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1.
A decade of studies of metal and nutrient inputs to the back-barrier area of Spiekeroog Island, NW German Wadden Sea, have concluded that pore water discharge provides a significant source of the enrichments of many components measured in the tidal channels during low tide. In this paper we add studies of radium isotopes to help quantify fluxes into and out of this system. Activities of radium isotopes in surface water from tidal channels in the back-barrier area exhibit pronounced changes in concert with the tide, with highest activities occurring near low tide. Other dissolved components: silica, total alkalinity (TA), manganese, and dissolved organic carbon (DOC) exhibit similar changes, with patterns matching the Ra isotopes. Uranium follows a reverse pattern with highest concentrations at high tide. Here we use radium isotope measurements in water column and pore water samples to estimate the fluxes of pore waters that enter the tidal channels during low tide. Using a flushing time of 4 days and the average activities of 224Ra, 223Ra, and 228Ra measured in the back-barrier surface and pore waters, we construct a balance of these isotopes, which is sustained by a deep pore water flux of (2-4) × 108 L per tidal cycle. This flux transports Ra and the other enriched components to the tidal channels and causes the observed low tide enrichments. An independent estimate of pore water recharge is based on the depletion of U in the tidal channels. The U-based recharge is about two times greater than the Ra-based discharge; however, other sinks of U could reduce the recharge estimate. The pore waters have wide ranges of enrichment in silica, alkalinity, manganese, DOC, and depletion of U with depth. We estimate concentrations of these components in pore water from the depth expected to contribute the majority of the pore water flux, 3.5 m, to determine fluxes of these components to the tidal channels. Samples from this depth have minimum concentrations of silica, alkalinity, manganese, and DOC. We also estimate the exports of these components (and import of U) due to mixing based on average measured concentrations in the tidal creeks and the 4-day flushing time. A comparison of these estimates reveals that the exports (negative in the case of U) equal or exceed the pore water fluxes. By using values slightly higher than the minimum concentrations at 3.5 m to calculate inputs, the two estimates could be forced to match. We conclude that pore water drainage is the major factor regulating fluxes of Ra isotopes, silica, alkalinity, manganese, DOC, and uranium in this system.  相似文献   

2.
Non-conservative behaviour of dissolved Mo was observed during specific time periods in the water column of the Wadden Sea of NW Germany. In July 2005 dissolved Mo declined within 36 h from a level only slightly below seawater (82 nM) to a minimum value of 30 nM, whereas in August 2002 dissolved Mo revealed a tidal cyclicity with maximum values up to 158 nM at low tide. In contrast, cruises in August 2003 and 2004 displayed an almost conservative behaviour of Mo. The decrease in dissolved Mo during July 2005 and elevated values in August 2002 were accompanied by Mo enrichments on aggregates in the water column of the Wadden Sea. Along with Mo, dissolved Mn showed unusual concentration patterns in July 2005, with values distinctly below the common summer level (by a factor of five). A direct relation between the loss of Mo and scavenging by freshly formed MnOx phases could not be inferred from our data because both metals revealed inverse patterns. Parallel to decreasing dissolved Mo concentrations dissolved Mn showed an increasing trend while particulate Mn decreased. Such finding is compatible with the formation of oxygen-depleted zones in aggregates, which provide suitable conditions for the rapid fixation of Mo and parallel release of Mn by chemically and/or microbially mediated processes. Our assumption is supported by biological (e.g. number of aggregate-associated bacteria) and sedimentological (e.g. aggregate abundance and size) parameters. The production of organic components (e.g. TEP) during breakdown of an algae bloom in July 2005 led to the formation of larger Mo-enriched aggregates, thus depleting the water column in dissolved Mo. After deposition on and incorporation into sandy tidal flats these aggregates are rapidly decomposed by microbial activity. Pore water profiles document that during microbial decomposition of these aggregates, substantial amounts of Mo are released and may replenish and even enrich Mo in the open water column. We postulate a conceptual model for the observed non-conservative behaviour of Mo in coastal waters, which is based on the tight coupling of geochemical, biological, and sedimentological processes.  相似文献   

