Evaluation of <Emphasis Type="Italic">smtA</Emphasis> expression and <Emphasis Type="Italic">E. coli</Emphasis> survival against cadmium ions

Cadmium and other heavy metals lead to environmental danger, and these heavy metals are a great threat to human and other animal’s health. Investigation of the relationship between survival of E. coli and metallothionein smtA gene expression against cadmium ion is the goal of this research. Survival of recombinant bacteria containing smtA gene was analyzed against various concentrations of cadmium chloride salt using optical density (OD). At the resistive range, recombinant bacteria were subjected to different treatments. At the logarithmic phase of bacterial growth, sampling, RNA extraction and cDNA synthesis were performed and smtA gene expression was then analyzed by real-time PCR using designed primers for smtA gene and Amp resistance (as the calibrator gene). Relative gene expression was calculated using the ??C_t method. The resistive range against cadmium chloride was 0.5–0.7 mM (minimum inhibitory concentration (MIC = 0.5 mM)). Survival and gene expression analysis showed that in induced bacteria, smtA expression was increased significantly that in turn conferred resistance to cadmium chloride prominently. There was a direct relationship between increased smtA gene expression and survival of the recombinant bacteria. Therefore, our result may help to confront to cadmium metal environmental pollution using overexpression of smtA gene expression in recombinant bacteria.     

Effects of heavy metals as stress factors on anaerobic digestion processes and biogas production from biomass

Heavy metals affect the biochemical reactions that take place during anaerobic digestion processes of organic matter. In this review, the different effects observed in anaerobic digestion processes and during the production of biomethane and biohydrogen from several substrates contaminated with and/or inheriting heavy metals from the substrates themselves were discussed. It has been found that heavy metals exert important roles in biochemical reactions. Heavy metals like copper, nickel, zinc, cadmium, chromium and lead have been overwhelmingly reported to be inhibitory and under certain conditions toxic in biochemical reactions depending on their concentrations. Heavy metals like iron may also exhibit stimulatory effects, but these effects have been scantily observed. This review also concludes that the severity of heavy metal inhibition depends upon factors like metal concentration in a soluble, ionic form in the solution, type of metal species, and amount and distribution of biomass in the digester or chain of biochemical reactions which constitute the anaerobic digestion process. A majority of studies have demonstrated that the toxic effect of heavy metals like chromium, cadmium and nickel is attributable to a disruption of enzyme function and structure by binding of the metal ions with thiol and other groups on protein molecules or by replacing naturally occurring metals in enzyme prosthetic groups. This review has not found published data on the effects of heavy metals on the hydrolysis stage of anaerobic digestion process chemistry, and hence further studies are required to depict any changes.     

Remediation technologies for metal-contaminated soils and groundwater: an evaluation

Metals including lead, chromium, arsenic, zinc, cadmium, copper and mercury can cause significant damage to the environment and human health as a result of their mobilities and solubilities. The selection of the most appropriate soil and sediment remediation method depends on the site characteristics, concentration, types of pollutants to be removed, and the end use of the contaminated medium. The approaches include isolation, immobilization, toxicity reduction, physical separation and extraction. Many of these technologies have been used full-scale. This paper will review both the full-scale and developing technologies that are available. Contaminants can be isolated and contained to minimize further movement, to reduce the permeability of the waste to less than 1×10⁻⁷ m/s (according to U.S. guidelines) and to increase the strength or bearing capacity of the waste. Physical barriers made of steel, cement, bentonite and grout walls can be used for isolation and minimization of metal mobility. Another method is solidification /stabilization, which contains the contaminants in an area by mixing or injecting agents. Solidification encapsulates contaminants in a solid matrix while stabilization involves formation of chemical bonds to reduce contaminant mobility. Another approach is size selection processes for removal of the larger, cleaner particles from the smaller more polluted ones. To accomplish this, several processes are used. They include: hydrocyclones, fluidized bed separation and flotation. Addition of special chemicals and aeration in the latter case causes these contaminated particles to float. Electrokinetic processes involve passing a low intensity electric current between a cathode and an anode imbedded in the contaminated soil. Ions and small charged particles, in addition to water, are transported between the electrodes. This technology have been demonstrated in the U.S. full-scale, in a limited manner but in Europe, it is used for copper, zinc, lead, arsenic, cadmium, chromium and nickel. The duration of time that the electrode remains in the soil, and spacing is site-specific. Techniques for the extraction of metals by biological means have been not extensively applied up to this point. The main methods include bioleaching and phytoremediation. Bioleaching involves Thiobacillus sp. bacteria which can reduce sulphur compounds under aerobic and acidic conditions (pH 4) at temperatures between 15 and 55°C. Plants such as Thlaspi, Urtica, Chenopodium, Polygonum sachalase and Alyssim have the capability to accumulate cadmium, copper, lead, nickel and zinc and can therefore be considered as an indirect method of treating contaminated soils. This method is limited to shallow depths of contamination. Soil washing and in situ flushing involve the addition of water with or without additives including organic and inorganic acids, sodium hydroxide which can dissolve organic soil matter, water soluble solvents such as methanol, nontoxic cations, complexing agents such as ethylenediaminetetraacetic acid (EDTA), acids in combination with complexation agents or oxidizing/reducing agents. Our research has indicated that biosurfactants, biologically produced surfactants, may also be promising agents for enhancing removal of metals from contaminated soils and sediments.

