Microbial activity and biogeochemical cycling in a nutrient-rich meromictic acid pit lake

Microbial activity, abundance and biomass, and biogeochemical cycling of iron, sulphur and carbon were studied in the extremely acidic (pH 2.5-4.3), meromictic, nutrient-rich pit lake Cueva de la Mora in Spain. The goal was to find out (1) if the relatively high nutrient content influenced plankton abundance in the water column and alkalinity-producing microbial processes in the sediments compared to other acid pit lakes, and (2) if sediments in the shallow, mixed and the deep, stagnant parts of the lake exhibited differences in microbial activities and geochemical sediment composition related to meromixis. We hypothesised that redox cycling was more intense in the mixed part and higher amounts of reduced components would accumulate in the stagnant part. Especially phytoplankton biomass, CO₂ production, and sulphate reduction were indeed higher than reported from typical acid pit lakes and were rather within the range of neutral or weakly acidic lakes, which can be attributed to the relatively high nutrient contents of Cueva de la Mora. Even in the monimolimnion, anaerobic processes occurred mainly in the sediments. Sediments from the mixed and stagnant parts of the lake differed markedly in their biogeochemistry. Mixolimnetic sediments showed high iron and sulphate reduction rates, and they appeared to undergo substantial recycling, as supported by reactive Fe, relation between gross sulphate reduction rate and net accumulation of reduced sulphur, and viable counts of iron and sulphur bacteria. Monimolimnetic sediments exhibited lower anaerobic microbial activities, and surprisingly they accumulated more Fe(II) than mixolimnetic sediments, but less reduced sulphur and carbon. This might be explained by a strong separation of the two water bodies, resulting in comparably less input of energy (light) and allochthonous matter into the monimolimnion. Regarding the total extent of alkalinity-generating microbial processes, their net effect is not sufficient to neutralise the lake within decades.     

Relationships between microbial communities and groundwater chemistry in two pristine confined groundwater aquifers in central China

This study explores linkages between the microbial composition and hydrochemical variables of pristine groundwater to identify active redox conditions and processes. Two confined aquifers underlying the city of Qianjiang in the Jianghan Plain in China were selected for this study, having different recharge sources and strong hydrochemical gradients. Typical methods for establishing redox processes according to threshold concentration criteria for geochemical parameters suggest iron or sulphate reduction processes. High‐throughput 16S rRNA sequencing was used to obtain diversity and taxonomic information on microbial communities. Instead of revealing iron‐ and sulphate‐reducing bacteria, salt‐ and alkali‐tolerant bacteria, such as the phylum Firmicutes and the class Gammaproteobacteria, and in particular, the family Bacillaceae, were dominant in the downstream groundwater of the first aquifer that had high ion concentrations caused by the dissolution of calcite and dolomite; meanwhile, the heterotrophic microaerophilic families Comamonadaceae and Rhodocyclaceae prevailed in the upstream groundwater of the first aquifer. Sulphate‐reducing bacteria were extremely abundant in the upstream groundwater of the second aquifer, as the SO₄^2? concentration was especially high. Methanogens and methanotrophs were predominant in the downstream groundwater of the second aquifer even though the concentration of SO₄^2? was much higher than 0.5 mg L^?1. The microbial communities, together with the geochemical parameters, indicated that the upstream region of the first aquifer was suboxic, that Fe(III) and Mn(IV) reductions were not the main redox processes in the downstream groundwater of the first aquifer with high Fe and Mn concentrations, and that the redox processes in the upstream and downstream regions of the second confined aquifer were SO₄^2? reduction and methanogenesis, respectively. This study expands understanding of the linkages between microbial communities and hydrogeochemistry in pristine groundwaters and provides more evidence for identifying active redox conditions and processes.     

Microbial iron reduction during passive in situ remediation of an acidic mine pit lake mesocosm

