Radionuclide partitioning across great lakes natural interfaces

Several water and surface microlayer samples from Lake St. Clair, the Niagara River, and the North Shore of Lake Ontario collected during 1983–1986 have been assayed for a variety of radionuclides. In addition, the foam accumulating in the pool just below Niagara Falls was also analyzed and found to be the most efficient aqueous phase collector of¹³⁷Cs,²¹⁰Pb, and²²⁶Ra.The order of radioisotope specific activities from highest to lowest is: Lake Ontario sediment, Niagara River suspended solids, Niagara River foam, surface microlayer water, and subsurface water. Radiological dose rates to the sediments from¹³⁷Cs,²²⁶Ra, and²²⁸Th total about 5 mGy/y.     

Gross-beta activity in ground water: natural sources and artifacts of sampling and laboratory analysis

Gross-beta activity has been used as an indicator of beta-emitting isotopes in water since at least the early 1950s. Originally designed for detection of radioactive releases from nuclear facilities and weapons tests, analysis of gross-beta activity is widely used in studies of naturally occurring radioactivity in ground water. Analyses of about 800 samples from 5 ground-water regions of the United States provide a basis for evaluating the utility of this measurement. The data suggest that measured gross-beta activities are due to (1) long-lived radionuclides in ground water, and (2) ingrowth of beta-emitting radionuclides during holding times between collection of samples and laboratory measurements.Although⁴⁰K and²²⁸Ra appear to be the primary sources of beta activity in ground water, the sum of⁴⁰K plus²²⁸Ra appears to be less than the measured gross-beta activity in most ground-water samples. The difference between the contribution from these radionuclides and gross-beta activity is most pronounced in ground water with gross-beta activities > 10 pCi/L, where these 2 radionuclides account for less than one-half the measured ross-beta activity. One exception is groundwater from the Coastal Plain of New Jersey, where⁴⁰K plus²²⁸Ra generally contribute most of the gross-beta activity. In contrast,⁴⁰K and²²⁸Ra generally contribute most of beta activity in ground water with gross-beta activities < 1 pCi/L.The gross-beta technique does not measure all beta activity in ground water. Although³H contributes beta activity to some ground water, it is driven from the sample before counting and therefore is not detected by gross-beta measurements. Beta-emitting radionuclides with half-lives shorter than a few days can decay to low values between sampling and counting. Although little is known about concentrations of most short-lived beta-emitting radionuclides in environmental ground water (water unaffected by direct releases from nuclear facilities and weapons tests), their activities are expected to be low.Ingrowth of beta-emitting radionuclides during sample holding times can contribute to gross-beta activity, particularly in ground water with gross-beta activities > 10 pCi/L. Ingrowth of beta-emitting progeny of²³⁸U, specifically²³⁴Pa and²³⁴Th, contributes much of the measured gross-beta activity in ground water from 4 of the 5 areas studied. Consequently, gross-beta activity measurements commonly overestimate the abundance of beta-emitting radionuclides actually present in ground water. Differing sample holding times before analysis lead to differing amounts of ingrowth of the two progeny. Therefore, holding times can affect observed gross-beta measurements, particularly in ground water with²³⁸U activities that are moderate to high compared with the activity of⁴⁰K plus²²⁸Ra. Uncertainties associated with counting efficiencies for beta particles with different energies further complicate the interpretation of gross-beta measurements.     

Genetic variation in the oyster,Crassostrea virginica (Gmelin), in relation to environmental variation

Four polymorphic loci in seven natural oyster (Crassostrea virginica Gmelin) populations of the Chesapeake Bay were analyzed by protein-gel electrophoresis for genetic variation. Samples of about 100 each were taken in 1977 along environmental gradients from stations in the James and Potomac rivers. The distribution of genotypes at four loci for each of the stations was nog significantly different from Hardy-Weinberg expectations. At two loci (Pgi andLap-2), a pool of all seven stations was also in equilibrium. Significant genetic differentiation between rivers was detected for two other loci (Pgm-1 andLap-1), and frequency of one genotype (Lap-1 ^95/95) was significantly correlated with mean temperature over the water monitoring period (1972–1977).     

