红树林沉积物中微生物驱动硫循环研究进展

红树林滨海湿地是在周期性咸水、淡水作用下形成的特殊生态系统,其沉积物中有机质含量丰富,微生物驱动的营养物质循环活跃。由于红树林沉积物中硫酸盐含量高、硫化物种类多,因此红树林是研究硫元素生物地球化学循环过程和机制的理想系统。本文综述了红树林生态系统中主要的硫元素循环过程,重点总结了硫氧化和硫酸盐还原过程及其功能微生物,分析了影响硫氧化和硫酸盐还原的主要环境因素,并对红树林沉积物中微生物驱动硫循环的重点研究方向进行了展望。鉴于微生物驱动的硫循环过程耦合碳、氮和金属元素循环,本文可为深入探究微生物驱动的生物地球化学元素循环耦合机制提供参考。     

红树林沉积物中微生物驱动硫循环研究进展北大核心CSCD

红树林滨海湿地是在周期性咸水、淡水作用下形成的特殊生态系统,其沉积物中有机质含量丰富,微生物驱动的营养物质循环活跃。由于红树林沉积物中硫酸盐含量高、硫化物种类多,因此红树林是研究硫元素生物地球化学循环过程和机制的理想系统。本文综述了红树林生态系统中主要的硫元素循环过程,重点总结了硫氧化和硫酸盐还原过程及其功能微生物,分析了影响硫氧化和硫酸盐还原的主要环境因素,并对红树林沉积物中微生物驱动硫循环的重点研究方向进行了展望。鉴于微生物驱动的硫循环过程耦合碳、氮和金属元素循环,本文可为深入探究微生物驱动的生物地球化学元素循环耦合机制提供参考。     

红树林湿地硫酸盐还原菌的多样性及其参与驱动的元素耦合机制

红树林生态系统是热带和亚热带地区重要的滨海湿地,具有营养物质形态多样化和高效动态变化的特征,是驱动碳、氮、硫等元素循环的热区。硫酸盐还原菌(sulfate-reducing prokaryotes,SRPs)是地球最古老的微生物生命形式之一,在推动早期地球地质演化以及现代生物地球化学循环中发挥关键作用,但其在红树林湿地还缺乏全面深入研究。本文基于Genome Taxonomy Database中原核生物基因组的挖掘,系统总结了硫酸盐还原菌的类群,梳理了近年来国内外红树林中硫酸盐还原菌的分布情况及影响其分布的因素,分析了硫酸盐还原菌在红树林生态系统的碳、氮、硫及铁等元素地球化学循环中的作用,并对硫酸盐还原菌未来的研究方向进行了展望,以期为深入研究硫酸盐还原菌参与驱动的元素生物地球化学循环及其耦合机制提供参考。     

海岸盐沼湿地土壤硫循环中的微生物及其作用

硫及硫化合物的动态循环是海岸盐沼湿地的重要组成部分,硫酸盐还原菌(SRB)和硫氧化菌(SOB)是推动硫循环的重要微生物。硫酸盐还原菌把硫酸盐还原为硫化物,同时消耗土壤中的有机物质;硫氧化菌把还原性硫化合物氧化为硫酸盐,缓解土壤中硫化物的积累,它们共同维持硫循环的动态平衡。本文综述了海岸盐沼湿地土壤中硫的存在形式、硫的地球化学循环以及在硫循环过程中扮演重要角色的硫酸盐还原菌和硫氧化菌的生物多样性、活性测定方法及其生态学意义等的最新研究进展,并提出了存在的问题及研究展望。     

水稻土中硫酸盐还原微生物研究进展

硫是水稻必需的营养元素之一.硫酸盐还原是硫元素生物地球化学循环中的关键步骤,在稻田土壤表层和水稻根际都十分活跃.介导硫酸盐还原过程的硫酸盐还原菌(sulfate- reducing bacteria, SRB)是稻田土壤中重要的功能菌群.它们不仅是硫元素生物地球化学循环的重要参与者,也是土壤中有机污染物降解的主要力量之一,发挥着重要的生态和环境功能.综述了稻田土壤中微生物参与的硫酸盐还原过程、SRB的生物多样性以及目前研究稻田土壤SRB主要采用的分子生态学方法,如末端限制性片段长度多样性(T-RFLP)、变性梯度凝胶电泳(DGGE)、实时荧光定量PCR(real-time PCR)、荧光原位杂交(FISH),并对水稻土壤中SRB的分子生态学研究方向进行了展望.     

