Register      Login
Crop and Pasture Science Crop and Pasture Science Society
Plant sciences, sustainable farming systems and food quality
RESEARCH ARTICLE

Tensile properties of seminal and nodal roots and their relationship with the root diameter and planting density of maize (Zea mays)

Sheng-qun Liu A B , Xiang-nan Li A , Xian-can Zhu A and Feng-bin Song A B
+ Author Affiliations
- Author Affiliations

A Laboratory of Black Soil Ecology, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, Changchun, 130102, P.R. China.

B Corresponding authors. Email: lsq@iga.ac.cn; songfb@iga.ac.cn

Crop and Pasture Science 69(7) 717-723 https://doi.org/10.1071/CP18005
Submitted: 14 December 2018  Accepted: 7 June 2018   Published: 28 June 2018

Abstract

The tensile property of roots is an important factor for anchorage and for resistance to root lodging. In this study, a root tensile test was applied to maize (Zea mays L.) grown in the field at three planting densities, 4.5 × 104, 6.75 × 104 and 9.0 × 104 plants ha–1, to quantify the maximum tensile force (Fmax) and tensile strength (Ts) of roots at the V10 stage (tenth leaf visible) and grain-filling stage. In addition, relationships among tensile properties, diameter and turgid weight : dry weight (TW : DW) ratio of roots were investigated. The results showed that the Fmax of primary and seminal adventitious roots was lower than of nodal roots. Among nodal roots, the Fmax of roots on upper nodes was higher. Planting density significantly affected the tensile force of nodal roots of the sixth to eighth tiers; their Fmax decreased with increasing planting density. A positive linear correlation between Fmax and root diameter and a power function between Ts and root diameter was observed. In addition, there was a positive linear correlation between the TW/DW ratio and root diameter and a negative exponential correlation between Ts and TW : DW ratio. Therefore, nodal roots with a lower TW : DW ratio could have a larger Ts, because their cells are smaller and cell walls are thicker. This result suggests that nodal roots with small and thick cells benefit the tensile properties of maize.

Additional keywords: axial root, primary root, root lodging, Zea mays.


References

Armstrong WP (2012) Stem and root anatomy: cellular structure of vascular plants. Wayne’s World. Available at: http://waynesword.palomar.edu/trjune99.htm#top (accessed 20 December 2012).

Bischetti GB, Chiaradia EA, Simonato T, Speziali B, Vitali B, Vullo P, Zocco A (2005) Root strength and root area ratio of forest species in Lombardy (Northern Italy). Plant and Soil 278, 11–22.
Root strength and root area ratio of forest species in Lombardy (Northern Italy).Crossref | GoogleScholarGoogle Scholar |

Bischetti GB, Chiaradia EA, Epis T, Morlotti E (2009) Root cohesion of forest species in the Italian Alps. Plant and Soil 324, 71–89.
Root cohesion of forest species in the Italian Alps.Crossref | GoogleScholarGoogle Scholar |

Burroughs ER, Thomas BR (1977) Declining root strength in Douglas fir after felling as a factor in slope stability. Research Paper INT-190, 27. Intermountain Forest and Range Experiment Station, Forest Service, United States Department of Agriculture, Ogden, UT, USA.

Chimungu JG, Loades KW, Lynch JP (2015) Root anatomical phenes predict root penetration ability and biomechanical properties in maize (Zea mays). Journal of Experimental Botany 66, 3151–3162.
Root anatomical phenes predict root penetration ability and biomechanical properties in maize (Zea mays).Crossref | GoogleScholarGoogle Scholar |

Commandeur PR, Pyles MR (1991) Modulus of elasticity and tensile strength of Douglas fir roots. Canadian Journal of Forest Research 21, 48–52.
Modulus of elasticity and tensile strength of Douglas fir roots.Crossref | GoogleScholarGoogle Scholar |

Crook MJ, Ennos AR, Sellers EK (1994) Structural development of the shoot and root systems of two winter wheat cultivars, Triticum aestivum L. Journal of Experimental Botany 45, 857–863.
Structural development of the shoot and root systems of two winter wheat cultivars, Triticum aestivum L.Crossref | GoogleScholarGoogle Scholar |

Cutler JM, Rains DW, Loomis RS (1977) The importance of cell size in the water relations of plants. Physiologia Plantarum 40, 255–260.
The importance of cell size in the water relations of plants.Crossref | GoogleScholarGoogle Scholar |

Ennos AR (2000) The mechanics of root anchorage. Advances in Botanical Research 33, 133–157.
The mechanics of root anchorage.Crossref | GoogleScholarGoogle Scholar |

Ennos AR, Fitter AH (1992) Comparative functional morphology of the anchorage systems of annual dicots. Functional Ecology 6, 71–78.
Comparative functional morphology of the anchorage systems of annual dicots.Crossref | GoogleScholarGoogle Scholar |

