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1.
The Bay of Concepcion (36°40′S; 73°02′W) is a semi-enclosed and shallow embayment in which biogeochemical processes are seasonally coupled to coastal upwelling during the austral spring and summer. The nutrient cycle in the bay is complex due to the combined effects of a pronounced O2 minimum layer and high nutrient concentrations both originating from subsurface equatorial water during coastal upwelling and a rapid rate of sediment nutrient recycling. The sediments are characterized by a high content of organic matter mainly due to the extremely high rates of phytoplankton production and deposition. During the upwelling period, a black flocculent layer frequently covers the sediment–water interface in the inner part of the bay where an extensive mat of Beggiatoa spp. develops. Three approaches are used to analyse the extent to which the benthic system recycles or retains nutrients at two stations, located at the centre (station C, St. C) and mouth (station B, St. B) of the bay for a 1-year period (March 1996–1997): (1) estimation of C and N remineralization rates based on SO42− reduction measurements, (2) calculation of C and N turnover rates using a diagenetic model applied to total organic carbon and total nitrogen vertical distributions and, (3) construction of C and N budgets from direct measurements of sedimentation (from a sediment trap) and estimates of the C and N burial rates. Depth-integrated SO42− reduction rates varied between 3.4 (winter) and 25.5 (summer) mmol m−2 d−1. Estimated C and N oxidation rates ranged between 7.9 and 87.8 mol C m−2 yr−1 and between 0.9 and 6.9 mol N m−2 yr−1, respectively. Each approach yielded minor differences in the C and N remineralization rates (and also minor differences between both studied stations), except when the kinetic model was applied to C and N distribution without including the presence of the flocculent layer. The rates of carbon oxidation and sulphate reduction were considerably higher than in other coastal sediments with similar depositional regime. The C and N burial rates were 2.23 and 0.21 (St. C) and 1.30 and 0.09 (St. B) mol m−2 yr−1, respectively. The C/N ratio of the buried fraction was ca. 10.6 at St. C and 14.4 at St. B. Because the observed differences in burial rates could not be ascribed to distinctive depositional (both stations have similar sediment accumulation rates) and oceanographic (similar O2 concentration and hydrography) conditions, differences may be due to in part spatial heterogeneity in the supply of organic matter. The degree of preservation of organic matter as plankton detritus and nitrogen accumulating bacterial biomass associated with Beggiatoa spp. at St. C may also be involved.  相似文献   

2.
Benthic oxygen uptake, sulphate reduction and benthic bacterial production were measured at two contrasting locations in the southern North Sea: the shallow and turbulent Broad Fourteens area in the Southern Bight, and the deeper Oyster Grounds, a deposition area, where thermohaline stratification occurs during summer. Oxygen uptake and sulphate reduction showed a clear seasonal pattern in the Broad Fourteens area, indicating a supply of carbon to the benthic system that is closely related to the standing stock of carbon in the water column. This close benthic-pelagic coupling is probably due to the influence of the tide in this part of the North Sea, which keeps the water column permanently mixed. At the Oyster Grounds, no seasonal pattern was observed. Peaks in oxygen uptake and sulphate reduction were found in winter. Irregularly occurring events, such as storms and fishery-related activities, are likely to affect the benthic mineralization patterns in this area. Annual benthic carbon mineralization rates estimated from oxygen uptake rates were 44 gC·m−2 at the Broad Fourteens, and 131 gC·m−2 at the Oyster Grounds, of which 26 and 28%, respectively, could be attributed to sulphate reduction (assuming an annual sulphide reoxidation rate of 100%). Although sulphate reduction rates in the southern North Sea are higher than previously suggested, aerobic respiration is the most important pathway for benthic carbon mineralization at the stations visited. Production rates of benthic bacterial carbon measured with labelled leucine were much higher than carbon mineralization rates based on oxygen uptake or sulphate reduction. This may either imply a very high bacterial carbon conversion efficiency, or point to shortcomings in the accuracy of the techniques. A critical evaluation of the techniques is recommended.  相似文献   

