都江堰地区丛枝菌根真菌多样性与生态研究

 调查了都江堰地区3个不同生境样地（般若寺、馒头山、龙池）中85种优势及常见植物的丛枝菌根真菌侵染率,其中78种植物（91.8%）被丛枝菌根真菌侵染。同时对其中58种植物根围土壤中丛枝菌根真菌的多样性进行分析,共分离到5属47种丛枝菌根真菌,其中球囊霉属（Glomus）35种,无梗囊霉属（Acaulospora）7种,原囊霉属（Archaeospora）1种,内养囊霉属（Entrophospora）2种,巨孢囊霉属（Gigaspora）2种。无梗囊霉属和球囊霉属是3个样地共有的优势属。光壁无梗囊霉（Acaulospora laevis）是龙池的优势种,而地表球囊霉（Glomus versiforme）是般若寺和馒头山的优势种。丛枝菌根真菌的孢子密度和种的丰度显著受到海拔相关因子影响,同时丛枝菌根真菌的种类组成也受较大影响。乔木砍伐没有显著影响丛枝菌根真菌的孢子密度和种的丰度,同时对种类组成影响也较小。根围土壤中丛枝菌根真菌的孢子密度与根系侵染率之间没有显著相关性（R2=0.024 8）。     

西双版纳热带雨林中丛枝菌根真菌的初步研究*

对西双版纳热带雨林中30个科的42种植物根系的丛枝菌根真菌定居情况进行了调查,并从这些植物的根际土壤中分离鉴定了分属于无梗囊霉属(Acaulospora)、球囊霉属(Glomus)和硬囊霉属(Sclerocystis)的25种丛枝菌根真菌。对热带雨林土壤中丛枝菌根真菌的孢子密度（spore density）、物种丰富度（species richness）以及已鉴定种的出现频率进行统计分析发现：热带雨林土壤中丛枝菌根真菌的孢子密度在每100g土壤116~1560个之间,平均478个;物种丰富度在2~7之间,平均为4.5;无梗囊霉属和球囊霉属真菌是热带雨林土壤中丛枝菌根真菌的优势类群。     

西双版纳热带次生林中的丛枝菌根调查

对西双版纳热带次生林中13个科的26种植物根系的丛枝菌根真菌（Arbuscular mycorrhizal fongii,AMF）侵染情况进行了研究,并从这些植物的根围土壤中分离鉴定了隶属于球囊霉属（Clomus）、巨孢囊霉属（Gigaspora）、盾巨孢囊霉属（Scutellospora）和无梗囊霉属（Acaulospora）的11种丛枝菌根真菌。该地次生林中AMF的孢子密度为13—29个／100g土壤,平均为19个;种的丰富度在4．9之间（平均为6）;平均频度为53．8％;相对多度为3．2％-26．5％;物种多样性指数和均匀度指数分别为0．94和0．93。丛枝菌根的侵染率达到44．8％．57．2％（平均为50．9％）;球囊霉属（Glomus）和无梗囊霉属（Acattlospora）是热带次生林根围土壤中菌根真菌的优势类群。     

西双版纳热带雨林中丛枝菌根真菌的初步研究

对西双版纳热带雨林中30个科的42种植物根系的丛枝菌根真菌定居情况进行了调查,并从这些植物的根际土壤中分离鉴定了分属于无梗囊霉属（Acaulospora)、球囊霉属（Glomus)和硬囊霉属（Sclerocystis)的25种丛枝菌根真菌,对热带雨林土壤中丛枝菌根真菌的孢子密度（spore density)、物种丰富度（species richness)以及已鉴定种的出现频率进行统计分析发现：热带雨林土壤中丛枝菌根真菌的孢子密度在每100g土壤116-1560个之间,平均478个;物种丰富度在2-7之间,平均为4.5;无梗囊霉属和球囊霉属真菌是热带雨林土壤中丛枝菌根真菌的优势类群。     

西双版纳地区龙脑香科植物AM真菌的初步研究

 对云南省西双版纳地区17种龙脑香科树种根系丛枝菌根（Arbuscular mycorrhiza, AM）真菌的定居情况进行了调查,并对根围土壤中AM真菌进行了分离和鉴定。结果表明,调查根样均有不同程度的菌根感染,感染率最高可达40%,调查揭示了西双版纳地区龙脑香科植物在自然条件下可形成丛枝菌根。初步从龙脑香科植物根际土壤中分离、鉴定出32种AM真菌,隶属于无梗囊霉属（Acaulospora）、球囊霉属（Glomus）、原囊霉属（Achaeospora）、拟球囊霉属（Paraglomus）和盾巨孢囊霉属（Scutellospora）,其中,无梗囊霉属和球囊霉属真菌为西双版纳地区龙脑香科植物AM真菌优势类群。     