Ferric iron reduction was studied in a pilot-scale enclosure experiment for passive biological remediation of an acidic mine pit lake in Lusatia, Germany. The metabolic properties of prokaryotes involved in Fe(III) reduction may be important for the outcome of biological remediation, as chemolithotrophic Fe(III) reduction can counteract the desired pH increase, but heterotrophic Fe(III) reduction will provide the necessary Fe(II) for precipitation of sulfide minerals following sulfate reduction. Therefore, vertical profiles of sediment parameters related to iron and sulfur cycling were determined in conjunction with viable counts of different ferric iron-reducing micro-organisms using selective media. Findings were compared to an untreated reference site. The addition of organic matter stimulated ferric iron reduction and sulfate reduction in the enclosure and led to elevated pH and accumulations of ferrous iron and reduced sulfur compounds. Numbers of neutrophilic heterotrophic Fe(III) reducers increased during treatment, those of acidophilic heterotrophic Fe(III) reducers remained similar, and those of acidophilic chemolithotrophic Fe(III) reducers decreased. Zones of ferric iron-reducing activity corresponded well with microbial depth profiles; however, viable counts of neutrophilic or acid-tolerant Fe(III) reducers must have been underestimated based on the corresponding observed activity levels. Ferric iron reduction by chemolithotrophic acidophiles seemed to be of minor importance, so a lowering of pH values due to Fe(III) reducing activity is unlikely.     

轮叶黑藻(Hydrilla verticillata)根系泌氧对沉积物中典型铁氧化菌和铁还原菌的影响

铁作为地壳中丰度最高的氧化还原敏感元素,对湖泊沉积物的氧化还原作用具有重要的指示意义.水生植物根系泌氧在根际形成微域的氧化圈,根际是氧化、还原同时发生的生物活跃区.以轮叶黑藻(Hydrilla verticillata)为研究对象,利用微电极和荧光定量PCR探讨根系泌氧作用对沉积物中典型铁氧化菌(嘉利翁氏菌)和典型铁还原菌(地杆菌)的影响.结果表明,轮叶黑藻生长迅速,通过根系泌氧作用影响沉积物中铁的价态和形态,是根际铁循环的重要参数,并对根际微区微生物有一定的影响.根系泌氧使根际嘉利翁氏菌和地杆菌数量增加,进一步影响根际微生物铁循环.实验结果可为微生物对根际铁循环的研究提供一定的理论基础.     

Very low-grade metamorphic study in the pre-Late Cretaceous terranes of New Caledonia (southwest Pacific Ocean)

Abstract   Pre-Late Cretaceous terranes from the central part of New Caledonia have been metamorphosed under very low-grade conditions by two high-pressure/low-temperature events. The present study investigates the metamorphic patterns with phyllosilicate crystallinities, electron microprobe analyses and petrography. The first metamorphic event is of Late Jurassic age and is characterized by very low (anchizone) to low-grade (epizone) conditions with a decrease of the illite Kübler Index (KI) and the chlorite Árkai Index (ÁI) values from northeast to southwest. This trend is also confirmed by chlorite thermometry. In the south of the area, un-metamorphosed sediments (diagenetic KI values) are observed in the Senonian 'formation à charbons', post-dating the metamorphism in this region. The second metamorphism is an Eocene high-pressure event, which overprints the Late Jurassic metamorphism in the northern part of the studied area. In this zone, the pattern of KI and ÁI indicates another gradient with increasing metamorphic conditions from southwest to northeast. Temperatures calculated by chlorite thermometry also indicate an evolution from southwest to northeast with slight increase of temperature from 298 ± 8°C to 327 ± 16°C. In both metamorphic zones, the K-white mica b cell dimension calculated on micas analyzed at electron microprobe are in good agreement with high-pressure/low-temperature metamorphic conditions (b₀ > 9.04 Å). A combination of chlorite thermometry and K-white mica b cell dimension allows estimation of a minimum pressure of 1.3 GPa in the Eocene zone (in excellent agreement with the 1.5 GPa registered in the northern part of New Caledonia) and a minimum of 1.1 GPa in the Late Jurassic metamorphic part.     

Magnetic signature of hydrocarbon-contaminated soils and sediments at the former oil field H?nigsen, Germany

Magnetic properties of hydrocarbon (HC) containing soils and sediments from two sites (Site A and B) of the former oil-field H?nigsen were analyzed in order to determine whether magnetic methods can be employed to delineate HC contamination of soils and sediments. Magnetic parameters such as magnetic susceptibility and induced isothermal remanent magnetizations, as well as soil and sediment properties such as pH, iron content and water content, HC content and most probable number counts of iron-metabolizing microorganisms were determined. The magnetic concentration-dependent parameters for HC contaminated samples were 25 times higher in soils from Site A than in sediment samples from Site B. However, at Site B the magnetic susceptibility was still four times higher in comparison to lithologically similar non-contaminated sediment samples from a third Site C. Newly formed magnetite containing mainly single domain particles was responsible for the magnetic enhancement, whereas superparamagnetic grains represented only a minor component. Site A had an acidic pH compared to neutral pH at Site B, and a higher crystalline and bioavailable total iron content. Nevertheless, Site B samples contained significant numbers of both iron(II)-oxidizing and iron(III)-reducing microorganisms indicating that microbial iron cycling might have taken place at this site and potentially played a role for iron mineral transformation, including magnetite (trans)formation. The content of total non-polar hydrocarbons (TNPH) at Site A was one order of magnitude higher than at Site B. Only at Site A magnetic susceptibility correlated well with TNPH. Our results demonstrate that HC contaminated samples had an enhanced magnetite content compared to non-contaminated soils and sediments. Therefore, magnetic methods may provide a quick and cost-effective way to assess HC contamination in soils and sediments. However, more field sites and laboratory investigations are needed to reveal the complex nature of the processes involved.     

