Method for isotope ratio drift correction by internal amplifier signal synchronization in MC-ICPMS transient signals

2014 ◽  
Vol 29 (9) ◽  
pp. 1607-1617 ◽  
Author(s):  
Alkiviadis Gourgiotis ◽  
Sylvain Bérail ◽  
Pascale Louvat ◽  
Hélène Isnard ◽  
Julien Moureau ◽  
...  

This work provides a simple method for isotope ratio drift correction in MC-ICPMS transient signals.


2020 ◽  
Vol 101 ◽  
pp. 105516
Author(s):  
Matteo Perini ◽  
Tiziana Nardin ◽  
Matteo Venturelli ◽  
Silvia Pianezze ◽  
Roberto Larcher


2017 ◽  
Vol 14 (5) ◽  
pp. 1305-1313 ◽  
Author(s):  
Mitchell Call ◽  
Kai G. Schulz ◽  
Matheus C. Carvalho ◽  
Isaac R. Santos ◽  
Damien T. Maher

Abstract. A new approach to autonomously determine concentrations of dissolved inorganic carbon (DIC) and its carbon stable isotope ratio (δ13C–DIC) at high temporal resolution is presented. The simple method requires no customised design. Instead it uses two commercially available instruments currently used in aquatic carbon research. An inorganic carbon analyser utilising non-dispersive infrared detection (NDIR) is coupled to a Cavity Ring-down Spectrometer (CRDS) to determine DIC and δ13C–DIC based on the liberated CO2 from acidified aliquots of water. Using a small sample volume of 2 mL, the precision and accuracy of the new method was comparable to standard isotope ratio mass spectrometry (IRMS) methods. The system achieved a sampling resolution of 16 min, with a DIC precision of ±1.5 to 2 µmol kg−1 and δ13C–DIC precision of ±0.14 ‰ for concentrations spanning 1000 to 3600 µmol kg−1. Accuracy of 0.1 ± 0.06 ‰ for δ13C–DIC based on DIC concentrations ranging from 2000 to 2230 µmol kg−1 was achieved during a laboratory-based algal bloom experiment. The high precision data that can be autonomously obtained by the system should enable complex carbonate system questions to be explored in aquatic sciences using high-temporal-resolution observations.



2003 ◽  
Vol 18 (5) ◽  
pp. 437-443 ◽  
Author(s):  
Mercedes Castillo Carrión ◽  
Jesús Reyes Andrés ◽  
Juan Antonio Martín Rubí ◽  
Håkan Emteborg


2012 ◽  
Vol 102 (3) ◽  
pp. 387a-388a
Author(s):  
Sang Hak Lee ◽  
Murat Baday ◽  
Marco Tjioe ◽  
Paul Dennis Simonson ◽  
Paul Ronald Selvin


2016 ◽  
Author(s):  
Mitchell Call ◽  
Kai G. Schulz ◽  
Matheus C. Carvalho ◽  
Isaac R. Santos ◽  
Damien T. Maher

Abstract. A new approach to autonomously determine concentrations of dissolved inorganic carbon (DIC) and its carbon stable isotope ratio (δ13C-DIC) at high temporal resolution is presented. The simple method requires no customised design. Instead it uses two commercially available instruments currently used in aquatic carbon research. An inorganic carbon analyser utilising non-dispersive infrared detection (NDIR) is coupled to a Cavity Ring-down Spectrometer (CRDS) to determine DIC and δ13C-DIC based on the liberated CO2 from acidified aliquots of water. Using a small sample volume of 2 ml, the precision and accuracy of the new method was comparable to standard isotope ratio mass spectrometry (IRMS) methods. The system achieved a sampling resolution of 16 mins, with a DIC precision of ±1.5 to 2 µmol kg−1 and δ13C-DIC precision of ±0.14 ‰ for concentrations spanning 1000 to 3600 µmol kg−1. Accuracy of 0.1 ± 0.06 ‰ based on DIC concentrations ranging from 2000 µmol kg−1 to 2230 µmol kg−1 was achieved during a laboratory-based algal bloom experiment. The high precision data that can be autonomously obtained by the system should enable complex carbonate system questions to be explored in aquatic sciences using high temporal resolution observations.



Author(s):  
K.-H. Herrmann ◽  
E. Reuber ◽  
P. Schiske

Aposteriori deblurring of high resolution electron micrographs of weak phase objects can be performed by holographic filters [1,2] which are arranged in the Fourier domain of a light-optical reconstruction set-up. According to the diffraction efficiency and the lateral position of the grating structure, the filters permit adjustment of the amplitudes and phases of the spatial frequencies in the image which is obtained in the first diffraction order.In the case of bright field imaging with axial illumination, the Contrast Transfer Functions (CTF) are oscillating, but real. For different imageforming conditions and several signal-to-noise ratios an extensive set of Wiener-filters should be available. A simple method of producing such filters by only photographic and mechanical means will be described here.A transparent master grating with 6.25 lines/mm and 160 mm diameter was produced by a high precision computer plotter. It is photographed through a rotating mask, plotted by a standard plotter.



Author(s):  
Dean A. Handley ◽  
Jack T. Alexander ◽  
Shu Chien

In situ preparation of cell cultures for ultrastructural investigations is a convenient method by which fixation, dehydration and embedment are carried out in the culture petri dish. The in situ method offers the advantage of preserving the native orientation of cell-cell interactions, junctional regions and overlapping configurations. In order to section after embedment, the petri dish is usually separated from the polymerized resin by either differential cryo-contraction or solvation in organic fluids. The remaining resin block must be re-embedded before sectioning. Although removal of the petri dish may not disrupt the native cellular geometry, it does sacrifice what is now recognized as an important characteristic of cell growth: cell-substratum molecular interactions. To preserve the topographic cell-substratum relationship, we developed a simple method of tapered rotary beveling to reduce the petri dish thickness to a dimension suitable for direct thin sectioning.



2010 ◽  
Vol 34 (8) ◽  
pp. S75-S75
Author(s):  
Weifeng Zhu ◽  
Zhuoqi Liu ◽  
Daya Luo ◽  
Xinyao Wu ◽  
Fusheng Wan


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