Celebrating the twentieth anniversary of EFM

Environmental Fluid Mechanics -     

Polonium (210Po) and lead (210Pb) in marine organisms and their transfer in marine food chains

The determination of ²¹⁰Po and ²¹⁰Pb was performed in marine organisms from the seashore to abyssal depths, encompassing a plethora of species from the microscopic plankton to the sperm whale. Concentrations of those radionuclides ranged from low values of about 5 × 10⁻¹ Bq kg⁻¹ (wet wt.) in jellyfish, to very high values of about of 3 × 10⁴ Bq kg⁻¹ (wet wt.) in the gut walls of sardines, with a common pattern of ²¹⁰Po > ²¹⁰Pb.These radionuclides are primarily absorbed from water and concentrated by phyto- and microzooplankton, and then are transferred to the next trophic level along marine food chains. Investigation in epipelagic, mesopelagic, bathypelagic and abyssobenthic organisms revealed that ²¹⁰Po is transferred in the marine food webs with transfer factors ranging from 0.1 to 0.7, and numerically similar to those of the energy transfer in the marine food chains. As ²¹⁰Po preferentially binds to amino acids and proteins, its transfer in food chains likely traces protein transfer and, thus, ²¹⁰Po transfer factors are similar to ecotrophic coefficients. ²¹⁰Pb is transferred less efficiently in marine food chains and this contributes to increased ²¹⁰Po:²¹⁰Pb activity ratios in some trophic levels.     

PCDD/Fs and dioxin-like PCBs in sediment and biota from the Mondego estuary (Portugal)

The concentrations of 17 polychlorinated dibenzo-p-dioxins and furans (PCDD/Fs), and 12 dioxin-like polychlorinated biphenyls (dl-PCBs) were measured in sediment and key species as an initial investigation on PCDD/Fs and dl-PCBs contamination in the Mondego estuary (Portugal). The results demonstrated that the values of the total PCDD/Fs (∑PCDD/Fs) concentrations were considerably lower than those of the sum of dl-PCBs (∑dl-PCBs) in all the studied samples. Regarding the contribution of individual congeners, OCDD was the predominant PCDD/F and the mono-ortho PCB 118 and PCB 105 were the dominant PCBs in the majority of the samples. Our results suggest that PCDD/Fs and PCBs behave quite differently along the aquatic food web: ∑PCDD/Fs concentrations were lower in higher trophic-level organisms with fish presenting a distinct PCDD/Fs congeners profile; on the contrary, the higher ∑dl-PCBs values were found in upper-level biota, although not exclusively, and quite similar dl-PCBs congener profiles were observed in nearly all the studied species.     

Penetrative convection in slender containers

An experimental study was conducted to investigate the penetration of a convective mixed layer into an overlying stably (solutally) stratified layer contained in a narrow, tall vessel when the fluid is subjected to a destabilizing heat flux from below. The interest was the evolution of the bottom mixed-layer height (\(h\)) with time (\(t\)) in the presence of side-wall effects, but without the formation of conventional double-diffusive layers. The side-wall effects are expected at small mixed-layer aspect ratios, \(\varGamma_{h} = (W/h)\), where \(W\) is the container width. This case has not been studied hitherto, although there are important environmental and industrial applications. The mixed-layer growth laws for low aspect ratio convection were formulated by assuming a balance between the vertical kinetic energy flux at the interface and the rate of change of potential energy of the fluid system due to turbulent entrainment. The effects of sidewalls were considered using similarity arguments, by taking characteristic rms velocities to be a function of \(\varGamma_{h}\), in addition to buoyancy flux (\(q_{0}\)) and \(h\). In all stages of evolution, the similarity variables \(\xi = h/W\) and \(t^{\prime } = Nt/A\), where \(A = N^{3} W^{2} /4q_{0}\) and \(N\) is the buoyancy frequency, scaled the mixed-layer evolution data remarkably well. Significant wall effects were noted when \(\varGamma_{h} < 1\), and for this case the interfacial vertical turbulent velocity and length scales were identified via scaling arguments and experimental data.     

