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1.
Fine scale distribution of nitrous oxide in marine sediments   总被引：1，自引：0，他引：1  
Vertical profiles of nitrous oxide and other inorganic nitrogen compounds in the sediments in Tokyo Bay and its vicinity were measured using the whole core squeezing method. Within the bay area, vertical profiles of nitrous oxide in the interstitial waters showed one or two distinctive peaks around the depth of 2–4 cm, which corresponded to the peaks of nitrite and nitrate. In situ formation of nitrous oxide through nitrification was suggested in those sediments, which was possibly activated by the presence of benthic animals. On the other hand, at the deep sediment off Tokyo Bay the profiles of nitrous oxide, nitrite and nitrate gave a monotonous single peak, indicating less bioturbated condition. Denitrification or dissimilatory nitrate reduction might be important for the formation of nitrous oxide peaks in the latter type of sediment.  相似文献   

2.
The presence of electrolytes (salts) in aqueous solution modifies the solubility and related properties of organic compounds in water. Reported data for salting-out constants (Setschenow constants) which relate solubility to the salt concentration of aromatic and alkane hydrocarbons, and their chlorinated derivatives, and some organic acids have been compiled for 25 aqueous salt solutions at 20–25 °C. The salting-out sequences for various electrolytes are discussed and it is shown that the salting-out effect is greater for organic solutes with large molar volumes. A compilation of salting-out constants for NaCl solutions and seawater (natural or synthetic) with a variety of solutes, shows that the Setschenow constants are similar for natural or artificial seawater (at salinity of 30–35%.) and NaCl solutions (at 3.0–3.5% or 0.5 M). A simple correlation is suggested for estimating the Setschenow constants for a variety of organic solutes in seawater which typically yields a reduction in solubility by a factor of 1.36. The hydrophobicity of organic solutes is therefore increased by this factor, as is the air-water partition coefficient, implying an increased partitioning from aqueous solution into air, organic carbon and lipid phases. The effect must be quantified when comparing the behavior of organic contaminants in freshwater and marine conditions.  相似文献   

3.
Joan D. Willey   《Marine Chemistry》1974,2(4):239-250
The solubility of amorphous silica in seawater at 0°C and from 1 to 1,220 atm. was found to be a linear function of pressure above 270 atm., but to deviate from linearity below that pressure. Using a quadratic derivation of Planck's equation, ΔV for the dissolution was found to be −16.5 cm3mole−1, and Δk was found to be −4.4 · 10−2 cm3 mole−1 atm−1∂Δk/∂P was found to be 27.2 · 10−5 cm3 mole−1 atm−2 which is too significant a factor to allow the commonly made assumption that ∂Δk/∂P =0. North's (1973) model of hydration suggests that this non-zero ∂Δk/∂P may indicate that the silicic acid molecule is more extensively hydrated at lower pressures.If the pressure in an experiment is suddenly lowered to atmospheric pressure after equilibrium solubility had been attained at the higher pressure, the precipitation that occurs to reduce the resulting supersaturation is complete within one hour in the experimental system used in this study.  相似文献   

