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1.
New perspectives on radium behavior within a subterranean estuary   总被引：2，自引：0，他引：2  
Over the past decade, radium isotopes have been frequently applied as tracers of submarine groundwater discharge (SGD). The unique radium signature of SGD is acquired within the subterranean estuary, a mixing zone between fresh groundwater and seawater in coastal aquifers, yet little is known about what controls Ra cycling in this system. The focus of this study was to examine controls on sediment and groundwater radium activities within permeable aquifer sands (Waquoit Bay, MA, USA) through a combination of field and laboratory studies. In the field, a series of sediment cores and corresponding groundwater profiles were collected for analysis of the four radium isotopes, as well as dissolved and sediment associated manganese, iron, and barium. We found that in addition to greater desorption at increasing salinity, radium was also closely tied to manganese and iron redox cycling within these sediments. A series of laboratory adsorption/desorption experiments helped elucidate the importance of 1) contact time between sediment and water, 2) salinity of water in contact with sediment, 3) redox conditions of water in contact with sediment, and 4) the chemical characteristics of sediment on radium adsorption/desorption. We found that these reactions are rapid (on the order of hours), desorption increases with increasing salinity and decreasing pH, and the presence of Fe and Mn (hydr)oxides on the sediment inhibit the release of radium. These sediments have a large capacity to sorb radium from fresh water. Combined with these experimental results, we present evidence from time series groundwater sampling that within this subterranean estuary there are cyclic periods of Ra accumulation and release controlled by changing salinity and redox conditions.  相似文献   

2.
A reverse phase High Performance Liquid Chromatography (HPLC) method was developed to detect soluble reactive phosphate (SRP) in marine and freshwater samples. This technique is scalable over a range of sample volumes from 10 μl to 10 ml, requires minimal sample preparation, and responds linearly from 1 nM to 100 μM (R2>0.964). Standard Murphy–Riley molybdenum blue reagents were used to react with phosphate in samples for analysis. Solid phase extraction tubes were used to clean the mixed complexing reagent prior to combining the reagent with samples. The method was applied to freshwater samples collected in July 2001 along an Andean mountain stream located in the Eastern Cordillera (2400 m) of Peru and marine samples collected in January 2002 within the low marsh of the estuarine Nueces Delta System, Texas Coastal Bend. For method comparison, field samples were analyzed using a standard manual spectrophotometric method. Field sample phosphate concentrations produced from each method were nearly identical. This method offers the advantages of low sample volume (1 ml or less) with high sensitivity, precision, and potential automation.  相似文献   

3.
Understanding trace metal behaviour in estuarine environments requires sampling strategies and analytical methods adapted to strong physical and geochemical gradients. In this study, we present a specific sampling strategy covering a wide range of hydrological conditions during nine cruises in 2003–2007 to characterise the behaviour of three dissolved metals (uranium, vanadium and molybdenum) in surface and bottom water along the salinity gradient of the highly turbid macrotidal Gironde Estuary using a solid–liquid extraction. Uranium behaved conservatively whatever the water discharges observed. The slight dissolved U depletion compared to the theoretical dilution line between the fluvial and marine end-members occasionally observed in the low salinity range (0–3) was attributed to the mixing of different water bodies of the Gironde tributaries. In contrast, dissolved V behaviour was largely influenced by the hydrological conditions, showing increasingly pronounced addition with decreasing freshwater discharges, (i.e. increasing residence times of water and particles in the estuary). This addition of dissolved V in the low- to mid-salinity range was attributed to desorption processes observed in the Maximum Turbidity Zone (MTZ). The distribution of dissolved Mo concentrations along the salinity gradient was highly variable. Apparent conservative, and non-conservative behaviours were observed and were related to the concomitance of desorption from SPM, inputs from sediments for additive distribution and biological uptake and removal into sediments for subtractive distribution. Based on the whole database (2003–2007), annual net fluxes to the coastal ocean were estimated for dissolved U (15.5–16.6 t yr−1) and V (31.3–36.7 t yr−1).  相似文献   