3.
Vertical gas profiles of N2, N2O and O2were obtained in intact sediment cores from a Tagus estuary salt marsh using membrane inlet mass spectrometry. This technique allows direct measurements of dissolved gas concentrations with minimal disturbance. O2concentrations decreased sharply with depth, becoming undetectable below 14mm. Denitrification products (N2and N2O) occurred in the surface layer of the sediment where O2was present. Diffusion of N2and N2O from the anaerobic zone, denitrification in anaerobic microsites and aerobic denitrification are possible explanations for this observation. N2was the sole product of denitrification in control sediment cores probably because of the great demand for electron acceptors in this sediment. The addition of NO3 − and CH3CO2 − increased the concentrations of N2and N2O in the sediment. Significantly higher concentrations in treated cores occurred between 1·5 and 2·0cm for N2and between 0·5 and 1·5cm for N2O. The peak in N2concentration occurred in the anaerobic zone of the sediment, close to the aerobic–anaerobic interface while the peak in N2O concentration occurred above this interface where concentrations of O2were approximately 10μM. This is indicative that, in this sediment, production of N2O is less sensitive to the presence of O2than reduction of N2O to N2.  相似文献   

4.
The characteristics of Mn(II) removal from sediment porewater and the potential role of manganese-oxidizing bacteria in this process were examined in sediments from a 335-m deep station in the Laurentian Trough of the St. Lawrence estuary. Manganese-oxidizing bacteria were most abundant in the thin layer of oxidized surface sediment, where Mn(II) removal rates were also fastest. The first-order rate constants for Mn(II) removal decreased from 1·2 × 103 day−1 to 6·6 day−1 over the first 30-mm depth. In experimental slurries, sediments removed Mn(II) from reduced zone porewater by a two-step process: a rapid saturation of Mn(II) binding sites was followed by a slower O2-enhanced removal rate which paralleled the apparent rate of Mn(II) oxidation. Sodium azide and mercuric chloride were tested specifically for their usefulness as bacterial poisons in sediment slurry systems. Sodium azide interfered with Mn(II) removal at low concentrations and was not an effective poison. Mercuric chloride inhibited bacterial activity at concentrations far lower than those at which significant interference of Mn(II) removal occurred. The response of sediment slurries treated with mercuric chloride indicated that the initial oxidation of sorbed Mn(II) was not bacterially-mediated under the experimental conditions tested.  相似文献   

5.
The influence of bioturbation on certain aspects of the biogeochemistry of sulfur and iron was examined in shallow-water sediments of Great Bay Estuary, New Hampshire. A bioturbated (JEL) and non-bioturbated (SQUAM) site were compared. Annual sulfate reduction measured with 35S, was 4·5 times more rapid at JEL. A significant portion of this difference was attributed to rapid rates which occurred throughout the upper 12 cm of sediment at JEL due to infaunal reworking activities. Sulfate reduction decreased rapidly with depth at SQUAM. FeS in the upper 2 cm at JEL increased in concentration from 3 to 45 μmol ml−1 from early May to late July while only increasing from 3 to 8 μmol ml−1 at SQUAM. Infaunal irrigation and reworking activities caused rapid and continous subsurface cycling of iron and sulfur at JEL. This maintained dissolved iron concentrations at 160–170 μM throughout the summer despite rapid sulfide production. Therefore, dissolved sulfide never accumulated in JEL pore waters. Although dissolved organic carbon (DOC) was generated during sulfate reduction, bioturbation during summer caused a net removal of DOC from JEL pore waters. Sulfate reduction rates, decomposition stoichiometry and nutrient concentrations were used to calculate turnover times of nutrients in pore waters. Nutrient turnover varied temporally and increased three-to five-fold during bioturbation. A secondary maximum in the abundance of recoverable sulfate-reducing bacteria occurred at 10 cm in JEL sediments only during periods of active bioturbation, demonstrating the influence of macrofaunal activities on bacterial distributions.  相似文献   

