The microfacies and sedimentary responses to the mass extinction during the Permian-Triassic transition at Yangou Section,Jiangxi Province,South China

A Permian-Triassic (P-Tr) boundary section of continuous carbonate facies, which well recorded the biotic and environmental processes through the great P-Tr transition in the shallow non-microbialite carbonate facies, has been studied in Yangou, Leping County, Jiangxi Province. The P-Tr sequence is well correlated with the Meishan section according to the conodont biostratigraphy and the excursion of carbon isotopes. A series of high-resolution thin-sections from the P-Tr boundary carbonate rocks at the Yangou section are studied to explore the interrelation between environmental change and biological evolution during the transitional time. Six microfacies have been identified based upon the observation of the thin-sections under a microscope on the grains and matrix and their interrelation. Combined with the data of fossils and carbon isotopes, Microfacies 4 (MF-4), coated-grain-bearing foraminifer oolitic sparitic limestone, and Microfacies 6 (MF-6), dark shelly micritic limestone, should be the different responses to the two episodes of mass extinction and environmental events that can be correlated throughout South China and even over the world. The oolitic limestone of MF-4 is the first finding from the latest Permian strata in South China and it might be a proxy of an unusual environmental condition of high pCO₂, low sulfate concentration and of microbial blooming in the aftermath of the latest Permian mass extinction. The micritic limestone of MF-6 containing rich micro-gastropods and ostracods probably represents the blooming event of disaster taxa in the earliest Triassic environment. The microfacies analysis at the Yangou section can well reveal the episodic process of the biological evolution and environmental change in the shallow non-microbialite carbonate facies throughout the great P-Tr transition, thus the Yangou section becomes an important complement to the Meishan section.     

Sulfur metabolism by marine heterotrophic bacteria involved in sulfur cycling in the ocean

Sulfur cycling in the biosphere is tightly interwoven with the cycling of carbon and nitrogen, through various biological and geochemical processes. Marine microorganisms, due to their high abundance, diverse metabolic activities, and tremendous adaptation potential, play an essential role in the functioning of global biogeochemical cycles and linking sulfur transformation to the cycling of carbon and nitrogen. Currently many coastal regions are severely stressed by hypoxic or anoxic conditions, leading to the accumulation of toxic sulfide. A number of recent studies have demonstrated that dissimilatory sulfur oxidation by heterotrophic bacteria can protect marine ecosystems from sulfide toxicity. Sulfur-oxidizing bacteria have evolved diverse phylogenetic and metabolic characteristics to fill an array of ecological niches in various marine habitats. Here, we review the recent findings on the microbial communities that are involved in the oxidation of inorganic sulfur compounds and address how the two elements of sulfur and carbon are interlinked and influence the ecology and biogeochemistry in the ocean. Delineating the metabolic enzymes and pathways of sulfur-oxidizing bacteria not only provides an insight into the microbial sulfur metabolism, but also helps us understand the effects of changing environmental conditions on marine sulfur cycling and reinforces the close connection between sulfur and carbon cycling in the ocean.     

Earliest microbially mediated pyrite oxidation in ~ 3.4 billion-year-old sediments

Pyrite (FeS₂) oxidation in modern sedimentary environments is neither a purely chemical nor purely microbial process, but it is significantly enhanced by the activity of microorganisms that use reduced forms of iron and sulphur in their metabolisms. On the early Earth, where oxygen levels were thought to be < 10^?5 of the present atmospheric level and chemical oxidants scarce, such biological mediation may have been critical in the redox cycles of iron and sulphur. Here, we show that detrital sedimentary pyrite grains in a ~ 3.4 billion-year-old sandstone were colonised by microbial communities. The detrital pyrite comes from the basal quartz arenite member of the 3.43–3.35 Ga Strelley Pool Formation (SPF) in the East Strelley greenstone belt of the Pilbara Craton, Western Australia. Rock chips and petrographic thin sections of black sandstones occurring on two ridges close to the SPF type locality of Strelley Pool were investigated using optical microscopy, SEM, TEM, laser Raman and NanoSIMS. The detrital pyrite grains exhibit laminated carbonaceous coatings of early Archean age, with localised enrichments of nitrogen that are interpreted as the in situ remains of biofilms growing on these nutrient-rich minerals. Pyrite surfaces contain spherical pits, chains of pits and channels that are morphologically distinct from abiotic alteration features. The pits and channels are widespread, have a clustered distribution typical of microbial colonisation, and are closely comparable to biologically mediated microstructures in the younger rock record and those created by extant Fe- and S-oxidising microbes in the laboratory. They are thus interpreted as trace fossils formed by the attachment of bacteria to the pyrite surfaces. A nano-layer and discreet nano-grains of secondary mineral precipitates, namely Fe-oxides belonging to the magnetite-maghaemite group, attest to pyrite oxidation. These are intimately associated with the biofilms and trace fossils, and are interpreted to represent the fossilised mineral products of biologically mediated pyrite oxidation. These data extend the geological range of microbes capable of metabolising reduced Fe and/or S compounds back to the early Archean and indicate that pyrite-rich sedimentary rocks provide promising targets in the search for extraterrestrial life.     

