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C.S. Martens

Publications and source records attributed to C.S. Martens.

5 recordsLinked to original sources
USGS2001

Overview of SAX99: Environmental considerations

A 1-km2 area located 2 km off the Florida Pan-handle (30??22.6???N; 86??38.7???W) was selected as the site to conduct high-frequency acoustic seafloor penetration, sediment propagation, and bottom scattering experiments [1]. Side scan, multibeam, and normal incidence chirp acoustic surveys as well as subsequent video surveys, diver observations, and vibra coring, indicate a uniform distribution of surficial and subbottom seafloor characteristics within the area. The site, in 18-19 m of water, is characterized by 1-2-m thick fine-to-medium clean sand and meets the logistic and scientific requirements specified for the acoustic experiments. This paper provides a preliminary summary of the meteorological, oceanographic, and seafloor conditions found during the experiments and describes the important physical and biological process that control the spatial distribution and temporal changes in these characteristics.

IEEE Journal of Oceanic Engineering↗
USGS1993

Sulfur isotope and porewater geochemistry of Florida escarpment seep sediments

Distributions of porewater constituents, SO 4 = , NH 4 + , Cl − , ∑CO 2 , and H 2 S, solid phase iron, and sulfur concentrations, and the sulfur isotopic composition of dissolved and solid phases were investigated in sediments from abyssal seeps at the base of the Florida escarpment. Despite the apparent similarity of seep sediment porewater chemistry to that of typical marine sediments undergoing early diagenesis, relationships between chemical distributions and isotopic measurements revealed that the distribution of pore fluid constituents was dominated by processes occurring within the platform rather than by in situ microbial processes. Ammonium and sulfate concentrations were linearly correlated with chloride concentrations, indicating that variations in porewater chemistry were controlled by the admixture of seawater and a sulfate depleted brine with a chlorinity of 27.5 ± 1.9%. and 2.2 ± 1.3 mM ammonium concentration. At sites dominated by seepage, dissolved sulfate isotopic composition remained near seawater values despite depletion in porewater concentrations. Porewater ∑CO 2 concentrations were found to be elevated relative to seawater, but not to the extent predicted from the observed sulfate depletion. Sediment solid phase sulfur was predominantly pyrite, at concentrations as high as 20% S by weight. In contrast to typical marine deposits, pyrite concentrations were not related to the quantity of sedimentary organic matter. Pyrite δ 34 S values ranged from −29%. to + 21%. (CDT). However, only positive δ 34 S values were observed at sites associated with high pyrite concentrations. Isotopically heavy pyrite was observed at sites with porewater sulfate of seawater-like isotopic composition. Isotopically light pyrite was associated with sites where porewater sulfate exhibited δ 34 S values greater than those in seawater, indicating the activity of in situ microbial sulfate reduction. Thus, dual sulfide sources are suggested to explain the range in sediment pyrite isotopic composition: a δ 34 S enriched (+10 to +20%.) source adverted from within the Florida platform, and a lighter 34 S depleted component generated in situ from microbial reduction of seawater sulfate. The degree of pyritization of seep sediments was as high as 0.9 and was controlled by pyrite concentrations, which varied over a wider range than did the non-pyrite solid phase iron concentrations. The highest non-sulfide solid phase iron concentrations were observed in sediments that are believed to be at the “front” of the advancing seep fluids (i.e., hemipelagic sediments newly exposed to the seep fluids), indicating that dissolution of hemipelagic background sediment may be the source of at least half of the iron to the highly pyritized seep sediments. Porewater sulfide concentrations were variable, reaching a maximum of 5.7 mM, and were not correlated with the degree of pyritization of the sediments, suggesting that iron was not particularly limiting to pyrite formation.

Geochimica et Cosmochimica Acta↗
USGS1987

Biogeochemical cycling in an organic-rich coastal marine basin. 7. Sulfur mass balance, oxygen uptake and sulfide retention

Sulfur and oxygen fluxes were quantified in the seasonally varying anoxic marine sedimentary system of Cape Lookout Bight, N.C., U.S.A. Over the three year study period, 1981–1983, the mean annual sulfate reduction rate was determined to be 18.2 ± 1.6 moles · m −2 · y −1 . This value, added to the estimate of the detrital sulfur input of 1.2 ± 4.4 gave a total sulfur input of 19.4 ± 4.7 moles · m −2 · y −1 . The sulfide flux to the sediment-water interface, measured in anaerobic benthic chambers was 4.6 ± 0.5 moles · m −2 · y −1 , and represented 37% of the annual oxygen uptake rate of 25.2 ± 2.8 moles · m −2 · y −1 . The sulfide burial rate, determined to be 15.5 ± 3.1 moles · m −2 · y −1 , was within 5% of the value predicted by summing the fluxes at the sediment-water interface. The C S "> CS weight ratio of sediment below the depth of diagenetic reaction was determined to be 2.75. The sulfide retention rate in these rapidly accumulating sediments (10 cm/yr) was 77 ± 19%. Comparison of this result with previous studies shows that rapid sediment accumulation and the lack of bioturbation control this unusually high degree of sulfide retention.

Geochimica et Cosmochimica Acta↗
USGS1987

Biogeochemical cycling in an organic-rich coastal marine basin. 8. A sulfur isotopic budget balanced by differential diffusion across the sediment-water interface

The sulfur isotopic composition of the sulfur fluxes occurring in the anoxic marine sediments of Cape Lookout Bight, N.C., U.S.A., was determined, and the result of isotopic mass balance was obtained via the differential diffusion model. Seasonal pore water sulfate δ 34 S measurements yielded a calculated sulfate input of 0.6%.. Sulfate transported into the sediments via diffusion appeared to be enriched in the lighter isotope because its concentration gradient was steeper, due to the increase in the measured isotopic composition of sulfate with depth. Similarly, the back diffusion of dissolved sulfide towards the sediment-water interface appeared enriched in the heavier isotope. The isotopic composition of this flux was calculated from measurements of the δ 34 S of dissolved sulfide and was determined to be 15.9%.. The isotopic composition of buried sulfide was determined to be −5.2%. and the detrital sulfur input was estimated to be −6.2%.. An isotope mass balance equation based upon the fluxes at the sediment-water interface successfully predicted the isotopic composition of the buried sulfur flux within 0.5%., thus confirming that isotopes diffuse in response to their individual concentration gradients.

Geochimica et Cosmochimica Acta↗