In summary, the main techniques that have been used for metal removal are solidification/stabilization, electrokinetics, and in situ extraction. Site characteristics are of paramount importance in choosing the most appropriate remediation method. Phytoremediation and bioleaching can also be used but are not as well developed.     

河南登封晚古生代含煤地层各煤组的古生物特征

<正> 河南登封位于华北地台的南缘,区内石炭二叠系厚度大,出露全,分布广泛。根据含煤地层的岩性特征、旋迴规律、煤层结构和煤质差异,近千米的煤系地层共分为九个煤组(表1)。通过11条剖面数千块标本的研究和综合分析,发现9个煤组的生物化石各具特色,易于区别。     

Application of artificial neural networks for estimating Cd,Zn, Pb removal efficiency from wastewater using complexation-microfiltration process

Complexation-microfiltration process for removal of heavy metal ions such as lead, cadmium and zinc from water had been investigated. Two soluble derivates of cellulose was selected as complexing agents. The dependence of the removal efficiency from the operating parameters (pH value, pressure, concentration of metal ion, concentration of complexing agent and type of counter ion) was established. Two approaches of preparation of input data and two different artificial neural network architectures, general regression neural network and back-propagation neural network have been used for modeling of experimental data. The extrapolation ability of selected architectures, i.e., the prediction of rejection coefficient with inputs beyond the calibration range of original model, was also determined. The predictions were successful, and after evaluation of performances, the models that were developed gave relatively good results of mean absolute percentage error from 4 to 14% and R-squared from 0.717 to 0.852 for general regression neural network and from 0.897 to 0.955 for back-propagation neural network.     

Distribution of protons and Cd between bacterial surfaces and dissolved humic substances determined through chemical equilibrium modeling

Bacteria and dissolved humic substances are capable of binding significant concentrations of metals in natural environments. Recent advances in understanding bacteria-metal and humic-metal complexation have provided a framework for directly comparing the binding capacities of these components. In this study, we use chemical equilibrium modeling to construct an internally consistent set of thermodynamic equilibrium constants for proton and Cd binding onto dissolved humic substances, using a variety of published data sets. Our modeling approach allows for the direct comparison of humic substance binding constants and site densities to those previously published for proton and Cd binding onto natural consortia of bacteria. We then combine these constants into a unified model that accounts for the competition between bacterial surfaces and humic and fulvic acids in order to determine the relative importance of each component on the total Cd budget. The combined model is used to examine the relative contributions of bacteria and dissolved humic substances to Cd complexation in natural settings. Calculations are performed for three representative systems: (1) one with a maximum realistic concentration of bacteria and a minimum realistic concentration of humic substance, (2) one with a maximum realistic concentration of humic substance and a minimum concentration of bacteria, and (3) one with an intermediate concentration of both components.Our modeling results indicate that dissolved humic substances have 2 orders of magnitude more available binding sites than bacterial surfaces (per gram). Humic substances also have a greater affinity than bacterial surfaces for binding Cd over circumneutral pH ranges. The combined model results demonstrate that, depending upon their relative concentrations, both Cd-humic and Cd-bacteria complexes are capable of dominating Cd-speciation in specific natural environments. This modeling approach is useful in that it can easily be extended to include other metals and binding ligands; however, thermodynamic data must be gathered on additional components to facilitate the modeling of more realistic systems.     

