Literature DB >> 25213652

Soil propagule banks of ectomycorrhizal fungi along forest development stages after mining.

Jian Huang1, Kazuhide Nara, Kun Zong, Chunlan Lian.   

Abstract

Ectomycorrhizal fungal (EMF) propagules play an important role in seedling establishment following disturbance. However, little is known about how the EMF propagule community changes with forest development. In this study, EMF propagules were examined using seedling bioassays in rhizosphere soils collected from a recently closed Pb-Zn tailing (Taolin Pb-Zn tailing (TLT)), a Cu tailing (Dexing Cu No. 2 tailing (DXT)) that had undergone 21 years of restoration, and a mature Masson pine (Pinus massoniana) forest (DXC) outside the Cu mining areas. The corresponding EMF communities colonizing Masson pine at each site were also investigated for comparison. After 8 months of running bioassays, ectomycorrhizal colonization was poor for seedlings grown in TLT (9.0 % ± 14.9 %) and DXT soils (22.4 % ± 17.7 %), while DXC seedlings were well colonized (47.5 % ± 24.9 %). Internal transcribed spacer sequencing revealed that EMF species richness increased with forest development in both the propagule bank (TLT, 6; DXT, 7; DXC, 12) and in the field (TLT, 8; DXT, 14; DXC, 26), though richness was lower in propagule banks. Several lineages, such as Cenococcum, Rhizopogon, Inocybe, Suillus, and Atheliaceae, were frequently encountered in propagule communities, but species assemblages were different among the three sites. Canonical correspondence analysis revealed that several soil parameters, i.e., N, EC, Cu, Pb, Zn, etc., were responsible for the distribution of EMF in the field and bioassay seedlings. The highest overlap in EMF species composition between the propagule bank and the field community was observed at the recently closed tailing (Morisita-Horn similarity = 0.71 for TLT), whereas the lowest overlap occurred at the mature forest (0.26 for DXC). These results indicate that EMF propagules in soil are less frequent and diverse in early primary succession and become more frequent and diverse along forest development, due mainly to the accumulation of dormant spores of Rhizopogon spp. and sclerotia of Cenococcum spp. Thus, EMF propagule communities in soil may diverge from those root-colonizing EMF communities along a gradient of forest development.

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Year:  2014        PMID: 25213652     DOI: 10.1007/s00248-014-0484-4

Source DB:  PubMed          Journal:  Microb Ecol        ISSN: 0095-3628            Impact factor:   4.552


  15 in total

1.  Bioavailability, mobility, and toxicity of Cu in soils around the Dexing Cu mine in China.

Authors:  Guangyong Guo; Tao Yuan; Wenhua Wang; Dan Li; Jinping Cheng; Yang Gao; Pei Zhou
Journal:  Environ Geochem Health       Date:  2010-08-10       Impact factor: 4.609

2.  UNITE: a database providing web-based methods for the molecular identification of ectomycorrhizal fungi.

Authors:  Urmas Kõljalg; Karl-Henrik Larsson; Kessy Abarenkov; R Henrik Nilsson; Ian J Alexander; Ursula Eberhardt; Susanne Erland; Klaus Høiland; Rasmus Kjøller; Ellen Larsson; Taina Pennanen; Robin Sen; Andy F S Taylor; Leho Tedersoo; Trude Vrålstad; Björn M Ursing
Journal:  New Phytol       Date:  2005-06       Impact factor: 10.151

3.  Ectomycorrhizal networks and seedling establishment during early primary succession.

Authors:  Kazuhide Nara
Journal:  New Phytol       Date:  2006       Impact factor: 10.151

4.  Germination and infectivity of ectomycorrhizal fungal spores in relation to their ecological traits during primary succession.

Authors:  Takahide A Ishida; Kazuhide Nara; Megumi Tanaka; Akihiko Kinoshita; Taizo Hogetsu
Journal:  New Phytol       Date:  2008-07-22       Impact factor: 10.151

5.  Inoculum potential of Rhizopogon spores increases with time over the first 4 yr of a 99-yr spore burial experiment.

Authors:  Thomas D Bruns; Kabir G Peay; Primrose J Boynton; Lisa C Grubisha; Nicole A Hynson; Nhu H Nguyen; Nicholas P Rosenstock
Journal:  New Phytol       Date:  2009-01       Impact factor: 10.151

Review 6.  Ectomycorrhizal lifestyle in fungi: global diversity, distribution, and evolution of phylogenetic lineages.