6.
The magnitude of the exchange flux at the water–sediment interface was determined on the basis of the ammonia concentration gradient at the near-bottom water–interstitial interface and Fick's first law. It was established that in Puck Bay, ammonia almost always passes from the sediment to water. Ammonia flux varied from 5 to 1434 μmol NH4-N m−2 day−1. In total,c. 138·2 tonneammonia year−1pass from sediments of Internal Puck Bay to near-bottom water, the equivalent value for External Puck Bay being 686·9 tonne year−1. In total, about 825 tonne ammonia year−1passes from the sediment to near-bottom water of Puck Bay. In interstitial waters, ammonia occurred in concentrations varying over a wide range (3–1084 μmol NH4-N dm−3).The basic factors affecting the magnitude of ammonia concentration in interstitial waters included: oxidation of organic matter, type of sediment, and inflow of fresh underground waters to the region examined.This paper involves preliminary studies only and constitutes a continuation of the studies on ionic macrocomponents and phosphorus in interstitial waters of Puck Bay undertaken previously.  相似文献   

7.
An intense diatom bloom developed within a strong meridional silicic acid gradient across the Antarctic Polar Front at 61°S, 170°W following stratification of the water column in late October/early November 1997. The region of high diatom biomass and the silicic acid gradient propogated southward across the Seasonal Ice Zone through time, with the maximum diatom biomass tracking the center of the silicic acid gradient. High diatom biomass and high rates of silica production persisted within the silicic acid gradient until the end of January 1998 (ca. 70 d) driving the gradient over 500 km to the south of its original position at the Polar Front. The bloom consumed 30 to >40 μM Si(OH)4 in the euphotic zone between about 60 and 66°S leaving near surface concentrations <2.5 μM and occasionally <1.0 μM in its wake. Integrated biogenic silica concentrations within the bloom averaged 410 mmol Si m−2 (range 162–793 mmol Si m−2). Average integrated silica production on two consecutive cruises in December 1997 and January 1998 that sampled the bloom while it was well developed were 27.5±6.9 and 22.6±20 mmol Si m−2 d−1, respectively. Those levels of siliceous biomass and silica production are similar in magnitude to those reported for ice-edge diatom blooms in the Ross Sea, Antarctica, which is considered to be among the most productive regions in the Southern Ocean. Net silica production (production minus dissolution) in surface waters during the bloom was 16–21 mmol Si m−2 d−1, which is sufficient for diatom growth to be the cause of the southward displacement of the silicic acid gradient. A strong seasonal change in silica dissolution : silica production rate ratios was observed. Integrated silica dissolution rates in the upper 100–150 m during the low biomass period before stratification averaged 64% of integrated production. During the bloom integrated dissolution rates averaged only 23% of integrated silica production, making 77% of the opal produced available for export to depth. The bloom ended in late January apparently due to a mixing event. Dissolution : production rate ratios increased to an average of 0.67 during that period indicating a return to a predominantly regenerative system.Our observations indicate that high diatom biomass and high silica production rates previously observed in the marginal seas around Antarctica also occur in the deep ocean near the Polar Front. The bloom we observed propagated across the latitudinal band overlying the sedimentary opal belt which encircles most of Antarctica implying a role for such blooms in the formation of those sediments. Comparison of our surface silica production rates with new estimates of opal accumulation rates in the abyssal sediments of the Southern Ocean, which have been corrected for sediment focusing, indicate a burial efficiency of 4.6% for biogenic silica. That efficiency is considerably lower than previous estimates for the Southern Ocean.  相似文献   