云南金顶铅锌矿区丛枝菌根真菌多样性的研究

对云南金顶铅锌矿区丛枝菌根真菌(Arbuscular mycorrhizal fungi,AMF)资源进行了调查,从32种植物的83个根际土壤样本中分离鉴定出5属36种丛枝菌根真菌,其中无梗囊霉属Acaulospora 5种、内养囊霉属Entrophospora 2种、巨孢囊霉属Gigaspora 1种、球囊霉属Glomus 24种及盾巨孢囊霉属Scutellospora 4种。球囊霉属和无梗囊霉属为金顶铅锌矿区中丛枝菌根真菌的优势属,沃克球囊霉Glomus walkeri是我国的新记录种。近明球囊霉Glomus claroideum、明球囊霉G.clarum、缩球囊霉G.constrictium、地球囊霉G.geosporum、摩西球囊霉G.mossaea、膨胀球囊霉G.pansihalos和疣突球囊霉G.verruculosum是金顶铅锌矿区的优势种;金顶铅锌矿区土壤中丛枝菌根真菌的孢子密度为495-11175个/100g土,平均3368±291(SE,标准误差)个/100g土,每种植物根际土壤中丛枝菌根真菌的物种丰富度为2-20种,平均11.5种;金顶铅锌矿区植物根际土壤中较高的AMF孢子密度和物种丰富度说明AMF对重金属污染具有较强的抗(耐受)性。     

金沙江干热河谷(元谋段)丛枝菌根真菌多样性研究*

从金沙江干热河谷(元谋段)75种植物的根际土壤中分离鉴定了44种丛枝菌根真菌, 分属无梗囊霉属Acaulospora、古孢霉属Archaeospora、内养囊霉属Entrophospora、巨孢囊霉属Gigaspora、球囊霉属Glomus和盾巨孢囊霉属Scutellospora, 其中,球囊霉属和无梗囊霉属为金沙江干热河谷中丛枝菌根真菌的优势属。齿状无梗囊霉A. denticulata、刺状无梗囊霉A. spinosa、瘤状无梗囊A. tuberculata,近明球囊霉Glomus claroideum、明球囊霉G. clarum、根内球囊霉G. intraradices、单孢球囊霉G. monosporum、弯丝球囊霉G. sinuosa是金沙江干热河谷(元谋段)的优势种。金沙江干热河谷土壤中丛枝菌根真菌的孢子密度为5~6400个/100g土壤,平均1504;每个根际土壤中丛枝菌根真菌的物种丰富度1~18种,平均9种。     

金沙江干热河谷(元谋段)丛枝菌根真菌多样性研究

从金沙江干热河谷(元谋段)75种植物的根际土壤中分离鉴定了44种丛枝菌根真菌, 分属无梗囊霉属Acaulospora、古孢霉属Archaeospora、内养囊霉属Entrophospora、巨孢囊霉属Gigaspora、球囊霉属Glomus和盾巨孢囊霉属Scutellospora, 其中,球囊霉属和无梗囊霉属为金沙江干热河谷中丛枝菌根真菌的优势属。齿状无梗囊霉A. denticulata、刺状无梗囊霉A. spinosa、瘤状无梗囊A. tuberculata,近明球囊霉Glomus claroideum、明球囊霉G. clarum、根内球囊霉G. intraradices、单孢球囊霉G. monosporum、弯丝球囊霉G. sinuosa是金沙江干热河谷(元谋段)的优势种。金沙江干热河谷土壤中丛枝菌根真菌的孢子密度为5~6400个/100g土壤,平均1504;每个根际土壤中丛枝菌根真菌的物种丰富度1~18种,平均9种。     