南京花神湖3种沉水植物表面附着微生物群落特征

沉水植物表面附着微生物系统是水生态的重要组成部分,然而当前对其了解仍不清楚.南京市花神湖是一个城市湖泊,沉水植物生长区域面积占湖面面积的40%左右.尽管花神湖的氮、磷营养盐水平很高,但最近未发生过藻类水华现象.本文以南京市花神湖中自然生长的优势种菹草(Potamogeton crispus)、伊乐藻(Elodea nuttallii)和金鱼藻(Ceratophyllum demersum)为研究对象,利用扫描电镜和荧光显微镜观测了叶表面附着微生物群落的分布特征,测定了植物表面附着微生物的密度及附生藻类的种类、密度和优势种群,并比较分析了不同水生植物之间附生藻类的差异性.结果表明,沉水植物表面微生物群落的分布与物种和叶龄有关.3种沉水植物中,菹草表面微生物群落结构最为复杂,微生境最为丰富.底部老叶片上面附着较多的微生物且表现出较高的生物多样性.植物表面附着微生物密度大小顺序为:菹草金鱼藻伊乐藻;植物表面附生藻类密度大小顺序为:菹草金鱼藻伊乐藻.总体来讲,沉水植物表面微生物总量大概比藻类数量高1~2个数量级.这为深入研究沉水植物及其表面微生物的生态功能奠定了基础.     

Suspended solids induce increasing microbial ammonium recycling along the river-estuary continuum of the Yangtze River

Many large rivers worldwide are enriched with high levels of suspended solids (SS), which are known to be hotspots of many nitrogen (N) transformation processes (e.g., denitrification, nitrification). However, the influence of SS on microbial ammonium (NH₄⁺) recycling remains unclear. Water column NH₄⁺ regeneration rates (REGs) and potential uptake rates (U_pots) as well as community biological NH₄⁺ demand (CBAD) was measured in the river-estuary continuum of the third longest river in the world—Yangtze River, which has dramatic SS gradients. We found that REGs, U_pots, and CBAD all increased downriver, with higher REGs, U_pots, and CBAD in the estuary than in the river sections. The regeneration and uptake of NH₄⁺ were nearly balanced in the river sections, while the positive CBAD in the estuary indicated obvious NH₄⁺ demand of microbes. Concentrations of SS, which also control the content of chemical oxygen demand and particulate N, were the main factor influencing NH₄⁺ recycling rates and CBAD. SS-induced regenerated NH₄⁺ in the river-estuary continuum of Yangtze River was estimated to be 11.02 × 10⁸ kg N yr⁻¹ and accounted for about 14% of total N inputs, suggesting that regenerated NH₄⁺ is an important N source for microbes and may influence nutrient dynamics in lower coasts. To our knowledge, this is the first study to report NH₄⁺ recycling in Yangtze River with an emphasis on its influencing factors and contribution to N budgets.     

