The qualities of a laser diffraction grain size analyser, the Coulter LS-100 (range claimed by the manufacturer: 0.4-900 mum in a single measurement), are evaluated on sediments of fluvial and lacustrine origin. Accuracy and resolution of measurement on standard latex spheres are excellent. Reproducibility of the results on natural sediments appears to be satisfactory, but the method underestimates the fraction of clay particles with an efficiency of detection (36-70%) proportional to the clay content determined from pipette analysis. This efficiency is somewhat higher than those reported from other instruments of the same generation. Comparison of the Coulter LS-100 with other sizing techniques shows good agreement with the sieving method but some differences appear with the electroresistance particle technique: median and mean size values measured by the Coulter Counter TA1 are systematically lower than those obtained by the Coulter LS-100. Analyses show good correlation with those of a Malvern Laser particle analyser but a discrepancy appears with very fine silt and clay sized sediments. The Coulter LS-100 detects a higher clay content than that measured with the Malvern Laser Sizer 2600. Except when precise measurements of clay content are needed, the Coulter LS-100 produces precise and accurate results in size ranges required for geological and environmental studies
During this century, the characteristics of the Upper Rhone River discharge, flowing into Lake Geneva, have been altered in response to the changes which have occurred in its watershed. Principally, numerous hydroelectric dams have been constructed on the course of the Rhone River tributaries. At present the major reservoirs can hold about 1220 10(6) m(3) of water, which represents 1/5 of the total annual Rhone River flow. Flow regime characteristics of the river have been modified by the dam operations. Water is released from reservoirs during winter and stored in summer. Large floods have also been reduced in amplitude and frequency. From the available literature data, sediment rating curves have been calculated and used to estimate the evolution of the sediment load from the Rhone River to Lake Geneva. They show that sediment input has decreased by at least a factor 2. This reduction has impacted the occurrence of underflows along the lake bottom, due to the reduction of sediment-laden floods, which in turn may have considerable negative effects on the reoxygenation of Lake Geneva deep waters
Abstract. Suspended sediment export from large Alpine catchments ( > 1000 km 2 ) over decadal timescales is sensitive to a number of factors, including long-term variations in climate, the activation-deactivation of different sediment sources (proglacial areas, hillslopes, etc.), transport through the fluvial system, and potential anthropogenic impacts on the sediment flux (e.g. through impoundments and flow regulation). Here, we report on a marked increase in suspended sediment concentrations observed near the outlet of the upper Rhône River Basin in the mid-1980s. This increase coincides with a statistically significant step-like increase in basin-wide mean air temperature. We explore the possible explanations of the suspended sediment rise in terms of changes in water discharge (transport capacity), and the activation of different potential sources of fine sediment (sediment supply) in the catchment by hydroclimatic forcing. Time series of precipitation and temperature-driven snowmelt, snow cover, and ice melt simulated with a spatially distributed degreeday model, together with erosive rainfall on snow-free surfaces, are tested to explore possible reasons for the rise in suspended sediment concentration. We show that the abrupt change in air temperature reduced snow cover and the contribution of snowmelt, and enhanced ice melt. The results of statistical tests show that the onset of increased ice melt was likely to play a dominant role in the suspended sediment concentration rise in the mid-1980s. Temperature-driven enhanced melting of glaciers, which cover about 10 % of the catchment surface, can increase suspended sediment yields through an increased contribution of sediment-rich glacial meltwater, increased sediment availability due to glacier recession, and increased runoff from sediment-rich proglacial areas. The reduced extent and duration of snow cover in the catchment are also potential contributors to the rise in suspended sediment concentration through hillslope erosion by rainfall on snow-free surfaces, and increased meltwater production on snow-free glacier surfaces. Despite the rise in air temperature, changes in mean discharge in the mid-1980s were not statistically significant, and their interpretation is complicated by hydropower reservoir management and the flushing operations at intakes. Overall, the results show that to explain changes in suspended sediment transport from large Alpine catchments it is necessary to include an understanding of the multitude of sediment sources involved together with the hydroclimatic conditioning of their activation (e.g. changes in precipitation, runoff, air temperature). In addition, this study points out that climate signals in suspended sediment dynamics may be visible even in highly regulated and human-impacted systems. This is particularly relevant for quantifying climate change and hydropower impacts on streamflow and sediment budgets in Alpine catchments.
