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1.
Benthic fluxes of dissolved inorganic nitrogen (NO3 and NH4+), dissolved organic nitrogen (DON), N2 (denitrification), O2 and TCO2 were measured in the tidal reaches of the Bremer River, south east Queensland, Australia. Measurements were made at three sites during summer and winter. Fluxes of NO3 were generally directed into the sediments at rates of up to −225 μmol N m−2 h−1. NH4+ was mostly taken up by the sediments at rates of up to −52 μmol N m−2 h−1, its ultimate fate probably being denitrification. DON fluxes were not significant during winter. During summer, fluxes of DON were observed both into (−105 μmol m−2 h−1) and out of (39 μmol m−2 h−1) the sediments. Average N2 fluxes at all sampling sites were similar during summer (162 μmol N m−2 h−1) and winter (153 μmol N m−2 h−1). Denitrification was fed both by nitrification within the sediment and NO3 from the water column. Sediment respiration rates played an important role in the dynamics of nitrification and denitrification. NO3 fluxes were significantly related to TCO2 fluxes (p<0.01), with a release of NO3 from the sediment only occurring at respiration rates below 1000 μmol C m−2 h−1. Rates of denitrification increased with respiration up to TCO2 fluxes of 1000 μmol C m−2 h−1. At sediment respiration rates above 1000 μmol C m−2 h−1, denitrification rates increased less rapidly with respiration in winter and declined during summer. On a monthly basis denitrification removed about 9% of the total nitrogen and 16% of NO3 entering the Bremer River system from known point sources. This is a similar magnitude to that estimated in other tidal river systems and estuaries receiving similar nitrogen loads. During flood events the amount of NO3 denitrified dropped to about 6% of the total river NO3 load.  相似文献   

2.
Wind-driven cyclonic eddies are hypothesized to relieve nutrient stress and enhance primary production by the upward displacement of nutrient-rich deep waters into the euphotic zone. In this study, we measured nitrate (NO3), particulate carbon (PC), particulate nitrogen (PN), their stable isotope compositions (δ15N-NO3, δ13C-PC and δ15N-PN, respectively), and dissolved organic nitrogen (DON) within Cyclone Opal, a mature wind-driven eddy generated in the lee of the Hawaiian Islands. Sampling occurred in March 2005 as part of the multi-disciplinary E-Flux study, approximately 4–6 weeks after eddy formation. Integrated NO3 concentrations above 110 m were 4.8 times greater inside the eddy (85.8±6.4 mmol N m−2) compared to the surrounding water column (17.8±7.8 mmol N m−2). Using N-isotope derived estimates of NO3 assimilation, we estimated that 213±59 mmol m−2 of NO3 was initially injected into the upper 110 m Cyclone Opal formation, implying that NO3 was assimilated at a rate of 3.75±0.5 mmol N m−2 d−1. This injected NO3 supported 68±19% and 66±9% of the phytoplankton N demand and export production, respectively. N isotope data suggest that 32±6% of the initial NO3 remained unassimilated. Self-shading, inefficiency in the transfer of N from dissolved to particulate export, or depletion of a specific nutrient other than N may have led to a lack of complete NO3 assimilation. Using a salt budget approach, we estimate that dissolved organic nitrogen (DON) concentrations increased from eddy formation (3.8±0.4 mmol N m−2) to the time of sampling (4.0±0.09 mmol N m−2), implying that DON accumulated at rate of 0.83±1.3 mmol N m−2 d−1, and accounted for 22±15% of the injected NO3. Interestingly, no significant increase in suspended PN and PC, or export production was observed inside Cyclone Opal relative to the surrounding water column. A simple N budget shows that if 22±15% of the injected NO3 was shunted into the DON pool, and 32±6% is unassimilated, then 46±16% of the injected NO3 remains undocumented. Alternative loss processes within the eddy include lateral exchange of injected NO3 along isopycnal surfaces, remineralization of PN at depth, as well as microzooplankton grazing. A 9-day time series within Cyclone Opal revealed a temporal depletion in δ15N-PN, implying a rapid change in the N source. A change in NO3 assimilation, or a shift from NO3 fueled growth to assimilation of a 15N-deplete N source, may be responsible for such observations.  相似文献   

