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1.
Temporal changes in nitrogen isotopic composition (δ15N) of the NO3 − pool in the water column below the pycnocline in Ise Bay, Japan were investigated to evaluate the effect of nitrification on the change in the δ15N in the water column. The δ15N of NO3 − in the lower layers varied from −8.5‰ in May to +8.4‰ in July in response to the development of seasonal hypoxia and conversion from NH4 + to NO3 −. The significantly 15N-depleted NO3 − in May most likely arose from nitrification in the water column. The calculated apparent isotopic discrimination for water column nitrification (ɛnit = δ15Nsubstrate − δ15Nproduct) was 24.5‰, which lies within the range of previous laboratory-based estimates. Though prominent deficits of NO3 − from hypoxic bottom waters due to denitrification were revealed in July, the isotopic discrimination of denitrification in the sediments was low (ɛdenit = ∼1‰). δ15NNO3 in the hypoxic lower layer mainly reflects the isotopic effect of water column nitrification, given that water column nitrification is not directly linked with sedimentary denitrification and the effect of sedimentary denitrification on the change in δ15NNO3 is relatively small.  相似文献   

2.
A method for the determination of the δ15N of nitrate in seawater described by Cline and Kaplan (1975) has been modified for application to low-level nitrate samples. We have minimized the reagent blank problem by replacing the Devarda's alloy with an aluminum reagent, and have also established a procedure that yields quantitative (93 ± 2%) extraction of nitrogen even at low nitrate levels. Though the amounts and the δ15N of the blank N varied from one reagent set to another, with these modifications, an overall N blank was reduced to approximately 0.80 ± 0.33 μmole N having an estimated δ15N value of −1.8‰. After blank and yield corrections, the measured isotopic composition of nitrate differed by approximately 0.1‰ from the actual value while the precision was within ±0.2‰ at the 1.25 μM level. The modified procedure was applied to seawater samples collected from the equatorial Pacific in order to compare the N blanks in field samples with those derived from laboratory experiments. The results support the suitability of the modified approach for isotopic analysis of oceanic nitrate in shallow water. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

3.
Spatial distribution of the carbon and nitrogen content and their isotopic enrichment in suspended matter and sediments were measured in the Godavari estuary to identify the sources and transformation mechanism of organic matter. Significant variability in isotopic distribution was found over the entire length of the Godavari estuary, suggesting multiple sources of organic matter. The mean isotopic ratios (δ13Csed −25.1 ± 0.9, δ13Csus −24.9 ± 1, δ15Nsed 8.0 ± 2 and δ15Nsus 6.5 ± 0.9‰) and elemental concentrations (Csed 0.45 ± 0.2%, Csus 0.9 ± 0.7%, Nsed 0.07 ± 0.05% and Nsus 0.16 ± 0.1%) support a predominantly terrigenous source. Significant enrichment in the isotopic ratios of δ13C from the upper to lower estuary in both suspended (−27.5 and −24.3‰, respectively) and sedimentary (−26.2 and −24.9‰, respectively) phases indicates a decrease in the influence of terrigeneous material toward the mouth of the estuary. A significant positive relationship exists between the δ13C of suspended and sediment, which indicates that these two organic carbon pools are likely coupled in the form of a significant exchange between the two phases. A positive relationship exists between chlorophyll a and suspended organic matter, which may mean that a significant source of organic carbon is the in situ produced phytoplankton. But, applying a simple mixing model to our isotopes, data yielded about 46% as the contribution of the terrestrial source to suspended matter, which may support the excessive heterotrophic activity in the Godavari estuary reported earlier.  相似文献   

