Effect of diurnal temperature alternations on plant morphology in some greenhouse crops. A mini review

Abstract In recent decades, chemical growth retardants have been used to control plant morphology in many greenhouse crops. Research is currently underway to find other practical means of regulating plant morphology. Efforts have concentrated on temperature control, which could result in well-shaped plants without a delay in flowering. The difference (DIF) between day temperature ( DT ) and night temperature ( NT ) influences internode length, plant height, leaf orientation, shoot orientation, chlorophyll content, lateral branching and petiole and flower stalk elongation in plants. Internode length increases as DIF increases. The response of stem elongation to DIF is greater when DIF increases from zero to positive, than from negative to zero DIF. DIF has the greatest effect on plant height during the period of rapid growth in determinant crops. Furthermore, the responses to DIF are rapid, and most plants respond to a change in DT and NT within 24 h. The effects of DIF on stem elongation and leaf expansion are a result of increased cellular elongation rather than division. In some long day plants (LDP), DIF has only a minor influence on flower initiation. The effect of negative DIF on flowering is different in the shortday plant poinsettia, where negative DIF delays flowering significantly. DIF interacts with light quality, light intensity, photoperiod and growth retardants, but not with water stress. A physiological explanation for the effects of DIF suggests that DIF may elicit responses through affecting the concentration of endogenous gibberellins (GAs). Stem elongation is also sensitive to a temperature drop in the last 2 h of the night or the first 2 h of the day. In Begonia × hiemalis Fortsch., temperature drop interacts with irradiance. Interaction between growth factors may be the reason that the effects of DIF and temperature drop on plant morphogenesis differ between research reports. Average daily temperature (ADT) can influence internode elongation in some species. Leaf unfolding rate is affected by ADT and not by DIF. The plant stem elongation rate is not constant during a day/night cycle and this knowledge can be used for control of plant morphogenesis and flowering by DT and NT alternations. This review shows that DIF and temperature drop can reduce or eliminate the use of growth retardants in many greenhouse crops.

[1]  S. Grimstad,et al.  Effect of different day and night temperature regimes on greenhouse cucumber young plant production, flower bud formation and early yield , 1993 .

[2]  R. Moe TEMPERATURE AND DAYLENGTH RESPONSES IN DIANTHUS CARTHUSIANORUM CV. NAPOLEON III , 1983 .

[3]  EFFECT OF TEMPERATURE ON DEVELOPMENT RATE AND LENGTH INCREASE OF TOMATO, CUCUMBER AND SWEET PEPPER. , 1992 .

[4]  R. Moe,et al.  CONTROL OF PLANT HEIGHT IN POINSETTIA BY TEMPERATURE DROP AND GRAPHICAL TRACKING. , 1992 .

[5]  Royal D. Heins,et al.  Control of plant morphogenesis and flowering by light quality and temperature. , 1990 .

[6]  L. Mortensen,et al.  Stem elongation and keeping quality in poinsettia (Euphorbia pulcherrima Willd.) as affected by temperature and supplementary lighting , 1992 .

[7]  F. W. Went,et al.  The Experimental Control of Plant Growth , 1958 .

[8]  F. Went Plant growth under controlled conditions. II. Thermoperiodicity in growth and fruiting of the tomato , 1944 .

[9]  A. D. Koning,et al.  The effect of different day/night temperature regimes on growth, development and yield of glasshouse tomatoes , 1988 .

[10]  M. Karlsson,et al.  Growth and Development of Petunia × hybrids as a Function of Temperature and Irradiance , 1991 .

[11]  R. Moe Effect of day and night temperature alternations and of plant growth regulators on stem elongation and flowering of the long-day plant Campanula isophylla Moretti. , 1990 .

[12]  T. Kristoffersen Interactions of photoperiod and temperature in growth and development of young tomato plants : lycopersicon esculentum mill. , 1963 .

[13]  R. Heins,et al.  Thermomorphogenesis in Lilium longiflorum , 1989 .

[14]  R. Moe,et al.  Stem elongation and flowering of the long-day plant Campanula isophylla Moretti in response to day and night temperature alternations and light quality , 1991 .

[15]  R. Pharis,et al.  Gibberellins and Reproductive Development in Seed Plants , 1985 .

