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1.
Submarine groundwater discharge (SGD) to coastal southern Rhode Island was estimated from measurements of the naturally-occurring radioisotopes 226Ra (t1/2 = 1600 y) and 228Ra (t1/2 = 5.75 y). Surface water and porewater samples were collected quarterly in Winnapaug, Quonochontaug, Ninigret, Green Hill, and Pt. Judith–Potter Ponds, as well as nearly monthly in the surface water of Rhode Island Sound, from January 2002 to August 2003; additional porewater samples were collected in August 2005. Surface water activities ranged from 12–83 dpm 100 L− 1 (60 dpm = 1 Bq) and 21–256 dpm 100 L− 1 for 226Ra and 228Ra, respectively. Porewater 226Ra activities ranged from 16–736 dpm 100 L− 1 (2002–2003) and 95–815 dpm 100 L− 1 (2005), while porewater 228Ra activities ranged from 23–1265 dpm 100 L− 1. Combining these data with a simple box model provided average 226Ra-based submarine groundwater fluxes ranging from 11–159 L m− 2 d− 1 and average 228Ra-derived fluxes of 15–259 L m− 2 d− 1. Seasonal changes in Ra-derived SGD were apparent in all ponds as well as between ponds, with SGD values of 30–472 L m− 2 d− 1 (Winnapaug Pond), 6–20 L m− 2 d− 1 (Quonochontaug Pond), 36–273 L m− 2 d− 1 (Ninigret Pond), 29–76 L m− 2 d− 1 (Green Hill Pond), and 19–83 L m− 2 d− 1 (Pt. Judith–Potter Pond). These Ra-derived fluxes are up to two orders of magnitude higher than results predicted by a numerical model of groundwater flow, estimates of aquifer recharge for the study period, and values published in previous Ra-based SGD studies in Rhode Island. This disparity may result from differences in the type of flow (recirculated seawater versus fresh groundwater) determined using each technique, as well as variability in porewater Ra activity.  相似文献   

2.
We measured significant activities of short-lived radium isotopes, 223Ra (half-life = 11 days) and 224Ra (half-life = 3.7 days), around the margins of the Hawaiian Islands to water depths of 3500 m. These measurements suggest fluid inputs from the basalt to the surrounding ocean. In general 223Ra activities were considerably greater than 224Ra in spite of the expected higher production rate of 224Ra activity in basalt. The 223Ra was not supported by dissolved 227Ac. The highest enrichments of 223Ra were measured over the Puna Ridge (2100 m depth) east of Hawaii. Here 223Ra activities reached 19 dpm/m3, similar to activities measured near sites of active submarine groundwater discharge in the South Atlantic Bight. To explain the high activities of 223Ra unaccompanied by 224Ra, we postulate that thermally-driven circulation of seawater through the Puna Ridge deposits 231Pa on basalt surfaces. With time the 231Pa produces 227Ac and 223Ra; and 223Ra desorbs into the circulating fluids. These fluids then transport 223Ra into the overlying ocean. Based on the inventory of 223Ra above the Puna Ridge, we estimate the flow of fluids through the ridge to be on the order of 20–60 cm3 cm− 2 day− 1. In less than 1000 years the incoming seawater could provide enough 231Pa to basalt surfaces to balance the inventory of 223Ra above the ridge if only 8% of the 223Ra was transported to the overlying water. These observations on the flanks of a volcanically-active ocean island have significant implications for quantifying fluid fluxes from the flanks of the mid-ocean ridge system. By mapping 223Ra inventories in the ocean above ridge flanks and measuring the activity of 223Ra in the emerging fluids, the fluid flux can be obtained.  相似文献   

