A simple method for calculating growth rates of petroleum hydrocarbon plumes

Consumption of aquifer Fe(III) during biodegradation of ground water contaminants may result in expansion of a contaminant plume, changing the outlook for monitored natural attenuation. Data from two research sites contaminated with petroleum hydrocarbons show that toluene and xylenes degrade under methanogenic conditions, but the benzene and ethylbenzene plumes grow as aquifer Fe(III) supplies are depleted. By considering a one-dimensional reaction front in a constant unidirectional flow field, it is possible to derive a simple expression for the growth rate of a benzene plume. The method balances the mass flux of benzene with the Fe(III) content of the aquifer, assuming that the biodegradation reaction is instantaneous. The resulting expression shows that the benzene front migration is retarded relative to the ground water velocity by a factor that depends on the concentrations of hydrocarbon and bioavailable Fe(III). The method provides good agreement with benzene plumes at a crude oil study site in Minnesota and a gasoline site in South Carolina. Compared to the South Carolina site, the Minnesota site has 25% higher benzene flux but eight times the Fe(III), leading to about one-sixth the expansion rate. Although it was developed for benzene, toluene, ethylbenzene, and xylenes, the growth-rate estimation method may have applications to contaminant plumes from other persistent contaminant sources.     

Determination of first-order degradation rate constants from monitoring networks

In this article, different strategies for estimating first-order degradation rate constants from measured field data are compared by application to multiple, synthetic, contaminant plumes. The plumes were generated by numerical simulation of contaminant transport and degradation in virtual heterogeneous aquifers. These sites were then individually and independently investigated on the computer by installation of extensive networks of observation wells. From the data measured at the wells, that is, contaminant concentrations, hydraulic conductivities, and heads, first-order degradation rates were estimated by three 1D centerline methods, which use only measurements located on the plume axis, and a two-dimensional method, which uses all concentration measurements available downgradient from the contaminant source. Results for both strategies show that the true rate constant used for the numerical simulation of the plumes in general tends to be overestimated. Overestimation is stronger for narrow plumes from small source zones, with an average overestimation factor of about 5 and single values ranging from 0.5 to 20, decreasing for wider plumes, with an average overestimation factor of about 2 and similar spread. Reasons for this overestimation are identified in the velocity calculation, the dispersivity parameterization, and off-centerline measurements. For narrow plumes, the one- and the two-dimensional strategies show approximately the same amount of overestimation. For wider plumes, however, incorporation of all measurements in the two-dimensional approach reduces the estimation error. No significant relation between the number of observation wells in the monitoring network and the quality of the estimated rate constant is found for the two-dimensional approach.     

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.     

Thermal DNAPL Source Zone Treatment Impact on a CVOC Plume

The tetrachloroethene (PCE) source zone at a site in Endicott, New York had caused a dissolved PCE plume. This plume was commingled with a petroleum hydrocarbon plume from an upgradient source of fuel oil. The plume required a system for hydraulic containment, using extraction wells located about 360 m downgradient of the source. The source area was remediated using in situ thermal desorption (ISTD). Approximately 1406 kilograms (kg) of PCE was removed in addition to 4082 kg of commingled petroleum‐related compounds. The ISTD treatment reduced the PCE mass discharge into the plume from an estimated 57 kg/year to 0.07 kg/year, essentially removing the source term. In the 5 years following the completion of the thermal treatment in early 2010, the PCE plume has collapsed, and the concentration of degradation products in the PCE‐series plume area has declined by two to three orders of magnitude. Anaerobic dechlorination is the suspected dominant mechanism, assisted by the presence of a fuel oil smear zone and a petroleum hydrocarbon plume from a separate source area upgradient of the PCE source. Based on the post‐thermal treatment groundwater monitoring data, the hydraulic containment system was reduced in 2014 and discontinued in early 2015.     