4.
The Patos–Mirim Lagoon system along the southern coast of Brazil is linked to the coastal ocean by a narrow mouth and by groundwater transport through a Holocene barrier. Although other groundwater systems are apparently active in this region, the hydraulic head of the lagoon, the largest in South America, drives groundwater transport to the coast. Water levels in wells placed in the barrier respond to changing water level in the lagoon. The wells also provide a measure of the nutrient concentrations of groundwater flowing toward the ocean. Additionally, temporary well points were used to obtain nutrient samples in groundwater on the beach face of the barrier. These samples revealed a subterranean freshwater–seawater mixing zone over a ca. 240 km shoreline. Previously published results of radium isotopic analyses of groundwater and of surface water from cross-shelf transects were used to estimate a water flux of submarine groundwater discharge (SGD) to nearshore surface waters of 8.5 × 107 m3/day. Using this SGD and the nutrient concentrations in different compartments, nutrient fluxes between groundwater and surface water were estimated. Fluxes were computed using both average and median reservoir (i.e. groundwater and surface water) nutrient concentrations. The SGD total dissolved inorganic nitrogen, phosphate and silicate fluxes (2.42, 0.52, 5.92 × 106 mol day− 1, respectively) may represent as much as 55% (total N) to 10% (Si) of the nutrient fluxes to the adjacent shelf environment. Assuming nitrogen limitation, SGD may be capable of supporting a production rate of ca. 3000 g C m2 year− 1in the nearshore surf zone in this region.  相似文献   

5.
This paper reports the initial results of a study of groundwater and coastal waters of southern Brazil adjacent to a 240 km barrier spit separating the Patos Lagoon, the largest coastal lagoon in South America, from the South Atlantic Ocean. The objective of this research is to assess the chemical alteration of freshwater and freshwater–seawater mixtures advecting through coastal permeable sands, and the influence of the submarine discharge of these fluids (SGD) on the chemistry of coastal waters. Here we focus on dissolved iron in this system and use radium isotopic tracers to quantify SGD and cross-shelf fluxes. Iron concentrations in groundwaters vary between 0.6 and 180 μM. The influence of the submarine discharge of these fluids into the surf zone produces dissolved Fe concentrations as high as several micromolar in coastal surface waters. The offshore gradient of dissolved Fe, coupled with results for Ra isotopes, is used to quantify the SGD flux of dissolved Fe from this coastline. We estimate the SGD flux to be 2 × 106 mol day− 1 and the cross-shelf flux to be 3.2 × 105 mol day− 1. This latter flux is equal to about 10% of the soluble atmospheric Fe flux to the entire South Atlantic Ocean. We speculate on the importance of this previously unrecognized iron input to regional ocean production and on the potential significance of this source to understanding variations in glacial–interglacial ocean production.  相似文献   

6.
Gordey  A. A.  Osadchiev  A. S. 《Oceanology》2022,62(2):171-181
Oceanology - The Patos Lagoon is located in southern Brazil and is the largest freshwater lagoon in the world; it is connected to the Atlantic Ocean by a narrow strait. Through this strait, saline...  相似文献   

7.
During three cruises in the Black Sea, organised in July 1995 and April–May 1997, biological and chemical parameters that can influence the carbon budget were measured in the water column on the NW shelf, particularly in the mixing zone with Danube River waters. We observed in early spring (end of April–May) conditions an important input of freshwater organisms that enhanced the microbial activity in the low salinity range. High bacterial activity regenerates nitrogen in the form of nitrates, but is also responsible for an important consumption of ammonium and phosphate, leading to a high N/P ratio and a strong deficit in phosphorus. The consequence is a limitation of phytoplankton development but also a production of carbohydrates that accumulate all along the salinity gradient. These mechanisms are responsible for a seasonal accumulation of dissolved organic carbon (DOC) that increases from 210 μM in winter to about 280 μM in summer. All this excess DOC disappears during winter, probably degraded by bacterial activity. The degradation of carbon-rich organic matter increases the phosphorus demand by bacteria bringing limitation to phytoplankton primary production.  相似文献   