4.
Dissolved oxygen in seawater has been determined by using the Winkler's reaction scheme for decades. An interference in this reaction scheme that has been heretofore overlooked is the presence of naturally occurring iodate in seawater. Each mole of iodate can result in an apparent presence of 1.5 mol of dissolved oxygen. At the concentrations of iodate in the surface and deep open ocean, it can lead to an overestimation of 0.52 ± 0.15 and 0.63 ± 0.05 μmol kg− 1 of oxygen in these waters respectively. In coastal and inshore waters, the effect is less predictable as the concentration of iodate is more variable. The solubility of oxygen in seawater was likely overestimated in data sources that were based on the Winkler's reaction scheme for the determination of oxygen. The solubility equation of García and Gordon [Garcia H.E., Gordon, L.I., 1992. Oxygen solubility in seawater: Better fitting equations. Limnol. Oceanogr. 37, 1307–1312] derived from the results of Benson and Krause [Benson, F.B., Krause, D. Jr., 1984. The concentration and isotopic fractionation of oxygen dissolved in freshwater and seawater in equilibrium with the atmosphere. Limnol. Oceanogr. 29, 620–632] is free from this source of error and is recommended for general use. By neglecting the presence of iodate, the average global super-saturation of oxygen in the surface oceans and the corresponding efflux of oxygen to the atmosphere both have been overestimated by about 8%. Regionally, in areas where the degree of super-saturation or under-saturation of oxygen in the surface water is small, such as in the tropical oceans, the net air–sea exchange flux can be grossly under- or overestimated. Even the estimated direction of the exchange can be reversed. Furthermore, the presence of iodate can lead to an overestimation of the saturation anomaly of oxygen in the upper ocean attributed to biological production by 0.23 ± 0.07%. AOU may have been underestimated by 0.52 ± 0.15 and 0.63 ± 0.05 μmol kg− 1 in the surface mixed layer and deep water, while preformed phosphate and preformed nitrate may have been overestimated by 0.004 ± 0.001 and 0.06 ± 0.02 μmol kg− 1 in the surface mixed layer, and 0.005 ± 0.0004 and 0.073 ± 0.006 μmol kg− 1 in the deep water. These are small but not negligible corrections, especially in areas where the values of these parameters are small. At the increasing level of sophistication in the interpretation of oxygen data, this source of error should now be taken into account. Nevertheless, in order to avoid confusion, an internationally accepted standard needs to be adopted before these corrections can be applied.  相似文献   

5.
The distributions, sources and atmospheric fluxes of nitrous oxide (N2O) in the seawater of Jiaozhou Bay were investigated during four surveys in 2003 to evaluate this area as a source of N2O to the atmosphere. N2O concentrations in both the surface and bottom waters of Jiaozhou Bay showed obvious variability with both seasons and tidal cycles. Atmospheric fluxes of N2O in Jiaozhou Bay showed seasonal and spatial variations, with the highest values occurring in summer and the lowest in winter. The annual emission of N2O from the bay was estimated to be 1.09 × 106–2.23 × 106 mol yr−1. N2O in the water column of Jiaozhou Bay was found to come from several external sources including riverine water, sewage water and groundwater input, among which the riverine input was dominant while the groundwater input was rather limited. The spatial variation in distribution and atmospheric fluxes of N2O in Jiaozhou Bay was influenced by the input of polluted river waters and sewage effluent along the eastern coast, which highlights the effects of human impacts on N2O emission rates.  相似文献   

6.
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7.
Biogeochemical ocean-atmosphere transfers in the Arabian Sea   总被引：2，自引：2，他引：2  
Transfers of some important biogenic atmospheric constituents, carbon dioxide (CO2), methane (CH4), molecular nitrogen (N2), nitrous oxide (N2O), nitrate , ammonia (NH3), methylamines (MAs) and dimethylsulphide (DMS), across the air–sea interface are investigated using published data generated mostly during the Arabian Sea Process Study (1992–1997) of the Joint Global Ocean Flux Study (JGOFS). The most important contribution of the region to biogeochemical fluxes is through the production of N2 and N2O facilitated by an acute, mid-water deficiency of dissolved oxygen (O2); emissions of these gases to the atmosphere from the Arabian Sea are globally significant. For the other constituents, especially CO2, even though the surface concentrations and atmospheric fluxes exhibit extremely large variations both in space and time, arising from the unique physical forcing and associated biogeochemical environment, the overall significance in terms of their global fluxes is not much because of the relatively small area of the Arabian Sea. Distribution and air–sea exchanges of some of these constituents are likely to be greatly influenced by alterations of the subsurface O2 field forced by human-induced eutrophication and/or modifications to the regional hydrography.  相似文献   

