Cosmopolitan Species As Models for Ecophysiological Responses to Global Change: The Common Reed Phragmites australis
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články, přehledy
PubMed
29250081
PubMed Central
PMC5715336
DOI
10.3389/fpls.2017.01833
Knihovny.cz E-zdroje
- Klíčová slova
- atmospheric CO2, climate change, eutrophication, global distribution, intraspecific variation, invasive species, salinity, temperature,
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Phragmites australis is a cosmopolitan grass and often the dominant species in the ecosystems it inhabits. Due to high intraspecific diversity and phenotypic plasticity, P. australis has an extensive ecological amplitude and a great capacity to acclimate to adverse environmental conditions; it can therefore offer valuable insights into plant responses to global change. Here we review the ecology and ecophysiology of prominent P. australis lineages and their responses to multiple forms of global change. Key findings of our review are that: (1) P. australis lineages are well-adapted to regions of their phylogeographic origin and therefore respond differently to changes in climatic conditions such as temperature or atmospheric CO2; (2) each lineage consists of populations that may occur in geographically different habitats and contain multiple genotypes; (3) the phenotypic plasticity of functional and fitness-related traits of a genotype determine the responses to global change factors; (4) genotypes with high plasticity to environmental drivers may acclimate or even vastly expand their ranges, genotypes of medium plasticity must acclimate or experience range-shifts, and those with low plasticity may face local extinction; (5) responses to ancillary types of global change, like shifting levels of soil salinity, flooding, and drought, are not consistent within lineages and depend on adaptation of individual genotypes. These patterns suggest that the diverse lineages of P. australis will undergo intense selective pressure in the face of global change such that the distributions and interactions of co-occurring lineages, as well as those of genotypes within-lineages, are very likely to be altered. We propose that the strong latitudinal clines within and between P. australis lineages can be a useful tool for predicting plant responses to climate change in general and present a conceptual framework for using P. australis lineages to predict plant responses to global change and its consequences.
Aquatic Biology Department of Bioscience Aarhus University Aarhus Denmark
College of Landscape Architecture and Forestry Qingdao Agricultural University Qingdao China
Department of Agricultural Sciences University of Bologna Bologna Italy
Department of Biological Sciences Louisiana State University Baton Rouge LA United States
Department of Biology Bryn Mawr College Bryn Mawr PA United States
Department of Ecology Faculty of Science Charles University Prague Czechia
Department of Entomology Kansas State University Manhattan KS United States
Department of Landscape Architecture and Horticulture Temple University Ambler PA United States
Department of Natural Resources Science University of Rhode Island Kingston RI United States
Department of Watershed Sciences and Ecology Center Utah State University Logan UT United States
Institute of Botany The Czech Academy of Sciences Průhonice Czechia
Institute of Ecology and Biodiversity School of Life Sciences Shandong University Jinan China
Smithsonian Environmental Research Center Edgewater MD United States
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Achenbach L., Brix H. (2013). Can differences in salinity tolerance explain the distribution of four genetically distinct lineages of DOI
Achenbach L., Brix H. (2014). Monitoring the short-term response to salt exposure of two genetically distinct DOI
Achenbach L., Eller F., Nguyen L. X., Brix H. (2013). Differences in salinity tolerance of genetically distinct DOI
Achenbach L., Lambertini C., Brix H. (2012). Phenotypic traits of PubMed DOI PMC
Afreen F., Zobayed S. M. A., Armstrong J., Armstrong W. (2007). Pressure gradients along whole culms and leaf sheaths, and other aspects of humidity-induced gas transport in PubMed DOI
Ainsworth E. A., Rogers A. (2007). The response of photosynthesis and a stomatal conductance to rising CO PubMed DOI
Allen W. J., Meyerson L. A., Cummings D., Anderson J., Bhattarai G. P., Cronin J. T. (2017). Biogeography of a plant invasion: drivers of latitudinal variation in enemy release. DOI
Almeida J. P., Montúfar R., Anthelme F. (2013). Patterns and origin of intraspecific functional variability in a tropical alpine species along an altitudinal gradient. DOI
