崇明岛不同土地利用类型河岸带土壤反硝化酶活性特征

以崇明岛河岸带为研究对象,采用乙炔抑制法,研究了不同土地利用类型河岸带(农田河岸带、林地河岸带、草地河岸带)土壤反硝化酶活性及其影响因素.结果表明：河岸带反硝化酶活性在(0.69±0.11)～(134.93±33.72) μg N·kg^-1·h^-1,不同土地类型河岸带土壤反硝化酶活性存在明显差异,整体趋势为林地河岸带>农田河岸带>草地河岸带.河岸带表层土壤(0～10 cm)反硝化酶活性与其他土层(10～30、30～50和50～70 cm)呈显著差异(P<0.05).反硝化酶活性与土壤有机碳、土壤全氮和土壤硝态氮呈极显著正相关关系(P<0.01).土地利用类型的变化主要通过改变河岸带土壤自然结构和理化性质、降低土壤有机质的积累、影响土壤氮素的转化,从而抑制河岸带土壤反硝化作用的发生.     

模拟咸水入侵对崇明岛河岸带根际土壤微生物及反硝化作用的影响

通过模拟咸水入侵,研究了其对崇明岛河岸带根际土壤微生物及其反硝化过程的影响.结果表明:模拟咸水入侵后4种不同植被型河岸带土壤根际微生物区系发生显著变化,除放线菌菌群数量稍有增加外,细菌、真菌以及硝化和反硝化细菌数量均出现不同程度下降,特别是反硝化功能细菌数量较对照平均下降51.8％,说明河岸带土壤不同微生物区系对咸水入侵的响应存在显著差异.模拟咸水入侵后,河岸带土壤与氮转换相关的酶活性普遍受到抑制,且抑制作用随酶类型不同而存在差异,亚硝酸还原酶对咸水入侵最敏感,其活性较对照平均下降了43.5％,脲酶活性次之,其降幅为37.4％,而脱氢酶受咸水影响较小,其活性平均下降29.5％.模拟咸水入侵明显削弱了河岸带土壤反硝化作用,其速率平均下降34.9％.不同植被型河岸带土壤微生物对咸水入侵的生态生理响应存在显著差异,与对照相比,茭白根际土壤微生物数量和酶活性受咸水入侵的平均抑制率最大,土壤反硝化速率最小,其次是菖蒲和芦苇.在模拟咸水入侵下,菖蒲与芦苇混合群落根际土壤微生物数量、酶活性和反硝化速率抑制率明显低于单一植物模式,表明混合植被群落根际土壤微生物过程及反硝化作用对咸水入侵具有较好的缓冲性能.     

施肥对设施菜地nirK型反硝化细菌群落结构和丰度的影响

采用末端限制性片段多态性分析(T-RFLP)和实时荧光定量PCR(real-time PCR)方法,研究了甘肃武威设施菜地不同施肥条件下0~20 cm、20~40 cm土层中土壤nirK型反硝化细菌群落结构和丰度的变化.结果表明:施肥对土壤中nirK型反硝化细菌的群落结构具有明显影响,且对70、156、190 bp片段所代表设施菜地土壤优势种群影响最显著.施肥对0~20cm土层nirK型反硝化细菌丰度有明显影响,其最大值出现在全有机肥(M)处理、为每克干土2.16×107个拷贝数,分别是对照(CK)和全化肥(NPK)处理的2.04和2.02倍.设施菜地土壤0~20 cm与20~40 cm土层nirK型反硝化细菌的优势种群及其基因丰度均存在显著差异,且设施菜地土壤中nirK型反硝化细菌的群落结构和丰度与大田差异明显.土壤pH值、有机质及硝酸盐含量均影响nirK型反硝化细菌的群落结构和丰度.系统发育分析结果表明,土壤中除存在与厌氧反硝化细菌亲缘相近的nirK型反硝化微生物外,还存在与好氧反硝化菌亲缘关系相近的nirK型反硝化微生物,如根瘤菌属、苍白杆菌属、土壤杆菌属等.     

