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. 2007 Oct 23;8:10. doi: 10.1186/1467-4866-8-10

Figure 2.

Figure 2

Plots of stable isotopes of aqueous sulfate. A) δ34SSO4 vs. δ18OSO4; δ34S of sulfide minerals shown as vertical bars; B) δ34SSO4 vs. dissolved copper concentration. Data points with error bars indicate non-detects for copper, for which symbols plotted at one-half of the method detection limit (MDL) and error bars extend upward to the MDL (0.003 mg L-1). Enrichment of δ34SSO4 in residual mine pool is likely caused by preferential reduction of 32SO4 by sulfate-reducing bacteria, producing H2S that scavenges aqueous copper from solution.