Oligocene sequence stratigraphy and basin development in the Danish North Sea sector based on log interpretations

Five sequences are defined in the Oligocene succession of the Danish North Sea sector. Two of the sequences, 4.1a and 4.3, have been identified onshore Denmark.Two types of prograding lowstand deposits are recognized. Sand-dominated deposits occur proximally, comprising sharp-based forced regressive deposits covered with prograding low-stand deposits. Clay-dominated prograding lowstand deposits occur distally in the sequences. The highstand deposits are proximally represented by thick prograding sandy deposits and distally by thin and condensed intervals.The main sediment input direction was from the north and the northeast. A succession oif lithofacies, from shallow marine facies dominated by sand to outer shelf facies dominated by clay, is mapped in each of the sequences. An overall southward progradation of the shoreline took place during the Oligocene, interrupted only by minor shoreline retreats.     

Petrogenesis of orthopyroxene- and amphibole-bearing andesites, Mustique, Grenadine Islands, Lesser Antilles Arc: Isotope, trace element and physical constraints

Abstract On the island of Mustique, fresh and propylitized olivine–plagioclase–clinopyroxene basalt, plagioclase–clinopyroxene–orthopyroxene and plagioclase–clinopyroxene–amphibole andesite lavas and minor intrusions are interbedded with Oligocene pyroclastic and epiclastic rocks. Chemical data show that two isotopically identical, but chemically different, suites of lava are present: (i) the OPXS (⁸⁷Sr/⁸⁶Sr 0.70403–0.70454; ¹⁴³Nd/¹⁴⁴Nd 0.512952–0.512986; δ¹⁸O_cpx 5.49 and 5.61), comprising basalts and orthopyroxene‐bearing andesites; and (ii) the AMPHS (⁸⁷Sr/⁸⁶Sr 0.70401–0.70457; ¹⁴³Nd/¹⁴⁴Nd 0.512981–0.513037; δ¹⁸O_cpx 5.54), made up of basalts and amphibole‐bearing andesites. The OPXS has higher contents of TiO₂, P₂O₅, light rare earth elements, Sm, Pb, Th, U, Zr, Y and Nb, and higher La/Yb ratios than the AMPHS. The isotopic data suggest that both suites formed from melts derived from the same subduction‐modified depleted mantle source as the volcanic rocks of nearby St Vincent and Bequia, and the northern islands of the Lesser Antilles Arc. The immobile trace element contents, and La/Yb ratios, of the OPXS are indicative of ～10% partial melting of the source, whereas those of the AMPHS are indicative of ～25% partial melting. The within‐suite chemical variation of the OPXS is consistent with ～45% fractional crystallization of its intratelluric mineral assemblages, and that of the AMPHS is consistent with the removal of ～65% of its intratelluric assemblages. Experimental evidence suggests that both suites of basalt crystallized at pressures <8 kbar from melts containing 1–2 wt% water. After extensive fractional crystallization, the andesites crystallized at pressures between approximately 5 and 2 kbar. The OPXS magmas appear to have lost more of their water content than the AMPHS magmas. Thus, the OPXS andesites formed from melts with an estimated water content of 2–3 wt%, whereas the AMPHS andesites formed from melts containing at least 4.5 wt% water.     

Comments on “Two-dimensional concentration distribution for mixing-controlled bioreactive transport in steady-state” by O.A. Cirpka and A.J. Valocchi

In this comment we present a re-analysis of the analytical solution presented by Cirpka and Valocchi for steady-state concentrations of dissolved bioreactive compounds and bacterial biomass in porous media. We discuss the validity range of the analytical solution. In particular, the criterion used to determine the sustainability of biomass is revisited. This re-analysis shows that the ω$\omega$ criterion used by Cirpka and Valocchi is only a necessary but not a sufficient criterion to determine the bioreactive zones. As a consequence, the analytical solution does not provide the exact distribution of compounds throughout the domain, but can serve as upper or lower boundaries for species concentrations at a given location. These conclusions are supported by the simulation results obtained from an established reactive transport model.     