大气CO2浓度增高对麦田土壤硝化和反硝化细菌的影响

硝化和反硝化细菌是土壤中与氮转化有关的微生物菌群 ,大气CO2 浓度升高可能对它们的数量产生影响。位于中国无锡的稻 麦轮作农田生态系统FACE平台 2 0 0 1年 6月开始运行。本试验在 2 0 0 3年小麦生长季研究了土壤 (0～ 5cm和 5～ 10cm土层 )中硝化和反硝化细菌在大气CO2 浓度升高条件下的变化。试验采用最大可能法 (MPN)计这两种微生物菌群的数量。结果表明 ,0～ 5cm土层硝化菌数拔节期和成熟期FACE低于对照 ,而孕穗期FACE高于对照 ,5～ 10cm土层硝化菌数越冬期与成熟期FACE低于对照 ,大气CO2 浓度升高使得麦田土壤硝化细菌数目减少。 0～ 5cm土层各个生长期反硝化菌数FACE与对照均没有明显差异 ,5～ 10cm土层反硝化菌数拔节期FACE低于对照 ,大气CO2 浓度升高对麦田土壤反硝化菌的影响不大。     

施肥对设施菜地nirK型反硝化细菌群落结构和丰度的影响

采用末端限制性片段多态性分析(T-RFLP)和实时荧光定量PCR(real-time PCR)方法,研究了甘肃武威设施菜地不同施肥条件下0～20 cm、20～40 cm土层中土壤nirK型反硝化细菌群落结构和丰度的变化.结果表明： 施肥对土壤中nirK型反硝化细菌的群落结构具有明显影响,且对70、156、190 bp片段所代表设施菜地土壤优势种群影响最显著.施肥对0～20 cm土层nirK型反硝化细菌丰度有明显影响,其最大值出现在全有机肥(M)处理、为每克干土2.16×10⁷个拷贝数,分别是对照(CK)和全化肥(NPK)处理的2.04和2.02倍.设施菜地土壤0～20 cm与20～40 cm土层nirK型反硝化细菌的优势种群及其基因丰度均存在显著差异,且设施菜地土壤中nirK型反硝化细菌的群落结构和丰度与大田差异明显.土壤pH值、有机质及硝酸盐含量均影响nirK型反硝化细菌的群落结构和丰度.系统发育分析结果表明,土壤中除存在与厌氧反硝化细菌亲缘相近的nirK型反硝化微生物外,还存在与好氧反硝化菌亲缘关系相近的nirK型反硝化微生物,如根瘤菌属、苍白杆菌属、土壤杆菌属等.
     

长期施肥制度对稻田土壤反硝化细菌群落活性和结构的影响

以中国科学院桃源农业生态试验站长期定位施肥试验为平台,研究了3种长期施肥制度(对照不施肥-CK,化学施肥-NPK,化学施肥+有机肥-NPKOM)下土壤反硝化速率的差异.同时,以硝酸还原酶基因(narG)作为反硝化细菌的功能标志物,分析了施肥对反硝化细菌群落结构和多样性的影响.结果表明,长期施用有机肥的土壤反硝化速率,反硝化菌多样性都高于对照和施用化肥处理.从3个处理的土壤样品中共获得35个narG基因的可操作分类单元(OTU)主要分布在两个簇,与变形菌门(Proteobacteria)和放线菌门(Actinobacteria)的反硝化细菌有一定的亲缘关系,均为首次从土壤中克隆.Shannon多样性指数显示,NPKOM处理的narG基因多样性最高,CK处理次之,NPK处理最低.LUBSHUFF软件对narG基因群落组成的分析显示,施有机肥后含narG基因的细菌群落组成与CK之间有显著性差异(P<0.05),而化肥(NPK)没有产生显著影响.实验结果为进一步研究亚热带地区水稻土反硝化作用及反硝化功能菌提供了重要的依据.     

