The isotopic composition of reduced organic carbon

The subterranean estuary: a reaction zone of ground water and sea water

Present-day production of CaCO3 in tne world ocean is calculated to be about 5 billion tons (bt) per year, of which about 3 bt accumulate in sediments; the other 40% is dissolved. Nearly half of the carbonate sediment accumulates on reefs, banks, and tropical shelves, and consists largely of metastable aragonite and magnesian calcite. Deep-sea carbonates, predominantly calcitic coccoliths and planktonic foraminifera, have orders of magnitude lower productivity and accumulation rates than shallow-water carbonates, but they cover orders of magnitude larger basin area. Twice as much calcium is removed from the oceans by present-day carbonate accumulation as is estimated to be brought in by rivers and hydrothermal activity (1.6 bt), suggesting that outputs have been overestimated or inputs underestimated, that one or more other inputs have not been identified, and/or that the oceans are not presently in steady state. One “missing” calcium source might be groundwater, although its present-day input is probably much smaller than that of rivers. If, as seems likely, CaCO3 accumulation presently exceeds terrestial and hydrothermal input, this imbalance presumably is offset by decreased accumulation and increased input during lowered sea level: shallow-water accumulation decreases by an order of magnitude with a 100 m drop in sea level, while groundwater influx increases because of heightened piezometric head and the diagenesis of metastable aragonite and magnesian calcite from subaerially exposed shallow-water carbonates.

Production and accumulation of calcium carbonate in the ocean: Budget of a nonsteady state

The exchange of groundwater between land and sea is a major component of the hydrological cycle. This exchange, called submarine groundwater discharge (SGD), is comprised of terrestrial water mixed with sea water that has infiltrated coastal aquifers. The composition of SGD differs from that predicted by simple mixing because biogeochemical reactions in the aquifer modify its chemistry. To emphasize the importance of mixing and chemical reaction, these coastal aquifers are called subterranean estuaries. Geologists recognize this mixing zone as a site of carbonate diagenesis and dolomite formation. Biologists have recognized that terrestrial inputs of nutrients to the coastal ocean may occur through subterranean processes. Further evidence of SGD comes from the distribution of chemical tracers in the coastal ocean. These tracers originate within coastal aquifers and reach the ocean through SGD. Tracer studies reveal that SGD provides globally important fluxes of nutrients, carbon, and metals to coastal waters.

https://moritz.botany.ut.ee/~olli/eutrsem/Moore_2010.pdf

The Effect of Submarine Groundwater Discharge on the Ocean

X-ray Diffraction Procedures for Clay Mineral Identification

The first broad program of scientific shallow drilling on the U.S. Atlantic continental shelf has delineated rocks of Pleistocene to Late Cretaceous age, including phosphoritic Miocene strata, widespread Eocene carbonate deposits that serve as reflective seismic markers, and several regional unconformities. Two sites, off Maryland and New Jersey, showed light hydrocarbon gases having affinity to mature petroleum. Pore fluid studies showed that relatively fresh to brackish water occurs beneath much of the Atlantic continental shelf, whereas increases in salinity off Georgla and beneath the Florida-Hatteras slope suggest buried evaporitic strata. The sediment cores showed engineering properties that range from good foundation strength to a potential for severe loss of strength through interaction between sediments and man-made structures.

U.s. Geological survey core drilling on the atlantic shelf.

In some calcium carbonate-bearing sandstones from the edge of the continental shelf off the northeast United States, the δC 13 range is from -30 and -60 per mil for both aragonite and high-magnesium calcite. The δC 13 of co-existing shells of Modiolus sp. is normal (+ 1.7 to -2.7 per mil). The δO 18 values of around + 3.5 per mil in all samples suggest deposition at temperatures around 0°C. Quaternary methane oxidized either chemically or microbiologically to carbon dioxide is the probable source of carbon in these carbonates.

John C. Hathaway

Papers

U.s. Geological survey core drilling on the atlantic shelf.

Methane-derived marine carbonates of pleistocene age.

A restudy of stevensite and allied minerals

Palygorskite: New X-Ray data

Regional Clay Mineral Fades in Estuaries and Continental Margin of the United States East Coast