Dynamics of Redox Changes of Iron Caused by Light–dark Variations in Littoral Sediment of a Freshwater Lake

Depth profiles of oxygen concentration and the redox status of acid-extractable iron were measured in littoral sediment cores of Lake Constance incubated under a light–dark regimen of 12 h. While oxygen penetrated to 3.4±0.2 mm depth in the dark, photosynthetic oxygen production shifted the oxic–anoxic interface down to 4.0±0.2 mm or 5.9±1.6 mm depth, at low or high light intensity, respectively, and caused a net oxygen efflux into the water column. After a light–dark or dark–light transition, the oxygen concentration at the sediment surface reached a new steady state within about 20 min. The redox state of the bioavailable iron was determined in 1-mm slices of sediment subcores. After a dark period of 12 h, 85% of the acid-extractable iron (10.5 μmol cm⁻³ total) in the uppermost 8 mm was in the reduced state. Within 12 h at low or high light intensity, the proportion of ferrous iron decreased to 82 or 75%, respectively, corresponding to net rates of iron oxidation in the range of 244 and 732 nmol cm⁻³ h⁻¹, respectively. About 55 or 82% of the iron oxidation at low or high light intensity occurred in the respective oxic zone of the sediment; the remaining part was oxidized in the anoxic zone, probably coupled to nitrate reduction. The areal rates of iron oxidation in the respective oxic layer (21 or 123 nmol cm⁻² h⁻¹ at low or high light intensity, respectively) would account for 4 and 23% of the total electron flow to oxygen, respectively. Light changes caused a rapid migration of the oxic–anoxic interface in the sediment, followed by a slow redox reaction of biologically available iron, thus providing temporal niches for aerobic iron oxidizers and anaerobic iron reducers.     

Effects of benthic filamentous algae on the sediment–water interface in an acidic mining lake

Natural alkalinity generation by microbial sulphate reduction in acidic lakes is usually inhibited by the low pH and a low primary production which results in a lack of suitable organic carbon sources. In some acidic mining lakes mass developments of filamentous benthic algae occur. The effects of this periphyton layer on the biogeochemistry of the sediment–water interface were investigated by in situ microsensor measurements and laboratory incubations in Mining Lake Grünewalder Lauch (Germany). Microsensor measurements showed that the oxic–anoxic boundary was located in the periphyton layer and was moving up and down depending on light triggered photosynthesis. The sediment itself was permanently anoxic. The diurnal redox shift and the maintenance of neutral conditions in the periphyton layer lead to an effective precipitation of iron and phosphorus. Under the periphyton layer very high sulphate reduction rates up to 265 nmol cm⁻³ d⁻¹ were measured in the sediment. These are the highest rates reported for mining lakes so far. The microbial activity was high enough to keep the pH in the surface sediment neutral and contributed to natural alkalinity production. Handling editor: L. Naselli-Flores     

Methanogenesis and microbial lipid synthesis in anoxic salt marsh sediments

In anoxic salt marsh sediments of Sapelo Island, GA, USA, the vertical distribution of CH₄ production was measured in the upper 20 cm of surface sediments in ten locations. In one section of high marsh sediments, the concentration and oxidation of acetate in sediment porewaters and the rate and amount of¹⁴C acetate and¹⁴CO₂ incorporation into cellular lipids of the microbial population were investigated. CH₄ production rates ranged from <1 to 493 nM CH₄ gram sediment⁻¹ day⁻¹ from intact subcores incubated under nitrogen. Replacement with H₂ stimulated the rate of methane release up to nine fold relative to N₂ incubations. Rates of lipid synthesis from CO₂ averaged 39.2 ×10⁻²nanomoles lipid carbon cm³ sediment⁻¹ hr⁻¹, suggesting that CO₂ may be an important carbon precursor for microbial membrane synthesis in marsh sediments under anoxic conditions. Qualitative measurements of lipid synthesis rates from acetate were found to average 8.7 × 10⁻² nanomoles. Phospholipids were the dominant lipids synthesized by both substrates in sediment cores, accounting for an average of 76.6% of all lipid radioactivity. Small amounts of ether lipids indicative of methanogenic bacteria were observed in cores incubated for 7 days, with similar rates of synthesis for both CO₂ and acetate. The low rate of ether lipid synthesis suggests that either methanogen lipid biosynthesis is very slow or that methanogens represent a small component of total microbial lipid synthesis in anoxic sediments. present address: The University of Maryland,, Chesapeake Biological Laboratory, Box 38, Solomons, MD 20688, USA     