3.
The short-lived radium isotopes, 223Ra (T1/2 = 11.4 days) and 224Ra (T1/2 = 3.66 days), have been successfully used as tracers of several environmental processes, e.g., submarine groundwater discharge, coastal mixing processes, and water residence times. In this paper, the uncertainties associated with 223Ra and 224Ra measurements using a Radium Delayed Coincidence Counter are determined on a detailed error propagation basis with a confidence interval of 1σ. From the data analyses of several groups of coastal water samples, the calculated relative uncertainties averaged 12% for the 223Ra and 7% for the 224Ra. These uncertainties can decrease for radium-enriched groundwater samples although asymptotic limits have been found at 7% relative uncertainty for 223Ra and 4% for 224Ra. In this paper, the influence of sampling and measurement parameters on the final radium uncertainties is evaluated in order to provide guidance to optimize these factors and obtain more reliable results.  相似文献   

4.
The distributions of dissolved organic carbon (DOC), Ba, U, and a suite of naturally occurring radionuclides in the U/Th decay series (222Rn, 223,224,226,228Ra) were studied during high- and low-discharge conditions in the Loxahatchee River estuary, Florida to examine the role of submarine groundwater discharge in estuarine transport. The fresh water endmember of this still relatively pristine estuary may reflect not only river-borne constituents, but also those advected during active groundwater/surface water (hyporheic) exchange. During both discharge conditions, Ba concentrations indicated slight non-conservative mixing. Such Ba excesses could be attributed either to submarine groundwater discharge or particle desorption processes. Estuarine dissolved organic carbon concentrations were highest at salinities closest to zero. Uranium distributions were lowest in the fresh water sites and mixed mostly conservatively with an increase in salinity. Suspended particulate matter (SPM) concentrations were generally lowest (< 5 mg L− 1) close to zero salinity and increased several-fold ( 18 mg L− 1; low discharge) toward the seaward endmember, which may be attributed to dynamic resuspension of bottom sediments within Jupiter Inlet.Surface water-column 222Rn activities were most elevated (> 28 dpm L− 1) at the freshwater endmember of the estuary and appear to identify regions of the river most influenced by the discharge of fresh groundwater. Activities of four naturally occurring isotopes of Ra (223,224,226,228Ra) in this estuary and select adjacent shallow groundwater wells yield mean estuarine water-mass transit times of less than 1 day; these values are in close agreement to those calculated by tidal prism and tidal frequency. Submarine groundwater discharge rates to the Loxahatchee River estuary were calculated using a tidal prism approach, an excess 226Ra mass balance, and an electromagnetic seepage meter. Average SGD rates ranged from 1.0 to 3.8 × 105 m3 d− 1 (20–74 L m− 2 d− 1), depending on river-discharge stage. Such calculated SGD estimates, which must include both a recirculated as well as fresh water component, are in close agreement with results obtained from a first-order watershed mass balance. Average submarine groundwater discharge rates yield NH4+ and PO4− 3 flux estimates to the Loxahatchee River estuary that range from 62.7 to 1063.1 and 69.2 to 378.5 μmol m− 2 d− 1, respectively, depending on river stage. SGD-derived nutrient flux rates are compared to yearly computed riverine total N and total P load estimates.  相似文献   

5.
The RaDeCC™ system has proved to be a robust method of measuring 223Ra and 224Ra extracted from natural waters. Samples ranging in size from < 1 to > 1000 L are first concentrated onto Mn-fiber. The Mn-fiber is partially dried and placed into a circulation system with helium as the carrier gas. Alpha decays of the radon daughters of 223Ra and 224Ra are recorded in a scintillation cell. These data are used to activate electronic gates in the delayed coincidence system, which separate events due to 223Ra from those due to 224Ra. The system combines a high detection efficiency with low background to accurately measure 223Ra and 224Ra at concentrations on the order of 5 atoms per liter. Since this system was first deployed, numerous improvements in electronics and technique have occurred. In this paper I present tests we have conducted to confirm certain assumptions and improve the overall technique of sample collection and measurement.  相似文献   