Radionuclides in ground water of the Carson River Basin,western Nevada and eastern California,U.S.A.

Ground water is the main source of domestic and public supply in the Carson River Basin. Ground water originates as precipitation primarily in the Sierra Nevada in the western part of Carson and Eagle Valleys, and flows down gradient in the direction of the Carson River through Dayton and Churchill Valleys to a terminal sink in the Carson Desert. Because radionuclides dissolved in ground water can pose a threat to human health, the distribution and sources of several naturally occurring radionuclides that contribute to gross-alpha and gross-beta activities in the study area were investigated. Generally, alpha and beta activities and U concentration increase from the up-gradient to down-gradient hydrographic areas of the Carson River Basin, whereas²²²Rn concentration decreases. Both²²⁶Ra and²²⁸Ra concentrations are similar throughout the study area. Alpha and beta activities and U concentration commonly exceed 100 pCi/l in the Carson Desert at the distal end of the flow system. Radon-222 commonly exceeds 2,000 pCi/l in the western part of Carson and Eagle Valleys adjacent to the Sierra Nevada. Radium-226 and²²⁸Ra concentrations are <5pCi/l. Four ground water samples were analyzed for²¹⁰Po and one sample contained a high concentration of 21 pCi/l. Seven samples were analyzed for²¹⁰Pb; six contained <3pCi/l and one contained 12 pCi/l. Thorium-230 was detected at concentrations of 0.15 and 0.20 pCi/l in two of four samples.Alpha-emitting radionuclides in the ground water originated from the dissolution of U-rich granitic rocks in the Sierra Nevada by CO₂, oxygenated water. Dissolution of primary minerals, mainly titanite (sphene) in the granitic rocks, releases U to the water. Dissolved U is probably removed from the water by adsorption on Fe- and Mn-oxide coatings on fracture surfaces and fine-grained sediment, by adsorption on organic matter, and by coprecipitation with Fe and Mn oxides. These coated sediments are transported throughout the basin by fluvial processes. Thus, U is transported as dissolved and adsorbed species. A rise in the water table in the Carson Desert because of irrigation has resulted in the oxidation of U-rich organic matter and dissolution of U-bearing coatings on sediments, producing unusually high U concentration in the ground water.Alpha activity in the ground water is almost entirely from the decay of U dissolved in the water. Beta activity in ground water samples is primarily from the decay of⁴⁰K dissolved in the water and ingrowth of²³⁸U progeny in the sample before analysis. Approximately one-half of the measured beta activity may not be present in ground water in the aquifer, but instead is produced in the sample after collection and before analysis. Potassium-40 is primarily from the dissolution of K-containing minerals, probably K-feldspar and biotite. Radon-222 is primarily from the decay of²²⁶Ra in the aquifer materials. Radium in the ground water is thought to be mainly from alpha recoil associated with the decay of Th in the aquifer material. Some Ra may be from dissolution (or desorption) or Ra-rich coatings on sediments.     

Origin and age of saline waters in Busko Spa (Southern Poland) determined by isotope,noble gas and hydrochemical methods: evidence of interglacial and pre-Quaternary warm climate recharges

In the Busko and Solec Spas, saline sulphide and sulphate waters are exploited at different depths. The shallow water system in Busko is related to an interglacial or interstadial period shown by the lack of tritium and¹⁴C and its δ¹⁸O and δD values equal to that of modern water. The noble gas temperatures (NGT) are somewhat lower than the present air temperatures, but the⁴He and⁴⁰Ar ages of about 90–480 ka confirm a Pleistocene recharge. The δ¹⁸O and δD values of the deep system are much heavier than those of local modern waters, which may mean the recharge of a warm pre-Quaternary climate. The⁴He,⁴⁰Ar and²¹Ne contents and the NGT values confirm the deep system to be recharged at the pre-Quaternary stages of the present hydrologic cycle, i.e. after the sea transgression in the Badenian. High SO₄²⁻ contents indicate that the Cl⁻ and SO₄²⁻ in both systems originated from simultaneous leaching of NaCl and gypsum. Other components can be explained by cation exchange between water and Badenian clay minerals in marls (e.g. Ca²⁺ for Mg²⁺ and Na⁺ for K⁺) and by the decay of marine organic matter supplying Br⁻, I⁻ and B.     