8.
Wet atmospheric deposition of dissolved N, P and Si species is studied in well-mixed coastal ecosystem to evaluate its potential to stimulate photosynthetic activities in nutrient-depleted conditions. Our results show that, during spring, seawater is greatly depleted in major nutrients: Dissolved Inorganic Nitrogen (DIN), Dissolved Inorganic Phosphorus (DIP) and Silicic acid (Si), in parallel with an increase of phytoplanktonic biomass. In spring (March–May) and summer (June–September), wet atmospheric deposition is the predominant source (>60%, relative to riverine contribution) for nitrates and ammonium inputs to this N-limited coastal ecosystem. During winter (October–February), riverine inputs of DIN predominate (>80%) and are annually the most important source of DIP (>90%). This situation allows us to calculate the possibility for a significant contribution to primary production in May 2003, from atmospheric deposition (total input for DIN ≈300 kg km−2 month−1). Based on usual Redfield ratios and assuming that all of the atmospheric-derived N (AD-N) in rainwater is bioavailable for phytoplankton growth, we can estimate new production due to AD-N of 950 mg C m−2 month−1, during this period of depletion in the water column. During the same episode (May 2003), photosynthetic activity rate, considered as gross primary production, was estimated to approximately 30 300 mg C m−2 month−1. Calculation indicates that new photosynthetic activity due to wet atmospheric inputs of nitrogen could be up to 3%.  相似文献   

9.
The solubility of iron, aluminium, manganese and phosphorus has been determined in aerosol samples collected between 49°N and 52°S during three cruises conducted in the Atlantic Ocean as part of the European Union funded IRONAGES programme. Solubilities (defined at pH 4.7) determined for Fe and Al in samples of Saharan dust were significantly lower (medians 1.7% and 3.0%, respectively) than the solubilities of these metals in aerosols from other source regions (whole dataset medians 5.2% and 9.0%, respectively). Mn solubility also varied with aerosol source, but the median solubility of Mn in Saharan dust was very similar to the median for the dataset as a whole (55% and 56%, respectively). The observed solubility of aerosol P was ∼ 32%, with P solubility in Saharan aerosol perhaps as low as 10%. Laboratory studies have indicated that aerosol Fe solubility is enhanced by acid processing. No relationship could be found between Fe solubility and the concentrations of acid species (non-seasalt SO42−, NO3−) nor the net acidity of the aerosol, so we are unable to confirm that this process is significant in the atmosphere. In terms of the supply of soluble Fe to oceanic ecosystems on a global scale, the observed higher solubility for Fe in non-Saharan aerosols is probably not significant because the Sahara is easily the dominant source of Fe to the Atlantic. On a smaller scale however, higher solubility for aerosol Fe may alter our understanding of Fe cycling in regions such as the remote Southern Ocean.  相似文献   

10.
The apparent (stoichiometric) solubility product of calcite in artificial seawater of salinity 35‰ was measured by a saturometer technique. The value of the apparent solubility product was found to be (4·59 ± 0·05) × 10−7 moles/(kilogram of seawater)2 at 25°C with a temperature coefficient of −0·0108 × 10−7/°C between 2 and 25°C. These values are significantly smaller than those found by MacIntyre (1965) and other workers. The effect of these results on the saturation of the oceans with respect to calcite is examined.  相似文献   

11.
DMS emitted into the atmosphere over the global oceans has a range of effects upon atmospheric composition (mediated through various oxidation products) that may be significant with regard to issues as important as climate regulation, and the trace gas oxidation capacity of the marine atmospheric boundary layer. The roles played by DMS oxidation products within these contexts are diverse and complex, and in many instances are not well understood. Here we summarize what is known, and suspected, about the couplings between the marine atmospheric sulfur cycle, other atmospheric chemical cycles, and the dynamics and microphysics of the marine atmospheric boundary layer. This overview focuses heavily on measurements carried out in clean Southern Ocean air masses in association with the Australian Baseline Air Pollution Station located at Cape Grim (40° 40′ 56″S, 144° 41′ 18″ E), Tasmania. The data confirm that in the remote marine atmosphere, DMS is a central player in a variety of important atmospheric processes, reinforcing the need to understand quantitatively the factors that regulate DMS emissions from the ocean to the atmosphere.  相似文献   

