PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2014 | 36 | 12 |

Tytuł artykułu

Interspecific differences in root architecture among maize and triticale genotypes grown under drought, waterlogging and soil compaction

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Environmental stresses (soil compaction, drought, waterlogging) cause changes in plants’ root system structure, also affecting the growth of above-ground parts. The aim of this study was to estimate phenotypic variation among maize and triticale genotypes in root penetration ability through petrolatum-wax-layer (RPA). Also, the effect of shortage or excess of soil water on dry matter of shoots and roots and morphological changes in root system structure in sensitive and resistant maize and triticale genotypes grown in low or high soil compaction level was evaluated. To estimate RPA index, the petrolatum-wax-layer method (PWL) was used. The strength of three petrolatum-wax concentrations 60, 50 and 40 % was 0.52, 1.07 and 1.58 MPa, respectively. High coefficients of variation (CV) were observed in 0.52 and 1.07 MPa and for maize were 19.2 and 21.7 %, and for triticale, 12.5 and 18.3 %, respectively. The data indicate that the use of PWL technique is an effective screening method, and makes it possible to divide the genotypes into resistant and sensitive groups. The second part of this study investigated a multistress effect of soil compaction combined with drought or waterlogging on root and shoot growth and morphological changes in root system structure of maize and triticale genotypes differing in susceptibility to environmental stresses. Seedlings were grown for 4 weeks in root-boxes under conditions of low (LSC 1.1 g cm⁻³) or severe (SSC 1.6 g cm⁻³) soil compaction. Drought or waterlogging stresses were applied for 2 weeks from 14th to 28th day. In comparison to LSC treatment, in SSC treatment the decrease in dry matter of shoots and roots was greater for sensitive genotypes of maize and triticale (Ancora, CHD-147). Soil drought or waterlogging caused greater decrease of dry matter of shoots and roots in seedlings grown in SSC in comparison to LSC. The root penetration index (RPI) was estimated as a ratio of root dry matter in 15–40 cm root-box layer to total root dry matter. On the basis of RPI it was possible to group the genotypes according to their ability to distribute roots in soil profile. In comparison to LSC, SSC exerted a strong influence on the length of seminal and seminal adventitious roots, as well as the number and length of L- and S-type lateral roots developed on seminal and nodal roots. In both species the restriction effect of soil compaction on number and length of roots was more severe in sensitive (Ankora, CHD-147) than in resistant (Tina, CHD-247) genotypes. The restriction in roots propagation was greater in triticale than in maize. Exposure to drought or waterlogging in the case of genotypes grown in LSC and SSC treatments caused a decrease in number and length of particular components of root system structure. In both species the decrease of root number and length in plants grown under waterlogging was greater than under drought. The observed changes in root system were greater in sensitive (Ankora, CHD147) than in resistant (Tina, CHD-247) genotypes. Statistically significant correlations were found between RPA and RPI and also between these indexes and soil compaction, drought and waterlogging susceptibility indexes. This indicates that genotypes resistant to soil compaction were resistant to drought or waterlogging and also that genotypes resistant to drought were resistant to waterlogging.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

36

Numer

12

Opis fizyczny

p.3249-3261,fig.,ref.

Twórcy

  • The F. Gorski Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, 30-231, Krakow, Poland
autor
  • The F. Gorski Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, 30-231, Krakow, Poland
autor
  • Department of Plant Physiology, Agriculture University, Podluzna 3, 30 254, Krakow, Poland
autor
  • Department of Plant Physiology, Institute of Biology, Pedagogical University, Podbrzezie 2, 30 054, Krakow, Poland
autor
  • The F. Gorski Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, 30-231, Krakow, Poland
autor
  • Department of Plant Physiology, Institute of Biology, Pedagogical University, Podbrzezie 2, 30 054, Krakow, Poland
autor
  • The F. Gorski Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, 30-231, Krakow, Poland
autor
  • The F. Gorski Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, 30-231, Krakow, Poland

