Register      Login
Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

Branch roots of young maize seedlings, their production, growth, and phloem supply from the primary root

Linda C. Enns A , Margaret E. McCully B D and Martin J. Canny C
+ Author Affiliations
- Author Affiliations

A Biology Department, University of Washington, Seattle, WA 98195, USA.

B CSIRO Plant Industry, PO Box 1600, Canberra, ACT 2601, Australia.

C Research School of Biological Sciences, Australian National University, Canberra, ACT 0200, Australia.

D Corresponding author. Email: margaret.mccully@csiro.au

Functional Plant Biology 33(4) 391-399 https://doi.org/10.1071/FP06029
Submitted: 7 February 2006  Accepted: 7 March 2006   Published: 3 April 2006

Abstract

Branch root development on the primary root of maize (Zea mays L.) seedlings was followed for 9 d after planting. This period includes the shift from seedling heterotrophy to autotrophy. Linear density of branches in the basal region ranged from ~38 cm–1 at the base to ~10 cm–1 beyond 10 cm. Branch roots in the first ~8 cm were produced before assimilate was available. Branch length decreased from ~26 mm at 1 cm along the primary root to ~8 mm at 10 cm from the base. Without the cotyledon, branch root density in the basal region was ~10 cm–1 and roots were short (~5 mm). Beyond 8–10 cm both measurements matched those of intact seedlings. Dark-grown seedlings had basal branch root densities higher than those without cotyledons but none beyond 10 cm. There were more and smaller diameter sieve tubes in the basal region of the primary root. These decreased distally in number but had larger diameters where branches formed after assimilate was available. Proliferation of basal branch roots in very young seedlings can have major advantages for successful seedling establishment in the field and could be screened for without difficulty.

Keywords: heterotrophy to autotrophy shift, lateral roots, nutrient sources for growth, seedling development, sieve tube diameter, seminal roots, Zea mays.


References


Begna SH, Dwyer LM, Cloutier D, Assemat L, DiTommaso A, Zhou X, Prithiviraj B, Smith DL (2002) Decoupling of light intensity effects on the growth and development of C3 and C4 weed species through sucrose supplementation. Journal of Experimental Botany 53, 1935–1940.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Bourdu R, Gregory N (1983) Étude comparé du début de la croissance chez divers génotypes de mais. Agronomie 3, 761–770. open url image1

Cahn MD, Zobel RW, Boulden DR (1989) Relationship between root elongation rate and diameter and duration of growth of lateral roots of maize. Plant and Soil 119, 271–279. open url image1

Chassot A, Richner W (2002) Root characteristics and phosphorus uptake of maize seedlings in a bilayered soil. Agronomy Journal 94, 118–127. open url image1

Cooper CS, MacDonald PW (1970) Energetics of early seedling growth in corn (Zea mays L.). Crop Science 10, 136–139. open url image1

Deleens E, Gregory N, Bourdu R (1984) Transition between seed reserve use and photosynthetic supply during development of maize seedlings. Plant Science Letters 37, 35–39.
Crossref | GoogleScholarGoogle Scholar | open url image1

Fusseder A (1987) The longevity and activity of the primary root of maize. Plant and Soil 101, 257–265. open url image1

Hochholdinger F, Woll K, Guo L, Schnable PS (2005) The accumulation of abundant soluble proteins changes early in the development of the primary roots of maize (Zea mays L.). Proteomics 5, 4885–4893.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Hund A, Fracheboud Y, Soldati A, Frascaroli E, Salvi S, Stamp P (2004) QTL controlling root and shoot traits of maize seedlings under cold stress. Theoretical and Applied Genetics 109, 618–629.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Leclerc J-C, Abd el Rahman N (1988) Crise de l’intensité de la photosynthèse au cours de la croissance de jeunes plantes de Maïs. Étude avec un appareillage nouveau. Comptes Rendues de l’Academie de Sciences, Paris. 306, 421–426. open url image1

Luxová M (1991) Mechanisms of reduction of the stelar pattern along barley roots. Botanica Acta 104, 163–168. open url image1

Maizlish NA, Fritton DD, Kendall WA (1980) Root morphology and early development of maize at varying levels of nitrogen. Agronomy Journal 72, 25–31. open url image1

Mandoli DF, Ford GA, Waldron LJ, Nemson JA, Briggs WR (1990) Some spectral properties of several soil types: implications for photomorphogenesis. Plant, Cell & Environment 13, 287–294. open url image1

McCully ME, Mallett JE (1993) The branch roots of Zea. 3. Vascular connections and bridges for nutrient recycling. Annals of Botany 71, 327–341.
Crossref | GoogleScholarGoogle Scholar | open url image1

Pagès L, Pellerin S (1994) Evaluation of parameters describing the root system architecture of field-grown maize plants (Zea mays L). II. Density, length, and branching of first-order lateral roots. Plant and Soil 164, 169–176. open url image1

Park WJ, Hochholdinger F, Gierl A (2004) Release of the benzoxazinoids defense molecules during lateral- and crown root emergence in Zea mays. Journal of Plant Physiology 161, 981–985.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Sun Q, Yoda K, Suzuki H (2005) Internal axial light conduction in the stems and roots of herbaceous plants. Journal of Experimental Botany 56, 191–203.
PubMed |
open url image1

Varney GT, Canny MJ, Wang XL, McCully ME (1991) The branch roots of Zea. I. First order branches, their number, sizes and division into classes. Annals of Botany 67, 357–364. open url image1

Watt M, McCully ME, Kirkegaard JA (2003) Soil strength and rate of root elongation alter the accumulation of Pseudomonas spp. and other bacteria in the rhizosphere of wheat. Functional Plant Biology 30, 483–491.
Crossref | GoogleScholarGoogle Scholar | open url image1

Watt M, Kirkegaard JA, Rebetzke GJ (2005) A wheat genotype developed for rapid leaf growth copes well with the physical and biological properties of unploughed soil. Functional Plant Biology 32, 695–706.
Crossref | GoogleScholarGoogle Scholar | open url image1

Zhu J, Lynch JP (2004) The contribution of lateral rooting to phosphorus acquisition in maize (Zea mays) seedlings. Functional Plant Biology 31, 949–958.
Crossref | GoogleScholarGoogle Scholar | open url image1