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1.
Application of a simple model describing regional variations in the contents of manganese and associated minor metals in deep-sea sediments suggests that solid manganese phases are being removed from the <0.5 μm fraction of seawater at ～1–7 · 1012g yr?1 in excess of the rate of stream-supplied manganese. This flux is consistent with: (1) the relative rates of sediment accumulation in the Atlantic and Pacific Oceans; (2) the contrast between the oceanic residence time of manganese calculated from stream-supply data (14 · 103 yr) and from the flux of manganese precipitating in marine sediments or as manganese nodules (0.38–2.4 · 103 yr); (3) the surplus mass of manganese revealed by geochemical balance calculations (22.9 · 102g). On this basis excess manganese is accumulating in deep-sea sediments at 0.2–2.0 · 10?6 g cm?2yr?1. Manganese supplied to the upper layers of marine sediments by diagenesis has been evaluated with the aid of vertical advection—diffusion—reaction models. The calculated diagenetic flux of manganese at the sediment surface in a near-shore environment is in agreement with the known accretion rate of manganese deposits (1.7 · 10?2 g cm?2 10?3 yr?1) and the regionally variable flux over the area assessed is consistent with the presence or absence of manganese nodules at or near the water-sediment interface. The diagenetic flux at the surface of deep-sea sediments has been calculated at 0.7 · 10?4 g cm?2 10?3 yr?1 when the upper, oxic, zone of the sediment is ～20 cm thick. A limiting factor on the in situ production flux of dissolved manganese in deep-sea sediments appears to be the availability of reducing agents for manganese dissolution rather than the rate of downward transport of manganese-rich sediment to a reaction boundary where dissolution takes place. Various estimates of the rate of upward-migrating manganese suggest that manganese precipitates in the oxic zone with a rate constant of ～10?7 sec?1 with the result that diagenetic processes cannot supply the flux of excess manganese through more than ～0.25 m of oxic sediment. However, estimates of the flux of manganese to the oceans by submarine volcanic processes (0.79–1.1 · 1012g yr?1) are similar to the surplus mass of manganese detected by geochemical balance calculations (0.7 · 1012g yr?1). If submarine hydrothermal solutions provide only 10% of this excess then their computed discharge rate (39 g cm?2 yr?1) and residence time in the upper layer of oceanic crust (130,000 yr) agree well with these parameters for continental thermal springs.  相似文献   

2.
Chemical extraction techniques show that the majority of the arsenic in North Atlantic deep-sea sediments is associated with an iron phase compositionally similar to that found in deep-sea ferromanganese nodules (As/Fe ～ 11 · 10?4) and is probably of seawater origin. Some sediments also contain As associated with Fe oxides produced by continental weathering. A minority (～8%) of the arsenic is of detrital origin but is not associated with Fe or Mn oxides; it has a content (1.7 ppm) similar to the average crustal abundance. In the Eastern Mediterranean Sea, near-shore sediments contain As associated with land-derived Fe oxides (As/Fe ～ 2 · 10?4), but As/Fe ratios increase to ～ 13 · 10?4 in deep-sea sediments as the contribution of seawater derived arsenic becomes dominant. Arsenic is enriched in metalliferous sediments (As/Fe ～ 20?50 · 10?4) but As/P ratios of metalliferous sediments, deep-sea ferromanganese nodules and deep-ocean water are all similar. Although a hydrothermal contribution cannot be discounted, it is likely that the arsenic is also of seawater origin, suggesting that hydrothermal iron oxyhydroxides remove As more efficiently from seawater than do iron phases (goethite) in deep-sea sediments and nodules. Arsenic accumulates in deep-sea sediments (～ 6 μg cm?2 10?3 yr?1) at sediments (～ 120 μg cm?2 10?3 yr?1) at rate sufficient to balance river input input (～3 · 1010 g yr?1). These estimates give an oceanic residence time for arsenic of 1–2 · 105 yr.  相似文献   

