Hydrocarbons in western North Atlantic surface sediments

High concentrations of hydrocarbons (500–3000 μg/g dry weight) together with a complex and wide molecular weight range of composition, and low ¹⁴C activity of δ¹⁴C = ?833 ± 50%. strongly indicate that fossil fuel hydrocarbons make up the bulk of hydrocarbons in and near the New York Bight dump site areas. The composition and concentrations of hydrocarbons in Hudson Channel sediments suggest some transport of dump site hydrocarbons to areas in the channel midway to the edge of the continental shelf. Sediments at 16 stations in other areas of the continental shelf, continental slope and abyssal plain have hydrocarbon concentrations and compositions indicating that no more than 1 μg/g dry weight of fossil fuel hydrocarbons are present.N-alkanes from land sources were among the most predominant hydrocarbons in all samples except those in the New York Bight region. Their presence in abyssal plain surface sediments documents transport of some land derived organic matter to these deep ocean areas. Two 25-carbon cycloalkenes are among the more predominant hydrocarbons in continental shelf surface sediments except for the dump site areas. These two compounds are present in lower concentrations in slope sediments and are not detected in abyssal plain sediments.     

Hydrocarbons in age-dated sediment cores from two basins in the Southern California Bight

The distributions of hydrocarbons in sediment cores dated by ²¹⁰Pb (1845–1977) from San Pedro and San Nicolas Basins in the Southern California Bight have been determined by gas Chromatographic and combined gas chromatographic-mass spectrometric analysis. The chromatograms of the hydrocarbons contain peaks of resolved alkanes and cycloalkanes, as well as an unresolved complex mixture which decrease in content with increasing depth in both of the cores. The concentrations of o,p' andp,p'-DDE are highest in the top 50 mm of the San Pedro core section. The 45–50 mm segment of this core was deposited in the 1945–1950 period when DDT (the precursor of DDE compounds) came into common use. The relatively high content of hydrocarbons and DDE in this core is attributable to the proximity of the site to the San Pedro Harbor which receives petroleum residues from shipping, sewage outfalls and industrial effluents. The presence of only traces of DDE throughout the San Nicolas core, and the low hydrocarbon content are explainable by the greater distance of this basin from anthropogenic inputs and probably a greater rate of degradation of deposited organic matter during bioturbation. δ¹³C, δ¹⁵N and electron-spin resonance analyses of kerogens and humic substances in these cores, indicate that most of this organic matter in these sediments is of a marine origin.     

Cluster analysis of marine sediments and waste deposits in New York bight

Cluster analysis of some chemical characteristics of marine sediments and associated waste deposits in the New York Bight reveals the existence of four cluster facies. Cluster facies I is the sediment containing dredged wastes from New York Harbor. Cluster facies II is the widespread sand and gravel deposit of the continental shelf. Cluster facies III is the finergrained material in the Hudson Channel and the material accumulated in the sewage sludge disposal area. Cluster facies IV is not easily identified; it may correspond to some relict sedimentary feature in the area. Editor's Note: Ali is now with the Department of Geology and Geophysics, Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543; Gross is now with Chesapeake Bay Institute. The Johns Hopkins University, Baltimore, Maryland 21218.     

Characterization and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in sediments in the Yellow River Estuary, China

Concentrations and sources of polycyclic aromatic hydrocarbons (PAHs) were investigated in surface sediments of the Yellow River Estuary (YRE). The isobath-parallel tidal and residual currents play important roles in the variation of PAH distribution, such that the contamination level of PAHs in fine-grained sediments is significantly higher than in the relatively coarse grain size sediments. Both diagnostic ratios and principal component analysis (PCA) with multivariate linear regression (MLR) were used to apportion sources of PAHs. The results revealed that pyrogenic sources are important sources of PAHs. Further analysis indicated that the contributions of coal combustion, traffic-related pollution and mixed sources (spills of oil products and vegetation combustion) were 35, 29 and 36 %, respectively, using PCA/MLR. Pyrogenic sources (coal combustion and traffic-related pollution) contribute 64 % of anthropogenic PAHs in sediments, which indicates that energy consumption could be a predominant factor in PAH pollution of YRE. Acenaphthylene and acenaphthene are the two main species of PAHs with more ecotoxicological concern in YRE.     