The effect of prehatch and posthatch exposure to cadmium on salinity tolerance of larval grass shrimp,Palaemonetes pugio

Groups of embryonic grass shrimp,Palaemonetes pugio, were exposed to 0.1 and 0.3 mg/l cadmium at 30 ppt salinity and 25°C for the last 1, 4 or 8 days prior to hatching. Other groups of embryos were cultured in uncontaminated seawater. Prehatch exposure to cadmium was found to have no additive effect on the sensitivity of the larvae to cadmium exposure and salinity stress for 14 days after hatching. Only one group of larvae, exposed to 0.1 mg/l cadmium for 4 days before hatching, and transferred to 10 ppt salinity water containing 0.1 mg/l cadmium after hatching, showed a significant (X ², P<0.05) decrease in survival, compared to control survival. No significant decreases in survival were observed for any larvae transferred to 15 and 30 ppt salinity at a pre- and posthatch cadmium concentration of 0.1 mg/l. At a pre- and posthatch cadmium concentration of 0.3 mg/l, significant decreases in survival were observed for all of the larvae transferred to 10 and 15 ppt salinity after hatching. Significant decreases in survival were observed for only 2 of the groups exposed before hatching and transferred to 30 ppt salinity and 0.3 mg/l cadmium after hatching.     

Biodiesel production using solid metal oxide catalysts

Biodiesel production is worthy of continued study and optimization of production procedures due to its environmentally beneficial attributes and its renewable nature. Heterogeneous transesterification is considered to be a green process. The process requires neither catalyst recovery nor aqueous treatment steps and very high yields of methyl esters can be obtained, close to the theoretical value. However, heterogeneously catalyzed transesterification generally requires more severe operating conditions, and the performance of heterogeneous catalysts is generally lower than that of the commonly used homogeneous catalysts. Heterogeneous catalysis for biodiesel production has been extensively investigated in the last few years. Many metal oxides have been studied for the transesterification process of oils; these include alkali earth metal oxides, transition metal oxides, mixed metal oxides and supported metal oxides. The use of solid metal oxides as catalysts in oil transesterification is well established, accordingly, researchers’ attempts are now focused on how to attain the highest catalyst activity. Catalyst activity is a function of its specific surface area, base strength and base site concentration. High specific surface area, strong base strength and high concentration of base sites are characteristics of an active transesterification catalyst. This review provides a brief overview of the different metal oxides frequently used in the process of transesterification of oils for the production of biodiesel with special reference to the various methods of catalyst preparation and catalyst characterization. Reaction conditions and catalyst leaching analysis are also highlighted. Finally, concluding remarks regarding catalyst selection and catalyst preparation steps are provided.     

Removal of cadmium and humic acid from aqueous solutions using surface modified nanozeolite A

The sorption of cadmium and humic acids from aqueous solutions using surface-modified nanozeolite A has been investigated under various examination conditions. The morphology of untreated and treated nanozeolite was studied under scanning electron microscope and transmission electron microscope. Isotherms of cadmium adsorption onto surface-modified nanozeolite A were studied at different pH, solid to liquid ratio, adsorbate concentration and interaction time. Kinetic and equilibrium studies were conducted and the equilibrium data have been analyzed using Langmuir and Freundlich isotherm models. The study revealed that experimental results were in agreement with the Freundlich model. The Langmuir monolayer adsorption capacity was found to be 1666.67 g cadmium and 6.75 g humic acid per gram of modified nanozeolite A, which is higher than that of reported value for other zeolites. The sorption ability was enhanced by surface modification and reduction in size and enabled the zeolite to adsorb cadmium. The adsorption of cadmium and humic acid on nanozeolite was found to be the highest at pH 6 and 3, respectively. Results showed that solid to liquid ratio and pH are the most important factors for cadmium and humic acid removal, respectively. Effect of competitive ions was studied and results showed that there is no competition between cadmium and humic acid sorption and presence of these ions.     

