Skip to main content

An ultrasonic humidification fluorescent tracing method for detecting unsaturated atmospheric water absorption by the aerial parts of desert plants

Abstract

Atmospheric water absorption by plants has been explored for more than two centuries, and the aerial parts of plants, particularly the leaves of certain species, have been demonstrated to have an ability to absorb and utilize saturated atmospheric water such as fog, dew and condensed water. So far, however, there have been few studies on the aerial parts of desert plants in their absorption of unsaturated water from the atmosphere. This study presents an ultrasonic humidification fluorescent tracing method of detecting unsaturated atmospheric water absorption by the aerial parts of desert plants. We constructed an organic glass room based on the sizes of field plants. Then, the aboveground parts of the plants were humidified in the sealed glasshouse using an ultrasonic humidifier containing fluorescent reagents. The humidity and wetting time were controlled by turning on or off the humidifier according to the reading of a thermo-hygrometer suspended in the glasshouse. Fluorescence microscopy was employed to observe these plant samples. This method can generate unsaturated atmospheric water vapor and incorporate other fluorescent reagents or water-soluble chemical reagents for gasified humidification. In addition, it can identify plant parts that absorb unsaturated atmospheric water from the air, detect water absorption sites on the surface of leaves or tender stems, and determine the ability of tissues or microstructure of aerial parts to absorb water. This method provides a direct visual evidence for the inspection of leaf or tender stem microstructure in response to unsaturated atmospheric water absorption. Moreover, this method shows that aqueous pores in the cuticles of leaves or tender stems of desert plants are large enough to allow the passage of ionic fluorescent brightener with a molecular weight of up to 917 g/mol. Thus, this paper provides an important approach that explores the mechanism by which desert plants utilize unsaturated atmospheric water.

This is a preview of subscription content, access via your institution.

References

  • Asbjornsen H, Mora G, Helmers M J. 2007. Variation in water uptake dynamics among contrasting agricultural and native plant communities in the Midwestern U.S. Agriculture, Ecosystem & Environment, 121(4): 343–356.

    Article  Google Scholar 

  • Barthlott W, Neinhuis C. 1997. Purity of the sacred lotus, or escape from contamination in biological surfaces. Planta, 202(1): 1–8.

    Article  Google Scholar 

  • Bauer L. 1953. Addressing the question of mass transport within the plant with specific emphasis on the migration of fluorochromes. Planta, 42(5): 367–451.

    Article  Google Scholar 

  • Bhushan B, Jung Y C. 2006. Micro- and nanoscale characterization of hydrophobic and hydrophilic leaf surfaces. Nanotechnology, 17(11): 2758–2772.

    Article  Google Scholar 

  • Breshears D D, McDowell N G, Goddard K L, et al. 2008. Foliar absorption of intercepted rainfall improves woody plant water status most during drought. Ecology, 89(1): 41–47.

    Article  Google Scholar 

  • Brezeale E L, McGeorge W T, Brezeale J F. 1950. Moisture absorption by plants from an atmosphere of high humidity. Plant Physiology, 25(3): 413–419.

    Article  Google Scholar 

  • Burgess S S O, Adams M A, Turner N C, et al. 1998. The redistribution of soil water by tree root systems. Oecologia, 115(3): 306–311.

    Article  Google Scholar 

  • Burgess S S O, Dawson T E. 2004. The contribution of fog to the water relations of Sequoia sempervirens (D. Don): foliar uptake and prevention of dehydration. Plant, Cell & Environment, 27(8): 1023–1034.

    Article  Google Scholar 

  • Burkhardt J. 2010. Hygroscopic particles on leaves: nutrients or desiccants? Ecological Monographs, 80(3): 369–399.

    Article  Google Scholar 

  • Burkhardt J, Basi S, Pariyar S, et al. 2012. Stomatal penetration by aqueous solutions—an update involving leaf surface particles. New Phytologist, 196(3): 774–787.

