Linking toluene degradation with specific microbial populations in soil

Phospholipid fatty acid (PLFA) analysis of a soil microbial community was coupled with (13)C isotope tracer analysis to measure the community's response to addition of 35 microg of [(13)C]toluene ml of soil solution(-1). After 119 h of incubation with toluene, 96% of the incorporated (13)C was detected in only 16 of the total 59 PLFAs (27%) extracted from the soil. Of the total (13)C-enriched PLFAs, 85% were identical to the PLFAs contained in a toluene-metabolizing bacterium isolated from the same soil. In contrast, the majority of the soil PLFAs (91%) became labeled when the same soil was incubated with [(13)C]glucose. Our study showed that coupling (13)C tracer analysis with PLFA analysis is an effective technique for distinguishing a specific microbial population involved in metabolism of a labeled substrate in complex environments such as soil.     

Bacteria and Fungi Respond Differently to Multifactorial Climate Change in a Temperate Heathland,Traced with 13C-Glycine and FACE CO2

It is vital to understand responses of soil microorganisms to predicted climate changes, as these directly control soil carbon (C) dynamics. The rate of turnover of soil organic carbon is mediated by soil microorganisms whose activity may be affected by climate change. After one year of multifactorial climate change treatments, at an undisturbed temperate heathland, soil microbial community dynamics were investigated by injection of a very small concentration (5.12 µg C g⁻¹ soil) of ¹³C-labeled glycine (¹³C₂, 99 atom %) to soils in situ. Plots were treated with elevated temperature (+1°C, T), summer drought (D) and elevated atmospheric carbon dioxide (510 ppm [CO2]), as well as combined treatments (TD, TCO2, DCO2 and TDCO2). The ¹³C enrichment of respired CO₂ and of phospholipid fatty acids (PLFAs) was determined after 24 h. ¹³C-glycine incorporation into the biomarker PLFAs for specific microbial groups (Gram positive bacteria, Gram negative bacteria, actinobacteria and fungi) was quantified using gas chromatography-combustion-stable isotope ratio mass spectrometry (GC-C-IRMS).Gram positive bacteria opportunistically utilized the freshly added glycine substrate, i.e. incorporated ¹³C in all treatments, whereas fungi had minor or no glycine derived ¹³C-enrichment, hence slowly reacting to a new substrate. The effects of elevated CO₂ did suggest increased direct incorporation of glycine in microbial biomass, in particular in G⁺ bacteria, in an ecosystem subjected to elevated CO₂. Warming decreased the concentration of PLFAs in general. The FACE CO₂ was ¹³C-depleted (δ¹³C = 12.2‰) compared to ambient (δ¹³C = ∼−8‰), and this enabled observation of the integrated longer term responses of soil microorganisms to the FACE over one year. All together, the bacterial (and not fungal) utilization of glycine indicates substrate preference and resource partitioning in the microbial community, and therefore suggests a diversified response pattern to future changes in substrate availability and climatic factors.     

南亚热带3种人工林土壤微生物生物量和微生物群落结构特征

以我国南亚热带格木、红椎和马尾松人工林为对象,采用氯仿熏蒸浸提法和磷脂脂肪酸法(PLFA)分析了林地土壤微生物生物量和微生物群落结构组成.结果表明: 林分和季节因素均显著影响土壤微生物生物量、总PLFAs量、细菌PLFAs量和真菌PLFAs量,且干季林分下的土壤微生物生物量、总PLFAs量、单个PLFA量均大于雨季.红椎人工林土壤微生物生物量碳(MBC)和总PLFAs量最高,而格木人工林土壤微生物生物量氮(MBN)最高.土壤pH值对土壤丛枝菌根真菌(16:1ω5c)的影响达到极显著正相关水平.土壤总PLFAs量、革兰氏阳性菌(G⁺)以及腐生真菌(18:2ω6,9c)、革兰氏阳性菌/革兰氏阴性菌(G⁺/G^-)与土壤有机碳、全氮和全磷显著相关,表明土壤有机碳、全氮、全磷含量是影响该地区土壤微生物数量和种类的重要因素.外生菌根真菌(18:1ω9c)和丛枝菌根真菌与土壤碳氮比值呈极显著相关.     

