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1.
Measurements of the concentration and vertical distribution of dissolved aluminium and silica, and of pH. in interstitial waters of recent marine sediments from the North Sea and the Mediterranean Sea were performed to evaluate the behaviour of aluminium during early diagenesis. The results suggest that thermodynamic equilibria alone do not control the concentrations of dissolved species in the system Al-Si-O2-H2O during early diagenesis. Rather, these concentrations are governed by dynamic factors involving mineral dissolution-precipitation reactions and diffusion.  相似文献   

2.
Numerous previous studies indicate that several different authigenic aluminosilicates form in the oceans. In this study we show, using dissolved Al distributions in sediments and waters from the nearshore regions of the East China Sea, that the process of aluminosilicate formation probably begins rapidly upon contact of detrital clays with seawater. Statistical analyses of dissolved Al-Si-H+ relations in surface sediments indicate that the minerals forming in East China Sea sediments low in dissolved Fe are dioctahedral chlorites with an average composition EX0.91Mg0.77Al5.0Si2.7O10(OH)8 (where EX = exchangeable + 1 cation). This composition is also consistent with dissolved Al and Si measurements as a function of salinity in turbid overlying waters. Results suggest a dissolution—reprecipitation mechanism for clay mineral reconstitution. This mechanism can help to explain why different authigenic clays are found in different areas of the oceans. In the East China Sea the total amount of authigenic clays present must constitute a very minor fraction of the bottom sediments. Thus, the formation of these minerals has a relatively small impact upon dissolved Si distributions. Clay mineral reconstitution in nearshore regions may provide a mechanism for buffering sediments and overlying waters with respect to pH, as the composition of minerals formed should be a direct function of the H+ activity in the surrounding environment.  相似文献   

3.
 The concentrations of N, P and Fe in surface sediments and interstitial and overlying (bottom and surface) waters of the Ashtamudi estuary located in the southwest coast of India are reported along with the various chemical species of N (NO2–N, NO3–N, NH3–N and total N) and P (organic P, inorganic P and total P) in interstitial and overlying waters and discussed in terms of the physico-chemical environment of the system. The interstitial water exhibits higher salinity values compared to bottom and surface waters, indicating the coupled effects of salt-wedge phenomena and gravitational convection of more saline-denser marine water downward through surface sediments. N, P and Fe as well as their chemical forms are enriched in the interstitial water compared to bottom and surface waters. However, the dissolved oxygen (DO) shows an opposite trend. The marked enrichment of NH3–N in the interstitial water and its marginal presence in bottom and surface waters, together with the substantial decrease in the DO concentrations of bottom water and consequent increase in the concentrations of NO2–N and NO3–N in interstitial and bottom waters, points to the nitrification process operating in the sediment-water interface of the Ashtamudi estuary. The enrichment of total N, P and Fe in the interstitial water compared to the overlying counterparts and the positive correlation of sediment N, P and Fe with mud contents as well as organic carbon indicate that these elements are liberated during the early diagenetic decomposition of organic matter trapped in estuarine muds. Received: 5 Oktober 1998 · Accepted: 9 February 1999  相似文献   

4.
Polychlorinated biphenyls (PCBs) were measured in interstitial waters and sediments at a site in New Bedford Harbor, Massachusetts, to study partitioning processes of hydrophobic organic compounds in marine sediments. Pore water concentrations of total PCBs, expressed as Aroclor 1254, increased with depth in the sediments with a maximum concentration of 17.1 μg/L at 9–11 cm. Apparent distribution coefficients of individual chlorobiphenyls decreased with depth and were related to dissolved organic carbon levels. Results from this site suggest that most of the PCBs in interstitial waters are sorbed to organic colloids. A simple three-phase equilibrium sorption model can explain many features of the data. Changes in the composition of individual chlorobiphenyls in the sediments were also apparent. Microbial degradation appears to be responsible for large relative depletions of several chlorobiphenyls with depth in the core.  相似文献   