    Article  Google Scholar 

  • Burton Z, Bhushan B. 2006. Surface characterization and adhesion and friction properties of hydrophobic leaf surfaces. Ultramicroscopy, 106(8–9): 709–719.

    Article  Google Scholar 

  • Dawson T E, Ehleringer J R. 1991. Streamside trees that do not use stream water. Nature, 350(6316): 335–337.

    Article  Google Scholar 

  • Eichert T, Burkhardt J. 2001. Quantification of stomatal uptake of ionic solutes using a new model system. Journal of Experimental Botany, 52(357): 771–781.

    Google Scholar 

  • Eichert T, Kurtz A, Steiner U, et al. 2008. Size exclusion limits and lateral heterogeneity of the stomatal foliar uptake pathway for aqueous solutes and water-suspended nanoparticles. Physiologia Plantarum, 134(1): 151–160.

    Article  Google Scholar 

  • Eller C B, Lima A L, Oliveira R S. 2013. Foliar uptake of fog water and transport belowground alleviates drought effects in the cloud forest tree species, Drimys brasiliensis (Winteraceae). New Phytologist, 199(1): 151–162.

    Article  Google Scholar 

  • Fahn A. 1986. Structural and functional properties of trichomes of xeromorphic leaves. Annals of Botany, 57(5): 631–637.

    Google Scholar 

  • Gotsch S G, Asbjornsen H, Holwerda F, et al. 2014. Foggy days and dry nights determine crown–level water balance in a seasonal tropical montane cloud forest. Plant, Cell & Environment, 37(1): 261–272.

    Article  Google Scholar 

  • Gouvra E, Grammatikopoulos G. 2003. Beneficial effects of direct foliar water uptake on shoot water potential of five chasmophytes. Canadian Journal of Botany, 81(12): 1278–1284.

    Article  Google Scholar 

  • Grammatikopoulos G, Manetas Y. 1994. Direct absorption of water by hairy leaves of Phlomis fruticosa and its contribution to drought avoidance. Canadian Journal of Botany, 72(12): 1805–1811.

    Article  Google Scholar 

  • Koch K, Bhushan B, Barthlott W. 2009. Multifunctional surface structures of plants: An inspiration for biomimetics. Progress in Materials Science, 54(2): 137–178.

    Article  Google Scholar 

  • Limm E B, Dawson T E. 2010. Polystichum munitum (Dryopteridaceae) varies geographically in its capacity to absorb fog water by foliar uptake within the redwood forest ecosystem. American Journal of Botany, 97(7): 1121–1128.

    Article  Google Scholar 

  • Liu Z Q, Gaskin R E. 2004. Visualisation of the uptake of two model xenobiotics into bean leaves by confocal laser scanning microscopy: diffusion pathways and implication in phloem translocation. Pest Management Science, 60(5): 434–439.

    Article  Google Scholar 

  • Maier-Maercker U. 1979. Peristomatal transpiration and stomatal movement: a controversial view III. Visible effects of peri stomatal transpiration on the epidermis. Journal of Plant Physiology, 91(3): 225–238.

    Google Scholar 

  • Martin C E, von Willert D J. 2000. Leaf epidermal hydathodes and the ecophysiological consequences of foliar water uptake in species of Crassula from the Namib Desert in Southern Africa. Plant Biology, 2(2): 229–242.

    Article  Google Scholar 

  • Mastroberti A A, de Araujo Mariath J E. 2008. Development of mucilage cells of Araucaria angustifolia (Araucariaceae). Protoplasma, 232(3–4): 233–245.

    Article  Google Scholar 

  • Mooney H A, Gulmon S L, Ehleringer J, et al. 1980. Atmospheric water uptake by an Atacama Desert shrub. Science, 209(4457): 693–694.

    Article  Google Scholar 

  • Munné-Bosch S, Alegre L. 1999. Role of dew on the recovery of water-stressed Melissa officinalis L. plants. Journal of Plant Physiology, 154(5–6): 759–766.

