In situ tensile fracture toughness of surficial cohesive marine sediments

This study reports the first in situ measurements of tensile fracture toughness, K _IC, of soft, surficial, cohesive marine sediments. A newly developed probe continuously measures the stress required to cause tensile failure in sediments to depths of up to 1 m. Probe measurements are in agreement with standard laboratory methods of K _IC measurements in both potter’s clay and natural sediments. The data comprise in situ depth profiles from three field sites in Nova Scotia, Canada. Measured K _IC at two muddy sites (median grain size of 23–50 μm) range from near zero at the sediment surface to >1,800 Pa m^1/2 at 0.2 m depth. These profiles also appear to identify the bioturbated/mixed depth. K _IC for a sandy site (>90% sand) is an order of magnitude lower than for the muddy sediments, and reflects the lack of cohesion/adhesion. A comparison of K _IC, median grain size, and porosity in muddy sediments indicates that consolidation increases fracture strength, whereas inclusion of sand causes weakening; thus, sand-bearing layers can be easily identified in K _IC profiles. K _IC and vane-measured shear strength correlate strongly, which suggests that the vane measurements should perhaps be interpreted as shear fracture toughness, rather than shear strength. Comparison of in situ probe-measured values with K _IC of soils and gelatin shows that sediments have a K _IC range intermediate between denser compacted soils and softer, elastic gelatin.     

Sulfate reduction in deep coastal marine sediments

Sulfate reduction rates in sediments of four deep stations in the Saguenay Fjord and the Laurentian Trough, Gulf of St. Lawrence, are among the lowest reported for the coastal environment. Maximum rates were 0.4–7.0 nmol cm⁻³ day⁻¹. The low rates are due to relatively low sedimentation rates and continuously low temperatures. Regional differences in both integrated and maximum sulfate reduction rates in the sediment correlate with sediment trap measurements of sedimentation rate and organic carbon flux.Sulfate reduction accounts for the degradation of 5–26% of the estimated downward flux of organic matter to these sediments. Unlike the absolute rate of sulfate reduction, the relative proportion of the carbon flux that is degraded via sulfate reduction is not directly correlated with the sedimentation rate but is a function of organic matter composition, intensity of bioturbation, and the abundance of sub-oxic electron acceptors. Thus, the lowest proportion of carbon degradation via sulfate reduction occurred at a Gulf site, where a combination of low sedimentation and bioturbation rates allowed a long residence time for organic matter near the sediment surface and, in consequence, a low flux of labile carbon into the sulfate reduction zone. The highest proportion was observed at a station with a similar organic carbon flux but with higher rates of sedimentation and bioturbation. At a third site, with the highest rates of sulfate reduction as well as the highest rates of sedimentation and bioturbation, the contribution of sulfate reduction to organic matter degradation was only intermediate. This is attributable to the exhaustion of the supply of porewater sulfate. In deep coastal environments the proportion of organic matter degraded via sulfate reduction can be highly variable both spatially and temporally.     

海底沉积物声学性质原位测量系统海上试验研究

提出了一种新的海底沉积物声学性质原位测量方法,介绍了新研制的海底沉积物声学性质原位测量系统。在青岛近海海域对该系统进行了海试,获得了各个站位的声速数据。将测得的各站位的声速与不同海域的沉积物声速进行对比分析,并对各个站位的声速与沉积物的平均粒径进行了相关性分析,发现与以往研究结果一致,沉积物声速与沉积物类型相关,不同类型的沉积物的声速有明显差异;声速与平均粒径相关性较好,粒径越大,声速越高。结果表明,利用海底沉积物声学性质原位测量系统测得的原位声速是正确的,它能快速准确地得到海底沉积物的声速值。     

Geotechnical sampling and testing of gas-charged marine sediments atin situ pressures

Gas-charged marine sediments were sampled using a pressure core barrel and a new technique involving standard wireline sampling procedures. Pressure core barrel sampling provides sediments atin situ pressures with no degassing. Analysis of gas content, geotechnical properties and microfabric were performed for samples atin situ pressures and compared with degassed results. Methane concentrations ranged from 3,450 to 137,140 ppm for pressurized samples. Microfabric analyses reveal highly nonoriented clay particles and grains in degassed samples. Degassing of these methane-rich sediments increases porosities and compression indices, while reducing undrained shear strengths and computed preconsolidation pressures.     