红壤侵蚀区芒萁对土壤微生物群落结构的影响

土壤微生物是反映土壤质量状况的重要指标,研究侵蚀地植被恢复后土壤微生物群落结构的变化对深入认识土壤质量的演变具有重要意义。对比分析了未治理地(Y0)、治理13年(Y13)和31年(Y31)的马尾松林(Pinus massoniana)林下芒萁(Dicranopteris dichotoma)覆盖地(NRd)、去除芒萁覆盖地(Rd)与林下裸地(CK)土壤微生物生物量和群落结构差异,结果表明:林下裸地土壤微生物生物量碳(MBC)、微生物生物量氮(MBN)和总微生物磷脂脂肪酸量(总PLFAs)的含量均显著低于芒萁覆盖地,且去除芒萁4个月后,MBC和总PLFAs均有降低趋势,表明芒萁覆盖对土壤微生物生物量具有重要影响;林下芒萁覆盖地土壤革兰氏阳性菌(GP)、革兰氏阴性菌(GN)、丛植菌根真菌(VAM)、真菌(Fungi)、放线菌(ACT)的PLFAs含量显著高于林下裸地(Y13例外),去除芒萁4个月后,各值均有有接近林下裸地的趋势;芒萁覆盖地真菌/细菌的比值(F/B)均显著高于林下裸地(P0.05),芒萁覆盖地革兰氏阳性菌/革兰氏阴性菌的比值(GP/GN)、饱和直链脂肪酸/单不饱和脂肪酸的比值(sat/mono)和(cy17:0+cy19:0ω8c)/(16:1ω7c+18:1ω7c)(cy/pre)显著小于林下裸地(P0.05),去除芒萁4个月后,芒萁覆盖地土壤cy/pre显著升高(P0.05)(Y13例外),意味着芒萁覆盖地土壤生态系统更稳定,土壤的养分可利用性更高,微生物生物量和群落结构更丰富,活性更强;皮尔逊相关分析和冗余分析发现,土壤理化性质与土壤微生物生物量和群落结构关系密切,土壤C/N、p H和氮素水平是调控芒萁覆盖下土壤微生物生物量和群落结构的主要生态因子。     

转Bt基因水稻根际土壤微生物多样性的磷脂脂肪酸(PLFAs)表征

以亲本水稻为对照,应用13C脉冲标记和磷脂脂肪酸技术,分析转Bt基因对水稻根际微生物多样性的影响.结果表明:转Bt基因水稻与亲本水稻根际均以饱和脂肪酸和支链脂肪酸为主,单不饱和脂肪酸次之,多不饱和脂肪酸最少.苗期、拔节期和抽穗期,转成基因水稻根际革兰氏阳性菌(G+)代表性磷脂脂肪酸含量显著低于亲本水稻;革兰氏阴性菌(G-)代表性磷脂脂肪酸含量显著高于亲本水稻.水稻各生育期,转Bt基因未对水稻根际土壤真菌、放线菌磷脂脂肪酸含量造成显著影响,且转Bt基因水稻与亲本水稻根际微生物磷脂脂肪酸13C含量无显著性差异.表明外源Bt基因插入仅对水稻根际微生物多样性造成短暂影响,不具有持续性.     

