The cone penetration test and 2D imaging resistivity as tools to simulate the distribution of hydrocarbons in soil

The purpose of geophysical electrical surveys is to determine the subsurface resistivity distribution by making measurements on the ground surface. From these measurements, the true resistivity of the subsurface can be estimated. The ground resistivity is related to various geological parameters, such as the mineral and fluid content, porosity and degree of water saturation in the rock. Electrical resistivity surveys have been used for many decades in hydrogeological, mining and geotechnical investigations. More recently, they have been used for environmental surveys. To obtain a more accurate subsurface model than is possible with a simple 1-D model, a more complex model must be used. In a 2-D model, the resistivity values are allowed to vary in one horizontal direction (usually referred to as the x direction) but are assumed to be constant in the other horizontal (the y) direction. A more realistic model would be a fully 3-D model where the resistivity values are allowed to change in all three directions. In this research, a simulation of the cone penetration test and 2D imaging resistivity are used as tools to simulate the distribution of hydrocarbons in soil.     

Promoted dissipation of phenanthrene and pyrene in soils by amaranth (<Emphasis Type="Italic">Amaranthus tricolor</Emphasis> L.)

A study was conducted to investigate the performance of amaranth, a known hyperaccumulator of cesium, on the promotion of the dissipation of soil phenanthrene and pyrene, which are PAHs (polycyclic aromatic hydrocarbons). Amaranthus tricolor L. een choi was the cultivar used. The presence of Amaranthus tricolor L. evidently enhanced the dissipation of these PAHs in soils with initial phenanthrene concentrations of 7.450–456.5 mg/kg dw (dw, dry weight) and pyrene of 8.010–488.7 mg/kg dw. At the end of the experiment (45 days), the residual concentrations of phenanthrene and pyrene in spiked soils with plants were generally higher than those with no plants. The loss of phenanthrene and pyrene in vegetated soils was 87.85–94.03% and 46.89–76.57% of the soil with these chemicals, which was 2.55–13.66% and 11.12–56.55% larger than the loss in non-vegetated soils, respectively. The accumulation of phenanthrene and pyrene by the plant was evident. Root and shoot concentrations of these chemicals monotonically increased with increasing soil PAH concentrations. Bioconcentration factors (BCFs), defined as the ratio of chemical concentrations in plants and in the soils (on a dry weight basis), of phenanthrene and pyrene by roots were 0.136–0.776 and 0.603–1.425, while by shoots were 0.116–0.951 and 0.082–0.517, respectively. BCFs of phenanthrene and pyrene tended to decrease with the increasing concentrations of soil phenanthrene and pyrene. Plant accumulation only accounted for less than 0.32% (for phenanthrene) and 0.33% (for pyrene) of the total amount enhancement of the dissipated PAHs in vegetated vs. non-vegetated soils. In contrast, plant-promoted microbial biodegradation was the predominant contribution to the plant-enhanced dissipation of soil phenanthrene and pyrene. These results suggested the feasibility of the radionuclide hyperaccumulator in phytoremediating the soil PAH contaminants.     

Light hydrocarbons in hydrothermal and magmatic fumaroles: hints of catalytic and thermal reactions

Volcanic gaseous mixtures emitted from active volcanoes frequently show variable amounts of saturated (alkanes), unsaturated (alkenes) and aromatic volatile hydrocarbons. Three major patterns of distributions can be recognized, apparently related to the chemical-physical environment of formation of the gas exhalations: alkane-rich, low-temperature gas emissions from recently active volcanic areas; aromatic-rich hydrothermal manifestations; and alkene-rich, magmatic fumaroles on active volcanoes. Thermodynamic data, together with theoretical and practical findings from the petroleum industry, point to two main types of reactions occurring in these volcanic environments: cracking and reforming. Cracking processes, mainly caused by thermal effects, occur when hydrocarbon-bearing hydrothermal fluids enter and mix with a hot and dry, rapidly rising magmatic gas phase. The most probable products are light alkenes with carbon numbers decreasing with increasing reaction temperatures. The presence of aromatic species in hydrothermal fluids can be linked to reforming processes, catalysed by several possible agents, such as smectites and zeolites, generally present in the hydrothermally altered volcanic terranes, and facilitated by long residence times in a hydrothermal envelope.     

