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1.
The extent of authigenic alteration of biogenic and reactive silica in Pearl River estuarine sediments has been estimated using wet-chemical digestion methods. Results show relatively constant distributions of biogenic and reactive Si horizontally and vertically. Based on three core measurements, the biogenic and total reactive Si average 77.91 and 264.77 μmol Si g−1, respectively. Their extents of authigenic alteration are correspondingly estimated as ~55.6 and ~70.6%. The average biogenic Si accumulation rate is calculated as 1.91 × 109 mol Si year−1, which translates into storage of ~7.15% of the annual riverine dissolved silica input. By contrast, the total reactive Si accumulation rate is as high as 6.49 × 109 mol Si year−1, improving annual riverine silicic acid storage to ~24.19%. Detailed investigation is required for a good understanding of early diagenetic process of biogenic and reactive silica in this subtropical area.  相似文献   

2.
Water column and seabed samples were obtained from 92 stations on the Amazon continental shelf during October of 1979. Uptake of silica near and southeast of the river mouth began at a salinity of 8%. and accounted for 17% of the riverine silica flux to this region. Uptake northwest of the river mouth began at a salinity of 20%. and resulted in 33% removal of the riverine silica flux. Examination of filtered suspended solids revealed abundant diatoms in the surface waters, including Coscinodiscus. Skeletonema, Synedra. and Thalassiosira. The biological uptake of silica appears to be dependent on three factors: turbidity, turbulence, and nutrient availability. There was no evidence of abiological removal of silica in the Amazon estuary. 75 to 88% of the silica removed from surface waters by diatoms dissolves prior to accumulation in the seabed. Based on the mean biogenic silica content of shelf sediment (0.25%) and estimates of rates of sediment accumulation, the biogenic silica accumulation rate on the shelf is 2 × 1012 g/yr, which represents only 4% of the dissolved silica supplied by the Amazon River. Biological uptake of silica in estuarine surface waters may not accurately reflect permanent removal of biogenic silica to the seabed because of dissolution which occurs in bottom waters and near the sediment-water interface.  相似文献   

3.
A critical assessment has been made of the processes of supply and removal of dissolved silicon in the ocean. The only sources of importance appear to be continental drainage (supplying 4.3 × 1014 g SiO2/yr), Antarctic weathering and migration from sediment pore waters. The magnitudes of the last two processes are uncertain but there is evidence that they may add significantly to the river input. The total input appears to lie uncertainly within the range of 5.12 × 1014 g SiO2/yr.Estimates of removal in estuarine mixing processes (less than 1 × 1014 g SiO2/yr) and in pelagic siliceous oozes (less than 2 × 1014 g SiO2/yr) suggest that deposition by these processes may not balance the input. Other removal processes could include biological deposition in coastal waters, but the hypothesis that some removal in the sea occurs by inorganic processes, such as reverse weathering reactions, cannot be discounted.  相似文献   

4.
Deltaic environments are commonly assumed to be relatively minor sites of biogenic silica burial because of the small quantities of opaline silica detected by most operational analytical techniques. Rapid conversion of biogenic silica into authigenic silicates is also often discounted as a significant control on oceanic silica budgets. A variety of evidence for extensive early diagenetic alteration of biogenic silica in rapidly accumulating Amazon delta sediments indicates that both of these general assumptions are unjustified. Apparent lack of significant biogenic silica storage in deltaic environments, particularly in the tropics, may be largely an artifact of operational definitions that do not include early diagenetic products of biogenic silica. Biogenic silica particles buried in suboxic Amazon delta deposits can be unaltered, partially dissolved, covered with aluminosilicate or metal-rich coatings, or completely reconstituted into authigenic K-Fe-rich aluminosilicate minerals. Pore water (K, Mg, F, Si) and solid-phase distributions, direct observations of particles, laboratory experiments, and depositional context indicate that authigenic clays form rapidly (<1 yr) in the seasonally reworked surface layer (∼ 0.5-2 m) of the delta topset and are disseminated during sediment remobilization. Fe, Al-oxide rich debris derived from the tropical drainage basin is an abundant reactant, and thus the supply of biogenic silica is a major control on the amount of clay formed.The mild 1% Na2CO3 alkaline leach procedure commonly used to estimate biogenic silica was modified to include an initial mild leach step with 0.1N HCl to remove metal oxide coatings and to activate poorly crystalline authigenic phases for alkaline dissolution. Well-crystallized clays are not significantly affected by this modification nor is bulk Amazon River bed sediment. The two-step procedure indicates that ∼90% of the biogenic silica originally present in deposits is converted to clay or otherwise altered, raising the effective quantity of biogenic silica stored from ∼33 to ∼296 μmol Si g−1 (∼1.8% SiO2). Biogenic Si stored in the delta increases away from the river mouth, across shelf and along the dispersal system where primary production is highest. The K/Si ratio of labile authigenic material is ∼0.19 mol mol−1, far higher than Amazon River suspended matter (∼0.07 mol mol−1). Diagenetic models indicate formation rates in the mobile sediment layer of ∼2.8 μmol K g−1 yr−1 (∼16 μmol Si g−1 yr−1). Inclusion of authigenic alteration products of biogenic silica in estimates of reactive Si burial increases the deltaic storage of riverine Si to ∼22% of the Amazon River input. The rapid formation of aluminosilicates from biogenic SiO2, seawater solutes, and remobilized Fe, Al-oxides represents a form of reverse weathering. Rapid reverse weathering reactions in tropical muds and deltaic deposits, the largest sediment depocenters on Earth, confirms the general importance of these processes in oceanic elemental cycles.  相似文献   