3.
This research tests the hypothesis that trace metals respond to the extent of reducing conditions in a predictable way. We describe pore water and sediment measurements of iron (Fe), manganese (Mn), vanadium (V), uranium (U), rhenium (Re), and molybdenum (Mo) along a transect off Washington State (USA). Sediments become less reducing away from the continent, and the stations have a range of oxygen penetration depths (depth to unmeasurable O2 concentration) varying from a few millimeters to five centimeters. When oxygen penetrates ∼1 cm or less, Fe is reduced in the pore waters but reoxidized near the sediment-water interface, preventing a flux of Fe2+ to overlying waters, whereas Mn oxides are reduced and Mn2+ diffuses to overlying waters. Both Re and U authigenically accumulate in sediments. Only at the most reducing location, where the oxygen penetrates 0.3 cm below the sediment-water interface, does the surface 30 cm of sediments become reducing enough to authigenically accumulate Mo.Stations in close proximity to the Juan de Fuca Ridge crest are enriched in Mn and Fe from hydrothermal plume processes. Both V and Mo clearly associate with Mn cycling, whereas U may be associating with either Mn oxides and/or Fe oxyhydroxides. Rhenium is uncomplicated by adsorption to Mn oxides and/or Fe oxyhydroxides, and Re accumulation in sediments appears to be due solely to the extent of reducing conditions. Therefore, authigenic sediment Re enrichment appears to be the best indicator for intermediate reducing conditions, where oxygen penetrates less than ∼1 cm below the sediment-water interface, when coupled with negligible authigenic Mo enrichment.  相似文献   

4.
The sediments of the Port Camargue marina (South of France) are highly polluted by Cu and As (Briant et al., 2013). The dynamics of these pollutants in pore waters was investigated using redox tracers (sulfides, Fe, Mn, U, Mo) to better constrain the redox conditions.In summer, pore water profiles showed a steep redox gradient in the top 24 cm with the reduction of Fe and Mn oxy-hydroxides at the sediment water interface (SWI) and of sulfate immediately below. Below a depth of 24 cm, the Fe, Mn, Mo and U profiles in pore waters reflected Fe and Mn reducing conditions and, unlike in the overlying levels, sulfidic conditions were not observed. This unusual redox zonation was attributed to the occurrence of two distinct sediment layers: an upper layer comprising muddy organic-rich sediments underlain by a layer of relatively sandy and organic-poor sediments. The sandy sediments were in place before the building of the marina, whereas the muddy layer was deposited later. In the muddy layer, large quantities of Fe and Mo were removed in summer linked to the formation of insoluble sulfide phases. Mn, which can adsorb on Fe-sulfides or precipitate with carbonates, was also removed from pore waters. Uranium was removed probably through reduction and adsorption onto particles. In winter, in the absence of detectable pore water sulfides, removal of Mo was moderate compared to summer.Cu was released into solution at the sediment water interface but was efficiently trapped by the muddy layer, probably by precipitation with sulfides. Due to efficient trapping, today the Cu sediment profile reflects the increase in its use as a biocide in antifouling paints over the last 40 years.In the sandy layer, Fe, Mn, Mo and As were released into solution and diffused toward the top of the profile. They precipitated at the boundary between the muddy and sandy layers. This precipitation accounts for the high (75 μg g−1) As concentrations measured in the sediments at a depth of 24 cm.  相似文献   

