Ocean accumulation

It is generally admitted that all these hydrocarbons derive from fossil organic substances synthesized by higher plants on land and by algae and plankton in the ocean, accumulated in depressions, partly modified by the... 

It is difficult to say from the 834S record of sedimentary sulfur-bearing minerals when the oceans accumulated significant oxidized sulfur. It is likely that the activity of photosynthetic green and purple sulfur-oxidizing bacteria produced the first free sulfate in the environment by reactions like... 

Organic Carbon and Productivity Of the total carbon fixed annually ( 120 X lO mol C yr ) nearly all is respired and oxidized. Only a very small fraction of the organic matter produced in the ocean accumulates in the sediments. On a geological time scale the organic carbon preserved in the sediments is eventually remineralized to CO2. 

Most commercial marine diatomite deposits exploit accumulations resulting from large blooms of diatoms that occurred ia the oceans during the Miocene geological epoch. Diatomite sediments older than the Jurassic period are rare in the fossil record. Commercial deposits of diatomite are accumulations of the fossil skeletons, which can occur in beds as thick as 900 m in some locations (5). Marine deposits must have been formed on the bottom of protected basins or other bodies of quiet water, undisturbed by strong currents, in an environment similar to the existing Santa Barbara Channel or Gulf of California (3,6). 

The formation and dissolution of CaCOa in the ocean plays a significant role in all of these effects (34)- CaCOa is produced by marine organisms at a rate several times the supply rate of CaCOa to the sea from rivers. Thus, for the loss of CaCOa to sediments to match the supply from rivers, most of the CaCOa formed must be redissolved. The balance is maintained through changes in the [COa] content of the deep sea. A lowering of the CO2 concentration of the atmosphere and ocean, for example by increased new production, raises the [COa] ion content of sea water. This in turn creates a mismatch between CaCOa burial and CaCOa supply. CaCOa accumulates faster than it is supplied to the sea. This burial of excess CaCOa in marine sediments draws down the [COa] - concentration of sea water toward the value required for balance between CaCOa loss and gain. In this way, the ocean compensates for organic removal. As a consequence of this compensation process, the CO2 content of the atmosphere would rise back toward its initial value. 

The sediment surface separates a mixture of solid sediment and interstitial water from the overlying water. Growth of the sediment results from accumulation of solid particles and inclusion of water in the pore space between the particles. The rates of sediment deposition vary from a few millimeters per 1000 years in the pelagic ocean up to centimeters per year in lakes and coastal areas. The resulting flux density of solid particles to the sediment surface is normally in the range 0.006 to 6 kg/m per year (Lerman, 1979). The corresponding flux density of materials dissolved in the trapped water is 10 to 10 kg/m per year. Chemical species may also be transported across the sediment surface by other transport processes. The main processes are (Lerman, 1979) ... 

Nearly all of the detrital particles sinking into the deep ocean decompose and release the associated P. A small percentage (approximately 8%), however, do survive and accumulate on the sea floor. This P is then buried in the sediments (F i) and represents the ultimate removal of P from the ocean. 

Estuaries exhibit physical and chemical characteristics that are distinct from oceans or lakes. In estuaries, water renewal times are rapid (10 to 10 years compared to 1 to 10 years for lakes and 10 years for oceans), redox and salinity gradients are often transient, and diurnal variations in nutrient concentrations can be significant. The biological productivity of estuaries is high and this, coupled with accumulation of organic debris within estuary boundaries, often produces anoxic conditions at the sediment-water interface. Thus, in contrast to the relatively constant chemical composition of the... 

It has been recognized for some time that fluids in motion, such as the atmosphere or the ocean, disperse added materials. This properly has been exploited by engineers in a variety of ways, such as the use of smoke stacks for boiler furnaces and ocean ontfalls for the release of treated wastewaters. It is now known that dilution is seldom the solution to an enviromnental problem the dispersed pollutants may accumulate to undesirable levels in certain niches in an ecosystem, be transformed by biological and photochemical processes to other pollntants, or have nnanticipated health or ecological effects even at highly dilute concentrations. It is therefore necessary to rmderstand the transport and transformation of chemicals in the natural environment and through the trophic chain ctrlminating in man. 

Bulk rock chemistry of hydrothermally altered midoceanic ridge basalt has been well studied and used to estimate the geochemical mass balances of oceans today (Wolery and Sleep, 1976 Humphris and Thompson, 1978 Mottl, 1983). In contrast, very few analytical data on hydrothermally altered volcanic rocks that recently erupted at back-arc basins are available. However, a large number of analytical data have been accumulated on the hydrothermally altered Miocene volcanic rocks from the Green tuff region in the Japanese Islands which are inferred to have erupted in a back-arc tectonic setting (section 1.5.3). 

If Vtii/Ptii = 1 then the accumulation of °Thxs in marine sediments would provide an assessment of their sedimentation rate. For instance, if Pm is N dpm m yr , and N dpm are found in the upper 1 cm of 1 m of seafloor, then the sedimentation rate must be lcmyr Sedimentation rate is an important variable in paleoceanographic reconstruction as it provides the timescale for the continuous record of environmental change recorded in marine sediments. Sedimentation rate is also a key geochemical variable as sediments are the major sink for most chemical species in the ocean. A tool allowing assessment of past sedimentation rates is therefore an appealing prospect. 

Marcantonio F, Anderson RF, Higgins S, Stute M, Schlosser P, Kubik PW (2001b) Sediment focusing in the central equatorial Pacific Ocean. Paleoceanography 16(3) 260-267 Marcantonio F, Kumar N, Stute M, Anderson RF, Seidl MA, Schlosser P, Mix A (1995) A comparative study of accumulation rates derived by He and Th isotope analysis of marine sediments. Earth Planet. Sci. Letters 133 549-555... 

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