Ennos AR, Crook MJ, Grimshaw C (1993) The anchorage mechanics of maize, Zea mays. Journal of Experimental Botany 44, 147–153.
The anchorage mechanics of maize, Zea mays.Crossref | GoogleScholarGoogle Scholar |

Feix G, Hochholdinger F, Park WJ (2002) Maize root system and genetic analysis of its formation. In ‘Plant roots: The hidden half’. 3rd edn (Eds Y Waisel, A Eshel, U Kalfkalfi) pp. 239–248. (Marcel Dekker: New York)

Fitter AH, Stickland TR (1991) Architectural analysis of plant root systems 2. Influence of nutrient supply on architecture in contrasting plant species. New Phytologist 118, 383–389.
Architectural analysis of plant root systems 2. Influence of nutrient supply on architecture in contrasting plant species.Crossref | GoogleScholarGoogle Scholar |

Genet M, Stokes A, Salin F, Mickovski SB, Fourcaud T, Dumail JF, Van Beck R (2005) The influence of cellulose content on tensile strength in tree roots. Plant and Soil 278, 1–9.
The influence of cellulose content on tensile strength in tree roots.Crossref | GoogleScholarGoogle Scholar |

Girardin P, Jordan M-O, Picard D, Terndel R (1986) Harmonisation des notations concernant la description morphologique d’un pied de maïs (Zea mays L.). Agronomie 6, 873–875.
Harmonisation des notations concernant la description morphologique d’un pied de maïs (Zea mays L.).Crossref | GoogleScholarGoogle Scholar |

Han SJ, Wang EH, Chen XW, Luo S (2016) Effects of tillage on compression and rebound behavior of topsoil in black soil region. Turang Xuebao 53, 646–653. [in Chinese]

Hébert Y, Guingo E, Loudet O (2001) The response of root/shoot partitioning and root morphology to light reduction in maize genotypes. Crop Science 41, 363–371.
The response of root/shoot partitioning and root morphology to light reduction in maize genotypes.Crossref | GoogleScholarGoogle Scholar |

Hochholdinger F, Woll K, Sauer M, Dembinsky D (2004) Genetic dissection of root formation in maize (Zea mays) reveals root-type specific developmental programmes. Annals of Botany 93, 359–368.
Genetic dissection of root formation in maize (Zea mays) reveals root-type specific developmental programmes.Crossref | GoogleScholarGoogle Scholar |

Hoppe DC, Mccully ME, Wenzel CL (1986) The nodal roots of Zea: their development in relation to structural features of the stem. Canadian Journal of Botany 64, 2524–2537.
The nodal roots of Zea: their development in relation to structural features of the stem.Crossref | GoogleScholarGoogle Scholar |

Jeronimidis G (1980) Wood, one of nature’s challenging composites. In ‘The mechanical properties of biological materials. Proceedings Society for Experimental Biology Symposia XXXIV’. (Eds JFV Vincent, JD Currey) pp. 169–182. (Cambridge University Press: Cambridge, UK)

Kamara AY, Kling JG, Menkir A, Ibikunle O (2003) Association of vertical root-pulling resistance with root lodging and grain yield in selected S1, maize lines derived from a tropical low-nitrogen population. Journal of Agronomy & Crop Science 189, 129–135.
Association of vertical root-pulling resistance with root lodging and grain yield in selected S1, maize lines derived from a tropical low-nitrogen population.Crossref | GoogleScholarGoogle Scholar |

Liang AZ, Zhang XP, Fang HJ, Yang XM, Drury CF (2007) Short-term effects of tillage practices on organic carbon in clay loam soil of Northeast China. Pedosphere 17, 619–623.
Short-term effects of tillage practices on organic carbon in clay loam soil of Northeast China.Crossref | GoogleScholarGoogle Scholar |

Liu F, Stützel H (2002) Leaf water relations of vegetable amaranth (Amaranthus spp.) in response to soil drying. European Journal of Agronomy 16, 137–150.
Leaf water relations of vegetable amaranth (Amaranthus spp.) in response to soil drying.Crossref | GoogleScholarGoogle Scholar |

Liu SQ, Song FB, Liu FL, Zhu XC, Xu HB (2012) Effect of planting density on root lodging resistance and its relationship to nodal root growth characteristics in maize (Zea mays L.). The Journal of Agricultural Science 4, 182–189.

