Seasonal variation of organogenetic activity and reserves allocation in the shoot apex of Pinus pinaster Ait.

BACKGROUND AND AIMS To understand better the basic growth characteristics of pines and the fundamental properties of the shoot apical meristem (SAM), variations within the shoot apex of buds were studied. METHODS A detailed structural comparison of meristem dimensions, organogenetic activity, and the presence of lipids, starch grains and tannins was performed on shoot apices of juvenile, and male and female adult Pinus pinaster at five different times in the annual growth cycle. KEY RESULTS There were significant correlations among traits and differences in the pattern for juvenile and adult shoots. In juvenile shoots, peaks of organogenesis were present in spring and autumn, but not in summer. In adult shoots, one peak, characterized by an increase in meristem dimensions, was present in summer. The accumulation of starch grains beneath the SAM and of tannin in sub-apical pith parenchyma were at their maximum when organogenetic activity was high in spring and autumn in juvenile plants, and in summer in adult plants. In juvenile and adult plants, lipids were stored within the SAM in autumn, filling a large part of the bud in winter, and were depleted in the cortical parenchyma and then in the pith during shoot elongation. CONCLUSIONS Depending on the sites of accumulation within the SAM and on the stage of the annual growth cycle, lipids, starch and tannins may be involved in different processes. In spring, energy and structural materials released by lipid hydrolysis may contribute to stem elongation and/or cell-to-cell communication. During organogenesis, energy and structural materials released by starch hydrolysis may influence developmental programmes in the SAM and adjacent cells. Tannins may be involved in cellular detoxification. At the end of the growing season, accumulation of lipid and starch is positively correlated with the onset of dormancy.

[1]  J. Obeso,et al.  The costs of reproduction in plants. , 2002, The New phytologist.

[2]  D. Murphy The biogenesis and functions of lipid bodies in animals, plants and microorganisms. , 2001, Progress in lipid research.

[3]  P. Rinne,et al.  The shoot apical meristem restores its symplasmic organization during chilling-induced release from dormancy. , 2001, The Plant journal : for cell and molecular biology.

[4]  M. Racchi,et al.  Histological and biochemical changes in Pinus spp. seeds during germination and post-germinative growth: triacylglycerol distribution and catalase activity , 2000 .

[5]  F. Humbert,et al.  Water-related Phenomena in Winter Buds and Twigs of Picea abies L. (Karst.) until Bud-burst: A Biological, Histological and NMR Study , 2000 .

[6]  P. Davis,et al.  Seasonal Changes in Perennial Nodules of Beach Pea (Lathyrus maritimus [L.] Bigel.) with Special Reference to Oleosomes , 2000, International Journal of Plant Sciences.

[7]  Sjef Smeekens,et al.  SUGAR-INDUCED SIGNAL TRANSDUCTION IN PLANTS. , 2000, Annual review of plant physiology and plant molecular biology.

[8]  R. Ceulemans,et al.  Effects of season, needle age and elevated atmospheric CO(2) on photosynthesis in Scots pine (Pinus sylvestris). , 2000, Tree physiology.

[9]  Sandra L. Stone,et al.  Structural and Biochemical Changes in Loblolly Pine (Pinus taeda L.) Seeds during Germination and Early Seedling Growth. II. Storage Triacylglycerols and Carbohydrates , 1999, International Journal of Plant Sciences.

[10]  J. Albrechtová,et al.  Histochemical detection and image analysis of non-specific esterase activity and the amount of polyphenols during annual bud development in Norway spruce , 1999 .

[11]  T. Oniki,et al.  A peroxidase/phenolics/ascorbate system can scavenge hydrogen peroxide in plant cells , 1997 .

[12]  J. Murphy,et al.  Starch synthesis and localization in post-germination Pinusedulis seedlings , 1994 .

[13]  J. Owens,et al.  SEASONAL CHANGES IN THE APICAL ZONATION AND ULTRASTRUCTURE OF COASTAL DOUGLAS FIR SEEDLINGS (PSEUDOTSUGA MENZIESII). , 1990, American journal of botany.

[14]  O. Monteuuis,et al.  Nucleotide and nucleic acid status in shoot tips from juvenile and mature clones of Sequoiadendron giganteum during rest and growth phases. , 1987, Tree physiology.

[15]  J. Willison,et al.  The ultrastructure of quiescent buds of Tilia europaea , 1980 .

[16]  F. Ledig,et al.  Episodic growth and relative shoot:root balance in loblolly pine seedlings , 1980 .

[17]  R. A. Cecich AN ELECTRON MICROSCOPIC EVALUATION OF CYTOHISTOLOGICAL ZONATION IN THE SHOOT APICAL MERISTEM OF PINUS BANKSIANA , 1977 .

[18]  H. Horner,et al.  AN ULTRASTRUCTURAL AND MICROSPECTROPHOTOMETRIC STUDY OF THE SHOOT APEX DURING THE INITIATION OF THE FIRST LEAF IN GERMINATING PINUS BANKSIANA , 1977 .

[19]  D. Durzan,et al.  Cytochemical and Subcellular Organization of the Shoot Apical Meristem of Dry and Germinating Jack Pine Embryos , 1974 .

[20]  E. M. Gifford,et al.  Histochemical changes occurring at the seedling shoot apex of Pinus radiata , 1973 .

[21]  R. Riding Early ontogeny of seedlings of Pinus radiata , 1972 .

[22]  N. Lersten,et al.  A CYTOPHOTOMETRIC STUDY OF NUCLEIC ACIDS AND PROTEINS IN THE SHOOT APEX OF WHITE SPRUCE , 1972 .

[23]  Marie-Noëlle Jordy Les variations saisonnières au sein des apex caulinaires du Pin maritime (Pinus pinaster Ait. ) depuis la graine jusqu'à l'état adulte , 2000 .

[24]  D. Greer,et al.  Frost hardening of Pinus radiata seedlings: effects of temperature on relative growth rate, carbon balance and carbohydrate concentration. , 2000, Tree physiology.

[25]  E. Haukioja,et al.  Intra-plant regulation of growth and plant-herbivore interactions , 1998 .

[26]  Joan Welkowitz,et al.  Introductory Statistics for the Behavioral Sciences , 1971 .

[27]  E. Debazac Les modalités de la croissance en longueur chez les Pins , 1966 .

[28]  L. Randolph A New Fixing Fluid and a Revised Schedule for the Paraffin Method in Plant Cytology , 1935 .