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Shahwani, Muhammad Naeem (2011) Studies on abiotic stress tolerance in Hordeum vulgare L ... PDF

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Shahwani, Muhammad Naeem (2011) Studies on abiotic stress tolerance in Hordeum vulgare L. genotypes from arid and temperate regions. PhD thesis. http://theses.gla.ac.uk/2775/ Copyright and moral rights for this thesis are retained by the author A copy can be downloaded for personal non-commercial research or study, without prior permission or charge This thesis cannot be reproduced or quoted extensively from without first obtaining permission in writing from the Author The content must not be changed in any way or sold commercially in any format or medium without the formal permission of the Author When referring to this work, full bibliographic details including the author, title, awarding institution and date of the thesis must be given. Glasgow Theses Service http://theses.gla.ac.uk/ [email protected] Studies on Abiotic Stress Tolerance in Hordeum vulgare L. Genotypes from Arid and Temperate Regions Muhammad Naeem Shahwani Thesis Submitted for the Degree of Doctor of Philosophy College of Medical, Veterinary and Life Sciences, School of Life Sciences University of Glasgow U.K. July, 2011 © M. N. Shahwani ABSTRACT Plants growing in arid regions often suffer from high shoot temperatures, low shoot water concentrations, low turgor pressures, and high salinity in the rhizosphere. To investigate which traits confer tolerance on plants in these areas a range of genotypes was studied. These included Local (an uncharacterized landrace grown in south western Pakistan), Soorab-96 and Awaran-2002 (both elite cultivars developed by ICARDA and commercially grown in Pakistan), and Optic (an elite European cultivar). Measurements on germination, growth, and yield suggested that landrace Local is significantly least affected by high salinity (p<0.05) compared with lines Soorab-96, Awaran-2002 and Optic. Further investigations on ion profiling established that landrace Local could maintain low Na+/K+ ratios. This appeared to arise from Local’s ability to prevent Na+ accumulation in the roots and shoots by enhanced exclusion or efflux or both. Probably this unique characteristic of landrace Local helped in maintaining its photosynthetic efficiency, plant water status, and stomatal conductance, which resulted in its better performance and survival in high salinity. There was no evidence that high tissue solute concentrations, high proline levels or life cycle strategies played a role in salt stress tolerance. In addition, there was no evidence that osmotic stress was responsible for the observed suppression of growth in any of the genotypes. The main conclusion from this study is that for glycophytes (which do not complete a full life cycle above 100 mM NaCl; this includes all of the world’s major crops), it is the ionic component of salinity stress that impairs growth processes and yield, not the osmotic component. Further research on salinity stress in crops should focus on understanding the processes that control ionic balance rather than osmoregulation. There is some evidence that long term exposure of plants in the preceding generations to moderately high salt concentrations (e.g. 100 mM NaCl) improves barley halotolerance in succeeding generations, i.e. halotolerance has a transgenerational, epigenetic basis, but there was also evidence that the improved halotolerance in the Local genotype was partly genetic. In another series of experiments the importance of short periods of high leaf temperatures (T ) on photosynthetic efficiency of barley genotypes Local, Optic, and leaf Soorab-96 was investigated. In all three genotypes light saturated carbon dioxide assimilation rates (A ) and the carboxylation coefficients (Φ , a measure of the sat CO2 efficiency of CO fixation) in the fourth fully expanded leaves were equally suppressed 2 to approximately 20 % of their pre-treatment levels immediately after a short period of i heat stress (T > 40.0 ± 0.5 °C for 20 minutes). Parallel measurements using a range of leaf techniques confirmed that the suppression of A and Φ was not attributable to sat CO2 changes in the light harvesting capacity (leaf absorptance and chla excitation spectra), maximum quantum efficiency of PSII (Φ , Fv/Fm), and to stomatal conductance (g ). PSII s It is unlikely that the suppression arose from damage to the electron transport chain¸ or to the capacity to develop or maintain non-photochemical quenching (NPQ, which is dependent on the transthylakoid ΔpH), but these possibilities cannot be dismissed. LC- MS and enzymic analysis of leaf metabolite levels showed that the pools of metabolites feeding into RuBisCO are not affected by heat stress whilst those of the metabolites flowing away from RuBisCO were significantly depleted. The implication is that short periods of heat stress severely impairs RuBisCO, RuBisCO Activase, or processes close to the carboxylation step. Five days after heat stress A and ΦCO had significantly sat 2 recovered to approximately 40 % (p<0.05) of their pre-stress levels in landrace Local, but no significant recovery was observed in any of the elite lines including those distributed by ICARDA for arid land production. These findings provide evidence that thermal damage may play a significant role in yield suppressions in arid regions and that there is a genetic basis for thermotolerance in barley1. 1 Some of the work presented in this thesis has been given as oral presentations at two international scientific meetings. 1. International Conference on Food Security and Climate Change in the Dry Areas, by ICARDA in Amman-Jordan from 1-4th February 2010. 