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Sample records for 14c 55fe 63ni

  1. Assessing deposition levels of 55Fe, 60Co and 63Ni in the Ignalina NPP environment.

    PubMed

    Gudelis, A; Druteikiene, R; Luksiene, B; Gvozdaite, R; Nielsen, S P; Hou, X; Mazeika, J; Petrosius, R

    2010-06-01

    Two RBMK-1500 reactor units operated in Lithuania in the 1987-2004 period (one of them was stopped for decommissioning in 2004). This study presents a preliminary investigation of surface deposition density levels of (55)Fe and (63)Ni in moss samples collected in the close vicinity of the Ignalina NPP. Non-destructive analysis by the HPGe gamma-spectrometry was followed by radiochemical separation. Radiochemical analysis was based on anion-exchange and extraction chromatography. (55)Fe and (63)Ni activities were measured by liquid scintillation counting (LSC). The results indicate that the deposition values of (55)Fe are generally higher than those of (60)Co and (63)Ni. PMID:18818005

  2. A compendium on the NIST radionuclide assays of the massic activity of {sup 63}Ni and {sup 55}Fe solutions used for an international intercomparison of liquid scintillation spectrometry techniques

    SciTech Connect

    Colle, R.; Zimmerman, B.E.

    1997-09-01

    The National Institute of Standards and Technology recently participated in an international measurement intercomparison for {sup 63}Ni and {sup 55}Fe, which was conducted among principal national radionuclidic metrology laboratories. The intercomparison was sponsored by EUROMET, and was primarily intended to evaluate the capabilities of liquid scintillation (LS) spectrometry techniques for standardizing nuclides that decay by low-energy {beta}-emission (like {sup 63}Ni) and by low-Z (atomic number) electron capture (like {sup 55}Fe). The intercomparison findings exhibit a very good agreement for {sup 63}Ni among the various participating laboratories, including that for NIST, which suggests that the presently invoked LS methodologies are very capable of providing internationally-compatible standardizations for low-energy {beta}-emitters. The results for {sup 55}Fe are in considerably poorer agreement, and demonstrated the existence of several unresolved problems. It has thus become apparent that there is a need for the various international laboratories to conduct rigorous, systematic evaluations of their LS capabilities in assaying radionuclides that decay by low-Z electron capture.

  3. Searches for massive neutrino emission in {sup 14}C beta and {sup 55}Fe electron-capture decays

    SciTech Connect

    Wietfeldt, F.E. |

    1994-05-01

    In 1985 Simpson reported evidence for the emission of a 17 keV mass neutrino in a small fraction of tritium beta decays. An experimental controversy ensued in which a number of both positive and negative results were reported. The beta spectrum of {sup 14}C was collected in a unique {sup 14}C-doped planar germanium detector and a distortion was observed that initially confirmed Simpson`s result. Further tests linked this distortion to a splitting of the collected charge between the central detector and the surrounding guard ring in a fraction of the events. A second {sup 14}C measurement showed no evidence for emission of a 17 keV mass neutrino. In a related experiment, a high statistics electron-capture internal-bremsstrahlung photon spectrum of {sup 55}Fe was collected with a coaxial germanium detector. A local search for departures from a smooth shape near the endpoint was performed, using a second-derivative technique. An upper limit of 0.65% (95% C.L.) for the mixing Of a neutrino in the mass range 5--25 keV was established. The upper limit on the mixing of a 17 keV mass neutrino was 0.14% (95% C.L.).

  4. Radioanalytical studies of fallout 63Ni.

    PubMed

    Holm, E; Roos, P; Skwarzec, B

    1992-01-01

    Fallout of Nickel-63 (T1/2 = 100 a) produced in small amounts at nuclear weapon tests following the neutron activation of weapon construction material was investigated by studying carpets of lichen collected during 1961 to 1988 at the Lake Rogen district in central Sweden (62.3 degrees N, 12.4 degrees E). The maximal level of 63Ni in the lichen carpet, which occurred in 1964, was about 0.6 Bq kg-1, dry weight, and decreased to 0.1 Bq kg-1 in 1988. The deposition pattern for 63Ni was similar to other fallout radionuclides such as 137Cs, 90Sr and 239 + 240Pu. The concentrations of stable Ni were relatively constant at 0.5 to 1.0 microgram g-1 throughout the years resulting in, for example, a specific activity (63Ni/stable Ni) of 0.5 Bq mg-1 in 1964 and 0.1 Bq mg-1 in 1988. The total area content of 63Ni was estimated to be 1.0 Bq m-2 and the activity ratio 63Ni/60Co was estimated to be 0.03 in 1966. The Chernobyl accident in April 1986 did not significantly increase the levels of 63Ni. For the measurement of these extremely low-levels of 63Ni, 200 g of dry material (about 1 kg fresh) were ashed and leached with aqua regia after hydroxides had been precipitated with ammonia, leaving Ni in the aqueous phase. Nickel was extracted as a dimethylglyoxime complex by chloroform and back-extracted with HCl. Finally, Ni was electroplated onto copper discs from an ammonium sulfate medium at high pH. The radiochemical yield was determined by atomic absorption spectrometry of stable Ni before and after electrodeposition.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:1310303

  5. 63Ni (n ,γ ) cross sections measured with DANCE

    NASA Astrophysics Data System (ADS)

    Weigand, M.; Bredeweg, T. A.; Couture, A.; Göbel, K.; Heftrich, T.; Jandel, M.; Käppeler, F.; Lederer, C.; Kivel, N.; Korschinek, G.; Krtička, M.; O'Donnell, J. M.; Ostermöller, J.; Plag, R.; Reifarth, R.; Schumann, D.; Ullmann, J. L.; Wallner, A.

    2015-10-01

    The neutron capture cross section of the s -process branch nucleus 63Ni affects the abundances of other nuclei in its region, especially 63Cu and 64Zn. In order to determine the energy-dependent neutron capture cross section in the astrophysical energy region, an experiment at the Los Alamos National Laboratory has been performed using the calorimetric 4 π BaF2 array DANCE. The (n ,γ ) cross section of 63Ni has been determined relative to the well-known 197Au standard with uncertainties below 15%. Various 63Ni resonances have been identified based on the Q value. Furthermore, the s -process sensitivity of the new values was analyzed with the new network calculation tool NETZ.

  6. Gallium arsenide 55Fe X-ray-photovoltaic battery

    NASA Astrophysics Data System (ADS)

    Butera, S.; Lioliou, G.; Barnett, A. M.

    2016-02-01

    The effects of temperature on the key parameters of a prototype GaAs 55Fe radioisotope X-ray microbattery were studied over the temperature range of -20 °C to 70 °C. A p-i-n GaAs structure was used to collect the photons from a 254 Bq 55Fe radioisotope X-ray source. Experimental results showed that the open circuit voltage and the short circuit current decreased with increased temperature. The maximum output power and the conversion efficiency of the device decreased at higher temperatures. For the reported microbattery, the highest maximum output power (1 pW, corresponding to 0.4 μW/Ci) was observed at -20 °C. A conversion efficiency of 9% was measured at -20 °C.

  7. Measurement of 59Ni and 63Ni by accelerator mass spectrometry at CIAE

    NASA Astrophysics Data System (ADS)

    Wang, Xiaoming; He, Ming; Ruan, Xiangdong; Xu, Yongning; Shen, Hongtao; Du, Liang; Xiao, Caijin; Dong, Kejun; Jiang, Shan; Yang, Xuran; Lan, Xiaoxi; Wu, Shaoyong; Zhao, Qingzhang; Cai, Li; Pang, Fangfang

    2015-10-01

    The long lived isotopes 59Ni and 63Ni can be used in many areas such as radioactive waste management, neutron dosimetry, cosmic radiation study, and so on. Based on the large accelerator and a big Q3D magnetic spectrometer, the measurement method for 59Ni and 63Ni is under development at the AMS facility at China Institute of Atomic Energy (CIAE). By using the ΔE-Q3D technique with the Q3D magnetic spectrometer, the isobaric interferences were greatly reduced in the measurements of 59Ni and 63Ni. A four anode gas ionization chamber was then used to further identify isobars. With these techniques, the abundance sensitivities of 59Ni and 63Ni measurements are determined as 59Ni/Ni = 1 × 10-13 and 63Ni/Ni = 2 × 10-12, respectively.

  8. Quantitative autoradiographic assessment of sup 55 Fe-RBC distribution in rat brain

    SciTech Connect

    Lin, S.Z.; Nakata, H.; Tajima, A.; Gruber, K.; Acuff, V.; Patlak, C.; Fenstermacher, J. )

    1990-11-01

    A simple in vivo technique of labeling erythrocytes (RBCs) with {sup 55}Fe was developed for quantitative autoradiography (QAR). This procedure involved injecting 5-6 ml of ({sup 55}Fe)ferrous citrate solution (1 mCi/ml) intraperitoneally into donor rats. The number of labeled RBCs reached a maximum at around 7 days and declined very slowly thereafter. Labeled RBCs were harvested from donor rats and used for RBC volume measurement in awake rats. Brain radioactivity was assayed by QAR, which yielded spatial resolution of greater than 50 microns. Tight nearly irreversible binding of {sup 55}Fe to RBCs was found in vivo and in vitro. More than 99.5% of the {sup 55}Fe in the blood of donor rats was bound to RBCs. Because of this, labeled blood can be taken from donors and injected into recipients without further preparation. The tissue absorption of {sup 55}Fe emissions was the same in gray and white matter. Microvascular RBC volumes measured with {sup 55}Fe-labeled RBCs agreed with those assayed with {sup 51}Cr-labeled RBCs for many, but not all, brain areas. In conclusion, {sup 55}Fe-RBCs can be readily prepared by this technique and accurately quantitated in brain tissue by QAR.

  9. Bioaccumulation of (63)Ni in the scleractinian coral Stylophora pistillata and isolated Symbiodinium using radiotracer techniques.

    PubMed

    Hédouin, Laetitia; Metian, Marc; Teyssié, Jean-Louis; Oberhänsli, François; Ferrier-Pagès, Christine; Warnau, Michel

    2016-08-01

    Development of nickel mining activities along the New Caledonia coasts threatens the biodiversity of coral reefs. Although the validation of tropical marine organisms as bioindicators of metal mining contamination has received much attention in the literature over the last decade, few studies have examined the potential of corals, the fundamental organisms of coral reefs, to monitor nickel (Ni) contamination in tropical marine ecosystems. In an effort to bridge this gap, the present work investigated the bioaccumulation of (63)Ni in the scleractinian coral Stylophora pistillata and in its isolated zooxanthellae Symbiodinium, using radiotracer techniques. Results highlight the high capacities of coral tissues (zooxanthellae and host tissues) to efficiently bioconcentrate (63)Ni compared to skeleton (Concentration Factors CF at 14 days of exposure are 3 orders of magnitude higher in tissues than in skeleton). When non-contaminated conditions were restored, (63)Ni was more efficiently retained in skeleton than in coral tissues, with biological half-lives (Tb½) of 44.3 and 6.5 days, respectively. In addition, our work showed that Symbiodinium bioconcentrated (63)Ni exponentially, with a vol/vol concentration factor at steady state (VCFSS) reaching 14,056. However, compilation of our results highlighted that despite efficient bioconcentration of (63)Ni in Symbiodinium, their contribution to the whole (63)Ni accumulation in coral nubbins represents less than 7%, suggesting that other biologically controlled processes occur in coral host allowing such efficient bioconcentration in coral tissues. PMID:27192479

  10. Ultra-separation of nickel from copper metal for the measurement of 63Ni by AMS

    NASA Astrophysics Data System (ADS)

    Marchetti, A. A.; Hainsworth, L. J.; McAninch, J. E.; Leivers, M. R.; Jones, P. R.; Proctor, I. D.; Straume, T.

    1997-03-01

    Measurements of 63Ni (t{1}/{2} = 100 yr) produced by the reaction 63Cu(n,p)63Ni could be used in the assessment of fast-neutron fluence from the Hiroshima atomic bomb. Such measurements would add new information to help resolve the current discrepancy between measured thermal neutron activation values and those calculated with the DS86 dosimetry system. It has been estimated that the 63Ni production at 5 m from the hypocenter was (1.4 ± 0.1) × 107 atoms/g Cu. Because of its sensitivity, accelerator mass spectrometry (AMS) is ideal for measurements at this low level. However, 63Ni has to be separated from large amounts of stable atomic isobar 63Cu (69% of pure Cu). In this study, a procedure is presented for the electrochemical separation of ultra-low amounts of Ni from Cu. The method was developed using samples of electrical Cu wire that were irradiated with fission neutrons from a 252Cf source. The wire samples were electrochemically dissolved in a solution containing 1 mg of Ni carrier. The Cu was selectively deposited on a cathode at controlled potential. Measurements of total Ni after electroseparation indicate ˜ 100% carrier recovery. To prevent Cu contamination, AMS targets were prepared by nickel carbonyl generation. The AMS results show a successful quantitative separation of ˜ 107 atoms of 63Ni from 2-20 g samples of Cu.