6.
Multiple tracers of groundwater input (salinity, Si, 223Ra, 224Ra, and 226Ra) were used together to determine the magnitude, character (meteoric versus seawater), and nutrient contribution associated with submarine groundwater discharge across the leeward shores of the Hawai'ian Islands Maui, Moloka'i, and Hawai'i. Tracer abundances were elevated in the unconfined coastal aquifer and the nearshore zone, decreasing to low levels offshore, indicative of groundwater discharge (near-fresh, brackish, or saline) at all locations. At several sites, we detected evidence of fresh and saline SGD occurring simultaneously. Conservative estimates of SGD fluxes ranged widely, from 0.02–0.65 m3 m− 2 d− 1at the various sites. Groundwater nutrient fluxes of 0.04–40 mmol N m− 2 d− 1 and 0.01–1.6 mmol P m− 2 d− 1 represent a major source of new nutrients to coastal ecosystems along these coasts. Nutrient additions were typically greatest at locations with a substantial meteoric component in groundwater, but the recirculation of seawater through the aquifer may provide a means of transferring terrestrially-derived nutrients to the coastal zone at several sites.  相似文献   

7.
There is increasing evidence that submarine groundwater discharge (SGD) in many areas represents a major source of dissolved chemical constituents to the coastal ocean. In Great South Bay, NY, previous studies have shown that the discharge of nutrients with SGD may cause harmful algal blooms. This study estimates SGD to Great South Bay during August 2006 by performing a mass balance for each of the dissolved Ra isotopes (224Ra, 223Ra, 228Ra, 226Ra). The budget indicates a major unknown source (between 30 and 60% of the total input) of Ra to the bay. This imbalance can be resolved by a flux of Ra-enriched groundwater on the order of 3.5–4.5 × 109 L d− 1, depending on the Ra isotope. The Ra-estimated SGD rates compare well with those previously estimated by models of flow that decreases exponentially away from shore. Compared to previous reports of fresh groundwater discharge to the bay, the Ra-estimated discharge must comprise approximately 90% recirculated seawater. The good agreement between Ra- and model-estimated flow rates indicates that the primary SGD endmember may be best sampled at shallow depths in the sediments a short distance bayward of the low tide line.  相似文献   

8.
In the framework of the KEOPS project (KErguelen: compared study of the Ocean and the Plateau in Surface water), we aimed to provide information on the water mass pathways and vertical mixing on the Kerguelen Plateau, Southern Ocean, based on 228Ra profiles. Because 228Ra activities are extremely low in this area (~ 0.1 dpm/100 kg or ~ 2.10− 18 g kg− 1), the filtration of large volumes of seawater was required in order to be able to detect it with minimal uncertainty. This challenging study was an opportunity for us to test and compare methods aimed at removing efficiently radium isotopes from seawater. We used Mn-fiber that retains radium and that allows the measurement of all four radium isotopes (226Ra, 228Ra, 223Ra, 224Ra). First, we used Niskin bottles or the ship's seawater intake to collect large volumes of seawater that were passed onto Mn-fiber in the laboratory. Second, we filled cartridges with Mn-fiber that we placed in tandem on in situ pumps. Finally, we fixed nylon nets filled with Mn-fiber on the frame of in situ pumps to allow the passive filtration of seawater during the pump deployment.Yields of radium fixation on the cartridges filled with Mn-fiber and placed on in situ pumps are ca. 30% when combining the two cartridges. Because large volumes of seawater can be filtered with these pumps, this yields to effective volumes of 177–280 kg (that is, higher than that recovered from fourteen 12-l Niskin bottles). Finally, the effective volume of seawater that passed through Mn-fiber placed in nylon nets and deployed during 4 h ranged between 125 and 364 kg. Consequently, the two techniques that separate Ra isotopes in situ are good alternatives for pre-concentrating radium from seawater. They can save ship-time by avoiding repeated CTD casts to obtain the large volumes of seawater. This is especially true when in situ pumps are deployed to collect suspended particles. However, both methods only provide 228Ra/226Ra ratios. The determination of the 228Ra specific activity is obtained by multiplying this ratio by the 226Ra activity measured in a discrete sample collected at the same water depth.  相似文献   