Biogeochemical evolution of a landfill leachate plume, Norman, Oklahoma

Leachate from municipal landfills can create groundwater contaminant plumes that may last for decades to centuries. The fate of reactive contaminants in leachate-affected aquifers depends on the sustainability of biogeochemical processes affecting contaminant transport. Temporal variations in the configuration of redox zones downgradient from the Norman Landfill were studied for more than a decade. The leachate plume contained elevated concentrations of nonvolatile dissolved organic carbon (NVDOC) (up to 300 mg/L), methane (16 mg/L), ammonium (650 mg/L as N), iron (23 mg/L), chloride (1030 mg/L), and bicarbonate (4270 mg/L). Chemical and isotopic investigations along a 2D plume transect revealed consumption of solid and aqueous electron acceptors in the aquifer, depleting the natural attenuation capacity. Despite the relative recalcitrance of NVDOC to biodegradation, the center of the plume was depleted in sulfate, which reduces the long-term oxidation capacity of the leachate-affected aquifer. Ammonium and methane were attenuated in the aquifer relative to chloride by different processes: ammonium transport was retarded mainly by physical interaction with aquifer solids, whereas the methane plume was truncated largely by oxidation. Studies near plume boundaries revealed temporal variability in constituent concentrations related in part to hydrologic changes at various time scales. The upper boundary of the plume was a particularly active location where redox reactions responded to recharge events and seasonal water-table fluctuations. Accurately describing the biogeochemical processes that affect the transport of contaminants in this landfill-leachate-affected aquifer required understanding the aquifer's geologic and hydrodynamic framework.     

Plume-lithosphere interactions in the ocean basins: constraints from the source mineralogy

Trace element relationships of near-primary alkalic lavas from La Grille volcano, Grande Comore, in the Indian Ocean, as well as those of the Honolulu volcanic series, Oahu, Hawaii, show that their sources contain amphibole and/or phlogopite. Small amounts of each mineral (2% amphibole in the source of La Grille and 0.5% phlogopite plus some amphibole in the source of the Honolulu volcanics) and a range of absolute degrees of partial melting from 1 to 5% for both series are consistent with the observed trace element variation. Amphibole and phlogopite are not stable at the temperatures of convecting upper mantle or upwelling thermal plumes from the deep mantle; however, they are stable at pressure-temperature conditions of the oceanic lithospheric mantle. Therefore, the presence of amphibole and/or phlogopite in the magma source region of volcanics is strong evidence for lithospheric melting, and we conclude that the La Grille and the Honolulu series formed by melting of the oceanic lithospheric mantle.

The identification of amphibole ± phlogopite in the source region of both series implies that the metasomatism by fluids or volatile-rich melts occurred prior to melting. The presence of hydrous phases results in a lower solidus temperature of the lithospheric mantle, which can be reached by conductive heating by the thermal plumes. Isotope ratios of the La Grille and the Honolulu series display a restricted range in composition and represent compositional end-members for each island. Larger isotopic variations in shield lavas, represented by the contemporaneous Karthala volcano on Grande Comore and the older Koolau series on Oahu, reflect interaction of the upwelling thermal plumes with the lithospheric mantle rather than the heterogeneity of deep-seated mantle plume sources or entrainment of mantle material in the rising plume. Literature OsSr isotope ratio covariations constrain the process of plume-lithosphere interaction as occurring through mixing of plume melts and low-degree melts from the metasomatized oceanic lithospheric mantle.

The characterization of the lithospheric mantle signature allows the isotopic composition of the deep mantle plume components to be identified, and mixing relationships show that the Karthala and Koolau plume end-members have nearly uniform isotopic compositions. Based on independent arguments, isotopic variations on Heard and Easter islands have been shown to be a result of mixing between deep plume sources having distinct isotopic compositions with lithosphere or shallow asthenospheric mantle. To the extent that these case studies are representative of oceanic island volcanism, they indicate that interaction with oceanic lithospheric mantle plays an important role in the compositions of lavas erupted during the shield-building stage of plume magmatism, and that isotopic compositions of deep mantle plume sources are nearly uniform on the scale that they are sampled by melting.     

