Literature DB >> 21642124

Salt tolerance and osmotic adjustment of Spartina alterniflora (Poaceae) and the invasive M haplotype of Phragmites australis (Poaceae) along a salinity gradient.

Edward A Vasquez1, Edward P Glenn, Glenn R Guntenspergen, J Jed Brown, Stephen G Nelson.   

Abstract

An invasive variety of Phragmites australis (Poaceae, common reed), the M haplotype, has been implicated in the spread of this species into North American salt marshes that are normally dominated by the salt marsh grass Spartina alterniflora (Poaceae, smooth cordgrass). In some European marshes, on the other hand, Spartina spp. derived from S. alterniflora have spread into brackish P. australis marshes. In both cases, the non-native grass is thought to degrade the habitat value of the marsh for wildlife, and it is important to understand the physiological processes that lead to these species replacements. We compared the growth, salt tolerance, and osmotic adjustment of M haplotype P. australis and S. alterniflora along a salinity gradient in greenhouse experiments. Spartina alterniflora produced new biomass up to 0.6 M NaCl, whereas P. australis did not grow well above 0.2 M NaCl. The greater salt tolerance of S. alterniflora compared with P. australis was due to its ability to use Na(+) for osmotic adjustment in the shoots. On the other hand, at low salinities P. australis produced more shoots per gram of rhizome tissue than did S. alterniflora. This study illustrates how ecophysiological differences can shift the competitive advantage from one species to another along a stress gradient. Phragmites australis is spreading into North American coastal marshes that are experiencing reduced salinities, while Spartina spp. are spreading into northern European brackish marshes that are experiencing increased salinities as land use patterns change on the two continents.

Entities:  

Year:  2006        PMID: 21642124     DOI: 10.3732/ajb.93.12.1784

Source DB:  PubMed          Journal:  Am J Bot        ISSN: 0002-9122            Impact factor:   3.844


  10 in total

1.  Biomass production, photosynthesis, and leaf water relations of Spartina alterniflora under moderate water stress.

Authors:  Kamel Hessini; Mohamed Ghandour; Ali Albouchi; Abdelaziz Soltani; Koyro Hans Werner; Chedly Abdelly
Journal:  J Plant Res       Date:  2008-04-04       Impact factor: 2.629

2.  High tolerance to salinity and herbivory stresses may explain the expansion of Ipomoea cairica to salt marshes.

Authors:  Gang Liu; Qiao-Qiao Huang; Zhen-Guang Lin; Fang-Fang Huang; Hui-Xuan Liao; Shao-Lin Peng
Journal:  PLoS One       Date:  2012-11-15       Impact factor: 3.240

Review 3.  Cosmopolitan Species As Models for Ecophysiological Responses to Global Change: The Common Reed Phragmites australis.

Authors:  Franziska Eller; Hana Skálová; Joshua S Caplan; Ganesh P Bhattarai; Melissa K Burger; James T Cronin; Wen-Yong Guo; Xiao Guo; Eric L G Hazelton; Karin M Kettenring; Carla Lambertini; Melissa K McCormick; Laura A Meyerson; Thomas J Mozdzer; Petr Pyšek; Brian K Sorrell; Dennis F Whigham; Hans Brix
Journal:  Front Plant Sci       Date:  2017-11-16       Impact factor: 5.753

4.  Ecophysiological response of native and exotic salt marsh vegetation to waterlogging and salinity: Implications for the effects of sea-level rise.

Authors:  Shi-Hua Li; Zhen-Ming Ge; Li-Na Xie; Wei Chen; Lin Yuan; Dong-Qi Wang; Xiu-Zhen Li; Li-Quan Zhang
Journal:  Sci Rep       Date:  2018-02-05       Impact factor: 4.379

5.  No evidence for local adaptation to salt stress in the existing populations of invasive Solidago canadensis in China.

Authors:  Junmin Li; Haiyan Liu; Ming Yan; Leshan Du
Journal:  PLoS One       Date:  2017-04-06       Impact factor: 3.240

6.  Spatial genetic structure in natural populations of Phragmites australis in a mosaic of saline habitats in the Yellow River Delta, China.

Authors:  Lexuan Gao; Shaoqing Tang; Liqiong Zhuge; Ming Nie; Zhu Zhu; Bo Li; Ji Yang
Journal:  PLoS One       Date:  2012-08-16       Impact factor: 3.240

7.  Interspecific interactions between Phragmites australis and Spartina alterniflora along a tidal gradient in the Dongtan wetland, Eastern China.

Authors:  Yue Yuan; Kaiyun Wang; Dezhi Li; Yu Pan; Yuanyuan Lv; Meixia Zhao; JinJin Gao
Journal:  PLoS One       Date:  2013-01-16       Impact factor: 3.240

8.  Using Transcriptomics to Identify Differential Gene Expression in Response to Salinity among Australian Phragmites australis Clones.

Authors:  Gareth D Holmes; Nathan E Hall; Anthony R Gendall; Paul I Boon; Elizabeth A James
Journal:  Front Plant Sci       Date:  2016-04-13       Impact factor: 5.753

9.  Competitive interactions between native Spartina alterniflora and non-native Phragmites australis depend on nutrient loading and temperature.

Authors:  Rene Legault; Gregory P Zogg; Steven E Travis
Journal:  PLoS One       Date:  2018-02-01       Impact factor: 3.240

10.  Transgene Pyramiding of Salt Responsive Protein 3-1 (SaSRP3-1) and SaVHAc1 From Spartina alterniflora L. Enhances Salt Tolerance in Rice.

Authors:  Hanamareddy Biradar; Ratna Karan; Prasanta K Subudhi
Journal:  Front Plant Sci       Date:  2018-09-12       Impact factor: 5.753

  10 in total

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