9.
Delayed coincidence counters (RaDeCC), used for measuring 223Ra and 224Ra preconcentrated from water onto MnO2-impregnated acrylic fiber (“Mn-fiber”), require a standard Mn-fiber column that has a precisely known activity of 224Ra for calibration. This may be done by adding an aged 228Th standard solution to adsorb both 228Th and its daughter 224Ra quantitatively onto a Mn fiber. We used both seawater and deionized water (DIW) for testing the adsorption efficiency of Th and Ra onto Mn fibers. Our experimental results show that more than 50% of thorium (232Th and 228Th) breaks through the Mn-fiber column when DIW is used as a medium. However, near quantitative recoveries are obtained if filtered (0.45 μm) seawater is used to prepare the standard. In the case of pure DIW, the pH (initial pH  5.3) rises to > 10 after passing through the column while seawater (initial pH  7.8) changes to  7.2. Thus, the lack of thorium adsorption in DIW may be attributed to this huge increase of pH and the consequent formation of Th(OH)4 and polyhydroxyl colloids. Based on these observations, we recommend that one should use either artificial seawater or natural seawater (which has negligible 224Ra and 228Th) as a loading solution after 0.45 μm filtration. In addition, the thorium adsorption efficiency should be confirmed either by thorium analysis of the effluent solution or long-term monitoring of the supported 224Ra on the Mn fiber using the RaDeCC. Similar cautions are likely necessary for making 223Ra standards by adsorption of 227Ac onto Mn fibers.  相似文献   

10.
Submarine groundwater discharge (SGD) is now recognized as an important pathway for water and chemical species fluxes to the coastal ocean. In order to determinate SGD to the Gulf of Lion (France), we measured the activities of 226Ra and 228Ra by thermal ionization mass spectrometry (TIMS) in coastal waters and in the deep aquifer waters of the Rhone deltaic plain after pre-concentration of radium by MnO2. Compared to conventional counting techniques, TIMS requires lower quantities of water for the analyses, and leads to higher analytical precision. Radium isotopes were thus measured on 0.25–2 L water samples containing as little as 20 fg of 226Ra and 0.2–0.4 fg of 228Ra with precision equal to 2%. We demonstrate that coastal surface waters samples are enriched in 226Ra and 228Ra compared to the samples further offshore. The high precision radium measurements display a small but significant 226Ra and 228Ra enrichment within a strip of circa 30 km from the coast. Radium activities decrease beyond this region, entrained in the northern current along the shelf break or controlled by eddy diffusion. The radium excess in the first 30 km cannot be accounted for by the river nor by the early diagenesis. The primary source of the radium enrichment must therefore be ascribed to the discharge of submarine groundwater. Using a mass-balance model, we estimated the advective fluxes of 226Ra and 228Ra through SGD to be 5.2 × 1010 and 21 × 1010 dpm/d respectively. The 226Ra activities measured in the groundwater from the Rhone deltaic plain aquifer are comparable to those from other coastal groundwater studies throughout the world. By contrast, 228Ra activities are higher by up to one order of magnitude. Taking those groundwater radium activities as typical of the submarine groundwater end-member, a minimum volume of 0.24–4.5 × 1010 l/d is required to support the excess radium isotopes on the inner shelf. This has to be compared with the average rivers water runoff of 15.4 × 1010 l/d during the study period (1.6 to 29% of the river flow).  相似文献   

