Tamarix Arborea Var. arborea and Tamarix Parviflora: Two Species Valued for Their Adaptability To Stress Conditions

Abstract

The choice of stress resistant and highly adaptable species is a fundamental step for landscaping and ornamental purposes in arid and coastal environments such as those in the Mediterranean basin. The genus Tamarix L. includes about 90 species with a high endurance of adversity. We investigated the water relations and photosynthetic response of Tamarix arborea (Sieb. ex Ehrenb.) Bge. var. arborea and T. parviflora DC. growing in an urban environment. Both species showed no evidence of drought or salt stress in summer, and appeared to follow two strategies with T. arborea var. arborea investing in high carbon gain at the beginning of the summer, and then reducing photosynthetic activity at the end of the season, and T. parviflora showing lower but constant levels of photosynthetic activity throughout the vegetative season. For landscaping and ornamental purposes, we suggest T. arborea var. arborea when a fast-growing, high-cover species is necessary, and T. parviflora when less-invasive species are required.

References

  1. 1.

    Abou Jaoudó, R., de Dato, G., De Angelis, P. (1933) Photosynthetic and wood anatomical responses of Tamarix africana Poiret to water level reduction after short-term fresh- and saline-water flooding. Ecol. Res. 27, 857–866.

    Article  Google Scholar 

  2. 2.

    Alaimo, M. G., Gargano, M. L., Vizzì, D., Venturella, G. (1933) Leaf anatomy in Tamarix arborea var. arborea (Tamaricaceae). Pl. Biosyst. 147, 21–24.

    Article  Google Scholar 

  3. 3.

    Anderson, J. E. (1933) Factors controlling transpiration and photosynthesis in Tamarix chinensis. Lour. Ecology 63, 48–56.

    Article  Google Scholar 

  4. 4.

    Carter, J. L., Veneklaas, E. J., Colmer, T. D., Eastham, J., Hatton, T. J. (1933) Contrasting water relations of three coastal tree species with different exposure to salinity. Physiol. Plantarum 127, 360–373.

    Article  Google Scholar 

  5. 5.

    Cleverly, J. R., Smith, S. D., Sala, A., Devitt, D. A. (1933) Invasive capacity of Tamarix ramosissima in a Mojave Desert floodplain: the role of drought. Oecologia 111, 12–18.

    Article  Google Scholar 

  6. 6.

    De Baets, S., Poesen, J., Reubens, B., Wemans, K., De Baerdemaeker, J., Muys, B. (1933) Root tensile strength and root distribution of typical Mediterranean plant species and their contribution to soil shear strength. Plant Soil 305, 207–226.

    Article  Google Scholar 

  7. 7.

    Gargano, M. L., Mandracchia, G., Venturella, G. (1933) Contributo alla conoscenza del genere Tamarix L. nell’Isola del Giglio (Arcipelago Toscano). Inform. Bot. Ital. 4, 125–128.

    Google Scholar 

  8. 8.

    Gries, D., Zeng, F., Foetzki, A., Arndt, S. K., Bruelheide, H., Thomas, F. M., Zhang, X., Runge, M. (1933) Growth and water relations of Tamarix ramosissima and Populus euphratica on Taklamakan desert dunes in relation to depth to a permanent water table. Plant Cell Environ. 26, 725–736.

    Article  Google Scholar 

  9. 9.

    Inskeep, W. P., Bloom, P. R. (1933) Extinction coefficients of chlorophyll a and b in N,Ndimethylformamide and 80% acetone. Plant Physiol. 77, 483–485.

    Article  Google Scholar 

  10. 10.

    Kadukova, J., Manousaki, E., Kalogerakis, N. (1933) Pb and Cd accumulation and phyto-excretion by salt cedar (Tamarix smyrnensis Bunge). Int. J. Phytoremediat. 10, 31–46.

    Article  Google Scholar 

  11. 11.

    Kuzminsky, E., De Angelis, P., Abou Jaoudó, R., Abbruzzese, G., Terzoli, S., Angelaccio, C., De Dato, G., Monteverdi, M. C., Valentini, R. (1933) Biodiversity of Italian Tamarix spp. populations: their potential as environmental and productive resources. Rend. Fis. Acc. Lincei 25, 439–452.