  11. 252Cf spectrum-averaged cross section for the 63Cu(n, p)63Ni reaction

    NASA Astrophysics Data System (ADS)

    Imamura, M.; Shibata, T.; Shibata, S.; Ohkubo, T.; Satoh, S.; Nogawa, N.

    1999-01-01

    The 63Ni produced by the 63Cu(n, p)63Ni reaction provides a unique measure to estimate the fast-neutron fluence of the Hiroshima/Nagasaki atomic bomb. In the similarity of the fission neutron spectrum of 252Cf to that of 235U, we have measured activation cross sections of the 63Cu(n, p)63Ni reaction averaged for the 252Cf fission spectrum.

  12. Al0.52In0.48P 55Fe x-ray-photovoltaic battery

    NASA Astrophysics Data System (ADS)

    Butera, S.; Lioliou, G.; Krysa, A. B.; Barnett, A. M.

    2016-09-01

    An Al0.52In0.48P 55Fe radioisotope microbattery is demonstrated over the temperature range  ‑20 °C to 160 °C. Al0.52In0.48P p+-i-n+ mesa structures were used to collect the photons from a 238 MBq 55Fe radioisotope x-ray source. The effects of temperature on the key microbattery parameters were studied. Increasing the temperature, the saturation current increased; whilst the open circuit voltage, the maximum power and the conversion efficiency decreased. An open circuit voltage of 0.97 V and a conversion efficiency of 22% were measured in a single p+-i-n+ mesa structure at  ‑20 °C. The highest total microbattery maximum output power using two mesa structures was 1.2 pW at  ‑20 °C.

  13. Low-level measurement of 63Ni by means of accelerator mass spectrometry

    NASA Astrophysics Data System (ADS)

    Rugel, G.; Arazi, A.; Carroll, K. L.; Faestermann, T.; Knie, K.; Korschinek, G.; Marchetti, A. A.; Martinelli, R. E.; McAninch, J. E.; Rühm, W.; Straume, T.; Wallner, A.; Wallner, C.

    2004-08-01

    The radionuclide 63Ni (T1/2=100.1 a) has been proposed as a fluence monitor for fast neutrons in copper samples from Hiroshima. Accelerator mass spectrometry (AMS) represents a powerful tool for the detection of this radionuclide, provided the isobaric interference of 63Cu can be sufficiently suppressed. In this paper, we report the first results from a study on the 63Cu background observed in different sets of control samples, and in a 127-year-old environmental copper sample which was directly exposed to cosmic radiation for about 80 years. The 63Ni/Ni ratios measured in the blank samples range up to about 2 × 10-13 corresponding to concentrations of a few times 10463Ni atoms/g Cu. These results provide information on the overall background of the applied methodology and, thus, on the possible sensitivity of 63Ni measurements in copper samples by means of AMS. In the environmental sample, a 63Ni concentration of (1.0 ± 0.3) × 10563Ni atoms/g Cu was observed which is not significantly different from the results obtained on commercially available copper material. A similar concentration would be expected in a copper sample located 1300 m from the hypocenter of the Hiroshima atomic bomb.

  14. Solution chemistry effects on sorption behavior of radionuclide 63Ni(II) in illite-water suspensions

    NASA Astrophysics Data System (ADS)

    Hu, Baowei; Cheng, Wen; Zhang, Hui; Yang, Shitong

    2010-11-01

    In this work, a naturally occurring illite was characterized by using FTIR and XRD to determine its chemical constituents and crystal structure. A series of batch experiments were carried out to investigate the effect of various environmental factors such as contact time, pH, ionic strength, foreign ions, coexisting humic substances and temperature on the sorption behavior of illite towards radionuclide 63Ni(II). The sorption of 63Ni(II) on illite was strongly dependent on pH and ionic strength. A positive effect of HA/FA on 63Ni(II) sorption was found at pH < 6.5, whereas a negative effect was observed at pH > 6.5. The Langmuir, Freundlich, and D-R models were used to simulate the sorption isotherms of 63Ni(II) at three different temperatures of 293, 313 and 333 K. The thermodynamic parameters (Δ H0, Δ S0 and Δ G0) of 63Ni(II) sorption on illite were calculated from the temperature dependent sorption isotherms, and the results indicated that the sorption of 63Ni(II) on illite was endothermic and spontaneous. At low pH, the sorption of 63Ni(II) was dominated by outer-sphere surface complexation and ion exchange with Na +/H + on illite surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. From the experimental results, it is possible to conclude that illite has good potentialities for cost-effective treatments of 63Ni(II)-contaminated wastewaters.

  15. 55Fe effect on enhancing ferritic steel He/dpa ratio in fission reactor irradiations to simulate fusion conditions

    SciTech Connect

    Liu, Haibo; Abdou, Mohamed A.; Greenwood, Lawrence R.

    2013-11-01

    How to increase the ferritic steel He(appm)/dpa ratio in a fission reactor neutron spectrum is an important question for fusion reactor material testing. An early experiment showed that the accelerated He(appm)/dpa ratio of about 2.3 was achieved for 96% enriched 54Fe in iron with 458.2 effective full power days (EFPD) irradiation in the High Flux Isotope Reactor (HFIR), ORNL. Greenwood suggested that the transmutation produced 55Fe has a thermal neutron helium production cross section which may have an effect on this result. In the current work, the ferritic steel He(appm)/dpa ratio is studied in the neutron spectrum of HFIR with 55Fe thermal neutron helium production taken into account. The available ENDF-b format 55Fe incident neutron cross section file from TENDL, Netherlands, is first input into the calculation model. A benchmark calculation for the same sample as used in the aforementioned experiment was used to adjust and evaluate the TENDL 55Fe (n, a) cross section values. The analysis shows a decrease of a factor of 6700 for the TENDL 55Fe (n, a) cross section in the intermediate and low energy regions is required in order to fit the experimental results. The best fit to the cross section value at thermal neutron energy is about 27 mb. With the adjusted 55Fe (n, a) cross sections, calculation show that the 54Fe and 55Fe isotopes can be enriched by the isotopic tailoring technique in a ferritic steel sample irradiated in HFIR to significantly enhance the helium production rate. The results show that a 70% enriched 54Fe and 30% enriched 55Fe ferritic steel sample would produce a He(appm)/dpa ratio of about 13 initially in the HFIR peripheral target position (PTP). After one year irradiation, the ratio decreases to about 10. This new calculation can be used to guide future isotopic tailoring experiments designed to increase the He(appm)/dpa ratio in fission reactors. A benchmark experiment is suggested to be performed to evaluate the 55Fe (n, a) cross section

  16. 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

  17. A measurement of the beta spectrum of 63Ni using a new type of cryogenic detector

    NASA Astrophysics Data System (ADS)

    Gaistkell, R. J.; Angrave, L. C.; Booth, N. E.; Hahn, A. D.; Salmon, G. L.; Swift, A. M.

    1996-02-01

    A precision measurement of the beta spectrum of 63Ni has been performed using a new type of cryogenic particle detector. This is the first nuclear physics experiment using this technique, and we discuss the principles of the method, its advantages and its shortcomings. Careful studies of detector stability, calibration, pulse pile-up and systematics have made it possible to collect large numbers of events (∼ 10 8) over long periods (∼ 28 days). The measurement is consistent with no 17 keV/c 2 neutrino admixture, giving a preferred value of (-0.05 ± 0.31)%.

  18. Application of ammonium pyrrolidinedithiocarbamate precipitation and X-ray spectrometry in the analysis of 55Fe in nuclear liquid wastes

    NASA Astrophysics Data System (ADS)

    Nečemer, M.; Kump, P.

    1999-04-01

    A new approach to radiochemical separation of 55Fe in waste waters of the Kr\\vsko Nuclear Power Plant (hereafter referred to as the NPPK) is described. The proposed sensitive, fast and simple method is based on the preconcentration of radionuclides present in the liquid sample with ammonium pyrrolidinedithiocarbamate (APDC). The precipitated carbamates were separated by filtration through a cellulose-nitrate filter and the thin deposit obtained on the filter was then measured by an X-ray spectrometer. The activity of 55Fe was determined from a calibration procedure which utilized a certified solution of this radionuclide.

  19. Measurement of {sup 63}Ni and {sup 59}Ni by accelerator mass spectrometry using characteristic projectile x-rays

    SciTech Connect

    McAninch, J.E.; Hainsworth, L.J.; Marchetti, A.A.

    1996-05-01

    The long-lived isotopes of nickel ({sup 59}Ni, {sup 63}Ni) have current and potential use in a number of applications including cosmic radiation studies, biomedical tracing, characterization of low-level radioactive wastes, and neutron dosimetry. Methods are being developed at LLNL for the routine detection of these isotopes by AMS. One intended application is in Hiroshima dosimetry. The reaction {sup 63}Cu(n,p){sup 63}Ni has been identified as one of a small number of reactions which might be used for the direct determination of the fast neutron fluence emitted by the Hiroshima bomb. AMS measurement of {sup 63}Ni(t{sub 1/2} = 100 y) requires the chemical removal of {sup 63}Cu, which is a stable isobar of {sup 63}Ni. Following the electrochemical separation of Ni from gram-sized copper samples, the Cu concentration is further lowered to < 2 x 10{sup -8} (Cu/Ni) using the reaction of Ni with carbon monoxide to form the gas Ni(CO){sub 4}. The Ni(CO){sub 4} is thermally decomposed directly in sample holders for measurement by AMS. After analysis in the AMS spectrometer, the ions are identified using characteristic projectile x-rays, allowing further rejection of remaining {sup 63}Cu. In a demonstration experiment, {sup 63}Ni was measured in Cu wires (2-20 g) which had been exposed to neutrons from a {sup 252}Cf source. We successfully measured {sup 63}Ni at levels necessary for the measurement of Cu samples exposed near the Hiroshima hypocenter. For the demonstration samples, the Cu content was chemically reduced by a factor of 10{sup 12} with quantitative retention of {sup 63}Ni. Detection sensitivity (3{sigma}) was {approximately}20 fg {sup 63}Ni in 1 mg Ni carrier ({sup 63}Ni/Ni {approx} 2 x 10{sup -11}). Significant improvements in sensitivity are expected with planned incremental changes in the methods. Preliminary results indicate that a similar sensitivity is achievable for {sup 59}Ni (t{sub 1/2} = 10{sup 5} y).

  20. Measurement of 63Ni and 59Ni by accelerator mass spectrometry using characteristic projectile X-rays

    NASA Astrophysics Data System (ADS)

    McAninch, J. E.; Hainsworth, L. J.; Marchetti, A. A.; Leivers, M. R.; Jones, P. R.; Dunlop, A. E.; Mauthe, R.; Vogel, J. S.; Proctor, I. D.; Straume, T.

    1997-03-01

    The long-lived isotopes of nickel (59Ni, 63Ni) have current and potential use in a number of applications including cosmic radiation studies, biomedical tracing, characterization of low-level radioactive wastes, and neutron dosimetry. Methods are being developed at LLNL for the routine detection of these isotopes by AMS. One intended application is in Hiroshima dosimetry. The reaction 63Cu(n,p)63Ni has been identified as one of a small number of reactions which might be used for the direct determination of the fast neutron fluence emitted by the Hiroshima bomb. AMS measurement of 63Ni (t{1}/{2} = 100 y) requires the chemical removal of 63Cu, which is a stable isobar of 63Ni. Following the electrochemical separation of Ni from gram-sized copper samples, the Cu concentration is further lowered to < 2 × 10-8 ({Cu}/{Ni}) using the reaction of Ni with carbon monoxide to form the gas Ni(CO)4. The Ni(CO)4 is thermally decomposed directly in sample holders for measurement by AMS. After analysis in the AMS spectrometer, the ions are identified using characteristic projectile X-rays, allowing further rejection of remaining 63Cu. In a demonstration experiment, 63Ni was measured in Cu wires (2-20 g) which had been exposed to neutrons from a 252Cf source. We successfully measured 63Ni at levels necessary for the measurement of Cu samples exposed near the Hiroshima hypocenter. For the demonstration samples, the Cu content was chemically reduced by a factor of 1012 with quantitative retention of 63Ni. Detection sensitivity (3σ) was ˜ 20 fg 63Ni in 1 mg Ni carrier ({63Ni}/{Ni} ≈ 2 × 10-11). Significant improvements in sensitivity are expected with planned incremental changes in the methods. Preliminary results indicate that a similar sensitivity is achievable for 59Ni (t{1}/{2} = 105 y). Initial work has been undertaken on the application of this isotope as a biomedical tracer in living systems.

