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Roots and Uptake of Water and Nutrients

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Glossary

Fibrous root system :

root system formed by various root axis of similar size, typical of cereals.

Lateral roots :

are the roots formed from the pericycle cells of other roots. The first-order laterals referrer to the roots emerging from the primary and secondary root axes. Second-order laterals emerge from the first-order laterals, third-order laterals from the second-order lateral, and so on. Usually lateral branching is limited to the fifth-order laterals.

Primary roots :

often called seminal roots, are the first root axes to develop arising from the coleorhizae of the seed.

Rhizosphere :

volume of soil immediately adjacent to plant roots (usually between 10 and 20 mm), which is affected by their growth, secretions, respiration, nutrient and water, and associated soil microorganisms.

Root architecture :

describes the spatial configuration of the root system as a whole. Since it describes multiple root axes, it subsumes both topology and distribution.

Root cap...

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Bibliography

Primary Literature

  1. Lutz W, Sanderson W, Scherbov S (2001) The end of world population growth. Nature 412(6846):543–545

    Article  CAS  Google Scholar 

  2. Hamilton R (2009) Agriculture’s sustainable future: breeding better crops. In: Scientific American. http://www.scientificamerican.com/article.cfm?id=agricultures-sustainable-future

    Article  Google Scholar 

  3. Hirel B, Le Gouis J, Ney B, Gallais A (2007) The challenge of improving nitrogen use efficiency in crop plants: towards a more central role for genetic variability and quantitative genetics within integrated approaches. J Exp Bot 58(9):2369–2387

    Article  CAS  Google Scholar 

  4. Cattivelli L, Rizza F, Badeck F-W, Mazzucotelli E, Mastrangelo AM, Francia E, Marë C, Tondelli A, Stanca AM (2008) Drought tolerance improvement in crop plants: an integrated view from breeding to genomics. Field Crop Res 105(1–2):1–14

    Article  Google Scholar 

  5. Raun WR, Solie JB, Johnson GV, Stone ML, Mullen RW, Freeman KW, Thomason WE, Lukina EV (2002) Improving nitrogen use efficiency in cereal grain production with optical sensing and variable rate application. Agron J 94:815–820

    Article  Google Scholar 

  6. O’toole JC, Bland WL (1987) Genotypic variation in crop plant-root systems. Adv Agron 41:91–145

    Article  Google Scholar 

  7. Hoad SP, Russell G, Lucas ME, Bingham IJ (2001) The management of wheat, barley and oat root systems. In: Advances in agronomy, vol 74. Elsevier Academic Press Inc., San Diego, pp 193–246

    Chapter  Google Scholar 

  8. Gregory PJ (2006) Plant roots: growth, activity, and interaction with soils. Blackwell Publishing, Oxford

    Book  Google Scholar 

  9. Palta J, Watt M (2009) Vigorous crop root systems: form and function for improving the capture of water and nutrients. In: Sadras V (ed) Crop physiology – applications for genetic improvement and agronomy. Elsevier, San Diego

    Google Scholar 

  10. Reynolds M, Dreccer F, Trethowan R (2007) Drought-adaptive traits derived from wheat wild relatives and landraces. J Exp Bot 58(2):177–186

    Article  CAS  Google Scholar 

  11. Yoshida S, Hasegawa S (1982) The rice root system: its development and function. In: Drought resistance in crops with emphasis on rice. pp. 97–114, International Rice Research Institute, Los Baños, Philippines

    Google Scholar 

  12. Gahoonia TS, Nielsen NE (2004) Barley genotypes with long root hairs sustain high grain yields in low-P field. Plant Soil 262(1):55–62

    Article  CAS  Google Scholar 

  13. Richards RA, Passioura JB (1989) A breeding program to reduce the diameter of the major xylem vessel in the seminal roots of wheat and its effect on grain yield in rain-fed environments. Aust J Agric Res 40(5):943–950

    Article  Google Scholar 

  14. Fitter AH (1985) Functional significance of root morphology and root system architecture. In: Fitter AH, Atkinson D, Read DJ, Usher MB (eds) Ecological interactions in soil: plants, microbes and animals. Blackwell Scientific Publications, Oxford, pp 87–106

    Google Scholar 

  15. Lynch J (1995) Root architecture and plant productivity. Plant Physiol 109:7–13

    Article  CAS  Google Scholar 

  16. Gregory PJ, Crawford DV, Mcgowan M (1979) Nutrient relations of winter wheat: 2. Movement of nutrients to the root and their uptake. J Agric Sci 93:495–504

    Article  CAS  Google Scholar 

  17. Key JM (1973) The wheat root. In: Sears ER, Sears LMS (eds) 4th international wheat genetics symposium. University of Missouri/Agricultural Experiment Station, College of Agriculture, Columbia, pp 827–842

    Google Scholar 

  18. Gregory PJ, Mcgowan M, Biscoe PV, Hunter B (1978) Water relations of winter wheat: 1. Growth of root system. J Agric Sci 91:91–102

    Article  Google Scholar 

  19. Rich SM, Watt M (2013) Soil conditions and cereal root system architecture: review and considerations for linking Darwin and Weaver. J Exp Bot 64:1193–1208

    Article  CAS  Google Scholar 

  20. Hamblin A, Tennant D (1987) Root length density and water uptake in cereals and grain legumes: how well are they correlated? Aust J Agric Res 38:513–527

    Article  Google Scholar 

  21. Klepper B, Belford RK, Rickman RW (1984) Root and shoot development in winter wheat. Agron J 76(1):117–122

    Article  Google Scholar 

  22. Barraclough PB, Weir AH, Kuhlmann H (1991) Factors affecting the growth and distribution of winter wheat roots under UK field conditions. Develop Agric Manag-For Ecol 24:410–441

    Google Scholar 

  23. Barraclough PB, Weir AH (1988) Effects of compacted subsoil layer on root and shoot growth, water use and nutrient uptake of winter wheat. J Agric Sci 110:207–216

    Article  Google Scholar 

  24. Siddique KHM, Belford RK, Tennant D (1990) Root: shoot ratios of old and modern, tall and semidwarf wheats in a mediterranean environment. Plant Soil 121(1):89–98

    Article  Google Scholar 

  25. Barraclough PB (1984) The growth and activity of winter-wheat roots in the field - root-growth of high-yielding crops in relation to shoot growth. J Agric Sci 103:439–442

    Article  Google Scholar 

  26. Brouwer R (1983) Functional equilibrium: sense or nonsense? Neth J Agric Sci 31(4):335–348

    Google Scholar 

  27. Gregory PJ, Palta JA, Batts GR (1997) Root systems and root:mass ratio – carbon allocation under current and projected atmospheric conditions in arable crops. Plant Soil 187(2):221–228

    Article  Google Scholar 

  28. Gerwitz A, Page ER (1974) An empirical mathematical model to describe plant root systems. J Appl Ecol 11(2):773–781

    Article  Google Scholar 

  29. Gale MR, Grigal DF (1987) Vertical root distributions of northern tree species in relation to successional status. Can J For Res-Revue Canadienne De Recherche Forestiere 17(8):829–834

    Article  Google Scholar 

  30. Robertson MJ, Fukai S, Hammer GL, Ludlow MM (1993) Modelling root growth of grain sorghum using the CERES approach. Field Crop Res 33:113–130

    Article  Google Scholar 

  31. Zhuang J, Yu GR, Nakayama K (2001) Scaling of root length density of maize in the field profile. Plant Soil 235:135–142

