Temporal variability of Pb fluxes and bioturbation in shelf sediments beneath the high primary production area off Concepción, central-southern Chile (36°S)

We estimated monthly fluxes of ²¹⁰Pb in shelf sediments beneath a high productivity area off central-southern Chile (36°S) during 1 year (September 2002-August 2003). Sediment cores were obtained using a multiple corer and were analyzed mainly for ²¹⁰Pb, total pigments, and macrofauna abundance. The ²¹⁰Pb inventories and fluxes were estimated for surface sediments (0-5 cm) and bioturbation coefficients were inferred using chlorophyll-a (reactive) profiles. In general, ²¹⁰Pb content was inversely correlated with phytodetritus fluxes. High photosynthetic pigment contents in surface sediments were consistently associated with lower ²¹⁰Pb contents. Macrofaunal activity responded to oxygen and organic matter supplies at the sediment surface, generally concentrated in the first centimeters, but particularly so during months of high organic matter fluxes and deficient bottom water oxygen conditions. At this study site, several processes involved in the ²¹⁰Pb surface distribution make it difficult to accurately estimate ages at the surface. We postulate that the organic fluxes promote changes in the faunal activity, which, in combination with sediment resuspension and water circulation over the shelf, produce seasonal variations in the ²¹⁰Pb inventories.     

底部边界层颗粒态物质迁移特征的放射性核素分析方法

利用颗粒态放射性核素携带的颗粒物历经过程信息,我们提出用泥沙扩散方程和颗粒态放射性核素扩散方程联解底部边界层颗粒态物质迁移参数的方法。分析实例的样品取自荷兰Waden Sea南部Balgzand潮滩(砂坪)和Mok湾潮滩(泥坪)的两个站位(BG1和Mok2)。示踪核素为~(234)Th,~(210)Pb和~(137)Cs,其放射性比度由r能谱测出。     

Inputs of dissolved and particulate 226Ra to lakes and implications for 210Pb dating recent sediments

Gamma spectroscopy was used to measure radioisotope (²¹⁰Pb, ²²⁶Ra, ¹³⁷Cs) activities in sediment cores from 20 lakes and a wetland in Florida, USA. Nine profiles display relatively low (<5 dpm g^–1) and constant ²²⁶Ra activities, whereas 12 show high (>5 dpm g^–1) and variable ²²⁶Ra activities. In the latter group, most display up-core increases in activity. Upper sediments from two lakes (Round and Rowell) possess very high (>20 dpm g^–1) ²²⁶Ra activities that exceed total ²¹⁰Pb activities, clearly illustrating disequlibrium between ²²⁶Ra and supported ²¹⁰Pb. Supported ²¹⁰Pb activity is generally thought to come from in situ, ²²⁶Ra-containing detrital mineral particles, and is typically assumed to be in secular equilibrium with ²²⁶Ra activity. Since 1966, Round Lake has been augmented hydrologically with ²²⁶Ra-rich (6.2 dpm L^–1) groundwater pumped from the local deep aquifer. Adsorption of dissolved ²²⁶Ra to recent Round Lake sediments probably accounts for the high measured ²²⁶Ra activities and the pronounced disequilibrium between ²²⁶Ra and supported ²¹⁰Pb in topmost deposits. We suspect that many Florida waterbodies receive some ²²⁶Ra-rich runoff and seepage from groundwater pumped for irrigation, residential use, industrial applications, and mining. This may account for up-core increases in ²²⁶Ra activity measured in sediment cores from some Florida lakes. Significant groundwater pumping began within the last century, and there has been insufficient time for supported ²¹⁰Pb to come into equilibrium with adsorbed ²²⁶Ra in uppermost deposits. Input of ²²⁶Ra-rich groundwater to lakes may occur in any geographic region where local bedrock contains ²³⁸U and its daughters. When dissolved ²²⁶Ra adsorbs to recent sediments, it complicates accurate estimation of supported ²¹⁰Pb activity, and confounds calculation of unsupported ²¹⁰Pb activity that is used in dating models.     