5.
This study examined the removal of U, Mo, and Re from seawater by sedimentary processes at a shallow-water site with near-saturation bottom water O2 levels (240-380 μmol O2/L), very high organic matter oxidation rates (annually averaged rate is 880 μmol C/cm2/y), and shallow oxygen penetration depths (4 mm or less throughout the year). Under these conditions, U, Mo, and Re were removed rapidly to asymptotic pore water concentrations of 2.2-3.3 nmol/kg (U), 7-13 nmol/kg (Mo), and 11-14 pmol/kg (Re). The depth order in which the three metals were removed, determined by fitting a diffusion-reaction model to measured profiles, was Re < U < Mo. Model fits also suggest that the Mo profiles clearly showed the presence of a near-interface layer in which Mo was added to pore waters by remineralization of a solid phase. The importance of this solid phase source of pore water Mo increased from January to October as the organic matter oxidation rate increased, bottom water O2 decreased, and the O2 penetration depth decreased. Experiments with in situ benthic flux chambers generally showed fluxes of U and Mo into the sediments. However, when the overlying water O2 concentration in the chambers was allowed to drop to very low levels, Mn and Fe were released to the overlying water along with the simultaneous release of Mo and U. These experiments suggest that remineralization of Mn and/or Fe oxides may be a source of Mo and perhaps U to pore waters, and may complicate the accumulation of U and Mo in bioturbated sediments with high organic matter oxidation rates and shallow O2 penetration depths.Benthic chamber experiments including the nonreactive solute tracer, Br−, indicated that sediment irrigation was very important to solute exchange at the study site. The enhancement of sediment-seawater exchange due to irrigation was determined for the nonreactive tracer (Br−), TCO2, , U and Mo. The comparisons between these solutes showed that reactions within and around the burrows were very important for modulating the Mo flux, but less important for U. The effect of these reactions on Mo exchange was highly variable, enhancing Mo (and, to a lesser extent, U) uptake at times of relatively modest irrigation, but inhibiting exchange when irrigation rates were faster. These results reinforce the observation that Mo can be released to and removed from pore waters via sedimentary reactions.The removal rate of U and Mo from seawater by sedimentary reactions was found to agree with the rate of accumulation of authigenic U and Mo in the solid phase. The fluxes of U and Mo determined by in situ benthic flux chamber measurements were the largest that have been measured to date. These results confirm that removal of redox-sensitive metals from continental margin sediments underlying oxic bottom water is important, and suggest that continental margin sediments play a key role in the marine budgets of these metals.  相似文献   

6.
《Applied Geochemistry》2002,17(11):1495-1502
Oxidation measurements of nonvolatile dissolved organic carbon (DOC) have been determined by high temperature combustion for pore waters from sediments of Middle Valley and Escanaba Trough, Northeastern Pacific, sampled by the Ocean Drilling Program (ODP) Legs 139 and 169, as well as for overlying and near bottom seawater. The DOC values in the interstitial waters are generally greater than those in the overlying water column, ranging from 0.1 to 158 mg of C per liter (mg C/L). Some of the profiles of DOC in the pore waters are similar to total organic C and total inorganic C profiles. DOC maxima at shallow depths of Site 858 are probably enriched due to higher temperature alteration of organic matter. At Sites 856 and 1035, the DOC increases at greather depths due to the hydrothermal activity. The DOC values correlate with MnO and MgO profiles in Hole 856B. The changes below 30 mbsf in the DOC depth profiles of Sites 858 and 1036 parallel those of the volatile hydrocarbon gases. The reference Site 1037 in Escanaba Trough has DOC values that increase with depth according to the increase in thermal stress.  相似文献   

7.
The Sepik River is a major contributor of water, sediment and associated organic loads to the coastal waters of northern New Guinea. With a narrow continental shelf and strong coastal currents, much of this exported material is available for long distance transport into the Bismarck Sea and beyond. CTD casts and associated instrument data showed that the river signature was visible in optical measurements of deep profiles from the Sepik Canyon. Discrete water samples were collected in clean Niskin bottles for organic analysis. Additional high volume samples for lipid classes were collected with Infiltrex samplers deployed on a floating mooring, along with two sediment trap arrays set at 100 and 260 m depth. The Infiltrex samplers were set at 55, 180, 200 and 220 m depth in an effort to target the surface layers and those of westward flowing water in the New Guinea Coastal Undercurrent (NGCUC). The samplers allowed analysis of lipid classes in both dissolved and particulate phases.Analyses of lignin phenols, hydrocarbons, fatty acids, sterols, and n-alcohols in the samples were used to estimate the cycling of the organic input from the river system to the coastal waters and possible entrainment in the NGCUC. The molecular biomarkers confirmed the Sepik River as a significant source of reduced carbon in the near coastal zone influenced by the plume. They indicated that ca. 90% of the organic carbon delivered to the coastal zone is dispersed or degraded, with only about 10% of terrestrial carbon being deposited on to the narrow shelf of coastal sediments. The dissolved lignin phenols provided evidence for desorption of organics from particles with increasing depth. However, this desorption process did not change the C/N ratio of the dissolved organic carbon (DOC) in the deep water of the Sepik Canyon. The hydrocarbons, sterols and fatty acids showed the change from lipid content dominated by phytoplankton in surface layers to zooplankton and bacterial biomarkers in deeper waters. The organic biomarkers provided evidence that some of the dissolved organic input from the Sepik River was injected into fast moving undercurrents. However, concentrations of terrestrial biomarkers were diluted and/or degraded to non-detectable levels within 100 km of the source.  相似文献   