    Article  CAS  Google Scholar 

  32. King J, Gay A, Sylvester-Bradley R, Bingham I, Foulkes J, Gregory P, Robinson D (2003) Modelling ceral root systems for water and nitrogen capture: towards an economic optimum. Ann Bot 91:383–390

    Article  CAS  Google Scholar 

  33. Thomas GA, Fukai S, Hammer GL (1995) Growth and yield response of barley and chickpea to water stress under three environments in Southeast Queensland. II* root growth and soil wate extraction pattern. Aust J Agric Res 46:35–48

    Article  Google Scholar 

  34. Monteith JL (1986) How do crops manipulate water-supply and demand. Philos Trans R Soc Lond Ser A Math Phys Eng Sci 316(1537):245–259

    Article  Google Scholar 

  35. Robertson MJ, Fukai S, Ludlow MM, Hammer GL (1993) Water extraction by grain sorghum in a sub-humid environment. II. Extraction in relation to root growth. Field Crop Res 33:99–112

    Article  Google Scholar 

  36. Eissenstat DM (1991) On the relationship between specific root length and the rate of root proliferation – a field-study using citrus rootstocks. New Phytol 118(1):63–68

    Article  Google Scholar 

  37. Welbank PJ, Gibb MJ, Taylor PJ, Williams ED (1974) Root growth of cereal crops. Rothamsted experimental station report, 1973, Part 2, pp 26–66

    Google Scholar 

  38. Barraclough PB, Leigh RA (1984) The growth and activity of winter wheat roots in the field: the effect of sowing date and soil type on root growth of high yielding crops. J Agric Sci 103:59–74

    Article  Google Scholar 

  39. Van Noordwijk M, Brouwer G (1991) Review of quantitative root length data in agriculture. Elsevier, Amsterdam, PAYS-BAS

    Book  Google Scholar 

  40. Ryser P (1996) The importance of tissue density for growth and life span of leaves and roots: a comparison of five ecologically contrasting grasses. Funct Ecol 10(6):717–723

    Article  Google Scholar 

  41. Wahl S, Ryser P (2000) Root tissue structure is linked to ecological strategies of grasses. New Phytol 148:459–471

    Article  Google Scholar 

  42. Valenzuela-Estrada LR, Vera-Caraballo V, Ruth LE, Eissenstat DM (2008) Root anatomy, morphology, and longevity among root orders in Vaccinium corymbosum (Ericaceae). Am J Bot 95(12):1506–1514

    Article  Google Scholar 

  43. Eissenstat DM (1992) Costs and benefits of constructing roots of small diameter. J Plant Nutr 15(6–7):763–782

    Article  Google Scholar 

  44. Fitter AH (1996) Characteristics and functions of root systems. In: Waisel Y, Eshel A, Kafkafi U (eds) Plant roots: the hidden half. Marcel Dekker, New York, pp 1–20

    Google Scholar 

  45. Hetrick BAD, Leslie JF, Wilson GT, Kitt DG (1988) Physical and topological assessment of effects of a vesicular-arbuscular mycorrhizal fungus on root architecture of big bluestem. New Phytol 110(1):85–96

    Article  Google Scholar 

  46. Ryser P (1998) Intra- and interspecific variation in root length, root turnover and the underlying parameters. In: Lambers H, Poorter H, van Vuuren MMI (eds) Inherent variation in plant growth. Physiological mechanisms and ecological consequences. Backhuys Publishers, Leiden

    Google Scholar 

  47. de Dorlodot S, Forster B, Pages L, Price A, Tuberosa R, Draye X (2007) Root system architecture: opportunities and constraints for genetic improvement of crops. Trends Plant Sci 12:474–481

    Article  CAS  Google Scholar 

  48. Den Herder G, Van Isterdael G, Beeckmam T, De Smet I (2010) The roots of a new green revolution. Trends Plant Sci 15:600–607

    Article  CAS  Google Scholar 

  49. Zhu J, Iingram PA, Benfey PN, Elich T (2011) From lab to field, new approaches to phenotyping root system architecture. Curr Opin Plant Biol 14:310–317

    Article  Google Scholar 

  50. Ehdaie B, Waines JG (2003) 1RS translocation increases root biomass in Veery-type wheat isogenic lines and associates with grain yield. In: Pogna NE, Romano M, Pogna EA, Galterio G (eds) Proceedings of the 10th international wheat genetics symposium. Rome, ISC, Paestum, pp 693–695

    Google Scholar 

  51. Hamblin A, Tennant D, Perry MW (1990) The cost of stress – dry-matter partitioning changes with seasonal supply of water and nitrogen to dryland wheat. Plant Soil 122(1):47–58

    Article  Google Scholar 

  52. Barraclough PB, Kuhlmann H, Weir AH (1989) The effects of prolonged drought and nitrogen-fertilizer on root and shoot growth and water-uptake by winter-wheat. J Agron Crop Sci 163(5):352–360

    Article  Google Scholar 

  53. Zenisceva L (1990) The importance of the root-system in adaptation of spring barley genotypes to the conditions of environment. Rostlinna Vyroba 36:937–945

    Google Scholar 

  54. Palta JA, Gregory PJ (1997) Drought affects the fluxes of carbon to roots and soil in C-13 pulse-labelled plants of wheat. Soil Biol Biochem 29(9–10):1395–1403

    Article  CAS  Google Scholar 

  55. Martino DL, Shaykewich CF (1994) Root penetration profiles of wheat and barley as affected by soil penetration resistance in field conditions. Can J Soil Sci 74:193–200

    Article  Google Scholar 

  56. Kramer PJ (1983) Water relations of plants. Academic Press, Inc. Ltd., London

    Google Scholar 

  57. Karrou M, Maranville JW (1994) Response of wheat cultivars to different soil nitrogen and moisture regimes: I. Dry matter partitioning and root growth. J Plant Nutr 17(5):729–744

    Article  CAS  Google Scholar 

  58. Davidson RL (1969) Effect of root/leaf temperature differentials on root/shoot ratios in some pasture grasses and clover. Ann Bot 33(3):561–569

    Article  Google Scholar 

  59. Gregory PJ (1994) Root growth and activity. In: Boote KJ, Bennett JM, Sinclair TR, Paulsen GM (eds) Physiology and determination of crop yield. Soil Science Society of America, Madison, pp 65–93

    Google Scholar 

  60. Sharp RE, Davies WJ (1979) Solute regulation and growth by roots and shoots of water-stressed maize plants. Planta 147(1):43–49

    Article  CAS  Google Scholar 

  61. Li F-M, Yan X, Li F-R, Guo A-H (2001) Effects of different water supply regimes on water use and yield performance of spring wheat in a simulated semi-arid environment. Agric Water Manag 47(1):25–35

    Article  Google Scholar 

  62. Robinson D (1994) Resource capture by single roots. In: Monteith JL (ed) Resource capture by crops. Nottingham University Press, Loughborough, pp 53–76

    Google Scholar 

  63. Baburai nagesh AK (2006) The physiological and genetic bases of water-use efficiency in winter wheat. PhD thesis, The University of Nottingham

    Google Scholar 

  64. Ebrahim NM (2008) Responses of root and shoot growth of durum wheat (Triticum turgidum L. var durum) and barley (Hordeum vulgare L.) plants to different water and nitrogen levels. University of Jorda