3.
Rates of sediment accumulation and microbial mineralization were examined at three Kandelia candel forests spanning the intertidal zone along the south coastline of the heavily urbanized Jiulongljiang Estuary, Fujian Province, China. Mass sediment accumulation rates were rapid (range: 10–62 kg m−2 y−1) but decreased from the low- to the high-intertidal zone. High levels of radionuclides suggest that these sediments originate from erosion of agricultural soils within the catchment. Mineralization of sediment carbon and nitrogen was correspondingly rapid, with total rate of mineralization ranging from 135 to 191 mol C m−2 y−1 and 9 to 11 mol N m−2 y−1; rates were faster in summer than in autumn/winter. Rates of mineralization efficiency (70–93% for C; 69–92% for N) increased, as burial efficiency (7–30% for C; 8–31% for N) decreased, from the low-to the high-intertidal mangroves. Sulphate reduction was the dominant metabolic pathway to a depth of 1 m, with rates (19–281 mmol S m−2 d−1) exceeding those measured in other intertidal deposits. There is some evidence that Fe and Mn reduction-oxidation cycles are coupled to the activities of live roots within the 0–40 cm depth horizon. Oxic respiration accounted for 5–12% of total carbon mineralization. Methane flux was slow and highly variable when detectable (range: 5–66 μmol CH4 m−2 d−1). Nitrous oxide flux was also highly variable, but within the range (1.6–106.5 μmol N2O m−2 d−1) measured in other intertidal sediments. Rates of denitrification were rapid, ranging from 1106 to 3780 μmol N2 m−2 d−1, and equating to 11–20% of total sediment nitrogen inputs. Denitrification was supported by rapid NH4 release within surface deposits (range: 3.6–6.1 mmol m−2 d−1). Our results support the notion that mangrove forests are net accumulation sites for sediment and associated elements within estuaries, especially Kandelia candel forests receiving significant inputs as a direct result of intense human activity along the south China coast.  相似文献   

4.
Rates of net nitrification were calculated for four large (13 m3) estuarine-based microcosms that had been subjected to inorganic nutrient enrichment. Calculated rates were based on two years of weekly nitrate and nitrite measurements and ranged from a maximum of 0·55 μmol NO2+3 produced l−1 day−1 in the control tank (no enrichment) to over 13 μmol NO2+3 produced l−1 day−1 in the most enriched tank (receiving 18·6 μmol NH4 l−1 day−1). Almost all NO2+3 production was pelagic, little was benthic. Net NO3 production or net NO2 production dominated the net nitrification rates during different seasons. Good correlations were found between various oxidation rates and substrate concentrations. The calculated net nitrite production rates were 10 to 1000 times higher than previously reported rates for open ocean systems, demonstrating the potential importance of nitrification to estuarine systems.  相似文献   

