Summary1 Genetic differences among populations of a keystone species may affect ecosystem functional properties. We tested this by planting Spartina alterniflora from different geographical regions in a newly created salt marsh in Delaware, USA. 2 Spartina alterniflora plants from morphologically distinct short-form (back marsh) populations were originally collected from Massachusetts (41 ° 34 ′ Ν ), Delaware (38 ° 47 ′ Ν ), and Georgia (31 ° 25 ′ Ν ) in the USA and vegetatively propagated for 6 years in a salt water-irrigated common garden in Delaware before transfer to a newly created salt marsh. 3 The magnitude of the expression of marsh functions in the created marsh, measured over 5 years, remained distinct in patches of each ecotype. End of season aerial biomass, below-ground biomass, root and rhizome distribution, canopy height, stem density, and carbohydrate reserves were closer to values reported for the plants' native sites than to those typical of Delaware. Thus, many of the plant features characteristic of particular latitudes appear to be under genetic control. Such ecotypic differentiation influences ecosystem function through keystone resource and keystone modifier activities. 4 Respiration of the microbial community associated with either dead shoots or the soil varied with plant ecotype in the created wetland and the patterns reflected those reported for their native sites. High edaphic respiration under the Massachusetts ecotype was correlated with the high percentage of sugar in the rhizomes. Edaphic chlorophyll was greater under the canopies of the Massachusetts and Delaware ecotypes than under the Georgia canopy and exhibited a relationship similar to that of algal production rates reported for the native sites. Larval fish were most abundant in pit traps in the Massachusetts ecotype.

Phragmites australis is considered the most invasive plant in marsh and wetland communities in the eastern United States. Although allelopathy has been considered as a possible displacing mechanism in P. australis, there has been minimal success in characterizing the responsible allelochemical. We tested the occurrence of root-derived allelopathy in the invasiveness of P. australis. To this end, root exudates of two P. australis genotypes, BB (native) and P38 (an exotic) were tested for phytotoxicity on different plant species. The treatment of the susceptible plants with P. australis root exudates resulted in acute rhizotoxicity. It is interesting to note that the root exudates of P38 were more effective in causing root death in susceptible plants compared to the native BB exudates. The active ingredient in the P. australis exudates was identified as 3,4,5-trihydroxybenzoic acid (gallic acid). We tested the phytotoxic efficacy of gallic acid on various plant systems, including the model plant Arabidopsis thaliana. Most tested plants succumbed to the gallic acid treatment with the exception of P. australis itself. Mechanistically, gallic acid treatment generated elevated levels of reactive oxygen species (ROS) in the treated plant roots. Furthermore, the triggered ROS mediated the disruption of the root architecture of the susceptible plants by damaging the microtubule assembly. The study also highlights the persistence of the exuded gallic acid in P. australis's rhizosphere and its inhibitory effects against A. thaliana in the soil. In addition, gallic acid demonstrated an inhibitory effect on Spartina alterniflora, one of the salt marsh species it successfully invades.

The C‐4 salt marsh grass, Spartina patens, thrives in the upper portion of the marsh where soil salinities may be equal to coastal seawater. Spartina patens was grown in hydroponic culture in a greenhouse at 0, 340, and 510 mM NaCl, and measured for growth, tissue cation content, and root plasma membrane (PM) lipid composition. From 0 to 340 and 510 mM, the shoot growth decreased, but root growth was not affected. The Na+ content increased in both shoots and roots when plants were grown in salt, while the shoots had a decreased K+ content and the roots had a decreased Ca2+ content. Spartina patens root plasma membrane was isolated with an aqueous polymer two‐phase system. The purity of the plasma membrane was verified with cytochemical tests on membrane enzyme markers. Plasma membrane lipids were stable relative to the membrane protein content. Molar percentages of sterols (including free sterols) and phospholipid decreased with increasing salinity. However, glycolipid showed a statistically significant increase in the total lipid as salinity in the medium was increased from 0 to 510 mM. Even at a salinity of 510 mM, the plasma membrane sterol/phospholipid ratio was unaffected by NaCl. When the plants were grown in NaCl media, the plasma membrane had a decreased phosphatidylcholine (PC) and phosphatidylethanolamine (PE) content, but the PC/PE ratios were not affected. The plasma membrane molar percentage of sitosterol in total free sterol increased when plants were grown in salt media. The predominant membrane fatty acids were C11 and C14, and the major unsaturated one was C14:1. An increase in growth medium salinity resulted in a decreased root plasma membrane fluidity.

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