The Fe/Mn ratio in MORB and OIB determined by ICP-MS

نویسندگان

  • Liping Qin
  • Munir Humayun
چکیده

Variations in the abundance of iron in the mantle may have important consequences for mantle dynamics and geochemistry. The abundance of iron in lavas derived from mantle source regions varies during partial melting and subsequent fractionation, so that source heterogeneities are not easily resolved in iron abundances alone. However, manganese is a geochemically similar element, so that the planetary Fe/Mn ratio is approximately constant. Here, we report new Fe/Mn results for mid-oceanic ridge basalts (MORBs), oceanic island basalts (OIBs) and komatiites using a precise inductively coupled plasma mass spectrometric (ICP-MS) method to measure Fe/Mn to better than 0.5% (2r). As a measure of reproducibility of Fe/Mn, five olivine and five orthopyroxene grains from a Kilbourne Hole peridotite xenolith yielded Fe/Mn 69.8 ± 0.4 and 44.3 ± 0.2, respectively. To avoid ubiquitous secondary Fe–Mn oxides, Fe/Mn ratios in Pacific, Atlantic, and Indian MORBs were determined by Laser Ablation ICP-MS. MORB Fe/Mn (53–56) corrected for crystal fractionation yielded a value of 54.0 ± 1.2 (1r). Icelandic basalts and picrites (MgO 10–29%) had Fe/Mn ratios 56–61, with a single exception. Six relatively fresh komatiites from Belingwe (MgO 20–29%) yielded Fe/Mn values of 58.3 ± 0.2 (1r). Basalts from Tahiti and Reunion exhibited high Fe/Mn (>65), like Hawaii. This implies that the mantle source regions of Tahiti and Reunion lavas may have been enriched in Fe relative to other mantle reservoirs (e.g., MORBs, Iceland, Belingwe). Combined with previous results for Hawaii, we now find that Fe/Mn > 65 is characteristic of at least two plumes from the Pacific Superswell. It is conceivable that this is evidence for excess Fe due to core–mantle interaction in these mantle plumes, although partial melting of secondary pyroxenites may cause similar variations in Fe/Mn. Heterogeneity of Fe/Mn in mantle-derived lavas is now clearly documented. 2008 Elsevier Ltd. All rights reserved.

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تاریخ انتشار 2008