[16]  R. Heins,et al.  Modeling Temperature and Photoperiod Effects on Growth and Development of Dahlia , 1993 .

[17]  L. Mortensen,et al.  THERMOMORPHOGENESIS IN POT PLANTS , 1992 .

[18]  M. J. Pinthus,et al.  Effects of the Reversal of Day and Night Temperatures on Tillering and on the Elongation of Stems and Leaf Blades of Wheat , 1979 .

[19]  F. Went The Effect of Temperature on Plant Growth , 1953 .

[20]  Royal D. Heins,et al.  Thermomorphogenic and photoperiodic responses of Nephrolepis exaltata 'Dallas Jewel'. , 1990 .

[21]  L. Mortensen,et al.  Effects of CO2 enrichment and different day/ night temperature combinations on growth and flowering of Rosa L. and Kalanchoe blossfeldiana v. poelln. , 1992 .

[22]  R. Moe,et al.  Effects of temperature-drop and a short dark interruption on stem elongation and flowering in Begonia × hiemalis Fotsch , 1994 .

[23]  G. F. Kramer,et al.  INFLUENCE OF INVERSE DAY/NIGHT TEMPERATURE ON OZONE SENSITIVITY AND SELECTED MORPHOLOGICAL AND PHYSIOLOGICAL RESPONSES OF CUCUMBER , 1993 .

[24]  N. Zieslin,et al.  Regulation of stem elongation of lilies by temperature and the effect of gibberellin , 1988 .

[25]  J.V.M. Vogelezang,et al.  DIF AND TEMPERATURE DROP FOR SHORT-DAY POT PLANTS , 1992 .

[26]  B. Norkrans,et al.  Studies on Growth of Rhizina undulata Fr. and Its Production of Cellulose‐ and Pectin‐ Decomposing Enzymes , 1963 .

[27]  Royal D. Heins,et al.  Temperature effects on lily development rate and morphology from the visible bud stage until anthesis. , 1990 .

[28]  R. Berghage,et al.  PHOTOPERIOD INFLUENCES LEAF CHLOROPHYLL CONTENT IN CHRYSANTHEMUM GROWN WITH A NEGATIVE DIF TEMPERATURE REGIME , 1991 .

[29]  R. Moe,et al.  Temperature and Photoperiod Effects on Fuchsia × hybrida Morphology , 1991 .

[30]  S. Grimstad,et al.  The effect of a daily low temperature pulse on growth and development of greenhouse cucumber and tomato plants during propagation , 1993 .

[31]  Royal D. Heins,et al.  Temperature and Photosynthetic Photon Flux Influence Chrysanthemum Shoot Development and Flower Initiation under Short-day Conditions , 1989, Journal of the American Society for Horticultural Science.

[32]  R. Heins,et al.  Understanding and applying DIF , 1990 .

[33]  R. Berghage,et al.  The relationship between day and night temperature influences photosynthesis but not light compensation point or flower longevity of Easter lily, Lilium longiflorum Thunb. , 1990 .

[34]  L. Bertram,et al.  STEM ELONGATION OF DENDRANTHEMA AND TOMATO PLANTS IN RELATION TO DAY AND NIGHT TEMPERATURES , 1992 .

[35]  H. Tangerås MODIFYING EFFECTS OF ANCYMIDOL AND GIBBERELLINS ON TEMPERATURE INDUCED ELONGATION IN FUCHSIA X HYBRIDA , 1979 .

[36]  A. Halevy CRC Handbook of Flowering , 2019 .

[37]  M. G. Jones,et al.  The effect of photoperiod on the levels of seven endogenous gibberellins in the long-day plant Agrostemma githago L. , 1980, Planta.

[38]  A. Lecharny,et al.  Stem Extension Rate in Light-Grown Plants : Effects of Photo- and Thermoperiodic Treatments on the Endogenous Circadian Rhythm in Chenopodium rubrum. , 1985, Plant physiology.

[39]  L. Hendriks,et al.  EFFECTS OF INTENSITY, DURATION AND TIMING OF A TEMPERATURE DROP ON THE GROWTH AND FLOWERING OF EUPHORBIA PULCHERRIMA WILLD. EX KLOTZSCH , 1992 .