3.
The photolysis of nitrate in seawater by sunlight has been re-examined using abiotic seawater and naturally occurring concentrations. Photochemical formation of nitrite from nitrate was observed. First-order nitrate photolysis rate coefficients calculated from nitrite appearance (corrected for concomitant nitrite photolysis) ranged from 0 to 2.3 yr?1, median 0.7 yr?1. The coefficients did not correlate well with water chemistry, but decreased with increasing light dose. A first-order rate coefficient of 0.4 yr?1 was calculated for the primary photochemical process NO3? + hυ = NO2? + O(3P) under sea surface equatorial insolation and cloudiness conditions. However, no significant nitrate concentration decreases could be detected, suggesting an upper limit for the net first-order nitrate loss rate coefficient of 0.3 yr?1. The data thus imply some conversion in the reverse sense: NO2? + hυ →→ NO3?.If our median rate estimate applies to surface oceanic conditions, nitrate photolysis proceeds at roughly 0.02–0.5% of the rate of N incorporation during primary production. It is thus not a significant NO3-N sink. Since such reactive species as oxygen atoms, nitrogen dioxide, and hydroxyl radicals are produced, the reaction may have significant consequences in seawater. However, nitrite photolysis is almost certainly a more significant process.The results show internal inconsistencies and our rates are markedly different from those calculated using data from other studies. Nitrate photolysis rates are theoretically concentration- and light dose-dependent. Whether these dependencies explain the apparent discrepancies is unclear, as methodological effects may also be involved. The system requires further study.  相似文献   

4.
Excess 210Pb in a core from a Mexican Coastal Lagoon, which has no connection with the sea shows a small but measurable decay over the length of the core, when different approaches were compared (excess and corrected 210Pb activity with depth, total and inorganic cumulative weights) significant differences in the values for the sedimentation rate are obtained. The best coefficient correlation was calculated when corrected 210Pb activity for the uneven distribution of organic matter and cumulative inorganic weight is considered (ω = 0·93 cm yr?1, R = ?0·86; ω = 0·51 cm yr?1 for the top 13 cm, R = ?0·90 and 1·52 cm yr?1 for the interval 14–46 with R = ?0·96).Time frames in the sedimentary column were in agreement between the 210Pb calculated time and the appearance of shells fragments probably associated with the disturbances caused by the 1961 hurricane Tara.The surface accumulation rate is equivalent to a mean deposition of 262·5 g m?2 yr?1 or organic matter which is minor but comparable to some salt marshes of United States.  相似文献   

5.
Volumes of seawater filtered through the intertidal zone were measured on three modally reflective microtidal beaches in Western Australia. The filtered volumes were large, 19 m3 m?1 day?1 and 73 m3 m?1 day?1 on two ‘clean’ beaches but only 0·4 m3 m?1 per tidal cycle on a beach covered in kelp and seagrass wrack. The mean residence times of this water in the interstitial system and its percolation paths were both short, 1–7 h and 2–5 m respectively. Water input was greater across a beach cusp horn than across a cusp embayment. Most input occurred in the upper swash zone where the water table was less than 20 cm deep. Tidal variations in input volumes were evident even with tide ranges of only 20 cm. The inshore zone off these beaches filters on average 0·07 m3 m?2 day?1 at an average depth of 5·5 m under 0·4 m waves of 6·5 s duration. The importance of these procedures in the mineralization of organic materials and the regeneration of nutrients for an inshore ‘lagoon ecosystem’ is estimated and discused.  相似文献   

6.
A chemiluminescent analysis technique for the determination of nanomolar quantities of nitrate, nitrate plus nitrite or nitrite alone in seawater is described. The method depends on the selective reduction of these species to nitric oxide which is then determined by its chemiluminescent reaction with ozone, using a commercial nitrogen oxides analyzer. The necessary equipment is compact and sufficiently sturdy to allow shipboard use. A precision of ±2 nM is claimed with analytical rates of 10–12 samples h?1, and modifications are discussed to allow doubling the analytical rate.  相似文献   