12.
The degree of atmospheric saturation for O2, Ar, and N2 gases in water can be determined to accuracies of ±0.1–0.3% using mass spectrometry to determine the gas ratios and Winkler titrations for oxygen analysis. We describe methods used to obtain this level of accuracy and precision. Oxygen accuracy of ±0.1% can be obtained by careful attention to standardization using KIO3 standards that have been corrected for impurities. Accurate O2/Ar and O2/N2 gas ratios (±0.1–0.2%) are obtainable by measuring the mass ratios against the atmosphere if the effect of different gas concentrations on the performance of the mass spectrometer are taken into account. Oxygen and argon saturation values have been determined previously to accuracies of less than or equal to ±0.1%, but published estimates of the saturation value for nitrogen differ by more than 1%. We have redetermined the N2 saturation value at 19°C and zero salinity to be 0.92% greater than the results reported in the work of Weiss (1970).  相似文献   

13.
Fossil methane from the large and dynamic marine gas hydrate reservoir has the potential to influence oceanic and atmospheric carbon pools. However, natural radiocarbon (14C) measurements of gas hydrate methane have been extremely limited, and their use as a source and process indicator has not yet been systematically established. In this study, gas hydrate-bound and dissolved methane recovered from six geologically and geographically distinct high-gas-flux cold seeps was found to be 98 to 100% fossil based on its 14C content. Given this prevalence of fossil methane and the small contribution of gas hydrate (≤ 1%) to the present-day atmospheric methane flux, non-fossil contributions of gas hydrate methane to the atmosphere are not likely to be quantitatively significant. This conclusion is consistent with contemporary atmospheric methane budget calculations.In combination with δ13C- and δD-methane measurements, we also determine the extent to which the low, but detectable, amounts of 14C (~ 1–2% modern carbon, pMC) in methane from two cold seeps might reflect in situ production from near-seafloor sediment organic carbon (SOC). A 14C mass balance approach using fossil methane and 14C-enriched SOC suggests that as much as 8 to 29% of hydrate-associated methane carbon may originate from SOC contained within the upper 6 m of sediment. These findings validate the assumption of a predominantly fossil carbon source for marine gas hydrate, but also indicate that structural gas hydrate from at least certain cold seeps contains a component of methane produced during decomposition of non-fossil organic matter in near-surface sediment.  相似文献   

14.
An improved model is presented for the calculation of the solubility of carbon dioxide in aqueous solutions containing Na+, K+, Ca2+, Mg2+, Cl−, and SO42− in a wide temperature–pressure–ionic strength range (from 273 to 533 K, from 0 to 2000 bar, and from 0 to 4.5 molality of salts) with experimental accuracy. The improvements over the previous model [Duan, Z. and Sun, R., 2003. An improved model calculating CO2 solubility in pure water and aqueous NaCl solutions from 273 to 533K and from 0 to 2000 bar. Chemical Geology, 193: 257–271] include: (1) By developing a non-iterative equation to replace the original equation of state in the calculation of CO2 fugacity coefficients, the new model is at least twenty times computationally faster and can be easily adapted to numerical reaction-flow simulator for such applications as CO2 sequestration and (2) By fitting to the new solubility data, the new model improved the accuracy below 288 K from 6% to about 3% of uncertainty but still retains the high accuracy of the original model above 288 K. We comprehensively evaluate all experimental CO2 solubility data. Compared with these data, this model not only reproduces all the reliable data used for the parameterization but also predicts the data that were not used in the parameterization. In order to facilitate the application to CO2 sequestration, we also predicted CO2 solubility in seawater at two-phase coexistence (vapor–liquid or liquid–liquid) and at three-phase coexistence (CO2 hydrate–liquid water–vapor CO2 [or liquid CO2]). The improved model is programmed and can be downloaded from the website http://www.geochem-model.org/programs.htm.  相似文献   