8.
This paper deals with dissolved inorganic carbon (DIC) and organic carbon (DOC) in pore waters from a 150 m deep hole drilled through the carbonate barrier reef of Tahiti and its underlying basalt basement. Alkalinity-pH measurements were used to calculate the DIC species concentration, and DOC was analysed according to the high temperature catalytic oxidation technique. Salinity was used as a conservative tracer to help identify water origin and mixing within the hole. Water mixing, calcium carbonate dissolution and mineralization of organic carbon combined to form three distinct groups of pore water. In the deeper basalt layers, pore water with alkalinity of 1.4 meq kg–1 pH of 7.6 and p(CO2) of 1.2 mAtm was undersaturated with respect to both aragonite and calcite. In the intermediate carbonate layer, pore water with alkalinity of more than 2.0 meq kg–1, pH of 7.70 and p(CO2) of 1.4 mAtm was supersaturated with respect to both aragonite and calcite. The transition zone between those two groups extended between 80 and 100 m depth. The shift from aragonite undersaturation to supersaturation was mainly attributed to the mixing of undersaturated pore waters from the basalt basement with supersaturated pore waters from the overlaying limestone. In the top of the reef, inputs from a brackish water lens further increased p(CO2) up to 5.6 times the atmospheric P(CO2).  相似文献   

9.
Water samples from eight major Texas rivers were collected at different times during 1997–1998 to determine the dissolved and particulate trace metal concentrations, expected to show differences in climate patterns, river discharge and other hydrochemical conditions, and human activities along the different rivers. Specifically, two eastern Texas rivers (Sabine, Neches) lie in a region with high vegetation, flat topography, and high rainfall rates, while four Central Texas rivers (Trinity, Brazos, Colorado, and San Antonio) flow through large population centers. Relatively high dissolved organic carbon (DOC) concentrations in the eastern Texas rivers and lower pH led to higher Fe and Mn concentrations in river waters. The rivers that flow through large population centers showed elevated trace metal (e.g., Cd, Pb, Zn) concentrations partly due to anthropogenically produced organic ligands such as ethylenediaminetetraacetic acid (EDTA) present in these rivers. Trace metal levels were reduced below dams/reservoirs along several Texas rivers. Statistical analysis revealed four major factors (suspended particulate matter [SPM], EDTA, pH, and DOC) that can explain most of the observed variability of trace metal concentrations in these rivers. SPM concentrations directly controlled particulate metal contents. Variation in pH correlated with changes of dissolved Co, Fe, Mn, and Ni, and particulate Mn concentrations, while DOC concentrations were significantly related to dissolved Fe concentrations. Most importantly, it was found that, more than pH, EDTA concentrations exerted a major control on dissolved concentrations of Cd and Zn, and, to a lesser extent, Cu, Ni, and Pb.  相似文献   

10.
This paper deals with dissolved inorganic carbon (DIC) and organic carbon (DOC) in pore waters from a 150 m deep hole drilled through the carbonate barrier reef of Tahiti and its underlying basalt basement. Alkalinity-pH measurements were used to calculate the DIC species concentration, and DOC was analysed according to the high temperature catalytic oxidation technique. Salinity was used as a conservative tracer to help identify water origin and mixing within the hole. Water mixing, calcium carbonate dissolution and mineralization of organic carbon combined to form three distinct groups of pore water. In the deeper basalt layers, pore water with alkalinity of 1.4 meq kg?1 pH of 7.6 and p(CO2) of 1.2 mAtm was undersaturated with respect to both aragonite and calcite. In the intermediate carbonate layer, pore water with alkalinity of more than 2.0 meq kg?1, pH of 7.70 and p(CO2) of 1.4 mAtm was supersaturated with respect to both aragonite and calcite. The transition zone between those two groups extended between 80 and 100 m depth. The shift from aragonite undersaturation to supersaturation was mainly attributed to the mixing of undersaturated pore waters from the basalt basement with supersaturated pore waters from the overlaying limestone. In the top of the reef, inputs from a brackish water lens further increased p(CO2) up to 5.6 times the atmospheric P(CO2).  相似文献   

