How Effective Is Thermal Remediation of DNAPL Source Zones in Reducing Groundwater Concentrations?

Dense nonaqueous phase liquid (DNAPL) source areas containing chlorinated volatile organic compounds (cVOCs) such as trichloroethene (TCE) and perchloroethene (PCE) often give rise to significant dissolved plumes in groundwater, leading to the closure of downgradient water supply wells and creating vapor intrusion issues in buildings located above the plume. Hydraulic containment via pump‐and‐treat has often been implemented to limit migration but must continue indefinitely. Removal of the DNAPL source area by means such as in situ thermal remediation (ISTR) offers the potential to diminish or end the need for hydraulic containment if the associated dissolved plume attenuates sufficiently following source removal. A question often raised is whether this occurs or whether the back diffusion of contaminants from secondary sources such as low‐permeability lenses in the dissolved plume precludes it. The authors conducted DNAPL source removal using ISTR at dozens of sites. This paper presents a compilation of cases—10 separate DNAPL source areas at five project sites—where data indicate that the implementation of a thorough ISTR in a DNAPL source area can result in the attenuation of the associated dissolved plume, such that in several cases, long‐standing pump‐and‐treat systems could be turned off. Our findings contrast with recent assertions that aggressive source remediation may not be justifiable because dissolved plume concentrations will not decline sufficiently. We show that the application of ISTR can result in the thorough removal of the DNAPL source, effective diminution of dissolved plume groundwater concentrations, and achievement of drinking water standards.     

Oxygen-Containing Compounds Identified in Groundwater from Fuel Release Sites Using GCxGC-TOF-MS

This research continues a 7-year study of oxygen-containing organic compounds present in groundwater at gasoline and diesel fuel release sites that are quantified as diesel-range “total petroleum hydrocarbons” when measured by methods utilizing solvent extraction and gas chromatography. Two-dimensional gas chromatography with time-of-flight mass spectrometry was used to tentatively identify 1162 compounds (TICs) in 113 groundwater samples from 22 sites. Samples were collected from wells either upgradient of the release, within the source zone, or downgradient of the source but still within the plume of dissolved organics associated with release. The names and formulas of all TICs found in samples from each well type are presented and the results from upgradient and downgradient locations are compared in detail. About 60% of the most frequently detected TICs in downgradient wells were also detected in upgradient wells. A majority of these were saturated straight chain alkyl acids, commonly called fatty acids, or fatty acid esters. Of TICs frequently detected in downgradient wells but not upgradient wells, over half were branched alkyl alcohols. Hierarchical cluster analysis results suggest about 80% of the chemical composition of downgradient samples is more similar to upgradient samples than to source area samples. This similarity is due to the presence of the same types of fatty acids and esters. Principal component analysis indicates a continuum of biodegradation between the source area and downgradient samples with the latter becoming more consistent with upgradient samples. Results suggest some TICs may not be petroleum degradation intermediates but compounds synthesized by microorganisms through secondary production and carbon cycling.     

Persistence of a Groundwater Contaminant Plume after Hydraulic Source Containment at a Chlorinated‐Solvent Contaminated Site

The objective of this study was to characterize the behavior of a groundwater contaminant (trichloroethene, TCE) plume after implementation of a source‐containment operation at a site in Arizona. The plume resides in a quasi‐three‐layer system comprising a sand/gravel unit bounded on the top and bottom by relatively thick silty clayey layers. The system was monitored for 60 months beginning at start‐up in 2007 to measure the change in contaminant concentrations within the plume, the change in plume area, the mass of the contaminant removed, and the integrated contaminant mass discharge (CMD). The concentrations of TCE in groundwater pumped from the plume extraction wells have declined significantly over the course of operation, as have concentrations for groundwater sampled from 40 monitoring wells located within the plume. The total CMD associated with operation of the plume extraction wells peaked at 0.23 kg/d, decreased significantly within 1 year, and thereafter began an asymptotic decline to a current value of approximately 0.03 kg/d. Despite an 87% reduction in contaminant mass and a comparable 87% reduction in CMD for the plume, the spatial area encompassed by the plume has decreased by only approximately 50%. This is much less than would be anticipated based on ideal flushing and mass‐removal behavior. Simulations produced with a simplified three‐dimensional (3D) numerical model matched reasonably well to the measured data. The results of the study suggest that permeability heterogeneity, back diffusion, hydraulic factors associated with the specific well field system, and residual discharge from the source zone are all contributing to the observed persistence of the plume, as well as the asymptotic behavior currently observed for mass removal and for the reduction in CMD.     

