253 resultados para arbuscular mycorrhiza
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Arbuscular mycorrhizal fungi (AMF), which is intrinsically present or may be introduced in soils by inoculation, is an example of natural and renewable resource to increase plant nutrient uptake. This kind of fungi produces structures (hyphae, arbuscles and sometimes vesicles) inside the plant root cortex. This mutualistic relationship promotes plant gains in terms of water and nutrient absorption (mainly phosphorus). Biochar can benefit plant interaction with AMF, however, it can contain potentially toxic compounds such as heavy metals and organic compounds (e.g. dioxins, furans and polycyclic aromatic hydrocarbons), depending on the feedstock and pyrolysis conditions, which may damage organisms. For these reasons, the present work will approach the impacts of biochar application on soil attributes, AMF-plant symbiosis and its responses in plant growth and phosphorus uptake. Eucalyptus biochar produced at high temperatures increases sorghum growth; symbiosis with AMF; and enhances spore germination. Enhanced plant growth in the presence of high temperature biochar and AMF is a response of root branching stimulated by an additive effect between biochar characteristics and root colonization. Biochar obtained at low temperature reduces AMF spore germination; however it does not affect plant growth and symbiosis in soil.
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2016
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Arbuscular mycorrhizal (AM) fungi, commonly found in long-term cane-growing fields in northern Queensland, are linked with both negative and positive growth responses by sugarcane (Saccharum spp.), depending on P supply. A glasshouse trial was established to examine whether AM density might also have an important influence on these growth responses. Mycorrhizal spores (Glomus clarum), isolated from a long-term cane block in northern Queensland, were introduced into a pasteurised low-P cane soil at 5 densities (0, 0.06, 0.25, 1, 4 spores/g soil) and with 4 P treatments (0, 8.2, 25, and 47 mg/kg). At 83 days after planting, sugarcane tops responded positively to P fertilizer, although responses attributable to spore density were rarely observed. In one case, addition of 4 spores/g led to a 53% yield response over those without AM at 8 mgP/kg, or a relative benefit of 17 mg P/kg. Root colonisation was reduced for plants with nil or 74 mg P/kg. For those without AM, P concentration in the topmost visible dewlap (TVD) leaf increased significantly with fertiliser P (0.07 v. 0.15%). However, P concentration increased further with the presence of AM spores. Irrespective of AM, the critical P concentration in the TVD leaf was 0.18%. This study confirms earlier reports that sugarcane is poorly responsive to AM. Spore density, up to 4 spores/g soil, appears unable to influence this responsiveness, either positively or negatively. Attempts to gain P benefits by increasing AM density through rotation seem unlikely to lead to yield increases by sugarcane. Conversely, sugarcane grown in fields with high spore densities and high plant-available P, such as long-term cane-growing soils, is unlikely to suffer a yield reduction from mycorrhizal fungi.
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The development of biotechnology techniques in plant breeding and the new commercial applications have raised public and scientific concerns about the safety of genetically modified (GM) crops and trees. To find out the feasibility of these new technologies in the breeding of commercially important Finnish hardwood species and to estimate the ecological risks of the produced transgenic plants, the experiments of this study have been conducted as a part of a larger project focusing on the risk assessment of GM-trees. Transgenic Betula pendula and Populus trees were produced via Agrobacterium mediated transformation. Stilbene synthase (STS) gene from pine (Pinus sylvestris) and chitinase gene from sugar beet (Beta vulgaris) were transferred to (hybrid) aspen and birch, respectively, to improve disease resistance against fungal pathogens. To modify lignin biosynthesis, a 4-coumarate:coenzyme A ligase (4CL) gene fragment in antisense orientation was introduced into two birch clones. In in vitro test, one transgenic aspen line expressing pine STS gene showed increased resistance to decay fungus Phellinus tremulae. In the field, chitinase transgenic birch lines were more susceptible to leaf spot (Pyrenopeziza betulicola) than the non-transgenic control clone while the resistance against birch rust (Melampsoridium betulinum) was improved. No changes in the content or composition of lignin were detected in the 4CL antisense birch lines. In order to evaluate the ecological effects of the produced GM trees on non-target organisms, an in vitro mycorrhiza experiment with Paxillus involutus and a decomposition experiment in the field were performed. The expression of a transgenic chitinase did not disturb the establishment of mycorrhizal symbiosis between birch and P. involutus in vitro. 4CL antisense transformed birch lines showed retarded root growth but were able to form normal ectomycorrhizal associations with the mycorrhizal fungus in vitro. 4CL lines also showed normal litter decomposition. Unexpected growth reductions resulting from the gene transformation were observed in chitinase transgenic and 4CL antisense birch lines. These results indicate that genetic engineering can provide a tool in increasing disease resistance in Finnish tree species. More extensive data with several ectomycorrhizal species is needed to evaluate the consequences of transgene expression on beneficial plant-fungus symbioses. The potential pleiotropic effects of the transgene should also be taken into account when considering the safety of transgenic trees.
