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1.
We measured fluxes of NH4+ and NO3 and δ15N of NH4+, sediment, and porewater NH4+ from incubated sediment cores along a nitrate gradient and in different seasons from Childs River, MA. NH4+ flux was low at the downstream site with the lowest concentration of organic matter (high salinity) but otherwise did not differ along the estuary. The δ15N of regenerated NH4+ ranged from +6.1‰ to +15.3‰ but did not vary significantly with season or salinity; the mean for the entire estuary was +10.4 ± 0.5‰. Based on differences between the δ15N of regenerated NH4+ and sediment, and expected isotopic fractionation due to remineralization, we concluded that nitrification occurred after remineralization of NH4+. Differences between the δ15N of regenerated NH4+ and the δ15N of porewater NH4+ provided further evidence of nitrification. We estimated that 11% to 48% of remineralized NH4+ underwent coupled nitrification–denitrification before release into the water column. In spite of losses to denitrification, NH4+ flux released 1.4 mol N m−2 year−1 to the water column and could provide 42% of phytoplankton nitrogen requirements.  相似文献   

2.
We examined the effects of seasonal salinity changes on sediment ammonium (NH4 +) adsorption and exchange across the sediment–water interface in the Parker River Estuary, by means of seasonal field sampling, laboratory adsorption experiments, and modeling. The fraction of dissolved NH4 + relative to adsorbed NH4 + in oligohaline sediments rose significantly with increased pore water salinity over the season. Laboratory experiments demonstrated that small (∼3) increases in salinity from freshwater conditions had the greatest effect on NH4 + adsorption by reducing the exchangeable pool from 69% to 14% of the total NH4 + in the upper estuary sediments that experience large (0–20) seasonal salinity shifts. NH4 + dynamics did not appear to be significantly affected by salinity in sediments of the lower estuary where salinities under 10 were not measured. We further assessed the importance of salinity-mediated desorption by constructing a simple mechanistic numerical model for pore water chloride and NH4 + diffusion for sediments of the upper estuary. The model predicted pore water salinity and NH4 + profiles that fit measured profiles very well and described a seasonal pattern of NH4 + flux from the sediment that was significantly affected by salinity. The model demonstrated that changes in salinity on several timescales (tidally, seasonally, and annually) can significantly alter the magnitude and timing of NH4 + release from the sediments. Salinity-mediated desorption and fluxes of NH4 + from sediments in the upper estuary can be of similar magnitude to rates of organic nitrogen mineralization and may therefore be important in supporting estuarine productivity when watershed inputs of N are low.  相似文献   

3.
In this study rates of oxygen, ammonium (NH4 +), nitrate (NO3 ), nitrite (NO2 ), and nitrous oxide (N2O) fluxes, nitrogen (N) fixation, nitrification, and denitrification were compared between two intertidal sites for which there is an abundant global literature, muddy and sandy sediments, and two sites representing the rocky intertidal zone where biogeochemical processes have scarcely been investigated. In almost all sites oxygen production rates greatly exceeded oxygen consumption rates. During daylight, NH4 + and NO3 uptake rates together with ammonification could supply the different N requirements of the primary producer communities at all four sites; N assimilation by benthic or epilithic primary producers was the major process of dissolved inorganic nitrogen (DIN) removal; N fixation, nitrification, and denitrification were minor processes in the overall light DIN cycle. At night, distinct DIN cycling processes took place in the four environments, denitrification rates ranged from 9 ± 2 to 360 ± 30 μmol N2 m−2 h−1, accounting for 10–48% of the water column NO3 uptake; nitrification rates varied from 0 to 1712 ± 666 μmol NH4 + m−2 h−1. A conceptual model of N cycle dynamics showed major differences between intertidal sediment and rocky sites in terms of the mean rates of DIN net fluxes and the processes involved, with rocky biofilm showing generally higher fluxes. Of particular significance, the intertidal rocky biofilms released 10 times the amount of N2O produced in intertidal sediments (up to 17 ± 6 μmol N2O m−2 h−1), representing the highest N2O release rates ever recorded for marine systems. The biogeochemical contributions of intertidal rocky substrata to estuarine and coastal processes warrant future detailed investigation.  相似文献   

