Performance of the In Situ Microcosm Technique for Measuring the Degradation of Organic Chemicals in Aquifers

An in situ microcosm (ISM) consists of a stainless steel cylinder isolating about 2 L of the aquifer and is equipped with valves allowing for loading and sampling from the ground surface. During the last five years, this technique has been used frequently to study the degradation of organic chemicals in polluted and pristine aquifers representing different redox environments. The ISM technique has great potential for providing field-relevant degradation potentials and rate constants, but care must be taken in using the equipment and interpreting the results. This paper provides details concerning the installation and operation of an ISM and presents experiences concerning data interpretation and monitoring of redox conditions.     

Time dependence of organic matter decay and mixing processes in Framvaren, a permanently anoxic fjord in South Norway

Three different layers have been identified in Framvaren, which has a maximum water depth of 184 m. One oxic layer above the redoxcline at 18–20 m. One anoxic layer from 20 to 100 m which is occasionally ventilated by a flow over the sill (which has a depth of 2.5 m), and finally a stagnant layer below 100 m. Using the release rate of silica from the bottom and measurements of the concentration of HTO it is possible to make some calculations on the annual volume of interleaving in the layers 25–50 m, 50–75 m, and 75–100 m together with the advective flows. Reliable values of the sulfide concentration were obtained by precipitating and weighing HgS together with careful protection of all anoxic water samples with argon. The light yellow color of the precipitate in the depth range 25 to 80 m indicates that the occasional ventilation will cause such reactions as 0.50₂ + H₂S S(colloidal) + H₂O. The elemental sulfur, being stabilized with HS^–, is set free upon the precipitation of HgS. The new data for the concentration of sulfide give an acceptable stoichiometry for the decay reaction of organic matter. This is not the case with the data of Yao and Millero. The mean values for the concentrations of ammonium and phosphate agree with the new data of Yao and Millero. The mol/mol C/N ratio of 10.1 found in trapped material by Naess and coworkers (1988) agrees with the stoichiometry of the dissolved constituents, i.e. C/N = 9.92 ± 0.45. A denitrification reaction is suggested to explain the high values of C/N. The vertical diffusion coefficient at 100 m calculated from the depth profile of silica was 0.92 × 10^–6 m² s^–1 which lies in the range of values given by Fröyland. Finally, the ¹⁴C age of the total dissolved inorganic carbon (Ct) in the water below 90 m was about 1600 years indicating a bioproduction in the period 8000 years B.P. to A.D. 1853 when a channel was opened between the fjord outside (Helvikfjord) and Framvaren.     

Gold in the volcanogenic mercury-rich sulfide deposit Långsele,Skellefte ore district,northern Sweden

The mineralogy of gold from a volcanogenic sulfide deposit in northern Sweden (Långsele) was studied. The enrichment of gold and silver in massive ore occurs associated with an intrusive metadolerite vein which can be traced across the ore. The emplacement of this vein mobilized the precious metals together with galena and Pb-Sb sulfosalts into fractures and low pressure zones. A high mercury content at L»ngsele (average 250 ppm) has influenced the gold mineralogy. Thus, gold occurs as Au-Ag amalgam, native gold and rarely as aurostibite (AuSb₂). The results of microprobe analyses of amalgam cluster around Au_0.45Ag_0.45Hg_0.10. The composition of ternary amalgam is discussed in connection with the synthetic Au-Ag-Hg system. Furthermore, native gold was found myrmekitically integrown with stibnite which has been interpreted as a breakdown product of aurostibite at low temperature.     

