Lacustrine basin hydrocarbon exploration – current thoughts

Although much of the world's petroleum resource-base is associated with marine systems, regionally lacustrine petroleum systems are important. Individual accumulations may exceed several billion barrels. In each of these cases the oil is derived from a lacustrine source rock and may be produced from either nonmarine or marine reservoir rocks. The purpose of this paper is to describe the factors that control lacustrine source rock development and the nature of lacustrine reservoirs. Lacustrine oils display different physical and chemical characteristics than their marine counterparts. These differences can be related to the nature of their precursor material. Although the nature of the products are different, the geochemical threshold criteria for defining source rocks in both settings are the same because of common expulsion requirements. Commercially significant lacustrine systems require the presence of large, long-lived lakes. Such lake settings are tectonic in origin and restricted to climatic settings where precipitation exceeds evaporation. Within these large lake systems three primary factors determine source rock potential and quality. These factors are primary productivity level, organic preservation potential, and matrix sedimentation rate, which controls the dilution of preserved organic matter. Source rock potential is maximized where both productivity and preservation potential are maximized and sedimentation rate is minimized. To some degree these factors can compensate for each other. Hydrocarbon reservoir potential within lacustrine basins is partially impacted by overall tectonic setting. Within extensional settings, transport distances tend to be limited, with much of the sediment being transported away from the basin. The sediments delivered to the lake are poorly sorted and sedimentologically immature, commonly resulting in poor reservoirs due to both primary properties and their susceptibility to diagenesis. Within rifts better reservoirs tend to develop along platform or flexural margins. Stacking of reservoirs is important in lacustrine systems but baffles and barriers are often present between individual sand units. These barriers form as a result of lake level fluctuations. In compressional settings transport distances tend to be longer, resulting in more mature, better sorted sediments leading to higher quality reservoirs. These reservoirs typically develop in fluvial-deltaic and wave-dominated shoreline settings. Lacustrine carbonate reservoirs are locally important. These carbonates tend to develop during lake level lowstands and are dependent on diagenesis (dissolution and karstification) for porosity and permeability development. Lacustrine reservoirs are often stratigraphically and areally limited and display low individual well production rates. Within pure lacustrine systems exploration opportunities appear to be often restricted by either reservoir presence or quality (i.e., production rates). The best exploration opportunities in lacustrine basins appear to be associated with hybrid systems where a lacustrine source and marine reservoir exist.     

Chloride in precipitation and streamwater for the upland catchment of river severn,mid-wales; some consequences for hydrochemical models

Variations in the concentration of Cl in rainfall and stream runoff are presented for two catchments in the Hafren forest of mid-Wales, Great Britain. Despite the large fluctuations in rainfall concentrations, Cl in the streamwater remains relatively constant. Using the two-reservoir Birkenes model, an attempt was made to simulate observed Cl in streamwater. The original model was unable to reproduce the observations and several modifications are suggested to provide better simulations. The resulting model is not the only one capable of reproducing the observations; other hydrochemical models will most probably also achieve this although emphasis will in each case be placed on different aspects. In this paper, it is suggested that the stochastic properties of water movement and chemical processes can account for the streamwater chemistry responses observed. On the catchment scale these processes will lead to an apparently deterministic behaviour that may well be described by simple relationships.     

On the Relevance of $$\ln (z_{0} /z_{0T})= kB^{-1}$$

The assumption that the roughness Reynolds number \(( Re_{*})\) can be used as a basis for quantifying the boundary-layer property \({ kB}^{-1} (= \ln (z_{0}/z_{0T}))\) as in some modern numerical models is questioned. While \({ Re}_{*}\) is a useful property in studies of pipe flow, it appears to have only marginal applicability in the case of treeless terrain, as studied in the two experimental situations presented here. For both the daytime and night-time cases there appears to be little correlation between \({ kB}^{-1}\) and \({ Re}_{*}\). For daytime, the present studies indicate that the assumption \({ kB}^{-1} \approx 2\) is acceptable, while for night-time, the scatter involved in relating \({ kB}^{-1}\) to \({ Re}_{*}\) suggests there is little reason to assume a direct relationship. However, while the scatter affecting all of the night-time results is large, there remains a significant correlation between the heat and momentum fluxes upon which an alternative methodology for describing bulk air–surface exchange at night could be constructed. The friction coefficient (\(C_{f}\)) and the turbulent Stanton number \(({ St}_{*})\) are discussed as possible alternatives for describing bulk properties of the air layer adjacent to the surface. While describing the surface roughness in terms of the friction coefficient provides an attractive simplification relative to the conventional methodologies based on roughness length and stability considerations, use of the Stanton number shares many of uncertainties that affect \({ kB}^{-1}\). The transitions at dawn and dusk remain demanding situations to address.     

Increasing Iron Concentrations in UK Upland Waters

Iron distributions in rainfall, streams, soils and groundwaters are described for the Upper River Severn catchment of mid-Wales. Iron is mainly supplied from within-catchment sources with highest concentrations occurring under reducing conditions. Iron concentrations have doubled over the past 20 years (~5.0 μg yr⁻¹ for the forest and ~3.7 μg yr⁻¹ for the moorland). For the forested sites, the gradients are particularly high post-1993. UK rivers/lakes monitored by the UK Acid Waters Monitoring Network show similar increases. Generally, Fe correlates with dissolved organic carbon (DOC). The greatest rates of Fe increase coincide with those for DOC. Thermodynamic modelling using WHAM/Model VI indicates that Fe(III) is mainly in microparticulate form (probably oxyhydroxides) apart from under reducing conditions. It is proposed that Fe increases for surface waters are associated with increased microparticulate Fe(III) due to stabilisation against aggregation by binding of DOM to its surface. The results relate to acidification declines and deforestation leading to land disturbance and wetter conditions within the soil. There will be greater acidification reversal following tree harvesting due to lowering of atmospheric SO_x scavenging and this may have resulted in the greater increase in Fe in the later years of the study.     