4.
To determine the removal of regenerated nitrogen by estuarine sediments, we compared sediment N2 fluxes to the stoichiometry of nutrient and O2 fluxes in cores collected in the Childs River, Cape Cod, Massachusetts. The difference between the annual PO4 3− (0.2 mol P m−2 yr−1) and NH4 + (1.6 mol N m−2 yr−1) flux and the Redfield N∶P ratio of 16 suggested an annual deficit of 1.5 mol N m−2 yr−1. Denitrification predicted from O2∶NH4 + flux ratios and measured as N2 flux suggested a nitrogen sink of roughly the same magnitude (1.4 mol N m−2 yr−1). Denitrification accounted for low N∶P ratios of benthic flux and removed 32–37% of nitrogen inputs entering the relatively highly nutrient loaded Childs River, despite a relatively brief residence time for freshwater in this system. Uptake of bottom water nitrate could only supply a fraction of the observed N2 flux. Removal of regenerated nitrogen by denitrification in this system appears to vary seasonally. Denitrification efficiency was inversely correlated with oxygen and ammonium flux and was lowest in summer. We investigated the effect of organic matter on denitrification by simulating phytoplankton deposition to cores incubated in the lab and by deploying chambers on bare and macroaglae covered sediments in the field. Organic matter addition to sediments increased N2 flux and did not alter denitrification efficiency. Increased N2 flux co-varied with O2 and NH4 + fluxes. N2 flux (261±60 μmol m−2 h−1) was lower in chambers deployed on macroalgal beds than deployed on bare sediments (458±70 μmol m−2 h−1), and O2 uptake rate was higher in chambers deployed on macroalgal beds (14.6±2.2 mmol m−2 h−1) than on bare sediments (9.6±1.5 mmol m−2 h−1). Macroalgal cover, which can retain nitrogen in the system, is a link between nutrient loading and denitrification. Decreased denitrification due to increasing macroalgal cover could create a positive feedback because decreasing denitrification would increase nitrogen availability and could increase macroalgae cover.  相似文献   

5.
Electrical conductivity of saturated soil extracts (ECe) in three reclaimed tideland (RTL) soils on the west coast of Korea decreased with time since reclamation, indicating natural desalinization through leaching of salts by precipitation water. Soil N concentration increased with decreasing ECe. With the increase in soil N concentration, the δ15N decreased, likely caused by the input of 15N-depleted N sources. As N2-fixing plant species were found in the oldest RTL, atmospheric N2 fixation likely contributed to the increase in soil N concentration in the oldest RTL. Negative δ15N (−7.1 to −2.0‰) of total inorganic N (NH4 ++NO3 ) and published data on N deposition near the study area indicate that atmospheric N deposition might be another source of N in the RTLs. Meanwhile, the consistently negative δ15N of soil NO3 excluded N input from chemical fertilizer through groundwater flow as a potential N source, since NO3 in groundwater generally have a positive δ15N. The patterns of δ15N of NH4 + (+2.3 to +5.1‰) and NO3 (−9.2 to −5.0‰) suggested that nitrification was an active process that caused 15N enrichment in NH4 + but denitrification was probably minimal which would otherwise have caused 15N enrichment in NO3 . A quantitative approach on N budget would provide a better understanding of soil N dynamics in the studied RTLs.  相似文献   

6.
The Nauset Marsh estuary is the most extensive (9.45 km2) and least disturbed salt marsh/estuarine system within the Cape Cod National Seashore, even though much of the 19 km2 watershed area of the estuary is developed for residential or commercial purposes. Because all of the Nauset watershed is serviced by on-site individual sewage disposal systems, there is concern over the potential impact of groundwater-derived nutrients passing from these systems to the shallow receiving waters of the estuary. The purpose of this study was to determine whether denitrification (the bacterial conversion of nitrate to gaseous nitrogen) in estuarine sediments could effectively remove the nitrate from contaminated groundwater before it passed from the watershed to the estuary. Rates of denitrification were measured both in situ and in sediment cores, in areas of active groundwater discharge, in relatively pristine locations, and in areas situated down-gradient of moderate to heavily developed regions of the watershed. Denitrification rates for 47 sediment cores taken over an annual cycle at 5 stations ranged from non-detectable to 47 μmol N2 m−2 h. Mean denitrification rates were positively correlated with sediment organic content, and varied seasonally due to changes in sediment organic content and to the effect of water temperatures on sediment oxygen penetration depths. There was no correlation between observed denitrification rates and corresponding nitrate concentrations in groundwater. A comparison of in situ denitrification rates (supported by groundwater nitrate) with denitrification rates observed in sediment cores (supported by remineralized nitrate) showed that groundwater-driven denitrification rates were small, and not in excess of denitrification rates supported by remineralized nitrate. Most of the denitrification in Nauset sediments was apparently fueled by remineralized nitrate through coupled nitrification/denitrification. Denitrification did not contribute significantly to the direct loss of nitrate from incoming groundwater at Nauset Marsh estuary. Groundwater flow was rapid, and much of it occurred in freshwater springs and seeps through very coarse, sandy, well-oxygenated sediments of limited organic content. There was little opportunity for denitrification to occur during groundwater passage through these sediments. These results have important management implications because they suggest that the majority of nitrogen from contaminated groundwater crosses the sediment/water interface and arrives at Nauset Estuary, where it is available to primary producers. Preliminary budget calculations suggest that while denitrification was not an effective mechanism for the direct removal of nitrate in contaminated groundwater flowing to Nauset Marsh estuary, it may contribute to significant nitrogen losses from the estuary itself.  相似文献   

