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41.
Mg isotope fractionation in biogenic carbonates of deep-sea coral, benthic foraminifera, and hermatypic coral 总被引:1,自引:0,他引:1
Yoshimura T Tanimizu M Inoue M Suzuki A Iwasaki N Kawahata H 《Analytical and bioanalytical chemistry》2011,401(9):2755-2769
High-precision Mg isotope measurements by multiple collector inductively coupled plasma mass spectrometry were applied for
determinations of magnesium isotopic fractionation of biogenic calcium carbonates from seawater with a rapid Mg purification
technique. The mean δ26Mg values of scleractinian corals, giant clam, benthic foraminifera, and calcite deep-sea corals were −0.87‰, −2.57‰, −2.34‰,
and −2.43‰, suggesting preferential precipitation of light Mg isotopes to produce carbonate skeleton in biomineralization.
Mg isotope fractionation in deep-sea coral, which has high Mg calcite skeleton, showed a clear temperature (T) dependence from 2.5 °C to 19.5 °C: 1,000 × ln(α) = −2.63 (±0.076) + 0.0138 (±0.0051) × T(R
2 = 0.82, p < 0.01). The δ26Mg values of large benthic foraminifera, which are also composed of a high-Mg calcite skeleton, can be plotted on the same
regression line as that for deep-sea coral. Since the precipitation rates of deep-sea coral and benthic foraminifera are several
orders of magnitude different, the results suggest that kinetic isotope fractionation may not be a major controlling factor
for high-Mg calcite. The Mg isotope fractionation factors and the slope of temperature dependence from deep-sea corals and
benthic foraminifera are similar to that for an inorganically precipitated calcite speleothem. Taking into account element
partitioning and the calcification rate of biogenic CaCO3, the similarity among inorganic minerals, deep-sea corals, and benthic foraminiferas may indicate a strong mineralogical
control on Mg isotope fractionation for high-Mg calcite. On the other hand, δ26Mg in hermatypic corals composed of aragonite has been comparable with previous data on biogenic aragonite of coral, sclerosponges,
and scaphopad, regardless of species differences of samples. 相似文献
42.
Sogawa K Watanabe M Sato K Segawa S Ishii C Miyabe A Murata S Saito T Nomura F 《Analytical and bioanalytical chemistry》2011,400(7):1905-1911
In a clinical diagnosis microbiology laboratory, the current method of identifying bacterial isolates is based mainly on phenotypic
characteristics, for example growth pattern on different media, colony morphology, Gram stain, and various biochemical reactions.
These techniques collectively enable great accuracy in identifying most bacterial isolates, but are costly and time-consuming.
In our clinical microbiology laboratory, we prospectively assessed the ability of matrix-assisted laser desorption ionization–time
of flight mass spectrometry (MALDI–TOF MS) to identify bacterial strains that were routinely isolated from clinical samples.
Bacterial colonies obtained from a total of 468 strains of 92 bacterial species isolated at the Department of Clinical Laboratory
at Chiba University were directly placed on target MALDI plates followed by addition of CHCA matrix solution. The plates were
then subjected to MALDI–TOF MS measurement and the microorganisms were identified by pattern matching with the libraries in
the BioTyper 2.0 software. Identification success at the species and genus levels was 91.7% (429/468) and 97.0% (454/468),
respectively. MALDI–TOF MS is a rapid, simple, and high-throughput proteomic technique for identification of a variety of
bacterial species. Because colony-to-colony differences and effects of culture duration on the results are minimal, it can
be implemented in a conventional laboratory setting. Although for some pathogens, preanalytical processes should be refined,
and the current database should be improved to obtain more accurate results, the MALDI–TOF MS based method performs, in general,
as well as conventional methods and is a promising technology in clinical laboratories. 相似文献
43.
Motohashi S Nagase K Nakakita T Matsuo T Yoshida Y Kawakubo T Miura M Toriyama M Barybin MV 《The Journal of organic chemistry》2011,76(10):3922-3936
Enantiomerically pure (Z)-β-sulfinyl allylic alcohols of either handedness can be readily prepared from (Z)-β-sulfinyl enones using NaBH(4) or DIBAL reductants in the presence of LaCl(3) as a chelating agent. A chiral sulfoxide auxiliary induces the remote 1,2-asymmetric reduction (1,4-induction) to afford various chiral allylic alcohols in high yields with excellent stereoselectivities (up to 100% de). 相似文献
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46.
Masahiko Ishino Anatoly Y. Faenov Momoko Tanaka Satoshi Tamotsu Noboru Hasegawa Masaharu Nishikino Tatiana A. Pikuz Takeshi Kaihori Tetsuya Kawachi 《Applied Physics A: Materials Science & Processing》2013,110(1):179-188
To study the interactions between picosecond soft x-ray laser (SXRL) beams and material surfaces, gold (Au), copper (Cu), and silicon (Si) surfaces were irradiated with SXRL pulses having a wavelength of 13.9 nm and a duration of ~7 ps. Following irradiation, the surfaces of the substrates were observed using a scanning electron microscope and an atomic force microscope. With single pulse irradiation, ripple-like structures were formed on the Au and Cu surfaces. These structures were different from previously investigated conical structures formed on an Al surface. In addition, it was confirmed that the development of modified structures, i.e., growth of hillocks on the Au and Cu surfaces, was observed after multiple SXRL pulse exposures. However, on the Si surface, deep holes that seemed to be melted structures induced by the accumulation of multiple pulses of irradiations were found. Therefore, it was concluded that SXRL beam irradiation of various material surfaces causes different types of surface modifications, and the changes in the surface behaviors are attributed to the differences in the elemental properties, such as the attenuation length of x-ray photons. 相似文献
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