5.
The dissolved silica concentration in waters of Lake Superior probably is in a steady state because it is not influenced significantly by man, and the climate, topography and vegetation in the drainage area of the lake have been stable for the past 4000 years. Therefore the rate at which dissolved silica is introduced to the lake should equal the output rate.The primary inputs are: tributaries (4.1–4.6 × 108kgSiO2/yr), diffusion from sediment pore waters (0.21?0.78 × 108kgSiO2/yr) and atmospheric loading (0.26 × 108kgSiO2/yr). Silica is lost from the lake waters by: outflow through the St. Marys River, diatom deposition, adsorption onto particulates in the sediments, and authigenic formation of new silicate minerals. Tributary outflow accounts for less than one half the annual input of silica, and diatom deposition and silica adsorption withdraw less than 10% of the annual input. Therefore the formation of new silicate phases must be the dominant sink for dissolved silica in Lake Superior. The specific phases formed are not identified in the bottom sediments. X-ray diffraction studies suggest that smectite is one product, and amorphous ferroaluminum silicates may be another product.Mathematical modeling of the dissolved silica response to lake eutrophication suggests that the phosphate loading to Lake Superior would have to increase by about 250-fold to cause a silica depletion rate equal to that reported for Lake Michigan, assuming no change in the rate of upwelling of deep waters.  相似文献   

6.
《Applied Geochemistry》1999,14(1):41-52
Concentrations of S, organic C and Fe were investigated in profiles of sediments from two estuarine systems in the SW of Western Australia. In marine-affected sediments, inorganic S dominates total S and concentrations of total S correlate with Fe and not with organic C. In freshwater sediments, organic S dominates total S and concentrations of total S correlate with organic C and not with Fe. Molar Fe/S ratios in the estuarine sediments decrease with increasing salinity and approach unity for marine conditions. Net accumulation rates of S in sediments were estimated with a numerical computer model, calibrated with published data on profiles of marine sediments for diffusion of SO2−4, sedimentation rates and distributions of S. Measured depth-integrated reduction rates of SO2−4 in the marine-affected estuarine sediments approach those obtained for Fe-limited marine conditions at similar rates of sedimentation. Measured concentrations of inorganic S in anoxic freshwater sediments fit a numerically calculated relationship between inorganic S and sedimentation rate.  相似文献   

7.
Core A9-EB2 from the eastern Bransfield Basin, Antarctic Peninsula, consists of pelagic (diatom ooze-clay couplets and bioturbated diatom ooze) and hemipelagic (bioturbated mud) sediments interbedded with turbidites (homogeneous mud and silt–clay couplets). The cyclic and laminated nature of these pelagic sediments represents alternation between the deposition of diatom-rich biogenic sediments and of terrigenous sediments. Sediment properties and geochemical data explain the contrasting lamination, with light layers being finer-grained and relatively rich in total organic carbon and biogenic silica content. Also, the high-resolution magnetic susceptibility (MS) variations highlight distinct features: high MS values coincide with clastic-rich sections and low MS values correspond to biogenic sections. The chronology developed for core A9-EB2 accounts for anomalous ages associated with turbidites and shows a linear sedimentation rate of approximately 87 cm/103 yr, which is supported by an accumulation rate of 80 cm/103 yr calculated from 210Pb activity. The late Holocene records clearly identify Neoglacial events of the Little Ice Age (LIA) and Medieval Warm Period (MWP). Other unexplained climatic events comparable in duration and amplitude to the LIA and MWP events also appear in the MS record, suggesting intrinsically unstable climatic conditions during the late Holocene in the Bransfield Basin of Antarctic Peninsula.  相似文献   

