Sorption and anaerobic biodegradation of soluble aromatic compounds during groundwater transport. 1. Laboratory column experiments

. This paper deals with sorption and anaerobic biodegradation of the soluble aromatic fraction of jet fuel and how it is influenced by pore-water velocity during transport in a groundwater aquifer. The study was carried out as controlled laboratory column experiments. A binary mixture of toluene and 1,2,4-trimethylbenzene with a concentration ratio of 2:1 was used through the entire investigations. The column experiments were conducted with contaminated sediments and groundwater, taken from wells at a field research site. The columns were operated anaerobically under continuous-flow conditions at 10 °C in a temperature-controlled refrigerator. Two percent sodium azide was added to the injection solution of two of the columns to prevent biodegradation of the studied organic mixture. Chloride was used as a conservative tracer to characterize the hydrodynamic parameters such as dispersivity and porosity of the columns. The results showed that both compounds in the mixture were attenuated because of sorption and biodegradation processes in the columns. 1,2,4-trimethylbenzene was attenuated more significantly than toluene. Biodegradation of toluene was coupled mainly with the microbial reduction of ferric iron, whereas 1,2,4-trimethylbenzene, in contrast, was mostly sorbed. Their sorption and biodegradation were studied with different pore-water velocities, and a mass balance approach was applied to calculate biodegradation rates. The biodegradation rates of toluene were –0.16, –0.21, and –0.26 (unit: mM day^–1) for pore-water velocities of 96, 82.4, and 54.9 (unit: cm day^–1), respectively. This indicates that a decrease in the pore-water velocity significantly enhanced the biodegradation of toluene, consistent with other reports in the literature. For 1,2,4-trimethylbenzene the biodegradation rates were –0.05, –0.13 (unit: mM day^–1) for pore-water velocities of 96 and 82.4 (unit: cm day^–1), respectively. The biodegradation rate of 1,2,4-trimethylbenzene did not increase at the lowest pore water velocity as expected. This might be a result of substrate competition.     

The effect of copper-treated net pens on farmed salmon (Salmo salar) and other marine organisms and sediments

Samples of Atlantic salmon (Salmo salar), saithe (Pollacius virens), blue mussel (Mytilus edulis), brown seaweed (Ascophyllum nodosum) and sediment were collected from six different fish farms. Five of the farms used net pens treated with copper-containing coatings, whereas one farm did not use copper-containing coating (this was used as a reference location). Samples of muscle, liver and gills of Atlantic salmon and saithe, blue mussel and brown seaweed were freeze dried, homogenised, wet digested and analysed for copper by flame atomic absorption spectrometry. The results showed no significant differences in copper concentrations among the samples from the different locations. The copper contents of some of the samples appeared to be in the upper part of the normal concentration range. From a nutritional point of view, the use of copper-coatings on net pens did not affect the quality of the seafood products either within, or around the net pen.     

Coastal profile response to sea level rise: a process‐based approach

Prevailing ideas and calculations of coastal response to sea level rise (SLR) are often based on the Bruun model (Bruun P., Sea‐level rise as a cause of shore erosion, Journal Waterways Harbors Division, ASCE 88 : 117–130, 1962) that predicts upward and landward transfer of an equilibrium profile during SLR through offshore sediment transport on the shoreface. The model is based on a number of assumptions of questionable validity as well as outdated concepts on how sediment is transported across the shoreface. This contribution takes a numerical modelling approach that is based on first‐order processes contributing to the movement of sediment across the shoreface. Using a wave transformation model that predicts hydrodynamic processes driving cross‐shore sediment transport and an energetics‐based model for the coupling between hydrodynamics and sediment transport, we show that cross‐shore sediment transport is mainly onshore directed at the boundary between the lower and the upper shoreface, in agreement with the model proposed by Davidson‐Arnott (Conceptual model of the effects of sea level rise on sandy coasts, Journal of Coastal Research 21 : 1166–1172, 2005). The transition from onshore to offshore directed transport is located well within the surf zone and with a rising sea level this transition point becomes displaced landward and upward. Tests also show that substrate slope is of fundamental importance to the manner in which beaches react to rising sea level. Copyright © 2012 John Wiley & Sons, Ltd.     