Seasonal changes of concentrations of inorganic and organic nitrogen in coastal marine sediments

The seasonal fluctuations of the concentration of nitrogenous compounds in sediments was investigated for three regions of the Seto Inland Sea in Japan; the variation of nitrogenous compounds in sediments was also studied in a laboratory experiment.The amounts of ammonium, dissolved organic nitrogen, nitrite and nitrate, as percentages of the dissolved total nitrogen of the interstitial water, were in the ranges of 47–99%, 10–50%, 0·1–0·6% and 0·3–4·1%, respectively. Ammonium was the major component and organic nitrogen was the next most important. The concentrations of these nitrogenous compounds changed seasonally: dissolved total nitrogen was higher in the warm month of September than in May; ammonium increased in warm months and decreased in cold months, but nitrite and nitrate increased in cold months. It was possible to explain the seasonal fluctuation of nitrogenous compounds in terms of the rates of the metabolic pathways of nitrogen in the sediments.Ammonium was not necessarily correlated with dissolved organic nitrogen. From this, it was considered that ammonium did not occur from solubilization of particulate organic nitrogen followed by mineralization, but from direct mineralization of particulate organic nitrogen in sediments.For the sediments of Suho Nada, Hiuchi Nada and station B-47 in Beppu Bay, the ratio of dissolved ammonium to adsorbed ammonium in the sediments was in the range 10–25%, but the ratio was 60–70% of adsorbed ammonium in the considerably anaerobic sediments at station B-45 in Beppu Bay. The ratio of dissolved ammonium to adsorbed ammonium increased with the increase of the concentration of sulfide in sediments. It was recognized that the anaerobic conditions of the sediments led to the dissolution of adsorbed ammonium.     

Assessment of copper,cadmium and zinc remobilization in Mediterranean marine coastal sediments

The remobilization of copper, cadmium and zinc in sediments of three selected coastal microenvironments of the Aegean Sea (Eastern Mediterranean) is assessed. Various analytical methods and techniques were employed providing concentrations, profiles and forms of metals and organic matter in sediments and pore waters.     

In situ velocity profiles in gassy sediments: Kiel Bay

Acoustic behavior of gas-bearing sediments is significantly different from that of gas-free sediments. In situ velocity profiles and acoustic signal characteristics in gas-bearing sediments of the upper several meters of the sea floor in Kiel Bay are presented in this study. Observed velocities in gas-bearing sediments are both higher and lower than those of the gas-free sediments. Small amounts of gas appear to cause signal reverberation without much attenuation. whereas large amounts of gas cause substantial attenuation.     

In situ measurements of near-surface porosity in shallow-water marine sands

An in situ resistivity profiler was developed to measure with minimal disruption, the near-surface porosity of shallow-water marine sands. Results from a siliciclastic site off NW Florida and two Bahamian carbonate sites (an ooid shoal and coral reef sand flat) suggest the following general features. First, there is a 5- to 15-mm thick zone of elevated porosity adjacent to the sediment-water interface. Porosity in this layer was from 0.05 to 0.25 (decimal porosity) greater than the subjacent values, and would be difficult to resolve using traditional measurement techniques. Second, average porosity at >10-mm depth was 0.38 /spl plusmn/ 0.01 at the siliciclastic site, 0.39 /spl plusmn/ 0.01 at the ooid shoal site, and 0.49 /spl plusmn/ 0.02 at the coral reef sand flat site; consistent with literature values. Third, individual profiles exhibited 0.05-0.15 fluctuations about the mean, with vertical length scales of 5-15 mm. These fluctuations may be the result of grain packing heterogeneities caused by hydrodynamic sorting during deposition and subsequent physical and biological mixing or could be artifacts caused by disruption of the grain framework. Fourth, ripple troughs at the siliciclastic sand site had a significantly higher near-surface porosity compared to ripple crests, due most likely to the presence of detrital material in the troughs.     

A comparison of non-hydrolytic methods for extracting amino acids and proteins from coastal marine sediments