5.
As part of a study of early diagenesis in anaerobic lake sediments the major ions and P, Fe, Mn, pS, p? and pH were measured in interstitial waters of cores from eutrophic Greifensee in north-central Switzerland. A guide for the interpretation of such data is thermodynamic equilibrium between the dissolved species and mineral phases. The results show that CaCO3, which precipitates from the lake water, dissolves rapidly in the CO2-rich interstitial waters resulting in equilibrium with calcite in the top few centimeters of sediment. Siderite, on the other hand, is nearly ten-fold supersaturated 20–30 cm below the surface. Iron monosulfides are metastable in the surface 10–20 cm of sediment and pS and p? results indicate equilibrium between polysulfides and orthorhombic sulfur. Vivianite appears to be limiting the solubility of phosphate below a few centimeters of sediment.The above processes are highly interactive, especially in the case of ferrous iron, with one result being a two order of magnitude decrease in dissolved phosphate in a depth interval of 20cm in the interstitial waters.  相似文献   

6.
Subterranean estuary occupies the transition zone between hypoxic fresh groundwater and oxic seawater, and between terrestrial and marine sediment deposits. Consequently, we hypothesize, in a subterranean estuary, biogeochemical reactions of Fe respond to submarine groundwater discharge (SGD) and sea level rise. Porewater and sediment samples were collected across a 30-m wide freshwater discharge zone of the Indian River Lagoon (Florida, USA) subterranean estuary, and at a site 250 m offshore. Porewater Fe concentrations range from 0.5 μM at the shoreline and 250 m offshore to about 286 μM at the freshwater-saltwater boundary. Sediment sulfur and porewater sulfide maxima occur in near-surface OC-rich black sediments of marine origin, and dissolved Fe maxima occur in underlying OC-poor orange sediments of terrestrial origin. Freshwater SGD flow rates decrease offshore from around 1 to 0.1 cm/day, while bioirrigation exchange deepens with distance from about 10 cm at the shoreline to about 40 cm at the freshwater-saltwater boundary. DOC concentrations increase from around 75 μM at the shoreline to as much as 700 μM at the freshwater-saltwater boundary as a result of labile marine carbon inputs from marine SGD. This labile DOC reduces Fe-oxides, which in conjunction with slow discharge of SGD at the boundary, allows dissolved Fe to accumulate. Upward advection of fresh SGD carries dissolved Fe from the Fe-oxide reduction zone to the sulfate reduction zone, where dissolved Fe precipitates as Fe-sulfides. Saturation models of Fe-sulfides indicate some fractions of these Fe-sulfides get dissolved near the sediment-water interface, where bioirrigation exchanges oxic surface water. The estimated dissolved Fe flux is approximately 0.84 μM Fe/day per meter of shoreline to lagoon surface waters. Accelerated sea level rise predictions are thus likely to increase the Fe flux to surface waters and local primary productivity, particularly along coastlines where groundwater discharges through sediments.  相似文献   

7.
Two sediment cores retrieved at the northern slope of Sakhalin Island, Sea of Okhotsk, were analyzed for biogenic opal, organic carbon, carbonate, sulfur, major element concentrations, mineral contents, and dissolved substances including nutrients, sulfate, methane, major cations, humic substances, and total alkalinity. Down-core trends in mineral abundance suggest that plagioclase feldspars and other reactive silicate phases (olivine, pyroxene, volcanic ash) are transformed into smectite in the methanogenic sediment sections. The element ratios Na/Al, Mg/Al, and Ca/Al in the solid phase decrease with sediment depth indicating a loss of mobile cations with depth and producing a significant down-core increase in the chemical index of alteration. Pore waters separated from the sediment cores are highly enriched in dissolved magnesium, total alkalinity, humic substances, and boron. The high contents of dissolved organic carbon in the deeper methanogenic sediment sections (50-150 mg dm−3) may promote the dissolution of silicate phases through complexation of Al3+ and other structure-building cations. A non-steady state transport-reaction model was developed and applied to evaluate the down-core trends observed in the solid and dissolved phases. Dissolved Mg and total alkalinity were used to track the in-situ rates of marine silicate weathering since thermodynamic equilibrium calculations showed that these tracers are not affected by ion exchange processes with sediment surfaces. The modeling showed that silicate weathering is limited to the deeper methanogenic sediment section whereas reverse weathering was the dominant process in the overlying surface sediments. Depth-integrated rates of marine silicate weathering in methanogenic sediments derived from the model (81.4-99.2 mmol CO2 m−2 year−1) are lower than the marine weathering rates calculated from the solid phase data (198-245 mmol CO2 m−2 year−1) suggesting a decrease in marine weathering over time. The production of CO2 through reverse weathering in surface sediments (4.22-15.0 mmol CO2 m−2 year−1) is about one order of magnitude smaller than the weathering-induced CO2 consumption in the underlying sediments. The evaluation of pore water data from other continental margin sites shows that silicate weathering is a common process in methanogenic sediments. The global rate of CO2 consumption through marine silicate weathering estimated here as 5-20 Tmol CO2 year−1 is as high as the global rate of continental silicate weathering.  相似文献   