Feasibility of CO<Subscript>2</Subscript> adsorption by solid adsorbents: a review on low-temperature systems

In the last few decades of industrialization, the concentration of CO₂ in the atmosphere had increased rapidly. Different organizations have invested considerable funds in research activities worldwide for CO₂ capture and storage. To date, significant work has been done and various technologies have been proposed for CO₂ capture and storage. Both adsorption and absorption are promising techniques for CO₂ capture, but low-temperature adsorption processes using solid adsorbents are the prevailing technique nowadays. In this review paper, a variety of adsorbents such as carbonaceous materials, dry alkali metal-based sorbents, zeolites, metal–organic frameworks (MOFs) and microporous organic polymers (MOPs) have been studied. Various methods of chemical or physical modification and the effects of supporting materials have been discussed to enhance CO₂ capture capacity of these adsorbents. Low-temperature (<100 °C) adsorption processes for CO₂ capture are critically analyzed and concluded on the basis of information available so far in the literature. All the information in CO₂ adsorption using different routes has been discussed, summarized and thoroughly presented in this review article. The most important comparative study of relatively new material MOFs and MOPs is carried out between the groups and with other sorbent as well.     

Raw and calcination-modified coal waste as adsorbents to remove cadmium from simulated mining wastewater

The adsorption of cadmium from simulated mining wastewater by coal waste (CW) and calcination-modified coal waste (MCW) was investigated. Effects of pH, initial concentration, particle size of adsorbent, adsorbent dosage and temperature were studied in batch experiments. The adsorption efficiency for cadmium increased with increasing pH, and the optimum pH for cadmium adsorption onto MCW and CW was 6.0 and 6.5, respectively. Kinetic experiments showed that the adsorption equilibrium was reached within 120 min and followed pseudo-second-order model well. The adsorption isotherm data fit Langmuir and Freundlich models, and the adsorption capacity of cadmium on the two adsorbents increased with increasing temperature from 298 to 318 K. MCW had a higher adsorption capacity of cadmium than CW, because calcination treatment can make CW to have more loose structure and higher specific surface area. Thermodynamic parameters, the Gibbs free energy change (?G⁰), enthalpy change (?H⁰) and entropy change (?S⁰), were calculated and the results showed that the adsorption of cadmium on CW and MCW was spontaneous and endothermic. Fourier transform infrared studies indicated silanol and aluminol groups were responsible for cadmium binding. The desorption results indicated that the two adsorbents could be used repeatedly at least three times without significant decrease in the adsorption capacity for cadmium. The results suggested that modified CW could have high potential as low-cost adsorbent for cadmium removal.     

Surfactant-enhanced remediation of contaminated soil: a review

Extracting aqueous solutions with or without additives are employed to solubilize contaminants in soil. Since water solubility is the controlling removing mechanism, additives are used to enhance efficiencies. These additives can reduce the time to treat a site compared to the use of water alone. Additives must be of low toxicity and biodegradable. The research in this area has focussed mainly on halogenated volatile organic compounds (VOCs) and is still quite limited for metal removal. Additives include surfactants, organic and inorganic acids, sodium hydroxide, which can dissolve organic soil matter, water-soluble solvents such as methanol, displacement of cations with nontoxic ones, complexing agents such as EDTA, acids in combination with complexing agents or oxidizing/reducing agents. Cationic, anionic and nonionic surfactants are particularly used for soil washing or flushing. They contain both hydrophobic and hydrophilic portions, making them ideal for solubilization of hydrophobic compounds. Numerous studies have indicated that surfactants enhance recoveries of non-aqueous phase liquids (NAPLs). There have also been indications that pretreatment of soil with surfactant washing to solubilize hydrophobic compounds such as PAHs enhances biodegradation of these contaminants. A few in situ field studies have been performed with surfactants. Large-scale treatment has been done mostly for organic removal. Soil pH, soil type, cation exchange capacity (CEC), particle size, permeabilities and contaminants all affect removal efficiencies. High clay and organic matter contents are particularly detrimental. Understanding the chemistry of the binding of the contaminant and the hydrogeology of the site are very important. Once the water is pumped from the soil, it must be extracted and then treated to remove the hydrocarbons and metals. Several technologies exist such as sodium hydroxide or sodium sulfide precipitation, ion exchange, activated carbon adsorption, ultrafiltration, reverse osmosis, electrodialysis and biological processes. Recycling of the surfactants is desired to decrease treatment costs.

This paper will provide an overview of the laboratory research, field demonstration and full-scale application of surfactants for the remediation of contaminated soil. The majority of pilot scale in situ flushing tests, particularly in the United States, have involved the use of surfactants and co-solvents. There are only a few full-scale projects however. Recent laboratory scale efforts by the authors concerning the use of biosurfactants, biologically produced surfactants, to enhance the removal of copper, cadmium and zinc from contaminated soils and sediments are discussed. Three types of biosurfactants were evaluated for their effectiveness. They included a lipopeptide called surfactin from Bacillus subtilis, a rhamnolipid from Pseudomonas aeruginosa and a sophorolipid from Torulopsis bombicola. The results indicated the feasibility of removing the metals with the anionic biosurfactants even though the exchangeable fractions were not significant.     