若尔盖高原湿地泥炭沼泽土亚硝酸盐还原酶（nirK）反硝化细菌群落结构分析

若尔盖泥炭湿地是世界少有的低纬度永久冻土湿地,具有高海拔、高紫外辐射、高有机质的特点。该区域N2O的排放量对全球气候变暖有重要影响。对若尔盖高原湿地泥炭沼泽土中的亚硝酸盐还原酶(nir K)反硝化细菌群落结构多样性进行分析,以期揭示该区域N2O释放的微生物调控机制。基于若尔盖高原湿地泥炭沼泽土的理化性质和反硝化活性(PDA),结合限制性酶切片段长度多态性(Restriction fragment length polymorphism,RFLP)技术、克隆文库及分子测序对该生态系统中的nir K反硝化细菌群落结构及多样性进行分析。反硝化活性测定结果显示:阿西地区麦溪地区分区地区,反硝化活性与土壤有机碳、总氮和丰富度呈显著正相关(P0.05)。Shannon-wiener多样性指数以阿西最高、分区最低。3个样品中共测序15条nir K基因代表序列,系统发育表明若尔盖高原湿地优势nir K反硝化菌群为变形门菌群。其中,阿西地区主要为α-变形菌门,麦溪地区主要为β-变形菌门,分区地区无法确定优势种群。冗余分析(Redundancy analysis,RDA)显示:有效钾和有效磷是影响nir K反硝化细菌群落结构的关键环境因子。本论文显示,若尔盖高原湿地存在着明显的反硝化作用,调控这些反硝化作用的nir K反硝化细菌多样性较高,且与土壤有效钾和有效磷密切相关。     

黄土丘陵区不同植被土壤氮素转化微生物生理群特征及差异

采用最大或然计数法(most probable number, MPN)对黄土高原洞子沟流域不同植被恢复阶段土壤氮素微生物生理群(氨化细菌、亚硝化细菌、反硝化细菌)数量分布特征进行了测定,结果表明:1)土壤氨化细菌、亚硝化细菌和反硝化细菌数量随植被恢复而增加,三者最大值分别为最小值的74、4和31倍,其中氨化细菌和反硝化细菌的数量在铁杆蒿群落最低,辽东栎群落最高,亚硝化细菌数量在丁香群落最低,辽东栎群落最高;2)植被恢复对各氮素生理群影响不同,对氨化细菌影响最大,其次分别为反硝化细菌和亚硝化细菌;3)各氮素生理群数量差异较大,氨化细菌>反硝化细菌>亚硝化细菌。研究区氨化细菌占总数的75%-80%,反硝化细菌占20%-25%时,生态系统最为稳定;4)土壤理化性质与各功能菌关系紧密,其中,土壤容重和硝态氮含量与微生物数量相关性最大,全钾、矿化氮和微生物量氮也表现出很大的相关性。     

典型草原区不同生境反硝化菌群的空间特征

【背景】锡林河-河滨湿地-阶地草原是蒙古高原典型草原区代表性的水生-湿生-陆生生境,但不同生境中反硝化菌群的空间分布特征尚不明晰。【目的】阐明典型草原区不同生境反硝化菌群的组成、丰度、空间分布特征及异质性成因。【方法】利用16S rRNA基因测序研究锡林河流域水生、湿生、陆生生境6个样带沉积物/土壤细菌群落组成及相对丰度。基于2014年及以前文献报道的反硝化细菌及16S rRNA基因信息构建参比菌库,筛选生境关联的反硝化菌属。通过典范对应分析等探究反硝化菌群空间异质性成因。【结果】参比菌库包含80种反硝化细菌(65个属),6个样带测序获得的469个细菌属中36个为反硝化细菌属。3种生境共存的反硝化细菌有14个属,其中黄杆菌属(1.65%-14.17%)和噬氢菌属(1.56%-1.69%)是水生和湿生生境共有的优势菌,假单胞菌属(1.85%)是低河漫滩样带的优势菌。空间分布特征显示反硝化菌群沿水生-湿生-陆生生境呈现先升后降的分布趋势,在低河漫滩湿地达到最高值。典范对应分析表明:黄杆菌属、噬氢菌属、气单胞菌属、鞘氨醇单胞菌属等与pH值、水分及沙粒含量呈正相关关系,而芽孢杆菌属、链霉菌属、马杜拉放线菌属等与粘粒、粉粒、有机质、总氮含量等呈正相关关系。【结论】典型草原区反硝化菌群组成及丰度具有明显的生境异质性,低河漫滩湿地是反硝化细菌生长繁殖的最佳生境,由颗粒组成、水分含量和pH等环境因子共同驱动。     