7.
Porites panamensis is a hermatypic coral present in the eastern Pacific Ocean. Skeletal growth parameters have been reported, but studies of the relationship between annual calcification rates and environmental controls are scarce. In this study, we investigated three aspects of the annual calcification rates of P. panamensis: growth parameters among three P. panamensis populations; the sea surface temperature as a calcification rate control spanning a latitudinal gradient; and calcium carbonate production among three sites. Growth parameters varied among the sites due to the colony growth form. Massive colonies in the north showed a higher calcification rate than encrusting colonies in the south (mean: 1.22–0.49 g CaCO3 · cm?2 · yr?1), where variations in calcification rates were related to growth rate (0.91–0.38 cm · yr?1) rather than to skeletal density differences (overall mean ± SD, 1.31 ± 0.04 g CaCO3 · cm?3). Our results showed a positive linear relationship between annual calcification rates and sea surface temperatures within these P. panamensis populations. Differences were related to distinct oceanographic environments (within and at the entrance of the Gulf of California) with different sea surface temperature regimes and other chemical properties. Different populations calcified under different environmental conditions. Calcium carbonate production was dependent upon the calcification rate and coral cover and so carbonate production was higher in the north (coral cover 12%) than in the south (coral cover 3.5). Thus, the studied sites showed low calcium carbonate production (0.25–0.43 kg CaCO3 · m?2 · yr?1). Our results showed reduced calcification rates, regional temperature regime control over calcification rates, different growth forms, low coral cover and low calcium carbonate production rates in P. panamensis.  相似文献   

8.
Anchovy biomass and copepod standing stocks and growth rates on the Agulhas Bank were compared during the peak spawning period (November) in 1988 and 1989. In 1988, copepod biomass over the western Agulhas Bank was low (1,0 g dry mass·m?2) relative to anchovy biomass there (14,7 g dry mass·m?2). In November 1989 in the same area, fish biomass was much lower (5,7 g dry mass·m?2), following a recruitment failure, and copepod biomass was higher (2,4 g dry mass·m?2), possibly as a result of lesser predation by anchovy. By contrast, the eastern Agulhas Bank had a larger biomass of copepods (4–6 g dry mass·?2) and a lower biomass of anchovy during both years. Knowing, from laboratory studies, that a prey biomass of 0,78 g·m?2 is required for fish to obtain their daily maintenance ration, it is suggested that spawning on the western Agulhas Bank was food-limited in 1988. Copepods on the western Bank may be replaced by local growth or transport from the eastern Bank. Growth rates of copepods on the western Bank were 10–50 per cent of maximum in 1988, but total production (c. 100 mg dry mass·m?2·day?1) was low, primarily because biomass was low and less than the rate of consumption by anchovy (243 mg copepod dry mass·m?2·day?1). On the eastern Bank, copepod production exceeded anchovy consumption and it is concluded that the flux of copepod biomass onto the western Bank may be as important as local growth in replenishing copepod stocks there. Feeding conditions for anchovy on the western Agulhas Bank are often marginal compared to the situation on the eastern Bank, and it is suggested that the selection of the western Bank as the major spawning area is related more to the success of transport and survival of eggs and larvae on the West Coast recruiting grounds than to feeding conditions per se.  相似文献   

9.
The response of the exoproteolytic activity of seawater to proteolytic inhibitors suggests that metalloproteases are the main enzymes involved. The Km of exoproteolytic enzymes for the hydrolysis of indigenous proteins in coastal north seawater has been evaluated as 80 μg l−1 and the maximum rate of proteolysis lies in the range 0·1–0·35 μgC l−1-enzymatic-unit−1. Enrichment experiments suggest that both species selection and metabolic regulation may play a role in the exoproteolytic activity/biomass ratio. However, in situ exoproteolytic activity/biomass ratios observed in a broad range of natural marine environments lie in a very narrow range, which is intermediate between those observed after amino acid or protein enrichment.  相似文献   

