土壤食细菌线虫影响水稻根系生长的养分和激素作用机制
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
食细菌线虫作为土壤中重要的食细菌微型动物,与微生物相互作用对植物生长的影响已有大量研究报导。但关于食细菌线虫对植物根系生长影响的机理尚不明确。有些研究认为是其取食微生物所产生的直接或间接的养分作用(主要是氮素矿化)为植物生长提供更多有效氮,进而促进植物的生长。最近有研究表明:原生动物促进植物生长存在激素效应,而食细菌线虫在生理及生态上与原生动物很相似,因此有研究者推测食细菌线虫对植物生长的促进作用机理也可能存在激素效应。
     本文从土壤微生物及植物两条途径研究食细菌线虫对植物根系生长影响的机理。首先采用简化的悉生培养系统,研究食细菌线虫与不同产IAA细菌的相互作用及其对土壤IAA含量及氮素矿化的影响;并在同样模式下研究不同食细菌线虫与不同细菌的相互作用对水稻根系生长的影响,并采用实时荧光定量PCR(Quantitative Real-time qRT-PCR)检测激素IAA早期响应基因GH3-2在水稻根系内的表达,旨在揭示土壤食细菌线虫与细菌的相互作用对植物生长的激素作用机理。另一方面,在自然土培条件下,研究供试土壤土著食细菌线虫对水稻根系生长的影响,及根系内部响应基因对土壤IAA含量变化的响应,同时采用BIOLOG和PCR-DGGE两种方法研究了食细菌线虫对根际土壤微生物群落结构的影响,旨在进一步阐明土壤食细菌线虫与细菌的相互作用及其对植物生长的促进作用机理。所获主要研究结果如下:
     1.悉生培养(接种单一线虫和单一细菌)条件下,食细菌线虫(Cephalobus sp.)对不同产IAA细菌Pseudomonas sp.(P)和Burkholderia sp.(B)数量、活性及分泌IAA能力的影响
     在整个培养期,食细菌线虫的取食对土壤中细菌的数量虽无增殖作用,却促进了细菌的活性及分泌IAA的能力,且这种影响受采样时间和接种细菌种类的影响。接种线虫在培养第8天时显著促进了细菌P的活性,在20天时显著促进了细菌B的活性;接种线虫在培养14天显著增加了接种细菌P处理土壤IAA的含量,在20天时显著增加了接种细菌B处理土壤中IAA的含量。然而,不同的细菌种类也影响土壤中线虫的数量,除培养4天外,Cephalobus sp线虫的数量在接种P细菌处理中均高于接种B细菌处理,但两处理培养结束时线虫的数量都是起始数量的2倍以上。
     2.悉生培养条件下,不同食细菌线虫(Cephalobus sp.和C. elegans)与产IAA细菌(Pseudomonas sp和Burkholderia sp.)(?)司相互作用对水稻氮含量及根系生长的影响
     接种食细菌线虫[Cephalobus sp. (N1)和C. elegans(N2)]对产IAA细菌的数量均无明显促进作用,但是对产IAA细菌的活性都有显著影响,且因线虫种类、细菌种类和采样时间的不同而不同。接种线虫N1、N2对细菌P活性的促进作用在14天才表现出来;而接种线虫N2对细菌B活性的促进作用表现的更早,这种差异可能是由不同细菌特性的差异导致的。然而,不同产IAA细菌对接种线虫数量的影响也因线虫种类、细菌种类的不同有一定差异。接种线虫数量在接种细菌P处理中高于接种细菌B处理,且C. elegans线虫的数量高于Cephalobus sp线虫。食细菌线虫对水稻根系的总长度、根表面积及根尖数都有显著影响,且因接种细菌的种类及采样时间的不同而不同。接种线虫处理的水稻氮含量均高于单独接种细菌处理,且在接种细菌B处理的含量显著高于接种细菌P处理,而整个培养期内接种线虫种类对水稻氮含量无显著影响。
     3.悉生培养条件下,食细菌线虫对土壤IAA含量及水稻根系内GH3-2表达的影响
     接种食细菌线虫增加了土壤中IAA的含量,但是不同线虫和细菌的组合效应有所不同。与土壤中IAA含量的变化一致,水稻根系中IAA早期响应基因GH3-2的表达量也与土壤中接种的线虫与否及种类有明显的关系。土壤中IAA的含量与GH3-2基因的表达量之间存在显著的正相关关系(相关系数为0.663,P=0.019)。结合食细菌线虫对水稻根系形态的影响进一步从植物内在根系发育角度证明了食细菌线虫对根系生长的促进作用存在明显的激素作用。
     4.原位富化条件下,食细菌线虫对水稻根系生长的影响
     原位富化试验条件下,食细菌线虫使水稻的根系形态(根总长、根表面积、根平均直径和根尖数等)发生明显改变,使植物的根系都发育成了更长、有更多分支的根系系统,且这种影响受采样时间的影响很大。
     5.原位富化条件下,土壤食细菌线虫对土壤中氮素矿化的影响
     种植水稻系统中,有大量线虫富集处理(SM1)和有少量线虫富集处理(SM5)土壤中矿质氮(Mineral Nitrogen) 6勺含量均表现出先升高后降低的变化趋势。在培养10天时,SM1处理土壤中矿质氮的含量显著高于SM5处理土壤;随着培养时间的延长,两处理土壤中矿质氮含量均显著降低,且SM1处理MN的含量下降幅度为82.6%,显著高于SM5处理的50.5%。这一结果表明:食细菌线虫促进了土壤中氮的矿化,提高了其可利用性,而植物生长的吸收和固定氮素量的增加降低了土壤中矿质氮的含量,同时水稻对NH4+-N的偏好性使得土壤中NH4+-N和N03--N出现差异。
     6.食细菌线虫对根际土壤(种植水稻)微生物(细菌)群落结构的影响(Biolog和PCR-DGGE方法)
     Biolog结果表明:食细菌线虫影响了土壤微生物群落的总体活性(AWCD值表示),并显著地改变了土壤微生物群落结构(微生物对底物碳源的利用表征),但是这种影响随采样时间的不同而有所变化。在种植水稻20天后,食细菌线虫的存在增加了微生物碳源利用丰富度。种植水稻的土壤微生物群落结构DGGE分析结果也表明:培养20天时,SMl处理土壤微生物多样性指数和丰富度指数都显著高于SM5处理,这与Biolog方法得出的结果相同。培养30天时,两种方法得出的两个处理在多样性指数和丰富度指数的不一致性可能是因为BIOLOG和DGGE对微生物群落结构组成表征的方法不同,但是却从不同角度说明食细菌线虫改变了根际土壤微生物的群落结构组成。
     7.原位富化条件下,食细菌线虫对土壤IAA含量和植物体内GH3-2基因表达的影响
     与SM5处理相比,种植水稻的SM1处理土壤中IAA的含量及GH3-2基因在水稻根系内的表达量均显著提高。相关性分析得出二者的相关系数达0.865(p=0.0261),说明外源IAA含量的增加上调了GH3-2基因在水稻根系内的表达。这一结果从自然的土培试验,利用线虫原位富化的培养体系,进一步证实了悉生培养体系中食细菌线虫促进植物根系生长所存在的养分和激素作用。
     本研究从土壤微生物群落结构及植物内部相关基因的调控探讨了食细菌线虫对植物根系生长影响的养分效应和激素效应机理。本研究可为今后有效开发利用土壤有益线虫资源、改善土壤养分管理、提高作物生产提供理论依据和潜在的技术储备,有重要的理论意义和广阔的应用前景。
Bacterial-feeding nematodes, one of the primary grazers of soil bacteria, have been shown to affect root growth of different plant species. Most researches realized that the effects of bacterial-feeding nematodes on plant root growth resulted from direct or indirect nutrient effects (mainly nitrogen mineralization). Bacterial-feeding nematodes grazing on bacteria accelerate bacterial turnover and increase the turnover of soil organic matter, increased the nitrogen mineralization and improved the supply of inorganic nitrogen, and subsequently the plant growth was stimulated. Several researchers, however, have claimed that this process may not fully explain the mechanism of bacterial-feeding nematode stimulating plant growth. Considering the similarly of the physiology and zoology between bacterial-feeding nematodes and protozoa, and that the bacterial-feeding nematodes occur at equal or greater biomass in the rhizosphere than protozoa, it is believed that the activity of bacterial-feeding nematodes in the rhizosphere will also stimulate root proliferation by hormonal effects as seen for protozoan grazing.