8.
利用高精度的电感耦合等离子体质谱仪对2014年1月长江口表层水中溶解铀浓度及其234U/238U比值、2013年3月长江口表层沉积物中各矿物组分的铀含量及其234U/238U比值进行了测定,研究了其空间分布特征和影响因素。结果表明:除了长江径流和海水之外,长江口还有其他的溶解铀来源。水体中过剩铀与悬浮颗粒物浓度呈现显著相关性（r2=0.96）。对长江口表层沉积物进行的序列提取实验进一步表明,水体中悬浮颗粒物或沉积物中可解吸态和碳酸钙结合态铀可以在河口区域释放进入水体,而铁锰氧化物和有机物结合铀比较稳定,不受河口区混合过程的影响。每千克颗粒物或沉积物能够释放约2 μmol颗粒态铀,使其转化为溶解态。然而,铁氢氧化物和细颗粒物的絮凝吸附作用也可使溶解铀同时从河口水体中清除。在低盐度区,铀的清除和添加过程速率相近,使溶解铀呈现暂时的"伪保守"现象:颗粒态释放的铀具有明显低的234U/238U比值,导致水体的234U/238U低于保守混合值。在中高盐度区域,溶解铀呈现明显的富集现象。但是由于水相和颗粒相中的铀交换,可释放颗粒态铀的234U/238U接近溶解铀的234U/238U比值,从而导致水体的234U/238U比值呈现出保守性。长江口颗粒物的铀释放通量为（3.48±0.41）×105 mol/a,约占输入的总颗粒态铀通量（1.80±0.17）×106 mol/a的19.3%。长江口输入东海的溶解铀总通量（河流溶解态铀与河口添加铀之和）为（2.68±0.13）×106 mol/a,约为世界河流入海铀通量的11.7%。  相似文献   

9.
The horizontal distributions of reactive silicate and zinc in the Otago Harbour, New Zealand, a shallow, vertically well-mixed estuary, have been compared. Within the harbour silicate displayed a linear salinity profile on two sampling occasions in October and early November. Consideration of the silicate budget suggested some removal of freshwater silicate in the headwaters of the estuary. Zinc concentrations, measured using state-of-the-art clean laboratory techniques were orders of magnitude lower than previously published data for coastal waters. Typical values of 5–20 ng l−1 Zn were recorded in the seaward endmember. Zinc-salinity profiles were approximately linear. Relationships between zinc and silicate concentrations for the estuarine and freshwater samples suggest a coupling between the rates of supply of these elements to the ocean and their utilisation by plankton.  相似文献   

10.
This paper demonstrates the importance of advective transport of water through permeable estuarine and salt marsh sediments. This transport delivers significant quantities of radium and barium to the coastal ocean; and, in some cases may remove significant quantities of uranium. These conclusions are based on repeated analyses of seven river–estuarine systems from North Carolina to Florida. Fluxes of radium and barium from these river systems are shown to be inadequate to balance the dissolved inventories of these elements in the South Atlantic Bight. The strong interactions that occur between surface and subsurface waters as these rivers encounter coastal marshes lead us to consider these river mouths as marsh-dominated in terms of their chemical fluxes to the ocean. Such interactions between the river and coastal marsh must be considered when estimating fluxes of material between the land and ocean.  相似文献   

11.
The effects of a disturbance by sandbar opening on the zooplankton community were evaluated through a long-term study in an eutrophic and oligohaline system, Imboassica Lagoon, Rio de Janeiro, Brazil. Zooplankton samples and limnological data were collected monthly from March 2000 to February 2003. Before the sandbar was opened in February 2001, the lagoon showed eutrophic conditions, with high mean nutrient concentrations and low salinity (total nitrogen – TN = 190.28 μM, chlorophyll a content – Chl. a = 104.60 μg/L and salinity = 0.87′). During this period, the zooplankton species present, such as the rotifers Brachionus calyciflorus and Brachionus havanaensis, were typical of freshwater to oligohaline and eutrophic environments. After the sandbar opening, the lagoon changed to a lower trophic status and increased salinity (TN = 55.11 μM, Chl. a = 27.56 μg/L and salinity = 19.64′). As a result, the zooplankton community came to consist largely of the rotifer Brachionus plicatilis, marine copepods and meroplanktonic larvae, mainly Gastropoda. Salinity was the main force structuring the zooplankton community after the sandbar opening. Two years after this episode, the prior zooplankton community had not reestablished itself, indicating a low resilience to this disturbance. The conditions developed prior to a sandbar opening can be crucial to the community responses in the face of this disturbance and for the capacity of the original zooplankton community to re-establish itself.  相似文献   