World's Largest In Situ Thermal Desorption Project: Challenges and Solutions

This paper presents the largest In Situ Thermal Desorption (ISTD) project completed to date. The redevelopment of a former aerospace manufacturing facility adjacent to a commercial airport was the main driver, requiring relatively rapid reduction of several chlorinated volatile organic compounds (CVOC) in a 3.2‐acre source zone. The source zone was divided into four quadrants with differing treatment depths, heated simultaneously using a total of 907 thermal conduction heater wells. Five different depths were selected across the area, according to the depth of contaminant impact. Prior to implementation, a risk and optimization study led to placement of a vertical sheet‐pile wall around the treatment zone to minimize groundwater flow, and a pilot test of a novel direct‐drive method for installation of the heater casings. Because of a shallow water table, a layer of clean fill was placed over the treatment zone, and partial dewatering was necessary prior to heating. A network of vertical multiphase extraction wells and horizontal vapor extraction wells was used to establish hydraulic and pneumatic control and to capture the contaminants. The site was split into four decision units, each with a rigorous soil sampling program which included collecting a total of 270 confirmatory soil samples from locations with the highest pretreatment CVOC concentrations requiring reduction to below 1 mg/kg for each contaminant. Temperature monitoring and mass removal trends were used to trigger the sampling events. Eventually, a small area near the center of the site required the installation of four additional heaters before the soil goals were reached after 238 days of heating. The total energy usage for heating and treating the source area was 23 million kWh—slightly lower than the estimated 26.5 million kWh. Actual energy losses and the energy removal associated with the extracted steam were lower than anticipated. An estimated 13,400 kg (29,800 lbs) of CVOC mass was removed, and all soil goals were met. This paper presents the challenges associated with a project of this scale and describes the solutions to successfully complete the ISTD remedy.     

Removal of PCE DNAPL from Tight Clays Using In Situ Thermal Desorption

This paper presents a full‐scale thermal remediation of a brownfields site near San Francisco, California. In Situ Thermal Desorption (ISTD) was used for treatment of chlorinated solvents in a tight clay below the water table. The site had contaminants in concentrations indicating that a tetrachloroethene (PCE)‐rich DNAPL was present. A target volume of 5097 m³ of subsurface material to a depth of 6.2 m was treated for a period of 110 d of heating. Energy was delivered through 126 thermal conduction heater borings, and vapors were extracted from a combination of vertical and horizontal vacuum wells. Approximately 2540 kg of contaminants were recovered in the extracted vapors by the end of treatment. The PCE concentration in the clay was reduced from as high as 2700 mg/kg to an average concentration of 0.012 mg/kg within 110 d of heating (a reduction of >99.999%). Similar effectiveness was documented for TCE, cis‐1,2‐DCE, and vinyl chloride. A total of 2.2 million kWh of electric power was used to heat the site. Approximately 45% of this energy was used to heat the subsurface to the target temperature. Another 53% was necessary to boil approximately 41% of the groundwater within the treatment zone, creating approximately 600 pore volumes of steam by the end of the 110‐d heating and treatment period. Steam generation thus occurred within the clay. Partitioning of the contaminants into the steam and its removal comprised the dominant remedial mechanism. The steam migrated laterally toward the ISTD heaters, where it encountered a small dry region adjacent to each of the heaters, which served as a preferential pathway allowing the steam to migrate upward along the heaters to the more permeable vadose zone. There the steam was captured by a system of vertical and horizontal vacuum extraction wells. This vapor removal strategy facilitated effective thermal treatment of the tight clays located below the water table. Features of a robust design are extension of the heaters at least 1.2 m deeper than the treatment depth, and the installation of shallow horizontal vapor collection wells which allow for establishment of pneumatic control.     

Effects of a Dual‐Pump Crude‐Oil Recovery System,Bemidji, Minnesota,USA

A crude‐oil spill occurred in 1979 when a pipeline burst near Bemidji, MN. In 1998, the pipeline company installed a dual‐pump recovery system designed to remove crude oil remaining in the subsurface at the site. The remediation from 1999 to 2003 resulted in removal of about 115,000 L of crude oil, representing between 36% and 41% of the volume of oil (280,000 to 316,000 L) estimated to be present in 1998. Effects of the 1999 to 2003 remediation on the dissolved plume were evaluated using measurements of oil thicknesses in wells plus measurements of dissolved oxygen in groundwater. Although the recovery system decreased oil thicknesses in the immediate vicinity of the remediation wells, average oil thicknesses measured in wells were largely unaffected. Dissolved‐oxygen measurements indicate that a secondary plume was caused by disposal of the pumped water in an upgradient infiltration gallery; this plume expanded rapidly immediately following the start of the remediation in 1999. The result was expansion of the anoxic zone of groundwater upgradient and beneath the existing natural attenuation plume. Oil‐phase recovery at this site was shown to be challenging, and considerable volumes of mobile and entrapped oil remain in the subsurface despite remediation efforts.     

Methods to Estimate Source Zone Depletion of Fuel Releases by Groundwater Flow

We compare two methods for estimating the natural source zone depletion (NSZD) rate at fuel release sites that occurs by groundwater flow through the source zone due to dissolution and transport of biodegradation products. Dissolution is addressed identically in both methods. The “mass budget method”, previously proposed and applied by others, estimates the petroleum hydrocarbon biodegradation rate based on dissolved electron acceptor delivery and dissolved biodegradation product removal by groundwater flow. The mass budget method relies on assumed stoichiometry for the degradation reactions and differences in concentrations of dissolved species (oxygen, nitrate, sulfate, reduced iron, reduced manganese, nonvolatile dissolved organic carbon, methane) at monitoring locations upgradient and downgradient of the source zone. We illustrate a refinement to account for degradation reactions associated with loss of reduced iron from solution. The “carbon budget method,” a simplification of approaches applied by others, addresses carbon‐containing species in solution or lost from solution (precipitated) and does not require assumptions about stoichiometry or information about electron acceptors. We apply both methods to a fuel release site with unusually detailed monitoring data and discuss applicability to more typical and less thoroughly monitored sites. The methods, as would typically be applied, yield similar results but have different constraints and uncertainties. Overall, we conclude that the carbon budget method has greater practical utility as it is simpler, requires fewer assumptions, accounts for most iron‐reducing reactions, and does not include CO₂ that escapes from the saturated to the unsaturated zone.     

222Rn as Natural Tracer for LNAPL Recovery in a Crude Oil‐Contaminated Aquifer

The objective of this study was to investigate whether ²²²Rn in groundwater can be used as a tracer for light non‐aqueous phase liquid (LNAPL) quantification at a field site treated by dual‐phase LNAPL removal. After the break of a pipeline, 5 ha of soil in the nature reserve Coussouls de Crau in southern France was contaminated by 5100 m³ of crude oil. Part of this oil seeped into the underlying gravel aquifer and formed a floating oil body of about 3.9 ha. The remediation consists of plume management by hydraulic groundwater barriers and LNAPL extraction in the source zone. ²²²Rn measurements were performed in 21 wells in and outside the source zone during 15 months. In uncontaminated groundwater, the radon activity was relatively constant and remained always >11 Bq/L. The variability of radon activity measurements in wells affected by the pump‐and‐skim system was consistent with the measurements in wells that were not impacted by the system. The mean activities in wells in the source zone were, in general, significantly lower than in wells upgradient of the source zone, owing to partitioning of ²²²Rn into the oil phase. The lowest activities were found in zones with high non‐aqueous phase liquid (NAPL) recovery. LNAPL saturations around each recovery well were furthermore calculated during a period of high groundwater level, using a laboratory‐determined crude oil–water partitioning coefficient of 38.5 ± 2.9. This yielded an estimated volume of residual crude oil of 309 ± 93 m³ below the capillary fringe. We find that ²²²Rn is a useful and cheap groundwater tracer for finding zones of good LNAPL recovery in an aquifer treated by dual‐phase LNAPL removal, but that quantification of NAPL saturation using Rn is highly uncertain.     