     Two ways, which are soil microbilal and plant, were constructed to study the mechanisms of the effect of bacterial-feeding nematode on plant root growth. First, a gnotobiotic microcosm experiments were conducted to study the interactions between different bacterial-feeding nematodes and different IAA-producing bacteria and their effects on soil IAA content and nitrogen mineralization; Then, with the same system to study the effects of interactions between different bacterial-feeding nematodes and different IAA-producing bacteria on rice root growth and rice root intrinsic gene responding to alteration of IAA content in soil, which is then illustrate the mechanisms of the effect of bacterial-feeding nematodes on plant root growth. Then, experiments with natural soil (soil didn't sterile but directly incubated for enriched in soil native nematodes) were manipulated to determine the effects of bacterial-feeding nematodes on the root development of rice seedlings. Nematode grazing changing the microbial community was also discussed by physiology method Biolog and molecule method PCR-DGGE; Moreover, in order to illustrate the auxin effect of interactions between bacterial-feeding nematodes and bacteria on plant growth, the relative expression of the early auxin response genes GH3-2 in rice root was also measured by quantitative Real-time PCR. The main results were as follows:
     1. The effect of bacterial-feeding nematodes (Cephalobus sp.) on the number、activity and IAA production of IAA-producing bacteria (P and B) in gnotobiotic microcosm experiment
     The results showed that:Grazing on bacteria did not stimulate the growth of the bacteria; however, Grazing on bacteria stimulated bacteria activity and the ability of producing IAA significantly. They were influenced by bacteria species and sampling time; the presence of nematodes increased the activity of P bacteria after 8 days, while after 20 days for B bacteria; the nematodes increased soil IAA cntent after 14 days for P bacteria and 20 days after incubation for B bacteria. Meanwhile, the number of nematodes was influenced by bacteria species. The number of Cephalobus sp. in P bacteria was higher in B bacteria, but the number of the nematode was 2 times more than initial for both treatments.
     2. The effect of different bacterial-feeding nematodes (Cephalobus sp. and C. elegans) on IAA-producing bacteria (P and B) and the consequence of these interactions on rice plant growth in gnotobiotic microcosm experiment
     The results showed that the presence of nematodes affected the activity of IAA-producing acteria significantly, and the effects were varied with nematodes species, bacteria species and sampling time. C. elegans (N2) increased bacterial activity and soil IAA content much earlier than Cephalobus sp. (N1), which may be explained by different characteristic of nematode from different family. The effect of bacteria on the number of nematodes was different between different treatments. The number of nematodes in P treatment was higher than that in B treatment, and C. elegans was more than Cephalobus sp.. The presence of nematodes influences the root growth of rice including the total length, surface area and average diameter; the effects were varied with bacteria species and sampling time. The higher nitrogen uptake by the plant in the presence of nematodes than absence of nematodes, and the nitrogen content was higher in B treatment than that in P treatment. However, there was no significantly effect of nematode species on nitrogen uptake by the plant during the whole incubation.
     3. The effect of bacterial-feeding nematodes on soil IAA content and GH3-2 expression in rice root in gnotobiotic microcosm experiment
     The presence of nematodes increased soil IAA content, but the effect varied with different nematode and bacteria. Consistent with soil IAA content, the nematodes increased the GH3-2 expression in rice root. The correlations analysis showed that IAA correlate with the GH3-2 expression in rice root (r=0.663, P=0.019). Combined these results with the effects of bacterial-feeding nematodes on plant root proliferation and to some extent illustrated that bacterial-feeding nematodes affect plant root growth likely through the hormonal effects by intrinsic genetic program in plant root.
     4. The effect of bacterial-feeding nematodes on rice root growth
     Rice seedlings grown in the soils containing more bacterial-feeding nematodes developed a highly branched root system with longer roots; and the effects varied with sampling days. That may due to the difference growth period and sensitivity ability to variable environment of different species plant.
     5. The effect of bacterial-feeding nematodes on soil nitrogen mineralization
     In the system with rice, soil minerial nitrogen contents for both treatments with more bacterial-dfeeding nematodes and few bacterial-dfeeding nematodes were all increased during 0~10th day, and then decreased during 10~30th day. Soil minerial nitrogen contents in SM1 treatment were significant higher than SM5 treatment at day 10, with the increasing days of incubation, soil minerial nitrogen contents in SM1 treatment decreased (82.6%) more than that in SM5(50.5%). The results indicated that the nematodes increased soil nitrogen mineralization, increased the inorganic N available for uptake by the plant, thus decreased the content in soil. The results also showed that rice may be fond of different form of nitrogen, which induced the difference between NH4+-N and NO3--N contents in soil.
     6. The effect of bacterial-feeding nematodes on rhizosphere microbial community structure (Biolog and PCR-DGGE)
     The results showed that:Bacterial-feeding nematodes affect microbial activity (indicated by AWCD) and significantly changed the soil microbial community structure that the soil microbe's functions shifted evidently based on the sole carbon use pattern derived form Biolog method, and the effects varied with sampling time. The presence of nematodes significantly increased bacterial diversity in rice system. The results of DGGE showed that the richness index and diversity index, evenness index of soil microbe was increased during 10-20th day, decreased during 20th-30th day, and the diversity of soil microbe in SM1 were significantly higher than that in SM5 at day 20. The UPGMA analysis showed that the microbial community is similar between SM1 and SM5 at day 20 and 30, while different from day10. It is similar with the results got from Biolog. DGGE fingerprint showed that the nematode affect soil bacterial community structure via appearances or disappearance bands or alteration band intensity.
     7. The effect of bacterial-feeding nematodes on soil IAA content and GH3-2 expression in rice root
     Compared to the control soils (SM5), the soils containing more bacterial-feeding nematodes (SM1) significantly enhanced contents of IAA in soil planted with rice. The correlations analysis between IAA content in soil and GH3-2 expression measured by PT-PCR in rice root showed that IAA significantly correlated with the GH3 expression (P=0.0261, r=0.865), indicating that the GH3-2 was up regulated expression in rice root by increased exogenesis IAA. Combined these results with the effects of bacterial-feeding nematodes on plant root proliferation and to some extent illustrated that bacterial-feeding nematodes affect plant root growth likely through the hormonal effects by intrinsic genetic program in plant root.