Assessment of Water Quality in the Elbe River at Low Water Conditions Based on Factor Analysis

An assessment of water quality measurements during a long‐lasting low water period in the Elbe River is presented. Weekly samples were taken from May to December 2003 at a sampling site in the middle part of the Elbe River. For multivariate data analysis, 34 parameters of 46 samplings were considered. As a result of this analysis, 78% of the variance of the data set is explained by five factors. They can be assigned to the following latent variables: season (37.5%) > tributaries (12.7%) > re‐suspension (10.4%) > discharge (9.4%) > complexation (8.5%). For the investigated sampling site, two key processes were identified as dominating factors on the water quality during low water conditions. First, seasonal phytoplankton development caused changes in redox conditions with consequences for re‐solution of pollutants from sediments. Second, tributaries have a higher impact on the main stream, due to changes in mixing processes. Therefore, in addition to flood investigations, monitoring strategies, and management plans should be developed in order to survey changes in water quality during low water conditions.     

The clean development mechanism’s contribution to sustainable development: a review of the literature

The challenges of how to respond to climate change and ensure sustainable development are currently high on the political agenda among the world’s leading nations. The Clean Development Mechanism (CDM) is part of the global carbon market developing rapidly as part of the Kyoto response towards the mitigation of global warming. One of the aims of the CDM is to achieve sustainable development in developing countries, but uncertainty prevails as to whether the CDM is doing what it promises to do. Close to 200 studies on the CDM have been carried out since its birth in 1997 including peer-reviewed articles and reports from the grey literature. This review of the literature serves to assess the state of knowledge on how the CDM contributes to sustainable development (SD) including poverty alleviation. The main finding of the review is that, left to market forces, the CDM does not significantly contribute to sustainable development.     

Cycling of trace metals (Mn, Fe, Mo, U, V, Cr) in deep pore waters of intertidal flat sediments

Trace metals (Mn, Fe, Mo, U, Cr, V) were studied in pore waters of an intertidal flat located in the German Wadden Sea. The study system is an example of a permeable tidal flat system where pore water exchange is affected by tidal driven pressure gradients besides diffusion. Permanently installed in situ samplers were used to extract pore waters down to 5 m depth throughout one year. The samplers were either located close to the tidal flat margin or in central parts of the tidal flat. Despite dynamic sedimentological and hydrological conditions, the general trends with depth in deep tidal flat pore waters are remarkably similar to those observed in deep sea environments. Rates of trace metal cycling must be comparably large in order to maintain the observed pore water profiles. Trace metals further show similar general trends with depth close to the margin and in central parts of the tidal flat. Seasonal sampling revealed that V and Cr vary concurrent with seasonal changes in dissolved organic carbon (DOC) concentration. This effect is most notable close to the tidal flat margin where sulphate, DOC, and nutrients vary with season down to some metres depth. Seasonal variations of Mn, Fe, Mo, and U are by contrast limited to the upper decimetres of the sediment. Their seasonal patterns depend on organic matter supply, redox stratification, and particulate matter deposited on sediment surfaces. Pore water sampling within one tidal cycle provides evidence for pore water advection in margin sediments. During low tide pore water flow towards the creekbank is generated by a hydraulic gradient suggesting that deep pore waters may be seeping out of creekbank sediments. Owing to the enrichment of specific elements like Mn in pore water compared to sea water, seeping pore waters may have an impact on the chemistry of the open water column. Mass balance calculations reveal that the impact of deep pore waters on the Mn budget in the open water column is below 4%. Mn deep pore water discharge of the whole Wadden Sea is estimated to be about 9% of the total dissolved riverine Mn input into the Southern North Sea.     

Ulvöspinel in native iron-bearing assemblages and the origin of these assemblages in basalts from Ovifak,Greenland, and Bühl,Federal Republic of Germany

Euhedral crystals of ulvöspinel are found in many of the native-iron-bearing xenoliths from the basalt of Bühl near Kassel (West Germany) and Ovifak on Disko Island (West Greenland). The typical assemblage of these xenoliths at both localities is: native Fe, troilite, cohenite, ulvöspinel, ilmenite, olivine, and plagioclase, as well as silicate glass containing droplets of former Fe and troilite melt. The ulvöspinel subsolidus textures and intergrowths also indicate identical cooling histories for the xenoliths in both cases. Ulvöspinel crystallized after the formation of iron, but still above the Fe-FeS eutectic at 988° C. A subsequent strong drop in oxygen fugacity revealed partial breakdown of ulvöspinel according to the reaction .Microprobe analyses of a Bühl xenolith indicate that ulvöspinel contains up to 4.7 w.t.% MnO, while olivine compositions correspond to Fa_64–74Fo_12–24Te_12–15. The entire xenolith contains 1.9 w.t.% MnO. This fact, together with the geological evidence and the occurrence of corroded quartz relicts within some of the xenoliths provides clear evidence for reduction under near-surface conditions in a blast-furnace-like process. The reducing agent was coal from the Tertiary seams cut by the erupting basalt, while the xenolith source material most probably was spherosiderite, which is very common in the coals and would explain the high MnO content. Consequently, the presence of cohenite is not necessarily an indicator of high pressure.The analogies between the Bühl and Ovifak localities and their xenoliths strongly suggest a similar formation through near surface reduction and not derivation from the mantle.     