Modeling of Plume Capture by Continuous, Low-Permeability Barriers

Modeling was performed to simulate ground water flow through reactive barriers of lower hydraulic conductivity than the surrounding aquifer to determine the plume capture widths. As a plume approaches such a barrier, it spreads laterally. Therefore, to intercept an entire plume, the barrier must be wider than the upgradient width of the undisturbed plume. The results indicate that, for practical values of barrier thickness and plume width, hydraulic conductivities ten-fold less than that of the aquifer can be accommodated by making the width of the barrier approximately 20% greater than the upgradient width of the plume. Barrier hydraulic conductivities one-hundred-fold less than that of the aquifer may require barrier widths up to twice the width of the upgradient plume for plumes 100 feet wide (33 m) and as little as 1.1 times for plumes 1000 feet wide (325 m). The results presented here lend support to the view that novel emplacement methods that create zones of slightly lower hydraulic conductivity than the native aquifer may be viable alternatives to the excavation-and-backfill approaches which have thus far been used for installing permeable reactive barriers.     

Comparing Natural Source Zone Depletion Pathways at a Fuel Release Site

Natural source zone depletion (NSZD) refers to processes within chemically impacted vadose and saturated zones that reduce the mass of contaminants remaining in a defined source control volume. Studies of large petroleum hydrocarbon release sites have shown that the depletion rate by vapor phase migration of degradation products from the source control volume through the vadose zone (V‐NSZD) is often considerably higher than the rate of depletion from the source control volume by groundwater flow carrying dissolved petroleum hydrocarbons arising from dissolution, desorption, or back diffusion, and degradation products arising from biodegradation (GW‐NSZD). In this study, we quantified vadose zone and GW‐NSZD at a small unpaved fuel release site in California typical of those in settings with predominantly low permeability media. We estimated vadose zone using a dense network of efflux monitoring locations at four sampling events over 2 years, and GW‐NSZD using groundwater monitoring data downgradient of the source control volume in three depth intervals spanning up to 9 years. On average, vadose zone was 17 times greater than GW‐NSZD during the time interval of comparison, and vadose zone was in the range of rates quantified at other sites with petroleum hydrocarbon releases. Estimating vadose zone and GW‐NSZD rates is challenging but the vadose zone rate is the best indicator of overall source mass depletion, whereas GW‐NSZD rates may be useful as baselines to quantify progress of natural or engineered remediation in portions of the saturated zone in which there are impediments to loss of methane and other gases to the vadose zone.     

Method for Assessing Source Zone Natural Depletion at Chlorinated Aliphatic Spill Sites

This work focuses on the site‐specific assessment of source zone natural attenuation (SZNA) at chlorinated aliphatic hydrocarbon (CAH)‐impacted sites. The approach is similar in some ways, but different in other ways from recently proposed SZNA assessment paradigms for petroleum‐impacted sites. The similarities lie in the organization of the approach around determining: (1) whether or not SZNA is occurring, (2) the current SZNA rate, and (3) what is the future projection for SZNA rate changes and the final state of the source zone. Differences lie in how those rates are determined, especially with respect to the quantities measured and data reduction. Petroleum‐impacted site SZNA approaches emphasize quantifying fluxes of electron acceptors, while the proposed CAH assessment approach emphasizes quantifying parent and daughter compound fluxes. A paradigm for assessing SZNA at CAH sites is presented and its use is illustrated, for example former dry cleaner site, where the SZNA rate was approximately 3.5 kg/year as tetrachloroethylene (PCE) with about 80% of the mass loss attributed to groundwater flow and 20% attributed to vapor transport.     

