Photosynthetica

, Volume 55, Issue 2, pp 368–377 | Cite as

Response of stem sap flow and leaf photosynthesis in Tamarix chinensis to soil moisture in the Yellow River Delta, China

  • J. B. Xia
  • Z. G. Zhao
  • J. K. Sun
  • J. T. Liu
  • Y. Y. Zhao
Original Paper
  • 137 Downloads

Abstract

Soil moisture is the main limiting factor for vegetation growth at shell ridges in the Yellow River Delta of China. The objective of this study was to explore the soil moisture response of photosynthetic parameters and transpiration in Tamarix chinensis Lour., a dominant species of shell ridges. Leaf photosynthetic light-response parameters and sap flow were measured across a gradient of relative soil water content (RWC), from drought (23%) to waterlogging (92%) conditions. Leaf photosynthetic efficiency and stem sap flow of T. chinensis showed a clear threshold response to soil moisture changes. Leaf net photosynthetic rate, water-use efficiency (WUE), light-saturation point, apparent quantum yield, maximum net photosynthetic rate, and dark respiration rate peaked at moderately high RWC, decreasing towards high and low values of RWC. However, peak or bottom RWC values substantially differed for various parameters. Excessively high or low RWC caused a significant reduction in the leaf photosynthetic capacity and WUE, while the high photosynthetic capacity and high WUE was obtained at RWC of 73%. With increasing waterlogging or drought stress, T. chinensis delayed the starting time for stem sap flow in the early morning and ended sap flow activity earlier during the day time in order to shorten a daily transpiration period and reduce the daily water consumption. The leaf photosynthetic capacity and WUE of T. chinensis were higher under drought stress than under waterlogging stress. Nevertheless, drought stress caused a larger reduction of daily water consumption compared to waterlogging, which was consistent with a higher drought tolerance and a poor tolerance to waterlogging in this species. This species was characterized by the low photosynthetic capacity and low WUE in the range of RWC between 44 and 92%. The RWC of 49–63% was the appropriate range of soil moisture for plant growth and efficient physiological water use of T. chinensis seedlings.