贝壳砂改良土壤中反硝化细菌的分析

【目的】通过对一处经过长期使用贝壳砂进行改良的土壤中的反硝化细菌的多样性和细菌分离分析,研究该土壤中反硝化细菌的组成特征。【方法】采用454焦磷酸测序的方法分析了土壤样品中微生物群落的组成,选用Giltay培养基培养、鉴定从土壤中挑选的分离物的反硝化能力,并对具有反硝化能力的微生物进行了16S rRNA基因鉴定。【结果】该土壤样品中占据优势地位的为Proteobacteria、Acidobacteria、Bacteroidetes、Chloroflexi等门的微生物,属的水平上则有近70%尚未确立分类地位。所分离的细菌中,共得到12株厌氧条件下具有较高硝酸盐去除效率的微生物,分属Pseudomonas、Aeromonas、Serratia和Acinetobacter,均为γ变形菌纲的微生物。【结论】该土壤中具有较高的微生物多样性,包括很多未知类型的微生物和众多类型的反硝化细菌;分离到了11株具有反硝化能力的菌株,可用于该土壤的反硝化过程的进一步研究。     

不同季节艾比湖湿地盐角草根际nirS-型与nirK-型反硝化细菌群落组成分析

旨在了解艾比湖湿地盐生植物盐角草根际与非根际中不同类型反硝化细菌的分布及其随季节变化情况,为温带干旱地区荒漠盐化生态系统的代表-艾比湖湿地在生态植被恢复过程中,由微生物推动的土壤氮素循环过程提供数据支撑。采集了艾比湖湿地夏、秋、春三个季节的盐角草根际和非根际土壤样本,通过高通量测序技术,比较分析了nirS-型和nirK-型两种类型的反硝化细菌的多样性和群落结构特点;利用RDA (redundancy analysis)探究了土壤理化因素对反硝化细菌多样性及群落结构的影响。艾比湖湿地盐角草根际与非根际中,nirS-型和nirK-型反硝化细菌多样性最高的为秋季根际土壤样本;各土壤样本中的反硝化细菌多样性均呈现根际>非根际。盐角草各土壤样本中的nirS-型反硝化细菌在门分类水平上隶属于变形菌门(Proteobacteria),厚壁菌门(Firmicutes)和放线菌门(Actinobacteria),而nirK-型反硝化细菌在门水平上分类仅包括了Proteobacteria和Firmicutes。Proteobacteria在各土壤样本中的占比均较高;其中Gamma-Proteobacteria的盐单胞菌属(Halomonas)和假单胞菌属(Pseudomonas)是各土壤样本所共有的nirS-型反硝化菌的优势菌属,但它们在每个土壤样本中的相对丰度各有差异。Alpha-Proteobacteria的根瘤菌属(Rhizobium)是盐角草各土壤样本中较为广泛存在的nirK-型反硝化细菌。艾比湖湿地盐角草各土壤样本中的反硝化细菌群落结构存在着一定的差异。RDA结果显示含水量、有机质、全氮和铵态氮等对各土壤样本中的nirS-型反硝化细菌的多样性影响较大,含水量、有机质、全氮、碱解氮等是nirK-型反硝化细菌多样性的主要影响因素。土壤电导率、全磷、全钾、全氮和碱解氮协同影响nirS-型反硝化细菌的群落结构,有机质、速效钾、速效磷、pH和硝态氮是nirK-型反硝化细菌群落结构组成的主要影响因素。艾比湖湿地反硝化细菌呈现季节性变化,nirS-型和nirK-型反硝化细菌以不同的主要菌属,共同推进湿地反硝化作用。而对于湿地生态系统的保护,则需要进行长期而广泛的土壤状态评估和土壤反硝化微生物菌群的动态监测。     