Biogenic and abiogenic polynuclear aromatic hydrocarbons in sediments from two remote Adirondack lakes

Sediment cores from Sagamore Lake and Woods Lake in New York State's Adirondack Park, an area remote from industrial activities, were analyzed for polynuclear aromatic hydrocarbons (PAH) by high resolution gas chromatography/mass spectrometry (GC/MS). Their composition and distribution with depth in the sediment indicate that the parental PAH in the surface sediments are primarily produced by anthropogenic combustion of fossil fuels. Perylene in deep sediments is apparently transformed from natural precursors in the reducing environment, however, the exact precursors remain unknown. The rather even sediment distributions of the non-parental PAH differ from the parental, suggesting biogenic origins. Based on their chemical structures, retene and alkylated and partially hydrogenated phenanthrenes are believed to be biogenically converted from abietic acid; hydrochrysenes and hydropicenes, from pentacyclic triterpenes.     

Polycyclic aromatic hydrocarbons (PAHs) and Pb isotopic ratios in a sediment core from Shilianghe Reservoir,eastern China: Implying pollution sources

The history records of polycyclic aromatic hydrocarbons (PAHs), lead and its stable isotope ratios were determined in a sediment core to receive anthropogenic impacts on the Shilianghe Reservoir in eastern China. The historical changes of PAHs concentrations, PAHs fluxes, Pb/Al and Pb isotope ratios showed a synchronous trend throughout the core, suggesting changes in energy usage and correlating closely with the experience of a rapid economic and industrial development of the catchment, Linyi City in eastern China. PAHs isomer ratios results reveal PAHs in sediments are dominantly anthropogenic pyrogenic source, dominated by the combustion of coal and biomass. Furthermore, the Pb isotopic composition also clearly indicates that coal combustion dust mainly contributed to the Pb burden in the reservoir sediments. Based on mix end member model of Pb isotope ratios, coal combustion dust dominated anthropogenic Pb sources over fifty years contributing from 31% to 62% of total Pb in sediment. And the contribution of leaded gasoline was low than average 25%. In addition, a stable increase of coal combustion source was found in sediment core, while the contribution of leaded gasoline had declined in recent decades, with the phase-out of leaded gasoline in China.     

Response of hepatic trace element concentrations in fish exposed to elemental and organic contaminants

Multivariate analysis of contaminant data from a multi-year monitoring program demonstrates alterations in the hepatic chemistry of metals in fish exposed to organic contaminants. Metals (Ag, As, Cd, Cu, Fe, Hg, Mn, Ni, Pb, Se, Sn, Zn) and organic chemicals (PCBs, DDTs, chlordanes, dieldrins, PAHs) were measured in liver and associated sediments for winter flounder (Pleuronectes americanus) from 23 sites along the northeast Atlantic coast and for Atlantic croaker (Micropogonias undulatus) from 30 sites along the southeast Atlantic and Gulf of Mexico coasts of the United States. Concentrations of habitat contaminants varied from nil to levels signifying important anthropogenic inputs and thus provided a range in chronic exposures and related contaminant stress levels with which to investigate the response of hepatic chemistry in fish representative of viable populations. The data, analyzed by principal component, principal component regression, and biplot procedures, demonstrated an opposing relationship between micronutrient elements, principally Zn, and exposure to organic contaminants in winter flounder. This relationship was not present in Atlantic croaker that were resident in less contaminated habitats. Based on median concentrations in sediment, exposure of winter flounder to important organic contaminants (polycyclic aromatic hydrocarbons, polychlorinated biphenyls, DDTs) exceeded that for Atlantic croaker by 7 to 50 times. Coincident with depletion of hepatic Zn and Cd in winter flounder was accumulation of Hg and Ag. My results, in agreement with those of others, implicate the negative effects of hepatic detoxification of organic contaminants on metal binding in liver, which can cause depletion of essential elements while contaminant and potentially toxic elements accumulate.     

Evaluation of hydrocarbon pollution in marine sediments of Sfax coastal areas from the Gabes Gulf of Tunisia,Mediterranean Sea