     To summarize, the research discussed two main mechanisms of the effect of bacterial-feeding nematodes on plant growth by two ways, one is rhizosphere soil bacterial community structure, and the other is isintrinsic genetic program in plant root system. These findings supported theoretic knowledge and technical to host soil nematodes as an important bio-resource in soil nutrient management and plant growth. The present study may be valid not only for theory, but also for future application in agriculture.
引文
Abel S. and Theologis A.. Early genes and auxin action. Plant Physiol.,1996,111:9-17.
    Abrams B.I., Mitchell M.J. Role of nematode-bacterial interactions in heterotrophic systems with emphasis on sewage sludge decomposition. Oikos.,1980,35:404-410.
    Alphei J., Bonkowski M., Scheu S. Protozoa, Nematoda and Lumbricidae in the rhizosphere of Hordelymus europaers (Poaceae):Faunal interactions, response of microorganisms and effects on plant growth. Oecologia.,1996,106:111-126.
    Anderson J.P.E.. Soil respiration, in methods of soil analysis, part 2. chemical and microbiological properties (A.L. page. Ed.), Soil Science of Society of America, Madison., pp.1982,831-871.
    Anderson R.V., Coleman D.C., Cole C.V. et al. The use of soil microcosms in evaluating bacteriophagic nematode responses to other organisms and effects on nutrient cycling. International Journal of Environmental Studies.,1979,13:175-182.
    Anderson R.V., Elliott E.T., McClellan J.F.et al. Trophic interactions in soils as they affect energy and nutrient dynamics. Ⅲ. Biotic interactions of bacteria, amoebae and nematodes. Microbial Ecology., 1978,4:361-371.
    Anderson R.V., Gould W.D., Woods L.E. et al. Organic and inorganic nitrogenous losses by microbivorous nematodes in soil. Oikos.,1983,40:75-80.
    Anderson T.H., Domsch K.H. Application of eco-physiological quociente (qCO2 and Dq) on microbial biomasses from soils of different cropping histories. Soil Biology and Biochemistry,1990,22, 251-255.
    Arshad M., Frankenberger W.T. Plant growth-regulating substances in the rhizosphere:Microbial production and functions. Advances in Agronomy.,1998,62:45-151.
    Badalucco L. Protease and deaminase activities in wheat rhizosphere and their relation to bacterial and protozoa populations. Biology and Fertility of Soils.,1996,23:99-104.
    Bardgett R.D., Chan K.F. Experimental evidence that soil fauna enhance nutrient mineralization and plant nutrient uptake in montane grassland ecosystems. Soil Biology and Biochemistry.,1999,31: 1007-1014.
    Bardgett R.D., Keilier S., Cook R. et al. Dynamic interaction between soil animals and microorganisms in upland grassland soils amended with sheep dung:a microcosm experiment. Soil Biology and Biochemistry.,1998,30,531-539.
    Bashan L.E., de-Bashan. Bacteria/plant growth-promotion[C]//D Hillel. In Encyclopedia of soils in the environment.Vol 1. Oxford, UK.:Elsevier,2005:103-115.
    Baudoin E., Benizri E., Guckert A. Impact of artificial root exudates on the bacterial community structure in bulk soil andmaize rhizosphere. Soil Biology & Biochemistry.,2003,35:1183-1192.
    Beeckman T., Burssens, I. The peri cell cycle in Arabidopsis [J]. Journal of Expermimental BotGaz, 2001,52:403-411.
    Benkova E., Michniewicz M., Sauer M. Local efflux-dependent auxin gradients as acommon module for plant organ formation [J].Cell,2003,115:591-602.
    Bernard E.C. Soil nematode biodiversity. Biology and Fertility of Soils.,1992,14:99-103.
    Bird A.F., Ryder M.H. Feeding of the nematode Acrobeloides nanus on bacteria. Journal of Nematology.,1993,25:493-499.
    Blakely L.M. Expermiental studies lateral root formation in radish seed roots. I.General methods, developmetal stages, spontaneous formation of laterals [J].Botany,1982,143(3):34-352.
    Blakely L.M., Evans T.A. Cell dynamics studies on the pericycle of radish seedling roots [J].Plant Sci. Lett,1979,14:79-83.
    Blanc C.T, Sy M., Djigal D. et al. Nutrition on bacteria by bacterial-feeding nematodes and consequences on the structure of soil bacterial community. European Journal of Soil Biology,2006, 42, S70-S78.
    Bodelier P.L.E., Wijlhuizen A.G., Blom CWPM. et al. Effects of photoperiod on growth of and denitrification by Pseudomonas chlororaphis in the root zone of Glyceria maxima, studied in a gnotobiotiic microcosm. Plant and Soil.,1997,190:91-103.
    Boerjan W., Cevrera M.T., Delarue M.et al. Superroot, a recessive mutation in Arabidopsis, confers auxin over production. Plant Cell,1995,7:1405-1419.
    Bongers T. and Bongers M. Functional diversity of nematodes. Applied Soil Ecology,1998,10: 239-251.
    Bonkowski M, Brandt F. Do soil protozoa enhance plant growth by hormonal effects? Soil Biology and Biochemistry.,2002,34:1709-1715.
    Bonkowski M. Protozoa and plant growth:the microbial loop in soil revisited. New Phytologist.,2004, 162:617-631.
    Bonkowski M., Chen W.X., Griffiths B.S. et al. Microbiol-faunal interactions in the rhizosphere and effects on plant growth. European Journal of soil Biology.,2000b,36:135-147.
    Bonkowski M., Griffiths B.S., Scrimgeour C. Substrate heterogeneity and microfauna in soil organic'hotspots'as determinants of nitrogen capture and growth of rye-grass. Applied Soil Ecology., 2000a,4:37-53.
    Boukcim H., Pages L., Mousain D. Local NO3- or NH4+ supply modifies the root system architecture of Cedrus atlantica seedlings grown in a split-root device. Journal of Plant Physiology.,2006,163: 1293-1304.
    Bremner J. Inorganic forms of nitrogen. In:Black, C.A., Evans, D.D., White, J.L., Ensminger, L.E., Clark, F.E. (Eds.), Methods of Soil Analysis, Madison, WI.1965.
    Briones Jr A.M., Okabe S., Umemiya Y.et al. Ammonia-oxidising bacteria on root biofilms and their possible contribution to N use efficiency of different rice cultivars. Plant and Soil.,2003,250: 335-348.
    Calenza J.L., Grisafi P.L., Fink G.R. A pathway for lateral root formation in Arabidopsis thaliana. Gene Development.,1995,9:2131-2142.
    Campbell C.D., Grayston S.J., Hirst D.J. Use of rhizosphere carbon sources in sole carbon source tests to discriminate soil microbial communities. Journal of Microbiological Methods.,1997,30:33-41.
    Casero R.A., Pegg A.E. Spermidine/spermine N1-acetyltransferase-the turning point in polyamine metabolism. FASEBJ.1993,7(8):653-661.
    Casimriol, Marchnat A., Bhalerao R.P. Auxin transport Promotes Arabidopsis lateral root initiation. Plant Cell,2001,13:843-852.
    Casson S.A., Lindsey K. Genes and signaling in root development. New Phyrol.2003.,158:11-38.
    Celenza J.L. Jr Grisafi P.L., Fink G.R. A Pathway for lateral root formation in Arabidopsis thaliana. Genes Dev.,1995,9:2131-2142.
