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Australian Journal of Botany Australian Journal of Botany Society
Southern hemisphere botanical ecosystems
RESEARCH ARTICLE

Differential responses of accessions of native Australian Nicotiana species to water stress

Khondoker M. G. Dastogeer A B , Hua Li C , Krishnapillai Sivasithamparam C , Michael G. K. Jones C and Stephen J. Wylie C D
+ Author Affiliations
- Author Affiliations

A Department of Plant Pathology, Bangladesh Agricultural University, Mymensingh-2202.

B Present address: Plant Biotechnology Group, Western Australian State Agricultural Biotechnology Centre, School of Veterinary and Life Sciences, Murdoch University, Perth, WA 6150, Australia.

C Plant Biotechnology Group, Western Australian State Agricultural Biotechnology Centre, School of Veterinary and Life Sciences, Murdoch University, Perth, WA 6150, Australia.

D Corresponding author. Email: s.wylie@murdoch.edu.au

Australian Journal of Botany 66(3) 265-277 https://doi.org/10.1071/BT17148
Submitted: 14 August 2017  Accepted: 11 May 2018   Published: 19 June 2018

Abstract

Thirty-two accessions of four Nicotiana species (Nicotiana benthamiana Domin, Nicotiana occidentalis H.-M.Wheeler, Nicotiana simulans N. Burb. and Nicotiana umbratica N.T.Burb.) collected from wild plants in northern Australia were assessed for responses to water stress. Under moderate water stress conditions, shoot fresh weight, shoot dry weight, root fresh weight, root dry weight, root : shoot ratio, and relative water content of leaves were significantly affected. However, the degree to which the accessions were affected varied considerably. Some accessions of N. simulans, N. benthamiana and N. occidentalis were significantly more affected by water stress than others. There was significant variation between accessions in leaf and shoot tip wilting times. Initial symptom expression (leaf wilting) was significantly delayed in three accessions of N. benthamiana, and in one accession of N. umbratica. The least water stress tolerant lines, two accessions each of N. benthamiana, N. occidentalis and N. simulans, exhibited advanced symptoms of water stress (shoot tip wilting) within 14–17 days of cessation of watering. This stage was significantly delayed in three accessions of N. benthamiana and two accessions N. occidentalis and one accession of each of N. simulans and N. umbratica, which showed tip wilting only after 21–24 days. There were variations among the accessions of same Nicotiana species on their tolerance to water stress. Plant responses to water stress could not be predicted from their plant biomass and leaf relative water content under well-watered conditions. Leaf chlorophyll content was variable under water stress, but did not correlate with water stress tolerance.

Additional keywords: biomass, chlorophyll content, drought, leaf wilting, RWC, shoot tip wilting.


References

Allestrofa V (2014) Evaluation of drought adaptation of different tomato genotypes. Master thesis. University of Natural Resources and Life Sciences, Vienna.

Barrs HD (1968) Determination of water deficits in plant tissue. In ‘Water deficits and plant growth. Vol. 1’. (Ed. TT Kozlowski) pp. 235–368. (Academic Press: New York)

Beadle CL, Ludlow MM, Honeysett L (1993) Water relations. In ‘Photosynthesis and production in a changing environment’. (Eds DO Hall, JMO Scurlock, HR Bolhàr-Nordenkampf, RC Leegood, SP Long) pp. 113–127. (Chapman & Hall: London)

Blum A (1998) Improving wheat grain filling under stress by stem reserve mobilization. Euphytica 100, 77–83.
Improving wheat grain filling under stress by stem reserve mobilization.Crossref | GoogleScholarGoogle Scholar |

Bohnert HJ, Sheveleva E (1998) Plant stress adaptations-making metabolism move. Current Opinion in Plant Biology 1, 267–274.
Plant stress adaptations-making metabolism move.Crossref | GoogleScholarGoogle Scholar |

Chaves MM, Maroco JP, Pereira JS (2003) Understanding plant responses to drought – from genes to the whole plant. Functional Plant Biology 30, 239–264.
Understanding plant responses to drought – from genes to the whole plant.Crossref | GoogleScholarGoogle Scholar |

Chaves MM, Flexas J, Pinheiro C (2009) Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Annals of Botany 103, 551–560.
Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell.Crossref | GoogleScholarGoogle Scholar |

