Significance of Geological Parameters for Predicting Water Inflow in Hard Rock Tunnels

One of the most challenging aspects of tunnelling is prognostication of water inflows. More reliable prediction of groundwater inflow may give considerable economical saving for future tunnel projects and may also prevent damage of environment and installations on the surface. This paper is discussing the significance of eight hypotheses regarding geological parameters for predicting water inflow in tunnels. The respective hypotheses have been tested as part of a recent research project in Norway. Six Norwegian tunnels with different geological conditions were selected for the research; the Romeriksporten, Frøya, T-baneringen, Lunner, Skaugum, and Storsand tunnels. Based on detailed study of these tunnels, the hypotheses are tested by comparing water inflow with geological parameters and factors such as Q value, faulting, rock stress orientation, rock cover, thickness of permeable soil or depth of lake/sea above the tunnel, rock type, and width of weakness zones. It is found that four out of the eight tested hypotheses are supported, two have low to medium support and two are not supported. One unexpected result is that for the tunnels covered by this study, the water inflow was found to increase with rock cover.     

Hydrothermal alteration and zeolitization of the Fohberg phonolite,Kaiserstuhl Volcanic Complex,Germany

The subvolcanic Fohberg phonolite (Kaiserstuhl Volcanic Complex, Germany) is an economic zeolite deposit, formed by hydrothermal alteration of primary magmatic minerals. It is mined due to the high (>40 wt%) zeolite content, which accounts for the remarkable zeolitic physicochemical properties of the ground rock. New mineralogical and geochemical studies are carried out (a) to evaluate the manifestation of hydrothermal alteration, and (b) to constrain the physical and chemical properties of the fluids, which promoted hydrothermal replacement. The alkaline intrusion is characterized by the primary mineralogy: feldspathoid minerals, K-feldspar, aegirine–augite, wollastonite, and andradite. The rare-earth elements-phase götzenite is formed during the late-stage magmatic crystallization. Fluid-induced re-equilibration of feldspathoid minerals and wollastonite caused breakdown to a set of secondary phases. Feldspathoid minerals are totally replaced by various zeolite species, calcite, and barite. Wollastonite breakdown results in the formation of various zeolites, calcite, pectolite, sepiolite, and quartz. Zeolites are formed during subsolidus hydrothermal alteration (<150 °C) under alkaline conditions. A sequence of Ca–Na-dominated zeolite species (gonnardite, thomsonite, mesolite) is followed by natrolite. The sequence reflects an increase in \(\log [(a_{{{\text{Na}}^{ + } }} )/(a_{{{\text{H}}^{ + } }} )]\) and decrease in \(\log [(a_{{{\text{Ca}}^{2 + } }} )/(a_{{{\text{H}}^{ + } }}^{2} )]\) of the precipitating fluid. Low radiogenic ⁸⁷Sr/⁸⁶Sr values indicate a local origin of the elements necessary for secondary mineral formation from primary igneous phases. In addition, fractures cut the intrusive body, which contain zeolites, followed by calcite and a variety of other silicates, carbonates, and sulfates as younger generations. Stable isotope analysis of late-fracture calcite indicates very late circulation of meteoric fluids and mobilization of organic matter from surrounding sedimentary units.     

Effects of salinity on NH4 + adsorption capacity, nitrification, and denitrification in Danish estuarine sediments

The regulatory effect of salinity on nitrogen dynamics in estuarine sediments was investigated in the Randers Fjord estuary, Denmark, using sediment slurries and intact sediment cores and applying ¹⁵N-isotope techniques. Sediment was sampled at three representative stations varying in salinity, and all experiments were run at 0‰, 10‰, 20‰, and 30‰. The sediment NH₄ ⁺ adsorption capacity decreased markedly at all stations when salinity was increased from 0‰ to 10‰; further increase showed little effect. In situ nitrification and denitrification also decreased with increasing salinities, with the most pronounced reduction of approximately 50% being observed when the salinity was raised from 0‰ to 10‰. The salinity-induced reduction in NH₄ ⁺ adsorption capacity and stimulation of NH₄ ⁺ efflux has previously been argued to cause a reduction in nitrification activity since the nitrifying bacteria become limited by NH₄ ⁺ availability at higher salinities. However, using a potential nitrification assay where NH₄ ⁺ was added in excess, it was demonstrated that potential nitrification activity also decreased with increasing salinity, indicating that the inhibitory salinity effect may also be a physiological effect on the microorganisms. This hypothesis was supported by the finding that denitrification based on NO₃ ⁻ from the overlying water (D_w), which is independent of the nitrification process, and hence NH₄ ⁺ availability, also decreased with increasing salinity. We conclude that changes in salinity have a significant effect on nitrogen dynamics in estuarine sediments, which must be considered when nitrogen transformations are measured and evaluated.     