8.
The geochemistry of formation waters in the Molasse basin of Upper Austria has been investigated to ascertain the extent of meteoric water replacement of the connate interstitial fluids in these sediments. The chemistry, isotopic composition, and dissolved gas contents of the groundwaters and of oil and gas associated brines have been determined. The most superficial sediments of the basin, the Innviertel (Miocene), have been completely flushed by meteoric waters within the last 200 ka. The underlying Hall and Puchkirchen formations (Miocene/Oligocene) form gas reservoirs for biogenic methane, and the associated formation waters are chemically and isotopically modified connate brines of the original marine deposition. In the northeastern part of the basin, the connate brines of the deeper sediments (Cretaceous/Jurassic) have been partially or completely replaced by meteoric waters, whereas in the south of the basin these sediments contain high salinity fluids which are substantially of connate origin. These conclusions are supported by the stable isotope composition of the various brines. Oil-associated brines from the Eocene sediments contain large amounts of dissolved radiogenic40Ar, which suggests that the oils have migrated from high-temperature environments. This is in contrast with the Puchkirchen, for which the observed absence of radiogenic40Ar suggests that the biogenic methane has been formed in situ. The4He contents of these brines and of the Cretaceous/Jurassic groundwaters are, however, less than those in the overlying Puchkirchen formation and suggest that He has been removed from the deeper sediments as a result of flushing by meteoric water. The ratios of dissolved methane and nitrogen to argon increase with increasing ammonium content of the formation waters. All of these parameters may be used as indices for the maturation of the system. The heavy noble gases, Kr and Xe, are abnormally abundant in the dissolved gases, and this is attributed to geochemical concentration of these gases by adsorption onto shales in the sediment sequence. The overall geochemical situation confirms the existence of separate hydraulic systems with little interconnection in the several overlying geological horizons.  相似文献   

9.
The sedimentary geochemistry of dissolved Al is complicated by a number of different reactions. In this study we show that complexation by organic matter, adsorption to Fe-oxyhydroxides, and reaction with Si in solution have important effects on the distribution of dissolved Al in sediments. In the absence of physical resuspension of sediment into overlying waters, dissolved Al is rapidly consumed at the sediment-water interface and is subsequently released upon reduction of Fe-oxyhydroxides. This release does not cause noticeable perturbations in dissolved Al concentrations in sediments because of rapid consumption reactions which mask the true mobility of Al. Results suggest that one of the consumption reactions may be due to formation of an Fe-Al-silicate. The amount of authigenic aluminosilicate formed in estuarine sediments must be very small relative to the detrital component. In the deep-sea, however, the long residence time of Fe-oxyhydroxides at the sediment-water interface, with resulting greater accumulation of adsorbed Al may explain the abundance of Al in Fe-smectites reported from many different areas.  相似文献   

10.
The results of a study of the contribution of microbial metabolic products to total dissolved organic carbon (DOC) levels in coastal sediments are presented. The data indicate that acidic volatile compounds make up a substantial fraction of pore water DOC's in both oxic and anoxic pore waters of coastal marine sediments. Formic, acetic and butyric acids are the principal volatile species identified at levels exceeding 10 μM. Acid concentrations are up to five times higher in anoxic pore waters than in oxic waters. Volatile organic acids show promise as indicators of diagenetic processes in marine sediments and of the ecological succession of microorganisms, in particular.  相似文献   

