- 著者
 
          - 
             
             Yuji SANO
             
             Kotaro SHIRAI
             
             Naoto TAKAHATA
             
             Takafumi HIRATA
             
             Neil C. STURCHIO
             
          
 
          
          
          - 出版者
 
          - The Japan Society for Analytical Chemistry
 
          
          
          - 雑誌
 
          - Analytical Sciences (ISSN:09106340)
 
          
          
          - 巻号頁・発行日
 
          - vol.21, no.9, pp.1091-1097, 2005 (Released:2006-01-10)
 
          
          
          - 参考文献数
 
          - 34
 
          
          
          - 被引用文献数
 
          - 
             
             43
             
             
             45
             
             
          
        
 
        
        
        Concentrations of minor (Mg and Sr) and trace (Ba and U) elements in four natural calcium carbonate samples were first analyzed by inductively coupled plasma mass spectrometry (ICP-MS) after chemical dissolution and calibrated against a standard dolomite.  Their homogeneities were checked by in situ laser ablation (LA) ICP-MS with 10 - 20 spots.  The carbonate samples were measured by using a high lateral resolution secondary ion mass spectrometer (Nano-SIMS NS50).  A ∼4 nA O- primary beam was used to sputter a 5 - 6-µm diameter crater on the sample surface, and secondary positive ions were extracted for mass analysis using an accelerating voltage of 8 kV and a Mattauch-Herzog geometry.  A multi-collector system was adjusted to detect 26Mg+, 43Ca+, 88Sr+, 138Ba+, 238U16O+ and 238U16O2+ ions at the same time.  A resolving power of 2500 - 5000 at 10% peak height was attained by an entrance slit set at 40 µm, and each exit slit at 50 µm with adequate flat-topped peaks.  The observed 26Mg/43Ca, 88Sr/43Ca, 138Ba/43Ca and 238U16O2/43Ca ratios agreed well with those measured by LA-ICP-MS.  Foraminifera shells were analyzed at 5 - 6 µm scale by Nano-SIMS.  There was a large variation of the Mg/Ca ratios, up to ±38%, even in a single fragment of the shell, suggesting that although the ratios provide a useful paleoceanographic proxy at bulk scale, they may reflect a more complex pattern at <10 µm scale.