Upper lithospheric seismic velocity structure across the Pripyat Trough and the Ukrainian Shield along the EUROBRIDGE'97 profile

We present new results on the structure resulting from Palaeoproterozoic terrane accretion and later formation of one of the aulacogens in the East European Platform. Seismic data has been acquired along the 530-km-long, N–S-striking EUROBRIDGE'97 traverse across Sarmatia, a major crustal segment of the East European Craton. The profile extends across the Ukrainian Shield from the Devonian Pripyat Trough, across the Palaeoproterozoic Volyn Block and the Korosten Pluton, into the Archaean Podolian Block. Seismic waves from chemical explosions at 18 shot points at approximately 30-km intervals were recorded in two deployments by 120 mobile three-component seismographs at 3–4 km nominal station spacing. The data has been interpreted by use of two-dimensional tomographic travel time inversion and ray trace modelling. The high data quality allows modelling of the P- and S-wave velocity structure along the profile. There are pronounced differences in seismic velocity structure of the crust and uppermost mantle between the three main tectonic provinces traversed by the profile: (i) the Pripyat Trough is a ca. 4-km-deep sedimentary basin, fully located in the Osnitsk–Mikashevichi Igneous Belt in the northern part of the profile. The velocity structure is typical for a Precambrian craton, but is underlain by a ca. 5-km-thick lowest crustal layer of high velocity. The development of the Pripyat Trough appears to have only affected the upper crust without noticeable thinning of the whole crust; this may be explained by a rheologically strong lithosphere at the time of formation of the trough. (ii) Very high seismic velocity and Vp/Vs ratio characterise the Volyn Block and Korosten Pluton to a depth of 15 km and probably also the lowest crust. The values are consistent with an intrusive body of mafic composition in the upper crust that formed from bimodal melts derived from the mantle and the lower crust. (iii) The Podolian Block is close to a typical cratonic velocity structure, although it is characterised by relatively low seismic velocity and Vp/Vs ratio. A pronounced SW-dipping mantle reflector from Moho to at least 70 km depth may represent the Proterozoic suture between Sarmatia and Volgo–Uralia, the structure from terrane accretion, or a later shear zone in the upper mantle. The sub-Moho P-wave seismic velocity is high everywhere along the profile, with the exception of the area above the dipping reflector. This velocity change further supports a plate tectonic origin of the dipping mantle reflector. The profile demonstrates that structure from Palaeoproterozoic plate tectonic processes are still identifiable in the lithosphere, even where younger metamorphic equilibration of the crust has taken place.     

Intrinsic biodegradation of toluene coupled to the microbial reduction of ferric iron: laboratory column experiments

Intrinsic biodegradation of toluene coupled with the microbial reduction of ferric iron (Fe(III)) as the terminal electron acceptor was studied by using laboratory column experiments under continuous flow conditions. Columns were packed with contaminated aquifer sediment and N₂-purged groundwater taken from the western part of the Gardermoen aquifer. The columns were operated anaerobically at 8 °C (in-situ temperature). Chloride was initially used to characterize flow properties of the columns. Intrinsic biodegradation of toluene, including abiotic loss and biological loss, was estimated by comparing breakthrough curves of toluene for live columns and sterilized control columns based on mass balance in steady-state conditions. The column experiments were run at two different flow velocities. The estimated average intrinsic rate was -0.73 and -0.53 mM day^-1 for pore-water velocities of 1.75 and 2.68 cm h^-1, respectively, corresponding to -0.27 and -0.22 mM day^-1 in biological loss rate. The results indicate that intrinsic biodegradation of toluene could be used as an efficient remediation approach for contaminated groundwater at the Gardermoen fire-fighting training site.     

Sorption and anaerobic biodegradation of soluble aromatic compounds during groundwater transport. 2. Computer modeling

. The natural attenuation of a binary mixture of toluene and 1,2,4-trimethylbenzene, which was previously experimentally demonstrated in anaerobic column experiments, was simulated with the newly-developed PHREEQC model to reveal the biogeochemical processes involved. The processes considered in this model include advection, diffusion, sorption, redox reactions (e.g., oxidation of toluene and 1,2,4-trimethylbenzene coupled to the reduction of microbial ferric iron), precipitation of secondary minerals such as siderite and magnetite, and dissolution of hydrous ferric oxides, as well as other thermodynamic equilibrium reactions. The functions of advection and diffusion built into the PHREEQC were conventionally simulated. The sorption was kinetically simulated based on a bicontinuum model, whereas biodegradation was described using a multiple-term Monod model. The processes mentioned above were coupled with a geochemical equilibrium model. The consistency between the experimental and modeling results indicates that the processes defined and the controlling parameters chosen could describe the coupled interactions between transport and biogeochemical reactions for the studied system. The discrepancy between modeling and experimental observations, however, also revealed the limitation of the modeling approach. In general, the model approach, which incorporates simplified mathematical representations of the true physico-chemical dynamics of the sorption and biodegradation processes of toluene and 1,2,4-trimethylbenzene under anaerobic conditions is a very efficient and good predictive tool in management and remediation of contaminant groundwater aquifers.     