Assessment of organic pollutants in coastal sediments, UAE

Twenty-five stations were selected along the UAE coastal region to delineate the distribution and to determine the source of total petroleum hydrocarbon (TPH), total organic carbon (TOC), total Kjeldhal nitrogen (TKN), polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). The concentrations of TPH ranged between 46 and 223 mg/kg and the level of TOC was in the range from 0.044 to 17.8 wt%, while TPAHs occupied the range of 5–102.2 μg/kg. On the other hand, TPCBs showed values between 60 and 205 μg/kg and TKN ranged from 104 to 1,073 mg/kg. The present study shows that the distribution of organic compounds in UAE sediments were within safe limits comparing with previous studies. The present study revealed that TOC can be used as an indicator of oil pollution in heavily oiled sediments. The highest values of TOC, TPH, TPAHs and TPCBs related to the stations covered in fine sand due to adsorption properties and the large surface areas of the grains. The evaporation of low-boiling point compounds from surface layers leads to the enrichment of sediments with a thick residual. Al Sharjah-1 exhibited the highest values of TPH and TOC at Ras Al-Khaima-5, Umm Al-Quwen-1 and Dubai-1, while the highest values of TPAHs were at KhorFakkan-9, the highest value of TPCBs was at Ajman-2, and the highest values of TKN were at KhorFakkan-1, KhorFakkan-6 and Dubai-1.     

Oil migration through preferential petroleum migration pathway (PPMP) and polycyclic faults: A case study from the Shijiutuo Uplift,Bohai Bay basin,China

The Shijiutuo uplift is an oil enriched uplift in the offshore Bohai Bay Basin. Petroleum migration is a key factor for oil enrichment in Neogene reservoirs far away from the hydrocarbon kitchen. In this article, an integration of geological, geophysical and geochemical analyses are employed to investigate the petroleum migration and accumulation on the Shijiutuo uplift. Hydrocarbons in the QHD32-6 and QHD33 oilfields are mainly originated from the third (E₂s₃) and first (E₂s₁) member of the Shahejie Formation. The shallow traps have significant contributions of late-stage E₂s₁-derived oil. Lateral petroleum migration is a major mechanism forming large oilfields on the Shijiutuo uplift. The large oilfields have multiple hydrocarbon kitchens, multiple source rocks, and numerous preferential petroleum migration pathways (PPMPs). Once petroleum arrives at the structural highs on the Shijiutuo uplift through the Guantao Formation (N₁g) carrier-beds, neotectonic faults cutting through Guantao (N₁g) and Minghuazhen (N₁m^L) formations could serve as effective conduits for vertical petroleum migration. Neotectonic faults have experienced polycyclic fault activities. Fluid inclusions indicate episodic hydrocarbon charging. Crude oils display duplex properties of biodegradation and non-biodegradation, which is strong evidence for multiple and episodic oil charging on the Shijiutuo uplift. Finally, episodic petroleum charging along polycyclic neotectonic faults causes the late-stage E₂s₁-derived oils to occur in the shallow reservoirs.     

The synorogenic pegmatitic quartz veins of the Guacha Corral Shear zone (Sierra de Comechingones,Argentina): A textural,chemical, isotopic,cathodoluminescence and fluid inclusion study

The quartz veins and pegmatites of the Sierra de Comechingones (Sierras de Córdoba, NE Argentina) belong to the Comechingones Pegmatite field (CPF). For the quartz veins and the zoned pegmatites related parental granites are missing. The country rock of the quartz veins are mylonitic augengneisses in granulite to upper amphibolite facies. Field relations, microscopy, cathodoluminescence, radiometric age data, fluid inclusion, chemical and isotopic composition and literature define the quartz veins as synorogenic formed during the high-temperature phase of the Famatinian (480–460 Ma) event. During the Famatinian up to the Achalian (382–366 Ma) event the synorogenic quartz veins were subjected to high temperature ductile deformation documented by folding, boudinage and finally brittle shearing. K-Ar ages of illite from the shear zones of about 166 Ma document the final cooling of the Sierras Pampeanas below 100 °C. The long lasting thermal and deformational history of the study area is reflected by very different populations of fluid inclusions in vein quartz with remarkably high contents of thermogenic hydrocarbons in the early-formed fluid inclusions. LA–ICP–MS analysis reveals very low lattice-bound trace element contents, i.e. high purity quartz.     