热泉微生物驱动的氮循环研究进展及展望

热泉微生物是驱动热泉氮(N)循环的主导力量,开展热泉生态系统中驱动氮循环微生物种群构成及其与环境响应的研究,对于探索热泉中氮的生物地球化学循环、生命进化、生物修复等方面都具有重要的理论和应用价值。本文综合阐述了热泉生态系统驱动氮循环的功能微生物(如固氮菌、氨氧化菌、厌氧氨氧化菌、反硝化菌、异化硝酸盐还原菌)在系统发育学上的分布、功能基因的相对丰度、活性及其与环境因子(如温度、pH)的相关性等方面的研究现状和亟待解决的问题。并展望了热泉生境中驱动氮循环微生物未来的研究方向。     

湿地土壤硫组分特征及其影响因素的研究进展

硫是湿地中重要的生命元素, 硫对环境变化极为敏感, 在生源要素生物地球化学循环中扮演着重要角色。硫的价态多样, 形式复杂, 湿地垦殖使土地利用方式等发生显著改变, 进而影响到土壤硫组分的变化。垦殖背景下, 目前对湿地硫组分及其微生物驱动机制的研究尚不够深入。硫稳定同位素技术(δ34S)逐渐地被应用到硫生物地球化学循环过程的研究中, 可以探究硫素的来源。硫氧化菌(Sulfate oxidizing bacteria, SOB)和硫酸盐还原菌(Sulfate reduction bacteria, SRB)是硫组分形态转化的主要驱动者, 在湿地硫循环中发挥着重要的作用。土壤芳基硫酸酯酶是参与土壤硫循环的重要酶类, 是反映湿地土壤质量的一个重要生物学指标。该研究主要从湿地土壤硫组分的分布特征、影响因素、硫同位素来源示踪和微生物驱动机制4个方面, 综述了湿地土壤硫组分影响因素的研究动态。最后, 文章总结了当前研究中存在的问题, 提出了该领域今后深入探讨的一些建议。     

湖泊微生物反硝化过程及速率研究进展

湖泊中微生物介导的反硝化过程对于区域乃至全球的气候环境变化有着深远的影响。因此,研究湖泊微生物反硝化过程及速率有助于我们深刻理解湖泊氮元素生物地球化学循环规律,全面认识湖泊生境对全球氮循环的贡献。本文综述了湖泊生境中反硝化过程(包括典型的反硝化过程及与其他物质循环耦合的反硝化过程,如与有机氮耦合的共反硝化作用、与碳循环耦合的硝酸盐/亚硝酸盐依赖型厌氧甲烷氧化、与铁循环耦合的硝酸盐依赖型铁氧化、与硫循环耦合的硝酸盐还原硫氧化)的速率、驱动微生物及其影响因素。最后对湖泊反硝化过程研究现状和未来发展方向提出总结与展望。     

硫氧化细菌的种类及硫氧化途径的研究进展

硫,作为生物必需的大量营养元素之一,参与了细胞的能量代谢与蛋白质、维生素和抗生素等物质代谢。自然界中,硫以多种化学形态存在,包括单质硫、还原性硫化物、硫酸盐和含硫有机物。硫氧化是硫元素生物地球化学循环的重要组成部分,通常是指单质硫或还原性硫化物被微生物氧化的过程。硫氧化细菌种类繁多,其硫氧化相关基因、酶和途径也多种多样。近几年,相关方面的研究已取得很多进展,但在不同层面仍存在一些尚未解决的科学问题。本文主要围绕硫氧化细菌的种类及硫氧化途径的研究进展进行了综述。     