长期施用有机无机肥对潮土微生物群落的影响

微生物群落结构是土壤生态系统变化的预警及敏感指标,可用于表征土壤质量及其生态功能变化。本文用磷脂脂肪酸法研究了有机肥和NPK肥料长期施用对华北平原潮土微生物群落结构的影响及其变化特征。结果表明：长期施用有机和无机肥不仅提高了土壤有机碳、全氮、速效磷和速效钾等含量,改善了土壤酸碱度,而且显著增加了土壤微生物生物量,其中以有机肥的效果最为明显,增幅达到15.4%。长期施用肥料有机肥也改变了土壤微生物的群落结构,提高了细菌数量,降低了放线菌含量,而对真菌数量没有明显影响,导致真菌与细菌的比值下降。主成分分析表明,长期施用有机肥的土壤,细菌以含a19:0、br14:0、16:1w5c和17:1w9而真菌以含18:1w10c的微生物为优势种群,NPK处理土壤中细菌以含18:1w7、i19:0、br18:0、16:1w7t和a15:0的微生物为优势种群,CK处理中没有明显的优势种群。     

Linking Toluene Degradation with Specific Microbial Populations in Soil

Phospholipid fatty acid (PLFA) analysis of a soil microbial community was coupled with ¹³C isotope tracer analysis to measure the community’s response to addition of 35 μg of [¹³C]toluene ml of soil solution⁻¹. After 119 h of incubation with toluene, 96% of the incorporated ¹³C was detected in only 16 of the total 59 PLFAs (27%) extracted from the soil. Of the total ¹³C-enriched PLFAs, 85% were identical to the PLFAs contained in a toluene-metabolizing bacterium isolated from the same soil. In contrast, the majority of the soil PLFAs (91%) became labeled when the same soil was incubated with [¹³C]glucose. Our study showed that coupling ¹³C tracer analysis with PLFA analysis is an effective technique for distinguishing a specific microbial population involved in metabolism of a labeled substrate in complex environments such as soil.     

川西亚高山不同林龄云杉人工林土壤微生物群落结构

以川西亚高山云杉人工林林地土壤为对象,采用磷脂脂肪酸(PLFA)法研究了4种不同林龄(50、38、27和20年)的人工林土壤微生物多样性和群落结构特征.结果表明: 随着林龄的增加,土壤有机碳和全氮含量逐步增加;土壤微生物Shannon多样性和Pielou均匀度指数则呈现先增后减的趋势.土壤微生物总PLFAs量、细菌PLFAs量、真菌PLFAs量、放线菌PLFAs量以及丛枝菌根真菌PLFAs量均表现为随林龄的增加而增加.主成分分析(PCA)表明,不同林龄人工林的土壤微生物群落结构之间存在显著差异,其中,第1主成分(PC1)和第2主成分(PC2)共同解释了土壤微生物群落结构总变异的66.8%.冗余分析(RDA)表明,对土壤微生物群落结构产生显著影响的环境因子分别为土壤有机碳、全氮、全钾以及细根生物量.随着人工造林时间的延长,土壤肥力和微生物生物量增加,森林生态系统的恢复进程稳定.     

模拟氮沉降和灌草去除对杉木人工林地土壤微生物群落结构的影响

土壤微生物是陆地生态系统重要的分解者和地上-地下相互作用的纽带。本文以亚热带杉木(Cunninghamia lanceolateata)人工林为对象, 通过模拟林冠层氮沉降和林下灌草去除, 设置4种处理, 包括: 对照(CK)、灌草去除(UR)、氮沉降(N)和氮沉降加灌草去除(N × UR)的野外控制实验, 研究土壤微生物群落结构的响应。本实验分别于2016年4月(春季)和10月(秋季)采集0-10 cm层土壤样品, 运用磷脂脂肪酸法(PLFAs)分析土壤微生物群落结构。结果表明: (1) 10月份土壤微生物总PLFAs量及其他类群土壤微生物PLFAs量显著高于4月份(P < 0.05), 真菌/细菌比值没有显著差异。土壤微生物PLFAs中细菌占优势, 其次为真菌, 放线菌的占比最小; (2)相比CK处理, UR处理下土壤微生物总PLFAs量、细菌PLFAs量、革兰氏阴性菌PLFAs量和放线菌PLFAs量有增加趋势, 但未达到显著差异水平(P > 0.05); (3)相对CK, UR、N和N × UR处理降低了4月份土壤微生物多样性(H°)和均匀度指数(J), 但提高了10月份土壤微生物多样性指数; (4)冗余分析表明, 土壤硝态氮和总磷含量与土壤微生物群落之间呈现显著相关。本研究表明土壤微生物PLFAs在各处理下都表现出明显的季节动态; 短期内林下灌草去除对土壤微生物PLFAs影响表现出一定的促进作用, 氮沉降对土壤微生物群落影响还不甚明显, 需要长期的监测研究来评估两者及其交互作用对土壤微生物群落及其功能的影响。     

