concentration ([BC]). These correlated significantly with ship activity at the port and with the fraction of time during which the wind blew from the port. The average [V] when the wind was predominantly from the port was 0.52 ng m-3 (87%) higher than the average for all wind directions and 0.83 ng m-3 (280%) higher than that for the lowest vanadium yielding wind direction considered to approximate the natural background. Shipping was found to be the main source of V impacting urban air quality in Brisbane. However, contrary to the stated hypothesis, increases in PNC related measures did not correlate with ship emission indicators or ship traffic. Hence at this site ship emissions were not found to be a major contributor to PNC compared to other fossil fuel combustion sources such as road traffic, airport and refinery emissions.

  6. Carbon content of common airborne fungal species and fungal contribution to aerosol organic carbon in a subtropical city

    NASA Astrophysics Data System (ADS)

    Cheng, Jessica Y. W.; Chan, Chak K.; Lee, C.-T.; Lau, Arthur P. S.

    Interest in the role and contribution of fungi to atmospheric aerosols and processes grows in the past decade. Substantial data or information such as fungal mass or carbon loading to ambient aerosols is however still lacking. This study aimed to quantify the specific organic carbon content (OC per spore) of eleven fungal species commonly found airborne in the subtropics, and estimated their contribution to organic carbon in aerosols. The specific OC contents showed a size-dependent relationship ( r = 0.64, p < 0.05) and ranged from 3.6 to 201.0 pg carbon per spore or yeast cell, giving an average of 6.0 pg carbon per spore (RSD 51%) for spore or cell size less than 10 μm. In accounting for natural variations in the composition and abundance of fungal population, weighted-average carbon content for field samples was adopted using the laboratory determined specific OC values. An average of 5.97 pg carbon per spore (RSD 3.8%) was enumerated from 28 field samples collected at the university campus. The mean fungal OC concentration was 3.7, 6.0 and 9.7 ng m -3 in PM 2.5, PM 2.5-10 and PM 10, respectively. These corresponded to 0.1%, 1.2% and 0.2% of the total OC in PM 2.5, PM 2.5-10 and PM 10, respectively. In the study period, rain provided periods with low total OC but high fungal prevalence and fungi contributed 7-32% OC in PM 2.5-10 or 2.4-7.1% OC in PM 10. More extensive studies are deserved to better understand the spatial-, temporal- and episodic dependency on the fungal OC contribution to the atmospheric aerosols.

  7. Application of 14C analyses to source apportionment of carbonaceous PM 2.5 in the UK

    NASA Astrophysics Data System (ADS)

    Heal, Mathew R.; Naysmith, Philip; Cook, Gordon T.; Xu, Sheng; Duran, Teresa Raventós; Harrison, Roy M.

    2011-05-01

    Determination of the radiocarbon ( 14C) content of airborne particulate matter yields insight into the proportion of the carbonaceous material derived from fossil and contemporary carbon sources. Daily samples of PM 2.5 were collected by high-volume sampler at an urban background site in Birmingham, UK, and the fraction of 14C in both the total carbon, and in the organic and elemental carbon fractions, determined by two-stage combustion to CO 2, graphitisation and quantification by accelerator mass spectrometry. OC and EC content was also determined by Sunset Analyzer. The mean fraction contemporary TC in the PM 2.5 samples was 0.50 (range 0.27-0.66, n = 26). There was no seasonality to the data, but there was a positive trend between fraction contemporary TC and magnitude of SOC/TC ratio and for the high values of these two parameters to be associated with air-mass back trajectories arriving in Birmingham from over land. Using a five-compartment mass balance model on fraction contemporary carbon in OC and EC, the following average source apportionment for the TC in these PM 2.5 samples was derived: 27% fossil EC; 20% fossil OC; 2% biomass EC; 10% biomass OC; and 41% biogenic OC. The latter category will comprise, in addition to BVOC-derived SOC, other non-combustion contemporary carbon sources such as biological particles, vegetative detritus, humic material and tyre wear. The proportion of total PM 2.5 at this location estimated to derive from BVOC-derived secondary organic aerosol was 9-29%. The findings from this work are consistent with those from elsewhere in Europe and support the conclusion of a significant and ubiquitous contribution from non-fossil biogenic sources to the carbon in terrestrial aerosol.

  8. 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

  9. Low-level (submicromole) environmental 14C metrology

    NASA Astrophysics Data System (ADS)

    Currie, L. A.; Kessler, J. D.; Marolf, J. V.; McNichol, A. P.; Stuart, D. R.; Donoghue, J. C.; Donahue, D. J.; Burr, G. S.; Biddulph, D.

    2000-10-01

    Accelerator mass spectrometry (AMS) measurements of environmental 14C have been employed during the past decade at the several micromole level (tens of μg carbon), but advanced research in the atmospheric and marine sciences demands still higher (μg) sensitivity, an extreme example being the determination of 14C in elemental or "black" carbon (BC) at levels of 2-10 μg per kg of Greenland snow and ice (Currie et al., 1998). A fundamental limitation for 14C AMS is Poisson counting statistics, which sets in at about 1 μg modern-C. Using the small sample (25 μg) AMS target preparation facility at NOSAMS (Pearson et al., 1998), and the microsample combustion-dilution facility at NIST, we have demonstrated an intrinsic modern-C quantification limit ( mQ) of ca. 0.9 μg, based on a 1-parameter fit to the empirical AMS variance function. (For environmental 14C, the modern carbon quantification limit is defined as that mass ( mQ) corresponding to 10% relative standard deviation (rsd) for the fraction of modern carbon, σ( fM)/ fM.) Stringent control, required for quantitative dilution factors (DL), is achieved with the NIST on-line manometric/mass spectrometry facility that compensates also for unsuspected trace impurities from vigorous chemical processing (e.g., acid digestion). Our current combustion blank is trivial (mean: 0.16 ± 0.02 μg C, n=13) but lognormally distributed (dispersion [σ]: 0.07 ± 0.01 μg). An iterative numerical expression is introduced to assess the quantitative impacts of fossil and modern carbon blank components on mQ; and a new "clean chemistry" BC processing system is described for the minimization of such blanks. For the assay of soot carbon in Greenland snow/ice, the overall processing blank has been reduced from nearly 7 μg total carbon to less than 1 μg, and is undetectable for BC.

  10. Airborne radioactivity survey of the Miller Hill area, Carbon county, Wyoming

    USGS Publications Warehouse

    Meuschke, J.L.; Moxham, R.M.

    1953-01-01

    The accompanying map shows the results of an airborne radioactivity survey covering 65 square miles northwest of Miller Hill, Carbon county, Wyoming. The survey was made by the U.S. Geological Survey as part of a cooperative program with the U.S. Atomic Energy Commission. At 500 feet above the ground, the width of the zone from which anomalous radioactivity is measured varies with the intensity of radiation of the source and, for strong sources, the width would be as much as 1,400 feet. Quarter-mile spacing of the flight paths of the aircraft should be adequate to detect anomalies from strong sources of radioactivity. However, small areas of considerable radioactivity midway between flight paths may not be noted. The approximate location of each radioactivity anomaly is shown on the accompanying map. The plotted position of an anomaly may be in error by as much as a quarter of a mile owing to errors in the available base maps up to several square miles in which it is impossible to find and plot recognizable landmarks. The radioactivity anomalies shown on the accompanying map cannot be interpreted in terms of either the radioactive content or the extent of the source materials. The present technique of airborne radioactivity measurement does not permit distinguishing between activity due to thorium and that due to uranium. An anomaly, therefore, may represent radioactivity due entirely to uranium, or to thorium, or to a combination of uranium and thorium. The radioactivity that is recorded by airborne measurements at 500 feet above the ground can be caused by: 1. A moderately large area in which the rocks and soils are slightly more radioactive than the rocks and soils of the surrounding area. 2. A smaller area in which the rocks and soils are considerably more radioactive than rocks and soils in the surrounding area. 3. A very small area in which to rocks and soils are much more radioactive than the rocks and soils of the surrounding area. Any particular anomaly

  11. Characterization and Control of Airborne Particles Emitted During Production of Epoxy / Carbon Nanotube Nanocomposites

    PubMed Central

    Cena, Lorenzo G.; Peters, Thomas M.

    2016-01-01

    This work characterized airborne particles that were generated from the weighing of bulk, multi-wall carbon nanotubes (CNTs) and the manual sanding of epoxy test samples reinforced with CNTs. It also evaluated the effectiveness of three local exhaust ventilation (LEV) conditions (no LEV, custom fume hood, and biosafety cabinet) for control of particles generated during sanding of CNT-epoxy nanocomposites. Particle number and respirable mass concentrations were measured using an optical particle counter (OPC) and a condensation particle counter (CPC), and particle morphology was assessed by transmission electron microscopy. The ratios of the geometric mean (GM) concentrations measured during the process to that measured in the background (P/B ratios) were used as indices of the impact of the process and the LEVs on observed concentrations. Processing CNT-epoxy nanocomposites materials released respirable size airborne particles (P/B ratio: weighing = 1.79; sanding = 5.90) but generally no nanoparticles (P/B ratiô1). The particles generated during sanding were predominately micron-sized with protruding CNTs and very different from bulk CNTs that tended to remain in large (>1 μm) tangled clusters. Respirable mass concentrations in the operator’s breathing zone were lower when sanding was performed in the biological safety cabinet (GM = 0.20 μg/m3) compared to those with no LEV (GM = 2.68 μg/m3) or those when sanding was performed inside the fume hood (GM = 21.4 μg/m3; p-value < 0.0001). The poor performance of the custom fume hood used in this study may have been exacerbated by its lack of a front sash and rear baffles and its low face velocity (0.39 m/sec). PMID:21253981

  12. Characterization and control of airborne particles emitted during production of epoxy/carbon nanotube nanocomposites.

    PubMed

    Cena, Lorenzo G; Peters, Thomas M

    2011-02-01

    This work characterized airborne particles generated from the weighing of bulk, multiwall carbon nanotubes (CNTs) and the manual sanding of epoxy test samples reinforced with CNTs. It also evaluated the effectiveness of three local exhaust ventilation (LEV) conditions (no LEV, custom fume hood, and biosafety cabinet) for control of particles generated during sanding of CNT-epoxy nanocomposites. Particle number and respirable mass concentrations were measured using an optical particle counter (OPC) and a condensation particle counter (CPC), and particle morphology was assessed by transmission electron microscopy. The ratios of the geometric mean (GM) concentrations measured during the process to that measured in the background (P/B ratios) were used as indices of the impact of the process and the LEVs on observed concentrations. Processing CNT-epoxy nanocomposites materials released respirable size airborne particles (P/B ratio: weighing = 1.79; sanding = 5.90) but generally no nanoparticles (P/B ratio ∼1). The particles generated during sanding were predominantly micron sized with protruding CNTs and very different from bulk CNTs that tended to remain in large (>1 μm) tangled clusters. Respirable mass concentrations in the operator's breathing zone were lower when sanding was performed in the biological safety cabinet (GM = 0.20 μg/m(3) compared with those with no LEV (GM = 2.68 μg/m(3) or those when sanding was performed inside the fume hood (GM = 21.4 μg/m(3); p-value < 0.0001). The poor performance of the custom fume hood used in this study may have been exacerbated by its lack of a front sash and rear baffles and its low face velocity (0.39 m/sec). PMID:21253981

  13. Airborne sulfur trace species intercomparison campaign: Sulfur dioxide, dimethylsulfide, hydrogen sulfide, carbon disulfide, and carbonyl sulfide

    NASA Technical Reports Server (NTRS)

    Gregory, Gerald L.; Hoell, James M., Jr.; Davis, Douglas D.

    1991-01-01

    Results from an airborne intercomparison of techniques to measure tropospheric levels of sulfur trace gases are presented. The intercomparison was part of the NASA Global Tropospheric Experiment (GTE) and was conducted during the summer of 1989. The intercomparisons were conducted on the Wallops Electra aircraft during flights from Wallops Island, Virginia, and Natal, Brazil. Sulfur measurements intercompared included sulfur dioxide (SO2), dimethylsulfide (DMS), hydrogen sulfide (H2S), carbon disulfide (CS2), and carbonyl sulfide (OCS). Measurement techniques ranged from filter collection systems with post-flight analyses to mass spectrometer and gas chromatograph systems employing various methods for measuring and identifying the sulfur gases during flight. Sampling schedules for the techniques ranged from integrated collections over periods as long as 50 minutes to one- to three-minute samples every ten or fifteen minutes. Several of the techniques provided measurements of more than one sulfur gas. Instruments employing different detection principles were involved in each of the sulfur intercomparisons. Also included in the intercomparison measurement scenario were a host of supporting measurements (i.e., ozone, nitrogen oxides, carbon monoxide, total sulfur, aerosols, etc.) for purposes of: (1) interpreting results (i.e., correlation of any noted instrument disagreement with the chemical composition of the measurement environment); and (2) providing supporting chemical data to meet CITE-3 science objectives of studying ozone/sulfur photochemistry, diurnal cycles, etc. The results of the intercomparison study are briefly discussed.

  14. Airborne Detection and Dynamic Modeling of Carbon Dioxide and Methane Plumes

    NASA Astrophysics Data System (ADS)

    Jacob, Jamey; Mitchell, Taylor; Whyte, Seabrook

    2015-11-01

    To facilitate safe storage of greenhouse gases such as CO2 and CH4, airborne monitoring is investigated. Conventional soil gas monitoring has difficulty in distinguishing gas flux signals from leakage with those associated with meteorologically driven changes. A low-cost, lightweight sensor system has been developed and implemented onboard a small unmanned aircraft that measures gas concentration and is combined with other atmospheric diagnostics, including thermodynamic data and velocity from hot-wire and multi-hole probes. To characterize the system behavior and verify its effectiveness, field tests have been conducted over controlled rangeland burns and over simulated leaks. In the former case, since fire produces carbon dioxide over a large area, this was an opportunity to test in an environment that while only vaguely similar to a carbon sequestration leak source, also exhibits interesting plume behavior. In the simulated field tests, compressed gas tanks are used to mimic leaks and generate gaseous plumes. Since the sensor response time is a function of vehicle airspeed, dynamic calibration models are required to determine accurate location of gas concentration in (x , y , z , t) . Results are compared with simulations using combined flight and atmospheric dynamic models. Supported by Department of Energy Award DE-FE0012173.

  15. Making Carbon Emissions Remotely Sensible: Flux Observations of Carbon from an Airborne Laboratory (FOCAL), its Near-Surface Survey of Carbon Gases and Isotopologues on Alaska's North Slope

    NASA Astrophysics Data System (ADS)

    Dobosy, R.; Dumas, E. J.; Sayres, D. S.; Healy, C. E.; Munster, J. B.; Baker, B.; Anderson, J. G.

    2014-12-01

    Detailed process-oriented study of the mechanisms of conversion in the Arctic of fossil carbon to atmospheric gas is progressing, but necessarily limited to a few point locations and requiring detailed subsurface measurements inaccessible to remote sensing. Airborne measurements of concentration, transport and flux of these carbon gases at sufficiently low altitude to reflect surface variations can tie such local measurements to remotely observable features of the landscape. Carbon dioxide and water vapor have been observable for over 20 years from low-altitude small aircraft in the Arctic and elsewhere. Methane has been more difficult, requiring large powerful aircraft or limited flask samples. Recent developments in spectroscopy, however, have reduced the power and weight required to measure methane at rates suitable for eddy-covariance flux estimates. The Flux Observations of Carbon from an Airborne Laboratory (FOCAL) takes advantage of Integrated Cavity-Output Spectroscopy (ICOS) to measure CH4, CO2, and water vapor in a new airborne system. The system, moreover, measures these gases' stable isotopologues every two seconds or faster helping to separate thermogenic from biogenic emissions. Paired with the Best Airborne Turbulence (BAT) probe developed for small aircraft by NOAA's Air Resources Laboratory and a light twin-engine aircraft adapted by Aurora Flight Sciences Inc., the FOCAL measures at 6 m spacing, covering 100 km in less than 30 minutes. It flies between 10 m and 50 m above ground interspersed with profiles to the top of the boundary layer and beyond. This presentation gives an overview of the magnitude and variation in fluxes and concentrations of CH4, CO2, and H2O with space, time, and time of day in a spatially extensive survey, more than 7500 km total in 15 flights over roughly a 100 km square during the month of August 2013. An extensive data set such as this at low altitude with high-rate sampling addresses features that repeat on 1 km scale

  16. No evidence for a deglacial intermediate water Δ 14C anomaly in the SW Atlantic

    NASA Astrophysics Data System (ADS)

    Sortor, Rachel N.; Lund, David C.

    2011-10-01

    The last deglaciation was characterized by an increase in atmospheric pCO 2 and decrease in atmospheric radiocarbon activity. One hypothesis is that these changes were due to out-gassing of 14C-depleted carbon from the abyssal ocean. Reconstructions of foraminiferal Δ 14C from the eastern tropical Pacific, Arabian Sea, and high latitude North Atlantic show that severe depletions in 14C occurred at intermediate water depths during the last deglaciation. It has been suggested that 14C-depleted water from the abyss upwelled in the Southern Ocean and was then carried by Antarctic Intermediate Water (AAIW) to these sites. However, locations in the South Pacific in the direct path of modern-day AAIW do not exhibit the Δ 14C excursion and therefore cast doubt upon the AAIW mechanism ( De Pol-Holz et al., 2010; Rose et al., 2010). Here we evaluate whether or not a deglacial 14C anomaly occurred at intermediate depths in the Southwest Atlantic. We find that the deglacial benthic Δ 14C trend at our site is similar to the atmospheric Δ 14C trend. Our results are also largely consistent with results from U/Th-dated corals at shallower water depths on the Brazil Margin (Mangini et al., 2010). We find no evidence in the southwestern Atlantic of a ~ 300‰ decrease in intermediate water Δ 14C from 18 to 14 kyr BP like that observed in the eastern tropical Pacific ( Marchitto et al., 2007). When our results are paired with those from the South Pacific, it appears AAIW did not carry a highly 14C-depleted signal during the deglaciation. Another source of carbon is apparently required to explain the intermediate-depth Δ 14C anomalies in the North Atlantic, Indian, and Pacific Oceans.

  17. A high-resolution record of atmospheric 14C based on Hulu Cave speleothem H82

    NASA Astrophysics Data System (ADS)

    Southon, John; Noronha, Alexandra L.; Cheng, Hai; Edwards, R. Lawrence; Wang, Yongjin

    2012-02-01

    The development of a calibration of atmospheric radiocarbon (∆14C) is a significant scientific goal because it provides the means to link the numerous 14C dated paleoclimate records to a common timescale with absolutely dated records, and thereby improve our understanding the relationships between the carbon cycle and climate change. Currently, few calibration datasets that directly sample the atmospheric 14C reservoir are available beyond the end of the dendro-dated Holocene tree ring record at 12.6 kyr BP (Before 1950 AD). In the absence of suitable true atmospheric records, 14C calibrations beyond this age limit are based largely on marine data, that are complicated by the marine reservoir effect, which may have varied over the glacial cycle. In this paper, we present a high-resolution record of U-Th series and 14C measurements from Hulu Cave speleothem H82, spanning 10.6-26.8 kyr BP. Corrections for detrital 230Th are negligible, and the contribution of 14C-free geologic carbon to the speleothem calcite is small (5-6%) and is stable across major climate shifts. The time series provides a 16 kyr record of atmospheric ∆14C as well as an updated age model for the existing Hulu Cave δ18O record. The 14C data are in good overall agreement with existing marine and terrestrial 14C records, but comparisons with the Cariaco Basin marine ∆14C record through the deglacial interval reveal that the Cariaco reservoir age appears to have varied during parts of the Younger Dryas and Heinrich Stadial 1 cold events. This highlights the importance of developing extended high-resolution marine and terrestrial 14C records as a means of detecting changes in ocean circulation over the glacial cycle.

  18. Atmospheric 14C variations derived from tree rings during the early Younger Dryas

    NASA Astrophysics Data System (ADS)

    Hua, Quan; Barbetti, Mike; Fink, David; Kaiser, Klaus Felix; Friedrich, Michael; Kromer, Bernd; Levchenko, Vladimir A.; Zoppi, Ugo; Smith, Andrew M.; Bertuch, Fiona

    2009-12-01

    Atmospheric radiocarbon variations over the Younger Dryas interval, from ˜13,000 to 11,600 cal yr BP, are of immense scientific interest because they reveal crucial information about the linkages between climate, ocean circulation and the carbon cycle. However, no direct and reliable atmospheric 14C records based on tree rings for the entire Younger Dryas have been available. In this paper, we present (1) high-precision 14C measurements on the extension of absolute tree-ring chronology from 12,400 to 12,560 cal yr BP and (2) high-precision, high-resolution atmospheric 14C record derived from a 617-yr-long tree-ring chronology of Huon pine from Tasmania, Australia, spanning the early Younger Dryas. The new tree-ring 14C records bridge the current gap in European tree-ring radiocarbon chronologies during the early Younger Dryas, linking the floating Lateglacial Pine record to the absolute tree-ring timescale. A continuous and reliable atmospheric 14C record for the past 14,000 cal yr BP including the Younger Dryas is now available. The new records indicate that the abrupt rise in atmospheric Δ 14C associated with the Younger Dryas onset occurs at ˜12,760 cal yr BP, ˜240 yrs later than that recorded in Cariaco varves, with a smaller magnitude of ˜40‰ followed by several centennial Δ 14C variations of 20-25‰. Comparing the tree-ring Δ 14C to marine-derived Δ 14C and modelled Δ 14C based on ice-core 10Be fluxes, we conclude that changes in ocean circulation were mainly responsible for the Younger Dryas onset, while a combination of changes in ocean circulation and 14C production rate were responsible for atmospheric Δ 14C variations for the remainder of the Younger Dryas.

  19. Regional prediction of soil organic carbon content over croplands using airborne hyperspectral data

    NASA Astrophysics Data System (ADS)

    Vaudour, Emmanuelle; Gilliot, Jean-Marc; Bel, Liliane; Lefebvre, Josias; Chehdi, Kacem

    2015-04-01

    This study was carried out in the framework of the Prostock-Gessol3 and the BASC-SOCSENSIT projects, dedicated to the spatial monitoring of the effects of exogenous organic matter land application on soil organic carbon storage. It aims at identifying the potential of airborne hyperspectral AISA-Eagle data for predicting the topsoil organic carbon (SOC) content of bare cultivated soils over a large peri-urban area (221 km2) with both contrasted soils and SOC contents, located in the western region of Paris, France. Soils comprise hortic or glossic luvisols, calcaric, rendzic cambisols and colluvic cambisols. Airborne AISA-Eagle data (400-1000 nm, 126 bands) with 1 m-resolution were acquired on 17 April 2013 over 13 tracks which were georeferenced. Tracks were atmospherically corrected using a set of 22 synchronous field spectra of both bare soils, black and white targets and impervious surfaces. Atmospherically corrected track tiles were mosaicked at a 2 m-resolution resulting in a 66 Gb image. A SPOT4 satellite image was acquired the same day in the framework of the SPOT4-Take Five program of the French Space Agency (CNES) which provided it with atmospheric correction. The land use identification system layer (RPG) of 2012 was used to mask non-agricultural areas, then NDVI calculation and thresholding enabled to map agricultural fields with bare soil. All 18 sampled sites known to be bare at this very date were correctly included in this map. A total of 85 sites sampled in 2013 or in the 3 previous years were identified as bare by means of this map. Predictions were made from the mosaic spectra which were related to topsoil SOC contents by means of partial least squares regression (PLSR). Regression robustness was evaluated through a series of 1000 bootstrap data sets of calibration-validation samples. The use of the total sample including 27 sites under cloud shadows led to non-significant results. Considering 43 sites outside cloud shadows only, median

  20. Improving estimation of tree carbon stocks by harvesting aboveground woody biomass within airborne LiDAR flight areas

    NASA Astrophysics Data System (ADS)

    Colgan, M.; Asner, G. P.; Swemmer, A. M.

    2011-12-01

    The accurate estimation of carbon stored in a tree is essential to accounting for the carbon emissions due to deforestation and degradation. Airborne LiDAR (Light Detection and Ranging) has been successful in estimating aboveground carbon density (ACD) by correlating airborne metrics, such as canopy height, to field-estimated biomass. This latter step is reliant on field allometry which is applied to forest inventory quantities, such as stem diameter and height, to predict the biomass of a given tree stem. Constructing such allometry is expensive, time consuming, and requires destructive sampling. Consequently, the sample sizes used to construct such allometry are often small, and the largest tree sampled is often much smaller than the largest in the forest population. The uncertainty resulting from these sampling errors can lead to severe biases when the allometry is applied to stems larger than those harvested to construct the allometry, which is then subsequently propagated to airborne ACD estimates. The Kruger National Park (KNP) mission of maintaining biodiversity coincides with preserving ecosystem carbon stocks. However, one hurdle to accurately quantifying carbon density in savannas is that small stems are typically harvested to construct woody biomass allometry, yet they are not representative of Kruger's distribution of biomass. Consequently, these equations inadequately capture large tree variation in sapwood/hardwood composition, root/shoot/leaf allocation, branch fall, and stem rot. This study eliminates the "middleman" of field allometry by directly measuring, or harvesting, tree biomass within the extent of airborne LiDAR. This enables comparisons of field and airborne ACD estimates, and also enables creation of new airborne algorithms to estimate biomass at the scale of individual trees. A field campaign was conducted at Pompey Silica Mine 5km outside Kruger National Park, South Africa, in Mar-Aug 2010 to harvest and weigh tree mass. Since

  1. ARM-ACME V: ARM Airborne Carbon Measurements V on the North Slope of Alaska Science and Implementation Plan

    SciTech Connect

    Biraud, S

    2015-05-01

    Atmospheric temperatures are warming faster in the Arctic than predicted by climate models. The impact of this warming on permafrost degradation is not well understood, but it is projected to increase carbon decomposition and greenhouse gas production (CO₂ and/or CH₄) by arctic ecosystems. Airborne observations of atmospheric trace gases, aerosols, and cloud properties at the North Slope of Alaska are improving our understanding of global climate, with the goal of reducing the uncertainty in global and regional climate simulations and projections.

  2. A Nadir-adjusted Airborne Multi Spectral Imaging System (NAMSIS) for high-resolution remote sensing of carbon fluxes

    NASA Astrophysics Data System (ADS)

    Jiang, Z.; Scott, S.; Rahman, A. F.

    2012-12-01

    Satellite remote sensing is widely used in vegetation monitoring, water stress detection and carbon cycle modeling. However, image pixels from high temporal resolution satellite sensors (such as MODIS) have coarse spatial resolution, much larger than the canopies they are supposed to characterize. An alternative solution for on-demand high spatial resolution remote sensing is sensors onboard low-flying aircrafts. Airborne remote sensing has been traditionally used in crop management studies. In this presentation we demonstrate the application of a relatively low-cost airborne sensor system with customized spectral band combinations for studying forest carbon fluxes. Our team has developed an Inertia Measurement Unit (IMU) controlled automated system to detach aircraft movements (pitch and roll) and engine vibration from the six-band programmable imager, in order to maintain the sensor at nadir view at all times during the flight. Flight lines are configured by a GPS-controleld system to simulate MODIS pixels. A feature-based algorithm is used to automatically generate a mosaic of individual images along the flight lines. This algorithm eliminates the need to mosiac and georeference images manually. An empirical line method is used to calculate reflectance from the raw data. Images from this airborne system produce reflectance values that are comparable with MODIS reflectance product. These high spatial resolution (~0.5 m) images deliver detailed information about tree species and phenological conditions within each MODIS pixel, and thus permit a high resolution spatio-temporal assessment of forest carbon fluxes.

  3. Deglacial 14C plateau suites recalibrated by Suigetsu atmospheric 14C record - Revised 14C reservoir ages from three ocean basins corroborate extreme surface water variations

    NASA Astrophysics Data System (ADS)

    Sarnthein, M.; Balmer, S.; Grootes, P. M.

    2013-12-01

    Radiocarbon (14C) reservoir/ventilation ages (Δ14C) provide unique insights into the dynamics of ocean water masses over LGM and deglacial times. The 14C plateau-tuning technique enables us to derive both an absolute chronology for marine sediment records and a high-resolution record of changing Δ14C values for deglacial surface and deep waters (Sarnthein et al., 2007; AGU Monogr. 173, 175). We designate as 14C plateau a sediment section in the age-depth profile with several almost constant planktic 14C ages - variation less than ×100 to ×300 yr - which form a plateau-shaped scatter band that extends over ~5 to 50 and up to 200 cm in sediment cores with sedimentation rates of >10 cm/ky. Previously, a suite of >15 plateau boundary ages were calibrated to a joint reference record of U/Th-dated 14C time series measured on coral samples, the Cariaco sediment record, and speleothems (Fairbanks et al., 2005, QSR 24; Hughen et al., 2006, QSR 25; Beck et al., 2001, Science 292). We now used the varve-counted atmospheric 14C record of Lake Suigetsu (Ramsey et al., 2012, Science 338, 370) to recalibrate the boundary ages and average ages of 14C plateaus and apply the amended plateau-tuning technique to a dozen Δ14C records from the Atlantic and Indo-Pacific. Main results are: (1) The Suigetsu atmospheric 14C record reflects all 14C plateaus, their internal structures and relative length previously identified, but implies a rise in the average plateau age by <200 14C yr during the LGM, >700 yr at its end, and <200 yr in the Bølling-Allerød. (2) Based on different 14C ages of coeval atmospheric and planktic 14C plateaus surface water Δ14C may have temporarily dropped to an equivalent of 200 yr in low-latitude stratified waters, such as off northwestern South America, and in turn reached values corresponding to an age difference of >2500 14C yr in stratified subpolar regions and upwelled waters such as in the South China Sea, values that differ significantly from a

  4. May 14C be used to date contemporary art?

    NASA Astrophysics Data System (ADS)

    Fedi, M. E.; Caforio, L.; Mandò, P. A.; Petrucci, F.; Taccetti, F.

    2013-01-01

    The use of radiocarbon in forensics is by now widespread, thanks to the so-called bomb peak, which makes it possible to perform high-precision dating. Since 1955, 14C concentration in the atmosphere had strongly increased due to nuclear explosions, reaching its maximum value in 1963-1965. After the Nuclear Test Ban Treaty, 14C started to decrease as a consequence of the exchanges between atmosphere and the other natural carbon reservoirs. Nowadays, it is still slightly above the pre-bomb value. The work presented in this paper is based on the idea of exploiting the bomb peak to “precisely” date works of contemporary art, with the aim at identifying possible fakes. We analysed two kinds of materials from the 20th century: newspapers and painting canvases. Newspaper samples were taken because they might in principle be considered to represent dated samples (considering the date on the issues). Our data (28 samples) show a trend similar to atmospheric data in the literature, although with some differences; the paper peak is flatter and shifted towards more recent years (about five years) with respect to the atmospheric data. This can be explained by taking paper manufacturing processes into account. As to the canvas samples, the measured 14C concentrations were generally reasonably consistent with the expected concentrations (based on the year on the paintings). However, this does not indicate that the interpretation of the results is simpler and more straightforward. Obviously, we only measure the 14C concentration of the fibre used for the canvas, which does not necessarily measure the date the painting was manufactured. In this paper, sample preparation and experimental results will be discussed, in order to show the potential as well as the limitations of radiocarbon to date contemporary art.

  5. First Airborne Lidar Measurements of Methane and Carbon Dioxide Applying the MERLIN Demonstrator CHARM-F

    NASA Astrophysics Data System (ADS)

    Amediek, Axel; Büdenbender, Christian; Ehret, Gerhard; Fix, Andreas; Gerbig, Christoph; Kiemle, Chritstoph; Quatrevalet, Mathieu; Wirth, Martin

    2016-04-01

    CHARM-F is the new airborne four-wavelengths lidar for simultaneous soundings of atmospheric CO2 and CH4. Due to its high technological conformity it is also a demonstrator for MERLIN, the French-German satellite mission providing a methane lidar. MERLIN's Preliminary Design Review was successfully passed recently. The launch is planned for 2020. First CHARM-F measurements were performed in Spring 2015 onboard the German research aircraft HALO. The aircraft's maximum flight altitude of 15 km and special features of the lidar, such as a relatively large laser ground spot, result in data similar to those obtained by a spaceborne system. The CHARM-F and MERLIN lidars are designed in the IPDA (integrated path differential absorption) configuration using short double pulses, which gives column averaged gas mixing ratios between the system and ground. The successfully completed CHARM-F flight measurements provide a valuable dataset, which supports the retrieval algorithm development for MERLIN notably. Furthermore, the dataset allows detailed analyses of measurement sensitivities, general studies on the IPDA principle and on system design questions. These activities are supported by another instrument onboard the aircraft during the flight campaign: a cavity ring down spectrometer, providing in-situ data of carbon dioxide, methane and water vapor with high accuracy and precision, which is ideal for validation purposes of the aircraft lidar. For the near future, detailed characterizations of CHARM-F are planned, further support of the MERLIN design, as well as the scientific aircraft campaign CoMet.

  6. 17 CFR 240.14c-1 - Definitions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 17 Commodity and Securities Exchanges 3 2011-04-01 2011-04-01 false Definitions. 240.14c-1 Section 240.14c-1 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION (CONTINUED) GENERAL... Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) §...

  7. 17 CFR 240.14c-5 - Filing requirements.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 17 Commodity and Securities Exchanges 3 2012-04-01 2012-04-01 false Filing requirements. 240.14c-5 Section 240.14c-5 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION (CONTINUED... Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) §...

  8. 17 CFR 240.14c-5 - Filing requirements.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 17 Commodity and Securities Exchanges 3 2013-04-01 2013-04-01 false Filing requirements. 240.14c-5 Section 240.14c-5 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION (CONTINUED... Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) §...

  9. 17 CFR 240.14c-5 - Filing requirements.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 17 Commodity and Securities Exchanges 3 2011-04-01 2011-04-01 false Filing requirements. 240.14c-5 Section 240.14c-5 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION (CONTINUED... Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) §...

  10. 17 CFR 240.14c-1 - Definitions.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 17 Commodity and Securities Exchanges 3 2012-04-01 2012-04-01 false Definitions. 240.14c-1 Section 240.14c-1 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION (CONTINUED) GENERAL... Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) §...

  11. 17 CFR 240.14c-5 - Filing requirements.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 17 Commodity and Securities Exchanges 4 2014-04-01 2014-04-01 false Filing requirements. 240.14c-5 Section 240.14c-5 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION (CONTINUED... Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) §...

  12. 17 CFR 240.14c-1 - Definitions.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 17 Commodity and Securities Exchanges 4 2014-04-01 2014-04-01 false Definitions. 240.14c-1 Section 240.14c-1 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION (CONTINUED) GENERAL... Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) §...

  13. 17 CFR 240.14c-1 - Definitions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 17 Commodity and Securities Exchanges 3 2010-04-01 2010-04-01 false Definitions. 240.14c-1 Section 240.14c-1 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION (CONTINUED) GENERAL... Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) §...

  14. 17 CFR 240.14c-1 - Definitions.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 17 Commodity and Securities Exchanges 3 2013-04-01 2013-04-01 false Definitions. 240.14c-1 Section 240.14c-1 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION (CONTINUED) GENERAL... Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) §...

  15. Analyzing carbon dioxide and methane emissions in California using airborne measurements and model simulations

    NASA Astrophysics Data System (ADS)

    Johnson, M. S.; Yates, E. L.; Iraci, L. T.; Jeong, S.; Fischer, M. L.

    2013-12-01

    Greenhouse gas (GHG) concentrations have increased over the past decades and are linked to global temperature increases and climate change. These changes in climate have been suggested to have varying effects, and uncertain consequences, on agriculture, water supply, weather, sea-level rise, the economy, and energy. To counteract the trend of increasing atmospheric concentrations of GHGs, the state of California has passed the California Global Warming Act of 2006 (AB-32). This requires that by the year 2020, GHG (e.g., carbon dioxide (CO2) and methane (CH4)) emissions will be reduced to 1990 levels. To quantify GHG fluxes, emission inventories are routinely compiled for the State of California (e.g., CH4 emissions from the California Greenhouse Gas Emissions Measurement (CALGEM) Project). The major sources of CO2 and CH4 in the state of California are: transportation, electricity production, oil and gas extraction, cement plants, agriculture, landfills/waste, livestock, and wetlands. However, uncertainties remain in these emission inventories because many factors contributing to these processes are poorly quantified. To alleviate these uncertainties, a synergistic approach of applying air-borne measurements and chemical transport modeling (CTM) efforts to provide a method of quantifying local and regional GHG emissions will be performed during this study. Additionally, in order to further understand the temporal and spatial distributions of GHG fluxes in California and the impact these species have on regional climate, CTM simulations of daily variations and seasonality of total column CO2 and CH4 will be analyzed. To assess the magnitude and spatial variation of GHG emissions and to identify local 'hot spots', airborne measurements of CH4 and CO2 were made by the Alpha Jet Atmospheric eXperiment (AJAX) over the San Francisco Bay Area (SFBA) and San Joaquin Valley (SJV) in January and February 2013 during the Discover-AQ-CA study. High mixing ratios of GHGs were

  16. The fate of 14C in glucose 6-phosphate synthesized from [1-14C]Ribose 5-phosphate by enzymes of rat liver.

    PubMed Central

    Williams, J F; Clark, M G; Blackmore, P F

    1978-01-01

    1. Glucose 5-phosphate was synthesized from ribose 5-phosphate by an enzyme extract prepared from an acetone-dried powder of rat liver. Three rates of ribose 5-phosphate utilization were observed during incubation for 17 h. An analysis of intermediates and products formed throughout the incubation revealed that as much as 20% of the substrate carbon could not be accounted for. 2. With [1-14C]ribose 5-phosphate as substrate, the specific radioactivity of [14C]glucose 6-phosphate formed was determined at 1, 2, 5 and 30 min and 3, 8 and 17 h. It increased rapidly to 1.9-fold the initial specific radioactivity of [1-14C]ribose 5-phosphate at 3 h and then decreased to a value approximately equal to that of the substrate at 6 h, and finally at 17 h reached a value 0.8-fold that of the initial substrate [1-14C]ribose 5-phosphate. 3. The specific radioactivity of [14C]ribose 5-phosphate decreased to approx. 50% of its inital value during the first 3 h of the incubation and thereafter remained unchanged. 4. The distribution of 14C in the six carbon atoms of [14C]glucose 6-phosphate formed from [1-14C]ribose 5-phosphate at 1, 2, 5 and 30 min and 3, 8 and 17 h was determined. The early time intervals (1--30 min) were characterized by large amounts of 14C in C-2 and in C-6 and with C-1 and C-3 being unlabelled. In contrast, the later time intervals (3--17 h) were characterized by the appearance of 14C in C-1 and C-3 and decreasing amounts of 14C in C-2 and C-6. 5. It is concluded that neither the currently accepted reaction sequence for the non-oxidative pentose phosphate pathway nor the 'defined' pentose phosphate-cycle mechanism can be reconciled with the labelling patterns observed in glucose 6-phosphate formed during the inital 3 h of the incubation. PMID:728109

  17. Respiration of [14C]alanine by the ectomycorrhizal fungus Paxillus involutus.

    PubMed

    Chalot, M; Brun, A; Finlay, R D; Söderström, B

    1994-08-01

    The ectomycorrhizal fungus Paxillus involutus efficiently took up exogenously supplied [14C]alanine and rapidly converted it to pyruvate, citrate, succinate, fumarate and to CO2, thus providing direct evidence for the utilisation of alanine as a respiratory substrate. [14C]alanine was further actively metabolised to glutamate, glutamine and aspartate. Exposure to aminooxyacetate completely suppressed 14CO2 evolution and greatly reduced the flow of carbon from [14C]alanine to tricarboxylic acid cycle intermediates and amino acids, suggesting that alanine aminotransferase plays a pivotal role in alanine metabolism in Paxillus involutus. PMID:8082830

  18. Intracavity Optogalvanic Spectroscopy, A New Ultra-sensitive Analytical Technique for 14C Analysis

    PubMed Central

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

    2009-01-01

    We show a new ultra-sensitive laser based analytical technique, intracavity optogalvanic spectroscopy, allowing extremely high sensitivity for detection of 14C labeled carbon dioxide. Capable of replacing large accelerator mass spectrometers, the technique quantifies attomoles of 14C 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 14C:12C ratios are obtained. Using a 15W 14CO2 laser, a linear calibration with samples from 10-15 to >2 × 10-12 in 14C:12C ratios, as determined by accelerator mass spectrometry, is demonstrated. Possible applications include microdosing studies in drug development, individualized sub-therapeutic 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. PMID:18533685

  19. ARM Airborne Carbon Measurements (ARM-ACME) and ARM-ACME 2.5 Final Campaign Reports

    SciTech Connect

    Biraud, S. C.; Tom, M. S.; Sweeney, C.

    2016-01-01

    We report on a 5-year multi-institution and multi-agency airborne study of atmospheric composition and carbon cycling at the Atmospheric Radiation Measurement (ARM) Climate Research Facility’s Southern Great Plains (SGP) site, with scientific objectives that are central to the carbon-cycle and radiative-forcing goals of the U.S. Global Change Research Program and the North American Carbon Program (NACP). The goal of these measurements is to improve understanding of 1) the carbon exchange of the Atmospheric Radiation Measurement (ARM) SGP region; 2) how CO2 and associated water and energy fluxes influence radiative-forcing, convective processes, and CO2 concentrations over the ARM SGP region, and 3) how greenhouse gases are transported on continental scales.

  20. Carbon stocks and cycling in the Amazon basin: Measurement and modeling of natural disturbance and recovery using airborne LIDAR

    NASA Astrophysics Data System (ADS)

    Hunter, Maria O'Healy

    Forest structure, the three dimensional distribution of living and dead plant material including live crowns, understory vegetation and coarse woody debris, is the concrete physical form of carbon storage, the framework for biodiversity, and the instantaneous manifestation of disturbance and recovery processes. The frequency of disturbance and rate of decomposition drives the fractions of living and dead biomass, and the size of and intensity of disturbance drives the rate and species composition of forest recovery; both are primary sinks and sources in the carbon cycle. To improve understanding of disturbance and recovery processes, high-resolution airborne LIDAR (light detection and ranging) data from the Amazon region is combined with field measurements to analyze forest structure. These measurements are incorporated into a simple model to estimate light availability and the associated changes in carbon stocks. This work improves the understanding of Amazon forest dynamics and its role in the carbon cycle.

  1. Testing of a Two-Micron Double-Pulse IPDA Lidar Instrument for Airborne Atmospheric Carbon Dioxide Measurement

    NASA Astrophysics Data System (ADS)

    Yu, J.; Petros, M.; Refaat, T. F.; Remus, R.; Singh, U. N.

    2015-12-01

    Utilizing a tunable two-micron double-pulse laser transmitter, an airborne IPDA lidar system has been developed at NASA Langley Research Center for atmospheric carbon dioxide column measurements. The instrument comprises a receiver with 0.4 m telescope and InGaAs pin detectors coupled to 12-bit, 200 MS/s waveform digitizers. For on-site ground testing, the 2-μm CO2 IPDA lidar was installed inside a trailer located where meteorological data and CO2 mixing ratio profiles were obtained from CAPABLE and LiCoR in-suite sampling, respectively. IPDA horizontal ground testing with 860 m target distance indicated CO2 sensitivity of 2.24 ppm with -0.43 ppm offset, while operating at 3 GHz on-line position from the R30 line center. Then, the IPDA lidar was integrated inside the NASA B-200 aircraft, with supporting instrumentation, for airborne testing and validation. Supporting instruments included in-situ LiCoR sensor, GPS and video recorder for target identification. Besides, aircraft built-in sensors provided altitude, pressure, temperature and relative humidity sampling during flights. The 2-mm CO2 IPDA lidar airborne testing was conducted through ten daytime flights (27 hours flight time). Airborne testing included different operating and environmental conditions for flight altitude up to 7 km, different ground target conditions such as vegetation, soil, ocean, snow and sand and different cloud conditions. Some flights targeted power plant incinerators for investigating IPDA sensitivity to CO2 plums. Relying on independent CO2 in-situ sampling, conducted through NOAA, airborne IPDA CO2 sensitivity of 4.15 ppm with 1.14 ppm offset were observed at 6 km altitude and 4 GHz on-line offset frequency. This validates the 2-μm double-pulse IPDA lidar for atmospheric CO2 measurement.

  2. Taking stock of circumboreal forest carbon by combining inventory plot measurements with airborne and spaceborne LiDAR

    NASA Astrophysics Data System (ADS)

    Neigh, C. S.; Nelson, R. F.; Ranson, J.; Margolis, H. A.; Montesano, P. M.; Sun, G.; Kharuk, V.; Næsset, E.; Wulder, M. A.; Andersen, H.

    2013-12-01

    The boreal forest accounts for one-third of global forests, but remains largely inaccessible to ground-based measurements and monitoring. It contains large quantities of carbon in its vegetation and soils, and research suggests that it will be subject to increasingly severe climate-driven disturbance. We employ a suite of ground-, airborne- and space-based measurement techniques to derive the first satellite LiDAR-based estimates of aboveground carbon for the entire circumboreal forest biome. Incorporating these inventory techniques with uncertainty analysis, we estimate total aboveground carbon of 38 × 3.1 Pg. This boreal forest carbon is mostly concentrated from 50 to 55° N in eastern Canada and from 55 to 60° N in eastern Eurasia. Both of these regions are expected to warm > 3 °C by 2100, and monitoring the effects of warming on these stocks is important to understanding its future carbon balance. Our maps establish a baseline for future quantification of circumboreal carbon and the described technique should provide a robust method for future monitoring of the spatial and temporal changes of the aboveground carbon content. Circumboreal forest. a, aboveground carbon. b,c Error estimates of carbon density.

  3. Bioconversion of alpha-[14C]zearalenol and beta-[14C]zearalenol into [14C]zearalenone by Fusarium roseum 'Gibbosum'.

    PubMed Central

    Richardson, K E; Hagler, W M; Hamilton, P B

    1984-01-01

    Cultures of Fusarium roseium 'Gibbosum' on rice were treated with [14C]zearalenone, alpha[14C]zearalenol, or beta-[14C]zearalenol to determine whether a precursor-product relationship exists among these closely related fungal metabolites. Culture extracts were purified by silica gel column chromatography and fractionated by high-pressure liquid chromatography, and the level of radioactivity was determined. Within 7 days, the beta-[14C]zearalenol was converted to zearalenone, and no residual beta-[14C]zearalenol was detectable. Most of the alpha-[14C]zearalenol added was also converted into zearalenone with 14 days. In cultures treated with [14C]zearalenone, no radioactivity was noted in any other components. PMID:6742839

  4. An analytical method for 14C in environmental water based on a wet-oxidation process.

    PubMed

    Huang, Yan-Jun; Guo, Gui-Yin; Wu, Lian-Sheng; Zhang, Bing; Chen, Chao-Feng; Zhang, Hai-Ying; Qin, Hong-Juan; Shang-Guan, Zhi-Hong

    2015-04-01

    An analytical method for (14)C in environmental water based on a wet-oxidation process was developed. The method can be used to determine the activity concentrations of organic and inorganic (14)C in environmental water, or total (14)C, including in drinking water, surface water, rainwater and seawater. The wet-oxidation of the organic component allows the conversion of organic carbon to an inorganic form, and the extraction of the inorganic (14)C can be achieved by acidification and nitrogen purging. Environmental water with a volume of 20 L can be used for the wet-oxidation and extraction, and a detection limit of about 0.02 Bq/g(C) can be achieved for water with carbon content above 15 mg(C)/L, obviously lower than the natural level of (14)C in the environment. The collected carbon is sufficient for measurement with a low level liquid scintillation counter (LSC) for typical samples. Extraction or recovery experiments for inorganic carbon and organic carbon from typical materials, including analytical reagents of organic benzoquinone, sucrose, glutamic acid, nicotinic acid, humic acid, ethane diol, et cetera., were conducted with excellent results based on measurement on a total organic carbon analyzer and LSC. The recovery rate for inorganic carbon ranged tween 98.7%-99.0% with a mean of 98.9(± 0.1)%, for organic carbon recovery ranged between 93.8% and 100.0% with a mean of 97.1(± 2.6)%. Verification and an uncertainty budget of the method are also presented for a representative environmental water. The method is appropriate for (14)C analysis in environmental water, and can be applied also to the analysis of liquid effluent from nuclear facilities. PMID:25590997

  5. Synthesis of. beta. -sitosterol-/sup 14/C

    SciTech Connect

    Askinazi, B.Z.; Kivokurtseva, L.N.; Bobrova, N.S.; Kozarinskaya, N.Ya.

    1986-08-01

    The method of synthesis of ..beta..-sitosterol-4-/sup 14/C starting with the enolactone 4-oxa-5-sitosten-3-one is discussed. Methyl-/sup 14/C magnesium iodide is utilized for the introduction of the label. The authors selected this method for the isolation of ..beta..-sitosterol-/sup 14/C, introducing a series of changes into the original method. The authors discuss obtaining sitostenone, the ketoacid of sitostenone, the enol-lactone of the ketoacid of sitostenone, sitostenone-4-/sup 14/C (by different methods), the enol-acetate of sitostenone-/sup 14/C, and ..beta.. sitosterol-4-/sup 14/C.

  6. Human folate metabolism using 14C-accelerator mass spectrometry

    SciTech Connect

    Clifford, A. J.; Arjomand, A.; Duecker, S. R.; Johnson, H.; Schneider, P. D.; Zulim, R. A.; Bucholz, B. A.; Vogel, J. S.