8.
The burial characteristics and toxicity risks associated with n-alkanes and polycyclic aromatic hydrocarbons (PAHs) in the riverine and estuarine sediments of the Daliao River watershed were investigated based on three sediment cores. The sum of the n-alkane and PAH concentrations, normalized to organic carbon (OC), ranged from 0.27 to 63.09 μg g?1OC?1 and 6.60 to 366.20 μg g?1OC?1, respectively. The features and the history of industrial activities, such as the oil and chemical industries and port activities near the river and estuary, resulted in different distributions and sources of hydrocarbons. The sources of pollution were identified based on n-alkane indexes and on diagnostic ratios of PAHs. The diagnostic ratios indicated that the n-alkanes were derived from both biogenic and petrogenic sources in different proportions and that the PAHs were derived primarily from petrogenic combustion sources. A hierarchical cluster analysis grouped the core samples into two clusters. The first cluster, river sediments, corresponded to industrial activities; the second cluster, estuarine sediments, corresponded to port shipping activities. The toxic potency of the PAHs in the cores was assessed in terms of toxic equivalents (TEQs) of dibenzo[a,h]anthracene and benzo[a]pyrene. The top layer of the sediment in the cores had a relatively high toxicity. The TEQ values for benzo(a)pyrene (TEQBaP) and dioxins (TEQTCDD) furnished a consistent assessment of the PAHs in the sediment cores.  相似文献   

9.
High‐resolution gravity cores and box cores from the North Icelandic shelf have been studied for palaeoceanographic history based on lithological and biostratigraphical foraminiferal data. Results from two outer shelf cores covering the last 13.6 k 14C yr BP are presented in this paper. The sediments accumulated in north–south trending basins on each side of the Kolbeinsey Ridge at water depths of ca. 400 m. Sedimentation rates up to 1.5 m kyr−1 are observed during the Late‐glacial and Holocene. The Vedde and Saksunarvatn tephras are present in the cores as well as the Hekla 1104. A new tephra, KOL‐GS‐2, has been identified and dated to 13.4 k 14C yr BP, and another tephra, geochemically identical to the Borrobol Tephra, has been found at the same level. At present, the oceanographic Polar Front is located on the North Icelandic shelf, which experiences sharp oceanographic surface boundaries between the cold East Icelandic Current and the warmer Irminger Current. Past changes in sedimentological and biological processes in the study area are assumed to be related to fluctuations of the Polar Front. The area was deglaciated before ca. 14 kyr BP, but there is evidence of ice rafting up to the end of the GS‐1 (Greenland Stadial 1, Younger Dryas) period, increasing again towards the end of the Holocene. Foraminiferal studies show a relatively strong GS‐2 (pre‐13 kyr BP) palaeo‐Irminger Current, followed by severe cooling and then by unstable conditions during the remainder of the GI‐1 (Greenland Interstadial 1, Bølling–Allerød) and GS‐1 (Younger Dryas). Another cooling event occurred during the Preboreal before the Holocene current system was established at about 9 kyr BP. After a climatic optimum between 9 and 6 kyr BP the climate began to deteriorate and fluctuate. Copyright © 2000 John Wiley & Sons, Ltd.  相似文献   

10.
Vertical distributions of particulate silica, and of production and dissolution rates of biogenic silica, were determined on two N-S transects across the Pacific sector of the Antarctic Circumpolar Current during the austral spring of 1978. Particulate silica profiles showed elevated levels in surface water and near the bottom, with low (35–110 nmol Si · 1?1) and vertically uniform values through the intervening water column. Both the particulate silica content of the upper 200 m and the production rate of biogenic silica in the photic zone increased from north to south, reaching their highest values near the edge of the receding pack ice. A significant, but variable, fraction (18–58%) of the biogenic silica produced in the surface layer was redissolving in the upper 90–98 m. Net production of biogenic silica in the surface layer (production minus dissolution) was proceeding at a mean rate of ca. 2 mmol Si · m?2 · day?1. This is ca. 4 times greater than the most recent estimate of the mean accumulation rate of siliceous sediments beneath the ACC. We estimate, based on mass balance, that the mean dissolution rate of biogenic silica in subsurface water column in the Southern Ocean is 1.2–2.9 mmol Si · m?2 · day?1.  相似文献   