Photochemical generation of reactive intermediates from urban-waste bio-organic substances under UV and solar irradiation

Singlet oxygen (¹O₂), hydroxyl radicals (^•OH), and excited triplet states of organic matter (³OM^*) play a key role in the degradation of pollutants in aquatic environments. The formation rates and quantum yields (Φ) of these reactive intermediates (RI) through photosensitized reactions of dissolved organic matter (DOM) have been reported in the literature for decades. Urban biowaste-derived substances (UW-BOS), a form of organic matter derived from vegetative and urban waste, have recently been shown to be efficient sensitizers in the photo-degradation of different contaminants. Nevertheless, no quantitative measurements of photo-oxidant generation by UW-BOS have been reported. In this study, the formation quantum yields of ¹O₂ and ^•OH, as well as quantum yield coefficients of TMP degradation (indicative of ³OM^* formation), were quantified for two UW-BOS samples, under 254-nm UV radiation or simulated sunlight and compared to a DOM standard from the Suwanee River (SRNOM). Values of Φ for UW-BOS samples ranged from Φ(+¹O₂) = 8.0 to 8.8 × 10⁻³, Φ(+^•OH) = 4.1 to 4.3 × 10⁻⁶, and f _TMP = 1.22 to 1.23 × 10² L Einstein⁻¹ under simulated sunlight and from Φ(+¹O₂) = 1.4 to 2.3 × 10⁻², Φ(+^•OH) = 1.3 to 3.5 × 10⁻³, and f _TMP = 3.3 to 3.9 × 10² L Einstein⁻¹ under UV. Although UW-BOS are not necessarily better than natural DOM regarding photosensitizing properties, they do sensitize the production of RI and could potentially be used in engineered treatment systems.

     

The effects of different CCS technological scenarios on EU low-carbon generation mix

Carbon capture and storage technology (CCS), a technology to reduce the emissions in coal and gas power generation plants, will play an important role in the achievement of the European Union emissions reduction objective. In the European Union, energy policies are articulated around three different elements: measures to promote renewable energy technologies, the emissions certificates system and both energy-saving and energy-efficiency policies. The succession of directives and communications from the EU Commission on renewable technology generation share targets and the implementation of the European Emissions Market exemplify the serious EU commitment to a more environmentally friendly future. CCS technologies—together with RES technologies—are thus key to achieve the European emissions reduction target. Although the CCS commercial availability is not guaranteed—due to a slow technological development—some institutions, such as the Institute for Prospective Technological Studies, assume, for 2030 horizon, a quick development of this technology, growing until a maximum participation of an 18 % over the fossil fuels total generation. An eventual non-availability of these technologies in 2030 could increase the cost of this objective in a 70 %. Therefore, the achievement of pollutant emissions reduction targets depends on a correct design of the European generation technologies mix, which should include CCS technologies. Nevertheless, the uncertainty about the final costs and economic risk of these technologies makes a question about their future role to arise. This paper analyses the effects of different variations in the cost and risk of the CCS technologies (scenarios) over the European power technologies mix. The results confirm the need of the availability of these technologies in 2030, beyond the potential costs and risks of both options. The reason lies in the methodological approach of portfolio theory, which allows an analysis from an efficient portfolio point of view.     

Hydroclimatic changes and drivers in the Sava River Catchment and comparison with Swedish catchments

In this study, we investigate long-term hydroclimatic changes and their possible relation to regional changes in climate, land-use and water-use over the twentieth century in the transboundary Sava River Catchment (SRC) in South Eastern Europe. In a hydropower dominated part of the SRC, unlike in an unregulated part, we find increase in average annual evapotranspiration and decrease in temporal runoff variability, which are not readily explainable by observed concurrent climate change in temperature and precipitation and may be more related to landscape-internal change drivers. Among the latter investigated here, results indicate hydropower developments as most closely related to the found hydroclimatic shifts, consistent with previous such indications in studies of Swedish hydropower catchments. Overall, the present results have quantitatively framed the recent history and present state of hydroclimate in the SRC, of relevance for water resources in several countries and for a majority of their populations. This provides a useful basis for further assessment of possible future hydroclimatic changes, under different scenarios of climate change and land/water-use developments in the region.