8.
Concentrations of U and Th isotopes in Okinawa Trough and East China Sea sediment cores were determined by isotope dilution inductively coupled plasma-mass spectrometry (ID-ICP-MS) to investigate the behavior of redox sensitive uranium in suboxic hemipelagic sediments and determine their significance in oceanic uranium balance. 238U concentrations and 238U/232Th activity ratios in the East China Sea sediments showed no remarkable variation with depth. However, 238U and 238U/232Th ratios in the Okinawa Trough sediments were low in the surface oxidizing layer but increased where the suboxic condition was encountered. The distribution profiles of 230Th and 232Th concentrations were relatively constant with depth in both the Okinawa Trough and East China Sea sediment cores. These results suggested that there has been post-depositional precipitation of authigenic uranium within the suboxic Okinawa Trough sediment column. The post-depositional precipitation rates of authigenic uranium were estimated to be 47 ± 5 to >62 ± 8 ng cm−2 yr−1; these rates were comparable to those previously reported for several anoxic sediments. A mechanism controlling precipitation of uranium may be the downward diffusion of uranium U(VI), reduction to U(IV) and finally precipitation onto the solid phase. The accumulation rate of uranium for the Okinawa Trough sediments was approximately eight times higher than the world average rate reported for suboxic sediments. This removal of uranium in the oceanic budget increases the importance of the suboxic sediment sink.  相似文献   

9.
Sulfate reduction in deep coastal marine sediments   总被引：1，自引：0，他引：1  
Sulfate reduction rates in sediments of four deep stations in the Saguenay Fjord and the Laurentian Trough, Gulf of St. Lawrence, are among the lowest reported for the coastal environment. Maximum rates were 0.4–7.0 nmol cm−3 day−1. The low rates are due to relatively low sedimentation rates and continuously low temperatures. Regional differences in both integrated and maximum sulfate reduction rates in the sediment correlate with sediment trap measurements of sedimentation rate and organic carbon flux.Sulfate reduction accounts for the degradation of 5–26% of the estimated downward flux of organic matter to these sediments. Unlike the absolute rate of sulfate reduction, the relative proportion of the carbon flux that is degraded via sulfate reduction is not directly correlated with the sedimentation rate but is a function of organic matter composition, intensity of bioturbation, and the abundance of sub-oxic electron acceptors. Thus, the lowest proportion of carbon degradation via sulfate reduction occurred at a Gulf site, where a combination of low sedimentation and bioturbation rates allowed a long residence time for organic matter near the sediment surface and, in consequence, a low flux of labile carbon into the sulfate reduction zone. The highest proportion was observed at a station with a similar organic carbon flux but with higher rates of sedimentation and bioturbation. At a third site, with the highest rates of sulfate reduction as well as the highest rates of sedimentation and bioturbation, the contribution of sulfate reduction to organic matter degradation was only intermediate. This is attributable to the exhaustion of the supply of porewater sulfate. In deep coastal environments the proportion of organic matter degraded via sulfate reduction can be highly variable both spatially and temporally.  相似文献   

10.
A carbon flux study was carried out off the coast of Morocco, at 31°N, in a region characterized by the presence of a persistent cyclonic eddy. Two short-term (4 and 3 day) deployments of free-floating sediment traps were combined with water column sampling and rate process measurements as the ship followed the traps. For a period of 36 h between trap deployments, a hydrographic section was run along 31°30'N as part of a larger scale survey being carried out simultaneously on the R.V. A. von Humboldt. The first trap deployment was near the eastern margin of the eddy and the traps moved to the north and west in a frontal jet associated with its northern boundary. After the second deployment, which was at the recovery point of the first, the traps moved to the west and then to the southwest. Throughout the study, chlorophyll concentrations varied between 27 and 125 mg m−2 (0–100 m), with highest concentrations in the upwelled water nearest the coast and in upwelled water generated within the cyclonic eddy. Particulate organic carbon (POC) and particulate organic nitrogen (PON) concentrations were relatively uniform (13.6±1.8 and 1.63±28 g m−2 with phytoplankton carbon accounting for 16–85% of total POC. Bacterial carbon was 5% of total POC and mesozooplankton carbon concentrations were equivalent to 9% of total POC. Microzooplankton biomass was not assessed but POC:PON ratios in the water column were often high, suggesting there was sometimes a large detrital component in the POC. Primary production rates varied between 1.0 and 2.5 g C m−2 day−1. Bacterial consumption accounted for 50% of primary production. Metabolic rates suggested that copepods were ingesting more than 0.4 g C m−2 day−1. while filtration rates suggested that ingestion of phytoplankton carbon was only 0.2 g C m−2day−1, even when phytoplankton constituted 85% of the POC. f-ratios (based on uptake rates for 15N-nitrate and ammonia) were between 0.1 and 0.4, and excretion by mesozooplankton could account for 40% of the daily ammonium uptake by phytoplankton. HPLC pigment analysis showed that when chlorophyll biomass was high, diatoms were dominant, whereas when it was low, small prymnesiophytes, chlorophytes and diatoms were all important. The composition of the fluoresecent pigments in material in the sediment traps indicated that intact phytoplankton and copepod faecal pellets were the main sources but the relative rates of sedimentation of pigment, POC and PON for the two trapping periods did not reflect differences that were observed in the overlying water column. This was likely to be the result of spatial heterogeneity and strong horizontal currents heterogeneity and strong horizontal currents within the euphotic zone. Thus, material collected at 100 m probably did not originate in the water column immediately overlying the traps and trapping efficiencies might also have been variable.  相似文献   