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Soil incorporation of metalaxyl [methyl N-(2-methoxyacetyl)-N-(2,6,xylyl)-DL-alaninate] significantly enhanced root colonization of the vesicular-arbuscular (VA) mycorrhizal fungi Glomus fasciculatum associated with wheat. The stimulatory response of VA mycorrhizal fungi to low concentration of metalaxyl resulted in increased plant biomass production, nutrient uptake and grain yield of wheat. However, higher concentrations of metalaxyl, particularly 2.5 ppm of metalaxyl affected the mycorrhizal infection and seed yield of wheat, Addition of urban compost to an extent ameliorated the toxic effect of fungicide on VA mycorrhizal colonization, plant growth and yield of wheat when compared to unamended soil.
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Three species of bacteria, 8 species of fungi and 3 species of VAM-fungi were isolated from the soil substrata supporting Avicennia marina which comprises the majority of mangrove vegetation along the Karachi coast. The species abundances for fungi and bacteria were greater at one site (Sandspit) supporting healthy mangrove growth with soil pH 7.8, EC 16.2mmhos/cm², TSS 2.57% and available phosphorus 0.008% than at the other site (Korangi creek) with stunted growth of mangrove where the soil samples showed pH 7.9, EC 18.8mmhos/cm², TSS 1.45% and available phosphorus 0.001%. Symbiotic association by vasicular-arbuscular mycorrhizal (VAM) fungi in the roots of mangrove plants was also observed on a small scale at Korangi creek where the substratum was undergoing microbial degradation.
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杜鹃花属(Rhododendron L.)植物分布广泛,研究发现所有的杜鹃花科植物都能形成一种特殊的菌根——杜鹃花类菌根(Ericoid Mycorrhiza)。杜鹃花类菌根对杜鹃花科植物在营养胁迫的环境下生长起到重要的作用。近几年,对杜鹃花类菌根的生物学和生态功能的研究越来越重视。我国是杜鹃花属植物资源最为丰富的国家,因此研究杜鹃花属植物菌根真菌多样性,充分利用杜鹃花特有的菌根资源,促进杜鹃花迁地保护成功具有重大的意义。 本研究以分布较广并且是中国特有的杜鹃花属植物——大白花杜鹃(Rhododendron decorum Franch.)的野生植株为研究对象,应用直接扩增根中真菌ITS区的分子鉴定方法和T-RFLP(末端限制性片段长度多态性)的分析方法,来研究其菌根真菌的多样性;并结合生态化学计量学特征分析、宿主遗传相似性及其群落组成分析等内容,探讨大白花杜鹃的菌根真菌-宿主植物-根际土壤三者之间的关系。主要结果如下: (1)通过用直接扩增真菌ITS区序列,揭示了大白花杜鹃根部真菌的多样性,本研究发现,野生大白杜鹃根部的真菌种类比较丰富,至少有26个ITS-taxa,包括子囊菌和担子菌共5个真菌目:Helotiales、Lecanorales(≡Agyriales)、Onygenales、Sebacinales和Thelephorales,其中包括典型的ERM真菌——树粉孢属Oidiodendron sp.(Myxotrichaceae)真菌。另外还发现了黑色有隔内生菌(Dark septate endophyte,DSE)以及一些未命名的子囊菌。担子菌在本研究中占有较大比例,尤其是蜡壳耳菌目真菌;此外还有较典型的外生菌根真菌——革菌目真菌。 (2)大白花杜鹃野生植株与栽培植株在菌根真菌种类组成上,有一定的相似性;在忽略种源差异等条件下相较而言,前者的物种丰富度远高于后者。 (3)大白花杜鹃菌根真菌多样性和丰富度同它的根际土壤与叶片的C、N、P含量以及C/N、N/P、土壤pH值、宿主的海拔高度等都没有显著的相关关系。 (4)在大白花杜鹃的菌根真菌群落组成方面,整体上保持了相当程度的相似性,同时还保持了一定水平的差异;大白杜鹃菌根真菌的种类是丰富的,优势度指数表明其多样性水平很高。 (5)大白花杜鹃的遗传距离与其菌根真菌群落组成结构有极显著的相关关系,宿主的种内遗传差异可能对菌根真菌群落物种组成产生选择偏好。 (6)大白花杜鹃的群落组成与其菌根真菌群落组成有极为显著的关联性,伴生种的菌根类型可能会影响宿主植物菌根真菌的物种组成结构。