11.
Bulk chemical, mineralogical and selective leach analyses have been made on a suite of abyssal ferromanganese nodules and associated sediments from the S.W. equatorial Pacific Ocean. Compositional relations between nodules, sediment oxyhydroxides and nearby ferromanganese encrustations are drawn assuming that the crusts represent purely hydrogenetic ferromanganese material. Crusts, δMnO2-rich nodules and sediment oxyhydroxides are compositionally similar and distinct from diagenetic todorokitebearing nodules. Compared to Fe-Mn crusts, sediment oxyhydroxides are however slightly enriched, relative to Mn and Ni, in Fe, Cu, Zn, Ti and Al, and depleted in Co and Pb, reflecting processes of non-hydrogenous element supply and diagenesis. δMnO2 nodules exhibit compositions intermediate between Fe-Mn crusts and sediment oxyhydroxides and thus are considered to accrete oxides from both the water column and associated sediments.Deep ocean vertical element fluxes associated with large organic aggregates, biogenic calcite, silica and soft parts have been calculated for the study area. Fluxes associated with organic aggregates are one to three orders of magnitude greater than those associated with the other phases considered, are in good agreement with element accumulation rates in sediments, and are up to four orders of magnitude greater than element accumulation rates in nodules. Metal release from labile biogenic material in surface sediments can qualitatively explain the differences between the composition of Fe-Mn crusts and sediment oxyhydroxides.Todorokite-rich diagenetic nodules are confined to an eastwards widening equatorial wedge. It is proposed that todorokite precipitates directly from interstitial waters. Since the transition metal chemistry of interstitial waters is controlled dominantly by reactions involving the breakdown of organic carbon, the supply and degradation rate of organic material is a critical factor in the formation of diagenetic nodules. The wide range of (trace metal/Mn) ratios observed in marine todorokite reflects a balance between the release of trace metals from labile biogenic phases and the reductive remobilisation of Mn oxide, both of which are related to the breakdown of organic carbon.  相似文献   

12.
Behavior of Uranium in the Yellow River Plume (Yellow River Estuary)   总被引：2，自引：0，他引：2  
The Yellow River (Huanghe) is the second largest river in China and is known for its high turbidity. It also has remarkably high levels of dissolved uranium (U) concentrations (up to 38 nmol 1-1). To examine the mixing behavior of dissolved U between river water and seawater, surface water samples were collected along a salinity gradient from the Yellow River plume during September 2004 and were measured for dissolved U concentration,234U:238U activity ratio, phosphate (PO4 3–), and suspended particulate matter. Laboratory experiments were also conducted to simulate the mixing process in the Yellow River plume using unfiltered Yellow River water and filtered seawater. The results showed a nonconservative behavior for dissolved U at salinities < 20 with an addition of U to the plume waters estimated at about 1.4 X 105 mol yr–1. A similarity between variations in dissolved U and PO4 3– with salinity was also found. There are two major mechanisms, desorption from suspended sediments and diffusion from interstitial waters of bottom sediments, that may cause the elevated concentrations of dissolved U and PO4 3– in mid-salinity waters. Mixing experiments indicate that desorption seems more responsible for the elevated dissolved U concentrations, whereas diffusion influences more the enrichment of PO4 3–.  相似文献   

13.
Six Deep Sea Drilling Project (DSDP) Sites (252, 285, 315, 317, 336, 386) were examined for the chemical composition of the dissolved salts in interstitial waters, the oxygen isotopic composition of the interstitial waters, and the major ion composition of the bulk solid sediments. An examination of the concentration-depth profiles of dissolved calcium, magnesium, potassium, and H218O in conjunction with oxygen isotope mass balance calculations confirms the hypothesis that in DSDP pelagic drill sites concentration gradients in Ca. Mg. K, and H218O are largely due to alteration reactions occurring in the basalts of Layer 2 and to alteration reactions involving volcanic matter dispersed in the sediment column. Oxygen isotope mass balance calculations require substantial alteration of Layer 2 (up to 25% of the upper 1000 m). but only minor exchange of Ca, Mg, and K occurs with the overlying ocean. This implies that alteration reactions in Layer 2 are almost isochemical.  相似文献   