15.
Ship hull drag reduction using bottom air injection   总被引：1，自引：0，他引：1  
The idea of bottom air injection to reduce ship hull resistance is not new. Early patents envisioned planing hull applications. Recent planing hull tests speed realized an increase of 7–12 knots. River barges and ship fitted with an air injection system results are presented to show a 10–15% reduction in the frictional resistance. Graphs for making initial estimates for displacement hulls with bottom air injection are presented. It is clear from these results that improvements in high speed planing catamarans and full form hull resistance can be realized by using bottom air injection.  相似文献   

16.
From late 1995 through early 2001, three major interannual climate events occurred in the tropical Pacific; the 1995–97 La Niña (LN), 1997–98 El Niño (EN), and 1998–2001 LN. We analyze atmospheric and upper oceanic anomalies in the northeast Pacific (NEP) during these events, and compare them to anomalies both elsewhere in the north and tropical Pacific, and to typical EN and LN anomaly patterns. The atmospheric and oceanic anomalies varied strongly on intraseasonal and interannual scales. During the 1995–97 LN and 1997–98 EN, the Northeast Pacific was dominated by negative SLP and cyclonic wind anomalies, and by upper ocean temperature and sea surface height (SSH) anomalies. The latter were positive along the North American west coast and in the NEP thermal anomaly pool (between Hawaii, Vancouver Island, and Baja California), and negative in the central north Pacific. This atmospheric/oceanic anomaly pattern is typical of EN. An eastward shift in the atmospheric teleconnection from east Asia created EN-like anomalies in the NEP during the 1995–97 LN, well before the 1997–98 EN had begun. The persistence of negative sea-level pressure (SLP) and cyclonic wind anomalies in the NEP during the 1997–98 EN intensified pre-existing upper oceanic anomalies. Atmospheric anomalies were shifted eastward during late 1996–early 1998, leading to a similar onshore shift of oceanic anomalies. This produced exceptionally strong positive upper ocean temperature and SSH anomalies along the west coast during the 1997–98 EN, and explains the unusual coastal occurrences of several species of large pelagic warm-water fishes. The growth and eastward shift of these pre-existing anomalies does not appear to have been linked to tropical Pacific EN anomalies until late 1997, when a clear atmospheric teleconnection between the two regions developed. Prior to this, remote atmospheric impacts on the NEP were primarily from east Asia. As the 1998–2001 LN developed, NEP anomalies began reversing toward the typical LN pattern. This led to predominantly negative SLP and cyclonic wind anomalies in the NEP, and upper ocean temperature and SSH anomalies that were mainly negative along the west coast and positive in the central north Pacific. The persistence of these anomalies into mid-2001, and a number of concurrent biological changes in the NEP, suggest that a decadal climate shift may have occurred in late 1998.During 1995–2001, NEP oceanic anomalies tracked the overlying atmospheric anomalies, as indicated by the maintenance of a characteristic spatial relationship between these anomalies. In particular, wind stress curl and SSH anomalies in the NEP maintained an inverse relationship that strengthened and shifted eastward toward the west coast during late 1996–early 1998. This consistent relationship indicates that anomalous Ekman transport driven by regional atmospheric forcing was an important contributor to temperature and SSH anomalies in the NEP and CCS during the 1997–98 EN. Other studies have shown that coastal propagations originating from the tropical Pacific also may have contributed to coastal NEP anomalies during this EN. Our results indicate that at least some of this coastal anomaly signal may have been generated by regional atmospheric forcing within the NEP.  相似文献   

