Nutrient exchange across the sediment-water interface in the Potomac River estuary

The flux of ammonia, phosphate, silica and radon-222 from Potomac tidal river and estuary sediments is controlled by processes occurring at the sediment-water interface and within surficial sediment. Calculated diffusive fluxes range between 0·6 and 6·5 mmol m^?2 day^?1 for ammonia, 0·020 and 0·30 mmol m^?2 day^?1 for phosphate, and 1·3 and 3·8 mmol m^?2 day^?1 for silica. Measured in situ fluxes range between 1 and 21 mmol m^?2 day^?1 for ammonia, 0·1 and 2·0 mmol m^?2 day^?1 for phosphate, and 2 and 19 mmol m^?2 day^?1 for silica. The ratio of in situ fluxes to diffusive fluxes (flux enhancement) varied between 1·6 and 5·2 in the tidal river, between 2·0 and 20 in the transition zone, and from 1·3 to 5·1 in the lower estuary. The large flux enhancements from transition zone sediments are attributed to macrofaunal irrigation. Nutrient flux enhancements are correlated with radon flux enhancements, suggesting that fluxes may originate from a common region and that nutrients are regenerated within the upper 10–20 cm of the sediment column.The low fluxes of phosphate from tidal viver sediments reflect the control benthic sediment exerts on phosphorus through sorption by sedimentary iron oxyhydroxides. In the tidal river, benthic fluxes of ammonia and phosphate equal one-half and one-third of the nutrient input of the Blue Plains sewage treatment plant. In the tidal Potomac River, benthic sediment regeneration supplies a significant fraction of the nutrients utilized by primary producers in the water column during the summer months.     

Deposition of organic material in a coral reef lagoon,One Tree Island,Great Barrier Reef

Deposition of organic material was measured at four sites on One Tree Island coral reef using fixed sediment traps. Although no reliable data were obtained for the reef crest area because of problems of resuspension, mean deposition in the backreef area amounted to some 4 g organic C m⁻² day⁻¹ whereas in the lagoon it was about 1·5 g C m⁻² day⁻¹. This amounted to mean nitrogen deposition rates of 160 and 95 mg N m⁻² day⁻¹, respectively. As primary production by turf algae, the principal producers at One Tree Island, has been estimated at about 2·3 g C m⁻² day⁻¹ for the whole reef system and the weighted mean carbon deposition is estimated at 2·2 g C m⁻² day⁻¹, it is clear that the carbon produced by plants is largely retained in the system. Nitrogen deposition, on the other hand, amounted to only about 60% of that produced by turf algae and it must be assumed that much of this leached into the water during sedimentation. Losses of nitrogen may be minimized by incorporation of dissolved nitrogen by pelagic microheterotrophs which may in turn be consumed by filter feeders before they leave the reef.     

Dissolved nutrient fluxes from the nearshore sediments of Bowling Green Bay,central Great Barrier Reef Lagoon (Australia)

The fluxes of dissolved inorganic N, P, and Si from the nearshore sediments of the Great Barrier Reef Lagoon are significantly lower than those reported from sediments in temperate regions at similar temperatures. The directly measured fluxes range from −23 to +28, −154 to +890, and −990 to +1750 μmol m⁻² day⁻¹ for PO₄³⁻, ΣN(=NH₄⁺ + NO₂⁻ + NO₃⁻) and Si, respectively. Estimates suggest that sediments are the major source of dissolved N to near-shore waters of the Lagoon greatly exceeding the dissolved flux from rivers. Resuspension of up to 1 cm of sediment during storms would have a very small effect on the PO₄³⁻ or Si(OH)₄ concentration of the overlying water, but would significantly raise the ΣN concentration. The productivity of these waters may be controlled at various times by the balance between the steady-state sedimentary flux of nutrients, the fluvial input, and storm resuspension.     