14.
The oxidation of sulfide-rich rocks, mostly leftover debris from Cu mining in the early 20th century, is contributing to metal contamination of local coastal environments in Prince William Sound, Alaska. Analyses of sulfide, water, sediment, precipitate and biological samples from the Beatson, Ellamar, and Threeman mine sites show that acidic surface waters generated from sulfide weathering are pathways for redistribution of environmentally important elements into and beyond the intertidal zone at each site. Volcanogenic massive sulfide deposits composed of pyrrhotite and (or) pyrite + chalcopyrite + sphalerite with subordinate galena, arsenopyrite, and cobaltite represent potent sources of Cu, Zn, Pb, As, Co, Cd, and Hg. The resistance to oxidation among the major sulfides increases in the order pyrrhotite ? sphalerite < chalcopyrite ? pyrite; thus, pyrrhotite-rich rocks are typically more oxidized than those dominated by pyrite. The pervasive alteration of pyrrhotite begins with rim replacement by marcasite followed by replacement of the core by sulfur, Fe sulfate, and Fe–Al sulfate. The oxi dation of chalcopyrite and pyrite involves an encroachment by colloform Fe oxyhydroxides at grain margins and along crosscutting cracks that gradually consumes the entire grain. The complete oxidation of sulfide-rich samples results in a porous aggregate of goethite, lepidocrocite and amorphous Fe-oxyhydroxide enclosing hydrothermal and sedimentary silicates. An inverse correlation between pH and metal concentrations is evident in water data from all three sites. Among all waters sampled, pore waters from Ellamar beach gravels have the lowest pH (∼3) and highest concentrations of base metals (to ∼25,000 μg/L), which result from oxidation of abundant sulfide-rich debris in the sediment. High levels of dissolved Hg (to 4100 ng/L) in the pore waters probably result from oxidation of sphalerite-rich rocks. The low-pH and high concentrations of dissolved Fe, Al, and SO4 are conducive to precipitation of interstitial jarosite in the intertidal gravels. Although pore waters from the intertidal zone at the Threeman mine site have circumneutral pH values, small amounts of dissolved Fe2+ in the pore waters are oxidized during mixing with seawater, resulting in precipitation of Fe-oxyhydroxide flocs along the beach–seawater interface. At the Beatson site, surface waters funneled through the underground mine workings and discharged across the waste dumps have near-neutral pH (6.7–7.3) and a relatively small base-metal load; however, these streams probably play a role in the physical transport of metalliferous particulates into intertidal and offshore areas during storm events. Somewhat more acidic fluids, to pH 5.3, occur in stagnant seeps and small streams emerging from the Beatson waste dumps. Amorphous Fe precipitates in stagnant waters at Beatson have high Cu (5.2 wt%) and Zn (2.3 wt%) concentrations that probably reflect adsorption onto the extremely high surface area of colloidal particles. Conversely, crystalline precipitates composed of ferrihydrite and schwertmannite that formed in the active flow of small streams have lower metal contents, which are attributed to their smaller surface area and, therefore, fewer reactive sorption sites. Seeps containing precipitates with high metal contents may contribute contaminants to the marine environment during storm-induced periods of high runoff. Preliminary chemical data for mussels (Mytilus edulis) collected from Beatson, Ellamar, and Threeman indicate that bioaccumulation of base metals is occurring in the marine environment at all three sites.  相似文献   

15.
The ion activity product of Fe and phosphate in interstitial waters from four sediment cores taken from Greifensee, Switzerland indicate the presence of vivianite [Fe3(PO4)2 · 8 H2O] in the solid phase. Analysis of the sediment using an electron microprobe and by electron microscopy revealed P-rich grains to be also enriched in Fe. The combined methods provide strong evidence that vivianite is forming authigenically in the sediments. Thermodynamic stability calculations demonstrate that the most stable Fe and phosphate minerals (pyrite, siderite and apatite) are not the ones controlling the pore water chemistry. The results emphasize the importance of rate processes of mineral formation in early diagenesis.Calculations based on the sediment phosphate concentration, and the degree of supersaturation of Fe and phosphate in the upper portion (0–15 cm) of the pore waters, indicate that the rate of vivianite mineral growth is controlled by a surface reaction rather than a diffusion mechanism. The response time of dissolved phosphate in the sediment pore waters with respect to mineral precipitation is on the order of 1–20 days. Less than 15% of the phosphate released by organic matter degradation at the sediment-water interface and below is retained in the sediments.  相似文献   

