Skip to main content
Log in

Stress responses in Salix gracilistyla cuttings subjected to repetitive alternate flooding and drought

  • Original Paper
  • Published:
Trees Aims and scope Submit manuscript

Abstract

To determine the tolerance of Salix gracilistyla to repetitive alternate flooding and drought, we measured leaf stomatal conductance, pre-dawn water potential, osmotic adjustment, and biomass production under greenhouse conditions. We used a control and nine crossed treatments (F1-D1–F3-D3) in which we combined 1-, 2-, or 3-week floodings (F) and droughts (D). Leaf stomatal conductance was lowest in 3 weeks of flooding or drought when the preceding event (flood or drought) was also of a 3-week duration. Leaf pre-dawn water potential was reduced in 3 weeks of drought when preceded by 2 or 3 weeks of flooding. Cuttings had slight osmotic adjustments in repetitions of long floodings and droughts. During longer durations of drought in crossed experiments, plants had low root and shoot mass, few hypertrophic lenticels, and reduced leaf mass; when flooding duration increased in crossed experiments, root mass was reduced, there were more hypertrophic lenticels, and the leaf area was reduced. Cuttings achieved stress tolerance by inhibition of transpiration, osmotic adjustment, reduction of transpiration area, and development of hypertrophic lenticels. Stress tolerance was weak when repetitive 2- or 3-week floodings were combined with 3-week droughts. The duration of flooding and drought periods under which S. gracilistyla achieves stress tolerance may be critical in determining distributions along riverbanks.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Angeles G, Evert RF, Kozlowski TT (1986) Development of lenticels and adventitious roots in flooded Ulmus americana seedlings. Can J For Res 16:585–590

    Article  Google Scholar 

  • Armstrong W, Drew MC (2002) Root growth and metabolism under oxygen deficiency. In: Waisel Y, Eshel A, Kafkafi U (eds) Plant roots: the hidden half. Marchel Dekker, USA, pp 729–761

    Google Scholar 

  • Bertani A, Brambilla I (1982) Effect of decreasing oxygen concentration on wheat roots: growth and induction of anaerobic metabolism. Z Pflanzenphysiol 108:283–288

    CAS  Google Scholar 

  • Braatne JH, Hinckley TM, Stettler RF (1992) Influence of soil-water on the physiological and morphological components of plant water balance in Populus trichocarpa, Populus deltoides and their F1 hybrids. Tree Physiol 11:325–339

    PubMed  Google Scholar 

  • Crawford RMM (1982) Physiological responses to flooding. In: Lange OL, Nobel PS, Osmond CB, Ziegler H (eds) Physiological plant ecology II water relations and carbon assimilation. Springer, Berlin, pp 453–477

    Google Scholar 

  • Dat JF, Capelli N, Folzer H, Bourgeade P, Badot PM (2004) Sensing and signalling during plant flooding. Plant Physiol Biochem 42:273–282

    Article  CAS  PubMed  Google Scholar 

  • Dichio B, Xiloyannis C, Sofo A, Montanaro G (2006) Osmotic regulation in leaves and roots of olive trees during a water deficit and rewatering. Tree Physiol 26:179–185

    Article  PubMed  Google Scholar 

  • Domingo R, Perez-Pastor A, Ruiz-Sanchez C (2002) Physiological responses of apricot plants grafted on two different rootstocks to flooding conditions. J Plant Physiol 159:725–732

    Article  CAS  Google Scholar 

  • Drew MC (1990) Sensing soil oxygen. Plant Cell Environ 13:681–696

    Article  CAS  Google Scholar 

  • Everard JD, Drew MC (1989) Mechanisms controlling changes in water movement through the roots of Helianthus annuus L. during continuous exposure to oxygen deficiency. J Exp Bot 40:95–104

