Literature DB >> 24408640

Wintertime changes in the ultrastructure and metabolism of the microsporangiate strobili of the Scotch pine.

S Kupila-Ahvenniemi1, S Pihakaski, K Pihakaski.   

Abstract

Terminal buds of Pinus silvestris L. containing microsporangiate strobilus primordia were collected once a month throughout the winter. The electron microscopic studies indicated that in October and December, the cells of the strobili contained a large number of vacuoles, a portion of which was supposedly autophagic, and stacked rough endoplasmic reticulum. By February, the amount of these had decreased, and instead, a large population of dense bodies was visible. Additional phenomena, characteristic at this state, were the occurrences of highly uneven contours of the plasmalemma and of inclusions of various kinds between the plasmalemma and the cell wall. In March, autolysis was visible in a portion of cells outside the sporangia. In the sporangia the ground cytoplasm was thin but the number of organelles was increasing. In the April collections, cell divisions were visible. The amount of protein per dry weight increased during the winter reaching a peak in February. The activity of RNases, having optima of pH 5.0 and pH 7.5, was measured in two successive years. Both series showed a period of high activity during the middle of the winter. The exact timing of this period depended on the year in question. On the basis of these observations, the dormant period of the microsporangiate strobili of the Seotch pine is divided into three sub-periods. It is also suggested that the definition of dormancy of these structures should include a mentioning of alterations in the metabolical machinery of the cells.

Entities:  

Year:  1978        PMID: 24408640     DOI: 10.1007/BF00385003

Source DB:  PubMed          Journal:  Planta        ISSN: 0032-0935            Impact factor:   4.116


  7 in total

1.  Localization of Acid hydrolases in protoplasts: examination of the proposed lysosomal function of the mature vacuole.

Authors:  H C Butcher; G J Wagner; H W Siegelman
Journal:  Plant Physiol       Date:  1977-06       Impact factor: 8.340

2.  Vacuolar protein in apical and flower-petal cells.

Authors:  L K Shumway; V Cheng; C A Ryan
Journal:  Planta       Date:  1972-12       Impact factor: 4.116

3.  A simple methylene blue-azure II-basic fuchsin stain for epoxy-embedded tissue sections.

Authors:  C D Humphrey; F E Pittman
Journal:  Stain Technol       Date:  1974-01

4.  Determination of protein: a modification of the Lowry method that gives a linear photometric response.

Authors:  E F Hartree
Journal:  Anal Biochem       Date:  1972-08       Impact factor: 3.365

5.  Effect of gibberellic Acid and actinomycin d on the formation and distribution of rough endoplasmic reticulum in barley aleurone cells.

Authors:  E L Vigil; M Ruddat
Journal:  Plant Physiol       Date:  1973-03       Impact factor: 8.340

6.  Tannin inclusions in cell suspension cultures of white spruce.

Authors:  S C Chafe; D J Durzan
Journal:  Planta       Date:  1973-09       Impact factor: 4.116

7.  [Polyvinylpyrrolidone as protective substance against inhibition of enzyme systems caused by tannins].

Authors:  V Schneider; U W Hallier
Journal:  Planta       Date:  1970-06       Impact factor: 4.116

  7 in total
  3 in total

1.  Pollen development in Rhododendron in relation to winter dormancy and bloom time.

Authors:  Olga E Mirgorodskaya; Nuria K Koteyeva; Alexandra V Volchanskaya; Evgeny A Miroslavov
Journal:  Protoplasma       Date:  2015-02-03       Impact factor: 3.356

2.  Development of secretory cells and crystal cells in Eichhornia crassipes ramet shoot apex.

Authors:  Guo Xin Xu; Chao Tan; Xiao Jing Wei; Xiao Yan Gao; Hui Qiong Zheng
Journal:  Protoplasma       Date:  2010-05-12       Impact factor: 3.356

3.  Ultrastructural changes in the endoplasmic reticulum during dormancy release of apple embryos (Pyrus malus L.).

Authors:  M Bouvier-Durand; J Dereuddre; D Côme
Journal:  Planta       Date:  1981-01       Impact factor: 4.116

  3 in total

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