7.
Concentration profiles of O2, NH4 +, NO3 , and PO4 3− were measured at high spatial resolution in a 12-cm thick benthic mat of the filamentous macroalga Chaetomorpha linum. Oxygen and nutrient concentration profiles varied depending on algal activity and water turbulence. High surface irradiance stimulated O2 production in the surface layers and introduced O2 to deeper parts of the mat while the bottom layers of the mat and the underlying sediment were anoxic. Nutrient concentrations were highest in the bottom layers of the mat directly above the sediment nutrient source and decreased towards the surface layers due to algal assimilation and enhanced mixing with the overlying water column. Increased turbulence during windy periods resulted in more homogeneous oxygen and nutrient concentration profiles and shifted the oxic-anoxic interface downward. Denitrification within the mat, as measured by the isotope pairing technique on addition of 15NO3 , was found to take place directly below the oxic-anoxic interface. Denitrification activity was always due to coupled nitrification-denitrification, whereby nitrifiers in the mat utilize NH4 + diffusing from below and O2 diffusing from above. The denitrification rate in the mat ranged from 22 μmol m−2 h−1 to 28 μmol m−2 h−1, approximately equivalent to that measured in the surrounding nonvegetated sediment. Although sediment denitrification is suppressed when the sediment surface is covered by a dense macroalgal mat, the denitrification zone may migrate up into the mat. In eutrophic estuaries with a large area of macroalgal cover, the physical structure and growth stage of algal mats may thus play an important role in the regulation of nitrogen removal by denitrification.  相似文献   

8.
The applicability of the natural abundance of nitrogen gas isotope ratios was used to indicate the spatial distribution of nitrogen transformations in the water column and sediment pore waters of Lake Ngapouri, a small (area 0.19 km2), monomictic, eutrophic lake in the Taupo Volcanic Zone, North Island, New Zealand. Samples were collected from the epilimnion, hypolimnion, benthic boundary layer and at 5-cm intervals from the sediment pore waters at monthly intervals for 1 year. Values of δ15N [N2] ranged from −1 to 0.28‰ in the epilimnion, −1.5 to 1.25‰ in the hypolimnion, −1.8 to 12.2‰ in the benthic boundary layer and −0.7 to 3.5‰ in sediment pore waters. Values of δ15N [N2] showed a strong seasonal pattern that was related to the loss of dissolved oxygen in the hypolimnion during seasonal stratification. Increases in 15N-enriched dinitrogen take place in the benthic boundary layer during the periods of anoxia (taken to be dissolved oxygen concentrations <6.3 μM) and may be related to abundant ammonium substrate (up to 275 μM) to support denitrification. Nitrate concentrations increased up to 36 μM with increasing duration of anoxia. We hypothesise that an alternative electron acceptor besides oxygen is required to support the nitrification needed for the production of nitrate. Iron and manganese hydroxides and oxides from material sedimenting out of the water column may have induced chemo-nitrification sufficient to oxidise ammonium in the anoxic benthic boundary layer. The nitrate formed would mostly be rapidly denitrified so that the δ15N [N2] would continue to become enriched during the presence of anoxia, as observed in hypolimnion and benthic boundary layer of Lake Ngapouri. The changes in δ15N [N2] values indicate the potential use of isotope ratios to identify and quantify potential chemo-nitrification/denitrification in the water column and sediment pore waters of lakes.  相似文献   