Inferring upwelling rates in the equatorial Atlantic using Be measurements in the upper ocean

Ocean upwelling rates are difficult to measure because of the relatively small velocities involved, and therefore are typically inferred from indirect methods such as heat budget estimates or tracer observations. Here we present the first results using a novel technique, based on the isotope ⁷Be, to infer rates of upwelling along the equator. Beryllium-7 (half-life=53.3 d) is a cosmic-ray produced radioactive nuclide that is deposited by rainfall upon the ocean surface and subsequently enriched and homogenized within the mixed layer. Previous investigations have utilized the penetration of characteristically high mixed layer concentrations into the upper thermocline to trace ocean ventilation and subduction over seasonal timescales. Here, the tracer is used in a reverse sense; that is, the ⁷Be concentration in the usually ⁷Be-rich surface mixed layer will be diluted from penetration of ⁷Be “dead” water upwelled from below. This dilution provides a means to infer upwelling rates. Furthermore, with knowledge of upwelling rates, ⁷Be profiles can be used to constrain vertical diffusivity within the upper thermocline. These ideas were tested with samples collected during the Tropical Atlantic Climate Experiment (TACE) cruise (May 22-June 27, 2009). The observations indicated a nearly linear relationship between ⁷Be inventory and mixed layer temperature, as with increased upwelling, lower mixed layer temperatures correspond to greater ⁷Be dilution from depth. With this data, upwelling rates were estimated at a number of stations near the equator between 0°E and 30°W within and adjacent to the equatorial cold tongue. The derived upwelling rates ranged from 0 to 2.2 m/d, with maximum values found between the equator and 2°S. The corresponding K_z values derived for the upper thermocline were in the range 1-4×10⁻⁴ m²/s.     

The off-site implications of deforestation on sedimentation rates and pollution in Abkenar open water (Anzali Lagoon,Caspian Sea) using radionuclide techniques and sediment quality indices

Abkenar open water(AOW)has a 35 km²distribution and is the largest part of the Anzali Lagoon in the southern coastal zone of the Caspian Sea.The effects of deforestation in the upstream basin of the AOW were assessed by measuring the rate of sedimentation,sediment contamination,and ecological risk for aquatic life and end-users using radioisotopes Cesium-137 and Lead-210.The chronology of the AOW sediment column was studied using the Constant Rate of Supply model.Correlations between environmental changes and the sedimentary regime of the study area highlight the contribution of the AOW authorized international and local wood harvesting companies pre-and-post 1950 in the catchment in terms of the rate of sediment supply and the influx of toxic metals.Historical evidence shows that two specific layers formed during World Wars I and II with the mean rates of 0.185±0.04(±STD)and 0.32±0.02 kg/(m²·y),respectively.The highest influx of alkali elements and toxic metals(nickel,cadmium,lead,zinc,and copper)into the basin occurred in 1945.Two layers of gray mud(16-50 cm)and organic-rich dark loss mud(0-16 cm)correlated well with the programmed wood harvesting projects.These layers accumulated from 1953 to 2000 with a mean rate of 0.6±0.2 and 2±0.7 kg/(m²·y).Thus,aquatic life and end-users have been exposed to moderate to extremely high levels of toxic metals and a moderate level of contamination since the 1950s.     

Using GC-MS/Combustion/IRMS to determine the C/C ratios of individual hydrocarbons produced from the combustion of biomass materials--application to biomass burning

