Abstract
We have studied fluctuations in membrane PD in Chara australis at frequencies between 1 and 500 mHz, by classical noise analysis and by inspection of the PD time-course. The former shows (1) a quasi-Lorentzian (1/f 2) rise of noise power as frequency falls, and (2) a marked increase in noise power when the cell is exposed to high salinity (Chara australis is a salt-sensitive species). The latter shows that, as well as initiating depolarization, exposure to 50 mM Na as either chloride or sulfate usually initiates a continuous but random series of small depolarizations which gives rise to the increase in noise and whose mechanism is discussed.
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Bisson MA, Walker NA (1980) The Chara plasmalemma at high pH. Electrical measurements show rapid specific passive uniport of H+ or OH−. J Membr Biol 56:1–7
Bloomfield P (2000) Fourier analysis of time series: an introduction. Wiley, New York
Coster HGL, Smith JR (1977) Low-frequency impedance of Chara corallina:simultaneous measurements of the separate plasmalemma and tonoplastcapacitance and conductance. Aust J Plant Physiol 4:667–674
Cramer GR (2002) Sodium–calcium interactions under salinity stress. In: Lauchli A, Luttge U (eds) Salinity: environment–plants–molecules. Kluwer, Dordrecht, pp 205–227
Ferrier JM, Morvan C, Lucas WJ, Dainty J (1979) Plasmalemma voltage noise in Chara corallina. Plant Physiol 63:709–714
Findlay GP, Hope AB (1964) Ionic relations of cells of Chara australis: VII. The separate electrical characteristics of the plasmalemma and tonoplast. Aust J Biol Sci 17:62–77
Fisahn J, Mikschl E, Hansen U-P (1986) Separate oscillations of the electrogenic pump and of a K+ channel in Nitella as revealed by simultaneous measurement of membrane potential and of resistance. J Exp Bot 37:34–47
Gradmann D (2001) Models for oscillations in plants. Aust J Plant Physiol 28:577–590
Hansen U-P (1978) Do light-induced changes in the membrane potentialof Nitella reflect the feed-back regulation of a cytoplasmic parameter? J Membr Biol 41:197–224
Hayashi H, Hirakawa K (1979) The instability in the membrane potential of the Nitella internodal cell. J Phys Soc Japan 47:345–346
Hayashi H, Hirakawa K (1980) Nitella fluctuation and instability in the membrane potential near threshold. Biophys J 31:31–44
Hill SE, Osterhout WJV (1938) Nature of the action current in Nitella. IV. Production of quick action currents by exposure to NaCl. J Gen Physiol 22:91–106
Kay SM, Marple SL (1981) Spectrum analysis—a modern perspective. Proc IEEE 69:1380–1419
Kishimoto U (1966) Repetitive action potentials in Nitella internodes. Plant Cell Physiol 7:547–558
Korff H-M, Grahn J, Warncke J, Hansen U-P (1980) The noise spectrum of the membrane potential in Nitella. In: Spanswick RM, Lucas WJ, Dainty J (eds) Plant membrane transport: current conceptual issues. Elsevier, Amsterdam, pp 605–606
Ogata K, Chilcott TC, Coster HGL (1983) Spatial variation of the electrical properties of Chara australis. I. External potentials and membrane conductance. Aust J Plant Physiol 10:339–351
Osterhout WJV (1917) Antagonism and permeability. Science 45:1153–1197
Ross S, Dainty J (1985) Membrane electrical noise in Chara corallina, I. A low frequency spectral component. Plant Physiol 79:1021–1025
Ross S, Dainty J (1986) Membrane electrical noise in Chara corallina, II. Effects of inhibitors on the low frequency spectral component. Plant Physiol 81:758–761
Shabala S, Shabala L, Gradmann D, Chen Z-H, Newman I, Mancuso S (2006) Oscillations in plant membrane transport: model predictions, experimental validation and physiological implications. J Exp Bot 57:171–184
Shepherd VA, Beilby MJ, Al Khazaaly S, Shimmen T (2008) Mechano-perception in Chara cells: the influence of salinity and calcium on touch-activated receptor potentials, action potentials and ion transport. Plant Cell Environ 31:1575–1591. doi:10.1111/j.1365-3040.2008.01866.x
Spear DG, Barr JK, Barr GE (1969) Localization of hydrogen ion and chloride ion fluxes in Nitella. J Gen Physiol 54:397–414. doi:10.1085/jgp.54.3.397
Toko K, Iiyama S, Yamafuji K (1984) Band-type dissipative structure in ion transport systems with cylindrical shape. J Phys Soc Japan 53:4070–4082. doi:10.1143/JPSJ.53.4070
Tyerman SD, Skerrett M, Garrill A, Findlay GP, Leigh RA (1997) Pathways for the permeation of Na+, and Cl− into protoplasts derived from the cortex of wheat roots. J Exp Bot 48:459–480
Wacke M, Thiel G (2001) Electrically triggered all-or-none Ca2+ liberation during action potential in the giant alga Chara. J Gen Physiol 118:11–21. doi:10.1085/jgp.118.1.11
Wacke M, Thiel G, Hutt M-T (2003) Ca2+ dynamics during membrane excitation of green alga Chara: model simulations and experimental data. J Membr Biol 191:179–192. doi:10.1007/s00232-002-1054-0
Yao X, Bisson MA (1993) Passive proton conductance is the major reason for membrane depolarization and conductance increase in Chara buckellii in high-salt conditions. Plant Physiol 103:197–203
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“Proteins, membranes and cells: the structure-function nexus”. Contributions from the annual scientific meeting (including a special symposium in honour of Professor Alex Hope of Flinders University, South Australia) of the Australian Society for Biophysics held in Canberra, ACT, Australia, 28 September–1 October 2008.
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Al Khazaaly, S., Alan Walker, N., Beilby, M.J. et al. Membrane potential fluctuations in Chara australis: a characteristic signature of high external sodium. Eur Biophys J 39, 167–174 (2009). https://doi.org/10.1007/s00249-009-0485-2
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DOI: https://doi.org/10.1007/s00249-009-0485-2