10.
Monosaccharides were determined in waters and sediment pore waters from a wide variety of environments and locations. Desalting was performed by electrodialysis and concentrated extracts were analyzed by two forms of liquid chromatography. At least 12 sugars were identified. Glucose and fructose were the dominant monosaccharides in nearly all samples examined. Analyses of over 150 seawater and sediment pore water samples showed that fructose is highly significantly correlated (>0.99) with glucose concentrations. Laboratory kinetic experiments on the epimerization reaction, glucose ? fructose, in sterilized natural seawater in the dark, yielded a forward rate constant, k1, of 1.2 × 10?5 h?1 at 25°C and 1.6 × 10?7 h?1 at 2°C. The approximate time required to attain equilibrium at 25°C was 1.1 y and at 2°C, 15.4 y; the measured equilibrium constant was in the range 0.3–0.4. The actual ratio of fructose to glucose in natural water samples was usually in the range 1.0–1.4/l, independent of the total monosaccharide concentrations, which varied in the samples by a factor of ～100. Several possible explanations for the apparent discrepancy in the determined and found ratios are discussed: the presence of universal, as yet, undiscovered major biological sources for fructose in marine environments; preferential utilization of glucose; preferential incorporation of fructose into or onto inorganic colloids; and preferential formation of fructose-transition metal ion associations.  相似文献   

11.
The bivalve molluscs Mytilus californianus and Crassostrea gigas were exposed to filtered seawater containing the isotope 95mTc added as pertechnetate (TcO4?) to study the biokinetic behaviour of this element. Whole body concentration factors for both organisms at equilibrium were small (CF = 1·3–1·5); individual organ concentration factors were highest for the visceral mass in both. Loss rates determined both in the laboratory and under field conditions were biphasic for both molluscs; initial loss of Tc was rapid with slightly more than 50 % of the initial label being lost within 10 days. Thereafter, loss rates decreased and whole body biological half-lives ranged from 80 to 134 days. Neither I? nor IO3? affected the uptake of Tc by M. californianus even when concentrations of these anions exceeded those normally present in seawater by two orders of magnitude.  相似文献   

12.
From July 1981 to July 1982 Umbonium vestiarium (L.) on a north Penang sand shore numbered 573–11 077 m?2 (mean 4126 or 53·1 g dry tissue) near MLWN and 2164–12 414 m?2 (mean 6500 or 59·8 g dry tissue) further downshore. Heavy recruitment of young became evident in June and July 1982 and a closely corresponding cohort of young was present in July 1981. Progression of this cohort indicated that young settling in May–June grew to full size (11–13 mm diameter) by January–March the following year and that virtually all died during their second year, presumably having spawned in March–May. Recruitment of young was chiefly on the lower shore but adults came to be more abundant and predominant on the upper shore. There is some evidence of migration upshore during growth.Production is estimated at 105·4 g dry tissue m?2 y?1 (2118 kj) at the lower shore level and this is almost double the 58·8 g m?2 y?1 (1176·6 kj) at the higher level. These values represent almost the entire secondary production across much of the sand flats.Possible causes of such a marked annual cycle in the very weakly seasonal tropics of the Malacca Strait are considered and it is suggested that monsoonal changes in wind, wave action and salinity might be involved.  相似文献   

13.
The flux of ammonia, phosphate, silica and radon-222 from Potomac tidal river and estuary sediments is controlled by processes occurring at the sediment-water interface and within surficial sediment. Calculated diffusive fluxes range between 0·6 and 6·5 mmol m?2 day?1 for ammonia, 0·020 and 0·30 mmol m?2 day?1 for phosphate, and 1·3 and 3·8 mmol m?2 day?1 for silica. Measured in situ fluxes range between 1 and 21 mmol m?2 day?1 for ammonia, 0·1 and 2·0 mmol m?2 day?1 for phosphate, and 2 and 19 mmol m?2 day?1 for silica. The ratio of in situ fluxes to diffusive fluxes (flux enhancement) varied between 1·6 and 5·2 in the tidal river, between 2·0 and 20 in the transition zone, and from 1·3 to 5·1 in the lower estuary. The large flux enhancements from transition zone sediments are attributed to macrofaunal irrigation. Nutrient flux enhancements are correlated with radon flux enhancements, suggesting that fluxes may originate from a common region and that nutrients are regenerated within the upper 10–20 cm of the sediment column.The low fluxes of phosphate from tidal viver sediments reflect the control benthic sediment exerts on phosphorus through sorption by sedimentary iron oxyhydroxides. In the tidal river, benthic fluxes of ammonia and phosphate equal one-half and one-third of the nutrient input of the Blue Plains sewage treatment plant. In the tidal Potomac River, benthic sediment regeneration supplies a significant fraction of the nutrients utilized by primary producers in the water column during the summer months.  相似文献   

