2021
DOI: 10.1007/s11104-021-05147-w
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Colonization status and community structure of arbuscular mycorrhizal fungi in the coniferous tree, Cryptomeria japonica, with special reference to root orders

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Cited by 19 publications
(13 citation statements)
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“…This discrepancy can be explained by the use of different hosts, sites, seasons, AMF quantification proxies, and overall approaches [ 2 , 4 , 8 ], which varied among prior studies but were controlled in this work. In previous studies of the AMF communities of Cj and Co [ 19 , 20 , 38 ], root and soil OTU richness were not both evaluated, thus precluding comparison of intra- and extraradical AMF communities. In Venn diagrams, the number of AMF OTUs exclusive to the roots of Cj or Co decreased when data from all sites were considered (Online Resource 2 ).…”
Section: Discussionmentioning
confidence: 99%
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“…This discrepancy can be explained by the use of different hosts, sites, seasons, AMF quantification proxies, and overall approaches [ 2 , 4 , 8 ], which varied among prior studies but were controlled in this work. In previous studies of the AMF communities of Cj and Co [ 19 , 20 , 38 ], root and soil OTU richness were not both evaluated, thus precluding comparison of intra- and extraradical AMF communities. In Venn diagrams, the number of AMF OTUs exclusive to the roots of Cj or Co decreased when data from all sites were considered (Online Resource 2 ).…”
Section: Discussionmentioning
confidence: 99%
“…However, no study has assessed Co root colonization. Furthermore, few studies such as those by Zou et al [ 19 ], Matsuda et al [ 20 ], and Djotan et al [ 10 ] have investigated the AMF communities associated with Cj. To our knowledge, no study has compared the AMF community of the roots and surrounding soil of Cj and Co.…”
Section: Introductionmentioning
confidence: 99%
“…According to the MaarjAM, the VTX166 and VTX159 have been detected in various host plants from liverworts to seed plants on six continents. It has also been reported that VTX166 corresponded to one of the dominant OTUs in Japanese temperate forests (Miyake, Ishitsuka, Taniguchi, & Yamato, 2020;Matsuda, Kita, Kitagami, & Tanikawa, 2021). It was suggested that mycoheterotrophic plants preferentially target AM fungi that are well connected to many surrounding autotrophic plants (Gomes et al, 2022).…”
Section: Discussionmentioning
confidence: 90%
“…Genomes of some other types of ascoand basidiomycetous pathogens, such as some on leaves (Dhillon et al 2015;Duplessis et al 2011a;Zhu et al 2012) and of wilt-, blight-and cancer-pathogens in bark and xylem are available, including those of several insect-associated fungal species (Alamouti et al 2011;Comeau et al 2015;Crouch et al 2020;Demené et al 2022;Dhillon et al 2015;Ibarra Caballero et al 2019;Sbaraini et al 2017;Schuelke et al 2017;Stauber et al 2020;Stenlid et al 2017;Yin et al 2015). There is also a growing collection of genomes of symbiotic ECM species (e.g., Kohler et al 2015;Lofgren et al 2021;Looney et al 2022;Martin et al 2008Martin et al , 2010Martino et al 2018;Miyauchi et al 2020b;Peter et al 2016;Wagner et al 2015), some ericoid mycorrhizal ascomycetous fungi (Kohler et al 2015;Martino et al 2018;Perotto et al 2018), an arbuscular mycorrhizal fungus from the conifer Cryptomeria japonica (Matsuda et al 2021), and of a few tree endophytes (Gazis et al 2016;Knapp et al 2018;Schlegel et al 2016) while plant litter decay fungi and in general saprotrophic soil fungi have so far rather been neglected (Barbi et al 2020).…”
Section: Fungal Genomes and Transcriptomesmentioning
confidence: 99%