11.
Sediment characteristics, sediment respiration (oxygen uptake and sulphate reduction) and sediment–water nutrient exchange, in conjunction with water column structure and phytoplankton biomass were measured at five stations across the western Irish Sea front in August 2000. The transition from thermally stratified (surface to bottom temperature difference of 2.3 °C) to isothermal water (14.3 °C) occurred over a distance of 13 km. The influence of the front on phytoplankton biomass was limited to a small region of elevated near surface chlorophyll (2.23 mg m−3; 50% > biomass in mixed waters). The front clearly marked the boundary between depositional sediments (silt/clays) with elevated sediment pigment levels (≈60 mg m−2) on the western side, to pigment impoverished (<5 mg m−2) sand, through to coarse sand and shell fragments on the eastern side. Maximal rates of sedimentary respiration on the western stratified side of the front e.g. oxygen uptake S2 (852 μmol O2 m−2 h−1) and sulphate reduction at S1 (149 μmol SO42− m−2 h−1), coupled to significant efflux of nitrate and silicate at the western stations indicate closer benthic–pelagic coupling in the western Irish Sea. Whether this simply reflects the input of phytodetritus from the overlying water column or entrapment and settlement of pelagic production from other regions of the Irish Sea cannot yet be resolved.  相似文献   

12.
Thirty-one surficial sediment samples were collected from the floor of Izmit Bay with a grab onboard the R/V Bilim in summer 1987 and analysed for their grain size, total carbonate, and organic carbon distribution.Low calcareous-terrigenous mud (2–45% CaCO3) with a relatively high silt percentage was the principal sediment type found on the floor of Izmit Bay. Sediments rich in sand and gravel usually occur in the narrow and shoal areas of the bay, where biogenic and topography-related hydrodynamic conditions are dominant factors controlling the nature of bottom deposits. The carbonates are made up almost entirely of the remains of calcareous organisms. Organic carbon concentrations of the sediments (0·35-1·62%) are probably associated with the high primary production rates in this region. Thus, the rates of sedimentation in the Izmit Bay calculated from the organic carbon and primary productivity data are estimated to be up to 70 cm/1000 years.  相似文献   

13.
Mussels (Mytilus edulis L.) were exposed to North Sea crude oil, microencapsulated oil and dispersants, singly and in combination, and growth rates measured at 24–48 h intervals.Exposure to microencapsulated pure oil (2·0–2·1 mg litre−1) and to microencapsulated mixtures of oil (2·2−2·5 mg litre-1+5 % of the different dispersants (FINASOL OSR 5, COREXIT 9527, DISPOLENE 36 S) gave approximately the same reduction in growth rate (80–90%) within 170h.Oil chemically dispersed with DISPOLENE 36 S and a pure oil mechanically dispersed in water were significantly less toxic. In high concentrations (2 mg litre−1) all disperants are toxic, DISPOLENE 36 S ssignificantly more than the others.Mussels exposed for 170 h to microencapsulated oil and to microencapsulated oil dispersant mixtures recovered to control growth within 300 h in clean seawater, while in those given pure oil-in-water suspension, the recovery was slower.It is concluded that the toxicity of oil is mainly related to size and concentration of oil particles, while the effect of 5% dispersants added is negligible.  相似文献   