Climate tipping-point potential and paradoxical production of methane in a changing ocean

The global warming potential of methane (CH₄) is about 30 times stronger than that of carbon dioxide (CO₂) over a century timescale. Methane emission is hypothesized to have contributed to global climate change events and mass extinctions during Earth’s history. Therefore, the study of CH₄ production processes is critically important to the understanding of global climate change. It has been a dogma that biogenic CH₄ detectable in the oceans originates exclusively from the anaerobic metabolic activity of methanogenic archaea in hypoxic and anoxic environments, despite reports that many oxic surface and near-surface waters of the world’s oceans are CH₄-supersaturated, thereby rendering net sea-to-air emissions of CH₄. The phenomenon of CH₄ production in oxic marine waters is referred to as the “ocean methane paradox”. Although still not totally resolved, recent studies have generated several hypotheses regarding the sources of CH₄ production in oxic seawater. This review will summarize our current understanding of the importance of CH₄ in the global climate and analyze the biological processes and their underpinning mechanisms that lead to the production of CH₄ in oxic seawater environments. We will also tentatively explore the relationships of these microbial metabolic processes with global changes in climate and environment.     

Microbial roles equivalent to geological agents of high temperature and pressure in deep Earth

Microbes not only show sensitive responses to environmental changes but also play important roles in geochemical and geophysical systems. It is well known that microbes have caused major changes in surface environments and biogeochemical cycles through Earth history. Microbial processes can also induce the synthesis of certain minerals under Earth-surface conditions that previously were believed to form only under high temperatures and pressures in the deep Earth. For example, microbes can promote the conversion of smectite to illite, synthesis of authigenic plagioclase, precipitation of dolomite, and biotransformation of geolipids. These effects of microbes are due to their large surface/volume ratios, enzyme production, and abundant functional groups. Microbial catalyzation of chemical reactions proceeds through reaction-specific enzymes, a decrease in Gibbs’s free energy, and/or break through the dynamics reaction thresholds via their metabolisms and physiology. Microbes can lower the surface free energy of mineral nuclei via biophysical adsorption due to their large surface/volume ratios and abundant functional groups. The mineral precipitation and transformation processes induced by microbes are functionally equivalent to geological processes operating at high temperatures and pressures in the deep Earth, suggesting that microbial processes can serve as analogs to deep abiotic processes that are difficult to observe.     

VARIABILITY IN THE CHEMICAL COMPOSITION OF IN SITU SUBGLACIAL MELTWATERS

Meltwaters collected from boreholes drilled to the base of the Haut Glacier d'Arolla, Switzerland have chemical compositions that can be classified into three main groups. The first group is dilute, whereas the second group is similar to, though generally less concentrated in major ions, than contemporaneous bulk glacial runoff. The third group is more concentrated than any observed bulk runoff, including periods of flow recession. Waters of the first group are believed to represent supraglacial meltwater and ice melted during drilling. Limited solutes may be derived from interactions with debris in the borehole. The spatial pattern of borehole water levels and borehole water column stratification, combined with the chemical composition of the different groups, suggest that the second group represent samples of subglacial waters that exchange with channel water on a diurnal basis, and that the third group represent samples of water draining through a ‘distributed’ subglacial hydraulic system. High NO⁻₃ concentrations in the third group suggest that snowmelt may provide a significant proportion of the waters and that the residence time of the waters at the bed in this particular section of the distributed system is of the order of a few months. The high NO⁻₃ concentrations also suggest that some snowmelt is routed along different subglacial flowpaths to those used by icemelt. The average SO²⁻₄: (HCO⁻₃ + SO²⁻₄) ratio of the third group of meltwaters is 0.3, suggesting that sulphide oxidation and carbonate dissolution (which gives rise to a ratio of 0.5) cannot provide all the HCO⁻₃ to solution. Hence, carbonate hydrolysis may be occurring before sulphide oxidation, or there may be subglacial sources of CO₂, perhaps arising from microbial oxidation of organic C in bedrock, air bubbles in glacier ice or pockets of air trapped in subglacial cavities. The channel marginal zone is identified as an area that may influence the composition of bulk meltwater during periods of recession flow and low diurnal discharge regimes. © 1997 by John Wiley & Sons, Ltd.     