Engelbrecht BMJ, Comita L, Condit R, Kursar TA, Tyree MT, Turner BL, Hubbell SP (2007) Drought sensitivity shapes species distribution patterns in tropical forests. Nature 447, 80–82.
Drought sensitivity shapes species distribution patterns in tropical forests.Crossref | GoogleScholarGoogle Scholar |

Garcia-Mazcorro JF, Castillo-Carranza SA, Guard B, Gomez-Vazquez JP, Dowd SE, Brigthsmith DJ (2017) Comprehensive molecular characterization of bacterial communities in feces of pet birds using 16S marker sequencing. Microbial Ecology 73, 224–235.
Comprehensive molecular characterization of bacterial communities in feces of pet birds using 16S marker sequencing.Crossref | GoogleScholarGoogle Scholar |

Goodin MM, Zaitlin D, Naidu RA, Lommel SA (2008) Nicotiana benthamiana: its history and future as a model for plant–pathogen interactions. Molecular Plant-Microbe Interactions 21, 1015–1026.
Nicotiana benthamiana: its history and future as a model for plant–pathogen interactions.Crossref | GoogleScholarGoogle Scholar |

Hammer Ø, Harper DAT, Ryan PD (2001) PAST: paleontological statistics software package for education and data analysis. Palaeontologia Electronica 4, 4

Hereford J (2009) A quantitative survey of local adaptation and fitness trade-offs. American Naturalist 173, 579–588.
A quantitative survey of local adaptation and fitness trade-offs.Crossref | GoogleScholarGoogle Scholar |

Hirsch PR, Jhurreea D, Williams JK, Murray PJ, Scott T, Misselbrook TH, Goulding KW, Clark IM (2017) Soil resilience and recovery: rapid community responses to management changes. Plant and Soil 412, 283–297.
Soil resilience and recovery: rapid community responses to management changes.Crossref | GoogleScholarGoogle Scholar |

IBM (2012) ‘IBM SPSS statistics for Windows.’ (24th edn) (IBM Corp: Armonk, NY, USA)

Ings J, Mur LAJ, Robson PRH, Bosch M (2013) Physiological and growth responses to water deficit in the bioenergy crop Miscanthus × giganteus. Frontiers in Plant Science 4, 468
Physiological and growth responses to water deficit in the bioenergy crop Miscanthus × giganteus.Crossref | GoogleScholarGoogle Scholar |

IPCC (2007) ‘Climate change 2007: the physical science basis.’ (Cambridge University Press: Cambridge, UK)

Kalloo G (1991) Breeding for environmental stress resistance in tomato. In ‘Genetic improvement of tomato’. (Ed. G Kalloo) pp. 153–165. (Springer: Berlin)

Kirkham MB (2005) ‘Principles of soil and plant water relations.’ (Elsevier Academic Press: Burlington, MA, USA)

Larcher W (2003) ‘Physiological plant ecology.’ (4th edn) (Springer-Verlag: Berlin)

Lazcano-Ferrat I, Lovat CJ (1999) Relationship between relative water content, nitrogen pools, and growth of Phaseolus vulgaris L. and P. acutifoolius A. Gray during water deficit. Crop Science 39, 467–475.
Relationship between relative water content, nitrogen pools, and growth of Phaseolus vulgaris L. and P. acutifoolius A. Gray during water deficit.Crossref | GoogleScholarGoogle Scholar |

Ledbetter CA, Peterson S, Palmquist D (1996) In vitro osmotic tolerance of six clonally propagated Prunus accessions. Journal of Genetics & Breeding 50, 1–6.

Li RH, Guo PG, Baum M, Grando S, Ceccarelli S (2006) Evaluation of chlorophyll content and fluorescence parameters as indicators of drought tolerance in barley. Agricultural Sciences in China 5, 751–757.
Evaluation of chlorophyll content and fluorescence parameters as indicators of drought tolerance in barley.Crossref | GoogleScholarGoogle Scholar |

Malyshev AV (2015) Plant growth responses to winter climate change: from among-and within-species variation to plant–soil interactions. PhD thesis, Faculty of Biology, Chemistry and Earth Sciences, Universität Bayreuth, Bayreuth, Germany.