    Article  Google Scholar 

  • Garcia-Sánchez F, Syvertsen JP, Gimeno V, Botia P, Perez-Perez JG (2007) Responses to flooding and drought stress by two citrus rootstock seedlings with different water-use efficiency. Physiol Plantarum 130:532–542

    Article  Google Scholar 

  • Hiron RWP, Wright STC (1973) The role of endogenous abscisic acid in the response of plants to stress. J Exp Bot 24:769–781

    Article  CAS  Google Scholar 

  • Hook DD, Brown CL, Kormanik PP (1970) Lenticels and water root development of swamp tupelo under various flooding condition. Bot Gaz 131:217–224

    Article  Google Scholar 

  • Ishikawa S (1982) Ecological studies of the floodplain willow forests in the Tohoku district (in Japanese with English abstract). Res Rep Kochi Univ Natur Sci 31:95–104

    Google Scholar 

  • Ishikawa S (1997) Distribution behavior of riparian plants and species diversity of the vegetation on rocky river banks in the Yoshino River in Shikoku, Japan. Mem Fac Sci Kochi Univ Ser D (Biol) 18:1–7

    Google Scholar 

  • Jackson MB (1985) Ethylene and the responses of plants to soil waterlogging and submergence. Annu Rev Plant Physiol 36:145–174

    Article  CAS  Google Scholar 

  • Jackson MB (1991) Regulation of water relationships in flooded plants by ABA from leave, roots and xylem sap. In: Davies WJ, Jones HG (eds) Abscisic acid: physiology and biochemistry. Bios Scientific Publishers, Oxford, pp 217–226

    Google Scholar 

  • Jackson MB, Attwood PA (1996) Roots of willow (Salix viminalis L.) show marked tolerance to oxygen shortage in flooded soils and in solution culture. Plant Soil 187:37–45

    Article  CAS  Google Scholar 

  • Kludze HK, De Laune RD (1994) Methane emission and growth of Spartina patens in response to soil redox intensity. Soil Sci Soc Am J 58:1838–1845

    Article  CAS  Google Scholar 

  • Kludze H, Pezeshki SR, De Laune RD (1994) Evaluation of root oxygenation and growth in baldcypress in response to short-term soil hypoxia. Can J For Res 24:804–809

    Article  Google Scholar 

  • Kozlowski TT (1984) Flooding and Plant Growth. Academic Press, Orlando

    Google Scholar 

  • Kozlowski TT (1997) Responses of woody plants to flooding and salinity. Tree Physiol Monogr 1:1–29

    Google Scholar 

  • Kozlowski TT (2000) Responses of woody plants to human-induced environmental stresses: issues, problems and strategies for alleviating stress. Crit Rev Plant Sci 19:91–170

    Article  Google Scholar 

  • Kramer PJ (1940) Causes of decreased absorption of water by plants in poorly aerated media. Am J Bot 27:216–220

    Article  CAS  Google Scholar 

  • Kramer PJ, Jackson WJ (1954) Causes of injury to flooded tobacco plants. Plant Physiol 29:241–249

    Article  CAS  PubMed  Google Scholar 

  • Larcher W (1980) Physiological plant ecology. Springer, Berlin

    Google Scholar 

  • Li S, Pezeshki SR, Goodwin S, Shields FD (2004) Physiological responses of black willow (Salix nigra) cuttings to a range of soil moisture regimes. Photosynthetica 42:585–590

    Article  CAS  Google Scholar 

  • Liu ZJ, Dickmann DI (1993) Responses of 2 hybrid Populus clones to flooding, drought, and nitrogen availability. II. Gas-exchange and water relations. Can J Bot 71:927–938

    Article  CAS  Google Scholar 

  • Marron N, Dreyer E, Boudouresque E, Delay D, Petit JM, Delmotte FM, Brignolas F (2003) Impact of successive drought and re-watering cycles on growth and specific leaf area of two Populus x canadensis (Moench) clones, ‘Dorskamp’ and ‘Luisa_Avanzo’. Tree Physiol 23:1225–1235