    Charlton S.J, Brown C.A., Weisman G.A. et al. Cloned and transfected PZY4 receptors:characterization of a suramin and PPADS-insensitive response to UTP. Br J Phamraeol.1996,119(7):1301-1303.
    Cheng W.X., Zhang Q.L., Coleman D.C. et al. Is available carbon limiting microbial respiration in the rhizosphere. Soil Biology & Biochemistry.,1996,28:1283-1288.
    Choi K.H., Dobbs F.C. Comparison of two kinds of Biolog microplates (GN and ECO) in their ability to distinguish among aquatic microbial communities. Journal of Microbiological Methods.,1999,36: 203-213.
    Christensen H., Griffiths B.S., Christensen S. Bacterial incorporation of tritiated thymidine and populations of bacteriophagous fauna in the rhizosphere of wheat. Soil Biology and Biochemistry., 1992a,24:703-709.
    Christensen S., Griffiths B.S., Ekelund F. et al. Huge increase in bacterivores on freshly killed barley roots. FEMS Microbiology Ecology.,1992b,86:303-310.
    Cocking E.C. Endophytic colonization of plant roots by nitrogen-fixing bacteria. Plant and Soil.,2003, 252:169-175.
    Cole L. Enchytraeid worms (Oligochaeta) enhance mineralization of carbon in organic upland soils. Europen Journal of Soil Science.,2000,51:185-192.
    Coleman D.C. The role of microfloral and faunal interactions in affecting soil processes. In:Mitchell MJ, Nakas JP, eds. Microfloral and fauna interaction in natural and agro-ecosystems. Martinus Nijhoff/Dr W.Junk Publishers, Dordrecht,1986, p:317-348.
    Coleman D.C., Cole C.V., Anderson R.V. et al. An analysis of rhizosphere saprophage interactions in terrestrial ecosystems. In:Lohm UL, Persson T. eds. Soil organisms as components of ecosystems. Ecological Bulletins-NFR.,1977,25:299-309.
    Coleman D.C., Reid C.P.P., Cole C.V. Biological strategies of nutrient cycling in soil systems. Advances in Ecological Research.,1983,13:1-55.
    Couteaux M.M., Bottner P. Biological interactions between fauna and the microbial community in soils. In:Ritz K et al., eds. Beyond the biomass. Composition and functional analysis of soil microbial communities. John Wiley and Sons, Baffins Lane, Chichester, UK.,1994.
    Crawford N.M.A.D., Glass M. Molecular and Physiological aspect of nitrogen uptake in Plants. Trends Plant Sci.,1998,3(10):389-395.
    Culman S.W., Duxbury J.M., Lauren J.G.. et al. Microbial community response to soil solarization in Nepal's rice-wheat cropping system. Soil Biology and Biochemistry,2006,38:3359-3371.
    de Neergard A., Magid J. Influence of the rhizosphere on microbial biomass and recently formed organic matter. European Journal of Soil Science.,2001,52:377-384.
    De Smet I., Signora L., Beeckman T.et al. An abscisic acid- sensitive checkpoint in lateral root development of Arabidopsis. Plant J.2003,33(3):543-555.
    Djigal D., Brauman A., Diop T.A. et al. Influence of bacterial-feeding nematodes (Cephalobidae) on soil microbial communities during maize growth. Soil Biology and Biochemistry.,2004:323-331.
    Drew M.C. Comparison of the effects of a localized supply of phosphate, nitrate, ammonium and potassium on the growth of the seminal root system, and the shoot in barley. New Phytologist.,1975, 75:479-490.
    Duineveld B.M. Analysis of bacterial communities in the rhizosphere of chrysanthemum via denaturing gradient gel electrophoresis of PCR-amplified 16S rRNA as well as DNA fragments coding for 16S rRNA. Applied Environmental Microbiology.,2001,67:172-178.
    Edqards C.A., Stinner B.R. Interactions between soil-inhabiting invertebrates and microorganisms in relation to plant growth and ecosystem processes:an introduction. Agriculture, Ecosystems and Environment.,1988,24:1-3.
    Eichner C.A., Erb R.W., Timmis K.N. et al. Thermal gradient gel electrophoresis analysis of bioprotection from pollutant shocks in the activated sludge microbial community. Applied and Environmental Microbiology,1999,65:102-109.
    Epstein S.S., Shiaris M.P. Size-selective grazing of coastal bacterioplankton by natural assemblages of pigmented flagellates. Colorless flagellates and ciliates. Microbial Ecology.,1992,23:211-225.
    Ferris H., Venette R.C., Lau S.S. Population energetics of bacterial-feeding nematodes:carbon and nitrogen budgets. Soil Biology and Biochemistry.,1997,29:1183-1194.
    Ferris H., Venette R.C., van der Meulen H.R. et al. Nitrogen mineralization by bacterial-feeding nematodes:verification and measurement. Plant and Soil.,1998,203:159-171.
    Fisk M.C., Rurther K.F., Yavitt J.B. Microbial activity and function composition among northern peatland ecosystem. Soil Biology and Biochemistry,2003,35:591-602.
    Francisco S.S., Houdusse F., Zamarreno A.M. et al. Effects of IAA and IAA precursors on the development, mineral nutrition, IAA content and free polyamine content of pepper plants cultivated in hydroponic conditions. Scientia Horticulturae.,2005,106:38-52.
    Fu S.L., Ferris H., Brown D., Plant R. Does the positive feedback effect of nematodes on the biomass and activity of their bacteria prey vary with nematode species and population size? Soil Biology and Biochemistry.,2005,37:1979-1987.
    Fukai S., Cooper M. Development of drought-resistant cultivars using physio-morphological traits in rice. Field Crop Research.,1995,40:67-86.
    Fukaki H., Okushima Y., Tasaka M. et al. Auxin-mediated lateral root formation in higherplants. Int RevCytol.,2007,256:111-137.
    Garland J.L. Analysis and interpretation of community-level physiological profiles in microbial ecology. FEMS Microbiology Ecology.,1997,24:289-300.
    Garland J.L., Mills A.L. Classification and characterization of heterotrophic microbial communities on the basis of patterns of community-level sole-carbon-source utilization. Applied Environmental Microbiology.,1991,57:2351-2359.
    Germida J.J., Sicillano S.D., Defreitas J.R. et al. Diversity of root-associated bacteria associated with field-grown canola (Brassica napus L.) and wheat (Triticum aestivum L.). FEMS of Microbial Ecology.,1998,26:43-50.
    Goodfriend W.L., Olsen W.L., Frye R.J. Soil microfloral and microfaunal response to Salicornia bigelovii planting density and soil residue amendment. Plant and Soil.,2000,223:23-32.
    Gray W.M. Hormonal regulation of plant growth and development. PLoS Biol.,2004,2:1270-1273.
    Grayston S.J., Griffith G.S., Mawdsley J.L. et al. Accounting for variability in soil microbial communities of temperate upland grassland ecosystem. Soil Biology and Biochemistry.,2001,33: 533-551.
    Grayston S.J., Vaughan D., Jones D. Rhizosphere carbon flow in trees in comparison with annual plants: the importance of root exudation and its impact on microbial activity and nutrient availability. Applied Soil Ecology.,1996,5:29-56.