    Google Scholar 

  65. Fitter AH (1987) An architectural approach to the comparative ecology of plant root systems. New Phytol 106:61–77

    Article  Google Scholar 

  66. Li FM, Liu XL, Li SQ (2001) Effects of early soil water distribution on the dry matter partition between roots and shoots of winter wheat. Agric Water Manag 49(3):163–171

    Article  Google Scholar 

  67. Pardales JR, Kono Y (1990) Development of sorghum root system under increasing drought stress. Jpn J Crop Sci 59:752–761

    Article  Google Scholar 

  68. Sjharp R, Silk W, Hsiao T (1988) Growth of the maize primary root at low water potentials. I. Spatial distribution of expansive growth. Plant Physiol 87:50–57

    Article  Google Scholar 

  69. Salim MH, Todd GWS, M A (1965) Root development of wheat, oats and barley under conditions of soil moisture stress. Agron J 57:603–607

    Article  Google Scholar 

  70. Stasovski E, Peterson CA (1991) The effects of drought and subsequent rehydration on the structure and vitality of Zea Mays seedling roots. Can J Bot 69:1170–1178

    Article  Google Scholar 

  71. Sharp RE, Davies WJ (1979) Solute regulation and growth by roots and shoots of water-stressed maize plants. Planta 147:43–49

    Article  CAS  Google Scholar 

  72. Takahashi H (1997) Hydrotropism: the current state of our knowledge. J Plant Res 110:163–169

    Article  CAS  Google Scholar 

  73. Eapen D, Barroso ML, Ponce G, Campos ME, Cassab GI (2005) Hydrotropism: root growth responses to water. Trends Plant Sci 10:44–50

    Article  CAS  Google Scholar 

  74. Takahashi H, Scott TK (1991) Hydrotropism and its interaction with gravitropism in maize roots. Plant Physiol 96:558–564

    Article  CAS  Google Scholar 

  75. Turner NC, Begg JE (1981) Plant-water relations and adaptation to stress. Plant Soil 58(1–3):97–131

    Article  Google Scholar 

  76. Kramer PJ (1988) Changing concepts regarding plant water relations. Plant Cell Environ 11(7):565–568

    Article  Google Scholar 

  77. Hsiao TC, Frensch J, Rojas-Lara BAR (1998) The pressure-jump technique shows maize leaf growth to be enhanced by increases in turgor only when water status is not too high. Plant Cell Environ 21(1):33–42

    Article  Google Scholar 

  78. Passioura JB (1988) Changing concepts regarding plant water relations – response. Plant Cell Environ 11(7):569–571

    Article  Google Scholar 

  79. Passioura JB (1988) Root signals control leaf expansion in wheat seedlings growing in drying soil. Aust J Plant Physiol 15(5):687–693

    Article  Google Scholar 

  80. Gowing DJG, Davies WJ, Jones HG (1990) A positive root-sourced signal as an indicator of soil drying in apple, Malus x domestica Borkh. J Exp Bot 41(233):1535–1540

    Article  Google Scholar 

  81. Davies WJ, Tardieu F, Trejo CL (1994) How do chemical signals work in plants that grow in drying soil? Plant Physiol 104(2):309–314

    Article  CAS  Google Scholar 

  82. Taylor IB, Burbidge A, Thompson AJ (2000) Control of abscisic acid synthesis. J Exp Bot 51(350):1563–1574

    Article  CAS  Google Scholar 

  83. Zhang J, Davies WJ (1990) Changes in the concentration of aba in xylem sap as a function of changing soil-water status can account for changes in leaf conductance and growth. Plant Cell Environ 13(3):277–285

    Article  CAS  Google Scholar 

  84. Davies WJ, Zhang J (1991) Root signals and the regulation of growth and development of plants in drying soil. Annu Rev Plant Physiol Plant Mol Biol 42(1):55–76

    Article  CAS  Google Scholar 

  85. Hartung W, Jeschke WD (1999) Abscisic acid: a long-distance stress signal in salt-stressed plants. In: Lerner HR (ed) Plant responses to environmental stresses. Marcel Dekker Inc., New York, pp 333–348

    Google Scholar 

  86. Gollan T, Passioura JB, Munns R (1986) Soil water status affects the stomatal conductance of fully turgid wheat and sunflower leaves. Aust J Plant Physiol 13(4):459–464

    Article  Google Scholar 

  87. Aphale SL (2004). Role of root to shoot signalling in coordinating responses to nitrogen deficiency. PhD thesis, University of Nottingham

    Google Scholar 

  88. Munns R, Passioura JB, Guo JM, Chazen O, Cramer GR (2000) Water relations and leaf expansion: importance of time scale. J Exp Bot 51(350):1495–1504

    Article  CAS  Google Scholar 

  89. StikiĆ R, Davies WJ (2000) Stomatal reactions of two different maize lines to osmotically induced drought stress. Biol Plant 43(3):399–405

    Article  Google Scholar 

  90. Novoa R, Loomis RS (1981) Nitrogen and plant production. Plant Soil 58(1–3):177–204

    Article  CAS  Google Scholar 

  91. Dreccer M, Schapendonk A, Slafer G, Rabbinge R (2000) Comparative response of wheat and oilseed rape to nitrogen supply: absorption and utilisation efficiency of radiation and nitrogen during the reproductive stages determining yield. Plant Soil 220(1):189–205

    Article  CAS  Google Scholar 

  92. Mengel K, Kirkby EA (2001) Principles of plant nutrition. Kluwer Academic, London

    Book  Google Scholar 

  93. Reich PB (2002) Root-shoot relations: optimality in acclimation and adaptation or the: “Emperor’s new clothes”? In: Waisel Y, Eshel A, Kafkafi U (eds) Plant roots: the hidden half. Marcel Dekker, New York, pp 205–220

    Chapter  Google Scholar 

  94. Robinson D (2001) Root proliferation, nitrate inflow and their carbon costs during nitrogen capture by competing plants in patchy soil. Plant Soil 232(1–2):41–50

    Article  CAS  Google Scholar 

  95. Robinson D, Hodge A, Griffiths BS, Fitter AH (1999) Plant root proliferation in nitrogen-rich patches confers competitive advantage. Proc R Soc Lond Ser B Biol Sci 266(1418):431–435

    Article  Google Scholar 

  96. Jackson RB, Caldwell MM (1989) The timing and degree of root proliferation in fertile-soil microsites for 3 cold-desert perennials. Oecologia 81(2):149–153

    Article  CAS  Google Scholar 

  97. Drew MC, Saker LR, Ashley TW (1973) Nutrient supply and the growth of the seminal root system in barley: I. The effect of nitrate concentration on the growth of axes and laterals. J Exp Bot 24(6):1189–1202

    Article  CAS  Google Scholar 

  98. Drew MC, Saker LR (1975) Nutrient supply and the growth of the seminal root system in barley: II. Localized, compensatory increases in lateral root growth and rates op nitrate uptake when nitrate supply is restricted to only part of the root system. J Exp Bot 26(1):79–90

    Article  CAS  Google Scholar 

  99. Drew MC, Saker LR (1978) Nutrient supply and the growth of the seminal root system in barley: III. Compensatory increases in growth of lateral roots, and in rates of phosphate uptake, in response to a localized supply of phosphate. J Exp Bot 29(2):435–451

    Article  CAS  Google Scholar 

  100. Zhang HM, Forde BG (1998) An Arabidopsis MADS box gene that controls nutrient-induced changes in root architecture. Science 279(5349):407–409

