2004 Denver Annual Meeting (November 7–10, 2004)

Paper No. 9
Presentation Time: 3:30 PM

WHERE HAS ALL THE ARAGONITE GONE? MINERALOGY OF HOLOCENE NERITIC COOL-WATER CARBONATES, SOUTHERN AUSTRALIA


JAMES, Noel P.1, KYSER, T. Kurtis1 and BONE, Yvonne2, (1)Geological Sciences and Geological Engineering, Queen's Univ, Kingston, ON K7L 3N6, (2)School of Earth and Environmental Sciences, Univ of Adelaide, Adelaide, 5005, Australia, james@geol.queensu.ca

Surficial carbonate sediments on the southern continental shelf of Australia are cool-water in aspect and composed of biogenic particles produced largely during the late Quaternary. Current understanding is that such sediments are calcite-dominated, as were their older Cenozoic counterparts. The Holocene fraction of these sediments in modern open-shelf, neritic environments between 30 and 300 meters water depth is, however, 50% to 80% aragonite. Scant evidence of significant former aragonite in cool-water carbonate sedimentary rocks implies that most aragonite is lost before such sediments exit the marine diagenetic environment. Although marine dissolution must be taking place, the conundrum is exacerbated because seawater is saturated with respect to aragonite throughout the region. It is proposed that the aragonite, from skeletons of gastropods, infaunal bivalves, and certain bryozoans, is dissolved in the shallow subsurface as the byproduct of bacterial degradation of sedimentary organic matter. As a consequence, the geological and paleontological record of cool-water carbonates is strongly biased, and the inferred original calcitic composition of such sediments is the product of early diagenetic taphonomic loss, not selective biogenic productivity. The net result is not only dissolution of aragonite but also neomorphism of Mg-calcite to calcite with a marine geochemical signature. Synsedimentary aragonite loss, by removing CaCO3 that is usually available for calcite cementation during meteoric diagenesis, leads to retarded lithification of cool-water carbonates until deeply buried. Such removal of a significant carbonate fraction during deposition likely contributes to the low rates of cool-water sediment accumulation.