A study of234U/238U ratios in groundwaters of Taiyuan area,Shanxi Province

Uranium contents and²³⁴U/²³⁸U ratios have been determined on 29 water samples from the Taiyuan area, Shanxi Province. The results show that the same artesian aquifer has similar uranium contents and²³⁴U/²³⁸U activity ratios, and the deeper aquifers have higher A. R. values but lower uranium contents. The A. R. values increase slightly towards groundwater flow in the artesian aquifers dominated by oxidizing ground waters. The Lancun Spring and the famous Jinci Spring belong to two different karst groundwater systems, i.e., the east and west karst groundwater systems. The recharge area of the Lancun Spring should cover the wide limestone outcrops of middle Ordovician in the northeast. The Ordovician fissure-karst ground water to the Jinci Spring is extensively mixed with fissure water in Carboniferous-Jurassic formations and seepage water from the Fenhe River.     

Factors controlling the groundwater transport of U, Th, Ra, and Rn

A model for the groundwater transport of naturally occurring U, Th, Ra, and Rn nuclides in the²³⁸U and²³²Th decay series is discussed. The model developed here takes into account transport by advection and the physico-chemical processes of weathering, decay, α-recoil, and sorption at the water-rock interface. It describes the evolution along a flowline of the activities of the²³⁸U and²³²Th decay series nuclides in groundwater. Simple sets of relationships governing the activities of the various species in solution are derived, and these can be used both to calculate effective retardation factors and to interpret groundwater data. For the activities of each nuclide, a general solution to the transport equation has been obtained, which shows that the activities reach a constant value after a distance ϰ_i, characteristic of each nuclide. Where ϰ_i is much longer than the aquifer length, (for²³⁸U,²³⁴U, and²³²Th), the activities grow linearly with distance. Where gKⁱ is short compared to the aquifer length, (for²³⁴Th,²³⁰Th,²²⁸Th,²²⁸Ra, and²²⁴Ra), the activities rapidly reach a constant or quasi-constant activity value. For²²⁶Ra and²²²Rn, the limiting activity is reached after 1 km. High δ²³⁴U values (proportional to the ratio^ɛ234Th/^W238U) can be obtained through high recoil fraction and/or low weathering rates. The activity ratios²³⁰Th/²³²Th,²²⁸Ra/²²⁶Ra and²²⁴Ra/²²⁶Ra have been considered in the cases where either weathering or recoil is the predominant process of input from the mineral grain. Typical values for weathering rates and recoil fractions for a sandy aquifer indicate that recoil is the dominant process for Th isotopic ratios in the water. Measured data for Ra isotope activity ratios indicate that recoil is the process generally controlling the Ra isotopic composition in water. Higher isotopic ratios can be explained by different desorption kinetics of Ra. However, the model does not provide an explanation for²²⁸Ra/²²⁶Ra and²²⁴Ra/²²⁶Ra activity ratios less than unity. From the model, the highest²²²Rn emanation equals 2ɛ. This is in agreement with the hypothesis that²²²Rn activity can be used as a first approximation for input by recoil (Krishnaswamiet al 1982). However, high²²²Rn emanation cannot be explained by production from the surface layer as formulated in the model. Other possibilities involve models including surface precipitation, where the surface layer is not in steady-state.     