Methanogenesis and microbial lipid synthesis in anoxic salt marsh sediments

In anoxic salt marsh sediments of Sapelo Island, GA, USA, the vertical distribution of CH₄ production was measured in the upper 20 cm of surface sediments in ten locations. In one section of high marsh sediments, the concentration and oxidation of acetate in sediment porewaters and the rate and amount of¹⁴C acetate and¹⁴CO₂ incorporation into cellular lipids of the microbial population were investigated. CH₄ production rates ranged from <1 to 493 nM CH₄ gram sediment⁻¹ day⁻¹ from intact subcores incubated under nitrogen. Replacement with H₂ stimulated the rate of methane release up to nine fold relative to N₂ incubations. Rates of lipid synthesis from CO₂ averaged 39.2 ×10⁻²nanomoles lipid carbon cm³ sediment⁻¹ hr⁻¹, suggesting that CO₂ may be an important carbon precursor for microbial membrane synthesis in marsh sediments under anoxic conditions. Qualitative measurements of lipid synthesis rates from acetate were found to average 8.7 × 10⁻² nanomoles. Phospholipids were the dominant lipids synthesized by both substrates in sediment cores, accounting for an average of 76.6% of all lipid radioactivity. Small amounts of ether lipids indicative of methanogenic bacteria were observed in cores incubated for 7 days, with similar rates of synthesis for both CO₂ and acetate. The low rate of ether lipid synthesis suggests that either methanogen lipid biosynthesis is very slow or that methanogens represent a small component of total microbial lipid synthesis in anoxic sediments. present address: The University of Maryland,, Chesapeake Biological Laboratory, Box 38, Solomons, MD 20688, USA     

The rates of sediment-water exchange of oxygen and sediment bioturbation in Lough Neagh,Northern Ireland

Oxygen is transported 30 mm into the sediment at an 8 m depth site in eutrophic Lough Neagh by the irrigational activities of the benthic fauna. Faunal activity also mixes the upper 20 mm of sediment. Sediment oxygen uptake rate, redox potential-depth profile and the chlorophylla concentration were measured in the upper sediment layers from February to November 1979. Chlorophylla input to the sediment, following the Spring phytoplankton maximum, remained in the 0–1 cm sediment layer but did cause the redox potential profile to change from one with potentials around 400 mV in the upper 50 mm to one with a strong gradient over the 0–30 mm region. The start of benthic faunal activity in May caused the chlorophylla to be mixed into the 1–2 cm layer and also caused oxygen to be transported into the sediment at a rate sufficient to change the redox potential back to its initial state. The biodiffusion coefficient for solids in the upper 20 mm was estimated to be 6 × 10⁻⁸ cm² s⁻¹. Oxygen transport in the pore, waters of the upper sediment layers was considered to be best described as advection, caused by the irrigational activities of the benthic fauna.     

Temperature dependence of sediment-water exchange in Lake Grevelingen,SW Netherlands

Extended abstract Lake Grevelingen is a brackish water lake in the SW Netherlands. The lake has an area of 108 km², a mean depth of 5.3 m (maximum 48 m), a mean chlorinity of 13 to 16%0 Cl⁻, and a hydraulic residence time of about 8 years. Mass budget studies have shown a consistent seasonal pattern in the phosphorus sediment-water exchange in Lake Grevelingen (Kelderman 1980). From May to August a P mobilization from the sediment takes place, estimated atca. 12.5 mg P · m⁻² · day⁻¹. The sediment accumulatesca. 5.5 mg P · m⁻² · day⁻¹ during the rest of the year. Temperature may be an important factor in establishing this pattern. Sediment-water exchange was studied by means of laboratory experiments under specified conditions. Sediment cores (30 cm depth, 11 cm diameter) were taken at four stations in the lake, with sediment types varying from medium- to muddy sand (Fig. 1). The cores with overlying water (ca. 21) were placed in the dark at 5 °C in thermostatically controlled water baths. After a week's incubation time the temperature was slowly raised, such that after three weeks eight cores (four sediment types, duplicates) were at 5 °C, eight were at 10 °C, eight at 15 °C and eight at 20 °C. The same procedure was applied to the four control cores, containing lake water.     