  1. Neutron-induced 63Ni activity and microscopic observation of copper samples exposed to the Hiroshima atomic bomb

    NASA Astrophysics Data System (ADS)

    Shizuma, Kiyoshi; Endo, Satoru; Shinozaki, Kenji; Fukushima, Hiroshi

    2013-05-01

    Fast neutron activation data for 63Ni in copper samples exposed to the Hiroshima atomic bomb are important in evaluating neutron doses to the survivors. Up to until now, accelerator mass spectrometry and liquid scintillation counting methods have been applied in 63Ni measurements and data were accumulated within 1500 m from the hypocenter. The slope of the activation curve versus distance shows reasonable agreement with the calculation result, however, data near the hypocenter are scarce. In the present work, two copper samples obtained from the Atomic bomb dome (155 m from the hypocenter) and the Bank of Japan building (392 m) were utilized in 63Ni beta-ray measurement with a Si surface barrier detector. Additionally, microscopic observation of the metal surfaces was performed for the first time. Only upper limit of 63Ni production was obtained for copper sample of the Atomic bomb dome. The result of the 63Ni measurement for Bank of Japan building show reasonable agreement with the AMS measurement and to fast neutron activation calculations based on the Dosimetry System 2002 (DS02) neutrons.

  2. Identification of 63Ni and 60Co produced in a steel sample by thermal neutrons from the Hiroshima atomic bomb

    NASA Astrophysics Data System (ADS)

    Shizuma, K.; Iwatani, K.; Hasai, H.; Oka, T.; Hoshi, M.; Shibata, S.; Imamura, M.; Shibata, T.

    1997-02-01

    Long-lived residual radioactivity 63Ni produced by the (n, γ) reaction was detected for the first time from a steel plate sampled at near the hypocenter of the Hiroshima atomic bomb. Nickel and cobalt were chemically separated and enriched from the steel sample. Low energy beta rays of 63Ni were measured with a low-background liquid scintillation counter and gamma-rays of 60Co were measured with a low background Ge detector. Specific activities were determined as 0.0063±0.0004 Bq mg -1 for {63Ni}/{Ni} and 8.70±0.46 Bq mg -1 for {60Co}/{Co} at the time of the bomb explosion. Comparisons with the calculated yield based on the current dosimetry system DS86 neutrons were also given.

  3. Accelerator mass spectrometry of 63Ni using a gas-filled magnet at the Munich Tandem Laboratory

    NASA Astrophysics Data System (ADS)

    Rugel, G.; Faestermann, T.; Knie, K.; Korschinek, G.; Marchetti, A. A.; McAninch, J. E.; Rühm, W.; Straume, T.; Wallner, C.

    2000-10-01

    The detection of 63Ni ( T1/2=100.1 yr) by means of accelerator mass spectrometry (AMS) using a gas-filled magnet (GFM) is described. The experimental setup includes a dedicated ion source, a 14 MV MP tandem, a GFM and a multi-anode ionization chamber. First results indicate a background level of 63Ni/Ni ratios as low as 2×10 -14. This sensitivity will allow - for the first time ever - to detect 63Ni induced by fast neutrons in copper samples from Hiroshima and Nagasaki, even for distances beyond 1500 m from the hypocenters. Thus, it will be possible to reconstruct experimentally the neutron doses of the A-bomb survivors from Hiroshima and Nagasaki.

  4. Measuring the X-ray quantum efficiency of a hybrid CMOS detector with 55Fe

    NASA Astrophysics Data System (ADS)

    Bongiorno, S. D.; Falcone, A. D.; Prieskorn, Z.; Griffith, C.; Burrows, D. N.

    2015-06-01

    Charge coupled devices (CCDs) are currently the workhorse focal plane arrays operating aboard many orbiting astrophysics X-ray telescopes, e.g. Chandra, XMM-Newton, Swift, and Suzaku. In order to meet the count rate, power, and mission duration requirements defined by next-generation X-ray telescopes, future detectors will need to be read out faster, consume less power, and be more resistant to radiation and micrometeoroid damage than current-generation devices. The hybrid CMOS detector (HCD), a type of active pixel sensor, is currently being developed to meet these requirements. With a design architecture that involves bump bonding two semiconductor substrates together at the pixel level, these devices exhibit both the high read speed and low power consumption of CMOS readout circuitry and the high quantum efficiency (QE) of a deeply depleted silicon absorber. These devices are expected to exhibit the same excellent, high-energy quantum efficiency (QE) as deep-depletion CCDs (QE > 0.9 at 6 keV), while at the same time exhibiting superior readout flexibility, power consumption, and radiation hardness than CCDs. In this work we present a QE model for a Teledyne Imaging Sensors HyViSI HCD, which predicts QE=96% at 55Fe source energies (5.89 and 6.49 keV). We then present a QE measurement of the modeled device at the same energies, which shows QE=97±5% and is in good agreement with the model.

  5. Tracer diffusion of /sup 60/Co and /sup 63/Ni in amorphous NiZr alloy

    SciTech Connect

    Hoshino, K.; Averback, R.S.; Hahn, H.; Rothman, S.J.

    1987-01-01

    Tracer diffusion of /sup 60/Co and /sup 63/Ni in equiatomic amorphous NiZr alloy in the temperature range between 486 and 641/sup 0/K can be described by: D/sub Co/sup */ = 3.7 x 10/sup -7/ exp(-(135 +- 14) kJ mole/sup -1//RT) m/sup 2//sec and D/sub Ni//sup */ = 1.7 x 10/sup -7/ exp(-(140 +- 9) kJ mole/sup -1//RT) m/sup 2//sec. The values of D/sub Ni//sup */ are in reasonable agreement with those measured by the Rutherford backscattering technique. The measured diffusivities were independent of time, indicating that no relaxation took place during diffusion. 27 refs., 2 tabs.

  6. Neutron capture cross section of unstable 63Ni: implications for stellar nucleosynthesis.

    PubMed

    Lederer, C; Massimi, C; Altstadt, S; Andrzejewski, J; Audouin, L; Barbagallo, M; Bécares, V; Bečvář, F; Belloni, F; Berthoumieux, E; Billowes, J; Boccone, V; Bosnar, D; Brugger, M; Calviani, M; Calviño, F; Cano-Ott, D; Carrapiço, C; Cerutti, F; Chiaveri, E; Chin, M; Colonna, N; Cortés, G; Cortés-Giraldo, M A; Diakaki, M; Domingo-Pardo, C; Duran, I; Dressler, R; Dzysiuk, N; Eleftheriadis, C; Ferrari, A; Fraval, K; Ganesan, S; García, A R; Giubrone, G; Gómez-Hornillos, M B; Gonçalves, I F; González-Romero, E; Griesmayer, E; Guerrero, C; Gunsing, F; Gurusamy, P; Jenkins, D G; Jericha, E; Kadi, Y; Käppeler, F; Karadimos, D; Kivel, N; Koehler, P; Kokkoris, M; Korschinek, G; Krtička, M; Kroll, J; Langer, C; Leeb, H; Leong, L S; Losito, R; Manousos, A; Marganiec, J; Martínez, T; Mastinu, P F; Mastromarco, M; Meaze, M; Mendoza, E; Mengoni, A; Milazzo, P M; Mingrone, F; Mirea, M; Mondelaers, W; Paradela, C; Pavlik, A; Perkowski, J; Pignatari, M; Plompen, A; Praena, J; Quesada, J M; Rauscher, T; Reifarth, R; Riego, A; Roman, F; Rubbia, C; Sarmento, R; Schillebeeckx, P; Schmidt, S; Schumann, D; Tagliente, G; Tain, J L; Tarrío, D; Tassan-Got, L; Tsinganis, A; Valenta, S; Vannini, G; Variale, V; Vaz, P; Ventura, A; Versaci, R; Vermeulen, M J; Vlachoudis, V; Vlastou, R; Wallner, A; Ware, T; Weigand, M; Weiß, C; Wright, T J; Zugec, P

    2013-01-11

    The 63Ni(n,γ) cross section has been measured for the first time at the neutron time-of-flight facility n_TOF at CERN from thermal neutron energies up to 200 keV. In total, capture kernels of 12 (new) resonances were determined. Maxwellian averaged cross sections were calculated for thermal energies from   kT=5-100  keV with uncertainties around 20%. Stellar model calculations for a 25M⊙ star show that the new data have a significant effect on the s-process production of 63Cu, 64Ni, and 64Zn in massive stars, allowing stronger constraints on the Cu yields from explosive nucleosynthesis in the subsequent supernova. PMID:23383895

  7. Sorption properties of new composite materials suitable for radioanalytical determination of 59Ni and 63Ni

    NASA Astrophysics Data System (ADS)

    Fišera, O.; Šebesta, F.

    2006-01-01

    Results of the study of new and cheaper composite materials for selective separation and radioanalytical determination of radionickel (59,63Ni) in radioactive waste are presented in this work. Chelating agents dimethylglyoxime (DMG) and diphenylglyoxime (DPG) as active components were immobilized in porous matrix of binding polymer polyacrylonitrile (PAN). Sorption properties of these materials were compared with commercial Ni Resin (Eichrom Technologies, USA). Weight distribution ratios, sorption kinetics and operating capacities were investigated during the experiments performed. The highest weight distribution ratios were found for the material DPG-PAN. The sorbent DMG-PAN has the highest operating capacity. The fastest kinetics of nickel sorption was determined for the Ni Resin. Elution of nickel with nitric acid solution allows subsequent and direct determination of radionickel by liquid scintillation counting.

  8. Application of TDCR-Geant4 modeling to standardization of 63Ni.

    PubMed

    Thiam, C; Bobin, C; Chauvenet, B; Bouchard, J

    2012-09-01

    As an alternative to the classical TDCR model applied to liquid scintillation (LS) counting, a stochastic approach based on the Geant4 toolkit is presented for the simulation of light emission inside the dedicated three-photomultiplier detection system. To this end, the Geant4 modeling includes a comprehensive description of optical properties associated with each material constituting the optical chamber. The objective is to simulate the propagation of optical photons from their creation in the LS cocktail to the production of photoelectrons in the photomultipliers. First validated for the case of radionuclide standardization based on Cerenkov emission, the scintillation process has been added to a TDCR-Geant4 modeling using the Birks expression in order to account for the light-emission nonlinearity owing to ionization quenching. The scintillation yield of the commercial Ultima Gold LS cocktail has been determined from double-coincidence detection efficiencies obtained for (60)Co and (54)Mn with the 4π(LS)β-γ coincidence method. In this paper, the stochastic TDCR modeling is applied for the case of the standardization of (63)Ni (pure β(-)-emitter; E(max)=66.98 keV) and the activity concentration is compared with the result given by the classical model. PMID:22436447

  9. Determination of 63Ni and 59Ni in spent ion-exchange resin and activated charcoal from the IEA-R1 nuclear research reactor.

    PubMed

    Taddei, M H T; Macacini, J F; Vicente, R; Marumo, J T; Sakata, S K; Terremoto, L A A

    2013-07-01

    A radiochemical method has been adapted to determine (59)Ni and (63)Ni in samples of radioactive wastes from the water cleanup system of the IEA-R1 nuclear research reactor. The process includes extraction chromatographic resin with dimethylglyoxime (DMG) as a functional group. Activity concentrations of (59)Ni and (63)Ni were measured, respectively, by X-ray spectrometry and liquid scintillation counting, whereas the chemical yield was determined by ICP-OES. The average ratio of measured activity concentrations of (63)Ni and (59)Ni agree well with theory. PMID:23524230

  10. Temperature effect on betavoltaic microbatteries based on Si and GaAs under 63Ni and 147Pm irradiation

    NASA Astrophysics Data System (ADS)

    Wang, Hao; Tang, Xiao-bin; Liu, Yun-Peng; Xu, Zhi-Heng; Liu, Min; Chen, Da

    2015-09-01

    The effect of temperature on the output performance of four different types of betavoltaic microbatteries was investigated experimental and theoretical. Si and GaAs were selected as the energy conversion devices in four types of betavoltaic microbatteries, and 63Ni and 147Pm were used as beta sources. Current density-voltage curves were determined at a temperature range of 213.15-333.15 K. A simplified method was used to calculate the theoretical parameters of the betavoltaic microbatteries considering the energy loss of beta particles for self-absorption of radioactive source, the electron backscatter effect of different types of semiconductor materials, and the absorption of dead layer. Both the experimental and theoretical results show that the short-circuit current density increases slightly and the open-circuit voltage (VOC) decreases evidently with the increase in temperature. Different combinations of energy conversion devices and beta sources cause different effects of temperature on the microbatteries. In the approximately linear range, the VOC sensitivities caused by temperature for 63Ni-Si, 63Ni-GaAs, 147Pm-Si, and 147Pm-GaAs betavoltaic microbatteries were -2.57, -5.30, -2.53, and -4.90 mV/K respectively. Both theoretical and experimental energy conversion efficiency decreased evidently with the increase in temperature.

