(Table 1) Sr isotopes and chemical composition of DSDP Hole 61-462A basalts

Sixteen elemental abundances and 87Sr/86Sr ratio of the Nauru Basin basalt (Cores 75 to 90: sub-bottom depths 950 m to 1050 m) from Hole 462A have been determined by inductively coupled plasma-optical emission spectroscopy and mass spectrometry. The result indicates that the basalt is a new type of oceanic tholeiite, elementally similar to normal mid-oceanic ridge basalts and isotopically similar to oceanic island-type basalts.

(Table 1) Interstitial-water chemistry at DSP Leg 58 Holes

Interstitial waters from several sites drilled during Leg 58 have been analyzed for major constituents. Data for Sites 442, 443, and 444 in Shikoku Basin indicate that only small changes occur in the chemical composition. We did not note any influence on the interstitial water chemistry resulting from reactions taking place in the underlying basalts. Site 445 data indicate that reactions must occur in the sediment column, leading to decreases in dissolved magnesium and increases in dissolved calcium. In addition, a source of dissolved calcium appears in the underlying basalts. At Site 446, changes appear in dissolved-calcium and -magnesium concentrations, resulting mainly from alteration reactions in the basalts. Dissolved potassium has its main sink in deeper-lying sediments or basalts. Changes in dissolved strontium at Sites 445 and 446 can be explained in terms of carbonate recrystallization. At all sites, changes in dissolved manganese and lithium appear to be related to the presence of biogenic silica in the sediments.

(Table 1) Mineralogy of veins in basalts at DSDP Hole 61-462A

Numerous veins are present in basalts recovered from Hole 462A, Leg 61 of the Deep Sea Drilling Project. Three mineral assemblages are recognized and stratigraphically controlled. These assemblages are (1) a zeolite-bearing, quartz-poor assemblage which occurs from Core 44 to the bottom of the hole and contains smectite, clinoptilolite, calcite, pyrite, ± chabazite, ± analcime, ± quartz, ± apophyllite, ± talc (?); (2) a quartz-rich, pyrite-bearing assemblage, found between Cores 19 and 29, which contains smectite, calcite, quartz, and pyrite; and (3) a quartz-rich, celadonite-bearing assemblage which occurs from Cores 14 through 17 and contains smectite, calcite, quartz, celadonite, and Fe oxide. These data are interpreted to represent two episodes of vein mineral formation with an oxidative overprint on the more recent. The first episode followed the outpourings of basaltic lavas onto the sea floor. Zeolite-bearing veins were formed at elevated temperatures under low PCO2 while the thermal gradient was high and before a cover of calcareous sediments had formed. The second mineralization episode followed injection of basalt and microdiabase sills into a thick layer of sediments, and produced all the vein minerals now occurring between Cores 14 and 29. These veins formed at lower temperature and higher PCO2 than zeolite-bearing veins. The presence of pyrite indicates a nonoxidative environment. After the initial formation of these veins, oxygenated seawater diffused through the sedimentary cover and oxidized the pyrite and smectite, forming celadonite and Fe oxides.