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丛枝菌根是自然生态系统中分布最广的内生菌根,在促进植物生存与生长、植被恢复以及生物多样性保护等方面有着非常重要的作用。 随着现代分子生物学技术的不断发展,丛枝菌根真菌研究得到空前发展。大量DNA分析新技术在丛枝菌根真菌的分子遗传、分类鉴定、种间及种内亲缘关系、菌株持久性等方面得到应用,与传统菌根研究方法相比,表现出巨大的优越性。 本项研究利用分子生物学技术和研究方法对中国吉林长白山地区非豆科固氮植物以及东北地区固氮树木的丛枝菌根真菌DNA分子多态性及其与宿主植物之间的相互关系等进行初步研究,旨在利用分子生态学理论和研究方法揭示丛枝菌根真菌多样性及其与宿主植物之间相互适应和协同进化的一般规律,为更好地保护和利用这一重要的微生物资源提供理论依据。 通过比较与筛选,建立起丛枝菌根真菌痕量DNA快速、简便、高效的提取纯化方法——改良CTAB法。经PCR检测,所得DNA满足进一步研究的要求。 根据丛枝菌根真菌18s rRNA 小亚基核基因片段的特点,利用“科”特异性引物进行半巢式标记PCR (Labelled Primers-PCR,LP-PCR) 及单链构象多态性(Single-Stranded Conformation Polymorphism,SSCP)分析技术研究了长白山赤杨在属水平上表现出的多样性。另外,利用巢式PCR-RFLP技术,分别对来源于长白山不同海拔的四种赤杨菌根样品的AMF侵染情况及其系统进化进行了研究。利用AMF特异性PCR技术对我国东北地区四种非豆科树木和5种豆科树木菌根侵染情况和系统发育规律进行了研究 研究结果显示:赤杨根内AMF存在丰富的基因多样性。AMF的侵染有从宿主混乱性向宿主专一性发展的趋势。 长白山地区赤杨属植物至少有东北赤杨、西伯利亚赤杨和色赤杨三个树种在其“属”的水平上与共生的球囊霉科(Glomaceae)至少一个“种” 的丛枝菌根真菌,即根内球囊霉(Glomus intraradix),在“种”的水平上表现出不相关于宿主海拔高度的某种相互选择性。 东北赤杨AMF菌的宿主专一性水平最强,球囊霉属已成为东北赤杨的优势侵染类群;对于其余三种赤杨,AMF则出现宿主混乱现象。宿主因素比海拔因素对AMF侵染特异性的影响更为重要。 豆科与非豆科样本的混乱性都比较强,在特定植物和AMF属之间无特异侵染规律,相对来说,非豆科树木比豆科树木对于AMF的选择性要更强一些,更倾向于和球囊霉属与无梗孢囊霉属的AMF构建共生体。
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丛枝菌根是自然生态系统中分布最广的内生菌根,在促进植物生存与生长、植被恢复以及生物多样性保护等方面有着非常重要的作用。 随着现代分子生物学技术的不断发展,丛枝菌根真菌研究得到空前发展。大量DNA分析新技术在丛枝菌根真菌的分子遗传、分类鉴定、种间及种内亲缘关系、菌株持久性等方面得到应用,与传统菌根研究方法相比,表现出巨大的优越性。 本项研究利用分子生物学技术和研究方法对中国吉林长白山地区非豆科固氮植物以及东北地区固氮树木的丛枝菌根真菌DNA分子多态性及其与宿主植物之间的相互关系等进行初步研究,旨在利用分子生态学理论和研究方法揭示丛枝菌根真菌多样性及其与宿主植物之间相互适应和协同进化的一般规律,为更好地保护和利用这一重要的微生物资源提供理论依据。 通过比较与筛选,建立起丛枝菌根真菌痕量DNA快速、简便、高效的提取纯化方法——改良CTAB法。经PCR检测,所得DNA满足进一步研究的要求。 根据丛枝菌根真菌18s rRNA 小亚基核基因片段的特点,利用“科”特异性引物进行半巢式标记PCR (Labelled Primers-PCR,LP-PCR) 及单链构象多态性(Single-Stranded Conformation Polymorphism,SSCP)分析技术研究了长白山赤杨在属水平上表现出的多样性。另外,利用巢式PCR-RFLP技术,分别对来源于长白山不同海拔的四种赤杨菌根样品的AMF侵染情况及其系统进化进行了研究。利用AMF特异性PCR技术对我国东北地区四种非豆科树木和5种豆科树木菌根侵染情况和系统发育规律进行了研究 研究结果显示:赤杨根内AMF存在丰富的基因多样性。AMF的侵染有从宿主混乱性向宿主专一性发展的趋势。 长白山地区赤杨属植物至少有东北赤杨、西伯利亚赤杨和色赤杨三个树种在其“属”的水平上与共生的球囊霉科(Glomaceae)至少一个“种” 的丛枝菌根真菌,即根内球囊霉(Glomus intraradix),在“种”的水平上表现出不相关于宿主海拔高度的某种相互选择性。 东北赤杨AMF菌的宿主专一性水平最强,球囊霉属已成为东北赤杨的优势侵染类群;对于其余三种赤杨,AMF则出现宿主混乱现象。宿主因素比海拔因素对AMF侵染特异性的影响更为重要。 豆科与非豆科样本的混乱性都比较强,在特定植物和AMF属之间无特异侵染规律,相对来说,非豆科树木比豆科树木对于AMF的选择性要更强一些,更倾向于和球囊霉属与无梗孢囊霉属的AMF构建共生体.
