Sedimentary processes and trace metal contaminants in the buccaneer oil/gas field,northwestern gulf of Mexico

Sediments are the ultimate sink for contaminants in the marine environment, and physical processes of sedimentation influence the distribution and accumulation of these contaminants. Evaluation of contaminant levels in sediments is one approach to assessing environmental impact; data interpretation depends on consideration of sediment texture and mineralogy, however, which profoundly influence chemical composition. In this study, comparison of potentially contaminated sediments from the production field with control populations was done only within the context of similar (as to texture and organic carbon and carbonate content) sample groups as determined by cluster analysis. Ba, Cd, and Sr are identified as contaminants. Supported by the identification of a well-crystallized expandable clay—possibly bentonite—drilling fluids are a potential source of Ba. Ba and Sr may be unnaturally high because of their abundance in discharged produced formation waters, but may also be naturally controlled by the unique faunal assemblage associated with the structures. Cd is probably derived from corrosion of the structures and assorted debris on the seafloor. In general, contamination is limited to an area within 100 m of the platforms. Furthermore, substantial erosion around platforms has probably effectively removed and dispersed the bulk of the contaminants introduced into the marine environment by the offshore exploration/production operations.     

Autochthonous inheritance of zircon through Cretaceous partial melting of Carboniferous plutons: the Arthur River Complex,Fiordland, New Zealand

TIMS and SHRIMP U–Pb analyses of zircons from Milford Orthogneiss metadiorite (P = 1–1.4 GPa; T ≥ 750°C) of the Arthur River Complex of northern Fiordland reveal a bimodal age pattern. Zircons are predominantly either Paleozoic (357.0 ± 4.2 Ma) and prismatic with oscillatory zoning, or Cretaceous (133.9 ± 1.8 Ma) and ovoid with sector or patchy zoning. The younger age component is not observed overgrowing older grains. Most grains of both ages are overgrown by younger Cretaceous (~120 Ma) metamorphic zircon with very low U and Th/U (0.01). We interpret the bimodal ages as indicating initial igneous emplacement and crystallisation of a dioritic protolith pluton at ~357 Ma, followed by Early Cretaceous granulite-facies metamorphism at ~134 Ma, during which a significant fraction (~60%) of the zircon grains dissolved, and subsequently reprecipitated, effectively in situ, in partial melt pockets. The remaining ~40% of original Paleozoic grains were apparently not in contact with the partial melt, remained intact, and show only slight degrees of Pb loss. Sector zoning of the Cretaceous grains discounts their origin by solid state recrystallisation of Paleozoic grains. The alternative explanation—that the Paleozoic component represents a 40% inherited component in an Early Cretaceous transgressive dioritic magma—is considered less likely given the relatively high solubility of zircon in magma of this composition, the absence of 134 Ma overgrowths, the single discrete age of the older component, equivalent time-integrated ¹⁷⁷Hf/¹⁷⁶Hf compositions of both age groups, and the absence of the Cambrian-Proterozoic detrital zircon that dominates regional Cambro-Ordovician metasedimentary populations. Similar bimodal Carboniferous-Early Cretaceous age distributions are characteristic of the wider Arthur River Complex; 8 of 12 previously dated dioritic samples have a Paleozoic component averaging 51%. Furthermore, the age and chemical suite affinity of these and several more felsic rocks can be matched with those of the relatively unmetamorphosed Carboniferous plutonic terrane along the strike of the Mesozoic margin in southern Fiordland, also supporting the in situ derivation of the Carboniferous “inherited” component.     

Mineralogy and geochemistry of lateritic soil profiles in Kerala, India

Lateritic soils near Calicut, Kerala, contain halloysite of intermediate hydration, kaolinite, goethite, gibbsite and quartz. The presence of halloysite is responsible for relatively high plasticity and cation-exchange capacity. Fe-hydroxide colloids along with halloysite contribute to significant phosphate uptake by this soil. Composition of local groundwater is consistent with weathering of sodic plagioclase to gibbsite, kaolinite and metastable halloysite.     