    1999-03-25

    Folate is a water soluble vitamin required for optimal health, growth and development. It occurs naturally in various states of oxidation of the pteridine ring and with varying lengths to its glutamate chain. Folates function as one-carbon donors through methyl transferase catalyzed reactions. Low-folate diets, especially by those with suboptimal methyltransferase activity, are associated with increased risk of neural tube birth defects in children, hyperhomocysteinemic heart disease, and cancer in adults. Rapidly dividing (neoplastic) cells have a high folate need for DNA synthesis. Chemical analogs of folate (antifolates) that interfere with folate metabolism are used as therapeutic agents in cancer treatment. Although much is known about folate chemistry, metabolism of this vitamin in vivo in humans is not well understood. Since folate levels in blood and tissues are very low and methods to measure them are inadequate, the few previous studies that have examined folate metabolism used large doses of radiolabeled folic acid in patients with Hodgkin's disease and cancer (Butterworth et al. 1969, Krumdieck et al. 1978). A subsequent protocol using deuterated folic acid was also insufficiently sensitive to trace a physiologic folate dose (Stites et al. 1997). Accelerator mass spectrometry (AMS) is an emerging bioanalytical tool that overcomes the limitations of traditional mass spectrometry and of decay counting of long lived radioisotopes (Vogel et al. 1995). AMS can detect attomolar concentrations of 14 C in milligram-sized samples enabling in vivo radiotracer studies in healthy humans. We used AMS to study the metabolism of a physiologic 80 nmol oral dose of 14 C-folic acid (1/6 US RDA) by measuring the 14 C-folate levels in serial plasma, urine and feces samples taken over a 150-day period after dosing a healthy adult volunteer.

  7. Modelling above-ground carbon dynamics using multi-temporal airborne lidar: insights from a Mediterranean woodland

    NASA Astrophysics Data System (ADS)

    Simonson, W.; Ruiz-Benito, P.; Valladares, F.; Coomes, D.

    2016-02-01

    Woodlands represent highly significant carbon sinks globally, though could lose this function under future climatic change. Effective large-scale monitoring of these woodlands has a critical role to play in mitigating for, and adapting to, climate change. Mediterranean woodlands have low carbon densities, but represent important global carbon stocks due to their extensiveness and are particularly vulnerable because the region is predicted to become much hotter and drier over the coming century. Airborne lidar is already recognized as an excellent approach for high-fidelity carbon mapping, but few studies have used multi-temporal lidar surveys to measure carbon fluxes in forests and none have worked with Mediterranean woodlands. We use a multi-temporal (5-year interval) airborne lidar data set for a region of central Spain to estimate above-ground biomass (AGB) and carbon dynamics in typical mixed broadleaved and/or coniferous Mediterranean woodlands. Field calibration of the lidar data enabled the generation of grid-based maps of AGB for 2006 and 2011, and the resulting AGB change was estimated. There was a close agreement between the lidar-based AGB growth estimate (1.22 Mg ha-1 yr-1) and those derived from two independent sources: the Spanish National Forest Inventory, and a tree-ring based analysis (1.19 and 1.13 Mg ha-1 yr-1, respectively). We parameterised a simple simulator of forest dynamics using the lidar carbon flux measurements, and used it to explore four scenarios of fire occurrence. Under undisturbed conditions (no fire) an accelerating accumulation of biomass and carbon is evident over the next 100 years with an average carbon sequestration rate of 1.95 Mg C ha-1 yr-1. This rate reduces by almost a third when fire probability is increased to 0.01 (fire return rate of 100 years), as has been predicted under climate change. Our work shows the power of multi-temporal lidar surveying to map woodland carbon fluxes and provide parameters for carbon

  8. Modelling above-ground carbon dynamics using multi-temporal airborne lidar: insights from a Mediterranean woodland

    NASA Astrophysics Data System (ADS)

    Simonson, W.; Ruiz-Benito, P.; Valladares, F.; Coomes, D.

    2015-09-01

    Woodlands represent highly significant carbon sinks globally, though could lose this function under future climatic change. Effective large-scale monitoring of these woodlands has a critical role to play in mitigating for, and adapting to, climate change. Mediterranean woodlands have low carbon densities, but represent important global carbon stocks due to their extensiveness and are particularly vulnerable because the region is predicted to become much hotter and drier over the coming century. Airborne lidar is already recognized as an excellent approach for high-fidelity carbon mapping, but few studies have used multi-temporal lidar surveys to measure carbon fluxes in forests and none have worked with Mediterranean woodlands. We use a multi-temporal (five year interval) airborne lidar dataset for a region of central Spain to estimate above-ground biomass (AGB) and carbon dynamics in typical mixed broadleaved/coniferous Mediterranean woodlands. Field calibration of the lidar data enabled the generation of grid-based maps of AGB for 2006 and 2011, and the resulting AGB change were estimated. There was a close agreement between the lidar-based AGB growth estimate (1.22 Mg ha-1 year-1) and those derived from two independent sources: the Spanish National Forest Inventory, and a~tree-ring based analysis (1.19 and 1.13 Mg ha-1 year-1, respectively). We parameterised a simple simulator of forest dynamics using the lidar carbon flux measurements, and used it to explore four scenarios of fire occurrence. Under undisturbed conditions (no fire occurrence) an accelerating accumulation of biomass and carbon is evident over the next 100 years with an average carbon sequestration rate of 1.95 Mg C ha-1 year-1. This rate reduces by almost a third when fire probability is increased to 0.01, as has been predicted under climate change. Our work shows the power of multi-temporal lidar surveying to map woodland carbon fluxes and provide parameters for carbon dynamics models. Space

  9. Identifying a Sea Breeze Circulation Pattern Over the Los Angeles Basin Using Airborne In Situ Carbon Dioxide Measurements

    NASA Astrophysics Data System (ADS)

    Brannan, A. L.; Schill, S.; Trousdell, J.; Heath, N.; Lefer, B. L.; Yang, M. M.; Bertram, T. H.

    2014-12-01

    The Los Angeles Basin in Southern California is an optimal location for a circulation study, due to its location between the Pacific Ocean to the west and the Santa Monica and San Gabriel mountain ranges to the east, as well as its booming metropolitan population. Sea breeze circulation carries air at low altitudes from coastal to inland regions, where the air rises and expands before returning back towards the coast at higher altitudes. As a result, relatively clean air is expected at low altitudes over coastal regions, but following the path of sea breeze circulation should increase the amount of anthropogenic influence. During the 2014 NASA Student Airborne Research Program, a highly modified DC-8 aircraft completed flights from June 23 to 25 in and around the LA Basin, including missed approaches at four local airports—Los Alamitos and Long Beach (coastal), Ontario and Riverside (inland). Because carbon dioxide (CO2) is chemically inert and well-suited as a conserved atmospheric tracer, the NASA Langley Atmospheric Vertical Observations of CO2 in the Earth's Troposphere (AVOCET) instrument was used to make airborne in situ carbon dioxide measurements. Combining measured wind speed and direction data from the aircraft with CO2 data shows that carbon dioxide can be used to trace the sea breeze circulation pattern of the Los Angeles basin.

  10. 17 CFR 240.14c-101 - Schedule 14C. Information required in information statement.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...-101. Item 1. Information required by Items of Schedule 14A (17 CFR 240.14a-101). Furnish the information called for by all of the items of Schedule 14A of Regulation 14A (17 CFR 240.14a-101) (other than... 17 Commodity and Securities Exchanges 3 2011-04-01 2011-04-01 false Schedule 14C....

  11. Liquid scintillation counting of /sup 14/C for differentiation of synthetic ethanol from ethanol of fermentation

    SciTech Connect

    Martin, G.E.; Noakes, J.E.; Alfonso, F.C.; Figert, D.M.

    1981-09-01

    Samples containing ethanol are fractionated on a column so that the resultant ethanol content is > 93%. Determination of /sup 14/C by liquid scintillation counting on the ethanol fraction differentiates ethanol produced by fermentation from synthetic ethanol produced from fossil fuel sources. Twenty-seven samples were fractionated and analyzed for the /sup 14/C isotope. Six samples were synthetic ethanol derived from ethylene gas (direct and indirect process), and yielded a mean value for /sup 14/C isotope of 0.167 dpm/g carbon with a standard deviation (SD) of 0.066 dpm/g carbon (disintegrations per minute per gram of carbon). The remaining samples were ethanol derived from the fermentation of natural materials, such as corn, pear, sugar cane, grape, cherry, and blackberry, and yielded a mean value for /sup 14/C isotope of 16.11 dpm/g carbon with an SD of 1.27. The /sup 14/C values for specific mixtures of a synthetic and a natural ethanol compare favorably with the analytical values obtained by this procedure.

  12. Enhancement of radioactivity of /sup 14/C-/sup 12/C mixtures via partial reduction

    SciTech Connect

    Stevenson, G.R.; Lauricella, T.L.

    1986-08-20

    The solution electron affinities of perdeuterated polyaromatics are less than those of the protiated materials. This observation prompted the investigation of the possibility of increasing the radioactivity of benzophenone-carbonyl-/sup 14/C (BZO-14C)-cold benzophenone (BZO-12C) mixtures via the partial reduction of these mixtures to the ketyls. The /sup 14/C-depleted benzophenones left in the reaction vessel in the form of Na/sup +/(NH/sub 3/)BZO/sup -/ can be recovered by simply adding a solution of I/sub 2/ in tetrahydrofuran to the solid salt. Further, there is no theoretical limit as to how much the radioactivity of the sample can be enhanced by passing /sup 14/C-enhanced material through this process consecutively, up to the point where the pure carbon-14 compound is obtained.

  13. Sequestration of atmospheric CO2 in a weathering-derived, serpentinite-hosted magnesite deposit: 14C tracing of carbon sources and age constraints for a refined genetic model

    NASA Astrophysics Data System (ADS)

    Oskierski, H. C.; Dlugogorski, B. Z.; Jacobsen, G.

    2013-12-01

    The Attunga magnesite deposit is texturally and geochemically distinct from other spatially associated, serpentinite-hosted magnesite deposits in the Great Serpentinite Belt, New South Wales, Australia, such as the hydrothermal Piedmont magnesite deposit or widespread silica-carbonate alteration zones. Cryptocrystalline magnesite at Attunga predominantly occurs in nodular masses and irregular, desiccated veins that occupy pre-existing cracks and pore spaces resulting from fracturing and weathering of the host rock. Incipient weathering of the serpentinite host rock is accompanied by a decrease in volume and the mobilisation of MgO and CaO from the serpentinite. Pore spaces and permeability created during weathering and fracturing of the host rock provide access for CO2-, MgO- and CaO-bearing meteoric waters which led to an increase of volume during carbonation. SiO2 is only mobilised during more advanced stages of weathering and late stage infiltration of SiO2-bearing waters and precipitation of opal-A lead to local silicification of the serpentinite. Stable carbon and oxygen isotope signatures show that nodular magnesite at Attunga has formed under near-surface conditions incorporating carbon from C3-photosynthetic plants and oxygen from meteoric waters. Radiocarbon concentrations in the magnesite preclude subducted carbonaceous sediments as the source of carbon and, together with distinct stable carbon and oxygen isotope signatures, indicate that magnesite at Attunga precipitated from low temperature, supergene fluids. Even though there is no direct geochemical and isotopic evidence, some textural observations and field relationships for weathering-derived magnesite deposits suggest the prior existence of a possibly Early Triassic, hydrothermal magnesite deposit at Attunga. The presence of a pre-existing magnesite deposit may entail the localised formation of the weathering-derived magnesite at Attunga, but the predominance of weathering-related textures and

  14. 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.

  15. 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.

  16. The distribution of 14c from [U-14c]glucose in mice using whole-body autoradiography.

    PubMed

    Shimada, M; Kihara, T; Watanabe, M; Kurimoto, K

    1976-04-01

    Tissue distribution of radioactive carbon from [U-14C]glucose in the mouse in vivo was studied by whole-body autoradiography. The mice were frozen with Dry-Ice-acetone at 0.5, 1, 5 and 30 min, 1 and 24 hr and 1 and 3 weeks after intraperitoneal injection of [U-14C]glucose. Whole-sagittal sections of the frozen mouse, obtained by using a microtome in a cryostat, were dried in a cryostat and autoradiographed. The resulting dry autoradiographs are called untreated autoradiographs in the present work. The sections were then fixed in cold 6% (w/v) HClO4, dried at room temperature and again autoradiographed. Autoradiographs that have undergone this process are referred to as treated autoradiographs. In both untreated and treated autoradiographs, within 1 min following injection of the labeled glucose, the abdominal cavity had the highest autoradiographic density. At 1 hr, density became highest in Harder's, sublingual and duodenal glands, large intestinal mucosa and tongue, and after 3 weeks, no autoradiographic denisty was present. PMID:1270794

  17. A Model-based Interpretation of Low-frequency Changes in the Carbon Cycle during the Last 120,000 years and its Implications for the Reconstruction of Atmospheric (delta) 14-C

    NASA Technical Reports Server (NTRS)

    Koehler, Peter; Muscheler, Raimund; Fischer, Hubertus

    2006-01-01

    A main caveat in the interpretation of observed changes in atmospheric (Delta)C-l4 during the last 50,000 years is the unknown variability of the carbon cycle, which together with changes in the C-14 production rates determines the C-14 dynamics. A plausible scenario explaining glacial/interglacial dynamics seen in atmospheric CO2 and (delta)C-13 was proposed recently (Kohler et al., 2005a). A similar approach that expands its interpretation to the C-14 cycle is an important step toward a deeper understanding of (Delta)C-14 variability. This approach is based on an ocean/atmosphere/biosphere box model of the global carbon cycle (BICYCLE) to reproduce low-frequency changes in atmospheric CO2 as seen in Antarctic ice cores. The model is forced forward in time by various paleoclimatic records derived from ice and sediment cores. The simulation results of our proposed scenario match a compiled CO2 record from various ice cores during the last 120,000 years with high accuracy (r(sup 2) = 0.89). We analyze scenarios with different C-14 production rates, which are either constant or based on Be-10 measured in Greenland ice cores or the recent high-resolution geomagnetic field reconstruction GLOPIS-75 and compare them with the available (Delta)C-14 data covering the last 50,000 years. Our results suggest that during the last glacial cycle in general less than 110%0o f the increased atmospheric (Delta)C-14 is based on variations in the carbon cycle, while the largest part (5/6) of the variations has to be explained by other factors. Glacial atmospheric (Delta)C-14 larger than 700% cannot not be explained within our framework, neither through carbon cycle-based changes nor through variable C-14 production. Superimposed on these general trends might lie positive anomalies in atmospheric (Delta)C-14 of approx. 50% caused by millennial-scale variability of the northern deep water production during Heinrich events and Dansgaard/Oeschger climate fluctuations. According to our

  18. Predicting the cropland soil organic carbon (SOC) distribution on a regional scale using airborne spectroscopy and topographic features

    NASA Astrophysics Data System (ADS)

    Doetterl, S.; Stevens, S.; Van Wesemael, B.; Quine, T. A.; Van Oost, K.

    2012-04-01

    The effects of soil redistribution on the carbon cycle have recently been receiving growing attention. In eroding agricultural landscapes, carbon gets transported from erosional to depositional landscape features forming a heterogeneous pattern in quantity and quality of the distributed carbon. At present, methods and research to characterize this horizontal (across the earth surface) and vertical (with depth) variability are focused on local slope scales. Approaches linking detailed local assessments to larger scales are limited. This significantly hampers our ability to understand the impact of soil redistribution processes on the global C cycle that occur at larger spatial and temporal scales. Here, we present a method to predict the SOC distribution on a regional scale for high-input cropping systems using a combination of airborne spectroscopy, GIS-based analysis of a digital elevation model (DEM) and calibration with empirical data. For a North/South transect in Luxembourg, spatial modeling is used to integrate soil surface SOC data from airborne image spectroscopy (2m resolution), vertical SOC gradients from high resolution (0.10m) soil sampling and derivates of a high-res elevation model (5m resolution). This allows the prediction of the 3D distribution of cropland soil C to be interpolated over an area of c. 150 km2 in Luxemburg which is characterized by intensive agricultural land use, a high variability in soils and a complex topography. The model is able to predict patterns of C stock distribution for cropland on a regional scale using simple hydrologic and geomorphologic parameters and provides new insights into the spatial heterogeneity of soil carbon storage covering a large area. Eroding positions have a sharper decline of carbon content with depth than stable and especially depositional sites, which in contrast store high amounts of carbon in greater depths. Relative root mean square errors range between 23-49 % and the model is in good agreement

  19. 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.

  20. Evaluation of Airborne Particle Emissions from Commercial Products Containing Carbon Nanotubes

    PubMed Central

    Huang, Guannan; Park, Jae Hong; Cena, Lorenzo G.; Shelton, Betsy L.; Peters, Thomas M.

    2012-01-01

    The emission of the airborne particles from epoxy resin test sticks with different CNT loadings and two commercial products were characterized while sanding with three grit sizes and three disc sander speeds. The total number concentrations, respirable mass concentrations, and particle size number/mass distributions of the emitted particles were measured using a condensation particle counter, an optical particle counter, and a scanning mobility particle sizer. The emitted particles were sampled on a polycarbonate filter and analyzed using electron microscopy. The highest number concentrations (arithmetic mean = 4670 particles/cm3) were produced with coarse sandpaper, 2% (by weight) CNT test sticks and medium disc sander speed, whereas the lowest number concentrations (arithmetic mean = 92 particles/cm3) were produced with medium sandpaper, 2% CNT test sticks and slow disc sander speed. Respirable mass concentrations were highest (arithmetic mean = 1.01 mg/m3) for fine sandpaper, 2% CNT test sticks and medium disc sander speed and lowest (arithmetic mean = 0.20 mg/m3) for medium sandpaper, 0% CNT test sticks and medium disc sander speed. For CNT-epoxy samples, airborne particles were primarily micrometer-sized epoxy cores with CNT protrusions. No free CNTs were observed in airborne samples, except for tests conducted with 4% CNT epoxy. The number concentration, mass concentration, and size distribution of airborne particles generated when products containing CNTs are sanded depends on the conditions of sanding and the characteristics of the material being sanded. PMID:23204914

  1. Influence of increasing combustion temperature on the AMS 14C dating of modern crop phytoliths

    PubMed Central

    Yin, Jinhui; Yang, Xue; Zheng, Yonggang

    2014-01-01

    Several attempts have been made to directly date phytoliths, but most 14C results are not consistent with other independent chronologies. Due to the limited dataset, there is not a clear explanation for these discrepancies. Herein, we report the 14C ages of phytolith-occluded carbon (PhytOC) from contemporary rice and millet crops that were combusted at different temperatures to investigate the relationship between the combustion temperature and resulting 14C age. Our results show that the 14C age of PhytOC increases directly with combustion temperature (up to 1100°C) and results in age overestimations of hundreds of years. Considerably older ages are observed at higher temperatures, suggesting that it may be possible to distinguish between two fractions of organic carbon in phytoliths: labile and recalcitrant carbon. These findings challenge the assumption that PhytOC is homogeneous, an assumption made by those who have previously attempted to directly date phytoliths using 14C. PMID:25288281

  2. 17 CFR 240.14c-101 - Schedule 14C. Information required in information statement.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... required by Items of Schedule 14A (17 CFR 240.14a-101). Furnish the information called for by all of the items of Schedule 14A of Regulation 14A (17 CFR 240.14a-101) (other than Items 1(c). 2, 4 and 5 thereof... 17 Commodity and Securities Exchanges 3 2012-04-01 2012-04-01 false Schedule 14C....

  3. 17 CFR 240.14c-101 - Schedule 14C. Information required in information statement.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... required by Items of Schedule 14A (17 CFR 240.14a-101). Furnish the information called for by all of the items of Schedule 14A of Regulation 14A (17 CFR 240.14a-101) (other than Items 1(c). 2, 4 and 5 thereof... 17 Commodity and Securities Exchanges 4 2014-04-01 2014-04-01 false Schedule 14C....

  4. 17 CFR 240.14c-101 - Schedule 14C. Information required in information statement.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... required by Items of Schedule 14A (17 CFR 240.14a-101). Furnish the information called for by all of the items of Schedule 14A of Regulation 14A (17 CFR 240.14a-101) (other than Items 1(c). 2, 4 and 5 thereof... 17 Commodity and Securities Exchanges 3 2013-04-01 2013-04-01 false Schedule 14C....

  5. Investigation of {sup 14}C release in an engineered low-level waste disposal facility

    SciTech Connect

    Yim, M.S.; Simonson, S.A.; Sullivan, T.M.

    1996-05-01

    Atmospheric releases of {sup 14}C from a generic engineered low-level waste (LLW) disposal facility and its radiological impacts are investigated. A computer model that describes microbial gas generation and the transport has been developed and used to analyze the generation of {sup 14}C contaminated gases and subsequent migration in a facility. Models are based on a chemical kinetic description of aerobic and anaerobic decomposition of organic materials coupled with attending models of oxygen transport and consumption within waste containers in a facility. Effects of radiolysis on gas generation are addressed based on the estimated dose rate for class B and C wastes. Estimates predict that annual atmospheric release of {sup 14}C due to atmospheric pressure variations could range between {approximately}2.6 {times} 10{sup 8} and 5.5 {times} 10{sup 11} Bq as a result of microbial gas generation based on a volume of 48 000 m{sup 3} LLW disposed in a facility. The associated dose to a maximally exposed individual is estimated to be dominated by ingestion pathway and strongly depends on the fraction of the food imported from an uncontaminated outside area. Dose rates are expected to be <0.04 mSv/yr, considering a reasonable distance between the facility and the exposed population. The depletion through airborne releases of {sup 14}C inventory that is available for transport through other pathways is not expected to be a significant issue.

  6. Uptake and distribution of /sup 14/C during and following exposure to (/sup 14/C)methyl isocyanate

    SciTech Connect

    Ferguson, J.S.; Kennedy, A.L.; Stock, M.F.; Brown, W.E.; Alarie, Y.

    1988-06-15

    Guinea pigs were exposed to (/sup 14/C)methyl isocyanate (/sup 14/CH/sub 3/-NCO, /sup 14/C MIC) for periods of 1 to 6 hr at concentrations of 0.5 to 15 ppm. Arterial blood samples taken during exposure revealed immediate and rapid uptake of /sup 14/C. Clearance of /sup 14/C was then gradual over a period of 3 days. Similarly /sup 14/C was present in urine and bile immediately following exposure, and clearance paralleled that observed in blood. Guinea pigs fitted with a tracheal cannula and exposed while under anesthesia showed a reduced /sup 14/C uptake in blood indicating that most of the /sup 14/C MIC uptake in normal guinea pigs occurred from retention of this agent in the upper respiratory tract passages. In exposed guinea pigs /sup 14/C was distributed to all examined tissues. In pregnant female mice similarly exposed to /sup 14/C MIC, /sup 14/C was observed in all tissues examined following exposure including the uterus, placenta, and fetus. While the form of /sup 14/C distributed in blood and tissues has not yet been identified, these findings may help to explain the toxicity of MIC or MIC reaction products on organs other than the respiratory tract, as noted by several investigators.

  7. Airborne detection of diffuse carbon dioxide emissions at Mammoth Mountain, California

    USGS Publications Warehouse

    Gerlach, T.M.; Doukas, M.P.; McGee, K.A.; Kessler, R.

    1999-01-01

    We report the first airborne detection of CO2 degassing from diffuse volcanic sources. Airborne measurement of diffuse CO2 degassing offers a rapid alternative for monitoring CO2 emission rates at Mammoth Mountain. CO2 concentrations, temperatures, and barometric pressures were measured at ~2,500 GPS-referenced locations during a one-hour, eleven-orbit survey of air around Mammoth Mountain at ~3 km from the summit and altitudes of 2,895-3,657 m. A volcanic CO2 anomaly 4-5 km across with CO2 levels ~1 ppm above background was revealed downwind of tree-kill areas. It contained a 1-km core with concentrations exceeding background by >3 ppm. Emission rates of ~250 t d-1 are indicated. Orographic winds may play a key role in transporting the diffusely degassed CO2 upslope to elevations where it is lofted into the regional wind system.We report the first airborne detection of CO2 degassing from diffuse volcanic sources. Airborne measurement of diffuse CO2 degassing offers a rapid alternative for monitoring CO2 emission rates at Mammoth Mountain. CO2 concentrations, temperatures, and barometric pressures were measured at approximately 2,500 GPS-referenced locations during a one-hour, eleven-orbit survey of air around Mammoth Mountain at approximately 3 km from the summit and altitudes of 2,895-3,657 m. A volcanic CO2 anomaly 4-5 km across with CO2 levels approximately 1 ppm above background was revealed downwind of tree-kill areas. It contained a 1-km core with concentrations exceeding background by >3 ppm. Emission rates of approximately 250 t d-1 are indicated. Orographic winds may play a key role in transporting the diffusely degassed CO2 upslope to elevations where it is lofted into the regional wind system.

  8. The metabolism of [14C]nicotine in the cat

    PubMed Central

    Turner, D. M.

    1969-01-01

    The metabolism of [2′-14C]nicotine given as an intravenous injection in small doses to anaesthetized and unanaesthetized cats has been studied. A method is described for the quantitative determination of [14C]nicotine and [14C]cotinine in tissues and body fluids. Nanogram amounts of these compounds have been detected. After a single dose of 40μg. of [14C]nicotine/kg., 55% of the injected radioactivity was excreted in the urine within 24hr., but only 1% of this radioactivity was unchanged nicotine. [14C]Nicotine is metabolized extremely rapidly, [14C]cotinine appearing in the blood within 2·5min. of intravenous injection. [14C]Nicotine accumulates rapidly in the brain and 15min. after injection 90% of the radioactivity still represents [14C]nicotine. Metabolites of [14C]nicotine have been identified in liver and urine extracts. [14C]Nicotine-1′-oxide has been detected in both liver and urine. PMID:5360723

  9. Seasonal variations of 14C and δ13C for cave drip waters in Ryugashi Cave, Shizuoka Prefecture, central Japan

    NASA Astrophysics Data System (ADS)

    Minami, Masayo; Kato, Tomomi; Horikawa, Keiji; Nakamura, Toshio

    2015-11-01

    Speleothem 14C has recently emerged as a potentially powerful proxy for hydrology changes in comparison with atmospheric 14C calibration curve, rather than as a direct dating tool, apart from a time marker using bomb peak of 14C. Some possible causes for the relationship between speleothem 14C content (or dead carbon fraction: DCF) and karst hydrology have been proposed, such as changes in temperature, precipitation, drip water flow dynamics, cave air ventilation, soil air pCO2. In this study, we investigated seasonal variation in 14C and δ13C of drip water in Ryugashi Cave, Shizuoka Prefecture, central Japan, to examine the causes of the 14C and δ13C variations in a speleothem. The results show that different 14C concentrations and δ13C values of drip water from the Ryugashi Cave, were exhibited at different sites of the Caves No. 1, No. 3, and No. 4, which have different temperature, air pCO2, and flow paths. Further, the 14C and δ13C of drip waters showed seasonal variations at all sites, which were lower in fall and winter, and higher in spring and summer, though the extent of the variations was different among the sites. The 14C in drip waters tended to be correlated with the drip rates: 14C tended to be higher in drip waters with higher drip rates, and also correlated with rainfall amount around the Ryugashi Cave, especially for the drip waters in Cave No. 3, which are considered to have simpler flow paths. The increase in rainfall amount could bring the increase in drip rate of drip water, and then the decrease in interaction between solution and karst, resulting in 14C increase (DCF decrease) in drip water. Accordingly, the reconstruction of precipitation could be performed using 14C variation in a speleothem formed by drip water with simple flow dynamics.

  10. The use of airborne laser scanning to develop a pixel-based stratification for a verified carbon offset project

    PubMed Central

    2011-01-01

    Background The voluntary carbon market is a new and growing market that is increasingly important to consider in managing forestland. Monitoring, reporting, and verifying carbon stocks and fluxes at a project level is the single largest direct cost of a forest carbon offset project. There are now many methods for estimating forest stocks with high accuracy that use both Airborne Laser Scanning (ALS) and high-resolution optical remote sensing data. However, many of these methods are not appropriate for use under existing carbon offset standards and most have not been field tested. Results This paper presents a pixel-based forest stratification method that uses both ALS and optical remote sensing data to optimally partition the variability across an ~10,000 ha forest ownership in Mendocino County, CA, USA. This new stratification approach improved the accuracy of the forest inventory, reduced the cost of field-based inventory, and provides a powerful tool for future management planning. This approach also details a method of determining the optimum pixel size to best partition a forest. Conclusions The use of ALS and optical remote sensing data can help reduce the cost of field inventory and can help to locate areas that need the most intensive inventory effort. This pixel-based stratification method may provide a cost-effective approach to reducing inventory costs over larger areas when the remote sensing data acquisition costs can be kept low on a per acre basis. PMID:22004847

  11. Accurate lacustrine and wetland sediment accumulation rates determined from 14c activity of bulk sediment fractions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In the absence of identifiable macrofossils in lacustrine sediments, 14C dating must rely on pollen or bulk sediment fractions. Bulk sediment fractions are not generally preferred because they contain an unknown mixture of organic material of variable age, they may contain dead carbon such as ligni...

  12. Effects of insulin on the utilization of 14C-glycerol and 14C-glucose in hepatectomized nephrectomized rats.

    PubMed

    Mampel, T; Herrera, E

    1985-04-01

    Insulin (i.v.) administration to functionally hepatectomized-nephrectomized rats did not alter circulating levels of glycerol and only slightly affected plasma radioactivity when animals received (U-14C)-glycerol, whereas after (U-14C)-glucose administration insulin enhanced hypoglycemia and greatly accelerated the rate of radioactivity loss from plasma. At 15 min after i.v. injection of (U-14C)-glycerol, radioactivity in total lipids was reduced in heart and lungs by insulin administration and enhanced in carcass and brown adipose tissue. These effects involved the 14C-glyceride glycerol fraction in the case of heart and 14C-fatty acids in carcass and adipose tissue. When (U-14C)-glucose was administered, insulin enhanced the appearance of 14C-water-soluble material in heart and carcass and 14C-total lipids in heart, carcass, and both brown and white adipose tissue. The effect in heart corresponded mainly to the 14C-glyceride glycerol fraction whereas it corresponded to the 14C-fatty acids in the other tissues. Therefore, insulin effects on glycerol metabolism substantially differ from those on glucose. Opposite effects on heart and lung glycerol utilization as compared to those in carcass and brown adipose tissue may account for the difficulties in observing changes in plasma glycerol levels after insulin treatment. PMID:3891443

  13. Distribution of aged atrazine related 14C-residues in natural soil following incubation with the earthworm Apporectodea caliginosa.

    NASA Astrophysics Data System (ADS)

    Andreou, K.; Jablonowski, N.; Jones, K.; Burauel, P.; Semple, K.

    2009-04-01

    The distribution and localisation of atrazine related 14C-residues into the different physical fractions of soil may reveal information on processes taking place in soil. Soils amended with 14C-atrazine, were aged for 22 years under environmental conditions in a lysimeter in Germany. The soil was sampled and subjected to physical and chemical fractionation before and after incubation for 7 days with the earthworm Apporectodea caliginosa. No significant change in the soil physical and chemical fractionation of the atrazine related 14C-residues and organic carbon was observed in this study due to the activity of the A. caliginosa. The smaller size soil fractions (Microaggregates and Colloids) were highly enriched with aged atrazine 14C-residues equivalents and organic carbon. Also the humic acid extracted using a simple alkaline extraction have were also enriched with aged atrazine 14C-residues equivalents. The low organic carbon content of the soil, the absence of relatively fresh organic matter and the long ageing time might explain the limited bioavailability of the atrazine related 14C-residues to the earthworm. This finding is of particular importance given that the soil used here was aged under natural environmental conditions compared to laboratory studies. Earthworms are important species in soil ecology and thus, the question of the bioavailability of aged pesticide residues to such organism is critical. The bioavalability of the atrazine 14C-residues equivalent was absent in the current study illustrating that those aged residues posed minimal risk to earthworms.

  14. Distribution of aged atrazine related 14C-residues in natural soil following incubation with the earthworm Apporectodea caliginosa

    NASA Astrophysics Data System (ADS)

    Andreou, Kostas; Semple, Kirk; Jones, Kevin

    2010-05-01

    The distribution and localisation of atrazine related 14C-residues into the different physical fractions of soil may reveal information on processes taking place in soil. Soils amended with 14C-atrazine, were aged for 22 years under environmental conditions in a lysimeter in Germany. The soil was sampled and subjected to physical and chemical fractionation before and after incubation for 7 days with the earthworm Apporectodea caliginosa. No significant change in the soil physical and chemical fractionation of the atrazine related 14C-residues and organic carbon was observed in this study due to the activity of the A. caliginosa. The smaller size soil fractions (Microaggregates and Colloids) were highly enriched with aged atrazine 14C-residues equivalents and organic carbon. Also the humic acid extracted using a simple alkaline extraction have were also enriched with aged atrazine 14C-residues equivalents. The low organic carbon content of the soil, the absence of relatively fresh organic matter and the long ageing time might explain the limited bioavailability of the atrazine related 14C-residues to the earthworm. This finding is of particular importance given that the soil used here was aged under natural environmental conditions compared to laboratory studies. Earthworms are important species in soil ecology and thus, the question of the bioavailability of aged pesticide residues to such organism is critical. The bioavalability of the atrazine 14C-residues equivalent was absent in the current study illustrating that those aged residues posed minimal risk to earthworms.

  15. Airborne Observations of the Spatial and Temporal Variability of Tropospheric Carbon Dioxide during the INTEX-B Campaign

    NASA Technical Reports Server (NTRS)

    Vay, Stephanie A.; Choi, Younghoon; Woo, Jung-Hun; Barrick, John D.; Sachse, Glen W.; Blake, Donald; Avery, Melody A.; Fuelberg, Henry; Nolf, Scott

    2006-01-01

    The Intercontinental Chemical Transport Experiment-North America (INTEX-NA) is an international field campaign envisioned to investigate the transport and transformation of gases and aerosols on transcontinental/intercontinental scales and assess their impact on air quality and climate. Phase B (INTEX-B) of the mission was conducted during a 10- week period from March 1 to May 15, 2006 and focused initially on pollution outflow from the Mexico City Metropolitan Area, later addressing the transport of pollution from Asia to North America during springtime meteorological conditions. During the deployment, fast-response (1-s resolution) CO2 measurements were recorded aboard the NASA DC-8 providing valuable regional-scale information on carbon sources and sinks over sparsely sampled areas of North America and adjacent ocean basins. When coupled with the enormously sophisticated chemistry payload on the DC-8, these measurements collectively afford extremely powerful multi-tracer constraints for carbon source/sink attribution. Preliminary examination of the two data sets from the INTEX-B campaign, acquired one month apart, reveals not only the influence of the CO2 seasonal cycle, but also the preponderance of human population and industrial activity in the northern hemisphere. In this presentation, a synergy of the ensemble of airborne and surface observations, bottomup emission inventories, as well as transport history are invoked in a GIS framework to elucidate the source/sink processes reflected in the observations. The airborne CO2 data, along with simultaneous surface measurements (e.g. NOAA ESRL), are examined to establish the vertical distribution and variability of CO2 as a function of location. The role of localized sources, long-range transport, the biosphere, stratospheric exchange, and dynamical processes on the CO2 spatial variability observed throughout the tropospheric column will be discussed.

  16. Behaviour of (14)C-sulfadiazine and (14)C-difloxacin during manure storage.

    PubMed

    Lamshöft, Marc; Sukul, Premasis; Zühlke, Sebastian; Spiteller, Michael

    2010-03-01

    The persistence of sulfadiazine, difloxacin, and their metabolites has been investigated in stored manure. The manure collected from sulfadiazine ((14)C-SDZ) and difloxacin ((14)C-DIF) treated pigs contained N-acetylsulfadiazine (Ac-SDZ), 4-hydroxy-SDZ (4-OH-SDZ), and sarafloxacin (SARA) as the main metabolites, respectively along with their parent compounds. Manures were stored separately at 10 degrees C and 20 degrees C at various moisture levels. About 96-99% of the radioactivity remained in extractable parent compounds and their metabolites after 150d of storage. The formation of non-extractable residue and the rate of mineralization were both negligible in manure containing SDZ and DIF. During storage SDZ concentration increased as a result of the deacetylation of Ac-SDZ, whose concentration decreased proportionally. Hence the environmental effects may be underestimated if the parent compound alone is considered for environmental risk assessment. About 11% and 14% of 4-OH-SDZ were lost after 20 and 40d of storage; thereafter its concentration increased relatively, highlighting hydroxylation of SDZ. DIF degraded very slowly (7% loss after 150d) during the storage of manure; in contrast the concentration of SARA decreased rapidly (72-90% loss after 150d). Dilution of manure and storage at higher temperatures for a reasonable period of time enhanced the rate of reactions of SDZ, DIF and their related metabolites. PMID:20022355

  17. Synthesis of 14C-labeled perfluorooctanoic and perfluorodecanoic acids; Purification of perfluorodecanoic acid

    SciTech Connect

    Reich, I.L.; Reich, H.J.; Menahan, L.A.; Peterson, R.E.

    1987-01-01

    Perfluorooctanoic and -decanoic acids are representative of a series of perfluorinated acids that have been used for a variety of industrial purposes primarily due to their surfactant properties. The toxicity of these compounds is being investigated in a number of laboratories. 14C-labeled materials would be useful in these studies but are not commercially available. Johncock prepared unlabeled PFOA in low yield by carbonation of the unstable perfluoroheptyllithium at -90 degrees Centigrade. We anticipated several problems in applying this procedure to the synthesis of the 14C-labeled material. Johncock's procedure was run on a fairly large scale (10 mmol) with excess CO2.

  18. Δ14C level of annual plants and fossil fuel derived CO2 distribution across different regions of China

    NASA Astrophysics Data System (ADS)

    Xi, X. T.; Ding, X. F.; Fu, D. P.; Zhou, L. P.; Liu, K. X.

    2013-01-01

    The 14C level in annual plants is a sensitive tracer for monitoring fossil fuel derived CO2 in the atmosphere. Corn leave samples were selected from different regions of China, including high mountains in the Tibetan Plateau, grassland in Inner Mongolia, and inland and coastal cities during the summer of 2010. The 14C/12C ratio of the samples was measured with the NEC compact AMS system at the Institute of Heavy Ion Physics, Peking University. The fossil fuel derived CO2 was estimated by comparing the measured Δ14C values of corn leave samples to background atmospheric Δ14C level. The influences of topography, meteorological conditions and carbon cycling processes on the fossil fuel derived CO2 concentration are considered when interpreting the data. Our results show a clear association of the low Δ14C values with regions where human activities are intensive.

  19. Enzymatic method for the synthesis of (/sup 14/C)pyridoxal 5-phosphate from (/sup 14/C)pyridoxine

    SciTech Connect

    Yagi, T.; Takasugi, M.; Yamamoto, S.; Nozaki, M.

    1986-10-01

    A new enzymatic method for the synthesis of (/sup 14/C)pyridoxal 5-phosphate is presented. (/sup 14/C)Pyridoxal 5'-phosphate was synthesized from (/sup 14/C)pyriodoxine through the successive actions of pyridoxal kinase and pyrdoxamine 5'-phosphate oxidase in a reaction mixture containing ATP, (/sup 14/C)pyridoxine, and both enzymes. (/sup 14/C)Pyridoxal 5'-phosphate was isolated by omega-aminohexyl-Sepharose 6B column chromatography. The overall yield of the product was more than 60%, starting from 550 nmol of (/sup 14/C)pyridoxine. The radiochemical purity of the products, as determined by thin-layer and ion-exchange chromatography, was greater than 98%.

  20. Low-level 14C methane oxidation rate measurements modified for remote field settings

    NASA Astrophysics Data System (ADS)

    Pack, M. A.; Pohlman, J.; Ruppel, C. D.; Xu, X.

    2012-12-01

    Aerobic methane oxidation limits atmospheric methane emissions from degraded subsea permafrost and dissociated methane hydrates in high latitude oceans. Methane oxidation rate measurements are a crucial tool for investigating the efficacy of this process, but are logistically challenging when working on small research vessels in remote settings. We modified a low-level 14C-CH4 oxidation rate measurement for use in the Beaufort Sea above hydrate bearing sediments during August 2012. Application of the more common 3H-CH4 rate measurement that uses 106 times more radioactivity was not practical because the R/V Ukpik cannot accommodate a radiation van. The low-level 14C measurement does not require a radiation van, but careful isolation of the 14C-label is essential to avoid contaminating natural abundance 14C measurements. We used 14C-CH4 with a total activity of 1.1 μCi, which is far below the 100 μCi permitting level. In addition, we modified field procedures to simplify and shorten sample processing. The original low-level 14C-CH4 method requires 6 steps in the field: (1) collect water samples in glass serum bottles, (2) inject 14C-CH4 into bottles, (3) incubate for 24 hours, (4) filter to separate the methanotrophic bacterial cells from the aqueous sample, (5) kill the filtrate with sodium hydroxide (NaOH), and (6) purge with nitrogen to remove unused 14C-CH4. Onshore, the 14C-CH4 respired to carbon dioxide or incorporated into cell material by methanotrophic bacteria during incubation is quantified by accelerator mass spectrometry (AMS). We conducted an experiment to test the possibility of storing samples for purging and filtering back onshore (steps 4 and 6). We subjected a series of water samples to steps 1-3 & 5, and preserved with mercuric chloride (HgCl2) instead of NaOH because HgCl2 is less likely to break down cell material during storage. The 14C-content of the carbon dioxide in samples preserved with HgCl2 and stored for up to 2 weeks was stable

  1. Bound sup 14 C residues in stored wheat treated with ( sup 14 C)deltamethrin and their bioavailability in rats

    SciTech Connect

    Khan, S.U.; Kacew, S. ); Akhtar, M.H. )

    1990-04-01

    Wheat grains treated with radiolabeled deltamethrin ((S)-{alpha}-cyano-3-phenoxybenzyl (1R,3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate) and stored in the laboratory for 168 days formed bound (nonextractable) {sup 14}C residues. The amount of bound {sup 14}C residues formed was about 11% of the total {sup 14}C in stored grain. Br{sub 2}CA (3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylic acid) and 3-PBacid (3-phenoxybenzoic acid) were present in the form of bound {sup 14}C residues in addition to some radiolabeled product of unknown composition. The stored wheat containing bound {sup 14}C was fed to rats. The {sup 14}C residues were excreted in urine and feces in nearly equal proportion. The {sup 14}C residues identified in urine were Br{sub 2}CA, 3-PBacid, and conjugated compounds of 4{prime}-OH-3-PBacid (3-(4-hydroxyphenoxy)benzoic acid). Most of the {sup 14}C residues excreted in feces were extractable with methanol. Trace amounts of {sup 14}C residues were also present in lungs, kidney, and liver. The results suggest that bound residues in stored wheat treated with deltamethrin when fed to rats are highly bioavailable.

  2. Changes in Atmospheric 14C Between 55 and 42 ky BP Recorded in a Stalagmite From Socotra Island, Indian Ocean

    NASA Astrophysics Data System (ADS)

    Weyhenmeyer, C. E.; Burns, S. J.; Fleitmann, D.; Kramers, J. D.; Matter, A.; Waber, H. N.; Reimer, P. J.

    2003-12-01

    A record of atmospheric radiocarbon (14C) variations for a part of the last glacial period was obtained from a 1.7 m long stalagmite, M1-2, from Socotra Island in the Indian Ocean. The stalagmite radiocarbon values were corrected for 14C-free carbon added by water-rock interaction (dead carbon fraction), by using del 13C values of the calcite as a constraint. An age-depth model was developed from 25 high-precision U/Th measurements. The base of the stalagmite dates to 54.7 ky BP and it stopped growing around 42.2 ky BP. The difference between U/Th and 14C ages shows a smooth, steady increase from about 5,000 years at the base of the stalagmite to about 8,000 years at its top. Correspondingly, Delta 14C values increase from 500 per mil to about 1300 per mil, which indicates that concentrations of atmospheric 14C steadily increased between 55 and 42 yr BP. The record from Socotra Island does not show the large and rapid D14C changes previously recorded in a stalagmite from the Bahamas (Beck et al, Science 2001). The D14C values estimated from M1-2 are significantly higher than those estimated from a marine 14C record (foraminifera) from Cariaco Basin for the same time period (Hughen et al. in prep). In the latter, D14C values decrease to near 0 at about 44 ky BP. The most likely reason for this discrepancy are the two different time scales used; the Cariaco Basin is matched to the GISP2 timescale, which is approximately 5000 years younger than indicated by the stalagmite U/Th chronology (Burns et al, Science 2003). When the Cariaco basin record is adjusted to the M1-2 timescale, the D14C values for both datasets are similar.

  3. Comparison of Varve and 14C Chronologies from Steel Lake, Minnesota, USA

    SciTech Connect

    Tian, J; Brown, T A; Hu, F S

    2004-12-29

    Annually laminated sediments (varves) offer an effective means of acquiring high-quality paleoenvironmental records. However, the strength of a varve chronology can be compromised by a number of factors, such as missing varves, ambiguous laminations, and human counting error. We assess the quality of a varve chronology for the last three millennia from Steel Lake, Minnesota, through comparisons with nine AMS {sup 14}C dates on terrestrial plant macrofossils from the same core. These comparisons revealed an overall 8.4% discrepancy, primarily because of missing/uncountable varves within two stratigraphic intervals characterized by low carbonate concentrations and obscure laminations. Application of appropriate correction factors to these two intervals results in excellent agreement between the varve and {sup 14}C chronologies. These results, together with other varve studies, demonstrate that an independent age-determination method, such as {sup 14}C dating, is usually necessary to verify, and potentially correct, varve chronologies.

  4. Abundance of {sup 14}C in biomass fractions of wastes and solid recovered fuels

    SciTech Connect

    Fellner, Johann Rechberger, Helmut

    2009-05-15

    In recent years thermal utilization of mixed wastes and solid recovered fuels has become of increasing importance in European waste management. Since wastes or solid recovered fuels are generally composed of fossil and biogenic materials, only part of the CO{sub 2} emissions is accounted for in greenhouse gas inventories or emission trading schemes. A promising approach for determining this fraction is the so-called radiocarbon method. It is based on different ratios of the carbon isotopes {sup 14}C and {sup 12}C in fossil and biogenic fuels. Fossil fuels have zero radiocarbon, whereas biogenic materials are enriched in {sup 14}C and reflect the {sup 14}CO{sub 2} abundance of the ambient atmosphere. Due to nuclear weapons tests in the past century, the radiocarbon content in the atmosphere has not been constant, which has resulted in a varying {sup 14}C content of biogenic matter, depending on the period of growth. In the present paper {sup 14}C contents of different biogenic waste fractions (e.g., kitchen waste, paper, wood), as well as mixtures of different wastes (household, bulky waste, and commercial waste), and solid recovered fuels are determined. The calculated {sup 14}C content of the materials investigated ranges between 98 and 135 pMC.

  5. Abundance of (14)C in biomass fractions of wastes and solid recovered fuels.

    PubMed

    Fellner, Johann; Rechberger, Helmut

    2009-05-01

    In recent years thermal utilization of mixed wastes and solid recovered fuels has become of increasing importance in European waste management. Since wastes or solid recovered fuels are generally composed of fossil and biogenic materials, only part of the CO(2) emissions is accounted for in greenhouse gas inventories or emission trading schemes. A promising approach for determining this fraction is the so-called radiocarbon method. It is based on different ratios of the carbon isotopes (14)C and (12)C in fossil and biogenic fuels. Fossil fuels have zero radiocarbon, whereas biogenic materials are enriched in (14)C and reflect the (14)CO(2) abundance of the ambient atmosphere. Due to nuclear weapons tests in the past century, the radiocarbon content in the atmosphere has not been constant, which has resulted in a varying (14)C content of biogenic matter, depending on the period of growth. In the present paper (14)C contents of different biogenic waste fractions (e.g., kitchen waste, paper, wood), as well as mixtures of different wastes (household, bulky waste, and commercial waste), and solid recovered fuels are determined. The calculated (14)C content of the materials investigated ranges between 98 and 135pMC. PMID:19157836

  6. Progress report on a novel in situ14C extraction scheme at the University of Cologne

    NASA Astrophysics Data System (ADS)

    Fülöp, R.-H.; Wacker, L.; Dunai, T. J.

    2015-10-01

    We present initial results of in situ14C system blank and calibration sample measurements obtained using the in situ14C extraction scheme developed at the University of Cologne. The 14C extraction scheme specifically exploits the phase transformation of quartz to cristobalite in order to quantitatively extract the carbon as CO2 and follows a scheme that is different to that of existing extraction systems. Features are offline furnace extraction, single pass catalytic oxidation using mixed copper (I,II) oxide as catalyst, the use of UHV-compatible components and of vacuum annealed copper tubing. The design allows a relatively rapid sample throughput - two samples per day as opposed to the current 2 days per sample that can be done on other lines - and can accommodate samples ranging between 0.5 and 4 g of clean quartz. Following extraction and cleaning, the CO2 gas is measured using the gas ion source of the MICADAS AMS facility at ETH Zurich. The extraction system yields low systems blanks (10 +16/-10 × 103 atoms 14C, ±1 σ) and the initial results indicate that further improvements are achievable. Measurements of the CRONUS-A standard sample show a good reproducibility and results are consistent with published values. We also present the first in situ14C results for the CRONUS-R standard material.