Translocation and turnover of rhizodeposit carbon within soil microbial communities of an extensive grassland ecosystem

Background and Aims

A substantial amount of photosynthesized plant-C is allocated belowground in grassland ecosystems where it influences the structure and function of the soil microbial community with potential implications for C cycling and storage. We applied stable isotope probing of microbial PLFAs and repeated soil sampling in a grassland over a period of 1 year to assess the role of microbial communities in the cycling of rhizodeposit-C.

Methods

Pulse-labeling with ¹³CO₂ was performed in a grassland site near Gent (Belgium). Soil samples were taken 24 h, 1 week, 1 month, 4 months, 9 months and 1 year following labeling and analyzed for ¹³C in soil, roots and microbial PLFAs.

Results

C enrichment of PLFAs occurred rapidly (within 24 h) but temporally varied across microbial groups. PLFAs indicative for fungi and gram-negative bacteria showed a faster ¹³C uptake compared to gram-positive bacteria and actinomycetes. However, the relative ¹³C concentrations of the latter communities increased after 1 week, while those of fungi decreased and those of gram-negative bacteria remained constant. PLFA ¹³C mean residence times were much shorter for fungi compared to bacteria and actinomycetes.

Conclusions

Our results indicate temporally varying rhizodeposit-C uptake by different microbial groups, and faster turnover rates of mycorrhizal versus saprotrophic fungi and fungi versus bacteria. Fungi appeared to play a major role in the initial processing and possible rapid channeling of rhizodeposit-C into the soil microbial community. Actinomycetes and gram-positive bacteria appeared to have a delayed utilization of rhizodeposit-C or to prefer other C sources upon rhizodeposition.     

Use of 13C labeling to assess carbon partitioning in transgenic and nontransgenic (parental) rice and their rhizosphere soil microbial communities

Photosynthetic assimilation of CO₂ is a primary source of carbon in soil and root exudates and can influence the community dynamics of rhizosphere organisms. Thus, if carbon partitioning is affected in transgenic crops, rhizosphere microbial communities may also be affected. In this study, the temporal effects of gene transformation on carbon partitioning in rice and rhizosphere microbial communities were investigated under greenhouse conditions using the ¹³C pulse-chase labeling method and phospholipid fatty acid (PLFA) analysis. The ¹³C contents in leaves of transgenic (Bt) and nontransgenic (Ck) rice were significantly different at the seedling, booting and heading stages. There were no detectable differences in ¹³C distribution in rice roots and rhizosphere microorganisms at any point during rice development. Although a significantly lower amount of Gram-positive bacterial PLFAs and a higher amount of Gram-negative bacterial PLFAs were observed in Bt rice rhizosphere as compared with Ck at all plant development stages, there were no significant differences in the amount of individual ¹³C-PLFA between Bt and Ck rhizospheres at any growing stage. These findings indicate that the insertion of cry1Ab and marker genes into rice had no persistent or adverse effect on the photosynthate distribution in rice or the microbial community composition in its rhizosphere.     

Estimating high-affinity methanotrophic bacterial biomass, growth, and turnover in soil by phospholipid fatty acid 13C labeling