Alvarez M. G., Tron F., Mauchamp A. (2005). Sexual versus asexual colonization by DOI
Antonielli M., Pasqualini S., Batini P., Ederli L., Massacci A., Loreto F. T. I. (2002). Physiological and anatomical characterisation of DOI
Araki R., Mori M., Mori M., Hasegawa H. (2005). Genetic differences in nitrate uptake in two clones of the common reed, DOI
Armstrong J., Armstrong W. (1991). A convective through-flow of gases in DOI
Armstrong J., Armstrong W., Armstrong I. B., Pittaway G. R. (1996a). Senescence, and phytotoxin, insect, fungal and mechanical damage: factors reducing convective gas-flows in DOI
Armstrong J., Armstrong W., Beckett P. M., Halder J. E., Lythe S., Holt R., et al. (1996b). Pathways of aeration and the mechanisms and beneficial effects of humidity- and Venturi-induced convections in DOI
Armstrong W., Armstrong J., Beckett P. M. (1996c). Pressurized aeration in wetland macrophytes: some theoretical aspects of humidity-induced convection and thermal transpiration. DOI
Aspinwall M. J., Lowry D. B., Taylor S. H., Juenger T. E., Hawkes C. V., Johnson M. V. V., et al. (2013). Genotypic variation in traits linked to climate and aboveground productivity in a widespread C PubMed DOI
Baldwin A. H., Kettenring K. M., Whigham D. F. (2010). Seed banks of DOI
Bart D., Hartman J. M. (2003). The role of large rhizome dispersal and low salinity windows in the establishment of common reed, DOI
Bastlová D., Bastl M., Cizkova H., Kvet J. (2006). Plasticity of DOI
Beckett L. H., Baldwin A. H., Kearney M. S. (2016). Tidal marshes across a chesapeake bay subestuary are not keeping up with sea-level rise. PubMed DOI PMC
Bender M. A., Knutson T. R., Tuleya R. E., Sirutis J. J., Vecchi G. A., Garner S. T., et al. (2010). Modeled impact of anthropogenic warming on the frequency of intense Atlantic hurricanes. PubMed DOI
Bernal B., Megonigal J. P., Mozdzer T. J. (2017). An invasive wetland grass primes deep soil carbon pools. PubMed DOI
Bhattarai G. P., Cronin J. T. (2014). Hurricane activity and the large-scale pattern of spread of an invasive plant species. PubMed DOI PMC
Bhattarai G. P., Meyerson L. A., Anderson J., Cummings D., Allen W. J., Cronin J. T. (2017a). Biogeography of a plant invasion: genetic variation and plasticity in latitudinal clines for traits related to herbivory. DOI
Bhattarai G. P., Meyerson L. A., Cronin J. T. (2017b). Geographical variation in apparent competition between native and invasive PubMed DOI
Bodensteiner L. R., Gabriel A. O. (2003). Response of mid-water common reed stands to water level variations and winter conditions in Lake Poygan, Wisconsin, United States. DOI
Bolnick D. I., Amarasekare P., Arau jo M. S., Bürger R., Levine J. M., Novak M. (2011). Why intraspecific trait variation matters in community ecology. PubMed DOI PMC
Bradshaw A. D. (1965). Evolutionary significance of phenotypic plasticity in plants. DOI
Bragato C., Brix H., Malagoli M. (2006). Accumulation of nutrients and heavy metals in PubMed DOI
Bräutigam A., Gowik U. (2016). Photorespiration connects C PubMed DOI
Brisson J., Paradis E., Bellavance M. E. (2008). Evidence of sexual reproduction in the invasive common reed ( DOI
Brix H. (1989). Gas-Exchange through dead culms of reed, DOI
Brix H. (1997). Do macrophytes play a role in constructed treatment wetlands?
Brix H. (1999a). Genetic diversity, ecophysiology and growth dynamics of reed (
Brix H. (1999b). The European research project on reed die-back and progression (EUREED). DOI
Brix H., Schierup H. H. (1989). The use of aquatic macrophytes in water-pollution control.
Brix H., Sorrell B. K., Lorenzen B. (2001). Are DOI
Brix H., Sorrell B. K., Orr P. T. (1992). Internal pressurization and convective gas flow in some emergent freshwater macrophytes. DOI
Brix H., Sorrell B. K., Schierup H. H. (1996). Gas fluxes achieved by in situ convective flow in DOI
Burdick D. M., Buchsbaum R., Holt E. (2001). Variation in soil salinity associated with expansion of PubMed DOI PMC
Burdick D. M., Konisky R. A. (2003). Determinants of expansion for DOI
Caplan J. S., Hager R. N., Megonigal J. P., Mozdzer T. J. (2015). Global change accelerates carbon assimilation by a wetland ecosystem engineer. DOI
Caplan J. S., Wheaton C. N., Mozdzer T. J. (2014). Belowground advantages in construction cost facilitate a cryptic plant invasion. PubMed DOI PMC
Chambers R., Osgood D., Bart D., Montalto F. (2003). DOI
Chambers R. M., Meyerson L. A., Saltonstall K. (1999). Expansion of DOI
Chambers R. M., Mozdzer T. J., Ambrose J. C. (1998). Effects of salinity and sulfide on the distribution of DOI
Chapman D. S., Haynes T., Beal S., Essl F., Bullock J. M. (2014). Phenology predicts the native and invasive range limits of common ragweed. PubMed DOI