14.
Nitrification in a closed prawn-culture system was well established and followed the classical oxidation sequence of ammonia via nitrite to nitrate. Ammonia levels were in the range 4,8–68,7 μg-at N·??1 nitrite 0,15–891 μg-at N·??1 and nitrate approached a maximum of 9 898 μg-at N·??1 after 22 weeks. Marine nitrifying bacteria were enumerated by the most probable number (MPN) technique. The maximum MPN estimate of either group of nitrifying bacteria in the filter was 1,73 × 107·cm?3 while the maximum MPN estimate of their counterparts in the culture water was approximately 500 times lower. To establish mean incubation times for the accurate enumeration of nitrifying bacteria, incubations were carried out over a period of 130 days. Maximum estimates of MPN of ammonia-oxidizing bacteria were obtained after an incubation period of 20 days with a mean of 15 days. Nitrite-oxidizing bacteria required a maximum of 65 days with a mean incubation period of 30,3 days.  相似文献   

15.
The stability constants of the ion pairs NaSO4?, KSO4?, MgSO4?, CaSO4, MgCl+ and CaCl+ were determined at 25°C and 0.7 M formal ionic strength, by measuring the solubility of gypsum (CaSO4 · 2H2O) in different media. The media used contained one or two of the following electrolytes: NaCl, KCl, MgCl2, NaClO4, Mg(ClO4)2, Na2SO4. Values for the stability constants are 1.22, 1.84, 12.3, 30.6, 0.48 and 1.20 M?1, respectively, and the solubility product for gypsum is 2.87 · 10?4M2. The distribution of the main constituents of seawater was calculated using these results and the values of the carbonate and bicarbonate constants given by Dyrssen and Hansson (1972–1973). The solubility of gypsum in seawater as calculated and determined experimentally was 21.43 mM and 21.10 mM, respectively.  相似文献   

16.
A widely used method for determining iodate in seawater involves reaction of the IO3? with excess I?, under acid conditions, to form I2 which is measured colorimetrically. It is known that when the acidification is by mineral acid, nitrite can interfere with the method by oxidising I? to I2 in an analogous way to IO3?. Some workers have used sulphamic acid for acidification since it is reported to destroy nitrite in solution.We have investigated the extent of nitrite interference in the colorimetric determination of iodate using both mineral acid and sulphamic acid for acidifying the reaction mixture. In seawater the extent of the interference is equivalent to 0.212 μM 1?1 IO3? per μM 1?1 NO2? with sulphuric acid, and 0.128 μM 1?1 IO3? per μM 1?1 NO2? with sulphamic acid. This means that for a seawater containing 0.31 μM 1?1 (39 μg 1?1) IO3?, the presence of 0.5 μM 1?1 NO2? will lead to an error of 25% in the iodate determined colorimetrically in methods using sulphuric acid, and 15% in methods in which sulphamic acid is used.  相似文献   

17.
Free-living marine nematodes at two littoral sites near Vancouver, Canada were studied over a 1-year period. Sixty-four species were found at a Belcarra Park site, with a maximum nematode density of 6·7 × 105 m?2 and 24 species at Iona Island, with a maximum density of 1·6 × 105 m?2. At both sites most of the nematodes occurred in the upper 2 cm of the 6 cm depth of sediment examined, and the vertical distribution of most species remained constant during the year. The distribution of the nematodes in relation to some physical parameters is discussed. The occurrence of certain species suggests that they have a worldwide distribution.  相似文献   