Plutonium and radiocesium in the water column of the Hudson River estuary

Isotopes of plutonium (Pu), cesium (Cs), and cobalt (Co) introduced into the Hudson River Estuary from fallout deposition, the erosion of fallout-contaminated surface soils, and nuclear reactor effluent (isotopes of Cs and Co only) have been measured in water column samples collected from 1975 to 1980 Isotopic measurements conducted independently by two research groups utilizing different sampling and analytical techniques have been summarized. The major conclusions drawn from the work are that for water samples collected by the two laboratories over similar time periods, the mean concentrations of nonfilterable^239,240Pu (<0.45 μm) were identical at 0.13 fCi/l, mean concentrations of both¹³⁷Cs and^239,240Pu in suspended particulates were more divergent at 2,270±920 pCi/kg (±1 SD) and 1,430±430 pCi/kg for¹³⁷Cs, and 19±8 pCi/kg and 12±4 pCi/kg for^239,240Pu The behavior of^239,240Pu and¹³⁷Cs within the water column is shown to diverge within brackish waters Specifically, the magnitude of the¹³⁷Cs distribution coefficient (K _d ) can be expressed as an inverse power function of the chloride ion concentrations for chlorinities between 0.1 and 4 g Cl⁻/l No difference in the^239,240PuK _d has been observed between fresh and brackish waters Based on the expected inventories of^239,240Pu and¹³⁷Cs within watershed soils, the current downstream transport of these radionuclides represents fractional mobilization rates on the order of 1–4 (×10⁻⁴) per year     

Transport and sediment accumulation of210Pb and137Cs in two Southeast Alaskan fjords

Sediment profiles of²¹⁰Pb and¹³⁷Cs in cores collected at increasing distances from the heads of Smeaton Bay and Boca de Quadra fjords indicate that watersheds influence the inventories of radioisotopes present and that the steep topographies of the fjords enhance sediment redistribution. Episodic deposition of terrestrially derived sediment was responsible for roughly 50% of the¹³⁷Cs and 45% of the²¹⁰Pb inventories in shallower (less than 180 m) locations in Wilson and Bakewell arms of Smeaton Bay.²¹⁰Pb sedimentation rates at shallower sites when corrected for episodic deposition were less than sedimentation rates obtained in the deep basins of the fjords where sediment focusing and increased primary productivity in the overlying water column occur. Higher fluxes of dissolved Mn from surficial sediments and subsequent reoxidation in the overlying water may have enhanced scavenging of²¹⁰Pb in basin locations, resulting in higher inventories. Episodic events have occurred frequently in Smeaton Bay and Boca de Quadra suggesting that steady-state conditions with respect to sedimenting particles can be achieved only when averaged over long time periods approaching the time over which¹³⁷Cs and²¹⁰Pb are useful.     

Historical trace element distribution in sediments from the Mississippi River delta

Five sediment cores were collected on the shelf of the inner Mississippi Bight in June 2003 for a suite of radionuclides to establish geochronologies and trace elements to examine patterns of contaminant deposition and accumulation. Core sites were chosen to reflect a matrix of variable water depths, proximity to the Mississippi River mouth as the primary source for terrigenous particles, and extent and duration of summertime water column hypoxia. The vertical distribution of^239,240Pu and²¹⁰Pb_xs(=²¹⁰Pb_total−²²⁶Ra) provided reliable geochronological age constraints to develop models for mass accumulation rates and historic trace element inputs and variations. Mass accumulation rates ranged from 0.27 to 0.87 g cm⁻²yr⁻¹ and were internally consistent using either²¹⁰Pb_xs or^239,240Pu. Measured inventories of¹³⁷Cs,^239,240Pu, and²¹⁰Pb_xs were compared to atmospheric deposition rates to quantify potential sediment focusing or winnowing. Observed variability in calculated mass accumulation rates may be attributed foremost to site-specific proximity to the river mouth (i.e., sediment source), variability in water depth, and enhanced sediment focusing at the Mississippi River canyon site. Trace element concentrations were first normalized to Al, and then Al-normalized enrichment factors (ANEF) were calculated based on preanthropogenic and crustal trace element abundances. These ANEFs were typically >1 for V and Ba, while for most other elements studied, either no enrichment or depletion was observed. The enrichment of Ba may be related, in part, to the seasonal occurrence of oxygen-depleted subsurface waters off the Mississippi River delta, as well as being an ubiquitous byproduct of the petroleum industry.     

