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Plant function and evolutionary biology
RESEARCH ARTICLE

Water loss from leaf mesophyll stripped of the epidermis

Martin Canny
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Plant Science Division, Research School of Biology, RN Robertson Building, The Australian National University, Canberra, ACT 0200, Australia. Email: martin.canny@anu.edu.au

Functional Plant Biology 39(5) 421-434 https://doi.org/10.1071/FP11265
Submitted: 28 November 2011  Accepted: 22 March 2012   Published: 9 May 2012

Abstract

Water vapour flux (rate of water loss) from the mesophyll of isolated Agapanthus praecox Willd. leaf pieces without an epidermis was investigated by loss of mass into unstirred air at relative humidities (RHs) of 0.993–0.850, compared with the rate from a water atmometer (rate of evaporation). The point at which relative evaporation (RE, the rate of water loss divided by the rate of evaporation) reaches <1 inadequately identifies the onset of mesophyll regulation because values >1 were found. For RHs of 0.993–0.967, RE varied in daily cycles from 0.6 to ~3, with a period of ~24 h, maxima at mid-afternoon, minima at or near dawn. For RH < 0.950, the cycles were suppressed. An initial rate of RE ≈1.2, RE declined towards zero. In leaf pieces supplied with water via vascular strands (rate of transpiration), the daily cycle persisted down to RH 0.850, where maximal RE ≈ 2. Transpiration from one surface of field leaves gave the rate of transpiration in the same range. These data require the maximum RE for each vapour pressure deficit as the value identifying the onset of mesophyll regulation (possibly by aquaporins), which produces cyclic changes in the rates of water loss and transpiration. At RH < 0.95, the decline of RE below 1 is probably regulated by cell wall water status. Possible functions of the two types of regulation are discussed.

Additional keywords: aquaporins, cell wall regulation, circadian rhythm, leaf intercellular relative humidity, mesophyll regulation, water reference atmometer.


References

Ackerson RC, Krieg R (1977) Stomatal and nonstomatal regulation of water use in cotton, corn, and sorghum. Plant Physiology 60, 850–853.
Stomatal and nonstomatal regulation of water use in cotton, corn, and sorghum.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3cnht1ekug%3D%3D&md5=97d3c7ec7e736d218a0151947becbc01CAS |

Ackerson RC, Krieg DR, Haring CL, Chang N (1977) Effects of plant water status on stomatal activity, photosynthesis, and nitrate reductase activity of field grown cotton. Crop Science 17, 81–84.
Effects of plant water status on stomatal activity, photosynthesis, and nitrate reductase activity of field grown cotton.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE2sXhsFalurg%3D&md5=bcaa946ae2658c883ec921a4a9fd80a9CAS |

Bange GGJ (1953) On the quantitative explanation of stomatal transpiration. Acta Botanica Neerlandica 2, 255–257.

Bierhuizen JF, Slatyer RO, Rose CW (1965) A porometer for laboratory and field operation. Journal of Experimental Botany 16, 182–191.
A porometer for laboratory and field operation.Crossref | GoogleScholarGoogle Scholar |

Canny MJ, Huang CX (2006) Leaf water content and palisade cell size. New Phytologist 170, 75–85.
Leaf water content and palisade cell size.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD287ltFymtw%3D%3D&md5=2abd32561211c4eb3df079fcea622409CAS |

Canny MJ, Wong CS, Huang CX, Miller C (2011) Differential shrinkage of mesophyll cells in transpiring cotton leaves: implications for static and dynamic pools of water, and for water transport pathways. Functional Plant Biology 39, 91–102.
Differential shrinkage of mesophyll cells in transpiring cotton leaves: implications for static and dynamic pools of water, and for water transport pathways.Crossref | GoogleScholarGoogle Scholar |

Cochard H, Venisse J-S, Barigah TS, Brunel N, Herbette S, Guillot A, Tyree MT, Saki S (2007) Putative role of aquaporins in variable hydraulic conductance of leaves in response to light. Plant Physiology 143, 122–133.
Putative role of aquaporins in variable hydraulic conductance of leaves in response to light.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXpt1OgtQ%3D%3D&md5=85464d98836efb4bb726fecff23a3e4dCAS |

Cowan IR, Milthorpe FL (1968) Plant factors influencing the water status of plant tissues. In ‘Water deficits and plant growth. Vol. 1’ (Ed. TT Kozlowski) pp. 137–193. (Academic Press: New York)

Darwin F, Pertz DMM (1911) On a new method of estimating the aperture of stomata. Proceedings of the Royal Society of London. Series B, Containing Papers of a Biological Character 84, 136–154.
On a new method of estimating the aperture of stomata.Crossref | GoogleScholarGoogle Scholar |

England WE, McCully ME, Huang CX (1997) Solvent vapour lock: an extreme case of the problems caused by lignified and suberized cell walls during resin infiltration. Journal of Microscopy 185, 85–93.
Solvent vapour lock: an extreme case of the problems caused by lignified and suberized cell walls during resin infiltration.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2sXhsFertb8%3D&md5=ce48b0f710cbbd6f9dc50fa5005489e3CAS |