11.
Measurements of bromoform (CHBr3), diiodomethane (CH2I2), chloroiodomethane (CH2ICl) and bromoiodomethane (CH2IBr) were made in the water column (5–100 m depth) of the Southern Ocean within 0–40 km of the Antarctic sea ice during the ANTXX1/2 transect of the German R/V Polarstern, at five locations between 70–72°S and 9–11°W in the Antarctic spring/summer of 2003–2004. Some of the profiles exhibited a very pronounced layer of surface sea-ice meltwater, as evidenced by salinity minima and temperature maxima, along with surface maxima in concentrations of CHBr3, CH2I2, CH2ICl and CH2IBr. These results are consistent with in situ surface halocarbon production by ice algae liberated from the sea ice, although production within the sea ice followed by transport cannot be entirely ruled out. Additional sub-surface maxima in halocarbons occurred between 20 and 80 m. At a station further from shore and not affected by surface sea-ice meltwater, surface concentrations of CH2I2 were decreased whereas CH2ICl concentrations were increased compared to the stations influenced by meltwater, consistent with photochemical conversion of CH2I2 to CH2ICl, perhaps during upward mixing from a layer at  70 m enhanced in iodocarbons. Mean surface (5–10 m) water concentrations of halocarbons in these coastal Antarctic waters were 57 pmol l− 1 CHBr3 (range 44–78 pmol l− 1), 4.2 pmol l− 1 CH2I2 (range 1.7–8.2 pmol l− 1), 0.8 pmol l− 1 CH2IBr (range 0.2–1.4 pmol l− 1), and 0.7 pmol l− 1 CH2ICl (range 0.2–2.4 pmol l− 1). Concurrent measurements in air suggested a sea-air flux of bromoform near the Antarctic coast of between 1 and 100 (mean 32.3, median 10.4) nmol m− 2 day− 1 and saturation anomalies of 557–1082% (mean 783%, median 733%), similar in magnitude to global shelf values. In surface samples affected by meltwater, CH2I2 fluxes ranged from 0.02 to 6.1 nmol m− 2 day− 1, with mean and median values of 1.9 and 1.1 nmol m− 2 day− 1, respectively.  相似文献   

12.
The four naturally-occurring radium isotopes (223Ra, 224Ra, 226Ra and 228Ra) were used to estimate the submarine groundwater discharge (SGD) in the Isola La Cura marsh area in the northern Venice Lagoon (Italy). By determining the radium contributors to the study area (river, coastal ocean and sediments) the radium excess in the lagoon water was quantified through a mass balance model. This radium excess is attributed to a submarine groundwater discharge source and represents the most important input of radium. Possible endmembers were considered from analysis of groundwater samples (subtidal and marsh piezometers, marsh wells and seepage meters) that were enriched in Ra by one to two orders of magnitude relative to surface waters. In particular, a permeable layer at 80 cm depth in the surrounding marsh is considered to be representative of the most likely SGD source, although similar radium activities were measured in other subtidal porewater samples collected in the Isola La Cura area. The estimated SGD flux to the study area ranged from 1 · 109 to 6 · 109 L·d− 1, the same order of magnitude as the overall riverine input to the lagoon (3 · 109 L·d− 1). A major fraction of this SGD flux is likely recirculated seawater, as evidenced by the endmember salinity. The water residence time of 2 days was estimated by both using the shortest-lived radium isotope and estimating the volume of water exchanged between the lagoon and the open sea during a tidal cycle (tidal prism approach). This SGD flux could be used to estimate the input of other chemical species (metals, nutrients, etc.) via SGD which might affect the Venice Lagoon ecosystem.  相似文献   