西藏羌塘盆地的深部构造与含油气远景评价

羌塘盆地是目前国内石油勘探的热点地区之一,作者综合研究了羌塘盆地的地球物理、石油地质调查资料及INDEPTH-3深部调查结果,得出:1, 盆地内烃源层、储集层、盖层及其组合条件很好, 局部构造发育,有利于形成和保存油气藏,断裂不会成为致命问题,提出了今后工作的主要目的层为上三叠世-中侏罗系组成的中构造层;2,对盆地二级构造作了新的划分,否定羌中隆起,提出盆地表层的主要构造方向为北西-南东向,成“三凹三隆”及“一深凹”的地壳结构特征,其中主沉降带内部及其两侧是最有利的找油气远景地带;3,本区壳幔之间的相互作用较强,盆地北部火山及热活动多,对油气远景评价有较大影响,而盆地南部沉积厚度大,受深层热影响相对较小,是找油气的更有利的地段。4,强调查明深部地层物性、油气赋存状况,烃类物质的来源和上下构造符合情况是当务之急。重点是加强点上的调查和评价研究;5,提出不能轻视伦坡拉陆相第三系盆地找油前景,它可能汇聚有两侧海相地层的油气。     

Crude Oil at the Bemidji Site: 25 Years of Monitoring,Modeling, and Understanding

The fate of hydrocarbons in the subsurface near Bemidji, Minnesota, has been investigated by a multidisciplinary group of scientists for over a quarter century. Research at Bemidji has involved extensive investigations of multiphase flow and transport, volatilization, dissolution, geochemical interactions, microbial populations, and biodegradation with the goal of providing an improved understanding of the natural processes limiting the extent of hydrocarbon contamination. A considerable volume of oil remains in the subsurface today despite 30 years of natural attenuation and 5 years of pump‐and‐skim remediation. Studies at Bemidji were among the first to document the importance of anaerobic biodegradation processes for hydrocarbon removal and remediation by natural attenuation. Spatial variability of hydraulic properties was observed to influence subsurface oil and water flow, vapor diffusion, and the progression of biodegradation. Pore‐scale capillary pressure‐saturation hysteresis and the presence of fine‐grained sediments impeded oil flow, causing entrapment and relatively large residual oil saturations. Hydrocarbon attenuation and plume extent was a function of groundwater flow, compound‐specific volatilization, dissolution and biodegradation rates, and availability of electron acceptors. Simulation of hydrocarbon fate and transport affirmed concepts developed from field observations, and provided estimates of field‐scale reaction rates and hydrocarbon mass balance. Long‐term field studies at Bemidji have illustrated that the fate of hydrocarbons evolves with time, and a snap‐shot study of a hydrocarbon plume may not provide information that is of relevance to the long‐term behavior of the plume during natural attenuation.     

The effects of vertical barrier walls on the hydraulic control of contaminated groundwater

We present explicit analytic solutions describing the hydraulic head and discharge vector for two-dimensional, steady groundwater flow past an impermeable barrier embedded in a regional flow field. We use the solution to investigate the effects of open vertical barriers on the flow field; in particular, we examine the hydraulic containment of contaminant plumes or source zones by combination of a vertical barrier wall and extraction wells. We quantify the local reduction in discharge rates due to the barrier wall and the local increase in the size of the capture zone of an extraction well near an open, up-gradient barrier. We find that the combination of an open vertical barrier with down-gradient extraction wells can be very effective in decreasing the well discharge rate necessary to control a contaminant plume or source area. Design charts are presented for quantifying the effects of the barrier wall on the hydraulic control of the groundwater flow field and for estimating the jump in head across a barrier. The charts are appropriate for use in the preliminary design and cost estimating of remedial systems, and for the design of dewatering systems.     