Farquhar GD, Raschke K (1978) On the resistance to transpiration of the sites of evaporation within the leaf. Plant Physiology 61, 1000–1005.
On the resistance to transpiration of the sites of evaporation within the leaf.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3cnht1GrsQ%3D%3D&md5=c6393d8cc3bf316571a2dba745cb0d6cCAS |

Fischer RA (1968) Resistance to water loss in the mesophyll of leek (Allium porrum). Journal of Experimental Botany 19, 135–145.
Resistance to water loss in the mesophyll of leek (Allium porrum).Crossref | GoogleScholarGoogle Scholar |

Frank AB, Power JF, Willis WO (1973) Effect of temperature and plant water stress on photosynthesis, diffusion resistance, and leaf water potential in spring wheat. Agronomy Journal 65, 777–780.
Effect of temperature and plant water stress on photosynthesis, diffusion resistance, and leaf water potential in spring wheat.Crossref | GoogleScholarGoogle Scholar |

Gale J, Poljakoff-Mayber A, Kahane I (1967) The gas diffusion porometer technique and its application to the measurement of leaf mesophyll resistance. Israel Journal of Botany 16, 187–204.

Hagemeyer J, Waisel Y (1983) An endogenous circadian rhythm of transpiration in Tamarix aphylla. Physiologia Plantarum 70, 133–138.
An endogenous circadian rhythm of transpiration in Tamarix aphylla.Crossref | GoogleScholarGoogle Scholar |

Hultquist JH (1973) Photosynthesis and resistance to water loss as related to maturity stage in grain sorghum. Proceedings of the 8th Biennial Program of Grain Sorghum Research Utility Conference, pp. 80–83.

Jarvis PG, Slatyer RO (1970) The role of the mesophyll cell wall in leaf transpiration. Planta 90, 303–322.
The role of the mesophyll cell wall in leaf transpiration.Crossref | GoogleScholarGoogle Scholar |

Jones HG, Higgs KH (1980) Resistance to water loss from the mesophyll cell surface in plant leaves. Journal of Experimental Botany 31, 545–553.
Resistance to water loss from the mesophyll cell surface in plant leaves.Crossref | GoogleScholarGoogle Scholar |

Jones HG, Norton TA (1979) Internal factors controlling the rate of evaporation from fronds of some intertidal algae. New Phytologist 83, 771–781.
Internal factors controlling the rate of evaporation from fronds of some intertidal algae.Crossref | GoogleScholarGoogle Scholar |

Kaldenhoff R, Ribas-Carbo MK, Sans JF, Lovisolo C, Heckwolf M, Uehlein N (2008) Aquaporins and plant water balance. Plant, Cell & Environment 31, 658–666.
Aquaporins and plant water balance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXlvFehur8%3D&md5=61730cdefb00e44e211c0cb575646a22CAS |

Klemm G (1956) Untersuchungen über den Transpirationswiderstand der Mesophyllmembranen und seine Bedeutung als Regulator für die stomatäre Transpiration. Planta 47, 547–587.
Untersuchungen über den Transpirationswiderstand der Mesophyllmembranen und seine Bedeutung als Regulator für die stomatäre Transpiration.Crossref | GoogleScholarGoogle Scholar |

Livingston BE (1935) Atmometers of porous porcelain and paper, their use in physiological ecology. Ecology 16, 438–472.
Atmometers of porous porcelain and paper, their use in physiological ecology.Crossref | GoogleScholarGoogle Scholar |

Livingston BE, Brown WH (1912) Relation of the daily march of transpiration to variations in the water content of foliage leaves. Botanical Gazette (Chicago, Ill.) 53, 309–330.
Relation of the daily march of transpiration to variations in the water content of foliage leaves.Crossref | GoogleScholarGoogle Scholar |

Maximov NA (1929) ‘The plant in relation to water’ Transl. R.H. Yapp. (George Allen and Unwin: London)

McCully ME, Canny MJ, Huang CX (2009) Cryo-scanning electron microscopy (CSEM) in the advancement of functional plant biology. Morphological and anatomical applications. Functional Plant Biology 36, 97–124.
Cryo-scanning electron microscopy (CSEM) in the advancement of functional plant biology. Morphological and anatomical applications.Crossref | GoogleScholarGoogle Scholar |

McCully ME, Canny MJ, Huang CX, Miller C, Brink F (2010) Cryo-scanning electron microscopy (CSEM) in the advancement of functional plant biology: energy dispersive X-ray microanalysis (CEDX) applications. Functional Plant Biology 37, 1011–1040.
Cryo-scanning electron microscopy (CSEM) in the advancement of functional plant biology: energy dispersive X-ray microanalysis (CEDX) applications.Crossref | GoogleScholarGoogle Scholar |

Nardini A, Salleo S, Andri S (2005) Circadian regulation of leaf hydraulic conductance in sunflower (Helianthus annuus L. cv Margot). Plant, Cell & Environment 28, 750–759.
Circadian regulation of leaf hydraulic conductance in sunflower (Helianthus annuus L. cv Margot).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXmvVaku7o%3D&md5=e18cf47b418708908727a4aeee90c3b0CAS |

Nobel PS (1991) ‘Physicochemical and environmental plant physiology’. (Academic Press: New York)

Pearce JN, Nelson AF (1932) The vapour pressures of aqueous solutions of lithium nitrate and the activity coefficients of some alkali salts in solutions of high concentration at 25°. Journal of Physical Chemistry 54, 3544–3555.