Exceptionally Long MTBE Plumes of the Past Have Greatly Diminished

Studies published in the late 1990s and early 2000s identified the presence of exceptionally long methyl tert‐butyl ether (MTBE) plumes (more than 600 m or 2000 feet) in groundwater and have been cited in technical literature as characteristic of MTBE plumes. However, the scientific literature is incomplete in regard to the subsequent behavior and fate of these MTBE plumes over the past decade. To address this gap, this issue paper compiles recent groundwater monitoring records for nine exceptional plumes that were identified in prior studies. These nine sites exhibited maximum historical MTBE groundwater plume lengths ranging from 820 m (2700 feet) to 3200 m (10,500 feet) in length, exceeding the lengths of 99% of MTBE plumes, as characterized in multiple surveys at underground storage tank sites across the United States. Groundwater monitoring data compiled in our review demonstrate that these MTBE plumes have decreased in length over the past decade, with five of the nine plumes exhibiting decreases of 75% or more compared to their historical maximum lengths. MTBE concentrations within these plumes have decreased by 93% to 100%, with two of the nine sites showing significant decreases (98% and 99%) such that the regulatory authority has subsequently designated the site as requiring no further action.     

Cone Penetrometer Tests and HydroPunch® Sampling: A Screening Technique for Plume Definition

Cone penetrometer tests and HydroPunch® sampling were used to define the extent of volatile organic compounds in ground water. The investigation indicated that the combination of these techniques is effective for obtaining ground water samples for preliminary plume definition. HydroPunch samples can be collected in unconsolidated sediments and the analytical results obtained from these samples are comparable to those obtained from adjacent monitoring wells. This sampling method is a rapid and cost-effective screening technique for characterizing the extent of contaminant plumes in soft sediment environments. Use of this screening technique allowed monitoring wells to be located at the plume boundary, thereby reducing the number of wells installed and the overall cost of the plume definition program.     

Review of Quantitative Surveys of the Length and Stability of MTBE,TBA, and Benzene Plumes in Groundwater at UST Sites

Quantitative information regarding the length and stability condition of groundwater plumes of benzene, methyl tert‐butyl ether (MTBE), and tert‐butyl alcohol (TBA) has been compiled from thousands of underground storage tank (UST) sites in the United States where gasoline fuel releases have occurred. This paper presents a review and summary of 13 published scientific surveys, of which 10 address benzene and/or MTBE plumes only, and 3 address benzene, MTBE, and TBA plumes. These data show the observed lengths of benzene and MTBE plumes to be relatively consistent among various regions and hydrogeologic settings, with median lengths at a delineation limit of 10 µg/L falling into relatively narrow ranges from 101 to 185 feet for benzene and 110 to 178 feet for MTBE. The observed statistical distributions of MTBE and benzene plumes show the two plume types to be of comparable lengths, with 90th percentile MTBE plume lengths moderately exceeding benzene plume lengths by 16% at a 10‐µg/L delineation limit (400 feet vs. 345 feet) and 25% at a 5‐µg/L delineation limit (530 feet vs. 425 feet). Stability analyses for benzene and MTBE plumes found 94 and 93% of these plumes, respectively, to be in a nonexpanding condition, and over 91% of individual monitoring wells to exhibit nonincreasing concentration trends. Three published studies addressing TBA found TBA plumes to be of comparable length to MTBE and benzene plumes, with 86% of wells in one study showing nonincreasing concentration trends.     

Tomographic reconstruction of gas plumes using scanning DOAS

This paper presents a method to reconstruct the gas distribution inside a vertical cross section of a gas plume by combining data from two or more scanning DOAS instruments using a tomographic algorithm. The method can be applied to gas plumes from any single, elevated point source, such as a volcano or industrial chimney. Such two-dimensional concentration distributions may prove to be useful for example in plume chemistry, dispersion and environmental impact studies. Here we show the case with one scanning DOAS instrument located on each side of the plume, which is the easiest and most economic setup as well as the most useful in routine monitoring of e.g. volcanic gas emissions. The paper investigates the conditions under which tomographic reconstructions can be performed and discusses limitations of this setup. The proposed method has been studied theoretically by numerical simulations and has been experimentally tested during two field campaigns, with measurements of SO₂ emissions from a volcano and a power plant. The simulations show that, under good measurement conditions, the algorithm presented performs well, which is further confirmed by the experimental results.     

