Photosynthetica 2018, 56(4):1353-1364 | DOI: 10.1007/s11099-018-0846-0

Morphological and ecophysiological plasticity in dioecious plant Populus tomentosa under drought and alkaline stresses

Y. W. Lu1,2, X. L. Miao1, Q. Y. Song1, S. M. Peng3, B. L. Duan2,*
1 School of Life Sciences, Liaocheng University, Liaocheng, China
2 Key Laboratory of Mountain Surface Processes and Ecological Regulation, Institute of Mountain Hazards and Environment, Chinese Academy of Sciences, Chengdu, China
3 College of Materials and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu, China

Morphological and ecophysiological traits showed by male and female Populus tomentosa Carr. trees were studied under various degrees of water and alkaline stresses. The results showed that different adaptations to drought and alkaline stresses were adopted by each gender; males possessed a much higher tolerance to both stresses compared to females. In contrast to females, the males exhibited a lower inhibition in total biomass, total leaf area, net photosynthetic rate, stomatal conductance, leaf carbon and nitrogen concentrations as well as water- and nitrogen-use efficiency in response to drought and alkaline stresses. Nevertheless, compared to the males, the females showed a higher plasticity in root biomass/shoot biomass ratio, fine root/coarse root ratio, and intrinsic water-use efficiency, indicating that the males and females differed in some of trade-offs between growth and stress defence to maximize water and nitrogen gains under both stress conditions.

Keywords: alkaline stress; cuttings; drought; gender; plasticity index; poplar

Received: August 24, 2017; Accepted: March 9, 2018; Prepublished online: December 1, 2018; Published: November 1, 2018Show citation

ACS AIP APA ASA Harvard Chicago IEEE ISO690 MLA NLM Turabian Vancouver
Lu, Y.W., Miao, X.L., Song, Q.Y., Peng, S.M., & Duan, B.L. (2018). Morphological and ecophysiological plasticity in dioecious plant Populus tomentosa under drought and alkaline stresses. Photosynthetica56(4), 1353-1364. doi: 10.1007/s11099-018-0846-0.
Download citation