Trace Element Partitioning between Taenite and Kamacite; Relationship to the Cooling Rates of Iron Meteorites

Abstract— Instrumental neutron activation analysis (INAA) was used to determine Ni, Co, Cu, Ga, As, Au, W, Re and Ir in taenite lamellae isolated by acid dissolution from eight iron meteorites from groups IA, IIIAB and IVA. Taenite is enriched in Ni, Cu, Ga, As, Au, W, Re and Ir relative to kamacite, whereas taenite is depleted in Co. Taenite/kamacite partition ratios in slowly cooled IAB meteorites are farther from unity than those in rapidly cooled IVA meteorites. Taenite/kamacite partition ratios for Cu, Ir, Au and Co may be sensitive cooling rate indicators.     

New multifunctional hunting landscapes in Denmark

Between 1992 and 2008 subsidization of mandatory set aside land under the EU Common Agricultural Policy (CAP) gave rise to the establishment of a characteristic type of multifunctional hunting landscapes in Denmark, primarily located on fallow land in tilled valley bottoms. A national survey of these landscapes in 2006 has been carried out and 1061 hunting areas have been identified nationwide. Subsidies relating to set aside land acted as a supplementary type of income, which supported the development of multifunctional land use on marginal soils where the income from hunting and subsidies in combination was a viable alternative to monofunctional rotational agriculture. Hunting landscapes developed as the consequence of landscape management strategies designed to comply with the requirements of the CAP while improving habitat conditions for wildlife and increasing income from hunting rental activities. Forty-seven percent of the hunting landscapes in 2006 were in rotational production in 2010 while 19% were used for other agricultural purposes and 34% were taken out of the subsidy regime and removed from the general agricultural register. In 2012, a total of 431 such areas ? 41% of the areas identified in 2006 ? were still used for hunting. The number and geographical distribution of the hunting landscapes seems closely related to the potential average hunting rent, the level of urbanisation and the occurrence of manorial estates with traditions for multifunctional land use as part of their economic strategy. Implications for the ongoing discussion on land use policy concerning land sharing vs. land sparing is discussed.     

On the potential for CO2 mineral storage in continental flood basalts – PHREEQC batch- and 1D diffusion–reaction simulations

Continental flood basalts (CFB) are considered as potential CO₂ storage sites because of their high reactivity and abundant divalent metal ions that can potentially trap carbon for geological timescales. Moreover, laterally extensive CFB are found in many place in the world within reasonable distances from major CO₂ point emission sources. Based on the mineral and glass composition of the Columbia River Basalt (CRB) we estimated the potential of CFB to store CO₂ in secondary carbonates. We simulated the system using kinetic dependent dissolution of primary basalt-minerals (pyroxene, feldspar and glass) and the local equilibrium assumption for secondary phases (weathering products). The simulations were divided into closed-system batch simulations at a constant CO₂ pressure of 100?bar with sensitivity studies of temperature and reactive surface area, an evaluation of the reactivity of H₂O in scCO₂, and finally 1D reactive diffusion simulations giving reactivity at CO₂ pressures varying from 0 to 100?bar. Although the uncertainty in reactive surface area and corresponding reaction rates are large, we have estimated the potential for CO₂ mineral storage and identified factors that control the maximum extent of carbonation. The simulations showed that formation of carbonates from basalt at 40?C may be limited to the formation of siderite and possibly FeMg carbonates. Calcium was largely consumed by zeolite and oxide instead of forming carbonates. At higher temperatures (60 ?C 100?C), magnesite is suggested to form together with siderite and ankerite. The maximum potential of CO₂ stored as solid carbonates, if CO₂ is supplied to the reactions unlimited, is shown to depend on the availability of pore space as the hydration and carbonation reactions increase the solid volume and clog the pore space. For systems such as in the scCO₂ phase with limited amount of water, the total carbonation potential is limited by the amount of water present for hydration of basalt.