金沙江干热河谷（元谋段）丛枝菌根真菌多样性研究

从金沙江干热河谷(元谋段)75种植物的根际土壤中分离鉴定了44种丛枝菌根真菌,分属无梗囊霉属Acaulospora、古孢霉属Archaeospora、内养囊霉属Entrophospora、巨孢囊霉属Gigaspora、球囊霉属Glomus和盾巨孢囊霉属Scutellospora,其中,球囊霉属和无梗囊霉属为金沙江干热河谷中丛枝菌根真菌的优势属。齿状无梗囊霉A．denticulata、刺状无梗囊霉A．spinosa、瘤状无梗囊A．tuberculata,近明球囊霉Glomus claroideum、明球囊霉G．clarum、根内球囊霉G．intraradices、单孢球囊霉Gmonosporum、弯丝球囊霉G．sinuosa是金沙江干热河谷(元谋段)的优势种。金沙江干热河谷土壤中丛枝菌根真菌的孢子密度为5-6400个／100g土壤,平均1504;每个根际土壤中丛枝菌根真菌的物种丰富度1～18种,平均9种。     

三峡库区消落带常见野生植物AM真菌

从三峡库区消落带3种常见野生植物的15个根际土壤样本中共分离鉴定出24种丛枝菌根真菌（Arbuscular mycorrhizal fungi,AMF）,包括球囊霉属Glomus 15种、无梗囊霉属Acaulospora 3种、近明球囊霉属Claroideoglomus 2种和多样孢霉属Diversispora、内养囊霉属Entro phospora、巨孢囊霉属Gigaspora及类球囊霉属Paraglomus各1种。其中地表多样孢囊霉D. epigaea 和伯氏类球囊霉P. pernambucanum是我国的新记录种。研究发现这3种植物根际土壤中丛枝菌根真菌的优势属为球囊霉属,优势种为地球囊霉G. geosporum、单孢球囊霉G. monosporum、地表球囊霉G. versiforme、副冠球囊霉G. coronatum 和黄孢球囊霉G. flavisporum。研究还发现在这3种植物根际土壤中丛枝菌根真菌的孢子密度平均为839±170个/100g土,物种丰富度在14-22种之间,Shannon-Wiener多样性指数和均匀度分别在1.97-2.21、0.409-0.479之间波动。结果表明三峡库区消落带是一个AMF多样性研究的资源库。     

Nested multiplex PCR——A feasible technique to study partial community of arbuscular mycorrhizal fungi in field-growing plant root

Plant can be infected by different arbuscular mycorrhizal fungi, but little is known about the interaction between them within root tissues mainly because different species cannot be distinguished on the basis of fungal structure. Accurate species identification of Arbuscular mycorrhizal fungi (AMF) colonized in plant roots is the comerstone of mycorrhizal study, yet this fundamental step is impossible through its morphological character alone. For accurate, rapid and inexpensive detection of partial mycorrhizal fungal community in plant roots, a nested multiplex polymerase chain reaction (PCR) was developed in this study. Five discriminating primers designed based on the variable region of the 5′ end of the large ribosomal subunit were used in the experiment for testing their specificity and the sensitivity in nested PCR by using spores from Glomus mosseae (BEG12), Glomus intraradices (BEG141), Scutellospora castaneae (BEG1) and two unidentified Glomus sp. HAUO3 and HAUO4. The feasibility assay of nested multiplex PCR was conducted by use of spore mixture, Astragalus sinicum roots co-inoculated with 4 species of arbuscular mycorrhizal fungi from pot cultures and 15 different field-growing plant roots respectively after analyses of the compatibility of primers. The result indicated that the sensitivity was in the same range as that of the corresponding single PCR reaction. Overall accuracy was 95%. The efficiency and sensitivity of this multiplex PCR procedure provided a rapid and easy way to simultaneously detect several of arbuscular mycorrhizal fungal species in a same plant root system.     

Nested multiplex PCR—A feasible technique to study partial community of arbuscular mycorrhizal fungi in field-growing plant root

Plant can be infected by different arbuscular mycorrhizal fungi, but little is known about the interaction between them within root tissues mainly because different species cannot be distinguished on the basis of fungal structure. Accurate species identification of Arbuscular mycorrhizal fungi (AMF) colonized in plant roots is the comerstone of mycorrhizal study, yet this fundamental step is impossible through its morphological character alone. For accurate, rapid and inexpensive detection of partial mycorrhizal fungal community in plant roots, a nested multiplex polymerase chain reaction (PCR) was developed in this study. Five discriminating primers designed based on the variable region of the 5′ end of the large ribosomal subunit were used in the experiment for testing their specificity and the sensitivity in nested PCR by using spores from Glomus mosseae (BEG12), Glomus intraradices (BEG141), Scutellospora castaneae (BEG1) and two unidentified Glomus sp. HAUO3 and HAUO4. The feasibility assay of nested multiplex PCR was conducted by use of spore mixture, Astragalus sinicum roots co-inoculated with 4 species of arbuscular mycorrhizal fungi from pot cultures and 15 different field-growing plant roots respectively after analyses of the compatibility of primers. The result indicated that the sensitivity was in the same range as that of the corresponding single PCR reaction. Overall accuracy was 95%. The efficiency and sensitivity of this multiplex PCR procedure provided a rapid and easy way to simultaneously detect several of arbuscular mycorrhizal fungal species in a same plant root system.     