5.
Uptake of inorganic carbon and ammonium by the plankton community of three North Carolina estuaries was measured using 14C and 15N isotope methods. At 0% light, C appeared to be lost via respiration, and at increasing light levels uptake of inorganic carbon increased linearly, saturated (mean Ik = 358±30 μEin m−2 s−1), and frequently showed inhibition at the highest light intensities. At 0% light NH4+ uptake was significantly greater than zero and was frequently equivalent to uptake in the light (light independent); at increasing light levels NH4+ uptake saturated (mean Ik = 172±44 μEin m−2 s−1) and frequently indicated strong inhibition. Light-saturated uptake rates of inorganic carbon and NH4+ were a function of chlorophyll a (r2 = 0·7−0·9); average assimilation numbers were 625 nmol CO2 (μg chl. a)−1 h−1 and 12·9 nmol NH4+ (μg chl. a)−1 h−1 and were positively correlated with temperature (r2 = 0·3−0·7). The ratio of dark to light-saturated NH4+ uptake tended to be near 1·0 for large algal populations at low NH4+ concentrations, indicating near light independence of uptake; whereas the ratio was lower for the opposite conditions. These data are interpreted as indicative of nitrogen stress, and it is suggested that uptake of NH4+ deep in the euphotic zone and at night are mechanisms for balancing the C:N of cellular pools. A 24-h study using summed short-term incubations confirmed this; the cumulative C:N of CO2 and NH4+ uptake during the daylight period was 10–20, whereas over the 24-h period the ratio was 6 due to dark NH4+ uptake. Annual carbon and nitrogen primary productivity were respectively estimated as 24 and 4·0 mol m−2 year−1 for the South River estuary, 42 and 7·3 mol m−2 year−1 for the Neuse River estuary, and 9·6 and 1·6 mol m−2 year−1 for the Newport River estuary.  相似文献   

6.
The concentration and distribution of dissolved nitrogenous compounds was studied in the Greenland Sea in June 1991. Dissolved organic (DON) and inorganic nitrogen (DIN) were determined in seawater of different origin and depth. Dissolved organic matter was isolated on XAD-2 resin and fractionated into its non-humic hydrophilic (H1), and so-called humic components (hydrophobic acid, HbA, and hydrophobic neutral, HbN). From all fractions the DON content was subsequently determined. Total DON concentrations were about 5 μmol Ni−1 in the surface and 3 μmol NI−1 below depths of 150–200 m. DIN varied between 1.5 and 1.6 μmol NI−1. There was a highly significant inverse correlation (r = −0.75) between DON and DIN suggesting a close coupling in the uptake and release of the different forms of nitrogen. The mean DON concentrations of the XAD-fractions were for HI = 2.3 μmol Ni−1, for HbA = 0.8 μmol NI and for HbN = 1.0 μmol NI−1. The average percentage contributions were, respectively, 56%, 19% and 25%. This means that about 56% of the total DON does not belong to the ‘humic fraction’. The HbN fraction was evenly distributed in the water column, without any obvious relationship with water masses, depth, or nutrient status. In contrast, the HbA fraction showed a significant correlation with total DON.  相似文献   

7.
N2O Production, Nitrification and Denitrification in an Estuarine Sediment   总被引:1,自引:0,他引:1  
The mechanisms regulating N2O production in an estuarine sediment (Tama Estuary, Japan) were studied by comparing the change in N2O production with those in nitrification and denitrification using an experimental continuous-flow sediment–water system with15N tracer (15N-NO−3 addition). From Feburary to May, both nitrification and denitrification in the sediment increased (246 to 716 μmol N m−2 h−1and 214 to 1260 μmol N m−2 h−1, respectively), while benthic N2O evolution decreased slightly (1560 to 1250 nmol N m−2 h−1). Apparent diffusion coefficients of inorganic nitrogen compounds and O2at the sediment–water interface, calculated from the respective concentration gradients and benthic fluxes, were close to the molecular diffusion coefficients (0·68–2·0 times) in February. However, they increased to 8·8–52 times in May except for that of NO−2, suggesting that the enhanced NO−3 and O2supply from the overlying water by benthic irrigation likely stimulated nitrification and denitrification. Since the progress of anoxic condition by the rise of temperature from February to May (9 to 16 °C) presumably accelerated N2O production through nitrification, the observed decrease in sedimentary N2O production seems to be attributed to the decrease in N2O production/occurrence of its consumption by denitrification. In addition to the activities of both nitrification and denitrification, the change in N2O metabolism during denitrification by the balance between total demand of the electron acceptor and supply of NO−3+NO−2 can be an important factor regulating N2O production in nearshore sediments.  相似文献   