Comparison of isotope pairing and N2:Ar methods for measuring sediment denitrification—Assumption, modifications, and implications

Denitrification has been measured during the last few years using two different methods in particular: isotope pairing measured on a triple-collector isotopic ratio mass spectrometer and N₂:Ar ratios measured on a membrane inlet mass spectrometer (MIMS). This study compares these two techniques in short-term batch experiments. Rates obtained using the original N₂∶Ar method were up to 3 to 4 times higher than rates obtained using the isotope pairing technique due to O₂ reacting with the N₂ during MIMS analysis. Oxygen combines with N₂ within the mass spectrometer ion source forming NO⁺ which reduces the N₂ concentration. The decrease in N₂ is least at lower O₂ concentrations and since oxygen is typically consumed during incubations of sediment cores, the result is often a pseudo-increase in N₂ concentration being interpreted as denitrification activity. The magnitude of this ocygen effect may be instrument specific. The reaction of O₂ with N₂ and the subsequent decrease in N₂ was only partly correctly using an O₂ correction curve for the relationship between N₂ and O₂ concentrations. The O₂ corrected N₂∶Ar denitrification rates were lower, but still did not match the isotope pairing rates and the variability between replicates was much higher. Using a copper reduction column heated to 600°C to remove all of the O₂ from the sample before MIMS analysis resulted in comparable rates (slightly lower), and comparable variability between replicates, to the isotope pairing technique. The N₂:Ar technique determines the net N₂ production as the difference between N₂ production by denitrification and N₂ consumption by N-fixation, while N-fixation has little effect on the isotope pairing technique which determines a rate very close to the gross N₂ production. When the two different techniques were applied on the same sediment, the small difference in rates obtained by the two methods seemed to reflect N-fixation as also supported from measurements of ethylene production in acetylene enriched sediment cores. The N₂:Ar and isotope pairing techniques may be combined to provide simultaneous measurements of denitrification and N-fixation. Both techniques have several assumptions that must be met to achieve accurate rates; a number of tests are outlined that can be applied to demonstrate that these assumptions are being meet.     

Spatial variation of overbank aggradation rate and its influence on avulsion frequency

Abstract River avulsions are commonly considered to be driven by the aggradation and growth of alluvial ridges, and the associated increase in cross‐valley slope relative to either the down‐channel slope or the down‐valley slope (the latter is termed the slope ratio in the present paper). Therefore, spatial patterns of overbank aggradation rate over stratigraphically relevant time scales are critical in avulsion‐dominated models of alluvial architecture. Detailed evidence on centennial‐ to millennial‐scale floodplain deposition has, to date, been largely unavailable. New data on such long‐term overbank aggradation rates from the Rhine–Meuse and Mississippi deltas demonstrate that the rate of decrease of overbank deposition away from the channel belt is much larger than has been supposed hitherto, and can be similar to observations for single overbank floods. This leads to more rapid growth of alluvial ridges and more rapid increase in slope ratios, potentially resulting in increased avulsion frequencies. A revised input parameter for overbank aggradation rate was used in a three‐dimensional model of alluvial architecture to study its effect on avulsion frequency. Realistic patterns of avulsion and interavulsion periods (≈1000 years) were simulated with input data from the Holocene Rhine River, with avulsions occurring when the slope ratio is in the range 3–5. However, caution should be practised with respect to uncritical use of these numbers in different settings. Evidence from the two study areas suggests that the avulsion threshold cannot be represented by one single value, irrespective of whether critical slope ratios are used, as in the present study, or superelevation as has been proposed by other investigators.     