A time series phospholipid fatty acid (PLFA) 13C-labeling study was undertaken to determine methanotrophic taxon, calculate methanotrophic biomass, and assess carbon recycling in an upland brown earth soil from Bronydd Mawr (Wales, United Kingdom). Laboratory incubations of soils were performed at ambient CH4 concentrations using synthetic air containing 2 parts per million of volume of 13CH4. Flowthrough chambers maintained a stable CH4 concentration throughout the 11-week incubation. Soils were analyzed at weekly intervals by gas chromatography (GC), GC-mass spectrometry, and GC-combustion-isotope ratio mass spectrometry to identify and quantify individual PLFAs and trace the incorporation of 13C label into the microbial biomass. Incorporation of the 13C label was seen throughout the experiment, with the rate of incorporation decreasing after 9 weeks. The delta13C values of individual PLFAs showed that 13C label was incorporated into different components to various extents and at various rates, reflecting the diversity of PLFA sources. Quantitative assessments of 13C-labeled PLFAs showed that the methanotrophic population was of constant structure throughout the experiment. The dominant 13C-labeled PLFA was 18:1omega7c, with 16:1omega5 present at lower abundance, suggesting the presence of novel type II methanotrophs. The biomass of methane-oxidizing bacteria at optimum labeling was estimated to be about 7.2 x 10(6) cells g(-1) of soil (dry weight). While recycling of 13C label from the methanotrophic biomass must occur, it is a slower process than initial 13CH4 incorporation, with only about 5 to 10% of 13C-labeled PLFAs reflecting this process. Thus, 13C-labeled PLFA distributions determined at any time point during 13CH4 incubation can be used for chemotaxonomic assessments, although extended incubations are required to achieve optimum 13C labeling for methanotrophic biomass determinations.     

Microbial 13C utilization patterns via stable isotope probing of phospholipid biomarkers in Mojave Desert soils exposed to ambient and elevated atmospheric CO2

Changes in plant inputs under changing atmospheric CO₂ can be expected to alter the size and/or functional characteristics of soil microbial communities which can determine whether soils are a C sink or source. Stable isotope probing was used to trace autotrophically fixed ¹³C into phospholipid fatty acid (PLFA) biomarkers in Mojave Desert soils planted with the desert shrub, Larrea tridentata. Seedlings were pulse‐labeled with ¹³CO₂ under ambient and elevated CO₂ in controlled environmental growth chambers. The label was chased into the soil by extracting soil PLFAs after labeling at Days 0, 2, 10, 24, and 49. Eighteen of 29 PLFAs identified showed ¹³C enrichment relative to nonlabeled control soils. Patterns of PLFA enrichment varied temporally and were similar for various PLFAs found within a microbial functional group. Enrichment of PLFA ¹³C generally occurred within the first 2 days in general and fungal biomarkers, followed by increasingly greater enrichment in bacterial biomarkers as the study progressed (Gram‐negative, Gram‐positive, actinobacteria). While treatment CO₂ level did not affect total PLFA‐C concentrations, microbial functional group abundances and distribution responded to treatment CO₂ level and these shifts persisted throughout the study. Specifically, ratios of bacterial‐to‐total PLFA‐C decreased and fungal‐to‐bacterial PLFA‐C increased under elevated CO₂ compared with ambient conditions. Differences in the timing of ¹³C incorporation into lipid biomarkers coupled with changes in microbial functional groups indicate that microbial community characteristics in Mojave Desert soils have shifted in response to long‐term exposure to increased atmospheric CO₂.     

Flooding forested groundwater recharge areas modifies microbial communities from top soil to groundwater table

Subsurface microorganisms are crucial for contaminant degradation and maintenance of groundwater quality. This study investigates the microbial biomass and community composition [by phospholipid fatty acids (PLFAs)], as well as physical and chemical soil characteristics at woodland flooding sites of an artificial groundwater recharge system used for drinking water production. Vertical soil profiles to c . 4 m at two watered and one nonwatered site were analyzed. The microbial biomass was equal in watered and nonwatered sites, and considerable fractions (25–42%) were located in 40–340 cm depth. The microbial community structure differed significantly between watered and nonwatered sites, predominantly below 100 cm depth. Proportions of the bacterial PLFAs 16:1ω5, 16:1ω7, cy17:0 and 18:1ω9t, and the long-chained PLFAs 22:1ω9 and 24:1ω9 were more prominent at the watered sites, whereas branched, saturated PLFAs (iso/anteiso) dominated at the nonwatered site. PLFA community indices indicated stress response ( trans / cis ratio), higher nutrient availability (unsaturation index) and changes in membrane fluidity (iso/anteiso ratio) due to flooding. In conclusion, water recharge processes led to nutrient input and altered environmental conditions, which resulted in a highly active and adapted microbial community residing in the vadose zone that effectively degraded organic compounds.     