A rapid assessment of the sedimentary buffering capacity towards free sulphides

Combined field surveys and laboratory studies were conducted in two Italian coastal lagoons, which differ for geomorphology, hydrodynamics and eutrophication degree (Sacca di Goro and Lesina lagoons, Adriatic Sea). Research aimed at assessing with a rapid technique the potential buffering capacity of sedimentary iron towards sulphides. In Spring and Summer 2004, the main pools of iron and sulphides were analysed in the uppermost sediment horizon (0–5 cm) at four stations in each lagoon. In parallel, experiments with laboratory incubations of sediment slurries were carried out at two sites in each lagoon in order to assess the sediment capacity of binding and retaining sulphides. Sediment slurries were kept stirred and anoxic with N₂ purging. Aliquots of dissolved sulphides (DS) were then added and DS concentrations were monitored until they were undetectable. On average, the total reactive iron (RFe), extracted with 6 N HCl, ranged from 170 to 400 μmol cm⁻³ in the Sacca di Goro stations, and comprised between 40 and 150 μmol cm⁻³ in the Lesina sites. The labile iron ferric quota (LFe: extractable with 0.5 N HCl) is considered representative of the microbially reducible iron fraction and was highest in spring in Sacca di Goro (up to 20 μmol cm⁻³). Differences among stations evidenced by PCA analysis, can be inferred from RFe, LFe and AVS, which represent the iron buffer and its saturation status, respectively. The sedimentary DS uptake was 6 μmol cm⁻³ of fresh sediment in Lesina and 8–12 μmol cm⁻³ in Sacca di Goro, indicating a direct relationship between DS removal and iron availability. Guest editors: A. Razinkovas, Z. R. Gasiūnaitė, J. M. Zaldivar & P. Viaroli European Lagoons and their Watersheds: Function and Biodiversity     

Annual cycles of benthic community oxygen uptake in a deep oligotrophic lake (Attersee,Austria)

Benthic community oxygen uptake of Lake Attersee sediments was measured between 1976 and 1979, along two profiles at 25, 50 and 100 m depth. Profile I was situated in the bay of Unterach into which the main tributary, Mondsee-Ache, discharges a high load of organic matter. Profile II was chosen at Weyregg to avoid the eutrophying effect of Mondsee-Ache. Oxygen uptake rates of Unterach sediments at 25 and 50 m depth were found to be higher when compared to the other sites (mean rates: Unterach 25 m = 15.56, 50 m = 11.05 mg O₂ · m⁻² · h⁻¹; Weyregg 25 m = 6.43, 50 m = 5.14 mg O₂ · m⁻² · h⁻¹). Organic content of the uppermost sediment layer was also higher in the bay of Unterach than at Weyregg. Oxygen uptake rates of undisturbed sediment cores vary considerably throughout the year, but no simple correlation existed with variations in organic content of the sediments. Peaks of organic matter were found to concur with following peaks of oxygen uptake rates, which implies that a certain time span is necessary for transforming freshly sedimented organic matter into a state digestable for the benthic community. The retardation between increasing organic matter of the sediment and the corresponding increase of benthic oxygen uptake was different at Unterach and Weyregg respectively, which is explained by the different quality of sedimenting material.     