Biogeochemistry of iron in an acidic lake

In this paper, the fate of iron in Lake Cristallina, an acidic lake in the Alps of Switzerland, is discussed. A simple conceptual model is developed in order to explain the observed diel variation in dissolved iron(II) concentration. Biotite weathering provides reduced iron that is oxidized and subsequently precipitated in the lake. The amorphous Fe(III)hydroxide (FeOOH xH₂O), found in the sediments of Lake Cristallina, is an Fe(II) oxidation product. This oxygenation reaction is most probably catalyzed by bacteria surfaces, as indicated by the relatively high estimated oxidation rate compared to the oxidation rate of the homogeneous oxidation of inorganic Fe(II) species at the ambient pH of Lake Cristallina (pH 5.4 at 4 °C) and by the scanning electron micrograph pictures. Under the influence of light, these amorphous iron(III)hydroxide phases are reductively dissolved. The net concentration of Fe(II) reflects the balance of the reductive dissolution and the oxidation/precipitation reactions and tends to parallel the light intensity, leading to a diurnal variation in the Fe(II) concentration. The rate of the photochemical reductive dissolution of Lake Cristallina iron(III)hydroxides is greatly enhanced in situ and in the laboratory by addition of oxalate to the lake water.     

Sediments,porewaters and diagenesis in an urban water body,Salford, UK: impacts of remediation

Contaminated sediments deposited within urban water bodies commonly exert a significant negative effect on overlying water quality. However, our understanding of the processes operating within such anthropogenic sediments is currently poor. This paper describes the nature of the sediment and early diagenetic reactions in a highly polluted major urban water body (the Salford Quays of the Manchester Ship Canal) that has undergone remediation focused on the water column. The style of sedimentation within Salford Quays has been significantly changed as a result of remediation of the water column. Pre‐remediation sediments are composed of a range of natural detrital grains, predominantly quartz and clay, and anthropogenic detrital material dominated by industrial furnace‐derived metal‐rich slag grains. Post‐remediation sediments are composed of predominantly autochthonous material, including siliceous algal remains and clays. At the top of the pre‐remediation sediments and immediately beneath the post‐remediation sediments is a layer significantly enriched in furnace‐derived slag grains, input into the basin as a result of site clearance prior to water‐column remediation. These grains contain a high level of metals, resulting in a significantly enhanced metal concentration in the sediments at this depth. Porewater analysis reveals the importance of both bacterial organic matter oxidation reactions and the dissolution of industrial grains upon the mobility of nutrient and chemical species within Salford Quays. Minor release of iron and manganese at shallow depths is likely to be taking place as a result of bacterial Fe(III) and Mn(IV) reduction. Petrographic analysis reveals that the abundant authigenic mineral within the sediment is manganese‐rich vivianite, and thus Fe(II) and Mn(II) released by bacterial reactions may be being taken up through the precipitation of this mineral. Significant porewater peaks in iron, manganese and silicon deeper in the sediment column are most probably the result of dissolution of furnace‐derived grains in the sediments. These species have subsequently diffused into porewater above and below the metal‐enriched layer. This study illustrates that the remediation of water quality in anthropogenic water bodies can significantly impact upon the physical and chemical nature of sedimentation. Additionally, it also highlights how diagenetic processes in sediments derived from anthropogenic grains can be markedly different from those in sediments derived from natural detrital material. Copyright © 2003 John Wiley & Sons, Ltd.     