11.
The vertical distribution of dissolved Al in interstitial waters of recent marine sediments has been determined using a fluorimetric analytical method adapted for interstitial water analysis. The results suggest that diagenetic reactions occur in the sediment soon after deposition. A narrow depth zone acting as a source of dissolved Al is found in each core. Outside this zone Al appears to be removed from solution and its concentration decreases to values of 1.5 μgAl/l or less, comparable to those of open ocean waters. Dissolved Al and SiO2 concentrations in interstitial waters close to the sediment-seawater interface are linearly correlated in most cases, suggesting that the geochemistry of Al may be related to the behaviour of biogenic silica in marine sediments.  相似文献   

12.
A 20 kyr long sediment sequence from the Congo deep sea fan (core GeoB 6518-1), one of the world’s largest deep sea river fans, has been analysed for bulk and molecular proxies in order to reconstruct the marine, soil and plant organic carbon (OC) contributions to these sediments since the last glacial maximum. The bulk proxies applied, C/N ratio and δ13Corg, ranged from 10 to 12.5 and from −24.5 to −21‰ VPDB, respectively. As molecular proxies, concentrations of marine derived alkenones and terrestrial derived odd-numbered n-alkanes were used, which varied between 0.2 and 4 μg/g dry weight sediment. In addition, the branched vs. isoprenoid tetraether (BIT) index, a proxy for soil organic matter input, was used, which varied from 0.3 to 0.5 in this core.Application of binary mixing models, based on the different individual proxies, showed estimates for terrestrial OC input varying by up to 50% due to the heterogeneous nature of the OC. Application of a three end-member mixing model using the δ13Corg content, the C/N ratio and the BIT index, enabled the distinction of soil and plant organic matter as separate contributors to the sedimentary OC pool. The results show that marine OC accounts for 20% to 40% of the total OC present in the deep sea fan sediments over the last 20 kyr and that soil OC accounts for about half (∼45% on average) of the OC present. This suggests that soil OC represents the majority of the terrestrial OC delivered to the fan sediments.Accumulation rates of the plant and soil OC fractions over the last 20 kyr varied by a factor of up to 5, and are strongly related to sediment accumulation rates. They showed an increase starting at ca. 17 kyr BP, a decline during the Younger Dryas, peak values during the early Holocene and lower values in the late Holocene. This pattern matches with reconstructions of past central African humidity and Congo River discharge from the same core and revealed that central African precipitation patterns exert a dominant control on terrestrial OC deposition in the Congo deep sea fan. Marine OC accumulation rates are only weakly related to sediment accumulation rates and vary only little over time compared to the terrigenous fractions. These variations are likely a result of enhanced preservation during times of higher sedimentation rates and of relative small fluctuations in primary production due to wind-driven upwelling.  相似文献   

13.
Silicic acid (H4SiO4) flux from the sediment, H4SiO4 concentration and river flow were used to obtain an annual dissolved silicon budget for Chesapeake Bay. H4SiO4 concentrations vary seasonally in the estuary: for a 12-year period, mean H4SiO4 concentrations in the mesohaline region were high both in spring and in late summer to early fall, and were low in late spring—occasionally approaching levels potentially limiting to diatom growth. Most of the annual allochthonous H4SiO4 supply to the estuary derives from the three major rivers, but regenerative H4SiO4 flux from the sediment to the water column exceeds the total riverine input by a factor of at least five. Sediment H4SiO4 efflux exhibits seasonality and averages approximately 2–3 mol Si m?2 yr?1. The high rates of sediment dissolution and efflux appear to maintain high levels of H4SiO4 in the mesohaline region, and Si-limitation of diatom growth there seems unlikely. The relative rates of biogenic silica formation and dissolution do not vary synchronously: seasonal variations in diatom productivity, sedimentary release of H4SiO4 and river flow all contribute to the observed late winter and late summer seasonal maxima and late spring minimum in water column H4SiO4 concentrations. If the only source of Si to support sedimentary H4SiO4 efflux is biogenic particulate silica recently deposited from the water column and this silica in turn was produced by diatoms in a ratio of 8C:1 Si, the minimum annual primary production by diatoms is at least 260 g C m?2, approximately half of annual total plankton primary production. This estimate would be revised upwards according to the amount of particulate biogenic silica dissolving in the water column. Burial of biogenic silica amounts to from 2 to 84% of the sediment efflux of H4SiO4, depending on location in the bay. On an annual basis, burial represents from 60 to 100% of fluvial H4SiO4-Si inputs.  相似文献   