  11. A method to detect low-level 63Ni activity for estimating fast neutron fluence from the Hiroshima atomic bomb.

    PubMed

    Ito, Y; Shibata, T; Imamura, M; Shibata, S; Nogawa, N; Uwamino, Y; Shizuma, K

    1999-06-01

    The Hiroshima and Nagasaki atomic bombs resulted in the worst reported exposure of radiation to the human body. The data of survivors have provided the basis for the risk estimation for ionizing radiation, and thus are widely used as the basis of radiation safety. In this report we have studied a new method to detect the low-level 63Ni activity in copper samples in order to estimate the fast neutron fluence from the Hiroshima atomic bomb. Only 0.8 x 10(-3) Bq g(-1) of 63Ni is expected to be produced by the atomic bomb in a copper sample with the 63Cu(n, p)63Ni reaction at a distance of 500 m from the hypocenter. Our method has the required level of sensitivity for determination of the fast neutron fluence out to distances of at least 500 m, and perhaps as far as 1,000 m. We have already investigated and collected some bomb-irradiated copper samples for further study. PMID:10334579

  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. Facile synthesis of (55)Fe-labeled well-dispersible hematite nanoparticles for bioaccumulation studies in nanotoxicology.

    PubMed

    Huang, Bin; Xiao, Lin; Yang, Liu-Yan; Ji, Rong; Miao, Ai-Jun

    2016-06-01

    Although water-dispersible engineered nanoparticles (ENPs) have a wide range of applications, the ENPs used in many nanotoxicological studies tend to form micron-sized aggregates in the exposure media and thus cannot reflect the toxicity of real nanoparticles. Here we described the synthesis of bare hematite nanoparticles (HNPs-0) and two poly(acrylic acid) (PAA)-coated forms (HNPs-1 and HNPs-2). All three HNPs were well dispersed in deionized water, but HNPs-0 quickly aggregated in the three culture media tested. By contrast, the suspensions of HNPs-1 and HNPs-2 remained stable, with negligible amounts of PAA and Fe(3+) liberated from either one under the investigated conditions. To better quantify the accumulation of the coated HNPs, a relatively innocuous (55)Fe-labeled form of HNPs-2 was synthesized as an example and its accumulation in three phytoplankton species was tested. Consistent with the uptake kinetics model for conventional pollutants, the cellular accumulation of HNPs-2 increased linearly with exposure time for two of the three phytoplankton species. These results demonstrate the utility of (55)Fe-labeled well-dispersible HNPs as a model material for nanoparticle bioaccumulation studies in nanotoxicology. PMID:27038212

  14. Measurement of 55Fe(n ,p ) cross sections by the surrogate-reaction method for fusion technology applications

    NASA Astrophysics Data System (ADS)

    Pandey, Bhawna; Desai, V. V.; Suryanarayana, S. V.; Nayak, B. K.; Saxena, A.; Mirgule, E. T.; Santra, S.; Mahata, K.; Makawana, R.; Abhangi, M.; Basu, T. K.; Rao, C. V. S.; Jakhar, S.; Vala, S.; Sarkar, B.; Agrawal, H. M.; Kaur, G.; Prajapati, P. M.; Pal, Asim; Sarkar, D.; Kundu, A.

    2016-02-01

    We have measured the proton decay probabilities of the *56Fe and *47Ti compound systems which are populated by the transfer reactions 52Cr(6Li,d ) *56Fe (surrogate of n +55Fe→*56Fe→p +55Mn ) and 45Sc(6Li,α ) *47Ti (surrogate of n +46Ti→47Ti*→p +46Sc ) reactions, respectively. The 55Fe(n ,p ) cross sections were then obtained in the equivalent neutron energy range of 7.9 to 20.1 MeV within the framework of the surrogate-reaction method. The measured results were compared with predictions of the empire-3.2.3 statistical model code and various recent evaluated data libraries. The experimental cross-section data on 55Fe(n ,p ) are in reasonable agreement with EAF-2010, while the TENDL-2014 and ROSFOND-2010 data show some discrepancies. This study demonstrates the possibility of determining neutron-induced charged particle emission cross sections for unstable radionuclides relevant to fusion technology applications by the surrogate-reaction method.

  15. 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

  16. 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

  17. 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

  18. Accelerator mass spectrometry of 63Ni at the Munich Tandem Laboratory for estimating fast neutron fluences from the Hiroshima atomic bomb.

    PubMed

    Rühm, W; Knie, K; Rugel, G; Marchetti, A A; Faestermann, T; Wallner, C; McAninch, J E; Straume, T; Korschinek, G

    2000-10-01

    After the release of the present dosimetry system DS86 in 1987, measurements have shown that DS86 may substantially underestimate thermal neutron fluences at large distances (>1,000 m) from the hypocenter in Hiroshima. This discrepancy casts doubts on the DS86 neutron source term and, consequently, the survivors' estimated neutron doses. However, the doses were caused mainly by fast neutrons. To determine retrospectively fast neutron fluences in Hiroshima, the reaction 63Cu(n, p)63Ni can be used, if adequate copper samples can be found. Measuring 63Ni (half life 100 y) in Hiroshima samples requires a very sensitive technique, such as accelerator mass spectrometry (AMS), because of the relatively small amounts of 63Ni expected (approximately 10(5)-10(6) atoms per gram of copper). Experiments performed at Lawrence Livermore National Laboratory have demonstrated in 1996 that AMS can be used to measure 63Ni in Hiroshima copper samples. Subsequently, a collaboration was established with the Technical University of Munich in view of its potential to perform more sensitive measurements of 63Ni than the Livermore facility and in the interest of interlaboratory validation. This paper presents the progress made at the Munich facility in the measurement of 63Ni by AMS. The Munich accelerator mass spectrometry facility is a combination of a high energy tandem accelerator and a detection system featuring a gas-filled magnet. It is designed for high sensitivity measurements of long-lived radioisotopes. Optimization of the ion source setup has further improved the sensitivity for 63Ni by reducing the background level of the 63Cu isobar interference by about two orders of magnitude. Current background levels correspond to a ratio of 63Ni/Ni<2x10(-14) and suggest that, with adequate copper samples, the assessment of fast neutron fluences in Hiroshima and Nagasaki is possible for ground distances of up to 1500 m, and--under favorable conditions--even beyond. To demonstrate this

  19. 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

  20. 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) §...

  1. 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) §...

  2. 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) §...

  3. 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) §...

  4. 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) §...

  5. 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) §...

  6. 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) §...

  7. 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) §...

  8. 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) §...

  9. Neutron-induced 63Ni in copper samples from Hiroshima and Nagasaki: a comprehensive presentation of results obtained at the Munich Maier-Leibnitz Laboratory.

    PubMed

    Rühm, W; Carroll, K L; Egbert, S D; Faestermann, T; Knie, K; Korschinek, G; Martinelli, R E; Marchetti, A A; McAninch, J E; Rugel, G; Straume, T; Wallner, A; Wallner, C; Fujita, S; Hasai, H; Hoshi, M; Shizuma, K

    2007-11-01

    Those inhabitants of Hiroshima and Nagasaki who were affected by the A-bomb explosions, were exposed to a mixed neutron and gamma radiation field. Few years later about 120,000 survivors of both cities were selected, and since then radiation-induced late effects such as leukemia and solid tumors are being investigated in this cohort. When the present study was initiated, the fast neutron fluences that caused the neutron doses of these survivors had never been determined experimentally. In principle, this would have been possible if radioisotopes produced by fast neutrons from the A-bomb explosions had been detected in samples from Hiroshima and Nagasaki at distances where the inhabitants survived. However, no suitable radioisotope had so far been identified. As a contribution to a large international effort to re-evaluate the A-bomb dosimetry, the concentration of the radionuclide (63)Ni (half-life 100.1 years) has been measured in copper samples from Hiroshima and Nagasaki. These measurements were mainly performed at the Maier-Leibnitz-Laboratory in Munich, Germany, by means of accelerator mass spectrometry. Because the (63)Ni had been produced in these samples by fast A-bomb neutrons via the reaction (63)Cu(n,p)(63)Ni, these measurements allow direct experimental validation of calculated neutron doses to the members of the LSS cohort, for the first time. The results of these efforts have already been published in a compact form. A more detailed discussion of the methodical aspects of these measurements and their results are given in the present paper. Eight copper samples that had been significantly exposed to fast neutrons from the Hiroshima A-bomb explosion were investigated. In general, measured (63)Ni concentrations decreased in these samples with increasing distance to the hypocenter, from 4 x 10(6 ) (63)Ni nuclei per gram copper at 391 m, to about 1 x 10(5 ) (63)Ni nuclei per gram copper at about 1,400 m. Additional measurements performed on three large

  10. 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

  11. 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.

  12. 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

  13. 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....

  14. Amendments to (63)Ni production calculation for Hiroshima by Takamiya et al. and DS02 fluence data by Egbert et al.

    PubMed

    Takamiya, K; Imanaka, T; Egbert, S D; Rühm, W

    2011-05-01

    In a previous paper, Takamiya et al. calculated (63)Ni production in copper samples exposed to the Hiroshima atomic bomb. More specifically, they used their experimental cross-section values of the (63)Cu(n,p)(63)Ni reaction and compared the result with that of the corresponding calculation in the radiation dosimetry system DS02, which used another set of cross-section values. These results were different, and the following two reasons were found: typographical errors in several energy boundary values in the DS02 report that was also used in the calculation by Takamiya et al. and an inappropriate assumption on the cross-section values of the low neutron energy region in the calculation by Takamiya et al. These two issues are described and amended in the present report. PMID:21327808

  15. 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....

  16. 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....

  17. 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....

  18. 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.

  19. 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

  20. 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

  1. 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

  2. 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%.

  3. 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.

  4. 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

  5. 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.

  6. 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

  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. 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

  9. 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...

  10. 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.

  11. 5.9-keV Mn K-shell X-ray luminosity from the decay of 55Fe in Type Ia supernova models

    NASA Astrophysics Data System (ADS)

    Seitenzahl, I. R.; Summa, A.; Krauß, F.; Sim, S. A.; Diehl, R.; Elsässer, D.; Fink, M.; Hillebrandt, W.; Kromer, M.; Maeda, K.; Mannheim, K.; Pakmor, R.; Röpke, F. K.; Ruiter, A. J.; Wilms, J.

    2015-02-01

    We show that the X-ray line flux of the Mn Kα line at 5.9 keV from the decay of 55Fe is a promising diagnostic to distinguish between Type Ia supernova (SN Ia) explosion models. Using radiation transport calculations, we compute the line flux for two three-dimensional explosion models: a near-Chandrasekhar mass delayed detonation and a violent merger of two (1.1 and 0.9 M⊙) white dwarfs. Both models are based on solar metallicity zero-age main-sequence progenitors. Due to explosive nuclear burning at higher density, the delayed-detonation model synthesizes ˜3.5 times more radioactive 55Fe than the merger model. As a result, we find that the peak Mn Kα line flux of the delayed-detonation model exceeds that of the merger model by a factor of ˜4.5. Since in both models the 5.9-keV X-ray flux peaks five to six years after the explosion, a single measurement of the X-ray line emission at this time can place a constraint on the explosion physics that is complementary to those derived from earlier phase optical spectra or light curves. We perform detector simulations of current and future X-ray telescopes to investigate the possibilities of detecting the X-ray line at 5.9 keV. Of the currently existing telescopes, XMM-Newton/pn is the best instrument for close (≲1-2 Mpc), non-background limited SNe Ia because of its large effective area. Due to its low instrumental background, Chandra/ACIS is currently the best choice for SNe Ia at distances above ˜2 Mpc. For the delayed-detonation scenario, a line detection is feasible with Chandra up to ˜3 Mpc for an exposure time of 106 s. We find that it should be possible with currently existing X-ray instruments (with exposure times ≲5 × 105 s) to detect both of our models at sufficiently high S/N to distinguish between them for hypothetical events within the Local Group. The prospects for detection will be better with future missions. For example, the proposed Athena/X-IFU instrument could detect our delayed

  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. 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

  15. 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.

  16. 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.

  17. 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.

  18. 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.

  19. 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.

  20. 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.

  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. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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...

  7. 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...

  8. 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...

  9. 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...

  10. 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...

  11. 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...

  12. 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...

  13. 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...

  14. 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...

  15. 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...

  16. 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...

  17. 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...

  18. 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...

  19. 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...

  20. 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...