9.
Benthic metabolism and nutrient exchange across the sediment-water interface were examined over an annual cycle at four sites along a freshwater to marine transect in the Parker River-Plum Island Sound estuary in northeastern Massachusetts, U.S. Sediment organic carbon content was highest at the freshwater site (10.3%) and decreased along the salinity gradient to 0.2% in the sandy sediments at the marine end of the estuary. C:N ratios were highest in the mid estuary (23:1) and lowest near the sea (11:1). Chlorophyll a in the surface sediments was high along the entire length of the estuary (39–57 mg chlorophyll a m−2) but especially so in the sandy marine sediments (172 mg chlorophyll a m−2). Chlorophyll a to phaeophytin ratios suggested most chlorophyll is detrital, except at the sandy marine site. Porewater sulfide values varied seasonally and between sites, reflecting both changes in sulfate availability as overlying water salinity changed and sediment metabolism. Patterns of sediment redox potential followed those of sulfide. Porewater profiles of inorganic N and P reflected strong seasonal patterns in remineralization, accumulation, and release. Highest porewater NH4 + values were found in upper and mid estuarine sediments, occasionally exceeding 1 mM N. Porewater nitrate was frequently absent, except in the sandy marine sediments where concentrations of 8 μM were often observed. Annual average respiration was lowest at the marine site (13 mmol O2 m−2 d−1 and 21 mmol TCO2 m−2 d−1) and highest in the mid estuary (130 mmol O2 m−2 d−1 and 170 mmol TCO2 m−2 d−1) where clam densities were also high. N2O and CH4 fluxes were low at all stations throughout the year: Over the course, of a year, sediments varied from being sources to sinks of dissolved organic C and N, with the overall spatial pattern related closely to sediment organic content. There was little correlation between PO4 3− flux and metabolism, which we attribute to geochemical processes. At the two sites having the lowest salinities, PO4 3− flux was directed into the sediments. On average, between 22% and 32% of total system metabolism was attributable to the benthos. The mid estuary site was an exception, as benthic metabolism accounted for 95% of the total, which is attributable to high densities of filter-feeding clams. Benthic remineralization supplied from less than 1% to over 190% of the N requirements and 0% to 21% of the P requirements of primary producers in this system. Estimates of denitrification calculated from stoichiometry of C and N fluxes ranged from 0% for the upper and mid estuary site to 35% for the freshwater site to 100% of sediment organic N remineralization at the marine site. We hypothesize that low values in the upper and mid estuary are attributable to enhanced NH4 + fluxes during summer due to desorption of exchangeable ammonium from rising porewater salinity. NH4 + desorption during summer may be a mechanism that maintains high rates of pelagic primary production at a time of low inorganic N inputs from the watershed.  相似文献   

10.
To characterize the isotopic composition of organisms at the base of the food web and the controls on their variability, the concentration and δ13C isotopic composition of dissolved inorganic carbon (DIC) and plankton δ13C, δ15N, and δ34S were measured. The measurements were made during periods of high and low river flow in Apalachicola Bay, Florida, United States, over 3 yr. DIC concentration and δ13C values were related to salinity, indicating that conservative mixing of riverine and marine waters was responsible for the overall distributions. The usefulness of DIC δ13C data for characterizing the trophic processes within the estuary was dependent upon the residence time of water within the season. Plankton δ13C values varied from −22‰ to −30‰ and were directly related to estuarine DIC δ13C, offset by a factor of roughly −20‰. This offset factor varied with salinity. Values of δ34S in estuarine plankton (station means ranged from 11.4‰ to 13.1‰) were depleted relative to marine plankton (17.7±0.4‰) possibly due to the admixture of34S-depleted sedimentary sulfide with estuarine samples. Values of δ34S in plankton were not related to δ13C values of plankton and were only weakly correlated to the salinity of the water from which the plankton were collected, indicating that marine sulfate was the primary source of planktonic sulfur. Values of δ15N in plankton varied from 5.5‰ to 10.7‰ and appeared related to dominance of the sample by phytoplankton or zooplankton. Estuarine plankton was15N enriched relative to offshore plankton and estuarine sediment.  相似文献   