NAPL source zone depletion model and its application to railroad-tank-car spills

We developed a new semi-analytical source zone depletion model (SZDM) for multicomponent light nonaqueous phase liquids (LNAPLs) and incorporated this into an existing screening model for estimating cleanup times for chemical spills from railroad tank cars that previously considered only single-component LNAPLs. Results from the SZDM compare favorably to those from a three-dimensional numerical model, and from another semi-analytical model that does not consider source zone depletion. The model was used to evaluate groundwater contamination and cleanup times for four complex mixtures of concern in the railroad industry. Among the petroleum hydrocarbon mixtures considered, the cleanup time of diesel fuel was much longer than E95, gasoline, and crude oil. This is mainly due to the high fraction of low solubility components in diesel fuel. The results demonstrate that the updated screening model with the newly developed SZDM is computationally efficient, and provides valuable comparisons of cleanup times that can be used in assessing the health and financial risk associated with chemical mixture spills from railroad-tank-car accidents.     

Small Purge Method to Sample Vapor from Groundwater Monitoring Wells Screened Across the Water Table

Groundwater monitoring wells are present at most hydrocarbon release sites that are being assessed for cleanup. If screened across the vadose zone, these wells provide an opportunity to collect vapor samples that can be used in the evaluation of vapor movement and biodegradation processes occurring at such sites. This paper presents a low purge volume method (modified after that developed by the U.S. EPA) for sampling vapor from monitoring wells that is easy to implement and can provide an assessment of the soil gas total petroleum hydrocarbon (TPH) and O₂ concentrations at the base of the vadose zone. As a result, the small purge method allows for sampling of vapor from monitoring wells to support petroleum vapor intrusion (PVI) risk assessment. The small purge volume method was field tested at the Hal's service station site in Green River, Utah. This site is well‐known for numerous soil gas measurements containing high O₂ and high TPH vapor concentrations in the same samples which is inconsistent with well‐accepted biodegradation models for the vapor pathway. Using the low purge volume method, monitoring wells were sampled over, upgradient, and downgradient of the light nonaqueous phase liquid (LNAPL) footprint. Results from our testing at Hal's show that vapor from monitoring wells over LNAPL contained very low O₂ and high TPH concentrations. In contrast, vapor from monitoring wells not over LNAPL contained high O₂ and low TPH concentrations. The results of this study show that a low purge volume method is consistent with biodegradation models especially for sampling at sites where low permeability soils exist in and around a LNAPL source zone.     

Geochemical Indicators of Intrinsic Bioremediation

A detailed field investigation has been completed at a gasoline-contaminated aquifer near Rocky Point, NC, to examine possible indicators of intrinsic bioremediation and identify factors that may significantly influence the rate and extent of bioremediation. The dissolved plume of benzene, toluene, ethylbenzene, and xylene (BTEX) in ground water is naturally degrading. Toluene and o-xylene are most rapidly degraded followed by m-, p-xylene, and benzene. Ethylbenzene appears to degrade very slowly under anaerobic conditions present in the center of the plume. The rate and extent of biodegradation appears to be strongly influenced by the type and quantity of electron acceptors present in the aquifer. At the upgradient edge of the plume, nitrate, ferric iron, and oxygen are used as terminal electron acceptors during hydrocarbon biodegradation. The equivalent of 40 to 50 mg/I of hydrocarbon is degraded based on the increase in dissolved CO₂ relative to background ground water. Immediately downgradient of the source area, sulfate and iron are the dominant electron acceptors. Toluene and o-xylene are rapidly removed in this region. Once the available oxygen, nitrate, and sulfate are consumed, biodegradation is limited and appears to be controlled by mixing and aerobic biodegradation at the plume fringes.     

Evaluation of Seasonal Factors on Petroleum Hydrocarbon Vapor Biodegradation and Intrusion Potential in a Cold Climate