Cadmium absorption and accumulation in different parts of kidney beans, radishes and pumpkins

This study is done to measure the absorption and distribution of cadmium in different parts of kidney beans, radishes and pumpkins. Three parts of a field was chosen. In one part 65 ppm of cadmium nitrate was added to water and in the other part 130 ppm, the last part was irrigated with normal water. Samples were digested by EPA 3050 method. Cadmium concentration was measured by Unicam 919 absorption unit. Beans accumulate cadmium mostly in root (70 ppm) and a little amount is mobilized through upper parts (12–16ppm), but kidneys did not accumulate a significant amount. In radishes the roots did not accumulate a significant amount of cadmium but stems had 4 ppm and leaves had 25 ppm. Cadmium concentration in soil does not affect its concentration in different parts of pumpkins and beside the stems and leaves (4 ppm) the other parts' concentrations were insignificant. In regard to the results of this study the cadmium concentrations in edible parts of the samples (kidney beans, radish roots and pumpkin fruit) were less than the U.S. EPA standards for agriculture and human beings.     

扬子地块西南缘铅锌矿床Cd、Ge与Ga富集规律初步研究

扬子地块西南缘分布着大量富含Cd、Ge与Ga的铅锌矿床，已成为我国Pb、Zn及Cd、Ge与Ga矿产资源的重要生产基地。对代表性铅锌矿床进行野外地质调查和系统采样鉴定后．应用电子探针微区分析手段，研究主要矿石矿物闪锌矿、方铅矿和黄铁矿中分散元素的富集特征。结果显示．各类矿床中闪锌矿均相对富集Cd，方铅矿富集Ge与Ga，而黄铁矿中Cd、Ge与Ga的富集系数均相对较低．未呈现出选择性富集的趋势；赋存于震旦纪一寒武纪地层且以脉状、网脉状产出的矿体中闪锌矿的Cd含量明显高于赋存于晚古生代并以层状产出的矿体中闪锌矿的Cd含量。     

Microbial sources of intact polar diacylglycerolipids in the Western North Atlantic Ocean

Intact polar membrane lipids are essential components of microbial membranes and recent work has uncovered a diversity of them occurring in the ocean. While it has long been understood that lipid composition varies across microbial groups, the microbial origins of the intact polar lipids in the surface ocean remain to be fully explained. This study focused on identifying the microbial sources of intact polar diacylglycerolipids (IP-DAGs) in the surface waters of the western North Atlantic Ocean. We used three approaches to define these microbial sources: (i) ¹³C tracing to identify photoautotrophic and heterotrophic production of the major classes of IP-DAGs, (ii) cell sorting flow cytometry of Prochlorococcus, Synechococcus and heterotrophic bacteria to determine IP-DAG composition and (iii) regrowth incubations targeting IP-DAG production by heterotrophic bacteria. Stable isotope tracing indicated that sulfoquinovosyldiacylglycerol (SQDG) and diacylglyceryl-trimethyl-homoserine (DGTS) were produced predominantly by photoautotrophs, while phosphatidylglycerol (PG) production was dominated by heterotrophic bacteria. Of the cells sorted with flow cytometry, Prochlorococcus and Synechococcus were found to have abundant glycolipids, while heterotrophic bacteria were dominated by phospholipids. The regrowth incubations showed that the growth of heterotrophic bacteria correlated with an increase in the concentration of PG, phosphatidylethanolamine (PE) and monoglycosyldiacylglycerol (MGDG). The finding of MGDG in heterotrophic bacteria differs from previous work, which had asserted that the membranes of heterotrophic bacteria in this environment were composed entirely of phospholipids. Overall, our findings indicate that phytoplankton are the primary source of SQDG and DGTS, while heterotrophic bacteria are the dominant source of PG, making these three compounds promising biomarkers for the study of microbes in the surface ocean.     