11.
The isotopic composition of dissolved boron, in combination with the elemental concentrations of B, Cl and salinities in freshwater-seawater mixed samples taken from the estuary of the Changjiang River, the largest one in China, was investigated in detail in this study. Brackish water and seawater samples from the estuary of the Changjiang River were collected during low water season in November, 1998. Boron isotopic compositions were determined by the Cs2BO^+2-graphite technique with a analytical uncertainty of 0.2‰ for NIST SRM 951 and an average analytical uncertainty of 0.8‰ for the samples. The isotopic compositions of boron, expressed in δ^11B, and boron concentrations in the Changjiang River at Nanjing and seawater from the open marine East Sea, China, are characterized by δ^11B values of -5.4‰ and 40.0‰, as well as 0.0272 and 4.43 mg B/L, respectively. Well-defined correlations between δ^11B values, B concentrations and Cl concentrations are interpreted in terms of binary mixing between fiver input water and East Sea seawater by a process of straightforward dilution. The offsets of δ^11B values are not related to the contents of clastic sediment and to the addition of boron. These relationships favor a conservative behavior of boron at the estuarine of the Changjiang River.  相似文献   

12.
Quantifying Sediment Nitrogen Releases Associated with Estuarine Dredging   总被引:1,自引:0,他引:1  
Experimental studies of sediment pore water NH4 + chemistry, adsorbed NH4 + concentrations, sediment?Cwater NH4 + exchange and N2?CN flux were carried out to quantify the mass of labile N that can be released during large-scale dredging activities. Pore water NH4 + concentrations below 0.5-m sediment depth averaged 5 ± 2 mmol L?1 with average adsorbed NH4 + concentrations of 11 ??mol g?1. Elevated NH4 + concentrations found in rapidly accreting dredge channels are partly a result of the rapid advective burial of both reactive organic matter and pore water. Elutriate tests, a dilution of sediment with site water, yielded adsorbed NH4 + concentrations very similar to those using the more typical KCl extraction. Intact deep sediment sections exposed to overlying water, used to simulate postdredging conditions, showed high initial fluxes of ammonium and no development of coupled nitrification?Cdenitrification under the cold incubation conditions. Despite high concentrations and effluxes of NH4 + during dredging, the amount of NH4 + release during dredging was <0.5% of northern Chesapeake Bay sediment fluxes. The likelihood of large environmental effects of nitrogen release during the dredging of navigational channels in the Chesapeake Bay is low.  相似文献   

13.
A “snap shot” survey of the Mississippi estuary was made during a period of low river discharge, when the estuarine mixing zone was within the deltaic channels. Concentrations of H+, Ca2+, inorganic phosphorus and inorganic carbon suggest that the waters of the river and the low salinity (<5‰) portion of the estuary are near saturation with respect to calcite and sedimentary calcium phosphate. An input of oxidized nitrogen species and N2O was observed in the estuary between 0 and 4‰ salinity. The concentrations of dissolved NH4 + and O2, over most of the estuary, appeared to be influenced by decomposition of terrestrial organic matter in bottom sediments. The estuarine bottom also appears to be a source of CH4 which has been suggested to originate from petroleum shipping and refining operations. Estuarine mixing with offshore Gulf waters was the dominant influence on distributions of dissolved species over most of the estuary (i.e., from salinities >5‰). The phytoplankton abundance (measured as chlorophylla) increased as the depth of the mixed layer decreased in a manner consistent with that expected for a light-limited ecosystem. Fluxes of NO3 ?+NO2 ? and soluble inorganic phosphorus to the Gulf of Mexico were estimated to be 3.4±0.2×103 g N s?1 and 1.9±0.2 g P s?1 respectively, at the time of this study.  相似文献   

14.
The distilling effect of evaporation and the diluting effect of precipitation on salinity at two estuarine sites in the humid subtropical setting of the Indian River Lagoon, Florida, were evaluated based on daily evaporation computed with an energy-budget method and measured precipitation. Despite the larger magnitude of evaporation (about 1,58 mm yr−1) compared to precipitation (about 1,180 mm yr−1) between February 2002 and January 2004, the variability of monthly precipitation induced salinity changes was more than twice the variability of evaporation induced changes. Use of a constant, mean value of evaporation, along with measured values of daily precipitation, were sufficient to produce simulated salinity changes that contained little monthly (root-mean-square error = 0.33‰ mo−1 and 0.52‰ mo−1 at the two sites) or cumulative error (<1‰ yr−1) compared to simulations that used computed daily values of evaporation. This result indicates that measuring the temporal variability in evaporation may not be critical to simulation of salinity within the lagoon. Comparison of evaporation and precipitation induced salinity changes with measured salinity changes indicates that evaporation and precipitation explained only 4% of the changes in salinity within a flow-through area of the lagoon; surface water and ocean inflows probably accounted for most of the variability in salinity at this site. Evaporation and precipitation induced salinity changes explained 61% of the variability in salinity at a flow-restricted part of the lagoon.  相似文献   

