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1.
Ammonia-oxidizing bacteria (AOB) and ammonia-oxidizing archaea (AOA) play important roles in nitrification in various environments. They may also be key communities for ammonia oxidation in composting systems, although few studies have discussed their presence. We investigated the relative diversity and abundance of AOB and AOA using cloning procedures, denaturing gradient gel electrophoresis analysis, and real-time PCR during several stages in the process of cattle manure composting. Our results revealed that the AOB community structure changed during the process. At the high-temperature stage (>60°C), a member of the Nitrosomonas europaea/eutropha cluster dominated while the uncultured Nitrosomonas spp. cluster appeared after the temperature decreased. Additionally, our analysis indicated that AOA sequences, which were classified into a soil/sediment cluster, were present after the temperature decreased during the composting process. At these stages, the number of the archaeal amoA gene copies (3.2 or 3.9?×?107 copies per gram freeze-dried compost) was significantly higher than that of bacterial amoA gene copies (2.2–7.2?×?106 copies per gram freeze-dried compost). Our results suggest that both AOB and AOA are actively involved in nitrification of composting systems.  相似文献   

2.
The cold springs underlain by gas hydrates on the Qinghai-Tibet Plateau (QTP) are similar to deep-sea cold seeps with respect to methane biogeochemistry. Previous studies have shown that ammonia oxidizing bacteria (AOB) and archaea (AOA) are actively present and play important roles in the carbon/nitrogen cycles in cold seeps. Studying AOA and AOB communities in the QTP cold springs will be of great importance to our understanding of carbon and nitrogen cycling dynamics related to the underlying gas hydrates on the QTP. Thus, the abundance and diversity of AOB and AOA in sediments of four cold springs underlain by gas hydrates on the QTP were determined by using quantitative polymerase chain reaction and amoA gene (encoding ammonia monooxygenase involved in ammonia oxidation) phylogenetic analysis. The results showed that the AOB and AOA amoA gene abundances were at 103–104 copies per gram of the sediments in the investigated cold springs. The AOB population consisted of Nitrosospira and Nitrosomonas in contrast with the mere presence of Nitrosospira in marine cold seeps. The AOB diversity was higher in cold springs than in cold seeps. The AOA population was mainly composed of Nitrososphaera, in contrast with the dominance of Nitrosopumilus in cold seeps. The terrestrial origin and high level of dissolved oxygen of the cold springs may be the main factors accounting for the observed differences in AOB and AOA populations between the QTP cold springs and marine cold seeps.  相似文献   

3.
The impact of heavy-metal contamination on archaean communities was studied in soils amended with sewage sludge contaminated with heavy metals to varying extents. Fluorescent in situ hybridization showed a decrease in the percentage of Archaea from 1.3% ± 0.3% of 4′,6-diamidino-2-phenylindole-stained cells in untreated soil to below the detection limit in soils amended with heavy metals. A comparison of the archaean communities of the different plots by denaturing gradient gel electrophoresis revealed differences in the structure of the archaean communities in soils with increasing heavy-metal contamination. Analysis of cloned 16S ribosomal DNA showed close similarities to a unique and globally distributed lineage of the kingdom Crenarchaeota that is phylogenetically distinct from currently characterized crenarchaeotal species.  相似文献   

4.
研究不同施肥制度对水稻土氨氧化古菌(AOA)群落结构和垂直分布特征的影响,可以深入认识不同施肥制度下的石灰性紫色水稻土氮素循环特征及微生物驱动机制,为该地区科学施肥、培肥地力提供理论依据。利用化学分析和变性梯度凝胶电泳(DGGE)对不同施肥制度下石灰性紫色水稻土理化性质和AOA群落结构进行了分析。结果显示:相对于无肥处理,施肥会降低石灰性紫色水稻土pH和硝氮含量,而增加土壤有机质、全氮和氨氮含量。伴随土壤深度增加,土壤pH增加,全氮和硝氮含量降低,氨氮含量变化趋势不明显。不同施肥制度在不同土壤深度对石灰性紫色水稻土AOA群落结构产生不同的胁迫效应,不同施肥制度下的AOA群落结构在0—20 cm处差异不明显;土壤深度增加,不同施肥制度下的AOA群落结构表现出明显差异,CK和N肥处理下的AOA群落结构较简单。AOA群落结构多样性指数和丰富度随土壤深度增加而减小。石灰性紫色水稻土AOA与来自不同土壤和水体环境的AOA具有明显相似性。冗余梯度分析(RDA)显示pH(P=0.012)是造成石灰性紫色水稻土AOA群落结构差异的主要原因。研究揭示石灰性紫色水稻土中的AOA群落结构受施肥制度明显影响并表现出明显的垂直分布特征。  相似文献   