  7. Development of an Airborne Triple-Pulse 2-Micron Integrated Path Differential Absorption Lidar (IPDA) for Simultaneous Airborne Column Measurements of Carbon Dioxide and Water Vapor in the Atmosphere

    NASA Technical Reports Server (NTRS)

    Singh, Upendra N.; Petros, Mulugeta; Refaat, Tamer F.; Yu, Jirong; Antill, Charles W.; Remus, Ruben

    2016-01-01

    This presentation will provide status and details of an airborne 2-micron triple-pulse integrated path differential absorption (IPDA) lidar being developed at NASA Langley Research Center with support from NASA ESTO Instrument Incubator Program. The development of this active optical remote sensing IPDA instrument is targeted for measuring both atmospheric carbon dioxide and water vapor in the atmosphere from an airborne platform. This presentation will focus on the advancement of the 2-micron triple-pulse IPDA lidar development. Updates on the state-of-the-art triple-pulse laser transmitter will be presented including the status of seed laser locking, wavelength control, receiver and detector upgrades, laser packaging and lidar integration. Future plan for IPDA lidar system for ground integration, testing and flight validation will also be presented.

  8. 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

  9. Substrate metabolism in isolated rat jejunal epithelium. Analysis using /sup 14/C-radioisotopes

    SciTech Connect

    Mallet, R.T.

    1986-01-01

    The jejunal epithelium absorbs nutrients from the intestinal lumen and is therefore the initial site for metabolism of these compounds. The purpose of this investigation is to analyze substrate metabolism in a preparation of jejunal epithelium relatively free of other tissues. Novel radioisotopic labelling techniques allow quantitation of substrate metabolism in the TCA cycle, Embden-Meyerhof (glycolytic) pathway, and hexose monophosphate shunt. For example, ratios of /sup 14/CO/sub 2/ production from pairs of /sup 14/C-pyruvate, and /sup 14/C-succinate radioisotopes (CO/sub 2/ ratios) indicate the probability of TCA cycle intermediate efflux to generate compounds other than CO/sub 2/. With (2,3-/sup 14/C)succinate as tracer, the ratio of /sup 14/C in carbon 4 + 5 versus carbon 2 + 3 of citrate, the citrate labelling ratio, equals the probability of TCA intermediate flux to the acetyl CoA-derived portion of citrate versus flux to the oxaloacetate-derived portion. The principal metabolic substrates for the jejunal epithelium are glucose and glutamine. CO/sub 2/ ratios indicate that glutamine uptake and metabolism is partially Na/sup +/-independent, and is saturable, with a half-maximal rate at physiological plasma glutamine concentrations. Glucose metabolism in the jejunal epithelium proceeds almost entirely via the Embden-Meyerhof pathway. Conversion of substrates to multi-carbon products in this tissue allows partial conservation of reduced carbon for further utilization in other tissues. In summary, metabolic modeling based on /sup 14/C labelling ratios is a potentially valuable technique for analysis of metabolic flux patterns in cell preparations.

  10. Comparison of 14C ages of hydrothermal petroleums

    USGS Publications Warehouse

    Simoneit, B.R.T.; Kvenvolden, K.A.

    1994-01-01

    In order to set limits on the time frame of formation of hydrothermal petroleum, we have obtained 14C ages on samples from three diverse regions; Gulf of California (Guaymas Basin), Northeast Pacific Ocean (Escanaba Trough and Middle Valley), and the East African Rift (Tanganyika Trough). The results date the source of carbon and therefore provide maximum ages for the formation and emplacement of the hydrothermal petroleums. The youngest petroleum occurs iin the Souther Trough of Guaymas Basin (3200-6600 yr, mean 4692 yr); in the Northern Trough the petroleum is slightly older (7400 yr). Significantly older hydrothermal petroleum occurs in Escanaba Trough (17,000 yr) and Middle Valley (29,000 yr). A continental example from the East African Rift has an age of 25,000 yr, comparable to the ages observed in the oceanic samples from the Northeast Pacific Ocean. These ages affirm that hydrothermal petroleum formation is a very rapid process and took place some time between the latest Pleistocene and the present in these active hydrothermal systems. ?? 1994.

  11. Impact of liming and drying municipal sewage sludge on the amount and availability of (14)C-acetyl sulfamethoxazole and (14)C-acetaminophen residues.

    PubMed

    Geng, Chunnu; Bergheaud, Valérie; Garnier, Patricia; Zhu, Yong-Guan; Haudin, Claire-Sophie

    2016-01-01

    Acetyl Sulfamethoxazole (AC-SMX) and acetaminophen (ACM) can be found in municipal sewage sludge, and their content and availability may be influenced by sludge treatments, such as drying and liming. A sludge similarly centrifuged with/without a flocculant was spiked with (14)C-labelled AC-SMX or ACM. Then, it was either limed (20% CaO) or/and dried under different laboratory conditions (1 week at ambient temperature; and 48 h at 40 or 80 °C). The total amount and distribution of the (14)C-compounds among several chemical fractions, based on the sludge floc definition, were assessed at the end of the treatments. All the (14)C-activity brought initially was recovered in the limed and/or dried sludges for AC-SMX but only between 44.4 and 84.9% for ACM, with the highest rate obtained for the limed sludge. Drying at 80 °C or liming increased the percentage of the sludge total organic carbon recovered in the extracts containing soluble extracellular polymeric substances (S-EPS) and the percentage of the total (14)C-activity extracted simultaneously. The non-extractable residues represented only 3.9-11.6% of the total (14)C-activity measured in the treated sludges for AC-SMX and 16.9-21.8% for ACM. The presence of AC-SMX and ACM residues in the treated sludges, after liming and drying under different conditions, was shown using some (14)C-labelled molecules. At this time scale and according to the extraction method selected, most of the (14)C-residues remained soluble and easily extractable for both compounds. This result implies that certain precautions should be taken when storing sludges before being spread on the field. Sludge piles, particularly the limed sludge, should be protected from rain to limit the production of lixiviates, which may contain residues of AC-SMX and ACM. PMID:26492342

  12. First Airborne IPDA Lidar Measurements of Methane and Carbon Dioxide Applying the DLR Greenhouse Gas Sounder CHARM-F

    NASA Astrophysics Data System (ADS)

    Amediek, A.; Ehret, G.; Fix, A.; Wirth, M.; Quatrevalet, M.; Büdenbender, C.; Kiemle, C.; Loehring, J.; Gerbig, C.

    2015-12-01

    First airborne measurement using CHARM-F, the four-wavelengths lidar for simultaneous soundings of atmospheric CO2 and CH4, were performed in Spring 2015 onboard the German research aircraft HALO. The lidar is designed in the IPDA (integrated path differential absorption) configuration using short double pulses, which gives column averaged gas mixing ratios between aircraft and ground. HALO's maximum flight altitude of 15 km and special features of the lidar, such as a relatively large laser ground spot, enable the CHARM-F system to be an airborne demonstrator for future spaceborne greenhouse gas lidars. Due to a high technological conformity this applies in particular to the French-German satellite mission MERLIN, the spaceborne methane IPDA lidar. The successfully completed flight measurements provide a valuable dataset, which supports the retrieval algorithm development for MERLIN notably. The flights covered different ground cover types, different orography types as well as the sea. Additionally, we captured different cloud conditions, at which the broken cloud case is a matter of particular interest. This dataset allows detailed analyses of measurement sensitivities, general studies on the IPDA principle and on technical details of the system. These activities are supported by another instrument onboard: a cavity ring down spectrometer, providing in-situ data of carbon dioxide, methane and water vapor with high accuracy and precision, which is ideal for validation purposes of the lidar. Additionally the onboard instrumentation of HALO gives information about pressure and temperature for cross-checking the ECMWF data, which are intended to be used for calculating the weighting function, the key quantity for the retrieval of gas column mixing ratios from the measured gas optical depths. In combination with dedicated descents into the boundary layer and subsequent ascents, a self-contained dataset for characterizations of CHARM-F is available.

  13. Domestic airborne black carbon levels and 8-isoprostane in exhaled breath condensate among children in New York City☆

    PubMed Central

    Rosa, Maria Jose; Yan, Beizhan; Chillrud, Steven N.; Acosta, Luis M.; Divjan, Adnan; Jacobson, Judith S.; Miller, Rachel L.; Goldstein, Inge F.; Perzanowski, Matthew S.

    2015-01-01

    Background Exposure to airborne black carbon (BC) has been associated with asthma development, respiratory symptoms and decrements in lung function. However, the mechanism through which BC may lead to respiratory symptoms has not been completely elucidated. Oxidative stress has been suggested as a potential mechanism through which BC might lead to adverse health outcomes. Exhaled breath condensate (EBC) allows for the non-invasive collection of airway lining fluid containing biomarkers of oxidative stress like 8-isoprostane, a stable by-product of lipid peroxidation. Therefore, we sought to characterize the association between domestic airborne BC concentrations and 8-isoprostane in EBC. Materials and methods Seven- and eight-year-old children participated in an asthma case–control study in New York City. During home visits, air samples and EBC were collected. Seven day averages of domestic levels of particulate matter <2.5 µm (PM2.5), BC and environmental tobacco smoke (ETS) were measured. Urea and 8-isoprostane were measured by liquid chromatography tandem mass spectrometry (LC/MS/MS) in EBC. Results In univariate models, PM2.5 and BC, but not ETS, were significantly associated with increases in 8-isoprostane in the EBC (β = 0.006 and β = 0.106 respectively, p < 0.05 for both). These associations remained statistically significant for both PM2.5 and BC after adjustment for covariates. In a co-pollutant model including PM2.5, BC and ETS, only BC remained a statistically significant predictor of 8-isoprostane (p < 0.05). Conclusions Our findings suggest the BC fraction of PM might contain exposure relevant to increased oxidative stress in the airways. PMID:25262082

  14. 14C-age tracers in global ocean circulation models

    NASA Astrophysics Data System (ADS)

    Koeve, W.; Wagner, H.; Kähler, P.; Oschlies, A.

    2015-07-01

    The natural abundance of 14C in total CO2 dissolved in seawater (DIC) is a property applied to evaluate the water age structure and circulation in the ocean and in ocean models. In this study we use three different representations of the global ocean circulation augmented with a suite of idealised tracers to study the potential and limitations of using natural 14C to determine water age, which is the time elapsed since a body of water has been in contact with the atmosphere. We find that, globally, bulk 14C-age is dominated by two equally important components, one associated with ageing, i.e. the time component of circulation, and one associated with a "preformed 14C-age". The latter quantity exists because of the slow and incomplete atmosphere-ocean equilibration of 14C particularly in high latitudes where many water masses form. In the ocean's interior, preformed 14C-age behaves like a passive tracer. The relative contribution of the preformed component to bulk 14C-age varies regionally within a given model, but also between models. Regional variability in the Atlantic Ocean is associated with the mixing of waters with very different end members of preformed 14C-age. Here, variations in the preformed component over space and time mask the circulation component to an extent that its patterns are not detectable from bulk 14C-age. Between models, the variability of preformed 14C-age can also be considerable (factor of 2), related to the combination of physical model parameters, which influence circulation dynamics or gas exchange. The preformed component was found to be very sensitive to gas exchange and moderately sensitive to ice cover. In our model evaluation, the choice of the gas-exchange constant from within the currently accepted range of uncertainty had such a strong influence on preformed and bulk 14C-age that if model evaluation would be based on bulk 14C-age, it could easily impair the evaluation and tuning of a model's circulation on global and regional

  15. Development and Preliminary Tests of an Open-Path Airborne Diode Laser Absorption Instrument for Carbon Dioxide

    NASA Astrophysics Data System (ADS)

    Diskin, G. S.; DiGangi, J. P.; Yang, M. M.; Rana, M.; Slate, T. A.

    2015-12-01

    Carbon dioxide (CO2) is well known for its importance as an atmospheric greenhouse gas, with many sources and sinks around the globe. Understanding the fluxes of carbon into and out of the atmosphere is a complex and daunting challenge. One tool applied by scientists to measure the vertical flux of CO2 near the surface uses the eddy covariance technique, most often from towers but also from aircraft flying specific patterns over the study area. In this technique, variations of constituents of interest are correlated with fluctuations in the local vertical wind velocity. Measurement requirements are stringent, particularly with regard to precision, sensitivity to small changes, and temporal sampling rate. In addition, many aircraft have limited payload capability, so instrument size, weight, and power consumption are also important considerations. We report on the development and preliminary application of an airborne sensor for the measurement of atmospheric CO2. The instrument, modeled on the successful DLH (Diode Laser Hygrometer) series of instruments, has been tested in the laboratory and on the NASA DC-8 aircraft. Performance parameters such as accuracy, precision, sensitivity, specificity, and temporal response are discussed in the context of typical atmospheric variability and suitability for flux measurement applications. On-aircraft, in-flight intercomparison data have been obtained and will be discussed as well. Performance of the instrument has been promising, and continued flight testing is planned during 2016.

  16. Development and Preliminary Tests of an Open-Path Airborne Diode Laser Absorption Instrument for Carbon Dioxide

    NASA Technical Reports Server (NTRS)

    Diskin, Glenn S.; DiGangi, Joshua P.; Yang, Melissa; Slate, Thomas A.; Rana, Mario

    2015-01-01

    Carbon dioxide (CO2) is well known for its importance as an atmospheric greenhouse gas, with many sources and sinks around the globe. Understanding the fluxes of carbon into and out of the atmosphere is a complex and daunting challenge. One tool applied by scientists to measure the vertical flux of CO2 near the surface uses the eddy covariance technique, most often from towers but also from aircraft flying specific patterns over the study area. In this technique, variations of constituents of interest are correlated with fluctuations in the local vertical wind velocity. Measurement requirements are stringent, particularly with regard to precision, sensitivity to small changes, and temporal sampling rate. In addition, many aircraft have limited payload capability, so instrument size, weight, and power consumption are also important considerations. We report on the development and preliminary application of an airborne sensor for the measurement of atmospheric CO2. The instrument, modeled on the successful DLH (Diode Laser Hygrometer) series of instruments, has been tested in the laboratory and on the NASA DC-8 aircraft. Performance parameters such as accuracy, precision, sensitivity, specificity, and temporal response are discussed in the context of typical atmospheric variability and suitability for flux measurement applications. On-aircraft, in-flight data have been obtained and are discussed as well. Performance of the instrument has been promising, and continued flight testing is planned during 2016.

  17. Transport of sup 14 C-IAA and sup 14 C-ACC within floral organs of Ipomoea nil

    SciTech Connect

    Kiss, H.G. ); Maurice, H.R. ); Koning, R.E. ); Daie, J. )

    1989-04-01

    The transport of {sup 14}C-IAA {sup 14}C-ACC from agarose donor blocks applied to I. nil filaments their recovery as {sup 14}C-accumulation into floral organs was examined. The accumulation of the isotopes in the corolla tissue was greater when {sup 14}C-ACC was applied than {sup 14}C-IAA in intact isolated flower buds. Greater levels of the isotopes accumulated in the pistil, with minimal levels in receptacle and calyx tissues from isolated buds. With intact buds, greater levels of the isotopes were recovered in pistil, calyx receptacle tissues. This study provides further evidence for the role of the filaments as transport vectors for IAA ACC for the production of ethylene.

  18. Quantitative Identification of Biogenic Nonextractable Pesticide Residues in Soil by (14)C-Analysis.

    PubMed

    Poßberg, Claudia; Schmidt, Burkhard; Nowak, Karolina; Telscher, Markus; Lagojda, Andreas; Schaeffer, Andreas

    2016-06-21

    Quantification of nonextractable residues (NER) of pesticides in soil is feasible by use of radioactively labeled compounds, but structural information on these long-term stabilized residues is usually lacking. Microorganisms incorporate parts of the radiolabeled ((14)C-) carbon from contaminants into microbial biomass, which after cell death enters soil organic matter, thus forming biogenic nonextractable residues (bioNER). The formation of bioNER is not yet determinable in environmental fate studies due to a lack of methodology. This paper focuses on the development of a feasible analytical method to quantify proteinaceous carbon, since proteins make up the largest mass portion of bacterial cells. The test substance (14)C-bromoxynil after 56 days forms more than 70% of NER in soil. For further characterization of NER the amino acids were extracted, purified, and separated by two-dimensional thin-layer chromatography (TLC). Visualization of the (14)C-amino acids was performed by bioimaging, unambiguous identification by GC-MS and LC-MS/MS. Our analysis revealed that after 56 days of incubation about 14.5% of the (14)C-label of bromoxynil was incorporated in amino acids. Extrapolating this content based on the amount of proteins in the biomass (55%), in total about 26% of the NER is accounted for by bioNER and thus is not environmentally relevant. PMID:27192605

  19. Measurement of 14C emission rates from a pressurised heavy water reactor.

    PubMed

    Joshi, M L; Ramamirtham, B; Soman, S D

    1987-06-01

    Carbon-14 is produced in pressurised heavy water reactors (PHWR), mainly as an activation product in the fuel. It is also produced in the heavy water used as the primary coolant and moderator, and is produced in the air in the annular space between the pressure tube and calandria tubes as well as in the free space in the calandria vault. The production rates in different systems of a PHWR are calculated on the basis of design parameters. During a period of 3 y, 14C released through the gaseous route has been measured at Rajasthan Atomic Power Station, Kota, India, a PHWR unit. These releases have been found to be mainly 14CO2. This reduced form of 14C is less than 5% of the releases. The normalised releases of 14C have a geometric mean of 5.17 TBq GWe-1 y-1 and a geometric standard deviation of 1.52. The 14C present in the form of carbonates in liquid effluents has also been measured and is 0.14% of the gaseous releases. PMID:3583743

  20. Estimating Carbon STOCK Changes of Mangrove Forests Using Satellite Imagery and Airborne LiDAR Data in the South Sumatra State, Indonesia

    NASA Astrophysics Data System (ADS)

    Maeda, Y.; Fukushima, A.; Imai, Y.; Tanahashi, Y.; Nakama, E.; Ohta, S.; Kawazoe, K.; Akune, N.

    2016-06-01

    The purposes of this study were 1) to estimate the biomass in the mangrove forests using satellite imagery and airborne LiDAR data, and 2) to estimate the amount of carbon stock changes using biomass estimated. The study area is located in the coastal area of the South Sumatra state, Indonesia. This area is approximately 66,500 ha with mostly flat land features. In this study, the following procedures were carried out: (1) Classification of types of tree species using Satellite imagery in the study area, (2) Development of correlation equations between spatial volume based on LiDAR data and biomass stock based on field survey for each types of tree species, and estimation of total biomass stock and carbon stock using the equation, and (3) Estimation of carbon stock change using Chronological Satellite Imageries. The result showed the biomass and the amount of carbon stock changes can be estimated with high accuracy, by combining the spatial volume based on airborne LiDAR data with the tree species classification based on satellite imagery. Quantitative biomass monitoring is in demand for projects related to REDD+ in developing countries, and this study showed that combining airborne LiDAR data with satellite imagery is one of the effective methods of monitoring for REDD+ projects.

  1. Spatial distribution and characterization of long-term aged 14C-labeled atrazine residues in soil.

    PubMed

    Jablonowski, Nicolai D; Koeppchen, Stephan; Hofmann, Diana; Schaeffer, Andreas; Burauel, Peter

    2008-10-22

    The long-term behavior of the herbicide atrazine and its metabolites in the environment is of continued interest in terms of risk assessment and soil quality monitoring. Aqueous desorption, detection, and quantification of atrazine and its metabolites from an agriculturally used soil were performed 22 years after the last atrazine application. A lysimeter soil containing long-term aged atrazine for >20 years was subdivided into 10 and 5 cm layers (at the lysimeter bottom: soil 0-50 and 50-55 cm; fine gravel 55-60 cm depth, implemented for drainage purposes) to identify the qualitative and quantitative differences of aged (14)C-labeled atrazine residues depending on the soil profile and chemico-physical conditions of the individual soil layers. Deionized water was used for nonexhaustive cold water shaking extraction of the soil. With increasing soil depth, the amount of previously applied (14)C activity decreased significantly from 8.8% to 0.7% at 55-60 cm depth whereas the percentage of desorbed (14)C residues in each soil layer increased from 2% to 6% of the total (14)C activity in the sample. The only metabolite detectable by means of LC-MS/MS was 2-hydroxyatrazine while most of the residual (14)C activity was bound to the soil and was not desorbed. The amount of desorbed 2-hydroxyatrazine decreased with increasing soil depth from 21% to 10% of the total desorbed (14)C residue fraction. The amount of (14)C residues in the soil layers correlated well with the carbon content in the soil and in the aqueous soil extracts ( p value = 0.99 and 0.97, respectively), which may provide evidence of the binding behavior of the aged atrazine residues on soil carbon. The lowest coarse layer (55-60 cm) showed increased residual (14)C activity leading to the assumption that most (14)C residues were leached from the soil column over time. PMID:18808141

  2. Airborne measurements of Black Carbon using miniature high-performance Aethalometers during global circumnavigation campaign GLWF 2012

    NASA Astrophysics Data System (ADS)

    Močnik, Griša; Drinovec, Luka; Vidmar, Primož; Lenarčič, Matevž

    2013-04-01

    While ground-level measurements of atmospheric aerosols are routinely performed around the world, there exists very little data on their vertical and geographical distribution in the global atmosphere. This data is a crucial requirement for our understanding of the dispersion of pollutant species of anthropogenic origin, and their possible effects on radiative forcing, cloud condensation, and other phenomena which can contribute to adverse outcomes. Black Carbon (BC) is a unique tracer for combustion emissions, and can be detected rapidly and with great sensitivity by filter-based optical methods. It has no non-combustion sources and is not transformed by atmospheric processes. Its presence at altitude is unequivocal. Recent technical advances have led to the development of miniaturized instruments which can be operated on ultra-light aircraft, balloons or UAV's. From January to April 2012, a 'Pipistrel Virus' single-seat ultra-light aircraft flew around the world on a photographic and environmental-awareness mission. The flight track covered all seven continents; crossed all major oceans; and operated at altitudes around 3000 m ASL and up to 8900 m ASL. The aircraft carried a specially-developed high-sensitivity miniaturized dual-wavelength Aethalometer, which recorded BC concentrations with very high temporal resolution and sensitivity (see Reference below). We present examples of data from flight tracks over remote oceans, uninhabited land masses, and densely populated areas. Back-trajectories are used to show transport of polluted air masses. Measuring the dependence of the aerosol absorption on the wavelength, we show that aerosols produced during biomass combustion can be transported to high altitude in high concentrations. 1. __, Carbon Sampling Takes Flight, Science 2012, 335, 1286. 2. G. Močnik, L. Drinovec, M. Lenarčič, Airborne measurements of Black Carbon during the GLW Flight using miniature high-performance Aethalometers, accessed 8 January 2013

  3. {sup 14}C depth profiles in Apollo 15 and 17 cores and lunar rock 68815

    SciTech Connect

    Jull, A.J.T.; Cloudt, S.; Donahue, D.J.; Sisterson, J.M.; Reedy, R.C.; Masarik, J.

    1998-09-01

    Accelerator mass spectrometry (AMS) was used to measure the activity vs. depth profiles of {sup 14}C produced by both solar cosmic rays (SCR) and galactic cosmic rays (GCR) in Apollo 15 lunar cores 15001-6 and 15008, Apollo 17 core 76001, and lunar rock 68815. Calculated GCR production rates are in good agreement with {sup 14}C measurements at depths below {approximately}10 cm. Carbon-14 produced by solar protons was observed in the top few cm of the Apollo 15 cores and lunar rock 68815, with near-surface values as high as 66 dpm/kg in 68815. Only low levels of SCR-produced {sup 14}C were observed in the Apollo 17 core 76001. New cross sections for production of {sup 14}C by proton spallation on O, Si, Al, Mg, Fe, and Ni were measured using AMS. These cross sections are essential for the analysis of the measured {sup 14}C depth profiles. The best fit to the activity-depth profiles for solar-proton-produced {sup 14}C measured in the tops of both the Apollo 15 cores and 68815 was obtained for an exponential rigidity spectral shape R{sub 0} of 110--115 MV and a 4 {pi} flux (J{sub 10}, Ep > 10 MeV) of 103--108 protons/cm{sup 2}/s. These values of R{sub 0} are higher, indicating a harder rigidity, and the solar-proton fluxes are higher than those determined from {sup 10}Be, {sup 26}Al, and {sup 53}Mn measurements.

  4. Determination of 14C residue in eggs of laying hens administered orally with [14C] sulfaquinoxaline.

    PubMed

    Shaikh, B; Rummel, N; Smith, D

    2004-06-01

    Ten layer hens were dosed for 5 consecutive days with 6.2 mg kg(-1) [14C] sulfaquinoxaline (SQX). Eggs were collected from the hens during the 5-day dosing period and during a 10-day post-dose withdrawal period. Egg yolk and albumen were separated and assayed for total radioactive residues (TRR) using a combustion oxidizer and liquid scintillation counting techniques. Significant amounts of radioactivity were detected on the second day of dosing (greater than 24h after the initial dose) in both egg yolk and albumen. First eggs were collected about 8 h after dosing; the second-day eggs were collected during 8-h period after the second dose. Radioactive residues reached a maximum on the fifth day of dosing in albumen, whereas on the second day of withdrawal in egg yolk, the peak TRR levels in albumen were about threefold higher than in yolk. Thereafter, the TRR levels declined rapidly in albumen and were detectable up to withdrawal day 6, whereas the TRR levels in egg yolk declined more slowly and were detectable up to withdrawal day 10. High-performance liquid chromatography analysis indicated that the parent drug sulfaquinoxaline was the major component in both the egg albumen and yolk. Additionally, this work suggests that egg yolk is the appropriate matrix for monitoring SQX residues PMID:15204532

  5. Identification of Biodegradation Pathways in a Multi-Process Phytoremediation System (MPPS) Using Natural Abundance 14C Analysis of PLFA

    NASA Astrophysics Data System (ADS)

    Cowie, B. R.; Greenberg, B. M.; Slater, G. F.

    2008-12-01

    Optimizing remediation of petroleum-contaminated soils requires thorough understanding of the mechanisms and pathways involved in a proposed remediation system. In many engineered and natural attenuation systems, multiple degradation pathways may contribute to observed contaminant mass losses. In this study, biodegradation in the soil microbial community was identified as a major pathway for petroleum hydrocarbon removal in a Multi-Process Phytoremediation System (MPPS) using natural abundance 14C analysis of Phospholipid Fatty Acids (PLFA). In contaminated soils, PLFA were depleted in Δ14C to less than -800‰, directly demonstrating microbial uptake and utilization of petroleum derived carbon14C = -992‰) during bioremediation. Mass balance indicated that more than 80% of microbial carbon was derived from petroleum hydrocarbons and a maximum of 20% was produced from metabolism of modern carbon sources. In contrast, in a nearby uncontaminated control soil, the microbial community maintained a nearly modern 14C signature, suggesting preferential degradation of more labile, recent carbon. Mass balance using δ13C and Δ14C of soil CO2 demonstrated that mineralization of petroleum carbon contributed 60-65% of soil CO2 at the contaminated site. The remainder was derived from atmospheric (27-30%) and decomposition of non- petroleum natural organic carbon (5-10%). The clean control exhibited substantially lower CO2 concentrations that were derived from atmospheric (55%) and natural organic carbon (45%) sources. This study highlights the value of using multiple carbon isotopes to identify degradation pathways in petroleum- contaminated soils undergoing phytoremediation and the power of natural abundance 14C to detect petroleum metabolism in natural microbial communities.

  6. Impact of cement renders on airborne ozone and carbon dioxide concentrations

    NASA Astrophysics Data System (ADS)

    Taylor-Lange, Sarah C.; Juenger, Maria C. G.; Siegel, Jeffrey A.

    2013-05-01

    The uptake of pollutants by building surfaces can potentially improve both indoor and outdoor air quality. Cement renders provide a unique opportunity for passive pollutant removal because they can cover large surface areas. This study investigated the passive removal of carbon dioxide and ozone by cement renders having varied binder compositions and curing durations. The results from this study demonstrated shorter curing durations resulted in greater pollutant uptake. However, the use of the supplementary cementitious material, metakaolin, in the cement render increased the carbon dioxide ingress while decreasing the ozone uptake. Therefore, the adaptation of the render composition for the best effective application may result in valuable indoor air quality or carbon savings consequences.

  7. 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.

  8. Long-term Airborne Black Carbon Measurements on a Lufthansa Passenger Aircraft

    NASA Astrophysics Data System (ADS)

    Cheng, Y.; Su, H.; Ditas, J.; Scharffe, D.; Wang, S.; Zhang, Y.; McMeeking, G. R.; Brenninkmeijer, C. A. M.; Poeschl, U.

    2015-12-01

    Aerosol particles containing black carbon are the most absorbing component of incoming solar radiation and exert a significant positive radiative forcing thus forming next to CO2 the strongest component of current global warming. Nevertheless, the role of black carbon particles and especially their complex interaction with clouds needs further research which is hampered by the limited experimental data, especially observations in the free troposphere, and in the UTLS (upper troposphere and lower stratosphere). In August 2014, a single particle soot photometer (SP2) was included in the extensive scientific payload of the CARIBIC (Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrument Container) project. CARIBIC is in operation since 1997 and carries out systematic observations of trace gas and aerosol sampling and on-line analyses, as well as DOAS remote sensing system at 10-12 km altitude. For this a special air freight container combining different instruments is transported on a monthly basis using a Lufthansa Airbus A340-600 passenger aircraft with destinations from 120°W to 120°E and 10°N to 75°N. The integration of a SP2 offers the possibility for the first long-term measurement of global distribution of black carbon. Up to date the SP2 measurements have been analyzed for 392 flights hours over four continents (Fig. 1). The first measurements show promising results of black carbon including periods when background concentrations in the UTLS were encountered. Beside a general distribution of number and mass of black carbon particles, peak events were detected with up to 20 times higher concentrations compared to the background. Moreover, high concentration plumes have been observed continuously over a range of 10,000 km. Interestingly, our results show also a generally lower amount of black carbon mass in the tropics compared to the mid latitude northern hemisphere.

  9. Long-term airborne black carbon measurements on a Lufthansa passenger aircraft

    NASA Astrophysics Data System (ADS)

    Ditas, Jeannine; Su, Hang; Scharffe, Dieter; Wang, Siwen; Zhang, Yuxuan; Brenninkmeijer, Carl; Pöschl, Ulrich; Cheng, Yafang

    2016-04-01

    Aerosol particles containing black carbon are the most absorbing component of incoming solar radiation and exert a significant positive radiative forcing thus forming next to CO² the strongest component of current global warming (Bond, 2013). Nevertheless, the role of black carbon particles and especially their complex interaction with clouds needs further research which is hampered by the limited experimental data, especially observations in the free and upper troposphere, and in the UTLS (upper troposphere and lower stratosphere). Many models underestimate the global atmospheric absorption attributable to black carbon by a factor of almost 3 (Bond, 2013). In August 2014, a single particle soot photometer was included in the extensive scientific payload of the CARIBIC (Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrument Container) project. CARIBIC is in operation since 1997 (with an interruption for 2002-2005) and carries out systematic observations at 10-12 km altitude. For this a special air freight container combining different instruments is transported on a monthly basis using a Lufthansa Airbus A340-600 passenger aircraft with destinations from 120°W to 120°E and 10°N to 75°N. The container has equipment for trace gas analyses and sampling and aerosol analyses and sampling and is connected to an inlet system that is part of the aircraft which contains a camera and DOAS remote sensing system. The integration of a single particle soot photometer (SP2) offers the possibility for the first long-term measurement of global distribution of black carbon and so far flights up to November 2015 have been conducted with more than 400 flight hours. So far the SP2 measurements have been analysed for flights over four continents from Munich to San Francisco, Sao Paulo, Tokyo, Beijing, Cape Town, Los Angeles and Hong Kong). The first measurements show promising results of black carbon measurements. Background concentrations in the UTLS

  10. 14C-age tracers in global ocean circulation models

    NASA Astrophysics Data System (ADS)

    Koeve, W.; Wagner, H.; Kähler, P.; Oschlies, A.

    2014-10-01

    The natural abundance of 14C in total CO2 dissolved in seawater is a property applied to evaluate the water age structure and circulation in the ocean and in ocean models. In this study we use three different representations of the global ocean circulation augmented with a suite of idealised tracers to study the potential and limitations of using natural 14C to determine water age, the time elapsed since a body of water had contact with the atmosphere. We find that, globally, bulk 14C-age is dominated by two equally important components, one associated with aging, i.e. the time component of circulation and one associated with a "preformed 14C-age". This latter quantity exists because of the slow and incomplete atmosphere/ocean equilibration of 14C in particular in high latitudes where many water masses form. The relative contribution of the preformed component to bulk 14C-age varies regionally within a given model, but also between models. Regional variability, e.g. in the Atlantic Ocean is associated with the mixing of waters with very different end members of preformed 14C-age. In the Atlantic, variations in the preformed component over space and time mask the circulation component to an extent that its patterns are not detectable from bulk 14C-age alone. Between models the variability of age can also be considerable (factor of 2), related to the combinations of physical model parameters, which influence circulation dynamics, and gas exchange in the models. The preformed component was found to be very sensitive to gas exchange and moderately sensitive to ice cover. In our model evaluation exercise, the choice of the gas exchange constant from within the current range of uncertainty had such a strong influence on preformed and bulk 14C-age that if model evaluation would be based on bulk 14C-age it could easily impair the evaluation and tuning of a models circulation on global and regional scales. Based on the results of this study, we propose that considering

  11. Using airborne HIAPER Pole-to-Pole Observations (HIPPO) to evaluate model and remote sensing estimates of atmospheric carbon dioxide

    NASA Astrophysics Data System (ADS)

    Frankenberg, Christian; Kulawik, Susan S.; Wofsy, Steven C.; Chevallier, Frédéric; Daube, Bruce; Kort, Eric A.; O'Dell, Christopher; Olsen, Edward T.; Osterman, Gregory

    2016-06-01

    In recent years, space-borne observations of atmospheric carbon dioxide (CO2) have been increasingly used in global carbon-cycle studies. In order to obtain added value from space-borne measurements, they have to suffice stringent accuracy and precision requirements, with the latter being less crucial as it can be reduced by just enhanced sample size. Validation of CO2 column-averaged dry air mole fractions (XCO2) heavily relies on measurements of the Total Carbon Column Observing Network (TCCON). Owing to the sparseness of the network and the requirements imposed on space-based measurements, independent additional validation is highly valuable. Here, we use observations from the High-Performance Instrumented Airborne Platform for Environmental Research (HIAPER) Pole-to-Pole Observations (HIPPO) flights from 01/2009 through 09/2011 to validate CO2 measurements from satellites (Greenhouse Gases Observing Satellite - GOSAT, Thermal Emission Sounder - TES, Atmospheric Infrared Sounder - AIRS) and atmospheric inversion models (CarbonTracker CT2013B, Monitoring Atmospheric Composition and Climate (MACC) v13r1). We find that the atmospheric models capture the XCO2 variability observed in HIPPO flights very well, with correlation coefficients (r2) of 0.93 and 0.95 for CT2013B and MACC, respectively. Some larger discrepancies can be observed in profile comparisons at higher latitudes, in particular at 300 hPa during the peaks of either carbon uptake or release. These deviations can be up to 4 ppm and hint at misrepresentation of vertical transport. Comparisons with the GOSAT satellite are of comparable quality, with an r2 of 0.85, a mean bias μ of -0.06 ppm, and a standard deviation σ of 0.45 ppm. TES exhibits an r2 of 0.75, μ of 0.34 ppm, and σ of 1.13 ppm. For AIRS, we find an r2 of 0.37, μ of 1.11 ppm, and σ of 1.46 ppm, with latitude-dependent biases. For these comparisons at least 6, 20, and 50 atmospheric soundings have been averaged for GOSAT, TES, and AIRS

  12. Energy metabolism used as a tool to model the transfer of 14C and 3H in animals.

    PubMed

    Melintescu, A; Galeriu, D

    2010-11-01

    The transfer through the environment of (3)H and (14)C must be modelled differently than that of other radionuclides released from nuclear reactors because hydrogen and carbon enter straight into the life cycle. A solid understanding of the behaviour of (3)H and (14)C in the food chain is essential because (3)H may be released in large quantities from future thermonuclear reactors, and (14)C accumulates in the environment because of its long half-life. For the present study, the hypothesis that both (3)H and (14)C metabolism in mammals can be modelled based on the understanding of energy metabolism has been tested. Recently published results demonstrate that the loss rate of organically bound tritium and (14)C from tissues of laboratory and farm animals can be assessed based upon their specific metabolic rates and enthalpy of combustion; the same is true for human beings. The improved model presented here relates the dynamics of organically bound tritium and (14)C within organs to the whole body and has been expanded to account for the growth of ruminants. The improved model has been expanded and applied for (14)C transfer in wild mammals and has been modified to apply to birds. PMID:20532542

  13. Local variations in 14C - How is bomb-pulse dating of human tissues and cells affected?

    NASA Astrophysics Data System (ADS)

    Stenström, Kristina; Skog, Göran; Nilsson, Carl Magnus; Hellborg, Ragnar; Svegborn, Sigrid Leide; Georgiadou, Elisavet; Mattsson, Sören

    2010-04-01

    Atmospheric nuclear weapons testing in the late 1950s and early 1960s almost doubled the amount of 14C in the atmosphere. The resulting 14C "bomb-pulse" has been shown to provide useful age information in e.g. forensic and environmental sciences, biology and the geosciences. The technique is also currently being used for retrospective cell dating in man, in order to provide insight into the rate of formation of new cells in the human body. Bomb-pulse dating relies on precise measurements of the declining 14C concentration in atmospheric CO 2 collected at clean-air sites. However, it is not always recognized that the calculations can be complicated in some cases by significant local variations in the specific activity of 14C in carbon in the air and foodstuff. This paper presents investigations of local 14C variations in the vicinities of nuclear installations and laboratories using 14C. Levels of 14C in workers using this radioisotope are also discussed.

  14. 14-C-NAPHTHYL, 14-C-METHYL AND 14-C-CARBONYL CARBARYL DISTRIBUTION IN THE PREGNANT MOUSE AND RAT

    EPA Science Inventory

    The distribution of carbaryl labeled with 14C in the ring, methyl or carbonyl groups was determined in pregnant mice and rats. Three identical concurrent experiments were performed using each of the three radiolabeled compounds in each of the species so that the different moietie...

  15. Decay width measurements of excited states in 14C

    NASA Astrophysics Data System (ADS)

    Haigh, P.; Ashwood, N.; Bloxham, T.; Curtis, N.; Freer, M.; Price, D.; Ziman, V.; Bohlen, H.; Kokalova, T.; Schulz, C.; von Oertzen, W.; Weldon, C.; Catford, W.; Harlin, C.

    2008-05-01

    Various excited states in 14C, above the α-decay threshold, are believed to possess a geometric arrangement of three α-particles covalently bound by the two delocalised valence neutrons. The 12C(16O, 14O)14C* reaction was studied at a beam energy of 234 MeV, at the ISL facility at the Hahn-Meitner-Institut (HMI), Berlin. The 14O ejectile was detected by a Q3D spectrometer at forward angles. The energies and angles of the excited 14C recoil break-up fragments were measured in coincidence using a double sided silicon strip detector array comprised of four detectors at backwards angles. A complete kinematic reconstruction of the reaction was performed to reconstruct the 14C* → 10Be + α and 14C* → 13C + n decay channels and the branching ratios of these decays were calculated. Neutron emission was found to be favoured for the 12.96, 14.87, 16.72 and 18.6 MeV states. Evidence for α-decay was found for the 14.87, 18.6 and 21.4 MeV states; which are candidates for the three bodied molecular cluster structure of 14C.

  16. Tracking airborne CO2 mitigation and low cost transformation into valuable carbon nanotubes.

    PubMed

    Ren, Jiawen; Licht, Stuart

    2016-01-01

    Primary evidence of the direct uptake of atmospheric CO2 and direct transformation into carbon nanotubes, CNTs, is demonstrated through isotopic labeling, and provides a new high yield route to mitigate this greenhouse gas. CO2 is converted directly to CNTs and does not require pre-concentration of the airbone CO2. This C2CNT (CO2 to carbon nanotube) synthesis transforms CO2-gas dissolved in a 750 °C molten Li2CO3, by electrolysis, into O2-gas at a nickel electrode, and at a steel cathode into CNTs or carbon or nanofibers, CNFs. CNTs are synthesized at a 100-fold price reduction compared to conventional chemical vapour deposition, CVD, synthesis. The low cost conversion to a stable, value-added commodity incentivizes CO2 removal to mitigate climate change. The synthesis allows morphology control at the liquid/solid interface that is not available through conventional CVD synthesis at the gas/solid interface. Natural abundance (12)CO2 forms hollow CNTs, while equivalent synthetic conditions with heavier (13)CO2 favours closed core CNFs, as characterized by Raman, SEM and TEM. Production ease is demonstrated by the first synthesis of a pure (13)C multiwalled carbon nanofiber. PMID:27279594

  17. Tracking airborne CO2 mitigation and low cost transformation into valuable carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Ren, Jiawen; Licht, Stuart

    2016-06-01

    Primary evidence of the direct uptake of atmospheric CO2 and direct transformation into carbon nanotubes, CNTs, is demonstrated through isotopic labeling, and provides a new high yield route to mitigate this greenhouse gas. CO2 is converted directly to CNTs and does not require pre-concentration of the airbone CO2. This C2CNT (CO2 to carbon nanotube) synthesis transforms CO2-gas dissolved in a 750 °C molten Li2CO3, by electrolysis, into O2-gas at a nickel electrode, and at a steel cathode into CNTs or carbon or nanofibers, CNFs. CNTs are synthesized at a 100-fold price reduction compared to conventional chemical vapour deposition, CVD, synthesis. The low cost conversion to a stable, value-added commodity incentivizes CO2 removal to mitigate climate change. The synthesis allows morphology control at the liquid/solid interface that is not available through conventional CVD synthesis at the gas/solid interface. Natural abundance 12CO2 forms hollow CNTs, while equivalent synthetic conditions with heavier 13CO2 favours closed core CNFs, as characterized by Raman, SEM and TEM. Production ease is demonstrated by the first synthesis of a pure 13C multiwalled carbon nanofiber.

  18. Tracking airborne CO2 mitigation and low cost transformation into valuable carbon nanotubes

    PubMed Central

    Licht, Stuart

    2016-01-01

    Primary evidence of the direct uptake of atmospheric CO2 and direct transformation into carbon nanotubes, CNTs, is demonstrated through isotopic labeling, and provides a new high yield route to mitigate this greenhouse gas. CO2 is converted directly to CNTs and does not require pre-concentration of the airbone CO2. This C2CNT (CO2 to carbon nanotube) synthesis transforms CO2-gas dissolved in a 750 °C molten Li2CO3, by electrolysis, into O2-gas at a nickel electrode, and at a steel cathode into CNTs or carbon or nanofibers, CNFs. CNTs are synthesized at a 100-fold price reduction compared to conventional chemical vapour deposition, CVD, synthesis. The low cost conversion to a stable, value-added commodity incentivizes CO2 removal to mitigate climate change. The synthesis allows morphology control at the liquid/solid interface that is not available through conventional CVD synthesis at the gas/solid interface. Natural abundance 12CO2 forms hollow CNTs, while equivalent synthetic conditions with heavier 13CO2 favours closed core CNFs, as characterized by Raman, SEM and TEM. Production ease is demonstrated by the first synthesis of a pure 13C multiwalled carbon nanofiber. PMID:27279594

  19. The LLNL Accelerator Mass Spectrometry System for Biochemical 14C-Measurements

    SciTech Connect

    Ognibene, T J; Bench, G; Brown, T A; Vogel, J S

    2002-10-31

    We report on recent improvements made to our 1 MV accelerator mass spectrometry system that is dedicated to {sup 14}C quantification of biochemical samples. Increased vacuum pumping capacity near the high voltage terminal has resulted in a 2-fold reduction of system backgrounds to 0.04 amol {sup 14}C/mg carbon. Carbon ion transmission through the accelerator has also improved a few percent. We have also developed tritium measurement capability on this spectrometer. The {sup 3}H/{sup 1}H isotopic ratio of a milligram-sized processed tap water sample has been measured at 4 {+-} 1 x 10{sup -16} (430 {+-} 110 {micro}Bq/mg H). Measurement throughput for a typical biochemical {sup 3}H sample is estimated to be {approx}10 minutes/sample.

  20. Formation of Bound Residues during Microbial Degradation of [14C]Anthracene in Soil

    PubMed Central

    Kästner, M.; Streibich, S.; Beyrer, M.; Richnow, H. H.; Fritsche, W.

    1999-01-01

    Carbon partitioning and residue formation during microbial degradation of polycyclic aromatic hydrocarbons (PAH) in soil and soil-compost mixtures were examined by using [14C]anthracenes labeled at different positions. In native soil 43.8% of [9-14C]anthracene was mineralized by the autochthonous microflora and 45.4% was transformed into bound residues within 176 days. Addition of compost increased the metabolism (67.2% of the anthracene was mineralized) and decreased the residue formation (20.7% of the anthracene was transformed). Thus, the higher organic carbon content after compost was added did not increase the level of residue formation. [14C]anthracene labeled at position 1,2,3,4,4a,5a was metabolized more rapidly and resulted in formation of higher levels of residues (28.5%) by the soil-compost mixture than [14C]anthracene radiolabeled at position C-9 (20.7%). Two phases of residue formation were observed in the experiments. In the first phase the original compound was sequestered in the soil, as indicated by its limited extractability. In the second phase metabolites were incorporated into humic substances after microbial degradation of the PAH (biogenic residue formation). PAH metabolites undergo oxidative coupling to phenolic compounds to form nonhydrolyzable humic substance-like macromolecules. We found indications that monomeric educts are coupled by C-C- or either bonds. Hydrolyzable ester bonds or sorption of the parent compounds plays a minor role in residue formation. Moreover, experiments performed with 14CO2 revealed that residues may arise from CO2 in the soil in amounts typical for anthracene biodegradation. The extent of residue formation depends on the metabolic capacity of the soil microflora and the characteristics of the soil. The position of the 14C label is another important factor which controls mineralization and residue formation from metabolized compounds. PMID:10223966

  1. Formation of bound residues during microbial degradation of [{sup 14}C]anthracene in soil

    SciTech Connect

    Kaestner, M.; Streibich, S.; Beyrer, M.; Fritsche, W.; Richnow, H.H.

    1999-05-01

    Carbon partitioning and residue formation during microbial degradation of polycyclic aromatic hydrocarbons (PAH) in soil and soil-compost mixtures were examined by using [{sup 14}C]anthracenes labeled at different positions. In native soil 43.8% of [9-{sup 14}C]anthracene was mineralized by the autochthonous microflora and 45.4% was transformed into bound residues within 176 days. Addition of compost increased the metabolism and decreased the residue formation (20.7% of the anthracene was transformed). Thus, the higher organic carbon content after compost was added did not increase the level of residue formation. [{sup 14}C]anthracene labeled at position 1,2,3,4,4a,5a was metabolized more rapidly and resulted in formation of higher levels of residues (28.5%) by the soil-compost mixture than [{sup 14}C]anthracene radiolabeled at position C-9 (20.7%). Two phases of residue formation were observed in the experiments. In the first phase the original compound was sequestered in the soil, as indicated by its limited extractability. In the second phase metabolites were incorporated into humic substances after microbial degradation of the PAH (biogenic residue formation). PAH metabolites undergo oxidative coupling to phenolic compounds to form nonhydrolyzable humic substance-like macromolecules. The authors found indications that monomeric educts are coupled by C-C- or either bonds. Hydrolyzable ester bonds or sorption of the parent compounds plays a minor role in residue formation. Moreover, experiments performed with {sup 14}CO{sub 2} revealed that residues may arise from CO{sub 2} in the soil in amounts typical for anthracene biodegradation. The extent of residue formation depends on the metabolic capacity of the soil microflora and the characteristics of the soil. The position of the {sup 14}C label is another important factor which controls mineralization and residue formation from metabolized compounds.

  2. Airborne remote sensing of photosynthetic light use efficiency and carbon uptake along an Arctic transect in Finland

    NASA Astrophysics Data System (ADS)

    Atherton, J.; Hill, T. C.; Prieto-Blanco, A.; Wade, T.; Clement, R.; Moncrieff, J.; Williams, M. D.; Disney, M.; Nichol, C. J.

    2009-12-01

    It is critical to understand the dynamics of ecosystem carbon uptake through seasonal changes and in response to environmental drivers. In this study we utilised aircraft based remote sensing and CO2/H2O flux monitoring systems to quantify changes in photosynthesis along an Arctic transect. The University of Edinburgh's (UK) research aircraft (a Diamond HK 36 TTC-ECO Dimona) was deployed in the Arctic during summer 2008 to carry out a series of transect-flights over a birch-mire mosaic site near Kevo, Finland as part of the Arctic Biosphere Atmosphere Coupling at Multiple Scales (ABACUS) project. The aircraft is equipped with automated dual field-of-view (hyperspectral) radiometers and CO2/H2O flux and meteorological instrumentation. Vegetation indices known to be related to photosynthetic light use efficiency (LUE), including the well established Photochemical Reflectance Index (PRI) and Solar-induced Fluorescence (SiF) as well as the Normalized Difference Vegetation Index (NDVI) were calculated from the spectral data and matched in space to the CO2 flux measurements. We explored spatial relationships between NDVI and CO2 flux, LUE (CO2 flux / Absorbed Photosynthetically Active Radiation) and PRI and finally SiF (calculated using the Fraunhofer infilling method) and relevant environmental drivers. Our results highlight the unique ability of an airborne platform to quantify ecosystem physiology across a landscape and demonstrate how such measurements can bridge the spatial gap between ground and satellite-based observations.

