Co-action of temperature and phosphate in inducing turion formation in Spirodela polyrhiza (Great duckweed)

Increased phosphate concentration, higher temperature and addition of glucose all increased the number of fronds and turions of the duckweed Spirodela polyrhiza formed under in vitro conditions. Increasing the number of turions by increasing the plant biomass does not mean that the developmental process (switch of the programme of the primordia from vegetative fronds toward resting turions) has been specifically influenced. The specific turion yield (STY; number of turions formed by one frond) and the time of onset of turion formation have been used as more specific measures of turion induction. At more than 30 µm initial phosphate the STY was increased by lower temperature (15 °C) and became independent of the phosphate concentration. Between 10 and 30 µm and at higher temperatures (25  °C) the STY was increased by lower phosphate levels. The stimulatory effect of lower temperature was more pronounced than that of lower phosphate concentrations. Decreased phosphate concentration highly accelerated the formation of the first turions. The influence of low temperature was small at lower phosphate concentration but became dominant at higher concentrations (especially in autotrophic cultures). Low phosphate levels (e.g. 10 µm) and low temperatures (e.g. 15 °C) both represent specific turion-inducing factors having significant interactive effects. In S. polyrhiza, these signals may replace the interactive effects of photoperiods and low temperature known from other hydrophytes in turion induction under natural conditions.

[1]  Daniel J. Crawford,et al.  Phylogeny and Systematics of Lemnaceae, the Duckweed Family , 2009 .

[2]  J. Browse,et al.  Temperature sensing and cold acclimation. , 2001, Current opinion in plant biology.

[3]  K. Appenroth,et al.  Light-induced Starch Degradation in Non-dormant Turions of Spirodela polyrhiza¶ , 2001 .

[4]  P. Palonen,et al.  Changes in carbohydrates and freezing tolerance during cold acclimation of red raspberry cultivars grown in vitro and in vivo , 2000 .

[5]  I. Ciereszko,et al.  Sucrose metabolism in leaves and roots of bean (Phaseolus vulgaris L.) during phosphate deficiency , 2000 .

[6]  A. J. Underwood,et al.  Experiments in Ecology. , 1997 .

[7]  W. T. Haller,et al.  Short-day Exposure Period For Subterranean Turion Formation in Dioecious Hydrilla , 1997 .

[8]  M. Netherland Turion ecology of hydrilla. , 1997 .

[9]  A. Rychter,et al.  Assimilate translocation in bean plants (Phaseolus vulgaris L.) during phosphate deficiency , 1996 .

[10]  A. Fleming,et al.  The Physiological Role of Abscisic Acid in Eliciting Turion Morphogenesis , 1995, Plant physiology.

[11]  G. May,et al.  Phosphate Modulates Transcription of Soybean VspB and Other Sugar-Inducible Genes. , 1994, The Plant cell.

[12]  A. Fleming,et al.  A plant gene with homology to D-myo-inositol-3-phosphate synthase is rapidly and spatially up-regulated during an abscisic-acid-induced morphogenic response in Spirodela polyrrhiza. , 1993, The Plant journal : for cell and molecular biology.

[13]  K. Appenroth,et al.  Photophysiology of turion germination in Spirodela polyrhiza (L.) schleiden. XI. Structural changes during red light induced responses , 1993 .

[14]  K. Appenroth,et al.  Phytochrome Control of Turion Formation in Spirodela polyrhiza L. Schleiden , 1990 .

[15]  K. Appenroth,et al.  PHOTOPHYSIOLOGY OF TURION GERMINATION IN Spirodela polyrhiza (L.) SCHLEIDEN–V. DEMONSTRATION OF A CALCIUM‐REQUIRING PHASE DURING PHYTOCHROME‐MEDIATED GERMINATION , 1990 .

[16]  R. J. V. Wijk Ecological studies on Potamogeton pectinatus L. V. Nutritional ecology, in vitro uptake of nutrients and growth limitation , 1989 .

[17]  A. Srivastava,et al.  Effect of Cadmium on Turion Formation and Germination of Spirodela polyrrhiza L. , 1989 .

[18]  F. Jungnickel,et al.  Influence of Nutrient Deficiency and Light on Turion Formation in Spirodela polyrhizass (L.) SCHLEIDEN , 1989 .

[19]  J. Thullen Production of axillary turions by the dioecious Hydrilla verticillata , 1989 .

[20]  J. Tillberg,et al.  Carbohydrate partitioning, photosynthesis and growth in Lemna gibba G3. I: Effects of nitrogen limitation , 1987 .

[21]  D. Spence,et al.  PHOTOCONTROL OF TURION FORMATION BY POTAMOGETON CRISPUS L. IN THE LABORATORY AND NATURAL WATER , 1985 .

[22]  E. Cossins,et al.  Senescence, turion development, and turion germination in nitrate- and sulfate-deficient Spirodela polyrhiza. Relationships between nutrient availability and exogenous cytokinins , 1983 .

[23]  A. Trewavas,et al.  Abscisic‐acid‐induced turion formation in Spirodela polyrrhiza L. I. Production and development of the turion , 1983 .

[24]  Y. Oda,et al.  Heterogeneity of dormancy in the turions of Spirodela polyrrhiza , 1979 .

[25]  R. Newton,et al.  TURION FORMATION AND GERMINATION IN SPIRODELA POLYRHIZA , 1978 .

[26]  L. Noodén,et al.  Environmental and hormonal control of turion formation in Myriophyllum verticillatum , 1976 .

[27]  G. Stewart Abscisic Acid and Morphogenesis in Lemna polyrhiza L. , 1969, Nature.

[28]  T. Perry Dormancy, Turion Formation, and Germination by Different Clones of Spirodela polyrrhiza. , 1968, Plant physiology.

[29]  A. Henssen Die Dauerorgane von Spirodela Polytthiza (L.) Schleid. in physiologischer Betrachtung , 1954 .

[30]  D. L. Jacobs An Ecological Life‐History of Spirodela Polyrhiza (Greater Duckweed) with Emphasis on the Turion Phase , 1947 .