5.
The response of soil ammonia-oxidizing bacterial (AOB) and archaeal (AOA) communities to individual environmental variables (e.g., pH, temperature, and carbon- and nitrogen-related soil nutrients) has been extensively studied, but how these environmental conditions collectively shape AOB and AOA distributions in unmanaged agricultural soils across a large latitudinal gradient remains poorly known. In this study, the AOB and AOA community structure and diversity in 26 agricultural soils collected from eastern China were investigated by using quantitative PCR and bar-coded 454 pyrosequencing of the amoA gene that encodes the alpha subunit of ammonia monooxygenase. The sampling locations span over a 17° latitude gradient and cover a range of climatic conditions. The Nitrosospira and Nitrososphaera were the dominant clusters of AOB and AOA, respectively; but the subcluster-level composition of Nitrosospira-related AOB and Nitrososphaera-related AOA varied across the latitudinal gradient. Variance partitioning analysis showed that geography and climatic conditions (e.g., mean annual temperature and precipitation), as well as carbon-/nitrogen-related soil nutrients, contributed more to the AOB and AOA community variations (∼50% in total) than soil pH (∼10% in total). These results are important in furthering our understanding of environmental conditions influencing AOB and AOA community structure across a range of environmental gradients.  相似文献   

6.
Diversity and abundance of ammonia-oxidizing archaea (AOA) and bacteria (AOB) in samples of the northern South China Sea subsurface sediment were assessed by analyzing the amoA gene sequences retrieved from the samples. The microbial diversity was assessed using rarefaction and phylogenetic analyses. The deep-sea subsurface sediments harbored diverse and distinct AOA and AOB communities, but the abundance of AOA was lower than that of AOB, consistent with many other studies about bacteria and archaea in subsurface sediments. Diversity of AOA shown in the OTUs and Shannon index was correlated with the concentration of nitrite in the Pearson analysis, but no obvious relationships between the diversity or abundance of AOB and the physicochemical parameters could be identified in the present study, indicating the concentration of ammonium may not be an important factor to determine the diversity and abundance of ammonia-oxidizing prokaryotes in the subsurface sediments. Additionally, Nitrosomonas-like AOB was found to be dominant in subsurface sediments of the northern South China Sea showing a different adaption strategy comparing with some Nitrosospira-like AOB lineages. Concentration of nitrite was correlated with diversity of AOA, but no correlations between diversity and abundance of AOB and the physicochemical parameters were established in the study. Supplementary materials are available for this article. Go to the publisher's online edition of Geomicrobiology Journal to view the free supplemental files.  相似文献   