14.
A sediment disk reactor was tested in once flow-through mode to retrieve kinetic parameters for the Monod rate law that describes sulfate reduction. The experimental method was compared with a previously described procedure by the authors where a sediment plug-flow reactor was operated in a recirculation mode. In recirculation mode, accumulation of metabolic byproducts in certain cases may result in negative feedback, thus preventing accurate determination of kinetic information. The method described in this article provides an alternative to the recirculation sediment plug-flow-through reactor technique for retrieving kinetic parameters of microbially mediated reactions in aquatic sediments.For sulfate reduction in a saltmarsh site, a maximum estimate of the half-saturation concentration, Ks, of 204±26 μM and a maximum reaction rate, Rm, of 2846±129 nmol cm(wetsediment)3 d−1 was determined. The Ks value obtained was consistent with the one estimated previously (Ks=240±20 μM) from a different site within the same saltmarsh mud flat using a recirculating reactor. From the Rm value and reduction rates determined using 35SO42− incubation experiments, we infer that sulfate reduction is limited in the field. Substrate availability is not the main contributor for the limitation, however. Competition from other microbes, such as iron reducers affects the activity of sulfate reducers in the suboxic to anoxic zones, whereas aerobes compete in the oxic zone. High sulfide concentration in the pore water may also have acted as a toxin to the sulfate reducers in the field.  相似文献   

15.
Lagrangian time series of dimethylsulfide (DMS) concentrations from a cyclonic and an anticyclonic eddy in the Sargasso Sea were used in conjunction with measured DMS loss rates and a model of vertical mixing to estimate gross DMS production in the upper 60 m during summer 2004. Loss terms included biological consumption, photolysis, and ventilation to the atmosphere. The time- and depth (0–60 m)-averaged gross DMS production was estimated to be 0.73±0.09 nM d−1 in the cyclonic eddy and 0.90±0.15 nM d−1 in the anticyclonic eddy, with respective DMS replacement times of 5±1 and 6±1 d. The higher estimated rate of gross production and lower measured loss rate constants in the anticyclonic eddy were equally responsible for this eddy's 50% higher DMS inventory (0–60 m). When normalized to chlorophyll and total dimethylsulfoniopropionate (DMSP), estimated gross production in the anticyclonic eddy was about twice that in the cyclonic eddy, consistent with the greater fraction of phytoplankton that were DMSP producers in the anticyclonic eddy. Higher rates of gross production were estimated below the mixed layer, contributing to the subsurface DMS maximum found in both eddies. In both eddies, gas exchange, microbial consumption, and photolysis were roughly equal DMS loss terms in the surface mixed layer (0.2–0.4 nM d−1). Vertical mixing was a substantial source of DMS to the surface mixed layer in both eddies (0.2–0.3 nM d−1) owing to the relatively high DMS concentrations below the mixed layer. Estimated net biological DMS production rates (gross production minus microbial consumption) in the mixed layer were substantially lower (by almost a factor of 3) than those estimated in a previous study of the Sargasso Sea, which may explain the relatively low mixed-layer DMS concentrations found here during July 2004 (3 nM) compared to previous summers (4–6 nM).  相似文献   

16.
The sediments of Southampton Water were analysed for petroleum hydrocarbons to determine the fate of petrochemical refinery waste in the estuary. Much of the petroleum hydrocarbons appears to be removed by adsorption onto estuarine sediments close to source. Surface sediment concentrations range from 3·1mg/g dry weight near a refinery to 0·5 mg/g dry weight at locations distant from the refinery.The absence of any change with depth in total hydrocarbon concentrations from some sediment cores and the presence of distinct ‘oil’ horizons in others suggests that mixing of sediments in the area is very random. Sedimentation rates in areas where a distinct oil horizon was observed ranged from 1 to 3cm a year.  相似文献   