    Grayston S.J., Wang S.Q., Campbell C.D. et al. Selective influence of plant soecies on microbial diversity in the rhizosphere. Soil Biology and Biochemistry.,1998,30:369-378.
    Grewel P.S. Influence of bacteria and temperature on the reproduction of Caenorhabditis elegans (Nematoda:Rhabditidae) infesting mushrooms (Agaricus bisporus). Nematologica.,1991,37:72-82.
    Grewel P.S., Wright D.J. Migration of Caenorhabditis elegans (Nematoda Rhabditidae) larvae towards bacteria and the nature of the bacterial stimulus. Fund. Appl. Nematol.,15:159-166.
    Griffiths B.S, Bonkowski M., Dobson G.et al. Changes in soil microbial community structure in the presence of microbial-feeding nematodes and protozoa. Pedobiologia.,1999,43:297-304.
    Griffiths B.S. A comparison of microbial feeding nematodes and protozoa in the rhizosphere of different plants. Biology and Fertility of Soils.,1990,9:83-88.
    Griffiths B.S. Microbial-feeding nematodes and protozoa in soil:Their effects on microbial activity and nitrogen mineralization in decomposition hotspots and the rhizosphere. Plant and Soil.,1994, 164:25-33.
    Griffiths B.S. The role of bacterial-feeding nematodes and protozoa in rhizosphere nutrient cycling. Aspects of Applied Biology.,1989,22:141-145.
    Griffiths B.S., Bardgett R.D. Interactions between micro-feeding invertebrates and soil microorganisms. In:van Elsas JD, Wellington E, Trevors JT. eds. Modern Soil Microbiology. Marcell Dekker, New York.,1997,165-182.
    Griffiths B.S., Bengough A.G., Neilson R. et al. The extent to which nematode communities are affected by soil factors-a pot experiment. Nematology.,2002,4:943-952.
    Griffiths B.S., Bonkowski M., Dobson G.et al. Changes in soil microbial community structure in the presence of microbial-feeding nematodes and protozoa. Pedobiologia.,1999,43:297-304.
    Griffiths B.S., Caul S. Migration of bacterial-feeding nematodes, but not protozoa, to decomposing grass residues. Biology and Fertility of Soils.,1993,15:201-207.
    Griffiths B.S., Ritz K., Wheatley R.E. Nematodes as indicators of enhanced microbiological activity in a Scottish organic farming system. Soil Use and Management.,1994,10:20-24.
    Griffiths B.S., Welschen R., Van Arendonk J.C.M.et al. The effect of nitrate-nitrogen supply on bacteria and bacterial-feeding fauna in the rhizosphere of different grass species. Oecologia.,1992,91: 253-259.
    Griffiths B.S., Wheatley R.E., Olesen T.et al. Dynamics of nematodes and protozoa following the experimental addition of cattle or pig slurry to soil. Soil Biology & Biochemistry.,1998,30: 1379-1387.
    Griffiths B.S., Young I.M., Boag B. Nematodes associated with the rhizosphere of barly (Hordeum vulgare). Pedobiologia.,1991,35:265-272.
    Guilfoyle T.J. Auxin-regulated genes and promoters. In:Hooykaas PJJ, Hall MA, Libbenga KR(eds)Biochemistry and molecular biology of plant hormones.Amsterdam:Elsevier,1999, 423-459.
    Guiran de C., Bonnel L., Abriached M. Landspreading of pig manures. Ⅳ. Effect on soil nematodes. In Gasser JKR ed. Effluences from Livestock. Applied Science Publishers Ltd., London.,1980, pp 109-119.
    Hackett C.A., Griffiths B.S. Statistical analysis of the time-course of Biolog substrate utilization. Journal of Microbiological Methods.,1997,30:63-69.
    Hagen G., Guilfoyle T.J. Auxin-responsive gene expression:genes, promoters and regulatory factors. PlantMol Biol.,2002,49:373-385.
    Hagen G. and Guilfoyle T.J. Rapid induction of selective transcription by auxin. MOI. Cell. Biol.,1985, 5:1197-1203.
    Hanson P.J., Edwards N.T., Garten C.T., Andrews JA. Separating root and soil microbial contributions to soil respiration:a review of methods and observation. Biogeochemistry.,2000,48:115-146.
    Hedlund K., Augustsson A. Effects of Enchytraeid grazing on fungal growth and respiration. Soil Biology and Biochemistry.,1995,27:905-909.
    Hedrick D.B., Peacock A., Stephen J.R.et al. Measuring soil microbial community diversity using polar lipid fatty acid and denaturing gradient gel electrophoresis data. Journal of Microbiological Methods, 2000,41:235-248.
    Hobbie L. and Estelle M. The axr4 auxin-resistant mutants of Arabidposis thaliana define a gene important for root gravitropism and lateral root initiation. Plant J.1995,7:211-220.
    Hodge A., Robinson D., Griffiths B.S.et al. Why plants bother:root proliferation results in increased nitrogen capture from an organic patch when two grasses compete. Plant, Cell and Environment., 1999,22:811-820.
    Hofman T.W., s'Jacob J.J. Distribution and dynamics of mycophagous and microbivorous nematodes in potato fields and their relationship to some food sources. Annual Applied Biology.,1989,115: 291-298.
    Huttl R.F., Schneider B.U. Forest ecosystem degradation and rehabilitation. Ecological Engineering., 1998,10:19-31.
    Ibekwe A.M., Kennedy A.C. Fatty acid methyl ester (FAME) profiles as a tool to investigate community composition of two agricultural soils. Plant and Soil.,1998,206:151-161.
    Iijima M., Kono Y. Interspecific differences of the root system structures of four cereal species as affected by soil compaction. Japanese Journal of Crop Science.,1991,60:130-138.
    Ingham R.E., Anderson R.V., Gould W.D.et al. Vertical distribution of nematodes in a short grass prairie. Pedobiologia.,1985b,28:155-160.
    Ingham R.E., Trofymow J.A., Ingham E.R.et al. Interactions of bacteria, fungi and their nematode grazers:effects on nutrient cycling and plant growth. Ecological Monographs.,1985a,55:119-140.
    Jentschke G., Bonkowski M., Godbold D.L.et al. Soil protozoa and forest tree growth:Non-nutritional effects and interaction with mycorrhizas. Biology and Fertility of Soils.,1995,20:263-269.
    Joseph C.M., Phillips D.A. Metabolites from soil bacteria affect plant water relations. Plant Physiology and Biochemistry.,2003,41:189-192.
    Kandeler E., Marschner P., Tsherko D. et al. Microbial community composition and functional diversity in the rhizosphere of maize. Plant and Soil.,2002,238:301-312.
    Khan S,Stone JM.Arabidopsis thaliana GH3.9 influences primary root growth.Planta,2007,226:21-34.
    Khan S., Stone J.M. Arabidopsis thaliana GH3.9 influences primary root growth. Planta,2007, 226:21-34.
    King J.J., Stimart D.P., Fisher R.H. et al. A Mutation altering Auxin Homeostasis and Plant Morphology in Arabidopsis. PlantCell.,1995,7(12):2023-2037.
    Kinner N.E., Harvey R.W., Blakeslee K.et al. Size-selective predation on ground-water bacteria by nanoflagellates in an organic contaminated aquifer. Applied and Environmental Microbiology.,1998, 64:618-625.
    Knox O.G.G., Killham K., Artz R.R.E.et al. Effect of nematodes on rhizosphere colonization by seed-applied bacteria. Applied and Environmental Microbiology.,2004,70:4666-4671.