Radioisotope dynamics - the origin and fate of nuclides in groundwater

The use of radionuclides as clocks for groundwater dating and as probes to investigate the geometry and spatial extent of the contact area between rocks and water is reviewed. Subsurface production rates for²²²Rn³⁷Ar,⁸⁵Kr,³⁹Ar,³⁶CI,³He,⁴He and⁴⁰Ar in various rock types are listed. Measured Rn fluxes from the surface of sandstone grains and from pieces of granite point to scale-dependent diffusion coefficients. The temporal evolution of subsurface-produced²²²Rn-,³⁷Ar-,⁸⁵Kr- and³⁹Ar-activities in groundwaters yields radionuclide escape factors between 0.1 % and 9% for the Stripa granite (Sweden) and between 1% and 4% for the Milk River sandstone (Canada). The combination of³H,⁸⁵Kr,³⁹Ar,¹⁴C,³⁶CI,⁴He in the UK Triassic sandstone aquifer allows groundwater dating up to 40 000 a. Very old groundwaters can be studied using Cl,³⁶Cl and⁴He evolution as demonstrated in the Milk River aquifer in Canada.     

Geochemical evidence of preferential flow of water through fractures in unsaturated tuff,Apache Leap,Arizona

The occurrence and significance of aqueous flow through fractures in unsaturated tuff was investigated at the Apache Leap Research Site near Superior, Arizona. Water samples for geochemical and isotopic analysis were collected from water seeping from fractures in a mine haulage tunnel, from the saturated zone in a vertical borehole (USW UZP-4), and from both the unsaturated and saturated zones in an angled borehole (DSB). The geochemistry and¹⁴C activity of water samples from the DSB suggest that most of the recharge to the saturated zone has occurred through fractures, especially beneath the ephemeral streams. Evidence of substantial recent recharge through fractures was found in saturated-zone samples from the mine haulage tunnel using ³H, δ³⁴S and SO₄²⁻/Cl⁻ analyses. Evidence of partial imbibition of fracture flow into the rock matrix was found at multiple depths throughout the 147 m unsaturated zone at the DSB using geophysical measurements from the borehole, water-content analyses from core samples, and ¹⁴C and ³H analyses from pore water extracted from preserved core samples. Post-bomb ¹⁴C activity was measured in pore water near fractures just above the saturated zone.     

A study on cosmogenic nuclides in the Jilin meteorite and its irradiation history

44 samples of the Jilin meteorite were analyzed by various laboratories for spallogenic, radiogenic, and trapped rare gases. A non-uniform distribution has been found for the rare gases of different origins. There have been found correlations among the spallogenic rare gases, with apparent depth effects. 43 samples were analyzed for their cosmogenic radionuclides⁶⁰Co,²⁶Al,³⁶Cl,⁴⁰K,⁵³Mn,⁵⁴Mn, and²²Na. Correlations have been found between⁶⁰Co and⁵³Mn and between⁶⁰Co and²¹Ne. The Jilin meteorite has a complex history of cosmic-ray irradiation. According to the two-stage model and the other fragments have a burying depth two stages,T ₁=11 m.y. andT ₂=0.3 m.y. The burying depth of all samples in the parent body can be obtained by the content of²¹Ne. Jilin meteorite No. 1 is located 20–142 cm from the surface, No. 4 ranges from 106–134 cm, and the other fragments have a burying depth between 15 and 150 cm. The equation of the reference plane for the surface of the 1-stage Jilin meteoroid is 0.24x+0.81y+0.53z+0.5=0. Use can also be made of⁶⁰Co to determine the burying depth of all samples in the 2-stage Jilin meteoroid (under a geometry of 4π), and further to restore the preatmospheric form and size of the parent body. During its atmospheric passage, the Jilin had an ablation rate of ca. 30%. On the basis of the two-stage model and the concentration of²¹Ne and⁶⁰Co in the samples, we propose a scheme to restore the relative position of all samples in the parent body. 12 sample-distribution regions can be sketched out. Also can be restored the relative position of all the samples in the parent body during the two stages.     