References

  1. Adams T.S., McCormack M.L., Eissenstat D.M.: Foraging strategies in trees of different root morphology: the role of root lifespan.-Tree Physiol. 33: 940-948, 2013. Go to original source...
  2. Behnke K., Ghirardo A., Janz D.I. et al.: Isoprene function in two contrasting poplars under salt and sunflecks.-Tree Physiol. 33: 562-578, 2013. Go to original source...
  3. Berendse F., Aerts R.: Nitrogen-use-efficiency: a biologically meaningful definition?-Funct Ecol. 1: 293-296, 1987.
  4. Bernacchi C.J., Thompson J.N., Coleman J.S. et al.: Allometric analysis reveals relatively little variation in nitrogen versus biomass accrual in four plant species exposed to varying light, nutrients, water and CO2.-Plant Cell Environ. 30: 1216-1222, 2007. Go to original source...
  5. Bonal D., Sabatier D., Montpied P. et al.: Interspecific variability of d13C among trees in rainforests of French Guiana: functional groups and canopy integration.-Oecologia 124: 454-468, 2000. Go to original source...
  6. Bongers F., Schnitzer S.A., Traore D.: The importance of lianas and consequences for forest management in west Africa.-Bioterre 1: 59-70, 2002.
  7. Bouma T.J., Broekhuysen A.G.M., Veen B.W.: Analysis of root respiration of Solanum tuberosum as related to growth, ion uptake, and maintenance of biomass.-Plant Physiol. Bioch. 34: 795-806, 1996.
  8. Cepeda-Cornejo V., Dirzo R.: Sex-related differences in reproductive allocation, growth, defense and herbivory in three dioecious neotropical palms.-PLoS ONE 5: e9824, 2010. Go to original source...
  9. Chen J., Dong T.F., Duan B.L. et al.: Sexual competition and N supply interactively affect the dimorphism and competiveness of opposite sexes in Populus cathayana.-Plant Cell Environ. 38: 1285-1298, 2015. Go to original source...
  10. Dawson T.E., Bliss L.C.: Patterns of water use and tissue water relations in the dioecious shrub, Salix arctica: the physiological basis for habitat partitioning between the sexes.-Oecologia 79: 332-343, 1989. Go to original source...
  11. Dawson T.E., Ehleringer J.R.: Gender-specific physiology, carbon isotope discrimination, and habitat distribution in discrimination, and habitat distribution in boxelder, Acer negundo.-Ecology 74: 798-815, 1993. Go to original source...
  12. Dawson T.E., Geber M.A.: Sexual dimorphism in physiology and morphology.-In: Geber M.A., Dawson T.E., Delph L.F. (ed.): Gender and Dimorphism of Flowering Plants. Pp. 175-216. Springer, Berlin 1999. Go to original source...
  13. Delph L.F.: Sex-differential resource-allocation patterns in the subdioecious shrub Hebe subalpina.-Ecology 71: 1342-1351, 1990. Go to original source...
  14. Dijkstra F.A., Carrillo Y., Aspinwall M.J. et al.: Water, nitrogen and phosphorus use efficiencies of four tree species in response to variable water and nutrient supply.-Plant Soil 406: 187-199, 2016. Go to original source...
  15. Dong T.F., Li J.Y., Zhang Y.B. et al.: Partial shading of lateral branches affects growth, and foliage nitrogen-and water-use efficiencies in the conifer Cunninghamia lanceolata growing in a warm monsoon climate.-Tree Physiol. 35: 632-643, 2015. Go to original source...
  16. Dudley L.S.: Ecological correlates of secondary dimorphism in Salix glauca (Salicaceae).-Am. J. Bot. 93: 1775-1783, 2006. Go to original source...
  17. Eissenstat D.M., Yanai R.D.: The ecology of root lifespan.-Adv. Ecol. Res. 27: 1-60, 1997.
  18. Eissenstat D.M., Wells C.E., Yanai R.D. et al.: Building roots in a changing environment: implications for root longevity.-New Phytol. 147: 33-42, 2000. Go to original source...
  19. Farquhar G.D., Ehleringer J.R., Hubick K.T.: Carbon isotope discrimination and photosynthesis.-Annu. Rev. Plant Phys. 40: 503-537, 1989. Go to original source...
  20. Field C., Merino J., Mooney H.A.: Compromises between wateruse efficiency and nitrogen-use efficiency in five species of California evergreens.-Oecologia 60: 384-389, 1983. Go to original source...
  21. Garrish V., Cernusak L.A., Winter K. et al.: Nitrogen to phosphorus ratio of plant biomass versus soil solution in atropical pioneer tree, Ficus insipida.-J. Exp. Bot. 61: 3735-3748, 2010. Go to original source...