2. SEB Annual Conference, Prague, 30th June-3rd July 2010. ii In the Name of Almighty Allah (God), Most Gracious, Most Merciful ACKNOWLEDGEMENTS: First and foremost countless thanks and praises to Almighty Allah (Subhana-u- watahala) for his granted bounties (i.e. observe, analyse and interpret). Then to His beloved Messenger Muhammad (PBUH) for prioritizing the knowledge for the benefit of all humanity. I am indebted to my supervisor Dr. Peter Dominy, for his unfailing support and encouragement, the kindness, the opportunity and help to allow me independence ‘no words can describe his assistance’. He also helped me a lot to believe in my self and in possibility to reach my goals. I have not only learned material facts, but also focus and organization. His supervision has provided an ideal intellectual environment to learn science for which I will always be grateful and his enthusiasm and encouragement have persisted and sustained me over the last three years. Special thanks to all staff members and scholars of the Dominy group, in particular, and other groups from the Plant Sciences Discipline in general, for the warmth and kindness shown to me. It will be an injustice if I do not pay thanks to Dr. Stéphanie Arrivault (The Max Planck Institute of Molecular Plant Physiology, Am Muehlenberg, Germany) for her incredible help in analyzing my plant samples for C3 cycle metabolite pools. I thank all friends specially Dr. Peter Meadows and Dr. Azra Meadows for their incredible help and support during my studies. I would like to thank the people of Islamic Republic of Pakistan, the administration of BUITEMS, and the Higher Education Commission of Pakistan for their continuous encouragement, well wishes, and financial support. Last but not least. I would like to express my sincere thanks to my Parents for their sincere love and good wishes, to my wife Saiqa for playing a great role during my scholastic studies. I also thank my children Tayeba, Anam, Iqra, Momina, and Malaika for their patience during my long absence from home and for creating a warm and rewarding environment when I returned home tired. Finally, I am extremely grateful to my brothers, sisters, and close relatives for their encouragement and support. Without the help of Almighty Allah and the help of all these people mentioned above this work would not have been completed. iii TABLE OF CONTENTS Sections....................................................................................................................... Page Title Page...........................................................................................................................0 Abstract...............................................................................................................................i Acknowledgements..........................................................................................................iii Table of Contents.............................................................................................................iv List of Figures..................................................................................................................xi List of Tables..................................................................................................................xiv Abbreviations..................................................................................................................xv Declaration....................................................................................................................xvii 1 Chapter 1: Introduction.........................................................................................1 1.1 Food Supply and Population Growth in the 21st Century.........................1 1.2 Abiotic Stress: A Worldwide Problem in Agriculture..............................2 1.2.1 Soil Salinity...............................................................................................3 1.2.1.1 The Effect of Salinity on Agriculture...................................................4 1.2.1.2 Classification of Plants According to Their Tolerance of Salinity.......4 1.2.1.3 The Deleterious Effects of High Salinity on Plants..............................5 1.2.1.4 Strategies for Coping with High Salinity..............................................6 1.2.1.5 The Importance of Turgor.....................................................................7 1.2.1.6 Na+ Uptake Mechanisms.......................................................................8 1.2.1.7 Salt Stress Sensing in Plants...............................................................10 1.2.1.8 Na+ Sequestration................................................................................10 1.2.2 Thermal Stress.........................................................................................12 1.2.2.1 Effects of Heat Stress on Plants..........................................................13 1.2.2.2 Plant Responses to Heat Stress...........................................................14 1.2.2.2.1 Morpho-Anatomical Responses....................................................14 1.2.2.2.2 Physiological Responses...............................................................15 1.2.2.3 Mechanisms of Thermotolerance........................................................18 1.3 Thermotolerance Studies in Barley.........................................................21 1.4 Background of the Study.........................................................................22 1.4.1 Plant Material and Area..........................................................................22 1.4.2 Hypothesis Behind Current Study...........................................................23 1.4.3 Aims and Objectives of the Study...........................................................25 iv 2 Chapter 2: Materials and Methods.....................................................................26 2.1 Halotolerance..........................................................................................26 2.1.1 Plant Material..........................................................................................26 2.1.2 Agronomic Characterization of Barley Genotypes Under High Salt Concentrations........................................................................................................28 2.1.2.1 Germination........................................................................................28 