17.
The products of 35S-sulphate reduction by sedimentary bacteria were measured at two sites in a salt marsh on the east coast of England. Non-acid-volatile products were measured, after acid-volatile sulphide was removed, by their reduction to sulphide by digestion with tin. The proportion of the sulphate reduced to tin-reducible products varied between 25% in a salt marsh pan and 61% in creek sediment, over a 0–25 cm depth profile. There were also variations with depth at each site in the proportions of sulphate reduced to tin-reducible products. Further examination revealed differences in the proportions of sulphate which were reduced to free sulphide, acid-volatile sulphide, sulphur or pyrite at the two sites. The data suggest that previous work which did not measure non-acid-volatile products underestimated sulphate reduction rates by three-fold in the creek site, but by only one third in the pan.  相似文献   

18.
Proper sample storage and analytical techniques are required when analyzing anoxic sediment for acid volatile sulfide (AVS), because a change in redox state may alter sediment parameters. The goal of this study was to determine the optimum sample handling, storage, and analytical techniques to adopt when determining AVS concentrations in sediment. To determine the correct handling and storage protocols for use with anoxic sediment, samples of three different AVS levels were manipulated under a combination of the following handling and storage plans: handled on benchtop or under nitrogen atmosphere; preserved with zinc acetate (ZnAc) or not preserved, and stored at 4 °C or frozen (< − 20 °C). The data indicate that sulfide levels are best maintained when samples are handled under a nitrogen atmosphere, stored at 4 °C or frozen, and analyzed within 2 weeks of collection. To determine the best analytical procedure for the determination of AVS in sediment, the following methods were compared: colorimetric, gravimetric, ion-selective electrode, and photoionization detection. The colorimetric method was preferred.  相似文献   

19.
The small frenulate pogonophores (Annelida: Pogonophora a.k.a. Siboglinidae) typically inhabit muddy sediments on the continental slope, although a few species occur near hydrothermal vents and cold seeps. We present data on the distribution and habitat characteristics of several species on the European continental shelf and slope from 48°N to 75°N and show how the animals interact with the chemistry of the sediments. The environments inhabited include: shallow (30 m), organic-rich, fjord sediments; slope sediments (1000–2200 m) and methane seeps at 330 m depth. All the species studied obtain nutrition from endosymbiotic bacteria. They take up reduced sulphur species, or in one case, methane, through the posterior parts of their tubes buried in the anoxic sediment. We conclude that most species undertake sulphide ‘mining’, a mechanism previously demonstrated in the bivalves Lucinoma borealis and Thyasira sarsi. These pogonophores participate in the sulphur cycle and effectively lower the sulphide content of the sediments. Our results show that the abundance of frenulate pogonophores increases with increasing sedimentation and with decreasing abundance of other benthos, particularly bioturbating organisms. The maximum sustainable carrying capacity of non-seep sediments for frenulate pogonophores is limited by the rate of sulphate reduction.  相似文献   

20.
The use of dissolved organic matter fluorescence as a tracer of river-sea mixing was examined in two South Carolina estuaries. Fluorescence declined linearly with seawater dilution in laboratory mixing studies, and also behaved conservatively in an estuary where a single river emptied into a bay. Fluorescence-salinity relationships were also studied in another estuary where a piedmont river (high suspended sediment, low fluorescence) and a coastal plains river (low sediment, high fluorescence) mixed with ocean water. The factor of 2 or greater difference in fluorescence between the two rivers allowed their relative contribution to the estuarine water mass to be distinguished. Petroleum hydrocarbons, measured in estuarine water at 0·7-1·8 μg l−1 concentrations, contributed negligibly to water fluorescence.  相似文献   

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