Methane Release through Resuspension of Littoral Sediment

Sediment in the littoral zone of lakes is frequently disturbed by wave action or bioturbation, resulting in sediment resuspension. In undisturbed sediment, methanotrophic bacteria efficiently reduce the diffusive flux of methane into the water column. In a microcosm study, the resuspension of littoral sediment was simulated in sediment cores for a winter (n = 3) and a summer situation (n = 3). The erosion of surface sediment resulted in a large flux of methane into the overlying water (207 ± 176 μmol h⁻¹ m⁻² in winter and 73 ± 18 μmol h⁻¹ m⁻² in summer). Only a minor part (16 ± 7%) of the methane released was oxidized by methanotrophic bacteria, whereas the major part escaped into the water column. Only 6–16% of the littoral zone has to be resuspended to reach the same flux as from undisturbed littoral sediment. For the daily flux, a sediment resuspension has to last 1–4 h to reach the undisturbed daily flux. The study reveals the important role of sediment resuspension in the littoral methane cycle as an intense but variable source of methane of largely unknown magnitude.     

Seasonal Rates of Methane Oxidation in Anoxic Marine Sediments

Methane concentrations and rates of methane oxidation were measured in intact sediment cores from an inshore marine sediment at Jutland, Denmark. The rates of methane oxidation, determined by the appearance of ¹⁴CO₂ from injected ¹⁴CH₄, varied with sediment depth and season. Most methane oxidation was anoxic, but oxygen may have contributed to methane oxidation at the sediment surface. Cumulative rates (0- to 12-cm depth) for methane oxidation at Kysing Fjord were 3.34, 3.48, 8.60, and 17.04 μmol m⁻² day⁻¹ for April (4°C), May (13°C), July (17°C), and August (21°C), respectively. If all of the methane was oxidized by sulfate, it would account for only 0.01 to 0.06% of the sulfate reduction. The data indicate that methane was produced, in addition to being oxidized, in the 0- to 18-cm sediment stratum.     

Seasonal variation in sulfate reduction and methanogenesis in peaty sediments of eutrophic Lake Loosdrecht,The Netherlands

During one year, concentration profiles of sulfate and methane were measured in sediment cores of eutrophic Lake Loosdrecht. Sulfate concentrations decreased exponentially with depth towards a constant threshold value of 7.6 ± 6.1 μM. Concentration profiles were used to calculate fluxes of sulfate and methane and to estimate the anaerobic mineralization rate. Anaerobic mineralization was highest in autumn which was probably due to an increased sedimentation of easily degradable organic carbon. At high rates (>600 μ mol organic carbon .m⁻².h⁻¹), sulfate reduction appeared to be limited by sulfate and methanogenesis accounted for over 80% of the anaerobic mineralization. At low anaerobic mineralization rates, measured in winter and spring, sulfate reduction was predominant. There was little methanogenesis below 5 cm depth in the sediment which indicated a rapid decrease of degradable organic matter with depth. There was a remarkable difference, especially in winter, between methane fluxes which were measured in batch experiments and those calculated from the concentration profiles in the sediment. These differences may be due to methane diffusing upward from deep layers.     

Effects of the burrowing mayfly,Hexagenia, on nitrogen and sulfur fractions in lake sediment microcosms

Effects of the burrowing mayfly, Hexagenia, on nitrogen and sulfur fractions of sediment, and overlying water were determined. Laboratory microcosms were used to reproduce the benthic environment. The activities of Hexagenia increased sediment Eh (1.98 ± 0.486 (22) mV · day ⁻¹), and decreased pH in sediment (−0.007 ± 0.001 (22) day ⁻¹) and overlying water(-0.024 ± 0.004 (10) day⁻¹). In the control, Eh decreased and pH did not change. The presence of Hexagenia also markedly increased ammonia in sediment (5.46 ± 0.14 (22) ppm N · day⁻¹) and overlying water (0.792 ± 0.154 (10) ppm N · day⁻¹), while the control did not change. In addition, the sulfate fraction of sediment (0.177 ± 0.006 (17)% dry mass) and water (50.0 ± 4.9 (5) mg · I⁻¹) in microcosms with Hexagenia was greater than that of the control (0.151 ± 0.005 (16)% dry mass; 14.7 ± 1.71 (3) mg · 1⁻¹) at the termination of the experiment. Hexagenia may also stimulate the mineralization of carbon-bonded sulfur. The general role of Hexagenia in altering sediment chemistry is discussed.     

