996 resultados para Calcium carbonate


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Physical properties measurements provide a relatively inexpensive and fast way to obtain high-resolution estimates of the variations in sedimentological properties. To better resolve the validity and cause of the geophysical signals measured by the Ocean Drilling Program (ODP) shipboard multisensor track (MST) instruments, 223 x 10 cm**3 core samples were collected at 4 cm intervals in Core 167-1016B-17H at the California Margin Conception Transect for the measurements of index properties, carbonate content, and opal content. This core was chosen because hole-to-hole stratigraphic correlation of MST data suggested that Core 17H corresponds to a depth interval that displays the greatest range of amplitude of many physical properties.

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Site 722 provides high resolution records of percent CaCO3, magnetic susceptibility, d18O, organic carbon, and coarse fraction for the past 3.4 m.y. from the crest of the Owen Ridge, northwestern Arabian Sea. Within this time interval, most of the carbonate percent variations can be attributed to terrigenous dilution and do not reflect changes in the carbonate system. From the late Pliocene to Present, the average rate of calcium carbonate accumulation increases from 1 to 3 g/cm**2/k.y. and the average accumulation of organic carbon decreases from 75 to 30 mg/cm**2/k.y. The carbonate component is more dissolved in the older interval. The long-term variations in carbonate accumulation may reflect a greater input of organic matter in the late Pliocene, which decomposes to produce CO2 and dissolve carbonate. Magnetic susceptibility and % noncarbonate (100 - CaCO3%) reflect changes in the amount of the lithogenic component in the sediments. The period of variation of lithogenic material is the same period as the original forcing of the regional summer monsoon, however, the timing matches global aridity patterns and global ice volume (sea level) changes. This preliminary analysis suggests that the high frequency variation of lithogenic material persists for at least the last 3.4 m.y. Within the last million years, calcium carbonate accumulation has a large amplitude signal that covaries with major changes in ice volume. Both calcium carbonate and noncarbonate (mostly terrigenous) accumulation are greatest during glacial stages. Interglacial intervals are characterized by low mass accumulation rates, increased foraminifer fragmentation, and increased opal concentration. The accumulation of organic carbon matches the high frequency changes in sedimentation rates. We attribute this high correlation to enhanced preservation of organic carbon by increased sedimentation rate. Of the three major biological components studied, only opal exhibits the variations expected for a biological productivity system forced by monsoonal upwelling driven by changes in northern hemisphere summer radiation.

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A total of 776 sediment samples were measured for percent CaCO3 using a coulometer. These data are compared with percent blue reflectance (450-550 nm) measured with the Oregon State University split-core analysis track. In previous studies percent blue reflectance has been an excellent proxy for percent CaCO3 and in this study shows many of the main depositional trends (i.e., a 100-k.y. cycle, with a 55% reflectance range is evident in the upper 900 k.y., underlain by sediments exhibiting a 40-k.y. cycle with only a 30% reflectance range). Between ~21 and 5 Ma the average percent reflectance decreases from ~35% to ~8%. A similar decrease is also recorded between ~24 and 22 Ma. Percent CaCO3 trends closely match those of the percent blue spectral reflectance. This is especially well shown in the 100-k.y. cyclicity and in the interval between 24.5 and 21.5 Ma. In both intervals CaCO3 analyses are abundant. An exception occurs in the interval between 2 and 5 meters composite depth (~193 and 240 k.y.). There, percent CaCO3 and percent reflectance are out of phase. The lack of agreement is not likely to be due to a very wet core, in which water would dominate the spectral reflectance instead of sediment, or to problems with the composite depth slice. The discrepancy remains unexplained and provides clear evidence that when noninvasive measurements are used as proxies for chemical measurements they must be substantiated by the actual chemical or physical measurements.

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