4.
N2 fixation is an important biological process that adds new nitrogen to oceans and plays a key role in modulating the oceanic nitrate inventory. However, it is not known how, when, and where N2 fixation rates have varied in response to past climate changes. This study presents a new record of nitrogen isotopic composition (δ15N) over the last 83 kyr from a sediment core (KH02-4 SUP8) taken in the Sulu Sea in the western equatorial Pacific region; data allow the N2 fixation variability in the sea to be reconstructed. Sediments, sinking, and suspended particulate organic matter (POM) all have lighter isotopic values compared to the δ15N values of substrate nitrate (av. 5.8‰) in North Pacific Intermediate Water. These lighter δ15N values are regarded as reflecting N2 fixation in the Sulu Sea surface water. A δ15N mass balance model shows that N2 fixation rates were significantly enhanced during 54–34 kyr in MIS-3 and MIS-2. It has been speculated that higher interglacial denitrification rates in the Arabian Sea and the eastern tropical Pacific would have markedly decreased the global oceanic N inventory and contributed to the increase in N2 fixation in oligotrophic regions, but such a model was not revealed by our study. It is possible that changes in N2 fixation rates in the Sulu Sea were regional response, and accumulation of phosphate in the surface waters due to enhanced monsoon-driven mixing is thought to have stimulated enhancements of N2 fixation during MIS-3 and MIS-2.  相似文献   

5.
Surface sediment from the coastal bays of Gwangyang and Masan in South Korea were analyzed for their contents and isotopic values of organic carbon and total nitrogen. The sources and diagenetic alteration of organic matter were also assessed. Total organic carbon varied from 0.22% to 3.48% (average = 1.40%, n = 75), and C/N ratios varied from 2.4 to 15.2 (average = 8.79, n = 75). δ13Corg ranged from −19.92‰ to −25.86‰ (average = −21.21‰, n = 75), and δ15NTN ranged from 8.57‰ to 3.93‰ (average = 6.49‰, n = 75). Total organic carbon in both areas was associated with grain-size, with higher contents in finer grained sediment. The high carbon content observed in Masan Bay sediment correlated with its higher C/N ratio. δ13Corg and δ15NTN varied widely, attributable to various influences such as the input of terrestrial organic matter and diagenetic alteration. The depleted δ13Corg and higher δ15NTN observed in the sediment of Gwangyang Bay reflected terrestrial supply, implying that biogeochemical processes, i.e. bacterial degradation, were more active in Masan Bay sediment, which showed less depleted δ13Corg and higher δ15NTN than Gwangyang Bay sediment. δ15NTN was the more useful indicator of biogeochemical processes in the highly anoxic sediment. These results indicate that the δ13Corg and δ15NTN of sedimentary organic matter in coastal bays can indicate the source and degree of diagenetic alteration of sedimentary organic matter.  相似文献   

6.
Concentrations of particulate organic nitrogen (PN), dissolved inorganic nitrogen (DIN), and their nitrogen isotope ratios (δ 15N) in the Kiso-Sansen Rivers were determined from monthly observations over the course of a year to assess variations in the form and sources of riverine nitrogen discharged into Ise Bay. The δ 15N values of NO3 − observed in the Kiso-Sansen Rivers showed a logarithmic decreasing trend from 8 to 0‰, which varied with the river discharge, indicating mixing between point sources with high δ 15N and non-point sources with low δ 15N. The influence of isotope fractionation of in situ biogeochemical processes (mainly DIN assimilation by phytoplankton) on δ 15N of NO3 − was negligible, because sufficient concentrations of NH4 + for phytoplankton demand would inhibit the assimilation of NO3 −. A simple relationship between river discharge and δ 15N of NO3 − showed that the fraction of total NO3 − flux arising from point sources increased from 4.0–6.3% (1.1–1.8 tN day−1) during higher discharge (>600 m3 s−1) to 30.2–48.3% (2.6–4.1 tN day−1) during lower discharge (<300 m3 s−1). Riverine NO3 − discharge from the Kiso-Sansen Rivers can explain 75% of the variations in surface NO3 − at the head of Ise Bay over the year.  相似文献   