A comparative study on the illite crystallinity and the clay mineral reflectance spectral index for subdividing the very low-grade metamorphic belt along the Lizhou-Hekou geological section in the Youjiang sedimentary basin, Guangxi, China

To examine the application potential of hyperspectral remote sensing techniques in classifying very low-grade metamorphic belts, the composition of clay minerals and the cyrstallinity of illite from mudstones were measured using XRD and VIS-SWIR (400-2500 nm) reflectance spectroscopy. Based on the illite cyrstallinity, Kubler Index (KI), the Early Triassic LuoLou Group and the Middle Triassic lower Baifeng Formation were classified as the lower Epizone with KI△2θ° ranging from 0.22 to 0.25, the upper Baifeng Formation as upper anchizone with KI△2θ°ranging from 0.26 to 0.33, and the Hekou Formation as lower anchizone with KI△2θ° ranging from 0.38 to 0.40. According to a KI△2θ° value of 0.43, it is possible that there may exist a local diagenetic zone in the upper strata. The illite cyrstallinity Kubler index and the metamorphic grade increase from the bottom to the top of the stratigraphic sequence. The metamorphic grade boundaries nearly match the stratigraphic boundaries, indicating a burial metamorphism nature for the stratigraphic sequence. From the bottom to the top of the sequence, the spectral absorption band center of clay minerals from fresh rocks is around 2200 nm. The absorption band centers change towards shorter wavelengths: the Luolou Group being at 2220 nm, the Baifeng Formation at 2217-2213 nm, the lower member of the Hekou Formation at 2214-2206 nm, and the upper member of the Hekou Formation at 2205-2197 nm. The spectral absorption band center of illite shows the same change pattern. These results indicate that very low-grade metamorphic belts can be subdivided using spectral indices of clay minerals, which are measured by using field portable spectroradiometers. However, it may not work well with satellite and airborne sensors.     

Kinetics of redox cycling of iron coupled with fulvic acid

The kinetics of conversion of iron(III) (hydr)oxides to ferrous iron mediated by fulvic acid have been investigated in order to improve the understanding of the redox cycling of iron at the oxic-anoxic boundary in natural waters. Under the conditions similar to natural waters, fulvic acid is able to reduce the iron(III) (hydr)oxide. The kinetics of the reaction depend on the reactivity of iron(III) (hydr)oxides and the reducing power of the fulvic acid. The rate of reaction is 60 nm/h obtained under following conditions: total concentration of Fe(III) 1.0 × 10^–4 M, pH 7.5, fulvic acid 5 mg/L. The rate is considered as a net result of reduction and oxidation in the > Fe^III-OH/Fe(II) wheel coupled with fulvic acid. In a real natural water system, reductants other than fulvic acid may be of importance. The results obtained in the laboratory, however, provide evidence that the Fe(OH)₃(s)/Fe(II) redox couple is able to act as an electron-transfer mediator for the oxidation of natural organic substances, such as fulvic acid by molecular oxygen either in the absence of microorganisms or as a supplement to microbial activity.     

Toxicity assessments of nanoscale zerovalent iron and its oxidation products in medaka (Oryzias latipes) fish

Iron-based nanotechnologies are increasingly used for environmental remediation; however, toxicologic impacts of iron nanoparticles on the aquatic ecosystem remain poorly understood. We treated larvae of medaka fish (Oryzias latipes) with thoroughly characterized solutions containing carboxymethyl cellulose (CMC)-stabilized nanoscale zerovalent iron (nZVI), aged nanoscale iron oxides (nFe-oxides) or ferrous ion (Fe[II]) for 12-14 days' aqueous exposure to assess the causal toxic effect(s) of iron NPs on the fish. With the CMC-nZVI solution, the dissolved oxygen level decreased, and a burst of reactive oxygen species (ROS) was generated as Fe(II) oxidized to ferric ion (Fe[III]); with the other two iron solutions, these parameters did not significantly change. CMC-nZVI and Fe(II) solutions caused acute lethally and sublethally toxic effects in medaka larvae, with nFe-oxide-containing solutions causing the least toxic effects. We discuss modes of toxic action of iron NPs and chronic toxic effects in terms of hypoxia, Fe(II) toxicity and ROS-mediated oxidative damage.     

The Role of Microorganisms in Uranium Behavior in the Water–Rock System

Geochemical processes involving redox reactions and leading to either formation or transformation of geochemical barriers may be largely induced or enhanced by microbial activity. The microbial reduction of uranium is studied as a strategy for rehabilitation of uranium-containing groundwater. The bioremediation mechanism converts dissolved uranium(VI) into low-solubility U(IV). The processes involving dissimilatory reducing bacteria, which facilitate the reduction and retention of U(VI) in soils and rocks, are considered. The diversity of microorganisms involved in anaerobic reduction of uranium is shown. The geochemical conditions that may affect the rate of microbial reduction of U(VI) are specified, i.e., the presence of nitrate ions, phosphate ions, calcium ions, and iron oxides. The mechanisms of their action are examined. Geochemical barriers with the participation of microorganisms are proposed for the rehabilitation of groundwater with uranium removed from groundwater and deposited locally as a result of microbial reduction of U(VI).     