    Article  CAS  Google Scholar 

  101. Robinson D (1994) The responses of plants to non-uniform supplies of nutrients. New Phytol 127(4):635–674

    Article  CAS  Google Scholar 

  102. Brown SC, Keatinge JDH, Gregory PJ, Cooper PJM (1987) Effects of fertilizer, variety and location on barley production under rainfed conditions in northern Syria 1. Root and shoot growth. Field Crop Res 16:53–66

    Article  Google Scholar 

  103. Herrera JM, Stamp P, Liedgens M (2005) Dynamics of root development of spring wheat genotypes varying in nitrogen use efficiency. In: Foulkes J, Russel G, Hawkesford M, Gooding M, Sparkes D, Stockdale E (eds) Roots and the soil environment II. Associatin of Applied Biologists, Warwick, pp 197–201

    Google Scholar 

  104. Ryser P, Lambers H (1995) Root and leaf attributes accounting for the performance of fast- and slow-growing grasses at different nutrient supply. Plant Soil 170:251–265

    Article  CAS  Google Scholar 

  105. Foulkes MJ, Hawkesford MJ, Barraclough PB, Holdsworth MJ, Kerr S, Kightley S, Shewry PR (2009) Identifying traits to improve the nitrogen economy of wheat: recent advances and future prospects. Field Crop Res 123:139–152

    Google Scholar 

  106. Doussan C, Pages L, Pierret A (2003) Soil exploration and resource acquisition by plant roots: an architectural and modelling point of view. Agronomie 23(5–6):419–431

    Article  Google Scholar 

  107. Kramer PJ, Boyer JS (1995) Water relations of plants and soils. Academic Press, San Diego

    Google Scholar 

  108. Van Noordwijk M (1983) Functional interpretation of root densities in the field for nutrient and water uptake. In: Böhm W, Kutschera L, Lichtenegger E (eds) Root ecology and its practical application, international symposium on gumpenstein 1982. Irdning, Bundesanstalt Gumpenstein, pp 207–226

    Google Scholar 

  109. Gregory PJ, Brown SC (1989) Root growth, water use and yield of crops in dry environments: what characteristics are desirable? Asp Appl Biol 22:235–243

    Google Scholar 

  110. Pantuwan G, Fukai S, Cooper M, O’toole JC, Sarkarung S (1997) Root traits to increase drought resistance in rainfed lowland rice. Breeding Strategies for Rainfed Lowland Rice in Drought-Prone Environments 77:170–179

    Google Scholar 

  111. Lilley JM, Fukai S (1994) Effect of timing and severity of water deficit on four diverse rice cultivars I. Rooting pattern and soil water extraction. Field Crop Res 37(3):205–213

    Article  Google Scholar 

  112. Siopongco J, Yamauchi A, Salekdeh H, Bennett J, Wade LJ (2005) Root growth and water extraction response of doubled-haploid rice lines to drought and rewatering during the vegetative stage. Plant Prod Sci 8(5):497–508

    Article  Google Scholar 

  113. Ford KE, Gregory PJ, Gooding MJ, Pepler S (2006) Genotype and fungicide effects on late-season root growth of winter wheat. Plant Soil 284(1–2):33–44

    Article  CAS  Google Scholar 

  114. Christopher JT, Manschadi AM, Hammer GL, Borrell AK (2008) Developmental and physiological traits associated with high yield and stay-green phenotype in wheat. Aust J Agric Res 59(4):354–364

    Article  Google Scholar 

  115. Bengough AG, Bransby MF, Hans J, Mckenna SJ, Roberts TJ, Valentine TA (2006) Root responses to soil physical conditions; growth dynamics from field to cell. J Exp Bot 57(2):437–447

    Article  CAS  Google Scholar 

  116. Kato Y, Abe J, Kamoshita A, Yamagishi J (2006) Genotypic variation in root growth angle in rice (Oryza sativa L.) and its association with deep root development in upland fields with different water regimes. Plant Soil 287:117–129

    Article  CAS  Google Scholar 

  117. Uga Y, Okiuno K, Yano M (2011) Dro1, a major QTL involved in deep rooting of rice under upland field conditions. J Exp Bot 62:2485–2494

    Article  CAS  Google Scholar 

  118. Manscadi A, Hammer G, Christopher J, De Voil P (2008) Genotypic variation in seedling root architectural traits and implications for drought adaptation in wheat (Triticum aestivum L.) Plant Soil 303:115–129

    Article  CAS  Google Scholar 

  119. Manschadi AM, Christopher JT, Hammer GL, de Voil P (2010) Experimental and modelling studies of drought-adaptive root architectural traits in wheat (Triticum aestivum L.) Plant Biosyst 144:458–462

    Article  Google Scholar 

  120. Olivares-Villegas JJ, Reynolds MP, McDonald GK (2007) Drought-adaptive attributes in the Seri/Babax hexaploid wheat population. Funct Plant Biol 34:189–203

    Article  Google Scholar 

  121. Oyanagi A, Nakamoto T, Wada M (1993) Relationship between root growth angle of seedlings and vertical distribution of roots in the field in wheat cultivars. Jpn J Crop Sci 62:565–570

    Article  Google Scholar 

  122. Trachsel S, Kaeppler SM, Brown KM, Lynch JP (2013) Maize root growth angles become steeper under low N conditions. Field Crop Res 140:18–31

    Article  Google Scholar 

  123. Lynch JP (2013) Steep, cheap and deep: an ideotype to optimize water and N acquisition by maize root systems. Ann Bot 112:347–357

    Article  CAS  Google Scholar 

  124. Kirk GJD (2003) Rice root properties for internal aeration and efficient nutrient acquisition in submerged soil. New Phytol 159(1):185–194

    Article  CAS  Google Scholar 

  125. Eapen D, Barroso ML, Ponce G, Campos ME, Cassab GI (2005) Hydrotropism: rootgrowthresponsestowater. Trends Plant Sci 10:44–50. https://doi.org/10.1016/j.tplants.2004.11.004

    Article  CAS  Google Scholar 

  126. Takashashi H, Miyazawa Y, Fujii N (2009) Hormonal interactions during root tropic growth: hydrotropism versus gravitropism. Plant Mol Biol 69:489–502. https://doi.org/10.1007/s11103-008-9438-x

    Article  CAS  Google Scholar 

  127. Cassab GI, Eapen D, Camjpos ME (2013) Root hydrotropism: an update. Am J Bot 100:14–24

    Article  CAS  Google Scholar 

  128. Takahashi N, Goto N, Okada K, Takahashi H (2002) Hydrotropism in abscisic acid, wavy, and gravitropic mutants of Arabidopsis thaliana. Planta 216:203–211

    Article  CAS  Google Scholar 

  129. Kaneyasu T, Kobayashi A, Nakayama M, Fujii N, Takahashi H, Miyazawa Y (2007) Auxin response, but not its polar transport, plays a role in hydrotropism of Arabidopsis roots. J Exp Bot 58:1143–1150

    Article  CAS  Google Scholar 

  130. Koevoets IT, Venema JH, Elzenga JTM, Testerink C (2016) Roots withstanding their environment: exploiting root system architecture responses to abiotic stress to improve crop tolerance. Front Plant Sci 7:1335

    Article  Google Scholar 

  131. Moriwaki T, Mitazawa Y, Kobayashi A, Takahashi H (2013) Molecular mechanisms of hydrotropism in seedling roots of Arabidopsis thaliana (Brassicaceae). Am J Bot 100:25–34

    Article  CAS  Google Scholar 

  132. Takahashi H, Scott TK (1991) Hydrotropism and its interactions with gravitropism in maize roots. Plant Physiol 96:558–564

