Abstract
Boron and Pb isotopic compositions together with B–U–Th–Pb concentrations were determined for Pacific and Indian mantle-type mid-ocean ridge basalts (MORB) obtained from shallow drill holes near the Australian Antarctic Discordance (AAD). Boron contents in the altered samples range from 29.7 to 69.6 ppm and are extremely enriched relative to fresh MORB glass with 0.4–0.6 ppm B. Similarly the δ 11B values range from 5.5‰ to 15.9‰ in the altered basalts and require interaction with a δ 11B enriched fluid similar to seawater ∼ 39.5‰ and/or boron isotope fractionation during the formation of secondary clays. Positive correlations between B concentrations and other chemical indices of alteration such as H 2O CO 2, K 2O, P 2O 5, U and 87Sr/ 86Sr indicate that B is progressively enriched in the basalts as they become more altered. Interestingly, δ 11B shows the largest isotopic shift to + 16‰ in the least altered basalts, followed by a continual decrease to + 5–6‰ in the most altered basalts. These observations may indicate a change from an early seawater dominated fluid towards a sediment-dominated fluid as a result of an increase in sediment cover with increasing age of the seafloor. The progression from heavy δ 11B towards lighter values with increasing degrees of alteration may also reflect increased formation of clay minerals (e.g., saponite). A comparison of 238U/ 204Pb and 206Pb/ 204Pb in fresh glass and variably altered basalt from Site 1160B shows extreme variations that are caused by secondary U enrichment during low temperature alteration. Modeling of the U–Pb isotope system confirms that some alteration events occurred early in the 21.5 m.y. history of these rocks, even though a significant second pulse of alteration happened at ∼ 12 Ma after formation of the crust. The U–Pb systematics of co-genetic basaltic glass and variably low temperature altered basaltic whole rocks are thus a potential tool to place age constraints on the timing of alteration and fluid flow in the ocean crust.
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