11.
汪寿松  陈昌明  Irion  G 《沉积学报》1988,6(2):78-96
本文目的在于说明有限区域内潮坪小环境沉积物的矿物学和地球化学特点及沉积过程的改造作用。沉积物样品取自汪额诺格岛与联邦德国的德国湾南岸之间的障壁潮坪。粒度分析表明,障壁潮坪由大体平行于大陆的泥坪、混合坪到砂坪三个带组成。粘土矿物以伊利石为主,其次为蒙脱石、高岭石和绿泥石,与北海粘土矿物组合一致。粘土矿物组成和重金属Fe、Mn、Cu、Pb、Zn含量在潮坪不同部位相差无几,说明沉积物受到潮汐水流反覆侵蚀和再沉积作用的混合作用。近潮口附近有机碳含量增高是潮汐水流从北海通过进潮口携入有机物的结果。  相似文献   

12.
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13.
Analytical data for the Atlantis II and Discovery deeps in the Red Sea are given. The data were collected in March and June 1976 during the 22nd cruise of R/V Akademik Kurchatov in the Indian Ocean. On board analyses were performed of density, chlorinity, Mg, Ca, Sr and trace elements. The salinity, calculated from the density, is related to the chlorinity by S = 1.67 Cl + 4.02. The Ca-salinity relation is linear for both deeps showing that intermediate waters are formed by mixing of the brines with Red Sea water (RSDW). The hot brine (62°C) in the Atlantis II deep contains approx. 80 mg/kg of Fe and Mn while the warm brine (45°C) in the Discovery deep has a very low concentration of Fe and approx. 50 mg/kg of Mn. Mixing of RSDW containing 2 ml/l of oxygen with the anoxic deep brines causes precipitation of hydrous Mn(IV) and Fe(III) hydroxides. These two processes occur at different depths in the two deeps due to the formation of the warm (48–49°) intermediate brine in the Atlantis II deep. The oxidation-hydrolysis reactions proposed are supported by alkalinity-depth profiles and measurements of pH. These reactions also explain most of the trace element distributions and the composition of the SiO2-Fe(III) hydroxide slurry recovered by some water samplers in the Atlantis II deep.  相似文献   

14.
Vertical profiles from the water column, including the maximum turbidity zone (MTZ) to the consolidated sediment were sampled in September 2000 in the freshwater reaches of the Gironde Estuary during a complete neap tide-spring tide cycle. The vertical distributions of dissolved major redox parameters and metals (Mn, Fe, Cd, Cu, V, Co, Ni, Mo, and U) were determined. Reactive particulate metal fractions were also determined from selective leaching. The studied system is characterized by density layers functioning at different time-scales, consisting of two mobile layers, i.e., the liquid (LM) and the soft mud (SM), overlying consolidated sediments (CS). This results in a three-zone diagenetic regime where (1) O2 dynamics are fast enough to show depletion in the rapidly mixed LM sequence (tidal time-scale), (2) denitrification occurs on the weekly time-scale mixing SM sequence, and (3) the Mn, Fe, and sulfate cycling occurs in the CS layer (annual time-scale). The studied trace metals show differential behavior during early diagenesis: (1) Cd, Cu, and V are released into pore water preferentially from organic matter in the SM, (2) Co, Ni, and U are released in the CS from Mn and Fe oxides during reductive dissolution, and (3) Mo from both processes. Transient conditions (i.e., oscillations of redox fronts and reoxidation processes), due to the dynamics of the mobile layers, strongly influence the trace metal distributions as inducing resolubilization (Cd, Cu, and Mo). In the CS, authigenic metal phases accumulate, either by direct precipitation with sulfides (Cu, Cd) or co-precipitation with Fe-sulfides (Mo). Microbially mediated reduction of Fe oxides is proposed to control U removal from pore water by reduction of U(VI) to U(IV) at depth. However, a significant fraction of the trace metals is trapped in the sediment in exchangeable forms, and therefore is susceptible to be mobilized due to resuspension of estuarine sediment during strong river flood periods and/or dredging activities.  相似文献   