12.
Results of the chemical investigation on the Bannock and Tyro Basins are reported.Both basins were found to be hypersaline ( 10 times higher than salinity of normal seawater) and anoxic. In all investigated basins a region of transition, a few meters thick, was identified at depths > 3327 dbar. It is characterized by a sharp gradient of salinity, and all concentrations of analysed species increase strongly except for dissolved oxygen and nitrate, which immediately drop to zero. This region appears as a sharp boundary that prevents mixing. As a result, in the presence of organic matter, an anoxic condition developed with the complete depletion of dissolved oxygen. At the same time, hydrogen sulphide and ammonium accumulated within the brine. Between the Bannock and the Tyro brines differences occur in the measured concentrations of H2S, SO2−4, Ca2+ and NH3. There are some differences also within the Bannock area sub-basins.The Libeccio sub-basin, in the Bannock area, contains a double-layered brine: the upper layer is 140 dbar thick and the lower layer is 300 dbar thick. A second interface between upper and lower brines develops at a depth of 3500 dbar. Nearly all of the measured concentrations vs. depth show the double layer, with the exception of ammonium, the concentration of which remains nearly constant throughout the anoxic column. Profiles of the other species analyzed show remarkable differences on passing from the upper to the lower brine. Hydrogen sulphide, sulphate and fluoride concentrations appear constant and then increase at the second interface. The calcium concentration is also constant in the upper brine, but decreases at the second interface. Total alkalinity and phosphate concentrations show a maximum peak just below the first interface. However, after passing through the second interface all the chemical parameters exhibit an almost constant behaviour down to the bottom.Hypersaline conditions are attributed to the dissolution of Messinian evaporite, and anoxia is suggested to originate from the oxidation of organic matter present in sediments and from the absence of bottom water circulation in such a deep and enclosed environment.The chemical conditions can be summarized as follows: in the Libeccio Basin the values for the species analysed have the ranges: 39–321 psu for ‘salinity’, 8.2−6.5 for pH, 2.7–4.0 mM for total alkalinity, 0.2-0 mM for dissolved oxygen, 0–1669 μM for hydrogen sulphide, 0–198 μM for thiol, 31–99 mM for sulphate, 11–21 mM for calcium, 7–100 μM for fluoride, 0.2–3080 μM for ammonium, 5.8-0 μM for nitrite, 0.2–12 μM for phosphate and 8–130 μM for silicate.  相似文献   

13.
Field observation was conducted to monitor phosphate concentrations in groundwater and seawater mixing at two sandy beaches in Futtsu and Miura in Tokyo Bay, Japan. Dissolved phosphate concentrations were measured along transects from fresh groundwater aquifer to seawater adjacent the beaches. The concentrations were often high (up to 46 µM) in fresh groundwater samples (Cl– < 0.2). Coastal seawater, on the other hand, exhibited low phosphate concentrations (1.5 µM or less). Along the transects, phosphate generally displayed non-conservative behavior during mixing of fresh and saline waters in the aquifer; concentrations as high as 100 µM were found around the upper limit of seawater intrusion (Cl– = 2). Laboratory experiments were executed to identify the processes that control the phosphate behavior in the mixing processes. The results revealed that adsorption-desorption processes by the aquifer sand particles could significantly control the phosphate concentrations in the groundwater. Furthermore, the adsorption and/or desorption was found to be a function of salinity; the equilibrium concentration of dissolved phosphate in slurry of sand and water was the highest in freshwater and decreased considerably in saline water. The extreme concentration of phosphate may be caused by release from sand particles coinciding with the rapid change in salinity with tide.  相似文献   