Chaves M. M., Pereira J. S., Maroco J., Rodrigues M. L., Ricardo C. P. P., Osório M. L., et al. (2002). How plants cope with water stress in the field? Photosynthesis and growth. PubMed DOI PMC
Chen K. M., Gong H. J., Chen G. C., Wang S. M., Zhang C. L. (2003). Up-regulation of glutathione metabolism and changes in redox status involved in adaptation of reed ( PubMed DOI
Christin P. A., Salamin N., Kellogg E. A., Vicentini A., Besnard G. (2009). Integrating phylogeny into studies of C PubMed DOI PMC
Chu H., Cho W. K., Jo Y. (2011). Identification of natural hybrids in Korean Phragmites using haplotype and genotype analyses. DOI
Čížková H., Brix H., Kopecky J., Lukavska J. (1999). Organic acids in the sediments of wetlands dominated by DOI
Cizkova-Koncalova H., Kvet J., Thompson K. (1992). Carbon starvation: a key to reed decline in eutrophic lakes. DOI
Clevering O. A. (1998). Effects of litter accumulation and water table on morphology and productivity of DOI
Clevering O. A. (1999). Between-and within-population differences in PubMed DOI
Clevering O. A., Brix H., Lukavská J. (2001). Geographic variation in growth responses in PubMed DOI
Clevering O. A., Lissner J. (1999). Taxonomy, chromosome numbers, clonal diversity and population dynamics of DOI
Colautti R. I., Alexander J. M., Dlugosch K. M., Keller S. R., Sultan S. E. (2017). Invasions and extinctions through the looking glass of evolutionary ecology. PubMed DOI PMC
Coomes D. A., Grubb P. J. (2000). Impacts of root competition in forests and woodlands: a theoretical framework and review of experiments. DOI
Coops H., van den Brink F. W. B., van der Velde G. (1996). Growth and morphological responses of four helophyte species in an experimental water-depth gradient. DOI
Cronin J. T., Bhattarai G. P., Allen W. J., Meyerson L. A. (2015). Biogeography of a plant invasion: plant-herbivore interactions. PubMed DOI
Crutsinger G. M., Souza L., Sanders N. J. (2008). Intraspecific diversity and dominant genotypes resist plant invasions. PubMed
Cui B., Hua Y., Wang C., Liao X., Tan X., Tao W. (2010). Estimation of ecological water requirements based on habitat response to water level in Huanghe River Delta, China. DOI
Den Hartog C., Květ J., Sukopp H. (1989). Reed. A common species in decline. DOI
Douhovnikoff V., Hazelton E. L. (2014). Clonal growth: Invasion or stability? A comparative study of clonal architecture and diversity in native and introduced lineages of PubMed DOI
Drenovsky R. E., Grewell B. J., D’Antonio C. M., Funk J. L., James J. J., Molinari N., et al. (2012). A functional trait perspective on plant invasion. PubMed DOI PMC
Dukes J. S., Mooney H. A. (1999). Does global change increase the success of biological invaders? PubMed
Dykyjová D., Ondok J. P., Priban K. (1970). Seasonal changes in productivity and vertical structure of reed-stands (
Eid I. M., Shaltout K. H., Al-Sodany Y. M., Kai Jensen K. (2010). Effects of abiotic conditions on DOI
Elhaak M. A., Eldin A. S., Sammour R. H. (1993). Response of
Eller F., Brix H. (2012). Different genotypes of DOI
Eller F., Lambertini C., Nguyen L. X., Achenbach L., Brix H. (2013). Interactive effects of elevated temperature and CO DOI
Eller F., Lambertini C., Nguyen L. X., Brix H. (2014a). Increased invasive potential of non-native PubMed
Eller F., Lambertini C., Nielsen M. W., Radutoiu S., Brix H. (2014b). Expression of major photosynthetic and salt-resistance genes in invasive reed lineages grown under elevated CO PubMed DOI PMC
Engels J. G., Jensen K. (2010). Role of biotic interactions and physical factors in determining the distribution of marsh species along an estuarine salinity gradient. DOI
Engloner A. I. (2004). Annual growth dynamics and morphological differences of reed ( DOI
Engloner A. I. (2009). Structure, growth dynamics and biomass of reed ( DOI
Engloner A. I., Major A. (2011). Clonal diversity of DOI
Engloner A. I., Szego D. (2016). Genetic diversity of riverine reed stands indicating the water regime of the habitat. DOI
Erdei L., Horváth F., Tari I., Pécsváradi A., Szegletes Z., Dulai S. (2001). Differences in photorespiration, glutamine synthetase and polyamines between fragmented and closed stands of DOI
Franks S. J., Weber J. J., Aitken S. N. (2014). Evolutionary and plastic responses to climate change in terrestrial plant populations. PubMed DOI PMC
Galloway J. N., Dentener F. J., Capone D. G., Boyer E. W., Howarth R. W., Seitzinger S. P., et al. (2004). Nitrogen cycles: past, present, and future. DOI
Gao L., Tang S., Zhuge L., Nie M., Zhu Z., Li B., et al. (2012). Spatial genetic structure in natural populations of PubMed DOI PMC