    PubMed  Google Scholar 

  • Maruyama Y, Morikawa Y (1983) Measurement of leaf water relations using the pressure–volume technique. J Jpn For Soc 65:23–28

    Google Scholar 

  • Metcalfe JC, Davies WJ, Pereira JS (1990) Leaf growth of Eucalyptus globulus seedlings under water deficit. Tree Physiol 6:221–227

    PubMed  Google Scholar 

  • Milborrow BV (1974) The chemistry and physiology of abscisic acid. Annu Rev Plant Physiol 25:259–307

    Article  CAS  Google Scholar 

  • Nakai A, Kisanuki H (2007a) Effect of elevation above the waterline on the growth of current-year Salix gracilistyla seedlings on a gravel bar (in Japanese with English abstract). J Jpn For Soc 89:1–6

    Article  Google Scholar 

  • Nakai A, Kisanuki H (2007b) Effect of inundation duration on Salix gracilistyla density and size on a gravel bar. J For Res 12:365–370

    Article  Google Scholar 

  • Nakai A, Yurugi Y, Kisanuki H (2009) Growth responses of Salix gracilistyla cuttings to a range of substrate moisture and oxygen availability. Ecol Res 24:1057–1065

    Article  Google Scholar 

  • Niiyama K (1987) Distribution of salicaceous species and soil texture of habitats along the Ishikari River (in Japanese with English abstract). Jpn J Ecol 37:163–174

    Google Scholar 

  • Pezeshki SR (2001) Wetland plant responses to soil flooding. Environ Exp Bot 46:299–312

    Article  Google Scholar 

  • Pezeshki SR, Anderson PH, Shields FDJ (1998) Effects of soil moisture regimes on growth and survival of black willow (Salix nigra) posts (cuttings). Wetlands 18:460–470

    Article  Google Scholar 

  • Ponnamperuma FN (1972) The chemistry of submerged soil. Adv Agron 24:29–96

    Article  CAS  Google Scholar 

  • Schaff SD, Pezeshki SR, Shields FDJ (2003) Effects of soil conditions on survival and growth of black willow cuttings. Environ Manag 31:748–763

    Article  Google Scholar 

  • Topa MA, McLeod KW (1988) Promotion of aerenchyma formation in Pinus serotina seedlings by ethylene. Can J For Res 18:276–280

    CAS  Google Scholar 

  • van Splunder I, Voesenek LACJ, Coops H, de Vries XJA, Blom CWPM (1996) Morphological responses of seedlings of four species of Salicaceae to drought. Can J Bot 74:1988–1995

    Article  Google Scholar 

  • Wikbergi J, Ogreni E (2007) Variation in drought resistance, drought acclimation and water conservation in four willow cultivars used for biomass production. Tree Physiol 27:1339–1346

    Google Scholar 

  • Williams JL, Levine JM (2004) Small-scale variation in growing season length affects size structure of scarlet monkeyflower. Oikos 106:131–137

    Article  Google Scholar 

  • Yamamoto F, Sakata T, Terazawa K (1995a) Growth, morphology, stem anatomy and ethylene production in flooded Alnus japonica seedlings. IAWA J 16:47–59

    Google Scholar 

  • Yamamoto F, Sakata T, Terazawa K (1995b) Physiological, anatomical and morphological responses of Fraxinus mandshurica seedlings to flooding. Tree Physiol 15:713–719

    PubMed  Google Scholar 

Download references

Acknowledgments

The authors thank their colleagues for their assistance with the survey.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Arisa Nakai.

Additional information

Communicated by E. Beck.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nakai, A., Yurugi, Y. & Kisanuki, H. Stress responses in Salix gracilistyla cuttings subjected to repetitive alternate flooding and drought. Trees 24, 1087–1095 (2010). https://doi.org/10.1007/s00468-010-0481-2

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00468-010-0481-2

Keywords

Navigation