Manganese and Iron Oxidation During Benthic Oxygenic Photosynthesis

The effect of benthic oxygenic photosynthesis on sediment-water fluxes of manganese and iron was studied for an intertidal sediment. Undisturbed sediments were incubated at an incident surface irradiance of 250 μE m⁻² s⁻¹at 26 °C. Oxygenic photosynthesis was selectively inhibited by adding [3-(3,4-dichloro)-1,1-dimethyl-urea] (DCMU). Benthic fluxes were determined experimentally from the change in manganese and iron concentrations in the overlying water, and were predicted from the pore water concentration gradients at the sediment-water interface assuming molecular diffusion as the transport mechanism. The experimental fluxes of manganese and iron in DCMU-treated cores amounted to −0·84 and −0·59 mmol m⁻²day⁻¹, respectively, and were directed from the sediment towards the overlying water. In the control cores, showing high rates of benthic oxygenic photosynthesis, the fluxes of manganese and iron were directed towards the sediment, 0·06 and 0·01 mmol m⁻²day⁻¹, respectively. Mass balances for the 0·1–0·14 cm thick oxic zone, calculated from the experimental fluxes and the predicted fluxes, suggest a minimum areal reoxidation of 0·6 mmol m⁻²day⁻¹for manganese and of 0·48 mmol m⁻²day⁻¹for iron in cores showing benthic photosynthesis. The estimated turnover times for dissolved Mn²⁺and dissolved Fe²⁺in the oxic surface layer during benthic photosynthesis were 0·8 and 0·25 h, respectively. Sediment oxygen microprofiles and the sediment pH profiles suggest that chemical precipitation and reoxidation dominates the retention of manganese and iron during benthic oxygenic photosynthesis in shallow intertidal sediments.     

Microbial nitrogen transformations in sediments and inorganic nitrogen fluxes across the sediment/water interface on the South Island West Coast,New Zealand

In January 1982, sediment microbial N transformations and inorganic N fluxes across the sediment/water interface were studied at nine sites off the South Island West Coast, New Zealand. The sediments showed a great variety in physical, chemical and biological properties. The sediment organic matter had a molar $\text{C}\text{N}$ ratio of 5.9–10.9, and the total $\text{N}\text{P}$ ratio was 1.2–4.0. The denitrification capacity in the top 7.5 cm of sediment was 0.1–77.2 mmol N m^?2 day^?1 and generally declined with increasing sediment depth. The in situ denitrification rate was 0.02–1.84 mmol N m^?2 day^?1 and highest activities were generally found in surface sediments and at 6–7.5 cm depth. Denitrification accounted for 82–100% of total nitrate reduction. Net N mineralization was indirectly estimated at 0.6–2.4 mmol N m^?2 day^?1, and the experimental determination of this N transformation gave 0.6–3.2 mmol N m^?2 day^?1. Denitrification accounted for 3–75% of net N mineralization. The diffusive flux of ammonium and nitrate across the sediment/water interface was 0.1–0.7 and 0.1–0.6 mmol N m^?2 day^?1, respectively.     

Composition and bacterial utilization of free amino acids in tropical mangrove sediments

The composition and bacterial utilization of dissolved free amino acids (DFAA) in tropical mangrove sediments was examined. Amino acid concentrations (300–900 ng total DFAA ml⁻¹) and composition were similar to that of other organic-rich, anaerobic sediments with lowest and highest concentrations in the low and mid intertidal zones, respectively. The non-protein amino acid, β-glutamic acid, rarely reported in previous studies, was found as a major component of the interstitial DFAA pool. Intracellular amino acids from some cultured strains of sulphate-reducing bacteria (e.g. Desulfobacter app) showed the presence of β-glutamic acid as a major cellular constituent suggesting that these bacteria may be a source of this amino acid in mangrove pore waters. In high intertidal sediments, bacterial growth rates (μ) correlated significantly with total DFAA concentrations with depth.Amino acid concentrations and composition differed significantly between sediments and overlying tidal waters. Flux chamber experiments showed negligible amino acid flux out of the sediments in untreated chambers, but rates of amino acid flux ranged from 27 to 69 mgN m⁻² day⁻¹ (= 81–207 mg C.m⁻² day⁻¹) in chambers where poisons were applied to the sediment surface. Such fluxes could account for between 9–38% and 5–19% of the nitrogen and carbon required to support the levels of bacterial productivity measured in surface (0–1 cm) sediments. These experiments suggest that bacterial populations in surface sediments are capable of utilizing all of the amino acid flux to the sediment-water interface in tropical mangroves.     