Mass extinction and Pangea integration during the Paleozoic-Mesozoic transition

The greatest Phanerozoic mass extinction happened at the end-Permian to earliest Triassic.About 95%species,82%genera,and more than half families became extinct,constituting the sole macro-mass extinction in geological history.This event not only caused the great extinction but also destroyed the 200 Myr-long Paleozoic marine ecosystem,prompted its transition to Mesozoic ecosystem,and induced coal gap on land as well as reef gap and chert gap in ocean.The biotic crisis during the Paleozoic-Mesozoic transition was a long process of co-evolution between geospheres and biosphere.The event sequence at the Permian-Triassic boundary(PTB)reveals two-episodic pattern of rapidly deteriorating global changes and biotic mass extinction and the intimate relationship between them.The severe global changes coupling multiple geospheres may have affected the Pangea integration on the Earth’s surface spheres,which include:the Pangea integration→enhanced mountain height and basin depth,changes of wind and ocean current systems;enhanced ocean basin depth→the greatest Phanerozoic regression at PTB,disappearance of epeiric seas and subsequent rapid transgression;the Pangea integration→thermal isolation effect of continental lithosphere and decrease of mid-ocean ridges→development of continental volcanism;two-episode volcanism causing LIPs of the Emeishan Basalt and the Siberian Trap(259–251 Ma)→global warming and mass extinction;continental aridification and replacement of monsoon system by latitudinal wind system→destruction of vegetation;enhanced weathering and CH4emission→negative excursion ofδ13C;mantle plume→crust doming→regression;possible relation between the Illawarra magnetic reversal and the PTB extinction,and so on.Mantle plume produced the Late Permian LIPs and mantle convection may have caused the process of the Pangea integration.Subduction,delamination,and accumulation of the earth’s cool lithospheric material at the"D"layer of CMB started mantle plume by heat compensation and disturbed the outer core thermo-convection,and the latter in turn would generate the mid-Permian geomagnetic reversal.These core and mantle perturbations may have caused the Pangea integration and two successive LIPs in the Permian,and probably finally the mass extinction at the PTB.     

Atmospheric carbon dioxide and the long-term control of the Earth’s climate

A CO₂-weathering model has been used to explore the possible evolution of the Earth’s climate as the Sun steadily brightened throughout geologic time. The results of the model calculations can be described in terms of three, qualitatively different, “Megaclimates”. Mega-climate 1 resulted from a period of rapid outgassing in the early Archean, with high, but declining, temperatures caused by the small weathering rates on a largely water-covered planet. Mega-climate 2 began about 3 Gyear ago as major continental land masses developed, increasing the weathering rate in the early Proterozoic and thereby depleting the atmospheric CO₂ concentration. This process produced the first Precambrian glaciations about 2.3 Gyear ago. During Mega-climate 2, evolutionary biological processes increased the surface weatherability in incremental steps and plate tectonics modulated the CO₂ outgassing rate with an estimated period of 150 Myear (approximately one-half the period for the formation and breakup of super continents). Throughout Mega-climate 2 the surface temperature was controlled by variations in the atmospheric CO₂ level allowing transitions between glacial and non-glacial conditions. The results of the model for Mega-climate 2 are in agreement with the occurrence (and absence) of glaciations in the geologic record. Extending the model to the future suggests that CO₂ control of the Earth’s temperature will no longer be able to compensate for a solar flux that continues to increase. The present level of atmospheric CO₂ is so small that further reduction in CO₂ cannot prevent the Earth from experiencing Mega-climate 3 with steadily increasing surface temperatures caused by the continued brightening of the Sun. During Mega-climate 3, the main danger to the biosphere would come not from an increasing temperature but from a decreasing (rather than an increasing) CO₂ level which could, in time, fall below 0.5 PAL, causing serious damage to the biosphere. Fortunately, the rates of change due to solar brightening are slow enough that Mega-climate 3 appears to pose no threat to the biosphere for the next 0.5-2 Gyear.     

