Determination of natural Cu-isotope variation by plasma-source mass spectrometry: implications for use as geochemical tracers

Abstract Techniques for the high precision measurement of 65 Cu/ 63 Cu ratios by multiple-collector plasma-source mass spectrometry has been developed. Two approaches, namely Zn-doping and “sample-standard bracketing”, have been exploited. By using the “sample-standard bracketing” technique, a range of samples including native copper, Cu-carbonate and Cu-sulphides from terrestrial and marine environments have been analysed. An overall variation in 65 Cu/ 63 Cu of 22 parts per 10 4 (22 e units) is observed. This is more than 30 times the 2 σ analytical uncertainty of the technique employed, and thus demonstrates the great potential for using stable Cu isotopes as tracers in geological and planetary processes. The variations in e 65 Cu values observed in this study display some regularity. Those samples involving formation through low temperature aqueous solutions display large differences in e 65 Cu values even at a single locality, whereas chalcopyrite samples hosted in igneous rocks show similar Cu-isotope compositions worldwide. This indicates that the e 65 Cu variations arise principally through mass fractionation in low temperature aqueous processes, rather than through source heterogeneity. In contrast to continental sulphides, chalcopyrites from black smoker sulphide chimneys on the ocean floor show large variations in e 65 Cu values. Relative to active high temperature hydrothermal vents, the old inactive vent deposits are enriched in 63 Cu and show smaller variations in e 65 Cu values. Within in a single active chimney, Cu isotopes become lighter from bottom to top. This variation pattern is explained tentatively by means of a two-stage-process model, which involves: (1)the preferential leachin 65 g of 65 Cu by hydrothermal processes, and (2)subsequent isotopic exchange between the early formed Cu-sulphides and 65 Cu-depleted late-stage hydrothermal fluids. This new capability for Cu-isotope measurement is expected to have a major impact across disciplines ranging from cosmochemistry and geochemistry through biogeochemistry to biochemistry and alimentology.

[1]  K. Gillis,et al.  Lithium isotopic composition of submarine basalts: implications for the lithium cycle in the oceans , 1992 .

[2]  E. Scott,et al.  Ion microprobe analysis of olivine in pallasite meteorites for nickel , 1979 .

[3]  W. Shanks,et al.  Sulfur isotope study of chimney minerals and vent fluids from 21°N, East Pacific Rise: Hydrothermal sulfur sources and disequilibrium sulfate reduction , 1988 .

[4]  R. Hékinian,et al.  Age dating of sulfide deposits from axial and off-axial structures on the East Pacific Rise near 12°50′N , 1985 .

[5]  M. Rehkämper,et al.  Early evolution of the Earth and Moon: new constraints from Hf-W isotope geochemistry , 1996 .

[6]  W. Seyfried,et al.  The effect of temperature on metal mobility in subseafloor hydrothermal systems: constraints from basalt alteration experiments , 1990 .

[7]  M. Frank,et al.  A new variable dispersion double-focusing plasma mass spectrometer with performance illustrated for Pb isotopes , 1998 .

[8]  E. Boyle,et al.  Low Blank Preconcentration Technique for the Determination of Lead, Copper, and Cadmium in Small-Volume Seawater Samples by Isotope Dilution ICPMS. , 1997, Analytical chemistry.

[9]  R. Dietz Sudbury Structure as an Astrobleme , 1964, The Journal of Geology.

[10]  Francis Albarède,et al.  Precise analysis of copper and zinc isotopic compositions by plasma-source mass spectrometry , 1999 .

[11]  A. Halliday,et al.  Precise determinations of the isotopic compositions and atomic weights of molybdenum, tellurium, tin and tungsten using ICP magnetic sector multiple collector mass spectrometry , 1995 .

[12]  B. Murton,et al.  Mineralogy and sulphur isotope geochemistry of the Broken Spur sulphides, 29°N, Mid-Atlantic Ridge , 1995, Geological Society, London, Special Publications.

[13]  R. Grieve,et al.  The Sudbury Structure: Constraints on its genesis from Lithoprobe results , 1994 .

[14]  A. Schultz,et al.  Mid-Ocean Ridge Hydrothermal Fluxes and the Chemical Composition of the Ocean , 1996 .

[15]  J. Edmond,et al.  A lithium isotope study of hot springs and metabasalts from Mid‐Ocean Ridge Hydrothermal Systems , 1993 .

[16]  William E Seyfried,et al.  The effect of redox on the relative solubilities of copper and iron in Cl-bearing aqueous fluids at elevated temperatures and pressures: An experimental study with application to subseafloor hydrothermal systems , 1993 .

[17]  R. K. O’nions,et al.  SIMS ANALYSIS OF U-PB ISOTOPES IN MONAZITE : MATRIX EFFECTS , 1998 .

[18]  M. Rehkämper,et al.  Applications of Multiple Collector-ICPMS to Cosmochemistry, Geochemistry, and Paleoceanography , 1998 .

[19]  C. German,et al.  Continuation of the hydrothermal fluid chemistry time series at TAG, and the effects of ODP drilling , 1996 .

[20]  A. J. Walder,et al.  Communication. Isotopic ratio measurement using a double focusing magnetic sector mass analyser with an inductively coupled plasma as an ion source , 1992 .

[21]  S. S. Goldich Natural Variations in the Abundance Ratio and the , 1965 .

[22]  A. Basu,et al.  Origin of the Sudbury Complex by Meteoritic Impact: Neodymium Isotopic Evidence , 1985, Science.

[23]  A. J. Walder,et al.  Isotope ratio measurement of lead, neodymium and neodymium–samarium mixtures, Hafnium and Hafnium–Lutetium mixtures with a double focusing multiple collector inductively coupled plasma mass spectrometer , 1993 .

[24]  J. Eiler,et al.  SIMS analysis of oxygen isotopes: matrix effects in complex minerals and glasses , 1997 .