Microbial photosynthesis in coral reef sediments (Heron Reef, Australia)

We investigated microphytobenthic photosynthesis at four stations in the coral reef sediments at Heron Reef, Australia. The microphytobenthos was dominated by diatoms, dinoflagellates and cyanobacteria, as indicated by biomarker pigment analysis. Conspicuous algae firmly attached to the sand grains (ca. 100 μm in diameter, surrounded by a hard transparent wall) were rich in peridinin, a marker pigment for dinoflagellates, but also showed a high diversity based on cyanobacterial 16S rDNA gene sequence analysis. Specimens of these algae that were buried below the photic zone exhibited an unexpected stimulation of respiration by light, resulting in an increase of local oxygen concentrations upon darkening. Net photosynthesis of the sediments varied between 1.9 and 8.5 mmol O₂ m⁻² h⁻¹ and was strongly correlated with Chl a content, which lay between 31 and 84 mg m⁻². An estimate based on our spatially limited dataset indicates that the microphytobenthic production for the entire reef is in the order of magnitude of the production estimated for corals. Photosynthesis stimulated calcification at all investigated sites (0.2–1.0 mmol Ca²⁺ m⁻² h⁻¹). The sediments of at least three stations were net calcifying. Sedimentary N₂-fixation rates (measured by acetylene reduction assays at two sites) ranged between 0.9 to 3.9 mmol N₂ m⁻² h⁻¹ and were highest in the light, indicating the importance of heterocystous cyanobacteria. In coral fingers no N₂-fixation was measurable, which stresses the importance of the sediment compartment for reef nitrogen cycling.     

The effect of salinity on the microbial mineralization of two polycyclic aromatic hydrocarbons in estuarine sediments

Sediments from the lower Hudson River estuary and two other coastal environments were examined experimentally for their ability to mineralize (convert to CO₂) the polycyclic aromatic hydrocarbons (PAHs) naphthalene and anthracene over a range of salinities. Routine assays employed 1:1 (vol fresh sed:vol water) sediment slurrys in order to overcome natural variability in mineralization rates among replicates. Mineralization rates were stimulated by about 2·5 fold, compared to unslurried controls, while the coefficient of variation fell from 13% to 3·5%.Rates of naphthalene mineralization in surface sediments from along the mainstem of the Hudson River (salinities from 2 to 27%) ranged from 0·011 to 1·5 nmol cm⁻³ day⁻¹ (pool turnover [T_n] from 60 to 2040 days) with no discernible trends along the estuarine gradient. For two stations examined experimentally (mile point 5, salinity 23%; mile point 26, salinity 5%), microbial assemblages appeared acclimated to broad salinity variations as alter rates of mineralization compared to controls.Sediments from two upstream marshes of the Hudson (mile points 36 and 45) showed rates of naphthalene mineralization from 0·007 to 0·15 nmol cm⁻³ day⁻¹ (T_n from 14 to 368 days), while sediments from a third marsh in freshwater (mile point 76) had high rates (66 nmol cm⁻³ day⁻¹; T_n 40 days). For the two upstream marsh stations which rarely experienced salt intrusion, there was a substantial decrease in mineralization of naphthalene and anthracene with increasing salinity.Consistently high rates of naphthalene mineralization (780 to 1600 nmol cm⁻³ day⁻¹; T_n 5 to 6 days) were observed in petroleum contaminated sediments from Port Jefferson Harbor (PJH) on the north shore of Long Island. PJH has a relatively constant salinity regime (about 27%) and imposed decreases in salinity effected decreases in rates of naphthalene and anthracene mineralization. Lowest rates of naphthalene mineralization (0·003 to 0·004 nmol cm⁻³ day⁻¹; T_n from 714 days to 833 days) were found in sediments from two stations in the relatively pristine Carmans River estuary on the south shore of Long Island.The ability of increases or decreases in salinity to affect the rate of model PAH mineralization appeared to be dependent on the natural variation in the salinity regime from which a sample was obtained. Data from all the environments studied indicated a strong positive correlation between PAH concentration and the rates of mineralization of naphthalene. Rates of PAH mineralization in all environments examined appear to be primarily controlled by the extent of pollutant loading and not by natural variations in the salinity regime.     