Ge Z. M., Zhang L. Q., Yuan L., Zhang C. (2014). Effects of salinity on temperature-dependent photosynthetic parameters of a native C DOI
Gigante D., Angiolini C., Landucci F., Maneli F., Nisi B., Vaselli O., et al. (2014). New occurrence of reed bed decline in southern Europe: do permanent flooding and chemical parameters play a role? PubMed DOI
Gioria M., Osborne B. A. (2014). Resource competition in plant invasions: emerging patterns and research needs. PubMed DOI PMC
Gong C. M., Bai J., Deng J. M., Wang G. X., Liu X. P. (2011). Leaf anatomy and photosynthetic carbon metabolic characteristics in DOI
Gorai M., Vadel A. M., Neffati M. (2006). Seed germination characteristics of
Gorenflot R., Hubac J. M., Jay M., Lalande P. (1983). “Geographic distribution, polyploidy and pattern of flavonoids in
Gries C., Kappen L., Losch R. (1990). Mechanism of flood tolerance in reed, DOI
Guo W.-Y., Lambertini C., Li X.-Z., Meyerson L. M., Brix H. (2013). Invasion of Old World PubMed
Guo W.-Y., Lambertini C., Nguyen L. X., Li X.-Z., Brix H. (2014). Preadaptation and post-introduction evolution facilitate the invasion of PubMed DOI PMC
Han Z., Cui B. (2016). Performance of macrophyte indicators to eutrophication pressure in ponds. DOI
Hanganu J., Mihail G., Coops H. (1999). Responses of ecotypes of DOI
Hansen D. L., Lambertini C., Jampeetong A., Brix H. (2007). Clone-specific differences in DOI
Haslam S. M. (1970). The performance of DOI
Haslam S. M. (1972). DOI
Haslam S. M. (1973). Some aspects of the life history and autecology of
Haslam S. M. (1975). The performance of DOI
Hauber D. P., Saltonstall K., White D. A., Hood C. S. (2011). Genetic variation in the common reed, DOI
Hauber D. P., White D. A., Powers S. P., Defrancesch F. R. (1991). Isozyme variation and correspondence with unusual infrared reflectance patterns in DOI
Hazelton E. L., Mozdzer T. J., Burdick D. M., Kettenring K. M., Whigham D. F. (2014). PubMed DOI PMC
Hazelton E. L. G., Knight T. J., Theodose T. A. (2010). Glutamine synthetase partitioning in native and introduced salt marsh grasses. DOI
Hellings S. E., Gallagher J. L. (1992). The effects of salinity and flooding on PubMed DOI
Henriques F. S., Webb M. E. (1989). Comparative study of two grasses from different habitats by scanning electron microscopy. DOI
Hernández-Crespo C., Oliver N., Bixquert J., Gargallo S., Martín M. (2016). Comparison of three plants in a surface flow constructed wetland treating eutrophic water in a Mediterranean climate. DOI
Hiesey W. M., Clausen J., Keck D. D. (1942). Relations between climate and intraspecific variation in plants. DOI
Holdredge C., Bertness M. D., von Wettberg E., Silliman B. R. (2010). Nutrient enrichment enhances hidden differences in phenotype to drive a cryptic plant invasion. DOI
Holmes G. D., Hall N. E., Gendall A. R., Boon P. I., James E. A. (2016). Using transcriptomics to identify differential gene expression in response to salinity among Australian PubMed DOI PMC
Hughes A. R., Schenck F. R., Bloomberg J., Hanley T. C., Feng D., Gouhier T. C., et al. (2016). Biogeographic gradients in ecosystem processes of the invasive ecosystem engineer DOI
Ikegami M., van Hal S., van Rheenen J. W. A., Whigham D. F., Werger M. J. A. (2008). Spatial division of labor of DOI
IPCC (2007).
IPCC (2014).
Irmak S., Kabenge I., Rudnick D., Knezevic S., Woodward D., Moravek M. (2013). Evapotranspiration crop coefficients for mixed riparian plant community and transpiration crop coefficients for Common reed, Cottonwood and Peach-leaf willow in the Platte River Basin, Nebraska-United States. DOI
Jackson M. B., Armstrong W. (1999). Formation of aerenchyma and the processes of plant ventilation in relation to soil flooding and submergence. DOI
Jump A. S., Peñuelas J. (2005). Running to stand still: adaptation and the response of plants to rapid climate change. PubMed DOI
Karunaratne S., Asaeda T., Yutani K. (2003). Growth performance of DOI
Kettenring K. M., de Blois S., Hauber D. P. (2012). Moving from a regional to a continental perspective of PubMed DOI PMC
Kettenring K. M., McCormick M. K., Baron H. M., Whigham D. F. (2010). DOI
Kettenring K. M., McCormick M. K., Baron H. M., Whigham D. F. (2011). Mechanisms of DOI
Kettenring K. M., Mock K. E. (2012). Genetic diversity, reproductive mode, and dispersal differ between the cryptic invader, DOI
Kettenring K. M., Mock K. E., Zaman B., McKee M. (2016). Life on the edge: reproductive mode and rate of invasive DOI
Kettenring K. M., Whigham D. F. (2009). Seed viability and seed dormancy of non-native DOI
Kettenring K. M., Whigham D. F., Hazelton E. L. G., Gallagher S. K., Weiner H. M. (2015). Biotic resistance, disturbance, and mode of colonization impact the invasion of a widespread, introduced wetland grass. PubMed DOI