  1. 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...

  2. 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.

  3. 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

  4. 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.

  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. 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

  7. 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

  8. 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

  9. 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

  10. 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.

  11. 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

  12. 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.

  13. 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

  14. 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.

  15. 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.

  16. Improved Analytical Performance of Negative 63Ni Ion Mobility Spectrometry for On-line Measurement of Propofol Using Dichloromethane as Dopant

    NASA Astrophysics Data System (ADS)

    Zhou, Qinghua; Hua, Lei; Wang, Changsong; Li, Enyou; Li, Haiyang

    2015-01-01

    On-line monitoring of propofol in exhaled air is a potential way to evaluate the anaesthesia depth for patients during surgery. In this study, a negative 63Ni ionization high resolution ion mobility spectrometer with Bradbury-Nielsen-Gate-Grid structure was built to measure propofol with reactant ions Cl-(H2O) n using dichloromethane as dopant. Instead of forming three propofol ions (M - H)-, M · O2 -, and (M2 - H)- with reactant ions O2 -(H2O) n , only product ion M · Cl- was produced when introducing dichloromethane gas. The peak-to-peak resolution ( R p-p) between reactant ions Cl-(H2O) n and product ion M · Cl- was 17.4, which was 1.6 times larger than that between O2 -(H2O) n and product ion. Furthermore, the linear response range using reactant ions Cl-(H2O) n was 3.5 times wider than that obtained with reactant ions O2 -(H2O) n .

  17. 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.

  18. Selective uptake, distribution, and redistribution of (109)Cd, (57)Co, (65)Zn, (63)Ni, and (134)Cs via xylem and phloem in the heavy metal hyperaccumulator Solanum nigrum L.

    PubMed

    Wei, Shuhe; Anders, Iwona; Feller, Urs

    2014-06-01

    The focus of this article was to explore the translocation of (109)Cd, (57)Co, (65)Zn, (63)Ni, and (134)Cs via xylem and phloem in the newly found hyperaccumulator Solanum nigrum L. Two experiments with the uptake via the roots and transport of (109)Cd, (57)Co, and (65)Zn labeled by roots, and the redistribution of (109)Cd, (65)Zn, (57)Co, (63)Ni, and (134)Cs using flap label in S. nigrum in a hydroponic culture with a standard nutrient solution were conducted. The results showed that (109)Cd added for 24 h to the nutrient medium of young plants was rapidly taken up, transferred to the shoot, and accumulated in the cotyledons and the oldest leaves but was not efficiently redistributed within the shoot afterward leading to a rather low content in the fruits. In contrast, (57)Co was more slowly taken up and released to the shoot, but afterward, this element was redistributed from older leaves to younger leaves and maturing fruits. (65)Zn was rapidly taken up and transferred to the shoot (mainly to the youngest leaves and not to the cotyledons). Afterward, this radionuclide was redistributed within the shoot to the youngest organs and finally accumulated in the maturing fruits. After flap labeling, all five heavy metals tested ((109)Cd, (57)Co, (65)Zn, (63)Ni, (134)Cs) were exported from the labeled leaf and redistributed within the plant. The accumulation in the fruits was most pronounced for (63)Ni and (65)Zn, while a relatively high percentage of (57)Co was finally found in the roots. (134)Cs was roughly in the middle of them. The transport of (109)Cd differed from that previously reported for wheat or lupin and might be important for the potential of S. nigrum to hyperaccumulate cadmium. PMID:24604268

  19. 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.

  20. 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.

  1. 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.

  2. 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

  3. 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.

  4. 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

  5. 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.

  6. 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.

  7. 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

  8. 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

  9. 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.

  10. 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.

  11. 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.

  12. 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.

  13. 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...

  14. 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

  15. 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.

  16. 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.

  17. 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.

  18. 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

  19. 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.

  20. 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.

  1. 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

  2. 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.

  3. 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.

  4. 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.

  5. Microwave Characterization of Pb0.45Ca0.55(Fe0.5Nb0.5)1-x Sn x O3 Multiferroics at X-Band

    NASA Astrophysics Data System (ADS)

    Singh, Charanjeet; Kaur, Randeep; Bindra Narang, S.; Puri, Maalti; Dhiman, Tanvi; Kaur, Harpreet

    2016-06-01

    The microwave characteristics of Pb0.45Ca0.55(Fe0.5Nb0.5)1-x Sn x O3 multiferroics (x = 0.03, 0.06, 0.09, 0.12, 0.15) have been investigated as a function of frequency (8-12 GHz) and thickness for different substitutions of Sn4+ ions. The absorber testing device method is used to study microwave properties in the rectangular slotted waveguide. The condition of microwave signal after passing through different compositions has been reported. The quarter wavelength criterion is used to evaluate the microwave absorption. The large microwave absorption is observed at lower as well as higher substitution. Maximum reflected power has been found at higher substitution. The different compositions for electromagnetic applications have also been put forth.

  6. 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

  7. 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

  8. 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.

  9. 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.

  10. 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

  11. (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

  12. (/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.

  13. 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.

  14. 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.

  15. 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.

  16. 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...

  17. 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.

  18. 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...

  19. 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...

  20. 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

  1. 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.

  2. 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.

  3. 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

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  11. 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.

  12. 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

  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. 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.

  16. 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

  17. 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

  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. 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. 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.

  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. 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.

  3. 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

  4. 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

  5. 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.

  6. 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.

  7. 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...

  8. ( 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. pylori-positivity. By taking advantage of the statistical probabilities, older patients could be accurately diagnosed with H. pylori at lower 14C values. We found that (14C)urea breath test to be both a sensitive and specific test that can be abbreviated to a 30-min examination (total test time). Moreover, our mathematical model indicates that a patient's age should be considered in order to optimize interpretation of the (14C)urea breath test, although further observations are needed to confirm this model.

  9. 17 CFR 240.14c-2 - Distribution of information statement.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 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. 17 CFR 240.14c-2 - Distribution of information statement.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 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...

  11. 17 CFR 240.14c-2 - Distribution of information statement.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 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...

  12. 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.

  13. Seasonally Resolved Surface Water (delta)14C Variability in the Lombok Strait: A Coralline Perspective

    SciTech Connect

    Guilderson, T P; Fallon, S J; Moore, M D; Schrag, D P; Charles, C D

    2008-04-23

    We have explored surface water mixing in the Lombok Strait through a {approx}bimonthly resolved surface water {Delta}{sup 14}C time-series reconstructed from a coral in the Lombok Strait that spans 1937 through 1990. The prebomb surface water {Delta}{sup 14}C average is -60.5{per_thousand} and individual samples range from -72{per_thousand} to 134{per_thousand}. The annual average post-bomb maximum occurs in 1973 and is 122{per_thousand}. The timing of the post-bomb maximum is consistent with a primary subtropical source for the surface waters in the Indonesian Seas. During the post-bomb period the coral records regular seasonal cycles of 5-20{per_thousand}. Seasonal high {Delta}{sup 14}C occur during March-May (warm, low salinity), and low {Delta}{sup 14}C occur in September (cool, higher salinity). The {Delta}{sup 14}C seasonality is coherent and in phase with the seasonal {Delta}{sup 14}C cycle observed in Makassar Strait. We estimate the influence of high {Delta}{sup 14}C Makassar Strait (North Pacific) water flowing through the Lombok Strait using a two endmember mixing model and the seasonal extremes observed at the two sites. The percentage of Makassar Strait water varies between 16 and 70%, and between 1955 and 1990 it averages 40%. During La Nina events there is a higher percentage of Makassar Strait (high {Delta}{sup 14}C) water in the Lombok Strait.

  14. Extraction of /sup 14/C-labeled photosynthate from aquatic plants with dimethyl sulfoxide (DMSO)

    SciTech Connect

    Filbin, G.J.; Hough, R.A.

    1984-03-01

    DMSO was tested as a solvent to extract /sup 14/C-labeled photosynthate from three species of aquatic plants in photosynthesis measurements and compared with the dry oxidation method for plant radioassay. Extraction efficiency was in the range of 96-99% of fixed /sup 14/C, and precision was comparable to, or better than, that obtained with dry oxidation. The method is simple and inexpensive, and for fresh tissue the same sample extracts can be used for chlorophyll analyses.

  15. Fate of 14C-acrylamide in roasted and ground coffee during storage.

    PubMed

    Baum, Matthias; Böhm, Nadine; Görlitz, Jessica; Lantz, Ingo; Merz, Karl Heinz; Ternité, Rüdiger; Eisenbrand, Gerhard

    2008-05-01

    Acrylamide (AA) is formed during heating of carbohydrate rich foods in the course of the Maillard reaction. AA has been classified as probably carcinogenic to humans. Storage experiments with roasted coffee have shown that AA levels decrease depending on storage time and temperature. In the present study the fate of AA lost during storage of roasted and ground (R&G) coffee was studied, using 14C-labeled AA as radiotracer. Radiolabel was measured in coffee brew, filter residue, and volatiles. In the brew, total (14)C-label decreased during storage of R&G coffee, while activity in the filter residue built up concomitantly. [2,3-14C]-AA (14C-AA) was the only 14C-related water extractable low molecular compound in the brew detected by radio-HPLC. No formation of volatile 14C-AA-related compounds was detected during storage and coffee brewing. Close to 90% of the radiolabel in the filter residue (spent R&G coffee, spent grounds) remained firmly bound to the matrix, largely resisting extraction by aqueous ammonia, ethyl acetate, chloroform, hexane, and sequential polyenzymatic digest. Furanthiols, which are abundant as aroma components in roasted coffee, have not been found to be involved in the formation of covalent AA adducts and thus do not contribute substantially to the decrease of AA during storage. PMID:18435440

  16. AMS studies of the long-term turnover of 14C-labelled fat in man

    NASA Astrophysics Data System (ADS)

    Gunnarsson, M.; Mattsson, S.; Stenström, K.; Leide-Svegborn, S.; Erlandsson, B.; Faarinen, M.; Hellborg, R.; Kiisk, M.; Nilsson, L.-E.; Nosslin, B.; Persson, P.; Skog, G.; Åberg, M.

    2000-10-01

    To estimate the biokinetics of 14C-labelled fatty acids and the associated radiation absorbed dose to man, long-term retention of 14C from oral intake of glycerol tri[1- 14C]oleate (triolein) has been studied using accelerator mass spectrometry (AMS). As a complement to earlier reported data for three individuals, we present here results for one person from measurements up to 4.6 yr after administration, now also including 14C-levels in fat, muscle and bone. In this subject, a total of 44% of the administered activity was recovered in the exhaled air. Fasting increased the exhalation of 14C. The "excess" 14CO2 due to fasting had a half-life of about 400 d. AMS measurements on fat, muscle and bone biopsies taken from the same subject 4.5 yr after ingestion indicated that a small fraction of the administered activity was still present in fat. Also, bone tissue had a higher 14C specific activity than the current environmental level. No significantly increased level was found in the muscle sample.

  17. Lack of tissue renewal in human adult Achilles tendon is revealed by nuclear bomb (14)C.

    PubMed

    Heinemeier, Katja Maria; Schjerling, Peter; Heinemeier, Jan; Magnusson, Stig Peter; Kjaer, Michael

    2013-05-01

    Tendons are often injured and heal poorly. Whether this is caused by a slow tissue turnover is unknown, since existing data provide diverging estimates of tendon protein half-life that range from 2 mo to 200 yr. With the purpose of determining life-long turnover of human tendon tissue, we used the (14)C bomb-pulse method. This method takes advantage of the dramatic increase in atmospheric levels of (14)C, produced by nuclear bomb tests in 1955-1963, which is reflected in all living organisms. Levels of (14)C were measured in 28 forensic samples of Achilles tendon core and 4 skeletal muscle samples (donor birth years 1945-1983) with accelerator mass spectrometry (AMS) and compared to known atmospheric levels to estimate tissue turnover. We found that Achilles tendon tissue retained levels of (14)C corresponding to atmospheric levels several decades before tissue sampling, demonstrating a very limited tissue turnover. The tendon concentrations of (14)C approximately reflected the atmospheric levels present during the first 17 yr of life, indicating that the tendon core is formed during height growth and is essentially not renewed thereafter. In contrast, (14)C levels in muscle indicated continuous turnover. Our observation provides a fundamental premise for understanding tendon function and pathology, and likely explains the poor regenerative capacity of tendon tissue. PMID:23401563

  18. 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.