Compositions and transport of lipid biomarkers through the water column and surficial sediments of the equatorial Pacific Ocean

A systematic investigation of fluxes and compositions of lipids through the water column and into sediments was conducted along the U.S. JGOFS EgPac transect from l2°N to l5°S at 140°W. Fluxes of lipids out of the euphotic zone varied spatially and temporally, ranging from ≈0.20 – 0.6 mmol lipid-C m⁻² day⁻¹. Lipid fluxes were greatly attenuated with increasing water column depth, dropping to 0.002-0.06 mmol lipid-C m⁻² day⁻¹ in deep-water sediment traps. Sediment accumulation rates for lipids were ≈ 0.0002 – 0.00003 mmol lipid-C m⁻² day⁻¹. Lipids comprised ≈ 11–23% of C_org in net-plankton, 10–30% in particles exiting the euphotic zone, 2–4% particles in the deep EgPac, and 0.1-1 % in sediments. Lipids were, in general, selectively lost due to their greater reactivity relative to bulk organic matter toward biogeochemical degradation in the water column and sediment. Qualitative changes in lipid compositions through the water column and into sediments are consistent with the reactive nature of lipids. Fatty acids were the most labile compounds, with polyunsaturated fatty acids (PUFAs) being quickly lost from particles. Branchedchain C₁₅ and C₁₇ fatty acids increased in relative abundance as particulate matter sank and was incorporated into the sediment, indicating inputs of organic matter from bacteria. Long-chain C₃₉ alkenones of marine origin and long-chain C₂₀-C₃₀ fatty acids, alcohols and hydrocarbons derived from land plants were selectively preserved in sediments. Compositional changes over time and space demonstrate the dynamic range of reactivities among individual biomarker compounds, and hence of organic matter as a whole. A thorough understanding of biogeochemical reprocessing of organic matter in the oceanic water column and sediments is, thus, essential for using the sediment record for reconstructing past oceanic environments.     

Oxygen fluxes involving the benthic micro- and macrophytic components in the Thau Lagoon under pre-anoxic conditions

Measurements of oxygen fluxes at the water-sediment interface (transparent and opaque enclosures) were made on bare sediments inhabited by microphytes on the one hand, and on sediments diversely colonized by macrophytes (macroalgae and seagrasses) on the other hand. Five stations, typical of different biotopes of a Mediterranean shallow lagoon were studied from May to July 1993 in order to observe an anoxic event which usually occurs at that time of the year. Average diurnal respiration of benthic communities ranged from 40 mg (or 1.25 mmol) O₂ m² h⁻¹ in bare sediments (31 % of the lagoon area) to 76 mg (or 2.37 mmol) O₂ m⁻² h⁻¹ in sediments with a medium coverage of macroalgae (37 % of the total area) and, finally, to 100 mg (or 3.12 mmol) O₂ m⁻²h⁻¹ in the denser macrophytic area (32 % of the total area). The highest diurnal gross production was observed in the zone colonized by macroalgae and seagrasses, and especially in corridors between shellfish-cultivation tables (300 mg O₂ m⁻² h⁻¹, or 9.37 mmol O₂m⁻² h⁻¹, equivalent to 113 mg C m⁻² h⁻¹). Overall, during this period, net bottom oxygen production was close to nil in ca. 30 %, and positive in 70 % of the lagoon area. The average net oxygen production for the whole lagoon in summer is thus in the order of 100 mg O₂ m⁻²h⁻¹. In 1993, at the end of July, an anoxic event was avoided due to a period of strong wind.     

