Iron is an important constituent of the rock-forming minerals that are produced at elevated temperatures experienced during magma genesis. Iron has four stable isotopes (54, 56, 57 and 58) and is an important constituent of the secondary minerals produced by alteration of the primary minerals, occurring in clay minerals and carbonates. Kinetic, equilibrium and nuclear processes fractionate the isotopes, in the same way as is commonly observed for other stable isotopes. At elevated temperatures, Fe isotopes display limited fractionation, detection and resolution of which requires a highly sensitive instrumentation, such as multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS). Stable Fe isotopes follow mass-dependent fractionation pattern. Standard delta notation is used to report Fe-isotope data in per mil (‰) and is defined as follows:
In the present work, we have measured bulk iron-isotope compositions of 12 Martian meteorites to ascertain variation in their
δ56Fe and
δ57Fe values. In addition, we have also analysed a set of terrestrial samples including Proterozoic basalts and granites from Southern India and sandstone samples from Antarctic dry valley (DV) regions, which may be considered Martian analogues (). The Martian meteorite samples selected in our study represent all the three major groups described earlier. The terrestrial basalt and granite samples were selected from the Harker collection of the University of Cambridge, UK. The mineralogy and petrology of these samples have previously been studied extensively (
Anand et al. 2003). The present-day climatic conditions in the DV regions of Antarctica represent an extreme end member of the range of conditions prevailing in the Earth today. This includes very cold temperatures and nearly no humidity, which presents a very harsh environment for the survival of life. Nevertheless, microbial communities, known as cryptoendoliths, have been found thriving within the sandstones of DV regions (
Friedmann 1982). A selection of cryptoendolithic-bearing sandstones and cryptoendolith-free sandstones were obtained from the collection of British Geological Survey.
Blackhurst et al. (2004) performed a detailed elemental study on bulk- and individual components of these samples and found some specific elemental fractionations associated with different portions of these samples. It was not clear if these elemental signatures were related to the maturity and diagenesis of the sandstone samples or if they could be ascribed to microbial activities. We chose three Antarctic sandstone samples from the study by
Blackhurst et al. (2004) to conduct Fe-isotope measurements. Two cryptoendolith-free sandstones, VH59 and MM45, were analysed for their bulk Fe-isotope compositions. The third sample, BP8 was a cryptoendolith-bearing sample which had very low bulk FeO content. Only the top layer, termed ‘crust’ in the
Blackhurst et al. (2004) study contained sufficient Fe to obtain Fe-isotopic composition.
| Table 1List of samples analysed for Fe isotopes in this study. (Samples beginning with BM are from the Natural History Museum collections. NIPR stands for National Institute for Polar Research, Japan. Two of the Martian meteorites were donated to one of the (more ...) |
The initial step of sample preparation involved acid digestion of
ca 200

mg powdered sample in HF–HClO
4–HCl medium, followed by ion-exchange chromatography to separate Fe from other matrix elements. Further details of the procedure followed here can be found in
Mullane et al. (2003). Subsequent to column chromatography, the Fe-isotope compositions were measured on a fixed resolution (
m/Δ
m=500) MC-ICP-MS (IsoProbe, GV Instruments, UK) with respect to the Fe isotope standard IRMM-014, using the sample-standard bracketing method (
Mullane et al. 2003). Blank subtraction is undertaken off-line. Correction for isobaric interference of
54Cr on
54Fe is made by monitoring the
52Cr signal and applying an on-line mathematical correction at mass 54. The ion-exchange chromatography strips out any Cr present in the sample. However, Cr can also be introduced during the analysis from the instrument components (e.g. cones) for which an online correction is usually applied as mentioned earlier. In typical cases, this correction is almost negligible (less than 0.0001% of the
54Fe signal) suggesting no significant isobaric interference of
54Cr on
54Fe. The other isobaric interference of
40Ar
16OH background at mass 57 is reduced by analysing solutions at a concentration of approximately 4–10

p.p.m. and sample and standard solutions were concentration-matched to within ±5%. Both these procedures are routine in various labs conducting Fe-isotope measurements by sample standard bracketing technique (
Mullane et al. 2003). The samples were run over a 15-month period and a number of industrial and natural standards were run to check the accuracy of the results. Fe solutions from other laboratories were also analysed for inter-laboratory comparisons. Each sample was run at least twice, usually, three to four times over a 15-month period. Each run consisted of six repeat measurements of
56/54Fe and
57/54Fe ratios with respect to international reference material, IRMM-014. The analytical set-up adopted in the present study was the same as that described by
Mullane et al. (2003). Only those parameters were different that vary on the daily basis for the optimum running of the machine, such as the rate of gas flow in the nebulizer and hexapole. lists the Fe-isotope compositions of some of the standard solutions that were run during this study. Typical external errors are less than 0.1‰ (2 sigma) in most cases.
| Table 2Fe isotopic composition of reference material analysed in this study. |