8.
We examined the effect of light on water column and benthic fluxes in the Pensacola Bay estuary, a river-dominated system in the northeastern Gulf of Mexico. Measurements were made during the summers of 2003 and 2004 on 16 dates distributed along depth and salinity gradients. Dissolved oxygen fluxes were measured on replicate sediment and water column samples exposed to a gradient of photosynthetically active radiation. Sediment inorganic nutrient (NH4+, NO3, PO43−) fluxes were measured. The response of dissolved oxygen fluxes to variation in light was fit to a photosynthesis–irradiance model and the parameter estimates were used to calculate daily integrated production in the water column and the benthos. The results suggest that shoal environments supported substantial benthic productivity, averaging 13.6 ± 4.7 mmol O2 m−2 d−1, whereas channel environments supported low benthic productivity, averaging 0.5 ± 0.3 mmol O2 m−2 d−1SE). Estimates of baywide microphytobenthic productivity ranged from 8.1 to 16.5 mmol O2 m−2 d−1, comprising about 16–32% of total system productivity. Benthic and water column dark respiration averaged 15.2 ± 3.2 and 33.6 ± 3.7 mmol O2 m−2 d−1, respectively Inorganic nutrient fluxes were generally low compared to relevant estuarine literature values, and responded minimally to light exposure. Across all stations, nutrient fluxes from sediments to the water column averaged 1.11 ± 0.98 mmol m−2 d−1 for NH4+, 0.58 ± 1.08 mmol m−2 d−1 for NO3, 0.01 ± 0.09 mmol m−2 d−1 for PO43−. The results of this study illustrate how light reaching the sediments is an important modulator of benthic nutrient and oxygen dynamics in shallow estuarine systems.  相似文献   

9.
10.
Appropriate conditions have been achieved for the accurate, rapid, and highly precise shipboard simultaneous determination of dissolved organic carbon and total dissolved nitrogen in seawater by high temperature catalytic oxidation. A nitrogen-specific Antek 705D chemiluminescence detector and a CO2-specific LiCor Li6252 IRGA have been coupled in-series with a Shimadzu TOC-5000 organic carbon analyser. Precision of both simultaneous measurements is ≤1.5%, i.e. ±1 μmol C l−1 and ±0.3 μmol N l−1, respectively. Quality of analysis is not compromised by vibrations associated with ocean going research vessels.  相似文献   

11.
Macroalgae biomass and concentrations of nitrogen, phosphorus and chlorophyll a were determined weekly or biweekly in water and sediments, during the spring-summer of 1985 in a hypertrophic area of the lagoon of Venice. Remarkable biomass production (up to 286 g m−2 day−1, wet weight), was interrupted during three periods of anoxia, when macroalgal decomposition (rate: up to 1000 g m−2 day−1) released extraordinary amounts of nutrients. Depending on the macroalgae distribution in the water column, the nutrients released in water varied from 3·3 to 19·1 μg-at litre−1 for total inorganic nitrogen and from 1·8 to 2·7 μg-at litre−1 for reactive phosphorus. Most nutrients, however, accumulated in the surficial sediment (up to 0·640 and to 3·06 mg g−1 for P and N respectively) redoubling the amounts already stored under aerobic conditions, Phytoplankton, systematically below 5 mg m−3 as Chl. a, sharply increased up to 100 mg m−3 only after the release of nutrients in water by anaerobic macroalgal decomposition. During the algal growth periods, the N:P atomic ratio in water decreased to 0·7, suggesting that nitrogen is a growth-limiting factor. This ratio for surficial sediment was between 6·6 and 13·1, similar to that of macroalgae (8·6–12·0).  相似文献   