14.
The mineral and chemical compositions and physical properties of diatomaceous clayey–siliceous sediments in the Sea of Okhotsk are studied. Absolute masses of silica accumulation are determined. Their compositional model based on the silica content is similar to that of Late Jurassic and Olenekian–middle Anisian cherts of the Sikhote Alin region. The thickness of the Holocene siliceous unit and the absolute mass of siliceous deposits depended on bioproductivity in the upper water column and the seafloor topography. Absolute masses of SiO2 am (0.05–5.7 g cm–2 ka–1) and SiO2 fr (0.5–11.6 g cm–2 ka–1) are minimal on seamounts and maximal in depressions near foothills. These values match absolute masses of SiO2 fr accumulations in Triassic and Late Jurassic basins of the Sikhote Alin region (0.33–3 g cm–2 ka–1). Comparison of the composition and absolute masses of silica shows that Triassic and Late Jurassic siliceous sequences of Sikhote Alin could be accumulated in the marginal marine basin near a continent.  相似文献   

15.
This first sedimentary interpretation of two incised-valley fills in the Gulf of Cádiz (southern Spain), which accumulated during the last fourth-order eustatic cycle in response to fluvial incision, changes of sea level, and correlative deposition, relates the filling of the estuarine basins and their barriers with four regional progradation phases, H1 to H4. The cases studied are the wave-dominated Guadalete, and the mixed, tide and wave-dominated Odiel-Tinto estuaries. The sequence boundary is a type-1 surface produced during the lowstand of the Last Glacial period ca. 18 000 14C yr BP. No fluvial lowstand deposits were found in the area. Due to rapid transgression the valley fills consist of transgressive and highstand sediments. The maximum landward advance of the estuarine barriers occurred ca. 6500–6000 14C yr BP during the maximum of the Flandrian transgression, but there is no evidence of sea level rising appreciably above the present. A large part of the estuaries was filled during H1 (ca. 6500–4400 14C yr BP) but ravinement by shifting tidal inlets destroyed most of the coeval barriers. During the H2 phase (ca. 4200–2550 14C yr BP) sedimentation was favoured by arid conditions and concentrated in the axial estuarine zones and the barriers. Between H2 and H3 prevailing winds changed from W to WSW, increasing spit growth to the east and south-east. Progradation of bay-head deltas and flood-plains during H3 (ca. 2300–800 14C yr BP) and H4 (500 yr ago to the present) further reduced the accommodation space in the largely-filled valleys, and sediment by-passed the estuaries and accumulated in the estuarine barriers as fast-growing spits. Arid conditions and increasing human activity have caused rapid coastal modifications.  相似文献   

16.
The distribution and rates of accumulation of Mo in marine deposits have been determined and compared with the same parameters for U and Mn. High concentrations of Mo are associated both with oxidizing environments represented by the presence of ferro-manganese oxide-rich sediments (where Mo/U ～- 3) and with reducing environments (where Mo/U is about unity). The supply of Mo by streams is more than adequate to balance the measured removal rate in normal deep-sea deposits and no submarine volcanic ‘emanations’ need be involved. On an ocean-wide basis, 4 · 3 μg Mo/cm2/1000 yr is supplied in solution by streams. Of this, 2·0 μg Mo/cm2/1000 yr is removed in deep-sea sediments and manganese nodules. The remaining 2·3 μg Mo/cm2/1000 yr is probably removed in primarily (but not exclusively) near-shore reducing sediments. The average Mo accumulation rate in these environments is about 1000 μg Mo/cm2/1000 yr; thus only 0·23 per cent of the world ocean area need be such reducing sites.  相似文献   