The Tunisian environmental legislation that follows the EC Directives requires monitoring of persistent, toxic and bio-accumulated substances commonly considered as hazardous substances. In order to comply with this requirement, samples of sea water, sediment and biota from the urbanized and industrialized coast line of Sfax city are investigated. This study presents the results of petroleum hydrocarbon content, distribution and probable origin (anthropogenic and/or biogenic) in 16 intertidal sediments of Sfax coastal area. Alkane distribution indices and hydrocarbon distribution patterns are used to identify natural and anthropogenic input. Non-aromatic hydrocarbons present a high concentration with a range varying from 180 to 1,400 μg/g of dry sediment. The total concentrations of polycyclic aromatic hydrocarbons (PAHs) varied from 0.41 to 5.6 μg/g dry weight. These concentrations are comparable to other marine areas that receive important inputs. n-Alkanes with carbon number ranging from 15 to 35 are identified to be derived from both biogenic and anthropogenic sources in varying proportions. Pristane/phytane ratio shows values lower than 1.4 suggesting the presence of petroleum contamination. This is confirmed by the presence of a large group of unresolved complex mixture and the identification of hopanes with predominant C29 and C30 compounds and steranes with predominance of C27 over C28 and C29 compounds. Ratios of selected PAH concentrations indicate petrogenic and pyrolytic origin of hydrocarbons. Anthropogenic hydrocarbon inputs were more apparent at sites associated with industrial discharges, shipping activities and sewage outfalls.     

The early diagenesis of aliphatic hydrocarbons and organic matter in sedimentary particulates from Dabob Bay,Washington

Aliphatic hydrocarbon compositions were quantitatively characterized in plankton, sediment trap-collected particulate materials and sediments from Dabob Bay using high resolution glass capillary gas chromatography. The average net accumulation of individual hydrocarbons measured in a 1-yr series of sediment traps was compared with the net accumulation of corresponding compounds measured in three depth intervals of ²¹⁰Pb-dated bottom sediments. Systematic and rapid decreases in the net accumulation of individual hydrocarbons were observed from the sediment traps to the sediments. Most pronounced decreases were measured for planktonically derived hydrocarbon constituents (e.g. pristane and two unsaturated compounds) which are rapidly remineralized at or near the sediment-water interface. Consequently, the amount of each compound measured in deposited sediments is not necessarily a quantitative indication of its initial flux to the sediments. The n-alkanes (C_25,27,29,31). characteristic of terrestrial plant waxes, are the predominant hydrocarbons measured by 4–6 cm depth in these sediments and show reasonably constant net accumulation below this interval.Significant diagenetic alteration of the bulk organic matter contained in the average sediment trap particulate material is also noted through comparison with bottom sediments on the basis of organic C/N and δ¹³C measurements. Organic matter elementally similar to marine plankton is preferentially remineralized upon deposition of the sedimentary particulates. The residual organic matter remaining and buried in the bottom sediments closely resembles terrestrial organic matter.     

Temporal trends of aliphatic and polyaromatic hydrocarbons in the Bohai Sea, China: Evidence from the sedimentary record

This work reports the historical trends and sources of aliphatic hydrocarbons (AHs) and polycyclic aromatic hydrocarbons (PAHs) in two ²¹⁰Pb dated sediment cores extracted from the central mud areas of Bohai Sea (Bohai). The TOC/TN ratio of the bulk organic matter (OM) and the composition of the n-alkanes suggest that the sedimentary organic matter was of mixed marine and terrigenous sources. The coarser sediment grain size and decreasing C/N ratios since ∼1976 could be attributed to the relocation of the Yellow River mouth causing a decreased influence of Yellow River derived sediments and associated OM into the central Bohai. The concentration of total 16 PAHs in the two cores ranged from 34.2-202 ng/g (mean, 91.5) for BC1, and from 53.3-186 ng/g (mean, 103) for BC2, with a high abundance of 2-3 ring PAHs. Perylene in the two cores mainly originated from terrigenous sources via riverine discharge and thus could be potentially related to changes in the sediment load from the Yellow River into the Bohai over time. Petroleum inputs could be revealed by ratios of methylphenanthrenes to phenanthrene (MP/P) and the patterns of more stable geochemical biomarkers (hopanes and steranes) along the two cores, in addition to the presence of unresolved complex mixtures (UCM) in the surface layers. Source diagnostic ratios of PAHs indicated a pyrogenic origin from biomass and coal combustion with a minor petroleum contribution. Downcore trends of compositional PAHs profiles were in agreement with the socio-economic development in China in the past decades. This temporal variation of sedimentary PAHs can also reflect a different evolution stage of energy structure in China as compared with those of the western developed countries.     