Failure and flow development of a complex slide: the 1993 Sesa landslide

Large landslides are often characterised by complex activity resulting from their ability to suddenly change behaviour. In fact, these landslides can pass from a slump to a flow characterised by relatively high mobility. This characteristic is a cause of extremely high severity and hazard in areas affected by such phenomena. An interesting case of a large slide in glacial deposits, which occurred in 1993 in the Valcamonica of the Italian Alps, is presented. Different approaches both to characterise the coarse frictional materials involved in the slide and to model the slide initiation and its evolution are adopted. The initial slide mass had a volume of almost 2 Mm³ and after its initial sliding motion along the slope, flowed for about 7 km down the main valley stream. Voight's method has been used to analyse measured slope displacements recorded for a few years before the slope failure. This analysis provided evidence that different times of failure could have been predicted beforehand by rigorous examination of the available data. Laboratory tests and image/processing techniques have been performed to characterise the landslide material as resembling a “bimrock” (block in matrix material). Slope stability analyses have been performed and a dynamic modelling method has been tested on the flow by comparing its results to those obtained by analysis of eyewitness statements and field observations on the mudline left by the flow. Finally, existing empirical approaches for hazard assessment on an alluvial fan have been applied and modified to produce a hazard zonation map for the alluvial fan area by considering maximum expected discharge, local geometry of the channel and the possibility of channel occlusion and subsequent avulsion.     

遥感水文应用中的尺度问题

遥感技术在水文科学中的广泛应用，极大地拓宽了其研究的领域和范围，增加了其研究的深度。但同时也应该看到，遥感信息的空间分辨率和时间分辨率，以及水文科学自身尺度问题的复杂性，一方面对遥感水文的应用产生困难和问题，限制了水文遥感的应用；另一方面又对水文尺度问题提供了新的技术手段，为遥感水文应用增添了新的亮点。从水文机理与空间尺度、遥感信息的空间分辨率、水文参数的空间延拓，以及遥感技术与水文科学的发展等 4个方面探讨了遥感水文的空间尺度问题；从瞬时遥感信息的时间拓展和遥感信息的时间分辨率 2个方面讨论了遥感水文的时间尺度问题。     

Indicator Variogram Models: Do We Have Much Choice?

Many variogram (or covariance) models that are valid—or realizable—models of Gaussian random functions are not realizable indicator variogram (or covariance) models. Unfortunately there is no known necessary and sufficient condition for a function to be the indicator variogram of a random set. Necessary conditions can be easily obtained for the behavior at the origin or at large distance. The power, Gaussian, cubic or cardinal-sine models do not fulfill these conditions and are therefore not realizable. These considerations are illustrated by a Monte Carlo simulation demonstrating nonrealizability over some very simple three-point configurations in two or three dimensions. No definitive result has been obtained about the spherical model. Among the commonly used models for Gaussian variables, only the exponential appears to be a realizable indicator variogram model in all dimensions. It can be associated with a mosaic, a Boolean or a truncated Gaussian random set. In one dimension, the exponential indicator model is closely associated with continuous-time Markov chains, which can also lead to more variogram models such as the damped oscillation model. One-dimensional random sets can also be derived from renewal processes, or mosaic models associated with such processes. This provides an interesting link between the geostatistical formalism, focused mostly on two-point statistics, and the approach of quantitative sedimentologists who compute the probability distribution function of the thickness of different geological facies. The last part of the paper presents three approaches for obtaining new realizable indicator variogram models in three dimensions. One approach consists of combining existing realizable models. Other approaches are based on the formalism of Boolean random sets and truncated Gaussian functions.     

我国北西部地区层间氧化带砂岩型铀矿床微生物与铀成矿作用研究初探

层间氧化带砂岩型铀矿床中微生物参与成矿现象和微生物活动证据越来越多,表明微生物对当今我国主攻的层间氧化带砂岩型铀矿床的形成起重要作用。本文利用分子生物学、活菌培养和实验室模拟等方法对新疆十红滩和蒙其古尔两个典型砂岩型铀矿床中微生物与铀成矿作用关系进行了探讨,结果表明不同地球化学环境带岩石中主要微生物类群的分布特征不同,表现出明显的生物地球化学分带性,从氧化带到还原带,喜氧菌数量逐渐减少,厌氧菌数量递增,各带细菌的分布受容矿层中有机碳含量、铁的存在形式及含量、所赋存地下水的溶解氧和硫酸盐含量等的控制。微生物对铀成矿的影响是综合性的,同时也受到各种环境因素的制约,微生物之间也存在着共生、互生、竞争和拮抗的关系,从而影响着矿床的发育。该类铀矿床微生物富集铀的机制是以间接的非代谢性生物吸附为主,而代谢性富集机制则是次要的。