    Knox O.G.G., Killham K., Wilson M.J. Nematode-enhanced microbial colonization of the wheat rhizosphere. FEMS Microbiology Letters,2003,225:227-233.
    Kreuzer K., Adamczyk J., Iijima M., Wagner M., Scheu S., Bonkowski M. Grazing of a common species of soil protozoa (Acanthamoeba castellanii) affects rhizosphere bacterial community composition and root architecture of rice (Oryza sativa L.). Soil Biology and Biochemistry.,2006,38:1665-1672.
    Krome K., Rosenberg K., Bonkowski M., Scheu S. Grazing of protozoa on rhizosphere bacteria alters growth and reproduction of Arabidopsis thaliana. Soil Biology and Biochemistry.,2009, 41:1866-1873.
    Kuikman P.J., Jansen A.G., Van Veen J.A. 15N nitrogen mineralization from bacteria by protozoan grazing at different soil moisture regimes. Soil Biology and Biochemistry.,1991,23:193-200.
    Kuikman P.J., Jansen A.G., Van Veen J.A.et al. Protozoan predation and the turnover of soil organic carbon and nitrogen in the presence of plants. Biology and Fertility of Soils.,1990,10:22-28.
    Lambrecht M., Okon Y., Broek A.V. Indole-3-acetic acid:a reciprocal signalling molecule in bacteria-plant interactions. Trends in Microbiology 2000,8:298-300.
    Larkin R.P. Characterization of soil microbial communities under different potato cropping systems by microbial population dynamics, substrate utilization, and fatty acid profiles. Soil Biology & Biochemistry.,2003,35:1451-1466.
    Laskowski M.J., Williams M.E., Nusbaum H. C. et al. Formation of lateral root meristems is a two-stage Process. DeveloPment,1995,121:3303-3310.
    Lavelle p. Faunua activities and soil process:adaptive strategies that determine ecosystem function. In: Transctions of 15# world congress of soil science,1994,1:189-220.
    Li C.G., Li X.M. and Wang J.G. Effect of soybean continuous cropping on bulk and rhizosphere soilmicrobial community function. Acta Ecologic Sinica,2006,26(4):1144-1150.
    Li H.X., Hu F. Effect of bacterial-feeding nematode inoculation on wheat growth and N and P uptake. Pedosphere.,2001,11(1):57-62.
    Li H.X., Kazuyuki I., Johji M. Effects of Temperature on Population Growth and N Mineralization of Soil Bacteria and Bacterial-feeding Nematode. Microbes and Environments.,2001,16 (3):141-146.
    Liang W.J, Mouratov S., Pinhasi-Adiv Y.et al. Seasonal variation in the nematode communities associated with two halophytes in a desert ecosystem. Pedobiologia.,2002,46:63-74.
    Liao H., Rubio G, Yan X.et al. Effect of phosphorus availability on basal root shallowness in common bean. Plant and Soil.,2001,232:69-79.
    Lynch J. Root architecture and plant productivity. Plant Physiol.,1995,109(1):7-13
    Lynch J.M. The rhizosphere. John Wiley and Sons, Chichester.,1990,458.
    Lynch J.M., Whipps J.M. Substrate flow in the rhizosphere. Plant and Soil.,1990,129:1-10.
    MacNaughton S.J., Stephen J.R., Venosa A.D.et al. Microbial population changes during bioremediation of an experimental oil spill. Applied and Environmental Microbiology,1999,65:3566-3574.
    Mahaffee W.F., Kloepper J.W. Bacterial communities of the rhizosphere and endorhiza associated with field-grown cucumber plants inoculated with a plant growth-promoting rhizobacterium or its genetically modified derivative. Canadian Journal of Microbiology.,1997,43:344-353.
    Malamy J.E. Intrinsic and environmental response pathways that regulate root system architecture. Plant, Cell and Environment.,2005,28:67-77.
    Malamy J.E., Benfey P.N. Organization cell diferentiation in lateral roots of Arabidopsis thaliana. Development 1997,124:33-44.
    Mamilov A.S., Byzov B.A., Zvyagintsev D.G., Dilly O.M. Predation on fungal and bacterial biomass in a soddy-podzolic soil amended with starch, wheat straw and alfalfa meal. Applied Soil Ecology., 2001,16:131-139.
    Mao X.F., Hu F., Griffiths B.S. Bacterial-feeding nematodes enhance root growth of tomato seedlings. Soil Biology and Biochemistry.,2006,38,1615-1622.
    Mao X.F., Hu F., Griffiths B.S. Do bacterial-feeding nematodes stimulate root proliferation through hormonal effects? Soil Biology and Biochemistry.,2007,39,1616-1619.
    Marschner H. Mineral nutrition of higher plants. Academic Press, New York,1995,889.
    Marschner P., Yang C.H., Lieberei R., Crowley D.E. Soil and plant specific effects on bacterial community composition in the rhizosphere. Soil Biology and Biochemistry.,2001,33:1437-1445.
    Martens D.A., Frankenberge Jr W.T. Assimilation of exogenous 2-14C-indole acetic acid and 3-14Ctryptophan exposed to roots of three wheat varieties. Plant and Soil.,1994,166:281-290.
    Matiru V.N., Dakora F.D. The rhizosphere signal molecule lumichrome alters seedling development in both legumes and cereals. New Phytologist.,2005,166:439-444.
    Merbach W., Mirus E., Knof G. et al. Release of carbon and nitrogen compounds by plant roots and their possible ecological importance. J. Plant Nutr. Soil Sci.,1999,162:373-383.
    Meuwly P., Pilet P. Local treatment with indole-3-acetic acid induces differential growth responses in Zea mays L. roots. Planta.,1991,185:58-64.
    Miethling R., Wieland G, Backhaus H.et al. Variation of microbial rhizosphere communities in response to crop species, soil origin, and inoculation with Sinorhizobium meliloti L. Microbial Ecology.,2000, 40:43-56.
    Morel C., Hinsinger P. Root induced modifications of the exchange of phosphate ion between soil solution and soil solid phase. Plant and Soil.,1999,211:103-110.
    Mukesh J., Navneet K., Akhilesh K. et al., The auxin-responsive GH3 gene family in rice (Oryza sativa). Funct. Integr. Genomics.,2006,6:36-46.
    Muyzer G., de Waal E.C., Uitterlinden A.G. Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes encoding for 16SrRNA. Applied and Environmental Microbiology.,1993,59:695-700.
    Nakazawa M.,Yabe N., Chikawa T, et al. DFL1, an auxin-responsive GH3 gene homologue,negatively regulates shoot cell elongation and lateral root formation,andpositively regulates the light response of hypocotyl length. Plant J,2001,25:213-221.
    Naseby D.C., Loccoz Y.M., Powell J., Gara F.O., Lynch J.M. Soil enzyme activities in the rhizosphere of field-grown sugar beet inoculated with the biocontrol agent Pseudomonas fluoresens F113. Biology and Fertility of Soils.,1998,27:39-43.
    Nikolyuk V.F., Tapilskaja N.V. Bodenamoben als Produzenten von biotisch aktiven Stoffen. Pedobiologia.,1969,9:182-187.
    Opperman M.H., Wood M., Harris P.J., Cherrett C.P. Nematode and nitrate dynamics in soils treated with cattle slurry. Soil Biology & Biochemistry.,1993,25:19-24.