Arbuscular mycorrhizal fungus-promoted accumulation of two new triterpenoids in cucumber roots

Cucumber (Cucumis sativus L.) roots were analyzed by HPLC and TLC for their levels of secondary metabolites upon inoculation with the arbuscular mycorrhizal fungus, Glomus caledonium. Three compounds in EtOAc extracts from the mycorrhizal roots showed significant increases six weeks after inoculation. These compounds were isolated by column chromatography and determined to be two novel triterpenes, 2beta-hydroxybryonolic acid (2beta,3beta-dihydroxy-D:C-friedoolean-8-en-29-oic acid) and 3beta-bryoferulic acid [3beta-O-trans-ferulyl-D:C-friedooleana-7,9(11)-diene-29-oic acid], and the known triterpene, bryonolic acid, by spectroscopic methods. Time-course experiments showed that the levels of the three terpenoids in cucumber roots were significantly increased by the application of a 53-microm sieving from a soil inoculum of the arbuscular mycorrhizal fungus containing soil microbes but no mycorrhizal fungi, and that mycorrhizal colonization further promoted the terpenoid accumulation. Inoculation with Glomus mosseae also enhanced the accumulation of the triterpenes, whereas no accumulation was observed by inoculating with the fungal pathogen, Fusarium oxysporum f. sp. cucumerinum. 2Beta-hydroxybryonolic acid was also isolated from the roots of melon and watermelon.     

Distribution of arbuscular mycorrhizal fungi in marshy and shoreline vegetation of Deepar Beel Ramsar Site of Assam,India

Arbuscular mycorrhizal fungal (AMF) symbiosis was thought to be rare in wetland plant roots, although several recent studies suggested that this association might be important in wetland ecosystems. In this research work we have studied the distribution of AMF in the marshy and shoreline vegetation of Deepar Beel Ramsar site of Assam, India. The study reveals the percentage of mycorrhizal colonization in the roots of different plant species which were observed from 20.89 to 86.47% and particularly found larger among the members of the family Poaceae. The Vetiveria zizanioides L. from the family Cyperaceae showed the highest (86.47%) percentage of root colonization, however, only one plant species viz. Scirpus lateriflorus Gmel. from the same family was found to be nonmycorrhizal. The rhizospheric soil samples of most of the plant species were found to be dominated by Glomus morphotypes. All total 18 AMF morphotypes were recorded which comprises four genera viz. Glomus (66.67%), Acaulospora (16.66%), Gigaspora (11.11%) and Scutellospora (5.56%). The observation of diversity of AMF in 25 different plant species among the wetland plants gives a glimpse of AMF diversity and their host selectivity in the said ecosystem.     

Arbuscular mycorrhiza of Arnica montana under field conditions—conventional and molecular studies

Two distinct populations of Arnica montana, an endangered medicinal plant, were studied under field conditions. The material was investigated using microscopic and molecular methods. The analyzed plants were always found to be mycorrhizal. Nineteen arbuscular mycorrhizal fungal DNA sequences were obtained from the roots. They were related to Glomus Group A, but most did not match any known species. Some showed a degree of similarity to fungi colonizing liverworts. Conventional analysis of spores isolated from soil samples allowed to identify different fungal taxa: Glomus macrocarpum, Glomus mosseae, Acaulospora lacunosa, and Scutellospora dipurpurescens. Their spores were also isolated from trap cultures.     

南方红豆杉丛枝菌根(AM)的研究

研究了南方红豆杉根部丛枝菌根真菌(AMF)侵染情况、菌根形态结构以及根际土中AMF孢子的种类与数量.结果显示:南方红豆杉可与AMF形成典型的丛枝-泡囊型菌根,侵染率在71.2%~94.4%,但是历山、蟒河自然保护区的侵染强度优于人工栽培区;在南方红豆杉根际土中共分离鉴定出5种AMF,无梗囊霉属1种、球囊霉属4种,分别是:光壁无梗囊霉、地表球囊霉、地球囊霉、缩球囊霉、明球囊霉,其中光壁无梗囊霉为优势种;南方红豆杉的根由表皮、外皮层、内皮层、中柱组成,AMF只侵染表皮层、内皮层,不能侵染中柱.这为将来利用AMF接种技术进行南方红豆杉的繁殖、移植栽培以及紫杉醇的积累等研究提供了理论依据.     