2.1.2.1.1 Experimental Design.....................................................................28 2.1.2.2 Growth of Mature Plants.....................................................................28 2.1.2.2.1 Plant Material................................................................................28 2.1.2.2.2 Experimental Design for Growth and Yield.................................30 2.1.2.2.3 Shoot and Root Length, Fresh and Dry Weight............................30 2.1.2.2.4 Tillers, Ears, Grains and Grain Weight Per Plant.........................30 2.1.2.3 Assessment of Development...............................................................30 2.1.2.3.1 Assessment of Ppd-H1 Flowering Locus......................................31 2.1.3 Physiological Characterization of Barley Genotypes under high salt concentrations.........................................................................................................33 2.1.3.1 Photosynthesis.....................................................................................33 2.1.3.1.1 CO Response Curve.....................................................................33 2 2.1.3.1.2 Light Response Curve...................................................................37 2.1.3.2 Water Potential....................................................................................40 2.1.3.3 Solute Potential...................................................................................40 2.1.3.3.1 Solute Potential of Tissue Cell Sap (Tissue ψ )................................40 s 2.1.3.3.2 Solute Potential of Exuded Xylem Sap (xylem ψ )..........................40 s 2.1.3.3.3 Proline Concentration...................................................................41 2.1.4 Ion Analysis............................................................................................41 2.1.4.1 Preparation of Barley Material for ICP-OES Analysis.......................41 2.1.4.1.1 Standard Solution..........................................................................42 2.1.4.1.2 Assessment of Ion Concentration in Plant Material......................42 2.2 High Temperature Thermotolerance.......................................................43 2.2.1 Plant Material..........................................................................................43 2.2.2 Exposure to Heat Stress..........................................................................43 2.2.2.1 ‘Incremental’ Heat Stress Experiments...............................................43 2.2.2.2 ‘Temperature Jump’ Heat Stress Experiments....................................43 2.2.3 Leaf Absorptance and Fluorescence Measurements...............................48 2.2.3.1 Measurement of Leaf Absorptance and Light harvesting Capacity....48 2.2.3.2 Measurement of Photosystem-II Quantum Yield (ΦPS-II) and Electron Transport Rates (ETR).............................................................48 2.2.4 Gas Exchange Measurements.................................................................50 2.2.5 Metabolite Pools Analysis......................................................................50 2.2.5.1 Preparation of Plant Extracts...............................................................50 v 2.2.5.2 Sample Extraction...............................................................................52 2.2.5.3 Analysis of Metabolite Pools..............................................................52 2.2.5.4 Synthesis of Deuterated G6P and G3P...............................................52 2.2.5.5 Ion Pair Chromatography – Triple Quadrupole MS...........................53 2.2.5.6 Detection and Validation of Signals in Plant Extracts........................54 2.2.5.7 Other Metabolite Assays.....................................................................54 2.2.6 Statistical Analysis..................................................................................56 3 Chapter 3: Characterization of Halotolerance in Barley Genotypes: Germination, Growth, Yield, and Development........................................................57 3.1 Germination............................................................................................57 3.2 Growth Parameters..................................................................................62 3.2.1 Phenotypic Representation of Barley Genotypes under High Salt Concentrations........................................................................................................62 3.2.2 Shoot and Root Length...........................................................................65 3.2.3 Shoot and Root Fresh Weight.................................................................65 3.2.4 Shoot and Root Dry Weight....................................................................69 3.2.4.1 Tillering...............................................................................................71 3.3 Yield Parameters.....................................................................................74 3.3.1 Ears and Grains per Plant........................................................................74 3.3.2 Grain Weight per Plant and 1000 Grain Weight.....................................76 3.4 The Effects of Salt Stress on the Development of Barley Genotypes ....78 3.4.1 The Effects of Salt Stress on Four Key Developmental Stages..............81 3.4.2 Assessment of Ppd-H1 Flowering Locus................................................84 3.5 Discussion...............................................................................................86 4 Chapter 4: Characterization of Halotolerance in Barley Genotypes: Physiological Responses................................................................................................90 4.1 Carbon Dioxide Supply and Photosynthesis...........................................90 4.1.1 Stomatal Conductance (gs).....................................................................91 4.1.2 CO Assimilation Rates and Quantum Efficiency..................................91 2 4.1.3 Carboxylation Efficiency (Φ CO )..........................................................95 2 4.1.4 Apparent Photorespiration (V ) and Dark Respiration (mitRd)...............95 o 4.1.5 Ratio of Internal CO (C) to Atmospheric CO Concentration (C ), and 2 i 2 a Assimilation versus Stomatal Conductance............................................................99 4.2 Plant Water Status.................................................................................102 4.2.1 Relative Water Content and Water Use Efficiency..............................102 vi 4.2.2 Leaf Water Potential (ψ ), Xylem Solute Potential (Xylemψ ) and Turgor H2O s Pressure ...............................................................................................................104 4.2.3 Leaf Tissue Solute Potential and Proline Concentrations.....................107 4.3 Ion Content Assessment........................................................................109 4.3.1 K+, Na+ Content and Na+/K+ Ratio of Barley Stem..............................109 4.3.2 K+, Na+ Content and Na+/K+ Ratio of Barley Root...............................113 4.3.3 K+, Na+ Content and Na+/K+ Ratio of Barley Green Leaves................116 4.3.4 K+, Na+ Content and Na+/K+ Ratio of Barley Desiccated Leaves........119 4.3.5 Distribution of K+ and Na+ Content in Shoots and Roots.....................119 4.4 Assessment of Sodium Uptake.............................................................123 4.4.1 Na+ and K+ Uptake by Barley Shoots....................................................123 4.4.2 Na+ and K+ Uptake by Barley Roots.....................................................125 4.4.3 Distribution of K+ and Na+ Content in Shoots and Roots.....................125 4.5 Mapping Loci Conferring Tolerance in Landrace Local......................128 4.6 Epigenetic Studies in Barley Genotypes...............................................130 4.6.1 The Effects of Parental Salt Stress on Seedling Growth.......................130 4.7 Discussion.............................................................................................134 5 Chapter 5: Characterization of Thermotolerance in Barley...........................139 5.1 ‘Incremental’ Heat Stress......................................................................139 5.1.1 Gas Exchange Measurements...............................................................139 5.1.1.1 Light Saturated CO Assimilation Rates (A ).................................140 2 sat 5.1.1.2 Transpiration Rates (E) and Stomatal Conductance (gs)..................140 5.1.1.3 Relationship of CO Assimilation (A) with Stomatal Conductance (gs) 2 under Incremental Heat Stress Events..................................................140 5.1.2 Leaf Absorptance..................................................................................145 5.1.2.1 Light Absorptance.............................................................................145 5.1.2.2 Chlorophyll Fluorescence Excitation Spectra...................................145 5.2 ‘Temperature Jump’ Heat Stress Experiments......................................148 5.2.1 Gas Exchange Measurements...............................................................148 5.2.1.1 Light Saturated CO Assimilation Rates (A ) and Carboxylation 2 sat Efficiency (Φ CO )...............................................................................148 2 5.2.1.2 Phenotypic Differences in Leaves After Heat Stress........................149 5.2.1.3 Transpiration (E) and stomatal Conductance (gs).............................155 5.2.1.4 CO Assimilation and Photorespiration vs. Stomatal Conductance..156 2 vii 5.2.1.5 Relationship of CO Assimilation (A) And Apparent Photorespiration 2 with Stomatal Conductance (gs) under Temperature Jump Heat Stress Events....................................................................................................157 5.2.1.6 Effects of Temperature Jump Heat Stress on the Ratio of Stomatal Conductance Before, Immediately After and 5 Days after...................159 5.2.1.7 Stomatal Densities in Leaves of Local and Optic.............................159 5.2.2 Fluorescence Measurements.................................................................161 5.2.2.1 Quantum Efficiency (Fv/Fm) and Non Photochemical Quenching (NPQ)....................................................................................................161 5.2.2.2 Steady State and Maximum Electron Transport Rates.....................165 5.2.3 C3 Cycle Metabolites............................................................................168 5.2.3.1 Effect of Heat Stress on Metabolite Pool Levels of Cytosol, Mitochondria and Plastid......................................................................168 5.3 Discussion.............................................................................................173 6 Chapter 6: General Discussion..........................................................................176 6.1 Comparison of Salt Stress in Barley Genotypes...................................176 6.1.1 Epigenetic Base of Halotolerance in Barley.........................................183 6.2 Comparison of Thermal Stress in Barley Genotypes............................184 6.3 Conclusions and Future Work...............................................................190 6.3.1 Salt Stress..............................................................................................190 6.3.2 Thermal Stress.......................................................................................190 6.3.3 General Conclusions.............................................................................191 7 References............................................................................................................192 8 Appendix....................................................................Error! 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2. SEB Annual Conference, Prague, 30th June-3rd July 2010. beloved Messenger Muhammad (PBUH) for prioritizing the knowledge for the benefit.
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