  22. Geber M.A., Dawson T.E., Delph L.F.: Gender and Sexual Dimorphism in Flowering Plants. Pp. 217-246. Springer, Berlin 1999. Go to original source...
  23. Godoy O., Valladares F., Castro-Díez P.: Multispecies comparison reveals that invasive and native plants differ in their traits but not in their plasticity.-Funct. Ecol. 25: 1248-1259, 2011. Go to original source...
  24. Guo D.L., Xia M.X., Wei X. et al.: Anatomical traits associated with absorption and mycorrhizal colonization are linked to root branch order in twenty-three Chinese temperate tree species.-New Phytol. 180: 673-683, 2008. Go to original source...
  25. Hawkins B.J.: Family variation in nutritional and growth traits in Douglas-fir seedlings.-Tree Physiol. 27: 911-919, 2007. Go to original source...
  26. He C.Z., Zhang Z.Y., Feng X.L. et al.: Variation of leaf characteristics in Populus tomentosa Carr.-For. Stud. China 7: 51-53, 2005. [In Chinese] Go to original source...
  27. James J.J., Tiller R.L., Richards J.H.: Multiple resources limit plant growth and function in a saline-alkaline desert community.-J. Ecol. 93: 113-126, 2005. Go to original source...
  28. Kalcsits L.A., Min X., Guy R.D.: Interspecific variation in leafroot differences in d15N among three tree species grown with either nitrate or ammonium.-Trees 29: 1069-1078, 2015. Go to original source...
  29. Li A., Guo D.L., Wang Z.Q. et al.: Nitrogen and phosphorus allocation in leaves, twigs, and fine roots across 49 temperate, subtropical and tropical tree species: a hierarchical pattern.-Funct. Ecol. 24: 224-232, 2010. Go to original source...
  30. Li C.Y., Berninger F., Koskela J. et al.: Drought responses of Eucalyptus microtheca provenances depend on seasonality of rainfall in their place of origin.-Aust. J. Plant Physiol. 27: 231-238, 2000.
  31. Li C.Y, Yin C.Y., Liu S.: Different responses of two contrasting Populus davidiana populations to exogenous abscisic acid application.-Environ. Exp. Bot. 51: 237-246, 2004. Go to original source...
  32. Li Y., Duan B.L., Chen J. et al.: Males exhibit competitive advantages over females of Populus deltoides under salinity stress.-Tree Physiol. 36: 1573-1584, 2016. Go to original source...
  33. Lu Y.W., Wang G.Q., Meng Q.J. et al.: Growth and physiological responses to arbuscular mycorrhizal fungi and salt stress in dioecious plant Populus tomentosa.-Can. J. Forest Res. 44: 1020-1031, 2014.
  34. McCormack M.L., Adams T.S., Smithwick E.A.H. et al.: Predicting fine root lifespan from plant functional traits in temperate trees.-New Phytol. 195: 823-831, 2012. Go to original source...
  35. McDowell N., Marshall J., Hooker T. et al.: Estimating CO2 flux from snowpacks at three sites in the Rocky Mountains.-Tree Physiol. 20: 745-753, 2000. Go to original source...
  36. Millard P., Grelet G.-A.: Nitrogen storage and remobilization by trees: ecophysiological relevance in a changing world.-Tree Physiol. 30: 1083-1095, 2010. Go to original source...
  37. Mitchell A.K.: Acclimation of Pacific yew (Taxus brevifolia) foliage to sun and shade.-Tree Physiol. 18: 749-757, 1998. Go to original source...
  38. Montesinos D., Villar-Salvador P., García-Fayos P. et al.: Genders in Juniperus thurifera have different functional responses to variations in nutrient availability.-New Phytol. 193: 705-712, 2012. Go to original source...
  39. Munns R.: Plant adaptations to salt and water stress: differences and commonalities.-Adv. Bot. Res. 57: 1-32, 2011. Go to original source...
  40. Nelson D.W., Sommers L.E.: Total carbon, organic carbon and organic matter.-In: Page A.L., Miller R.H., Keeney D.R. (ed.): Methods of Soil Analysis, Part 2. Chemical and Microbio logical Properties. Pp. 539-579. American Society of Agronomy, Madison 1982.
  41. Obeso J.R.: The cost of reproduction in plants.-New Phytol. 155: 321-348, 2002. Go to original source...
  42. Ometto J.P.H.B., Ehleringer J.R., Domingues T.F. et al.: The stable carbon and nitrogen isotopic composition of vegetation in tropical forests of the Amazon Basin, Brazil.-Biogeochemistry 79: 251-274, 2006. Go to original source...