7.
The abundance and diversity of archaeal ammonia monooxygenase subunit A (amoA) genes from hydrothermal vent chimneys at the Juan de Fuca Ridge were investigated. The majority of the retrieved archaeal amoA sequences exhibited identities of less than 95% to those in the GenBank database. Novel ammonia-oxidizing archaea may exist in the hydrothermal vent environments.Ammonia-oxidizing archaea (AOA) may play important roles in carbon and nitrogen cycles in various temperate environments (5, 7, 10, 12, 16). The frequent detection (23, 24) and successful enrichment (2, 6) of thermophilic AOA from terrestrial hot springs suggested a wide distribution of thermophilic AOA in geothermal environments. High concentrations of NH4+ (1, 9, 11) and high rates of ammonia oxidation (9, 22) have been observed at the Juan de Fuca Ridge. However, the presence of AOA in this deep-sea hydrothermal system has not been reported. Here, the abundance and diversity of AOA in three hydrothermal vent chimneys in the Endeavor segment of the Juan de Fuca Ridge were investigated by targeting the conserved amoA genes. This is also the first report on AOA from deep-sea hydrothermal vent chimneys.These vent chimneys were sulfide structures obtained in the fall of 2005 using the submersible Alvin on board the research vessel Atlantis (dive numbers 4143, 4136, and 4148). Chimney 4148 was an active black smoker venting at around 310°C in the Main Endeavor field (47°56.876′N, 129°5.915′W; depth, 2,192 m). Chimney 4143-1 was an active black smoker venting at 316°C in the Mothra field (47°55.424′N, 129°6.533′W; depth, 2,267 m). The outer layers (samples 4148-1A and 4143-1A) of these chimneys were used in this study. The sample from chimney 4136-1 was from a diffusive field (Clambed field) (47°57.909′N, 129°5.443′W; depth, 2,200 m), where the in situ temperature was measured as 29.2°C. The chimney samples were stored at −20°C on board, transported to the home laboratory on dry ice, and stored at −80°C until analyses were performed.Chimney samples were frozen in liquid nitrogen and milled upon thawing. This procedure was repeated three times to break down the solid sample into small particles, which were then mixed with DNA extraction buffer for DNA isolation as described before (25). The obtained crude DNA was purified by an E-Z N.A. Cycle-Pure kit (Omega Bio-Tek Inc., Norcross, GA). PCR amplifications for the archaeal 16S rRNA gene, the crenarchaeal marine group I (MGI) 16S rRNA gene, the archaeal amoA gene, and the bacterial amoA gene followed procedures previously described (Table (Table1)1) (3, 5, 10, 14). Quantitative PCR (Q-PCR) was performed using a model 7500 real-time system (Applied Biosystems, United Kingdom) and a 20-μl reaction mixture that consisted of 1 μl (1 to 10 ng) of DNA as the template, a 0.15 μM concentration of each primer, and 10 μl of Power SYBR green PCR master mix (Applied Biosystems, United Kingdom) with ROX and SYBR green I. The inserted PCR fragments of clones 4143-1A-71 (from the amoA gene library) and 4136-1-4 (from the archaeal 16S rRNA gene library) were amplified and purified to generate standard DNAs for amoA or archaeal 16S rRNA gene quantification. A serial dilution of standard DNAs was performed to generate calibration curves for sample quantification. A melting curve analysis was performed after amplification, and the cycle threshold was set automatically using system 7500 software, version 1.3.

TABLE 1.