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大气CO_2浓度升高对整个陆地生态系统产生巨大影响。微生物是土壤中重要而又活跃的组成部分,是自然界物质循环不可缺少的成员,行使着许多对陆地生命至关重要的功能。因此,了解土壤中微生物的变化,是了解整个陆地生态系统对大气CO_2浓度升高响应的关键。木文利用在江苏省无锡市建立的稻一麦轮作FACE系统研究平台,研究了CO_2浓度升高对农田土壤微生物及VA菌根的影响。结果发现在FACE条件下,土壤细菌、真菌和放线菌的数量都随着小麦和水稻的生长而发生变化,分别在小麦返青期和水稻拔节期偏大,随后均有所下降,与对照相比,CO_2浓度升高增加土壤细菌、真菌和放线菌的数量;小麦根区土壤中议菌根真菌的抱子以球囊霉属(Glomus)为优势属,以摩西球囊霉(Glomus mosseae)为优势种;在小麦拔节期和孕穗期观察到VA菌根真菌侵染,侵染率在拔节期偏高,后逐渐降低,CO_2浓度升高使小麦VA菌根侵染率增加,而在水稻根系没有观察到VA菌根真菌侵染;根系活力分别在小麦拔节期和水稻抽穗期偏高,到成熟期均降低,CO_2浓度升高使根系活力增强;小麦VA菌根侵染率与根系活力存在正相关关系。总之,大气CO_2浓度升高对农田土壤细菌、真菌和放线菌的数量、VA菌根侵染率及根系活力都表现出一定的促进作用。
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本实验表明:外生菌根真菌彩色豆马勃、劣味乳菇、丝膜菌对PH的适应范围较广,最适生长BH呈酸性。模拟酸雨对马尾松幼苗菌根的外部形态和内部结构有明显影响。在温室栽培中,模拟酸雨(PH2.0)显著抑制菌根侵染率,在田间实验中,对菌根侵染率有一定的影响。菌根PH和土壤PH值随模拟酸雨PH下降而逐渐降低,接种菌根菌可略提高菌根PH和土壤PH值。菌根真菌过氧化氢酶对培养基中PH的变化不敏感,模拟酸雨对菌根过氧化氢酶活性影响也不明显。但沙培中,模拟酸雨(PH2.0)显著抑制菌根过氧化氢酶活性。模拟酸雨(PH2.0)显著刺激菌根过氧化物酶活性,接种菌根菌可以降低菌根过氧化物酶活性。不同PH的培养基对菌体硝酸还原酶活性有明显影响,而且菌体生长速度与硝酸还原酶活性呈正相关。模拟酸雨(PH2.0)显著抑制菌根硝酸还原酶活性,而接种菌根菌明显提高根系硝酸还原酶活性。菌体酸性磷酸酶活性对培养基中PH变化不敏感,同样菌根酸性磷酸酶活性对模拟酸雨的影响也不明显,但是接种菌根菌可明显提高根系酸性磷酸酶活性。模拟酸雨对马尾松幼苗茎的高生长影响不显著。但是对幼苗茎、根系的干重和侧根总长度有显著抑制作用。轻度酸雨(PH4.5-3.0)对马尾松幼苗生长有促进作用,接种菌可提高幼苗生长。从菌根形态结构和生理活性上看,接种菌根菌可减轻模拟酸雨对马尾松幼苗根系的危害,增强对模拟酸雨的抗性。4dThe result of experiment showed that ectomycorrhizal fungi Pisolithus tinctorins. Lactarius insulsus. Cortinarius russus can be growth in broad PH rang in pure culture, the optimum growth PH is acidity. The external morphology and internal structure of ectomycorrhiza of P. massoniana are affected with simulated acid rain. In greenhouse, simulated acid rain (PH2.0) treatment caused significant decrease in the percent infection, but it's not marked in field. The PH of mycorrhizal and soil are reduced with reducing rainfall PH. These PH are slight higher for inoculation with ectomycorrhizal fungi. Catalase activity of ectomycorrhizal fungus is not sensitive to medium with different PH. Mycorrhiza catalase activiyt is not affected significantly with simulated acid rain, but it's inhibited significantly with simulated acid rain (PH2.0) in the sand culture. Peroxidase atcivity of mycorrhiza is enhanced significantly with simulated acid rain (PH2.0), but it's universally lower for inoculation with ectomycorrhizal fungus. Ectomycorrhizal fungus nitrate reductase activity is affected significantly to medium with differdnt PH, the rates of these fungi growth and nitrate reductase activity is significant correlation. Nitrate reductase activity of mycorrhiza is inhibited significantly with simulated acid rain (PH 2.0), but it's increased significantly for inocnlation with mycorrhizal fungi. Ectomycorrhizal fungas acid phosphatase activity is not affected to medium with different PH, Mycorrhiza acid phosphatase activity is not affected with simulated acid rain too, the acid phosphatase activity of roots inoculated with mycorrhizal fungas is increased significantly. The highest acidity level simulated rain reduced signhficantly root system biomass and the dry weight of stem. Iower acidity level simulated rain can stimulated the growth of P. massoniana, the growth of seedling inocnlated with mycorrhizal fungus can be increased.