  3. Biosynthesis of riboflavin. Enzymatic formation of the xylene moiety from [14C]ribulose 5-phosphate.

    PubMed

    Nielsen, P; Neuberger, G; Floss, H G; Bacher, A

    1984-02-14

    We have studied the enzymatic formation of the xylene ring of riboflavin using cell extracts from the flavinogenic yeast Candida guilliermondii. 5-Amino-6-ribitylamino-2,4(1H,3H)-pyrimidinedione or its 5'-phosphate could serve as substrates. In addition, a pentose phosphate or pentulose phosphate was required. Experiments with [14C]ribulose 5-phosphate gave evidence for the incorporation of the ribulose carbon atoms except C-4 into the xylene ring of the vitamin. PMID:6546684

  4. Synthesis of 2-(methylsulfonyl)-5-(4-(methylsulfonyl) phenyl)-4-phenyl-1H-[5-(14) C]imidazole, a selective COX-2 inhibitor, via asymmetrical benzoins.

    PubMed

    Shirvani, Gholamhossein; Shockravi, Abbas; Amini, Mohsen; Saemian, Nader

    2016-04-01

    4,5-Diarylimidazoles labeled with carbon-14 in the 5-position of the imidazole ring were prepared as a part of three-step sequence from 2-hydroxy-1-(4-(methylthio)phenyl)-2-phenyl[1-(14) C]ethanone as a key synthetic intermediate which has been synthesized from potassium [(14) C]cyanide. PMID:26916231

  5. Enzymatic aryl-O-methyl-/sup 14/C labeling of model lignin monomers

    SciTech Connect

    Frazer, A.C.; Bossert, I.; Young, L.Y.

    1986-01-01

    Aryl-O-methyl ethers are abundant in aerobic and anaerobic environments. In particular, lignin is composed of units of this type. Lignin monomers specifically radiolabeled in methoxy, side chain, and ring carbons have been synthesized by chemical procedures and are important in studies of lignin synthesis and degradation, humus formation, and microbial O-demethylation. In this paper attention is drawn to an enzymatic procedure for preparing O-methyl-/sup 14/C-labeled aromatic lignin monomers which has not previously been exploited in microbial ecology and physiology studies and which has several advantages compared with chemical synthesis procedures. O-(methyl-/sup 14/C)vanillic and O-(methyl-/sup 14/C)ferulic acids were prepared with S-(methyl-/sup 14/C)adenosyl-L-methionine as the methyl donor, using commercially obtained porcine liver catechol-O-methyltransferase (EC 2.1.1.6). The specific activity of the methylated products was the same as that of the methyl donor, a maximum of about 58 ..mu..Ci/..mu..mol, and the yields were 42% (vanillate) and 35% (ferulate). Thus lignin monomers are readily prepared as O-methylated products of the catechol-O-methyltransferase reaction and, with this enzyme method of preparation, would be more widely available than labeled compounds which require chemical synthesis.

  6. Test of AMS 14C dating of pollen concentrates using tephrochronology

    NASA Astrophysics Data System (ADS)

    Newnham, Rewi M.; Vandergoes, Marcus J.; Garnett, Mark H.; Lowe, David J.; Prior, Christine; Almond, Peter C.

    2007-01-01

    Previous attempts to radiocarbon date sediments >10 kyr from the high rainfall region of Westland, New Zealand, a critical location for investigation of interhemispheric patterns of climate change, have been problematic. This study, building on recent work by Vandergoes and Prior ([2003]), shows that AMS 14C dating of pollen concentrates has potential to provide more reliable ages than other sediment constituents, including plant macrofossils. The method was applied to sediments from three sites containing the 22.6k 14C yr Kawakawa Tephra, which provided an independent test of the 14C ages. Although some minor laboratory contamination was detected in tests on background standards, the modelled relationship between sample mass and measured 14C content permitted an appropriate correction to be determined. Improved pollen concentrations derived by density separation between 1.4 and 1.2 specific gravity and sieving in the range 10-50 m provided either older ages than other fractions of the same sample or, where in situ contamination was not evident, equivalent ages. Differences in degree of in situ contamination between depositional environments indicated that, in Westland, lake sites may be less susceptible to contamination by younger carbon than peat sites, where this process may be facilitated by root penetration into underlying sediments. Copyright

  7. Assessment of EDGAR emission inventory using carbon monoxide (CO) MOZAIC/IAGOS airborne measurements over Europe

    NASA Astrophysics Data System (ADS)

    Boschetti, Fabio; Chen, Huilin; Marshall, Julia; Gerbig, Christoph; Thouret, Valerie; Nedelec, Philippe

    2014-05-01

    The main advantage of using airborne data is their ability to collect mole fraction measurements covering most of the troposphere. However, mainly due to the cost of rental aircraft, the number of flights is usually quite limited, with direct consequences on measurement availability. Making use of commercial airliners, the MOZAIC/IAGOS program provides CO mole fraction measurements on a regular basis, avoiding this disadvantage. In this study MOZAIC/IAGOS measurements have been used together with a Lagrangian particle dispersion model (STILT) to evaluate the representativeness of the EDGAR version-4.2 emission inventory at 3 different locations (Frankfurt, Paris and Vienna) for the time frame 2004-2011. We make use of the concept of the mixed layer, where signals resulting from CO emissions are reasonable well mixed, and lead to an enhancement of CO within the mixed layer. We investigate the CO enhancement relative to values in the free troposphere (specifically at two km above the mixing height), for both the upper and lower half of the mixed layer. The hypothesis is that the CO enhancement in the upper half of the mixed layer is more representative for larger spatial scales, as the vertical distance to the surface and its emission sources is increased compared to that of the lower half. CO enhancements calculated from CO mole fractions modeled by STILT coupled with the emission inventory at 10 km horizontal resolution are compared with the corresponding values from observed CO mole fractions for both the lower and the upper half of the mixed layer. The transport model domain is roughly coincident with the EU territory; simulations show that most of the Lagrangian particles exit the domain to the north and to the west. On these sides of the domain, boundaries are represented by oceans, characterized by small CO vertical gradients. Modeled global CO fields from the MACC project will be used in this study as lateral boundary conditions. We found that the simulation

  8. Variability in 14C contents of soil organic matter at the plot and regional scale across climatic and geologic gradients

    NASA Astrophysics Data System (ADS)

    van der Voort, Tessa Sophia; Hagedorn, Frank; McIntyre, Cameron; Zell, Claudia; Walthert, Lorenz; Schleppi, Patrick; Feng, Xiaojuan; Eglinton, Timothy Ian

    2016-06-01

    Soil organic matter (SOM) forms the largest terrestrial pool of carbon outside of sedimentary rocks. Radiocarbon is a powerful tool for assessing soil organic matter dynamics. However, due to the nature of the measurement, extensive 14C studies of soil systems remain relatively rare. In particular, information on the extent of spatial and temporal variability in 14C contents of soils is limited, yet this information is crucial for establishing the range of baseline properties and for detecting potential modifications to the SOM pool. This study describes a comprehensive approach to explore heterogeneity in bulk SOM 14C in Swiss forest soils that encompass diverse landscapes and climates. We examine spatial variability in soil organic carbon (SOC) 14C, SOC content and C : N ratios over both regional climatic and geologic gradients, on the watershed- and plot-scale and within soil profiles. Results reveal (1) a relatively uniform radiocarbon signal across climatic and geologic gradients in Swiss forest topsoils (0-5 cm, Δ14C = 130 ± 28.6, n = 12 sites), (2) similar radiocarbon trends with soil depth despite dissimilar environmental conditions, and (3) micro-topography dependent, plot-scale variability that is similar in magnitude to regional-scale variability (e.g., Gleysol, 0-5 cm, Δ14C 126 ± 35.2, n = 8 adjacent plots of 10 × 10 m). Statistical analyses have additionally shown that Δ14C signature in the topsoil is not significantly correlated to climatic parameters (precipitation, elevation, primary production) except mean annual temperature at 0-5 cm. These observations have important consequences for SOM carbon stability modelling assumptions, as well as for the understanding of controls on past and current soil carbon dynamics.

  9. Double-pulse 2-μm integrated path differential absorption lidar airborne validation for atmospheric carbon dioxide measurement.

    PubMed

    Refaat, Tamer F; Singh, Upendra N; Yu, Jirong; Petros, Mulugeta; Remus, Ruben; Ismail, Syed

    2016-05-20

    Field experiments were conducted to test and evaluate the initial atmospheric carbon dioxide (CO2) measurement capability of airborne, high-energy, double-pulsed, 2-μm integrated path differential absorption (IPDA) lidar. This IPDA was designed, integrated, and operated at the NASA Langley Research Center on-board the NASA B-200 aircraft. The IPDA was tuned to the CO2 strong absorption line at 2050.9670 nm, which is the optimum for lower tropospheric weighted column measurements. Flights were conducted over land and ocean under different conditions. The first validation experiments of the IPDA for atmospheric CO2 remote sensing, focusing on low surface reflectivity oceanic surface returns during full day background conditions, are presented. In these experiments, the IPDA measurements were validated by comparison to airborne flask air-sampling measurements conducted by the NOAA Earth System Research Laboratory. IPDA performance modeling was conducted to evaluate measurement sensitivity and bias errors. The IPDA signals and their variation with altitude compare well with predicted model results. In addition, off-off-line testing was conducted, with fixed instrument settings, to evaluate the IPDA systematic and random errors. Analysis shows an altitude-independent differential optical depth offset of 0.0769. Optical depth measurement uncertainty of 0.0918 compares well with the predicted value of 0.0761. IPDA CO2 column measurement compares well with model-driven, near-simultaneous air-sampling measurements from the NOAA aircraft at different altitudes. With a 10-s shot average, CO2 differential optical depth measurement of 1.0054±0.0103 was retrieved from a 6-km altitude and a 4-GHz on-line operation. As compared to CO2 weighted-average column dry-air volume mixing ratio of 404.08 ppm, derived from air sampling, IPDA measurement resulted in a value of 405.22±4.15  ppm with 1.02% uncertainty and

  10. Airborne radioactivity survey of parts of Baggs SW and Baggs SE quadrangles, Carbon and Sweetwater counties, Wyoming

    USGS Publications Warehouse

    Henderson, J.R.

    1954-01-01

    The accompanying map shows the results of an airborne radioactivity survey in 151 square miles of Baggs SW and Baggs SE quadrangles, Wyoming. This area is part of a larger survey made in southern Carbon and Sweetwater counties by the U.S. Geological Survey, November 9-24, 1953. The work was undertaken as part of a cooperative program with the U.S. Atomic Energy Commission. The survey was made with scintillation detection equipment mounted in a C-47 aircraft and consisted of parallel east-west flight lines spaced at quarter mile intervals, flown approximately 500 feet above the ground. Aerial photographs were used for pilot guidance, and the flight path of the aircraft was recorded by a gyrostabilized, continuous-strip-film camera. The distance of the aircraft from the ground was measured with a continuously recording radio altimeter. The width of the zone on the ground form which the anomalous radiation is measured at the nominal 500 foot flight altitude varied with the areal extent and the intensity of radioactivity of the source. For strong sources of radioactivity the width of the zone may be as much as 1,400 feet. Thus, quarter mile spacing of the flight lines would be adequate to detect anomalies from strong sources of radioactivity; however, small areas of considerable radioactivity midway between flight lines may not be noted. The approximate locations of twelve radioactivity anomalies are shown on the accompanying map. The plotted position of the anomalies may be in error by as much as a quarter mile owing to the errors in available base maps or to the existence of areas on the base maps up to several square miles in which it is impossible to find and plot recognizable landmarks. The present technique of airborne radioactivity measurement does not permit distinguishing between activity due to thorium and that due to uranium. An anomaly, therefore, may represent radioactivity due entirely to one or to a combination of these elements. The radioactivity

  11. Characterization of 14C in Swedish light water reactors.

    PubMed

    Magnusson, Asa; Aronsson, Per-Olof; Lundgren, Klas; Stenström, Kristina

    2008-08-01

    This paper presents the results of a 4-y investigation of 14C in different waste streams of both boiling water reactors (BWRs) and pressurized water reactors (PWRs). Due to the potential impact of 14C on human health, minimizing waste and releases from the nuclear power industry is of considerable interest. The experimental data and conclusions may be implemented to select appropriate waste management strategies and practices at reactor units and disposal facilities. Organic and inorganic 14C in spent ion exchange resins, process water systems, ejector off-gas and replaced steam generator tubes were analyzed using a recently developed extraction method. Separate analysis of the chemical species is of importance in order to model and predict the fate of 14C within process systems as well as in dose calculations for disposal facilities. By combining the results of this investigation with newly calculated production rates, mass balance assessments were made of the 14C originating from production in the coolant. Of the 14C formed in the coolant of BWRs, 0.6-0.8% was found to be accumulated in the ion exchange resins (core-specific production rate in the coolant of a 2,500 MWth BWR calculated to be 580 GBq GW(e)(-1) y(-1)). The corresponding value for PWRs was 6-10% (production rate in a 2,775 MWth PWR calculated to be 350 GBq GW(e)(-1) y(-1)). The 14C released with liquid discharges was found to be insignificant, constituting less than 0.5% of the production in the coolant. The stack releases, routinely measured at the power plants, were found to correspond to 60-155% of the calculated coolant production, with large variations between the BWR units. PMID:18617793

  12. Measuring the 14C content in liquid scintillators

    NASA Astrophysics Data System (ADS)

    Enqvist, T.; Barabanov, I. R.; Bezrukov, L. B.; Gangapshev, A. M.; Gavrilyuk, Y. M.; Grishina, V. Yu; Gurentsov, V. I.; Hissa, J.; Joutsenvaara, J.; Kazalov, V. V.; Krokhaleva, S.; Kutuniva, J.; Kuusiniemi, P.; Kuzminov, V. V.; Kurlovich, A. S.; Loo, K.; Lubsandorzhiev, B. K.; Lubsandorzhiev, S.; Morgalyuk, V. P.; Novikova, G. Y.; Pshukov, A. M.; Sinev, V. V.; Słupecki, M.; Trzaska, W. H.; Umerov, Sh I.; Veresnikova, A. V.; Virkajärvi, A.; Yanovich, Y. A.; Zavarzina, V. P.

    2016-05-01

    We are going to perform a series of measurements where the 14C/12 C ratio will be measured from several liquid scintillator samples with a dedicated setup. The setup is designed with the aim of measuring ratios smaller than 10-18. Measurements take place in two underground laboratories: in the Baksan Neutrino Observatory, Russia and in the Pyhäsalmi mine, Finland. In Baksan the measurements started in 2015 and in Pyhäsalmi they start in the beginning of 2015. In order to fully understand the operation of the setup and its background contributions a development of simulation packages has also been started. Low-energy neutrino detection with a liquid scintillator requires that the intrinsic 14C content in the liquid is extremely low. In the Borexino CTF detector at Gran Sasso, Italy the 14C/12C ratio of 2 × 10-18 has been achieved being the lowest 14C concentration ever measured. In principle, the older the oil or gas source that the liquid scintillator is derived of and the deeper it situates, the smaller the 14C/12C ratio is supposed to be. This, however, is not generally the case, and the ratio is probably determined by the U and Th content of the local environment.

  13. Implications of ammonia emissions from post-combustion carbon capture for airborne particulate matter.

    PubMed

    Heo, Jinhyok; McCoy, Sean T; Adams, Peter J

    2015-04-21

    Amine scrubbing, a mature post-combustion carbon capture and storage (CCS) technology, could increase ambient concentrations of fine particulate matter (PM2.5) due to its ammonia emissions. To capture 2.0 Gt CO2/year, for example, it could emit 32 Gg NH3/year in the United States given current design targets or 15 times higher (480 Gg NH3/year) at rates typical of current pilot plants. Employing a chemical transport model, we found that the latter emission rate would cause an increase of 2.0 μg PM2.5/m(3) in nonattainment areas during wintertime, which would be troublesome for PM2.5-burdened areas, and much lower increases during other seasons. Wintertime PM2.5 increases in nonattainment areas were fairly linear at a rate of 3.4 μg PM2.5/m(3) per 1 Tg NH3, allowing these results to be applied to other CCS emissions scenarios. The PM2.5 impacts are modestly uncertain (±20%) depending on future emissions of SO2, NOx, and NH3. The public health costs of CCS NH3 emissions were valued at $31-68 per tonne CO2 captured, comparable to the social cost of carbon itself. Because the costs of solvent loss to CCS operators are lower than the social costs of CCS ammonia, there is a regulatory interest to limit ammonia emissions from CCS. PMID:25811231

  14. Does the 14C method estimate net photosynthesis? II. Implications from cyclostat studies of marine phytoplankton

    NASA Astrophysics Data System (ADS)

    Pei, Shaofeng; Laws, Edward A.

    2014-09-01

    Two species of marine phytoplankton, Isochrysis galbana and Chlorella kessleri, were grown in a continuous culture system on a 12-h:12-h light:dark cycle of illumination under nitrate-limited growth conditions. At growth rates of ~1 d-1, production rates estimated from 14C uptake were not significantly different from production rates estimated from changes in particulate organic carbon (POC) and total organic carbon (TOC). At growth rates of ~0.35 d-1, however, production rates based on uptake of 14C significantly (p<0.05) overestimated production rates based on changes in POC and TOC in all cases for C. kessleri and after 24 h for I. galbana. The ratio of production based on 14C uptake to production based on changes in POC and TOC concentrations was in all cases higher after 24 h than after 12 h. The extent of overestimation after a 24-h incubation at ~0.35 d-1 was about 23 and 40% in the cases of I. galbana and C. kessleri, respectively. Dark respiration rates estimated from changes in 14C activity during the dark period were lower than the rates estimated from changes of POC and TOC concentrations during the 12 h of darkness because only about 73% of the carbon respired during the dark period had been fixed during the previous 12-h photoperiod. The fact that the 14C method tends to overestimate net carbon assimilation by a greater percentage at low growth rates than at high growth rates probably reflects the greater efficiency of intracellular recycling of respired CO2 at high growth rates. The fact that the extent of overestimation is greater when cells are grown on a light:dark cycle probably reflects the fact that not all carbon respired in the dark was fixed during the previous photoperiod and that intracellular recycling of respired CO2 during the photoperiod is inefficient during some phases of the synchronized growth that tends to be entrained by light:dark cycles.

  15. The search for cluster structure in 14C with the prototype AT-TPC

    NASA Astrophysics Data System (ADS)

    Fritsch, Adam Louis

    Certain light nuclei are known to have inherent cluster structuring, and the nature of the triple-alpha structure of carbon isotopes is a subject of active discussion in nuclear physics. Clustering in neutron-rich nuclei is of particular interest as such work could shed light on how neutrons affect alpha clustering, making 14C a logical candidate for such a study. Cluster structure in 14C was investigated at the University of Notre Dame with the prototype Active Target-Time Projection Chamber (AT-TPC). A 38.2 MeV secondary beam of 10Be was incident on an active target volume containing He:CO2 90:10 gas at 1 atm, in which trajectories of beam particles and reaction products were measured using the tracking capabilities of the prototype AT-TPC. Angular correlations of 10Be and alpha particles were used to reconstruct kinematics of scattering. Excitation functions and angular distributions were measured in both elastic and inelastic channels, which unraveled a number of resonances in 14C. Spin-parity assignments have been made for the elastic resonances by R-matrix analysis. Evidence of a positive-parity rotational band has been indicated by the 14C resonances. The proposed level scheme and the strong resonance strength observed in the inelastic channel are in line with the prediction by the antisymmetrized molecular dynamics (AMD) method indicating linear-chain structure in 14C. The results also demonstrate unique and powerful potentials of active-target technology in radioactive-beam experiments and are an important step toward the construction of the full-scale AT-TPC for the ReA3 facility at NSCL.

  16. Reconciling Change in Oi-Horizon 14C With Mass Loss for an Oak Forest

    SciTech Connect

    Hanson, P J; Swanston, C W; Garten, Jr., C T; Todd, D E; Trumbore, S E

    2005-06-27

    First-year litter decomposition was estimated for an upland-oak forest ecosystem using enrichment or dilution of the {sup 14}C-signature of the Oi-horizon. These isotopically-based mass-loss estimates were contrasted with measured mass-loss rates from past litterbag studies. Mass-loss derived from changes in the {sup 14}C-signature of the Oi-horizon suggested mean mass loss over 9 months of 45% which was higher than the corresponding 9-month rate extrapolated from litterbag studies ({approx}35%). Greater mass loss was expected from the isotopic approach because litterbags are known to limit mass loss processes driven by soil macrofauna (e.g., fragmentation and comminution). Although the {sup 14}C-isotope approach offers the advantage of being a non-invasive method, it exhibited high variability that undermined its utility as an alternative to routine litterbag mass loss methods. However, the {sup 14}C approach measures the residence time of C in the leaf litter, rather than the time it takes for leaves to disappear; hence radiocarbon measures are subject to C immobilization and recycling in the microbial pool, and do not necessarily reflect results from litterbag mass loss. The commonly applied two-compartment isotopic mixing model was appropriate for estimating decomposition from isotopic enrichment of near-background soils, but it produced divergent results for isotopic dilution of a multi-layered system with litter cohorts having independent {sup 14}C-signatures. This discrepancy suggests that cohort-based models are needed to adequately capture the complex processes involved in carbon transport associated with litter mass-loss. Such models will be crucial for predicting intra- and interannual differences in organic horizon decomposition driven by scenarios of climatic change.

  17. 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. PMID:26555367

  18. What do we learn from EC (black carbon), OC and their Isotope Measurements in Fine Airborne PM over Canada?

    NASA Astrophysics Data System (ADS)

    Huang, L.; Zhang, W.; Sharma, S.; Brook, J.; Chan, T.; Leaitch, R.

    2009-04-01

    Elemental carbon and organic carbon (EC & OC) components in fine airborne carbonaceous particulate matter (PM) are major air pollutants existing in urban, rural and remote environments as well as key players in climate change (via radiative forcing). It is known that both EC (also called as black carbon or soot) and OC are released from various emission sources (e.g., fossil fuel combustion, biomass burning) and OC is also produced in the atmosphere through photochemical oxidations from gas phase organics. Tracking their spatial (e.g., from urban to rural to background air or latitudinal) and temporal (e.g. seasonal and inter-annual) distributions will provide valuable information to constraining emission sources and atmospheric transport/transformation mechanisms as well as to assessing effectiveness of mitigation for these pollutants. Sources/processes detecting and attributing are key aspects in both air quality and climate change research. Isotope measurements, as independent tools, can provide valuable insight to constrain those aspects. Duo to its inert nature, it is expected that the ^13C of EC won't be changed after emitting to the atmosphere, reflecting the signature of source, whereas the ^13Cof OC will have a various degree of changes through photochemical processes, depending on the history of the air mass. Therefore, an isotopic profile of ^13C in carbon components released at different temperature ranges can provide useful insight to the emission sources and formation processes in ambient PM. Quartz filter samples were collected at the five sites over Canada, from Toronto (a typical urban site), Egbert (a rural site, ~ 80 km northwest of Toronto), to Fraserdale, and Berm-TT (both are continental boreal forest sites), to Alert (an Arctic baseline site). EC and OC concentrations for those samples collected during the period (2006 - 2007) were determined using a thermal method (Totoal_900_EnCan) developed in Toronto lab at Environment Canada, which is

  19. Rapid, high-resolution 14C chronology of ooids

    NASA Astrophysics Data System (ADS)

    Beaupré, Steven R.; Roberts, Mark L.; Burton, Joshua R.; Summons, Roger E.

    2015-06-01

    Ooids are small, spherical to ellipsoidal grains composed of concentric layers of CaCO3 that could potentially serve as biogeochemical records of the environments in which they grew. Such records, however, must be placed in the proper temporal context. Therefore, we developed a novel acidification system and employed an accelerator mass spectrometer (AMS) with a gas accepting ion source to obtain radiocarbon (14C) chronologies extending radially through ooids within one 8-h workday. The method was applied to ooids from Highborne Cay, Bahamas and Shark Bay, Australia, yielding reproducible 14C chronologies, as well as constraints on the rates and durations of ooid growth and independent estimates of local 14C reservoir ages.

  20. The synthesis of [(14) C]AZD5122. Incorporation of an IV (14) C-microtracer dose into a first in human study to determine the absolute oral bioavailability of AZD5122.

    PubMed

    Hickey, Michael J; Allen, Paul H; Kingston, Lee P; Wilkinson, David J

    2016-05-30

    AZD5122, N-(2-(2,3-difluorobenzylthio)-6-((2R,3R)-3,4-dihydroxybutan-2-ylamino)pyrimidin-4-yl)azetidine-1-sulfonamide was under investigation as a potential chemokine receptor CXCR2 antagonist for the treatment for inflammatory diseases. To gain a better understanding of the human pharmacokinetic profile, an exploratory phase I IV microtracer study was conducted using carbon-14 radiolabelled AZD5122. [(14) C]AZD5122 was carbon-14 labelled in the pyrimidine ring in five steps in an overall radiochemical yield of 19% from [(14) C]thiourea. The absolute oral bioavailability of AZD5122 was assessed in healthy subjects by an oral administration of AZD5122, followed by a concomitant intravenous [(14) C]AZD5122 microdose. PMID:27169760

  1. Study of Rainbow Scattering in 16O + 14C System

    NASA Astrophysics Data System (ADS)

    Demyanova, A. S.; Glukhov, Yu. A.; Ogloblin, A. A.; Trzaska, W.; Bohlen, H. G.; Oertzen, W. Von; Goncharov, S. A.; Izadpanakh, A.; Maslov, V. A.; Penionzhkevich, Yu. E.; Sobolev, Yu. G.; Khlebnikov, S. V.; Tyurin, G. P.

    2005-09-01

    We carried out new measurements of the 16O+14C differential cross-sections at the 16O energy 281 MeV in the large angles interval at the Jyvaskyla University cyclotron and at the smallest angles at the cyclotron of Hahn-Meitner institute. The results of the experiment showed that clear rainbow structure in 16O + 14C scattering really takes place. The observed position of the main Airy minimum predicted but not observed in previous measurements fits well to the empirical systematization "angle - inverse energy", obtained for the system 16O + 12C.

  2. 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.

  3. Search for exotic cluster configurations in 14C nucleus

    NASA Astrophysics Data System (ADS)

    Korotkova, L. Yu; Chernyshev, B. A.; Gurov, Yu B.; Karpuhin, V. S.; Lapushkin, S. V.; Pritula, R. V.; Schurenkova, T. D.

    2016-02-01

    The analysis of 2-dimentional Dalitz’ diagram, measured in 14C(π-, pd)X reaction, allowed to distinguish the pion absorption by p intranuclear cluster and to obtain an indication on the existence of 3p + 11Li configuration in 14C nucleus. Highly excited states of 12,13Be isotopes were found with the energy of Ex ≈ 30 MeV for the first time. It was shown that these states decay as follows 12Be*→p + 11Li and 13Be*→d + 11Li.

  4. Origin of the Anomalous Long Lifetime of 14C

    SciTech Connect

    Dean, David Jarvis; Nam, Hai Ah; Maris, Pieter; Vary, J. P.; Navratil, Petr; Ormand, W. Erich

    2011-01-01

    We report the microscopic origins of the anomalously suppressed beta decay of 14C to 14N using the ab initio no-core shell model with the Hamiltonian from the chiral effective field theory including three-nucleon force terms. The three-nucleon force induces unexpectedly large cancellations within the p shell between contributions to beta decay, which reduce the traditionally large contributions from the nucleon-nucleon interactions by an order of magnitude, leading to the long lifetime of 14C.

  5. Role of biotransformation, sorption and mineralization of (14)C-labelled sulfamethoxazole under different redox conditions.

    PubMed

    Alvarino, T; Nastold, P; Suarez, S; Omil, F; Corvini, P F X; Bouju, H

    2016-01-15

    (14)C-sulfamethoxazole biotransformation, sorption and mineralization was studied with heterotrophic and autotrophic biomass under aerobic and anoxic conditions, as well as with anaerobic biomass. The (14)C-radiolabelled residues distribution in the solid, liquid and gas phases was closely monitored along a total incubation time of 190 h. Biotransformation was the main removal mechanism, mineralization and sorption remaining below 5% in all the cases, although the presence of a carbon source exerted a positive effect on the mineralization rate by the aerobic heterotrophic bacteria. In fact, an influence of the type of primary substrate and the redox potential was observed in all cases on the biotransformation and mineralization rates, since an enhancement of the removal rate was observed when an external carbon source was used as a primary substrate under aerobic conditions, while a negligible effect was observed under nitrifying conditions. In the liquid phases collected from all assays, up to three additional peaks corresponding to (14)C-radiolabelled residues were detected. The highest concentration was observed under anaerobic conditions, where two radioactive metabolites were detected representing each around 15% of the total applied radioactivity after 180 h incubation. One of the metabolites detected under anoxic and anaerobic conditions, is probably resulting from ring cleavage of the isoxazole ring. PMID:26546766

  6. 14C and {Th}/{U} dating of Pleistocene and Holocene stromatolites from East African paleolakes

    NASA Astrophysics Data System (ADS)

    Hillaire-Marcel, Claude; Carro, Odette; Casanova, Joel

    1986-05-01

    During recent humid episodes, stromatolites were built along paleolake margins, some 60 m above the modern water level of Lakes Natron and Magadi (southern Gregory Rift Valley). Three generations of stromatolites are observed, the more recent ones frequently covering pebbles and boulders eroded from the older ones. The youngest one yielded 14C ages ranging from approximately 12,000 to 10,000 yr B.P. Their δ 13C values (≥2.6%) suggest isotopic equilibrium between the paleolake total inorganic dissolved carbon and the atmospheric CO 2, thereby lending credence to the reliability of the 14C. An initial {230Th }/{232Th } ratio in the detrital component was determined by {Th}/{U} measurements on the 14C dated stromatolites. Using this value a {230Th }/{234U } chronology for the older stromatolites was calculated. Ages of ≥240,000 and 135,000 ± 10,000 yr were obtained for the first and second generations, respectively. A humid episode apparently characterized eastern Africa during each glacial-interglacial transition. 18O and 13C measurements on stromatolites, when compared to values on modern waters and carbonates, provide paleohydrological information. Long residence time of the paleolake waters and less seasonally contrasted regimes are inferred.

  7. A procedure for batch separation of sup 14 C-hexose from sup 14 C-sucrose

    SciTech Connect

    Tarpley, L.; Vietor, D.M. )

    1991-05-01

    This presentation describes a method for separating {sup 14}C-hexose from {sup 14}C-sucrose in extracts of plant tissue. Portions of ethanol extracts are treated with activated charcoal in microcentrifuge tubes. Aliquots are removed, ethanol evaporated and replaced with reaction mixture that phosphorylates hexose (HEPPS, K{sub 2}HPO{sub 4}, Mg(C{sub 2}H{sub 3}O{sub 2}){sub 2}, ovalbumen, Na{sub 2}ATP, yeast hexokinase). After a time course, the hexokinase reaction is stopped (slowed considerably) to minimize effects of contamination enzyme activities. The stopping agent used is lyxose, a nonphosphorylable analogue of glucose. The strong anionic charge of phosphate introduced through the hexokinase action results in binding (> 95%) of hexose-phosphate to anion-exchange resin. Sucrose remains unbound (> 95%) in solution. This batch ion-exchange is performed in microcentrifuge tubes to allow many samples to be processed simultaneously. Recovery of radiolabel in extracts is complete (99%), and determinations are repeatable (cv = 23%). This method for routinely separating and quantifying {sup 14}C-hexose and {sup 14}C-sucrose in plant tissue extracts can contribute to the economy and feasibility of studies of {sup 14}C-photoassimilate partitioning to soluble sugars within and among plant tissues.

  8. Spatial patterns of vegetation biomass and soil organic carbon acquired from airborne lidar and hyperspectral imagery at Reynolds Creek Critical Zone Observatory

    NASA Astrophysics Data System (ADS)

    Will, R. M.; Li, A.; Glenn, N. F.; Benner, S. G.; Spaete, L.; Ilangakoon, N. T.

    2015-12-01

    Soil organic carbon distribution and the factors influencing this distribution are important for understanding carbon stores, vegetation dynamics, and the overall carbon cycle. Linking soil organic carbon (SOC) with aboveground vegetation biomass may provide a method to better understand SOC distribution in semiarid ecosystems. The Reynolds Creek Critical Zone Observatory (RC CZO) in Idaho, USA, is approximately 240 square kilometers and is situated in the semiarid Great Basin of the sagebrush-steppe ecosystem. Full waveform airborne lidar data and Next-Generation Airborne Visible/Infrared Imaging Spectrometer (AVIRIS-ng) collected in 2014 across the RC CZO are used to map vegetation biomass and SOC and then explore the relationships between them. Vegetation biomass is estimated by identifying vegetation species, and quantifying distribution and structure with lidar and integrating the field-measured biomass. Spectral data from AVIRIS-ng are used to differentiate non-photosynthetic vegetation (NPV) and soil, which are commonly confused in semiarid ecosystems. The information from lidar and AVIRIS-ng are then used to predict SOC by partial least squares regression (PLSR). An uncertainty analysis is provided, demonstrating the applicability of these approaches to improving our understanding of the distribution and patterns of SOC across the landscape.

  9. Airborne black carbon concentrations over an urban region in western India-temporal variability, effects of meteorology, and source regions.

    PubMed

    Bapna, Mukund; Sunder Raman, Ramya; Ramachandran, S; Rajesh, T A

    2013-03-01

    This study characterizes over 5 years of high time resolution (5 min), airborne black carbon (BC) concentrations (July 2003 to December 2008) measured over Ahmedabad, an urban region in western India. The data were used to obtain different time averages of BC concentrations, and these averages were then used to assess the diurnal, seasonal, and annual variability of BC over the study region. Assessment of diurnal variations revealed a strong association between BC concentrations and vehicular traffic. Peaks in BC concentration were co-incident with the morning (0730 to 0830, LST) and late evening (1930 to 2030, LST) rush hour traffic. Additionally, diurnal variability in BC concentrations during major festivals (Diwali and Dushera during the months of October/November) revealed an increase in BC concentrations due to fireworks displays. Maximum half hourly BC concentrations during the festival days were as high as 79.8 μg m(-3). However, the high concentrations rapidly decayed suggesting that local meteorology during the festive season was favorable for aerosol dispersion. A multiple linear regression (MLR) model with BC as the dependent variable and meteorological parameters as independent variables was fitted. The variability in temperature, humidity, wind speed, and wind direction accounted for about 49% of the variability in measured BC concentrations. Conditional probability function (CPF) analysis was used to identify the geographical location of local source regions contributing to the effective BC measured (at 880 nm) at the receptor site. The east north-east (ENE) direction to the receptor was identified as a major source region. National highway (NH8) and two coal-fired thermal power stations (at Gandhinagar and Sabarmati) were located in the identified direction, suggesting that local traffic and power plant emissions were likely contributors to the measured BC. PMID:22777610

  10. 17 CFR 240.14c-3 - Annual report to be furnished security holders.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... security holders. 240.14c-3 Section 240.14c-3 Commodity and Securities Exchanges SECURITIES AND EXCHANGE... Under the Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-3 Annual report to be furnished security holders. (a) If the information...

  11. 17 CFR 240.14c-7 - Providing copies of material for certain beneficial owners.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... for certain beneficial owners. 240.14c-7 Section 240.14c-7 Commodity and Securities Exchanges... Rules and Regulations Under the Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-7 Providing copies of material for certain beneficial...

  12. 17 CFR 240.14c-4 - Presentation of information in information statement.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... information statement. 240.14c-4 Section 240.14c-4 Commodity and Securities Exchanges SECURITIES AND EXCHANGE... Under the Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-4 Presentation of information in information statement. (a) The...

  13. 17 CFR 240.14c-7 - Providing copies of material for certain beneficial owners.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... for certain beneficial owners. 240.14c-7 Section 240.14c-7 Commodity and Securities Exchanges... Rules and Regulations Under the Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-7 Providing copies of material for certain beneficial...

  14. 17 CFR 240.14c-6 - False or misleading statements.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    .... 240.14c-6 Section 240.14c-6 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION... Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-6 False or misleading statements. (a) No information statement shall contain any statement...

  15. 17 CFR 240.14c-3 - Annual report to be furnished security holders.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... security holders. 240.14c-3 Section 240.14c-3 Commodity and Securities Exchanges SECURITIES AND EXCHANGE... Under the Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-3 Annual report to be furnished security holders. (a) If the information...

  16. 17 CFR 240.14c-6 - False or misleading statements.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    .... 240.14c-6 Section 240.14c-6 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION... Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-6 False or misleading statements. (a) No information statement shall contain any statement...

  17. 17 CFR 240.14c-7 - Providing copies of material for certain beneficial owners.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... for certain beneficial owners. 240.14c-7 Section 240.14c-7 Commodity and Securities Exchanges... Rules and Regulations Under the Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-7 Providing copies of material for certain beneficial...

  18. 17 CFR 240.14c-4 - Presentation of information in information statement.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... information statement. 240.14c-4 Section 240.14c-4 Commodity and Securities Exchanges SECURITIES AND EXCHANGE... Under the Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-4 Presentation of information in information statement. (a) The...

  19. 17 CFR 240.14c-3 - Annual report to be furnished security holders.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... security holders. 240.14c-3 Section 240.14c-3 Commodity and Securities Exchanges SECURITIES AND EXCHANGE... Under the Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-3 Annual report to be furnished security holders. (a) If the information...

  20. 17 CFR 240.14c-6 - False or misleading statements.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    .... 240.14c-6 Section 240.14c-6 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION... Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-6 False or misleading statements. (a) No information statement shall contain any statement...

  1. 17 CFR 240.14c-6 - False or misleading statements.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    .... 240.14c-6 Section 240.14c-6 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION... Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-6 False or misleading statements. (a) No information statement shall contain any statement...

  2. 17 CFR 240.14c-7 - Providing copies of material for certain beneficial owners.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... for certain beneficial owners. 240.14c-7 Section 240.14c-7 Commodity and Securities Exchanges... Rules and Regulations Under the Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-7 Providing copies of material for certain beneficial...

  3. 17 CFR 240.14c-4 - Presentation of information in information statement.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... information statement. 240.14c-4 Section 240.14c-4 Commodity and Securities Exchanges SECURITIES AND EXCHANGE... Under the Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-4 Presentation of information in information statement. (a) The...

  4. 17 CFR 240.14c-3 - Annual report to be furnished security holders.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... security holders. 240.14c-3 Section 240.14c-3 Commodity and Securities Exchanges SECURITIES AND EXCHANGE... Under the Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-3 Annual report to be furnished security holders. (a) If the information...

  5. 17 CFR 240.14c-6 - False or misleading statements.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    .... 240.14c-6 Section 240.14c-6 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION... Securities Exchange Act of 1934 Regulation 14c: Distribution of Information Pursuant to Section 14(c) § 240.14c-6 False or misleading statements. (a) No information statement shall contain any statement...

  6. Airborne tunable diode laser sensor for high-precision concentration and flux measurements of carbon monoxide and methane

    NASA Technical Reports Server (NTRS)

    Sachse, G. W.; Collins, J. E., Jr.; Hill, G. F.; Wade, L. O.; Burney, L. G.; Ritter, J. A.

    1991-01-01

    An airborne tunable diode laser instrument is described that is capable of operating in two measurement modes. One mode provides high precision (0.1 percent CH4; 1 percent CO) measurements of CH4 and CO with a 5 second response time, and a second mode achieves the very fast response time that is necessary to make airborne eddy correlation flux measurements. Examples of data from atmospheric expeditions of the Global Tropospheric Experiment are presented.

  7. Reassessment of sup 14 CO sub 2 compartmentation and of ( sup 14 C)formate oxidation in rat liver

    SciTech Connect

    Marsolais, C.; Lafreniere, F.; David, F.; Dodgson, S.J.; Brunengraber, H. )

    1989-11-25

    Our previous report had concluded that a fraction of ({sup 14}C)formate oxidation in liver occurs in the mitochondrion. This conclusion was based on the labeling patterns of urea and acetoacetate labeled via {sup 14}CO{sub 2} generated from ({sup 14}C)formate and other ({sup 14}C)substrates. We reassessed our interpretation in experiments conducted in (i) perifused mitochondria and (ii) isolated livers perfused with buffer containing ({sup 14}C)formate, ({sup 14}C)gluconolactone, {sup 14}CO{sub 2}, or NaH{sup 13}CO{sub 3}, in the absence and presence of acetazolamide, an inhibitor of carbonic anhydrase. Our data show that the cytosolic pools of bicarbonate and CO{sub 2} are not in isotopic equilibrium when {sup 14}CO{sub 2} is generated in the cytosol or is supplied as NaH{sup 14}CO3. We retract our earlier suggestion of a mitochondrial site of ({sup 14}C)formate oxidation.

  8. Hydrogen bond disruption in DNA base pairs from (14)C transmutation.

    PubMed

    Sassi, Michel; Carter, Damien J; Uberuaga, Blas P; Stanek, Christopher R; Mancera, Ricardo L; Marks, Nigel A

    2014-09-01

    Recent ab initio molecular dynamics simulations have shown that radioactive carbon does not normally fragment DNA bases when it decays. Motivated by this finding, density functional theory and Bader analysis have been used to quantify the effect of C → N transmutation on hydrogen bonding in DNA base pairs. We find that (14)C decay has the potential to significantly alter hydrogen bonds in a variety of ways including direct proton shuttling (thymine and cytosine), thermally activated proton shuttling (guanine), and hydrogen bond breaking (cytosine). Transmutation substantially modifies both the absolute and relative strengths of the hydrogen bonding pattern, and in two instances (adenine and cytosine), the density at the critical point indicates development of mild covalent character. Since hydrogen bonding is an important component of Watson-Crick pairing, these (14)C-induced modifications, while infrequent, may trigger errors in DNA transcription and replication. PMID:25127298

  9. ( sup 14 C)-Sucrose uptake by guard cell protoplasts of pisum sativum, argenteum mutant

    SciTech Connect

    Rohrig, K.; Raschke, K. )

    1991-05-01

    Guard cells rely on import for their supply with reduced carbon. The authors tested by silicone oil centrifugation the ability of guard cell protoplasts to accumulated ({sup 14}C)-sucrose. Uptake rates were corrected after measurement of {sup 14}C-sorbitol and {sup 3}H{sub 2}O spaces. Sucrose uptake followed biphasic kinetics, with a high-affinity component below 1 mM external sucrose (apparent K{sub m} 0.8 mM at 25C) and a low-affinity nonsaturable component above. Uptake depended on pH (optimum at pH 5.0). Variations in the concentrations of external KCl, CCCP, and valinomycin indicated that about one-half of the sucrose uptake rate could be related to an electrochemical gradient across the plasmalemma. Total uptake rates measured at 5 mM external sucrose seem to be sufficient to replenish emptied plastids with starch within a few hours.

  10. Incineration and monitoring of low-level 3H and 14C wastes at a biological research institution

    SciTech Connect

    Hamrick, P.E.; Knapp, S.J.; Parker, M.G.; Watson, J.E. Jr.

    1986-10-01

    Low-level radioactive waste containing liquid scintillation fluid and known amounts of /sup 14/C and /sup 3/H has been incinerated in a modified pathological incinerator with the incinerator effluent, refractory surface and ash being monitored. The study relates the activity monitored to that incinerated and discusses how this relation was affected by a modification of the incinerator and monitoring conditions. No significant activity was found to be associated with the ash, particulates or the refractory surface. These data suggest that most of the activity is released as tritiated water vapor and /sup 14/C-labeled carbon dioxide. However, incomplete oxidation may occur for short periods of time depending on the amount of liquid scintillation fluid incinerated, with the possible release of /sup 14/C-labeled carbon monoxide.

  11. Tritium and 14C background levels in pristine aquatic systems and their potential sources of variability.

    PubMed

    Eyrolle-Boyer, Frédérique; Claval, David; Cossonnet, Catherine; Zebracki, Mathilde; Gairoard, Stéphanie; Radakovitch, Olivier; Calmon, Philippe; Leclerc, Elisabeth

    2015-01-01

    Tritium and (14)C are currently the two main radionuclides discharged by nuclear industry. Tritium integrates into and closely follows the water cycle and, as shown recently the carbon cycle, as does (14)C (Eyrolle-Boyer et al., 2014a, b). As a result, these two elements persist in both terrestrial and aquatic environments according to the recycling rates of organic matter. Although on average the organically bound tritium (OBT) activity of sediments in pristine rivers does not significantly differ today (2007-2012) from the mean tritiated water (HTO) content on record for rainwater (2.4 ± 0.6 Bq/L and 1.6 ± 0.4 Bq/L, respectively), regional differences are expected depending on the biomass inventories affected by atmospheric global fallout from nuclear testing and the recycling rate of organic matter within watersheds. The results obtained between 2007 and 2012 for (14)C show that the levels varied between 94.5 ± 1.5 and 234 ± 2.7 Bq/kg of C for the sediments in French rivers and across a slightly higher range of 199 ± 1.3 to 238 ± 3.1 Bq/kg of C for fish. This variation is most probably due to preferential uptake of some organic carbon compounds by fish restraining (14)C dilution with refractory organic carbon and/or with old carbonates both depleted in (14)C. Overall, most of these ranges of values are below the mean baseline value for the terrestrial environment (232.0 ± 1.8 Bq/kg of C in 2012, Roussel-Debet, 2014a) in relation to dilution by the carbonates and/or fossil organic carbon present in aquatic systems. This emphasises yet again the value of establishing regional baseline value ranges for these two radionuclides in order to account for palaeoclimatic and lithological variations. Besides, our results obtained from sedimentary archive investigation have confirmed the delayed contamination of aquatic sediments by tritium from the past nuclear tests atmospheric fallout, as recently demonstrated from data chronicles (Eyrolle

  12. Extracting in situ cosmogenic 14C from olivine: significance for the CRONUS-Earth project

    NASA Astrophysics Data System (ADS)

    Pigati, J. S.; Lifton, N. A.; Quade, J.; Jull, A. T.

    2005-12-01

    One of the main goals of the Cosmic-Ray-prOduced NUclide Systematics on Earth (CRONUS-Earth) project is to compare production rates of in situ cosmogenic nuclides (CNs) at several well-dated locations in various rock types. Quartz is the most commonly used target mineral for several CNs (e.g., 10Be, 26Al, 21Ne, 14C), but is generally absent in mafic volcanic terrains, where flows of different ages can constrain temporal variations in CN production at a given location. Because of its short half-life (5.73 ka), in situ cosmogenic 14C (in situ 14C) can be particularly useful for elucidating temporal variations in CN production over much shorter time scales than other CNs. While CNs such as 36Cl and 21Ne can be measured in both mafic and felsic rocks, clearly it would be advantageous to measure in situ 14C in mafic rocks as well. As such, we have worked to develop reliable protocols to extract in situ 14C from olivine. We conducted numerous stepped combustion experiments testing the efficacy of various chemical pretreatments. We were able to extract a stable and reproducible in situ 14C component from olivine using a LiBO2 flux, following pretreatment with dilute HNO3. However, measured concentrations in olivine (normalized to SiO2 composition) from two known-age basalt flows, the Tabernacle Hill flow (17.3+/-0.4 ka in age) in central Utah and the McCarty's flow (3.0+/-0.2 ka in age) in western New Mexico, were 3 to 5 times lower than predicted in situ 14C concentrations based on measurements in quartz. This discrepancy appears to arise from (1) a synthetic spinel-like mineral formed during our extraction process by the chemical interaction of the Al2O3 sample boat and olivine dissolved within the LiBO2 flux, and (2) undissolved pyroxene phenocrysts (difficult to separate in quantity from olivines). Although we do not fully understand how the formation of the synthetic mineral may affect carbon atoms liberated from olivine, the concentration of in situ 14C atoms that

  13. 14C Terrestrial Ages of Meteorites from Desert Regions: Algeria and Australia

    NASA Astrophysics Data System (ADS)

    Jull, A. J. T.; Wlotzka, F.; Bevan, A. W. R.; Brown, S. T.; Donahue, D. J.

    1993-07-01

    The terrestrial age or residence time on the Earth's surface is important in determining the history of a meteorite. Carbon-14 has been used for a terrestrial-age indicator since 1962 [1,2]. Since 1984, small samples of meteorites of 0.1 to 0.5 g have been dated using accelerator mass spectrometry [3-5]. The precision of terrestrial age estimates is limited by the accuracy to which the saturated activity of ^14C in the meteorite is known. Jull et al. [4,5] used Bruderheim and some other chondrites to establish a saturated activity reference level. It is important to be aware that ^14C can vary with the depth and size of the object, and ^14C as a function of accurate depth has so far been measured only for one object, Knyahinya [7]. Carbon-14 is of particular interest in warmer climatic regions, where the storage time before a meteorite weathers away is expected to be much less than other locations, for example, Antarctica. This view was originally based on the work of Boeckl [7], who determined a "weathering half life" of some 3500 yr for chondrites from the southwestern U.S. This work was reinvestigated [5] and it was determined that the ^14C age distribution of the meteorites was longer than the earlier report. We have studied ^14C ages of meteorites from Roosevelt County, New Mexico [8], and from the western Libyan desert [9]. In both these areas meteorites of ages as old as 35,000 yr are observed, and the mean survival time at both locations is well over 10,000 yr. We have studied the ^14C age distribution of a large number of meteorites from Acfer, Algeria, and the Nullarbor Plain, Australia. Figure 1 presents the ^14C age distribution of Acfer samples compared to some other locations where a substantial number of ^14C ages have been obtained. The Algerian site shows a simple exponential dependence of terrestrial age vs. time, and no meteorites of >25 K.y. age. This is in contrast to the results from the southwestern U.S. [7] and from Roosevelt County [8]. One

  14. 14C-urea breath test in C pylori gastritis.