PCR primers and procedures used in this study
Target genePrimerSequence (5′→3′)PCR cycle conditionsReference
Archaeal amoAArch-amoAFSTAATGGTCTGGCTTAGACG5 min at 95°C; 30 cycles consisting of 45 s at 94°C, 1 min at 53°C, and 1 min at 72°C; 15 min at 72°CFrancis et al., 2005 (5)
Arch-amoARGCGGCCATCCATCTGTATGT
Archaeal 16S rRNA21FTTCCGGTTGATCCYGCCRG5 min at 95°C; 30 cycles consisting of 30 s at 94°C, 1 min at 54°C, and 1 min at 72°C; 10 min at 72°CDeLong, 1992 (3)
958RYCCGGCGTTGAMTCCAATT
Archaeal 16S rRNA (for Q-PCR)344FACGGGGCGCAGCAGGCGCGA10 min at 50°C, 2 min at 95°C; 40 cycles consisting of 15 s at 95°C and 1 min at 60°C; 15 s at 95°C, 1 min at 60°C, and 15 s at 95°C to make the melting curveØvreås et al., 1998 (15)
518RATTACCGCGGCTGCTGG
Archaeal amoA (for Q-PCR)amo196FGGWGTKCCRGGRACWGCMAC10 min at 50°C and 2 min at 95°C; 40 cycles consisting of 15 s at 95°C and 1 min at 60°C; 15 s at 95°C, 1 min at 60°C, and 15 s at 95°C to make the melting curveTreusch et al., 2005 (20)
amo277RCRATGAAGTCRTAHGGRTADCC
Bacterial amoAAmoA-1FGGGGTTTCTACTGGTGGT5 min at 95°C; 30 cycles consisting of 30 s at 94°C, 45 s at 54°C-50°C, and 45 s at 72°C; 10 min at 72°CStephen et al., 1998 (19)
AmoA-2RCCCCTCKGSAAAGCCTTCTTCRotthauwe et al., 1997 (17)
Crenarchaeal marine group I 16S rRNA771FACGGTGAGGGATGAAAGCT5 min at 95°C; 30 cycles consisting of 30 s at 95°C, 30 s at 54°C, and 30 s at 72°COchsenreiter et al., 2003 (14)
957RCGGCGTTGACTCCAATTG
Open in a separate windowTriplicate PCR products were pooled and clone libraries constructed following the manufacturer''s instructions (Takara Inc., Dalian, China). PCR clones from the libraries were randomly selected for sequencing (Sangon Inc., China). Phylogenetic trees were generated using the PHYLIP package (4) and the maximum-likelihood, neighbor-joining, and maximum-parsimony methods. Bootstrap analysis was used to estimate the reliability of phylogenetic tree constructions (200 replicates). Trees were created using the program Treeview (version 1.6.6).Positive and specific PCR bands were obtained for the archaeal amoA genes from all the three samples, while no PCR band was obtained for the bacterial amoA gene (for the primers and procedures used, see Table Table1).1). In addition, sample 4136-1 was found by Q-PCR analysis to contain the highest number of archaeal amoA genes (with 7.36 ± 0.37 × 104 copies per g of chimney), followed by samples 4143-1A (with 1.88 ± 0.08 × 104 copies per g of chimney) and 4148-1A (with 1.37 ± 0.07 × 102 copies per g of chimney).Clone libraries of archaeal amoA from the three samples were constructed. A total of 93 clones (33 from sample 4136-1, 30 from sample 4143-1A, and 30 from sample 4148-1A) were sequenced and divided into 33 operational taxonomic units (OTUs) based on 99% nucleotide identity. The majority (81.7%) of the retrieved archaeal amoA OTU sequences exhibited relatively low identity (≤94.56%) to other archaeal amoA sequences deposited in GenBank. The phylogenetic relationships among the retrieved amoA and some published amoA sequences are shown in Fig. Fig.1.1. The chimney archaeal amoA sequences fell into five clusters (chimney group I, chimney group II, sediment A-1, and water column A and B clusters), except the sequence of clone 4143-1A-10, which did not fall into any cluster and exhibited the highest identity (90%) to the sequence of clone HB_B_0805A06, which was derived from coastal sediment (18). Chimney group I contained 52 sequences (30 from sample 4148-1A, 11 from sample 4143-1A, and 11 from sample 4136-1); chimney group II contained 23 sequences (20 from sample 4136-1 and 3 from sample 4143-1A). Fourteen sequences from sample 4143-1A grouped into water column A and B clusters (5); and one sequence from sample 4143-1A grouped into the sediment A-1 cluster (13). The sequences from chimney group I exhibited the highest identity (94%) to clone CR-G3N006, derived from a cold seep of the Japan Sea (13). Sequences in chimney group II exhibited the highest identity to clone OA-MA-122 from a water column of a coastal aquarium biofilter, with 84% nucleotide identity (21). The sequences of chimney group II did not cluster with any other sequences. Although showing low bootstrap values (<50%), the chimney group II sequences always clustered into a separate group (Fig. (Fig.1)1) according to different calculation methods, including the maximum-likelihood, neighbor-joining, and maximum-parsimony methods.Open in a separate windowFIG. 1.Phylogenetic tree showing the affiliations of archaeal amoA gene sequences from chimneys (in bold), sediments, soil, water, and the isolated AOA. Bootstrap values were calculated from 200 replications with 585 characters. Maximum-likelihood (left), distance (middle), and parsimony (right) bootstrap values providing ≥50% support are indicated. The bar represents 100 expected substitutions for the archaeal amoA region analyzed. Bacterial amoA sequences were set as the outgroup.Sample 4136-1 contained the highest number of archaeal amoA gene copies. Q-PCR using primers 344F and 518R (15) showed that sample 4136-1 contained 1.10 ± 0.05 × 106 copies of archaeal 16S rRNA genes per g of chimney. Assuming that each crenarchaeal cell possessed only one copy of the amoA gene (8), the AOA constituted at least 6.1% of the archaeal community in sample 4136-1. To explore the potential sources of these amoA sequences in sample 4136-1, an archaeal 16S rRNA clone library was constructed and a total of 82 clones were sequenced. These sequences divided into 20 OTUs based on 98% nucleotide identity. Fifteen OTUs (accounting 76.8% of the total sequences) belonged to hyperthermophilic Desulfurococcales species, and two OTUs (accounting for 15.9% of the total number of sequences) belonged to hyperthermophilic Thermoproteales species of the Crenarchaeota phylum, whereas three OTUs (accounting 7.32% of the total number of sequences) belonged to Thermococcales species of the Euryarchaeota kingdom (Fig. (Fig.2).2). Members of the crenarchaeal MGI, which was thought to be the source of nonthermophilic AOA (6, 8), were not detected in this library. Therefore, PCR using MGI-specific primers was performed to further detect MGI species (for PCR primers and conditions, see Table Table11 and reference 14). MGI species were easily detected in sample 4143-1A, but not in samples 4136-1 and 4148-1A, by direct PCR amplification. A nested PCR method employing generic archaeal 16S rRNA gene primers was then performed for the first round of PCR followed by MGI-selective PCR primers for the second round of PCR. This procedure created a PCR band of the correct size for MGI species from sample 4136-1; that band was later shown by cloning and sequencing to represent an MGI 16S rRNA gene fragment (see Fig. S1 in the supplemental material). The data implied that some of the amoA genes detected in the chimney samples may have come from MGI species; however, to determine the origin of the amoA genes, especially those in the chimney groups I and II, isolation or enrichment of the organisms would be necessary.Open in a separate windowFIG. 2.Phylogenetic tree showing the affiliations of 16S rRNA gene sequences retrieved from hydrothermal vent chimney 4136-1 (in boldface) with selected reference sequences of the Archaea domain. Bootstrap values were calculated from 200 replications with 790 characters. Maximum-likelihood (left), distance (middle), and parsimony (right) bootstrap values providing ≥50% support are indicated. The bar represents 100 expected substitutions for the archaeal 16S rRNA gene analyzed. Bacterial 16S rRNA sequences were set as the outgroup. HWCGIII, hot water crenarchaeotic group III.  相似文献   

