Strontium isotope data from DSDP Sites 32-305 and 62-463 and ODP Sites 113-689 and 113-690

Fluctuations in oxygen (d18O) and carbon (d13C) isotope values of benthic foraminiferal calcite from the tropical Pacific and Southern Oceans indicate rapid reversals in the dominant mode and direction of the thermohaline circulation during a 1 m.y. interval (71-70 Ma) in the Maastrichtian. At the onset of this change, benthic foraminiferal d18O values increased and were highest in low-latitude Pacific Ocean waters, whereas benthic and planktic foraminiferal d13C values decreased and benthic values were lowest in the Southern Ocean. Subsequently, benthic foraminiferal d18O values in the Indo-Pacific decreased, and benthic and planktic d13C values increased globally. These isotopic patterns suggest that cool intermediate-depth waters, derived from high-latitude regions, penetrated temporarily to the tropics. The low benthic d13C values at the Southern Ocean sites, however, suggest that these cool waters may have been derived from high northern rather than high southern latitudes. Correlation with eustatic sea-level curves suggests that sea-level change was the most likely mechanism to change the circulation and/or source(s) of intermediate-depth waters. We thus propose that oceanic circulation during the latest Cretaceous was vigorous and that competing sources of intermediate- and deep-water formation, linked to changes in climate and sea level, may have alternated in importance.

Calcium carbonate and organic carbon at DSDP Leg 62 Holes

Percent CaCO3 was determined in selected samples aboard the ship by the carbonate-bomb technique (Müller and Gastner, 1971). Results of these analyses are listed in Table 1 and plotted in Figures 1, 3, 4, and 5 as plus signs (+). Samples collected specifically for analyses of CaCO3 and organic carbon were analyzed at three shore-based laboratories. Concentrations of total carbon, organic carbon, and CaCO3 were determined in some samples at the DSDP sediment laboratory, using a Leco carbon analyzer, by personnel of the U.S. Geological Survey, under the supervision of T. L. Valuer. Most of these samples were collected from lithologic units containing relatively high concentrations of organic carbon. Sample procedures are outlined in Boyce and Bode (1972). Precision and accuracy are both ±0.3% absolute for total carbon, ±0.06% absolute for organic carbon, and ±3% absolute for CaCO3.