    PubMed Central

    Rauws, E A; Royen, E A; Langenberg, W; Woensel, J V; Vrij, A A; Tytgat, G N

    1989-01-01

    14C-urea breath test was used to detect Campylobacter pylori colonisation in 129 consecutive non-ulcer dyspepsia patients. Fasting patients were given 3 microCi (110 kBq) of 14C-labelled urea after a test meal. Breath samples were collected at 10 minute intervals for 90 minutes and the C-14 activity was counted on a liquid scintillation analyser. Urea derived 14CO2 appears in the exhaled breath of Campylobacter pylori culture positive individuals within 20-30 minutes. Likelihood analysis revealed a most favourable cut off level of [0.07% dose 14C-urea/mmol CO2] multiplied by body weight at t = 40 minutes, to separate culture positive from culture negative subjects. Using this upper limit of normal, a positive likelihood ratio of 50 and a negative likelihood ratio of 0.05 was calculated. Sensitivity of the test was 95% and specificity 98%. The 14C-urea breath test is a simple, sensitive and non-invasive test, that detects viable C pylori microorganism and semiquantitatively assesses the bacterial load of C pylori colonisation. Administration of a single dose of colloidal bismuth subcitrate resulted in a rapid decrease in 14CO2 excretion, so this test can be used to confirm eradication of the bacterium in therapeutic trials without endoscopy, or need for culture. PMID:2753404

  15. Applications of AMS {sup 14}C on Climate and Archaeology

    SciTech Connect

    Gomes, P. R. S.

    2007-10-26

    We describe the Accelerator Mass Spectrometry (AMS) technique and two distinct applications of its use with {sup 14}C to study environmental problems in Brazil, such as forest fires and climate changes in the Amazon region and archaeological studies on the early settlements in the Southeast Brazilian coast.

  16. Excretion of radioactivity following the intraperitoneal administration of /sup 14/C-DDT, /sup 14/C-DDD, /sup 14/C-DDE and /sup 14/C-DDMU to the rat and Japanese Quail

    SciTech Connect

    Fawcett, S.C.; Bunyan, P.J.; Huson, L.W.; King, L.J.; Stanley, P.I.

    1981-09-01

    A study in progress to examine the metabolic fate of DDT in birds and mammals is discussed. The first phase of the study, which is reported in this article, has been to establish the rate of excretion of ratioactivity following the intraperitoneal administrations of /sup 14/C-DDT, /sup 14/C-DDE, /sup 14/C-DDD, and /sup 14/C-DDMU to male rats and male Japanese quail. The mean values from the three animals in each experimental group for the amount of radioactivity excreted daily are given, and it was found that the rats excreted the radioactivity administered as DDT, DDD, and DDE substantially faster than did the quail. DDMU was excreted relatively rapidly and at similar rates. This finding suggests that apparent differences in the rates of excretion of DDT by birds and mammals probably arise from differences in the conversion of DDT to DDD or DDE or in the degradation of these metabolites to DDMU. The Japanese quail differ from the rats in excreting substantial amounts of unchanged DDT, DDE, and DDD, which probably reflects the inability of the Japanese quail to readily metabolise these compounds.

  17. Airborne intercomparison of vacuum ultraviolet fluorescence and tunable diode laser absorption measurements of tropospheric carbon monoxide

    NASA Astrophysics Data System (ADS)

    Holloway, John S.; Jakoubek, Roger O.; Parrish, David D.; Gerbig, Christoph; Volz-Thomas, Andreas; Schmitgen, Sandra; Fried, Alan; Wert, Brian; Henry, Bruce; Drummond, James R.

    2000-01-01

    During the fall 1997 North Atlantic Regional Experiment (NARE 97), two separate intercomparisons of aircraft-based carbon monoxide measurement instrumentation were conducted. On September 2, CO measurements were simultaneously made aboard the National Oceanic and Atmospheric Administration (NOAA) WP-3 by vacuum ultraviolet (VUV) fluorescence and by tunable diode laser absorption spectroscopy (TDLAS). On September 18, an intercomparison flight was conducted between two separate instruments, both employing the VUV fluorescence method, on the NOAA WP-3 and the U.K. Meteorological Office C-130 Hercules. The results indicate that both of the VUV fluorescence instruments and the TDLAS system are capable of measuring ambient CO accurately and precisely with no apparent interferences in 5 s. The accuracy of the measurements, based upon three independent calibration systems, is indicated by the agreement to within 11% with systematic offsets of less than 1 ppbv. In addition, one of the groups participated in the Measurement of Air Pollution From Satellite (MAPS) intercomparison [Novelli et al., 1998] with a different measurement technique but very similar calibration system, and agreed with the accepted analysis to within 5%. The precision of the measurements is indicated by the variability of the ratio of simultaneous measurements from the separate instruments. This variability is consistent with the estimated precisions of 1.5 ppbv and 2.2 ppbv for the 5 s average results of the C-130 and the WP-3 instruments, respectively, and indicates a precision of approximately 3.6% for the TDLAS instrument. The excellent agreement of the instruments in both intercomparisons demonstrates that significant interferences in the measurements are absent in air masses that ranged from 7 km in the midtroposphere to boundary layer conditions including subtropical marine air and continental outflow with embedded urban plumes. The intercomparison of the two VUV instruments that differed widely

  18. Atmospheric profiles of Black Carbon at remote locations using light-weight airborne Aethalometers

    NASA Astrophysics Data System (ADS)

    Hansen, A. D.; Močnik, G.; Drinovec, L.; Lenarcic, M.

    2012-12-01

    While measurements of atmospheric aerosols are routinely performed at ground-level around the world, there is far less knowledge of their concentrations at altitude: yet this data is a crucial requirement for our understanding of the dispersion of pollutants of anthropogenic origin, with their associated effects on radiative forcing, cloud condensation, and other adverse phenomena. Black Carbon (BC) is a unique tracer for combustion emissions, and can be detected rapidly and with great sensitivity by filter-based optical methods. It has no non-combustion sources and is not transformed by atmospheric processes. Recent technical advances have developed light-weight miniaturized instruments which can be operated on light aircraft or carried aboard commercial passenger flights. From January to April 2012, a single-seat ultra-light aircraft flew around the world on a scientific, photographic and environmental-awareness mission. The flight track crossed all seven continents and all major oceans, with altitudes up to 8.9 km ASL. The aircraft carried a custom-developed high-sensitivity dual-wavelength light-weight Aethalometer, operating at 370 and 880 nm with special provision to compensate for the effects of changing pressure, temperature and humidity. The instrument recorded BC concentrations with high temporal resolution and sensitivity better than 5 ng/m3. We present examples of data from flight tracks over remote oceans, uninhabited land masses, and densely populated areas, analyzing the spectral dependence of absorption to infer the contributions to BC from fossil fuel vs. biomass combustion, and aggregating the data into vertical profiles. The regional and long range transport of BC may be investigated using back-trajectories. We have also operated miniature instruments in the passenger cabins of long-distance commercial aircraft. Since there are no combustion sources within the cabin, any BC in the ventilation air must necessarily have originated from the outside

  19. Reconstructing Ocean Circulation using Coral (triangle)14C Time Series

    SciTech Connect

    Kashgarian, M; Guilderson, T P

    2001-02-23

    We utilize monthly {sup 14}C data derived from coral archives in conjunction with ocean circulation models to address two questions: (1) how does the shallow circulation of the tropical Pacific vary on seasonal to decadal time scales and (2) which dynamic processes determine the mean vertical structure of the equatorial Pacific thermocline. Our results directly impact the understanding of global climate events such as the El Nino-Southern Oscillation (ENSO). To study changes in ocean circulation and water mass distribution involved in the genesis and evolution of ENSO and decadal climate variability, it is necessary to have records of climate variables several decades in length. Continuous instrumental records are limited because technology for continuous monitoring of ocean currents (e.g. satellites and moored arrays) has only recently been available, and ships of opportunity archives such as COADS contain large spatial and temporal biases. In addition, temperature and salinity in surface waters are not conservative and thus can not be independently relied upon to trace water masses, reducing the utility of historical observations. Radiocarbon in sea water is a quasi-conservative water mass tracer and is incorporated into coral skeletal material, thus coral {sup 14}C records can be used to reconstruct changes in shallow circulation that would be difficult to characterize using instrumental data. High resolution {Delta}{sup 14}C timeseries such as ours, provide a powerful constraint on the rate of surface ocean mixing and hold great promise to augment one time oceanographic surveys. {Delta}{sup 14}C timeseries such as these, not only provide fundamental information about the shallow circulation of the Pacific, but can also be directly used as a benchmark for the next generation of high resolution ocean models used in prognosticating climate. The measurement of {Delta}{sup 14}C in biological archives such as tree rings and coral growth bands is a direct record of

  20. Urinary metabolites of 14C-labeled thyroxine in man

    PubMed Central

    Pittman, Constance S.; Buck, Melvin W.; Chambers, Joseph B.

    1972-01-01

    Studies were carried out to determine the chemical structures of thyroxine metabolites after total deiodination. Normal subjects were given thyroxine labeled with 14C on the nonphenolic ring and the alanine side chain, 8-11 μg/day for 10 days. By paper chromatography of fresh urine, six or more 14C-labeled compounds were separated. The 14C-labeled metabolites were concentrated by passing the urine through a nonionic polymeric adsorbent. Two major thyroxine metabolites were identified. The identification was made by three different methods: (a) chromatography, (b) synthesis of derivatives, and (c) recrystallization to constant specific activity. One 14C-labeled metabolite was identified as thyroacetic acid or 4-phenoxy-(4′-hydroxy) phenyl-acetic acid. Another one was identified as thyronine. Of the total urinary 14C radioactivity, 43.7% was recovered as thyroacetic acid and 19.8% was recovered as thyronine. Approximately one-fifth of each of these metabolites was present in the urine in bound form which released the free metabolites during acid hydrolysis. The average daily excretion of thyroacetic acid was 13.7% of the renal disposal rate of thyroxine, or approximately 7.5 μg/day. The average daily excretion of thyronine was 6.5% of the renal disposal rate of thyroxine or approximately 3.9 μg/day while the urinary iodide made up 64.7% of the renal disposal rate of thyroxine. Our findings provide the needed proof that the major metabolic pathways of thyroxine remove the iodine atoms by substituting hydrogen for iodine and leave the diphenyl ether nucleus intact. PMID:5032524

  1. Does the 14C method estimate net photosynthesis? Implications from batch and continuous culture studies of marine phytoplankton

    NASA Astrophysics Data System (ADS)

    Pei, Shaofeng; Laws, Edward A.

    2013-12-01

    We carried out batch culture studies with seven species of marine phytoplankton and chemostat studies with two of the seven species to determine whether and to what extent 14C uptake approximated net photosynthesis. In two of seven cases, Isochrysis galbana and Dunaliella tertiolecta, cells uniformly labeled with 14C lost no activity when they were transferred to a 14C-free medium and allowed to grow in the light. In similar experiments with four other species, uniformly labeled cells lost activity when incubated in the light, but the loss rates were only a few percent per day. Thus these six species appear to respire primarily recently fixed carbon. In the case of the remaining species, Chlorella kessleri, loss rates of 14C in the light from uniformly labeled cells were about 29% per day, the apparent ratio of respiration to net photosynthesis being 0.4. Follow-up chemostat studies with I. galbana and C. kessleri grown under both light- and nitrate-limited conditions produced results consistent with the implications of the batch culture work: uptake of 14C by I. galbana after incubations of 24 h yielded estimates of photosynthetic carbon fixation equal to the product of the chemostat dilution rate and the concentration of organic carbon in the growth chamber. Similar experiments with C. kessleri produced 14C-based estimates of photosynthetic carbon fixation that exceeded the net rates of organic carbon production in the growth chamber by roughly 55%. Time-course studies with both species indicated that at high growth rates recently fixed carbon began to enter the respiratory substrate pool after a time lag of several hours, a result consistent with previous work with D. tertiolecta. The lag time appeared to be much shorter at low growth rates. The results with C. kessleri are similar to results previously reported for Chlorella pyrenoidosa and Amphidium carteri. Collectively these results suggest that 14C uptake by species with relatively high ratios of

  2. Evaluation of an airborne triple-pulsed 2 μm IPDA lidar for simultaneous and independent atmospheric water vapor and carbon dioxide measurements.

    PubMed

    Refaat, Tamer F; Singh, Upendra N; Yu, Jirong; Petros, Mulugeta; Ismail, Syed; Kavaya, Michael J; Davis, Kenneth J

    2015-02-20

    Water vapor and carbon dioxide are the most dominant greenhouse gases directly contributing to the Earth's radiation budget and global warming. A performance evaluation of an airborne triple-pulsed integrated path differential absorption (IPDA) lidar system for simultaneous and independent monitoring of atmospheric water vapor and carbon dioxide column amounts is presented. This system leverages a state-of-the-art Ho:Tm:YLF triple-pulse laser transmitter operating at 2.05 μm wavelength. The transmitter provides wavelength tuning and locking capabilities for each pulse. The IPDA lidar system leverages a low risk and technologically mature receiver system based on InGaAs pin detectors. Measurement methodology and wavelength setting are discussed. The IPDA lidar return signals and error budget are analyzed for airborne operation on-board the NASA B-200. Results indicate that the IPDA lidar system is capable of measuring water vapor and carbon dioxide differential optical depth with 0.5% and 0.2% accuracy, respectively, from an altitude of 8 km to the surface and with 10 s averaging. Provided availability of meteorological data, in terms of temperature, pressure, and relative humidity vertical profiles, the differential optical depth conversion into weighted-average column dry-air volume-mixing ratio is also presented. PMID:25968204

  3. Investigating δ13C and Δ14C within Mytilus californianus shells as proxies of upwelling intensity

    NASA Astrophysics Data System (ADS)

    Ferguson, J. E.; Johnson, K. R.; Santos, G.; Meyer, L.; Tripati, A.

    2013-06-01

    Along the west coast of North America, climate and marine productivity is affected by seasonal to interannual changes in coastal upwelling. Our understanding of upwelling variability in the past is limited by the short duration of instrumental records. Changes in upwelling intensity are expected to affect the 13C/12C (δ13C) and radiocarbon (∆14C) content of marine dissolved inorganic carbon (DIC) due to variable mixing of old, upwelled seawater into surface waters. If seasonal variations in the δ13C of DIC are recorded in marine bivalve shells, they may provide valuable information about the extent of upwelling in the past. Comparison of modern Mytilus californianus shells from South California with a 5 year time series of coastal seawater ∆14C and δ13C allows an assessment of the suitability of Mytilus shell ∆14C and δ13C as proxies of upwelling intensity. We show that both absolute values and the seasonal range in seawater ∆14C are preserved in shell ∆14C, allowing its use as an indicator of upwelling intensity. Interpretation of shell δ13C is more problematic, with the δ13C of shell carbonate lower than seawater DIC by variable amounts (ranging from 0.5‰ to 1.5‰) due to the incorporation of metabolic carbon. The spatial and temporal variability observed in specimens that grew during the severe El Niño event of 1997-1998 demonstrates how a transect of shells spanning the western North American coastline can be used to reconstruct large-scale patterns of seawater ∆14C variability for specific intervals of interest, such as those associated with El Niño Southern Oscillation-type phenomena.

  4. Methods for high precision 14C AMS measurement of atmospheric CO2 at LLNL

    SciTech Connect

    Graven, H D; Guilderson, T P; Keeling, R F

    2006-10-18

    Development of {sup 14}C analysis with precision better than 2{per_thousand} has the potential to expand the utility of {sup 14}CO{sub 2} measurements for carbon cycle investigations as atmospheric gradients currently approach traditional measurement precision of 2-5{per_thousand}. The AMS facility at the Center for Accelerator Mass Spectrometry, Lawrence Livermore National Laboratory, produces high and stable beam currents that enable efficient acquisition times for large numbers of {sup 14}C counts. One million {sup 14}C atoms can be detected in approximately 25 minutes, suggesting that near 1{per_thousand} counting precision is economically feasible at LLNL. The overall uncertainty in measured values is ultimately determined by the variation between measured ratios in several sputtering periods of the same sample and by the reproducibility of replicate samples. Experiments on the collection of one million counts on replicate samples of CO{sub 2} extracted from a whole air cylinder show a standard deviation of 1.7{per_thousand} in 36 samples measured over several wheels. This precision may be limited by the reproducibility of Oxalic Acid I standard samples, which is considerably poorer. We outline the procedures for high-precision sample handling and analysis that have enabled reproducibility in the cylinder extraction samples at the <2{per_thousand} level and describe future directions to continue increasing measurement precision at LLNL.

  5. Measurements of 14C in ancient ice from Taylor Glacier, Antarctica constrain in situ cosmogenic 14CH4 and 14CO production rates

    NASA Astrophysics Data System (ADS)

    Petrenko, Vasilii V.; Severinghaus, Jeffrey P.; Schaefer, Hinrich; Smith, Andrew M.; Kuhl, Tanner; Baggenstos, Daniel; Hua, Quan; Brook, Edward J.; Rose, Paul; Kulin, Robb; Bauska, Thomas; Harth, Christina; Buizert, Christo; Orsi, Anais; Emanuele, Guy; Lee, James E.; Brailsford, Gordon; Keeling, Ralph; Weiss, Ray F.

    2016-03-01

    Carbon-14 (14C) is incorporated into glacial ice by trapping of atmospheric gases as well as direct near-surface in situ cosmogenic production. 14C of trapped methane (14CH4) is a powerful tracer for past CH4 emissions from "old" carbon sources such as permafrost and marine CH4 clathrates. 14C in trapped carbon dioxide (14CO2) can be used for absolute dating of ice cores. In situ produced cosmogenic 14C in carbon monoxide (14CO) can potentially be used to reconstruct the past cosmic ray flux and past solar activity. Unfortunately, the trapped atmospheric and in situ cosmogenic components of 14C in glacial ice are difficult to disentangle and a thorough understanding of the in situ cosmogenic component is needed in order to extract useful information from ice core 14C. We analyzed very large (≈1000 kg) ice samples in the 2.26-19.53 m depth range from the ablation zone of Taylor Glacier, Antarctica, to study in situ cosmogenic production of 14CH4 and 14CO. All sampled ice is >50 ka in age, allowing for the assumption that most of the measured 14C originates from recent in situ cosmogenic production as ancient ice is brought to the surface via ablation. Our results place the first constraints on cosmogenic 14CH4 production rates and improve on prior estimates of 14CO production rates in ice. We find a constant 14CH4/14CO production ratio (0.0076 ± 0.0003) for samples deeper than 3 m, which allows the use of 14CO for correcting the 14CH4 signals for the in situ cosmogenic component. Our results also provide the first unambiguous confirmation of 14C production by fast muons in a natural setting (ice or rock) and suggest that the 14C production rates in ice commonly used in the literature may be too high.

  6. The metabolism of [14C]-debrisoquine in man.

    PubMed Central

    Idle, J R; Mahgoub, A; Angelo, M M; Dring, L G; Lancaster, R; Smith, R L

    1979-01-01

    1 The synthesis of [14C]-debrisoquine hydrochloride and 4-hydroxy-debrisoquine sulphate is described. 2 The metabolic fate and excretion profile in both urine and faeces of 14C-labelled debrisoquine was studied in five healthy human subjects. 3 Investigations showed that the drug is well-absorbed after a single oral dose of 32 mg and quantitatively eliminated from the body within three days. 4 4-Hydroxy-debrisoquine is the major metabolite of debrisoquine, although significant amounts of 5-,6-, 7- and 8-hydroxy-debrisoquine are also formed. 5 Electron-capture gas chromatography is a useful method for measuring debrisoquine and its five hydroxylated metabolites in urine at the pg level. PMID:371651

  7. Metabolism of U/sup 14/C palmitic and 1-/sup 14/C caproic acids by lettuce seeds during early germination

    SciTech Connect

    Salon, C.; Raymond, P.; Pradet, A.

    1986-04-01

    Germinating lettuce embryos (before radicule emergence) were fed with either U/sup 14/C palmitic acid or 1/sup 14/C caproic acid until a metabolic steady state was reached. The bulk of labelled caproate was evolved as respiratory CO/sub 2/ (52%) and incorporated into organic and amino acids (38%) and only a small part incorporated into lipids whereas most of labelled palmitic acid was found into lipids (92%) and only 8% evolved as CO/sub 2/ and incorporated into organic and amino acids. The label distribution at steady state in intermediates linked to the T.C.A. cycle was interpreted using a metabolic model. They found that the two fatty acids were degraded by ..beta..-oxidation and incorporated into the T.C.A. cycle as acetylCoA suggesting that ..beta..-oxidation is located in the mitochondria. The results also indicate that lipids contribute for at least 90% to the carbon supply to respiration.

  8. Integration of WorldView-2 and airborne LiDAR data for tree species level carbon stock mapping in Kayar Khola watershed, Nepal

    NASA Astrophysics Data System (ADS)

    Karna, Yogendra K.; Hussin, Yousif Ali; Gilani, Hammad; Bronsveld, M. C.; Murthy, M. S. R.; Qamer, Faisal Mueen; Karky, Bhaskar Singh; Bhattarai, Thakur; Aigong, Xu; Baniya, Chitra Bahadur

    2015-06-01

    Integration of WorldView-2 satellite image with small footprint airborne LiDAR data for estimation of tree carbon at species level has been investigated in tropical forests of Nepal. This research aims to quantify and map carbon stock for dominant tree species in Chitwan district of central Nepal. Object based image analysis and supervised nearest neighbor classification methods were deployed for tree canopy retrieval and species level classification respectively. Initially, six dominant tree species (Shorea robusta, Schima wallichii, Lagerstroemia parviflora, Terminalia tomentosa, Mallotus philippinensis and Semecarpus anacardium) were able to be identified and mapped through image classification. The result showed a 76% accuracy of segmentation and 1970.99 as best average separability. Tree canopy height model (CHM) was extracted based on LiDAR's first and last return from an entire study area. On average, a significant correlation coefficient (r) between canopy projection area (CPA) and carbon; height and carbon; and CPA and height were obtained as 0.73, 0.76 and 0.63, respectively for correctly detected trees. Carbon stock model validation results showed regression models being able to explain up to 94%, 78%, 76%, 84% and 78% of variations in carbon estimation for the following tree species: S. robusta, L. parviflora, T. tomentosa, S. wallichii and others (combination of rest tree species).

  9. Metabolic fate of the (14)C-labeled herbicide clodinafop-propargyl in soil.

    PubMed

    Jaquet, Jasmin; Weitzel, Pascal; Junge, Thorsten; Schmidt, Burkhard

    2014-01-01

    The metabolic fate of (14)C-phenyl-labeled herbicide clodinafop-propargyl (CfP) was studied for 28 days in lab assays using a soil from Germany (Ap horizon, silt loam, and cambisol). Mineralization amounted to 12.40% of applied (14)C after 28 days showing a distinct lag phase until day 7 of incubation. Portions of radioactivity extractable by means of 0.01 M CaCl2 solution (bioavailable fraction) decreased rapidly and were 4.41% after 28 days. Even immediately after application, only 57.31% were extracted with the aqueous solvent. Subsequent extraction using accelerated solvent extraction (ASE; acetonitrile/water 4:1, v/v) released 39.91% of applied (14)C with day 0 and 26.16% with day 28 of incubation from the samples. Non-extractable portions of radioactivity thus, increased with time amounting to 11.99% (day 0) and 65.00% (day 28). A remarkable increase was observed between 14 and 28 days correlating with the distinct increase of mineralization. No correlation was found throughout incubation with general microbial activity as determined by DMSO reduction. Analysis of the CaCl2 and ASE extracts by radio-TLC, radio-HPLC and GC/MS revealed that CfP was rapidly cleaved to free acid clodinafop (Cf), which was further (bio-) transformed; DT50 values (based on radio-TLC detection of the parent compound) were far below 1 day (CfP) and about 7 days (Cf). TLC analysis pointed to 2-(4-hydroxyphenoxy)-propionic acid as further metabolite. Due to fractionation of non-extractable residues, most of the (14)C was associated with fulvic and humic acids, portions in humin fractions and non-humics were moderate and low, respectively. Using a special strategy, which included pre-incubation of the soil with CfP and then mineralization of (14)C-CfP as criterion, a microorganism was isolated from the soil examined. The microorganism grew using CfP as sole carbon source with concomitant evolution of (14)CO2. The bacterium was characterized by growth on commonly used carbon

  10. Pediatric microdose and microtracer studies using 14C in Europe.

    PubMed

    Turner, M A; Mooij, M G; Vaes, W H J; Windhorst, A D; Hendrikse, N H; Knibbe, C A J; Kõrgvee, L T; Maruszak, W; Grynkiewicz, G; Garner, R C; Tibboel, D; Park, B K; de Wildt, S N

    2015-09-01

    Important information gaps remain on the efficacy and safety of drugs in children. Pediatric drug development encounters several ethical, practical, and scientific challenges. One barrier to the evaluation of medicines for children is a lack of innovative methodologies that have been adapted to the needs of children. This article presents our successful experience of pediatric microdose and microtracer studies using (14) C-labeled probes in Europe to illustrate the strengths and limitations of these approaches. PMID:26095095

  11. Retrieval of Vegetation Structure and Carbon Balance Parameters Using Ground-Based Lidar and Scaling to Airborne and Spaceborne Lidar Sensors

    NASA Astrophysics Data System (ADS)

    Strahler, A. H.; Ni-Meister, W.; Woodcock, C. E.; Li, X.; Jupp, D. L.; Culvenor, D.

    2006-12-01

    This research uses a ground-based, upward hemispherical scanning lidar to retrieve forest canopy structural information, including tree height, mean tree diameter, basal area, stem count density, crown diameter, woody biomass, and green biomass. These parameters are then linked to airborne and spaceborne lidars to provide large-area mapping of structural and biomass parameters. The terrestrial lidar instrument, Echidna(TM), developed by CSIRO Australia, allows rapid acquisition of vegetation structure data that can be readily integrated with downward-looking airborne lidar, such as LVIS (Laser Vegetation Imaging Sensor), and spaceborne lidar, such as GLAS (Geoscience Laser Altimeter System) on ICESat. Lidar waveforms and vegetation structure are linked for these three sensors through the hybrid geometric-optical radiative-transfer (GORT) model, which uses basic vegetation structure parameters and principles of geometric optics, coupled with radiative transfer theory, to model scattering and absorption of light by collections of individual plant crowns. Use of a common model for lidar waveforms at ground, airborne, and spaceborne levels facilitates integration and scaling of the data to provide large-area maps and inventories of vegetation structure and carbon stocks. Our research plan includes acquisition of Echidna(TM) under-canopy hemispherical lidar scans at North American test sites where LVIS and GLAS data have been or are being acquired; analysis and modeling of spatially coincident lidar waveforms acquired by the three sensor systems; linking of the three data sources using the GORT model; and mapping of vegetation structure and carbon-balance parameters at LVIS and GLAS resolutions based on Echidna(TM) measurements.

  12. Bioproduction of [14C]ochratoxin A in submerged culture.

    PubMed Central

    Lillehoj, E B; Aalund, O; Hald, B

    1978-01-01

    A number of Aspergillus and Penicillium species were tested for production of ochratoxin A (OA) in several media. After 8 days of static incubations of submerged cultures at 28 degrees C, toxin yields of 25 and 30 micrograms/ml were obtained with Aspergillus alliaceus NRRL 4181 in Ferreirás and 2% yeast extract-4% sucrose media, respectively. However, the largest production observed in the preliminary screening was 54 micrograms/ml; this highest level was produced by A. sulphureus NRRL 4077 in a modified Czapek solution. The medium contained the basal salts and sucrose of Czapek plus urea (3%) and corn steep liquor (0.5% solids). A time study of toxin production demonstrated maximum yield of 350 micrograms/ml by the A. sulphureus isolate in the modified Czapek medium after 11 days of static incubation at 28 degrees C. The optimal production conditions were employed in additional tests designed to measure the efficiency of 14C incorporation from sodium [1-14C]-acetate into OA. Samples (20 microCi) of sodium acetate were added to separate culture flasks at 24-h intervals during the initial 9 days of the fermentation. Addition of [14C]acetate on day 4 of incubation provided the maximum yield of labeled OA. The highest specific activity of labeled toxin obtained was 0.07 microCi/mg of OA and the maximum incorporation rate of labeled acetate was 5.3%. PMID:727787

  13. Airy structure in 16O+14C nuclear rainbow scattering

    NASA Astrophysics Data System (ADS)

    Ohkubo, S.; Hirabayashi, Y.

    2015-08-01

    The Airy structure in 16 O +14 C rainbow scattering is studied with an extended double-folding (EDF) model that describes all the diagonal and off-diagonal coupling potentials derived from the microscopic realistic wave functions for 16 O by using a density-dependent nucleon-nucleon force. The experimental angular distributions at EL=132 , 281, and 382.2 MeV are well reproduced by the calculations. By studying the energy evolution of the Airy structure, the Airy minimum around θ =76∘ in the angular distribution at EL=132 MeV is assigned as the second-order Airy minimum A 2 in contrast to the recent literature which assigns it as the third order A 3 . The Airy minima in the 90∘ excitation function is investigated in comparison with well-known 16 O +16 O and 12 C +12 C systems. Evolution of the Airy structure into the molecular resonances with the 16 O +14 C cluster structure in the low-energy region around Ec .m .=30 MeV is discussed. It is predicted theoretically for the first time for a non-4 N 16O +14 C system that Airy elephants in the 90∘ excitation function are present.

  14. Temporal variation in the interhemispheric 14C offset

    NASA Astrophysics Data System (ADS)

    McCormac, F. G.; Hogg, A. G.; Higham, T. F. G.; Lynch-Stieglitz, J.; Broecker, W. S.; Baillie, M. G. L.; Palmer, J.; Xiong, L.; Pilcher, J. R.; Brown, D.; Hoper, S. T.

    Contemporaneous tree-ring dated wood, from trees in the northern and southern hemispheres, gives different 14C dates. Previous studies [Vogel et al., 1986; 1993] using wood from South Africa and The Netherlands have shown depletion's of -4.56 ± 0.85‰ and -5.12±0.62‰ respectively. This translates to age differences of 36±7 and 41±5 years (yrs) with the southern hemisphere giving the older dates. More recently, Stuiver and Braziunas [1998] have shown that an offset of 23±4 yrs exists between combined 19th century wood measurements from Tasmania and Chile in the southern hemisphere and the west coast of the U.S. (Washington) in the northern hemisphere. In this study measurements on contemporaneous decadal samples of oak from the British Isles and cedar from New Zealand over the period 1725 to 1885 AD show a depletion of -3.4±0.58‰ (27.2±4.7 yrs). However, data after 1895 AD has a mean offset of 0.66±1.06‰ (-5.3±8.5 yrs) with increased variance compared to 19th century data. This, we believe, is attributable to anthropogenic fossil fuel, which, due to its long residence time in the earth, has long since lost any 14C component and when burned preferentially depletes the northern hemisphere atmosphere of 14C.

  15. Metabolic fate of the (14)C-labeled herbicide clodinafop-propargyl in a sediment-water system.

    PubMed

    Yuan, Ye; Weitzel, Pascal; Schäffer, Andreas; Schmidt, Burkhard

    2015-01-01

    was isolated from the sediment examined. It grew on (14)C-CfP as sole carbon source with evolution of (14)CO2. The bacterium was characterized by growth on commonly used carbon sources and 16S rDNA sequence analysis. Its sequence exhibited high similarity with that of Nocardioides aromaticivorans strain H-1 (98.85%; DSM 15131, JCM 11674). PMID:26065513

  16. Searching For A Suitable Gas Ion Source For 14C Accelerator Mass Spectrometry

    SciTech Connect

    Reden, Karl von; Roberts, Mark; Han, Baoxi; Schneider, Robert; Wills, John

    2007-08-10

    This paper describes the challenges facing 14C Accelerator Mass Spectrometry (AMS) in the effort to directly analyze the combusted effluent of a chromatograph (or any other continuous source of sample material). An efficient, low-memory negative gas ion source would greatly simplify the task to make this a reality. We discuss our tests of a microwave ion source charge exchange canal combination, present an improved design, and hope to generate more interest in the negative ion source community to develop a direct-extraction negative carbon gas ion source for AMS.

  17. A batch preparation method for graphite targets with low background for AMS [sup 14]C measurements

    SciTech Connect

    Kitagawa, Hiroyuki International Research Center for Japanese Studies, Nishikyp-ku, Kyoto ); Masuzawa, Toshiyuki; Matsumoto, Eiji ); Makamura, Toshio )

    1993-01-01

    The authors have developed a method of graphitization from CO[sub 2] samples for accurate [sup 14]C measurements by accelerator mass spectrometry. Their batch method, using a sealed Vycor tube, reduces the risk of contamination during graphitization and makes it possible to prepare many samples in a short time (typically 20 samples per day). They also describe details of the target-preparation method involving carbon isotopic fractionation during graphitization, yield of graphite from CO[sub 2], ion-beam intensity of the target, and background (or blank) level estimated using bituminous coal.

  18. Source apportionment of carbonaceous aerosol in Sao Paulo using 13C and 14C measurements

    NASA Astrophysics Data System (ADS)

    Oyama, Beatriz; Andrade, Maria de Fatima; Holzinger, Rupert; Röckmann, Thomas; Meijer, Harro A. J.; Dusek, Ulrike

    2016-04-01

    The Metropolitan Area of Sao Paulo is affected by high aerosol concentrations, which contain a large fraction of organic material. Up to date, not much is known about the composition and origin of the organic aerosol in this city. We present the first source apportionment of the carbonaceous aerosol fraction in Sao Paulo, using stable (13C) and radioactive carbon isotopes (14C). 14C provides a clear-cut distinction between fossil sources, which contain no 14C, and contemporary sources such as biofuels, biomass burning, or biogenic sources, which contain a typical contemporary 14C/12C ratio. 13C can be used to distinguish C3 plants, such as maize and sugarcane, from C4 plants. This can help to identify a possible impact of sugarcane field burning in the rural areas of Sao Paulo State on the aerosol carbon in the city. In the first part of the study, we compare two tunnel studies: Tunnel 1 is frequented only by light duty vehicles, which run mainly on mixtures of gasoline with ethanol (gasohol, 25% ethanol and 85% gasoline) or hydrated ethanol (5% water and 95% ethanol). Tunnel 2 contains a significant fraction of heavy-duty diesel vehicles, and therefore the fraction of biofuels in the average fleet is lower. Comparison of 14C in organic and elemental carbon (OC and EC) shows that in both tunnels there is no significant contribution of biofuels to EC. Combusting ethanol-gasoline fuels in a vehicle engine does apparently not result in significant EC formation from ethanol. Biofuels contribute around 45% to OC in Tunnel 1 an only 20% in Tunnel 2, reflecting a strong impact of diesel vehicles in Tunnel 2. In the second part of the study we conduct a source apportionment of ambient aerosol carbon collected in a field study during winter (July-August) 2012. Ambient EC has two main sources, vehicular emissions and biomass burning. We estimate a contribution of vehicular sources to EC of roughly 90% during weekdays and 80% during weekends, using the 14C values measured in

  19. In vitro O 2 fluxes compared with 14C production and other rate terms during the JGOFS Equatorial Pacific experiment

    NASA Astrophysics Data System (ADS)

    Bender, Michael; Orchardo, Joe; Dickson, Mary-Lynn; Barber, Richard; Lindley, Steven

    1999-04-01

    We report rates of gross and net O 2 production measured in vitro during JGOFS cruises in the equatorial Pacific in spring and fall, 1992. We scale O 2 productivities to net and gross C production. We then compare the calculated rates with 14C production and with new/export production measured by various techniques. 14C productivities in samples incubated for 24 h are about 45% of gross carbon production rates calculated from gross O 2 production. The difference is compatible with expected rates of the Mehler reaction, photorespiration, excretion, and community mitochondrial respiration. 14C production rates are similar to net carbon production rates in the upper half of the euphotic zone. At lower irradiances, where net C production can be zero or less, 14C productivities lie between net community production and gross primary production. Net carbon production rates in vitro are a factor of =4-20 times greater than estimates from drifting sediment trap and tracer transport studies. This difference probably reflects anomalous accumulation of POC in bottles because of the exclusion of grazers.

  20. Evaluation of iron and cobalt powders as catalysts for 14C-AMS target preparation

    NASA Astrophysics Data System (ADS)

    Santos, G. M.; Mazon, M.; Southon, J. R.; Rifai, S.; Moore, R.

    2007-06-01

    We present an evaluation of different brands of cobalt and iron powders used to catalyze CO2 reduction for 14C-AMS graphite targets at the KCCAMS/University of California, Irvine. The optimal catalyst is characterized by rapid graphitization, homogeneity and lack of sintering of the catalyst/carbon mixture, and contains minimal amounts of both "modern" and "dead" carbon. Fifteen catalyst powders were evaluated using these criteria. The results of this study indicate three good "catalyst-candidates" with backgrounds on processed coal (Argonne Premium coal POC#3) samples around 60 ka BP and modern and dead carbon contamination of ⩽0.2 μgC for 4-5 mg of catalyst.

  1. Estimating Aboveground Forest Carbon Stock of Major Tropical Forest Land Uses Using Airborne Lidar and Field Measurement Data in Central Sumatra

    NASA Astrophysics Data System (ADS)

    Thapa, R. B.; Watanabe, M.; Motohka, T.; Shiraishi, T.; shimada, M.

    2013-12-01

    Tropical forests are providing environmental goods and services including carbon sequestration, energy regulation, water fluxes, wildlife habitats, fuel, and building materials. Despite the policy attention, the tropical forest reserve in Southeast Asian region is releasing vast amount of carbon to the atmosphere due to deforestation. Establishing quality forest statistics and documenting aboveground forest carbon stocks (AFCS) are emerging in the region. Airborne and satellite based large area monitoring methods are developed to compliment conventional plot based field measurement methods as they are costly, time consuming, and difficult to implement for large regions. But these methods still require adequate ground measurements for calibrating accurate AFCS model. Furthermore, tropical region comprised of varieties of natural and plantation forests capping higher variability of forest structures and biomass volumes. To address this issue and the needs for ground data, we propose the systematic collection of ground data integrated with airborne light detection and ranging (LiDAR) data. Airborne LiDAR enables accurate measures of vertical forest structure, including canopy height and volume demanding less ground measurement plots. Using an appropriate forest type based LiDAR sampling framework, structural properties of forest can be quantified and treated similar to ground measurement plots, producing locally relevant information to use independently with satellite data sources including synthetic aperture radar (SAR). In this study, we examined LiDAR derived forest parameters with field measured data and developed general and specific AFCS models for tropical forests in central Sumatra. The general model is fitted for all types of natural and plantation forests while the specific model is fitted to the specific forest type. The study region consists of natural forests including peat swamp and dry moist forests, regrowth, and mangrove and plantation forests

  2. 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

  3. The TOCATTA-χ model for assessing 14C transfers to grass: an evaluation for atmospheric operational releases from nuclear facilities.

    PubMed

    Aulagnier, Céline; Le Dizès, Séverine; Maro, Denis; Hébert, Didier; Lardy, Romain; Martin, Raphael

    2013-06-01

    Radioactive (14)C is formed as a by-product of nuclear power generation and from the operation of nuclear fuel reprocessing plants like AREVA-NC La Hague (North France), which releases about 15 TBq per year of (14)C into the atmosphere. This article evaluates a recently improved radioecology model (TOCATTA-χ) to assess (14)C transfers to grassland ecosystems under normal operating conditions. The new version of the TOCATTA model (TOCATTA-χ) includes developments that were derived from PaSiM, a pasture model for simulating grassland carbon and radiocarbon cycling. The TOCATTA-χ model has been tested against observations of (14)C activity concentrations in grass samples collected monthly from six plots which are located around the periphery of the reprocessing plant. Simulated (14)C activities are consistent with observations on both intensively managed and poorly managed grasslands, but an adaptation of the mean turn-over time for (14)C within the plant is necessary in the model to account for different management practices. When atmospheric (14)C activity concentrations are directly inferred from observations, TOCATTA-χ performs better than TOCATTA (the root mean square error is decreased by 45%), but when atmospheric (14)C activity concentrations are not known and must be calculated, the uncertainty associated with the TOCATTA-χ model outcomes is estimated to be larger than the standard deviation of the observations. PMID:23466654

  4. Radiocarbon content of pre-bomb marine mollusks and variations in the 14C Reservoir age for coastal areas of the Barents and Kara Seas, Russia

    NASA Astrophysics Data System (ADS)

    Forman, Steven L.; Polyak, Leonid

    Fourteen mollusks, collected alive between 1900 and 1945 from the Russian Barents and Kara seas, were analyzed by AMS 14C dating to evaluate variations in the 14C marine reservoir for arctic coastal sites, which is important for correcting ages in paleoenvironmental time-series and advancing understanding of the exchange of carbon. The 14C ages on the mollusks reveal a range of marine reservoir values (R(t)) from 159 14C yr to 764 14C yr. The oldest R(t) values of 764 to 620 14C yr are for the bivalve Portlandia arctica, which often inhabit cold and low salinity waters and muddy substrates. The depleted 14C content for this bivalve reflects possibly the incorporation of old carbon from freshwater inputs and/or the consumption of old organic matter from the underlying sediments and pore waters. Other mollusks with sessile habitats and pelagic food sources gave significantly lower R(t) values between 159 and 344 14C yr. The youngest R(t) values indicate enrichment in 14C and may partially reflect enhanced transfer of 14C-enriched CO2 from the atmosphere to the ocean surface with wind-generated wave agitation. This study underscores that a variety of processes can lead to variable 14C depletion and enrichment of surface waters yielding a ca. 600 year age span for contemporaneous arctic mollusks. There may be added uncertainty in the 14C reservoir correction for deposit-feeder species such as Portlandia sp. and perhaps for certain benthic foraminifera (e.g. Nonion labradoricum) because these taxa often incorporate old organic matter from the substrate. A reservoir correction of ≥700 years may be more appropriate for infaunal, deposit-eater species, particularly in glacier-dominated environments. Mollusks and foraminifera with sessile habits and pelagic food sources should be selected preferentially for 14C dating, because their shells may more closely reflect the 14C content of the global-ocean mixed layer.

  5. 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 carbonates14C = -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).

  6. Autoradiographic disposition of (1-methyl-/sup 14/C)- and (2-/sup 14/C)caffeine in mice

    SciTech Connect

    Lachance, M.P.; Marlowe, C.; Waddell, W.J.

    1983-11-01

    Male, C57B1/6J mice received either (1-methyl-14C)caffeine or (2-14C)caffeine via the tail vein at a dose of 0.7 or 11 mg/kg, respectively. At 0.1, 0.33, 1, 3, 9, and 24 hr after treatment, the mice were anesthetized with ether and frozen by immersion in dry ice/hexane. The mice were processed for whole-body autoradiography by the Ullberg technique; this procedure does not allow thawing or contact with solvents. All autoradiographs revealed some retention of radioactivity at early time intervals in the lacrimal glands, seminal vesicle fluid, nasal and olfactory epithelium, and retinal melanocytes. The remaining portion of the animal was densitometrically uniform except for the lower levels noted in the CNS and adipose tissues. Excretion of radioactivity by the liver and kidneys seems to be the major routes of elimination. Localization in the liver at late time intervals was confined principally to the centrilobular region. Late sites of retention, observed only after (1-methyl-14C)caffeine administration, included the pancreas, minor and major salivary glands, splenic red pulp, thymal cortex, bone marrow, and gastrointestinal epithelium. Sites of localization present in both studies included the olfactory epithelium, lacrimal glands, hair follicles, and retinal melanocytes. Further studies are needed to determine whether the localization at these various sites is due to metabolic degradation, active transport, or possibly a specific receptor interaction.

  7. Pre to Post-Bomb Seawater 14C History in the Gulf of Alaska Inferred From a Deep Sea Coral: Isididae sp.

    NASA Astrophysics Data System (ADS)

    Roark, B.; Guilderson, T. P.; Fallon, S.; Dunbar, R. B.; McCulloch, M.

    2006-12-01

    Deep-sea corals are an important archive of intermediate and deep-water variability, and provide the means to explore decadal to century-scale ocean dynamics in regions and time periods heretofore unexplored. We present a reconstruction of pre to post-bomb surface and interior water Δ14C based on analysis of deep-sea Isididae (bamboo) corals collected live at ~700 meters in June 2002 at Warwick Seamount, Gulf of Alaska. Concurrent isotope analyses of polyp/tissue and outermost portion of the hard horny proteinaceous gorgonin nodes compared with in situ dissolved inorganic carbon indicates that the gorgonin portion is derived exclusively from recently fixed/exported particulate organic carbon and thus a record of the surface water 14C/12C history. This is in contrast to the carbonate internode portion which is primarily derived from in situ dissolved inorganic carbon, and thus a record of the in situ 14C/12C. Radiocarbon analysis of gorgonin nodal sections captures the surface water D14C evolution. Pre-bomb values are -105‰ reaching a maximum of 100‰ before decreasing to collection values of 20‰. We anticipate that the post-bomb maximum will be in the early 1970s consistent with other mid to high latitude records and that the pre/post bomb transition initiates near 1956. If we utilize the gorgonin pre/post bomb transition as a tie-point and assume a linear growth rate the Isididae used in this study are 75- 125 years old. Carbonate Δ14C shows a 25‰ increase from -215 to -190‰ reflecting the penetration of bomb-14C in the sub-polar North Pacific. To place the carbonate time-series on a fixed timescale we determined the minor element chemistry and tested the inter-species reproducibility. The distribution of Sr is quite homogenous whereas Mg is not with higher Mg concentrations associated with centers of calcification. Age estimates using what appear to be annual Sr/Ca cycles, which we hypothesize are related to biomineralization cycles associated with a

  8. A high resolution method for 14C analysis of a coral from South China Sea: Implication for "AD 775" 14C event

    NASA Astrophysics Data System (ADS)

    Ding, Ping; Shen, Chengde; Yi, Weixi; Wang, Ning; Ding, Xingfang; Liu, Kexin; Fu, Dongpo; Liu, Weiguo; Liu, Yi

    2015-10-01

    A pre-heating method that improves the background and precision of 14C dating significantly was applied for fossil coral dating with high resolution in our lab in Guangzhou Institute of Geochemistry, Chinese Academy of Sciences (GIGCAS). The reaction tube is heated under 300 °C in a vacuum line before it is used for graphitization. The method can reduce the contamination absorbed in TiH2, Zn and Fe power placed in the graphitization tube. With the pre-heating and average drilling method, bi-weekly resolution 14C dating in a fossil coral is carried out to investigate the "AD 775 14C spike event". Different from the tree ring 14C archives with the 14C spike of ∼15‰ (Δ14C), the 14C spike in the coral shows an abrupt peak of 45‰ and two smaller spikes of Δ14C > 20‰ in half a year in AD 776. And then, the 14C content in coral decreases gradually in AD 777. The peak time of the 14C spike event likely occurs in the summer of AD 776 according to the δ18O variation in coral. High-resolution dating of 14C in coral provides not only a more detail process of the event than that from tree rings, but also the first report of the event from sea ecosystem. Both of them suggest an extraterrestrial origin of the event cause.

  9. Assessment of the 14C-Glycocholic Acid Breath Test

    PubMed Central

    James, O. F. W.; Agnew, J. E.; Bouchier, I. A. D.

    1973-01-01

    The 1-(14C)-glycine-glycocholic-acid breath test has been performed on 104 subjects and a normal range established. Abnormal results due to bacterial deconjugation of bile salts were found not only in patients with the “contaminated bowel” syndrome and in those with ileal resection but also in a third group, patients with cholangitis. Abnormal results were also found in patients with gastrocolic fistula and staphylococcal enterocolitis, while mildly abnormal results were also found in some patients with liver disease. PMID:4718834

  10. Oxygen Effects on Photosynthesis and 14C Metabolism in Desert Plants

    PubMed Central

    Glacoleva, Tatyana A.; Zalensky, Oleg V.; Mokronosov, Adolf T.

    1978-01-01

    The effect of 1% and 21% O2 upon 14CO2 assimilation by desert plants exposed for 10 to 90 seconds has been studied. The plants studied can be divided into three groups with respect to O2. The C3 plants display the usual Warburg effect. No changes could be observed in the intensity of photosynthesis as a function of O2 content in another group of plants (showing signs of Crassulacean acid metabolism). In still another group of plants (C4 plants) the stimulating effect of O2 on photosynthesis could be detected. In C3 plants, O2 inhibits the processing of carbon through the Calvin cycle intermediates. The involvement of carbon in the glycolate pathway fails to explain completely the inhibiting effect of O2 on photosynthesis. It is assumed that O2 inhibits the enzymes of the Calvin cycle. In C4 plants O2 stimulates the incorporation of 14C into malate and aspartate. The incorporation of 14C into the intermediates of the Calvin cycle in C4 plants is inhibited much like that in typical C3 plants. PMID:16660486

  11. 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

  12. 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

  13. Using Airborne Microwave Remotely Sensed Root-Zone Soil Moisture and Flux Measurements to Improve Regional Predictions of Carbon Fluxes in a Terrestrial Biosphere Model

    NASA Astrophysics Data System (ADS)

    Zhang, K.; Antonarakis, A. S.; Medvigy, D.; Burgin, M. S.; Crow, W. T.; Milak, S.; Jaruwatanadilok, S.; Truong-Loi, M.; Moghaddam, M.; Saatchi, S. S.; Cuenca, R. H.; Moorcroft, P. R.