McKay C, Filipsson H, Romero O, Stuut JB, Björck S (2016) The interplay between the surface and bottom water environment within the Benguela Upwelling System over the last 70 ka. Paleoceanography 31, 266–285.
The interplay between the surface and bottom water environment within the Benguela Upwelling System over the last 70 ka.Crossref | GoogleScholarGoogle Scholar |

McWilliam JR (1986) The national and international importance of drought and salinity effects on agricultural production. Australian Journal of Plant Physiology 13, 1–13.
The national and international importance of drought and salinity effects on agricultural production.Crossref | GoogleScholarGoogle Scholar |

Morgan JM (1984) Osmoregulation and water stress in higher plants. Annual Review of Plant Physiology 35, 299–319.
Osmoregulation and water stress in higher plants.Crossref | GoogleScholarGoogle Scholar |

Nikolaeva MK, Maevskaya SN, Shugaev AG, Bukhov NG (2010) Effect of drought on chlorophyll content and antioxidant enzyme activities in leaves of three wheat cultivars varying in productivity. Russian Journal of Plant Physiology: a Comprehensive Russian Journal on Modern Phytophysiology 57, 87–95.
Effect of drought on chlorophyll content and antioxidant enzyme activities in leaves of three wheat cultivars varying in productivity.Crossref | GoogleScholarGoogle Scholar |

Pereira JS, Chaves MM (1993) ‘Plant water deficits in Mediterranean ecosystems.’ (Bios Scientific Publications: Oxford)

R Core Team (2015) ‘R: A language and environment for statistical computing.’ (R Foundation for Statistical Computing: Vienna, Austria) Available at http://www.R-project.org/ [Verified 6 May 2017]

Ramos MLG, Parsons R, Sprent JI, Games EK (2003) Effect of water stress on nitrogen fixation and nodule structure of common bean. Pesquisa Agropecuária Brasileira 38, 339–347.
Effect of water stress on nitrogen fixation and nodule structure of common bean.Crossref | GoogleScholarGoogle Scholar |

Schonfeld MA, Johnson RC, Carwer BF, Mornhinweg DW (1988) Water relations in winter wheat as drought resistance indicators. Crop Science 28, 526–531.
Water relations in winter wheat as drought resistance indicators.Crossref | GoogleScholarGoogle Scholar |

Stata Corp L (2017) ‘Stata statistical software release 15.’ (Stata Press Publication: College Station, TX, USA)

Vialet-Chabrand SR Matthews JS Simkin A Raines CA Lawson T 2017 Importance of fluctuations in light on pant photosynthetic acclimation. Plant Physiology. In press. 10.1104/pp.16.01767

Williams GC (1966) ‘Adaptation and natural selection: a critique of some current evolutionary thought.’ (Princeton University Press: Princeton, NJ, USA)

Wylie SJ, Zhang C, Long V, Roossinck MJ, Koh SH, Jones MG, Iqbal S, Li H (2015) Differential responses to virus challenge of laboratory and wild accessions of Australian species of Nicotiana, and comparative analysis of RDR1 gene sequences. PLoS One 10, e0121787
Differential responses to virus challenge of laboratory and wild accessions of Australian species of Nicotiana, and comparative analysis of RDR1 gene sequences.Crossref | GoogleScholarGoogle Scholar |

Xu P, Chen F, Mannas JP, Feldman T, Sumner LW, Roossinck MJ (2008) Virus infection improves drought tolerance. New Phytologist 180, 911–921.
Virus infection improves drought tolerance.Crossref | GoogleScholarGoogle Scholar |

Zaura E, Keijser BJ, Huse SM, Crielaard W (2009) Defining the healthy” core microbiome” of oral microbial communities. BMC Microbiology 9, 259
Defining the healthy” core microbiome” of oral microbial communities.Crossref | GoogleScholarGoogle Scholar |

Zhang C, Li H Shober A McGrath J (2015) Greenhouse gas emissions of corn fielded with broilers litter treated by ammonia control technology. In ‘NABEC Papers. NABEC 2015 annual meeting, Newark, Delaware, (American Society of Agricultural and Biological Engineers: St Joseph, MI, USA)