Geochemical fractionation of manganese in the Riogrande II reservoir, Antioquia, Colombia

The Riogrande II reservoir in Colombia has a total storage capacity of 240 million m³ and lies 2,270 m above sea level. The reservoir is used for power generation, water supply and environmental improvement. Dissolved manganese (Mn) is removed from reservoir water dedicated to domestic use by purification processes. Removal of Mn, however, poses a major challenge to purification processes and warrants the study of ways to naturally reduce dissolved Mn levels in the reservoir. The source of Mn within the reservoir is not well understood, however, presumably arises from sediment mobilization initiated by variation in pH, redox potential (ORP or Eh), dissolved oxygen (O₂) and ionic strength conditions. This study investigated conditions within the reservoir to further understand Mn transfer from the sediment into the water column. O₂, pH, oxidation–reduction potential (ORP or Eh), organic matter content and electric conductivity were measured in water samples and sediment from the reservoir. Sequential extraction (SE) procedures were used to test the specific effects exerted by each of these conditions on Mn mobilization from the sediments. The European Community Bureau of Reference (BCR) sequential extraction procedure was used to quantify metals in sediment (referred to as the BCR extraction below). Statistical analysis of geochemical data from water samples (both water column and sediment pore water) and sediments demonstrated the conditions under which Mn can be released from sediments into the water column. The results indicated a primarily oxic water column and anoxic reducing conditions in the sediment (ORP or Eh ≤ ?80 mV). The pH of water in contact with bottom sediments varied from 7.6 to 6.8. The pH of sedimentary pore water varied from 6.8 to 4.7. The sediments contained significant amounts of organic matter (20 %). Chemical extractions showed that the exchangeable fraction contained over 50 % of the total Mn within sediments. Microscopic analysis using scanning electron microscopy–energy dispersive spectroscopy (SEM–EDS) indicated that Mn does not occur within well-crystallized mineral phases in the Riogrande II sediments. A large proportion of Mn exists instead as material adsorbed onto the surfaces of recently deposited sediment particles. Bacterial oxidation of organic matter may cause the observed anoxic conditions at the bottom of the reservoir. Mineralization of organic matter therefore contributes to reducing conditions within the sediments. Mobilization of Mn from the sediment into the water column may result from reductive dissolution of this fraction. Manganese release by this mechanism diminishes the water quality of the Riogrande II reservoir and warrants further study.     

A sediment chronology of the eutrophication of Chesapeake Bay

Chesapeake Bay sediments were examined for biogeochemical evidence of eutrophication trends using two mesohaline sediment cores. Measurements of ²¹⁰Pb geochronology and sediment profiles of organic carbon, nitrogen, organic phosphorus, inorganic phosphorus, and biogenis silica (BSi) were used used to develop temporal concentration trends. Recent sediments have 2–3 times as much organic carbon and nitrogen as sediments from 80 to 100 yr ago, but the increases result from both changes in organic matter deposition and time-dependent changes in organic matter decomposition rates. Despite increases in phosphorus loading, no major changes in phosphorus concentration were noted throughout most of the century; anthropogenic phosphorus deposition, though not evident in sulfidic mid-bay sediments, must occur in more oxidizing sediment environments in both the northern and southern bays. Temporal trends in BSi concentrations are much less evident and the lack of substantial increases in this century suggest that BSi inputs may be capped by late spring-summer Si limitation.     

A sedimentological study of the dredged material deposit in the New York Bight

A variety of sediment types were identified in sediment cores taken at the dredged material dumpsite in the New York Bight. Black sandy mud is characteristic of dumped dredged material while glauconitic and quartzose sands are typical of the naturally deposited sediments underlying the deposit. The sedimentological investigation indicates that largescale differentiation of dumped material occurs at the dumpsite. Laminated sediments and discrete beds are typical of the central part of the deposit, the area that receives the bulk of direct dumping. Relatively homogeneous, fine-grained sediments, presumably derived from the area of direct dumping, are characteristic of the material present at the periphery of the deposit. Preferential transport of fine-grained material to the fringes of the deposit may be an important contaminant transport mechanism in the area. Incursion of glauconitic sand, derived from surrounding areas, onto the edges of the deposit is also believed to occur. Based on bathymetric surveys of the area conducted in 1936, 1973, and 1978, rates of dredged material accumulation at the dumpsite have been estimated for the period 1936–1978. The calculated rates range from 50 cm/yr at the apex of the deposit to 6 cm/yr at the periphery. Contribution 294 of the Marine Sciences Research Center (MSRC) of the State University of New York at Stony Brook.     