    2013-12-01

    North American ecosystems are critical components of the global carbon cycle, exchanging large amounts of carbon dioxide and other gases with the atmosphere. Net ecosystem exchange (NEE) of CO2 between atmosphere and ecosystems quantifies these carbon fluxes, but current continental-scale estimates contain high levels of uncertainty. Root-zone soil moisture (RZSM) and its spatial and temporal heterogeneity influences NEE and improved estimates can help reduce uncertainty in NEE estimates. We used the RZSM measurements from the Airborne Microwave Observatory of Subcanopy and Subsurface (AirMOSS) mission, and the carbon, water and energy fluxes observed by the eddy-covariance flux towers to constrain the Ecosystem Demography Model 2.2 (ED2.2) to improve its predictions of carbon fluxes. The parameters of the ED2.2 model were first optimized at seven flux tower sites in North America, which represent six different biomes, by constraining the model against a suite of flux measurements and forest inventory measurements through a Bayesian Markov-Chain Monte Carlo framework. We further applied the AirMOSS RZSM products to constrain the ED2.2 model to achieve better estimates of regional NEE. Evaluation against flux tower measurements and forest dynamics measurements shows that the constrained ED2.2 model produces improved predictions of monthly to annual carbon fluxes. The remote sensing based RZSM can further help improve the spatial patterns and temporal variations of model NEE. The results demonstrate that model-data fusion can substantially improve model performance and highlight the important role of RZSM in regulating the spatial and temporal heterogeneities of carbon fluxes.

  14. 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 carbonates14C = -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).

  15. Modelling the transfer of 14C from the atmosphere to grass: a case study in a grass field near AREVA-NC La Hague.

    PubMed

    Aulagnier, C; Le Dizès, S; Maro, D; Hébert, D; Lardy, R; Martin, R; Gonze, M-A

    2012-10-01

    Radioactive (14)C is formed as a by-product of nuclear power generation and from operation of nuclear fuel reprocessing plants like AREVA-NC La Hague (North France), which releases about 15 TBq per year of (14)C into the atmosphere. Since the autumn of 2006, (14)C activity concentrations in samples from the terrestrial environment (air, grass and soil) have been monitored monthly on grassland 2 km downwind of the reprocessing plant. The monitoring data provides an opportunity to validate radioecology models used to assess (14)C transfer to grassland ecosystems. This article compares and discusses the ability of two different models to reproduce the observed temporal variability in grass (14)C activity in the vicinity of AREVA-NC La Hague. These two models are the TOCATTA model which is specifically designed for modelling transfer of (14)C and tritium in the terrestrial environment, and PaSim, a pasture model for simulating grassland carbon and nitrogen cycling. Both TOCATTA and PaSim tend to under-estimate the magnitude of observed peaks in grass (14)C activity, although they reproduce the general trends. PaSim simulates (14)C activities in substrate and structural pools of the plant. We define a mean turn-over time for (14)C within the plant, which is based on both experimental data and the frequency of cuts. An adapted PaSim result is presented using the 15 and 20 day moving average results for the (14)C activity in the substrate pool, which shows a good match to the observations. This model reduces the Root Mean Square Error (RMSE) by nearly 40% in comparison to TOCATTA. PMID:22537618

  16. A First Look at Airborne Imaging Spectrometer (AIS) Data in an Area of Altered Volcanic Rocks and Carbonate Formations, Hot Creek Range, South Central Nevada

    NASA Technical Reports Server (NTRS)

    Feldman, S. C.; Taranik, J. V.; Mouat, D. A.

    1985-01-01

    Three flight lines of Airborne Imaging Spectrometer (AIS) data were collected in 128 bands between 1.2 and 2.4 microns in the Hot Creek Range, Nevada on July 25, 1984. The flight lines are underlain by hydrothermally altered and unaltered Paleozoic carbonates and Tertiary rhyolitic to latitic volcanics in the Tybo mining district. The original project objectives were to discriminate carbonate rocks from other rock types, to distinguish limestone from dolomite, and to discriminate carbonate units from each other using AIS imagery. Because of high cloud cover over the prime carbonate flight line and because of the acquisition of another flight line in altered and unaltered volcanics, the study has been extended to the discrimination of alteration products. In an area of altered and unaltered rhyolites and latites in Red Rock Canyon, altered and unaltered rock could be discriminated from each other using spectral features in the 1.16 to 2.34 micron range. The altered spectral signatures resembled montmorillonite and kaolinite. Field samples were gathered and the presence of montmorillonite was confirmed by X-ray analysis.

  17. Disposition of [14C]ruboxistaurin in humans.

    PubMed

    Burkey, Jennifer L; Campanale, Kristina M; Barbuch, Robert; O'Bannon, Douglas; Rash, James; Benson, Charles; Small, David

    2006-11-01

    Ruboxistaurin is a potent and specific inhibitor of the beta isoforms of protein kinase C (PKC) that is being developed for the treatment of diabetic microvascular complications. The disposition of [(14)C]ruboxistaurin was determined in six healthy male subjects who received a single oral dose of 64 mg of [(14)C]ruboxistaurin in solution. There were no clinically significant adverse events during the study. Whole blood, urine, and feces were collected at frequent intervals after dosing. Metabolites were profiled by high performance liquid chromatography with radiometric detection. The total mean recovery of the radioactive dose was approximately 87%, with the majority of the radioactivity (82.6 +/- 1.1%) recovered in the feces. Urine was a minor pathway of elimination (4.1 +/- 0.3%). The major route of ruboxistaurin metabolism was to the N-desmethyl ruboxistaurin metabolite (LY338522), which has been shown to be active and equipotent to ruboxistaurin in the inhibition of PKC(beta). In addition, multiple hydroxylated metabolites were identified by liquid chromatography-mass spectrometry in all matrices. Pharmacokinetics were conducted for both ruboxistaurin and LY338522 (N-desmethyl ruboxistaurin, 1). These moieties together accounted for approximately 52% of the radiocarbon measured in the plasma. The excreted radioactivity was profiled using radiochromatography, and approximately 31% was structurally characterized as ruboxistaurin or N-desmethyl ruboxistaurin. These data demonstrate that ruboxistaurin is metabolized primarily to N-desmethyl ruboxistaurin (1) and multiple other oxidation products, and is excreted primarily in the feces. PMID:16896067

  18. 14C Concentrations in the Northern Atlantic and Nordic Seas

    NASA Astrophysics Data System (ADS)

    Nadeau, M.-J.; Grootes, P. M.; Erlenkeuser, H.

    2003-04-01

    We report here more than 450 new Δ14C results from water samples from the North Atlantic and the Nordic Seas measured at the Leibniz-Labor, Christian-Albrechts Universität, Kiel, using accelerator mass spectrometry. The water samples were collected during three cruises of the RV Meteor: M36 in 1996 (65 measurements, 6 stations), M39 in 1997 (217 measurements, 11 stations) and M50 in 2001 (189 measurements, 10 stations). These results are compared to those of previous sampling campaigns: GEOSECS (1972) and TTO (1981) and of samples obtained from previous cruises of the RV Meteor (M18 in 1991 and M30 in 1994) measured by decay counting at the Institut für Umweltphysik in Heidelberg. Several stations from the cruise M50 are located along the WOCE A02 line from the western entrance of the English Channel to the tip of Newfoundland/Grand Banks. This transect also analysed during the M30 (1994) campaign provides the evolution of the penetration of atmospheric bomb 14C into these waters over a seven year period. Other samples were taken in the Labrador Sea, and North and South of Iceland. Comparison with CFC measurements, for some of the stations, also provides an insight in the penetration of both tracers into the ocean.

  19. Accelerator mass spectrometry analysis of 14C-oxaliplatin concentrations in biological samples and 14C contents in biological samples and antineoplastic agents

    NASA Astrophysics Data System (ADS)

    Toyoguchi, Teiko; Kobayashi, Takeshi; Konno, Noboru; Shiraishi, Tadashi; Kato, Kazuhiro; Tokanai, Fuyuki

    2015-10-01

    Accelerator mass spectrometry (AMS) is expected to play an important role in microdose trials. In this study, we measured the 14C concentration in 14C-oxaliplatin-spiked serum, urine and supernatant of fecal homogenate samples in our Yamagata University (YU) - AMS system. The calibration curves of 14C concentration in serum, urine and supernatant of fecal homogenate were linear (the correlation coefficients were ⩾0.9893), and the precision and accuracy was within the acceptance criteria. To examine a 14C content of water in three vacuum blood collection tubes and a syringe were measured. 14C was not detected from water in these devices. The mean 14C content in urine samples of 6 healthy Japanese volunteers was 0.144 dpm/mL, and the intra-day fluctuation of 14C content in urine from a volunteer was little. The antineoplastic agents are administered to the patients in combination. Then, 14C contents of the antineoplastic agents were quantitated. 14C contents were different among 10 antineoplastic agents; 14C contents of paclitaxel injection and docetaxel hydrate injection were higher than those of the other injections. These results indicate that our quantitation method using YU-AMS system is suited for microdosing studies and that measurement of baseline and co-administered drugs might be necessary for the studies in low concentrations.

  20. Human Vitamin B12 Absorption and Metabolism are Measured by Accelerator Mass Spectrometry Using Specifically Labeled 14C-Cobalamin

    SciTech Connect

    Carkeet, C; Dueker, S R; Lango, J; Buchholz, B A; Miller, J W; Green, R; Hammock, B D; Roth, J R; Anderson, P J

    2006-01-26

    There is need for an improved test of human ability to assimilate dietary vitamin B{sub 12}. Assaying and understanding absorption and uptake of B{sub 12} is important because defects can lead to hematological and neurological complications. Accelerator mass spectrometry (AMS) is uniquely suited for assessing absorption and kinetics of {sup 14}C-labeled substances after oral ingestion because it is more sensitive than decay counting and can measure levels of carbon-14 ({sup 14}C) in microliter volumes of biological samples, with negligible exposure of subjects to radioactivity. The test we describe employs amounts of B{sub 12} in the range of normal dietary intake. The B{sub 12} used was quantitatively labeled with {sup 14}C at one particular atom of the DMB moiety by exploiting idiosyncrasies of Salmonellametabolism. In order to grow aerobically on ethanolamine, S. entericamust be provided with either pre-formed B{sub 12} or two of its precursors: cobinamide and dimethylbenzimidazole (DMB). When provided with {sup 14}C-DMB specifically labeled in the C2 position, cells produced {sup 14}C-B{sub 12} of high specific activity (2.1 GBq/mmol, 58 mCi/mmol) and no detectable dilution of label from endogenous DMB synthesis. In a human kinetic study, a physiological dose (1.5 mg, 2.2 KBq/59 nCi) of purified {sup 14}C-B{sub 12} was administered and showed plasma appearance and clearance curves consistent with the predicted behavior of the pure vitamin. This method opens new avenues for study of B{sub 12} assimilation.

  1. Surrogate gas prediction model as a proxy for Δ14C-based measurements of fossil fuel CO2

    NASA Astrophysics Data System (ADS)

    Coakley, Kevin J.; Miller, John B.; Montzka, Stephen A.; Sweeney, Colm; Miller, Ben R.

    2016-06-01

    The measured 14C:12C isotopic ratio of atmospheric CO2 (and its associated derived Δ14C value) is an ideal tracer for determination of the fossil fuel derived CO2 enhancement contributing to any atmospheric CO2 measurement (Cff). Given enough such measurements, independent top-down estimation of U.S. fossil fuel CO2 emissions should be possible. However, the number of Δ14C measurements is presently constrained by cost, available sample volume, and availability of mass spectrometer measurement facilities. Δ14C is therefore measured in just a small fraction of samples obtained by flask air sampling networks around the world. Here we develop a projection pursuit regression (PPR) model to predict Cff as a function of multiple surrogate gases acquired within the NOAA/Earth System Research Laboratory (ESRL) Global Greenhouse Gas Reference Network (GGGRN). The surrogates consist of measured enhancements of various anthropogenic trace gases, including CO, SF6, and halocarbon and hydrocarbon acquired in vertical airborne sampling profiles near Cape May, NJ and Portsmouth, NH from 2005 to 2010. Model performance for these sites is quantified based on predicted values corresponding to test data excluded from the model building process. Chi-square hypothesis test analysis indicates that these predictions and corresponding observations are consistent given our uncertainty budget which accounts for random effects and one particular systematic effect. However, quantification of the combined uncertainty of the prediction due to all relevant systematic effects is difficult because of the limited range of the observations and their relatively high fractional uncertainties at the sampling sites considered here. To account for the possibility of additional systematic effects, we incorporate another component of uncertainty into our budget. Expanding the number of Δ14C measurements in the NOAA GGGRN and building new PPR models at additional sites would improve our understanding of

  2. Process-oriented dose assessment model for 14C due to releases during normal operation of a nuclear power plant.

    PubMed

    Aquilonius, Karin; Hallberg, Bengt

    2005-01-01

    Swedish nuclear utility companies are required to assess doses due to releases of radionuclides during normal operation. In 2001, calculation methods used earlier were updated due to new authority regulations. The isotope (14)C is of special interest in dose assessments due to the role of carbon in the metabolism of all life forms. Earlier, factors expressing the ratio between concentration of (14)C in air and in various plants were used. In order to extend the possibility to take local conditions into account, a process-oriented assessment model for uptake of carbon and doses from releases of (14)C to air was developed (POM(14)C). The model uses part of DAISY which has been developed to model the turnover of carbon in crops. [Hansen, S., Jensen, H.E., Nielsen, N.E., Svendsen, H., 1993. Description of the Soil Plant System Model DAISY, Basic Principles and Modelling Approach. Simulation Model for Transformation and Transport of Energy and Matter in the Soil Plant Atmosphere System. Jordbruksförlaget, The Royal Veterinary and Agricultural University, Copenhagen, Denmark]. The main objectives were to test model performance of the former method, and to investigate if taking site specific parameters into account to a greater degree would lead to major differences in the results. Several exposure pathways were considered: direct consumption of locally grown cereals, vegetables, and root vegetables, as well as consumption of milk and meat from cows having eaten fodder cereals and green fodder from the area around the nuclear plant. The total dose of the earlier model was compared with that of POM(14)C. The result of the former was shown to be slightly higher than the latter, but POM(14)C confirmed that the earlier results were of a reasonable magnitude. When full account of local conditions was taken, e.g. as regards solar radiation, temperature, and concentration of (14)C in air at various places in the surroundings of each nuclear plant, a difference in dose between

  3. A Process-based Study of Speleothem 14C Variability: Climatic Controls and Prospects for Speleothem-based Radiocarbon Calibration

    NASA Astrophysics Data System (ADS)

    Johnson, K. R.; Magana, A. L.; Hu, C.; Ruan, J.

    2011-12-01

    Recent studies have shown that speleothems may be useful for improving the 14C calibration curve, primarily because: (1) they can be absolutely dated with the U-Th method, (2) they obtain the majority of their carbon directly from the atmosphere, and (3) the "dead carbon fraction" (DCF) obtained from the carbonate bedrock has been shown to be fairly constant over long time periods. In order to assess the stability of DCF, and hence the validity of speleothem based calibration curves, however, it is necessary to conduct detailed studies in modern cave systems and on well-dated stalagmites that overlap with the tree-ring 14C record. We will present results of a study at Heshang Cave, Hubei Province, China (30°27'N, 110°25'E; 294 m), the site of ongoing, extensive modern calibration and paleoclimate reconstruction efforts. We have conducted a detailed study of C cycling in the modern cave system through collection and analysis of the δ13C and Δ14C composition of soil CO2, dripwater DIC, and monthly modern calcite samples to investigate how seasonal environmental changes impact speleothem DCF and δ13C. In addition, we have investigated climatic controls on DCF on longer timescales through high-resolution 14C analysis of an annually laminated, U-Th dated Holocene stalagmite. Modern calcite from a site near the cave entrance shows significant seasonal Δ14C variability, ranging from 30 to 65%, which may reflect seasonal variability in atmospheric Δ14C. This suggests that cave dripwater DIC may sometimes equilibrate with cave air CO2, prior to calcite precipitation. Despite a large range in the Δ14C values of dripwater DIC samples collected from throughout the cave, individual speleothem DCF appears quite constant over the Holocene, at 9.3 ± 1.9%, with an average age offset of 838 ± 187 years. Applying this constant DCF correction over the Holocene yields an excellent correlation with the IntCal09 curve (r2 = 0.99). While minor DCF variability could introduce

  4. AixMICADAS, the accelerator mass spectrometer dedicated to 14C recently installed in Aix-en-Provence, France

    NASA Astrophysics Data System (ADS)

    Bard, Edouard; Tuna, Thibaut; Fagault, Yoann; Bonvalot, Lise; Wacker, Lukas; Fahrni, Simon; Synal, Hans-Arno

    2015-10-01

    A compact AMS system dedicated to measuring 14C in ultra-small samples was installed at the CEREGE in Aix-en-Provence at the end of March 2014, together with an automated graphitization system. AixMICADAS operates at around 200 kV with carbon ion stripping in helium leading to a transmission of about 47%. The hybrid ion source works with graphite targets and CO2 gas. It is coupled to a versatile gas interface system that ensures stable gas measurements from different sources: a cracker for CO2 in glass ampoules, an elemental analyzer for combusting organic matter and an automated system to handle carbonate by wet chemistry. The analyses performed during the first half-year of operation show that a precision of about 2‰ is reached on modern samples of about 1 mg of carbon. Measurements of IAEA reference materials of various 14C ages show a good agreement with consensus values. Direct measurements of geological graphites indicate a machine background equivalent to an age of 68,000 years BP. AixMICADAS is thus limited solely by the 14C contamination of samples in the field and in the laboratory. The performances of the gas ion source and its gas interface system were tested with two CO2 production units: the elemental analyzer and the automated carbonate hydrolysis unit. These tests show that samples ranging between 10 and 100 μg C can produce a 12C- ion beam of the order of 10-15 μA during time spans ranging from 3 to 30 min depending on the sample mass. Coupling the automated hydrolysis system to the gas ion source of AixMICADAS, enables us to develop a method involving sequential leaching of carbonate samples with direct 14C measurements of the leached fractions and the residual sample. The main advantage is that all of steps leaching and hydrolysis are performed in the same vial for a particular sample. A sequential leaching was applied to a young carbonate sample (ca. 6600 years BP) whose 14C age agrees with previous determination and which shows no sign of

  5. 2-Micron Triple-Pulse Integrated Path Differential Absorption Lidar Development for Simultaneous Airborne Column Measurements of Carbon Dioxide and Water Vapor in the Atmosphere

    NASA Technical Reports Server (NTRS)

    Singh, Upendra N.; Petros, Mulugeta; Refaat, Tamer F.; Yu, Jirong

    2016-01-01

    For more than 15 years, NASA Langley Research Center (LaRC) has contributed in developing several 2-micron carbon dioxide active remote sensors using the DIAL technique. Currently, an airborne 2-micron triple-pulse integrated path differential absorption (IPDA) lidar is under development at NASA LaRC. This paper focuses on the advancement of the 2-micron triple-pulse IPDA lidar development. Updates on the state-of-the-art triple-pulse laser transmitter will be presented including the status of wavelength control, packaging and lidar integration. In addition, receiver development updates will also be presented, including telescope integration, detection systems and data acquisition electronics. Future plan for IPDA lidar system for ground integration, testing and flight validation will be presented.

  6. Solid-State 2-Micron Laser Transmitter Advancement for Wind and Carbon Dioxide Measurements From Ground, Airborne, and Space-Based Lidar Systems

    NASA Technical Reports Server (NTRS)

    Singh, Upendra N.; Kavaya, Michael J.; Koch, Grady; Yu, Jirong; Ismail, Syed

    2008-01-01

    NASA Langley Research Center has been developing 2-micron lidar technologies over a decade for wind measurements, utilizing coherent Doppler wind lidar technique and carbon dioxide measurements, utilizing Differential Absorption Lidar (DIAL) technique. Significant advancements have been made towards developing state-of-the-art technologies towards laser transmitters, detectors, and receiver systems. These efforts have led to the development of solid-state lasers with high pulse energy, tunablility, wavelength-stability, and double-pulsed operation. This paper will present a review of these technological developments along with examples of high resolution wind and high precision CO2 DIAL measurements in the atmosphere. Plans for the development of compact high power lasers for applications in airborne and future space platforms for wind and regional to global scale measurement of atmospheric CO2 will also be discussed.

  7. Fourth Airborne Geoscience Workshop

    NASA Technical Reports Server (NTRS)

    1991-01-01

    The focus of the workshop was on how the airborne community can assist in achieving the goals of the Global Change Research Program. The many activities that employ airborne platforms and sensors were discussed: platforms and instrument development; airborne oceanography; lidar research; SAR measurements; Doppler radar; laser measurements; cloud physics; airborne experiments; airborne microwave measurements; and airborne data collection.

  8. Airborne laser

    NASA Astrophysics Data System (ADS)

    Lamberson, Steven E.

    2002-06-01

    The US Air Force Airborne Laser (ABL) is an airborne, megawatt-class laser system with a state-of-the-art atmospheric compensation system to destroy enemy ballistic missiles at long ranges. This system will provide both deterrence and defense against the use of such weapons during conflicts. This paper provides an overview of the ABL weapon system including: the notional operational concept, the development approach and schedule, the overall aircraft configuration, the technologies being incorporated in the ABL, and the risk reduction approach being utilized to ensure program success.

  9. Metabolism and excretion of [14C] verruculogen in a sheep.

    PubMed

    Perera, K P; Mantle, P G; Penny, R H

    1982-05-01

    [14C] Verruculogen (75 micrograms/kg) was given intravenously to a sheep under barbiturate anaesthesia to prevent the severe tremor and convulsions which would otherwise have occurred. Two hours later 28 per cent of the tremorgenic mycotoxin was detected in the liver, bile and small intestine. Approximately 0.5 per cent was excreted in the urine. Trace amounts of radiolabel were detected in the cortex and corpus striatum of the brain. Verruculogen was metabolised by the liver and converted completely to four more polar products, including two isomeric forms of desoxy-verruculogen and the weakly tremorgenic mycotoxin TR-2. The principal and most polar metabolite excreted is probably an isomer of TR-2. PMID:7100651

  10. Structure of 19O from 9Be + 14C

    NASA Astrophysics Data System (ADS)

    Dungan, R.; Tabor, S. L.; Vonmoss, J.; Morrow, S.; Abromeit, B.; Kravvaris, K.; Parker, J. J., IV; Tai, P. L.; Tripathi, Vandana; Volya, A.

    2015-10-01

    The 9Be(14C, α γ) reaction at ELab = 30 and 35 MeV was used to study excited states of 19O. The Florida State University (FSU) γ detector array was used to detect γ radiation in coincidence with charged particles detected and identified with a silicon ΔE-E particle telescope. From α- γ- γ coincidences five new states of 19O have been identified and an additional three new γ transitions among known states have been observed. An additional previously unobserved state has been marked tentative from α- γ coincidences. These results are compared to shell model calculations using the USDA, WBP, and PSDU interactions. This work was supported in part by U.S. National Science Foundation Grant NSF-14-01574.

  11. Effect of endomycorrhizae on the bioavailability of bound sup 14 C residues to onion plants from an organic soil treated with ( sup 14 C)fonofos

    SciTech Connect

    Nelson, S.D.; Khan, S.U. )

    1990-03-01

    Uptake of bound {sup 14}C residues from an organic soil treated with radiolabeled fonofos (O-ethyl S-phenyl ethylphosphonodithioate) by selected Glomus endomycorrhiza and onion roots was studied. The hyphae of endomycorrhizal associations were capable of removing {sup 14}C residues from the soil and transporting them to onion plants. Bioavailability of soil-bound {sup 14}C residues, as measured by {sup 14}C residue content in onion, was increased 32 and 40% over that of nonmycorrhizal plants by hyphae of Glomus intraradices and Glomus vesiculiferium, respectively. The data suggest that under field conditions endomycorrhizal infection may greatly increase the bioavailability of soil-bound pesticide residues to plants.

  12. 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

  13. MEASUREMENTS OF PAST 14C LEVELS AND 13C/12C RATIOS IN THE SURFACE WATERS OF THE WORLD'S SUBPOLAR OCEANS.

    SciTech Connect

    Brown, T A

    2010-04-22

    Under this project we have developed methods that allow the reconstruction of past {sup 14}C levels of the surface waters of the subpolar North Pacific Ocean by measuring the {sup 14}C contents of archived salmon scales. The overall goal of this research was to reduce of the uncertainty in the uptake of fossil CO{sub 2} by the oceans and thereby improve the quantification of the global carbon cycle and to elucidate the fate of anthropogenic CO{sub 2}. Ocean General Circulation Models (OGCMs), with their three dimensional global spatial coverage and temporal modeling capabilities, provide the best route to accurately calculating the total uptake of CO{sub 2} by the oceans and, hence, to achieving the desired reduction in uncertainty. {sup 14}C has played, and continues to play, a central role in the validation of the OGCMs calculations, particularly with respect to those model components which govern the uptake of CO{sub 2} from the atmosphere and the transport of this carbon within the oceans. Under this project, we have developed time-series records of the {sup 14}C levels of the surface waters of three areas of the subpolar North Pacific Ocean. As the previously available data on the time-history of oceanic surface water {sup 14}C levels are very limited, these time-series records provide significant new {sup 14}C data to constrain and validate the OGCMs.

  14. Renewal rates of east Atlantic deep water estimated by inversion of /sup 14/C data

    SciTech Connect

    Schlitzer, R.

    1987-03-15

    The renewal of the deep water of the East Atlantic and its large-scale internal circulation are studied on the basis of the distributions of potential temperature, silicate, ..sigma..CO/sub 2/, and /sup 14/C. An isopycnal multibox model including advection, mixing, and sources and sinks is set up and described. Tracer data are input for the model, and balance equations for the various properties for the boxes of the model serve as constraints for the determination of water fluxes, mixing coefficients, and source parameters. Extremal values for various model parameters that are consistent with the tracer data (satisfy the balance equations within the estimated tolerances) are calculated by linear programming techniques. /sup 14/C data are seen to be valuable in determining absolute flow rates. Model results confirm the importance of the Romanche Fracture Zone for the renewal of east Atlantic deep water. Eastward flows through the Romanche Fracture Zone were found to be between 2.6 and 5.1 Sv. Flows through the Vema Fracture Zone amount to at most 20% of the Romanche Fracture Zone inflow. Contributions of Antarctic Bottom Water at the southern end of the East Atlantic and of Iceland Scotland Overflow Water at the northern end are very small (<5% of equatorial inflow). Diapycnal mixing coefficients are between 1 and 10 cm/sup 2//s, and values for the dissolution rates of silicate and carbon are in the expected range.

  15. Highly Sensitive 14C and 3H Quantification of Biochemical Samples Using Accelerator Mass Spectrometry

    SciTech Connect

    Ognibene, T J; Vogel, J S

    2003-10-23

    Accelerator Mass Spectrometry (AMS) is an isotope ratio mass spectrometer that quantifies low levels of rare isotopes with half-lives between 10 and 10{sup 8} years. Typical sensitivities are 10{sup 6} atoms in a milligram-sized sample. AMS was originally developed for use in the geosciences as a tool to carbon date archaeological artifacts, but has applications in many fields. In the biosciences, the extreme sensitivity of AMS is used to trace nutrients, toxins and therapeutics in humans and animals using less than {micro}g/kg doses containing between 1-100 nCi of {sup 14}C. This sensitivity is used to reduce sample size, reduce chemical exposures to environmental or physiological levels, reduce radiation exposures to subjects, and/or reduce radioactive (and ''mixed'') waste. Compared to decay counting, AMS provides for a much higher measurement throughput for low activity samples. For example, a milligram-sized sample containing 1 dpm of {sup 14}C can be measured to 3% precision in several seconds. That same sample would require approximately 1 week of decay counting to obtain similar precision.

  16. The direct absorption method of 14C assay—historical perspective and future potential

    NASA Astrophysics Data System (ADS)

    Vita-Finzi, Claudio; Leaney, Fred

    2006-05-01

    Radiocarbon dating by liquid scintillation counting of 14CO 2 absorbed into an alkaline liquid was first developed for groundwater research. In the 1980s it was applied to molluscs, barnacles, corals and other carbonates, and yielded dependable results within a few hours, with standard errors of ˜10% for ages <14 000 yr, at about 1/200 the price of commercial 14C dates. Although its cost has risen fivefold, the first-order approach remains useful in coastal neotectonics, where numerous low-precision determinations are often more useful than a few high-precision dates. Direct absorption (DA) 14C dating has now been improved and extended to include wood and charcoal samples, and provides ages in a variety of environments with standard errors similar to those reported by conventional radiometric laboratories and for ages spanning the last 30 000 years. The unit cost for a 'state of the art' DA determination is close to 50% of that by benzene synthesis, but the method is favoured in many hydrological and archaeological applications because it is robust and rapid.

  17. Radiochemically pure (1-/sup 14/C)valproic acid--a mixture of labeled structural isomers

    SciTech Connect

    Dickinson, R.G.; Wood, B.T.; Kluck, R.M.; Hooper, W.D.

    1986-01-01

    Ongoing studies of the disposition of valproic acid (VPA) and its glucuronide conjugate required the radiolabeled drug for greater sensitivity and tracing of oxidation metabolites. (1-/sup 14/C)VPA hereinafter called LABEL (radiochemical purity greater than 98% as determined by paper and thin layer chromatography) was purchased from Amersham International, U.K. Quantitative analysis of VPA and VPA-glucuronide in bile and urine samples from rats given VPA and tracer LABEL by our standard gas chromatographic assay showed gross discrepancies with the results obtained by liquid scintillation counting of the same extracts. Examination of the purity of LABEL was therefore undertaken. Equilibration of LABEL between various organic-aqueous solvent pairs was identical to that of authentic VPA. However, gas chromatographic-mass spectrometric analysis of the trimethylsilyl derivative of LABEL revealed it to be a mixture of labeled 2-methylheptanoic acid (approximately 60%), 2-ethylhexanoic acid (approximately 30%), and 2-propylpentanoic acid (i.e., VPA, 5-10%). The origin of the isomers of VPA in LABEL was logically traced to the synthetic procedure--coupling of the Grignard reagent of (an isomeric mixture of 2-, 3-, and 4-) chloroheptane(s) with (/sup 14/C)carbon dioxide. This result highlights the inadequacy of the quality control procedures used and reinforces the necessity for caution in accepting the quoted purity of radiolabeled drugs.

  18. Factors affecting the uptake of 14C-labeled organic chemicals by plants from soil

    SciTech Connect

    Topp, E.; Scheunert, I.; Attar, A.; Korte, F.

    1986-04-01

    The uptake of /sup 14/C from various /sup 14/C-labeled organic chemicals from different chemical classes by barley and cress seedlings from soil was studied for 7 days in a closed aerated laboratory apparatus. Uptake by roots and by leaves via the air was determined separately. Although comparative long-term outdoor studies showed that an equilibrium is not reached within a short time period, plant concentration factors after 7 days could be correlated to some physicochemical and structural substance properties. Barley root concentration factors due to root uptake, expressed as concentration in roots divided by concentration in soil, gave a fairly good negative correlation to adsorption coefficients based on soil organic carbon. Barley root concentration factors, expressed as concentration in roots divided by concentration in soil liquid, gave a positive correlation to the n-octanol/water partition coefficients. Uptake of chemicals by barley leaves via air was strongly positively correlated to volatilization of chemicals from soil. Both root and foliar uptake by barley could be correlated well to the molecular weight of 14 chemicals. Uptake of chemicals by cress differed from that by barley, and correlations to physicochemical substance properties mostly were poor.

  19. Photoperiodic control of soybean /sup 14/C-assimilate partitioning during the seed filling period

    SciTech Connect

    Morandi, E.N.

    1986-04-01

    Photoperiod not only controls the timing of flowering, but also affects later stages of seed development. To study its effect on assimilate partitioning, soybean plants were kept in short days (SD) or night interrupted (NI) during seed filling. The source-sink ratio was fixed to one leaflet-one pod per node. The node was girdle-isolated and its leaflet was pulse labelled with /sup 14/CO/sub 2/. SD plants partitioned more /sup 14/C into seeds, while NI plants showed higher proportions in the petiole, stem and carpel. Seed growth rate and final seed dry weight were increased by 40% in SD. The sugar/starch ratio was increased in cotyledons and decreased in leaves of SD plants. In contrast, NI plants showed more /sup 14/C incorporation into proteins. No changes were detected in carbon exchange ratio, dark respiration and total node dry weight. Thus, photoperiodic induced changes in carbohydrate and protein partitioning occurred without changes in the overall assimilatory process.

  20. Defective (U-14 C) palmitic acid oxidation in Duchenne muscular dystrophy

    SciTech Connect

    Carroll, J.E.; Norris, B.J.; Brooke, M.H.

    1985-01-01

    Compared with normal skeletal muscle, muscle from patients with Duchenne dystrophy had decreased (U-14 C) palmitic acid oxidation. (1-14 C) palmitic acid oxidation was normal. These results may indicate a defect in intramitochondrial fatty acid oxidation.

  1. Large spatial variations in coastal 14C reservoir age - a case study from the Baltic Sea

    NASA Astrophysics Data System (ADS)

    Lougheed, B. C.; Filipsson, H. L.; Snowball, I.

    2013-02-01

    Coastal locations are highly influenced by input from freshwater river runoff, including sources of terrestrial carbon, which can be expected to modify the 14C reservoir age, or R(t), associated with marine water. In this Baltic Sea case study, pre-bomb museum collection mollusc shells of known calendar age, from 30 locations across a strategic salinity transect of the Baltic Sea, were analysed for 14C, δ13C and δ18O. R(t) was calculated for all 30 locations. Seven locations, of which six are within close proximity of the coast, were found to have relatively higher R(t) values, indicative of hard-water effects. δ13Caragonite values were found to be indicative of hard-water influence only for certain locations, suggesting the possibility of different sources of old carbon in different locations. Whenever possible, the Macoma genus of mollusc was selected from the museum collections, in order to exclude species specific reservoir age effects as much as possible. When the Macoma samples are exclusively considered, and samples from hard-water locations excluded, a statistically significant correlation between Macoma R(t) and average salinity is found, indicating a two end-member linear mixing model between 14Cmarine and 14Crunoff. A map of Baltic Sea Macoma aragonite R(t) for the late 19th and early 20th centuries is produced. Such a map can provide an estimate for contemporary Baltic Sea Macoma R(t), although one must exercise caution when applying such estimates back in time or to 14C dates obtained from different sample material. A statistically significant correlation is also found between δ18Oaragonite and Macoma R(t), suggesting that δ18Oaragonite can be used to estimate Macoma palaeo-R(t). The results of this Baltic Sea case study, which show that R(t) is affected by hydrographic conditions and local carbon inputs, have important consequences for other coastal and estuarine locations, where R(t) is also likely to significantly vary on spatial and temporal

  2. Percutaneous absorption of ( sup 14 C)DDT and ( sup 14 C)benzo(a)pyrene from soil

    SciTech Connect

    Wester, R.C.; Maibach, H.I.; Bucks, D.A.; Sedik, L.; Melendres, J.; Liao, C.; DiZio, S. )

    1990-10-01

    The objective was to determine percutaneous absorption of DDT and benzo(a)pyrene in vitro and in vivo from soil into and through skin. Soil (Yolo County 65-California-57-8; 26% sand, 26% clay, 48% silt) was passed through 10-, 20-, and 48-mesh sieves. Soil then retained by 80-mesh was mixed with (14C)-labeled chemical at 10 ppm. Acetone solutions at 10 ppm were prepared for comparative analysis. Human cadaver skin was dermatomed to 500 microns and used in glass diffusion cells with human plasma as the receptor fluid (3 ml/hr flow rate) for a 24-hr skin application time. With acetone vehicle, DDT (18.1 +/- 13.4%) readily penetrated into human skin. Significantly less DDT (1.0 +/- 0.7%) penetrated into human skin from soil. DDT would not partition from human skin into human plasma in the receptor phase (less than 0.1%). With acetone vehicle, benzo(a)pyrene (23.7 +/- 9.7%) readily penetrated into human skin. Significantly less benzo(a)pyrene (1.4 +/- 0.9%) penetrated into human skin from soil. Benzo(a)pyrene would not partition from human skin into human plasma in the receptor phase (less than 0.1%). Substantivity (skin retention) was investigated by applying 14C-labeled chemical to human skin in vitro for only 25 min. After soap and water wash, 16.7 +/- 13.2% of DDT applied in acetone remained absorbed to skin. With soil only 0.25 +/- 0.11% of DDT remained absorbed to skin. After soap and water wash 5.1 +/- 2.1% of benzo(a)pyrene applied in acetone remained absorbed to skin. With soil only 0.14 +/- 0.13% of benzo(a)pyrene remained absorbed to skin.

  3. DISTRIBUTION OF 14C-ATRAZINE FOLLOWING AN ACUTE LACTATIONAL EXPOSURE IN THE WISTAR RAT.

    EPA Science Inventory

    The purpose of the present study was to examine the distribution of atrazine in the lactating dam and suckling neonate following an acute exposure to either 2 or 4 mg/kg 14C-atrazine (14C-ATR) by gavage. 14C-ATR was administered to the nursing dam on postnatal day 3 by oral gavag...

  4. Characterization of hemoglobin adduct formation in mice and rats after administration of ( sup 14 C)butadiene or ( sup 14 C)isoprene

    SciTech Connect

    Sun, J.D.; Dahl, A.R.; Bond, J.A.; Birnbaum, L.S.; Henderson, R.F. )

    1989-08-01

    Occupational exposures to 1,3-butadiene or isoprene occur through their use in the manufacture of rubber and other related polymer products. The purpose of this study was to determine if butadiene or isoprene administration would result in the formation of adducts with blood hemoglobin (Hb), and if such adducts can be used as a measure of previous exposure(s). Male B6C3F1 mice and male Sprague-Dawley rats were injected intraperitoneally with 1, 10, 100, or 1000 mumol (14C)butadiene or 0.3, 3.0, 300, 1000, or 3000 mumol (14C)isoprene per kilogram body weight. Animals were killed 24 hr later. Globin was isolated from blood samples and was analyzed for 14C by liquid scintillation spectroscopy. Hb adduct formation was linearly related to administered doses up to 100 mumol (14C)butadiene or 500 mumol (14C)isoprene per kilogram body weight for mice and rats, respectively. For (14C)butadiene, the efficiency of Hb adduct formation in mice and rats within the linear response range was 0.177 +/- 0.003 and 0.407 +/- 0.019 (pmol of 14C-adducts/mg globin)/(mumol of retained (14C)butadiene/kg body wt), respectively (mean +/- SE; n = 18). For (14C)isoprene, these values for mice and rats were 0.158 +/- 0.035 and 0.079 +/- 0.016 (pmol of 14C-adducts/mg globin)/(mumol of retained (14C)isoprene/kg body wt), respectively (mean +/- SE; n = 12). Hb adducts also accumulated linearly after repeated daily administration of 100 mumol (14C)butadiene or 500 mumol (14C)isoprene per kilogram body wt to mice and rats, respectively, for 3 days. (14C)Butadiene-derived Hb adducts in blood showed lifetimes of approximately 24 and approximately 65 days for mice and rats, respectively, which correlate with the reported lifetimes for red blood cells in these rodent species. Thus, levels of butadiene- or isoprene-derived adducts on Hb in circulating blood may be a useful measure of prior repeated exposures to these compounds.

  5. Imprint of CO2 emission in atmosphere and biosphere on the basis of 14C and 13C measurements

    NASA Astrophysics Data System (ADS)

    Pazdur, Anna; Gabryś, Alicja; Kuc, Tadeusz; Pawełczyk, Sławomira; Piotrowska, Natalia; Rakowski, Andrzej; Różański, Kazimierz; Sensuła, Barbara

    2015-04-01

    As is shown in the IPCC (Intergovernmental Panel on Climate Change) report, the observed climate changes are caused, among others, by human activity. Mainly emission of CO2 to the atmosphere coming from the burning of fossil fuels, can have dire consequences for life on Earth and development of humankind. The report uses, among others, data obtained from isotopic measurements in the biosphere. Measurements of 14C and 13C concentration in modern atmospheric carbon dioxide and biosphere allow the determination of the decrease of the concentration of this isotope. Furthermore, the magnitude of emission to the atmosphere of carbon dioxide not containing the isotope 14C can be estimated on this basis. Such emission stems from fossil fuel combustion - petroleum, natural gas and black coal. A sensitive bioindicator of the emission are annual tree rings. The measurements of 14C concentration in tree ring material using AMS allow to see its seasonal changes. Trees, treated as an archive of changes in conjunction with information about the isotopic composition of carbon can be used for monitoring of environment as sensitive bioindicators on local, as well as on the global scale. Regular investigations of isotopic composition of carbon in trees have been carried out in the GADAM Centre for the urban areas of both Poland and worldwide. This method can be applied in the study of the emission of CO2 to the atmosphere and its spatial and temporal distribution connected with the production of energy by power plants based on fossil fuel combustion for the area of southern Poland. Modelling of CO2 emission using both 14C and 13C carbon isotopes measured in pine tree rings on the background of climatic changes will be presented. The national ecological policy in the era of global warming requires the manufacturers of energy to get involved in the development of methods suitable for monitoring the state of the environment. Hence, the interest in the area of monitoring the fossil fuel

  6. Relative and absolute emissions of anthropogenic trace gases around the US based on paired atmospheric observations of fossil fuel CO2 from 14C

    NASA Astrophysics Data System (ADS)

    Miller, J. B.; Lehman, S.; Montzka, S. A.; Andrews, A. E.; Sweeney, C.; Miller, B. R.; Wolak, C.; Dlugokencky, E. J.; Southon, J. R.; Turnbull, J. C.; LaFranchi, B. W.; Guilderson, T. P.; Fischer, M. L.; Tans, P. P.

    2012-12-01

    The small radiocarbon fraction of atmospheric CO2 (~1:10^12 14C:C) has proven to be an ideal tracer for the fossil fuel derived component of observed CO2 (Cff) over large industrialized land areas. A growing number of 14CO2 measurements are now being made in air sampled from a network of tall towers and airborne profiling sites around the US alongside measurements of CO2, CO, CH4, N2O, SF6, and a large suite of halo- and hydro-carbons. Cff paired with boundary-layer enhancements of more than 20 other anthropogenic gases measured in the same samples allow us to determine apparent emissions ratios for each gas with respect to Cff (where apparent ratios refer to those at the time of observation rather than at the time of emission). Here we compare seasonal and spatial variability of apparent emissions ratios for regions of significant urban and industrial emissions around the US, including sites in California, Texas, the mid-west, south-east and north-east . Statistically significant and coherent spatial and seasonal patterns in apparent emissions ratios are determined for many gases over multiple years. These can in turn be combined with appropriate spatial footprints over which the emissions of fossil fuel derived CO2 has been independently determined based on inventories and process models in order to estimate absolute emissions of the correlate gases in different regions, following simple scaling methods we have outlined previously [Miller et al. 2012, J. Geophys. Res., doi:10.1029/2011JD017048]. This approach provides some of the first reliable "top down", observationally-based emissions estimates for these gases, many of which influence climate, air quality and stratospheric ozone. Unlike most "bottom up" inventories, our estimates of absolute trace gas emissions are accompanied by quantifiable estimates of uncertainty.

  7. Partitioning of Soil Respiration Sources Using 14C-Enriched Leaf Litter and Roots in a Temperate Forest, Oak Ridge, TN

    NASA Astrophysics Data System (ADS)

    Cisneros Dozal, L.; Trumbore, S.; Hanson, P.; Xu, X.

    2002-12-01

    Leaf litter enriched in 14C with values ranging from +952‰ to +1055 ‰ and control leaf litter with Δ14C of +215 ‰ to +230 ‰ were used to establish replicated plots on the Oak Ridge Reservation (ORR), Oak Ridge National Laboratory, Tennessee for tracking of soil carbon cycling. Our goal is to partition the heterotrophic and autotrophic components of total CO2 emission from the soil. Measurements have been carried out in the summer of 2001 and 2002 at two sites (Walker Branch and TVA) that are on the same soil type, but that have different initial levels of 14C resulting from a localized ecosystem-scale 14C release event in 1999. Measurements include total soil respiration rates using a chamber technique, trapping of CO2 evolved from chambers and from root respiration to determine 14C and 13C signatures, and incubations of soil and leaf litter in the laboratory to obtain rates of decomposition and 14C and 13C signatures from heterotrophic CO2 sources. Total C fluxes (mg C/m2-hr) varied among the sites by up to ~40%, with differences between enriched and control plots similar to site-to-site variation between TVA and Walker Branch. In May of 2002, the 14C signature of the total CO2 emitted from the enriched plots was always higher than that of the control plots in both sites, with averaged values of Δ14C of +493 ‰ and +357 ‰ in TVA and of +300 ‰ and +156 ‰ in Walker Branch, for the enriched and control plots respectively. We use the mass balance equation, Δ14Ctotal=FxΔ14C{leaf litter}+(1-F)x(Δ14C{root and soil decomposition} +Δ14C{roots respiration}) to estimate the contribution of leaf litter decomposition to the total CO2 flux (F). Within any one site, the difference in the 14C signature emitted from the soil between the two treatments should be directly proportional to the contribution of leaf litter decomposition only, since the other components (roots and soil decomposition and roots respiration) are assumed to remain the same for enriched

  8. Effects of Pseudomonas species on the release of bound sup 14 C residues from soil treated with ( sup 14 C)atrazine

    SciTech Connect

    Khan, S.U.; Behki, R.M. )

    1990-11-01

    The release of bound (nonextractable) {sup 14}C residues from soil previously treated with ({sup 14}C)atrazine was investigated by incubation of the solvent-extracted soil with two species of Pseudomonas capable of metabolizing atrazine. The two species, 192 and 194, released bound {sup 14}C residues from the soil. Addition of glucose, known to increase microbiological activities, to the incubated soil appeared to enhance the release of soil-bound {sup 14}C residues, in particular in the presence of Pseudomonas species 192. The {sup 14}C bound residues in soil, mainly present as the parent compound and its hydroxy and monodealkylated analogues, were released into the incubation mixture and were subsequently metabolized by the two species involving dechlorination and dealkylation.

  9. Photolysis of 14C-sulfadiazine in water and manure.

    PubMed

    Sukul, Premasis; Lamshöft, Marc; Zühlke, Sebastian; Spiteller, Michael

    2008-03-01

    Photolysis of 14C-sulfadiazine in aqueous solution under simulated sunlight followed first-order kinetics. The impact of H2O2, humic acid, fulvic acid and acetone to enhance the photodegradation of sulfadiazine (SDZ) was studied. Six photoproducts, 4-OH-SDZ, 5-OH-SDZ, N-formyl-SDZ, 4-[2-iminopyrimidine-1(2H)-yl] aniline, 2-aminopyrimidine, and aniline were identified. Extrusion of SO2 was found to be the main degradation process during irradiation. These photoproducts can occur in water and soil upon sunlight exposure, when soil is treated with SDZ contained in manure. Due to photodegradation the experimental half-life of the SDZ in water was 32h and in the presence of photosensitizers the half-life values were 19.3-31.4h, 17.2-31.4h, 12.6-29.8h, and 3.8-30.7h for H2O2, humic acid, fulvic acid, and acetone, respectively depending on the concentration of the photosensitizers. The presence of photosensitizers markedly reduced SDZ persistence, indicating that indirect photolytic processes are important factors governing the photodegradation of SDZ in aqueous environments. Investigation revealed further persistence behavior of SDZ in manure. The half-life value of SDZ in manure was 158h. PMID:18076971

  10. 14C determination in different bio-based products

    NASA Astrophysics Data System (ADS)

    Santos Arévalo, Francisco-Javier; Gómez Martínez, Isabel; Agulló García, Lidia; Reina Maldonado, María-Teresa; García León, Manuel

    2015-10-01

    Radiocarbon determination can be used as a tool to investigate the presence of biological elements in different bio-based products, such as biodiesel blends. These products may also be produced from fossil materials obtaining the same final molecules, so that composition is chemically indistinguishable. The amount of radiocarbon in these products can reveal how much of these biological elements have been used, usually mixed with petrol derived components, free of 14C. Some of these products are liquid and thus the handling at the laboratory is not as straightforward as with solid samples. At Centro Nacional de Aceleradores (CNA) we have tested the viability of these samples using a graphitization system coupled to an elemental analyzer used for combustion of the samples, thus avoiding any vacuum process. Samples do not follow any chemical pre-treatment procedure and are directly graphitized. Specific equipment for liquid samples related to the elemental analyzer was tested. Measurement of samples was performed by low-energy AMS at the 1 MV HVEE facility at CNA, paying special attention to background limits and reproducibility during sample preparation.

  11. Degredation of [{sup 14}C]-propargite in soil

    SciTech Connect

    Comezoglu, S.N.; Ly, V.T.; Wu, J.

    1996-10-01

    The degradation of {sup 14}C-labeled propargite in soil was investigated in three different test conditions, namely, aerobic soil, anaerobic soil, aerobic aquatic, and anaerobic aquatic. All studies were conducted at {approximately}25{degrees}C in the dark with treatment rates of either 5 ppm or 6 ppm and were conducted for a period of one year except the anaerobic soil and aerobic aquatic study which were conducted for two months and one month, respectively. The apparent T{sub 1/2} values observed were {approximately}38 days, {approximately}47 days, {approximately}67 days and {approximately}64 days for aerobic aquatic, anaerobic aquatic, aerobic soil and anaerobic soil studies, respectively. The soil and test systems were extracted with organic solvent followed by radiocounting and chromatographic analysis. Major metabolites were isolated and identified by co-chromatography as well as mass spectrometry (GC/MS and/or LC/MS). A number of products were detected which included p-tertiary butylphenoxy cyclohexanol (TBPC), 2-[4-(2-hydroxycyclohexoxy) phenyl]-2,2-dimethyl acetic acid (TBPC-acid), p-tertiarybutyl phenol (PTBP), and 2-(p-tertiarybutyl phenoxy) cyclohexanol sulfuric acid as the identified major products. The averaged overall recoveries for the test substance in all studies were excellent (>90%). Data indicated that the propargite degraded at a moderate rate in hydrosoils either aerobically or anaerobically while in terrestrial soil, the degradation was slowed down after several months of incubation.