Critical Assessment of Glyco- and Phospholipid Separation by Using Silica Chromatography

Phospholipid-derived fatty acids (PLFAs) are commonly used to characterize microbial communities in situ and the phylogenetic positions of newly isolated microorganisms. PLFAs are obtained through separation of phospholipids from glycolipids and neutral lipids using silica column chromatography. We evaluated the performance of this separation method for the first time using direct detection of intact polar lipids (IPLs) with high-performance liquid chromatography–mass spectrometry (HPLC-MS). We show that under either standard or modified conditions, the phospholipid fraction contains not only phospholipids but also other lipid classes such as glycolipids, betaine lipids, and sulfoquinovosyldiacylglycerols. Thus, commonly reported PLFA compositions likely are not derived purely from phospholipids and perhaps may not be representative of fatty acids present in living microbes.     

毛竹高速生长期土壤碳氮动态及其微生物特性

研究了典型毛竹林毛竹高速生长期间土壤碳氮动态及其微生物生态特性。结果表明:毛竹高速生长期间,3个试验地土壤全氮、碱解氮、铵态氮、硝态氮及总有机碳和水溶性有机碳(DOC)的含量均有不同幅度的下降,其中25℃蒸馏水提取DOC(25℃DOC)降幅分别达到51%、22%和223%,且25℃DOC下降幅度明显大于80℃DOC的下降幅度。随毛竹生长,土壤全氮和有机碳含量变化较为明显,相关分析表明两者呈极显著的正相关(R2=0.89**)。同时,土壤微生物量碳含量大幅度降低,由原来的800 mg/kg降到了525 mg/kg。采用PLFA法对土壤微生物群落结构进行了分析,代表细菌的饱和脂肪酸(14:0,16:0,18:0,20:0,i15:0,i16:0,i17:0,i18:0,a15:0,a17:0)基本上都分布在载荷图的右侧;代表真菌的不饱和脂肪酸(18:2w6,9c/18:0ANTE)分布在主成分载荷图的左侧,表明随着毛竹生长,土壤中细菌含量减少,真菌含量增加。说明毛竹的高速生长消耗了土壤中的碳氮,同时对土壤微生物群落结构产生了明显的影响。     

枯落物处理对格木林土壤碳氮转化和微生物群落结构的短期影响

以我国南亚热带格木人工纯林为研究对象,采用气压过程分离(BaPS)技术和磷脂脂肪酸(PLFAs)法研究了不同枯落物处理(对照、枯落物去除、枯落物加倍)下土壤碳氮转化速率和微生物群落结构的季节变化.结果表明:不同枯落物处理土壤呼吸和总硝化速率均呈现明显的季节动态,雨季显著高于旱季.枯落物处理初期,土壤呼吸和总硝化速率均随枯落物输入量的增加呈下降趋势,但随着枯落物处理时间的延长,二者随枯落物输入量的增加而增加.旱季不同枯落物处理土壤微生物PLFAs总量和各菌群PLFAs量均显著高于雨季,而雨季真菌PLFAs/细菌PLFAs明显高于旱季.在旱季,枯落物去除处理土壤微生物PLFAs总量、细菌PLFAs量、真菌PLFAs量和丛枝菌根真菌PLFAs量分别显著提高30.9%、28.8%、44.4%和31.6%.在雨季,枯落物去除处理细菌PLFAs量和丛枝菌根真菌PLFAs量分别显著降低10.6%和33.3%.土壤微生物群落结构受枯落物输入量处理和季节的双重影响,土壤微生物群落结构主要受土壤温度和铵态氮的影响.枯落物输入量处理在短期内显著影响了格木林土壤碳氮转化速率和微生物群落结构,这种影响因季节的不同而存在差异.     