Bibliografia

  • Andrade A, Wolfe DW, Ferens E (1993) Leaf expansion, photosynthesis and water relations of sunflower plants grown on compacted soil. Plant Soil 149:175–184
  • Ashraf M (2010) Inducing drought tolerance in plants: recent advances. Biotech Adv 28:199–238
  • Assaeed AM, McGowan M, Hebblethwaite PD, Brereton JC (1990) Effect of soil compaction on growth, yield and light interception of selected crops. Ann Appl Biol 117:653–667
  • Atwell BJ (1993) Response of roots to mechanical impedance. Environ Exp Bot 33:27–40
  • Busscher WJ, Sojka RE, Doty CW (1986) Residual effects of tillage on coastal plain soil strength. Soil Sci 2:144–148
  • Chan G, Weil RR (2010) Penetration of cover crop roots through compacted soil. Plant Soil 331:31–43
  • Chang TT, Armenta-soto JL, Mao CX, Peiris R, Loresto GC (1986) Genetic studies on the components of drought resistance in rice (Oryza sativa L.). In: Rice genetics IRRI. Los Banos, pp 389–398
  • Chaves MM, Pereira JS, Maroco J, Rodrigues ML, Ricardo CPP, Osorio LM, Carvalho I, Faria T, Pinheiro C (2002) How plants cope with water stress in the field? Photosynthesis and growth. Ann Bot 89:907–916
  • Clark LJ, Whalley WR, Barraclough PB (2003) How do roots penetrate strong soil. Plant Soil 255:93–104
  • Fageria NK, Balingar VC, Clark RB (2006) Physiology of crop production. The Haworth Press Inc., New York, London, Oxford, pp 23–60
  • Fischer RA, Maurer R (1978) Drought resistance in spring wheat cultivars. I. Grain yield response. Aust J Agric Res 29:897–907
  • Glinski J, Lipiec J (1990) Soil physical conditions and plant roots. CRC Press, Boca Raton
  • Golbashy M, Ebrahimi M, Khavari-Khorasani S, Choukan R (2010) Evaluation of drought tolerance of same corn (Zea mays L.) hybrids in Iran. Afr J Agric Res 5:2714–2719
  • Grzesiak S, Hura T, Grzesiak MT, Pieńkowski S (1999) The impact of limited soil moisture and waterlogging stress conditions on morphological and anatomical root traits in maize (Zea mays L.) hybrids of different drought tolerance. Acta Physiol Plant 21:305–315
  • Grzesiak S, Grzesiak MT, Filek W, Hura T, Stabryła J (2002) The impact of different soil moisture and soil compaction on the growth of triticale root system. Acta Physiol Plant 24:331–342
  • Grzesiak MT, Marcinska I, Janowiak F, Rzepka A, Hura T (2012) The relationship between seedling growth and grain yield under drought conditions in maize and triticale genotypes. Acta Physiol Plant 34:1757–1764
  • Grzesiak MT, Waligórski P, Janowiak F, Marcińska I, Hura K, Szczyrek P, Głąb T (2013) The relations between drought susceptibility index based on grain yield (DSIGY) and key physiological seedling traits in maize and triticale genotypes. Acta Physiol Plant 35:549–565
  • Grzesiak MT, Szczyrek P, Rut G, Ostrowska A, Hura K, Rzepka A, Hura T, Grzesiak S (2014) Interspecific differences in tolerance to a soil compaction, drought and waterlogging stresses among maize and triticale genotypes. J. Agric Crop Sci. JAC-04-2014-0108 (in press)
  • Hanson AD, Nelson ChE (1985) Water adaptation of crop to drought. In: Carlson PS (ed) The biology of crop productivity. Academic Press, New York, pp 79–149
  • Hillel D, van Bavel CHM (1976) Simulation of profile water storage as related to soil hydraulic properties. Soil Sci Soc Am J 40:807–815
  • Iijima M, Kono Y (1991) Interspecific differences of the root system structures of four cereal species as affected by soil compaction. Jpn J Crop Sci 60:130–138
  • Iijima M, Kono Y, Yamauchi A, Jr Pardales (1991) Effects of soil compaction on the development of rice and maize root system. Environ Exp Bot 30:333–342
  • Kasperbauer MJ, Busscher WJ (1991) Genotypic differences in cotton root penetration of a compacted subsoil layer. Crop Sci 31:1376–1378