13.
The measurement of short-lived 223Ra often involves a second measurement for supported activities, which represents 227Ac in the sample. Here we exploit this fact, presenting a set of 284 values on the oceanic distribution of 227Ac, which was collected when analyzing water samples for short-lived radium isotopes by the radium delayed coincidence counting system. The present work compiles 227Ac data from coastal regions all over the northern hemisphere, including values from ground water, from estuaries and lagoons, and from marine end-members. Deep-sea samples from a continental slope off Puerto Rico and from an active vent site near Hawaii complete the overview of 227Ac near its potential sources.The average 227Ac activities of nearshore marine end-members range from 0.4 dpm m− 3 at the Gulf of Mexico to 3.0 dpm m− 3 in the coastal waters of the Korean Strait. In analogy to 228Ra, we find the extension of adjacent shelf regions to play a substantial role for 227Ac activities, although less pronounced than for radium, due to its weaker shelf source. Based on previously published values, we calculate an open ocean 227Ac inventory of 1.35 * 1018 dpm 227Acex in the ocean, which corresponds to 37 moles, or 8.4 kg. This implies a flux of 127 dpm m−2 y− 1 from the deep-sea floor. For the shelf regions, we obtain a global inventory of 227Ac of 4.5 * 1015 dpm, which cannot be converted directly into a flux value, as the regional loss term of 227Ac to the open ocean would have to be included.Ac has so far been considered to behave similarly to Ra in the marine environment, with the exception of a strong Ac source in the deep-sea due to 231Paex. Here, we present evidence of geochemical differences between Ac, which is retained in a warm vent system, and Ra, which is readily released [Moore, W.S., Ussler, W. and Paull, C.K., 2008-this issue. Short-lived radium isotopes in the Hawaiian margin: Evidence for large fluid fluxes through the Puna Ridge. Marine Chemistry]. Another potential mechanism of producing deviations in 227Ac/228Ra and daughter isotope ratios from the expected production value of lithogenic material is observed at reducing environments, where enrichment in uranium may occur. The presented data here may serve as a reference for including 227Ac in circulation models, and the overview provides values for some end-members that contribute to the global Ac distribution.  相似文献   

14.
A mass balance for the naturally-occurring radium isotopes (224Ra, 223Ra, 228Ra, and 226Ra) in Jamaica Bay, NY, was conducted by directly estimating the individual Ra contributions of wastewater discharge, diffusion from fine-grained subtidal sediments, water percolation through marshes, desorption from resuspended particles, and water exchange at the inlet. The mass balance revealed a major unknown source term accounting for 19–71% of the total Ra input, which could only be resolved by invoking a source from submarine groundwater. Shallow (< 2 m depth) groundwater from permeable sediments in Jamaica Bay was brackish and enriched in Ra relative to surface bay waters by over two orders of magnitude. To balance Ra fluxes, a submarine groundwater input of 0.8 × 109–9.0 × 109 L d− 1 was required. This flux was similar for all four isotopes, with individual estimates varying by less than a factor of 2. Our calculated groundwater flux was 6- to 70-fold higher than the fresh groundwater discharge to the bay estimated by hydrological methods, but closely matched direct flow rates measured with seepage meters. This suggests that a substantial portion of the discharge consisted of recirculated seawater. The magnitude of submarine groundwater discharge varied seasonally, in the order: summer > autumn > spring. Chemical analyses suggest that the recirculated seawater component of submarine groundwater delivers as much dissolved nitrogen to the bay as the fresh groundwater flux.  相似文献   

15.
In the current study, low-background γ-spectrometry was employed to determine the 228Ra/226Ra activity ratio and 137Cs activity of 84 coastal water samples collected at six sites along the main island of Japan (Honshu Island) within the Sea of Japan, including the Tsushima Strait, and two other representative sites on Honshu Island (a Pacific shore and the Tsugaru Strait) at 1-month intervals in 2006.The 228Ra/226Ra ratio of coastal waters in the Sea of Japan exhibited similar patterns of seasonal variation, with minimum values during early summer (228Ra/226Ra = 0.6–0.8), maximum values during autumn (228Ra/226Ra = 1.5–3), and a time lag in their temporal changes ( 2.5 months and over  1300 km distance). However, the 2 other sites represented no clear periodic variation.In contrast to the positive correlation between 137Cs activity (0.6–1.7 mBq/L) and salinity (15–35), the 228Ra/226Ra ratio of coastal water samples from the Sea of Japan was not observed to correlate with salinity, and the increase in the 228Ra/226Ra ratio was not as marked (0.5–1; May–June 2004 and 2005) during the migration along Honshu Island. The input of land-derived water and/or the diffusion of radium from coastal sediments is unlikely to have affected the wide seasonal variation in the 228Ra/226Ra ratio observed in these water samples.The seasonal variation in the 228Ra/226Ra ratio recorded for the coastal waters of the Sea of Japan is considered to be mainly controlled by the remarkable changes in the mixing ratio of the 228Ra-poor Kuroshio and the 228Ra-rich continental shelf waters within the East China Sea (ECS). After passing through the Tsushima Strait, this water mass moves northeast along the coastline of the Sea of Japan as the Tsushima Coastal Branch Current (TCBC).  相似文献   