8.
Autotrophic ammonia-oxidizing communities, which are responsible for the rate-limiting step of nitrification in most soils, have not been studied extensively in semiarid ecosystems. Abundances of soil archaeal and bacterial amoA were measured with real-time polymerase chain reaction along an elevation gradient in northern Arizona. Archaeal amoA was the predominant form of amoA at all sites; however, ratios of archaeal to bacterial amoA ranged from 17 to more than 1,600. Although size of ammonia-oxidizing bacteria populations was correlated with precipitation, temperature, percent sand, and soil C/N, there were no significant relationships between ammonia-oxidizing archaea populations and any of the environmental parameters evaluated in this study. Our results suggest that in these soils, archaea may be the primary ammonia oxidizers, and that ammonia-oxidizing archaea and ammonia-oxidizing bacteria occupy different niches.  相似文献   

9.
Denitrification is an important microbial process in soils and leads to the emission of nitrous oxide (N2O). However, studies about the microbial community involved in denitrification processes in polluted paddy fields are scarce. Here, we studied two rice paddies which had been polluted for more than three decades by metal mining and smelter activities. Abundance and community composition were determined using real-time polymerase chain reaction (PCR) assay and denaturing gradient gel electrophoresis of nitrite reductase and nitrous oxide reductase gene amplicons (nirK and nosZ), while denitrifying activities were assessed by measuring potential denitrifier enzyme activity. We found that the community structure of both nirK and nosZ containing denitrifiers shifted under pollution in the two rice paddies. All the retrieved nirK sequences did not group into either α- or β-proteobacteria, while most of the nosZ species were affiliated with α-proteobacteria. While the abundance of both nirK and nosZ was significantly reduced in the polluted soils at “Dexing” (with relatively higher Cu levels), these parameters did not change significantly at “Dabaoshan” (polluted with Cd, Pb, Cu, and Zn). Furthermore, total denitrifying activity and N2O production and reduction rates also only decreased under pollution at “Dexing.” These findings suggest that nirK and nosZ containing denitrifier populations and their activities could be sensitive to considerable Cu pollution, which could potentially affect N2O release from polluted paddy soils.  相似文献   