Toxicity assessments of nanoscale zerovalent iron and its oxidation products in medaka (Oryzias latipes) fish

Iron-based nanotechnologies are increasingly used for environmental remediation; however, toxicologic impacts of iron nanoparticles on the aquatic ecosystem remain poorly understood. We treated larvae of medaka fish (Oryzias latipes) with thoroughly characterized solutions containing carboxymethyl cellulose (CMC)-stabilized nanoscale zerovalent iron (nZVI), aged nanoscale iron oxides (nFe-oxides) or ferrous ion (Fe[II]) for 12–14 days’ aqueous exposure to assess the causal toxic effect(s) of iron NPs on the fish. With the CMC-nZVI solution, the dissolved oxygen level decreased, and a burst of reactive oxygen species (ROS) was generated as Fe(II) oxidized to ferric ion (Fe[III]); with the other two iron solutions, these parameters did not significantly change. CMC-nZVI and Fe(II) solutions caused acute lethally and sublethally toxic effects in medaka larvae, with nFe-oxide-containing solutions causing the least toxic effects. We discuss modes of toxic action of iron NPs and chronic toxic effects in terms of hypoxia, Fe(II) toxicity and ROS-mediated oxidative damage.     

Bacterial symbiosis forming laminated iron‐rich deposits in Okuoku‐hachikurou hot spring,Akita Prefecture,Japan

Banded iron formations are the most characteristic of Archean–Paleoproterozoic sediment records. Laminated textures resembling banded iron formations can be observed in modern hot‐spring environments. Using sedimentological and microbiological techniques, we investigated the processes of laminar formation and considered the origin of lamination textures. An iron‐rich deposit at the Okuoku‐hachikurou hot spring in Japan exhibits sub‐millimeter laminations consisting of bacteria‐induced ferrihydrite and aragonite. The ferrihydrite particles are spherical and exhibit fine lamination, up to 100 µm thick in ferrihydrite‐rich parts. In aragonite‐rich parts, ferrihydrite particles form filamentous textures with diameters of 10–30 µm, but not laminations. Textural analysis using scanning electron microscopy and phylotype analysis using 16S rRNA indicated the bacterial contribution to ferrihydrite precipitation. A sheath‐like fabric showing a meshwork of nanometer‐order organic filaments, and sheath‐forming bacteria were observed in the deposit specimen etched by citric acid. Phylotype analysis detected in the iron‐rich deposits some bacterial types related to cyanobacteria, purple bacteria, and iron‐oxidizing bacteria. Iron‐oxidizing bacteria probably were responsible for precipitation of the ferrihydrite. Chemolithoautotrophic iron‐oxidizing bacteria are microaerophilic and thrive on Fe(II) in a redox gradient, but dissolved oxygen was not detected in the Okuoku‐hachikurou hot spring. Thus, a certain supply of oxygen is needed for metabolism of the microaerophilic iron‐oxidizing bacteria. The distribution of photosynthetic pigments in the iron‐rich parts indicates that the most likely source of oxygen is photosynthesis by cyanobacteria. This symbiotic relationship between cyanobacteria and iron‐oxidizing bacteria can explain the laminated texture of iron‐rich deposits in the Okuoku‐hachikurou hot spring. These laminations may reflect changes in photosynthetic intensity. There is presently some debate about the bacterial groups that may have played roles in precipitation of banded iron formations. This study presents a new bacterial model for iron precipitation and may provide a mechanism for sub‐millimeter laminations in banded iron formations deposited in shallow water.     