7.
We have developed an ecosystem model including two nitrogen isotopes (14N and 15N), and validated this model using an actual data set. A study of nitrogen isotopic ratios (δ15N) using a marine ecosystem model is thought to be most helpful in quantitatively understanding the marine nitrogen cycle. Moreover, the model study may indicate a new potential of δ15N as a tracer. This model has six compartments: phytoplankton, zooplankton, particulate organic nitrogen, dissolved organic nitrogen, nitrate and ammonium in a two-box model, and has biological processes with/without isotopic fractionation. We have applied this model to the Sea of Okhotsk and successfully reproduced the δ15N of nitrate measured in seawater and the seasonal variations in δ15N of sinking particles obtained from sediment trap experiments. Simulated δ15N of phytoplankton are determined by δ 15N of nitrate and ammonium, and the nitrogen f-ratio, defined as the ratio of nitrate assimilation by phytoplankton to total nitrogenous nutrient assimilation. Detailed considerations of biological processes in the spring and autumn blooms have demonstrated that there is a significant difference between simulated δ15N values of phytoplankton, which assimilates only nitrate, and only ammonium, respectively. We suggest that observations of δ 15N values of phytoplankton, nitrate and ammonium in the spring and autumn blooms may indicate the ratios of nutrient selectivity by phytoplankton. In winter, most of the simulated biogeochemical fluxes decrease rapidly, but nitrification flux decreases much more slowly than the other biogeochemical fluxes. Therefore, simulated δ15N values and concentrations of ammonium reflect almost only nitrification. We suggest that the nitrification rate can be parameterized with observations of δ15N of ammonium in winter and a sensitive study varying the parameter of nitrification rate.  相似文献   

8.
The stable nitrogen isotope ratio (δ 15N) in macroalgae is effectively used as a time-integrated bioindicator to record nitrogen sources for primary producers during their growing periods in aquatic ecosystems. However, the utility of this tool is limited because the occurrence of these organisms is often restricted in space and time. To investigate the potential of chemical composition in sedimentary organic matter (SOM) as a proxy for time-integrated environmental conditions, nitrogen (N) and carbon (C) contents and their stable isotope ratios (δ 15N and δ 13C) were determined, and systematically cross-checked against corresponding values in macroalgae at the Shiraho fringing reef in Okinawa, Japan. Preliminary trials showed that δ 15N in SOM processed by the “wash-out method” for δ 13C analysis yielded similar δ 15N values to the bulk sediment, despite the loss of some SOM during the process. The amounts of organic matter and the ratio of the HCl-insoluble portion were variable within the reef, probably reflecting local vegetation and subsequent decomposition. The distribution of δ 15N and δ 13C in SOM showed similar trends to those of macroalgae, with mostly constant differences of 1.4‰ and −6.7‰, respectively. These differences throughout the reef appeared to be explained in terms of mixed contributions from macrophyte and epibenthic microalgae growing in different seasons and years, with their debris undergoing diagenetic alteration. Therefore, macroalgae and SOM δ-values can be used in a complementary manner, over various time scales, as indicators of the integrated effect of dissolved inorganic nitrogen (DIN) sources on coral reef ecosystems.  相似文献   

9.
We present high-resolution isotopic records and cathodoluminescence studies of recently dead and live bivalve specimens from cold seeps, in an attempt to reconstruct environmental conditions during organism growth, and thereby the possible variability of fluid-venting activity at the seafloor. Shells of the burrowing lucinid Myrtea aff. amorpha were collected at three localities near actively venting methane seeps in the Eastern Mediterranean deep sea, using the Nautile submersible during two French oceanographic cruises: from the Kazan mud volcano, in the vicinity of the Anaximander mounts (MEDINAUT cruise, 1998), and from the central pockmark province and the Amon mud volcano of the Nile deep-sea fan (NAUTINIL cruise, 2003). The oxygen and carbon isotope compositions of 18 shells from the various localities, and also from different sites at the same locality show a rather strong scatter (1.8 < δ 18O‰ < 3.4; −10.2 < δ 13C‰ < 2.2), and values lower than those expected for carbonate precipitated at equilibrium with present-day bottom waters. This means that warm methane-rich fluids were mixed with bottom seawater during precipitation of shell carbonates. We have tried to determine ontogenetic age of two shells by using cathodoluminescence as a sclerochronological proxy, because the direct counting of carbonate increments was not possible in these specimens. There is a relatively good correspondence between cathodoluminescence trends and oxygen isotope profiles that might support the link between manganese incorporation during growth and temperature. Eight specimens of lucinid shells were selected for high-resolution isotopic profiling. A few shells exhibit decreasing δ 18O and δ 13C values from the umbo to the actively growing ventral shell margin, which can be attributed to the commonly observed physiologically controlled deceleration of growth with increasing organism age, this metabolic effect corresponding to the increase of incorporation of respiratory CO2. A few shells exhibit high-frequency δ 18O variations with an amplitude of about 1.5‰ that might be related to temperature variations controlled by fluid-venting activity. One shell from the pockmark province of the Nile deep-sea fan records a strong, sharp δ 13C decrease of about 9‰, and extending over a 5-mm interval in the shell that can be related to a major methane release event. Another shell from the Kazan mud volcano exhibits a progressive increase of δ 13C values from −10‰ to 0‰ with age, which might indicate decreasing methane flow throughout the organism’s life. This study has demonstrated that bivalve shells from deep-sea cold seeps represent good indicators of variability in seepage activity of methane-rich fluids, at various scales in both space and time. Although the precise chronology of the observed events was not established, because shell growth rate is not known in this case, this remains a priority for future studies in such environments.  相似文献   