Using chemical and microbiological indicators to track the impacts from the land application of treated municipal wastewater and other sources on groundwater quality in a karstic springs basin

Multiple chemical constituents (nutrients; N, O, H, C stable isotopes; 64 organic wastewater compounds, 16 pharmaceutical compounds) and microbiological indicators were used to assess the impact on groundwater quality from the land application of approximately 9.5 million liters per day of treated municipal sewage effluent to a sprayfield in the 960-km² Ichetucknee Springs basin, northern Florida. Enriched stable isotope signatures (δ¹⁸O and δ²H) were found in water from the effluent reservoir and a sprayfield monitoring well (MW-7) due to evaporation; however, groundwater samples downgradient from the sprayfield have δ¹⁸O and δ²H concentrations that represented recharge of meteoric water. Boron and chloride concentrations also were elevated in water from the sprayfield effluent reservoir and MW-7, but concentrations in groundwater decreased substantially with distance downgradient to background levels in the springs (about 12 km) and indicated at least a tenfold dilution factor. Nitrate-nitrogen isotope (δ¹⁵N–NO₃) values above 10 ‰ in most water samples were indicative of organic nitrogen sources except Blue Hole Spring (δ¹⁵N–NO₃ = 4.6–4.9 ‰), which indicated an inorganic source of nitrogen (fertilizers). The detection of low concentrations the insect repellent N,N-diethyl-metatoluamide (DEET), and other organic compounds associated with domestic wastewater in Devil’s Eye Spring indicated that leakage from a nearby septic tank drainfield likely has occurred. Elevated levels of fecal coliforms and enterococci were found in Blue Hole Spring during higher flow conditions, which likely resulted from hydraulic connections to upgradient sinkholes and are consistent with previoius dye-trace studies. Enteroviruses were not detected in the sprayfield effluent reservoir, but were found in low concentrations in water samples from a downgradient well and Blue Hole Spring during high-flow conditions indicating a human wastewater source. The Upper Floridan aquifer in the Ichetucknee Springs basin is highly vulnerable to contamination from multiple anthropogenic sources throughout the springs basin.     

A variable turbidity maximum in the Kennebec estuary, Maine

A turbidity maximum has been observed in the Kennebec estuary during mode rate and low flow conditions near the upstream limit of salinity intrusion. Hydrographic, ADCP, and transmissometer data were collected at different river flow levels and seasons during 1995–1998. The location of the tip of the salt intrusion changes dramatically and during high runoff may be flushed from the channel of the estuary along with the accumulated particles in the turbidity maximum. It is hypothesized that the estuarine turbidity maximum (ETM) was absent 18% of the time with occurrences in all seasons during 1993–1999 based on river flow volumes from the Kennebec and Androscoggin Rivers throughout the study period. When the flow is moderate and low, which occurred 73% of the time on average, a region of high turbidity can be found as far as 40 km upstream of the mouth. Suspended particulate loads are low in the ETM, on the order of tens of mg l⁻¹ and may vary with the length of time that the ETM has been present.     

A Compilation of New and Published Major and Trace Element Data for NIST SRM 610 and NIST SRM 612 Glass Reference Materials

Microanalytical trace element techniques (such as ion probe or laser ablation ICP-MS) are hampered by a lack of well characterized, homogeneous standards. Two silicate glass reference materials produced by National Institute of Standards and Technology (NIST), NIST SRM 610 and NIST SRM 612, have been shown to be homogeneous and are spiked with up to sixty one trace elements at nominal concentrations of 500 μg g-1 and 50 μg g-1 respectively. These samples (supplied as 3 mm wafers) are equivalent to NIST SRM 611 and NIST SRM 613 respectively (which are supplied as 1 mm wafers) and are becoming more widely used as potential microanalytical reference materials. NIST however, only certifies up to eight elements in these glasses. Here we have compiled concentration data from approximately sixty published works for both glasses, and have produced new analyses from our laboratories. Compilations are presented for the matrix composition of these glasses and for fifty eight trace elements. The trace element data includes all available new and published data, and summaries present the overall average and standard deviation, the range, median, geometric mean and a preferred average (which excludes all data outside ± one standard deviation of the overall average). For the elements which have been certified, there is a good agreement between the compiled averages and the NIST data. This compilation is designed to provide useful new working values for these reference materials.     

Observations and modeling of infrared and millimeter molecular lines towards GL2591

We have observed C₂H₂ and HCN rovibrational transitions near 13µm in absorption against GL2591. We also have observed rotational transitions at 0.6-3 mm of CS, HCN, H₂CO, and HCO⁺. Analysis of the rotational lines, which arise in the extended cloud around the source, shows that no single density model can explain all the data. Models with density and temperature gradients do much better; in particular models withn(r) r ^–1.5 can reproduce the observed pattern of emission line strengths. The abundances show significant depletion compared to models of gas-phase chemistry. The rovibrational data were analyzed in comparison to the absorption line analysis of CO by Mitchellet al. (1989). Our data are consistent with the C₂H₂ and HCN absorption arising in the same warm (200 K) and hot (1010 K) components seen in CO, but we see little evidence for the cold (38 K) component seen in CO. The rovibrational lines from higher states (J 21) indicate that the hot HCN deviates from LTE, leading to a density of about 3 × 10⁷ cm^–3. Comparison of the two data sets shows that the rovibrational absorption of HCN, rather than arising in the extended envelope, must come from a region with a small angular extent. A model in which early-time gas phase abundances are preserved on grain mantles and released at high temperature can explain the data.