Degradation of organic pollutants in near shore marine sediments: Part I—breakdown of pulp mill fibre

Cellulose levels in the sediments of Loch Linnhe and Loch Eil were measured over a period of years following the introduction of pulp mill effluent to system. Cellulose levels in experimental sediment systems subjected to pulp fibre inputs at levels simulating various possible loch input levels were measured and compared. No permanent build up of cellulose in either the loch systems or the experimental systems was observed, even at high input levels.Pulp fibre degradation rates were measured experimentally using two different techniques. No difference was found between the degradation rates of wet and predried fibre.Degradation rates equivalent to 0·2 g dry fibre m^?2 day^?1 were found in areas of low fibre input and 0·5 g dry fibre m^?2 day^?1 in areas of high input were recorded. These rates were of the same order as, but somewhat lower than, the probable input rates to the sediments in Loch Eil. Speculations as to possible reasons for this are advanced.     

Impact of macroalgal dredging on dystrophic crises and phototrophic bacterial blooms (red waters) in a brackish coastal lagoon

The Prévost lagoon (Mediterranean coast, France), was subject to annual dystrophic crises caused by the biodegradation of opportunistic macroalgae (Ulva lactuca) in the past. These crises result in anoxic waters with subsequent blooms of Purple Sulphur Bacteria (red waters) which, by oxidizing sulphide, contribute to the reestablishment of oxic conditions in the water column. Mechanical dredging of the macroalgal biomass has been carried out in the lagoon since 1991 with the aim of preventing the ecological and economic disturbances caused by such crises. Dredging began just before the phototrophic bloom when the water was already hypoxic (O₂ = 0.7 mg·L⁻¹) and contained sulphilde (H₂S = 7.3 mg·L⁻¹) and purple patches of phototrophic bacteria (Thiocapsa sp.) that were beginning to develop on decaying macroalgae at the sediment surface. The dredging prevented red water formation and drastically modified both phototrophic community structure and activity and biogeochemical sulphur cycling. The dredging permitted the reestablishment of oxic conditions for a short period only (1–13 August). Resuspension of the superficial sediment layers disturbed the phototrophic bacterial community, whose numbers decreased by one order of magnitude (from 2 × 10⁶ to 3.9 × 10⁵ CFU.mL⁻¹). The phototrophic community was no longer effective in reoxidizing the reduced sulphur compounds remaining in the sediments, as shown by a drastic sulphate depletion in the superficial sediment layers. Moreover, the increase in the specific bacteriochlorophyll a concentration of the phototrophic purple bacteria and the rapid development of Green Sulphur Bacteria (Prosthecochloris-like microorganisms) indicated that the phototrophic community was growing under severe light-limiting conditions due to the resuspension of sediment particles in the water. These conditions did not allow the phototrophic bacterial community to efficiently reoxidize the reduced sulphur compounds originating from the sediments. In consequence, hypoxic conditions (O₂ = 4.7 to 4.8 mg·L⁻¹) and low sulphide concentrations (H₂S = 0.4 to 0.7 mg·L⁻¹) were detected in the water column until September. The ecological balance in the lagoon was reestablished only in October, whereas, in previous years it had been restored in August.     

Export fluxes of particulate organic carbon in the Chukchi Sea: A comparative study using 234Th/238U disequilibria and drifting sediment traps