Application of226Ra,228Ra,223Ra, and224Ra in coastal waters to assessing coastal mixing rates and groundwater discharge to oceans

The fate of dissolved material delivered to the coastal ocean depends on its reactivity and the rate at which it is mixed offshore. To measure the rate of exchange of coastal waters, we employ two short-lived radium isotopes,²²³Ra and²²⁴Ra. Along the coast of South Carolina, shore-perpendicular profiles of²²³Ra and²²⁴Ra in surface waters show consistent gradients which may be modeled to yield eddy diffusion coefficients of 350–540 m²s⁻¹. Coupling the exchange rate with offshore concentration gradients yields estimates of offshore fluxes of dissolved materials. For systems in steady state, the offshore fluxes must be balanced by new inputs from rivers, groundwater, sewers or other sources. Two tracers that show promise in evaluating groundwater input are barium and²²⁶Ra. These tracers have high relative concentrations in the fluids and low-reactivity in the coastal ocean. Applying the eddy diffusion coefficients to the offshore gradient of²²⁶Ra concentration provides an estimate of the offshore flux of²²⁶Ra. Measuring the concentrations of²²⁶Ra in subsurface fluids provides an estimate of the fluid flux necessary to provide the²²⁶Ra. These estimates indicate that the volume of groundwater required to support these fluxes is of the order of 40% of the surface water flow.     

Seasonal and spatial distribution of the Carolina marsh clamPolymesoda caroliniana (Bosc) in a Mississippi tidal marsh

The abundance of the marsh clamPolymesoda caroliniana at four stations on a Mississippi tidal marsh was followed from February 1977 through April 1978. The stations varied with respect to inundation time and vegetative cover. The largest population was found in an area flooded 12% of the year (136 individuals per m²) and in an area flooded 3.2% of the year (126 individuals per m²). However, the latter area contained no large clams (>25.5 mm). Smaller populations were found in the upper reaches of a tidal creek draining the marsh (68 individuals per m²) and in an area flooded 5.8% of the year (73 individuals per m²). The average abundance of the clams on the marsh was 100 per m². At least three recruitment periods were apparent. In laboratory studies, clams larger than 15 mm survived longer than 30 days without water. Clams smaller than 12 mm survived less than 6 days without water. Several decapods (Callinectes sapidus, Uca longisignalis, andSesarma reticulatum) consumed clams smaller than 10 mm but were unable to eat larger clams under laboratory conditions.Polymesoda caroliniana may be important to the functioning of the marsh by removing large quantities of particulate matter from flooding water.     

Cosmogenic isotope and track records in meteorites and their implications to cosmic ray fluxes

Study of several cosmic ray effects, such as VH track density, spallogenic²⁶Al and⁵³Mn activity,²¹Ne and²²Ne/²¹Ne ratio, made in the same sample or in cores taken from different meteorites can identify parameters related to the exposure history of meteorites and cosmic ray flux variations. Meteorites with single or multiple exposure can be distinguished from a track production rate —²²Ne/²¹Ne correlation diagram and cosmic ray flux variations over 10⁶–10⁷ years can be deduced from a three-isotope correlation diagram of²⁶Al,⁵³Mn and²¹Ne. Isotopic data based on chondrites with simple, one-stage exposure are consistent with the same average galactic cosmic ray intensity over the past 2 million years as that during the past 10⁷ years.     

Annual cycle of radionuclide contamination on tide-washed pasture in the Mersey Estuary, NW England

The radionuclide burden of vegetation comprising a tide-washed pasture at Ince Marsh in the Mersey Estuary, U.K., derives mainly from adhered external particulates originating as suspended sediments in estuarine water. Radionuclide concentrations are dominated by the growth cycle of the vegetation, with the highest winter levels of contamination activity an order of magnitude greater than the lowest levels in mid-summer. A secondary effect due to sediment transfer during periods of severe flooding produces subsidiary features on this dominant seasonal profile. Radionuclide concentrations on vegetation are in the range¹³⁷Cs=8–191,¹³⁴Cs=0.3–0.9,²⁴¹Am=0.6–46,²³⁸Pu=0.1–1.5, and^239/240Pu=0.8–44 Bq kg⁻¹. These ranges reflect the relative concentrations of radionuclides in estuarine sediment (¹³⁷Cs=615,²⁴¹Am=202, and^239/240Pu=104 Bq kg⁻¹) rather than the values in filtered estuary water (¹³⁷Cs=0.4,²⁴¹Am=0.001, and^239/240Pu=0.001 Bq 1⁻¹). Median K_d values for these radionuclide species are Cs=1,400, Am=200,000, and Pu=80,000 1 kg⁻¹).     