Advances in analytical techniques now allow for the potential analysis of intact peptides and proteins isolated from marine sediments. However, there is no established technique for the extraction of macromolecular materials from marine sediments. Six different methods for extracting the amino acid component from coastal marine sediments were compared to the standard hot acid hydrolysis technique for their percent recovery and amino acid composition. The standard hot acid hydrolysis on dried, whole sediments released the greatest concentration of total amino acids (PS-THAA; 3.52 mg gdwt^− 1 ± 10% (SMD)), yet this only accounted for 22% of the total nitrogen in Puget Sound sediments (Washington, USA). Repeated hydrolysis of the same samples did not improve the recovery of nitrogen by more than an additional 10%. Base extraction (0.5 N NaOH) was the second best method for recovering amino acid nitrogen, releasing 60% of the Puget Sound total hydrolyzable amino acids (PS-THAA) (corresponding to 13% of the total sedimentary nitrogen), and has the advantage that it does not rely on peptide hydrolysis to free the nitrogenous component from the sediment matrix. The amino acid distribution of the 0.5 N NaOH extract was not significantly different than the initial THAA. Other non-hydrolyzing methods released lower yields of amino acids (Triton X-100 ≥ hot water > 50 mM NH₄HCO₃ > HF), but might prove to be of use to investigators interested in specific fractions of sedimentary organic nitrogen because these four methods had distinctly different amino acid compositions (enrichments in basic amino acids and depletions in acidic amino acids). Treatments with HF both before and after traditional hydrolysis and/or extractions with base did not release any more of the sedimentary nitrogen. Our results are consistent with the hypothesis that a large fraction of the sedimentary nitrogen (TN) is protected within an organic matrix.     

Scoping the effective marine environmental assessment of dredging and ocean disposal of coastal sediments in Korea

The application of scoping is reviewed to improve the efficiency and rationality of the marine environmental impact assessment system applied to the dredging of coastal sediments and the oceanic disposal of dredged material in Korea. Both the impact levels and those items requiring assessment vary in response to differing goals of the coastal activities involved and also to changes in the characteristics of different marine environments. As a consequence, different assessment fields need to be emphasized for evaluation of the impact that both dredging and dumping might have on the sites involved. The status of current assessment procedures is examined and its problems are diagnosed. Following a survey of interested parties and a review of case studies of the oceanic disposal of dredged sediment in other countries, checklists of core assessment items are proposed as part of a revamped review process, along with improvements to the assessment system.     

Molecular weight and trace metal distributions in fulvic and humic acid fractions of coastal marine sediments

Molecular weight and trace metal distributions of fulvic and humic acid fractions of marine sediments from the Seto Inland Sea were investigated by using a gel filtration technique in combination with atomic absorption and emission spectrometries. A binary molecular weight distribution was found both in the fulvic acid fraction and in the humic acid fraction. The fulvic acid fractions with molecular weights of less than 1.5×10³ and of 5×10³?10⁴ accounted for 38–57 % and 25–41 % of the total fulvic acids, respectively, and the humic acid fractions with molecular weights of 10²?10⁴ and of over 2×10⁵ accounted for 58–73 % and 16–27 % of the total humic acids, respectively. The components with molecular weights of over 1.5×10³ contained 54 %, on average, of the Fe, Zn and Cu in the fulvic acid fraction, and the components with molecular weights of over 10⁴ contained 58 %, on average, of these metals in the humic acid fraction.     

Hydrocarbons in Washington coastal sediments

The sources and distributions of polycyclic aromatic hydrocarbons (PAH) and aliphatic hydrocarbons are characterized in seventeen sediments from a highly river-influenced sedimentary environment off the southwestern coast of Washington. The major hydrocarbons are land-derived, introduced as preformed compounds and display long-term stability in sediment cores. A series of PAH of anthropogenic origin and two naturally derived compounds, retene and perylene, dominate the PAH composition in these sediments. Plantwax n-alkanes are the major aliphatic hydrocarbon constituents. Aliphatic hydrocarbons of marine origin, pristane and a series of four acyclic, multibranched C₂₅ polyolefins, are also observed in many sediments. The concentrations of these marine-derived hydrocarbons decrease to negligible levels rapidly with sediment depth from the sea-sediment interface, suggesting degradation.In general, the major land-derived hydrocarbons are concentrated in the midshelf silt deposit which extends northwestward along the continental shelf from the Columbia River mouth. A quantitatively more minor, natural series of phenanthrene homologs, also of terrestrial origin, is preferentially advected further offshore and deposited in continental slope sediments. These distributions are consistent with recognized particle associations for these compounds and sediment dispersal processes in this coastal environment. Sediment core records suggest the present pattern of dispersal has persisted for at least the past century and possibly since the Late Pleistocene.     

Grain-size parameters of marine sediments

In their average grain-size parameters (K _d , K _dl), recent sediments of the northern Caspian Sea and the Barents Sea shelf are similar, while the sediments of the Norwegian Sea are closer to their counterparts of the World Ocean. Seaward, the content of the subcolloidal fraction increases against the background of the decreasing proportions of coarse-and medium-grained pelite matter.     