15.
The concentrations of authigenic phases of Cd, Re, U, and Mo increase with depth in four 45-cm-long sediment box cores collected along the axis of the Laurentian Trough, Gulf of St. Lawrence. Average authigenic accumulation rates, estimated from element inventories, are similar to rates in other continental margin environments. Strong regional variations in sediment accumulation rate and sulfide concentration have little influence on the accumulation rates of Cd and Re. This suggests that slow precipitation kinetics controls the accumulation of Cd and Re in these sediments. The accumulation rate of authigenic U is more variable; it may be tied to the kinetics of microbially mediated U reduction and be controlled by the availability of reactive organic matter. Authigenic Mo is distinguished by a sharp subsurface concentration minimum, above which Mo cycles with manganese. Mo released to pore water upon reduction of Mn oxides diffuses downward and enriches the subsurface sediment. Mo accumulates most rapidly in the sediment with the highest sulfide content. Slow conversion of molybdate to thiomolybdate may explain the much slower Mo accumulation rate in the less sulfidic sediments. A component of authigenic Mo accumulates with pyrite in an approximately constant Mo:Fe ratio. The accumulation rate of pyrite and associated Mo is insensitive to AVS abundance. Pyrite formation may be limited by the reactivity of iron oxide minerals.  相似文献   

16.
为了更好地理解碳酸盐岩旋回沉积的形成机制,计算机模拟可谓是一种既直观又定量的好方法。我们重点选择了与沉积相有关的五个重要参数：（１）与水深相关的沉积速率;（２）时滞（Ｌａｇｔｉｍｅ）;（３）盆地线性沉降速率;（４）潮差;（５）海平面振荡幅度与周期等。由于碳酸盐岩沉积物对海平面变化非常敏感,因此研究中特别注意了海平面振荡幅度与周期的变化对碳酸盐岩旋回沉积的控制和影响。一个几米厚的潮坪旋回层序通常是由海平面的低幅振荡形成的,振荡幅度也就是几米,时滞亦较短。当海平面振荡幅度较大时,在海平面下降期间,滨线向海迁移的速率会超过潮坪的侧向加积速率,因此在内陆棚上缺乏潮坪沉积物。海平面振荡幅度的增加也能造成海平面下降快于潮坪的沉降,滨线向海迁移速率比潮坪进积的速率要快得多,从而在旋回层序内发育较厚的渗流带以及不整合界面。某些高幅振荡（１００ｍ或更大）还可造成碳酸盐岩台地的早期淹没以及沉积旋回内部的深水相与浅水相并置  相似文献   

17.
南海西部陆坡海域海底广泛发育麻坑,其规模和数量在世界范围内均属罕见,但关于它们目前的活动特征尚不清楚。通过对西沙隆起西南部麻坑区采集的两根沉积柱样孔隙水SO^2–4、K^＋、Mg^2＋、Ca^2＋、Sr^2＋以及溶解有机碳（DIC）含量随深度的变化特征的研究,揭示麻坑内与硫酸根消耗有关的生物地球化学过程,并推断麻坑目前的活动状况。采集于麻坑外的C9柱样SO^2–4浓度变化整体呈向下凹的形态降低,减少的硫酸根是被有机质硫酸盐还原作用消耗。采集于麻坑内的C14柱样SO^2–4浓度梯度呈现明显的三段式变化,0.00-0.66 m内SO2–4浓度变化主要受有机质硫酸盐还原作用控制,0.66-3.70 m受有机质硫酸盐还原和甲烷缺氧氧化共同控制,3.70 m以下部分主要受甲烷缺氧氧化作用的影响。根据C14柱样3.7 m以下孔隙水硫酸根浓度梯度计算的硫酸根-甲烷交接带（SMI）约在14.3 m处,甲烷向上扩散的通量约为0.0144 mol/（m^2·a）。此外,2个柱样沉积物孔隙水的Ca^2＋浓度均随深度明显降低,而Mg2＋浓度略微降低,主要与自生碳酸盐矿物沉淀有关。C14的Mg/Ca和Sr/Ca随深度变化指示该柱样沉积物中自生碳酸盐岩矿物主要为高镁方解石。2个柱样的孔隙水地球化学特征显示目前研究区麻坑活动不活跃, C14麻坑中含甲烷流体发生微弱渗漏,可能处于麻坑活动的衰落期。  相似文献   