Sewers as a Source and Sink of Chlorinated‐Solvent Groundwater Contamination,Marine Corps Recruit Depot,Parris Island,South Carolina

Groundwater contamination by tetrachloroethene and its dechlorination products is present in two partially intermingled plumes in the surficial aquifer near a former dry‐cleaning facility at Site 45, Marine Corps Recruit Depot, Parris Island, South Carolina. The northern plume originates from the vicinity of former above‐ground storage tanks. Free‐phase tetrachloroethene from activities in this area entered the groundwater. The southern plume originates at a nearby, new dry‐cleaning facility, but probably was the result of contamination released to the aquifer from a leaking sanitary sewer line from the former dry‐cleaning facility. Discharge of dissolved groundwater contamination is primarily to leaking storm sewers below the water table. The strong influence of sanitary sewers on source distribution and of storm sewers on plume orientation and discharge at this site indicates that groundwater‐contamination investigators should consider the potential influence of sewer systems at their sites.     

The geomagnetic field at the Paleozoic/Mesozoic and Mesozoic/Cenozoic boundaries and lower mantle plumes

The data on the amplitude of variations in the direction and paleointensity of the geomagnetic field and the frequency of reversals throughout the last 50 Myr near the Paleozoic/Mesozoic and Mesozoic/Cenozoic boundaries, characterized by peaks of magmatic activity of Siberian and Deccan traps, and data on the amplitude of variations in the geomagnetic field direction relative to contemporary world magnetic anomalies are generalized. The boundaries of geological eras are not fixed in recorded paleointensity, polarity, reversal frequency, and variations in the geomagnetic field direction. Against the background of the “normal” field, nearly the same tendency of an increase in the amplitude of field direction variations is observed toward epicenters of contemporary lower mantle plumes; Greenland, Deccan, and Siberian superplumes; and world magnetic anomalies. This suggests a common origin of lower mantle plumes of various formation times, world magnetic anomalies, and the rise in the amplitude of geomagnetic field variations; i.e., all these phenomena are due to a local excitation in the upper part of the liquid core. Large plumes arise in intervals of the most significant changes in the paleointensity (drops or rises), while no correlation exists between the plume generation and the reversal frequency: times of plume formation correlate with the very diverse patterns of the frequency of reversals, from their total absence to maximum frequencies, implying that world magnetic anomalies, variations in the magnetic field direction and paleointensity, and plumes, on the one hand, and field reversals, on the other, have different sources. The time interval between magmatic activity of a plume at the Earth’s surface and its origination at the core-mantle boundary (the time of the plume rise toward the surface) amounts to 20–50 Myr in all cases considered. Different rise times are apparently associated with different paths of the plume rise, “delays” in the plume upward movement, and so on. The spread in “delay” times of each plume can be attributed to uncertainties in age determinations of paleomagnetic study objects and/or the natural remanent magnetization, but it is more probable that this is a result of the formation of a series of plumes (superplumes) in approximately the same region at the core-mantle boundary in the aforementioned time interval. Such an interpretation is supported by the existence of compact clusters of higher field direction amplitudes between 300 and 200 Ma that are possible regions of formation of world magnetic anomalies and plumes.     