Kim J., Verma S. B., Billesbach D. P. (1998). Seasonal variation in methane emission from a temperate Phragmites-dominated marsh: effect of growth stage and plant-mediated transport. DOI
Kim S. Y., Kang H. (2008). Effects of elevated CO DOI
Knutson T. R., McBride J. L., Chan J., Emanuel K., Holland G., Landsea C., et al. (2010). Tropical cyclones and climate change. DOI
Kolada A. (2016). The use of helophytes in assessing eutrophication of temperate lowland lakes: Added value? DOI
Koppitz H. (1999). Analysis of genetic diversity among selected populations of DOI
Koppitz H. (2004). Effects of flooding on the amino acid and carbohydrate patterns of DOI
Koppitz H., Dewender M., Ostendorp W., Schmieder K. (2004). Amino acids as indicators of physiological stress in common reed DOI
Kriticos D. J., Webber B. L., Leriche A., Ota N., Bathols J., Macadam I., et al. (2012). CliMond: global high resolution historical and future scenario climate surfaces for bioclimatic modelling. DOI
Kühl H., Woitke P., Kohl J. G. (1997). Strategies of nitrogen cycling of DOI
Lambertini C. (2016). Heteroplasmy due to chloroplast paternal leakage: another insight into DOI
Lambertini C., Eller F. P., Achenbach L., Nguyen L. X., Guo W.-Y., Brix H. (2012a). “Revisiting
Lambertini C., Gustafsson M. H. G., Frydenberg J., Lissner J., Speranza M., Brix H. (2006). A phylogeographic study of the cosmopolitan genus DOI
Lambertini C., Mendelsshon I. A., Gustafsson M. G. H., Olesen B., Riis T., Sorrell B. K., et al. (2012b). Tracing the origin of Gulf Coast PubMed DOI
Lambertini C., Sorrell B. K., Riis T., Olesen B., Brix H. (2012c). Exploring the borders of European PubMed DOI PMC
Latzel V., Klimesova J. (2010). Transgenerational plasticity in clonal plants. DOI
Lavergne S., Molofsky J. (2004). Reed canary grass ( DOI
Lavergne S., Molofsky J. (2007). Increased genetic variation and evolutionary potential drive the success of an invasive grass. PubMed DOI PMC
Lee J., An S. (2015). Effect of dikes on the distribution and characteristics of DOI
Lessmann J. M., Brix H., Bauer V., Clevering O. A., Comín F. A. (2001). Effect of climatic gradients on the photosynthetic responses of four DOI
Li F., Xie Y., Chen X., Hou Z., Li X., Deng Z., et al. (2013). Succession of aquatic macrophytes in the modern Yellow River Delta after 150 years of alluviation. DOI
Lissner J., Schierup H. H. (1997). Effects of salinity on the growth of DOI
Lissner J., Schierup H. H., Comín F. A., Astorga V. (1999a). Effect of climate on the salt tolerance of two
Lissner J., Schierup H. H., Comín F. A., Astorga V. (1999b). Effect of climate on the salt tolerance of two DOI
Ma B., Lv X., Warren A., Gong J. (2013). Shifts in diversity and community structure of endophytic bacteria and archaea across root, stem and leaf tissues in the common reed, PubMed DOI
Mathiasen P., Premoli A. C. (2016). Living on the edge: adaptive and plastic responses of the tree PubMed DOI
Matoh T., Matsushita N., Takahashi E. (1988). Salt tolerance of the reed plant DOI
Mauchamp A., Methy M. (2004). Submergence-induced damage of photosynthetic apparatus in DOI
McCormick M. K., Kettenring K. M., Baron H. M., Whigham D. F. (2010a). Extent and mechanisms of DOI
McCormick M. K., Kettenring K. M., Baron H. M., Whigham D. F. (2010b). Spread of invasive DOI
Meadows R. E. (2006).
Meriste M., Kirsimäe K., Freiberg L. (2012). Relative sea-level changes at shallow coasts inferred from reed bed distribution over the last 50 years in Matsalu bay, the Baltic Sea. DOI
Meyerson L. A., Cronin J. T., Bhattarai G. P., Brix H., Lambertini C., Lucanova M., et al. (2016a). Do ploidy level and nuclear genome size and latitude of origin modify the expression of DOI
Meyerson L. A., Cronin J. T., Pyšek P. (2016b). DOI
Meyerson L. A., Lambert A. M., Saltonstall K. (2010a). A tale of three lineages: expansion of common reed ( DOI
Meyerson L. A., Lambertini C., McCormick M. K., Whigham D. F. (2012). Hybridization of common reed in North America? The answer is blowing in the wind. PubMed DOI PMC
Meyerson L. A., Saltonstall K., Windham L., Kiviat E., Findlay S. (2000). A comparison of DOI
Meyerson L. A., Viola D. V., Brown R. N. (2010b). Hybridization of invasive DOI
Milla R., Cornelissen J. H. C., van Logtestijn R. S. P., Toet S., Aerts R. (2006). Vascular plant responses to elevated CO DOI
Minchinton T. E. (2002). Precipitation during El Niño correlates with increasing spread of DOI
Mitsch W. J., Bernal B., Nahlik A. M., Mander Ü., Zhang L., Anderson C. J., et al. (2013). Wetlands, carbon, and climate change. DOI
Mitsch W. J., Gosselink J. G. (2007).