微生物硫循环网络的研究进展

硫元素是所有生物的基本组成成分,是生物体必需的营养元素之一。硫氧化还原微生物的数量多、分布广、代谢途径多样化,硫化合物之间的平衡依赖于微生物代谢网络中的各种硫转化反应与代谢过程。此外,硫循环与碳、氮循环紧密相关,对地球生态循环起到了至关重要的作用。本文综述了近期微生物硫循环网络的研究进展,包括所涉及的主要微生物、硫循环的生物化学途径、硫循环的环境意义和工业应用潜能等,深入了解自然和人工生态系统中存在的硫循环过程,可为控制工农业生产中硫元素的增减与利用提供理论基础与应用方案。     

南极冰下水生态系统微生物与生源元素循环研究进展

南极大陆冰盖下存在液态水,形成了由冰下湖、冰下河/溪、冰封湖和冰架下水体等组成的冰下水生态系统,具有低温、黑暗和寡营养等极端的环境条件特征。微生物主导了南极冰下水生态系统,其具有丰富多样的种群构成、功能形式和独特的适应机制,在生源元素生物地球化学循环过程中起了重要作用。研究南极冰下微生物群落的生态特征及其参与的生源元素地球化学循环过程,可为揭示地球生命演化和探索外星生命提供指示,具有重要的科学意义。本文综述了南极冰下水生态系统的极端环境条件、冰下微生物的多样性、冰下微生物参与的生物地球化学循环以及冰下微生物的适极机理,最后基于研究现状展望了南极冰下微生物的未来研究方向。     

Sedimentary pyrite sulfur isotope compositions preserve signatures of the surface microbial mat environment in sediments underlying low-oxygen cyanobacterial mats

The sedimentary pyrite sulfur isotope (δ³⁴S) record is an archive of ancient microbial sulfur cycling and environmental conditions. Interpretations of pyrite δ³⁴S signatures in sediments deposited in microbial mat ecosystems are based on studies of modern microbial mat porewater sulfide δ³⁴S geochemistry. Pyrite δ³⁴S values often capture δ³⁴S signatures of porewater sulfide at the location of pyrite formation. However, microbial mats are dynamic environments in which biogeochemical cycling shifts vertically on diurnal cycles. Therefore, there is a need to study how the location of pyrite formation impacts pyrite δ³⁴S patterns in these dynamic systems. Here, we present diurnal porewater sulfide δ³⁴S trends and δ³⁴S values of pyrite and iron monosulfides from Middle Island Sinkhole, Lake Huron. The sediment–water interface of this sinkhole hosts a low-oxygen cyanobacterial mat ecosystem, which serves as a useful location to explore preservation of sedimentary pyrite δ³⁴S signatures in early Earth environments. Porewater sulfide δ³⁴S values vary by up to ~25‰ throughout the day due to light-driven changes in surface microbial community activity that propagate downwards, affecting porewater geochemistry as deep as 7.5 cm in the sediment. Progressive consumption of the sulfate reservoir drives δ³⁴S variability, instead of variations in average cell-specific sulfate reduction rates and/or sulfide oxidation at different depths in the sediment. The δ³⁴S values of pyrite are similar to porewater sulfide δ³⁴S values near the mat surface. We suggest that oxidative sulfur cycling and other microbial activity promote pyrite formation in and immediately adjacent to the microbial mat and that iron geochemistry limits further pyrite formation with depth in the sediment. These results imply that primary δ³⁴S signatures of pyrite deposited in organic-rich, iron-poor microbial mat environments capture information about microbial sulfur cycling and environmental conditions at the mat surface and are only minimally affected by deeper sedimentary processes during early diagenesis.     

Molecular underpinnings for microbial extracellular electron transfer during biogeochemical cycling of earth elements

Microbial extracellular electron transfer(EET) is electron exchanges between the quinol/quinone pools in microbial cytoplasmic membrane and extracellular substrates. Microorganisms with EET capabilities are widespread in Earth hydrosphere, such as sediments of rivers, lakes and oceans, where they play crucial roles in biogeochemical cycling of key elements, including carbon,nitrogen, sulfur, iron and manganese. Over the past 12 years, significant progress has been made in mechanistic understanding of microbial EET at the molecular level. In this review, we focus on the molecular mechanisms underlying the microbial ability for extracellular redox transformation of iron, direct interspecies electron transfer as well as long distance electron transfer mediated by the cable bacteria in the hydrosphere.     