16.
In order to attempt to elucidate the nature of biogeochemical processes occurring at the water-sediment interface, sterols have been analysed in near bottom sea and interstitial waters collected in the eastern and western intertropical Atlantic ocean. Free and esterified sterol concentrations range from 0.2 to 82 μg l?1 and are much higher than those found in overlying sea water, which range from 0.2 to 1.7 μg l?1 for the dissolved fraction and from 0.01 to 0.07 μg l?1 for the particulate fraction. Cholest-5-en-3β-ol and 24-ethylcholest-5-en-3β-ol are the dominant sterols in sea and interstitial waters. The variability encountered for the relative importance of minor sterols such as 24-methylcholesta-5,24(28)-dien-3β-ol and stanols, 5α-cholest-22(E)-en-3β-ol, 5α-cholestan-3β-ol and 24-ethyl-5α-cholestan-3β-ol in interstitial water and their variation with depth is discussed in terms of diversity of inputs and bacterial activity. For sediments cored off the Mauritanian coast, a productive area characterized by an intense upwelling, the chemical signatures observed in interstitial water through stanol/stenol ratios occur at levels of very high heterotrophic aerobic bacterial biomass estimations. The study of the sterol composition of interstitial water could constitute a valuable tool in appreciating the intensity of chemical and biological processes occurring in the first few metres of recent marine sediments.  相似文献   

17.
The infinite dilution diffusion coefficient for Al(OH)4? necessary to calculate fluxes of dissolved Al between sediments and overlying waters, was determined at 25°C. Measurements were made using the diaphragm-cell method by diffusing Al(OH)4? spiked KBr solutions against KCL over a range of ionic strengths. The mean of 9 separate measurements gives 1.04 ± .02 × 10?5cm2/s as the infinite dilution diffusion coefficient for Al(OH)4? at 25°C.  相似文献   

18.
 Eh, pH, salinity, total alkalinity, dissolved O2, NO2 –, PO4 –3, SiO2 and NH4 + of waters from a mangrove forest, an estuary and a creek connecting the mangrove forest and the estuary have been measured. Further, the chemistry of interstitial waters of surficial and core sediments from the mangrove forest have been analyzed for the above parameters, except dissolved oxygen. To understand the flux of nutrients from the mangrove forest to the adjoining estuary, creek waters were monitored during tidal phases. PO4 –3, SiO2 and NH4 + were found to be at elevated levels in mangrove waters whereas NO2 – shows no variation compared to the estuary. Dissolved O2 is low in mangrove waters. PO4 –3, NH4 + and SiO2 are several times higher in interstitial waters than in overlying waters. Several fold enrichment of PO4 –3, NH4 + and, to some extent, SiO2 were measured in creek waters during ebbing relative to flooding, indicating that mangroves act as a perennial source for the above nutrients. Received: 26 May 1998 · Accepted: 21 July 1998  相似文献   

19.
Chemical analyses of pore waters from recent marine carbonate sediments, Devil's Hole, Harrington Sound, Bermuda, have been obtained at intervals over a four year period. Interstitial waters were systematically analyzed for pH, titration alkalinity, dissolved sulfides, NH4+, Ca2+, Mg2+ and Na+ or Cl?. Additional analyses on some cores included SO42?, PO43?, dissolved CH4 and N2, and C:N:H ratios in the detrital organic material. The following general trends with depth (to ～ 1 m) are observed: (1) major cations show little or no change; (2) pH decreases; (3) alkalinity, sulfides, NH4+ and PO43? increase; (4) dissolved CH4 is consistently low. The chemical changes with depth can be modelled theoretically and are consistent with experimental data.Significant seasonal changes in pore water chemistry are observed. The data suggest an annual exchange between the pore waters (to a depth of ～ 1 m) and the overlying water of Harrington Sound; the exchange occurs between August and January. The nutrient flux out of the sediments during this process may be a major factor in the plankton ecology of Harrington Sound.  相似文献   

20.
The Mn distribution in Panama Basin area sediments and interstitial waters is discussed. Striking surficial Mn enrichments produced by a well-known diagenetic recycling process characterize the sediments of the region. Thermodynamic solubility calculations indicate that in at least one core interstitial waters approach saturation with respect to MnCO3. A mixed carbonate phase of composition (Mn48 Ca47 Mg5)CO3 was recovered from an ash band in the same core. The association of this material with the coarse volcaniclastic debris is thought to result from facile manganous carbonate precipitation in sediment horizons of coarser mean grain size. Since sulphate reduction in the upper two metres of Panama Basin sediments is fairly minor, little increase in alkalinity is observed, and it is postulated that significant production of carbonate alkalinity is not a prerequisite for manganous carbonate generation in hemipelagic sediments. A more important factor appears to be the availability of Mn oxides for solution during early diagenesis. Stable C isotopic analyses indicate that little C of organic origin is used in the precipitation reaction in either Panama Basin or Loch Fyne (Scotland) sediments.  相似文献   

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