Roderick ML, Canny MJ (2005) A mechanical interpretation of pressure chamber measurements – what does the strength of the squeeze tell us? Plant Physiology and Biochemistry 43, 323–336.
A mechanical interpretation of pressure chamber measurements – what does the strength of the squeeze tell us?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXkt1Oju7w%3D&md5=30a0601b70081f8206d0b77db8bf8574CAS |

Sack L, Holbrook NM (2006) Leaf hydraulics. Annual Review of Plant Biology 57, 361–381.
Leaf hydraulics.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XosVKhtrs%3D&md5=c5dea6f9a90cbaf206906d650dedd1e2CAS |

Scheidegger C, Günthardt-Georg M, Matyssek R, Hatvani P (1991) Low-temperature scanning electron microscopy of birch leaves after exposure to ozone. Journal of Microscopy 161, 85–95.

Scholz F (1974) Zum Prinzip des Wassertransports in Kiefernadeln. Biochemie und Physiologie der Pflanzen 165, 253–263.

Scoffoni C, Pou A, Aasamaa K, Sack L (2008) The rapid light response of leaf hydraulic conductance: new evidence from two experimental methods. Plant, Cell & Environment 31, 1803–1812.
The rapid light response of leaf hydraulic conductance: new evidence from two experimental methods.Crossref | GoogleScholarGoogle Scholar |

Shane MW, McCully ME, Canny MJ (2000) Architecture of branch-root junctions in maize: structure of the connecting xylem and the porosity of pit membranes. Annals of Botany 85, 613–624.
Architecture of branch-root junctions in maize: structure of the connecting xylem and the porosity of pit membranes.Crossref | GoogleScholarGoogle Scholar |

Skaar Ch, Siau JF (1981) Thermal diffusion of bound water in wood. Wood Science and Technology 15, 105–112.
Thermal diffusion of bound water in wood.Crossref | GoogleScholarGoogle Scholar |

Slavik B (1958) The influence of water deficit on transpiration. Planta 11, 524–536.
The influence of water deficit on transpiration.Crossref | GoogleScholarGoogle Scholar |

Sresnevski BJ (1905) On evaporation from the surface of the human body and from plants. Proceedings of the 2nd Climatological and Hydrological Congress, St. Petersburg 1, 311–333.

Stålfelt MG (1932) Der stomatäre Regulation in der pflanzlichen Transpiration. Planta 17, 23–85.

Stålfelt MG (1956) Die cuticuläre Transpiration. In ‘Encyclopedia of plant physiology. Vol. III.’ Ed.W Ruhland, pp. 342–350. (Springer-Verlag: Berlin) [In German]

Stamm AJ (1959) Bound water diffusion into wood in the fiber direction. Forest Products Journal 9, 27–32.

Stamm AJ (1964) ‘Wood and cellulose science’. (Ronald Press: New York).

Turrell FM (1936) The area of the internal exposed surface of dicotyledon leaves. American Journal of Botany 23, 255–264.
The area of the internal exposed surface of dicotyledon leaves.Crossref | GoogleScholarGoogle Scholar |

Voicu MC, Zwiazek JJ, Tyree MT (2008) Light response of hydraulic conductance in bur oak (Quercus macrocarpa) leaves. Tree Physiology 28, 1007–1015.
Light response of hydraulic conductance in bur oak (Quercus macrocarpa) leaves.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXptFyrtb4%3D&md5=a019074447d2445528e655a4c0614d4bCAS |

Voicu MC, Cooke JEK, Zwiazek JJ (2009) Aquaporin gene expression and apoplastic water flow in bur oak (Quercus macrocarpa) leaves in relation to the light response of leaf hydraulic conductance. Journal of Experimental Botany 60, 4063–4075.
Aquaporin gene expression and apoplastic water flow in bur oak (Quercus macrocarpa) leaves in relation to the light response of leaf hydraulic conductance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXht1WqtLnJ&md5=f36499a68ade964bce4c3711a2a58301CAS |

Weyers JDB, Travis AJ (1981) Selection and preparation of leaf epidermis for experiments on stomatal physiology. Journal of Experimental Botany 32, 837–850.
Selection and preparation of leaf epidermis for experiments on stomatal physiology.Crossref | GoogleScholarGoogle Scholar |

Whitelaw-Weckert MA, Whitelaw ES, Rogiers SY, Quirk L, Clark AC, Huang CX (2011) Bacterial inflorescence rot of grapevine caused by Pseudomonas syringae pv. syringae. Plant Pathology 60, 325–337.
Bacterial inflorescence rot of grapevine caused by Pseudomonas syringae pv. syringae.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXkvVGruro%3D&md5=cbc298555e4c0b5c58644e27d6cf64aaCAS |