Characterising the distribution of near-shore submarine groundwater discharge along a coastline using 222Rn and electrical conductivity

The spatial and temporal distribution of near-shore fresh submarine groundwater discharge (SGD) was characterised from the coastal aquifers of the Willunga Basin, South Australia, an extensive aquifer system that supports an important viticultural region. Measurements of electrical conductivity (EC) and ²²²Rn (radon) activity were collected at 19 sites along the coastline during the Southern Hemisphere spring (2011) and summer (2013). At each site, samples were collected from the surf zone as well asporewater from beach sediment in the intertidal zone. Surf-zone radon activity ranged from <5 to 70mBq L^–1, and intertidal porewater radon ranged over two orders of magnitude (220–36 940 mBq L^–1) along the Willunga Basin coastline during both surveys. Overall, surf-zone and porewater EC was lower in the spring 2011 survey than in the summer 2013 survey. Porewater EC was similar to that of coastal water at most sites along the coastline, except at three sites where porewater EC was found to be lower than coastal water during both surveys, and three sites where evaporated seawater was observed in the summer survey. Based on the patterns in radon and EC along the coastline, two sites of localised fresh SGD were identified, in addition to a groundwater spring that is known to discharge to the coast. The results indicate that near-shore fresh SGD occurs as localised seeps rather than diffuse seepage along the entire coastline. The apparent absence of groundwater discharge at most locations is also consistent with current evidence suggesting that extensive groundwater pumping within the basin has resulted in seawater intrusion across much of the coastline. These observations also suggest that previous studies are likely to have over-estimated SGD rates from the Willunga Basin because they assumed that SGD occurred along the entire coastline.     

洋面冷锋的三维数值模拟──潜热释放对冷锋结构的影响

通过比较一次洋面冷锋过程的干、湿三维模拟结果，揭示潜热释放对冷锋结构的影响。结果表明：由于潜热释放的作用，冷锋区的温度梯度和风矢量的气旋性切变大大地加强了，冷锋附近的涡度场和垂直速度场呈现出更多的更加紧密的中尺度结构；锋面非地转直接环流在湿模拟中比在干模拟中发展得更加充分并且具有更高的组织性；潜热加热倾向于增加锋面环流的强度，尤其是其上升支的强度。研究表明，潜热释放过程是形成冷锋前沿上方低层大气中狭窄强上升气流区的关键因素之一。     

Atmospheric Correction Over Coastal Turbid Waters of Bay of Bengal Using OCEANSAT-I Ocean Colour Monitor (OCM) Data

Space-borne ocean-colour remote sensor-detected radiance is heavily contaminated by solar radiation backscattered by the atmospheric air molecules and aerosols. Hence, the first step in ocean-colour data processing is the removal of this atmospheric contribution from the sensor-detected radiance to enable detection of optically active oceanic constituents e.g. chlorophyll-a, suspended sediment etc. In standard atmospheric correction procedure for OCEANSAT-1 Ocean Colour Monitor (OCM) data, NIR bands centered at 765 and 865 nm wavelengths were used for aerosol characterization. Due to high absorption by water molecules, ocean surface in these two wavelengths acts as dark background, therefore, sensor detected radiance can be assumed to have major contribution from atmospheric scattering. For coastal turbid waters this assumption of dark surface fails due to the presence of highly scattering sediments which causes sufficient water-leaving radiance in NIR bands and lead to over-estimation of aerosol radiance resulting in negative water leaving radiance for λ < 700 nm. In the present study, for the turbid coastal waters in the northern Bay of Bengal, the concept of spatial homogeneity of aerosol and water leaving reflectance has been applied to perform atmospheric correction of OCAEANSAT-1 OCM data. The results of the turbid water atmospheric correction have also been validated using in-situ measured water-leaving radiance. Comparison of satellite derived water-leaving radiance for five coastal stations with in-situ measured radiance spectra, indicates an improvement over the standard atmospheric correction algorithm giving physically realistic and positive values. Root Mean Square Error (RMSE) between the in-situ measured and satellite derived water leaving radiance for wavelengths 412 nm, 443 nm, 490 nm, 512 nm and 555 nm was found to be 1.11, 0.718, 0.575, 0.611 and 0.651%, respectively, using standard atmospheric correction procedure. By the use of spatial homogeneity concept, this error was reduced to 0.125, 0.173, 0.176, 0.225, and 0.290 and the correlation coefficient arrived at 0.945, which is an improvement over the standard atmospheric correction procedure.     