Molina-Montenegro M. A., Galleguillos C., Oses R., Acuña-Rodríguez I. S., Lavín P., Gallardo-Cerda J., et al. (2016). Adaptive phenotypic plasticity and competitive ability deployed under a climate change scenario may promote the invasion of DOI
Molina-Montenegro M. A., Naya D. E. (2012). Latitudinal patterns in phenotypic plasticity and fitness-related traits: assessing the climatic variability hypothesis (CVH) with an invasive plant species. PubMed DOI PMC
Moore G. E., Burdick D. M., Peter C. R., Keirstead D. R. (2012). Belowground biomass of DOI
Morgan J. M. (1984). Osmoregulation and water stress in higher plants. DOI
Mozdzer T. J., Brisson J., Hazelton E. L. G. (2013). Physiological ecology and functional traits of North American native and Eurasian introduced DOI
Mozdzer T. J., Caplan J. S., Hager R. N., Proffitt C. E., Meyerson L. A. (2016a). Contrasting trait responses to latitudinal climate variation in two lineages of an invasive grass. DOI
Mozdzer T. J., Langley J. A., Mueller P., Megonigal J. P. (2016b). Erratum to: deep rooting and global change facilitate spread of invasive grass. DOI
Mozdzer T. J., Megonigal J. P. (2012). Jack-and-Master trait responses to elevated CO PubMed DOI PMC
Mozdzer T. J., Megonigal J. P. (2013). Increased methane emissions by an introduced DOI
Mozdzer T. J., Zieman J. C. (2010). Ecophysiological differences between genetic lineages facilitate the invasion of non-native DOI
Mozdzer T. J., Zieman J. C., McGlathery K. J. (2010). Nitrogen uptake by native and invasive temperate coastal macrophytes: importance of dissolved organic nitrogen. DOI
Munguia-Rosas M. A., Ollerton J., Parra-Tabla V., De-Nova J. A. (2011). Meta-analysis of phenotypic selection on flowering phenology suggests that early flowering plants are favoured. PubMed DOI
Münzbergová Z., Hadincová V. (2017). Transgenerational plasticity as an important mechanism affecting response of clonal species to changing climate. PubMed DOI PMC
Münzbergová Z., Hadincová V., Skálová H., Vandvik V. (2017). Genetic differentiation and plasticity interact along temperature and precipitation gradients to determine plant performance under climate change. DOI
Nada R. M., Khedr A. H. A., Serag M. S., El-Nagar N. A. (2015). Growth, photosynthesis and stress-inducible genes of DOI
Nakamura M., Nakamurac T., Tsuchiyaa T., Noguchi K. (2013). Functional linkage between N acquisition strategies and aeration capacities of hydrophytes for efficient oxygen consumption in roots. PubMed DOI
Naumann J. C., Young D. R., Anderson J. E. (2007). Linking leaf chlorophyll fluorescence properties to physiological responses for detection of salt and drought stress in coastal plant species. PubMed DOI
Nechwatal J., Wielgoss A., Mendgen K. (2008). Flooding events and rising water temperatures increase the significance of the reed pathogen DOI
Nguyen L. X., Lambertini C., Sorrell B. K., Eller F., Achenbach L., Brix H. (2013). Photosynthesis of co-existing DOI
Niu S., Luo Y., Li D., Cao S., Xia J., Li J., et al. (2014). Plant growth and mortality under climatic extremes: an overview. DOI
Oney B., Reineking B., O’Neill G., Kreyling J. (2013). Intraspecific variation buffers projected climate change impacts on PubMed DOI PMC
Ostendorp W. (1989). ‘Die-back’ of reeds in Europe - a critical review of Literature. DOI
Ostendorp W. (1999). Susceptibility of lakeside DOI
Ostendorp W., Dienst M. (2012). Geschichte der seeuferröhrichte in der grenzzone des Bodensee-Untersees.
Ostendorp W., Dienst M., Schmieder K. (2003). Disturbance and rehabilitation of lakeside DOI
Packer J. G., Meyerson L. A., Richardson D. M., Brundu G., Allen W. J., Bhattarai G. P., et al. (2017a). Global networks for invasion science: benefits, challenges and guidelines. DOI
Packer J. G., Meyerson L. A., Skalova H., Pysek P., Kueffer C. (2017b). Biological flora of the British isles: DOI
Packett C. R., Chambers R. M. (2006). Distribution and nutrient status of haplotypes of the marsh grass DOI
Pagter M., Bragato C., Brix H. (2005). Tolerance and physiological responses of DOI
Pagter M., Bragato C., Malagoli M., Brix H. (2009). Osmotic and ionic effects of NaCl and Na DOI
Pauca-Comanescu M., Clevering O. A., Hanganu J., Gridin M. (1999). Phenotypic differences among ploidy levels of DOI
Paul J., Kirk H., Freeland J. (2011). Genetic diversity and differentiation of fragmented reedbeds ( DOI
Pauls S. U., Nowak C., Balint M., Pfenninger M. (2013). The impact of global climate change on genetic diversity within populations and species. PubMed DOI
Poorter H., Niinemets U., Poorter L., Wright I. J., Villar R. (2009). Causes and consequences of variation in leaf mass per area (LMA): a meta-analysis. PubMed DOI
Post E. (2013).
Price A. L., Fant J. B., Larkin D. J. (2014). Ecology of native vs. introduced DOI
Pyšek P., Jarošík V., Hulme P. E., Pergl J., Hejda M., Schaffner U., et al. (2012). A global assessment of invasive plant impacts on resident species, communities and ecosystems: the interaction of impact measures, invading species’ traits and environment. DOI
Pyšek P., Pergl J., Essl F., Lenzner B., Dawson W., Kreft H., et al. (2017). Naturalized alien flora of the world: species diversity, taxonomic and phylogenetic patterns, geographic distribution and global hotspots of plant invasion. DOI
Raunkiaer C. (1893). En ny form af tagrør:
Rechav Y. (1967).