18.
Pore waters were collected from a sea-marginal, hypersaline pond in the Sinai and analyzed for dissolved organic carbon (DOC). The pore water DOC values ranged from 121 to 818 mg 1−1 with maxima between 15 and 54 cm deep. These values are some of the highest observed from recent sediments and probably reflect production via abiotic as well as biotic sources.  相似文献   

19.
As an essential nutrient for diatoms, silica plays a key role in the estuarine and coastal food web. High concentrations of dissolved silica (DSi) were found in the seepage water of tidal freshwater marshes, which were therefore assumed to contribute to the silica supply to estuarine waters in times of silica limitation. A comprehensive budget calculation for European salt marshes is presented in this study. Earlier, salt marshes were considered to have even higher silica recycling rates than tidal freshwater marshes. Between 2009 and 2011, concentrations, pools and fluxes of silica in two salt marshes at the German Wadden Sea coast were determined (in soil, pore water, aboveground vegetation, freshly deposited sediments and seepage water). Subsequently, a budget was calculated. Special emphasis was placed on the influence of grazing management on silica cycling. Our results show that the two salt marshes were sinks for silica. The average import of biogenic silica (BSi) with freshly deposited sediments (1,334 kmol km?2 year?1) largely exceeded the DSi and BSi exports with seepage water (80 kmol km?2 year?1). Grazing management can affect silica cycling of salt marshes by influencing hydrology and vegetation structure. Abandoned sites had larger DSi export rates than grazed sites. One third of all BSi imports occurred in only one major flooding, underlining the relevance of rare events in the silica budget of tidal marshes. This aspect has been widely neglected in earlier studies, what might have led to an underestimation of silica import rates to tidal marshes hitherto.  相似文献   

20.
Along a 2 km NW-SE transect along the energy gradient of an intertidal sand body of the back-barrier tidal flats of Spiekeroog island (German Wadden Sea, southern North Sea), three sets of closely spaced surface sediment samples were taken at different times to investigate whether the effects of progressive size sorting could be identified in the textural parameters and size-frequency curves of the sediments. Grain-sizes analyses were carried out with a high-resolution settling tube having an internal resolution of 1/50-psi intervals. The settling velocity data were subsequently transformed numerically into equivalent settling diameters on the basis of a quartz sphere standard. At this high resolution, it was possible to visualize subtle changes in textural parameters which would not have been resolved by standard 0.25-phi sieve analyses. The first two sample sets of 1992 and 1994 show similar trends of progressive fining in the sediment, combined with a slight decrease in skewness and sorting in the direction of decreasing energy. Ten years later, in 2003, the sediments were slightly coarser but still reflected the hydrodynamic energy gradient by a distinct fining trend along the transect. However, in contrast to the former data sets, the skewness values now remained constant, whereas the sorting values revealed the existence of two overlapping hydrodynamic energy regimes on the tidal flat. The better sorting in the coarser size fractions and the general coarsening trend in the central part of the tidal flat are interpreted to reflect an increase in the hydrodynamic energy level since the first two sample sets were collected. This observation suggests that some of the finer particles in the grain-size spectrum on the tidal flat were winnowed out by wave action without, however, completely obliterating the former trend. This interpretation is supported by an increase in the frequency and duration of strong winds as recorded by the national weather bureau since the early 1990s. The results of the study demonstrate that the intertidal sediments of the Wadden Sea respond rapidly and sensitively to gradual changes in the hydrodynamic energy regime.  相似文献   

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