    Article  CAS  Google Scholar 

  133. Mizuno H, Kobayashi A, Fijii N, Yamashita M, Takahashi H (2002) Hydrotropic response and expression pattern of auxin-inducible gene, CS-IAA1, in the primary roots of clinorotated cucumber seedlings. Plant Cell Physiol 43:793–801

    Article  CAS  Google Scholar 

  134. Takahashi H, Suge H (1991) Root hydrotropism of an agravitropic pea mutant, ageotropum. Physiol Plant 82:24–31

    Article  Google Scholar 

  135. Takahashi H, Takano M, Fijii N, Yamashita M, Suge H (1996) Induction of hydrotropism in clinorotated seedling roots of Alaska pea, Pisum sativum L. J Plant Res 109:335–337

    Article  CAS  Google Scholar 

  136. Shkolnik D, Kreiger G, Nuriel R, Fromm H (2016) Hydrotropism: root bending does not require auxin redistribution. Mol Plant 9:757–759

    Article  CAS  Google Scholar 

  137. Bao Y, Aggarwal P, Robbins NE, Stuttock CJ, Thompson MC, Tan HQ et al (2014) Plant roots use a patterning mechanism to position lateral root branches toward available water. Proc Natl Acad Sci USA 111:9319–9324

    Article  CAS  Google Scholar 

  138. Deak KI, Malamy J (2005) Osmotic regulation of root system architecture. Plant J 43:17–28

    Article  CAS  Google Scholar 

  139. Robinson D, Linehan DJ, Caul S (1991) What limits nitrate uptake from soil. Plant Cell Environ 14(1):77–85

    Article  CAS  Google Scholar 

  140. Cooper PJM, Gregory PJ, Keatinge JDH, Brown SC (1987) Effects of fertilizer, variety and location on barley production under rainfed conditions in Northern Syria. 2: soil water dyamics and crop water use. Field Crop Res 16:67–84

    Article  Google Scholar 

  141. Wiesler F, Horst WJ (1993) Differences among maize cultivars in the utilization of soil nitrate and the related losses of nitrate through leaching. Plant Soil 151:193–203

    Article  CAS  Google Scholar 

  142. Wiesler F, Horst WJ (1994) Root growth and nitrate utilization of maize cultivars under field conditions. Plant Soil 163:267–277

    Article  CAS  Google Scholar 

  143. Thorup-Kristensen K (1993) Root development of nitrogen catch crops and of a succeeding crop of broccoli. Acta Agric Scand Sect B Soil Plant Sci 43:58–64

    CAS  Google Scholar 

  144. Linkhor BI, Williamson LC, Fitter AH, Leyser HMO (2002) Nitrate and phosphate availability and distribution havedifferent effects on root system architecture of Arabidopsis. Plant J 29:751–760

    Article  Google Scholar 

  145. Gruber BD, Giehl RFH, Friede S, von Wiren N (2013) Plasticity of the Arabidopsis root system under nutrient deficiencies. Plant Physiol 163:161–179

    Article  CAS  Google Scholar 

  146. Saengwilai P, Tian X, Lynch JP (2014) Low crown root number enhances nitrogen acquisition from low-nitrogen soils in maize. Plant Physiol 166:581–589

    Article  CAS  Google Scholar 

  147. Fitter AH, Stickland TR (1991) Architectural analysis of plant-root systems: 2. Influence of nutrient supply on architecture in contrasting plant-species. New Phytol 118(3):383–389

    Article  Google Scholar 

  148. Cabrera-Bosquet L, Molero G, Bort J, Nogués S, Araus JL (2007) The combined effect of constant water deficit and nitrogen supply on WUE, NUE and D13C in durum wheat potted plants. Ann Appl Biol 151(3):277–289

    Article  CAS  Google Scholar 

  149. Pask A (2009) Optimising nitrogen storage in wheat canopies for genetic reduction in fertiliser nitrogen inputs. PhD thesis, The University of Nottingham

    Google Scholar 

  150. Dunbabin V, Diggle A, Rengel Z (2003) Is there an optimal root architecture for nitrate capture in leaching environments? Plant Cell Environ 26:835–844

    Article  Google Scholar 

  151. Forde BG, Clarkson DT (1999) Nitrate and ammonium nutrition of plants: physiological and molecular perspectives. In: Callow JA (ed) Advances in botanical research incorporating advances in plant pathology, vol 30. Academic Press Inc., San Diego, pp 1–90

    Chapter  Google Scholar 

  152. Crawford NM, Glass ADM (1998) Molecular and physiological aspects of nitrate uptake in plants. Trends Plant Sci 3(10):389–395

    Article  Google Scholar 

  153. Williams LE, Miller AJ (2001) Transporters responsible for the uptake and partitioning of nitrogenous solutes. Annu Rev Plant Physiol Plant Mol Biol 52:659–688

    Article  CAS  Google Scholar 

  154. Hawkesford MJ, Miller AJ (2004) Ion-coupled transport of inorganic solutes. In: Blatt MR (ed) Membrane transport in plants annual reviews 15. Blackwell CRC Press publishing, Oxford, pp 105–134

    Google Scholar 

  155. Lauter FR, Ninnemann O, Bucher M, Riesmeier JW, Frommer WB (1996) Preferential expression of an ammonium transporter and of two putative nitrate transporters in root hairs of tomato. Proc Natl Acad Sci USA 93(15):8139–8144

    Article  CAS  Google Scholar 

  156. Zhuo DG, Okamoto M, Vidmar JJ, Glass ADM (1999) Regulation of a putative high-affinity nitrate transporter (Nrt2;1At) in roots of Arabidopsis thaliana. Plant J 17(5):563–568

    Article  CAS  Google Scholar 

  157. Ono F, Frommer WB, Von Wiren N (2000) Coordinated diurnal regulation of low- and high-affinity nitrate transporters in tomato. Plant Biol 2(1):17–23

    Article  CAS  Google Scholar 

  158. Orsel M, Krapp A, Daniel-Vedele F (2002) Analysis of the NRT2 nitrate transporter family in Arabidopsis. Structure and gene expression. Plant Physiol 129(2):886–896

    Article  CAS  Google Scholar 

  159. Bucher M (2007) Functional biology of plant phosphate uptake at root and mycorrhiza interfaces. New Phytol 173(1):11–26

    Article  CAS  Google Scholar 

  160. Miller AJ, Shen Q, Xu G (2009) Freeways in the plant: transporters for N, P and S and their regulation. Curr Opin Plant Biol 12(3):284–290

    Article  CAS  Google Scholar 

  161. Gregory PJ (1994) Resource capture by root networks. In: Monteith JL, Scoot RK, Unsworth MH (eds) Resource capture by crops. Nottingham University Press, Nottingham, pp 77–97

    Google Scholar 

  162. Nielsen NE, Schjorring JK (1983) Efficiency and kinetics of phosphorus uptake from soil by various barley genotypes. Plant Soil 72(2–3):225–230

    Article  CAS  Google Scholar 

  163. López-Bucio J, Hernández-Abreu E, Sánchez-Calderón L, Nieto-Jacobo MF, Simpson J, Herrera-Estrella L (2002) Phosphate availability alters architecture and causes changes in hormone sensitivity in the Arabidopsis root system. Plant Physiol 129(1):244–256

    Article  CAS  Google Scholar 

  164. Poirier Y, Bucher M (2002) Phosphate transport and homeostasis in Arabidopsis. American Society of Plant Biologists, Rockville