Effect of major ion variations in the marine environment on the specific gravity-conductivity-chlorinity-salinity relationship

Partial equivalent conductances and partial equivalent volumes of the major constituents in seawater were used to evaluate the specific gravity-conductivity-chlorinity-salinity relationships in the marine environment. For example, in the open ocean, the relationships between Cl‰ and both S‰ and specific gravity are valid to within 0.014‰ and 0.014 σ_t, respectively. The relationships between conductivity and S‰ and specific gravity are valid to within 0.006‰ and 0.007 σ_t. In river diluted nearshore areas specific gravity anomalies inferred from Cl‰, can be as great as 0.06 σ_t and 0.04 σ_t when inferred from a conductivity ratio measurement.     

Comparison of three oxidation methods used for the analysis of the dissolved organic carbon in seawater

Three methods for the determination of dissolved organic carbon in seawater were compared. Samples were analysed using persulphate oxidation, high-temperature combustion, and ultraviolet photo-oxidation. The dissolved organic carbon content of the seawater samples ranged from 0.6 to 1.6 mg C/I. This study shows that results of high-temperature oxidation and photo-oxidation procedures differ by less than 5%, whereas results with persulphate oxidation are about 15% less than those obtained with the high-temperature oxidation. The relative merits of each of the oxidation techniques for the determination of organic matter in seawater are discussed.     

The sea as a source of atmospheric phosphorus

The geochemical fractionation of phosphorus on the drop produced by bubbles bursting in seawater has been studied using a field sampling system called the Bubble Interfacial Microlayer Sampler (BIMS). The droplets from bursting bubbles were collected on filter samples in Narragansett Bay, Rhode Island during the summer of 1975. Phosphorus was found to be fractionated by the bubble-bursting process. The enrichment factor ranged from 4 to 170. Enrichment was found to increase with decreasing phosphorus concentration at 20 cm depth while it decreases with increasing wind velocity. Enrichment was independent of bubbling depth. Together these facts suggest that the sea-surface microlayer is the source of the phosphorus on the ejected drops. Organic phosphorus on the filter samples was found to be enriched relative to surface-water phosphorus by factors of 100–200, while reactive phosphorus was enriched by factors of only 6–8. This suggests that surface-active organic phosphorus compounds are the source phosphorus in the microlayer.The organic phosphorus content of samples of atmospheric particulates collected over the phosphate-rich upwelling waters near the Peru coast was found to correlate significantly with sea-salt sodium. Enrichments calculated using the average phosphorus concentration of the surface water in this area agree well with the results of the BIMS study. Thus it appears that phosphorus fractionation does occur in nature and may be important in supplying this nutrient to some coastal regions of the world.     

Preservation of enzymic activity in marine plankton by low-temperature freezing

The measurement of enzymic activity in plankton communities is useful in the study of marine ecosystems. Such measurements can lead to a clearer understanding of the biological transformations in plankton communities at a particular time. However, the assays are somewhat time-consuming. To facilitate analysis of large numbers of samples, we have developed a method of quick-freezing of whole cells and of cell-free extracts of the diatom, Skeletonema costatum, followed by storage at ?60°C for up to one week. No loss in either the electron transport system (ETS) or the glutamate dehydrogenase (GDH) activity occurs. Similar conditions of storage can be used for the preservation of ETS activity in the marine copepod Calanus pacificus. Also, no measurable loss in either the GDH or the ETS activity is detectable after the quick-frozen whole cells of S. costatum have been kept frozen for over a year.