Inorganic and methylated germanium species were determlned at sub parts per trllllon levels by a comblnatlon of hydrlde generatlon and Inductively coupled argon plasma mass spectrometry (ICP-MS). The germanium species In solution were reduced to the correspondlng hydrides by sodium tetrahydroborate, transferred with a helium gas stream, and trapped In a liquid nitrogen cooled U-trap. The hydrides were evaporated and introduced into the ICP torch, and the Ion count at m / z = 74 was monitored. The reduction efficiencies for methylated germanium species in a malic acid matrix were more than 97 % . The absolute detection limits were 0.08 pg of Ge for lnorganlc germanlum (Ge,), 0.1 pg of Ge for monomethylgermanium (MMGe) and dlmethylgermanium (DMGe), and 0.09 pg of Ge for trimethylgermanium (TMGe). The dynamic ranges of the detection span 4 orders of magnitude. The proposed method was applied to natural waters and wastewaters, and Ge,, MMGe and DMGe were detected In all of the samples studied.
INTRODUCTIONChemical speciation of elements is indispensable to an understanding of the biological cycles of some elements in the environment (I). Recent studies have revealed that germanium in natural waters exists as both inorganic and organic chemical species a t sub-ng to ng L-' levels (2)(3)(4)(5)(6)(7)(8)(9). Two organogermanium species, monomethylgermanium (MMGe) and dimethylgermanium (DMGe), have been identified in natural waters by methods based on the hydride generation technique (5-7), and it should be noted that MMGe is the major germanium species in seawater. However, information on or-