12.
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   

13.
Seasonal and diurnal reduced sulfur gas emissions were measured along a salinity gradient in Louisiana Gulf Coast salt, brackish and freshwater marshes. Reduced sulfur gas emission was strongly associated with habitat and salinity gradient. The dominant emission component was dimethyl sulfide (average: 57·3 μg S m−2 h−1) in saltmarsh with considerable seasonal (max: 144·03 μg S m−2 h−1; min: 1·47 μg S m−2 h−1) and diurnal (max: 83·58 μg S m−2 h−1; min: 69·59 μg S m−2 h−1) changes in flux rates. Hydrogen sulfide was dominant (average: 21·2 μg S m−2 h−1, max: 79·2 μg S m−2 h−1; min: 5·29 μg S m−2 h−1) form in brackishmarsh and carbonyl sulfide (average: 1·09 μg S m−2 h−1; max: 3·42 μg S m−2 h−1; min: 0·32 μg S m−2 h−1) was dominant form in freshwater marsh. A greater amount of H2S was evolved from brackishmarsh (21·22 μg S m−2 h−1) as compared to the saltmarsh (2·46 μg S m−2 h−1) and freshwater marsh (0·30 μg S m−2 h−1). Emission of total reduced sulfur gases decreased with decrease in salinity and distance inland from the coast. Emission of total reduced sulfur gases over the study averaged 73·3 μg S m−2 h−1 for the saltmarsh, 32·1 μg S m−2 h−1 for brackishmarsh and 2·76 μg S m−2 h−1 for the freshwater marsh.  相似文献   

14.
The whole core squeezing method was used to simultaneously obtain profiles of nitrous oxide (N2O), nitrogenous nutrients, and dissolved oxygen in sediments of Koaziro Bay, Japan (coastal water), the East China Sea (marginal sea), and the central Pacific Ocean (open ocean). In the spring of Koaziro Bay, subsurface peaks of interstitial N2O (0.5–3.5 cm depth) were observed, at which concentrations were higher than in the overlying water. This was also true for nitrate (NO3) and nitrite (NO2) profiles, suggesting that the transport of oxic overlying water to the depth through faunal burrows induced in situ N2O production depending on nitrification. In the summer of Koaziro Bay, sediment concentrations of N2O, NO3 and NO2 were lower than in the overlying water. In most East China Sea sediments, both N2O and NO3 decreased sharply in the top 0.5–2 cm oxic layer (oxygen: 15–130 μM), which may have indicated N2O and NO3 consumption by denitrification at anoxic microsites. N2O peaks at subsurface depth (0.5–6.5 cm) implied in situ production of N2O and/or its supply from the overlying water through faunal burrows. However, the occurrence of the latter process was not confirmed by the profiles of other constituents. In the central Pacific Ocean, the accumulation of N2O and NO3 in the sediments likely resulted from nitrification. Nitrous oxide fluxes from the sediments, calculated using its gradient at the sediment–water interface and the molecular diffusion coefficient, were −45 to 6.9 nmolN m−2 h−1 in Koaziro Bay in the spring, −29 to −21 nmolN m−2 h−1 in the summer, −46 to 37 nmolN m−2 h−1 in the East China Sea, 0.17 to 0.23 nmolN m−2 h−1 in the equatorial Pacific, and <±0.2 nmolN m−2 h−1 in the subtropical North Pacific, respectively.  相似文献   

15.
Particle export from the upper waters of the oligotrophic ocean may play a crucial role in the global carbon cycle. Mesoscale eddies have been hypothesized to inject new nutrients into oligotrophic surface waters, thereby increasing new production and particle export in otherwise nutrient deficient regimes. The E-Flux Program was a large multidisciplinary project designed to investigate the physical, biological and biogeochemical characteristics of cold-core cyclonic eddies that form in the lee of the Hawaiian Islands. There, we investigated particle dynamics using 210Pb–210Po disequilibrium. Seawater samples for 210Pb and 210Po were collected both within (IN) and outside (OUT) of two cyclones, Noah and Opal, at different stages of their evolution as well as from the eddy generation region. Particulate carbon (PC), particulate nitrogen (PN) and biogenic silica (bSiO2) export fluxes were determined using water-column PC, PN, and bSiO2 inventories and the residence times of 210Po. PC and PN fluxes at 150 m ranged from 1.58±0.10 to 1.71±0.16 mmol C m−2 d−1 and 0.22±0.02 to 0.30±0.02 mmol N m−2 d−1 within Cyclones Opal and Noah. PC and PN fluxes at OUT stations sampled during both cruises were of similar magnitudes, 1.69±0.16 to 1.67±0.16 mmol C m−2 d−1 and 0.30±0.03 to 0.26±0.03 mmol N m−2 d−1. The bSiO2 fluxes within Cyclone Opal were 0.157±0.010 mmol Si m−2 d−1 versus 0.025±0.002 mmol Si m−2 d−1 at OUT stations. These results of minimal PC and PN export, but significant eddy-induced bSiO2 fluxes, agree very well with other studies that used a variety of direct and indirect methods. Thus, our results suggest that using elemental inventories and residence times of 210Po is another independent and robust method for determining particle export and should be investigated more fully.  相似文献   