14.
Particle-bound phosphorus along an urbanized coastal plain estuary   总被引：1，自引：0，他引：1  
The distribution of particle-bound phosphorus in the suspended sediment of the Delaware Estuary was examined with a sequential chemical leaching technique. The phosphorus content of particles was highest in the tidal river (140–250 μmol g−1) near major anthropogenic inputs. Despite this enrichment of river particles with phosphorus, suspended particles within the salinity gradient had a phosphorus content more similar to the world's average. Sequential chemical leaches revealed that particulate phosphorus was associated with organic matter, aluminum oxides, iron oxides, and apatite in all areas of the estuary. However, ‘excess’ particle-bound phosphorus in the tidal river was associated mainly with iron oxides (27%), aluminum oxides (23%), and organic matter (50%). Within the salinity gradient, particulate phosphorus associated with iron oxides, aluminum oxides, and apatite all decreased with increasing salinity. Estuarine mixing was simulated to determine whether the observed decreases in particle-bound phosphorus pools in field samples were due to release into solution. During simulated mixing, particulate phosphorus associated with iron and aluminum oxides decreased, but no change was observed in apatite-bound phosphorus. The results of the mixing study combined with the observed particle-bound phosphorus distributions suggest that phosphate concentrations along the Delaware Estuary may be partially ‘buffered’ by aluminum and iron oxide phases.  相似文献   

15.
Recent sediments and separated phosphate pellets ( 125–500 μm in diameter) from the Peru shelf have been analyzed for uranium decay-series isotopes and 14C in order to determine age relationships and mineralization rates. Uranium-series ages of pellets separated from one box core are significantly higher than AMS radiocarbon ages determined for the same pellets. These differences appear to be a consequence of mixing of an older generation of pellets with ones which are more recently formed. Postdepositional adsorption of reactive elements such as thorium and protactinium onto pellet surfaces may also contribute to the observed discordancy with radiocarbon ages.

Sediment radiocarbon and 210Pb sediment results, as well as some trends in the uranium-series data, suggest that high concentrations of phosphate pellets have accumulated in some Peru shelf sediments without extensive reworking. Individual pellets apparently form very quickly, on time scales of a few years. Estimated authigenic uptake rates of phosphorus into pellets ranges from 0.5 to 9.40 μmol-P cm− 2 yr− 1, somewhat higher than rates measured for nodules from the same area. This is consistent with observations that pelletal morphologies predominate over nodular forms within ancient phosphorite deposits.  相似文献   


16.
A high temperature catalytic oxidation (HTCO) technique was used to measure dissolved organic carbon (DOC) during seasonal surveys of the Tamar Estuary, U.K. At the time of the programme, the field of DOC analysis had been plagued by numerous analytical difficulties. However, using thorough calibration of the analytical systems and the systematic analysis of an internal reference material, a valuable estuarine DOC data set was produced. The range of DOC concentrations observed (478–110 μM C) is consistent with the published data for riverine and coastal sea waters respectively. The Tamar Estuary is a freshwater DOC-dominated system, with strong correlation between lateral DOC distribution and salinity. However, mixing behaviour was not strictly conservative. During tidal cycle studies at a fixed station, DOC concentrations appeared to be uncoupled from salinity, and were inversely related to turbidity. It is concluded that tidally-induced resuspension of bottom sediments provided the dominant control mechanism for DOC concentration. The Tamar Estuary shows contrasting behaviour to the larger, more heavily impacted, Severn Estuary. Hence it is likely that the behaviour of DOC in estuaries cannot be classified as typical per se, but is a function of the natural and anthropogenic characteristics of the catchment and hydrology.  相似文献   

