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1.
Measurements of the naturally occurring radioisotopes 223Ra (t1/2 = 11.4 days) and 224Ra (t1/2 = 3.66 days) in southern Rhode Island salt ponds were combined with a simple model to obtain independent estimates of the age of these coastal waters. 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, beginning January 2002 through August 2003. Surface water activities ranged from 1–78 dpm 100 L− 1 and 5–885 dpm 100 L− 1 for 223Ra and 224Ra, respectively. Porewater radium activities ranged from 3 to 715 dpm 100 L− 1 for 223Ra, and 57–4926 dpm 100 L− 1 for 224Ra. Results indicate seasonally varying water mass ages for Ninigret (5–12 days), Winnapaug (2–6 days) and Pt. Judith-Potter Ponds (1–9 days) and, in contrast, relatively constant ages for Green Hill (5–7 days) and Quonochontaug Ponds (3–6 days). 相似文献
2.
Patrick Ollivier Christelle Claude Olivier Radakovitch Bruno Hamelin 《Marine Chemistry》2008,109(3-4):337
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
3.
Estimating submarine groundwater discharge around Isola La Cura, northern Venice Lagoon (Italy), by using the radium quartet 总被引：1，自引：0，他引：1
E. Garcia-Solsona P. Masqu J. Garcia-Orellana J. Rapaglia A.J. Beck J.K. Cochran H.J. Bokuniewicz L. Zaggia F. Collavini 《Marine Chemistry》2008,109(3-4):292
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
4.
Short-lived radium isotopes in the Hawaiian margin: Evidence for large fluid fluxes through the Puna Ridge 总被引：2，自引：1，他引：1
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
5.
Caroline Schmidt Claudia Hanfland Pierre Regnier Philippe Van Cappellen Michael Schl��ter Ulrich Knauthe Ingrid Stimac Walter Geibert 《Geo-Marine Letters》2011,31(4):259-269
Activities of the naturally occurring radium nuclides 228Ra, 226Ra, 224Ra and 223Ra were determined in waters of the open German Bight and adjacent nearshore areas in the North Sea, in order to explore the
potential use of radium isotopes as natural tracers of land–ocean interaction in an environment characterised by extensive
tidal flats, as well as riverine and groundwater influx. Data collected at various tidal phases from the Weser Estuary (228Ra: 46.3 ± 4.6; 226Ra: 17.1 ± 1.1; 224Ra: 26.1 ± 8.2 to 36.5 ± 6.1; 223Ra: 1.8 ± 0.1 to 4.0 ± 0.4), tidal flats near Sahlenburg (228Ra: 39.3 ± 3.8 to 46.0 ± 4.5; 226Ra: 15.5 ± 1.5 to 16.5 ± 1.7; 224Ra: 34.3 ± 2.2 to 85.3 ± 6.3; 223Ra: 3.6 ± 0.5 to 8.0 ± 1.2), freshwater seeps on tidal flats near Sahlenburg (228Ra: 42.1 ± 4.1; 226Ra: 21.3 ± 2.2; 224Ra: 5.1 ± 0.9; 223Ra: 2.6 ± 1.3) and also in permanently inundated parts of the North Sea (228Ra: 23.0 ± 2.3 to 28.2 ± 2.8; 226Ra: 8.2 ± 0.8 to 11.8 ± 1.2; 224Ra: 3.1 ± 1.0 to 10.1 ± 0.9; 223Ra: 0.1 ± 0.02 to 0.9 ± 0.05; units: disintegrations per minute per 100 kg water sample) reveal that, except for the fresh
groundwater, the potential end-members of nearshore water mass mixing have quite similar radium signatures, excluding a simple
discrimination between the sources. However, the decreasing activities of the short-lived 224Ra and 223Ra isotopes recorded towards the island of Helgoland in the central German Bight show a potential to constrain fluxes of land-derived
material to the open North Sea. The largest source for all radium isotopes is generally found on the vast tidal flats and
in the Weser Estuary. Future work could meaningfully combine this so-called radium quartet approach with investigations of
radon activity. Indeed, preliminary data from a tidal flat site with fresh groundwater seepage reveal a 222Rn signal that is clearly lower in seawater. 相似文献
6.