Simultaneous mass spectral detection and stable carbon isotope analysis was performed on individual indigenous n-alkanes isolated from single C₄ and C³ plant species and on a series of aliphatic and polycyclic aromatic hydrocarbons (PAH) produced from the combustion of these same biomass materials. The analysis technique used a combined gas chromatograph-mass spectrometer/combustion/isotope ratio mass spectrometer (GC-MS/C/IRMS). Precision (2σ) for replicate measurements of individual compounds in standard solutions using this novel configuration ranged between 0.2 and 0.5‰ for n-alkanes and 0.3 and 0.8‰ for PAH. Accuracy of the n-alkane measurements ranged between 0.1 and 0.4‰ and that of the PAH measurements ranged between 0.2 and 0.9‰. Replicate GC-MS/C/IRMS measurements on the combustion-derived n-alkene/alkane pairs were performed to within a precision of between 0.1 and 1.1‰ and the precision for the combustion PAH was similar to the standard PAH solution. No notable isotopic effects were observed when altering the temperature of the combustion process from 900 to 700°C, or as a result of the individual n-alkenes/alkanes partitioning between the gaseous and condensate fractions. Combustion-derived n-alkenes/alkanes ranged from C₁₁ to C₃₁, and the C₄-derived n-alkenes/alkanes were approx. 8‰ more enriched in ¹³C than the C₃-derived compounds. Both the C₄ and C₃-derived n-alkenes/alkanes (C₂₀-C₃₀) were isotopically similar to the indigenous n-alkanes and were 2-3‰ more depleted in ¹³C than the lower mol. wt (C₁₁₁₁-C₁₉) n-alkenes/alkanes, suggesting an independent origin for the lower mol. wt compounds. Combustion-generated C₄ and C₃-derived 2-, 3-, and 4-ring PAH were also isotopically distinct (Δδ = 10‰). Unlike the n-alkenes/alkanes, no compound-to-compound variations were observed between the low and high mol. wt PAH. This study demonstrates that the isotopic composition of original plant biomass material is mainly preserved in the aliphatic hydrocarbons and PAH generated by its combustion. Consequently, analyses of these compounds in sediments impacted by fire occurrences may provide useful information about paleo-fire activity that may help elucidate the impact biomass burning may have had and could have on climate-biosphere interactions.     

Application of the chlorine-36 method for the delineation of groundwater infiltration of large river systems: example of the Danube River in western Hungary (Szigetköz area)

The gravel aquifer within the Szigetköz Plain in northern Hungary is mainly fed by the infiltration of the Danube River. This infiltration process can be identified using the tritium/helium method to a distance of about 30 km away from the infiltration area of the Danube. In this study, chlorine-36 analyses are used as additional method. This natural radioisotope was also produced by nuclear bomb tests in the atmosphere. It is an ideal, stable constituent for this particular study due to its very long half-life (300,000 years), and consequently acts as an independent check of the established model of aquifer recharge. The chlorine-36 data of the analysed selected groundwater samples of this area clearly show the effect of the atmospheric nuclear bomb tests, with enhanced ³⁶Cl/Cl ratios of up to a factor 10 higher than the unaffected groundwater of the pre-bomb period within the study area. Finally, the observed ³⁶Cl values were introduced into a transport model with dispersion/advection-type flow of groundwater to deduce the transport parameters.     

Hydrochemical and isotopic behaviour of a Saharan phreatic aquifer suffering severe natural and anthropic constraints (case of Oued-Souf region, Algeria)

An approach combining the use of water dissolved chemical species and isotopic fingerprints has been used to understand the behavior of a phreatic aquifer and to determine the origin of its different water components. This aquifer is located in the large sedimentary basin of the Great Oriental Erg (Algeria) and overlies two deeper aquifers: the Complexe Terminal (CT) and the Continental Intercalaire (CI). Besides the deterioration of its groundwater quality, its water table has risen during the last 20 years. A water budget surplus between 950 and 2500 l s^?1 was estimated. Down-gradient groundwater evolution (south-north) has shown that the mineralisation increases from 1.23 to 5.20 g l^?1 due to evaporite minerals dissolution. Chemical and isotopic data demonstrated that in addition to rainfall there is a contribution from the CT and CI aquifers. The latter are tritium-free and less mineralized than the phreatic aquifer. Their radiocarbon contents are very low (<10 pmC, percent modern Carbon) (Pleistocene recharge) whereas quite the contrary is observed for the superficial aquifer which exhibits fairly high and variable C-14 activities (50–100 pmC), evidence of recent recharge. On the basis of tritium contents, two groundwater groups were identified for the phreatic aquifer.