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A number of methods are available for those researchers considering the addition of molecular analyses of ectomycorrhizal (EcM) fungi to their research projects and weighing the various approaches they might take. Analyzing natural EcM fungal communities has traditionally been a highly skilled, time-consuming process relying heavily on exacting morphological characterization of EcM root tips. Increasingly powerful molecular methods for analyzing EcM communities make this area of research available to a much wider range of researchers. Ecologists can gain from the body of work characterizing EcM while avoiding the requirement for exceptional expertise by carefully combining elements of traditional methods with the more recent molecular approaches. A cursory morphological analysis can yield a traditional quantification of EcM fungi based on tip numbers, a unit with functional and historical significance. Ectomycorrhizal root DNA extracts may then be analyzed with molecular methods widely used for characterizing microbiota. These range from methods applicable only to the simple mixes resulting from careful morphotyping, to community-oriented methods that identify many types in mixed samples as well as provide an estimate of their relative abundances. Extramatrical hyphae in bulk soil can also be more effectively studied, extending characterization of EcM fungal communities beyond the rhizoplane. The trend toward techniques permitting larger sample sets without prohibitive labor and time requirements will also permit us to more frequently address the issues of spatial and temporal variability and better characterize the roles of EcM fungi at multiple scales.
Resumo:
A comunidade nativa de fungos micorrízicos arbusculares (FMA), presente em amostras de raiz e de solo rizosférico de 15 genótipos de milho contrastantes para eficiência no uso de fósforo, foi avaliada pela técnica de eletroforese em gel de gradiente desnaturante (DGGE). Foram amplificados fragmentos do DNA ribossomal com primers específicos para as famílias Acaulosporaceae e Glomeraceae. Os primers para a família Glomeraceae foram eficientes em diferenciar a estrutura da população de fungos micorrízicos, indicando grande diversidade da comunidade entre os genótipos. No DGGE específico para Glomeraceae, foram observadas bandas exclusivas nas linhagens eficientes L228-3 e L3, ambas cultivadas sob baixo teor de fósforo, indicando uma associação preferencial entre os genótipos e os simbiontes, que pode resultar em melhor eficiência na aquisição de fósforo. Além disso, a presença de Glomus clarum nestas duas linhagens eficientes, cultivadas sob baixo P, indica uma possível relação dessa espécie à tolerância ao estresse de P nesse solo. Com relação à família Acaulosporaceae, a técnica de DGGE detectou pouca variação entre os genótipos cultivados em baixo P, além de menor diversidade de fungos micorrízicos dessa família colonizando as raízes de milho.