  • Kono Y, Yamauchi A, Nonoyama T, Tatsumi T, Kawamura N (1987a) A revised system of root-soil interaction for laboratory work. Environ Control Biol 25:141–151
  • Kono Y, Yamauchi A, Kawamura AN, Tatsumi J (1987b) Interspecific differences of the capacities of waterlogging and drought tolerance among summer cereals. Jpn. J Crop Sci 56:115–129
  • Larsson S, Górny AG (1988) Grain yield and drought resistance indices of oat cultivars in field rain shelter and laboratory experiments. J Agron Crop Sci 161:277–286
  • Lipiec J, Ishioka T, Hatano R, Sakuma T (1993) Effects of soil structural discontinuity on root and shoot growth and water use in maize. Plant Soil 157:65–74
  • Lipiec J, Ishioka T, Szustak A, Pietrusiewicz J, Stępniewski W (1996) Effects of soil compaction and transient oxygen deficiency on growth, water use and stomatal resistance in maize. Acta Agric Scand Sect B Soil Plant Sci 46:186–191
  • Masle J (1992) Genetic variation in the effects of root impedance on the growth and transpiration rates of wheat and barley. Aust J Plant Physiol 19:109–125
  • Masle J (2002) High soil strength: mechanical forces at play on root morphogenesis and in root:shoot signaling. In: Waisel Y, Eshel A, Kafkafi U (eds) Plant roots the hidden half. Marcel Dekker Inc, New York, Basel, pp 807–819
  • Materechera SA, Alston AM, Kirby JM, Dexter AR (1992) Influence of root diameter on the penetration of the seminal roots into a compacted sub soil. Plant Soil 144:297–303
  • Nayyar H, Gupta D (2006) Differential sensitivity of C3 and C4 plants to water deficit stress: association with oxidative stress and antioxidants. Environ Exp Bot 58:106–113
  • O‘Toole JC, Cruz RT (1983) Genotypic variation in epicuticular wax of rice. Crop Sci 23:392–394
  • Royo C, Abaza M, Blaneo R, Gareia del Moral LF (2000) Triticale grain growth and morphometry as affected by drought stress, late sowing and simulated drought stress. Aust J Plant Physiol 27:1051–1059
  • Tardieu F (1991) Spatial arrangement of maize roots in the field. In: McMichael BL, Person H (eds) Plant roots and their environment. Elsevier, Amsterdam, pp 506–514
  • Tardieu F, Katerji N (1991) Plant response to soil water reserve: consequences of the root system environment. Irrig Sci 12:145–152
  • Taylor HM, Gardner HR (1960) Use of wax substrates in root penetration studies. Soil Sci Soc Am Proc 24:79–81
  • Tu JC, Tan CS (1991) Effect on soil compaction on growth, yield and root rots of white beans in clay loam and sand loam soil. Soil Biol Biochem 23:233–238
  • Whalley WR, Dexter AR (1994) Root development and earthworm movement in relation to soil strength and structure. Arch Agron Soil Sci 38:1–40
  • Winter SR, Musick JT, Porter KB (1988) Evaluation of screening techniques for breeding drought-resistant winter wheat. Crop Sci 28:512–516
  • Witta S, Galiciab L, Liseca J, Cairnsc J, Tiessend A, Araus JL, Palacios-Rojas N, Ferniea AR (2012) Metabolic and phenotypic responses of greenhouse-grown maize hybrids to experimentally controlled drought stress. Mol Plant 5:401–417
  • Yamauchi A (1993) Significance of root system structure in relation to stress tolerance in cereal crop. Low-input sustainable crop production system in Asia. Korean Soc Crop Sci, Korea, pp 347–360
  • Yoshida S, Hasegawa S (1982) The rice root system: its development and function. Drought resistance in crop with emphasis on rice. IRRI Los Banos, Philippines, pp 97–114
  • Yu LX, Ray JD, O‘Toole JC, Nguyen HT (1995) Use of waxpetrolatum layer for screening rice root penetration. Crop Sci 35:684–687
  • Zagdanska B (1992) Physiological criteria for estimation of plant resistance to drought. Biul Inst Hod i Aklim Roślin 183:11–19 (in Polish)

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-ffacc19a-5349-426d-92a8-b952bbd12c9d
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.