Mineralogy and stable oxygen isotope ratios of the Cretaceous-Tertiary boundary

Results of detailed mineralogical, chemical, and oxygen isotope analyses of the clay minerals and zeolites from two Cretaceous-Tertiary (K/T) boundary regions, Stevns Klint, Denmark, and Deep Sea Drilling Project (DSDP) Hole 465A in the north central Pacific Ocean, are presented. In the central part of the Stevns Klint K/T boundary layer, the only clay mineral detected by x-ray diffraction is a pure smectite with > 95 percent expandable layers. No detrital clay minerals or quartz were observed in the clay size fraction in these beds, whereas the clay minerals above and below the boundary layer are illite and mixed-layer smectite-illite of detrital origin as well as quartz. The mineralogical purity of the clay fraction, the presence of smectite only at the boundary, and the d18O value of the smectite (27.2 ± 0.2 per mil) suggest that it formed in situ by alteration of glass. Formation from impact rather than from volcanic glass is supported by its major element chemistry. The high content of iridium and other siderophile elements is not due to the cessation of calcium carbonate deposition and resulting slow sedimentation rates. At DSDP Hole 465A, the principal clay mineral in the boundary zone (80 to 143 centimeters) is a mixed-layer smectite-illite with >=90 percent expandable layers, accompanied by some detrital quartz and small amounts of a euhedral authigenic zeolite (clinoptilolite). The mixed-layer smectite-illite from the interval 118 to 120 centimeters in the zone of high iridium abundance has a very low rare earth element content; the negative cerium anomaly indicates formation in the marine environment. This conclusion is corroborated by the d18O value of this clay mineral (27.1 ± 0.2 per mil). Thus, this mixed-layer smectite-illite formed possibly from the same glass as the K/T boundary smectite at Stevns Klint, Denmark.

Isotopic composition of igneous rocks from DSDP Site 462

The tholeiitic basalts and microdolerites that comprise the Cretaceous igneous complex in the Nauru Basin in the western equatorial Pacific have moderate ranges in initial 87Sr/86Sr (0.70347 - 0.70356), initial 143Nd/144Nd (0.51278 - 0.51287), and measured 206Pb/204Pb (18.52 - 19.15), 207Pb/204Pb (15.48 - 15.66) and 208Pb/204Pb (38.28 - 38.81). These isotopic ratios overlap with those of both oceanic island basalts (OIB) and South Atlantic and Indian mid-ocean ridge basalts (MORB). However, the petrography, mineralogy, and bulk rock chemistry of the igneous complex are more similar to MORB than to OIB. Also, the rare earth element contents of Nauru Basin igneous rocks are uniformly depleted in light elements (La/Sm(ch) < 1) indicative of a mantle source compositionally similar to that of MORB. These results suggest that the igneous complex is the top of the original ocean crust in the Nauru Basin, and that the notion that the crust must be 15 to 35 m.y. older based on simple extrapolation and identification of the M-sequence magnetic lineations (Larson et al., 1981, doi:10.2973/dsdp.proc.61.1981; Moberly et al., 1985, doi:10.2973/dsdp.proc.81.1984) may be invalid because of a more complicated tectonic setting. The igneous complex most probably was extruded from an ocean ridge system located near the anomalously hot, volcanically active, and isotopically distinct region in the south central Pacific which has been in existence since c. 120 Ma.

Petrology and geochemistry of silicified upper Miocene chalk at DSDP Site 69-504

Chert, Porcellanite, and other silicified rocks formed in response to high heat flow in the lower 50 meters of 275 meters of sediments at Deep Sea Drilling Project Site 504, Costa Rica Rift. Chert and Porcellanite partly or completely replaced upper Miocene chalk and limestone. Silicified rock occurs as nodules, laminae, stringers, and casts of burrows, and consists of quartz and opal-CT in varying amounts, associated with secondary calcite. The secondary silica was derived from dissolution of opal-A (biogenic silica), mostly diatom frustules and radiolarian tests. Temperature data obtained at the site indicate that transformation of opal-A to opal-CT began at about 50°C, and transformation from opal-CT to quartz at about 55°C. Quartz is most abundant close to basement basalts. These silica transformations occurred over the past 1 m.y., and took place so rapidly that there was incomplete ordering of opal-CT before transformation to quartz; opal-CT formed initially with an uncommonly wide d spacing. Quartz shows poor crystallinity. Chemical data show that the extensively silicified rocks consist of over 96% SiO2; in these rocks, minor and trace elements decreased greatly, except for boron, which increased. Low Al2O3 and TiO2 contents in all studied rocks preclude the presence of significant volcanic or terrigenous detritus. Mn content increases with depth, perhaps reflecting contributions from basalts or hydrothermal solutions. Comparisons with cherts from oceanic plateaus in the central Pacific point to a more purely biogenic host sediment for the Costa Rica Rift cherts, more rapid precipitation of quartz, and formation nearer a spreading center. Despite being closer to continental sources of ash and terrigenous detritus, Costa Rica Rift cherts have lower Al2O3, Fe2O3, and Mn concentrations.