a b s t r a c tContinuous high-resolution sedimentary record of heavy metals (chromium (Cr), copper (Cu), lead (Pb), zinc (Zn), manganese (Mn), and mercury (Hg)), from lakes Lucerne and Meidsee (Switzerland), provides pollutant deposition history from two contrasting Alpine environments over the last millennia. The distribution of conservative elements (thorium (Th), scandium (Sc) and titanium (Ti)) shows that in absence of human disturbances, the trace element input is primarily controlled by weathering processes (i.e., runoff and erosion). Nonetheless, the enrichment factor (EF) of Pb and Hg (that are measured by independent methods), and the Pb isotopic composition of sediments from the remote lake Meidsee (which are proportionally more enriched in anthropogenic heavy metals), likely detect early mining activities during the Bronze Age. Meanwhile, the deposition of trace elements remains close to the range of natural variations until the strong impact of Roman activities on atmospheric metal emissions. Both sites display simultaneous increases in anthropogenic trace metal deposition during the Greek and Roman Empires (ca 300 BC to AD 400), the Late Middle Ages (ca AD 1400), and the Early Modern Europe (after ca AD 1600). However, the greatest increases in anthropogenic metal pollution are evidenced after the industrial revolution of ca AD 1850, at low and high altitudes. During the twentieth century, industrial releases multiplied by ca 10 times heavy metal fluxes to hydrological systems located on both sides of the Alps. During the last decades, the recent growing contribution of low radiogenic Pb further highlights the contribution of industrial sources with respect to wood and coal burning emissions.
As the methylation of inorganic mercury to neurotoxic methylmercury has been attributed to the activity of anaerobic bacteria, the formation of methylmercury in the oxic water column of marine ecosystems has puzzled scientists over the past years. Here we show for the first time that methylmercury can be produced in particles sinking through oxygenated water column of lakes. Total mercury and methylmercury concentrations were measured in the settling particles and in surface sediments of the largest freshwater lake in Western Europe (Lake Geneva). While total mercury concentration differences between sediments and settling particles were not significant, methylmercury concentrations were about ten-fold greater in settling particles. Methylmercury demethylation rate constants (k) were of similar magnitude in both compartments. In contrast, mercury methylation rate constants (k) were one order of magnitude greater in settling particles. The net potential for methylmercury formation, assessed by the ratio between the two rate constants (k k), was therefore up to ten fold greater in settling particles, denoting that in situ transformations likely contributed to the high methylmercury concentration found in settling particles. Mercury methylation was inhibited (∼80%) in settling particles amended with molybdate, demonstrating the prominent role of biological sulfate-reduction in the process.
Chlor-alkali plants using mercury (Hg) cell technology are acute point sources of Hg pollution in the aquatic environment. While there have been recent efforts to reduce the use of Hg cells, some of the emitted Hg can be transformed to neurotoxic methylmercury (MeHg). Here, we aimed (i) to study the dispersion of Hg in four reservoirs located downstream of a chlor-alkali plant along the Olt River (Romania) and (ii) to track the activity of bacterial functional genes involved in Hg methylation. Total Hg (THg) concentrations in water and sediments decreased successively from the initial reservoir to downstream reservoirs. Suspended fine size particles and seston appeared to be responsible for the transport of THg into downstream reservoirs, while macrophytes reflected the local bioavailability of Hg. The concentration and proportion of MeHg were correlated with THg, but were not correlated with bacterial activity in sediments, while the abundance of hgcA transcript correlated with organic matter and Cl− concentration, indicating the importance of Hg bioavailability in sediments for Hg methylation. Our data clearly highlights the importance of considering Hg contamination as a legacy pollutant since there is a high risk of continued Hg accumulation in food webs long after Hg-cell phase out
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.