Large-volume sampling of ²³⁴Th and drifting sediment trap deployments were conducted as part of the 2004 Western Arctic Shelf–Basin Interactions (SBI) spring (May 15–June 23) and summer (July 17–August 26) process cruises in the Chukchi Sea. Measurements of ²³⁴Th and particulate organic carbon (POC) export fluxes were obtained at five stations during the spring cruise and four stations during the summer cruise along Barrow Canyon (BC) and along a parallel shelf-to-basin transect from East Hanna Shoal (EHS) to the Canada Basin. ²³⁴Th and POC fluxes obtained with in situ pumps and drifting sediment traps agreed to within a factor of 2 for 70% of the measurements. POC export fluxes measured with in situ pumps at 50 m along BC were similar in spring and summer (average = 14.0 ± 8.0 mmol C m^− 2 day^− 1 and 16.5 ± 6.5 mmol C m^− 2 day^− 1, respectively), but increased from spring to summer at the EHS transect (average = 1.9 ± 1.1 mmol C m^− 2 day^− 1 and 19.5 ± 3.3 mmol C m^− 2 day^− 1, respectively). POC fluxes measured with sediment traps at 50 m along BC were also similar in both seasons (31.3 ± 9.3 mmol C m^− 2 day^− 1 and 29.1 ± 14.2 mmol C m^− 2 day^− 1, respectively), but were approximately twice as high as POC fluxes measured with in situ pumps. Sediment trap POC fluxes measured along the EHS transect also increased from spring to summer (3.0 ± 1.9 mmol C m^− 2 day^− 1 and 13.0 ± 6.4 mmol C m^− 2 day^− 1, respectively), and these fluxes were similar to the POC fluxes obtained with in situ pumps. Discrepancies in POC export fluxes measured using in situ pumps and sediment traps may be reasonably explained by differences in the estimated POC/²³⁴Th ratios that arise from differences between the techniques, such as time-scale of measurement and size and composition of the collected particles. Despite this variability, in situ pump and sediment trap-derived POC fluxes were only significantly different at a highly productive station in BC during the spring.     

Sulfide,iron, manganese,and phosphate in the deep water of the Chesapeake Bay during anoxia

Concentrations of dissolved oxygen and sulfide, and of dissolved and particulate iron, manganese, and phosphate were measured as functions of salinity at a station in the Chesapeake Bay during stratification and deep water anoxia in spring and summer, 1981. The observed concentration/salinity profiles showed that oxygen was transported in a direction opposite to that of salt, while dissolved sulfide was transported in the same direction as salt through the anoxic water to be oxidized in oxygen consumption zones located below the steepest parts of the halocline. Both oxygen and sulfide were transported conservatively on 18 June. Their fluxes were 1·2 and 2 mol m⁻² d⁻¹, respectively. The oxygen flux was 30% of that stoichiometrically needed to oxidize the sulfide transported, suggesting that the oxygen consumption zone was advancing to shallower, less saline water, thus increasing the volume of anoxic water. Although oxygen was transported conservatively, sulfide was produced as it was transported through the anoxic water on 8 July.The anoxic water was supersaturated with respect to ferrous sulfide on 18 June, but most of the anoxic water was saturated on 8 July. Precipitation of ferrous sulfide had little effect on the sulfide flux on 18 June. The manganese(II) concentration/salinity profile exhibited a maximum in the oxygen consumption zone on 18 June. On 8 July the profile was independent of salinity at high salinities. Iron(II) and manganese(II) consumed little if any oxygen in the oxygen consumption zone.Soluble reactive phosphate was transported conservatively through the anoxic water on 18 June. It was produced as it was transported on 8 July. All of the phosphate was consumed in the oxygen consumption zones by sulfide oxidizing bacteria. On 18 June its flux, estimated to be 2·8 mmol m⁻² d⁻¹, was less than 10% of that required for bacterial oxidation of the sulfide reaching the oxygen consumption zone. The rest was oxidized chemically. The growth and activity of the bacteria were limited by the rate at which soluble reactive phosphate was transported to the oxygen consumption zone.Little or none of the sulfide, iron(II), or phosphate originated in the bottom sediment at the station. The results indicate that they were transported into the water sampled from deeper more saline water downstream, suggesting that they originated in the deep trough that extends along the spine of the Bay. Manganese(II), however, resulted from the reduction and dissolution of oxidized manganese particles as they sank into the anoxic water.     