10.
Nitrogen isotope compositions of particulate organic matter and nitrate were analyzed for seawater sampled at five stations at the Alaskan Gyre, Western Subarctic Gyre and East China Sea, focusing on the samples from the surface to 5000 m water to characterize the nitrogen cycling in the subarctic North Pacific Ocean and its marginal sea. The 15N of particulate organic matter showed little agreement with a conceptual closed model that interprets isotopic variation as being caused by isotope discrimination on nitrate utilization. The 15N and 13C of particulate organic matter varied with the water depth. A correlation between isotope compositions and C/N elemental ratio was found generally at all stations, although some irregular data were also found in deep layers. We developed a hypothetical nitrogen balance model based on N2 fixation and denitrification in seawater and attempted to apply it to distinguish nutrient cycling using both 15N-NO3 – and N* variation in seawater. This model was applied to the observed data set of 15N-NO3 – and N* in the North Pacific water and estimated the 15N-NO3 – of primordial nitrate in the North Pacific deep water as 4.8. The North Pacific intermediate water for all stations showed similar 15N-NO3 – and N* values of 6 and –3 µmol/kg, respectively, suggesting a similar nitrogen biogeochemistry. In the East China Sea, analysis showed evidence of water exchange with the North Pacific intermediate water but a significant influence of nitrogen from the river runoff was found in depths shallower than 400 m.  相似文献   

11.
The Shenhu area is one of the most favorable places for the occurrence of gas hydrates in the northern continental slope of the South China Sea. Pore water samples were collected in two piston cores (SH-A and SH-B) from this area, and the concentrations of sulfate and dissolved inorganic carbon (DIC) and its carbon isotopic composition were measured. The data revealed large DIC variations and very negative δ 13C-DIC values. Two reaction zones, 0–3 mbsf and below 3 mbsf, are identified in the sediment system. At site SH-A, the upper zone (0–3 mbsf) shows relatively constant sulfate and DIC concentrations and δ 13C-DIC values, possibly due to bioturbation and fluid advection. The lower zone (below 3 mbsf) displays good linear gradients for sulfate and DIC concentrations, and δ 13C-DIC values. At site SH-B, both zones show linear gradients, but the decreasing gradients for δ 13C-DIC and SO4 2− in the lower zone below 3 mbsf are greater than those from the upper zone, 0–3 mbsf. The calculated sulfate-methane interface (SMI) depths of the two cores are 10.0 m and 11.1 m, respectively. The depth profiles of both DIC and δ 13C-DIC showed similar characteristics as those in other gas hydrate locations in the world oceans, such as the Blake Ridge. Overall, our results indicate an anaerobic methane oxidation (AMO) process in the sediments with large methane flux from depth in the studied area, which might be linked to the formation of gas hydrates in this area.  相似文献   

12.
 Ikaite crystals (CaCO3×6H2O) have been found at 232- to 238-cm sediment depth in R/V Polarstern core PS2460-4 from the Laptev Sea continental margin in a water depth of 204 m. δ13C values of this phase average −36.3±0.4‰ PDB (N=2), which is significantly outside the range of normal marine carbonates. The CO2 involved in the precipitation of the ikaite is most probably derived from methane, which has extremely depleted 13C isotope values. Two possible sources of methane in these sediments are: (1) methanogenesis (decomposition of organic matter under anaerobic conditions); and (2) gas hydrates, which are known to occur in the Siberian shelf regions. Received: 20 March 1996 / Revision received: 22 July 1996  相似文献   