Characterization and advanced oxidation treatment of dyeing effluent by Fenton’s reagent

Textile effluent from dyeing process has been a serious environmental threat for years. This study was intended to evaluate the performance of Fenton’s process for the removal of chemical oxygen demand (COD), colour and turbidity. Experiments were conducted by laboratory-scale reactors fed with cotton dyeing effluent. The Fenton process employs ferrous ions and hydrogen peroxide H₂O₂ under acidic pH conditions. The experimental variables studied include doses of iron salts and hydrogen peroxide, oxidation time, pH for oxidation and coagulation. The COD, color and turbidity removal reached a maximum of 97.2, 96.8 and 84.8% respectively at a reaction time of 20 min under optimum doses of H₂O₂ and Fe²⁺. Hydrogen peroxide dose ranging from 0.5 to 2.0 mL/500 mL and FeSO₄ · 7H₂O in the range of 0.5–4.0 gm/500 mL were selected to be examined at different reaction times between 10 and 30 min. Optimum dose of hydrogen peroxide and ferrous sulphate were 2.0 mL and 1.0 gm respectively for 500 mL of sample. In this study optimized pH 4.0 and 6.0 was found effective for oxidation and coagulation respectively.     

A ∼300-year record of environmental changes in Lake Issyk-Kul,Central Asia,inferred from lipid biomarkers in sediments

We measured lipid biomarkers (n-alkanes [n-ALKs] and n-alkanoic acids [n-FAs]) and other components of organic matter (total organic carbon [TOC] and total nitrogen [TN]) in a sediment core from Lake Issyk-Kul, Central Asia, to infer environmental changes in and around the lake during the last ∼300 years. Stratigraphic shifts in lipid biomarkers, TOC and TN, indicate three distinct environmental stages in the lake over the past three centuries: (1) Stage I (1670s–1790s, 51–36 cm sediment depth) corresponds to a period of stable hydrology in the lake, reflected by relatively constant concentrations of n-ALKs and n-FAs and values of related indexes. The interval was a period of relatively low trophic state. Natural factors were the main controls on environmental changes in and around the lake. (2) Stage II (1800s–1970s, 35–15 cm sediment depth) was a period when human activities began to exert influence on the environment in and around the lake. Enhanced agricultural exploitation and greater regional rainfall resulted in delivery to the lake of more land-derived lipids. Logging activity around the lake altered the vegetation, as revealed by shifts in C₂₇/C₃₃ ratios and the average chain length (ACL₂₇₋₃₃). A significant decline in lake level caused by excessive water consumption impacted aquatic macrophytes, as revealed by a reduction in macrophyte indicators. Lower nutrient concentrations were inferred for this period. (3) Stage III (1980s–present, 14–0 cm sediment depth) corresponds to a period of accelerating eutrophication. Before year 2000, lake level declined steadily as a result of low rainfall (drought) and high evaporation, which exerted a strong influence on the lake condition. In addition, anthropogenic activities contributed to lake eutrophication. After 2000, the lake experienced a dramatic increase in trophic state, characterized by high algal productivity, as indicated by greater TN, short-chain n-ALKs and short-chain n-FAs. The change was probably caused by flourishing tourism around the lake. In summary, environmental changes in and around Lake Issyk-Kul during the past ∼300 years were originally driven largely by natural factors such as shifts in regional precipitation amount. Human activities (e.g. logging, agriculture, water extraction, and more recently, tourism) took on increasingly important roles during the last two centuries, affecting watershed vegetation, the lake primary producer community and lake trophic status. Changes recorded in the lake sediments over the last ∼300 years are in good agreement with historical records.     

不同生态处理方法对黑臭河道底泥细菌多样性与群落结构的影响

底泥细菌代谢是城市河道底泥代谢物的主要来源,最终决定城市河道的生态状况.本文研究了黑臭河道底泥经添加硝酸钙、生物促生剂和种植沉水植物处理后底泥中细菌群落结构的响应,以期为城市黑臭河道细菌群落的改善和综合治理提供理论依据.实验结果表明:经过不同生态处理后,上覆水中,添加硝酸钙组总氮(TN)含量显著高于对照组,添加生物促生剂组溶解氧浓度显著高于对照组.沉积物中,所有处理组的氧化还原电位值(ORP)均显著高于对照组,种植沉水植物组和添加硝酸钙组TN含量均显著低于对照组,沉积物理化性质得到一定改善.对不同生态处理组底泥细菌群落的研究发现,处理组底泥细菌群落产生了较大变化,且不同处理组细菌群落变化不同,生物促生剂组底泥中细菌的Sobs指数和Chao 1指数显著高于对照组和硝酸钙组,且生物促生剂组Shannon指数和PD指数显著高于硝酸钙组.Proteobacteria(Deltaproteobacteria、Betaproteobacteria、Gammaproteobacteria)、Chloroflexi、Firmicutes、Bacteroidetes和Spirochaetae是各实验组的主要优势菌门;非度量多维尺度分析表明:硝酸钙和生物促生剂的投加可明显改变底泥细菌群落结构组成.在属水平上,uncultured_Anaerolineaceae、Ferribacterium、uncultured_Xanthomonadales_Incertae_Sedis是导致底泥细菌群落发生变化的主要菌属.冗余分析结果表明,底泥ORP的变化是驱动细菌群落结构变化的关键环境因素.     