牛场肥水灌溉对土壤nirK、nirS型反硝化微生物群落结构的影响

以徐水县梁家营长期定位施肥试验田为研究对象,利用末端限制性片段长度多态性(T-RFLP)分析和克隆文库构建,研究了5种施肥处理(清水灌溉CK、无机肥灌溉CF、牛场肥水不同浓度、不同次数灌溉T4、T5和T11)下土壤中nirK、nirS型反硝化细菌群落多样性及其群落结构的演变。结果表明,不同施肥处理下nirK、nirS型反硝化细菌群落多样性无显著差异,但群落结构却有明显变化:nirK型反硝化细菌群落结构既受施肥种类又受施肥量影响,优势种群尤其对施肥种类和施肥量响应显著;nirS型反硝化细菌则主要受施肥种类影响,施肥量影响微弱。牛场肥水处理和无机肥处理分别促进和抑制不同的nirS型反硝化细菌,群落主成分受无机肥促进、牛场肥水抑制。系统发育分析结果表明,土壤中nirK型反硝化细菌主要与假单胞菌属(Pseudomonas)、产碱杆菌属(Alcaligenes)和根瘤菌属(Rhizobium)的反硝化细菌具有较近的亲缘关系;nirS型反硝化细菌主要与劳尔氏菌(Ralstonia)和红长命菌属(Rubrivivax)有较近的亲缘关系。试验土壤中反硝化微生物多与目前已报道的好氧反硝化细菌亲缘关系较近,这可能与微生物分析取自表层土有关。     

Effect of Sulfadiazine on Abundance and Diversity of Denitrifying Bacteria by Determining nirK and nirS Genes in Two Arable Soils

Sulfadiazine (SDZ) is an antibiotic frequently used in agricultural husbandry. Via manuring of excrements of medicated animals, the drug reaches the soil and might impair important biochemical transformation processes performed by microbes, e.g., the nitrogen turnover. We studied the effect of pig manure and SDZ-spiked pig manure on denitrifying bacteria by quantifying nirK and nirS nitrite reductase genes in two arable soils. Addition of manure entailed mainly an increase of nirK-harboring denitrifiers in both soils, whereas in the SDZ-amended treatments, primarily the nirS denitrifiers increased in abundance after the bioavailable SDZ had declined. However, the community composition of nirS nitrite reducers investigated by denaturing gradient gel electrophoresis did not change despite the observed alterations in abundance.     

Community composition and functioning of denitrifying bacteria from adjacent meadow and forest soils

We investigated communities of denitrifying bacteria from adjacent meadow and forest soils. Our objectives were to explore spatial gradients in denitrifier communities from meadow to forest, examine whether community composition was related to ecological properties (such as vegetation type and process rates), and determine phylogenetic relationships among denitrifiers. nosZ, a key gene in the denitrification pathway for nitrous oxide reductase, served as a marker for denitrifying bacteria. Denitrifying enzyme activity (DEA) was measured as a proxy for function. Other variables, such as nitrification potential and soil C/N ratio, were also measured. Soil samples were taken along transects that spanned meadow-forest boundaries at two sites in the H. J. Andrews Experimental Forest in the Western Cascade Mountains of Oregon. Results indicated strong functional and structural community differences between the meadow and forest soils. Levels of DEA were an order of magnitude higher in the meadow soils. Denitrifying community composition was related to process rates and vegetation type as determined on the basis of multivariate analyses of nosZ terminal restriction fragment length polymorphism profiles. Denitrifier communities formed distinct groups according to vegetation type and site. Screening 225 nosZ clones yielded 47 unique denitrifying genotypes; the most dominant genotype occurred 31 times, and half the genotypes occurred once. Several dominant and less-dominant denitrifying genotypes were more characteristic of either meadow or forest soils. The majority of nosZ fragments sequenced from meadow or forest soils were most similar to nosZ from the Rhizobiaceae group in alpha-Proteobacteria species. Denitrifying community composition, as well as environmental factors, may contribute to the variability of denitrification rates in these systems.     