Role of Extrinsic Arbuscular Mycorrhizal Fungi in Heavy Metal-Contaminated Wetlands with Various Soil Moisture Levels

This study presents an efficient heavy metal (HM) control method in HM-contaminated wetlands with varied soil moisture levels through the introduction of extrinsic arbuscular mycorrhizal fungi (AMF) into natural wetland soil containing indigenous AMF species. A pot culture experiment was designed to determine the effect of two soil water contents (5–8% and 25–30%), five extrinsic AMF inoculants (Glomus mosseae, G. clarum, G. claroideum, G. etunicatum, and G. intraradices), and HM contamination on root colonization, plant growth, and element uptake of common reed (Phragmites australis (Cav.) Trin. ex Steudel) plantlets in wetland soils. This study showed the prevalence of mycorrhizae in the roots of all P. australis plantlets, regardless of extrinsic AMF inoculations, varied soil moisture or HM levels. It seems that different extrinsic AMF inoculations effectively lowered HM concentrations in the aboveground tissues of P. australis at two soil moisture levels. However, metal species, metal concentrations, and soil moisture should also be very important factors influencing the elemental uptake performance of plants in wetland ecosystems. Besides, the soil moisture level significantly influenced plant growth (including height, and shoot and root dry weight (DW)), and extrinsic AMF inoculations differently affected shoot DW.     

Mycorrhizal status and diversity of fungal endophytes in roots of common buckwheat (Fagopyrum esculentum) and tartary buckwheat (F. tataricum)

To determine the mycorrhizal status and to identify the fungi colonising the roots of the plants, common buckwheat (Fagopyrum esculentum) and tartary buckwheat (F. tataricum) were inoculated with an indigenous fungal mixture from a buckwheat field. Root colonisation was characterised by the hyphae and distinct microsclerotia of dark septate endophytes, with occasional arbuscules and vesicles of arbuscular mycorrhizal fungi. Sequences of arbuscular mycorrhizal fungi colonising tartary buckwheat clustered close to the Glomus species group A. Sequences with similarity to the Ceratobasidium/Rhizoctonia complex, a putative dark septate endophyte fungus, were amplified from the roots of both common and tartary buckwheat. To the best of our knowledge, this is the first report of arbuscular mycorrhizal colonisation in tartary buckwheat and the first molecular characterisation of these fungi that can colonise both of these economically important plant species.     

13C incorporation into signature fatty acids as an assay for carbon allocation in arbuscular mycorrhiza

The ubiquitous arbuscular mycorrhizal fungi consume significant amounts of plant assimilated C, but this C flow has been difficult to quantify. The neutral lipid fatty acid 16:1omega5 is a quantitative signature for most arbuscular mycorrhizal fungi in roots and soil. We measured carbon transfer from four plant species to the arbuscular mycorrhizal fungus Glomus intraradices by estimating (13)C enrichment of 16:1omega5 and compared it with (13)C enrichment of total root and mycelial C. Carbon allocation to mycelia was detected within 1 day in monoxenic arbuscular mycorrhizal root cultures labeled with [(13)C]glucose. The (13)C enrichment of neutral lipid fatty acid 16:1omega5 extracted from roots increased from 0.14% 1 day after labeling to 2.2% 7 days after labeling. The colonized roots usually were more enriched for (13)C in the arbuscular mycorrhizal fungal neutral lipid fatty acid 16:1omega5 than for the root specific neutral lipid fatty acid 18:2omega6,9. We labeled plant assimilates by using (13)CO(2) in whole-plant experiments. The extraradical mycelium often was more enriched for (13)C than was the intraradical mycelium, suggesting rapid translocation of carbon to and more active growth by the extraradical mycelium. Since there was a good correlation between (13)C enrichment in neutral lipid fatty acid 16:1omega5 and total (13)C in extraradical mycelia in different systems (r(2) = 0.94), we propose that the total amount of labeled C in intraradical and extraradical mycelium can be calculated from the (13)C enrichment of 16:1omega5. The method described enables evaluation of C flow from plants to arbuscular mycorrhizal fungi to be made without extraction, purification and identification of fungal mycelia.