17.
《Applied Geochemistry》1998,13(2):269-280
A slow flow, plug-through reactor was developed for measuring equilibrium and kinetic parameters of biogeochemical reactions on intact sections of sediment cores. The experimental approach was designed to preserve the structural, geochemical and microbiological integrity of the sediment sections and, hence, retrieve reaction parameters that apply to in-situ conditions.Inert tracer breakthrough experiments were performed on a variety of unconsolidated surface sediments from lacustrine, estuarine and marine depositional environments. The sediments studied cover wide ranges of composition, porosity (46–83%) and mean grain size (10−4−10−2 cm). Longitudinal dispersion coefficients were determined from the breakthrough curves of Br−. The curves were also used to check for early breakthrough or trailing, that is, features indicative of non-ideal flow conditions. Sediment plugs that exhibited these features were eliminated from further experiments.Dimensionless equilibrium adsorption coefficients (K) of NH4+, were calculated from measured retardation times between the breakthrough of NH4+ and Br−. The values of K at 5°C vary between 0.3 and 2.3, with the highest value obtained in a fine-grained marine sediment, the lowest in a coarse-grained lake sediment. The values for the marine and estuarine sediments agree with values reported in the literature. The dependencies of K on ionic strength (range 0.2-0.7m) and temperature (range 5–25°C) in an estuarine sediment confirm that the main sorption mechanism for NH4+ is ion exchange.The reactor was used in recirculation mode to measure steady-state rates of dissimilatory SO42− reduction in a salt-marsh sediment. Recirculation homogenizes solute concentrations within the reactor, hence facilitating the derivation of reaction rate expressions that depend on solution composition. The rate of microbial S04− reduction was found to be nearly independent of the dissolved SO42− concentration in the range of 2.2−1 mM. Fitting of the experimental rates to a Monod relationship resulted in a maximum estimate of the half-saturation concentration, Ks, of 240 μM. This value is comparable to those reported for a pure culture of SO42−-reducing bacteria, but is significantly smaller than the only other Ks value reported in the literature for SO42− utilization in a natural marine sediment.  相似文献   

18.
The record of the biogenic silica flux (BSF, g cm−2(103yr)−1) in Lake Biwa reflects changes in diatom productivity in the lake and provides information regarding changes in paleoclimatic conditions. The BSF record of Lake Biwa demonstrates five periods over the past ca. 145,000 yr when the BSF values were significantly greater than 7.5 g cm−2(103yr)−1, and five intervals when they were lower. The data imply that paleoclimatic conditions were warmer and wetter from ca. 123,000 to 115,000, 103,000 to 95,000, 88,000 to 72,000, 57,000 to 32,000 yr B.P., and around ca. 6000 yr B.P. when the BSF values were greater, and relatively dry and cold from ca. 141,000 to 123,000 yr B.P. and during intervals between two of the five warm and wet episodes when the BSF values were lower. Time series of the BSF record can be correlated with the record of biogenic silica content in Lake Baikal and the marine oxygen isotope stages 1 through 6. Furthermore, the BSF values varied with much higher amplitude during the last interglaciation than during the last glaciation, probably implying that the diatom productivity in Lake Biwa was likewise more variable and had a larger range under interglacial conditions than under glacial conditions.  相似文献   

19.
We present a model of estuarine mixing, removal, and input for dissolved constituents, and apply the model to 39 nutrient (P, N, Si) profiles collected over a 14-month period in a pristine river/ estuary: Ochlockonee Bay, Florida. Each profile is deconvolved into three component functions: linear mixing (conservative) first-order removal (biological productivity), and parabolic input (regeneration). After correction for temporal variations in the fluvial end-members, the model provides quantitative estimates of total estuarine primary production, net regeneration, and subsequent fluxes to the ocean over a year-long period. The modeled data set is internally self-consistent: virtually perfect mass balances are obtained for P and Si. All biological P-uptake is regenerated within the estuary so that virtually 100% of the fluvial reactive-P enters the ocean. One-third of the fluvial reactive-P enters the estuary as particles whose phosphate is released after deposition in estuarine sediments. About 20% of the dissolved fluvial silica flux is removed biologically; all of this biogenic silica dissolves in the estuary and enters the ocean. N cannot be mass balanced, probably because it enters and escapes the bay in unmeasured forms (as NH4 or via denitrification to N2 and N2O). In the Ochlockonee, biological productivity removes nutrients in the ratios N:P ? 9:1 and Si:P ? 20:1.  相似文献   

20.
Mercury concentrations (HgT) in fine-grained fraction (<63 μm) of core sediments of the Hugli–Matla–Bidyadhari estuarine complex, India were analyzed. Results revealed a wide range of spatial variations (<4–93 ng g−1 dry weight) with a definite enhancement level at the lower stretch of the estuarine complex infested with mangrove plants, which might act as a sink to HgT. An elevated concentration of Hg was encountered in surface/subsurface layer of the core in majority of the cases resulting from physical, biogenic and postdepositional diagenetic processes that remobilized and resuspended the metal from deeper sediments. A strong positive correlation was observed between the Hg and clay fraction content of the sediments, while the correlations of Hg with Al, Fe and Mn were poor. Based on the index of geoaccumulation (I geo) and effects range-low (ER-L) value, it is considered that the sediments are less polluted and thus there is less chance of ecotoxicological risk to organisms living in sediments.  相似文献   

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