云南抚仙湖窑泥沟复合湿地的除氮效果

为了延缓抚仙湖局部湖湾水体富营养化趋势,在北岸建设了净化面积1hm2.的复合人工湿地.综合利用生物氧化塘、水平潜流湿地和表面流湿地治理技术,对入湖河道窑泥沟污水中氮的去除效果进行了试验研究.试验结果表明,湿地系统的除氮效果十分明显,水力负荷年平均为437mm／d,氮负荷年平均为3.315 g／(m2·d),湿地系统氮滞留量年平均为1.91g／(m2·d).其中,通过植物吸收同化作用除氮量为0.142g／(m2·d),占总氮滞留量的7.5％左右.湿地系统对污水中硝酸盐及亚硝酸盐氮(NOX-)、氨氮(NH4+)、有机氮(TON)和总氮(TN)的去除率年平均分别为62.7％、53.8％、62.4％和57.5％.在湿地系统各功能区中,表面流人工湿地除氮效果最佳,氮去除率年平均为39.4％,硝化和反硝化作用均较强;生物净化塘除氮效果次之,氮去除率年平均为18.5％;潜流人工湿地氮去除率年平均为10.6％;沉淀池中氮去除率年平均只有3.6％.     

内陆水体好氧甲烷氧化过程研究进展

内陆水体是全球碳循环的关键组成部分,是大气中甲烷(CH_4)的重要来源,每年从内陆淡水与自然湿地排放进入大气的CH4约为185～357 Tg/a.通常,内陆水体中CH_4主要由分布于水层底部的厌氧区或沉积层内的产甲烷菌介导产生,其向水层表面传输的过程中易被甲烷氧化菌所氧化.甲烷氧化菌可分为好氧甲烷氧化菌和厌氧甲烷氧化菌,有氧条件下,由好氧甲烷氧化菌介导的好氧甲烷氧化过程是水体中甲烷氧化过程的主要形式,湖泊底部产生的CH_4总量中约有99%可以被上覆水体中的好氧甲烷氧化过程所消耗.本文收集文献综合分析阐明,好氧甲烷氧化过程是由水环境因子、水文条件以及不同内陆水体的生态系统特征共同调控,同时也表现在了好氧甲烷氧化菌的生境偏好上.复杂的调控过程构建了内陆水体向大气输送CH_4的动态平衡,并最终反映在内陆水体对全球CH_4循环、碳循环作出的贡献上.     

Estimating the influence of increased nitrate loads from wastewater on phosphorus mobility in river sediments

Research on the sediment‐surface water transition zone in three study site regions, different in hydrological conditions, was conducted to estimate to which extent nitrate in surface water can contribute to riverbed sediment oxidation and thus prevent release of sediment phosphorus to surface water. Consequently, the Du tch Flow Model (DUFLOW) based water quality model “Spreewald” and results from the emission model “ Mo delling N utrient E missions in Ri ver S ystems” (MONERIS) were used to estimate to which extent wastewater treatment plants (WWTPs) could contribute to the NO₃^– concentration in surface waters if they were operated without denitrification. It is demonstrated that an effective phosphorus retention in sediments by means of surface water NO₃^– is possible only under specific conditions, i. e. (i) a sufficient supply of surface water to the sediment by advective fluxes, (ii) a sufficient amount of sediment iron to provide phosphorus binding sites in the case of sediment oxidation, (iii) a redox system not leading to a rapid NO₃^– and FeOOH depletion and to phosphorus release from organic pools by high microbial activities. Model results show that in‐stream denitrification processes counteract a significant increase of NO₃^– surface water concentrations from WWTPs operated without denitrification during summer, when eutrophication risk through phosphorus is highest. The increase of NO₃^– surface water concentrations in winter due to decreased denitrification in the surface water is of minor relevance for phosphorus release from sediments.     