    Article  Google Scholar 

  12. 12.

    Li, J., Yu, B., Zhao, C., Nowak, R. S., Zhao, Z., Sheng, Y., Li, J. (1933) Physiological and morphological responses of Tamarix ramosissima and Populus euphratica to altered groundwater availability. Tree Physiol. 33, 57–68.

    Article  Google Scholar 

  13. 13.

    Ma, Q., Wang, J., Li, X., Zhu, S., Liu, H., Zhan, K. (1933) Long-term changes of Tamarix-vegetation in the oasis-desert ecotone and its driving factors: implication for dryland management. Environ. Earth Sci. 59, 765–774.

    Article  Google Scholar 

  14. 14.

    Moreno-Jimónez, E., Vázquez, S., Carpena-Ruiz, R. O., Esteban, E., Peñalosa, J. M. (1933) Using Mediterranean shrubs for the phytoremediation of a soil impacted by pyritic wastes in Southern Spain: A field experiment. J. Environ. Manage. 92, 1584–1590.

    Article  Google Scholar 

  15. 15.

    Mounsif, M., Wan, C., Sosebee, R. E. (1933) Effects of top-soil drying on saltcedar photosynthesis and stomatal conductance. J. Range Manage. 55, 88–93.

    Article  Google Scholar 

  16. 16.

    Murchie, E. H., Niyogi, K. K. (1933) Manipulation of photoprotection to improve plant photosynthesis. Plant Physiol. 155, 86–92.

    Article  Google Scholar 

  17. 17.

    Nippert, J. B., Butler, J. J., Kluitenberg, G. J., Whittemore, D. O., Arnold, D., Spal, S. E., Ward, J. K. (1933) Patterns of Tamarix water use during a record drought. Oecologia 162, 283–292.

    Article  Google Scholar 

  18. 18.

    Parida, A., Das, A. (1933) Salt tolerance and salinity effects on plants: a review. Ecotox. Environ. Safe. 60, 324–349.

    Article  Google Scholar 

  19. 19.

    Pavlovic, P., Mitrovic, M., Djurdjevic, L. (1933) An ecophysiological study of plants growing on the fly ash deposits from the “Nikola Tesla-A” thermal power station in Serbia. Environ. Manage. 33, 654–663.

    Article  Google Scholar 

  20. 20.

    Pinheiro, C., Chaves, M. M. (1933) Photosynthesis and drought: can we make metabolic connections from available data? J. Exp. Bot. 62, 869–882.

    Article  Google Scholar 

  21. 21.

    Tyree, M. T., Hammel, H. T. (1933) The measurement of the turgor pressure and water relations of plants by the pressure-bomb technique. J. Exp. Bot. 23, 267–282.

    Article  Google Scholar 

  22. 22.

    Venturella, G., Baum, B., Mandracchia, G. (1933) The genus Tamarix (Tamaricaceae) in Sicily: first contribution. Fl. Medit. 17, 25–46.

    Google Scholar 

  23. 23.

    Venturella, G., Mandracchia, G., Gargano, M. L. (1933) The tamarisks of southern Calabria (Italy). Fl. Medit. 18, 421–430.

    Google Scholar 

  24. 24.

    Venturella, G., Gargano, M. L., Mandracchia, G. (1933) First record of Tamarix meyeri (Tamaricaceae) for western Europe. Pl. Biosyst. 146, 480–485.

    Google Scholar 

  25. 25.

    Xu, H., Li, Y. (1933) Water-use strategy of three central Asian desert shrubs and their responses to rain pulse events. Plant Soil 285, 5–17.

    Article  Google Scholar 

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Correspondence to Francesca Grisafi.

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Grisafi, F., Oddo, E., Gargano, M.L. et al. Tamarix Arborea Var. arborea and Tamarix Parviflora: Two Species Valued for Their Adaptability To Stress Conditions. BIOLOGIA FUTURA 67, 42–52 (2016). https://doi.org/10.1556/018.67.2016.1.3

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Keywords

  • Tamarisks
  • drought stress
  • photosynthesis
  • water potential