Reich P. B., Oleksyn J. (2008). Climate warming will reduce growth and survival of Scots pine except in the far north. PubMed DOI
Rintamaki E., Aro E. M. (1985). Photosynthetic and photorespiratory enzymes in widely divergent plant-species with special reference to the moss DOI
Rodewald-Rudescu L. (1974).
Rodriguez M., Brisson J. (2016). Does the combination of two plant species improve removal efficiency in treatment wetlands? DOI
Rolletschek H., Hartzendorf T., Rolletschek A., Kohl J. G. (1999). Biometric variation in DOI
Romero J. A., Brix H., Comin F. A. (1999). Interactive effects of N and P on growth, nutrient allocation and NH4 uptake kinetics by DOI
Rooth J. E., Stevenson J. C., Cornwall J. C. (2003). Increased sediment accretion rates following invasion by DOI
Sage R. F. (2016). Tracking the evolutionary rise of C PubMed DOI PMC
Saltmarsh A., Mauchamp A., Rambal S. (2006). Contrasted effects of water limitation on leaf functions and growth of two emergent co-occurring plant species, DOI
Saltonstall K. (2002). Cryptic invasion by a non-native genotype of the common reed, PubMed DOI PMC
Saltonstall K. (2003). Microsatellite variation within and among North American lineages of PubMed DOI
Saltonstall K., Castillo H. E., Blossey B. (2014). Confirmed field hybridization of native and introduced PubMed DOI
Saltonstall K., Lambert A. (2015). What happens in Vegas, better stay in Vegas: DOI
Saltonstall K., Stevenson J. C. (2007). The effect of nutrients on seedling growth of native and introduced DOI
Schmid S. F., Stocklin J., Hamann E., Kesselring H. (2017). High-elevation plants have reduced plasticity in flowering time in response to warming compared to low-elevation congeners. DOI
Schöb C., Armas C., Guler M., Prieto I., Pugnaire F. I. (2013). Variability in functional traits mediates plant interactions along stress gradients. DOI
Scholefield P. A., Doick K. J., Herbert B. M. J., Hewitt C. N. S., Schnitzler J. P., Pinelli P., et al. (2004). Impact of rising CO DOI
Sciance M. B., Patrick C. J., Weller D. E., Williams M. N., McCormick M. K., Hazelton E. L. G. (2016). Local and regional disturbances associated with the invasion of Chesapeake Bay marshes by the common reed DOI
Sorrell B. K., Brix H., Schierup H. H., Lorenzen B. (1997). Die-back of DOI
Soukup A., Votrubova O., Cizkova H. (2000). Internal segmentation of rhizomes of DOI
Springate D. A., Kover P. X. (2014). Plant responses to elevated temperatures: a field study on phenological sensitivity and fitness responses to simulated climate warming. PubMed DOI PMC
Stebbins G. L. (1971). Adaptive radiation of reproductive characteristics in angiosperms, II: seeds and seedlings. DOI
Suda J., Meyerson L. A., Leitch I. J., Pyšek P. (2015). The hidden side of plant invasions: the role of genome size. PubMed DOI
Szczepanska W., Szczepanski A. (1976). Growth of
Takahashi R., Nishio T., Ichizen N., Takano T. (2007). High-affinity K PubMed DOI
Tang L., Gao Y., Wang C. H., Li B., Chen J. K., Zhao B. (2013). Habitat heterogeneity influences restoration efficacy: implications of a habitat-specific management regime for an invaded marsh. DOI
Tho B. T., Sorrell B. K., Lambertini C., Eller F., Brix H. (2016). Phragmites australis: how do genotypes of different phylogeographic origins differ from their invasive genotypes in growth, nitrogen allocation and gas exchange? DOI
Thuiller W., Lavorel S., Araujo M. B., Sykes M. T., Prentice I. C., Mooney H. A. (2005). Climate change threats to plant diversity in Europe. PubMed DOI PMC
Touchette B. W., Iannacone L. R., Turner G. E., Frank A. R. (2007). Drought tolerance versus drought avoidance: a comparison of plant-water relations in herbaceous wetland plants subjected to water withdrawal and repletion. DOI
Trenberth K. E., Dai A., van der Schrier G., Jones P. D., Barichivich J., Briffa K. R., et al. (2014). Global warming and changes in drought. DOI
Tripathee R., Schäfer K. V. R. (2014). Above- and belowground biomass allocation in four dominant salt marsh species of the eastern United States. DOI
Tulbure M. G., Ghioca-Robrecht D. M., Johnston C. A., Whigham D. F. (2012). Inventory and ventilation efficiency of nonnative and native DOI
Tulbure M. G., Johnston C. A. (2010). Environmental conditions promoting non-native DOI
Tulbure M. G., Johnston C. A., Auger D. L. (2007). Rapid invasion of a Great Lakes coastal wetland by non-native DOI
Tylová E., Steinbachová L., Soukup A., Gloser V., Votrubová O. (2013). Pore water N:P and NH DOI
Tylova-Munzarova E., Bent Lorenzen B., Hans Brix H., Olga Votrubova O. (2005). The effects of NH DOI
Ulrich K. E., Burton T. M. (1985). The effects of nitrate, phosphate and potassium fertilization on growth and nutrient uptake patterns of DOI