Potential capacity of coprecipitation of dissolved organic carbon (DOC) with iron(III) precipitates

Hypolimnetic anoxic water of Lake Onogawa was subjected to aeration experiments. When the samples were agitated by magnetic stirrers for 24 h, dissolved oxygen increased from 0 to more than 7.6 mg l⁻¹, dissolved iron decreased from 98% to about 5% of the initial total iron, and from 32% to 48% of the dissolved organic carbon (DOC) disappeared. On the other hand, when the anoxic waters were left unstirred, dissolved oxygen increased from 0 to 2.2 mg l⁻¹, dissolved iron decreased from 98% to 31%, and 20% of the DOC disappeared within 48 h. Further 24-h incubation had little effect on the DOC loss, although dissolved oxygen increased to 3.9 mg l⁻¹ and dissolved iron decreased to 5%. These rates of DOC disappearance are too large to be explained by bacterial decomposition. It is quite conceivable that a part of the DOC is coprecipitated with iron(III) precipitates. When Fe(II) in the anoxic hypolimnion is oxidized by autumnal water mixing, probably anoxic water is mixed with aerobic water. The anoxic water must receive oxygen from the aerobic water during this mixing and be simultaneously diluted with the aerobic water. Because the present experimental conditions, especially the stirred one, significantly differ from in situ conditions, the present results are thought to be a potential capacity of DOC coprecipitation.     

Distribution and Characteristics of Dissolved Organic Matter in Mangrove Sediment Pore Waters along the Coastline of French Guiana

Mangroves represent a major environment of tropical coasts. They are highly productive, and act both as a source and a sink of organic carbon. Concentrations and characteristics (fluorescence and hydrophobic–hydrophilic fractions) of dissolved organic matter (DOM) were investigated in relation to the organic content of sediments and to the chemistry of pore waters along the coastline of French Guiana. The pore waters studied were extracted (centrifugation, soil moisture sampler) from sediments cored beneath A. germinans mangrove stands representative of development stages: pioneer, mature and senescent. In order to asses the effects of seasonal changes, two cores were performed in each location, just after dry and wet seasons, respectively. Dissolved organic carbon (DOC) concentrations in pore waters of the upper sediment were found to increase, from 0.7 mmol l⁻¹ under the pioneers to 9 under senescent mangroves. The evolution of sedimentary organic carbon (SedOC) in the same sediment paralleled that of DOC, increasing from 0.7 to 28%. On the contrary, in the lower parts of sediment cores SedOC and DOC displayed contrasting vertical trends: SedOC decreased sharply with depth while DOC increased, reaching concentrations up to 30 mmol l⁻¹ at 50 cm in the older, senescent mangroves. In addition, the Fluorescence/DOC ratios and the hydrophobic contents of DOC were higher at greater depths in most cores, expressing changes in the DOC composition. These results suggest that the DOC of the upper layers originated directly from the SedOC of the enclosing sediment, while the hydrophobic and fluorescent DOC accumulated in the anoxic bottom layer. The mechanisms responsible for this accumulation at depth requires additional research to be fully understood. However, the anoxic conditions and high pH values prevailing in the lower sediment, by lessening DOM sorption and enhancing SedOC dissolution, may be partly responsible for the high DOC concentrations and fluorescences at depth. In addition, seasonal variation may be involved. During the rainy season, water sources were mixed resulting in lower DOC concentrations in the upper sediment, whereas during the dry season, increased evapotranspiration concentrate salts and DOC, which are transported vertically with percolating water.     