Additional key words

drought gas exchange light-use efficiency water consumption waterlogging 

Abbreviations

AQY

apparent quantum yield

DSF

daily cumulative sap flow

E

transpiration rate

LCP

light-compensation point

LSP

light-saturation point

PN

net photosynthetic rate

PNmax

light-saturated net photosynthetic rate

RD

dark respiration rate

RWC

relative soil water content

SWC

soil water content

WUE

water-use efficiency

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References

  1. Cui B.S., Yang Q.C., Zhang K.J. et al.: Responses of saltcedar (Tamarix chinensis) to water table depth and soil salinity in the Yellow River Delta, China. — Plant Ecol. 209: 279–290, 2010.CrossRefGoogle Scholar
  2. Du N., Guo W.H., Zhang X.R., Wang R.Q.: Morphological and physiological responses of Vitex negundo L. var. heterophylla (Franch.) Rehd. to drought stress. — Acta Physiol. Plant. 32: 839–848, 2010.CrossRefGoogle Scholar
  3. Farooq M., Wahid A., Kobayashi N. et al.: Plant drought stress: effects, mechanisms and management. — Agron. Sustain. Dev. 29: 185–212, 2009.CrossRefGoogle Scholar
  4. Farquhar G.D., Sharkey T.D.: Stomatal conductance and photosynthesis. — Annu. Rev. Physiol. 33: 317–345, 1982.CrossRefGoogle Scholar
  5. Gao S., Su P.X., Yan Q.D., Ding S.S.: Canopy and leaf gas exchange of Haloxylon ammodendron under different soil moisture regimes. — Sci. China Life Sci. 53: 718–728, 2010.CrossRefPubMedGoogle Scholar
  6. Gardian Z., Tichý J., Vácha F.: Structure of PSI, PSII and antenna complexes from yellow-green alga Xanthonema debile. — Photosynth. Res. 108: 25–32, 2011.CrossRefPubMedGoogle Scholar
  7. Gautam P., Lal B., Raja R. et al.: Effect of simulated flash flooding on rice and its recovery after flooding with nutrient management strategies. — Ecol. Eng. 77: 250–256, 2015.CrossRefGoogle Scholar
  8. Hsiao T.C.: Plant responses to water stress. — Annu. Rev. Plant Physiol. 24: 519–570, 1973.CrossRefGoogle Scholar
  9. Irvine J., Perks M.P., Magnani F. et al.: The response of Pinus sylvestris to drought: stomatal control of transpiration and hydraulic conductance. — Tree Physiol. 18: 393–402, 1998.CrossRefPubMedGoogle Scholar
  10. Jin X., Xu J., Bai K.D. et al.: [Comparison of drought strategies of three co-existing woody plants by their hydraulic structures.] — J. Beijing Forest. Univ. 33: 135–141, 2011. [In Chinese]Google Scholar
  11. Kiefer J., Wolfowitz J.: Stochastic estimation of the maximum of a regression function. — Ann. Math. Stat. 23: 462–466, 1952.CrossRefGoogle Scholar
  12. Lang Y., Wang M., Zhang G.C. et al.: Experimental and simulated light responses of photosynthesis in leaves of three tree species under different soil water conditions. — Photosynthetica 51: 370–378, 2013.CrossRefGoogle Scholar
  13. Li M.L., Zhou H.F., Sun P.F.: [Comparative study on the rule of stem-sap flow of Haloxylon ammodendron in the southern marginal zone of Junggar Basin.] — Arid Zone Res. 29: 101–108, 2012. [In Chinese]Google Scholar
  14. Maseda P.H., Fernández R.J.: Stay wet or else: three ways in which plants can adjust hydraulically to their environment. — J. Exp. Bot. 57: 3963–3977, 2006.CrossRefPubMedGoogle Scholar
  15. Meng F.J.: [Plant Physiology.] Pp. 63–65. Huazhong Univ. Sci. Technol. Press, Wuhan 2000. [In Chinese]Google Scholar
  16. Mitchell P.J., Veneklaas E.J., Lambers H., Burgess S.S.O.: Leaf water relations during summer water deficit: differential responses in turgor maintenance and variation in leaf structure among different plant communities in south-western Australia. — Plant Cell Environ. 31: 1791–1802, 2008.CrossRefPubMedGoogle Scholar
  17. Muller B., Pantin F., Génard M. et al.: Water deficits uncouple growth from photosynthesis, increase C content, and modify the relationships between C and growth in sink organs. — J. Exp. Bot. 62: 1715–1729, 2011.CrossRefPubMedGoogle Scholar
  18. Otieno D.O., Schmidt M.W.T., Kinyamario J.I. et al.: Responses of Acacia tortilis and Acacia xanthophloea to seasonal changes in soil water availability in the savanna region of Kenya. — J. Arid Environ. 62: 377–400, 2005.CrossRefGoogle Scholar
  19. Pataki D.E., Oren R.: Species differences in stomatal control of water loss at the canopy scale in a mature bottom land deciduous forest. — Adv. Water Resour. 26: 1267–1278, 2003.CrossRefGoogle Scholar
  20. Prior S.A., Runion G.B., Rogers H.H. et al.: Elevated atmospheric carbon dioxide effects on soybean and sorghum gas exchange in conventional and no-tillage systems. — J. Environ. Qual. 39: 596–608, 2010.CrossRefPubMedGoogle Scholar