A detailed seasonal study of soil vapor intrusion at a cold climate site with average yearly temperature of 1.9 °C was conducted at a house with a crawlspace that overlay a shallow dissolved‐phase petroleum hydrocarbon (gasoline) plume in North Battleford, Saskatchewan, Canada. This research was conducted primarily to assess if winter conditions, including snow/frost cover, and cold soil temperatures, influence aerobic biodegradation of petroleum vapors in soil and the potential for vapor intrusion. Continuous time‐series data for oxygen, pressure differentials, soil temperature, soil moisture, and weather conditions were collected from a high‐resolution monitoring network. Seasonal monitoring of groundwater, soil vapor, crawlspace air, and indoor air was also undertaken. Petroleum hydrocarbon vapor attenuation and biodegradation rates were not significantly reduced during low temperature winter months and there was no evidence for a significant capping effect of snow or frost cover that would limit oxygen ingress from the atmosphere. In the residual light nonaqueous phase liquid (LNAPL) source area adjacent to the house, evidence for biodegradation included rapid attenuation of hydrocarbon vapor concentrations over a vertical interval of approximately 0.9 m, and a corresponding decrease in oxygen to less than 1.5% v/v. In comparison, hydrocarbon vapor concentrations above the dissolved plume and below the house were much lower and decreased sharply within a few tens of centimeters above the groundwater source. Corresponding oxygen concentrations in soil gas were at least 10% v/v. A reactive transport model (MIN3P‐DUSTY) was initially calibrated to data from vertical profiles at the site to obtain biodegradation rates, and then used to simulate the observed soil vapor distribution. The calibrated model indicated that soil vapor transport was dominated by diffusion and aerobic biodegradation, and that crawlspace pressures and soil gas advection had little influence on soil vapor concentrations.     

渤海海域沙三段烃源灶演化特征研究

烃源灶是表征供烃中心的最合适的方法, 其迁移演化研究对油气勘探具有重要意义. 渤海海域为渤海湾盆地海域部分, 是中国主要富油气盆地之一. 沙河街组三段是古近系4套烃源岩中最重要的烃源岩. 本文在沉积、构造发育和热史研究成果的基础之上, 结合烃源岩地球化学参数模拟计算了沙三段烃源岩成熟生烃及生、排烃演化历史, 并以此研究渤海海域沙三段烃源灶的演化特征. 结果表明研究区具有早期的"双灶共存"和晚期"单灶为主, 多灶并存"的特征, 即早期(古近纪)为岐口和渤中凹陷烃源灶; 晚期(新近纪至今)以渤中凹陷烃源灶为主, 岐口、南堡、黄河口、辽中、辽西和秦南凹陷等烃源灶并存. 烃源灶为油气田的形成提供了物质基础, 渤海海域的大中型油气田分布在主要烃源灶周围的凸起区和斜坡带. 因而, 本文的研究可以为渤海海域油气的深入勘探决策提供基础.     

Impact of seasonal variations in hydrological stresses and spatial variations in geologic conditions on a TCE plume at an industrial complex in Wonju,Korea

Spatial and temporal variations in a trichloroethylene (TCE) plume at an industrial complex in Wonju, Korea, were examined based on hydrogeological data and seven rounds of groundwater quality data collected over a year. The site has considerable vertical heterogeneities; the top layer of soil is covered by impermeable paving material at several locations, followed by a series of reclaimed or residual soil layers, and with weathered rocks to the crystalline biotite granite at the bottom. Areal heterogeneity in the surface conditions plays an important role in controlling groundwater recharge. The heterogeneity structure is influenced by complex surface conditions paved with asphalt and concrete. Owing to the presence of limited recharge area and concentrated summer precipitation events, the effects of seasonal variations on groundwater hydraulics tend to diminish with distance from the recharge area. This result was established by analysing the influence of the contrasting surface recharge conditions between the near‐source zone and the far zone, and the seasonally concentrated precipitation on the transport patterns of a TCE plume. In addition, variations in the plume's downstream contaminant flux levels were also analysed along a transect line near the source zone. The results show that the general tendency of the TCE plume contaminant concentration and mass discharges were reproducible if we account for seasonal recharge variations and the associated changes in the groundwater level. During recharge events, the TCE concentration variations appear to be influenced by leaching of the residual dense non‐aqueous‐phase liquid (DNAPL) TCE trapped in the unsaturated zone. This result shows that seasonal variations in contaminant plume near the source zone is inevitable at this site, and that these variations indicate the presence of residual DNAPL at or above the water table, at least in some isolated locations. Copyright © 2011 John Wiley & Sons, Ltd.