    Article  Google Scholar 

  • Munné-Bosch S, Nogués S, Alegre L. 1999. Diurnal variations of photosynthesis and dew absorption by leaves in two evergreen shrubs growing in Mediterranean field conditions. New Phytologist, 144(1): 109–119.

    Article  Google Scholar 

  • Neinhuis C, Barthlott W. 1997. Characterization and distribution of water-repellent, self-cleaning plant surfaces. Annals of Botany, 79(6): 667–677.

    Article  Google Scholar 

  • O’Brien T P, McCully M E. 1981. The Study of Plant Structure: Principles and Selected Methods. Melbourne: Termarcarphi Pty. Ltd.

    Google Scholar 

  • Oliveira R S, Dawson T E, Burgess S S O. 2005. Evidence for direct water absorption by the shoot of the desiccation-tolerant plant Vellozia flavicans in the savannas of central Brazil. Journal of Tropical Ecology, 21(5): 585–588.

    Article  Google Scholar 

  • Otten A, Herminghaus S. 2004. How plants keep dry: a physicist’s point of view. Langmuir, 20(6): 2405–2408.

    Article  Google Scholar 

  • Phillips D L, Koch P L. 2002. Incorporating concentration dependence in stable isotope mixing models. Oecologia, 130(1): 114–125.

    Article  Google Scholar 

  • Phillips D L, Newsome S D, Gregg J W. 2005. Combining sources in stable isotope mixing models: alternative methods. Oecologia, 144(4): 520–527.

    Article  Google Scholar 

  • Schlegel T K, Schönherr J, Schreiber L. 2005. Size selectivity of aqueous pores in stomatous cuticles of Vicia faba leaves. Planta, 221(5): 648–655.

    Article  Google Scholar 

  • Schönherr J. 1976. Water permeability of isolated cuticular membranes: the effect of cuticular waxes on diffusion of water. Planta, 131(2): 159–164.

    Article  Google Scholar 

  • Schönherr J. 2006. Characterization of aqueous pores in plant cuticles and permeation of ionic solutes. Journal of Experimental Botany, 75(11): 2471–2491.

    Article  Google Scholar 

  • Schreiber L. 2005. Polar paths of diffusion across plant cuticles: new evidence for an old hypothesis. Annals of Botany, 95(7): 1069–1073.

    Article  Google Scholar 

  • Stone E C, Went F W, Young C L. 1950. Water absorption from the atmosphere by plants growing in dry soil. Science, 111(2890): 546–548.

    Article  Google Scholar 

  • Strugger S. 1939. Luminescence microscopical analysis of the parenchymatic plant transpiration stream. 3. Investigations on Helxine soleirolii Req. Biological Central Journal, 59: 409–442.

    Google Scholar 

  • Westhoff M, Zimmermann D, Zimmermann G, et al. 2009. Distribution and function of epistomatal mucilage plugs. Protoplasma, 235: 101–105.

    Article  Google Scholar 

  • Zhuang Y L, Ratchiffe S. 2012. Relationship between dew presence and Bassia dasyphylla plant growth. Journal of Arid Land, 4(1): 11–18.

    Article  Google Scholar 

  • Zimmermann D, Westhoff M, Zimmermann G, et al. 2007. Foliar water supply of tall trees: evidence for mucilage-facilitated moisture uptake from the atmosphere and the impact on pressure bomb measurements. Protoplasma, 232(1–2): 11–34.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Xiaohua Wang.

Rights and permissions

Reprints and Permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wang, X., Xiao, H., Ren, J. et al. An ultrasonic humidification fluorescent tracing method for detecting unsaturated atmospheric water absorption by the aerial parts of desert plants. J. Arid Land 8, 272–283 (2016). https://doi.org/10.1007/s40333-015-0018-z

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40333-015-0018-z

Keywords