  19. Disposition of 14C-alpha-cyclodextrin in germ-free and conventional rats.

    PubMed

    Van Ommen, B; De Bie, A T H J; Bär, A

    2004-06-01

    The absorption, disposition, metabolism, and excretion of uniformly (14)C-labeled alpha-cyclodextrin ((14)C-alpha-CD) was examined in four separate experiments with Wistar rats. In Experiment 1, (14)C-alpha-CD (25 microCi, 50 mg/kg bw) was administered intravenously to four male and four female conventional rats. In Experiment 2, (14)C-alpha-CD (25 microCi, 200 mg/kg bw) was given by gavage to four male and four female germ-free rats. In Experiments 3 and 4, (14)C-alpha-CD was given to groups of four male and four female conventional rats by gavage at different dose levels (100 microCi, 200 mg/kg bw; 25 microCi, 200 and 100 mg/kg bw). In all experiments, (14)C was measured in respiratory CO(2), urine, and feces over periods of 24-48 h, and in the contents of the gastrointestinal tract, blood, main organs, and residual carcass at termination of the experiments. The chemical identity of the (14)C-labeled compounds was examined by HPLC in blood (Experiment 1), urine (Experiments 1-4), feces (Experiments 2-4), and samples of intestinal contents (Experiments 2 and 4). Recovered (14)C was expressed as percentage of the administered dose. Experiment 1 showed that intravenously administered alpha-CD is excreted rapidly with urine. During the first 2h after dosing, plasma (14)C levels decreased rapidly (t(1/2), 26 and 21 min in male and female rats, respectively). About 13% of the administered (14)C dose (range 4.6-30.6) was detected in the feces, respiratory CO(2), organs, and carcass at the end of the experiment, i.e., 24 h after dosing. The presence of about 1.9% in the intestinal contents and feces suggests that a certain fraction of systemic alpha-CD is eliminated with the bile or saliva. Conclusive evidence, either positive or negative, for a hydrolysis and further metabolism of a small fraction of the administered alpha-CD by the enzymes of the mammalian body could not be gained from this experiment. Upon oral administration of (14)C-alpha-CD to germ-free rats

  20. 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

  1. The effects of the oral administration of fish oil concentrate on the release and the metabolism of (/sup 14/C)arachidonic acid and (/sup 14/C)eicosapentaenoic acid by human platelets

    SciTech Connect

    Hirai, A.; Terano, T.; Hamazaki, T.; Sajiki, J.; Kondo, S.; Ozawa, A.; Fujita, T.; Miyamoto, T.; Tamura, Y.; Kumagai, A.

    1982-11-01

    It has been suggested by several investigators that eicosapentaenoic acid (C20:5 omega 3, EPA) might have anti-thrombotic effects. In this experiment, the effect of the oral administration of EPA rich fish oil concentrate on platelet aggregation and the release and the metabolism of (/sup 1 -14/C)arachidonic acid and ((U)-/sup 14/C)eicosapentaenoic acid by human platelets was studied. Eight healthy male subjects ingested 18 capsules of fish oil concentrate (EPA 1.4 g) per day for 4 weeks. Plasma and platelet concentrations of EPA markedly increased, while those of arachidonic acid (C20:4 omega 6, AA) and docosahexaenoic acid (C22:6 omega 3, DHA) did not change. Platelet aggregation induced by collagen and ADP was reduced. Collagen induced (/sup 14/C)thromboxane B2 (TXB2) formation from (/sup 14/C)AA prelabeled platelets decreased. There was no detectable formation of (/sup 14/C)TXB3 from (/sup 14/C)EPA prelabeled platelets, and the conversion of exogenous (/sup 14/C)EPA to (/sup 14/C)TXB3 was lower than that of (/sup 14/C)AA to (/sup 14/C)TXB2. The release of (/sup 14/C)AA from (/sup 14/C)AA prelabeled platelets by collagen was significantly decreased. These observations raise the possibility that the release of arachidonic acid from platelet lipids might be affected by the alteration of EPA content in platelets.

  2. Persistence of the herbicides (/sup 14/C)chlorsulfuron and (/sup 14/C)metsulfuron methyl in prairie soils under laboratory conditions

    SciTech Connect

    Smith, A.E.

    1986-11-01

    Metsulfuron methyl, whose structure is closely related to that of chlorsulfuron, is currently being evaluated on the Canadian prairies as a postemergence treatment for the control of broadleaf weeds in cereal crops, in non-crop land and for brush control. Although applied postemergence, some of the herbicide will come into contact with the soil making it necessary to determine the fate of metsulfuron methyl in the soil. These studies were undertaken to investigate the rate of breakdown and the fate of (/sup 14/C)metsulfuron methyl in three soils under laboratory conditions where no leaching could occur. The rate of breakdown of (/sup 14/C)chlorsulfuron was also investigated in one of the soils.

  3. Measuring chlorophyll. cap alpha. and /sup 14/C-labeled photosynthate in aquatic angiosperms by the use of a tissue solubilizer. [/sup 14/C-labelled photosynthate

    SciTech Connect

    Beer, S.; Stewart, A.J.; Wetzel, R.G.

    1982-01-01

    A compound that quantitatively correlated with chlorophyll ..cap alpha.. could be measured fluorometrically in the extracts of leaves of three aquatic angiosperms (Myriophyllum heterophyllum Michx., Potamogeton crispus L., Elodea canadensis Michx.) treated with the tissue solubilizer BTS-450. Fluorescent characteristics of the solubilized plant tissues were stable for several weeks in the dark at temperatures up to 60/sup 0/C but rapidly degraded in sunlight or when acidified. /sup 14/C-Labeled photosynthate, which had been fixed by leaf discs during 1- to 10-hour exposure to H/sup 14/CO/sub 3/, was also readily extracted by the tissue solubilizer. Solubilizer extraction can, therefore, be used to determine both chlorophyll ..cap alpha.. content and /sup 14/C incorporation rates in the same leaf sample. The method is practical, because no grinding is required, the fluorescent characteristics of the extracts are stable, and analyses can be performed with very little plant material (about 3 milligrams).

  4. Progress in automated extraction and purification of in situ 14C from quartz: Results from the Purdue in situ 14C laboratory

    NASA Astrophysics Data System (ADS)

    Lifton, Nathaniel; Goehring, Brent; Wilson, Jim; Kubley, Thomas; Caffee, Marc

    2015-10-01

    Current extraction methods for in situ 14C from quartz [e.g., Lifton et al., (2001), Pigati et al., (2010), Hippe et al., (2013)] are time-consuming and repetitive, making them an attractive target for automation. We report on the status of in situ 14C extraction and purification systems originally automated at the University of Arizona that have now been reconstructed and upgraded at the Purdue Rare Isotope Measurement Laboratory (PRIME Lab). The Purdue in situ 14C laboratory builds on the flow-through extraction system design of Pigati et al. (2010), automating most of the procedure by retrofitting existing valves with external servo-controlled actuators, regulating the pressure of research purity O2 inside the furnace tube via a PID-based pressure controller in concert with an inlet mass flow controller, and installing an automated liquid N2 distribution system, all driven by LabView® software. A separate system for cryogenic CO2 purification, dilution, and splitting is also fully automated, ensuring a highly repeatable process regardless of the operator. We present results from procedural blanks and an intercomparison material (CRONUS-A), as well as results of experiments to increase the amount of material used in extraction, from the standard 5 g to 10 g or above. Results thus far are quite promising with procedural blanks comparable to previous work and significant improvements in reproducibility for CRONUS-A measurements. The latter analyses also demonstrate the feasibility of quantitative extraction of in situ 14C from sample masses up to 10 g. Our lab is now analyzing unknowns routinely, but lowering overall blank levels is the focus of ongoing research.

  5. Accelerator mass spectrometry measurements of the 13C (n ,γ )14C and 14N(n ,p )14C cross sections

    NASA Astrophysics Data System (ADS)

    Wallner, A.; Bichler, M.; Buczak, K.; Dillmann, I.; Käppeler, F.; Karakas, A.; Lederer, C.; Lugaro, M.; Mair, K.; Mengoni, A.; Schätzel, G.; Steier, P.; Trautvetter, H. P.

    2016-04-01

    The technique of accelerator mass spectrometry (AMS), offering a complementary tool for sensitive studies of key reactions in nuclear astrophysics, was applied for measurements of the 13C (n ,γ )14C and the 14N(n ,p )14C cross sections, which act as a neutron poison in s -process nucleosynthesis. Solid samples were irradiated at Karlsruhe Institute of Technology with neutrons closely resembling a Maxwell-Boltzmann distribution for k T =25 keV, and also at higher energies between En=123 and 182 keV. After neutron irradiation the produced amount of 14C in the samples was measured by AMS at the Vienna Environmental Research Accelerator (VERA) facility. For both reactions the present results provide important improvements compared to previous experimental data, which were strongly discordant in the astrophysically relevant energy range and missing for the comparably strong resonances above 100 keV. For 13C (n ,γ ) we find a four times smaller cross section around k T =25 keV than a previous measurement. For 14N(n ,p ), the present data suggest two times lower cross sections between 100 and 200 keV than had been obtained in previous experiments and data evaluations. The effect of the new stellar cross sections on the s process in low-mass asymptotic giant branch stars was studied for stellar models of 2 M⊙ initial mass, and solar and 1 /10th solar metallicity.

  6. Solar modulation of cosmic ray intensity and solar flare events inferred from (14)C contents in dated tree rings

    NASA Technical Reports Server (NTRS)

    Fan, C. Y.; Chen, T. M.; Yun, S. X.; Dai, K. M.

    1985-01-01

    The delta 14C values in 42 rings of a white spruce grown in Mackenzie Delta was measured as a continuing effort of tracing the history of solar modulation of cosmic ray intensity. The delta 14C values in six rings were measured, in search of a 14C increase due to two large solar flares that occurred in 1942. The results are presented.

  7. A Minute Dose of 14C-b-Carotene is Absorbed and Converted to Retinoids in Humans

    Technology Transfer Automated Retrieval System (TEKTRAN)

    We dosed 8 adults with 14C-all-trans [10,10',11,11'-14C]-B-carotene (1.01 nmol) to quantify its absorption and metabolism. We used accelerator mass spectrometry (AMS) to measure 14C eliminated in feces over 14 days, in urine over 30 days, and that was retained in plasma over 166 days since dose. We...

  8. 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

  9. 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

  10. In vitro synthesis and purification of UDP-( sup 14 C) galacturonate

    SciTech Connect

    Mitcham, E.J. ); Gross, K.C. ); Wasserman, B.P. )

    1989-04-01

    Pectins comprise a major component of the cell wall and much research has focused on degradation of pectins during ripening and senescence. However, little research has been conducted on pectin synthesis, partly due to a lack of commercial availability of UDP-({sup 14}C)galacturonic acid for use as a substrate in assaying galacturonan synthase. We report on the modification and integration of several procedures to synthesize UDP-({sup 14}C) galacturonic acid from commercially available UDP-({sup 14}C)glucuronic acid. A microsomal pellet containing UDP-D-glucuronate-4-epimerase was extracted from 5-day-old mung bean hypocotyls (Phaseolus aureus) and radish roots (Raphanus sativus L.) by ultracentrifugation at 30,000 rpm for 50 min. The UDP-({sup 14}C)galacturonic acid produced was separated from remaining UDP-({sup 14}C)glucuronic acid and other products by electrophoresis in pyridine:acetate:H{sub 2}O on silica gel. Spots were detected by autoradiography, eluted with 80% ethanol, and purified using anion exchange chromatography.

  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. 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

  13. 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.

  14. 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

  15. Release of aged 14C-atrazine residues from soil facilitated by dry-wet cycles

    NASA Astrophysics Data System (ADS)

    Jablonowski, N. D.; Yu, K.; Koeppchen, S.; Burauel, P.

    2012-04-01

    Intermittent dry-wet cycles may have an important effect on soil structure and aged pesticide residues release (1). A laboratory study was conducted to assess the maximum potential of water extractable aged atrazine residues influenced by soil drying and wetting. The used soil was obtained from an outdoor lysimeter (gleyic cambisol; Corg: 1.45%), containing environmentally aged (22 years) 14C-atrazine residues. For the experiment, soil from 0-10 cm depth was used since most residual 14C activity was previously found in this layer (2,3). Triplicate soil samples with a residual water content of approx. 8% were either dried (45° C) prior water addition or directly mixed with distilled water (soil+water: 1+2, w:w). The samples were shaken (150 rmp, 60 min, at 21° C), centrifuged (approx. 2000 g), and the supernatants were filtered. Water-extracted residual 14C activity was detected via liquid scintillation counter. The total water-extracted 14C activity (the amount of residual 14C activity in a sample equals 100%) was significantly higher (p

  16. Bioavailability of the Nano-Unit 14C-Agrochemicals Under Various Water Potential.

    PubMed

    Jung, S C; Kim, H G; Kuk, Y I; Ahn, H G; Senseman, S A; Lee, D J

    2015-08-01

    The study was conducted to investigate the effects of water potential on bioavailability of the nano-unit 14C-cafenstrole, 14C-pretilachlor, 14C-benfuresate, 14C-simetryn and 14C-oxyfluorfen applied with or without dimepiperate or daimuron under various water potential conditions. The highest bioavailable concentration in soil solution (BCSS) was found at 60% soil moisture, while the lowest occurred at 50% soil moisture for soil-applied alone or in combination. All water potential conditions differed significantly from each other with variations in total bioavailable amount in soil solution (TBSS) when either dimepiperate or daimuron were added to the soil, and changes were directly proportional to variations in water potential. Across all treatments, TBSS at 80% soil moisture was three to four times greater than that at 50% soil moisture when applied alone or in combination with dimepiperate or daimuron. Cafenstrole and simetryn had distribution coefficient (Kd) values <64 ml g-1 and a TBSS ranging from 10 to 44 ng g-1 soil, regardless of water potential conditions applied alone or in combination. Pretilachlor and benfuresate had Kd values <15 ml g-1 and a TBSS range of 38 to 255 ng g-1 soil when applied with or without dimepiperate or daimuron. PMID:26369226

  17. Special Analysis: Revised 14C Disposal Limits for the Saltstone Disposal Facility

    SciTech Connect

    Kaplan, D.I.

