Chemistry of minerals from ODP Leg 127/128 basalts

Suites of basalts drilled during Legs 127 and 128 can be distinguished by their mineral assemblages and compositions of phenocrysts and groundmass phases. An upper suite of plagioclase phyric basaltic sills with a groundmass composed of plagioclase, augite, and magnetite was recovered from Site 794. The upper, evolved part of this suite is highly plagioclase phyric, including calcic plagioclases (~An90). The most primitive, lower part of this upper suite, in addition, contains olivine, but lacks calcic plagioclase. A lower suite at Site 794 is plagioclase and olivine phyric to aphyric basaltic sills and flows with a groundmass of plagioclase, augite, olivine (~Fo75-83), and magnetite. At Site 795, plagioclase and augite phyric basalts and andesites were recovered. The relatively low Ti and Cr contents of augite of these basalts suggest typical arc tholeiitic parental magmas. Two suites of basalt were recovered from Site 797, an upper suite of plagioclase and olivine phyric to aphyric olivine basalts, and a lower suite of evolved plagioclase phyric basaltic sills. The most evolved sills at both sites lack olivine as phenocryst and groundmass phases, while this phase is present in the relatively primitive sills. The olivine-bearing suites contain plagioclase with relatively low potassium content and augite with relatively high sodium content. An exception is the olivine-bearing sills of the upper suite at Site 794 that contains plagioclase with relatively high potassium content similar to the associated olivine-free sills. The olivine-free suites contain plagioclase with high potassium content and augite with low sodium content and have the most evolved compositions of any of the Japan Sea rocks.

Mineralogy at DSDP Legs 58-60

Sediments recovered by drilling during Legs 58, 59, and 60 in the North and South Philippine Sea have been analyzed by X-ray diffractometry. The CaCO3 content was measured separately. The sites encompass several volcanic ridges and intervening inter-arc basin troughs as well as sites on the Mariana arc fore-arc sediment prism and the Mariana Trench. The sediments at all sites received major volcanogenic input from the various arcs; they tend to be rich in volcanic glass, with associated quartz, feldspar, pyroxenes and amphibole. Carbonate is a major component only at Site 445 at the southern end of the Daito Ridge, and at Site 448 on the Palau-Kyushu Ridge. All other sites were either deep relative to the carbonate compensation depth or had very high non-carbonate sedimentation rates. Clay minerals are mainly smectite and illite with lesser variable proportions of chlorite and kaolinite. Smectite predominates over illite except at sites in the Shikoku Basin and the Daito Ridge, and at one site in the Mariana Trench. At several sites, smectite increases and illite decreases with depth. Principal zeolites are phillipsite and clinoptilolite. Analcime occurs in some samples.

(Table 2) Mineralogy, stable isotopes, and mineral percentages of the carbonate fraction of samples from the South China Sea

Chemoherm carbonates, as well as numerous other types of methane seep carbonates, were discovered in 2004 along the passive margin of the northern South China Sea. Lithologically, the carbonates are micritic containing peloids, clasts and clam fragments. Some are highly brecciated with aragonite layers of varying thicknesses lining fractures and voids. Dissolution and replacement is common. Mineralogically, the carbonates are dominated by high magnesium calcites (HMC) and aragonite. Some HMCs with MgCO3 contents of between 30-38 mol%-extreme-HMC, occur in association with minor amounts of dolomite. All of the carbonates are strongly depleted in d13C, with a range from -35.7 to -57.5 per mil PDB and enriched in d18O (+ 4.0 to + 5.3 per mil PDB). Abundant microbial rods and filaments were recognized within the carbonate matrix as well as aragonite cements, likely fossils of chemosynthetic microbes involved in carbonate formation. The microbial structures are intimately associated with mineral grains. Some carbonate mineral grains resemble microbes. The isotope characteristics, the fabrics, the microbial structure, and the mineralogies are diagnostic of carbonates derived from anaerobic oxidation of methane mediated by microbes. From the succession of HMCs, extreme-HMC, and dolomite in layered tubular carbonates, combined with the presence of microbial structure and diagenetic fabric, we suggest that extreme-HMC may eventually transform into dolomites. Our results add to the worldwide record of seep carbonates and establish for the first time the exact locations and seafloor morphology where such carbonates formed in the South China Sea. Characteristics of the complex fabric demonstrate how seep carbonates may be used as archives recording multiple fluid regimes, dissolution, and early transformation events.

Carbonate record of ODP Leg 167 sites

One of the expected scientific results of Ocean Drilling Program Leg 167 was to reconstruct the Neogene history of biogenic calcium carbonate accumulation in the northeastern Pacific along the California margin (Lyle, Koizumi, Richter, et al., 1997). This aims to constrain inorganic carbon burial rates, deep-water hydrography in the North Pacific, and linkages between deep Atlantic and Pacific circulation and carbonate accumulation or dissolution patterns. Data are presented for four sites. Two of them are located in the California bight-East Cortez Basin (Site 1012: 32°16.970?N 118°23.024?W, 1773 m) and San Nicholas Basin (Site 1013: 32°48.040??, 118°53.992?W, 1564 m). The others are the dedicated Hole 1017E at Site 1017 (34°32.099?N, 121°6.430?W, 955 m) and Site 1019 in the Eel River Basin (41¢X40.972?N, 124°55.975?W, 977 m). Reconstruction of paleo-sea-surface temperatures (SST) by determining the alkenone unsaturation index of the extractable organic matter is an independent technique and helps to verify oxygen-isotope-based estimates. Results from the uppermost 600 cm of the dedicated Hole 1017E are expected to reveal the local temperature history of the last 30 k.y.

Carbonate chemistry, temperature and salinity of Lady Elliot Island Reef 2009-2010

Ocean acidification leads to changes in marine carbonate chemistry that are predicted to cause a decline in future coral reef calcification. Several laboratory and mesocosm experiments have described calcification responses of species and communities to increasing CO2. The few in situ studies on natural coral reefs that have been carried out to date have shown a direct relationship between aragonite saturation state (Omega arag) and net community calcification (Gnet). However, these studies have been performed over a limited range of Omega arag values, where extrapolation outside the observational range is required to predict future changes in coral reef calcification. We measured extreme diurnal variability in carbonate chemistry within a reef flat in the southern Great Barrier Reef, Australia. Omega arag varied between 1.1 and 6.5, thus exceeding the magnitude of change expected this century in open ocean subtropical/tropical waters. The observed variability comes about through biological activity on the reef, where changes to the carbonate chemistry are enhanced at low tide when reef flat waters are isolated from open ocean water. We define a relationship between net community calcification and Omega arag, using our in situ measurements. We find net community calcification to be linearly related to Omega arag, while temperature and nutrients had no significant effect on Gnet. Using our relationship between Gnet and Omega arag, we predict that net community calcification will decline by 55% of its preindustrial value by the end of the century. It is not known at this stage whether exposure to large variability in carbonate chemistry will make reef flat organisms more or less vulnerable to the non-calcifying physiological effects of increasing ocean CO2 and future laboratory studies will need to incorporate this natural variability to address this question.