Mathematical simulation of the diel O, S, and C biogeochemistry of a hypersaline microbial mat

The creation of a mathematical simulation model of photosynthetic microbial mats is important to our understanding of key biogeochemical cycles that may have altered the atmospheres and lithospheres of early Earth. A model is presented here as a tool to integrate empirical results from research on hypersaline mats from Baja California Sur (BCS), Mexico into a computational system that can be used to simulate biospheric inputs of trace gases to the atmosphere. The first version of our model, presented here, calculates fluxes and cycling of O(2), sulfide, and dissolved inorganic carbon (DIC) via abiotic components and via four major microbial guilds: cyanobacteria (CYA), sulfate reducing bacteria (SRB), purple sulfur bacteria (PSB) and colorless sulfur bacteria (CSB). We used generalized Monod-type equations that incorporate substrate and energy limits upon maximum rates of metabolic processes such as photosynthesis and sulfate reduction. We ran a simulation using temperature and irradiance inputs from data collected from a microbial mat in Guerrero Negro in BCS (Mexico). Model O(2), sulfide, and DIC concentration profiles and fluxes compared well with data collected in the field mats. There were some model-predicted features of biogeochemical cycling not observed in our actual measurements. For instance, large influxes and effluxes of DIC across the MBGC mat boundary may reveal previously unrecognized, but real, in situ limits on rates of biogeochemical processes. Some of the short-term variation in field-collected mat O(2) was not predicted by MBGC. This suggests a need both for more model sensitivity to small environmental fluctuations for the incorporation of a photorespiration function into the model.     

高温油藏生物膜内硫酸盐还原菌的腐蚀机理及防治策略

硫酸盐还原菌(sulfate-reducing bacteria,SRB)广泛分布于高温、高压及高盐的石油油藏中,在油藏硫循环中起主导作用。SRB能在油藏生物膜内生长,有微量低分子有机酸时利用硫酸盐为电子受体并将其还原成硫化氢。硫化氢会腐蚀管道,导致原油泄露等其他安全问题,每年造成的经济损失超过7 000亿元。本文首先总结了油藏生物膜内微生物菌群多样性,分析了生物膜内SRB及其相关菌群的协同腐蚀机理;然后讨论了高温油藏SRB介导的硫氮氢生物地球化学循环过程、胞外电子传递机制及其腐蚀作用,并通过几个高温油藏SRB生物膜内腐蚀的现场案例进一步阐明了SRB的腐蚀机制。在此基础上,提出了应对高温油藏生物膜内SRB腐蚀的生物纳米防治策略,这为高温油藏管道防腐提供了新思路。     

Abundance and diversity of aerobic anoxygenic phototrophic bacteria in saline lakes on the Tibetan plateau

Aerobic anoxygenic phototrophic (AAP) bacteria are heterotrophic prokaryotes that are capable of utilizing light as an energy source but are not capable of producing molecular oxygen. Recently, multiple studies have found that AAP bacteria are widely distributed in oceans and estuaries and may play an important role in carbon cycling. However, AAP bacteria in inland lake ecosystems have not been investigated in depth. In this study, the abundance and diversity of the pufL-M genes, encoding photosynthetic reaction centers of AAP bacteria, were determined in the oxic water column and anoxic sediments of saline lakes (Qinghai, Erhai, and Gahai Lakes) on the Tibetan Plateau, China. Our results indicated that AAP bacteria were abundant in inland lakes, with the proportion of AAP bacteria (in total bacteria) comparable to those in the oceans, but with a lower diversity. Salinity and pH were found to be potential factors controlling the AAP bacterial diversity and community composition. Our data have implications for a better understanding of the potential role of AAP bacteria in carbon cycling in inland lake ecosystems.     