Crystallographic orientations of high-angle grain boundaries in dynamically recrystallized quartz: First results

The crystallography and geometry of high-angle grain boundaries from dynamically recrystallized quartz have been studied. On the basis of combined electron backscatter diffraction and universal stage measurements, the complete crystallographic orientation of the grain boundaries could be calculated. The u-stage rotation of the grain boundaries to a vertical position reveals that they are never curved but always consist of straight segments. Our results show that these segments preferentially occupy rhombohedral, trapezohedral and bipyramidal orientations, i.e., orientations in a  25–50° girdle to the c-axis. A specific, albeit low, number of segments with special crystallographic orientation, with respect to a neighbouring quartz grain, often shows another special orientation with respect to the other neighbouring grain. Preferred combinations of grain boundary orientations related to both neighbouring grains are (i) low-index rhombohedral and high index trapezohedral, (ii) low-index bipyramidal and low-index trapezohedral or high-index rhombohedral, and (iii) low-index trapezohedral and low or high index trapezohedral. In certain cases, such as at triple junctions, the boundaries occupy specific trapezohedral orientations with a constant angle to the c-axis. This argues for energy isotropy of trapezohedral planes with the same angle to the quartz c-axis. In general, good match coincidence site lattice (CSL) orientations are not preferentially occupied so that most of the studied grain boundaries represent general boundaries. The formation of straight segments in special crystallographic orientations indicates the crystallographic control and implies an energy reduction of certain general boundaries.     

High‐resolution bathymetric mapping reveals subaqueous glacial landforms in the Arctic alpine lake Tarfala,Sweden

In Arctic alpine regions, glacio‐lacustrine environments respond sensitively to variations in climate conditions, impacting, for example,glacier extent and rendering former ice‐contact lakes into ice distal lakes and vice versa. Lakefloors may hold morphological records of past glacier extent, but remoteness and long periods of ice cover on such lakes make acquisition of high‐resolution bathymetric datasets challenging. Lake Tarfala and Kebnepakte Glacier, located in the Kebnekaise mountains, northern Sweden, comprise a small, dynamic glacio‐lacustrine system holding a climate archive that is not well studied. Using an autonomous surface vessel, a high‐resolution bathymetric dataset for Lake Tarfala was acquired in 2016, from which previously undiscovered end moraines and a potential grounding line feature were identified. For Kebnepakte Glacier, structure‐from‐motion photogrammetry was used to reconstruct its shape from photographs taken in 1910 and 1945. Combining these methods connects the glacial landform record identified at the lakefloor with the centennial‐scale dynamic behaviour of Kebnepakte Glacier. During its maximum 20^th century extent, attained c. 1910, Kebnepakte Glacier reached far into Lake Tarfala, but had retreated onto land by 1945, at an average of 7.9 m year^–1. Copyright © 2019 John Wiley & Sons, Ltd.     

Lake Søbygaard: a shallow lake in recovery after a reduction in phosphorus loading

The development and recovery of a shallow and hypertrophic lake following a reduction in the external phosphorus load has been documented. In spite of this reduction, phosphorus concentrations and phytoplankton biomass in the lake water are still very high. The reason for this development can be explained by three main factors: (1): the sediment has been accumulating a large phosphorus pool which is now causing a high internal phosphorus load, (2) due to the shallow conditions, resuspension of the upper sediment often takes place because of wind action and thereby increases the phosphorus loading from the sediment, (3) the development of a large population of planktivorous fish decreases the zooplankton biomass resulting in the development of a large phytoplankton biomass.     

Quartz Cement in Middle Jurassic Reservoir Sandstones in North Sea A Review. Part II： Duration and Silica Sources

The timing and duration of quartz cementation in sandstones have been mainly inferred from diagenetic texture, relationship between pore filling minerals, fluid inclusions and isotopic data. Fluid inclusion temperatures from North Sea reservoir sandstones indicate that most of the quartz cement forms at temperature exceeding 90℃ and is continually proceeding after oil emplacement, based on the fluid inclusion temperatures in quartz overgrowth which is approaching the bottom-hole temperatures. The duration of quartz cement after oil emplacement depends upon the saturation of porewater and the distribution of pore water film and the property of water-wet or oil-wet of the reactants. The leaching of K-feldspar by meteoric water requires pore water flow to move the released potassium and sodium and silica out the solution, which suggests the mechanism does not appear to be a major source of silica for quartz cementation. The quartz cementation coincidence with the compaction and pressure solution suggests the major source of silica. The alteration of feldspar by illitization of kaolinite may serve as another important source of silica at deep burial depth. External sources are not need to call on for illustrating the quartz cementation, because there is no evidences for large scale convection of pore water flow occurred in the burial history of reservoir sandstones of middle Jurassic in the North Sea.