  43. Ortiz P.L., Arista M., Talavera S.: Sex ratio and reproductive effort in the dioecious Juniperus communis subsp alpina (Suter) Celak. (Cupressaceae) along an altitudinal gradient.-Ann Bot.-London 89: 205-211, 2002. Go to original source...
  44. Paz E.Y., Gil K., Rebolledo L. et al.: Genetic diversity of Cuban pineapple germplasm assessed by AFLP markers.-Crop Breed. Appl. Biotechnol. 12: 104-110, 2012. Go to original source...
  45. Peñuelas J., Filella I., Lloret F. et al.: Effects of a severe drought on water and nitrogen use by Quercus ilex and Phillyrea latifolia.-Biol. Plantarum 43: 47-53, 2000. Go to original source...
  46. Poorter H., Niinemets U., Poorter L. et al.: Causes and consequences of variation in leaf mass per area (LMA): a metaanalysis.-New Phytol. 182: 565-588, 2009. Go to original source...
  47. Randriamanana T.R., Nybakken L., Lavola A. et al.: Sex-related differences in growth and carbon allocation to defence in Populus tremula as explained by currrent plant defence theories.-Tree Physiol. 34: 471-487, 2014. Go to original source...
  48. Rao P.S., Mishra B., Gupta S.R. et al.: Reproductive stage tolerance to salinity and alkalinity stresses in rice genotypes.-Plant Breed. 127: 256-261, 2008. Go to original source...
  49. Reich P.B., Walters M.B., Tabone T.J.: Response of Ulmus americana seedlings to varying nitrogen and water status. Water and nitrogen use efficiency in photosynthesis.-Tree Physiol. 5: 173-184,1989. Go to original source...
  50. Renner S.S., Ricklefs R.E.: Dioecy and its correlates in the flowering plants.-Am. J. Bot. 82: 596-606, 1995. Go to original source...
  51. Renninger H.J., Carlo N., Clark K.L. et al.: Physiological strategies of co-occurring oaks in a water-and nutrient-limited ecosystem.-Tree Physiol. 34: 159-173, 2014. Go to original source...
  52. Ripullone F., Lauteri M., Grassi G. et al.: Variation in nitrogen supply changes water-use efficiency of Pseudotsuga menziesii and Populus x euroamericana; a comparison of three approaches to determine water-use efficiency.-Tree Physiol. 24: 671-679, 2004. Go to original source...
  53. Stehlik I., Friedman J., Barrett S.C.H.: Environmental influence on primary sex ratio in a dioecious plant.-P. Natl. Acad. Sci. USA 105: 10847-10852, 2008. Go to original source...
  54. Sudmeyer R.A., Speijers J., Nicholas B.D.: Root distribution of Pinus pinaster, P. radiata, Eucalyptus globulus and E. kochii and associated soil chemistry in agricultural land adjacent to tree lines.-Tree Physiol. 24: 1333-1346, 2004. Go to original source...
  55. Sultan S.E.: What has survived of Darwin's theory? Phenotypic plasticity and the Neo-Darwinian legacy.-Evol. Trend Plant 6: 61-71,1992.
  56. Valladares F., Wright S.J., Lasso E. et al.: Plastic phenotypic response to light of 16 congeneric shrubs from a Panamanian rainforest.-Ecology 81: 1925-1936, 2000.
  57. Valladares F., Sánchez-Gómez D., Zavala M.A.: Quantitative estimation of phenotypic plasticity: bridging the gap between the evolutionary concept and its ecological applications.-J. Ecol. 94: 1103-1116, 2006. Go to original source...
  58. Wanek W., Zotz G.: Are vascular epiphytes nitrogen or phosphorus limited? A study of plant (15) N fractionation and foliar N:P stoichiometry with the tank bromeliad Vriesea sanguinolenta.-New Phytol. 192: 462-470, 2011. Go to original source...
  59. West-Eberhard M.J.: Phenotypic plasticity and the origins of diversity.-Annu. Rev. Ecol. Syst. 20: 249-278,1989. Go to original source...
  60. West-Eberhard M.J.: Developmental Plasticity and Evolution. Pp. 816. Oxford Univ. Press, New York 2003.
  61. Xu L.K., Baldocchi D.D.: Seasonal trends in photosynthetic parameters and stomatal conductance of blue oak (Quercus douglasii) under prolonged summer drought and high temperature.-Tree Physiol. 23: 865-877, 2003. Go to original source...
  62. Yanai R.D., Fahey T.J., Miller L.: Efficiency of nutrient acquisition by fine roots and mycorrhizae.-In: Smith W., Hinckley T.M. (ed.): Resource Physiology of Conifers. Pp. 75-103. Academic Press, New York 1995. Go to original source...
  63. Zhao H., Li Y., Zhang X. et al.: Sex-related and stagedependent source-to-sink transition in Populus cathayana grown at elevated CO2 and elevated temperature.-Tree Physiol. 32:1325-1338, 2012. Go to original source...