Lipid biomarkers in surface sediments from the Gulf of Genoa,Ligurian sea (NW Mediterranean sea) and their potential for the reconstruction of palaeo-environments

A series of molecular organic markers were determined in surface sediments from the Gulf of Genoa (Ligurian Sea) in order to evaluate their potential for palaeo-environmental reconstructions. Allochthonous input can be characterized by the distributions of n-C₂₉ and n-C₃₁ alkanes, n-C₂₆ and n-C₂₈ alkanols and branched glycerol dialkyl glycerol tetraethers (GDGTs), whose concentrations are generally highest near the river mouths. In the open basin however, terrestrial n-alkanes and n-alkanols may have an additional, eolian source. Autochthonous input is represented by crenarchaeol and isoprenoid GDGTs. Their concentrations are highest in the open basin showing the preference of Thaumarchaeota for oligotrophic waters. Indications of a significant degradation of sterols and C₃₇ alkenones exclude these lipids as reliable productivity proxies. Using terrestrial and aquatic lipids as end-members allows estimating the percentage of terrestrial organic matter between 20% and 58% in the coastal area decreasing to 1–30% in the deep basin. The spatial distribution of sea surface temperature (SST) estimates using the alkenone-based U^K′₃₇ index is very similar to the autumnal (November) mean satellite-based SST distribution. Conversely, TEX^H₈₆-derived SST estimates are close to winter SSTs in the coastal area and summer SSTs in the open basin. This pattern reflects presumably a shift in the main production of Thaumarchaeota from the coastal area in winter to the open basin in summer. This study represents a major prerequisite for the future application of lipid biomarkers on sediment cores from the Gulf of Genoa.     

四川盆地东北部海、陆相储层沥青组成特征及来源

本研究系统采集了四川盆地东北部大普光、元坝地区上三叠统须家河组、下三叠统飞仙关组、上二叠统长兴组和鄂西渝东地区中石炭统黄龙组储层固体沥青样品,进行了岩石热解、有机元素、碳同位素和饱和烃、芳烃组分GC/MS的分析,以确定其成因、性质和来源。这些沥青总体上具有低溶性(多数氯仿抽提物/TOC<8%)、高反射率(换算的Ro>1.4%)、低H/C原子比(<0.6)的性质,属焦沥青类,是古油藏原油或运移烃经热裂解成气的残留物。其中,飞仙关组、长兴组碳酸岩储层沥青的S/C原子比值普遍较高(主要在0.025~0.085范围),且硫同位素δ³⁴S值(主要在12‰~24‰)接近硬石膏,说明可能包含有部分TSR成因的沥青。这些高热演化沥青中饱和烃生物标志物的组成和分布出现了异常变化,基本失去了其常规应用意义。芳烃中2,6-/2,10-DMP(二甲基菲)、1,7-/1,9-DMP和4-/1-MDBT(甲基二苯并噻吩)比值,可用来指示沥青烃源岩的有机质生源构成和沉积环境性质。须家河组陆相沥青中这些芳烃比值较高,表征其烃源母质中陆源有机质占优势,且形成于氧化性的环境;而飞仙关组、长兴组及黄龙组海相沥青中这些参数值低得多,意味着其烃源岩有机质生源应以水生生物为主,并沉积于还原性环境。经沥青/烃源岩的碳同位素和二苯并噻吩系列组成对比,认为须家河组储层沥青来源于本层位烃源岩,飞仙关组和长兴组沥青同源于二叠系烃源层。鄂西渝东地区的黄龙组沥青碳同位素偏重(δ¹³C值为-23.2‰~-26.4‰),原始烃源可能主要来自中、下志留统韩家店组及小河坝组地层。