Geochemical weathering at the bed of Haut Glacier d'Arolla,Switzerland—a new model

Waters were sampled from 17 boreholes at Haut Glacier d'Arolla during the 1993 and 1994 ablation seasons. Three types of concentrated subglacial water were identified, based on the relative proportions of Ca²⁺, HCO₃^? and SO₄^2? to Si. Type A waters are the most solute rich and have the lowest relative proportion of Si. They are believed to form in hydrologically inefficient areas of a distributed drainage system. Most solute is obtained from coupled sulphide oxidation and carbonate dissolution (SO–CD). It is possible that there is a subglacial source of O₂, perhaps from gas bubbles released during regelation, because the high SO₄^2? levels found (up to 1200 µeq/L) are greater than could be achieved if sulphides are oxidized by oxygen in saturated water at 0 °C (c.414 µeq/L). A more likely alternative is that sulphide is oxidized by Fe³⁺ in anoxic environments. If this is the case, exchange reactions involving Fe^III and Fe^II from silicates are possible. These have the potential to generate relatively high concentrations of HCO₃^? with respect to SO₄^2?. Formation of secondary weathering products, such as clays, may explain the low Si concentrations of Type A waters. Type B waters were the most frequently sampled subglacial water. They are believed to be representative of waters flowing in more efficient parts of a distributed drainage system. Residence time and reaction kinetics help determine the solute composition of these waters. The initial water–rock reactions are carbonate and silicate hydrolysis, and there is exchange of divalent cations from solution for monovalent cations held on surface exchange sites. Hydrolysis is followed by SO–CD. The SO₄^2? concentrations usually are <414 µeq/L, although some range up to 580 µeq/L, which suggests that elements of the distributed drainage system may become anoxic. Type C waters were the most dilute, yet they were very turbid. Their chemical composition is characterized by low SO₄^2? : HCO₃^? ratios and high pH. Type C waters were usually artefacts of the borehole chemical weathering environment. True Type C waters are believed to flow through sulphide‐poor basal debris, particularly in the channel marginal zone. The composition of bulk runoff was most similar to diluted Type B waters at high discharge, and was similar to a mixture of Type B and C waters at lower discharge. These observations suggest that some supraglacial meltwaters input to the bed are stored temporarily in the channel marginal zone during rising discharge and are released during declining flow. Little of the subglacial chemical weathering we infer is associated with the sequestration of atmospheric CO₂. The progression of reactions is from carbonate and silicate hydrolysis, through sulphide oxidation by first oxygen and then Fe^III, which drives further carbonate and silicate weathering. A crude estimate of the ratio of carbonate to silicate weathering following hydrolysis is 4 : 1. We speculate that microbial oxidation of organic carbon also may occur. Both sulphide oxidation and microbial oxidation of organic carbon are likely to drive the bed towards suboxic conditions. Hence, we believe that subglacial chemical weathering does not sequester significant quantities of atmospheric CO₂ and that one of the key controls on the rate and magnitude of solute acquisition is microbial activity, which catalyses the reduction of Fe^III and the oxidation of FeS₂. Copyright © 2002 John Wiley & Sons, Ltd.     