18.
The solubilities and aqueous activity coefficients of polychlorinated biphenyls were measured in distilled and saline water (30? salinity). Solubilities in distilled water ranged from 3 · 10?4 g/l for dichlorobiphenyls to 6 · 10?6 g/l for heptachlorobiphenyls; values in artificial seawater were about five times lower than the corresponding values in distilled water. In both cases, the solubilities decreased regularly with increasing degree of chlorination. The corresponding activity coefficients are inversely proportional to the chlorine content and range from 4 · 107 to 4 · 109 in distilled water and from 3 · 108 to 1.5 · 1010 in saline water. Both the solubilities and activity coefficients agree well with those predicted from additivity considerations. The physical chemical aspects discussed in this paper can be applied in determining the solubility behavior of other stable organic molecules in the marine environment.  相似文献   

19.
A data base of 111 filter-collected marine atmospheric particulates is used to describe the distribution of lead over the North and South Atlantic, the Mediterranean Sea, the Red Sea, the Gulf of Aden and the northern and central Arabian Sea. The distribution of atmospheric Pb is assessed in terms of enrichment factor diagrams, and it is shown that over the marine regions studied in both the Northern and Southern Hemispheres the distribution of Pb in the atmosphere is controlled by the mixing of a background component, or components, with crustal material within certain concentration limits. For the Northern Hemisphere samples used in the investigation there is a reasonably well-defined Pb concentration minimum of ～ 0.6 ng m?3 of air; however, this will be severely decreased in more remote Northern Hemisphere marine regions. Geometric average Pb atmospheric concentrations vary from one marine region to another, ranging from ～ 0.98 ng m?3 of air for the South Atlantic westerlies to ～ 15 ng m?3 of air in the North Atlantic westerlies; although the latter reduces to ～ 7 ng m?3 of air when ‘polluted’ samples are excluded. Lead sea-surface deposition fluxes are calculated on the basis of two deposition velocities (0.25 and 1 cm s?1), the largest flux (220 ng Pb cm?2 yr?1) being found for the westerlies over the eastern margins of the North Atlantic. The distribution of lead over the North Atlantic is assessed in terms of the global lead budget and it is estimated that a maximum of ～ 24% of the total ‘natural’ lead injected annually into the World atmosphere, and ～ 3.5% of the anthropogenic lead injected annually into the Northern Hemisphere atmosphere, are deposited over the North Atlantic sea surface.  相似文献   

20.
By simulating an upwelling event in a laboratory microcosm, it was possible to promote the development of a natural and diverse planktonic community. An initial bacterioplankton community which developed in response to phytoplankton growth was dominated by small coccoid forms (0,14–0,2 μm3) of the genera Vibrio and Pseudomonas. This group was heavily exploited by the heterotrophic microflagellate Pseudobodo sp. (30 μm3). Later, the bacterioplankton community was dominated by large rods (0,7 μm3) which the flagellates seemed unable to exploit. A Lotka-Volterra predator-prey model fitted to the observed data indicated that the flagellates consumed 2,4 times their carbon body mass per day or 19 bacteria·flagellate?1·h?1 when prey were not limiting. Clearance rates were inversely proportional to prey density and ingestion rate, ranging from 2 × 10?3 to 20 × 10?3) μ?·flagellate?1·h?1. At typical field densities of bacteria and heterotrophic flagellates in the southern Benguela region, between 5 and 30 percent of the water column could be cleared per day. Specific growth rates of the flagellates were positively related to prey density, the maximal rate being 0,84 · d?1. Their initially faster growth rates allowed bacteria to increase in numbers despite predation. The growth yield of the flagellates (34–36 per cent) was also positively related to food density. Such low values suggest inefficient transfer of carbon to higher trophic orders but considerable nitrogen regeneration. Nitrogen excretion rates were approximately 6–7 μg N·mg dry weight?1·h?1, comparable to other flagellates but faster than ciliates. These rates are comparable with in situ measurements of NH+4-N excretion in pycnoclinal regions based on 15N isotope studies but are only about 20 per cent of measured rates in surface waters. This is interpreted to mean that, in pycnoclinal regions where the relative input of "new" nitrogen is high, there are few regenerative steps and the model describes them satisfactorily. In surface waters, observed rates of excretion can only be accounted for by many regenerative steps in a highly complex food chain in which the cumulative total of nitrogen excretion at each step amounts to that based on 15N labelling studies.  相似文献   

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