Loades K, Bengough A, Bransby M, Hallett P (2013) Biomechanics of nodal, seminal and lateral roots of barley: effects of diameter, waterlogging and mechanical impedance. Plant and Soil 370, 407–418.
Biomechanics of nodal, seminal and lateral roots of barley: effects of diameter, waterlogging and mechanical impedance.Crossref | GoogleScholarGoogle Scholar |

Lombardi F, Scippa GS, Lasserre B, Montagnoli A, Tognetti R, Marchetti M, Chiatante D (2017) The influence of slope on Spartium junceum root system: morphological, anatomical and biomechanical adaptation. Journal of Plant Research 130, 515–525.
The influence of slope on Spartium junceum root system: morphological, anatomical and biomechanical adaptation.Crossref | GoogleScholarGoogle Scholar |

Makarova OV, Cofie P, Koolen AJ (1998) Axial stress–strain relationships of fine roots of Beech and Larch in loading to failure and in cyclic loading. Soil & Tillage Research 45, 175–187.
Axial stress–strain relationships of fine roots of Beech and Larch in loading to failure and in cyclic loading.Crossref | GoogleScholarGoogle Scholar |

Mattia C, Bischetti GB, Gentile F (2005) Biotechnical characteristics of root systems of typical Mediterranean species. Plant and Soil 278, 23–32.
Biotechnical characteristics of root systems of typical Mediterranean species.Crossref | GoogleScholarGoogle Scholar |

Oladokun MA, Ennos AR (2006) Structural development and stability of rice Oryza sativa L. var. Nerica 1. Journal of Experimental Botany 57, 3123–3130.
Structural development and stability of rice Oryza sativa L. var. Nerica 1.Crossref | GoogleScholarGoogle Scholar |

Sanchez-Castillo L, Kubota T, Cantu-Silva I, Yanez-Diaz M, Pequeno-Ledezma M (2017) Comparisons of the root mechanical properties of three native Mexican tree species for soil bioengineering practices. Botanical Sciences 95, 259–269.
Comparisons of the root mechanical properties of three native Mexican tree species for soil bioengineering practices.Crossref | GoogleScholarGoogle Scholar |

Schwarz M, Cohen D, Or D (2010) Root-soil mechanical interactions during pullout and failure of root bundles. Journal of Geophysical Research 115, F04035
Root-soil mechanical interactions during pullout and failure of root bundles.Crossref | GoogleScholarGoogle Scholar |

Sjostrom E (1993) ‘Wood chemistry fundamentals and applications.’ 2nd edn (Academic Press: San Diego, CA, USA)

Stamp P, Kiel C (1992) Root morphology of maize and its relationship to root lodging. Journal of Agronomy & Crop Science 168, 113–118.
Root morphology of maize and its relationship to root lodging.Crossref | GoogleScholarGoogle Scholar |

Striker GG, Insausti P, Grimoldi AA, Vega AS (2007) Trade-off between root porosity and mechanical strength in species with different types of aerenchyma. Plant, Cell & Environment 30, 580–589.
Trade-off between root porosity and mechanical strength in species with different types of aerenchyma.Crossref | GoogleScholarGoogle Scholar |

Sylvain P (1993) Rate of differentiation and emergence of nodal maize roots. Plant and Soil 148, 155–161.
Rate of differentiation and emergence of nodal maize roots.Crossref | GoogleScholarGoogle Scholar |

Terzaghi M, Di Iorio A, Montagnoli A, Baesso B, Scippa GS, Chiatante D (2016) Forest canopy reduction stimulates xylem production and lowers carbon concentration in fine roots of European beech. Forest Ecology and Management 379, 81–90.
Forest canopy reduction stimulates xylem production and lowers carbon concentration in fine roots of European beech.Crossref | GoogleScholarGoogle Scholar |

Tetio-Kagho F, Gardner FP (1988) Responses of maize to plant population density. I. Canopy development, light relationships, and vegetative growth. Agronomy Journal 80, 930–935.
Responses of maize to plant population density. I. Canopy development, light relationships, and vegetative growth.Crossref | GoogleScholarGoogle Scholar |

Turmanina V (1965) On the strength of tree roots. Bulletin of Moscow Society of Naturalists. Biology Section 70, 36–45.

Vergani C, Schwarz M, Cohen D, Thormann JJ, Bischetti GB (2014) Effects of root tensile force and diameter distribution variability on root reinforcement in the Swiss and Italian Alps. Canadian Journal of Forest Research 44, 1426–1440.
Effects of root tensile force and diameter distribution variability on root reinforcement in the Swiss and Italian Alps.Crossref | GoogleScholarGoogle Scholar |

Yang Y, Chen L, Li N, Zhang Q (2016) Effect of root moisture content and diameter on root tensile properties. PLoS One 11, e0151791
Effect of root moisture content and diameter on root tensile properties.Crossref | GoogleScholarGoogle Scholar |

Zhang CB, Chen LH, Jiang J (2014) Why fine tree roots are stronger than thicker roots: The role of cellulose and lignin in relation to slope stability. Geomorphology 206, 196–202.
Why fine tree roots are stronger than thicker roots: The role of cellulose and lignin in relation to slope stability.Crossref | GoogleScholarGoogle Scholar |

Zhao J, Wang R (2013) Development process, problem and countermeasure of maize production in China. Journal of Agricultural Science and Technology 15, 1–6. [in Chinese]

Zhao M, Li JG, Zhang B, Dong ZQ, Wang MY (2006) The compensatory mechanism in exploring crop production potential. Acta Agronomica Sinica 32, 1566–1573. [in Chinese]