Aaron J. Beck John P. Rapaglia J. Kirk Cochran Henry J. Bokuniewicz Suhui Yang 《Marine Chemistry》2008,109(3-4):279
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
7.
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
8.
基于223Ra和224Ra的桑沟湾海底地下水排放通量 总被引：1，自引：0，他引：1
海底地下水排放（SGD）是陆地向海洋输送水量和营养物质的重要通道之一,对沿海物质通量及其生物地球化学循环有重要的影响,对生态环境起着不可忽视的作用。本文运用天然放射性同位素223Ra和224Ra示踪估算了我国北方典型养殖基地桑沟湾的海底地下水排放通量。结果表明,海底地下水样尤其是间隙水中Ra活度[224Ra=（968±31）dpm/（100 L）,223Ra=（31.4±4.9）dpm/（100 L）,n=9]远高于表层海水[224Ra=（38.7±2.0）dpm/（100 L）,223Ra=（1.70±0.50）dpm/（100 L）, n=21]。假设稳态条件下,考虑Ra的各源、汇项,利用Ra平衡模型,估算出桑沟湾SGD排放通量为（0.23~1.03）×107 m3/d。潮周期内的观测结果显示,涨潮时,水力梯度较小,SGD排放变弱,落潮时,水力梯度较大,导致了相对较多的SGD排放。在一个潮周期间,基于223Ra和224Ra得到的SGD排放通量平均为0.39×107 m3/d。潮汐动力下的SGD排放平均占总SGD排放的61%,因此桑沟湾沿岸的地下水排放主要受潮汐动力的影响,并对海水组成及海陆间物质交换有显著贡献。 相似文献
9.
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
10.
Sbastien Lamontagne Corinne Le Gal La Salle Gary J. Hancock Ian T. Webster Craig T. Simmons Andrew J. Love Julianne James-Smith Anthony J. Smith Jochen Kmpf Howard J. Fallowfield 《Marine Chemistry》2008,109(3-4):318
The input of groundwater-borne nutrients to Adelaide's (South Australia) coastal zone is not well known but could contribute to the ongoing decline of seagrass in the area. As a component of the Adelaide Coastal Waters Study (ACWS), the potential for using the radium quartet (223Ra, 224Ra, 226Ra and 228Ra) and 222Rn to evaluate submarine groundwater discharge (SGD) was evaluated. Potential isotopic signatures for SGD were assessed by sampling groundwater from three regional aquifers potentially contributing SGD to the ACWS area. In addition, intertidal groundwater was sampled at two sand beach sites. In general, the regional groundwaters were enriched in long-lived Ra isotopes (226Ra and 228Ra) and in 222Rn relative to intertidal groundwater. Radium activity (but not 222Rn activity) was positively correlated to salinity in groundwater from one of the regional aquifers and in intertidal groundwater. Radium isotope ratios (223Ra/226Ra, 224Ra/226Ra and 228Ra/226Ra) were less variable than individual Ra isotope activities within potential SGD sources. Recirculated seawater (estimated from the intertidal groundwater samples with seawater-like salinities) also had distinctly higher Ra isotope ratios than the regional groundwaters. The activities for all radioisotopes were relatively low in seawater. The activity of the short-lived 223Ra and 224Ra were highest at the shoreline and declined exponentially with distance offshore. In contrast, 228Ra and 226Ra activities had a weak linear declining trend with distance offshore. Rn-222 activity was at or near background in all seawater samples. The pattern of enrichment in short-lived Ra isotopes and the lack of 222Rn in seawater suggest that seawater recirculation is the main contributor to SGD in the ACWS area. Preliminary modeling of the offshore flux of 228Ra and 226Ra suggest that the SGD flux to the ACWS area ranges between 0.2 and 3 · 10− 3 m3 (m of shoreline)− 1 s− 1. 相似文献
11.