    Parkinson D., Gray T.R.G., Williams S.T. Methods for studying the ecology of soil micro-organisms. IBP Handbook,1971, No 19. Blackwell, Oxford.
    Phillips D.A., Ferris H., Cook D.R.et al. Molecular control points in rhizosphere food webs. Ecology., 2003,84:816-826.
    Phillips D.A., Fox T.C., King M.D.et al. Microbial products trigger amino acid exudation from plant roots. Plant Physiology.,2004,136:2887-2894.
    Phillips D.A., Joseph C.M., Yang G.P.et al. Identification of lumichrome as a Sinorhizobium enhancer of alfalfa root respiration and shoot growth. Proceedings of the National Academy of Science USA., 1999,96:12275-12280.
    Poonguzhali S., Madhaiyan M., Sa T. Quorum-sensing signals produced by plant-growth promoting Burkholderia strains under in vitro and in planta conditions. Research in Microbiology.,2007,158: 287-294.
    Price A.H., Tomos A.D., Virk D.S. Genetic dissection of root growth in rice (Oryza sativa L.):Ⅰ:a hydrophonic screen. Theoretical Applied Genetics.,1997,95:132-142.
    Puiter P.C., Moore J.C., Zwart K.B. Simulation of nitrogen mineralization in the below-ground food webs of two winter fields. Journal of Applied Ecology.,1993,30:95-106.
    Rahman A., Hosokawa S., Oono Y.et al. Auxin and ethylene response interactions during Arabidopsis root hair development dissected by auxin influx modulators. Plant Physiology.,2002,130: 1908-1917.
    Redinbaugh M.G., Campbell W.H. Higher plant responses to environmental nitrate. Physiologia Plantarum,1991,82:640-650.
    Reed R.C., Brady S.R., Muday G..K. Inhibition of auxin movement from the shoot into the root inhibits lateral root development in Arabidopsis. Plant physiol.,1998,118:1369-1378.
    Robinson D. The responses of plants to non-uniform supplies of nutrients. New Phytologist.,1994,127: 635-674.
    Rogg L.E., Lasswell J., Bartel B. A gain-of function mutation in IAA28 suppresses lateral root development. Plant Cell,2001,13:465-480.
    R(?)nn R. Spatial distribution and successional pattern of microbial activit and miro-faunal populations on decomposing barley roots. Journal of Applied Ecology.,1996,33:662-672.
    Rouatt J.W. et al. Statistical evaluation of the rhizosphere effect. Soil Science Society of America, Proceedings.,1960,24:271-273.
    Ruegger M., Dewey E., Hobbie, L. et al. Reduced naphthylPhthalamic acid binding in the tir3 mutant of Arabidopsis associated with a reduction in polar auxin transport and diverse morphological defects. Plant Cell,1997,9:745-757.
    Sattelmacher B., Gerendas J., Thoms K.et al. Interaction between root growth and mineral nutrition. Environ. ExP. Biol.,1993,33:63-73.
    Scheible W.R., A.Gonz61ez-Fontes, Lauerer M., Muller-Rober B., Caboche M., Stitt M. Nitrate acts as a signal to induce organic acid metabolism and repress starch metabolism in tobacco.Plant Cell,1997a, 9:783-798.
    Scheible W.R., Lauerer M., Sehulze E.D., Caboehe M., Stitt M. Accumulation of nitrate in the shoot acts as a signal to regulate shoot-root allocation in tobacco. Plant J.,1997b,11(4):671-691.
    Scheible W.R., Lauerer M., Sehulze E.D.et al. Accumulation of nitrate in the shoot acts as a signal to regulate shoot-root allocation in tobacco. Plant J.,1997b,11 (4):671-691.
    Sherr B.F., Sherr E.B., McDaniel J. Effect of protistan grazing on the frequency of dividing cells in bacterioplankton assemblages. Applied and Environmental Microbiology.,1992,58:2381-2385.
    Signora L., De Smet I., Foyer C.H. et al. ABA plays a central role in mediating the regulatory effects of nitrate on root branching in Arabidopsis. Plant J.2001,28:655-662.
    Singh B.K., Millard P., Whiteley A.S.et al. Unravelling rhizosphere-microbial interactions:opportunities and limitations. Trends in Microbiology.,2004,12(8):286-293.
    Smet I., Tetsumura T., Rybel B. et al. Auxin-dependent regulation of lateral root positioning in the basal meristem of Arabidopsis [J].Development,2007,134(4):681-690.
    Snyder R.A. Chemoattraction of a bacterivorous ciliates to bacteria surface compounds. Hydrobiologia., 1991,215:205-213.
    Soderberg K.H., Jumpponen A., Baath E. The microbial community in the rhizosphere determined by community level-physiological profile (CLPP) and direct soil- and cfu-PLFA techniques. Applied Soil Ecology.,2004,25:135-145.
    Sohlenius B., Sandor A. Vertical distribution of nematodes in arable soil under grass (Festuca pratensis) and barley (Hordeum vulgare). Biology and Fertility of Soils.,1987,3:19-25.
    Sonnemann I., Dogan H., Klein A.et al. Response of soil microflora to changes in nematode abundance-evidence for large scale effects in grassland soil. Journal of Plant Nutrient of Soil Science.,1999,162:38-391.
    Staswick PE,Serban B,Rowe M,et al.Characterization of an Arabidopsis enzyme family that conjugates amino acids to indole-3-acetic acid.Plant Cell,2005,17:616-627.
    Staswick PE,Tiryaki I,Rowe ML.Jasmonate response locus JAR1 and several related Arabidopsis genes encode enzymes of the firefly luciferase superfamily that show activity on jasmonic, salicylic, and indole-3-acetic acids in an assay for adenylation.Plant Cell,2002,14:1405-1415.
    Steer J., Harris J.A. Shifts in the microbial community in rhizosphere and non-rhizosphere soils during the growth of Agrostis stolonifera, Soil Biology and Biochemistry.,2000,32:869-878.
    Strom L. Root exudation of organic acids:importance to nutrient availability and the calcifuge and calcicole behaviour of plants. Oikos.,1997.80:459-466.
    Sulkava P., Huhta V., Laakso J. Impact of soil faunal structure on decomposition and N-mineralization in relation to temperature and moisture in forest soil. Pedebiologia.,1996,40:505-513.
    Sundin P., Valeur A., Olsson S., Odham G Interactions between bacteria-feeding nematodes and bacteria in the rape rhizosphere:effects on root exudation and distribution of bacteria. FEMS Microbiology Ecology.,1990,73:13-22.
    Swarup K., Benkova E., Swaru p R. et al. The auxin influx carrier LAX3 promotes lateral root emergence [J].Nat Cell Biol.,2008,10:946-954.
    Tapilskaja N.V. Amoeba albida Na'gler und ihre Beziehungen zu dem Pilz Verticillum dahliae Kleb, dem Erreger der Welkekrankheit von Baumwollpflanzen. Pedobiologia.,1967,7:156-165.
    Terol J., Domingo C., Talon M. The GH3 family in plants:Genome wide analysis in rice and evolutionary history based on EST analysis.Gene,2006,371:279-290.
    Theron J., Cloete T.E. Molecular techniques for determining microbial diversity and community structure in natural environments. Critical Reviews in Microbiology,2000,26:37-57.