Behavior of Hydrocarbons in the Mouth Parts of Arctic Rivers

The paper reviews data (acquired in 2007–2016) on aliphatic and polycyclic aromatic hydrocarbons in comparison with data on concentrations of lipids, C_org, and chlorophyll a in the water and bottom sediments the river–sea geochemical barrier (for the Northern Dvina, Ob, Yenisei, and Lena rivers). It was established that the concentrations of anthropogenic hydrocarbons decrease and these compounds precipitate like other organic compounds and particulate matter, where riverine and marine waters mix. Relatively pure water flows in the pelagic zones of seas. In spite of low temperatures in the Arctic, anthropogenic hydrocarbons transform so rapidly that natural compounds dominate in the water and bottom sediments: autochthonous in the seawater and allochthonous in the bottom sediments.     

Evaluating the influence of lake morphology,trophic status and diagenesis on geochemical profiles in lake sediments

Recent geochemical studies provide evidence that changes in vertical distributions of nutrients in lake sediments are driven by anthropogenic activities, based primarily on trends of increasing concentrations in upper sediment layers. However, the present study shows that vertical concentration profiles of C, N and P in lake sediments can be higher in the upper, most recently deposited sediment strata, driven largely by natural diagenetic processes and not eutrophication alone. Sediment cores from 14 different lakes in New Zealand and China were examined ranging from oligotrophic to highly eutrophic and shallow to deep, and it was found that the shape of vertical profiles of total P, a key nutrient for lake productivity, can be similar in sediments across gradients of widely differing trophic status. Empirical and mechanistic diagenesis steady state profile models were derived and applied to describe the vertical distribution of C, N and P in the sediments. These models, which focus on large scale temporal (decades) and spatial (up to 35 cm in the vertical) processes, revealed that density-differentiated burial and biodiffusive mixing, were strongly correlated with vertical concentration gradients of sediment C, N and P content, whereas lake trophic status was not. A sensitivity analysis of parameters included in the diagenetic model further showed that the processes including flux of organic matter to the sediment–water interface, burial (net sedimentation), breakdown of organic matter and biodiffusion all can significantly influence the vertical distribution of sediment P content. It was concluded that geochemical studies attempting to evaluate drivers of the vertical distribution of sediment C, N and P content in lake sediments should also account for the natural diagenetic drivers of vertical concentration gradients, assisted with application of similar models to those presented in this study. This would include quantification of key sediment diagenesis model parameters to separate out the influence of anthropogenic activities.     

Factors affecting dissolved organic matter dynamics in mixed-redox to anoxic coastal sediments

Mixed-redox (suboxic, or oscillating between oxidizing and reducing conditions) to anoxic marine sediments from the Raritan -New York Bay complex and the Inner New York Bight of the eastern U.S. were studied to investigate the factors controlling the accumulation of pore-water dissolved organic carbon (DOC). DOC increased with depth at each of four study sites, but accumulation was generally limited in the mixed-redox zone relative to the anoxic zone. Humic-like fluorescence intensity also differed between mixed-redox and anoxic zones of the sediment, such that anoxic pore waters were relatively enriched in fluorescent, humic-like compounds.A pore-water DOC model was tested for its capacity to explain these geochemical patterns. Model results for a heavily irrigated and a non-bioturbated site both suggest that, excluding the uppermost few cm of the sediment column, pore-water DOC is predominantly comprised of poorly-reactive material with estimated degradation rate constants on the order of 10⁻³ yr⁻¹. Model results are also consistent with the suggestion that DOC accumulation is suppressed in the mixed-redox compared to the anoxic zones of the sediment due to rapid oxidation of high-molecular-weight DOC, and limited production and enhanced oxidation of the less reactive polymeric low-molecular-weight component of the DOC pool. An assessment of sorptive behavior of DOC in the surface sediments of the study area suggests that sorption can influence pore-water DOC distributions under conditions of high sedimentation and low bioirrigation.     

Identification of specific organic contaminants for estimating the contribution of the Elbe river to the pollution of the German Bight

GC/MS analyses have been applied to sediment samples of the German Bight in order to document the state of organic contamination as well as to identify specific molecular markers that are appropriate to estimate the discharge of anthropogenic compounds derived from the Elbe river. Detailed screening analyses revealed a wide variety of organic lipophilic compounds of biogenic, petrogenic as well as anthropogenic origin. Potential marker compounds indicating the contribution of the Elbe river could be attributed mainly to the chlorinated aromatic contaminants. Specifically, these include tetra- to hexachlorobenzenes, mono- to dichloronaphthalenes, hexachlorobutadiene, tetrabutyl tin, alkylsulfonic acid phenylesters, 1,2,3,6,7,8-hexahydro-1,1,6,6-tetramethyl-4-isopropyl-as-indacene and 4,4′-dichlorodiphenylsulfide. These compounds are suitable to indicate the spatial distribution of Elbe river derived organic matter.     