16.
Fluxes contributing to the particulate carbonate system in deep-sea sediments were investigated at the BENGAL site in the Porcupine Abyssal Plain (Northeast Atlantic). Deposition fluxes were estimated using sediment traps at a nominal depth of 3000 m and amounted to 0.37±0.1 mmol C m−2 d−1. Dissolution of carbonate was determined using flux of total alkalinity from in situ benthic chambers, is 0.4±0.1 mmol C m−2 d−1. Burial of carbonate was calculated from data on the carbonate content of the sediment and sedimentation rates from a model age based on 14C dating on foraminifera (0.66±0.1 mmol C m−2 d−1). Burial plus dissolution was three times larger than particle deposition flux which indicates that steady-state is not achieved in these sediments. Mass balances for other components (BSi, 210Pb), and calculations of the focusing factor using 230Th, show that lateral inputs play only a minor role in this imbalance. Decadal variations of annual particle fluxes are also within the uncertainty of our average. Long-term change in dissolution may contribute to the imbalance, but can not be the main reason because burial alone is greater than the input flux. The observed imbalance is thus the consequence of a large change of carbonate input flux which has occured in the recent past. A box model is used to check the response time of the solid carbonate system in these sediments and the time to reach a new steady-state is in the order of 3 kyr. Thus it is likely that the system has been perturbed recently and that large dissolution and burial rates reflect the previously larger particulate carbonate deposition rates. We estimate that particulate carbonate fluxes have certainly decreased by a factor of at least 3 and that this change has occurred during the last few centuries.  相似文献   

17.
The effect of a sudden increase in salinity from 10 to 37 in porewater concentration and the benthic fluxes of ammonium, calcium and dissolved inorganic carbon were studied in sediments of a small coastal lagoon, the Albufera d'Es Grau (Minorca Island, Spain). The temporal effects of the changes in salinity were examined over 17 days using a single diffusion-reaction model and a mass-balance approach. After the salinity change, NH4+-flux to the water and Ca-flux toward sediments increased (NH4+-flux: 5000–3000 μmol m−2 d−1 in seawater and 600/250 μmol m−2 d−1 in brackish water; Ca-flux: −40/−76 meq m−2 d−1 at S=37 and −13/−10 meq m−2 d−1 at S=10); however, later NH4+-flux decreased in seawater, reaching values lower than in brackish water. In contrast, Ca-flux presented similar values in both conditions. The fluxes of dissolved inorganic carbon, which were constant at S=10 (55/45 mmol m−2 d−1), increased during the experiment at S=37 (from 30 mmol m−2 d−1 immediately after salinity increase to 60 mmol m−2 d−1 after 17 days).In brackish conditions, NH4+ and Ca2+ fluxes were consistent with a single diffusion-reaction model that assumes a zero-order reaction for NH4+ production and a first-order reaction for Ca2+ production. In seawater, this model explained the Ca-flux observed, but did not account for the high initial flux of NH4+.The mass balance for 17 days indicated a higher retention of NH4+ in porewater in the littoral station in seawater conditions (9.5 mmol m−2 at S=37 and 1.6 mmol m−2 at S=10) and a significant reduction in the water consumption at both sites (5 mmol m−2 at S=37; 35/23 mmol m−2 at S=10). In contrast, accumulation of dissolved inorganic carbon in porewater was lower in seawater incubations (−10/−1 meq m−2 at S=37; 50/90 meq m−2 at S=10) and was linked to a higher efflux of CO2 to the atmosphere, because of calcium carbonate precipitation in water (675/500 meq m−2). These results indicate that increased salinity in shallow coastal waters could play a major role in the global carbon cycle.  相似文献   