Localization of iron-reducing activity in paddy soilby profile studies

Profiles of iron speciations (porewaterFe(II) and Fe(III), solid-phase Fe(II) andFe(III)) have been studied to localize both ironreduction and oxidation in flooded paddy soil. Sulfateand nitrate were determined to analyze interactions ofredox reactions involved in the iron cycle with thoseof the sulfur and nitrogen cycle. The development ofthe iron(II) and iron(III) profiles was observed inmicroscale over a time period of 11 weeks. After 11weeks the profiles were stable and showed lowestconcentrations of solid-phase iron(II) on the soilsurface with increasing concentrations to a soil depthof 10 mm ( 100 µmol/cm³). Profilesof iron(III) showed a maximum of iron(III) at a depthof 2 to 4 mm ( 100--200 µmol/cm³).Porewater iron(II) concentrations were three orders ofmagnitude lower than extracted iron(II) and indicatedthat most iron(II) was adsorbed to the solid-phase orimmobilized as siderite and vivianite. Diffusive lossof iron from the soil was indicated by iron recovery(0.3 µmol gdw^–1) in the flooding water after12 weeks. The organic content of the soil influencedthe concentrations of solid-phase iron(II) in deepersoil layers (> 6 mm); higher Fe(II) concentrationsin soil with limiting amounts of electron donors mayindicate lower consumption of CO₂ by methanogenicbacteria and therefore a higher sideriteprecipitation. Soil planted with rice showed similariron(II) profiles of fresh paddy soil cores. However,maximal iron(III) concentrations ( 350µmol/cm³) were present in planted soil at adepth of 1 to 2.5 mm where oxygen is provided by a matof fine roots. Sulfate and nitrate concentrations inthe porewater were highest on the soil surface (10µM NO₃ ^–, 40 µM SO₄ ^2–) anddecreased with depth. Similar profiles were detectedfor malate, acetate, lactate, and propionate, theconcentrations decreased gradually from the surface toa depth of 4 mm. Profiles of oxygen showed highestconcentrations at the surface due to photosyntheticproduction and a depletion of oxygen below 3 mm depth.Methane production rates measured from soil layersincubated separately in closed vessels were zero atthe soil surface and increased with depth. In soildepths below 4 mm where iron(III) concentrationsdecreased higher methane production rates werefound.     

Growth of <Emphasis Type="Italic">Pseudomonas chloritidismutans</Emphasis> AW-1<Superscript>T</Superscript> on <Emphasis Type="Italic">n</Emphasis>-alkanes with chlorate as electron acceptor

Microbial (per)chlorate reduction is a unique process in which molecular oxygen is formed during the dismutation of chlorite. The oxygen thus formed may be used to degrade hydrocarbons by means of oxygenases under seemingly anoxic conditions. Up to now, no bacterium has been described that grows on aliphatic hydrocarbons with chlorate. Here, we report that Pseudomonas chloritidismutans AW-1^T grows on n-alkanes (ranging from C7 until C12) with chlorate as electron acceptor. Strain AW-1^T also grows on the intermediates of the presumed n-alkane degradation pathway. The specific growth rates on n-decane and chlorate and n-decane and oxygen were 0.5 ± 0.1 and 0.4 ± 0.02 day⁻¹, respectively. The key enzymes chlorate reductase and chlorite dismutase were assayed and found to be present. The oxygen-dependent alkane oxidation was demonstrated in whole-cell suspensions. The strain degrades n-alkanes with oxygen and chlorate but not with nitrate, thus suggesting that the strain employs oxygenase-dependent pathways for the breakdown of n-alkanes.     

Short-term spatial and temporal variation of sediment oxygen dynamics in a tropical tidal salt flat

Short-term spatial and temporal heterogeneity of oxygen dynamics and net primary production were studied in a tree day diurnal variation at a tidal tropical salt flat in the estuarine system of Sepetiba/Guaratiba coastal plain, Rio de Janeiro, Brazil. Oxygen concentrations were measured in situ with high temporal and spatial resolution oxygen microsensors. The results showed a remarkable heterogeneity of both oxygen penetration depth (from 0.18 to 0.85 cm) and net primary production (from −0.085 to 0.115 μmol O₂ cm⁻² s⁻¹) at different stations and sampling periods. Fast variations in abiotic factors like salinity and light due to the variable rainy weather were possibly the drivers of the high heterogeneity. In conclusion, short-term temporal changes could have a remarkable influence in sediment microalgae primary production. Not considering these changes can lead to wrong conclusions concerning the role and importance of sediment microalgae on tidal salt flats.     