Valladares F., Matesanz S., Guilhaumon F., Araujo M. B., Balaguer L., Benito-Garzon M., et al. (2014). The effects of phenotypic plasticity and local adaptation on forecasts of species range shifts under climate change. PubMed DOI
van der Putten W. H. (1997). Die-back of DOI
Van der Toorn J. (1972). Variability of
van Kleunen M., Dawson W., Essl F., Pergl J., Winter M., Weber E., et al. (2015). Global exchange and accumulation of non-native plants. PubMed DOI
Vartapetian B. B., Jackson M. B. (1997). Plant adaptations to anaerobic stress. DOI
Vasquez E. A., Glenn E. P., Brown J. J., Guntenspergen G. R., Nelson S. G. (2005). Salt tolerance underlies the cryptic invasion of North American salt marshes by an introduced haplotype of the common reed DOI
Vasquez E. A., Glenn E. P., Guntenspergen G. R., Brown J. J., Nelson S. G. (2006). Salt tolerance and osmotic adjustment of PubMed DOI
Vermaat J. E., Bos B., van der Burg P. (2016). Why do reed beds decline and fail to re-establish? A case study of Dutch peat lakes. DOI
Vilà M., Espinar J. L., Hejda M., Hulme P. E., Jarošík V., Maron J. L., et al. (2011). Ecological impacts of invasive alien plants: a meta-analysis of their effects on species, communities and ecosystems. PubMed DOI
Violle C., Enquist B. J., McGill B. J., Jiang L. I. N., Albert C. H., Hulshof C., et al. (2012). The return of the variance: intraspecific variability in community ecology. PubMed DOI
Visser M. E. (2016). Phenology: interactions of climate change and species. PubMed DOI
Vretare V., Weisner S. E. B., Strand J. A., Graneli W. (2001). Phenotypic plasticity in DOI
Vymazal J. (2013). Emergent plants used in free water surface constructed wetlands: a review. DOI
Wang H., Hao L., Wen J., Zhang C., Liang H. (1998). Differential expression of photosynthesis-related genes of reed ecotypes in response to drought and saline habitats. DOI
Wang W., Wang C., Sardans J., Tong C., Jia R., Zeng C., et al. (2015). Flood regime affects soil stoichiometry and the distribution of the invasive plants in subtropical estuarine wetlands in China. DOI
Weisner S. E. B., Strand J. A. (1996). Rhizome architecture in DOI
White S. D., Deegan B. M., Ganf G. G. (2007). The influence of water level fluctuations on the potential for convective flow in the emergent macrophytes DOI
White S. D., Ganf G. G. (2002). A comparison of the morphology, gas space anatomy and potential for internal aeration in DOI
Whyte R. S., Trexel-Kroll D., Klarer D. M., Shields R., Francko D. A. (2008). The invasion and spread of DOI
Wilson E. O. (eds) (1988). “The current state of biological diversity,” in
Windham L., Meyerson L. A. (2003). Effects of common reed ( DOI
Winkel A., Pedersen O., Ella E., Ismail A. M., Colmer T. D. (2014). Gas film retention and underwater photosynthesis during field submergence of four contrasting rice genotypes. PubMed DOI PMC
Wright J. P., Jones C. G. (2004). Predicting effects of ecosystem engineers on patch-scale species richness from primary productivity. DOI
Wu C. A., Murray L. A., Heffernan K. E. (2015). Evidence for natural hybridization between native and introduced lineages of PubMed DOI
Xiang J., Jiang A. N., Fang Y. P., Huang L. B., Zhang H. (2012). Effects of soil water gradient on stress-resistant enzyme activities in DOI
Yamasaki S., Tange I. (1981). Growth responses of DOI
Yarwood S. A., Baldwin A. H., Mateu M. G., Buyer J. S. (2016). Archeal rhizosphere communities differ between the native and invasive lineages of the wetland plant DOI
Yu J., Wang X., Ning K., Li Y., Wu H., Fu Y., et al. (2012). Effects of salinity and water depth on germination of DOI
Zemlin R., Kühl H., Kohl J. G. (2000). Effects of seasonal temperature on shoot growth dynamics and shoot morphology of common reed ( DOI
Zhai X. (2013).
Zhang G., Deng C. (2012). Gas exchange and chlorophyll fluorescence of salinity-alkalinity stressed
Zhao Y. J., Qing H., Zhao C. J., Zhou C. F., Zhang W. G., Xiao Y., et al. (2010). Phenotypic plasticity of DOI
Zheng W. J., Zheng X. P., Zhang C. L. (2000). A survey of photosynthetic carbon metabolism in 4 ecotypes of DOI
Zhu X., Chen G., Zhang C. (2001). Photosynthetic electron transport, photophosphorylation, and antioxidants in two ecotypes of reed ( DOI
Zhu X. Y., Jing Y., Chen G. C., Wang S. M., Zhang C. L. (2003a). Solute levels and osmoregulatory enzyme activities in reed plants adapted to drought and saline habitats. DOI
Zhu X. Y., Wang S. M., Zhang C. L. (2003b). Composition and characteristic differences in photosynthetic membranes of two ecotypes of reed ( DOI
Zhu X. Y., Xia W. X., Chen L. J. (2012). Leaf anatomy and C DOI
Metabolomic Evenness Underlies Intraspecific Differences Among Lineages of a Wetland Grass