Soil and water conservation measures improve soil carbon sequestration and soil quality under cashews

Land degradation is becoming a serious problem in the west coast region of India where one of the world's eight biodiversity hotspots,the‘Western Ghats’,is present.Poor land management practices and high rainfall have led to increasing problems associated with land degradation.A long-term(13-year)experiment was done to evaluate the impact of soil and water conservation measures on soil carbon sequestration and soil quality at three different depths under cashew nut cultivation on a 19%slope.Five soil and water conservation measures-continuous contour trenches,staggered contour trenches,halfmoon terraces,semi-elliptical trenches,and graded trenches all with vegetative barriers of Stylosanthes scabra and Vetiveria zizanoides and control were evaluated for their influence on soil properties,carbon sequestration,and soil quality under cashews.The soil and water conservation measures improved significantly the soil organic carbon,soil organic carbon stock,carbon sequestration rate and microbial activity compared to the control condition(without any measures).Among the measures tested,continuous contour trenches with vegetative barriers outperformed the others with respect to soil organic carbon stock,sequestration rate,and microbial activity.The lower metabolic quotient with the measures compared to the control indicated alleviation of environmental stress on microbes.Using principal component analysis and a correlation matrix,a minimum dataset was identified as the soil available nitrogen,bulk density,basal soil respiration,soil pH,acid phosphatase activity,and soil available boron and these were the most important soil properties controlling the soil quality.Four soil quality indices using two summation methods(additive and weighted)and two scoring methods(linear and non-linear)were developed using the minimum dataset.A linear weighted soil quality index was able to statistically differentiate the effect of soil and water conservation measures from that of the control.The highest value of the soil quality index of 0.98 was achieved with continuous contour trenches with a vegetative barrier.The results of the study indicate that soil and water conservation measures for cashews are a potential strategy to improve the soil carbon sequestration and soil quality along with improving crop productivity and reducing the erosion losses.     

Oxidation of Benzo(a) Pyrene Catalyzed by Phenol Oxidases of Alga Nitella sp. and Potato Tubers

The kinetics of oxidation of carcinogenic benzo(a)pyrene (0.1 nM solution in phosphate buffer) catalyzed by enzyme protein of soil and water plants (potato tubers and alga Nitella sp.) has been studied. The benzo(a)pyrene oxidation rate is determined by the phenoloxidase activity of the enzyme protein from both sources to an equal degree and expressed by the Michaelis-Menten equation. The values for k_cat and apparent K_m were (0.97 ± 0.14) Ms^?1 and 33 ± 6 μM, respectively. The presence of other compounds (including protein substances) in acetone preparations of potato tubers considerably suppresses its catalytic activity in relation to benzo(a)pyrene. Consequently, in the polluted biosphere some water plants, such as alga Nitella sp., and potato tuber can transform carcinogenic benzo(a)pyrene (BP). As oxidation products, all three BP-quinones, i.e. 1,6-, 3,6-and 6,12-diones, were identified.     

城市河流沉积物中氮素与好氧甲烷氧化菌群落特征响应关系

由于人类活动的影响大量未经处理的废污水汇入城市河流,高浓度的污染物影响了河流中微生物对生物地球化学物质迁移和转化的介导作用.本文选取典型的城市河流——北运河作为研究区域,分析了北运河沉积物中氮素形态以及含量的空间和季节差异性,并结合克隆文库分子生物学的方法,探讨了氮素形态和含量的差异对好氧甲烷氧化菌(aerobic methane-oxidizing microorganisms,MOB)群落特征的影响.结果表明:北运河沉积物中铵态氮(NH_4~+-N)为氮素的主要存在形态,存在显著的空间差异,其含量在下游显著高于上游,但季节差异不显著.NH_4~+-N含量的空间差异对MOB的群落结构和群落分布有显著影响,对群落多样性影响不显著.NH_4~+-N含量的空间分布特征与MOB的群落聚类特征一致,NH_4~+-N对MOB群落分布的影响显著高于其他形态的氮素,其含量越高,则与MOB群落分布的响应关系越紧密.北运河中NH_4~+-N的来源影响了沉积物中MOB的主要来源,MOB高同源性菌群的来源与NH_4~+-N等主要污染物的来源一致.沉积物中MOB物种之间联系的紧密程度依赖于氮素的主要存在形态及其含量水平.NH_4~+-N含量较高的下游沉积物中微生物彼此之间关系及集聚程度更强,受外界环境变化的干扰程度更强,受人类活动引起环境变化的敏感程度更高.城市河流中氮素的形态和含量差异对甲烷的氧化过程有显著影响.探究城市河流沉积物中高含量的NH_4~+-N对甲烷产生及消耗的影响过程是控制河流温室气体排放的关键.