Deoxygenation and remineralization above the sediment-water interface; an in situ experimental study

An in situ chamber of volume 3881 and bottom area 0·64 m² was used to determine the flux of oxygen and inorganic nutrients across an estuarine sediment-water interface over a 65-day period. Over the first 7 days, oxygen uptake was 378 mg m^?2 day^?1 and the rates of ammonium and phosphate release were 2·22 and 0·34 mg at. m^?2 day^?1, respectively. The water became anoxic in 14 days.The rates of flux in a similar chamber containing only detritus recently settled from the water column were 371 mg m^?2 day^?1 (oxygen), 1·66 mg at. m^?2 day^?1 (ammonium) and 0 12 mg at. m^?2 day^?1 (phosphate), demonstrating that detritus contributes substantially to exchange across the sediment-water interface.The evolution of the two chambers was similar over the latter part of the experimental period. A third chamber containing only water exhibited very minor changes.The role of detritus in nutrient recycling at the sediment-water interface is discussed in relation to the productivity of shallow water bodies such as the estuary in which the experiment was conducted, which itself undergoes periodic deoxygenation during prolonged stratification. The measured flux of nitrogen across the interface was found to represent approximately 31% of the mean daily phytoplankton requirement.     

Formation of chemogenic calcite in super-anoxic seawater — Framvaren, southern Norway

Framvaren, a super-anoxic fjord in southern Norway, contains 7–8 mmoll⁻¹ of sulphide and a total carbonate concentration of 18.5 mmol kg⁻¹ in the bottom water. The chemistry of calcium has been studied, considering sources, biogenic and chemical processes and sedimentary sinks. Calcium associated with the bacteria biomass at the redox interface (18m depth) appears to be the primary source of dissolved calcium in the deep, anoxic water. Excess calcium and high total carbonate cause supersaturation of calcite, which is precipitated chemogenically. Calcite (and presumably some aragonite) is identified both in sediment trap material and the bottom sediments below the depth of supersaturation.     

Organic carbon accumulation and sulfate reduction rates in slope and basin sediments of the Ulleung Basin,East/Japan Sea

This study investigated the organic carbon accumulation rates (OCARs) and sulfate reduction rates (SRRs) in slope and basin sediments of the Ulleung Basin, East/Japan Sea. These sediments have high organic contents at depths greater than 2,000 m; this is rare for deep-sea sediments, except for those of the Black Sea and Chilean upwelling regions. The mean organic carbon to total nitrogen molar ratio was estimated to be 6.98 in the Ulleung Basin sediments, indicating that the organic matter is predominantly of marine origin. Strong organic carbon enrichment in the Ulleung Basin appears to result from high export production, and low dilution by inputs of terrestrial materials and calcium carbonate. Apparent sedimentation rates, calculated primarily from excess ²¹⁰Pb distribution below the zone of sediment mixing, varied from 0.033 to 0.116 cm year⁻¹, agreeing well with previous results for the basin. OCARs fluctuated strongly in the range of 2.06–12.5 g C m⁻² year⁻¹, these rates being four times higher at the slope sites than at the basin sites. Within the top 15 cm of the sediment, the integrated SRRs ranged from 0.72 to 1.89 mmol m⁻² day⁻¹, with rates approximately twice as high in the slope areas as in the basin areas. SRR values were consistently higher in areas of high sedimentation and of high organic carbon accumulation, correlating well with apparent sedimentation rates and OCARs. The sulfate reduction rates recorded in the basin and slope sediments of the Ulleung Basin are higher than those reported for other parts of the world, with the exception of the Peruvian and Chilean upwelling regions. This is consistent with the high organic carbon contents of surface sediments of the Ulleung Basin, suggesting enhanced organic matter fluxes.     