Bifurcation of volcanic plumes in a crosswind

Bent-over buoyant jets distorted by a crosscurrent develop a vortex pair structure and can bifurcate to produce two distinct lobes which diverge from one another downwind. The region downwind of the source between the lobes has relatively low proportions of discharged fluid. Factors invoked by previous workers to cause or enhance bifurcation include buoyancy, release of latent heat at the plume edge by evaporating water droplets, geometry and orientation of the source, and the encounter with a density interface on the rising path of the plume. We suggest that the pressure distribution around the vortex pair of a rising plume may initially trigger bifurcation. We also report new experimental observations confirming that bifurcation becomes stronger for stronger bent-over plumes, identifying that bifurcation can also occur for straight-edged plumes but gradually disappears for stronger plumes which form a gravity current at their final level and spread for a significant distance against the current. Observations from satellites and the ground are reviewed and confirm that volcanic plumes can show bifurcation and a large range of bifurcation angles. Many of the bifurcating plumes spread out at the tropopause level and suggest the tropopause may act on the plumes as a density interface enhancing bifurcation. Even for quite moderate bifurcation angles, the two plume lobes become rapidly separated downwind by distances of tens of kilometers. Such bifurcating plumes drifting apart can only result in bilobate tephra fall deposits. The tephra fall deposit from the 16 km elevation, SE spreading, bifurcating volcanic plume erupted on 15 May 1981 from Mt Pagan was sampled by previous workers and clearly displayed bilobate characteristics. Examples of bilobate tephra fall deposits are reviewed and their origin briefly discussed. Bilobate deposits are common and may result from many causes. Plume bifurcation should be considered one of the possible mechanisms which can account for come examples of bilobate tephra fall deposits.     

Monitoring In Situ Biodegradation of MTBE Using Multiple Rounds of Compound‐Specific Stable Carbon Isotope Analysis

At a large industrial facility, methyl tert‐butyl ether (MTBE) was released to the subsurface and dispersed into the light, non‐aqueous phase liquids (LNAPL), in the first aquifer, with the LNAPL serving as a continuous source of MTBE in groundwater. Compound‐specific isotope analysis was conducted on both MTBE and tert‐butyl alcohol (TBA) in groundwater samples collected in 2008, 2011, and 2013 from wells located along and off the center line of the MTBE plume. The study demonstrated the onset and progress of biodegradation of MTBE between 2008 and 2013. The TBA observed in 2008 appears to be derived only in part from MTBE transformation while a significant portion of TBA might be contributed directly from LNAPL sources. In 2011 to 2013, the dominant source of TBA in the mid‐gradient plume was MTBE transformation. A contribution of an offsite LNAPL source, in particular to the down‐gradient area of the plume, is possible but could not be unequivocally confirmed. The time series provided direct evidence for MTBE biodegradation, but also a valuable insight on the sources of TBA.     

Geophysical Discovery of a New LNAPL Plume at the Former Wurtsmith AFB, Oscoda, Michigan

Alight nonaqueous phase liquid (LNAPL) ground water contaminant plume has been discovered by purely geophysical means at the former Wurtsmith Air Force Base (AFB) near Oscoda, Michigan. It is located near another plume called FT-02, which is a well-studied area undergoing natural bioremediation. The plume was discovered by ground penetrating radar (GPR) profiling while extending a long line from FT-02 to establish background variability around that plume. The new plume was apparent because of a high-conductivity "shadow' or GPR reflection attenuation observed below the conductive zone at the top of the aquifer, identical to the pattern observed at the FT-02 plume. Further GPR surveys were conducted by students of a Western Michigan University geophysics field course to outline the proximal part of the plume. The GPR survey was supplemented by an electromagnetic induction (EM) survey which showed a group of four cables crossing the area. Finally, a magnetometer survey was conducted to search for any buried steel objects which might have been missed by the EM survey. The results of the three geophysical surveys were then used by students of a University of Michigan field course to guide subsurface soil and fluid sampling, which verified the presence of residual LNAPL product and ground water with conductivities 2.5 to 3.3 times above background. The plume source is in the vicinity of a vaulted underground storage tank (UST) formerly used for the collection of waste solvents and fuels for subsequent use in the fire training exercises at FT-02. This newly discovered LNAPL plume, along with other "mature' plumes, fits the electrical model which predicts conductive ground water below the decomposing but electrically resistive LNAPLs. Finally, this is a fine example of the cooperative use of a dedicated research site for training by students of two different universities.     