13.
The δ18O, δ13C and trace element composition of pearls collected from Ago Bay, Japan, were investigated in order to evaluate biomineralization in the cultured pearl oyster (Pinctada fucata martensii). The oxygen isotopic data suggest that the pearls were produced around 23–24°C, mainly in June to early July, which is consistent with their occurrence in the field. Therefore the pearls were produced under or close to isotopic equilibrium conditions, although they showed high calcification rates (higher than 0.2–1.0 g cm− 2yr−1) under which, for example, coral skeletons (calcification rate ∼0.28 g cm− 2yr−1) often show non-equilibrium isotope partitioning. The δ13C values were ∼− 2.9‰ lower than those calculated for offshore waters under equilibrium conditions. This may be due to low-δ13C bottom waters resulting from the degradation of organic matter (OM) or to a contribution of low-δ 13C food. In the latter case, a simple mass balance calculation gives a respiration component of 14%. Twelve trace elements of bulk pearl samples were classified into four groups on the basis of their enrichment/depletion patterns relative to seawater and inter-element relationships: group 1, Co, Cr, Pb; group 2, Ba, Cs, U; group 3, Cu, Sn, V, and group 4, Mn, Rb, Mo. Comparison with coral skeletons suggests that Ba and Mn (groups 2 and 4) were definitely much enriched in proteinaceous OM relative to aragonite crystals in pearls and that V (group 3) in pearls showed only slight enrichment in the organicrich layer. By contrast, the other elements showed small differences between both layers (enrichment factor of <3), suggesting that these elements occur largely in aragonite crystals.  相似文献   

14.
This paper reports all available geochemical data on sediments and pore waters from the Xisha Trough on the northern continental margin of the South China Sea. The methane concentrations in marine sediments display a downhole increasing trend and their carbon isotopic compositions (δ 13C = −25 to −51‰) indicate a thermogenic origin. Pore water Cl− concentrations show a range from 537 to 730 mM, and the high Cl− samples also have higher concentrations of Br−, Na+, K+, and Mg2+, implying mixing between normal seawater and brine in the basin. The SO4 2− concentrations of pore waters vary from 19.9 to 36.8 mM, and show a downhole decreasing trend. Calculated SMI (sulfate-methane interfaces) depths and sulfate gradients are between 21 and 47 mbsf, and between −0.7 and −1.7 mM/m, respectively, which are similar to values in gas hydrate locations worldwide and suggest a high methane flux in the basin. Overall, the geochemical data, together with geological and geophysical evidence, such as the high sedimentation rates, high organic carbon contents, thick sediment piles, salt and mud diapirs, active faulting, abundant thermogenic gases, and occurrence of huge bottom simulating reflector (BSR), are suggestive of a favorable condition for occurrence of gas hydrates in this region.  相似文献   

15.
Compared to oxygen isotopes, the carbon isotope composition of biogenic carbonates is less commonly used as proxy for palaeoenvironmental reconstructions because shell δ13C is derived from both dissolved inorganic (seawater) and organic carbon sources (food), and interactions between these two pools make it difficult to unambiguously identify any independent effect of either. The main purpose of this study was to demonstrate any direct impact of variable food supply on bivalve shell δ13C signatures, using low/high rations of a 13C-light mixed algal diet fed to 14-month-old (adult) cultured Japanese Crassostrea gigas under otherwise essentially identical in vitro conditions during 3 summer months (May, June and July 2003, seawater temperature means at 16, 18 and 20 °C respectively) in experimental tanks at the Argenton laboratory along the Brittany Atlantic coast of France. At a daily ration of 12% (versus 4%) oyster dry weight, the newly grown part of the shells (hinge region) showed significantly lower δ13C values, by 3.5‰ (high ration: mean of −5.8  ± 1.1‰, n = 10; low ration: mean of −2.3  ± 0.7‰, n = 6; ANOVA Scheffe’s test, p < 0.0001). This can be explained by an enhanced metabolic activity at higher food supply, raising 13C-depleted respiratory CO2 in the extrapallial cavity. Based on these δ13C values and data extracted from the literature, and assuming no carbon isotope fractionation between food and shell, the proportion of shell metabolic carbon would be 26  ± 7 and 5  ± 5% for the high- and low-ration C. gigas shells respectively; with carbon isotope fractionation (arguably more realistic), the corresponding values would be 69  ± 14 and 24  ± 9%. Both groups of cultured shells exhibited lower δ13C values than did wild oysters from Marennes-Ol éron Bay in the study region, which is not inconsistent with an independent influence of diet type. Although there was no significant difference between the two food regimes in terms of δ18O shell values (means of 0.1  ± 0.3 and 0.4  ± 0.2‰ at high and low rations respectively, non-significant Scheffe’s test), a positive δ13C vs. δ18O relationship recorded at high rations supports the interpretation of a progressive temperature-mediated rise in metabolic activity fuelled by higher food supply (in this case reflecting increased energy investment in reproduction), in terms not only of δ13C (metabolic signal) but also of δ18O (seawater temperature signal). Overall, whole-shell δ18O trends faithfully recorded summer/winter variations in seawater temperature experienced by the 17-month-old cultured oysters.  相似文献   