10.
The phylogenetic diversity and species richness of ammonia-oxidizing archaea (AOA) and bacteria (AOB) were examined with aquarium biofiltration systems. Species richness, deduced from rarefaction analysis, and diversity indices indicated that the phylogenetic diversity and species richness of AOA are greater than those of AOB; the diversity of AOA and of AOB is minimized in cold-water aquaria. This finding implies that temperature is a key factor influencing the population structure and diversity of AOA and AOB in aquarium biofiltration systems.  相似文献   

11.
12.
Nitrifying biofilters are used in aquaria and aquaculture systems to prevent accumulation of ammonia by promoting rapid conversion to nitrate via nitrite. Ammonia-oxidizing archaea (AOA), as opposed to ammonia-oxidizing bacteria (AOB), were recently identified as the dominant ammonia oxidizers in most freshwater aquaria. This study investigated biofilms from fixed-bed aquarium biofilters to assess the temporal and spatial dynamics of AOA and AOB abundance and diversity. Over a period of four months, ammonia-oxidizing microorganisms from six freshwater and one marine aquarium were investigated at 4–5 time points. Nitrogen balances for three freshwater aquaria showed that active nitrification by aquarium biofilters accounted for ≥81–86% of total nitrogen conversion in the aquaria. Quantitative PCR (qPCR) for bacterial and thaumarchaeal ammonia monooxygenase (amoA) genes demonstrated that AOA were numerically dominant over AOB in all six freshwater aquaria tested, and contributed all detectable amoA genes in three aquarium biofilters. In the marine aquarium, however, AOB outnumbered AOA by three to five orders of magnitude based on amoA gene abundances. A comparison of AOA abundance in three carrier materials (fine sponge, rough sponge and sintered glass or ceramic rings) of two three-media freshwater biofilters revealed preferential growth of AOA on fine sponge. Denaturing gel gradient electrophoresis (DGGE) of thaumarchaeal 16S rRNA genes indicated that community composition within a given biofilter was stable across media types. In addition, DGGE of all aquarium biofilters revealed low AOA diversity, with few bands, which were stable over time. Nonmetric multidimensional scaling (NMDS) based on denaturing gradient gel electrophoresis (DGGE) fingerprints of thaumarchaeal 16S rRNA genes placed freshwater and marine aquaria communities in separate clusters. These results indicate that AOA are the dominant ammonia-oxidizing microorganisms in freshwater aquarium biofilters, and that AOA community composition within a given aquarium is stable over time and across biofilter support material types.  相似文献   

13.
Ant communities were surveyed along an elevational gradient in the Philippines extending from lowland dipterocarp forest (250 m elevation) to mossy forest (1750 m). Standardized pitfall trapping in arboreal and terrestrial microhabitats at seven sites yielded 51 species. Collecting by hand at five of the sites yielded 48 species. The two methods produced substantially different assemblages, with only 22 species (29%) taken in common. Only a fraction of the total ant community appeared to be sampled at most of the sites. Measures of species richness and relative abundance peaked at mid-elevations and declined sharply with increasing elevation. Ants were extremely rare above 1500 m elevation. Arboreal ants were trapped much less frequently than terrestrial ants at all sites. Ant species that were abundant had broader elevational distributions than those that were less common, but most species were rare and occurred at only one or two sites. The elevational patterns for ants are largely the inverse of those documented for Philippine small mammals which reach their greatest diversity and abundance at high elevations where ants are rare. This suggests that the two groups may interact competitively. Some of the patterns observed or inferred from this study may apply to tropical ant communities in general, and are presented as series of testable hypotheses as a guide and stimulus for future research.  相似文献   