    Google Scholar 

  165. Lynch JP, Brown KM (2001) Top soil foraging – an architectural adaptation of plants to low phosphorus availability. Plant Soil 237:225–237

    Article  CAS  Google Scholar 

  166. Peret B, Clement M, Nussaume L, Desnos T (2011) Root developmental adaptation to phosphate starvation: better safe than sorry. Trends Plant Sci 16:442–450

    Article  CAS  Google Scholar 

  167. Williamson LC (2001) Phosphate availability regulates root system architecture in Arabidopsis. Plant Physiol 126:875–882

    Article  CAS  Google Scholar 

  168. Zhu J, Lynch JP (2004) The contribution of lateral rooting to phosphorus acquisition efficiency in maize (Zea mays) seedlings. Funct Plant Biol 31:949–958

    Article  CAS  Google Scholar 

  169. Gahoonia TS, Nielsen NE, Joshi PA, Jahoor A (2001) A root hairless barley mutant for elucidating genetic of root hairs and phosphorus uptake. Plant Soil 235:211–219

    Article  CAS  Google Scholar 

  170. Koltai H (2011) Strigolactones are regulators of root development. New Phytol 190:545–549

    Article  CAS  Google Scholar 

  171. Ruyter-Spira C, Kohlen W, Charnikhova T, van Zeiil A, van Bezouwen L, de Ruijter N et al (2011) Physiological effects of the synthetic strigolactone analog GR24 on root system architecture in Arabidopsis: another below ground role for strigolactones? Plant 155:721–734

    CAS  Google Scholar 

  172. Mayzlish-Gati E, De-Cuyper C, Goormachtig S, Beeckman T, Vuylsteke M, Brewer PB et al (2012) Strigolactones are involved in root response to low phosphate conditions in Arabidopsis. Plant Physiol 160:1329–1341

    Article  CAS  Google Scholar 

  173. Matthys C, Walton A, Struk S, Stes E, Boyer FD, Gevaert K et al (2016) The whats, the wheres and the hows of strigolactone action in the roots. Planta 243:1327–1337

    Article  CAS  Google Scholar 

  174. Kapulnik Y, Resnick N, Mayzlish-Gati E, Kaplan Y, Wininger S, Hherhemhorn J et al (2011) Strigolactones interact with ethylene and auxin in regulating root-hair elongationin Arabidopsis. J Exp Bot 62:2915–2924

    Article  CAS  Google Scholar 

  175. Bonser AM, Lynch J, Snapp S (1995) Effect of phosphorus availability on basal root-growth angle in bean. Plant Physiol 108:112

    Google Scholar 

  176. Hurd EA (1974) Phenotype and drought tolerance in wheat. Agric Meteorol 14(1–2):39–55

    Article  Google Scholar 

  177. Mackey J (1973) The wheat root. In: Sears ER, Sears LMS (eds) Proceedings 4th international wheat genetics symposium, Columbia, pp 827–842

    Google Scholar 

  178. Briggle LW, Vogel LW (1968) Breeding short-statured, disease resistant wheats in the United States. Suppl Euphytica 1:107–130

    Google Scholar 

  179. Subbiah BV, Katayal JC, Narasinham RL, Dakshinamuri C (1968) Preliminary investigations on root distribution of high yielding wheat varieties. Int J Appl Radioact Isot 19:385–390

    Article  Google Scholar 

  180. Viemani SM (1971) Rooting patterns of dwarf wheats. Indian J Agron 61:33–36

    Google Scholar 

  181. Gupta AP, Virmani SM (1973) Note on the rooting pattern of three-gene-dwarf wheats. Indian J Agric Sci 43:971–973

    Google Scholar 

  182. Holbrook FS (1973) Rooting depths of selected wheat cultivars. MSc thesis, Colorado State University

    Google Scholar 

  183. Cholick FA, Welsh JR, Cole CV (1977) Rooting patterns of semi-dwarf and tall winter wheat cultivars under dryland field conditions. Crop Sci 17:637–639

    Article  Google Scholar 

  184. Bingham IJ, Foulkes MJ, Gay AP, Gregory PJ, King JA, Robinson D, Bradley RS (2002) ‘Balancing’ root and canopy growth. In: Authority HGC (ed) R & D conference: agronomic intelligence: the basis for profitable production, pp 6.1–6.14

    Google Scholar 

  185. Ehdaie B, Waines JG (1994) Growth and transpiration efficiency of near isogenic lines for height in a spring wheat. Crop Sci 34:1443–1451

    Article  Google Scholar 

  186. Haberle J, Svoboda P, Blaha L (1995) The comparison of shoot and root production in old and new cultivars of winter cereals. Roslinna Vyroba 41:511–551

    Google Scholar 

  187. Miralles DJ, Slafer GA, Lynch V (1997) Rooting patterns in near-isogenic lines of spring wheat for dwarfism. Plant Soil 197(1):79–86

    Article  CAS  Google Scholar 

  188. Troughton A, Whittington WJ (1968) The significance of genetic variation in root systems. In: Whittington WJ (ed) Root growth. Proceedings of the 15th Easter school in agricultural sciences. University of Nottingham/Plenum, New York, pp 296–314

    Google Scholar 

  189. Ehdaie B, Hall AE, Farquhar GD, Nguyen HT, Waines JG (1991) Water-use efficiency and carbon isotope discrimination in wheat. Crop Sci 31:1282–1288

    Article  Google Scholar 

  190. Ehdaie B, Waines JG (1993) Variation in water-use efficiency and its components in wheat. I. Well-watered pot experiment. Crop Sci 33:294–299

    Article  Google Scholar 

  191. Ehdaie B, Waines JG (1997) Growth and evapotranspiration efficiency in landrace and dwarf spring wheats. J Genet Breed 51:201–209

    Google Scholar 

  192. Ehdaie B (1995) Variation in water-use efficiency and its components in wheat. II. Pot and field experiments. Crop Sci 35:1617–1626

    Article  Google Scholar 

  193. Waines JG, Ehdaie B (2007) Domestication and crop physiology: roots of green-revolution wheat. Ann Bot 100:991–998

    Article  Google Scholar 

  194. Dreccer MF, Ogbonnaya FC, Borgognone MG (2004) Sodium exclusion in primary synthetic wheats. In: Black CK, Panozzo JF, Rebetzke GJ (eds) Proceedings of the 54th Australian cereal chemistry conference and 11th wheat breeders assembly, Sept 2004. Canberra Cereal Chemistry Division, RACI, pp 118–121

    Google Scholar 

  195. Lopes MS, Reynolds MP (2011) Drought adaptive traits and wide adaptation in elite lines derived from resynthesized hexaploid wheat. Crop Sci 51:1617–1626

    Article  Google Scholar 

  196. Mercjuck-Ovnat L, Fahima T, Ephrath JE, Krugman T, Saranga Y (2017) Ancestral QTL alleles from wild emmer wheat enhance root development under drought in modern wheat. Front Plant Sci 8:703

    Article  Google Scholar 

  197. Yu LX, Ray JD, O’toole JC, Nguyen HT (1995) Use of wax-petrolatum layers for screening rice root penetration. Crop Sci 35:684–687

    Article  Google Scholar 

  198. Bushamuka VN, Zobel RW (1998) Maize and soybean tap, basal, and lateral root responses to a stratified acid, aluminium toxic soil. Crop Sci 38:416–421