春季冻融期兴安落叶松林土壤微生物的时间动态及其影响因子

春季冻融期土壤微生物动态会影响生长季的碳和养分循环.在春季冻融期,每隔3~7d取样一次,采用磷脂脂肪酸法(PLFA)研究了兴安落叶松林4种土壤基质的微生物群落时间动态.结果表明:1)土壤微生物PLFAs总量、各类群的PLFAs量和相对丰度、革兰氏阳性细菌/革兰氏阴性细菌(G^+/G^-)、饱和脂肪酸/不饱和脂肪酸(S/NS)和细菌/总真菌(真菌+丛枝菌根真菌)(B/F)均存在显著的取样时间差异;2)在冻融前期土壤总有机碳(TOC)和土壤全氮(TN)是影响土壤微生物的主要因子,在冻融中期土壤湿度和土壤TOC、TN含量是主要影响因子,在冻融后期土壤微生物受到土壤温湿度、土壤TOC、TN含量及土壤碳氮比(C/N)的共同影响;3)土壤微生物PLFAs总量、各类群的PLFAs量和相对丰度(细菌丰度除外)、B/F、G^+/G^-、S/NS在土壤基质间均存在显著差异,土壤TOC、TN和C/N的不同是引起差异的主要环境因素.春季冻融期土壤温湿度和资源有效性是影响土壤微生物群落的主要因子,但影响程度因冻融阶段和微生物类群的不同而存在差异.     

Transpiration and metabolisation of TCE by willow plants – a pot experiment

Willows were grown in glass cylinders filled with compost above water-saturated quartz sand, to trace the fate of TCE in water and plant biomass. The experiment was repeated once with the same plants in two consecutive years. TCE was added in nominal concentrations of 0, 144, 288, and 721 mg l^?1. Unplanted cylinders were set-up and spiked with nominal concentrations of 721 mg l^?1 TCE in the second year. Additionally, ¹³C-enriched TCE solution (δ¹³C = 110.3 ‰) was used. Periodically, TCE content and metabolites were analyzed in water and plant biomass. The presence of TCE-degrading microorganisms was monitored via the measurement of the isotopic ratio of carbon (¹³C/¹²C) in TCE, and the abundance of ¹³C-labeled microbial PLFAs (phospholipid fatty acids). More than 98% of TCE was lost via evapotranspiration from the planted pots within one month after adding TCE. Transpiration accounted to 94 to 78% of the total evapotranspiration loss. Almost 1% of TCE was metabolized in the shoots, whereby trichloroacetic acid (TCAA) and dichloroacetic acid (DCAA) were dominant metabolites; less trichloroethanol (TCOH) and TCE accumulated in plant tissues. Microbial degradation was ruled out by δ¹³C measurements of water and PLFAs. TCE had no detected influence on plant stress status as determined by chlorophyll-fluorescence and gas exchange.     

中亚热带地区米槠天然林土壤微生物群落结构的多样性

为了解土壤微生物群落的结构,采用磷脂脂肪酸方法对武夷山和建瓯的米槠(Castanopsis carlesii)天然林土壤微生物群落的结构多样性进行了研究。结果表明,两地米槠天然林的土壤微生物群落组成十分丰富,多样性指数、丰富度指数和均匀度指数分别为2.92~3.01、25.84~28.23 和0.88~0.90。0~10 cm土层的磷脂脂肪酸总量、细菌特征脂肪酸、真菌特征脂肪酸、放线菌特征脂肪酸、革兰氏阳性菌和阴性菌特征脂肪酸含量均高于10~20 cm土层的,且建瓯万木林自然保护区的高于武夷山国家级自然保护区。10~20 cm土层的革兰氏阳性菌/革兰氏阴性菌高于0~10 cm土层的;细菌特征脂肪酸含量显著高于真菌,表明细菌在土壤微生物群落结构中处于优势地位。主成分分析表明,土壤微生物群落结构的差异主要是由采样地点的不同引起。