    2004-03-19

    The Saltstone Special Analysis calculated a limit for 14C based on the atmospheric pathway of 52 pCi/mL using some very conservative assumptions. This was compared to the estimated Low Curie Salt concentration of 0.45 pCi/mL and since the limit was two orders of magnitude greater than the estimated concentration, the decision was made that no further analysis was needed. The 14C concentration in Tank 41 has been found to be much greater than the estimated concentration and to exceed the limit derived in the Special Analysis. A rigorous analysis of the release of 14C via the air pathway that considers the chemical effects of the Saltstone system has shown that the flux of 14C is significantly less than that assumed in the Special Analysis. The net result is an inventory limit for 14C that is significantly higher than that derived in the Special Analysis that will also meet the performance objectives of DOE Order 435.1.

  18. Intestinal absorption and tissue distribution of ( sup 14 C)pyrroloquinoline quinone in mice

    SciTech Connect

    Smidt, C.R.; Unkefer, C.J.; Houck, D.R.; Rucker, R.B. )

    1991-05-01

    Pyrroloquinoline quinone (PQQ) functions as a cofactor for prokaryotic oxidoreductases, such as methanol dehydrogenase and membrane-bound glucose dehydrogenase. In animals fed chemically defined diets, PQQ improves reproductive outcome and neonatal growth. Consequently, the present study was undertaken to determine the extent to which PQQ is absorbed by the intestine, its tissue distribution, and route of excretion. About 28 micrograms of PQQ (0.42 microCi/mumol), labeled with {sup 14}C derived from L-tyrosine, was administered orally to Swiss-Webster mice (18-20 g) to estimate absorption. PQQ was readily absorbed (62%, range 19-89%) in the lower intestine, and was excreted by the kidneys (81% of the absorbed dose) within 24 hr. The only tissues that retained significant amounts of ({sup 14}C)PQQ at 24 hr were skin and kidney. For kidney, it was assumed that retention of ({sup 14}C)PQQ represented primarily PQQ destined for excretion. For skin, the concentration of ({sup 14}C)PQQ increased from 0.3% of the absorbed dose at 6 hr to 1.3% at 24 hr. Furthermore, most of the ({sup 14}C)PQQ in blood (greater than 95%) was associated with the blood cell fraction, rather than plasma.

  19. 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.

  20. Uptake and metabolism of (14C)-aspartate by developing kernels of maize (Zea mays L. )

    SciTech Connect

    Muhitch, M.J. )

    1990-05-01

    Pulse-chase experiments were performed to determine the metabolic fate of (14C)-aspartate in the pedicel region and subsequent uptake into the endosperm. Kernels were removed from the cob, leaving the pedicel attached but removing glumes, palea, and lemma. The basal tips were incubated in (14C)-aspartate for 0.5 h, followed by a 2 h chase period with unlabeled aspartate. In contrast to a previous study in which 70% of the 14C from aspartate was recovered in the organic acid fraction (Lyznik, et al., Phytochemistry 24: 425, 1985), only 20 to 25% of the radioactivity found in the 2 h chase period. While a small amount of the 14C transiently appeared in alanine at the beginning of the chase period, the most heavily labeled non-fed amino acid was glutamine, which accounted for 21% of the radioactivity within the pedicel amino acid fraction by 0.5 h into the chase period. There was no evidence for asparagine synthesis within the pedicel region of the kernel. 14C recovered from the endosperm in the form of amino acids were aspartate (60%), glutamine (20%), glutamate (15%), and alanine (5%). These results suggest that some of the maternally supplied amino acids undergo metabolic conversion to other amino acids before being taken up by the endosperm.

  1. 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.

  2. 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.

  3. Uptake and transfer of14C-simetryne through the laboratory freshwater food chain

    NASA Astrophysics Data System (ADS)

    Xu, Ying; Lay, J. P.; Zhang, Yongyuan

    1989-03-01

    This paper deals with the bioconcentration of14C-simetryne from water by aquatic test organisms: green algae— Monoraphidium minutum, rotifers— Brachionus rubens, daphnids— Daphnia magna, and fish— Brachydanio rerio. The chemical was bioconcentrated rapidly in all test species during the first 48 hours of experiment. The BCF values (bioconcentration factor) from all uptake studies show that simetryne has higher accumulation in algae than in rotifers, daphnids and zebra fish. The logarithm of the n-octanol/water partition coefficient of simetryne measured as 2.06±0.05 was correlated with the BCFs in the organisms as based on the lipid contents. 14C-simetryne uptake via the food-chain amounted to only 22% to 42% of the bioconcentration from water. Clearance of14C-derived residues from fish was rapid with a half-life of 2.1 days.

  4. Mobility Studies of (14)C-Chlorpyrifos in Malaysian Oil Palm Soils.

    PubMed

    Halimah, Muhamad; Ismail, B Sahid; Nashriyah, Mat; Maznah, Zainol

    2016-01-01

    The mobility of (14)C-chlorpyrifos using soil TLC was investigated in this study. It was found that chlorpyrifos was not mobile in clay, clay loam and peat soil. The mobility of (14)C-chlorpyrifos and non-labelled chlorpyrifos was also tested with silica gel TLC using three types of developing solvent hexane (100%), hexane:ethyl acetate (95:5, v/v); and hexane:ethyl acetate (98:2, v/v). The study showed that both the (14)C-labelled and non-labelled chlorpyrifos have the same Retardation Factor (Rf) for different developing solvent systems. From the soil column study on mobility of chlorpyrifos, it was observed that no chlorpyrifos residue was found below 5 cm depth in three types of soil at simulation rainfall of 20, 50 and 100 mm. Therefore, the soil column and TLC studies have shown similar findings in the mobility of chlorpyrifos. PMID:26546229

  5. Distribution of 14C-TNT and derivatives in different biochemical compartments of Phaseolus vulgaris.

    PubMed

    Sens, C; Scheidemann, P; Klunk, A; Werner, D

    1998-01-01

    (14)C-TNT was used to quantify the uptake rate and metabolic turnover of TNT in Phaseolus vulgaris. Seventeen plants were analysed by a special cell fractionation method with polar and nonpolar solvents and enzymes. We obtained three cytoplasmic fractions and five cell wall derived fractions. The recovery rate was 72% as measured by liquid scintillation counting. (14)C partitioned almost in equal amounts with approximately 50% in the cytoplasm and in the cell wall. The majority of the TNT-metabolites are present in the cytoplasm as was shown by GC/ECD and thin layer chromatography. The(14)C in the cell wall is bound probably resulting in long-term immobilisation of these metabolites. We conclude that plants may also be a model for nitroaromatic turnover and immobilisation in soil components. PMID:19002633

  6. A climatic record from 14C-dated wood fragments from southwestern Colorado

    USGS Publications Warehouse

    Epstein, S.; Xu, X.; Carrara, P.

    1999-01-01

    Deuterium concentrations in trees are related to the climatic temperature at which the trees grew. Deuterium analyses were made on all available (39) 14C-dated (all 14C dates cited are uncorrected) wood fragments collected from Lake Emma sediments. The 14C dates range from 9600 to 5400 'B.P.'. Tree line was above Lake Emma at 9600 'B.P.', was at Lake Emma at about 5000 'B.P.', and is 80 m below Lake Emma at the present time. The isotopic records at the various intervals of time coincide very well with this history. The range of ??D values is maximum at 9600 'B.P.' and is minimum at about 5400 'B.P.'. These data allow us to estimate the temperature range for the area between tree line and Lake Emma between these times. These results confirm previously observed cooling trends from several sources in the Western Hemisphere.

  7. {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.

  8. 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

  9. Effect of foliar treatments on distribution of /sup 14/C-glyphosate in Convolvulus arvensis L

    SciTech Connect

    Lauridson, T.C.

    1986-01-01

    Field bindweed is a perennial weed which produces shoots from buds on its roots. Herbicides, such as glyphosate (N-(phosphonomethyl)glycine) used for control of field bindweed usually do not kill all shoot buds on the roots, thus field bindweed often reinfests areas within 3 to 6 weeks of treatment. This dissertation deals with the development of a technique to change glyphosate distribution in field bindweed roots and could result in less shoot regrowth after glyphosate application. In field studies eight plant growth regulators were applied in September, 3 days before 2.24 kg/ha of 2.4-D((2,4-dichlorophenoxy) acetic acid) or 1.68 kg/ha of glyphosate. Eight months later, regrowth of shoots was least where glyphosate was applied at 0.028 kg/ha as a pretreatment, followed by a standard rate of 1.68 kg/ha. In subsequent greenhouse studies, typical patterns of shoot growth and /sup 14/C-glyphosate distribution in isolated root sections taken from 15-week-old intact plants were determined. In subsequent growth chamber studies, plants were decapitated to observe the effect of shoot apical dominance on /sup 14/C-glyphosate translocation. After /sup 14/C-glyphosate was applied, intact plants had about twice as much /sup 14/C in distal root sections as in proximal or middle root sections. Decapitated plants had more /sup 14/C in proximal and middle root sections than in distal sections, and about twice as much /sup 14/C was translocated to roots of decapitated plants than intact plants. Eight concentrations of 2,4,-D or glyphosate from 1 to 5000 ppm were applied in logarithmic series to 6-week old plants.

  10. A numerical approach to 14C wiggle-match dating of organic deposits: best fits and confidence intervals

    NASA Astrophysics Data System (ADS)

    Blaauw, Maarten; Heuvelink, Gerard B. M.; Mauquoy, Dmitri; van der Plicht, Johannes; van Geel, Bas

    2003-06-01

    14C wiggle-match dating (WMD) of peat deposits uses the non-linear relationship between 14C age and calendar age to match the shape of a sequence of closely spaced peat 14C dates with the 14C calibration curve. A numerical approach to WMD enables the quantitative assessment of various possible wiggle-match solutions and of calendar year confidence intervals for sequences of 14C dates. We assess the assumptions, advantages, and limitations of the method. Several case-studies show that WMD results in more precise chronologies than when individual 14C dates are calibrated. WMD is most successful during periods with major excursions in the 14C calibration curve (e.g., in one case WMD could narrow down confidence intervals from 230 to 36 yr).

  11. 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

  12. In situ 14C depth profile of subsurface vein quartz samples from Macraes Flat New Zealand

    NASA Astrophysics Data System (ADS)

    Kim, K. J.; Lal, D.; Englert, P. A. J.; Southon, J.

    2007-06-01

    We present results of measurements of cosmogenic in situ 14C produced in a quartz vein from Macraes Flat, East Otago, New Zealand, where concentrations of in situ produced 10Be and 26Al were previously studied by Kim and Englert [Earth Planet. Sci. Lett. 223 (2004) 113]. 14C was extracted from the quartz samples up to depths of 400 g cm-2 using a low temperature wet extraction method [D. Lal, A.J.T. Jull, Nucl. Instr. and Meth. B 92 (1994) 291]. Based on the results for 10Be and 26Al, we expected that the 14C activity in the samples would be at saturation levels, in equilibrium with erosion. The surface exposure age of this site was found to be about 25 000 years using 10Be and 26Al at the surface, with a surface erosion rate of at least 10-3 cm/y [K.J. Kim, P.A.J. Englert, Earth Planet. Sci. Lett. 223 (2004) 113]. The measured 14C activities were compared with those expected from spallation of Si and O in quartz by energetic neutrons and fast muons, and from capture of negative muons in O in quartz [B. Heisinger, A.J.T. Jull, D. Lal, P. Kubik, S. Ivy-Ochs, K. Knie, E. Nolte, Earth Planet. Sci. Lett. 200 (2002) 357; B. Heisinger, D. Lal, A.J.T. Jull, P. Kubik, S. Ivy-Ochs, S. Neumaier, K. Knie, V. Lazarev, E. Nolte, Earth Planet. Sci. Lett. 200 (2002) 345]. Surprisingly, we found that the 14C activities were significantly greater than those expected, by factors of 2 3, especially in samples of depths <200 g cm-2. We suspect that the excess 14C probably resulted from capture of thermal neutrons in nitrogen present in the fluid inclusions in quartz. This study shows that great care has to be taken in measurements of in situ 14C in quartz, especially in samples exposed near sea level and greater depths, where rates of spallation produced 14C are low.