    Article  CAS  Google Scholar 

  199. Sharma S, Xu S, Ehdaie B, Hoops A, Close TJ, Lukassewski AJ, Waines JG (2011) Dissection of QTL effects for root traits using a chromosome arm-specific mapping population in bread wheat. Theor Appl Genet 122:759–769

    Article  Google Scholar 

  200. Bai C, Liang Y, Hawkesford MJ (2013) Identification of QTLs associated with seedling root traits and their correlation with plant height in wheat. J Exp Bot 64:1745–1753

    Article  CAS  Google Scholar 

  201. Atkinson JA, Wingen LU, Griffiths M, Pound MP, Gaju O, Foulkes MJ, Le Gouis J, Griffiths S, Bennett MJ, King J, Wells DM (2015) Phenotyping pipeline reveals major seedling root growth QTL in hexaploid wheat. J Exp Bot 66:2283–2292

    Article  CAS  Google Scholar 

  202. Price AH, Steele KA, Moore BJ, Jones RGW (2002) Upland rice grown in soil-filled chambers and exposed to contrasting water-deficit regimes: II. Mapping quantitative trait loci for root morphology and distribution. Field Crop Res 76:25–43

    Article  Google Scholar 

  203. Courtois B, Ahmadi N, Khowaja F, Price AH, Rami J-F, Frouin J, Hamelin C, Ruiz M (2009) Rice root genetic architecture: meta-analysis from a drought QTL database. Rice 2:115–128

    Article  Google Scholar 

  204. Mai CD, Phung NTP, Truong HTM, Gonin M, Hoang GT, Nguyen KL, Do VN, Courtois B, Gantet P (2014) Genes controlling root development in rice. Rice J 7:30

    Article  Google Scholar 

  205. Price AH, Steele KA, Moore BJ, Barraclough PP, Clark LJ (2000) A combined RFLP and AFLP linkage map of upland rice (Oryza sativa L.) used to identify QTLs for root-penetration ability. Theor Appl Genet 100:49–56

    Article  CAS  Google Scholar 

  206. Ray JD, Yu L, Mccouch SR, Champoux MC, Wang G, Nguyen HT (1996) Mapping quantitative trait loci associated with root penetration ability in rice (Oryza sativa L.) Theor Appl Genet 92:627–636

    Article  CAS  Google Scholar 

  207. Champoux M, Wang G, Sarkarung S, Mackill DJ, O’Toole JC, Huang N, Mccouch SR (1995) Locating genes associated with root morphology and drought avoidance in rice via linkage to molecular marker. Theor Appl Genet 90:969–981

    Article  CAS  Google Scholar 

  208. Liu H, Wang S, Yu X, Yu J, He X, Zhang S, Shou H, Wu P (2005) ARL1, a LOB domain protein required for adventitious root formation in rice. Plant J 43:47–56

    Article  CAS  Google Scholar 

  209. Shen L, Courtois B, McNally K, Robin S, Li Z (2001) Evaluation of near-isogenic lines of rice introgressed with QTLs for root depth through marker-aided selection. Theor Appl Genet 103:75–83

    Article  CAS  Google Scholar 

  210. Steele KA, Price AH, Witcombe JR, Shrestha R, Singh BN, Gibbons JM, Virk DS (2013) QTLs associated with root traits increase yield in upland rice when transferred through marker-assisted selection. Theor Appl Genet 126:101–108

    Article  CAS  Google Scholar 

  211. Suji KK, Prince KSJ, Mankhar PS, Kanagaraj P, Poornima R, Amutha K, Kavitha S, Biji KR, Gomez SM, Chandra Babu R (2012) Evaluation of rice near isogenic lines with root QTLs for plant production and root traits in rainfed target populations of environment. Field Crop Res 137:89–96

    Article  Google Scholar 

  212. Steele KA, Price AH, Shashidhar HE, Witcombe JR (2006) Marker-assisted selection to introgress rice QTLs controlling root traits into an Indian upland rice variety. Theor Appl Genet 112(2):208–221

    Article  CAS  Google Scholar 

  213. Gamuyao R, Chin JH, Pariasca-Tanaka J, Pesaresi P, Catausan S, Dalid C, Slamet-Loedin I, Tecson-Mendoza EM, Wissuwa M, Heuer S (2012) The protein kinase Pstol1 from traditional rice confers tolerance of phosphorus deficiency. Nature 488:535–539

    Article  CAS  Google Scholar 

  214. Hochholdinger F, Tuberosa R (2009) Genetic and genomic dissection of maize root development and architecture. Curr Opin Plant Biol 12:172–177

    Article  CAS  Google Scholar 

  215. Coudert Y, Dievart A, Droc G, Gantet P (2013) ASL/LBD phylogeny suggests that genetic mechanisms of root initiation downstream of auxin are distinct in lycophytes and euphyllophytes. Mol Biol Evol 30:569–572

    Article  CAS  Google Scholar 

  216. Zhao Y, Hu Y, Dai M, Huang L, Zhou DX (2009) The WUSCHEL-related homeobox gene WOX11 is required to activate shoot-borne crown root development in rice. Plant Cell 21:736–748

    Article  CAS  Google Scholar 

  217. Ogbonnaya FC, Seah S, Delibes A, Jahier J, Lopez-Brana I, Eastwood RF, Lagudah ES (2001) Molecular-genetic characterisation of a new nematode resistance gene in wheat. Theor Appl Genet 102(4):623–629

    Article  CAS  Google Scholar 

  218. Manschadi A, Hammer G, Christopher J, Devoil P (2008) Genotypic variation in seedling root architectural traits and implications for drought adaptation in wheat (Triticum aestivum L.) Plant Soil 303(1):115–129

    Article  CAS  Google Scholar 

  219. Hund A, Ruta N, Liedgens M (2009) Rooting depth and water use efficiency of tropical maize inbred lines, differing in drought tolerance. Plant Soil 318:311–325

    Article  CAS  Google Scholar 

  220. Wojciechowski T, Gooding MJ, Ramsay L, Gregory PJ (2009) The effects ofdwarfing genes on seedling root growth of wheat. J Exp Bot 60:2565–2573

    Article  CAS  Google Scholar 

  221. Gregory PJ, Bengough AG, George TS, Hallett PD (2013) Rhizosphere engineering by plants: quantifying soil-root Interactions. In: Timlin D, Ahuja, LR (eds) Enhancing understanding and quantification of soil-root growth interactions. Book Series, Advances in Agricultural Systems Modeling-Transdisciplinary Research Synthesis and Applications Volume 4, pp. 1–31, Soil Science Society of America, Inc., Madison, WI, USA

    Google Scholar 

  222. Passioura JB (2006) The perils of pot experiments. Funct Plant Biol 33:1075–1079

    Article  Google Scholar 

  223. Passioura JB (2010) Scaling up: the essence of effective agricultural research. Funct Plant Biol 37:585–591

    Article  Google Scholar 

  224. Poorter H, Bühler J, Van Dusschoten D, Climent J, Postma JA (2012) Pot size matters: a meta-analysis of the effects of rooting volume on plant growth. Funct Plant Biol 39:839–850

    Article  Google Scholar 

  225. Gregory PJ, Gooding MJ, Ford KE, Hendriks PW, Kirkegaard JA, Rebetzke GJ (2005) Genotypic and environmental influences on the performance of wheat root systems. Asp Appl Biol 73:1–10

    Google Scholar 

  226. Gregory PJ, Hutchison DJ, Read DB, Jenneson PM, Gilboy WB, Morton EJ (2003) Non-invasive imaging of roots with high resolution X-ray micro-tomography. Plant Soil 255:351–359