18.
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   

19.
W. Koeve   《Marine Chemistry》2001,74(4):96
Observations of wintertime nutrient concentrations in surface waters are scarce in the temperate and subarctic North Atlantic Ocean. Three new methods of their estimation from spring or early summer observations are described and evaluated. The methods make use of a priori knowledge of the vertical distribution of oxygen saturation and empirical relationships between nutrient concentrations and oxygen saturation. A south–north increase in surface water winter nutrient concentration is observed. Winter nitrate concentrations range from very low levels of about 0.5 μmol dm−3 at 33°N to about 13.5 μmol dm−3 at 60°N. Previous estimates of winter nitrate concentrations have been overestimates by up to 50%. At the Biotrans Site (47°N, 20°W), a typical station in the temperate Northeast Atlantic, a mean winter nitrate concentration of 8 μmol dm−3 is estimated, compared to recently published values between 11 and 12.5 μmol dm−3. It is shown that most of the difference is due to a contribution of remineralised nitrate that had not been recognized in previous winter nutrient estimates. Mesoscale variation of wintertime nitrate concentrations at Biotrans are moderate (less than ±15% of the regional mean value of about 8 μmol dm−3). Interannual variation of the regional mean is small, too. In the available dataset, there was only 1 year with a significantly lower regional mean winter nitrate concentration (7 μmol dm−3), presumably due to restricted deep mixing during an atypically warm winter. The significance of winter nitrate estimates for the assessment of spring-bloom new production and the interpretation of bloom dynamics is evaluated. Applying estimates of wintertime nitrate concentrations of this study, it is found that pre-bloom new production (0.275 mol N m−2) at Biotrans almost equals spring-bloom new production (0.3 mol N m−2). Using previous estimates of wintertime nitrate yields unrealistically high estimates of pre-bloom new production (1.21–1.79 mol N m−2) which are inconsistent with observed levels of primary production and the seasonal development of biomass.  相似文献   

20.
Fatty acids and hydrocarbons of sedimenting particles were investigated in the northeastern Adriatic Sea from November 1988 to December 1989. Particles were collected at approximately monthly intervals, using sediment traps deployed at 30 m depth (2 m above bottom). Seasonal changes in sedimentation of particulate matter were very pronounced. Hydrocarbon fluxes and concentrations were found to vary significantly depending on the season. They averaged 2.69 ± 1.44 mg m−2 day−1 and 232.4 ± 90.93 μg g−1 in winter, respectively. In late spring-early summer the corresponding values amounted to 0.045 ± 0.015 mg m−2 day−1 and 13.72 ± 5.56 μg g−1, and they increased towards autumn, when mean values of 0.517 ± 0.228 mg m−2 day−1 and 98.86 ± 48.72 μg g−1 were obtained. In contrast, fatty acid fluxes and concentrations were low during winter (0.26 ± 0.08 mg m−2 day−1 and 21.95 ± 3.35 μg g−1), increased slightly towards the summer (0.48 ± 0.12 mg m−2 day−1 and 139.9 ± 44.6 μ g−1) and reached maximum rate and concentration in autumn, when average values were 1.98 ± 1.30 mg m2 day−1 and 489.1 ± 186.7 μg g−1, respectively. The differences in composition, concentrations and fluxes of the fatty acids and hydrocarbons were related to the sources of sedimenting material, reflecting the influence of resuspension of bottom sediments during winter and the appearance of mucus aggregates during summer and their subsequent deposition in autumn.  相似文献   

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