14.
陆彦春 《生态学杂志》1989,8(3):63-66,F004
稻田土壤主要分布于淮河以南地区。随着农田水利条件的改善,土壤生态环境发生变化,其耕作制度也随之不断改革。如在北部的徐淮地区大面积的旱改水,稻田面积增加,粮食产量大幅度上升。据调查统计,全省稻田土壤约占总耕地面积的60%左右,而生产的粮食约占粮食总产量的75%左右。稻田土壤因水分特点与土体构型的不同,可分为爽水、滞水、囊水、漏水与测渗五个类型。爽水水稻土主要分布于太湖平原与里下河  相似文献   

15.
Bacteria and nutrients were determined in upper soil samples collected underneath and between canopies of the dominant perennial in each of three sites along a steep precipitation gradient ranging from the Negev desert in the south of Israel to a Mediterranean forest in the north. Bacterial abundance, monitored by phospholipid fatty acid analysis, was significantly higher under the shrub canopy (compared to barren soils) in the arid and semi-arid sites but not in the Mediterranean soils. Bacterial community composition, determined using terminal restriction fragment length polymorphism and clone libraries, differed according to the sample’s origin. Closer examination revealed that in the arid and semi-arid sites, α-Proteobacteria are more abundant under the shrub canopy, while barren soils are characterized by a higher abundance of Actinobacteria. The bacterial communities in the Mediterranean soils were similar in both patch types. These results correspond to the hypothesis of “resource islands”, suggesting that shrub canopies provide a resource haven in low-resource landscapes. Yet, a survey of the physicochemical parameters of inter- and under-shrub soils could not attribute the changes in bacterial diversity to soil moisture, organic matter, or essential macronutrients. We suggest that in the nutrient-poor soils of the arid and semi-arid sites, bacteria occupying the soil under the shrub canopy may have longer growth periods under favorable conditions, resulting in their increased biomass and altered community composition.  相似文献   

16.
In order to characterize the vertical variation of abundance and community composition of ammonia-oxidizing archaea (AOA) and ammonia-oxidizing bacteria (AOB) in sediments of a eutrophic lake, Lake Taihu, molecular techniques including real-time PCR, clone library, and sequencing were carried out in this study. Abundances of archaeal amoA gene (ranged from 2.34 × 106 to 4.43 × 107 copies [g dry sediment]?1) were higher than those of bacterial amoA gene (ranged from 5.02 × 104 to 6.91 × 106 copies [g dry sediment]?1) for all samples and both of them exhibited negative correlations with the increased depths. Diversities of archaeal and bacterial amoA gene increased with the elevated depths. There were no significant variations of AOB community structures derived from different sediment depths, whereas obvious differences were observed for the AOA community compositions. The information acquired in this study would be useful to elucidate the roles of AOA and AOB in the nitrogen cycling of freshwater ecosystems.  相似文献   

17.
To unravel the existence of dominant bacterial population in the paddy fields of Eastern Uttar Pradesh, India and their relation to the prevailing soil physicochemistry using multivariate statistical analyses, a cumulative culture-independent 16S rRNA based Polymerase chain reaction-Denaturing gradient gel electrophoresis (PCR-DGGE) and a 16S-23S ribosomal intergenic spacer analysis (RISA) have been performed. Detrended correspondence analysis (DCA) and principal component analysis (PCA) biplot analyses were used to assess the relation between soil bacterial population and its physicochemistry. DCA analysis exhibited a strong dependence of bacterial existence on the soil physicochemical variables, such as organic matter, total nitrogen, inorganic nutrients, temperatures, and moisture status. Soil dehydrogenase activity (DHA) was assessed to check the metabolic activity of all soil samples which showed a range of 0.012–0.050 nmol TPF g?1 min?1 with significant variation (p < 0.01). Out of 96 bands excised, 45 different phylotypes were obtained using both techniques which elucidated the abundance of Cyanobacteria over other soil bacterial population. Scytonema sp., Leptolyngbya sp. and different uncultured cyanobacterial species were the major genera found. Profiling data obtained through PCR-DGGE and RISA were used in alpha diversity and rarefaction curve analysis suggested site 6 (Chandauli) as the most diversity rich site. Thus extensive dataset of weighted and unweighted variables generated through DGGE and RISA coupled with metabolic functioning of soil and multivariate analyses provided an excellent opportunity to map the soil microbial structure in paddy fields and their regulation with existing soil environment.  相似文献   