Transition probability/Markov chain analyses of DNAPL source zones and plumes

At sites where a dense nonaqueous phase liquid (DNAPL) was spilled or released into the subsurface, estimates of the mass of DNAPL contained in the subsurface from core or monitoring well data, either in the nonaqueous or aqueous phase, can be highly uncertain because of the erratic distribution of the DNAPL due to geologic heterogeneity. In this paper, a multiphase compositional model is applied to simulate, in detail, the DNAPL saturations and aqueous-phase plume migration in a highly characterized, heterogeneous glaciofluvial aquifer, the permeability and porosity data of which were collected by researchers at the University of Tübingen, Germany. The DNAPL saturation distribution and the aqueous-phase contaminant mole fractions are then reconstructed by sampling the data from the forward simulation results using two alternate approaches, each with different degrees of sampling conditioning. To reconstruct the DNAPL source zone architecture, the aqueous-phase plume configuration, and the contaminant mass in each phase, one method employs the novel transition probability/Markov chain approach (TP/MC), while the other involves a traditional variogram analysis of the sampled data followed by ordinary kriging. The TP/MC method is typically used for facies and/or hydraulic conductivity reconstruction, but here we explore the applicability of the TP/MC method for the reconstruction of DNAPL source zones and aqueous-phase plumes. The reconstructed geometry of the DNAPL source zone, the dissolved contaminant plume, and the estimated mass in each phase are compared using the two different geostatistical modeling approaches and for various degrees of data sampling from the results of the forward simulation. It is demonstrated that the TP/MC modeling technique is robust and accurate and is a preferable alternative compared to ordinary kriging for the reconstruction of DNAPL saturation patterns and dissolved-phase contaminant plumes.     

动态金幔柱模式──兼论金星上小型冠状构造的浅起源

热和组分密度异常共同驱动的动态金幔柱解析模式给出金幔柱在金幔中上升的历史．当金幔柱到达岩石层底时其头部的特征量是5个独立变量的函数：（1）金幔柱起源的深度;（2）金幔粘性系数;（3）源温度异常值;（4）源组分与热密度异常之比;（5）金幔柱的浮力通量．基于新的Mapellan数据,金星表面上有360多个冠状和类冠状构造已被发现,其中65％直径小于300km．这类小型冠状构造被认为是由具有下述特征的较小的金幔柱所形成：（1）最大直径小于300km;（2）当其头部到达岩石层底时,过剩温度足以产生部分熔融层,应高于150K;（3）被冠状构造下面的金幔柱带上来的总浮力有能力支撑冠状构造隆起的总质量．用这3个条件分析数值结果并约束金幔柱的源参数,根据本文的数值实验结果,金星上的小型冠状构造可能是起源于上金幔小于1000km深度的动态金幔柱形成的．     

Mass and flux distributions from DNAPL zones in sandy aquifers

At three industrial sites in Ontario, New Hampshire, and Florida, tetrachloroethylene (PCE) and trichloroethylene (TCE), released decades ago as dense nonaqueous phase liquids (DNAPLs), now form persistent source zones for dissolved contaminant plumes. These zones are suspended below the water table and above the bottoms of their respective, moderately homogeneous, unconfined sandy aquifers. Exceptionally detailed, depth-discrete, ground water sampling was performed using a direct-push sampler along cross sections of the dissolved-phase plumes, immediately downgradient of these DNAPL source zones. The total plume PCE or TCE mass-discharge through each cross section ranged between 15 and 31 kg/year. Vertical ground water sample spacing as small as 15 cm and lateral spacing typically between 1 and 3 m revealed small zones where maximum concentrations were between 1% and 61% of solubility. These local maxima are surrounded by much lower concentration zones. A spacing no larger than 15 to 30 cm was needed at some locations to identify high concentration zones, and aqueous VOC concentrations varied as much as four orders of magnitude across 30 cm vertical intervals. High-resolution sampling at these sites showed that three-quarters of the mass-discharge occurs within 5% to 10% of the plume cross sectional areas. The extreme spatial variability of the mass-discharge occurs even though the sand aquifers are nearly hydraulically homogeneous. Depth-discrete field techniques such as those used in this study are essential for finding the small zones producing most of the mass-discharge, which is important for assessing natural attenuation and designing remedial options.     