Alkane and PAH biomarkers as tracers of terrigenous organic carbon in Arctic Ocean sediments

We present the first sedimentary biomarker study encompassing the entire Arctic Ocean. A large data set of organic markers for terrigenous, petroleum and combustion inputs [alkanes, hopanes and steranes, parent and alkyl polycyclic aromatic hydrocarbons (PAHs)] is examined for patterns in space and time using principal components analysis (PCA) and partial least squares (PLS). Biomarker patterns reveal the central Arctic Ocean basin sediments to be compositionally distinct from those of the Mackenzie River/Beaufort Sea and Barents Sea, but similar to those of the Laptev Sea. PAH distributions reflected in PAH ratios and PCA projections demonstrate that Arctic Ocean sediment is dominated by natural inputs to the extent that anthropogenic combustion PAHs are not significant. We find only modest changes between the glacial and post-glacial sediments for atmospherically transported hydrocarbon biomarkers, while particle associated biomarkers were captured strongly at basin edges during the glacial period, and much more evenly transported across basins during the post-glacial period. The orders of magnitude decreases in particle associated petrogenic alkanes and PAHs in central basins during glacial times, coupled with the uniformity of most petrogenic biomarker parameters for most basin and shelf locations, reflect a massive reduction in ice transport that makes the margins the most likely source of petrogenic material for the Pleistocene/Holocene central Arctic basins. The proximity of large coal deposits of various maturity levels along the Lena River, the overlap in PAH and biomarker composition of the Laptev Sea and surficial sediments from the central Arctic Ocean and the location of the Laptev Sea at the origin of the main Transpolar Drift all point to eroded coals from the Lena River/Laptev Sea as the likely source of petrogenic hydrocarbons to the central Arctic Ocean. The ubiquitous presence of allochthonous coal in Arctic Ocean surface sediments provides a major constraint on the use of petrogenic biomarkers to infer the presence of subsurface petroleum reserves.     

Polycyclic aromatic hydrocarbon fingerprints in the Pichavaram mangrove–estuarine sediments,southeastern India

The sources and historical deposition of 16 polycyclic aromatic hydrocarbons (PAHs) were investigated in dated sediment cores from the Pichavaram mangrove–estuarine complex. The ΣPAH flux in mangrove and estuarine sediments was 0.064 ± 0.031 μg/cm²/yr and 0.043 ± 0.020 μg/cm²/yr, respectively. The PAH flux in sediments increased up-core, coinciding with rapid urbanization since the 1970s. The flux showed a decrease in recent years (since 1990), coinciding with less riverine discharge, and perhaps more effective implementation of environmental regulations. The sediments were dominated by low molecular weight PAHs, suggesting anthropogenic input. Ratios of specific PAH isomer pairs suggested a greater input of petrogenic vs. pyrogenic derived PAHs. Notably, the deposition of high molecular weight PAHs increase in mangrove surface sediments was due to lignite and firewood combustion. Because of their overall low concentration in sediments it is unlikely these PAHs pose an immediate ecological hazard.     

Benthic Oxygen Consumption and Organic Matter Turnover in Organic-poor, Permeable Shelf Sands

The high permeability of sediments and strong near-bottom currents cause seawater to infiltrate the surface layers of Middle Atlantic Bight shelf deposits. In this study, sandy sediment cores from 11 to 12 m water depth were percolated with filtered seawater on shipboard. Sedimentary oxygen consumption (SOC) increased non-linearly with pore water flow, approaching maximum rates of 120 mmol m⁻² d⁻¹ (May 2001) or 75 mmol m⁻² d⁻¹(July 2001). The addition of acetate to the inflowing water promptly enhanced the release of dissolved inorganic carbon (DIC) from the cores. DIC production rates were a linear function of acetate concentration, ranging from 100 to 300 mmol m⁻² d⁻¹ without substrate addition to 572 mmol m⁻² d⁻¹ with 100 mM acetate. The sediments also hydrolyzed a glucose pseudopolymer, and the liberated glucose prompted an increase of SOC. Our results suggest that decomposition rates of organic matter in permeable sands can exceed those of fine-grained, organic-rich deposits, when water currents cause advective interstitial flow, supplying the subsurface microbial community with degradable material and electron acceptors. We conclude that the highly permeable sand beds of the Middle Atlantic Bight are responsive within minutes to hours and efficiently operate as biocatalytical filters.