Small-scale spatial variations of natural radionuclide and trace metal distributions in sediments from the Hudson River estuary

Multiple sediment cores were collected in June 1994 in the turbidity maximum zone of the Hudson River estuary off Manhattan, New York. Results from X-radiography of the sediments and measurements of natural radionuclides (²³⁴Th,⁷Be, and²¹⁰Pb) and trace metals (Ag, Cd, Cu, Pb, and Zn) show significant spatial variability of sediment composition and structure and patchy distributions of radionuclides activities and trace metal concentrations in this small area (0.6 km × 0.5 km). Radionuclide and trace metal analyses confirm prior work (Olsen et al. 1978; Olsen et al. 1981; Hirschberg et al. 1996) that show the western margin area of the river acts as a repository of these chemical constituents at least for the short-term period (0.5–1 yr), and the mid-channel area is not a depositional area for sediments and associated chemical constituents.⁷Be profiles reveal short-term sediment deposition rates ranging from 6 cm yr^?1 to 26 cm yr^?1 in the western margin area. Significant spatial variations in excess²³⁴Th and⁷Be inventories (up to a factor of 10 and 5 for²³⁴Th and⁷Be, respectively) are found in the western margin depositional area, although the inventories are balanced, on average, with in situ production in water column and atmospheric supply. The spatial variation of surficial excess²¹⁰Pb and trace metal concentrations in depositional areas of the western margin are ≤10% for Ag, Cu, Pb, and Zn and 29% for Cd. However, the variations in the transition zone range from 28% to 93%. This variability is likely related to variations in tidal current velocity, bottom shear stress, and river channel morphology.     

Age of Saurashtra miliolites by U-Th decay series methods: possible implications to their origin

The miliolite deposits of Saurashtra have been dated by²³⁴U,²³⁰Th,²³¹Pa and¹⁴C methods. Concordant ages of 10⁵ years using the U decay series isotopes are obtained which agree with the ages of the coral reefs of Okha-Dwaraka coast suggesting a contemporaneous origin for both. The lower¹⁴C ages (≤40,000 years) may be due to a recent influx of seawater or ground water. Quartz and clay minerals together constitute only ≤10% by weight, as such the aeolian characteristics of quartz grains may not be relevant to the origin of the miliolites.     

Sources and history of heavy metal contamination and sediment deposition in Tivoli South Bay, Hudson River, New York

Persistent inorganic constitutents preserved in sediments of aquatic ecosystems record temporal variability of biogeochemical functioning and anthropogenic impacts.²¹⁰Pb and¹³⁷Cs dating techniques were used to study the past variations of heavy metals (Pb, Cu, and Zn) and accumulation rates of sediments for Tivoli South Bay, in the Hudson River National Estuarine Research Reserve ecosystem. South Bay, a tidal freshwater embayment of the Hudson, may play an important role in the sediment dynamics of this important river. The measured sedimentation rate range of 0.59 to 2.92 cm yr⁻¹ suggests that rapid accumulation occurred during the time period represented by the length of the cores (approximately the past 50 yr). Direct measurements of sediment exchange with the Hudson River reveal high variability in the sediment flux from one tidal cycle to the next. Net exchange does not seem to be adequate to explain sediment accumulation rates in the bay as measured by²¹⁰Pb and¹³⁷Cs. The difference may be supplied from upland streams or the Hudson River during storm events. Concentrations of the metals Pb, Cu and Zn were found to be well correlated with each other within individual cores at five of six sites tested. This suggests a common proximate source for the three metals at a specific site. The evidence is consistent with mixing in some environmental compartment before delivery to the bay. While metals self-correlate within individual cores, absolute concentrations, depth distribution patterns, and ratios of the metals to each other vary among the cores collected at different locations within the bay. Organic matter, Fe content, and particle size distribution of sediments do not account for the intercore variations in metal concentration. It is likely that cores collected from different sites may have derived metals from different sources, such as watershed streams and tidal exchange with the Hudson River.