16.
Natural iron fertilization processes are occurring around the Crozet Islands (46°26′S–52°18′E), thus relieving the water masses from the normally encountered High Nutrients Low Chlorophyll (HNLC) conditions of the Southern Ocean. During austral summers 2004/2005 and 2005/2006, iron and aluminium concentrations were investigated in large particles (> 53 µm) collected from just below the mixed layer at stations under the influence of island inputs, and also in adjacent HNLC waters. These large particles are anticipated to sink out of the mixed layer, and to reflect the net effects of input and cycling of these elements in the overlying mixed layer. Labile and refractory fractions were determined by a two-stage leaching technique. Data showed that water masses downstream of the islands were enriched in total iron and aluminium (0.25–2.68 nmol L− 1 and 0.34–3.28 nmol L− 1 respectively), relative to the southern HNLC control sites (0.15–0.29 nmol L− 1 for Fe and 0.12–0.29 nmol L− 1 for Al), with only a small fraction (typically < 1%) being acid leachable in both environments. Particulate iron predominantly derived from the island system represents a significant fraction of the total water column iron inventory and may complement dissolved Fe inputs that help support the high summer productivity around the Crozet islands.  相似文献   

17.
In order to estimate submarine groundwater discharge (SGD) and SGD-driven nutrient fluxes, we measured the concentrations of nutrients, 224Ra, and 226Ra in seawater, river water, and coastal groundwater of Yeongil Bay (in the southeastern coast of Korea) in August 2004 and February 2005. The bottom sediments over the shallow areas of this bay are composed mainly of coarse sands. Large excess concentrations of 224Ra, 226Ra, and Si supplied from SGD were observed in August 2004, while these excess concentrations were not apparent in February 2005. Based on the mass balance for 224Ra, 226Ra, and Si, which showed conservative mixing behavior in seawater, SGD was estimated to be approximately 6 × 106 m3 day− 1 (seepage rate = 0.2 m day− 1) in shallow areas (< 9 m water depth) in August 2004, which is much higher than the SGD level typically found in other coastal regions worldwide. During the summer period, SGD-driven nutrients in this bay contributed approximately 98%, 12%, and 76% of the total inputs for dissolved inorganic nitrogen (DIN), phosphorus (DIP), and silicate (DSi), respectively. Our study implies that the ecosystem in this highly permeable bed coastal zone is influenced strongly by SGD during summer, while such influences are negligible in winter.  相似文献   

18.
The concentrations of228Ra in surface waters of the Seto Inland Sea were determined. Surface waters from the central region of the Seto Inland Sea, Hiuchi Nada and Bingo Nada, contained concentrations of228Ra of 655–811 dpm/1000 l which were 100 times higher than those obtained in the Pacific Ocean. These high concentrations of228Ra must be supported by a228Ra flux from the bottom sediment. The lower limit of this flux was estimated to be more than 0.16 dpm cm–2 y–1. The228Ra concentrations decreased markedly from central regions of the Seto Inland Sea to about 18 dpm/1000 l in the Kii and the Bungo Channels as salinity increased. Using a box model and the228Ra data, the mean residence time of sea water in the Seto Inland Sea with respect to the exchange with the open ocean water was estimated to be less than 10 y, and the most probable value is the order of several years.  相似文献   