  21. Soares M.L.G., Tognella M.M.P., Cuevas E., Medina E.: Photosynthetic capacity and intrinsic water-use efficiency of Rhizophora mangle at its southernmost western Atlantic range. — Photosynthetica 53: 464–470, 2015.CrossRefGoogle Scholar
  22. Sofo A., Dichio B., Montanaro G. et al.: Photosynthetic performance and light response of two olive cultivars under different water and light regimes. — Photosynthetica 47: 602–608, 2009.CrossRefGoogle Scholar
  23. Talaat N.B., Shawky B.T., Ibrahim A.S.: Alleviation of droughtinduced oxidative stress in maize (Zea mays L.) plants by dual application of 24-epibrassinolide and spermine. — Environ. Exp. Bot. 113: 47–58, 2015.CrossRefGoogle Scholar
  24. Tika T.E., Hutchinson J.N.: Ring shear tests on soil from the Vaiont landslide slip surface. — Géotechnique 49: 59–74, 1999.CrossRefGoogle Scholar
  25. Wang R.R., Xia J.B., Yang J.H. et al.: [Comparison of light response models of photosynthesis in leaves of Periploca sepium under drought stress in sand habitat formed from seashells.] — Chin. J. Plant Ecol. 37: 111–121, 2013. [In Chinese]CrossRefGoogle Scholar
  26. Wang Z.X., Wei H., Li C.X. et al.: [Effect of soil moisture variations on photosynthetic charanteristics of slash pine seedlings.] — Acta Bot. Boreali-Occident. Sin. 32: 980–987, 2012. [In Chinese]Google Scholar
  27. Xia J.B., Zhang G.C., Sun J.K., Liu X.: [Threshold effects of photosynthetic and physiological parameters in Prunus sibirica to soil moisture and light intensity.] — Chin. J. Plant Ecol. 35: 322–329, 2011a. [In Chinese]CrossRefGoogle Scholar
  28. Xia J.B., Zhang G.C., Wang R.R. et al.: Effect of soil water availability on photosynthesis in Ziziphus jujuba var. spinosus in a sand habitat formed from seashells: Comparison of four models. — Photosynthetica 52: 253–261, 2014.CrossRefGoogle Scholar
  29. Xia J.B., Zhang S.Y., Zhang G.C. et al.: Critical responses of photosynthetic efficiency in Campsis radicans (L.) Seem. to soil water and light intensities. — Afr. J. Biotechnol. 10: 17748–17754, 2011b.CrossRefGoogle Scholar
  30. Xia J.B., Zhang S.Y., Zhu L.P. et al.: [Response characteristics of stem sap flow and leaf photosynthesis of Ziziphus jujuba var. spinosus in response to soil moisture in Shell Ridge Island.] — Sci. Silvae Sin. 50: 24–32, 2014. [In Chinese]Google Scholar
  31. Xu H., Zhang X.M., Yan H.L., Yao S.J.: [Stem sap flow and water consumption of Tamarix ramosissima in hinterland of Taklimakan Desert.] — Chin. J. Appl. Ecol. 18: 735–741, 2007. [In Chinese]Google Scholar
  32. Ye Z.P., Kang H.J.: [Study on biological significance of coefficients in modified model of photosynthesis–irradiance.] — J. Yangzhou Univ.-Agric. Life Sci. Edit. 33: 51–57, 2012. [In Chinese]Google Scholar
  33. Ye Z.P.: A new model for relationship between irradiance and the rate of photosynthesis in Oryza sativa. — Photosynthetica 45: 637–640, 2007.CrossRefGoogle Scholar
  34. Yue G.Y., Zhang T.H., Liu X.P., Yi X.Y.: [Development and application of thermal methods in measuring stem sap flow.] — Sci. Silvae Sin. 42: 102–108, 2006. [In Chinese]Google Scholar
  35. Zhang S.Y., Xia J.B., Zhang G.C. et al.: Threshold effects of photosynthetic efficiency parameters of wild jujube in response to soil moisture variation on shell beach ridges, Shandong, China. — Plant Biosyst. 148: 140–149, 2014.CrossRefGoogle Scholar
  36. Zhang S.Y., Zhang G.C., Gu S.Y. et al.: Critical responses of photosynthetic efficiency of Goldspur apple tree to soil water variation in semiarid loess hilly area. — Photosynthetica 48: 589–595, 2010.CrossRefGoogle Scholar
  37. Zhou C.M., Zhao P., Ni G.Y. et al.: [Whole-tree water use characteristics of Schima superba in wet and dry seasons based on sap flow and soil-leaf water potential gradient analysis.] — Chin. J. Ecol. 30: 2659–2666, 2011. [In Chinese]Google Scholar
  38. Zong Y.Z., Wang W.F., Xue Q.W., Shangguan Z.P.: Interactive effects of elevated CO2 and drought on photosynthetic capacity and PSII performance in maize. — Photosynthetica 52: 63–70, 2014.CrossRefGoogle Scholar

Copyright information

© The Institute of Experimental Botany 2017

Authors and Affiliations

  • J. B. Xia
    • 1
  • Z. G. Zhao
    • 1
  • J. K. Sun
    • 1
  • J. T. Liu
    • 1
  • Y. Y. Zhao
    • 1
  1. 1.Department of Life ScienceBinzhou University, Shandong Provincial Key Laboratory of Eco-Environmental Science for Yellow River DeltaBinzhouChina

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