Alkaline fluid circulation in ultramafic rocks and formation of nucleotide constituents: a hypothesis

Seawater is constantly circulating through oceanic basement as a low-temperature hydrothermal fluid (<150°C). In cases when ultramafic rocks are exposed to the fluids, for instance during the initial phase of subduction, ferromagnesian minerals are altered in contact with the water, leading to high pH and formation of secondary magnesium hydroxide, among other – brucite, that may scavenge borate and phosphate from seawater. The high pH may promote abiotic formation of pentoses, particularly ribose. Pentoses are stabilized by borate, since cyclic pentoses form a less reactive complex with borate. Analyses have shown that borate occupies the 2' and 3' positions of ribose, thus leaving the 5' position available for reactions like phosphorylation. The purine coding elements (adenine, in particular) of RNA may be formed in the same general hydrothermal environments of the seafloor.     

An Open,Object-Based Framework for Generating Anisotropy in Sedimentary Subsurface Models

The spatial distribution of hydraulic properties in the subsurface controls groundwater flow and solute transport. However, many approaches to modeling these distributions do not produce geologically realistic results and/or do not model the anisotropy of hydraulic conductivity caused by bedding structures in sedimentary deposits. We have developed a flexible object-based package for simulating hydraulic properties in the subsurface—the Hydrogeological Virtual Realities (HyVR) simulation package. This implements a hierarchical modeling framework that takes into account geological rules about stratigraphic bounding surfaces and the geometry of specific sedimentary structures to generate realistic aquifer models, including full hydraulic-conductivity tensors. The HyVR simulation package can create outputs suitable for standard groundwater modeling tools (e.g., MODFLOW), is written in Python, an open-source programming language, and is openly available at an online repository. This paper presents an overview of the underlying modeling principles and computational methods, as well as an example simulation based on the Macrodispersion Experiment site in Columbus, Mississippi. Our simulation package can currently simulate porous media that mimic geological conceptual models in fluvial depositional environments, and that include fine-scale heterogeneity in distributed hydraulic parameter fields. The simulation results allow qualitative geological conceptual models to be converted into digital subsurface models that can be used in quantitative numerical flow-and-transport simulations, with the aim of improving our understanding of the influence of geological realism on groundwater flow and solute transport.     

Geochemistry of groundwater in front of a warm‐based glacier in Southeast Greenland

Groundwater in front of warm‐based glaciers is likely to become a more integrated part of the future proglacial hydrological system at high latitudes due to global warming. Here, we present the first monitoring results of shallow groundwater chemistry and geochemical fingerprinting of glacier meltwater in front of a warm‐based glacier in Southeast Greenland (Mittivakkat Gletscher, 65° 41′ N, 37° 48′ W). The groundwater temperature, electrical conductivity and pressure head were monitored from August 2009 to August 2011, and water samples were collected in 2009 and analyzed for major ions and water isotopes (δD, δ¹⁸O). The 2 yrs of monitoring revealed that major outbursts of glacier water during the ablation season flushed the proglacial aquifer and determined the groundwater quality for the next 2–8 weeks until stable chemical conditions were reached again. Water isotope composition shows that isotopic fractionation occurs in both groundwater and glacier meltwater, but fractionation due to evaporation from near‐surface soil moisture prior to infiltration has the most significant effect. This study shows that groundwater in Low Arctic Greenland is likely to possess a combined geochemical and isotopic composition, which is distinguishable from other water sources in the proglacial environment. However, the shallow groundwater composition at a given time is highly dependent on major outbursts of glacier water in the previous months.