16.
Natural marine gas hydrate was discovered in Korean territorial waters during a 2007 KIGAM cruise to the central/southwestern Ulleung Basin, East Sea. The first data on the geochemical characterization of hydrate-bound water and gas are presented here for cold seep site 07GHP-10 in the central basin sector, together with analogous data for four sites (07GHP-01, 07GHP-02, 07GHP-03, and 07GHP-14) where no hydrates were detected in other cores from the central/southwestern sectors. Hydrate-bound water displayed very low concentrations of major ions (Cl−, SO42−, Na+, Mg2+, K+, and Ca2+), and more positive δD (15.5‰) and δ18O (2.3‰) signatures compared to seawater. Cl– freshening and more positive isotopic values were also observed in the pore water at gas hydrate site 07GHP-10. The inferred sulfate–methane interface (SMI) was very shallow (<5 mbsf) at least at four sites, suggesting the widespread occurrence of anaerobic oxidation of methane (AOM) at shallow sediment depths, and possibly high methane flux. Around the SMI, pore water alkalinity was very high (>40 mM), but the carbon isotopic ratios of dissolved inorganic carbon (δ13CDIC) did not show minimum values typical of AOM. Moreover, macroscopic authigenic carbonates were not observed at any of the core sites. This can plausibly be explained by carbon with high δ13C values diffusing upward from below the SMI, increasing alkalinity via deep methanogenesis and eventually escaping as alkalinity into the water column, with minor precipitation as solid phase. This contrasts, but is not inconsistent with recent reports of methane-fuelled carbonate formation at other sites in the southwestern basin sector. Methane was the main hydrocarbon component (>99.85%) of headspace, void, and hydrate-bound gases, C1/C2+ ratios were at least 1,000, and δ13CCH4 and δDCH4 values were in the typical range of methane generated by microbial reduction of CO2. This is supported by the δ13CC2H6 signatures of void and hydrate-bound gases, and helps clarify some contradictory interpretations existing for the Ulleung Basin as a whole. In combination, these findings suggest that deep biogenic gas and pore waters migrate upward through pathways such as hydrofractures, and measurably influence the shallow carbon cycle. As a result, cation-adjusted alkalinity/removed sulfate diagrams cannot always serve to estimate the degree of alkalinity produced by sulfate reduction and AOM in high methane flux areas.  相似文献   

17.
A method has been developed for determination of15N isotope ratio in nitrate nitrogen, which is a major analytical step in tracer experiments for studies of nitrate metabolism in the marine environment. The method is based on diazotization of nitrite with sulfanilic acid following reduction of nitrate to nitrite by a cadmium-copper column. The diazonium compound is then subject to the azo coupling reaction with 2-naphthol, and the azo dye formed is extracted by a solid phase extraction column. The dye eluted from the column is collected, and total nitrogen and15N content of the dye are determined by mass spectrometry. Sulfanilic acid can also remove preexisting nitrite by heating the sample under acidic conditions before passing through the cadmium-copper reduction column. The average recovery of nitrate nitrogen was 86%. A procedure for reducing the background nitrogen that derives from the analytical operations has been developed; background nitrogen was limited to about 0.25 μg-atomN. The variation in the background nitrogen levels reflects the range of error in15N determination of nitrate nitrogen by this method. Application of the present method to a15NO3 − isotope dilution experiment for determination of nitrification rate in sea water is demonstrated.  相似文献   