17.
1 Introduction Estuaries have been subject to intense anthro- pogenic influences over recent decades by inputs of ni- trogen as a consequence of fertilizer usage and sewage/waste input (Howarth et al., 1996). Thus, the capacity of an estuary to buffer or alleviate additional nutrients is of importance in modifying the load of ni- trogen in the marine ecosystem. The role of microor- ganisms in regulating fluxes of nitrogen from land to sea through estuaries has received increased attention (Ni…  相似文献   

18.
The seasonal and interannual variability of the air–sea CO2 flux (F) in the Atlantic sector of the Barents Sea have been investigated. Data for seawater fugacity of CO2 (fCO2sw) acquired during five cruises in the region were used to identify and validate an empirical procedure to compute fCO2sw from phosphate (PO4), seawater temperature (T), and salinity (S). This procedure was then applied to time series data of T, S, and PO4 collected in the Barents Sea Opening during the period 1990–1999, and the resulting fCO2sw estimates were combined with data for the atmospheric mole fraction of CO2, sea level pressure, and wind speed to evaluate F.The results show that the Atlantic sector of the Barents Sea is an annual sink of atmospheric CO2. The monthly mean uptake increases nearly monotonically from 0.101 mol C m− 2 in midwinter to 0.656 mol C m− 2 in midfall before it gradually decreases to the winter value. Interannual variability in the monthly mean flux was evaluated for the winter, summer, and fall seasons and was found to be ± 0.071 mol C m− 2 month− 1. The variability is controlled mainly through combined variation of fCO2sw and wind speed. The annual mean uptake of atmospheric CO2 in the region was estimated to 4.27 ± 0.68 mol C m− 2.  相似文献   

19.
Atmospheric and dissolved methane (CH4) and nitrous oxide (N2O) were measured in the unique coastal ecosystem of theBoddenwaters, including the western Oder estuary, (southern Baltic Sea) during five campaigns between 1994 and 1997. The CH4saturations, ranging from 105–15 500%, showed great spatial and temporal variability with maximum values in September and minimum values in December. The N2O saturations were in the range of 91–312% with a maximum in March. Enhanced concentrations of both gases were observed only in the western Oder estuary near the mouth of the Peene River. Thus, we conclude that the distributions of CH4and N2O in the investigatedBoddenwaters are, directly or indirectly, linked to the Peene River runoff and not to the Oder River. Our estimate of the annual CH4emissions from theBoddenwaters to the atmosphere indicates a significant contribution (c. 17%) to the overall CH4emissions from the Baltic Sea. In contrast, theBoddenwaters represent only a small source for atmospheric N2O.CH4production rates estimated from sediment slurry experiments revealed a significant spatial variability and indicated that methanogenic activity was related to acetate consumption in the surface sediment layer. Sedimentary CH4production might depend on different amounts of accumulation of organic material.  相似文献   

20.
The nitrogen inputs from atmospheric deposition and bottom water entrainment to the surface layer were modelled in the summer period (May–September) over a 11-year period (1989–1999) and compared to investigate the significance of these fluxes for generating blooms in the Kattegat. In the summer periods the average atmospheric deposition was 2.81 mg N m−2 d−1 compared to average entrainment fluxes of 5.42 mg N m−2 d−1, 1.21 mg N m−2 d−1 and 1.15 mg N m−2 d−1 for the northern, central and southern part of the Kattegat, respectively. Atmospheric nitrogen deposition alone could not sustain biomass increases associated with observed blooms and entrainment fluxes dominated the high nitrogen inputs to the surface layer. The potential for a bloom through growth was typically obtained after several days of high nitrogen inputs from entrainment in the frontal area of the northern Kattegat and to some extent from atmospheric deposition. The modelled nitrogen input in this area could account directly for 30% of the observed blooms in the Northern sub-basin, and through advective transport 24% and 19% of the observed blooms in the central and southern Kattegat. The direct nitrogen inputs through atmospheric deposition and entrainment to the central and southern sub-basins were small and could not be linked to any bloom observation.  相似文献   

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