  12. Distribution of 14C cylindrospermopsin in vivo in the mouse.

    PubMed

    Norris, R L; Seawright, A A; Shaw, G R; Smith, M J; Chiswell, R K; Moore, M R

    2001-01-01

    Radiolabelled 14C cylindrospermopsin (CYN) has been prepared and used to investigate the distribution and excretion of CYN in vivo in male Quackenbush mice. At a dose of 0.2 mg/kg (i.e., approx. median lethal dose) the following mean (SD) urinary and faecal recoveries (cumulative) were obtained, respectively: (0-6 hours, n = 4) 48.2 (29.3)%, 11.9 (21.4)%; (0-12 hours, n = 12) 66.0 (27.1)%, 5.7 (5.6)%; (0-24 hours, n = 12) 68.4 (26.7)%, 8.5 (8.1)%. Mean (SD) recoveries from livers at 6 hours were 20.6 (6.4)% (n = 4), at 48 hours 13.1 (7.7)% (n = 8), and 5-7 days were 2.1 (2.1)% (n = 8). A substantial amount (up to 23%) can be retained in the liver for up to 48 hours with a lesser amount retained in the kidneys. The excretion patterns show substantial interindividual variability between predominantly faecal or urinary excretion, but these patterns are not related in any simple manner to the outcome in terms of toxicity. There is at least one methanol-extractable metabolite as well as a nonmethanol-extractable metabolite in the liver. The methanol-extractable metabolite was not found in the kidney and is more hydrophilic than CYN itself on reverse phase. PMID:11769247

  13. Large spatial variations in coastal 14C reservoir age - a case study from the Baltic Sea

    NASA Astrophysics Data System (ADS)

    Lougheed, B. C.; Filipsson, H. L.; Snowball, I.

    2013-05-01

    Coastal locations are highly influenced by input from freshwater river runoff, including sources of terrestrial carbon, which can be expected to modify the 14C reservoir age, or R (t), associated with marine water. In this Baltic Sea case study, pre-bomb museum collection mollusc shells of known calendar age, from 30 locations across a strategic salinity transect of the Baltic Sea, were analysed for 14C, δ13C and δ18O. R (t) was calculated for all 30 locations. Seven locations, of which six are within close proximity of the coast, were found to have relatively higher R (t) values, indicative of hard-water effects. Whenever possible, the Macoma genus of mollusc was selected from the museum collections, in order to exclude species specific reservoir age effects as much as possible. When the Macoma samples are exclusively considered, and samples from hard-water locations excluded, a statistically significant correlation between Macoma R (t) and average salinity is found, indicating a two end-member linear mixing model between 14Cmarine and 14Crunoff. A map of Baltic Sea Macoma aragonite R (t) for the late 19th and early 20th centuries is produced. Such a map can provide an estimate for contemporary Baltic Sea Macoma R (t), although one must exercise caution when applying such estimates back in time or to 14C dates obtained from different sample material. A statistically significant correlation is found between δ18Oaragonite and Macoma R (t), suggesting that δ18Oaragonite can be used to estimate Macoma palaeo-R (t), due to the δ18Oaragonite signal being dominated by the salinity gradient of the Baltic Sea. A slightly increased correlation can be expected when δ18Oaragonite is corrected for temperature fractionation effects. The results of this Baltic Sea case study, which show that R (t) is affected by hydrographic conditions and local carbon inputs, have important consequences for other coastal and estuarine locations, where R (t) is also likely to significantly

  14. Deposition of bomb 14C in continental slope sediments of the Mid-Atlantic Bight: assessing organic matter sources and burial rates

    NASA Astrophysics Data System (ADS)

    DeMaster, D. J.; Thomas, C. J.; Blair, N. E.; Fornes, W. L.; Plaia, G.; Levin, L. A.

    As part of the Ocean Margins Program (OMP), organic carbon 14C measurements have been made on benthic fauna and kasten core sediments from the North Carolina continental slope. These analyses are used to evaluate the nature and burial flux of organic matter in the OMP study area off Cape Hatteras. Despite the fact that surface sediment 14C contents ranged from -41 to -215 per mil, the benthic fauna (primarily polychaetes) all contained significant amounts of bomb- 14C (body tissue 14C contents ranging from +20 to +82 per mil). Bomb- 14C clearly is reaching the seabed on the North Carolina slope, and the labile planktonic material carrying this signal is a primary source of nutrition to the benthic ecosystem. The enrichment of 14C in benthic faunal tissue relative to the 14C content of bulk surface-sediment organic matter (a difference of ˜150 per mil) is attributed to a combination of particle selection and selective digestive processes. Organic carbon burial rates from 12 stations on the North Carolina slope varied from 0.02 to 1.7 mol of C m -2 yr -1, with a mean value of 0.7 mol of C m -2 yr -1. The accumulation of organic matter on the upper slope accounts for <1% of the primary production in the entire continental margin system. The North Carolina margin was deliberately selected because of its potential for offshore transport and high sediment deposition rates, and even in this environment, burial of organic carbon accounts for a very small fraction of the primary production occurring in surface waters.

  15. Understanding the production and retention of in situ cosmogenic 14C in polar firn

    NASA Astrophysics Data System (ADS)

    Hmiel, B.; Petrenko, V. V.; Smith, A.; Buizert, C.; Harth, C. M.; Beaudette, R.; Place, P., Jr.; Hua, Q.; Yang, B.; Vimont, I.; Weiss, R. F.; Severinghaus, J. P.; Brook, E.; White, J. W. C.

    2014-12-01

    Radiocarbon in CO2, CO and CH4 trapped in polar ice is of interest for dating of ice cores, studies of past solar activity and cosmic ray flux, as well as studies of the paleoatmospheric CH4 budget. The major difficulty with interpreting 14C measurements in ice cores stems from the fact that the measured 14C represents a combination of trapped paleoatmospheric 14C and 14C that is cosmogenically produced within the ice matrix. This in situ cosmogenic 14C component in ice is at present poorly understood. Prior ice core 14C studies show conflicting results with regard to the retention of cosmogenic 14C in polar firn and partitioning of this 14C among CO2, CO and CH4. Our new study aims to comprehensively characterize the 14C of CO2, CO, and CH4 in both the air and the ice matrix throughout the firn column at Summit, Greenland. We will present new measurements of 14C in Summit firn air (the first phase of this study) and discuss the implications for in situ cosmogenic 14C production and retention.

  16. 14C-labeled substrate catabolism by human diploid fibroblasts derived from infants and adults

    SciTech Connect

    Rhead, W.J.; Moon, A.; Roettger, V.; Henkle, K.

    1985-10-01

    Untransformed diploid skin fibroblasts from eight normal adults, aged 24 to 74 years, catabolized several 14C-labeled substrates less effectively than cells from ten normal male infants. 14C-labeled substrate metabolism was quantitated either by measuring the evolution of 14CO2 from the 14C-labeled compounds or the incorporation of 14C into cellular protein via transamination of tricarboxylic acid cycle intermediates derived from the 14C-labeled substrates. With these methods, adult cells catabolized (1-14C)butyrate, (1-14C)octanoate, and 1-(2-14C)leucine at rates 44 to 64% of those found in infant cells. The oxidation of (1,4-14C)succinate and (U-14C)malate was identical in both infant and adult cells, while (2,3-14C)succinate catabolism was mildly decreased in adult cells (65-80% of control). These observations parallel those made in rat tissues and confirm that the same phenomenon occurs in cultured human fibroblasts.

  17. COCA: deriving urban emissions and the carbon exchange of a forested region using airborne CO2 and CO observations

    NASA Astrophysics Data System (ADS)

    Geiss, H.; Schmitgen, S.; Ciais, P.; Neininger, B.; Baeumle, M.; Brunet, Y.; Kley, D.

    2002-05-01

    A crucial challenge in measuring the partitioning of sources and sinks of atmospheric CO2 is the separation of regional anthropogenic CO2 sources from biogenic activity. The aim of the COCA project is to quantify the fossil fuel and biogenic CO2 fractions using continuous airborne CO2 and CO measurements, where CO acts as a tracer for anthropogenic CO2. At first part of the project COCA an attempt was made to measure daytime biogenic CO2 fluxes over a forest area (about 15 by 30 km size). The campaign took place around the CARBOEUROFLUX site ``Le Bray'' (Pinus pinaster) close to Bordeaux in France end of June 2001 Based on continuous airborne CO2, H2O and CO flux and concentration measurements a Lagrangian budgeting approach was chosen to measure regional CO2 deposition fluxes. The objective is to determine the CO2 uptake of the extended forest area from the CO2/CO gradients up- and downwind of the ecosystem, using CO as air mass tracer and such estimating the influence of anthropogenic CO2 advected into the area First results of the summer flight on June 23rd will be shown, where fair wind speeds (~5 m/s) and a low CBL height led to the observation of a clear decrease in CO2 at the downwind flight stacks with basically constant CO concentrations. For other summer flights with very low wind speeds, local effects dominate the observations leading to a larger variability in the observations. Both, correlations and anti-correlations of CO2 with the anthropogenic tracer CO have been observed. Positive correlations indicate fresh plumes of anthropogenic CO2. Negative correlations are indicative of entrainment of free tropospheric air, that was marked by relatively higher CO2 and lower CO concentrations than the average CBL concentrations. During a second campaign the variance of anthropogenic CO and CO2 emissions of a large city unaffected by biogenic processes has been studied. This campaign was carried out on February 16 and 17, 2002 over the Paris metropolitan area

  18. In vivo distribution of organophosphate antidotes: autoradiography of (/sup 14/C)HI-6 in the rat

    SciTech Connect

    Ligtenstein, D.A.; Moes, G.W.; Kossen, S.P.

    1988-02-01

    In order to visualize the distribution of HI-6 in the rat after iv administration, autoradiographic experiments were carried out with (/sup 14/C)HI-6, labeled at the carbon of the carboxamide moiety. Autoradiography clearly confirms penetration of HI-6 into the central nervous system. Considerable radioactivity was found in the cerebrum, the cerebellum, and the choroid plexus. No significant activity was detected in the pontomedullary region or the spinal cord. Peripherally, (/sup 14/C)HI-6 is observed in large amounts in kidneys, heart, liver, nose, bladder, testes, and marrow-containing bone. The gastrointestinal tract was largely devoid of any radioactivity. The relative absence of HI-6 in the pontomedullary region renders centrally mediated influences of HI-6 on hemodynamic and respiratory parameters less likely.

  19. Excretion of 14C-labeled cyanide in rats exposed to chronic intake of potassium cyanide

    SciTech Connect

    Okoh, P.N.

    1983-09-15

    The excretion of an acute dose of 14C-labeled cyanide in urine, feces, and expired air was studied in rats exposed to daily intake of unlabeled KCN in the diet for 6 weeks. Urinary excretion was the main route of elimination of cyanide carbon in these rats, accounting for 83% of the total excreted radioactivity in 12 hr and 89% of the total excreted radioactivity in 24 hr. The major excretion metabolite of cyanide in urine was thiocyanate, and this metabolite accounted for 71 and 79% of the total urinary activity in 12 hr and 24 hr, respectively. The mean total activity excreted in expired air after 12 hr was only 4%, and this value did not change after 24 hr. Of the total activity in expired air in 24 hr, 90% was present as carbon dioxide and 9% as cyanide. When these results were compared with those observed for control rats, it was clear that the mode of elimination of cyanide carbon in both urine and breath was not altered by the chronic intake of cyanide.

  20. Establishing chronologies for loess records within 40 ka by AMS 14C-dating of small mollusc shells

    NASA Astrophysics Data System (ADS)

    Ujvari, Gabor; Molnar, Mihaly; Novothny, Agnes; Kovacs, Janos

    2014-05-01

    The key objective of the INTIMATE project is to determine whether abrupt climatic changes during the period of 60 to 8 ka, as reflected in a range of proxy records, were regionally synchronous or whether there were significant 'leads' and 'lags' between the atmospheric, marine, terrestrial and cryospheric realms. Such goals require precisely dated records of paleoenvironmental change for this period. Although wind-blown loess deposits are regarded as key terrestrial archives of millennial or even centennial scale environmental changes, these records are mostly poorly dated and/or their age-depth models have uncertainties of millennial magnitude. This prevents us from addressing issues like synchroneity of abrupt climatic/environmental events on millennial time scales. Two different means of dating are commonly applied for loess sequences: luminescence and radiocarbon dating. Major problems are low precision of luminescence ages and the general lack of organic macrofossils (e.g. charcoal) in loess that can reliably be dated using 14C. Other datable phases in loess are mollusc shells, rhizoliths and organic matter. While organic matter 14C ages are often seriously compromised by rejuvenation in loess sequences, rhizolites consistently yield very young ages as first demonstrated in German loess profiles. Indeed, hypocatings (rhizolites) gave Holocene ages from three different depths (4.00 m: 9744-10156 2σ age range in cal yr BP, 5.00 m: 8013-8167 cal yr BP and 6.00 m: 9534-9686 cal yr BP) in the Dunaszekcső loess record we investigated. Mollusc shells are the only remaining phases for dating, but these are usually regarded as unreliable material for 14C-dating, as they may incorporate 14C-deficient (or dead) carbon from the local carbonate-rich substrate during shell formation, thereby producing anomalously old ages by up to 3000 years. Recent studies, however, indicated that reliable ages can be obtained by radiocarbon dating of molluscs having comparatively small (

  1. The effect of composition on stability ((14)C activity) of soil organic matter fractions from the albic and black soils.

    PubMed

    Jin, Jie; Sun, Ke; Wang, Ziying; Han, Lanfang; Wu, Fengchang; Xing, Baoshan

    2016-01-15

    The importance of the composition of soil organic matter (SOM) for carbon (C) cycling is still under debate. Here a single soil source was used to examine the specific influence of its composition on stability ((14)C activity) of SOM fractions while constraining other influential C turnover factors such as mineral, climate and plant input. The following SOM fractions were isolated from two soil samples: four humic acids, two humins, non-hydrolyzable carbon, and the demineralized fraction. We examined the isotope ratios of SOM fractions in relation to composition (such as aliphatic and aromatic C content) using solid state (13)C nuclear magnetic resonance (NMR) and thermal analysis. The Δ(14)C values of the fractions isolated from both an albic soil (SOMs-A) and a black soil (SOMs-B) correlated negatively with their peak temperature of decomposition and the temperature where half of the total heat of reaction was evolved, implying a potential link between thermal and biogeochemical stability of SOM fractions. Aryl C contents of SOMs-A determined using (13)C NMR varied inversely with δ(15)N values and directly with δ(13)C values, suggesting that part of aryl C of SOMs-A might be fire-derived. The Δ(14)C values of SOMs-A correlated positively with aliphatic C content and negatively with aromatic C content. We therefore concluded that fire-derived aromatic C in SOMs-A appeared to be more stable than microbially-derived aliphatic C. The greater decomposition of SOMs-B fractions weakened the relationship of their Δ(14)C values with alkyl and aryl C contents. Hence, the role of the composition of SOM fractions in regulating stability might be dependent on the source of specific C forms and their stage of decomposition. PMID:26402480

  2. A new 14C calibration data set for the last deglaciation based on marine varves

    SciTech Connect

    Hughen, K A; Kashgarian, M; Lehman, S J; Overpeck, J T; Peterson, L C; Southon, J R

    1999-02-22

    Varved sediments of the tropical Cariaco basin provide a new {sup 14}C calibration data set for the period of deglaciation (10,000 to 14,500 years before present: 10-14.5 cal ka BP). Independent evaluations of the Cariasco Basin calendar and {sup 14}C chronologies were based on the agreement of varve ages with the GISP2 ice core layer chronology for similar high-resolution paleoclimate records, in addition to {sup 14}C age agreement with terrestrial {sup 14}C dates, even during large climatic changes. These assessments indicate that the Cariaco Basin {sup 14}C reservoir age remained stable throughout the Younger Dryas and late Alleroed climatic events and that the varve and {sup 14}C chronologies provide an accurate alternative to existing calibrations based on coral U/Th dates. The Cariaco Basin calibration generally agrees with coral-derived calibrations but is more continuous and resolves century-scale details of {sup 14}C change not seen in the coral records. {sup 14}C plateaus can be identified at 9.6, 11.4, and 11.7 {sup 14}C ka BP, in addition to a large, sloping plateau during the Younger Dryas ({approximately}10 to 11 {sup 14}C ka BP). Accounting for features such as these is crucial to determining the relative timing and rates of change during abrupt global climate changes of the last deglaciation.

  3. 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 C.; Lubbe, H. J. L.; Davies, Gareth R.

    2016-01-01

    Accurate geochronologies are crucial for reconstructing the sensitivity of brackish and estuarine environments to dynamic external impacts of the past. Radiocarbon (14C) dating is commonly used for palaeoclimate studies, 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 behavioral 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 (using GIS) and species-specific 14C effects, we demonstrate the use of 87Sr/86Sr ratios for quantifying R(t) in ubiquitous mollusc shell material, leading to almost an order of magnitude increase in Baltic Sea 14C geochronological precision over the current state of the art. We propose that similar proxy methods can be developed for other brackish water bodies worldwide.

  4. Free flow electrophoresis separation and AMS quantitation of 14C-naphthalene-protein adducts

    NASA Astrophysics Data System (ADS)

    Buchholz, Bruce A.; Haack, Kurt W.; Sporty, Jennifer L.; Buckpitt, Alan R.; Morin, Dexter

    2010-04-01

    Naphthalene is a volatile aromatic hydrocarbon to which humans are exposed from a variety of sources including mobile air sources and cigarette smoke. Naphthalene produces dose-(concentration)dependent injury to airway epithelial cells of murine lung which is observed at concentrations well below the current occupational exposure standard. Toxicity is dependent upon the cytochrome P450 mediated metabolic activation of the parent substrate to unstable metabolites which become bound covalently to tissue proteins. Nearly 70 proteins have been identified as forming adducts with reactive naphthalene metabolites using in vitro systems but very little work has been conducted in vivo because reasonably large amounts (100 μCi) of 14C labeled parent compound must be administered to generate detectable adduct levels on storage phosphor screens following separation of labeled proteins by 2D gel electrophoresis. The work described here was done to provide proof of concept that protein separation by free flow electrophoresis followed by AMS detection of protein fractions containing protein bound reactive metabolites would provide adducted protein profiles in animals dosed with trace quantities of labeled naphthalene. Mice were administered 200 mg/kg naphthalene intraperitoneally at a calculated specific activity of 2 DPM/nmol (1 pCi/nmol) and respiratory epithelial tissue was obtained by lysis lavage 4 h post injection. Free flow electrophoresis (FFE) separates proteins in the liquid phase over a large pH range (2.5-11.5) using low molecular weight acids and bases to modify the pH. The apparatus separates fractions into standard 96-well plates that can be used in other protein analysis techniques. The buffers of the fractions have very high carbon content, however, and need to be dialyzed to yield buffers compatible with 14C-AMS. We describe the processing techniques required to couple FFE to AMS for quantitation of protein adducts.

  5. Online coupling of pure O2 thermo-optical methods - 14C AMS for source apportionment of carbonaceous aerosols

    NASA Astrophysics Data System (ADS)

    Agrios, Konstantinos; Salazar, Gary; Zhang, Yan-Lin; Uglietti, Chiara; Battaglia, Michael; Luginbühl, Marc; Ciobanu, Viorela Gabriela; Vonwiller, Matthias; Szidat, Sönke

    2015-10-01

    This paper reports on novel separation methods developed for the direct determination of 14C in organic carbon (OC) and elemental carbon (EC), two sub-fractions of total carbon (TC) of atmospheric air particulate matter. Until recently, separation of OC and EC has been performed off-line by manual and time-consuming techniques that relied on the collection of massive CO2 fractions. We present here two on-line hyphenated techniques between a Sunset OC/EC analyzer and a MICADAS (MIni radioCArbon DAting System) accelerator mass spectrometer (AMS) equipped with a gas ion source. The first implementation facilitates the direct measurement in the low sample size range (<10 μg C) with high throughput on a routine basis, while the second explores the potential for a continuous-flow real-time CO2 gas feed into the ion source. The performance achieved with reference materials and real atmospheric samples will be discussed to draw conclusions on the improvement offered in the field of 14C aerosol source apportionment.

  6. Airborne Fiber Size Characterization in Exposure Estimation: Evaluation of a Modified Transmission Electron Microcopy Protocol for Asbestos and Potential Use for Carbon Nanotubes and Nanofibers

    PubMed Central

    Dement, John M.; Kuempel, Eileen D.; Zumwalde, Ralph D.; Ristich, Anna M.; Fernback, Joseph E.; Smith, Randall J.

    2015-01-01

    Background Airborne fiber size has been shown to be an important factor relative to adverse lung effects of asbestos and suggested in animal studies of carbon nanotubes and nanofibers (CNT/CNF). Materials and Methods The International Standards Organization (ISO) transmission electron microscopy (TEM) method for asbestos was modified to increase the statistical precision of fiber size determinations, improve efficiency, and reduce analysis costs. Comparisons of the fiber size distributions and exposure indices by laboratory and counting method were performed. Results No significant differences in size distributions by the ISO and modified ISO methods were observed. Small but statistically-significant inter-lab differences in the proportion of fibers in some size bins were found, but these differences had little impact on the summary exposure indices. The modified ISO method produced slightly more precise estimates of the long fiber fraction (>15 μm). Conclusions The modified ISO method may be useful for estimating size-specific structure exposures, including CNT/CNF, for risk assessment research. PMID:25675894

  7. Impact of air-borne or canopy-derived dissolved organic carbon (DOC) on forest soil solution DOC in Flanders, Belgium

    NASA Astrophysics Data System (ADS)

    Verstraeten, Arne; De Vos, Bruno; Neirynck, Johan; Roskams, Peter; Hens, Maarten

    2014-02-01

    Dissolved organic carbon (DOC) in the soil solution of forests originates from a number of biologically and/or biochemically mediated processes, including litter decomposition and leaching, soil organic matter mineralization, root exudation, mucilage and microbial activity. A variable amount of DOC reaches the forest floor through deposition, but limited information is available about its impact on soil solution DOC. In this study, trends and patterns of soil solution DOC were evaluated in relation to deposition of DOC over an 11-year period (2002-2012) at five ICP Forests intensive monitoring plots in Flanders, northern Belgium. Trend analysis over this period showed an increase of soil solution DOC concentrations for all observed depth intervals. Fluxes of DOC increased in the organic layer, but were nearly stable in the mineral soil. Annual leaching losses of DOC were higher in coniferous (55-61 kg C ha-1) compared to deciduous plots (19-30 kg C ha-1) but embody less than 0.05% of total 1-m soil organic C stocks. Temporal deposition patterns could not explain the increasing trends of soil solution DOC concentrations. Deposition fluxes of DOC were strongly correlated with soil solution fluxes of DOC, but their seasonal peaks were not simultaneous, which confirmed that air-borne or canopy-derived DOC has a limited impact on soil solution DOC.

  8. 14C content in vegetation in the vicinities of Brazilian nuclear power reactors.

    PubMed

    Dias, Cíntia Melazo; Santos, Roberto Ventura; Stenström, Kristina; Nícoli, Iêda Gomes; Skog, Göran; da Silveira Corrêa, Rosangela

    2008-07-01

    (14)C specific activities were measured in grass samples collected around Brazilian nuclear power reactors. The specific activity values varied between 227 and 299 Bq/kg C. Except for two samples which showed (14)C specific activities 22% above background values, half of the samples showed background specific activities, and the other half had a (14)C excess of 1-18%. The highest specific activities were found close to the nuclear power plants and along the main wind directions (NE and NNE). The activity values were found to decrease with increasing distance from the reactors. The unexpectedly high (14)C excess values found in two samples were related to the local topography, which favors (14)C accumulation and limits the dispersion of the plume. The results indicate a clear (14)C anthropogenic signal within 5 km around the nuclear power plants which is most prominent along northeastwards, the prevailing wind direction. PMID:18308434

  9. Airborne measurements of sulfur dioxide, dimethyl sulfide, carbon disulfide, and carbonyl sulfide by isotope dilution gas chromatography/mass spectrometry

    NASA Technical Reports Server (NTRS)

    Bandy, Alan R.; Thornton, Donald C.; Driedger, Arthur R., III

    1993-01-01

    A gas chromatograph/mass spectrometer is described for determining atmospheric sulfur dioxide, carbon disulfide, dimethyl sulfide, and carbonyl sulfide from aircraft and ship platforms. Isotopically labelled variants of each analyte were used as internal standards to achieve high precision. The lower limit of detection for each species for an integration time of 3 min was 1 pptv for sulfur dioxide and dimethyl sulfide and 0.2 pptv for carbon disulfide and carbonyl sulfide. All four species were simultaneously determined with a sample frequency of one sample per 6 min or greater. When only one or two species were determined, a frequency of one sample per 4 min was achieved. Because a calibration is included in each sample, no separate calibration sequence was needed. Instrument warmup was only a few minutes. The instrument was very robust in field deployments, requiring little maintenance.

  10. Assessing in situ mineralization of recalcitrant organic compounds in vadose zone sediments using delta13C and 14C measurements.

    PubMed

    Kirtland, Brian C; Aelion, C Marjorie; Stone, Peter A

    2005-01-01

    Few techniques exist to measure the biodegradation of recalcitrant organic compounds such as chlorinated hydrocarbons (CHC) in situ, yet predictions of biodegradation rates are needed for assessing monitored natural attenuation. Traditional techniques measuring O2, CO2, or chemical concentrations (in situ respiration, metabolite and soil air monitoring) may not be sufficiently sensitive to estimate biodegradation rates for these compounds. This study combined isotopic measurements (14C and delta13C of CO2 and delta13C of CHCs) in conjunction with traditional methods to assess in situ biodegradation of perchloroethylene (PCE) and its metabolites in PCE-contaminated vadose zone sediments. CHC, ethene, ethane, methane, O2, and CO2 concentrations were measured over 56 days using gas chromatography (GC). delta13C of PCE, trichloroethylene (TCE) and cis-1,2-dichloroethylene (DCE), delta13C and 14C of vadose zone CO2 and sediment organic matter, and delta13C, 14C, and deltaD of methane were measured using a GC-isotope ratio mass spectrometer or accelerator mass spectrometer. PCE metabolites accounted for 0.2% to 18% of CHC concentration suggesting limited reductive dechlorination. Metabolites TCE and DCE were significantly enriched in (13)C with respect to PCE indicating metabolite biodegradation. Average delta13C-CO2 in source area wells (-23.5 per thousand) was significantly lower compared to background wells (-18.4 per thousand) indicating CHC mineralization. Calculated CHC mineralization rates were 0.003 to 0.01 mg DCE/kg soil/day based on lower 14C values of CO2 in the contaminated wells (63% to 107% modern carbon (pMC)) relative to the control well (117 pMC). Approximately 74% of the methane was calculated to be derived from in situ CHC biodegradation based on the 14C measurement of methane (29 pMC). 14C-CO2 analyses was a sensitive measurement for quantifying in situ recalcitrant organic compound mineralization in vadose zone sediments for which limited

  11. 14C AMS measurements of the bomb pulse in N- and S-hemisphere tropical trees

    NASA Astrophysics Data System (ADS)

    Murphy, J. O.; Lawson, E. M.; Fink, D.; Hotchkis, M. A. C.; Hua, Q.; Jacobsen, G. E.; Smith, A. M.; Tuniz, C.

    1997-03-01

    The 14C bomb-pulse signature has been measured by AMS on cross-dateable teak samples from N- and S-hemisphere locations in the tropics. Excellent agreement is found with the atmospheric 14C content in the period 1955 to 1980 for the respective hemispheres. These results demonstrate that 14C measurements can be used to facilitate growth rate determinations in tropical trees.

  12. Absorption, distribution and excretion of 14C-pilocarpine following oral administration to rats.

    PubMed

    Omori, Yasuhiro; Endo, Takuro; Hara, Yoshiki; Nishiyama, Masahiko; Midgley, Ian; Smart, Clair I; John, Alexandra J; Chasseaud, Leslie F; McBurney, Alan; John, Brian A

    2004-01-01

    The absorption, distribution and excretion of pilocarpine (CAS 92-13-7) were studied after single oral doses of 14C-pilocarpine hydrochloride (CAS 54-71-7) to the Sprague-Dawley rat, administered in aqueous solution mainly at a dose level of 0.3 mg/kg. Rats also received single intravenous doses at 0.3 mg/kg so as to compare 14C pharmacokinetics and excretion. The oral 14C-dose was rapidly and almost completely absorbed from the duodenum and small intestine within 30 min in the male rat and 14C concentrations in plasma declined biexponentially with a terminal half-life of about 9 h. Over the oral dosage range studied, i.e. 0.1-1.0 mg/kg, there was no evidence of significant non-proportionality for Cmax of 14C, whereas there was some such evidence for AUG24. Tissue 14C concentrations in male and pregnant female (Day 18) rats peaked at 0.5 h and mostly declined in parallel with those in the plasma. Excluding tissues concerned with drug absorption and elimination, 14C concentrations in most tissues were similar to, or lower than, those in the plasma. The extent of placental transfer of 14C was small and less than 0.09% of a maternal dose reached a foetus. 14C diffused into maternal milk at concentrations similar to those in the plasma. The 14C-dose was rapidly excreted in male rats, mostly in the urine (about 80%) during 6 h post dose. Recoveries of 14C in mass balance (excretion) studies were in the range 96-100%. There were no apparent gender differences in the disposition of 14C-pilocarpine in the rat. PMID:15112864

  13. Transient response of the CO2 airborne fraction to fluctuations in emissions: the role of climate-carbon feedbacks versus emissions growth rate

    NASA Astrophysics Data System (ADS)

    Landers, J. P.; Terenzi, F.; Khatiwala, S.

    2010-12-01

    The airborne fraction (AF), the proportion of anthropogenic CO2 emissions remaining in the atmosphere, has stayed remarkably constant over the past several decades. Studies have speculated that this historical constancy may be an inherent characteristic of the carbon cycle, leading to recent reports of an apparent increase in AF over the past few decades being interpreted in terms of a decrease in the efficiency of the ocean and land sinks. If this decrease is a response to hypothesized climate-carbon cycle feedbacks--for example changes in ocean circulation in the Southern Ocean due to global warming-induced increase in Westerlies--then it suggests an earlier than anticipated shift in the uptake capacity of the principal sinks that play a key role in mitigating the impact of human CO2 emissions on the climate system. Before invoking such mechanisms, however, it is important to distinguish variability due to feedbacks from that due to the intrinsic behavior of the system. Specifically, we believe that the large increase in emissions growth rate between the 1990s and the present decade -- from ~1% per year to over 3% per year -- may also serve as a viable explanation for decadal variability in the AF. Here, we use an ocean carbon cycle model driven by a state-of-the-art circulation state estimate coupled with an atmosphere and land biosphere, to explore and quantify the response of the AF to different idealized emission histories. The model closely reproduces the observed atmospheric and oceanic inventory of CO2 when forced with historical emissions. We find that the AF displays a complex transient behavior, taking on the O(100 y) to ``spin up'' to equilibrium. Moreover, its final steady state value depends sensitively on the shape of the emission history and, in particular, the rate-of-increase of the emissions. These results, which are qualitatively consistent with recent studies based on conceptual models (Gloor et al, 2010; Terenzi, PhD. Thesis, 2009), suggest

  14. 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.

  15. (/sup 14/C)chloroacetylcholine as an advantageous affinity label of the acetylcholine receptor

    SciTech Connect

    Bodmer, D.M.; Sin-Ren, A.C.; Waser, P.G.

    1987-01-01

    The alkylating agent (/sup 14/C)chloroacetylcholine perchlorate ((/sup 14/C) ClACh) was synthesized and used for affinity labelling of the nicotinic acetylcholine receptor from Torpedo marmorata. Solubilized and affinity-purified receptor proteins were reduced and alkylated according to the bromoacetylcholine-method. Covalent binding of (/sup 14/C) ClACh to the cholinergic receptor proved to be specific and saturable, and occurred exclusively to the alpha-subunit. Halogen substitution of acetylcholine by chlorine and insertion of a /sup 14/C-isotope instead of the widely used /sup 3/H resulted in favorable properties of the affinity label.

  16. (14C)acetate assimilation by a type I obligate methylotroph, Methylococcus capsulatus.

    PubMed Central

    Patel, R N; Hoare, S L; Hoare, D S; Taylor, B F

    1977-01-01

    Methanol and formate oxidation supported the assimilation of [14C]acetate by cell suspensions of Methylococcus capsulatus; oxidation of other primary alcohols, except ethanol, did not. The extent of [1-14C]acetate assimilation supported by methanol oxidation was decreased in the presence of primary alcohols, except ethanol. Potassium cyanide (0.33 mM) completely inhibited the oxidation of formate and its stimulation of [1-14C]acetate assimilation. The amount of [1-14C]acetate assimilation supported by methanol oxidation was significantly inhibited by cyanide. PMID:412469

  17. Regional prediction of soil organic carbon content over temperate croplands using visible near-infrared airborne hyperspectral imagery and synchronous field spectra

    NASA Astrophysics Data System (ADS)

    Vaudour, E.; Gilliot, J. M.; Bel, L.; Lefevre, J.; Chehdi, K.

    2016-07-01

    This study aimed at identifying the potential of Vis-NIR airborne hyperspectral AISA-Eagle data for predicting the topsoil organic carbon (SOC) content of bare cultivated soils over a large peri-urban area (221 km2) with both contrasted soils and SOC contents, located in the western region of Paris, France. Soil types comprised haplic luvisols, calcaric cambisols and colluvic cambisols. Airborne AISA-Eagle data (400-1000 nm, 126 bands) with 1 m-resolution were acquired on 17 April 2013 over 13 tracks. Tracks were atmospherically corrected then mosaicked at a 2 m-resolution using a set of 24 synchronous field spectra of bare soils, black and white targets and impervious surfaces. The land use identification system layer (RPG) of 2012 was used to mask non-agricultural areas, then calculation and thresholding of NDVI from an atmospherically corrected SPOT image acquired the same day enabled to map agricultural fields with bare soil. A total of 101 sites sampled either in 2013 or in the 3 previous years and in 2015 were identified as bare by means of this map. Predictions were made from the mosaic AISA spectra which were related to topsoil SOC contents by means of partial least squares regression (PLSR). Regression robustness was evaluated through a series of 1000 bootstrap data sets of calibration-validation samples, considering 74 sites outside cloud shadows only, and different sampling strategies for selecting calibration samples. Validation root-mean-square errors (RMSE) were comprised between 3.73 and 4.49 g Kg-1 and were ∼4 g Kg-1 in median. The most performing models in terms of coefficient of determination (R2) and Residual Prediction Deviation (RPD) values were the calibration models derived either from Kennard-Stone or conditioned Latin Hypercube sampling on smoothed spectra. The most generalizable model leading to lowest RMSE value of 3.73 g Kg-1 at the regional scale and 1.44 g Kg-1 at the within-field scale and low bias was the cross-validated leave

  18. The AMS 14C dating of Iron Age rice chaff ceramic temper from Ban Non Wat, Thailand: First results and its interpretation

    NASA Astrophysics Data System (ADS)

    Higham, Charles F. W.; Kuzmin, Yaroslav V.; Burr, G. S.

    2010-04-01

    Pottery tempered with rice chaff from the early Iron Age cemetery of Ban Non Wat site, northeast Thailand, has been subjected to direct AMS 14C dating, using low temperature combustion with oxygen as originally developed by authors. The carbon yield (0.2-0.5%) testifies the suitability of this pottery for dating. However, not all the results are in agreement with expected archaeological ages and other 14C dates from the studied site and neighboring site of Noen U-Loke. This calls for a thorough analysis and interpretation of pottery temper dates from the region.

  19. Effect of lonidamine on the utilization of /sup 14/C-labeled glucose by human astrocytoma cells

    SciTech Connect

    Paggi, M.G.; Zupi, G.; Fanciulli, M.; Del Carlo, C.; Giorno, S.; Laudonio, N.; Silvestrini, B.; Caputo, A.; Floridi, A.

    1987-10-01

    The effect of lonidamine (LND), 1-(2,4-dichlorobenzyl)-1H-indazol-3 carboxylic acid, on the utilization of carbon from /sup 14/C-labeled glucose by cell cultures of the permanent strain LI derived from a human glioblastoma multiforme (astrocytoma) has been investigated. The results may be summarized as follows. Aerobic glycolysis is the main energy-yielding process as shown by the fact that the greatest part of glucose carbon atoms is incorporated into lactate. Nevertheless, the amount of glucose converted accounts for only 63% of the lactate produced, indicating the presence of an elevated endogenous aerobic glycolysis. The amount of glucose carbon atoms incorporated into CO/sub 2/, lipids, nucleic acid, and supporting structures is low. LND decreased the incorporation of /sup 14/C activity in all the above mentioned isolated compounds because of its ability to inhibit glucose phosphorylation. Consequently, there is a lower concentration of glucose-6-phosphate which, in turn, affects the rate of formation of several metabolites in glycolytic and pentose phosphate pathways. Experiments with (1-/sup 14/C)-2-deoxy-D-glucose further substantiate the idea of glucose phosphorylation as a main target of LND and strongly suggest the presence of a mitochondrially bound hexokinase. The higher inhibition of glucose phosphorylation in exponentially growing cells indicates a further shift of the enzyme toward mitochondria-bound form and confirms the importance of the energy status of the cell in eliciting the response to LND. The reduced capacity of LND-treated cells to synthetize ATP and glucose-6-phosphate reflects the decreased synthesis of proteins and nucleic acids, which affects cell growth and duplication.

  20. A Comparison of Rapid-Screen 14C Dates and U/Th Dates from Fossil Corals: Implications for Paleoclimate Reconstruction

    NASA Astrophysics Data System (ADS)

    Grothe, P. R.; Cobb, K. M.; Bush, S.; Cheng, H.; Santos, G.; Southon, J. R.; Edwards, R. L.

    2014-12-01

    Paleoclimate records from fossil corals provide valuable benchmarks for climate model simulations of tropical climate variability. Unfortunately, the number of such reconstructions is limited by the rarity of the relatively large fossil coral heads that are targeted for paleoclimate studies. Abundant, albeit shorter (5-10yrs-long) fossil coral sequences could be used to generate a more robust, quasi-continuous reconstruction of tropical climate with built-in uncertainty estimates, but the large number of radiometric dates required is costly. A new rapid-screen 14C dating method, with a nominal precision of ±1.8% (1σ) for young carbonates (Bush et al., 2013), is roughly 10 times faster than high-precision U/Th dating, making it well-suited to screening a large number of corals. In this study, we compare rapid-screen 14C dates to both high-precision 14C dates and U/Th dates from well-characterized mid- to late-Holocene fossil corals collected from Christmas and Fanning Islands (2-4°N, 157-160°W) (Cobb et al., 2013). Our results show that most rapid-screen 14C dates agree with high-precision 14C dates (N=3) and U/Th dates (N=42), within combined uncertainties. However, two samples that contain 15 and 23% calcite (as determined by XRD) are associated with large discrepancies in calibrated 14C vs published U/Th ages (5065-5579 yBP (2σ) versus 6350 ±13 yBP (2σ) and 4868-5424 yBP (2σ) vs 6598 ±13 yBP (2σ)), respectively (Cobb et al., 2013). The 14C-U/Th mismatches, as well as poor reproducibility of replicate U/Th dates from these samples, are consistent with diagenetic alteration indicated by the presence of calcite. Mass balance calculations indicate that the dating discrepancies can be explained by a combination of 14C addition and U removal, both of which can occur through calcite recrystallization during freshwater diagenesis. Results illustrate that the rapid-screen 14C dating method is well-suited to surveying a large number (~100's) of fossil coral

  1. 14C age of the "Museum Breccia" (Campi Flegrei) and its relevance for the origin of the Campanian Ignimbrite

    USGS Publications Warehouse

    Lirer, L.; Rolandi, G.; Rubin, M.

    1991-01-01

    Field stratigraphic investigations and AMS 14C dating of carbon particles in paleosols has resulted in a framework of the sequence and age of the pyroclastic products in the Campi Flegrei area of Southern Italy. The Museum Breccia cannot be the early phase of the Campanian Ignimbrite, as was previously believed, but is from a smaller and later eruption with an age of approximately 17,900 y B.P. This date also precludes its correlation with the Neapolitan Yellow Tuff (12,000 y B.P.). ?? 1991.

  2. Comparison of nonabsorbable markers Poly R-478 and (14C)PEG-4,000 for use in developmental absorption studies

    SciTech Connect

    Stahl, G.E.; Fayer, J.C.; Ling, S.C.; Watkins, J.B. )

    1991-05-01

    To determine the utility of Poly R-478, a stable, polymeric dye (MW, 40,000), as a nonabsorbable marker for studies in the developing small intestine, it was validated by comparison to carbon 14-labeled polyethylene glycol, MW 4,000 (( 14C)PEG-4,000) in rats from 14 to 40 days of age. The recovery and quantification of Poly R-478 from biological samples is simple and rapid compared to other nonradioactive nonabsorbable markers. In 40-day-old rats simultaneously given Poly R-478 and (14C)PEG, total recoveries were similar, the percentages of the Poly R-478 dose and the (14C)PEG dose recovered per segment were identical, and taurocholate absorption rates calculated using each marker were comparable. Recovery of Poly R-478 from flushed intestinal segments, determined by a one-step extraction, was equivalent to that of (14C)PEG in 40-day-old rats (96.5 {plus minus} 3.7% versus 102.7 {plus minus} 10.1%; NS) but was superior to that of (14C)PEG in 21-day-old rats (98.0 {plus minus} 6.2% versus 63.4 {plus minus} 5.5%; p less than 0.001) and 14-day-old rats (97.8 {plus minus} 6.7% versus 56.7 {plus minus} 12.6%; p less than 0.001). Within each age group, the distribution of Poly R-478 within the intestine was similar to that of (14C)PEG. In addition, total taurocholate absorption in the presence of Poly R-478 was comparable to that in the presence of (14C)PEG. Complete recovery of Poly R-478 from a suspension of liver particles and from mixtures with two commercial infant formulas was demonstrated in vitro, suggesting that Poly R-478 may be used when foods are present in the intestine.

  3. Continuous lake-sediment records of glaciation in the Sierra Nevada between 52,600 and 12,500 14C yr B.P.

    USGS Publications Warehouse

    Benson, L.V.; May, Howard M.; Antweiler, R.C.; Brinton, T.I.; Kashgarian, Michaele; Smoot, J.P.; Lund, S.P.

    1998-01-01

    The chemistry of the carbonate-free clay-size fraction of Owens Lake sediments supports the use of total organic carbon and magnetic susceptibility as indicators of stadial-interstadial oscillations. Owens Lake records of total organic carbon, magnetic susceptibility, and chemical composition of the carbonate-free, clay-size fraction indicate that Tioga glaciation began ~24,500 and ended by ~13,600 14C yr B.P. Many of the components of glacial rock flour (e.g., TiO2, MnO, BaO) found in Owens Lake sediments achieved maximum values during the Tioga glaciation when valley glaciers reached their greatest extent. Total organic carbon and SiO2 (amorphous) concentrations reached minimum values during Tioga glaciation, resulting from decreases in productivity that accompanied the introduction of rock flour into the surface waters of Owens Lake. At least 20 stadial-interstadial oscillations occurred in the Sierra Nevada between 52,600 and 14,000 14C yr B.P. Total organic carbon data from a Pyramid Lake sediment core also indicate oscillations in glacier activity between >39,500 and ~13,600 14C yr B.P. Alpine glacier oscillations occurred on a frequency of ???1900 yr in both basins, suggesting that millennial-scale oscillations occurred in California and Nevada during most of the past 52,600 yr.

  4. Airborne measurements of black carbon aerosol over the Southeastern U.S. during the Southeast Atmosphere Study (SAS) experiment

    NASA Astrophysics Data System (ADS)

    Markovic, M. Z.; Perring, A. E.; Schwarz, J. P.; Fahey, D. W.; Gao, R.; Watts, L.; Holloway, J.; Graus, M.; Warneke, C.; De Gouw, J. A.; Veres, P. R.; Roberts, J. M.; Middlebrook, A. M.; Welti, A.; Liao, J.

    2013-12-01

    The Southeast Atmosphere Study (SAS) field campaign was a large-scale, collaborative project, which took place in the Southeastern U.S. in June and July of 2013. The goal of the campaign was to investigate the impacts of biogenic and anthropogenic gases and aerosols on the formation of haze and anomalous climate cooling in the region. During SAS, a NOAA Single Particle Soot Photometer (SP2) instrument was utilized onboard NOAA WP-3D research aircraft for measurements of black carbon (BC) aerosol mass and microphysical properties. BC aerosol is emitted into the atmosphere from biomass burning (BB) and incomplete combustion of fossil and biofuel. Hence, BC sources are strongly linked to anthropogenic activity. BC aerosol is currently the second largest anthropogenic climate forcing agent after CO2(g), and its climate impacts, which depend on vertical burden and internal mixing, are not fully understood. In the Southeast, BC aerosol is expected to provide surface area for the condensation of semi-volatile products of VOC oxidation and subsequent formation of secondary organic aerosol (SOA). Hence, BC is expected to impact the haze formation and regional climate. In this work we present an overview of BC measurements during Southeast Nexus (SENEX) study, the NOAA contribution to SAS. Geographical variations in mass mixing ratios, mass size distributions, and mixing state of BC over the Southeast U.S. are discussed. Relationships of BC with carbon monoxide (CO), acetonitrile (ACN) and other trace gases are used to investigate the impacts of urban, BB, natural gas development, and power plant emissions on the distribution and properties of BC aerosol in the region. Among studied urban centers, St. Louis and Atlanta were determined to be the largest source regions of BC. A clear weekend effect in BC mass mixing ratios and microphysical properties was observed in the metropolitan Atlanta region. Compared to BB and urban centers, power plants and natural gas developments

  5. Infrared airborne spectroradiometer survey results in the western Nevada area

    NASA Technical Reports Server (NTRS)

    Collins, W.; Chang, S. H.; Kuo, J. T.

    1982-01-01

    The Mark II airborne spectroradiometer system was flown over several geologic test sites in western Nevada. The infrared mineral absorption bands were observed and recorded for the first time using an airborne system with high spectral resolution in the 2.0 to 2.5 micron region. The data show that the hydrothermal alteration zone minerals, carbonates, and other minerals are clearly visible in the airborne survey mode. The finer spectral features that distinguish the various minerals with infrared bands are also clearly visible in the airborne survey data. Using specialized computer pattern recognition methods, it is possible to identify mineralogy and map alteration zones and lithologies by airborne spectroradiometer survey techniques.

  6. 17 CFR 240.14c-4 - Presentation of information in information statement.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 17 Commodity and Securities Exchanges 3 2010-04-01 2010-04-01 false Presentation of information in information statement. 240.14c-4 Section 240.14c-4 Commodity and Securities Exchanges SECURITIES AND EXCHANGE COMMISSION (CONTINUED) GENERAL RULES AND REGULATIONS, SECURITIES EXCHANGE ACT OF 1934 Rules and Regulations Under the Securities...

  7. 17 CFR 240.14c-4 - Presentation of information in information statement.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 17 Commodity and Securities Exchanges 3 2011-04-01 2011-04-01 false Presentation of information in... Section 14(c) § 240.14c-4 Presentation of information in information statement. (a) The information... type except that to the extent necessary for convenient presentation, financial statements and...

  8. Disposition of /sup 14/C tolrestat in laboratory animals and man

    SciTech Connect

    Ferdinandi, E.S.; Hicks, D.R.; Cayen, M.N.

    1986-03-01

    The disposition of the aldose reductase inhibitor tolrestat (T) was determined in the mouse, rat, dog, assemensis monkey, and man. Serum T and radioactivity ratios, and % of dose excreted after p.o. administration of /sup 14/C-T at a dose of 10 mk/kg (100 mg to man), are presented. Except for the rat and monkey, 55 to 95% of the urinary /sup 14/C was due to T and oxo-tolrestat (oxo-T, N-((5-(trifluoromethyl)-6-methoxy-1-napthalenyl)oxo-methyl)-N-methylglycine). Oxo-T is formed, in part, non-enzymatically from T; a potential intermediate in this transformation was detected in all the urine samples. In man and monkey, about 15% and 68%, respectively, of the urinary /sup 14/C was due to T-glucuronide. In rat urine, >90% of the /sup 14/C was due to polar metabolites; in bile, about 66% of the /sup 14/C was due to T. The composition of the serum /sup 14/C in the mouse and rat was determined. In conclusion, /sup 14/C-T was rapidly and well absorbed by all species. Except for the rat and dog, urine was the main excretion route for /sup 14/C. Urine/sup 14/ comprised mainly T, t-glucuronide of oxo-T in all the species except the rat.

  9. 17 CFR 240.14c-3 - Annual report to be furnished security holders.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... COMMISSION (CONTINUED) GENERAL RULES AND REGULATIONS, SECURITIES EXCHANGE ACT OF 1934 Rules and Regulations... 17 Commodity and Securities Exchanges 3 2010-04-01 2010-04-01 false Annual report to be furnished... Section 14(c) § 240.14c-3 Annual report to be furnished security holders. (a) If the information...