18.
Concentration and stable isotopic compositions (δ 18O) of dissolved O2 were measured in seawater samples collected from the Philippine Sea in June 2006. The in-situ O2 consumption rate and the isotopic fractionation factor (α r ) during dissolved O2 consumption were obtained from field observations by applying a vertical one-dimensional advection diffusion model to the deep water mass of about 1000–4000 m. The average O2 consumption rate and α r were, respectively, 0.11 ± 0.07 μmol kg−1yr−1 and 0.990 ± 0.001. These estimated values agree well with values from earlier estimations of Pacific deep water. The in-situ O2 consumption rates are two or more times higher north of 20°N, although the value of α r was not significantly different between the north and south. Its levels varied rapidly in the water mass of less about 2000 m depth. These results suggest that organic matter from the continent imparts a meaningful contribution to the upper water in the northern part of the area; it might produce the strong O2 minimum that is evident in the water mass from about 1000–2000 m in the northern part of the Philippine Sea.  相似文献   

19.
A 24 hour time series survey was carried out during a spring tide (tidal range ca.2 m) of May 1995 on a tidal estuary in the Seto Inland Sea, Japan, in the context of an integrated program planned to quantify the dynamics of biophilic elements (carbon, nitrogen and phosphorus) and the roles played by the macrobenthos on the processes. Three stations were set along a transect line of about 1.4 km, which linked the river to the rear to the innermost part of the subtidal zone. Every hour, at each station, measurements were made of surface water temperature, salinity and dissolved oxygen concentration, and surface water was collected for the determination of nutrients [NH4 +−N, (NO3 −+NO2 −)−N, PO4 3−−P and Si (OH)4−Si]. During the ebb flow, riverine input of silicate and nitrate+nitrite significantly increased the concentrations of both the intertidal and the subtidal stations. Conversely, during the high tide, river nutrient concentrations were lowered by the mixing of fresh water with sea water. As a result, best (inverse) correlations were found at the river station for salinity against silicate (y=-2.9 Sal.+110.7,r 2=0.879) and nitrate+nitrite (y=-1.3 Sal.+48.4,r 2=0.796). In contrast, ammonium nitrogen concentrations were higher at intermediate salinities. Indeed, no significant correlation was found between salinity and ammonium. The effect of the macrobenthos, which is abundant on the intertidal flat, is discussed as a biological component that influences the processes of nutrient regeneration within the estuary. The effect of the tidal amplitude is an important one in determining the extent of the variations in nutrient concentrations at all three stations, which were stronger between the lower low tide and the higher high tide.  相似文献   

20.
Organic matter in a tropical mangrove ecosystem was characterized by stable carbon and nitrogen isotopic analyze, conducted on various organic samples, including land and mangrove plants, soils, particulate organic matter (POM), and sea and river sediments along the southwestern coast of Thailand. The δ13C values of land plants and POM in river water can be explained in terms of a greater influence of C3 plants than C4 plants in this area. The POM and sediments from the Trang River and Ko Talibong area showed systematically higher δ15N values than those from Ko Muk and other coastal areas. Organic matter in the Trang River might be influenced by nitrogen released from agricultural or human waste, which could affect the isotopic composition of POM and sediments in the Trang River estuary and along the coast near the river mouth. We used a stochastic method to estimate the contributions of four organic end-members, identifiable by their δ13C and δ15N values. The results implied that seagrasses were a major source of sedimentary organic matter, contributing 42 ± 5% in the Ko Muk area and 36 ± 5% in the Ko Talibong area. The contribution of coastal POM to sediments was estimated to be only 13% in Ko Muk and 19% in Ko Talibong. Mangrove plants contributed approximately 23% in both areas. It was concluded that seagrasses are an important source of sedimentary organic matter in this coastal region of southwestern Thailand. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

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