Authors:  Leho Tedersoo; Tom W May; Matthew E Smith
Journal:  Mycorrhiza       Date:  2009-09-16       Impact factor: 3.387

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Journal:  FEMS Microbiol Ecol       Date:  2011-01-20       Impact factor: 4.194

8.  Host plant genus-level diversity is the best predictor of ectomycorrhizal fungal diversity in a Chinese subtropical forest.

Authors:  Cheng Gao; Nan-Nan Shi; Yue-Xing Liu; Kabir G Peay; Yong Zheng; Qiong Ding; Xiang-Cheng Mi; Ke-Ping Ma; Tesfaye Wubet; François Buscot; Liang-Dong Guo
Journal:  Mol Ecol       Date:  2013-06       Impact factor: 6.185

9.  Tricholoma matsutake in a natural Pinus densiflora forest: correspondence between above- and below-ground genets, association with multiple host trees and alteration of existing ectomycorrhizal communities.

Authors:  Chunlan Lian; Maki Narimatsu; Kazuhide Nara; Taizo Hogetsu
Journal:  New Phytol       Date:  2006       Impact factor: 10.151

10.  Impact of wildfire return interval on the ectomycorrhizal resistant propagules communities of a Mediterranean open forest.

Authors:  Erika Buscardo; Susana Rodríguez-Echeverría; María P Martín; Paolo De Angelis; João Santos Pereira; Helena Freitas
Journal:  Fungal Biol       Date:  2010-05-21
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  8 in total

1.  Soil propagule banks of ectomycorrhizal fungi share many common species along an elevation gradient.

Authors:  Yumiko Miyamoto; Kazuhide Nara
Journal:  Mycorrhiza       Date:  2015-08-01       Impact factor: 3.387

2.  Growth and photosynthetic responses of ectomycorrhizal pine seedlings exposed to elevated Cu in soils.

Authors:  Yahua Chen; Kazuhide Nara; Zhugui Wen; Liang Shi; Yan Xia; Zhenguo Shen; Chunlan Lian
Journal:  Mycorrhiza       Date:  2015-02-27       Impact factor: 3.387

3.  Soil spore bank communities of ectomycorrhizal fungi in endangered Chinese Douglas-fir forests.

Authors:  Zhugui Wen; Liang Shi; Yangze Tang; Lizhou Hong; Jiawang Xue; Jincheng Xing; Yahua Chen; Kazuhide Nara
Journal:  Mycorrhiza       Date:  2017-09-23       Impact factor: 3.387

4.  Ectomycorrhizal Fungal Communities in Urban Parks Are Similar to Those in Natural Forests but Shaped by Vegetation and Park Age.

Authors:  Nan Hui; Xinxin Liu; D Johan Kotze; Ari Jumpponen; Gaia Francini; Heikki Setälä
Journal:  Appl Environ Microbiol       Date:  2017-11-16       Impact factor: 4.792

5.  Ectomycorrhizal fungal communities in alpine relict forests of Pinus pumila on Mt. Norikura, Japan.

Authors:  Takahiko Koizumi; Masahira Hattori; Kazuhide Nara
Journal:  Mycorrhiza       Date:  2018-01-12       Impact factor: 3.387

6.  Hierarchical neighbor effects on mycorrhizal community structure and function.

Authors:  Holly V Moeller; Ian A Dickie; Duane A Peltzer; Tadashi Fukami
Journal:  Ecol Evol       Date:  2016-07-05       Impact factor: 2.912

7.  Ectomycorrhizal fungal communities in endangered Pinus amamiana forests.

Authors:  Masao Murata; Seiichi Kanetani; Kazuhide Nara
Journal:  PLoS One       Date:  2017-12-19       Impact factor: 3.240

8.  Soil propagule bank of ectomycorrhizal fungi associated with Masson pine (Pinus massoniana) grown in a manganese mine wasteland.

Authors:  Jian Huang; Qisheng Han; Junjian Li
Journal:  PLoS One       Date:  2018-06-05       Impact factor: 3.240

  8 in total

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