Fluxes of iron and manganese across the sediment–water interface under various redox conditions

Fluxes of dissolved forms of iron and manganese across the sediment–water interface were studied in situ in the Gulf of Finland and the Vistula Lagoon (Baltic Sea), and in the Golubaya Bay (Black Sea) from 2001 to 2005. Fluxes were measured using chamber incubations, and sediment cores were collected and sliced to assess the porewater and solid phase metal distribution at different depths. Measured and calculated benthic fluxes of manganese and iron were directed out of sediment for all sites and were found to vary between 70–4450 and 5–1000 µmole m^− 2 day^− 1 for manganese and iron, respectively. The behavior of the studied metals at various redox conditions in the near-bottom water and in the sediment was the main focus in this study. Our results show the importance of bottom water redox conditions for iron fluxes. We measured no fluxes at oxic conditions, intermediate fluxes at anoxic conditions (up to 200 μmole m^− 2 day^− 1) and high fluxes at suboxic conditions (up to 1000 μmole m^− 2 day^− 1). Total dissolved iron fluxes were generally dominated by iron(II). Contribution of iron(III) to the total iron flux did not exceed 20%. Obtained fluxes of manganese at all studied regions showed a linear correlation (r² = 0.97) to its concentration in the porewater of the top sediment layer (0–5 mm) and did not depend on dissolved oxygen concentrations of bottom water. Organically complexed iron and manganese were in most cases not involved in the benthic exchange processes.     

Negative effects of blue mussel (Mytilus edulis) presence in eelgrass (Zostera marina) beds in Flensborg fjord,Denmark

The effect of blue mussel (Mytilus edulis) presence in eelgrass (Zostera marina) beds was studied from June 2004 to July 2005 in Flensborg fjord, Denmark. The field experiments were conducted at two stations, one with only Z. marina (Eelgrass station) present and one where M. edulis were present in the Z. marina beds (Mixed station). Zostera marina parameters were measured (growth of leaves, shoot density, leaf length, and nutrient content) in combination with epiphyte cover and sediment parameters (sulphate reduction rates, sediment nutrient fluxes, organic content, C, N and P content) to examine possible positive and negative effects of the mussels on eelgrass performance. The fluxes of ammonium from the sediments were stimulated at all sampling dates at the Mixed station, and possibly stimulated epiphyte growth at this station. Further ¹⁵N signals in epiphytes from the Mixed station suggested that excretion products from the mussels were important nitrogen sources at this station. Sulphate reduction rates were enhanced at the Mixed station and also sediment sulphide concentrations increased under mussel influence, which may have resulted in sulphide toxicity and decreased growth of Z. marina at this station. The study indicates that for Z. marina beds in Flensborg Fjord the effects of M. edulis in seagrass beds are primarily negative, and raises the question whether this leads to negative effects on the stability and expansion of Z. marina beds.     

Dissolved organic carbon in sediments from the eastern North Atlantic

Profiles of dissolved organic carbon (DOC) were measured in the pore water of sediments from 1000, 2000 and 3500 m water depth in the eastern North Atlantic. A net DOC accumulation in the pore waters was observed, which followed closely the zonation of microbial respiration in these sediments. The concentration of pore water DOC in the zone of oxic respiration was elevated relative to that in the bottom ocean water. The resulting upward gradient across the sediment–water interface indicated a steady state diffusive benthic flux, F_DOC, of 0.25–0.44 mmol m⁻² day⁻¹ from these sediments. Subsequent increase in the concentration of DOC in the pore water occurred only in the sediments from 1000 and 2000 m water depth that supported anoxic respiration, leading to a deep concentration maximum. By contrast, in the sediments from 3500 m water depth, a deep concentration minimum was measured, coincident with minimal postoxic respiration in this near-abyssal setting. The gradient-based F_DOC represented approximately 14% of the total remineralized organic carbon (TCR=sum of F_DOC and depth-integrated organic carbon oxidation rate) in the sediments from 1000 and 2000 m water depth, while it was 36% of the TCR in the sediments from 3500 m water depth. A covariance of particulate organic carbon (POC) and pore water DOC with depth in the sediments was evident, more consistently at the deepest site. While the covariance can be related to biotic processes in these sediments, an alternative interpretation suggests a possible contribution of sorption to the biotic control on sedimentary organic carbon cycling. The steady state diagenetic conditions in which this may occur can be conceivable for some organic-poor deep-sea locations, but direct evidence is clearly required to validate them.