Holocene glacial history and sea-level changes on James Ross Island,Antarctic Peninsula

A reconstruction of deglaciation and associated sea-level changes on northern James Ross Island, Antarctic Peninsula, based on lithostratigraphical and geomorphological studies, shows that the initial deglaciation of presently ice-free areas occurred slightly before 7400 ¹⁴C yr BP. Sea-level in connection with the deglaciation was around 30 m a.s.l. A glacier readvance in Brandy Bay, of at least 7 km, with the initial 3 km over land, reached a position off the present coast at ca. 4600 yr BP. The culmination of the advance was of short duration, and by 4300 yr BP the coastal lowlands again were ice-free. A distinct marine level at 16–18 m a.s.l. was contemporaneous with or slightly post-dates the Brandy Bay advance, thus indicating the relative sea-level around 4600–4500 yr BP. Our results from James Ross Island confirm that over large areas in this part of Antarctica the last deglaciation occurred late. © 1997 John Wiley & Sons, Ltd.     

Run-up of tsunamis and long waves in terms of surf-similarity

In this paper we review and re-examine the classical analytical solutions for run-up of periodic long waves on an infinitely long slope as well as on a finite slope attached to a flat bottom. Both cases provide simple expressions for the maximum run-up and the associated flow velocity in terms of the surf-similarity parameter and the amplitude to depth ratio determined at some offshore location. We use the analytical expressions to analyze the impact of tsunamis on beaches and relate the discussion to the recent Indian Ocean tsunami from December 26, 2004. An important conclusion is that extreme run-up combined with extreme flow velocities occurs for surf-similarity parameters of the order 3–6, and for typical tsunami wave periods this requires relatively mild beach slopes. Next, we compare the theoretical solutions to measured run-up of breaking and non-breaking irregular waves on steep impermeable slopes. For the non-breaking waves, the theoretical curves turn out to be superior to state-of-the-art empirical estimates. Finally, we compare the theoretical solutions with numerical results obtained with a high-order Boussinesq-type method, and generally obtain an excellent agreement.     

Geochemistry of lead contaminated wetland soils amended with phosphorus

To remediate Pb contaminated soils it is proposed that phosphorus can be amended to the soils to transform the Pb into poorly soluble Pb-phosphate mineral phases. However, remediation strategies must account for variable Pb speciation and site-specific factors. In this study soil mineralogy and Pb speciation in soils from P-amended field trials at sites within the Coeur d’Alene River Basin in Idaho, USA were investigated. The soils are contaminated from mining activities and are enriched with Fe and Mn. Selective extraction of the soils indicated that the Fe oxides are poorly crystalline. XRD of the soil clay size fractions identified quartz, muscovite, kaolinite, siderite, lepidocrocite, and chlorite minerals. Amendment with P fertilizer dissolved the siderite. No Pb–phosphate minerals were detected by XRD. Electron microprobe analysis showed direct correlations between Pb, Fe, and Mn in the unamended soils, and negative correlations between Pb and Si. Lead and Mn were strongly correlated. In the amended soils Fe and P were strongly correlated. Results indicate that the Pb is associated with poorly crystalline Fe and Mn oxides, and that added P is primarily associated with Fe oxide phases. Comparisons of pore water Pb concentrations with chloropyromorphite and plumbogummite solubility suggest that in the phosphate-amended soils the pore waters are undersaturated in these phases, whereas several of the control soil pore waters were oversaturated, indicating the added phosphate suppressed the Pb solubility. Results from this research provide insight into the geochemistry occurring in the P-remediated soils that will help in making management and remediation decisions.