NirK and nirS Nitrite reductase genes from non-agricultural forest soil bacteria in Thailand

The genetic heterogeneity of the nitrite reductase gene (nirK and nirS) fragments from denitrifying prokaryotes in a non-agricultural forest soil in Thailand was investigated using soil samples from the Plant Germplasm-Royal Initiation Project area in Kanchanaburi Province, Thailand. Soil bacteria were screened for denitrification activity and 13 (from 211) positive isolates were obtained and further evaluated for their ability to reduce nitrate and to accumulate or reduce nitrite. Three species with potentially previously unreported denitrifying activities were recorded. Analysis of the partial nirK and nirS sequences of these 13 strains revealed a diverse sequence heterogeneity in these two genes within the same environment and even potentially within the same host species, the potential existence of lateral gene transfer and the first record of both nirK and nirS homologues in one bacterial species. Finally, isolates of two species of bacteria (Corynebacterium propinquum and Micrococcus lylae) are recorded as denitrifiers for the first time.     

Impact of Long-Term Fertilization on the Composition of Denitrifier Communities Based on Nitrite Reductase Analyses in a Paddy Soil

The effect of long-term fertilization on soil-denitrifying communities was determined by measuring the abundance and diversity of the nitrite reductase genes nirK and nirS. Soil samples were collected from plots of a long-term fertilization experiment started in 1990, located in Taoyuan (110°72″ E, 28°52″ N), China. The treatments were no fertilizer (NF), urea (UR), balanced mineral fertilizers (BM), and BM combined with rice straw (BMR). The abundance, diversity, and composition of the soil-denitrifying bacteria were determined by using real-time quantitative PCR, terminal restriction fragment length polymorphism (T-RFLP), and cloning and sequencing of nirK and nirS genes. There was a pronounced difference in the community composition and diversity of nirK-containing denitrifiers responding to the long-term fertilization regimes; however, less variation was observed in communities of nirS-containing denitrifiers, indicating that denitrifiers possessing nirK were more sensitive to the fertilization practices than those with nirS. In contrast, fertilization regimes had similar effects on the copy numbers of nirK and nirS genes. The BMR treatment had the highest copy numbers of nirK and nirS, followed by the two mineral fertilization regimes (UR and BM), and the lowest was in the NF treatment. Of the measured soil parameters, the differences in the community composition of nirK and the abundance of nir denitrifiers were highly correlated with the soil carbon content. Therefore, long-term fertilization resulted in a strong impact on the community structure of nirK populations only, and total organic carbon was the dominant factor in relation to the variations of nir community sizes.     

Community Composition and Functioning of Denitrifying Bacteria from Adjacent Meadow and Forest Soils

We investigated communities of denitrifying bacteria from adjacent meadow and forest soils. Our objectives were to explore spatial gradients in denitrifier communities from meadow to forest, examine whether community composition was related to ecological properties (such as vegetation type and process rates), and determine phylogenetic relationships among denitrifiers. nosZ, a key gene in the denitrification pathway for nitrous oxide reductase, served as a marker for denitrifying bacteria. Denitrifying enzyme activity (DEA) was measured as a proxy for function. Other variables, such as nitrification potential and soil C/N ratio, were also measured. Soil samples were taken along transects that spanned meadow-forest boundaries at two sites in the H. J. Andrews Experimental Forest in the Western Cascade Mountains of Oregon. Results indicated strong functional and structural community differences between the meadow and forest soils. Levels of DEA were an order of magnitude higher in the meadow soils. Denitrifying community composition was related to process rates and vegetation type as determined on the basis of multivariate analyses of nosZ terminal restriction fragment length polymorphism profiles. Denitrifier communities formed distinct groups according to vegetation type and site. Screening 225 nosZ clones yielded 47 unique denitrifying genotypes; the most dominant genotype occurred 31 times, and half the genotypes occurred once. Several dominant and less-dominant denitrifying genotypes were more characteristic of either meadow or forest soils. The majority of nosZ fragments sequenced from meadow or forest soils were most similar to nosZ from the Rhizobiaceae group in α-Proteobacteria species. Denitrifying community composition, as well as environmental factors, may contribute to the variability of denitrification rates in these systems.     