19.
We used naturally occurring radium isotopes as tracers of water exchange in Apalachicola Bay, a shallow coastal-plain estuary in northwestern Florida. The bay receives fresh water and radium from the Apalachicola River, and mixes with Gulf of Mexico waters through four inlets. We deployed moored buoys with attached Mn-fibers at several stations throughout the estuary during two summer and two winter periods. After deployment for at least one tidal cycle we measured the ratio of the two short-lived radium isotopes 223Ra (half-life = 11 d) and 224Ra (3.6 d) to estimate “radium ages” of the water in the bay.During our four seasonal deployments the river discharge ranged from 338 to 1016 m3 s− 1. According to our calculations the water turnover time in the bay during these samplings ranged from 6 to 12 days. Age contours in the bay showed that winds and tides as well as river discharge influence the water movement and the residence time of freshwater in the bay. We also calculated the mean age of river water in the bay which was between 5 to 9 days during the studied periods. We suggest that this approach can be used to quantify transport processes of dissolved substances in the bay. For example, soluble nutrient or pollutant transport rates from a point source could be examined. We conclude that the radium age technique is well suited for flushing rate calculations in river dominated shallow estuaries.  相似文献   

20.
Dissolved Cd (CdD) concentrations along the salinity gradient were measured in surface water of the Gironde Estuary during 15 cruises (2001–2007), covering a wide range of contrasting situations in terms of hydrology, turbidity and season. During all situations dissolved Cd concentrations displayed maximum values in the mid-salinity range, reflecting Cd addition by chloride-induced desorption and complexation. The daily net CdD fluxes from the Gironde Estuary to the coastal ocean were estimated using Boyle's method. Extrapolating CdD concentrations in the high salinity range to the freshwater end member using a theoretical dilution line produced 15 theoretical Cd concentrations (CdD0), each representative of one distinct situation. The obtained CdD0 concentrations were relatively similar (201 ± 28 ng L−1) when freshwater discharge Q was >500 m3 s−1 (508 ≤ Q ≤ 2600 m3 s−1), but were highly variable (340 ± 80 ng L−1; 247–490 ng L−1) for low discharge situations (169 ≤ Q ≤ 368 m3 s−1). The respective daily CdD net fluxes were 5–39 kg day−1, mainly depending on freshwater discharge. As this observation invalidates the existing method of estimating annual CdD net fluxes, we proposed an empirical model, using representative CdD0 values and daily freshwater discharges for the 2001–2007 period. Subsequent integration produced reliable CdD net flux estimates for the Gironde Estuary at the annual timescale that ranged between 3.8–5.0 t a−1 in 2005 and 6.0–7.2 t a−1 in 2004, depending on freshwater discharge. Comparing CdD net fluxes with the incoming CdD fluxes suggested that the annual net CdD addition in the Gironde Estuary ranged from 3.5 to 6.7 t a−1, without any clear temporal trend during the past seven years. The annual CdD net fluxes did not show a clearly decreasing trend in spite of an overall decrease by a factor 6 in Cd gross fluxes during the past decade. Furthermore, in six years out of seven (except 2003), the annual CdD net fluxes even exceeded river borne total (dissolved + particulate) gross Cd fluxes into the estuary. These observations were attributed to progressive Cd desorption from both suspended particles and bottom sediment during various sedimentation–resuspension cycles induced by tidal currents and/or continuous dredging (navigation channel) and diverse intra-estuarine sources (wet deposition, urban sources, and agriculture). Provided that gross fluxes remain stable over time, dissolved Cd exportation from the Gironde Estuary to the coastal ocean may remain at the present level for the coming decade and the estuarine sedimentary Cd stock is forecast to decrease slowly.  相似文献   

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