  13. In vivo survival of (14C)sucrose-loaded porcine carrier erythrocytes

    SciTech Connect

    DeLoach, J.R.

    1983-06-01

    Porcine carrier erythrocyte survival was measured in adult pigs. (14C)Sucrose-loaded erythrocytes had a biphasic survival curve, with as much as 50% of the cells removed from circulation in the first 24 hours. The remaining cells had a 35-day half-life. Encapsulation values were measured for porcine erythrocytes and entrapment of (14C)sucrose was greater than 45%. Addition of inosine and glucose to the dialyzed cells and to the final wash buffer before reinjection of autologous cells did not improve their survival.

  14. Variations of 14C around AD 775 and AD 1795 - due to solar activity

    NASA Astrophysics Data System (ADS)

    Neuhäuser, R.; Neuhäuser, D. L.

    2015-12-01

    The motivation for our study is the disputed cause for the strong variation of 14C around AD 775. Our method is to compare the 14C variation around AD 775 with other periods of strong variability. Our results are: (a) We see three periods, where 14C varied over 200 yr in a special way showing a certain pattern of strong secular variation: after a Grand Minimum with strongly increasing 14C, there is a series of strong short-term drop(s), rise(s), and again drop(s) within 60 yr, ending up to 200 yr after the start of the Grand Minimum. These three periods include the strong rises around BC 671, AD 775, and AD 1795. (b) We show with several solar activity proxies (radioisotopes, sunspots, and aurorae) for the AD 770s and 1790s that such intense rapid 14C increases can be explained by strong rapid decreases in solar activity and, hence, wind, so that the decrease in solar modulation potential leads to an increase in radioisotope production. (c) The strong rises around AD 775 and 1795 are due to three effects, (i) very strong activity in the previous cycles (i.e. very low 14C level), (ii) the declining phase of a very strong Schwabe cycle, and (iii) a phase of very weak activity after the strong 14C rise - very short and/or weak cycle(s) like the suddenly starting Dalton minimum. (d) Furthermore, we can show that the strong change at AD 1795 happened after a pair of two packages of four Schwabe cycles with certain hemispheric leadership (each package consists of two Gnevyshev-Ohl pairs, respectively two Hale-Babcock pairs). We show with several additional arguments that the rise around AD 775 was not that special. We conclude that such large, short-term rises in 14C (around BC 671, AD 775, and 1795) do not need to be explained by highly unlikely solar super-flares nor other rare events, but by extra-solar cosmic rays modulated due to solar activity variations.

  15. 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

  16. A study of placental transfer mechanisms in nonhuman primates using (/sup 14/C)phenylalanine

    SciTech Connect

    Pueschel, S.M.; Boylan, J.M.; Jackson, B.T.; Piasecki, G.J.

    1982-02-01

    Placental transfer mechanisms were investigated in pregnant Macaca Fascicularis and Macaca mulatta during the gestational age of 120 to 130 days. These primates underwent an operative procedure that allowed continuous fetal blood sampling. The administration of (/sup 14/C)phenylalanine into the maternal circulation revealed a significant increase of radioactive material in the fetal circulation, indicating an active placental transport mechanism unidirectional to the fetus. When (/sup 14/C)phenylalanine was injected into the fetus, radioactive aromatic amino acids in the maternal circulation increased only slightly over time, resembling a simple diffusion process.

  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. Percutaneous absorption of (7. 10-/sup 14/C)benzo(a)pyrene and (7,12-/sup 14/C)dimethylbenz(a)anthracene in mice

    SciTech Connect

    Sanders, C.L.; Skinner, C.; Gelman, R.A.

    1984-04-01

    The percutaneous penetration, tissue distribution, and excretion of /sup 14/C-labeled benzo(a)pyrene (BaP) and dimethylbenz(a)anthracene (DMBA) were studied in mice. Both BaP and DMBA rapidly penetrated the skin and were excreted more in the feces than in the urine. The proportion of BaP or DMBA absorbed was less with increasing applied dose due to apparent saturation of the uptake process. Uptake from the dorsal skin of the nose was similar to uptake from the dorsal nuchal skin. 24 references.

  19. Distribution of root exudates and mucilage in the rhizosphere: combining 14C imaging with neutron radiography

    NASA Astrophysics Data System (ADS)

    Holz, Maire; Carminati, Andrea; Kuzyakov, Yakov

    2015-04-01

    Water and nutrients will be the major factors limiting food production in future. Plant roots employ various mechanisms to increase the access to limited soil resources. Low molecular weight organic substances released by roots into the rhizosphere increase nutrient availability by interactions with microorganisms, while mucilage improves water availability under low moisture conditions. Though composition and quality of these substances have intensively been investigated, studies on the spatial distribution and quantification of exudates in soil are scarce. Our aim was to quantify and visualize root exudates and mucilage distribution around growing roots using neutron radiography and 14C imaging depending on drought stress. Plants were grown in rhizotrons well suited for neutron radiography and 14C imaging. Plants were exposed to various soil water contents experiencing different levels of drought stress. The water content in the rhizosphere was imaged during several drying/wetting cycles by neutron radiography. The radiographs taken a few hours after irrigation showed a wet region around the root tips showing the allocation and distribution of mucilage. The increased water content in the rhizosphere of the young root segments was related to mucilage concentrations by parameterization described in Kroener et al. (2014). In parallel 14C imaging of root after 14CO2 labeling of shoots (Pausch and Kuzyakov 2011) showed distribution of rhizodeposits including mucilage. Three days after setting the water content, plants were labeled in 14CO2 atmosphere. Two days later 14C distribution in soil was imaged by placing a phosphor-imaging plate on the rhizobox. To quantify rhizodeposition, 14C activity on the image was related to the absolute 14C activity in the soil and root after destructive sampling. By comparing the amounts of mucilage (neutron radiography) with the amount of total root derived C (14C imaging), we were able to differentiate between mucilage and root

  20. Kinetic study of benzyl [1-14C]acetate as a potential probe for astrocytic energy metabolism in the rat brain: Comparison with benzyl [2-14C]acetate.

    PubMed

    Okada, Maki; Yanamoto, Kazuhiko; Kagawa, Tomohiko; Yoshino, Keiko; Hosoi, Rie; Abe, Kohji; Zhang, Ming-Rong; Inoue, Osamu

    2016-02-01

    Brain uptake of [(14)C]acetate has been reported to be a useful marker of astrocytic energy metabolism. In addition to uptake values, the rate of radiolabeled acetate washout from the brain appears to reflect CO2 exhaustion and oxygen consumption in astrocytes. We measured the time-radioactivity curves of benzyl [1-(14)C]acetate ([1-(14)C]BA), a lipophilic probe of [1-(14)C]acetate, and compared it with that of benzyl [2-(14)C]acetate ([2-(14)C]BA) in rat brains. The highest brain uptake was observed immediately after injecting either [1-(14)C]BA or [2-(14)C]BA, and both subsequently disappeared from the brain in a single-exponential manner. Estimated [1-(14)C]BA washout rates in the cerebral cortex and cerebellum were higher than those of [2-(14)C]BA. These results suggested that [1-(14)C]BA could be a useful probe for estimating the astrocytic oxidative metabolism. The [1-(14)C]BA washout rate in the cerebral cortex of immature rats was lower than that of mature rats. An autoradiographic study showed that the washout rates of [1-(14)C]BA from the rat brains of a lithium-pilocarpine-induced status epilepticus model were not significantly different from the values in control rat brains except for the medial septal nucleus. These results implied that the enhancement of amino acid turnover rate rather than astrocytic oxidative metabolism was increased in status epilepticus. PMID:26661153

  1. 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

  2. DERMAL PENETRATION OF [14C] CAPTAN IN YOUNG AND ADULT RATS

    EPA Science Inventory

    Dermal penetration of [14C] Captan was determined in young (33 day old) and adult (82 day old) female Fischer 344 rats by an in vivo method and two in vitro methods. ermal penetration in vivo at 72 hours was about 9% of the dose in both young and adult rats. o significant differe...

  3. 14C dating of bone using (gamma) Carboxyglutamic Acid and Carboxyglycine (Aminomalonate)

    SciTech Connect

    Southon, J R; Burky, R T; Kirner, D L; Taylor, R E; Hare, P E

    1999-04-27

    Radiocarbon determinations have been obtained on {gamma}-carboxyglutamic acid [Gla] and {alpha}-carboxyglycine (aminomalonate) [Am] as well as acid- and base-hydrolyzed total amino acids isolated from a series of fossil bones. As far as they are aware, Am has not been reported previously in fossil bone and neither Gla nor Am {sup 14}C values have been measured previously. Interest in Gla, an amino acid found in the non-collagen proteins osteocalcin and matrix Gla-protein (MGP), proceeds from the suggestion that it may be preferentially retained and more resistant to diagenetic contamination affecting {sup 14}C values in bones exhibiting low and trace amounts of collagen. The data do not support these suggestions. The suite of bones examined showed a general tendency for total amino acid and Gla concentrations to decrease in concert. Even for bones retaining significant amounts of collagen, Gla (and Am extracts) can yield {sup 14}C values discordant with their expected age and with {sup 14}C values obtained on total amino-acid fractions isolated from the same bone sample.

  4. 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

  5. Astrophysical S-Factor of Radiative p 14C Capture at Low Energies

    NASA Astrophysics Data System (ADS)

    Dubovichenko, S. B.; Burtebaev, N.; Dzhazairov-Kakhramanov, A. V.; Alimov, D. K.

    2016-04-01

    The possibility of describing the available experimental data on the astrophysical S-factor for the reaction of p14C capture to the ground state of 15N at astrophysical energies within the framework of the modified potential cluster model is considered.

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

    PubMed

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

    2012-09-10

    A method is described to determine the time of death of elephants. This is accomplished by analysis of the radionuclides 14C, 90Sr and 228/232Th in known samples of ivory, and in samples of unknown age. The reliability of this method is considerably increased by multi nuclide analysis. PMID:22717552

  7. Accuracy of post-bomb 137Cs and 14C in dating fluvial deposits

    USGS Publications Warehouse

    Ely, L.L.; Webb, R.H.; Enzel, Y.

    1992-01-01

    The accuracy and precision of 137Cs and 14C for dating post-1950 alluvial deposits were evaluated for deposits from known floods on two rivers in Arizona. The presence of 137Cs reliably indicates that deposition occurred after intensive above-ground nuclear testing was initiated around 1950. There was a positive correlation between the measured level of 137Cs activity and the clay content of the sediments, although 137Cs was detected even in sandy flood sediments with low clay content. 137Cs is a valuable dating tool in arid environments where organic materials for 14C or tree-ring dating are scarce and observational records are limited. The 14C activity measured in different types of fine organic detritus yielded dates within 1 to 8 yr of a 1980 flood deposit, and the accuracy was species-dependent. However, undifferentiated mixtures of fine organic materials from several post-bomb deposits of various ages repeatedly yielded dates between 1958 and 1962, and detrital charcoal yielded a date range of 1676-1939. In semiarid environments, the residence time of most types of organic debris precludes accurate annual resolution of post-bomb 14C dates. ?? 1992.

  8. 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.

  9. Kinetic Distribution of 14C-Metsulfuron-methyl Residues in Paddy Soils under Different Moisture Conditions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Rice paddy soils undergo several cycles of drying and wetting during a growing season. A laboratory study was conducted to determine the effect of soil moisture conditions on the distribution and kinetics of extractable and bound residues of 14C-metsulfuron-methyl in six Chinese paddy soils during 8...

  10. Anaerobic oxidation of [1,2-14C]dichloroethene under Mn(IV)-reducing conditions

    USGS Publications Warehouse

    Bradley, P.M.; Landmeyer, J.E.; Dinicola, R.S.

    1998-01-01

    Anaerobic oxidation of [1,2-14C]dichloroethene to14CO2 under Mn(IV)-reducing conditions was demonstrated. The results indicate that oxidative degradation of partially chlorinated solvents like dichloroethene can be significant even under anoxic conditions and demonstrate the potential importance of Mn(IV) reduction for remediation of chlorinated groundwater contaminants.