Strontium and argon isotopic homogenization of pelitic sediments during low-grade regional metamorphism: The pan-African upper Damara sequence of Northern Namibia (South West Africa)

The fine mineral fractions < 2 μm extracted from pelitic sediments of the Eocambrian upper Damaran Mulden Group were subjected to a detailed isotopic study by the Rb-Sr and K-Ar methods in combination with a mineralogical analysis by X-ray diffractometry.The sediments contain two major parageneses of metamorphic origin which can be related to two separate low-grade regional metamorphic events of anchizonal intensity with temperatures between 250 and 300°C and pressures up to 2 kbar. These events are dated at about 535 m.y. and 455 m.y. respectively (with λ(⁸⁷Rb) = 1.42 × 10^?11 yr^?1).Anomalously high K-Ar ages on samples from specific stratigraphic horizons can be related to open system behaviour and K migration during the formation of stilpnomelane from ferromagnesian illites.This study shows that age dating of sedimentary rocks subjected to low-grade regional metamorphism can only yield meaningful results if the interpretation of isotopic analyses is based on a clear understanding of the mineralogical processes that led to the formation of those parageneses which characterize the rock unit dated.     

Onshore-offshore gradient in reductive early diagenesis in coastal marine sediments of the Ria de Vigo, Northwest Iberian Peninsula

Early diagenetic modification of magnetic properties is an important process in marine sediments, but temporal and spatial variability of diagenetic processes have rarely been reported for recent coastal sediments. The magnetic properties of sediments from the Ria de Vigo (NW Spain) define a marked three-part zonation with depth. The uppermost zone is magnetically dominated by (titano-)magnetite. In the intermediate zone, rapid down-core dissolution of (titano-)magnetite increases the relative influence of high-coercivity magnetic minerals, which react more slowly during reductive dissolution than (titano-)magnetite. This zone is characterized by the ubiquitous occurrence of framboidal iron sulphides. Pyrite is the dominant iron sulphide, but framboidal ferrimagnetic greigite is also frequently observed in association with pyrite. The lowermost zone is characterized by an almost complete depletion of magnetic minerals associated with progressive reduction of detrital iron oxides with depth. This zonation is controlled by organic matter diagenesis, which varies with water depth and wave-induced sediment resuspension and organic matter reoxidation in the water column. This leads to a shallowing and thinning of each zone with more intense reductive diagenesis toward the interior of the ria. Such a zonation seems to be a common feature in shallow water marine environments. If preserved, the described zonation and its spatial variability provide a potential tool for detecting estuarine-like environments in the geological record. Magnetic detection of current or past reductive conditions also has important implications for assessing paleoenvironmental proxies that are sensitive to diagenetic redox state.     

Environmental magnetism of nanophase iron minerals: Testing the biomineralization pathway

Nanoparticles of iron oxides and iron oxyhydroxides are sensitive proxies of environmental change near the earth's surface. Our research programme aims to provide information about the environmental control variables (temperature, rainfall, pH, as well as microbial type and concentration) for the process of Fe(III) to Fe(II) reduction and solid phase precipitation. Such solid phases of environmental change proxies (e.g., magnetite and maghemite) are being produced in the laboratory for calibration of field data. Low temperature magnetometry and Mössbauer spectra are shown to be extremely useful for characterization and granulometry of such nanophases. In addition, it appears that magnetism may also be a sensitive probe for physical–chemical properties of the outermost ‘skins’ of such nanoparticles, confirming Louis Néel's predictions for the magnetic behavior of such outermost layers.     

Biostimulation and Bioaugmentation to Enhance Reductive Dechlorination of TCE in a Long‐Term Flow Through Column Study

Large laboratory columns (15.2 cm diameter, 183 cm long) were fed with groundwater containing trichloroethylene (TCE), were biostimulated and bioaugmented, and were monitored for over 7.5 years. The objective of the study was to observe how the selection of the carbon and energy source, i.e., whey, Newman Zone^® standard surfactant emulsified oil and Newman Zone nonionic surfactant emulsified oil, affected the rate and extent of dechlorination. Column effluent was monitored for TCE and its degradation products, redox indicators (nitrate‐N, Fe(II), sulfate), and changes in iron mineralogy. Total bacteria and Dehalococcoides mccartyi strains were quantified using q‐PCR. Complete dechlorination was only observed in the whey treated columns, occurring 1 year after bioaugmentation with addition of a culture known to dechlorinate TCE to ethene, and 3 years later in the non‐bioaugmented column. The addition of the emulsified oils with or without bioaugmentation resulted in dechlorination only through cis‐DCE and vinyl chloride. While Dehalococcoides mccartyi strains are the only known bacteria that can fully dechlorinate TCE, their presence, either natural or augmented, was not the sole determiner of complete dechlorination. The establishment of a supporting microbial community and biogeochemistry that developed with continuous feeding of whey, in addition to the presence of D. mccartyi, were necessary to support complete reductive dechlorination. Results confirm that careful selection of a biostimulant is critical to the success of TCE dechlorination in complex soil environments.