18.
The link between similarity in amino acid sequence for ammonia monooxygenase (AMO) and isotopic discrimination for ammonia oxidation ( l AMO ) was investigated in g -subdivision ammonia-oxidizing bacteria. The isotope effects for ammonia oxidation in pure cultures of the nitrifying strains Nitrosomonas marina , Nitrosomonas C-113a, Nitrosospira tenuis , Nitrosomonas europaea , and Nitrosomonas eutropha ranged from 14.2 to 38.2. The differences in isotope effects could not be readily explained by differential rates of ammonia oxidation, transport of NH 4 + , or accumulation of NH 2 OH or N 2 O among the strains. The major similarities and differences observed in l AMO are, however, paralleled by similarities and differences in amino acid sequences for the f -subunit of AMO (AmoA). Robust differences in l AMO among nitrifying bacteria may be expected to influence the stable isotopic signatures of nitrous oxide (N 2 O) produced in various environments.  相似文献   

19.
Anaerobic ammonium-oxidizing (anammox) bacteria have been detected in many marine and freshwater ecosystems. However, little is known about the distribution, diversity, and abundance of anammox bacteria in terrestrial ecosystems. In this study, anammox bacteria were found to be present in various agricultural soils collected from 32 different locations in China. Phylogenetic analysis of the 16S rRNA genes showed “Candidatus Brocadia,” “Candidatus Kuenenia,” “Candidatus Anammoxoglobus,” and “Candidatus Jettenia” in the collected soils, with “Candidatus Brocadia” being the dominant genus. Quantitative PCR showed that the abundance of anammox bacteria ranged from 6.38 × 104 ± 0.42 × 104 to 3.69 × 106 ± 0.25 × 106 copies per gram of dry weight. Different levels of diversity, composition, and abundance of the anammox bacterial communities were observed, and redundancy analysis indicated that the soil organic content and the distribution of anammox communities were correlated in the soils examined. Furthermore, Pearson correlation analysis showed that the diversity of the anammox bacteria was positively correlated with the soil ammonium content and the organic content, while the anammox bacterial abundance was positively correlated with the soil ammonium content. These results demonstrate the broad distribution of diverse anammox bacteria and its correlation with the soil environmental conditions within an extensive range of Chinese agricultural soils.  相似文献   

20.
To quantify the spatial distribution of ammonia-oxidizing bacteria (AOB) and archaea (AOA) and to determine nitrification activity in soil aggregates along a landscape, soil samples were collected from three landscape positions (shoulder, backslope, and toeslope) at two pasture sites with contrasting climatic conditions. The abundance of AOB and AOA was estimated by quantifying their respective bacterial and archaeal amoA gene copies using real-time polymerase chain reaction. Soil organic C (SOC), total N (TN), and the potential nitrification rate (PNR) were measured in aggregate size ranges (4–1, 1–0.25, and 0.25–0.05 mm). At site 1, a decreasing trend in PNR was observed as the size of aggregates decreased. Both bacterial and archaeal amoA genes were higher in the macroaggregates (4–1 and 1–0.25 mm) than in the microaggregates (0.25–0.05 mm) along the landscape. At site 2, PNR was higher in the smallest size of aggregates. In the 0.25–0.05-mm fraction, the abundance of bacterial and archaeal amoA genes was equal to, or greater than, those found in larger aggregate sizes. The relative abundance of archaeal amoA gene and the PNR correlated with relative SOC and TN contents along the landscapes. The positive relationship between relative archaeal amoA gene abundance and PNR suggests that nitrification in the studied pastures is probably driven by ammonia-oxidizing Thaumarchaeota.  相似文献   

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