    Timpte C., Lincoln C., Pickett F. B.et al. The AXR1 and AUX1 genes of Arabidopsis function in separate auxin-response pathways. plantJ.1995,8(4):561-569.
    Torrey F.A. Congenital ichthyosifonn eyrthrodenna. AMA Arch Denn Syphliol.1950,62(6):931-933.
    Trevors J.T. Electron transport system activity in soil, sediment and pure cultures. CRC Critical Rev. Microbiol.,1984,11:83-100.
    Trofymow J.A., Coleman D.C. The role of bacterivorous and fungivorous nematodes in cellulose and chitin decomposition. In:Freckman DW, ed. Nematodes in soil ecosystems. University of Texas Press, Austin, Texas, USA.,1982,117-138.
    Tuberosa R., Sanguineti M.C., Landi P.et al. Identification of QTLs for root characteristics in maize grown in hydroponics and analysis of their overlap with QTLs for grain yield in the field at two water regimes. Plant Molecular Biology.,2002,48:683-695.
    Venette R.C., Ferris H. Influence of bacterial type and density on population growth of bacterial-feeding nematodes. Soil Biology and Biochemistry.,1998,30:949-960.
    Verhagen F.J.M., Hagemann P.E.J, Woldendorp J.W.et al. Competition for ammonium between nitrifying bacteria and plant roots in soil in pots; effects of grazing by flagellates and fertilization. Soil Biology & Biochemistry.,1994,26:89-96.
    Villenave C., Bongers T., Ekschmitt K.et al. Changes in nematode communities after manuring in millet fields in Senegal. Nematology.,2003,5(3):351-358.
    Wang J.R., Hu H., Wang G. H. et al. Expression of PIN Genes in Rice (Oryza sativa L.):Tissue Specificity and Regulation by Hormones. Molecular Plant,2009,1-9.
    Wang X.B., Wu P., Hu B., Chen Q.S. Effects of nitrate on the growth of lateral root and nitrogen absorption in rice.Acta Bot. Sin.,2002,44 (6):678-683.
    Wardle D.A. The influence of biotic interactions on soil biodiversity. Ecology Letters.2006,9,870-886.
    Westover K.M., Kennedy A.C., Kelley S.E. Patterns of rhizosphere microbial community composition associated with co-occurring plant species. Journal of Ecology.,1997,85:863-873.
    Whitford W.G, Freckman D.W., Santos P.F.et al. The role of nematodes in desert ecosystems. In: Nematodes in Soil Ecosystems (Freckman, D.W. and Wallwork, J.A., Eds.),1982, pp.98-115. University of Texas Press, Austin, TX.
    Woods L.E., Cole C.V., Elliott E.T. et al. Nitrogen transformations in soil as affected by bacterial-microfauna interactions. Soil Biology and Biochemistry.,1982,14:93-98.
    Xiao H.F., Griffiths B.S., Chen X.Y., Liu M.Q. et al. Influence of bacterial-feeding nematodes on nitrification and the ammonia-oxidizing bacteria (AOB) community composition. Applied Soil Ecology,2010, (in press).
    Yeates G.W., Bongers T., de Goede R.GM. et al. Feeding habits in soil nematode families and genera-an outline for soil ecologists. Journal of nematology.,1993,25:315-331.
    Young I.M., Griffiths B.S., Robertson W.M. Continuous foraging by bacterial-feeding nematodes. Nematologica.,1996,42:378-382.
    Zhang H., Forde B.G. An arabidopsis MADS box gene that controls nutrient-induced changes in root architecture. Science,1998,279:407-409.
    Zhang H., Forde B.G.. Regulation of Arabidopsis root development by nitrate availability. Journal of Experimental Botany,2000,51:51-59.
    Zhang H., Jennings A., Barlow P.W.et al. Dual pathways for regulation of root branching by nitrate. Proceeding of national academy of science,1999,96:6529-6536.
    Zhang H.M., Jennings A.J., Forde B.G Regulation of Arabidopsis root development by nitrate availability. Journal of experimental Botany,2000,51:51-59.
    Zielezny Y., Groeneweg J., Vereecken H.et al. Impact of sulfadiazine and chlorotetracycline on soil bacterial community structure and respiratory activity. Soil Biology and Biochemistry,2006,38: 2372-2380.
    Zwart K.B., Kuikman P.J., Van Veen J.A. Rhizosphere protozoa:their significance in nutrient dynamics. In:Darbyshire JF ed. Soil Protozoa. CAB International Wallingford Oxon,1994, p:93-121.
    陈晶.微生物多样性的研究方法概述,生物技术,2005,15(4):85-87。
    陈小云,李辉信,胡锋等.食细菌线虫对土壤微生物量和微生物群落结构的影响.生态学报,2004,24(12):2825-2831.
    崔丽娜,董树亭,高荣岐等.外源四环素对菜田土壤微生物活性及数量的影响.水土保持学报,2010,.24:214-218.
    胡锋,李辉信,武心齐等.杀灭土壤中线虫对小麦生长和吸收N、P的影响.应用生态学报.,1998a,9:419-424.
    胡锋,李辉信,武心齐等.接种线虫对土壤-作物系统中肥料 15N 去向的影响.南京农业大学学报.,1998b,21:125-127.
    胡锋,李辉信,史玉英等.两种基因型小麦根际土壤生物动态及根际效应.土壤通报.,1998c,29(3):133-135.
    胡锋,李辉信,谢涟琪等.土壤食细菌线虫与细菌的相互作用及其对N、P矿化-生物固定的影响及机理.生态学报.,1999,19:914-920.
    胡锋,林茂松,吴珊眉.赣中低丘红壤生态系统线虫种群特征.王明珠等主编.红壤生态系统研究(第二集).江西科技出版社,南吕,1992,p:177-182.
    胡锋,吴珊眉.土壤生态系统中生物的相互作用与碎屑食物网研究进展.徐琪,李永吕主编.土壤·资源·生态·环境.青岛海洋大学出版社,青岛,1992,p:28-32.
    胡佩,杨红,刘德辉等.高效液相色谱法测定蚓粪中的植物激素.分析实验室,2001,20(6):8-10.
    焦晓丹,吴凤芝.土壤微生物多样性研究方法的进展.土壤通报,2004,35(6):789-792.
    梁文举,史奕.农业生态系统线虫多样性研究进展.应用生态学报.,2000,11(增刊):1-4.
    廖红,严小龙.菜豆根构型对低磷胁迫的适应性变化及基因型差异。植物学报,2000,42(2):158-163.
    毛小芳,李辉信,龙梅等.不同食细菌线虫取食密度下线虫对细菌数量、活性及土壤氮素矿化的影响,应用生态学报,2005,16(6):1112-1116.
    史正军,樊小林,Klaus D.等.根系局部供氮对水稻根系形态的影响及其机理.中国水稻科学,2005,19(2):147-152.
    王涛.植物扦插繁殖技术[M].北京:北京科学技术出版社,1989
    章家恩,蔡燕飞,高爱霞等.土壤微生物多样性实验研究方法概述.土壤,2004,36(4):346-350.
    赵学强,施卫明.水稻根系生长对不同氮形态响应的动态变化.土壤(Soils),2007,39(5):766-771.
    郑华,欧阳志云,方治国等.BIOLOG在土壤微生物群落功能多样性研究中的应用.土壤学报,2004,41(3):456-461.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700