Formation and diagenesis of bedding cycles in uppermost Cretaceous chalks of the Dan Field, Danish North Sea

Metre-scale lithologic cycles, visible in core and on logs from Maastrichtian chalks of the Dan Field, were examined to determine their mechanisms of deposition and relation to hydrocarbon production. The lower parts of cycles consist of porous, cream-coloured, largely non-stylolitic, commonly laminated chalk with limited bioturbation (mainly escape burrows). Cycles are capped by thinner intervals of white to grey, hard, stylolitic chalk with concentrations of bioclastic material, intense burrowing and few preserved primary sedimentary structures. The cycle caps contain nearly twice as much Mg as compared to the more porous parts of cycles and also have slightly larger δ¹⁸O values (?4·1‰ for the caps; ?4·4‰ for porous zones). There is a significant reduction of average cycle thickness, as well as total thickness of the Maastrichtian chalk section, from SW to NE across the Dan Field. The cycle thinning largely results from a reduced thickness of porous chalks from the lower parts of cycles and thus is reflected in lower average porosity and permeability on the NE side of the field. These data indicate that episodic winnowing removed fine-grained constituents from highstanding northeastern areas. Porous cycle bases were deposited at relatively high rates that precluded complete bioturbation; preserved laminae, coupled with escape burrows, reflect episodic sediment influx in areas that flank the seafloor highs. Cycle tops apparently accumulated more slowly (throughout the region, but especially on seafloor highs), perhaps because of reduced productivity of planktic organisms. Slower sedimentation allowed more complete bioturbation and destruction of sedimentary structures, and also led to incipient high-magnesium calcite seafloor cementation (sufficient to yield firmer sediment and enhanced burrow preservation, but not to form true hardgrounds). Thus, the elevated magnesium contents and reduced porosity of the cycle caps reflect very early diagenetic processes that were only partially modified by burial diagenesis. Rates of chalk deposition, as inferred from physical and geochemical evidence, appear to be a significant control on reservoir characteristics in North Sea chalks. The highest average porosities and permeabilities are found in areas with the highest sediment accumulation rates where seafloor diagenesis is minimized. Topographic depressions at the time of sedimentation can thus be expected to have the best production characteristics, and synsedimentary topographic highs should have the thinnest sections and the poorest petrophysical properties.     

Refinement of Phosphorus Determination in Quartz by LA‐ICP‐MS through Defining New Reference Material Values

The aim of this study was to improve the quality of laser ablation inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) determination of phosphorus in crystalline quartz. Over the last decade, the Geological Survey of Norway has routinely performed trace element determinations on quartz from both operating and potential quartz deposits by LA‐ICP‐MS. The determined phosphorus concentrations were, with but few exceptions, consistently within the range of 10 to 30 μg g^?1, results that seemed to be both too high and too consistent. The multi‐material calibration curve obtained from a suite of reference materials (NIST SRM 610, 612, 614, 1830, BAM No. 1 amorphous SiO₂ glass) did not define a precise regression line. Published phosphorus concentrations for the reference materials are poorly constrained and the observed dispersions along the multi‐material calibration curve suggest that some of the reference values may be inaccurate. Furthermore, the calibration curve did not pass through the origin of the [(cps ³¹P/cps ³⁰Si) · cone. Si] vs. P concentration diagram; thus, in addition to the uncertainties of the literature values of phosphorus, it is difficult to define the calibration curve. Three reference materials (NIST SRM 614, 1830, synthetic quartz KORTH) were sent for phosphorus accelerator implantation, providing an independent and accurate (± 3%) approach for determining phosphorus concentrations in crystalline quartz. The intrinsic phosphorus concentrations of the three implanted samples plus those for NIST SRM 610 and 612 were determined by secondary ion mass spectrometry (SIMS), yielding new phosphorus values for NIST SRM 610, 612, 614 and 1830. Using these new values resulted in a better defined LA‐ICP‐MS calibration curve. However, the source of the ICP‐MS related background could not be defined, such that it must still be empirically corrected for.     

Temporal analysis of groundwater nitrate concentrations from wells in Prince Edward Island,Canada: application of a linear mixed effects model

Changes in nitrate concentration in groundwater from wells in Prince Edward Island, Canada were investigated over time using two datasets. Temporal trends in groundwater nitrate concentrations were assessed annually during 1981–1996 (1,299 observations), and both seasonally and monthly during 1988–1991 (1,868 observations). Data were analysed using linear mixed models with random effects and correlation structures. The average nitrate concentration in the monthly dataset was 3.99 mg/L as NO₃–N, with January, May, and November concentrations being higher (p?=?0.018). A seasonal effect was present when season was combined with land use type in an interaction term (p?=?0.004). Wells located in agricultural areas had greater nitrate concentrations than urban areas, which in turn, had greater values than low human-impact areas. Row-cropped areas had higher groundwater nitrate concentrations in the summer, whereas manure storage areas were higher in the spring and autumn. Nitrate in groundwater in areas with low human impact and with centralized sewage disposal infrastructure remained relatively low and stable throughout the seasons. There was no significant annual trend (p?=?0.954), but for individual sites, 9.6% significantly increased in nitrate concentration over time, and 6.6% significantly decreased over time.     

Development of a laboratory exposure system using marine fish to carry out realistic effect studies with produced water discharged from offshore oil production

A biotest system for environmentally realistic exposure of fish to produced water (PW) was developed and tested. Authentic PW was collected at an oil production platform in the North Sea and preserved by freezing in multiple aliquots a 25 L. After transport to the test laboratory onshore, daily PW aliquots were thawed, homogenised and administered to the test fish, Atlantic cod (Gadus morhua), in two diluted exposure concentrations, 0.1% and 0.5%, during a 15 d period, using a continuous flow-through exposure setup. Positive control groups were exposed to two crude oil treatments for comparison. Chemical analyses showed that alkylphenol (AP) and PAH concentrations in PW exposure waters were very low. Observations of significantly increased AP and PAH metabolite levels in PW exposed fish demonstrated the suitability of the biotest system for its use in biological exposure/effect studies of PW, and it also demonstrated the sensitivity of bile metabolites as PW exposure markers in fish. The relevance of the biotest system for PW effect studies and for validating modelled environmental risk estimates of PW dischargers from offshore oil production is discussed.