15.
Measurements of15N/14N in dissolved molecular nitrogen (N2), nitrate (NO 3 ) and nitrous oxide (N2O) and18O/16O in N2O [expressed as δ15N and δ18O, relative to atmospheric N2 and oxygen (O2), respectively] have been made in water column at several locations in the Arabian Sea, a region with one of the thickest and most intense O2 minima observed in the open ocean. Microbially-mediated reduction of NO 3 to N2 (denitrification) in the oxygen minimum zone (OMZ) appears to greatly affect the natural isotopic abundances. The δ15N of NO 3 increases from 6‰ in deep waters (2500 m) to 15‰ within the core of the denitrifying layer (250–350 m); the δ15N of N2 concurrently decreases from 0.6‰ to 0.20‰ Values of the isotopic fractionation factor (ε) during denitrification estimated using simple advection-reaction and diffusion-reaction models are 22‰ and 25‰, respectively. A strong decrease in δ15N of NO 3 is observed from ∼ 200m (> 11‰) to 80m (∼ 6‰); this is attributed to the input of isotopically light nitrogen through nitrogen fixation. Isotopic analysis of N2O reveals extremely large enrichments of both15N and18O within the OMZ, presumably due to the preferential reduction of lighter N2O to N2. However, isotopically light N2O is observed to accumulate in high concentrations above the OMZ indicating that the N2O emitted to the atmosphere from this region cannot be very heavy. The isotope data from the intense upwelling zone off the southwest coast of India, where some of the highest concentrations of N2O ever found at the sea surface are observed, show moderate depletion of15N, but slight enrichment of18O relative to air. These results suggest that the ocean-atmosphere exchange cannot counter inputs of heavier isotopes (particularly18O) associated with the stratospheric back flux, as proposed by previous workers. This calls for additional sources and/or sinks of N2O in the atmosphere. Also, the N2O isotope data cannot be explained by production through either nitrification or denitrification, suggesting a possible coupling between the two processes as an important mechanism of N2O production.  相似文献   

16.
This study demonstrates the feasibility of using direct N2 measurements in an estuary for determination of denitrification. High precision measurements of dinitrogen: argon ratios (N2∶Ar) were made by membrane inlet mass spectrometry on water samples taken along the length of the Chesapeake Bay in July and October 2004. The N2∶Ar ratio in low salinity surface water was elevated relative to air saturation by 0.3–0.5% with no systematic change along the length of the Bay. N2∶Ar in high salinity bottom water exhibited a linear increase in the landward direction along a 144-km longitudinal section. In this section of the Bay covering 20% of the main stem, the bottom water salinity was statistically uniform and the increase in N2∶Ar was in the direction of net residual current flow. The system was analyzed as a capped river with the assumption that N2 entered the water from the underlying sediment where denitrification is known to take place. The rate of denitrification needed to support the measured increase in N2 was calculated using an average residual current velocity and water column depth. The increase in N2 with distance (0.046μmol N l−1 km−1) equated to an average denitrification flux of 73 μmol N m−2 h−1. N2 fluxes determined on sediment cores taken from the source and terminus regions of the delineated water mass were 45±23 and 83±39 μmol N m−2 hr−1, respectively, which were not statistically different from the whole system estimate. The measured change in oxygen concentration within the bottom water was used to estimate nitrogen remineralization and the efficiency of denitrification. Denitrification efficiency (nitrogen denitrified/nitrogen remineralized) was estimated to be in the range of 22–28% for the bottom water sediment system and 30–37% considering the sediment zone alone.  相似文献   