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
12.
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
13.
Radium tracing of submarine groundwater discharge (SGD) and associated nutrient fluxes in a highly-permeable bed coastal zone, Korea 总被引：2，自引：0，他引：2
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
14.
Radium mass-balance in Jamaica Bay, NY: Evidence for a substantial flux of submarine groundwater 总被引：3，自引：3，他引：3
Aaron J. Beck John P. Rapaglia J. Kirk Cochran Henry J. Bokuniewicz 《Marine Chemistry》2007,106(3-4):419-441
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.
M. Bourquin P. van Beek J.-L. Reyss M. Souhaut M.A. Charette C. Jeandel 《Marine Chemistry》2008,109(3-4):226
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
16.
Evaluation of the flushing rates of Apalachicola Bay, Florida via natural geochemical tracers 总被引：4，自引：0，他引：4
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
17.
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
18.
Determination of residence time and mixing processes of the Ubatuba,Brazil, inner shelf waters using natural Ra isotopes 总被引：1，自引：0，他引：1
Coastal waters contain elevated dissolved activities of short-lived radium isotopes, 223Ra and 224Ra, having half-lives of 11.4 and 3.66 days, respectively. The input of these isotopes near the coast must be balanced by decay and mixing into the open ocean, where excess activities are zero. Since the decay rate is known, in the ideal case the mixing rate may be determined from the offshore distribution of these isotopes. This study found that samples collected in June 2000 followed the expected exponential decrease with distance offshore. We assign a dispersion coefficient of 28–39 m2 s−1 for this study. During January 2002 and November 2003, there was not a consistent decrease of activity with distance offshore. This is likely due to the ruggedness of the coastline, where many bays and small islands interrupt simple mixing patterns. To estimate exchange rates during 2002 and 2003, we used a model based on the decrease in the 224Ra/223Ra activity ratio (AR) with time for samples isolated from fresh inputs of Ra. This model yielded residence times of 1–2 weeks for samples collected within 20 km of the coast. We used this residence time to calculate the flux of 228Ra (half-life = 5.7 years) to the study area necessary to maintain the enrichment relative to ocean water. This enrichment is a factor of ten greater than the flux of 228Ra expected from submarine groundwater discharge (SGD) occurring within 50 m of shore. 相似文献
19.
《Marine Chemistry》2007,103(1-2):131-145
We have investigated submarine groundwater discharge to Nueces Bay (Texas) using naturally occurring Ra isotopes. Dissolved Ra activities in Nueces Bay are among the highest observed in coastal estuaries; as great as 2600 dpm m− 3 for 228Ra and 1000 dpm m− 3 for 226Ra. Using a combination of salt and Ra mass balances, we demonstrate that river discharge and bay bottom sediments cannot supply the Ra needed to balance tidal export. In the case of 226Ra there is an additional source of 218 × 106 ± 105% dpm day− 1 which is 9 times the maximum supply from bay bottom sediments and 50 times the Ra supplied by the Nueces River. A groundwater flux of 310,000 m3 day− 1 is required to supply the needed 226Ra, based on the measured maximum Ra activity of local groundwater. Though as little as 10% of this flux may be advecting terrestrial groundwater this would still represent 160% of the Nueces River discharge. This makes it unlikely that groundwater discharge alone is supplying all of the additional 226Ra. Oil-field brine could potentially account for the remainder. Leakage of 6290 m3 day− 1 of oil-field brine from the submerged petroleum wells and pipelines within the bay could supply all of the needed 226Ra. Such large fluxes of brackish groundwater and oil-field brine could significantly affect bay nitrogen budgets, salinities, and dissolved oxygen concentrations and should be considered when determining the freshwater inflow requirements for Nueces Bay and similar estuaries. 相似文献
20.
The release of dissolved actinium to the ocean: A global comparison of different end-members 总被引：1，自引：1，他引：0
Walter Geibert Matt Charette Guebuem Kim Willard S. Moore Joseph Street Megan Young Adina Paytan 《Marine Chemistry》2008,109(3-4):409
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