Electronic supplementary material

The online version of this article (doi:10.1007/s13280-015-0641-0) contains supplementary material, which is available to authorized users.     

An alternative supercritical fluid extraction system for aqueous matrices and its application in pesticides residue analysis

Abstract

Supercritical fluid extraction (SFE) is a rapid and convenient method for the isolation of organic compounds from environmental samples. This paper describes a supercritical carbon dioxide (CO₂) extraction system that uses a newly designed extraction cell to recover organic compounds from an aqueous matrix. Analysis of the extracts by gas chromatography‐electron capture detector (GC‐ECD) indicated that the herbicide trifluralin (2,6‐dinitro‐N,N‐dipropyl‐4‐trifluoromethylaniline) could be quantitatively extracted by using the SFE system proposed with small amounts of sample. The percentage of recovery obtained with the SFE system described was twice as high as the result obtained using a conventional solid‐phase extraction technique. Extraction by SFE was completed in a short period of time using a simple and low‐cost home‐made system that did not require the use of organic solvents.     

Low-level arsenic exposure is associated with bladder cancer risk and cigarette smoking: a case–control study among men in Tunisia

Although exposure to high levels of arsenic is associated with excess bladder cancer risk, lower exposures generally are not. This study represents the first biomonitoring of arsenic exposure in Tunisia and focuses on a possible association with bladder cancer risk. In this context, 124 male bladder cancer cases and 220 controls were recruited and blood samples were analyzed to determine the concentration of As. The study subjects were stratified into median groups based on concentrations of arsenic in their blood. Blood arsenic (B-As) was significantly two to threefold higher in bladder cancer cases than in controls (p?<?0.05). The arsenic concentrations were significantly higher among both smokers and workers in construction. However, neither drinking water nor seafood was found to be incriminated as exposure sources. The adjusted risk ratios for B-As concentration categories 0.1–0.67 and ≥0.67 μg/L were 0.18 (95% CI?=?0.014–2.95) and 2.44 (95% CI?=?1.11–5.35), respectively. Arsenic levels were not found to be associated with tumor grade or stage. The considerable risk in the category of highest cumulative exposure argues for an association between bladder cancer risk and low-level arsenic exposure. Future investigations with larger samples and using techniques that allow the distinction of the different arsenic species should better elucidate this association. Furthermore, the modulation of arsenic level according to the histological grade may be of potential to be used as a diagnostic marker of the disease process and its possible relationship etiologically.     

Field application of palladized iron for the dechlorination of trichloroethene

Palladized iron (Pd/Fe) has been tested under field conditions for the dechlorination of trichloroethene (TCE) in groundwater. Contaminated water was pumped from aquifers in Ohio (0.7– 1.5 mg/l TCE) and Missouri (2–9 mg/l TCE and 1,2-dichloroethene) and passed through columns of Pd/Fe. The experiments demonstrated that the dechlorination reaction occurs efficiently until the surface of the Pd/Fe becomes fouled. Regeneration of the surface with dilute (1M) hydrochloric acid is easily accomplished under laboratory conditions, but initially was unsuccessful in the field. Further experiments indicated, that reduced sulfur species, although not naturally present in the groundwater being treated, were permanently poisoning the palladium. Apparently, sulfur-reducing bacteria utilize the hydrogen produced by the Pd/Fe process and reduce the sulfate that is present. An anion exchange column was used to remove sulfate (20 mg/l) from groundwater at the Kansas City Plant in order to test this theory. Under these conditions, a column of Pd/Fe was repetitively regenerated for a 4-week period. A second column, not protected by sulfate removal, could not be regenerated. The results demonstrated that Pd/Fe could be used in a long-term field process if a material with more resistance to Fe and Pd losses is developed.