17.
Hurricanes and other major storms cause acute changes in salinity within Florida's streams and rivers. Winddriven tidal surges that increase salinities may have long-lasting effects on submersed aquatic vegetation (SAV) and the associated fauna. We investigated potential effects of salinity pulses on SAV in Kings Bay, Florida, by subjecting the three most common macrophytes,Vallisneria americana, Myriophyllum spicatum., andHydrilla verticillata, to simulated salinity pulses. In Kings Bay, we documented changes in salinity during three storms in September 2004 and measured biomass and percent cover before and after these storms. During experiments, macrophytes were exposed to salinities of 5‰, 15‰, or 25‰ for 1, 2, or 7 d, with a 28-d recovery period in freshwater. Relative to controls, plants subjected to salinities of 5‰ exhibited few significant decreases in growth and no increase in mortality. All three species exhibited decreased growth in salinities of 15‰ or 25‰.H. verticillata, exhibited 100% mortality at 15‰ and 25‰, irrespective of the duration of exposure.M. spicatum andV. american exhibited increased mortality after 7-d exposures to 15‰ or any exposure to 25‰ Maximum daily salinities in Kings Bay approached or exceeded 15‰ after each of the three storms, with pulses generally lasting less than 2 d. Total aboveground biomass and percent cover of vascular plants, were reduced following the storms.M. spicatum exhibited an 83% decrease in aboveground biomass and an 80% decrease in percent cover.H. verticillata exhibited a 47% and 15% decline in biomass and percent cover, respectively.V. americana, exhibited an 18% increase in aboveground biomass and a 37% increase in percent cover, which suggests greater tolerance of salinity pulses and release from competition with the invasiveH. verticillata andM. spicatum. Our results indicate that rapid, storm-induced pulses of high salinity can have important consequences for submersed aquatic vegetation, restoration efforts, and management of invasive species.  相似文献   

18.
In an annual cycle from March 2005 to February 2006, benthic nutrient fluxes were measured monthly in the Dongtan intertidal flat within the Changjiang (Yangtze River) Estuary. Except for NH4^+, there always showed high fluxes from overlying water into sediment for other four nutrients. Sediments in the high and middle marshes, covered with halophyte and consisting of macrofauna, demonstrated more capabilities of assimilating nutrients from overlying water than the low marsh. Sampling seasons and nutrient concentrations in the overlying water could both exert significant effects on these fluxes. Additionally, according to the model provided by previous study, denitrification rates, that utilizing NO3- transported from overlying water (Dw) in Dongtan sediments, were estimated to be from -16 to 193 μmol·h^-1·m^-2 with an average value of 63 μmol·h^-1·m^-2 (n=18). These estimated values are still underestimates of the in-situ rates owing to the lack of consideration of DN, i.e., denitrification supported by the local NO3^- production via nitrification.  相似文献   

19.
 The exchange and release properties of the natural phillipsite tuff from the Aritain area in Jordan were evaluated by studying the exchange properties of this natural zeolite in the NH4 +–Na+ system. Exchange isotherms at 18, 35, and 50  °C showed that phillipsite exchanged NH4 + preferably over Na+ at all temperatures. However, the selectivity coefficient for NH4 + decreased with decreasing temperature. The release of NH4 + from phillipsite saturated with ammonium sulfate took place in two stages characterized by different SO4 2– : NH4 + ratios. Aritain phillipsite from NE Jordan could be processed and used as NH4 + slow-release fertilizers. The use of NH4 +-phillipsite tuff offers an option to the widely used soluble NH4-fertilizers in agciculture to avoid environmental problems associated with nitrogen contamination of surface water and groundwater. Received: 19 December 1996 · Accepted: 13 May 1997  相似文献   

20.
Two sets of lab-scale sequencing batch reactors (SBR), i.e., control SBR and SBR using zeolite as carrier (zeo-SBR), were applied to assess nitrogen removal efficiency. The test results revealed that zeolite powder added in SBR could improve its performance. Due to the combination of zeolite adsorption for NH4 +–N and enhanced simultaneous nitrification and de-nitrification (SND), a higher removal ratio of ammonia nitrogen in wastewater was observed in the test reactor, and the introduction of zeolite powder was helpful to inhabit sludge bulging comparing with the control SBR, in other words, activated sludge immobilized by zeolite powder could remove NH4 +–N, COD, and PO4 significantly in a shorter cycle time. Applied two hydraulic retention times (HRTs) showed that the nitrogen and phosphorus removal could be improved while adapting to load variations.  相似文献   

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