Acoustic impedance of marine sediments

A heavy walled steel tube has been used as an impedance tube for measuring the acoustic impedance of marine sediments. The acoustic characteristics of the water filled tube were found to be satisfactory for the measurements. Values of acoustic velocity and attenuation in the sediments were determined from the acoustic impedance measurements and found to agree with previously published data.     

Evaluation of the indophenol method to measure NH4 in extracts from coastal marine sediments

It has been found that the measurement of NH₄⁺ in extracts of marine sediments was influenced by factors which inhibit the indophenol colour development, and through gel chromatography, diffusion, dilution and internal standard assays, it was possible to determine the extent of this interference. The measurement of NH₄⁺ in KCl extracts and porewater, using internal standards, indicated that colour development was inhibited 13% and 51%, respectively. Dilution of samples alleviated this inhibition, but more than five-fold dilution was necessary for some extracts. Diffusion of NH₃, collection and measurement generally gave concentrations comparable with those derived from the use of internal standards. These data suggest that the indophenol reagents should be added to sufficient diluted sediment extracts or to diffusates from extracts, to prevent interference to the colour development of NH₄⁺.     

The consolidation of soft marine sediments

This paper outlines the governing relationships of nonlinear finite strain consolidation. A short review of current literature is presented. Nonlinear finite strain consolidation theory is applied to the analysis of the slow deposition of Gulf of Mexico Holocene sediments. It is shown that the conventional means of calculating rates of sediment accumulation are highly inaccurate. It is further shown that the state of effective stress and excess pore-water pressure, as calculated by nonlinear finite strain theory, is substantially different than when calculated by conventional Terzaghi-Frohlich theory.     

In situ hydrocarbon concentrations from pressurized cores in surface sediments, Northern Gulf of Mexico

Two newly developed coring devices, the Multi-Autoclave-Corer and the Dynamic Autoclave Piston Corer were deployed in shallow gas hydrate-bearing sediments in the northern Gulf of Mexico during research cruise SO174 (Oct–Nov 2003). For the first time, they enable the retrieval of near-surface sediment cores under ambient pressure. This enables the determination of in situ methane concentrations and amounts of gas hydrate in sediment depths where bottom water temperature and pressure changes most strongly influence gas/hydrate relationships. At seep sites of GC185 (Bush Hill) and the newly discovered sites at GC415, we determined the volume of low-weight hydrocarbons (C₁ through C₅) from nine pressurized cores via controlled degassing. The resulting in situ methane concentrations vary by two orders of magnitudes between 0.031 and 0.985 mol kg^− 1 pore water below the zone of sulfate depletion. This includes dissolved, free, and hydrate-bound CH₄. Combined with results from conventional cores, this establishes a variability of methane concentrations in close proximity to seep sites of five orders of magnitude. In total four out of nine pressure cores had CH₄ concentrations above equilibrium with gas hydrates. Two of them contain gas hydrate volumes of 15% (GC185) and 18% (GC415) of pore space. The measurements prove that the highest methane concentrations are not necessarily related to the highest advection rates. Brine advection inhibits gas hydrate stability a few centimeters below the sediment surface at the depth of anaerobic oxidation of methane and thus inhibits the storage of enhanced methane volumes. Here, computerized tomography (CT) of the pressure cores detected small amounts of free gas. This finding has major implications for methane distribution, possible consumption, and escape into the bottom water in fluid flow systems related to halokinesis.     

Input of atmospheric lead to marine sediments in a south-east Pacific coastal area (approximately 36 degrees S)

Atmospheric input of Pb to coastal sediments in the south-east Pacific (approximately 36 degrees S) was estimated using: (1) a salt marsh (non-local emission sources) as a natural collector of atmospheric fluxes and (2) Pb concentrations in rain and air samples, both considered to be representative of the atmospheric input in the study area. A radioisotopic geochronology technique ((210)Pb) was used to estimate the total Pb atmospheric supply to the sediments. The results show that atmospheric input to Concepción Bay accounts for 13-68% of Pb in near shore sediments, evaluated through salt marsh and rain, both showing comparable results. Consequently, there are other relevant Pb sources to explain the higher concentrations in this area. Sediments in the shelf are subject to important influence of upwelling waters, estimated by Salamanca [Sources and sinks of (210)Pb in Concepción Bay, Chile (1993) PhD thesis, Marine Science Research Center, State University of New York at Stony Brook, USA] using (210)Pb. The atmospheric input, however, is mainly responsible for the total Pb input, since the salt marsh (natural atmospheric collector) shows similar Pb(xs) inventories than the shelf, corresponding to a regional-scale Pb emissions.