Succession of cable bacteria and electric currents in marine sediment

Filamentous Desulfobulbaceae have been reported to conduct electrons over centimetre-long distances, thereby coupling oxygen reduction at the surface of marine sediment to sulphide oxidation in sub-surface layers. To understand how these ‘cable bacteria'' establish and sustain electric conductivity, we followed a population for 53 days after exposing sulphidic sediment with initially no detectable filaments to oxygen. After 10 days, cable bacteria and electric currents were established throughout the top 15 mm of the sediment, and after 21 days the filament density peaked with a total length of 2 km cm⁻². Cells elongated and divided at all depths with doubling times over the first 10 days of <20 h. Active, oriented movement must have occurred to explain the separation of O₂ and H₂S by 15 mm. Filament diameters varied from 0.4–1.7 μm, with a general increase over time and depth, and yet they shared 16S rRNA sequence identity of >98%. Comparison of the increase in biovolume and electric current density suggested high cellular growth efficiency. While the vertical expansion of filaments continued over time and reached 30 mm, the electric current density and biomass declined after 13 and 21 days, respectively. This might reflect a breakdown of short filaments as their solid sulphide sources became depleted in the top layers of the anoxic zone. In conclusion, cable bacteria combine rapid and efficient growth with oriented movement to establish and exploit the spatially separated half-reactions of sulphide oxidation and oxygen consumption.     

Effects of Spilled Oil on Bacterial Communities of Mediterranean Coastal Anoxic Sediments Chronically Subjected to Oil Hydrocarbon Contamination

The effects of spilled oil on sedimentary bacterial communities were examined in situ at 20 m water depth in a Mediterranean coastal area. Sediment collected at an experimental site chronically subjected to hydrocarbon inputs was reworked into PVC cores with or without a massive addition of crude Arabian light oil (∼20 g kg⁻¹ dry weight). Cores were reinserted into the sediment and incubated in situ at the sampling site (20 m water depth) for 135 and 503 days. The massive oil contamination induced significant shifts in the structure of the indigenous bacterial communities as shown by ribosomal intergenic spacer analysis (RISA). The vertical heterogeneity of the bacterial communities within the sediment was more pronounced in the oiled sediments particularly after 503 days of incubation. Response to oil of the deeper depth communities (8–10 cm) was slower than that of superficial depth communities (0–1 and 2–4 cm). Analysis of the oil composition by gas chromatography revealed a typical microbial alteration of n-alkanes during the experiment. Predominant RISA bands in oiled sediments were affiliated to hydrocarbonoclastic bacteria sequences. In particular, a 395-bp RISA band, which was the dominant band in all the oiled sediments for both incubation times, was closely related to hydrocarbonoclastic sulfate-reducing bacteria (SRB). These bacteria may have contributed to the main fingerprint changes and to the observed biodegradation of n-alkanes. This study provides useful information on bacterial dynamics in anoxic contaminated infralittoral sediments and highlights the need to assess more precisely the contribution of SRB to bioremediation in oil anoxic contaminated areas.     

Distribution of microphytobenthic biomass in Martel Inlet,King George Island (Antarctica)

The spatial and temporal variation of microphytobenthic biomass in the nearshore zone of Martel Inlet (King George Island, Antarctica) was estimated at several sites and depths (10–60 m), during three summer periods (1996/1997, 1997/1998, 2004/2005). The mean values were inversely related to the bathymetric gradient: higher ones at 10–20 m depth (136.2 ± 112.5 mg Chl a m⁻², 261.7 ± 455.9 mg Phaeo m⁻²), intermediate at 20–30 m (55.6 ± 39.5 mg Chl a m⁻², 108.8 ± 73.0 mg Phaeo m⁻²) and lower ones at 40–60 m (22.7 ± 23.7 mg Chl a m⁻², 58.3 ± 38.9 mg Phaeo m⁻²). There was also a reduction in the Chl a/Phaeo ratio with depth, from 3.2 ± 3.2 (10–20 m) to 0.7 ± 1.0 (40–60 m), showing a higher contribution of senescent phytoplankton and/or macroalgae debris at the deeper sites and the limited light flux reaching the bottom. Horizontal differences found in the biomass throughout the inlet could not be clearly related to hydrodynamics or proximity to glaciers, but with sediment characteristics. An inter-summer variation was observed: the first summer presented the highest microphytobenthic biomass apparently related to more hydrodynamic conditions, which causes the deposition of allochthonous material.