Potential petroleum sources and exploration directions around the Manjar Sag in the Tarim Basin

Since the discovery of the Tahe oilfield, it has been controversial on whether the main source rock is in the Cambrian or Middle-Upper Ordovician strata. In this paper, it is assumed that the crude oil from the Wells YM 2 and TD 2 was derived from the Middle-Upper Ordovician and Cambrian source rocks, respectively. We analyzed the biomarkers of the crude oil, asphalt-adsorbed hydrocarbon and saturated hydrocarbon in bitumen inclusions from the Lunnan and Hade areas in the North Uplift of the Tarim Basin. Results show that the ratios of tricyclic terpane C₂₁/C₂₃ in the crude oil, asphalt-adsorbed hydrocarbon and saturated hydrocarbon in bitumen inclusions are less than 1.0, indicating that they might be from Upper Ordovician source rocks; the ratios of C₂₈/(C₂₇+C₂₈+C₂₉) steranes in the saturated hydrocarbon from reservoir bitumen and bitumen inclusions are higher than 25, suggesting that they might come from the Cambrian source rocks, however, the ratios of C₂₈/(C₂₇+C₂₈+C₂₉) steranes in oil from the North Uplift are less than 25, suggesting that they might be sourced from the Upper Ordovician source rocks. These findings demonstrate that the sources of crude oil in the Tarim Basin are complicated. The chemical composition and carbon isotopes of Ordovician reservoired oil in the Tarim Basin indicated that the crude oil in the North Uplift (including the Tahe oilfield) and Tazhong Depression was within mixture areas of crude oil from the Wells YM 2 and TD 2 as the end members of the Cambrian and Middle-Upper Ordovician sourced oils, respectively. This observation suggests that the crude oil in the Ordovician strata is a mixture of oils from the Cambrian and Ordovician source rocks, with increasing contribution from the Cambrian source rocks from the southern slope of the North Uplift to northern slope of the Central Uplift of the Tarim Basin. Considering the lithology and sedimentary facies data, the spatial distribution of the Cambrian, Middle-Lower Ordovician and Upper Ordovician source rocks was reconstructed on the basis of seismic reflection characteristics, and high-quality source rocks were revealed to be mainly located in the slope belt of the basin and were longitudinally developed over the maximum flooding surface during the progressive-regressive cycle. Affected by the transformation of the tectonic framework in the basin, the overlays of source rocks in different regions are different and the distribution of oil and gas was determined by the initial basin sedimentary structure and later reformation process. The northern slope of the Central Uplift-Shuntuo-Gucheng areas would be a recent important target for oil and gas exploration, since they have been near the slope area for a long time.     

Case Histories of Shallow Time Domain Electromagnetics in Environmental Site Assessment

Time domain electromagnetic (TDEM) soundings were utilized in site assessment studies for the purpose of accomplishing two objectives: (1) measuring the migration of brines from oil and gas field evaporation pits, and (2) mapping the continuity of clay strata. Both case histories are representative of common objectives in site assessment. The data for both examples were analyzed by one-dimensional ridge regression inversions.
Both case histories illustrate that TDEM is an effective method for determining the lateral and vertical resistivity distribution (geoelectric section) of the subsurface in the depth range from about 5 m to 100 m, and it is known from other investigations that depths of investigations up to 2500 m can be achieved with TDEM.
Frequently, the lateral extent of contaminant plumes emanating from localized sources are of limited areal extent. The case history involving the use of TDEM to map a brine plume shows that a TDEM measurement has a relatively small zone of influence, so that meaningful information about the lateral and vertical extent of the plume can be obtained. Both case histories demonstrate the ability of TDEM to determine geoelectric sections below layers of low resistivity.