    Article  CAS  Google Scholar 

  227. Lontoc-Roy M, Dutilleul P, Prasher SO, Han LW, Brouillet T, Smith DL (2006) Advances in the acquisition and analysis of CT scan data to isolate a crop root system from the soil medium and quantify root system complexity in 3-D space. Geoderma 137:231–241

    Article  Google Scholar 

  228. Hargreaves CE, Gregory PJ, Bengough AG (2009) Measuring root traits in barley (Hordeum vulgare ssp vulgare and ssp spontaneum) seedlings using gel chambers, soil sacs and X-ray microtomography. Plant Soil 316:285–297

    Article  CAS  Google Scholar 

  229. Mooney SJ, Pridmore TP, Helliwell J, Bennett MJ (2012) Developing X-ray computed tomography to non-invasively image 3-D root systems architecture in soil. Plant Soil 352:1–22

    Article  CAS  Google Scholar 

  230. Mairhofer SS, Zappala S, Tracy S, Sturrock C, Bennett MJ, Mooney SJ, Pridmore TP (2013) Recovering complete plant root system architectures from soil via X-ray mu-computed tomography. Plant Methods 9:1–7

    Article  Google Scholar 

  231. Metzner R, Eggert A, Vandusschoten D, Pflugfelder D, Gerth S, Schurr U et al (2015) Direct comparison of MRI and X-ray CT technologies for 3D imaging of root systems in soil: potential and challenges for root trait quantification. Plant Methods 11:1–11

    Article  Google Scholar 

  232. Macfall JS, Johnson GA (2012) Plants, seeds, roots, and soils as applications of magnetic resonance microscopy. In: Encyclopedia of magnetic resonance. Wiley, New York

    Google Scholar 

  233. Vamerali T, Bandiera M, Mosca G (2012) Minirhizotrons in modern root studies. In: Mancuso S (ed) Measuring roots. Springer, Berlin/Heidelberg, pp 341–362

    Chapter  Google Scholar 

  234. Nagel KA, Putz A, Gilmer F et al (2012) GROWSCREEN-Rhizo is a novel phenotyping robot enabling simultaneous measurements of root and shoot growth for plants grown in soil-filled rhizotrons. Funct Plant Biol 39:891–904

    Article  Google Scholar 

  235. Lobet G, Pages L, Draye X (2011) A novel image-analysis toolbox enabling quantitative analysis of root system architecture. Plant Physiol 157:29–39

    Article  CAS  Google Scholar 

  236. Manske GGB, Vlek PLG (2002) Root architecture – wheat as a model. In: Waisel Y, Eshel A (eds) Plant roots: the hidden half. Marcel Dekker, Inc, New York, pp 249–259

    Chapter  Google Scholar 

  237. Polomski J, Kuhn N (2002) Root research methods. In: Waisel Y, Eshel A, Kafkafi U (eds) Plant roots: the hidden half. Marcel Dekker, New York, pp 295–321

    Google Scholar 

  238. Köpke U (1979) In Vergleich von feldm sur bestimmung der wurzelwascht landwirtschaftlichn kurturpflazen. Agric, Gottingen

    Google Scholar 

  239. Manske GGB, Ortiz-Monasterio JI, Vlek PLD (2001) Thecniques for measuring genetic diversity in roots. In: Reynods MP, Ortiz-Monasterio JI, McNab A (eds) Application of physiology in wheat breeding. CIMMIYT, Mexico

    Google Scholar 

  240. Wasson AP, Rebetzke GJ, Kirkegaard JA, Christopher J, Richards RA, Watt M (2014) Soil coring at multiple field environments can directly quantify variation in deep root traits to select wheat genotypes for breeding. J Exp Bot 65(21):6231–6249

    Article  CAS  Google Scholar 

  241. Schneider CA, Rasband WS, Eliceiri KW (2012) NIH Image to ImageJ: 25 years of image analysis. Nat Methods 9:671–675

    Article  CAS  Google Scholar 

  242. Chun Y, Huang I, Kuchel H, Edwards J, Hall S, Parent B, Herdina PE, Hartley DM, Langridge P, Mckay AC (2013) A DNA-based method for studying root responses to drought in field-grown wheat genotypes. Sci Rep 3:3194

    Article  Google Scholar 

  243. Swarup K, Benkova E, Swarup R, Casimiro I, Peret B, Yang Y, Parry G, Nielsen E, De Smet I, Vanneste S, Levesque MP, Carrier D, James N, Calvo V, Ljung K, Kramer E, Roberts R, Graham N, Marillonnet S, Patel K, Jones JDG, Taylor CG, Schachtman DP, May S, Sandberg G, Benfey P, Friml J, Kerr I, Beeckman T, Laplaze L, Bennett MJ (2008) The auxin influx carrier LAX3 promotes lateral root emergence. Nat Cell Biol 10(8):946–954

    Article  CAS  Google Scholar 

Books and Reviews

  • Bassirirad H (2000) Kinetics of nutrient uptake by roots: responses to global change. New Phytol 147(1):155–169

    Article  CAS  Google Scholar 

  • Beeckman T (ed) (2010) Root development. Blackwell Publishing Ltd., Chichester

    Google Scholar 

  • Bingham IJ (2001) Soil-root-canopy interactions. Ann Appl Biol 138(2):243–251

    Article  Google Scholar 

  • Bingham IJ, Hoad SP (2000) Towards below ground management. In: HGCA conference: crop management into the Millennium. HGCA, Homerton College, Conference Centre, Cambridge, pp 7.1–7.8

    Google Scholar 

  • Bingham IJ, Foulkes MJ, Gay AP, Gregory PJ, King JA, Robinson D, Bradley RS (2002) ‘Balancing’ root and canopy growth. In: Authority HGC (ed) R & D conference: agronomic intelligence: the basis for profitable production, pp 6.1–6.14

    Google Scholar 

  • Blum A (ed) (2009) Plant stress. http://plantstress.com/

  • Dakora FD, Phillips DA (2002) Root exudates as mediators of mineral acquisition in low-nutrient environments. Plant Soil 245(1):35–47

    Article  CAS  Google Scholar 

  • Lynch J, Brown KM (eds) (2009) Root research methods. http://roots.psu.edu/en/methods

  • Lynch JP (2007) Roots of the second green revolution. Aust J Bot 55(5):493–512

    Article  Google Scholar 

  • Schachtman DP, Goodger JQD (2008) Chemical root to shoot signaling under drought. Trends Plant Sci 13(6):281–287

    Article  CAS  Google Scholar 

  • Smit AL, Bengough AG, Engels C, Noordwijk MV, Pllerin S, Geijn SCVD (eds) (2000) Root methods. A handbook. Springer, Berlin

    Google Scholar 

  • Van Noordwijk M, Martikainen P, Bottner P, Cuevas E, Rouland C, Dhillion SS (1998) Global change and root function. Glob Chang Biol 4:759–772

    Article  Google Scholar 

  • Waisel Y, Eshel A, Kafkafi U (eds) (2002) Plant roots: the hidden half. Marcel Dekker, New York

    Google Scholar 

  • Wang E, Smith CJ (2004) Modelling the growth and water uptake function of plant root systems: a review. Aust J Agric Res 55:501–523

    Article  Google Scholar 

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Carvalho, P., Foulkes, M.J. (2018). Roots and Uptake of Water and Nutrients. In: Meyers, R. (eds) Encyclopedia of Sustainability Science and Technology. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-2493-6_195-3

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