Indicators of Microbial Sulfate Reduction in Acidic Sulfide-Rich Mine Tailings

Sulfate-reducing bacteria (SRB) are thought to be actively involved in the cycling of sulfur in acidic mine tailings. However, most studies have used circumstantial evidence to assess microbial sulfate activity in such environments. In order to fully ascertain the role of sulfate-reducing bacteria (SRB) in sulfur cycling in acidic mine tailings, we measured sulfate reduction rates, sulfur isotopic composition of reduced sulfide fractions, porewaters and solid-phase geochemistry and SRB populations in four different Cu-Zn tailings located in Timmins, Ontario, Canada. The tailings were sampled in the summer and in the spring, shortly after snowmelt. The results first indicate that all four sites showed very high sulfate reduction rates in the summer (～100–1000 nmol cm^{? 3}d^?1), which corresponded to the presence of sulfide in the porewaters and to high SRB populations. In some of the sites, zones of microbial sulfate reduction also corresponded to a decline of organic carbon and to an apparent pyrite (with slightly negative δ³⁴S values) enrichment around the same depth. Microbial sulfate reduction was also important in permanently acidic (pH 2–3) mine tailings sites, suggesting that SRB can be active under very acidic conditions. Secondly, the results showed that microbial sulfate reduction was greatly reduced in the spring, suggesting that temperature might be a key factor in the activity of SRB. However, a closer look at the results indicated that temperature was not the sole factor and that acidic conditions and limited substrate availability in the spring appeared to be important as well in limiting microbial sulfate par reduction in sulfidic mine tailings. Finally, the results indicate that sulfur undergoes rapid cycling throughout the year and that microbial sulfate reduction and metal sulfide precipitation do not appear to be a permanent sink for metals.     

Characterization of Enrichment Cultures Involved in the Carbon,Sulfur and Iron Biogeochemical Cycles in French Guiana Mobile Muds

The fluidized sediment ecosystem off French Guiana is characterized by active physical reworking, diversity of electron acceptors and highly variable redox regime. It is well studied geochemically but little is known about specific microorganisms involved in its biogeochemistry. Based on the biogeochemical profiles and rate kinetics, several possible biotically mediated pathways of the carbon, sulfur and iron cycles were hypothesized. Enrichment studies were set up with a goal to culture microorganisms responsible for these pathways. Stable microbial consortia potentially capable of the following chemolithoautotrophic types were enriched from the environment and characterized: elemental sulfur/thiosulfate disproportionators, thiosulfate-oxidizing ferrihydrite and nitrate reducers, sulfide/ferrous sulfide oxidizers coupled with nitrate and microaerophilic iron oxidizers. Attempts to generate several enrichments (anoxic ammonia oxidation, and sulfide oxidizers with ferric iron or manganese oxide) were not successful. Heterotrophic sulfate and elemental sulfur reduction bacteria are prominent and dominate reductive sulfur transformations. We hypothesize that carbon dioxide fixation coupled with synthesis of organic matter happens mostly via sulfur disproportionation and sulfur species oxidation with iron oxidation playing a minor role.     

Contrasting taxonomic stratification of microbial communities in two hypersaline meromictic lakes

Hypersaline meromictic lakes are extreme environments in which water stratification is associated with powerful physicochemical gradients and high salt concentrations. Furthermore, their physical stability coupled with vertical water column partitioning makes them important research model systems in microbial niche differentiation and biogeochemical cycling. Here, we compare the prokaryotic assemblages from Ursu and Fara Fund hypersaline meromictic lakes (Transylvanian Basin, Romania) in relation to their limnological factors and infer their role in elemental cycling by matching taxa to known taxon-specific biogeochemical functions. To assess the composition and structure of prokaryotic communities and the environmental factors that structure them, deep-coverage small subunit (SSU) ribosomal RNA (rDNA) amplicon sequencing, community domain-specific quantitative PCR and physicochemical analyses were performed on samples collected along depth profiles. The analyses showed that the lakes harbored multiple and diverse prokaryotic communities whose distribution mirrored the water stratification patterns. Ursu Lake was found to be dominated by Bacteria and to have a greater prokaryotic diversity than Fara Fund Lake that harbored an increased cell density and was populated mostly by Archaea within oxic strata. In spite of their contrasting diversity, the microbial populations indigenous to each lake pointed to similar physiological functions within carbon degradation and sulfate reduction. Furthermore, the taxonomy results coupled with methane detection and its stable C isotope composition indicated the presence of a yet-undescribed methanogenic group in the lakes'' hypersaline monimolimnion. In addition, ultrasmall uncultivated archaeal lineages were detected in the chemocline of Fara Fund Lake, where the recently proposed Nanohaloarchaeota phylum was found to thrive.