Metabolic Profiles and Genetic Diversity of Denitrifying Communities in Activated Sludge after Addition of Methanol or Ethanol

External carbon sources can enhance denitrification rates and thus improve nitrogen removal in wastewater treatment plants. The effects of adding methanol and ethanol on the genetic and metabolic diversity of denitrifying communities in activated sludge were compared using a pilot-scale plant with two parallel lines. A full-scale plant receiving the same municipal wastewater, but without external carbon source addition, was the reference. Metabolic profiles obtained from potential denitrification rates with 10 electron donors showed that the denitrifying communities altered their preferences for certain compounds after supplementation with methanol or ethanol and that methanol had the greater impact. Clone libraries of nirK and nirS genes, encoding the two different nitrite reductases in denitrifiers, revealed that methanol also increased the diversity of denitrifiers of the nirS type, which indicates that denitrifiers favored by methanol were on the rise in the community. This suggests that there might be a niche differentiation between nirS and nirK genotypes during activated sludge processes. The composition of nirS genotypes also varied greatly among all samples, whereas the nirK communities were more stable. The latter was confirmed by denaturing gradient gel electrophoresis of nirK communities on all sampling occasions. Our results support earlier hypotheses that the compositions of denitrifier communities change during predenitrification processes when external carbon sources are added, although no severe effect could be observed from an operational point of view.     

罕山土壤微生物群落组成对植被类型的响应

选取分布在中国东北部地区的阔叶林-针叶林-亚高山草甸这一明显的植被垂直带谱来研究植被类型对土壤微生物群落组成的影响。选取5种植被类型-山杨(Populus davidiana)(1250—1300 m),山杨(P.davidiana)与白桦(Betula platyphylla)的混交林(1370—1550 m),白桦(B.platyphylla)(1550—1720 m),落叶松(Larix principis-rupprechtii)(1840—1890 m),亚高山草甸(1900—1951 m),采用磷脂脂肪酸(Phopholipid Fatty Acids,PLFAs)分析方法测定不同植被类型下的土壤微生物群落组成。分别采用主成分分析(Principal Components Analysis,PCA)以及冗余分析(Redundancy Analysis,RDA)来解释单种特征PLFAs的分异以及土壤理化指标与微生物PLFAs指标间的相关性。结果表明不同植被类型下土壤有机碳(SOC)对土壤微生物PLFAs总量,各类群(真菌(f)、细菌(b)、革兰氏阳性菌(G+)、革兰氏阴性菌(G-))生物量以及群落结构影响显著;土壤微生物PLFAs总量及各类群的生物量随土层加深总体上表现降低趋势,G+/G-和f/b分别随土层加深总体上表现升高趋势。不同植被类型下,阔叶混交林土壤PLFAs总量及各类群生物量总体上最高;针叶林比阔叶林下的f/b和G+/G-高;亚高山草甸下低的p H值对有机碳的可利用性有一定的抑制作用,导致f/b和G+/G-的值相对较高。总之,不同植被类型下SOC对土壤微生物群落组成的影响最为显著,而较低的p H对有机碳的可利用性有一定的抑制作用;真菌对植被类型的变化比细菌更敏感,而细菌更易受可利用性养分和p H变异的影响,这对预测不同林型下的土壤微生物群落组成有重要的启示作用。     

Diversity of Nitrite Reductase (nirK and nirS) Gene Fragments in Forested Upland and Wetland Soils

The genetic heterogeneity of nitrite reductase gene (nirK and nirS) fragments from denitrifying prokaryotes in forested upland and marsh soil was investigated using molecular methods. nirK gene fragments could be amplified from both soils, whereas nirS gene fragments could be amplified only from the marsh soil. PCR products were cloned and screened by restriction fragment length polymorphism (RFLP), and representative fragments were sequenced. The diversity of nirK clones was lower than the diversity of nirS clones. Among the 54 distinct nirK RFLP patterns identified in the two soils, only one pattern was found in both soils and in each soil two dominant groups comprised >35% of all clones. No dominance and few redundant patterns were seen among the nirS clones. Phylogenetic analysis of deduced amino acids grouped the nirK sequences into five major clusters, with one cluster encompassing most marsh clones and all upland clones. Only a few of the nirK clone sequences branched with those of known denitrifying bacteria. The nirS clones formed two major clusters with several subclusters, but all nirS clones showed less than 80% identity to nirS sequences from known denitrifying bacteria. Overall, the data indicated that the denitrifying communities in the two soils have many members and that the soils have a high richness of different nir genes, especially of the nirS gene, most of which have not yet been found in cultivated denitrifiers.