  10. Production of [14C]fumonisin B1 by Fusarium moniliforme MRC 826 in corn cultures.

    PubMed Central

    Alberts, J F; Gelderblom, W C; Vleggaar, R; Marasas, W F; Rheeder, J P

    1993-01-01

    Kinetics of growth and fumonisin production by Fusarium moniliforme MRC 826 in corn "patty" cultures were investigated, and a technique was developed for the production of [14C]fumonisin B1 ([14C]FB1) by using L-[methyl-14C]methionine as the precursor. A significant (P < 0.01) correlation exists between fungal growth and FB1 (r = 0.89) and FB2 (r = 0.87) production in corn patties, beginning after 2 days and reaching the stationary phase after 14 days of incubation. [14C]FB1 was produced by adding L-[methyl-14C]methionine daily to cultures during the logarithmic phase of production. Incorporation of the isotope occurred at C-21 and C-22 of the fumonism molecule and was enhanced in the presence of unlabeled L-methionine. Although the concentration of exogenous unlabeled methionine is critical for incorporation of the 14C label, optimum incorporation was achieved by adding 50 mg of unlabeled L-methionine and 200 mu Ci of L-[methyl-14C]methionine to a corn patty (30 g) over a period of 9 days, yielding [14C]FB1 with a specific activity of 36 mu Ci/mmol. PMID:8368853

  11. Dilute Nuclear States: {sup 12}C, {sup 10}Be and {sup 14}C

    SciTech Connect

    Freer, M.

    2008-11-11

    The experimental evidence for dilute {alpha}-particle states in {sup 12}C, {sup 10}Be and {sup 14}C is discussed. The question of the location of the 2{sup +} excitation of the 7.65 MeV {sup 12}C state remains unresolved, as does the existence of possible analogue states in {sup 14}C.

  12. Fine-root turnover patterns and their relationship to root diameter and soil depth in a 14C-labeled hardwood forest

    SciTech Connect

    Joslin, Jr., John D; Gaudinski, Julia B.; Torn, Margaret S.; Riley, W. J.; Hanson, Paul J

    2006-01-01

    Characterization of turnover times of fine roots is essential to understanding patterns of carbon allocation in plants and describing forest C cycling. We used the rate of decline in the ratio of 14C to 12C in a mature hardwood forest, enriched by an inadvertent 14C pulse, to investigate fine-root turnover and its relationship with fine-root diameter and soil depth. Biomass and ?14C values were determined for fine roots collected during three consecutive winters from four sites, by depth, diameter size classes (<0.5 or 0.5-2 mm), and live-or-dead status. Live-root pools retained significant 14C enrichment over 3 yr, demonstrating a mean turnover time on the order of years. However, elevated ?14C values in dead-root pools within 18 months of the pulse indicated an additional component of live roots with short turnover times (months). Our results challenge assumptions of a single live fine-root pool with a unimodal and normal age distribution. Live fine roots <0.5 mm and those near the surface, especially those in the O horizon, had more rapid turnover than 0.5-2 mm roots and deeper roots, respectively.

  13. A large drop in atmospheric [sup 14]C/[sup 12]C and reduced melting in the younger dryas, documented with [sup 230]Th ages of corals

    SciTech Connect

    Edwards, R.L.; Beck, J.W. ); Burr, G.S.; Donahue, D.J. ); Chappell, J.M.A. ); Bloom, A.L. ); Druffel, E.R.M. ); Taylor, F.W. )

    1993-05-14

    Paired carbon-14 ([sup 14]C) and thorium-230 ([sup 230]Th) ages were determined on fossil corals from the Huon Peninsula, Papua New Guinea. The ages were used to calibrate part of the [sup 14]C time scale and to estimate rates of sea-level rise during the last deglaciation. An abrupt offset between the [sup 14]C and [sup 230]Th ages suggests that the atmospheric [sup 14]C/[sup 12]C ratio dropped by 15 percent during the latter part of and after the Younger Dryas (YD). This prominent drop coincides with greatly reduced rates of sea-level rise. Reduction of melting because of cooler conditions during the YD may have caused an increase in the rate of ocean ventilation, which caused the atmospheric [sup 14]C/[sup 12]C ratio to fall. The record of sea-level rise also shows that globally averaged rates of melting were relatively high at the beginning of the YD. Thus, these measurements satisfy one of the conditions required by the hypothesis that the diversion of meltwater from the Mississippi to the St. Lawrence River triggered the YD event. 41 refs., 5 figs., 1 tab.

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

    SciTech Connect

    Kerr, L A; Andrews, A H; Cailliet, G M; Brown, T A; Coale, K H

    2006-06-08

    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 periodicity 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.

  15. Measurement of biocarbon in flue gases using 14C

    SciTech Connect

    Haemaelaeinen, K.M.; Jungner, H.; Antson, O.; Rasanen, J.; Tormonen, K.; Roine, J.

    2007-07-01

    A preliminary investigation of the biocarbon fraction in carbon dioxide emissions of power plants using both fossil- and biobased fuels is presented. Calculation of the biocarbon fraction is based on radiocarbon content measured in power plant flue gases. Samples were collected directly from the chimneys into plastic sampling bags. The C-14 content in CO{sub 2} was measured by accelerator mass spectrometry (AMS). Flue gases from power plants that use natural gas, coal, wood chips, bark, plywood residue, sludge from the pulp factory, peat, and recovered fuel were measured. Among the selected plants, there was one that used only fossil fuel and one that used only biofuel; the other investigated plants burned mixtures of fuels. The results show that C-14 measurement provides the possibility to determine the ratio of bio and fossil fuel burned in power plants.

  16. Multi-Year Dynamics of Upland-Oak Forest Organic Horizons: Observations Based on a Unique 14C-Tracer and a Mechanistic Model

    NASA Astrophysics Data System (ADS)

    Hanson, P. J.; Trumbore, S. E.; Swanston, C. W.; Garten, C. T.; Callaham, M. A.; Jardine, P.; Post, W. M.

    2005-12-01

    The Enriched Background Isotope Study (EBIS) was initiated on the Oak Ridge Reservation (ORR) near Oak Ridge, Tennessee in the fall of 2000 to collect and utilize unique 14C-labeled leaf litter for a multi-year, litter-replacement experiment. The goal of EBIS is to understand key mechanisms driving soil carbon cycling and to develop robust models for describing the fate and accumulation of carbon within organic and mineral soils of oak-dominated forests. EBIS uses a combination of high-to-low gradients of 14C-signatures within the soils, roots, and leaf litter across the ORR together with manipulated 14C-litter enrichments or dilutions to track litter-layer C movement through the organic and mineral soil horizons. Through 3-years of defined 14C-litter-additions, we have no evidence that canopy leaf litter is a near-term source of mineral soil carbon. Rather, the downward migration of leaf-litter carbon is driven by annual layering and gravity-induced packing of organic matter to the surface of the mineral horizons. The well-drained, acid soils of these upland sites studies support only low earthworm populations and, therefore, bioturbation is an ineffective mechanism for C transport in this ecosystem. Standard multi-component isotopic mixing models were shown to be inadequate for the prediction of the observed 14C-distributions within the organic horizons following multiple year litter additions. Models containing expanded spatial and temporal details were needed to successfully capture organic-layer C turnover and transport through the organic layers of these soils. Critical details required to model 14C-dynamics in these soils include: the tracking of individual litter-layer cohorts over time, daily time-step simulations of intra-annual litter and humus decomposition as a function of temperature and water content, and the simulation of DOC leaching as a mass-loss and differential 14C-transport process. Within only a short time span (3 to 4 years), the EBIS is

  17. Will there be a 14C minimum in the tropical Pacific in the 1990s

    SciTech Connect

    Toggweiler, J.R. )

    1990-01-09

    14C distributions measured during GEOSECS showed large minima in bomb 14C levels in the tropical belts of the major ocean basins. Broecker et al. (1978, JGR, 83) attributed the minima to upwelling of deep water which was free of bomb 14C. Wyrtki (1981, JPO, 11) countered that heat budgets constrain the water upwelling the the equator to be from the upper themocline. Druffel (1987, JMR, 45) built a model of the Pacific upwelling system incorporating Wyrtki's description of the upwelling system. Druffel showed that the GEOSECS 14C minimum could be reproduced with upwelled upper thermocline water because bomb 14C levels were still relatively low in the tropical thermocline at the time of GEOSECS. Druffel went on to predict that mid latitude and tropical surface 14C levels would approach a common value before the 1990s and upper thermocline water masses acquired more bomb 14C and atmospheric 14C levels declined. By studying pre-bomb coral 14C records and a model simulation in Toggweiler et al. (1989, JGR, 94), I have found confirmation that some older and colder water upwells in the tropical Pacific. Upper thermocline (22-24C) water has about the same pre-bomb 14C content as pre-bomb surface waters and cannot generate a low 14C singal prior to the bomb test. The appearance of the oldest upwelled water in the coral data is correlated in time with the cold phase of the ENSO cycle. Most of the low 14C water moves southward into the South Pacific. I will argue that intensified upwelling during the cold phase of ENSO pulls up 12-14C water from the lower layers of the Equatorial Undercurrent. Upwelling from this layer may represent an important closure mechanism for mode waters formed in the subantarctic. A source of older water makes it certain that the tropical 14C minimum will persist through the 1990s and the remainder of the post-bomb era.

  18. Excretion of 14C-edrophonium and its metabolites in bile

    PubMed Central

    Back, D. J.; Calvey, T. N.

    1972-01-01

    1. The metabolism and biliary excretion of 14C-edrophonium chloride was studied in Wistar rat. 2. Approximately 5% of the dose was recovered from bile in 6 hours. Most of the radioactivity was eliminated as 14C-edrophonium glucuronide. Small amounts of the unchanged drug were also detected in bile, particularly during the first hour after administration of the drug. 3. The concentration of 14C-edrophonium glucuronide in bile was approximately 15-20 times its concentration in plasma. 4. In contrast, the concentration of unchanged 14C-edrophonium was similar in bile and plasma. 5. Evidence is presented that unchanged 14C-edrophonium is transferred from plasma to bile via the peribiliary vascular plexus. PMID:5040663

  19. Revisiting a universal airborne light detection and ranging approach for tropical forest carbon mapping: scaling-up from tree to stand to landscape.

    PubMed

    Vincent, Grégoire; Sabatier, Daniel; Rutishauser, Ervan

    2014-06-01

    Airborne laser scanning provides continuous coverage mapping of forest canopy height and thereby is a powerful tool to scale-up above-ground biomass (AGB) estimates from stand to landscape. A critical first step is the selection of the plot variables which can be related to light detection and ranging (LiDAR) statistics. A universal approach was previously proposed which combines local and regional estimates of basal area (BA) and wood density with LiDAR-derived canopy height to map carbon at a regional scale (Asner et al. in Oecologia 168:1147-1160, 2012). Here we explore the contribution of stem diameter distribution, specific wood density and height-diameter (H-D) allometry to forest stand AGB and propose an alternative model. By applying the new model to a large tropical forest data set we show that an appropriate choice of input variables is essential to minimize prediction error of stand AGB which will propagate at larger scale. Stem number (N) and average stem cross-sectional area should be used instead of BA when scaling from tree to plot. Stand quadratic mean diameter above the census threshold diameter size should be preferred over stand mean diameter as it reduces the prediction error of stand AGB by a factor of ten. Wood density should be weighted by stem volume per species instead of BA. LiDAR-derived statistics should prove useful for estimating local H-D allometries as well as mapping N and the mean quadratic diameter above 10 cm at the landscape level. Prior stratification into forest types is likely to improve both estimation procedures significantly and is considered the foremost current challenge. PMID:24615493

  20. Disposition of 14C-β-carotene following delivery with autologous triacylglyceride-rich lipoproteins

    NASA Astrophysics Data System (ADS)

    Dueker, Stephen R.; Vuong, Le Thuy; Faulkner, Brian; Buchholz, Bruce A.; Vogel, John S.

    2007-06-01

    Following ingestion, a fraction of β-carotene is cleaved into vitamin A in the intestine, while another is absorbed intact and distributed among tissues and organs. The extent to which this absorbed β-carotene serves as a source of vitamin A is unknown in vivo. In the present study we use the attomole sensitivity of accelerator mass spectrometry (AMS) for 14C to quantify the disposition of 14C-β-carotene (930 ng; 60.4 nCi of activity) after intravenous injection with an autologous triacylglyceride-rich lipoprotein fraction in a single volunteer. Total 14C was quantified in serial plasma samples and also in triglyceride-rich, and low density lipoprotein, subfractions. The appearance of 14C-retinol, the circulating form of vitamin A in plasma, was determined by chromatographic separation of plasma retinol extracts prior to AMS analysis. The data showed that 14C concentrations rapidly decayed within the triglyceride-rich lipoprotein fractions after injection, whereas low density lipoprotein 14C began a significant rise in 14C 5 h post dose. Plasma 14C-retinol also appeared at 5 h post dose and its concentrations were maintained above baseline for >88 days. Based upon comparisons of 14C-retinol concentrations following an earlier study with orally dosed 14C-β-carotene, a molar vitamin A value of the absorbed β-carotene of 0.19 was derived, meaning that 1 mole of absorbed β-carotene provides 0.19 moles of vitamin A. This is the first study to show that infused β-carotene contributes to the vitamin A economy in humans in vivo.

  1. Uptake of anthropogenic CO/sub 2/ by lateral transport models of the ocean based on the distribution of bomb-produced /sup 14/C

    SciTech Connect

    Peng, T.H.

    1986-01-01

    The pattern of global water column inventories of bomb-produced /sup 14/C suggests that a sizeable portion of bomb /sup 14/C that entered the Antarctic, northern Pacific, and tropical oceans has been transported to adjacent temperate regions. Models of lateral transport of surface water in the Atlantic, Indian, and Pacific Oceans are based on this distribution pattern. Upwelling of bomb-/sup 14/C-free water from below takes place in the Antarctic, northern Pacific, and tropical regions; downwelling of surface water occurs in the temperate oceans and northern Atlantic. Uptake of excess CO/sub 2/ by these models is calculated using the observed Mauna Loa pCO/sub 2/ record as an input function. Results indicate that 35% of fossil fuel CO/sub 2/ is taken up by these model oceans during the period 1958-1980. Considering the observed airborne fraction of 0.55, it appears that ca 10% of the global fossil fuel CO/sub 2/ is still missing.

  2. Seasonal Aerosol Distributions at Summit, Greenland: EC, OC, 14C and Individual Particle Analysis

    NASA Astrophysics Data System (ADS)

    Klouda, G. A.; Conny, J. M.; McNichol, A. P.; Dibb, J. E.

    2011-12-01

    Aerosol is known to affect the Earth's atmosphere and surface albedo thus having an influence on climate. In the case of carbonaceous aerosol, organic carbon (OC) tends to scatter sunlight while elemental (soot) carbon (EC) aerosol absorbs light. Considering the importance of these aerosols on snow and ice albedo (Hansen and Nazarenko, 2004), PM2.5, PM2.5-10 and snow-melt filters were collected weekly at Summit, Greenland from August 2000 to August 2002 to measure particulate EC, OC, and 14C of total carbon; the latter to quantify natural and anthropogenic source contributions. The pattern of PM2.5 shows a spring-summer maxima in EC (~10 ng m-3) and OC (~ 100 ng m-3); with levels consistent with summer 2006 measurements reported by Hagler et al. (2007). For a subset of filters over the two year period, the average biogenic contribution to PM2.5 OC was estimated to be 20 ng m-3 considering an average percent modern carbon of 46 % (SD=18 %; n=21) and an average total carbon concentration of 50 ng m-3. A summer maximum was observed in PM2.5-10 OC (~ 1000 ng m-3), while for the most part EC concentrations were below detection (< 300 ng m-3; limited primarily by the volume of air sampled). To provide insight into scattering and absorption properties of aerosols at Summit, we used scanning electron microscopy (SEM) to investigate the size, shape, and chemistry of particle populations as well as individual particles from selected filters. Particles were migrated from the filters to polished silicon or germanium wafers using an electrostatically-assisted centrifugation technique. Particle populations were studied by employing secondary electron imaging and energy dispersive x-ray spectroscopy (EDX) with automated SEM and associated particle analysis software. The size, shape, and composition of individual particles were studied with field-emission SEM employing secondary and backscatter electron imaging, bright-field and dark-field scanning transmission electron microscopy

  3. The effect of 6-aminonicotinamide on the levels of brain amino acids and glucose, and their labeling with 14C after injection of (U-14C) glucose

    SciTech Connect

    Gaitonde, M.K.; Lewis, L.P.; Evans, G.; Clapp, A.

    1981-10-01

    The brains of rats paralysed at 4 hr after the administration of 6-aminonicotinamide were found to contain decreased levels of glutamate and gamma-aminobutyrate. The glucose content of the brain of the treated rats was several fold higher than in controls. The incorporation of 14C into brain amino acids at 30 min after the injection of (U-14C)glucose was decreased by 16%: this was attributed to mainly decreased labeling of glutamate and associated amino acids. The results are discussed in the light of previous findings that the administration of 6-aminonicotinamide resulted in the blockade of the direct oxidation of glucose by the pentose phosphate pathway.

  4. Post-bomb coral Δ14C record from Iki Island, Japan: possible evidence of oceanographic conditions on the northern East China Sea shelf

    NASA Astrophysics Data System (ADS)

    Mitsuguchi, Takehiro; Hirota, Masashi; Paleo Labo AMS Dating Group; Yamazaki, Atsuko; Watanabe, Tsuyoshi; Yamano, Hiroya

    2016-07-01

    In this study, a sea-surface water Δ14C record of AD 1966-2000 (i.e., after the atmospheric nuclear-bomb testing period of the mid-1950s to early 1960s) was reconstructed from a coral sample collected from Iki Island, western Japan. The island is located in the Tsushima Strait where the Tsushima Current flows from the East China Sea (ECS) continental shelf into the Sea of Japan, indicating a strong influence of the ECS shelf water on the island. It is widely accepted that the Tsushima Current originates in the area between the ECS shelf break and the Nansei Islands further offshore as a branch of the Kuroshio Current, although another possible origin is the Taiwan-Tsushima Current System. The Δ14C record from Iki Island shows the following evidence of a response to the atmospheric nuclear testing: (1) an increase from ~55‰ in 1966 to ~133‰ in 1970, (2) a plateau ranging between ~123 and ~142‰ during the 1970s to the late 1980s, and (3) a gradual decrease from ~115‰ in 1990 to ~83‰ in 2000. Comparison of this record with coral Δ14C records from the Nansei Islands (Okinawa Island, Ishigaki Island and Kikai Island), located ~160-280 km off the ECS shelf break and little influenced by the shelf water, suggests that the surface-water Δ14C around Iki Island was ~30-45‰ lower than that of the Nansei Islands from the mid-1960s to late 1970s, and that the Δ14C difference between Iki Island and the Nansei Islands decreased from the end of the 1970s to ~0-15‰ in the mid-1980s to 2000. The lower Δ14C around Iki Island can be explained as follows: (1) in contrast to the Nansei Islands area, the ECS shelf area is a vertically mixed, highly concentrated carbon reservoir significantly connected to subsurface and deeper waters outside the shelf area, strongly suggesting that the surface-water Δ14C of the shelf area (perhaps excepting very shallow innermost shelf areas) was significantly less sensitive to the atmospheric nuclear-bomb 14C spike than that of the

  5. 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.

  6. Fate of ( sup 14 C)monolinuron in potatoes and soil under outdoor conditions

    SciTech Connect

    Freitag, D.; Scheunert, I. )

    1990-12-01

    (phenyl-{sup 14}C)Monolinuron was applied (2.5 and 1.9 kg/ha) to the soil surface of an outdoor lysimeter in two successive years: then, potatoes were grown. Total recovery of {sup 14}C in soil, plants, and leached water was about 55% (of {sup 14}C applied) after the first growing period and about 43% after the second growing period. Radioactivity in soil contained 77.1% (based on total {sup 14}C recovered in soil) bound residues, 15% monolinuron, and the following conversion products: N-(4-hydroxyphenyl)-N'-methoxy-N'-methylurea, N-(4-chlorophenyl)-N'-methylurea. N-(4-chlorophenyl)methylcarbamate, N-(4-chlorophenyl)-N-methyl-methylcarbamate, and 4-chloroformanilide. The leachate contained 0.8% (based on total {sup 14}C recovered in leachate) N-(4-hydroxyphenyl)-N'-methoxy-N'-methylurea. Potato plants contained 0.106 mg/kg radioactive residues in peeled tubers after one growing period and 15.94 mg/kg in the tops; after two growing periods, peeled tubers contained 0.091 mg/kg and tops contained 18.87 mg/kg radioactive residues. These residues consisted of bound {sup 14}C (57.9% of total {sup 14}C recovered in plants), N-(4-hydroxyphenyl)-N'-methoxy-N'-methylurea, N-(4-chlorophenyl)-N'-methylurea, N-(4-chlorophenyl)methylcarbamate, N-(4-chlorophenyl)-N-methyl-methylcarbamate, and 4,4'-dichlorozobenzene.

  7. The distribution of Δ14C in Korea from 2010 to 2013

    NASA Astrophysics Data System (ADS)

    Park, J. H.; Hong, W.; Xu, X.; Park, G.; Sung, K. S.; Sung, Kilho; Lee, Jong-geol; Nakanishi, T.; Park, Hyo-Seok

    2015-10-01

    Δ14C values of leaves of a deciduous tree record to those of atmospheric CO2 within error and were used to map out Δ14C distribution in Korea. We collected ginkgo (Ginkgo biloba Linnaeus, a deciduous tree) leaf samples in mid-June to early July from 2009 to 2013 in Korea to obtain the regional distribution of Δ14C. Commonly CO2 emitted from fossil fuel consumption dilutes atmospheric 14C, while operations and accidents at nuclear power plants can increase it. The distribution maps of Δ14C from 2010 to 2013 in Korea shows that Δ14C values in the northwestern and southeastern parts of Korea are lower than those of the other parts of Korea, which is consistent with the population and industry patterns. Decrease rates of annually averaged Δ14C values in Korea over the study period are larger than those of Pt. Barrow, Alaska, USA (71.3°N, 156.5°W), so the difference between them and those of Pt. Barrow, Alaska, USA became larger annually. This may be due to the increase in fossil fuel consumption in Korea and China. The decrease rate between 2010 and 2011 was smaller than in other years. This could be the effect of the Fukushima power plant accident which occurred in March 11, 2011, but further study is needed to clarify it.

  8. Biokinetic and dosimetric investigations of 14C-labeled substances in man using AMS

    NASA Astrophysics Data System (ADS)

    Mattsson, Sören; Gunnarsson, Mikael; Svegborn, Sigrid Leide; Nosslin, Bertil; Nilsson, Lars-Erik; Thorsson, Ola; Valind, Sven; Åberg, Magnus; Östberg, Henrik; Hellborg, Ragnar; Stenström, Kristina; Erlandsson, Bengt; Faarinen, Mikko; Kiisk, Madis; Magnusson, Carl-Erik; Persson, Per; Skog, Göran

    2001-07-01

    Up to now, radiation dose estimates from radiopharmaceuticals, labeled with pure β-emitting radionuclides, e.g., 14C or 3H have been very uncertain. Using accelerator mass spectrometry (AMS) we have derived new and improved data for 14C-triolein and 14C-urea and are currently running a program related to the biokinetics and dosimetry of 14C-glycocholic acid and 14C-xylose. The results of our investigations have made it possible to widen the indications for the clinical use of the 14C-urea test for Helicobacter pylori infection in children. The use of ultra-low activities, which is possible with AMS (down to 1/1000 of that used for liquid scintillation counting), has opened the possibility for metabolic investigations on children as well as on other sensitive patient groups like new-borns, and pregnant or breast-feeding women. Using the full potential of AMS, new 14C-labeled drugs could be tested on humans at a much earlier stage than today, avoiding uncertain extrapolations from animal models.

  9. Discussion: Reporting and calibration of post-bomb 14C data

    SciTech Connect

    Reimer, P J; Brown, T A; Reimer, R W

    2004-10-11

    The definitive paper by Stuiver and Polach (1977) established the conventions for reporting of {sup 14}C data for chronological and geophysical studies based on the radioactive decay of {sup 14}C in the sample since the year of sample death or formation. Several ways of reporting {sup 14}C activity levels relative to a standard were also established, but no specific instructions were given for reporting nuclear weapons testing (post-bomb) {sup 14}C levels in samples. Because the use of post-bomb {sup 14}C is becoming more prevalent in forensics, biology, and geosciences, a convention needs to be adopted. We advocate the use of fraction modern with a new symbol F{sup 14}C to prevent confusion with the previously used Fm, which may or may not have been fractionation corrected. We also discuss the calibration of post-bomb {sup 14}C samples and the available datasets and compilations, but do not give a recommendation for a particular dataset.

  10. The biological fate of sup 14 C-dimercaptosuccinic acid in monkeys and rabbits

    SciTech Connect

    Tillotson, J.A.; Boswell, G.; Kincannon, L.; Speckman, C.L.

    1989-09-01

    The biological fate of {sup 14}C-labeled dimercaptosuccinic acid (DMSA) in monkeys and rabbits was determined by measuring the {sup 14}C activity in their urine, feces, and expired air ({sup 14}CO{sub 2}). Monkeys absorbed less than 20% DMSA from three oral dose levels (0.082, 0.16, and 0.5 mmol/kg) of {sup 14}C-DMSA, and the rabbits absorbed 32% DMSA or less from an oral dose of {sup 14}C-DMSA (0.5 mmol/kg). Although the bioavailability of DMSA was limited in either species, DMSA was detected in the blood of both species within minutes after oral dosing. In either species, most of the radiolabel from the absorbed {sup 14}C-DMSA was detected in the urine within 12 hours. We also developed a sensitive assay for directly measuring levels of DMSA (as free thiols) in blood. Intact DMSA was not detected in the blood of the monkeys or the rabbits more than 200 minutes after oral or intravenous dosing at 0.5 mmol DMSA/kg body weight. However, {sup 14}C activity in blood and urine of the monkeys was measurable 72 hours after this dose. Differences between measured {sup 14}C concentrations and intact DMSA concentrations in the blood suggest the presence of DMSA metabolites that have longer half-lives than DMSA. Consequently, until the biological activities of these compounds are identified, the pharmacokinetic analysis of DMSA may be incomplete.

  11. Flux Observations of Carbon from an Airborne Laboratory (FOCAL): Using Advances in Spectroscopy, Turbulent Wind Measurements, and Small, Commercial Aircraft to Create Eddy Covariance Flux Maps from the Air.

    NASA Astrophysics Data System (ADS)

    Sayres, D. S.; Allen, N.; Healy, C. E.; Munster, J. B.; Rivero, M.; Tuozzolo, C.; Wilkerson, J.; Dobosy, R.; Dumas, E. J.; Heuer, M.; Kochendorfer, J.; Meyers, T. P.; Baker, B.; Langford, J.; Anderson, J. G.

    2014-12-01

    Over the past decade improvements in high-sensitivity, cavity-enhanced spectroscopic techniques have allowed for near-real time acquisition of atmospherically important gases at rates fast enough for use in eddy covariance. We report on the development of a suite of spectrometers capable of in situ measurements of the carbon-13 isotopologues of methane and carbon dioxide at high acquisition rates (10 Hz). Coupled with a mature airborne turbulence probe and a small, economical, commercial aircraft flying at 10 m above the surface FOCAL provides region scale surface fluxes of these important greenhouse gases. We describe the instrumentation, with emphasis on how new technology is changing the way these types of measurements can be made. FOCAL was first flown over the North Slope of Alaska in August, 2013. We will present a regional view of methane and carbon dioxide fluxes over parts of the North Slope as well as comparisons to traditional eddy covariance methods.

  12. The application of carbon-14 analyses to the source apportionment of atmospheric carbonaceous particulate matter: a review.

    PubMed

    Heal, Mathew R

    2014-01-01

    Organic carbon (OC) and elemental carbon (EC) together constitute a substantial proportion of airborne particulate matter (PM). Insight into the sources of this major contributor to PM is important for policies to mitigate the impact of PM on human health and climate change. In recent years measurement of the abundance of the radioisotope of carbon ((14)C) in samples of PM by accelerator mass spectrometry has been used to help quantify the relative contributions from sources of fossil carbon and contemporary carbon. This review provides an introduction to the different sources of carbon within PM and the role of (14)C measurements, a description of the preparation of PM samples and of the instrumentation used to quantify (14)C, and a summary of the results and source apportionment methods reported in published studies since 2004. All studies report a sizable fraction of the carbonaceous PM as of non-fossil origin. Even for PM collected in urban locations, the proportions of non-fossil carbon generally exceed 30%; typically the proportion in urban background locations is around 40-60% depending on the local influence of biomass burning. Where values have been measured directly, proportions of non-fossil carbon in EC are lower than in OC, reflecting the greater contribution of fossil-fuel combustion to EC and the generally small sources of contemporary EC. Detailed source apportionment studies point to important contributions from biogenic-derived secondary OC, consistent with other evidence of a ubiquitous presence of heavily oxidized background secondary OC. The review concludes with some comments on current issues and future prospects, including progress towards compound-class and individual-compound-specific (14)C analyses. PMID:24136253

  13. Synthesis, storage, and stability of (4-/sup 14/C)oxaloacetic acid

    SciTech Connect

    Hatch, M.D.; Heldt, H.W.

    1985-03-01

    A simple procedure for preparing (4-/sup 14/C)oxaloacetic acid based on the reaction between (/sup 14/C)HCO-3 and phosphoenolpyruvate catalyzed by phosphoenolpyruvate carboxylase is described. A simple method for preparing highly purified phosphoenolpyruvate carboxylase from maize leaves is described and the degradation of oxaloacetate under conditions of varying pH and divalent metal ion concentration is reported. (4-/sup 14/C)Oxaloacetic acid is stable for several months in 0.1 M HCl solution at -80 degrees C.

  14. Comparison of (14)C liquid scintillation counting at NIST and NRC Canada.

    PubMed

    Bergeron, Denis E; Galea, Raphael; Laureano-Pérez, Lizbeth; Zimmerman, Brian E

    2016-03-01

    An informal bilateral comparison of (14)C liquid scintillation (LS) counting at the National Research Council of Canada (NRC) and the National Institute of Standards and Technology (NIST) has been completed. Two solutions, one containing (14)C-labeled sodium benzoate and one containing (14)C-labeled n-hexadecane, were measured at both laboratories. Despite observed LS cocktail instabilities, the two laboratories achieved accord in their standardizations of both solutions. At the conclusion of the comparison, the beta spectrum used for efficiency calculations was identified as inadequate and the data were reanalyzed with different inputs, improving accord. PMID:26585641

  15. Timing is Everything:The Boon and Bane of 14C Geochronology

    SciTech Connect

    Guilderson, T; Guilderson, T; Reimer, P J; Brown, T

    2004-10-29

    There are underappreciated limitations of the conversion of {sup 14}C-ages to the fixed, calendrical time-scale that bear directly upon our understanding of the dynamic climate system, or the relationship between the collapse of one civilization and it's neighbor's. In this paper we present a quantitative assessment of the limits of {sup 14}C-geochronology and calibration onto the absolute calendrical time-scale over the Holocene. We take into account not only the inherent limitations of the {sup 14}C-calendar calibration curve, but also analytical uncertainties.

  16. Distribution of /sup 14/C after oral administration of (1-/sup 14/C)linoleic acid in rats fed different levels of essential fatty acids

    SciTech Connect

    Becker, W.

    1984-09-01

    Rats from an inbred Sprague-Dawley strain were fed semisynthetic diets with a low (0.3 energy percent (en %)), normal (3 en %) or high (10 en %) content of essential fatty acids (EFA) for at least three generations. Twenty-nine- to 33-day-old male rats were given a single intragastric dose of (1-14C)linoleic acid in olive oil, and the respiratory CO2, urine and feces were collected for 46 hours (expt 1) or 20 hours (expt 2). The 14C activity in respiratory CO2, feces, urine and the carcass was determined in both experiments. In experiment 2 it was also measured in samples of the brown fat, liver, adrenals, white fat, skeletal muscles and brain. In both experiments the rats fed the low EFA diet retained significantly more 14C activity than the rats fed the normal or high EFA diets. In all groups the concentration of label was highest in the brown fat and the adrenals, but the above differences among the groups with respect to 14C retention were mainly observed in the liver, skeletal muscles and brain.

  17. Multidecadal variations in Southern Hemisphere atmospheric 14C: Evidence against a Southern Ocean sink at the end of the Little Ice Age CO2 anomaly

    NASA Astrophysics Data System (ADS)

    Turney, Chris S. M.; Palmer, Jonathan; Hogg, Alan; Fogwill, Christopher J.; Jones, Richard T.; Bronk Ramsey, Christopher; Fenwick, Pavla; Grierson, Pauline; Wilmshurst, Janet; O'Donnell, Alison; Thomas, Zoë A.; Lipson, Mathew

    2016-02-01

    Northern Hemisphere-wide cooling during the Little Ice Age (LIA; 1650-1775 Common Era, C.E.) was associated with a ~5 ppmv decrease in atmospheric carbon dioxide. Changes in terrestrial and ocean carbon reservoirs have been postulated as possible drivers of this relatively large shift in atmospheric CO2, potentially providing insights into the mechanisms and sensitivity of the global carbon cycle. Here we report decadally resolved radiocarbon (14C) levels in a network of tree-ring series spanning 1700-1950 C.E. located along the northern boundary of, and within, the Southern Ocean. We observe regional dilutions in atmospheric radiocarbon (relative to the Northern Hemisphere) associated with upwelling of 14CO2-depleted abyssal waters. We find the interhemispheric 14C offset approaches zero during increasing global atmospheric CO2 at the end of the LIA, with reduced ventilation in the Southern Ocean and a Northern Hemisphere source of old carbon (most probably originating from deep Arctic peat layers). The coincidence of the atmospheric CO2 increase and reduction in the interhemispheric 14C offset imply a common climate control. Possible mechanisms of synchronous change in the high latitudes of both hemispheres are discussed.

  18. Seasonal variations and sources of ambient fossil and biogenic-derived carbonaceous aerosols based on 14C measurements in Lhasa, Tibet

    NASA Astrophysics Data System (ADS)

    Huang, Jie; Kang, Shichang; Shen, Chengde; Cong, Zhiyuan; Liu, Kexin; Wang, Wei; Liu, Lichao

    2010-06-01

    A total of 30 samples of total suspended particles were collected at an urban site in Lhasa, Tibet from August 2006 to July 2007 for investigating carbonaceous aerosol features. The fractions of contemporary carbon ( fc) in total carbon (TC) of ambient aerosols are presented using radiocarbon ( 14C) measurements. The value of fc represents the biogenic contribution to TC, as the biosphere releases organic compounds with the present 14C/ 12C level ( fc = 1), whereas 14C has become extinct in anthropogenic emissions of fossil carbon ( fc = 0). The fc values in Lhasa ranging from 0.357 to 0.702, are higher than Beijing and Tokyo, but clearly lower than the rural region of Launceston, which indicates a major biogenic influence in Lhasa. Seasonal variations of fc values corresponded well with variations of pollutants concentrations (e.g. NO 2). Higher fc values appeared in winter indicating carbonaceous aerosol is more dominated by wood burning and incineration of agricultural wastes within this season. The lower fc values in summer and autumn may be caused by increased diesel and petroleum emissions related to tourism in Lhasa. δ13C values ranged from - 26.40‰ to - 25.10‰, with relative higher values in spring and summer, reflecting the increment of fossil carbon emissions.

  19. Diffusion of /sup 14/C-labeled formocresol and glutaraldehyde in tooth structures

    SciTech Connect

    Wemes, J.C.; Purdell-Lewis, D.; Jongebloed, W.; Vaalburg, W.

    1982-09-01

    /sup 14/C-Formocresol and /sup 14/C-glutaraldehyde were placed in the root canals of freshly extracted human teeth. The outward diffusion of labeled aldehydes was then measured and autoradiograms of cross-sections taken. No diffusion of glutaraldehyde was detectable within 72 hours, whereas there was a rapidly increasing outflow of formocresol during the same period. In a separate group normal root canal treatment was completed until 2 mm. short of the roentgenologic apex with glutaraldehyde as an irrigant. The walls of the root canals of some of the specimens were examined with electron microscopy and the outflow of /sup 14/C-formocresol which was later placed in some specimens was counted. The use of glutaraldehyde as an irrigant resulted in closure of the apical third of the root canal as indicated by the absence of /sup 14/C-formocresol diffusion.

  20. Metabolism of 14C-urea by T-strain mycoplasma.

    PubMed

    Ford, D K; McCandlish, K L; Gronlund, A F

    1970-05-01

    When (14)C-labeled urea was metabolized by T-strain mycoplasma, 94 to 95% of the radioactivity was recovered as (14)CO(2), and significant radioactivity was not incorporated into cellular material. PMID:5419267

  1. Fate of ( sup 14 C)arsanilic acid in pigs and chickens

    SciTech Connect

    Aschbacher, P.W.; Feil, V.J. )

    1991-01-01

    Arsanilic acid uniformly labeled with {sup 14}C in the benzene ring was used to determine the metabolic fate of oral arsanilic acid in pigs and chickens. Arsanilic acid was well absorbed in both species, and urine was the predominant route of excretion. The bile was a minor (< 5% of the dose) route of excretion in pigs; however, biliary excretion was not measured in roosters. Arsanilic acid, N-acetylarsanilic acid, and (4-acetamidophenyl)dimethylarsine oxide were isolated from pig urine (17-39%, 15-29%, and < 5% of urinary {sup 14}C, respectively). Only 25% of the {sup 14}C in pig feces was extractable, and no metabolites could be isolated. Arsanilic acid was the only radioactive compound isolated from urine of colostomized roosters, and there was no suggestion of other metabolites from the isolation scheme employed. No attempt was made to isolate {sup 14}C compounds in feces from colostomized roosters or in excreta from normal roosters.

  2. Use of [14C]lysine to detect microbial contamination in liquid foods.

    PubMed Central

    Mafart, P; Bourgeois, C; Duteurtre, B; Moll, M

    1978-01-01

    A radiometric method for microbiological control in food industries is suggested. This method, based on the labeling of cells by [14C]lysine, was tested by using nine species of yeast and two species of bacteria. PMID:354531

  3. An update on in situ cosmogenic 14C analysis at ETH Zürich

    NASA Astrophysics Data System (ADS)

    Hippe, K.; Kober, F.; Wacker, L.; Fahrni, S. M.; Ivy-Ochs, S.; Akçar, N.; Schlüchter, C.; Wieler, R.

    2013-01-01

    We present the improved performance of the modified in situ cosmogenic 14C extraction system at ETH Zürich. Samples are now processed faster (2 days in total) and are measured with a high analytical precision of usually <2% using the gas ion source of the MICADAS AMS facility. Measurements of the PP-4 standard sample show a good reproducibility and consistency with published values. Procedural blanks are very low at currently ∼4.0 × 10414C atoms. Analyses of samples from a ∼300 year old rock avalanche prove that we can successfully apply in situ14C exposure dating to very young surfaces. Additionally, we present a modified calculation scheme for in situ14C concentrations which differs from that used for conventional radiocarbon dating. This new approach explicitly accounts for the characteristics of in situ14C production.

  4. Performance of a scanning mobility particle sizer in measuring diverse types of airborne nanoparticles: Multi-walled carbon nanotubes, welding fumes, and titanium dioxide spray.

    PubMed

    Chen, Bean T; Schwegler-Berry, Diane; Cumpston, Amy; Cumpston, Jared; Friend, Sherri; Stone, Samuel; Keane, Michael

    2016-07-01

    Direct-reading instruments have been widely used for characterizing airborne nanoparticles in inhalation toxicology and industrial hygiene studies for exposure/risk assessments. Instruments using electrical mobility sizing followed by optical counting, e.g., scanning or sequential mobility particle spectrometers (SMPS), have been considered as the "gold standard" for characterizing nanoparticles. An SMPS has the advantage of rapid response and has been widely used, but there is little information on its performance in assessing the full spectrum of nanoparticles encountered in the workplace. In this study, an SMPS was evaluated for its effectiveness in producing "monodisperse" aerosol and its adequacy in characterizing overall particle size distribution using three test aerosols, each mimicking a unique class of real-life nanoparticles: singlets of nearly spherical titanium dioxide (TiO2), agglomerates of fiber-like multi-walled carbon nanotube (MWCNT), and aggregates that constitutes welding fume (WF). These aerosols were analyzed by SMPS, cascade impactor, and by counting and sizing of discrete particles by scanning and transmission electron microscopy. The effectiveness of the SMPS to produce classified particles (fixed voltage mode) was assessed by examination of the resulting geometric standard deviation (GSD) from the impactor measurement. Results indicated that SMPS performed reasonably well for TiO2 (GSD = 1.3), but not for MWCNT and WF as evidenced by the large GSD values of 1.8 and 1.5, respectively. For overall characterization, results from SMPS (scanning voltage mode) exhibited particle-dependent discrepancies in the size distribution and total number concentration compared to those from microscopic analysis. Further investigation showed that use of a single-stage impactor at the SMPS inlet could distort the size distribution and underestimate the concentration as shown by the SMPS, whereas the presence of vapor molecules or atom clusters in some test

  5. Performance of a Scanning Mobility Particle Sizer in Measuring Diverse Types of Airborne Nanoparticles: Multi-Walled Carbon Nanotubes, Welding Fumes, and Titanium Dioxide Spray

    PubMed Central

    Chen, Bean T.; Schwegler-Berry, Diane; Cumpston, Amy; Cumpston, Jared; Friend, Sherri; Stone, Samuel; Keane, Michael

    2016-01-01

    Direct-reading instruments have been widely used for characterizing airborne nanoparticles in inhalation toxicology and industrial hygiene studies for exposure/risk assessments. Instruments using electrical mobility sizing followed by optical counting, e.g., scanning or sequential mobility particle spectrometers (SMPS), have been considered as the “gold standard” for characterizing nanoparticles. An SMPS has the advantage of rapid response and has been widely used, but there is little information on its performance in assessing the full spectrum of nanoparticles encountered in the workplace. In this study, an SMPS was evaluated for its effectiveness in producing “monodisperse” aerosol and its adequacy in characterizing overall particle size distribution using three test aerosols, each mimicking a unique class of real-life nanoparticles: singlets of nearly spherical titanium dioxide (TiO2), agglomerates of fiber-like multi-walled carbon nanotube (MWCNT), and aggregates that constitutes welding fume (WF). These aerosols were analyzed by SMPS, cascade impactor, and by counting and sizing of discrete particles by scanning and transmission electron microscopy. The effectiveness of the SMPS to produce classified particles (fixed voltage mode) was assessed by examination of the resulting geometric standard deviation (GSD) from the impactor measurement. Results indicated that SMPS performed reasonably well for TiO2 (GSD = 1.3), but not for MWCNT and WF as evidenced by the large GSD values of 1.8 and 1.5, respectively. For overall characterization, results from SMPS (scanning voltage mode) exhibited particle-dependent discrepancies in the size distribution and total number concentration compared to those from microscopic analysis. Further investigation showed that use of a single-stage impactor at the SMPS inlet could distort the size distribution and underestimate the concentration as shown by the SMPS, whereas the presence of vapor molecules or atom clusters in

  6. Wine ethanol 14C as a tracer for fossil fuel CO2 emissions in Europe: Measurements and model comparison

    NASA Astrophysics Data System (ADS)

    Palstra, Sanne W. L.; Karstens, Ute; Streurman, Harm-Jan; Meijer, Harro A. J.

    2008-11-01

    14C (radiocarbon) in atmospheric CO2 is the most direct tracer for the presence of fossil-fuel-derived CO2 (CO2-ff). We demonstrate the 14C measurement of wine ethanol as a way to determine the relative regional atmospheric CO2-ff concentration compared to a background site ("regional CO2-ff excess") for specific harvest years. The carbon in wine ethanol is directly back traceable to the atmospheric CO2 that the plants assimilate. An important advantage of using wine is that the atmosphere can be monitored annually back in time. We have analyzed a total of 165 wines, mainly from harvest years 1990-1993 and 2003-2004, among which is a semicontinuous series (1973-2004) of wines from one vineyard in southwest Germany. The results show clear spatial and temporal variations in the regional CO2-ff excess values. We have compared our measured regional CO2-ff excess values of 2003 and 2004 with those simulated by the REgional MOdel (REMO). The model results show a bias of almost +3 parts per million (ppm) CO2-ff compared with those of the observations. The modeled differences between 2003 and 2004, however, which can be used as a measure for the variability in atmospheric mixing and transport processes, show good agreement with those of the observations all over Europe. Correcting for interannual variations using modeled data produces a regional CO2-ff excess signal that is potentially useful for the verification of trends in regional fossil fuel consumption. In this fashion, analyzing 14C from wine ethanol offers the possibility to observe fossil fuel emissions back in time on many places in Europe and elsewhere.

  7. Metabolism of L-(guanidinooxy-/sup 14/C)canavanine in the rat

    SciTech Connect

    Thomas, D.A.; Rosenthal, G.A.

    1987-12-01

    The metabolism of L-canavanine, a nonprotein amino acid with significant antitumor effects, was investigated. L-Canavanine, provided at 2.0 g/kg, was supplemented with 5 microCi of L-(guanidinooxy-/sup 14/C)canavanine (58 microCi/mumol) and administered iv, sc, or orally to female Sprague-Dawley rats weighing approximately 200 g. /sup 14/C recovery in the urine at 24 hr was 83, 68, or 61%, respectively, of the administered dose. Another 5-8% of the /sup 14/C was expired as /sup 14/CO/sub 2/. The gastrointestinal tract contained 21% of orally administered /sup 14/C. Serum, feces, tissues, and de novo synthesized proteins only accounted for a few percent of the original dose by any administrative route. Analysis of the /sup 14/C-containing urinary metabolites revealed that (/sup 14/C) urea accounted for 88% of the urinary radioactivity for an iv injection, 75% for sc administration, and 50% following an oral dose. By all routes of administration, (/sup 14/C)guanidine represented 5% of the radioactivity in the urine and (/sup 14/C)guanidinoacetic acid accounted for 2%. Serum and urine amino acid analysis showed a markedly elevated ornithine level. Basic amino acids such as histidine, lysine, and arginine were also higher in the urine. Plasma ammonia levels were determined following oral canavanine doses of 1.0, 2.0, and 4.0 g/kg. A rapid but transient elevation in plasma ammonia was observed only at the 4.0 g/kg dose. This indicates that elevated plasma ammonia is not a likely cause of canavanine toxicity at the drug concentrations used in this study.

  8. Fate of (14)C-organic pollutant residues in composted sludge after application to soil.

    PubMed

    Haudin, Claire-Sophie; Zhang, Yuhai; Dumény, Valérie; Lashermes, Gwenaëlle; Bergheaud, Valérie; Barriuso, Enrique; Houot, Sabine

    2013-08-01

    Organic micropollutants may be present in biosolids, leading to soil contamination when they are recycled in agriculture. A sludge spiked with (14)C-labelled glyphosate (GLY), sodium linear dodecylbenzene sulphonate (LAS), fluoranthene (FLT) or 4-n-nonylphenol (NP) was composted with green waste and the fate of the (14)C-micropollutant residues remaining after composting was assessed after the compost application to the soil. (14)C-residues were mineralised in the soil and represented after 140d 20-32% of the initial activity for LAS, 16-25% for GLY, 6-9% for FLT and 4-7% for NP. The (14)C-residues at the end of composting that could not be extracted with methanol or ammonia were minimally remobilised or even increased for FLT. After 140d, non-extractable residues represented 38-52% of all of the (14)C-residues remaining in the soil for FLT, 50-67% for GLY, 91-92% for NP and 94-97% for LAS and in most cases, less than 1% of the (14)C-residues were water soluble, suggesting a low direct availability for leaching and microbial or plant assimilation. FLT was identified as the main compound among the methanol-extractable (14)C-residues that may be potentially available. The fate of the (14)C-organic pollutant residues in composts after application to soil could be assessed through a sequential chemical extraction scheme and depended on the chemical nature of the pollutant. PMID:23545187

  9. 17 CFR 240.14c-2 - Distribution of information statement.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... Regulation S-K (17 CFR 229.901(c)) and is registered (or authorized to be registered) on Form S-4 (17 CFR 229.25) or Form F-4 (17 CFR 229.34), the information statement must be distributed to security holders no... statement. 240.14c-2 Section 240.14c-2 Commodity and Securities Exchanges SECURITIES AND EXCHANGE...

  10. ( sup 14 C)urea breath test for diagnosis of Helicobacter pylori

    SciTech Connect

    Ormand, J.E.; Talley, N.J.; Carpenter, H.A.; Shorter, R.G.; Conley, C.R.; Wilson, W.R.; DiMagno, E.P.; Zinsmeister, A.R.; Phillips, S.F. )

    1990-07-01

    H. pylori is a potent urease producer, a characteristic that has been exploited in the development of the (14C)- and (13C)urea breath tests. The prevalence of H. pylori infection also is known to increase with advancing age; however, the individual patient's age has not routinely been considered when interpreting urea breath test results. The aim of this study was to validate a short, age-adjusted (14C)urea breath test for use in diagnosing H. pylori infections. Forty-one subjects (28 volunteers, 13 patients) underwent esophagogastroduodenoscopy with biopsies. Subjects were defined as being H. pylori-positive if histology or culture was positive. In addition, all subjects completed a 120-min (14C)urea breath test. A logistic regression analysis adjusting for age was used to estimate the probability of H. pylori positivity as a function of the 14C values generated. Sixteen subjects were H. pylori-positive, and 25 were H. pylori-negative. The 14C values generated between 15 and 80 min were found to be equally predictive in identifying H. pylori-positive subjects. Advancing age was associated with a higher probability of H. p