17.
Temperature, pH, total alkalinity, dissolved oxygen, silicate, nitrate, phosphate and the Mn, Fe and Al contents of suspended particulate matter (SPM) were measured in the Rimouski River estuary as functions of chlorinity during the period May—September 1980.At any given time, total alkalinity (TA) is conservative within the estuary with respect to chlorinity. However, the total alkalinity (TA) of the freshwater is related to river flow. This is attributed to dilution of the river water with bicarbonate-poor rainwater.Generally, pH follows the same pattern observed for TA in freshwater. Dissolved oxygen is usually more concentrated in freshwater and decreases linearly with increasing chlorinity. Freshwater is always saturated or supersaturated with respect to O2. Seasonal fluctuations are attributed to temperature variations.There is no evidence for removal of soluble silicate from the freshwater entering the sea. The concentration of silicate in the freshwater is strongly influenced by rainfall. Soil leaching, conditioned by high rainfall increases the concentration of soluble silicate in freshwater. Nitrate behaves similarly whereas phosphate is complicated by the presence of sewage.Analysis of the Mn, Fe and Al contained in the SPM indicates dilution of river-borne particles rich in Mn by others less rich in this element. A decrease in Mn content with increasing chlorinity and SPM concentration as well as increasing concentrations of SPM with increasing chlorinity indicate that the composition is controlled primarily by physical mixing of material from two sources rather than by chemical processes. Within the analytical precision the Fe/Al ratio does not vary with the chlorinity.  相似文献   

18.
We measured benthic and water column fluxes in a hypersaline coastal system (Baffin Bay, Texas) in 1996–1997, a period of decreasing salinity (increased freshwater input) and turbidity. Salinity decreased from a mean of 60 to 32 practical salinity units (psu) and turbidity decreased from a mean of 78 to 25 NTU over the study period. Associated with hydrological changes, there were important changes in nutrient fluxes and metabolism. There was a shift of total respiration from the water column to the sediments and an increased amount of the benthic metabolism (2–67%) was attributed to sulfate reduction in this system when salinity was lowest, perhaps a consequence of increased benthic light levels and photosynthetic production of labile carbon in the sediments. The sediments were a large sink for both N and P. Sediment particulate C:N (9.8) and C:P (119) ratios were lower than those in the water column. However, ammonium:phosphate fluxes increased coincident with increased sulfate reduction rates and porewater sulfide concentrations. Efficient N-retention mediated through dissimilative nitrate reduction to ammonium, and high rates of N-fixation in shallow, hypersaline systems may facilitate transitions from N-limitation to P-limitation. During the most hypersaline period, seston exhibited some of the most extreme nutrient ratios ever reported for a marine ecosystem (C:N 10–37 and C:P 200–1200) and suggest that plankton are likely to be P-limited or are very well adapted to low P availability. When salinity and N:P and C:P ratios were highest, the plankton was dominated by a brown tide alga (Aureoumbra lagunensis), supporting evidence that this organism is adapted to low P, long residence time systems.  相似文献   

19.
The salinity maximum of the Warm Deep Water advecting into the Weddell Sea lies about 200 m below the temperature maximum and an NO minimum. The NO minimum is horizontally as well as vertically resolved on two sections towards the eastern and southern coast of the Weddell Sea, one towards Cap Norvegia, the other towards the Filchner Ice Shelf, whereas the temperature and salinity maxima are horizontally resolved on the former section only. Thus NO is a valuable complementary tool in studying the boundary current along the coast of the Weddell Sea. The NO signal indicates a non-continuity within the boundary current, as the minimum in the downstream section (less than 480 μmol kg−1 ) is deeper than the upstream one ( more than 490 μmol kg−1). The temperature maximum as well as the NO minimum descend from a depth of about 400 m in the Cap Norvegia section to about 600 m in the Filchner Ice Shelf section, the salinity maximum being correspondingly lowered. A plot of NO vs. salinity shows a continuous mixing line between Warm Deep Water and the freshest part of the Winter Water interval, thus essentially displaying Winter Water as itself lying on a mixing line. This indicates that Warm Deep Water is being advected well into the winter surface layer.  相似文献   

20.
Behaviour of silicate, nitrate and phosphate in the Mandovi Estuary was studied during the premonsoon season. The study shows that silicate is removed from the water column while nitrate showed an internal source. This nitrate source has been identified as the wash water from an iron ore screening plant which discharges the muddy waste directly into the river. Applying mixing relations, the distribution of this nitrate both up- and downstream of the outfall has been studied. Phosphate showed very low concentrations in the low salinity region; however, its concentration increased slightly towards the higher salinity region.  相似文献   

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